<\/p>\n
Structural formula<\/p>\n
None<\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n
CAS number:<\/b>96-37-7<\/p>\n
MDL number:<\/b>MFCD00001382<\/p>\n
EINECS number:<\/b>202-503-2<\/p>\n
RTECS number:<\/b>GY4640000<\/p>\n
BRN number:<\/b>1900214<\/p>\n
PubChem number:<\/b>24884699<\/p>\nPhysical property data<\/h2>\n
1. Properties: colorless liquid with gasoline smell. [1]<\/sup><\/p>\n2. Melting point (\u2103): -142.5[2]<\/sup><\/p>\n3. Boiling point (\u2103): 71.8[3]<\/sup><\/p>\n4. Relative density (water = 1): 0.75[4]<\/sup><\/p>\n5. Relative vapor Density (air=1): 2.9[5]<\/sup><\/p>\n6. Saturated vapor pressure (kPa): 18.4 (25\u2103)[6]<\/sup><\/p>\n7. Heat of combustion (kJ\/mol): -3938.1[7]<\/sup><\/p>\n8. Critical temperature (\u2103): 259.6[8] <\/sup><\/p>\n9. Critical pressure (MPa): 3.784[9]<\/sup><\/p>\n10. Octanol\/water partition coefficient: 3.37 [10]<\/sup><\/p>\n11. Flash point (\u2103): <-7 (CC) [11]<\/sup><\/p>\n12. Ignition temperature (\u2103): 258[12]<\/sup><\/p>\n13. Explosion upper limit (%): 8.4[13]<\/sup><\/p>\n14. Lower explosion limit (%): 1.2[14]<\/sup><\/p>\n15. Solubility: Insoluble in water, soluble in most organic solvents such as ethanol, ether, benzene, acetone and so on. [15]<\/sup><\/p>\n16. Critical compression factor: 0.272<\/p>\n17. Critical density (g\u00b7cm-3<\/sup>): 0.264<\/p>\n18. Critical volume (cm3<\/sup>\u00b7mol-1<\/sup>): 318<\/p>\n19. Eccentricity factor: 0.230<\/p>\n20. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 16.173<\/p>\n21. van der Waals area (cm 2<\/sup>\u00b7mol-1<\/sup>): 8.090\u00d7109<\/sup><\/p>\n22. van der Waals volume (cm 3<\/sup>\u00b7mol-1<\/sup>): 60.170<\/p>\n23. Gas phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3969.86<\/p>\n24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
2. Melting point (\u2103): -142.5[2]<\/sup><\/p>\n3. Boiling point (\u2103): 71.8[3]<\/sup><\/p>\n4. Relative density (water = 1): 0.75[4]<\/sup><\/p>\n5. Relative vapor Density (air=1): 2.9[5]<\/sup><\/p>\n6. Saturated vapor pressure (kPa): 18.4 (25\u2103)[6]<\/sup><\/p>\n7. Heat of combustion (kJ\/mol): -3938.1[7]<\/sup><\/p>\n8. Critical temperature (\u2103): 259.6[8] <\/sup><\/p>\n9. Critical pressure (MPa): 3.784[9]<\/sup><\/p>\n10. Octanol\/water partition coefficient: 3.37 [10]<\/sup><\/p>\n11. Flash point (\u2103): <-7 (CC) [11]<\/sup><\/p>\n12. Ignition temperature (\u2103): 258[12]<\/sup><\/p>\n13. Explosion upper limit (%): 8.4[13]<\/sup><\/p>\n14. Lower explosion limit (%): 1.2[14]<\/sup><\/p>\n15. Solubility: Insoluble in water, soluble in most organic solvents such as ethanol, ether, benzene, acetone and so on. [15]<\/sup><\/p>\n16. Critical compression factor: 0.272<\/p>\n17. Critical density (g\u00b7cm-3<\/sup>): 0.264<\/p>\n18. Critical volume (cm3<\/sup>\u00b7mol-1<\/sup>): 318<\/p>\n19. Eccentricity factor: 0.230<\/p>\n20. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 16.173<\/p>\n21. van der Waals area (cm 2<\/sup>\u00b7mol-1<\/sup>): 8.090\u00d7109<\/sup><\/p>\n22. van der Waals volume (cm 3<\/sup>\u00b7mol-1<\/sup>): 60.170<\/p>\n23. Gas phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3969.86<\/p>\n24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3. Boiling point (\u2103): 71.8[3]<\/sup><\/p>\n4. Relative density (water = 1): 0.75[4]<\/sup><\/p>\n5. Relative vapor Density (air=1): 2.9[5]<\/sup><\/p>\n6. Saturated vapor pressure (kPa): 18.4 (25\u2103)[6]<\/sup><\/p>\n7. Heat of combustion (kJ\/mol): -3938.1[7]<\/sup><\/p>\n8. Critical temperature (\u2103): 259.6[8] <\/sup><\/p>\n9. Critical pressure (MPa): 3.784[9]<\/sup><\/p>\n10. Octanol\/water partition coefficient: 3.37 [10]<\/sup><\/p>\n11. Flash point (\u2103): <-7 (CC) [11]<\/sup><\/p>\n12. Ignition temperature (\u2103): 258[12]<\/sup><\/p>\n13. Explosion upper limit (%): 8.4[13]<\/sup><\/p>\n14. Lower explosion limit (%): 1.2[14]<\/sup><\/p>\n15. Solubility: Insoluble in water, soluble in most organic solvents such as ethanol, ether, benzene, acetone and so on. [15]<\/sup><\/p>\n16. Critical compression factor: 0.272<\/p>\n17. Critical density (g\u00b7cm-3<\/sup>): 0.264<\/p>\n18. Critical volume (cm3<\/sup>\u00b7mol-1<\/sup>): 318<\/p>\n19. Eccentricity factor: 0.230<\/p>\n20. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 16.173<\/p>\n21. van der Waals area (cm 2<\/sup>\u00b7mol-1<\/sup>): 8.090\u00d7109<\/sup><\/p>\n22. van der Waals volume (cm 3<\/sup>\u00b7mol-1<\/sup>): 60.170<\/p>\n23. Gas phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3969.86<\/p>\n24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
4. Relative density (water = 1): 0.75[4]<\/sup><\/p>\n5. Relative vapor Density (air=1): 2.9[5]<\/sup><\/p>\n6. Saturated vapor pressure (kPa): 18.4 (25\u2103)[6]<\/sup><\/p>\n7. Heat of combustion (kJ\/mol): -3938.1[7]<\/sup><\/p>\n8. Critical temperature (\u2103): 259.6[8] <\/sup><\/p>\n9. Critical pressure (MPa): 3.784[9]<\/sup><\/p>\n10. Octanol\/water partition coefficient: 3.37 [10]<\/sup><\/p>\n11. Flash point (\u2103): <-7 (CC) [11]<\/sup><\/p>\n12. Ignition temperature (\u2103): 258[12]<\/sup><\/p>\n13. Explosion upper limit (%): 8.4[13]<\/sup><\/p>\n14. Lower explosion limit (%): 1.2[14]<\/sup><\/p>\n15. Solubility: Insoluble in water, soluble in most organic solvents such as ethanol, ether, benzene, acetone and so on. [15]<\/sup><\/p>\n16. Critical compression factor: 0.272<\/p>\n17. Critical density (g\u00b7cm-3<\/sup>): 0.264<\/p>\n18. Critical volume (cm3<\/sup>\u00b7mol-1<\/sup>): 318<\/p>\n19. Eccentricity factor: 0.230<\/p>\n20. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 16.173<\/p>\n21. van der Waals area (cm 2<\/sup>\u00b7mol-1<\/sup>): 8.090\u00d7109<\/sup><\/p>\n22. van der Waals volume (cm 3<\/sup>\u00b7mol-1<\/sup>): 60.170<\/p>\n23. Gas phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3969.86<\/p>\n24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
5. Relative vapor Density (air=1): 2.9[5]<\/sup><\/p>\n6. Saturated vapor pressure (kPa): 18.4 (25\u2103)[6]<\/sup><\/p>\n7. Heat of combustion (kJ\/mol): -3938.1[7]<\/sup><\/p>\n8. Critical temperature (\u2103): 259.6[8] <\/sup><\/p>\n9. Critical pressure (MPa): 3.784[9]<\/sup><\/p>\n10. Octanol\/water partition coefficient: 3.37 [10]<\/sup><\/p>\n11. Flash point (\u2103): <-7 (CC) [11]<\/sup><\/p>\n12. Ignition temperature (\u2103): 258[12]<\/sup><\/p>\n13. Explosion upper limit (%): 8.4[13]<\/sup><\/p>\n14. Lower explosion limit (%): 1.2[14]<\/sup><\/p>\n15. Solubility: Insoluble in water, soluble in most organic solvents such as ethanol, ether, benzene, acetone and so on. [15]<\/sup><\/p>\n16. Critical compression factor: 0.272<\/p>\n17. Critical density (g\u00b7cm-3<\/sup>): 0.264<\/p>\n18. Critical volume (cm3<\/sup>\u00b7mol-1<\/sup>): 318<\/p>\n19. Eccentricity factor: 0.230<\/p>\n20. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 16.173<\/p>\n21. van der Waals area (cm 2<\/sup>\u00b7mol-1<\/sup>): 8.090\u00d7109<\/sup><\/p>\n22. van der Waals volume (cm 3<\/sup>\u00b7mol-1<\/sup>): 60.170<\/p>\n23. Gas phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3969.86<\/p>\n24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
6. Saturated vapor pressure (kPa): 18.4 (25\u2103)[6]<\/sup><\/p>\n7. Heat of combustion (kJ\/mol): -3938.1[7]<\/sup><\/p>\n8. Critical temperature (\u2103): 259.6[8] <\/sup><\/p>\n9. Critical pressure (MPa): 3.784[9]<\/sup><\/p>\n10. Octanol\/water partition coefficient: 3.37 [10]<\/sup><\/p>\n11. Flash point (\u2103): <-7 (CC) [11]<\/sup><\/p>\n12. Ignition temperature (\u2103): 258[12]<\/sup><\/p>\n13. Explosion upper limit (%): 8.4[13]<\/sup><\/p>\n14. Lower explosion limit (%): 1.2[14]<\/sup><\/p>\n15. Solubility: Insoluble in water, soluble in most organic solvents such as ethanol, ether, benzene, acetone and so on. [15]<\/sup><\/p>\n16. Critical compression factor: 0.272<\/p>\n17. Critical density (g\u00b7cm-3<\/sup>): 0.264<\/p>\n18. Critical volume (cm3<\/sup>\u00b7mol-1<\/sup>): 318<\/p>\n19. Eccentricity factor: 0.230<\/p>\n20. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 16.173<\/p>\n21. van der Waals area (cm 2<\/sup>\u00b7mol-1<\/sup>): 8.090\u00d7109<\/sup><\/p>\n22. van der Waals volume (cm 3<\/sup>\u00b7mol-1<\/sup>): 60.170<\/p>\n23. Gas phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3969.86<\/p>\n24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
7. Heat of combustion (kJ\/mol): -3938.1[7]<\/sup><\/p>\n8. Critical temperature (\u2103): 259.6[8] <\/sup><\/p>\n9. Critical pressure (MPa): 3.784[9]<\/sup><\/p>\n10. Octanol\/water partition coefficient: 3.37 [10]<\/sup><\/p>\n11. Flash point (\u2103): <-7 (CC) [11]<\/sup><\/p>\n12. Ignition temperature (\u2103): 258[12]<\/sup><\/p>\n13. Explosion upper limit (%): 8.4[13]<\/sup><\/p>\n14. Lower explosion limit (%): 1.2[14]<\/sup><\/p>\n15. Solubility: Insoluble in water, soluble in most organic solvents such as ethanol, ether, benzene, acetone and so on. [15]<\/sup><\/p>\n16. Critical compression factor: 0.272<\/p>\n17. Critical density (g\u00b7cm-3<\/sup>): 0.264<\/p>\n18. Critical volume (cm3<\/sup>\u00b7mol-1<\/sup>): 318<\/p>\n19. Eccentricity factor: 0.230<\/p>\n20. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 16.173<\/p>\n21. van der Waals area (cm 2<\/sup>\u00b7mol-1<\/sup>): 8.090\u00d7109<\/sup><\/p>\n22. van der Waals volume (cm 3<\/sup>\u00b7mol-1<\/sup>): 60.170<\/p>\n23. Gas phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3969.86<\/p>\n24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
8. Critical temperature (\u2103): 259.6[8] <\/sup><\/p>\n9. Critical pressure (MPa): 3.784[9]<\/sup><\/p>\n10. Octanol\/water partition coefficient: 3.37 [10]<\/sup><\/p>\n11. Flash point (\u2103): <-7 (CC) [11]<\/sup><\/p>\n12. Ignition temperature (\u2103): 258[12]<\/sup><\/p>\n13. Explosion upper limit (%): 8.4[13]<\/sup><\/p>\n14. Lower explosion limit (%): 1.2[14]<\/sup><\/p>\n15. Solubility: Insoluble in water, soluble in most organic solvents such as ethanol, ether, benzene, acetone and so on. [15]<\/sup><\/p>\n16. Critical compression factor: 0.272<\/p>\n17. Critical density (g\u00b7cm-3<\/sup>): 0.264<\/p>\n18. Critical volume (cm3<\/sup>\u00b7mol-1<\/sup>): 318<\/p>\n19. Eccentricity factor: 0.230<\/p>\n20. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 16.173<\/p>\n21. van der Waals area (cm 2<\/sup>\u00b7mol-1<\/sup>): 8.090\u00d7109<\/sup><\/p>\n22. van der Waals volume (cm 3<\/sup>\u00b7mol-1<\/sup>): 60.170<\/p>\n23. Gas phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3969.86<\/p>\n24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
9. Critical pressure (MPa): 3.784[9]<\/sup><\/p>\n10. Octanol\/water partition coefficient: 3.37 [10]<\/sup><\/p>\n11. Flash point (\u2103): <-7 (CC) [11]<\/sup><\/p>\n12. Ignition temperature (\u2103): 258[12]<\/sup><\/p>\n13. Explosion upper limit (%): 8.4[13]<\/sup><\/p>\n14. Lower explosion limit (%): 1.2[14]<\/sup><\/p>\n15. Solubility: Insoluble in water, soluble in most organic solvents such as ethanol, ether, benzene, acetone and so on. [15]<\/sup><\/p>\n16. Critical compression factor: 0.272<\/p>\n17. Critical density (g\u00b7cm-3<\/sup>): 0.264<\/p>\n18. Critical volume (cm3<\/sup>\u00b7mol-1<\/sup>): 318<\/p>\n19. Eccentricity factor: 0.230<\/p>\n20. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 16.173<\/p>\n21. van der Waals area (cm 2<\/sup>\u00b7mol-1<\/sup>): 8.090\u00d7109<\/sup><\/p>\n22. van der Waals volume (cm 3<\/sup>\u00b7mol-1<\/sup>): 60.170<\/p>\n23. Gas phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3969.86<\/p>\n24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
10. Octanol\/water partition coefficient: 3.37 [10]<\/sup><\/p>\n11. Flash point (\u2103): <-7 (CC) [11]<\/sup><\/p>\n12. Ignition temperature (\u2103): 258[12]<\/sup><\/p>\n13. Explosion upper limit (%): 8.4[13]<\/sup><\/p>\n14. Lower explosion limit (%): 1.2[14]<\/sup><\/p>\n15. Solubility: Insoluble in water, soluble in most organic solvents such as ethanol, ether, benzene, acetone and so on. [15]<\/sup><\/p>\n16. Critical compression factor: 0.272<\/p>\n17. Critical density (g\u00b7cm-3<\/sup>): 0.264<\/p>\n18. Critical volume (cm3<\/sup>\u00b7mol-1<\/sup>): 318<\/p>\n19. Eccentricity factor: 0.230<\/p>\n20. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 16.173<\/p>\n21. van der Waals area (cm 2<\/sup>\u00b7mol-1<\/sup>): 8.090\u00d7109<\/sup><\/p>\n22. van der Waals volume (cm 3<\/sup>\u00b7mol-1<\/sup>): 60.170<\/p>\n23. Gas phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3969.86<\/p>\n24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
11. Flash point (\u2103): <-7 (CC) [11]<\/sup><\/p>\n12. Ignition temperature (\u2103): 258[12]<\/sup><\/p>\n13. Explosion upper limit (%): 8.4[13]<\/sup><\/p>\n14. Lower explosion limit (%): 1.2[14]<\/sup><\/p>\n15. Solubility: Insoluble in water, soluble in most organic solvents such as ethanol, ether, benzene, acetone and so on. [15]<\/sup><\/p>\n16. Critical compression factor: 0.272<\/p>\n17. Critical density (g\u00b7cm-3<\/sup>): 0.264<\/p>\n18. Critical volume (cm3<\/sup>\u00b7mol-1<\/sup>): 318<\/p>\n19. Eccentricity factor: 0.230<\/p>\n20. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 16.173<\/p>\n21. van der Waals area (cm 2<\/sup>\u00b7mol-1<\/sup>): 8.090\u00d7109<\/sup><\/p>\n22. van der Waals volume (cm 3<\/sup>\u00b7mol-1<\/sup>): 60.170<\/p>\n23. Gas phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3969.86<\/p>\n24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
12. Ignition temperature (\u2103): 258[12]<\/sup><\/p>\n13. Explosion upper limit (%): 8.4[13]<\/sup><\/p>\n14. Lower explosion limit (%): 1.2[14]<\/sup><\/p>\n15. Solubility: Insoluble in water, soluble in most organic solvents such as ethanol, ether, benzene, acetone and so on. [15]<\/sup><\/p>\n16. Critical compression factor: 0.272<\/p>\n17. Critical density (g\u00b7cm-3<\/sup>): 0.264<\/p>\n18. Critical volume (cm3<\/sup>\u00b7mol-1<\/sup>): 318<\/p>\n19. Eccentricity factor: 0.230<\/p>\n20. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 16.173<\/p>\n21. van der Waals area (cm 2<\/sup>\u00b7mol-1<\/sup>): 8.090\u00d7109<\/sup><\/p>\n22. van der Waals volume (cm 3<\/sup>\u00b7mol-1<\/sup>): 60.170<\/p>\n23. Gas phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3969.86<\/p>\n24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
13. Explosion upper limit (%): 8.4[13]<\/sup><\/p>\n14. Lower explosion limit (%): 1.2[14]<\/sup><\/p>\n15. Solubility: Insoluble in water, soluble in most organic solvents such as ethanol, ether, benzene, acetone and so on. [15]<\/sup><\/p>\n16. Critical compression factor: 0.272<\/p>\n17. Critical density (g\u00b7cm-3<\/sup>): 0.264<\/p>\n18. Critical volume (cm3<\/sup>\u00b7mol-1<\/sup>): 318<\/p>\n19. Eccentricity factor: 0.230<\/p>\n20. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 16.173<\/p>\n21. van der Waals area (cm 2<\/sup>\u00b7mol-1<\/sup>): 8.090\u00d7109<\/sup><\/p>\n22. van der Waals volume (cm 3<\/sup>\u00b7mol-1<\/sup>): 60.170<\/p>\n23. Gas phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3969.86<\/p>\n24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
14. Lower explosion limit (%): 1.2[14]<\/sup><\/p>\n15. Solubility: Insoluble in water, soluble in most organic solvents such as ethanol, ether, benzene, acetone and so on. [15]<\/sup><\/p>\n16. Critical compression factor: 0.272<\/p>\n17. Critical density (g\u00b7cm-3<\/sup>): 0.264<\/p>\n18. Critical volume (cm3<\/sup>\u00b7mol-1<\/sup>): 318<\/p>\n19. Eccentricity factor: 0.230<\/p>\n20. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 16.173<\/p>\n21. van der Waals area (cm 2<\/sup>\u00b7mol-1<\/sup>): 8.090\u00d7109<\/sup><\/p>\n22. van der Waals volume (cm 3<\/sup>\u00b7mol-1<\/sup>): 60.170<\/p>\n23. Gas phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3969.86<\/p>\n24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
15. Solubility: Insoluble in water, soluble in most organic solvents such as ethanol, ether, benzene, acetone and so on. [15]<\/sup><\/p>\n16. Critical compression factor: 0.272<\/p>\n17. Critical density (g\u00b7cm-3<\/sup>): 0.264<\/p>\n18. Critical volume (cm3<\/sup>\u00b7mol-1<\/sup>): 318<\/p>\n19. Eccentricity factor: 0.230<\/p>\n20. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 16.173<\/p>\n21. van der Waals area (cm 2<\/sup>\u00b7mol-1<\/sup>): 8.090\u00d7109<\/sup><\/p>\n22. van der Waals volume (cm 3<\/sup>\u00b7mol-1<\/sup>): 60.170<\/p>\n23. Gas phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3969.86<\/p>\n24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
16. Critical compression factor: 0.272<\/p>\n
17. Critical density (g\u00b7cm-3<\/sup>): 0.264<\/p>\n18. Critical volume (cm3<\/sup>\u00b7mol-1<\/sup>): 318<\/p>\n19. Eccentricity factor: 0.230<\/p>\n20. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 16.173<\/p>\n21. van der Waals area (cm 2<\/sup>\u00b7mol-1<\/sup>): 8.090\u00d7109<\/sup><\/p>\n22. van der Waals volume (cm 3<\/sup>\u00b7mol-1<\/sup>): 60.170<\/p>\n23. Gas phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3969.86<\/p>\n24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
18. Critical volume (cm3<\/sup>\u00b7mol-1<\/sup>): 318<\/p>\n19. Eccentricity factor: 0.230<\/p>\n20. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 16.173<\/p>\n21. van der Waals area (cm 2<\/sup>\u00b7mol-1<\/sup>): 8.090\u00d7109<\/sup><\/p>\n22. van der Waals volume (cm 3<\/sup>\u00b7mol-1<\/sup>): 60.170<\/p>\n23. Gas phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3969.86<\/p>\n24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
19. Eccentricity factor: 0.230<\/p>\n
20. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup>: 16.173<\/p>\n21. van der Waals area (cm 2<\/sup>\u00b7mol-1<\/sup>): 8.090\u00d7109<\/sup><\/p>\n22. van der Waals volume (cm 3<\/sup>\u00b7mol-1<\/sup>): 60.170<\/p>\n23. Gas phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3969.86<\/p>\n24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
21. van der Waals area (cm 2<\/sup>\u00b7mol-1<\/sup>): 8.090\u00d7109<\/sup><\/p>\n22. van der Waals volume (cm 3<\/sup>\u00b7mol-1<\/sup>): 60.170<\/p>\n23. Gas phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3969.86<\/p>\n24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
22. van der Waals volume (cm 3<\/sup>\u00b7mol-1<\/sup>): 60.170<\/p>\n23. Gas phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3969.86<\/p>\n24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
23. Gas phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3969.86<\/p>\n24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
24. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -106.2<\/p>\n25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
25. Gas phase standard entropy (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 339.9<\/p>\n26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
26. Gas phase standard formation free energy (kJ\u00b7mol-1<\/sup>): 36.7<\/p>\n27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
27. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 109.5<\/p>\n28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
28. Liquid phase standard combustion heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -3938.15<\/p>\n29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
29. Liquid phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): -137.9<\/p>\n30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
30. Liquid phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>) : 247.94<\/p>\n31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
31. Liquid phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 31.97<\/p>\n32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
32. Liquid phase standard hot melt (J\u00b7 mol-1<\/sup>\u00b7K-1<\/sup>): 158.70<\/p>\n<\/p>\nToxicological data<\/h2>\n\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
\n 1. Acute toxicity<\/strong> No data available<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
2. Irritation<\/strong> No data available<\/p>\n3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3. Others [16]<\/sup><\/strong><\/strong> LCLo: 95g\/m3<\/sup> (mouse inhalation)<\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3 .Non-biodegradability[17]<\/sup><\/strong> <\/strong>In the air, when hydroxyl groups are free\ufffdWhen the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 2.3d (theoretical). <\/strong><\/p>\n4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
4. Bioconcentration[18]<\/sup><\/strong><\/strong> BCF: 210 (theory) <\/p>\n5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
5. Other harmful effects[19]<\/sup><\/strong><\/strong> This substance is harmful to the environment. Special attention should be paid to surface water, Pollution of soil, air and drinking water. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 27.76<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
1. Molar refractive index: 27.76<\/p>\n
2. Molar volume (cm3<\/sup>\/mol): 108.7<\/p>\n3. Isotonic specific volume (90.2K ): 239.5<\/p>\n4. Surface tension (dyne\/cm): 23.5<\/p>\n5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 6<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 33.3<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3. Isotonic specific volume (90.2K ): 239.5<\/p>\n
4. Surface tension (dyne\/cm): 23.5<\/p>\n
5. Polarizability (10-24cm3): 11.00<\/p>\n<\/p>\n
1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n
2. Number of hydrogen bond donors: 0<\/p>\n
3. Number of hydrogen bond acceptors: 0<\/p>\n
4. Number of rotatable chemical bonds: 0<\/p>\n
5. Number of tautomers: none<\/p>\n
6. Topological molecule polar surface area 0<\/p>\n
7. Number of heavy atoms: 6<\/p>\n
8. Surface charge: 0<\/p>\n
9. Complexity: 33.3<\/p>\n
10. Number of isotope atoms: 0<\/p>\n
11. Determine the number of atomic stereocenters: 0<\/p>\n
12. Uncertain number of atomic stereocenters: 0<\/p>\n
13. Determine the number of chemical bond stereocenters: 0 <\/p>\n
14. Number of uncertain chemical bond stereocenters: 0<\/p>\n
15. Number of covalent bond units: 1<\/p>\n<\/p>\n
1. Stability[20]<\/sup><\/strong><\/strong> Stable<\/p>\n2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
2. Incompatible substances [21]<\/sup><\/strong><\/strong> Strong oxidants, strong acids, strong bases, halogens<\/p>\n3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3. Polymerization hazards[22] <\/sup><\/strong><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
\n Storage Precautions[23]<\/sup><\/strong><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37\u2103. Keep container tightly sealed. should be kept away from oxidizer, do not store together. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency spill treatment equipment and suitable containment materials.\n <\/p>\nSynthesis method<\/h2>\nMethylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
Methylcyclopentane mainly exists in industrial hexane, accounting for about 5%. However, because its boiling point is close to that of n-hexane (68.74\u00b0C), it is difficult to completely separate it using general distillation methods. Therefore, using azeotropic distillation with methanol, methylcyclopentane with a purity of more than 99% can be obtained. <\/p>\n<\/p>\n
Used as solvent and standard material for chromatographic analysis, and also used in organic synthesis. [24]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/67.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/non-silicone-silicone-oil\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-2273-43-0\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/734<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nn-dicyclohexylmethylamine-2\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/11.jpg<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/catalyst-pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/pt303\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/niax-nmm-tertiary-amine-catalysts-momentive\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
Structural formula Business number 02B2 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48811,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15310],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48812"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48812\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48811"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48812"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48812"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48812"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
![\"Methylcyclopentane](\"http:\/\/www.newtopchem.com\/wp-content\/uploads\/2024\/05\/bf6561cca89a4a51ab11c723ed5a2032.gif\")
<\/p>\n<\/p>\n![https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg<\/a><\/br>extended-reading:](\"https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/115-1.jpg\"){kind=link}
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