<\/p>\n
Structural formula<\/p>\n
Seaiodoform,<\/p>\n
yellow iodine,<\/p>\n
iodoform,<\/p>\n
IPG Dry Adhesive Strips,<\/p>\n
Carbon triiodide,<\/p>\n
Triiodomethane<\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n
CAS number:<\/b>75-47-8<\/p>\n
MDL number:<\/b>MFCD00001069<\/p>\n
EINECS number:<\/b>200-874-5<\/p>\n
RTECS number:<\/b>PB7000000<\/p>\n
BRN number:<\/b>1697010<\/p>\n
PubChem number:<\/b>24881012<\/p>\nPhysical property data<\/h2>\n
1. Characteristics: yellow powder or crystal with unpleasant odor. [1]<\/sup><\/p>\n2. Melting point (\u2103): 115~120[2]<\/sup><\/p>\n3. Boiling point (\u2103) :218[3]<\/sup><\/p>\n4. Relative density (water = 1): 4.01[4]<\/sup><\/p>\n5. Relative Vapor density (air = 1): 13.0[5]<\/sup><\/p>\n6. Octanol\/water partition coefficient: 3.03[6]<\/sup><\/p>\n7. Solubility: Slightly soluble in water, soluble in benzene, ether and acetone. [7]<\/sup><\/p>\n8. Crystal phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): 141.0<\/p>\n 9. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): 210.9<\/p>\n10. Gas phase standard entropy (J\u00b7mol-1<\/sup> \u00b7K-1<\/sup>): 355.62<\/p>\n11. Gas phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 178.0<\/p>\n12. Vapor phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 75.07<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[8]<\/sup><\/strong><\/p>\nLD50: 355mg\/kg (rat oral); 1184mg\/kg (rabbit dermal )<\/p>\nLC50: 2657mg\/m3<\/sup> (mouse inhalation, 7h)<\/p>\n2. Irritation<\/strong> No information available<\/p>\n3. Mutagenicity [9]<\/sup> <\/strong>Microbial mutagenicity: Salmonella typhimurium 67\u03bcg\/dish. Unprogrammed DNA synthesis and sister chromosome exchange in hamster embryos: 1mg\/L. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[10]<\/sup> <\/strong>LC50: 2.92mg\/L (96h) (fathead minnow, dynamic)<\/p>\n 2. Biodegradability <\/strong>No data yet<\/p>\n3. Non-biodegradability [11]<\/sup> <\/strong>In the air, when the concentration of hydroxyl radicals When the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 55d (theoretical). <\/strong><\/p>\n4. Other harmful effects [12]<\/sup> <\/strong>This substance is harmful to the environment and attention should be paid to atmospheric pollution. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 45.54<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 101.8<\/p>\n3. Isotonic specific volume (90.2K ): 291.2<\/p>\n4. Surface tension (dyne\/cm): 66.7<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
2. Melting point (\u2103): 115~120[2]<\/sup><\/p>\n3. Boiling point (\u2103) :218[3]<\/sup><\/p>\n4. Relative density (water = 1): 4.01[4]<\/sup><\/p>\n5. Relative Vapor density (air = 1): 13.0[5]<\/sup><\/p>\n6. Octanol\/water partition coefficient: 3.03[6]<\/sup><\/p>\n7. Solubility: Slightly soluble in water, soluble in benzene, ether and acetone. [7]<\/sup><\/p>\n8. Crystal phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): 141.0<\/p>\n 9. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): 210.9<\/p>\n10. Gas phase standard entropy (J\u00b7mol-1<\/sup> \u00b7K-1<\/sup>): 355.62<\/p>\n11. Gas phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 178.0<\/p>\n12. Vapor phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 75.07<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[8]<\/sup><\/strong><\/p>\nLD50: 355mg\/kg (rat oral); 1184mg\/kg (rabbit dermal )<\/p>\nLC50: 2657mg\/m3<\/sup> (mouse inhalation, 7h)<\/p>\n2. Irritation<\/strong> No information available<\/p>\n3. Mutagenicity [9]<\/sup> <\/strong>Microbial mutagenicity: Salmonella typhimurium 67\u03bcg\/dish. Unprogrammed DNA synthesis and sister chromosome exchange in hamster embryos: 1mg\/L. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[10]<\/sup> <\/strong>LC50: 2.92mg\/L (96h) (fathead minnow, dynamic)<\/p>\n 2. Biodegradability <\/strong>No data yet<\/p>\n3. Non-biodegradability [11]<\/sup> <\/strong>In the air, when the concentration of hydroxyl radicals When the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 55d (theoretical). <\/strong><\/p>\n4. Other harmful effects [12]<\/sup> <\/strong>This substance is harmful to the environment and attention should be paid to atmospheric pollution. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 45.54<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 101.8<\/p>\n3. Isotonic specific volume (90.2K ): 291.2<\/p>\n4. Surface tension (dyne\/cm): 66.7<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3. Boiling point (\u2103) :218[3]<\/sup><\/p>\n4. Relative density (water = 1): 4.01[4]<\/sup><\/p>\n5. Relative Vapor density (air = 1): 13.0[5]<\/sup><\/p>\n6. Octanol\/water partition coefficient: 3.03[6]<\/sup><\/p>\n7. Solubility: Slightly soluble in water, soluble in benzene, ether and acetone. [7]<\/sup><\/p>\n8. Crystal phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): 141.0<\/p>\n 9. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): 210.9<\/p>\n10. Gas phase standard entropy (J\u00b7mol-1<\/sup> \u00b7K-1<\/sup>): 355.62<\/p>\n11. Gas phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 178.0<\/p>\n12. Vapor phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 75.07<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[8]<\/sup><\/strong><\/p>\nLD50: 355mg\/kg (rat oral); 1184mg\/kg (rabbit dermal )<\/p>\nLC50: 2657mg\/m3<\/sup> (mouse inhalation, 7h)<\/p>\n2. Irritation<\/strong> No information available<\/p>\n3. Mutagenicity [9]<\/sup> <\/strong>Microbial mutagenicity: Salmonella typhimurium 67\u03bcg\/dish. Unprogrammed DNA synthesis and sister chromosome exchange in hamster embryos: 1mg\/L. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[10]<\/sup> <\/strong>LC50: 2.92mg\/L (96h) (fathead minnow, dynamic)<\/p>\n 2. Biodegradability <\/strong>No data yet<\/p>\n3. Non-biodegradability [11]<\/sup> <\/strong>In the air, when the concentration of hydroxyl radicals When the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 55d (theoretical). <\/strong><\/p>\n4. Other harmful effects [12]<\/sup> <\/strong>This substance is harmful to the environment and attention should be paid to atmospheric pollution. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 45.54<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 101.8<\/p>\n3. Isotonic specific volume (90.2K ): 291.2<\/p>\n4. Surface tension (dyne\/cm): 66.7<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
4. Relative density (water = 1): 4.01[4]<\/sup><\/p>\n5. Relative Vapor density (air = 1): 13.0[5]<\/sup><\/p>\n6. Octanol\/water partition coefficient: 3.03[6]<\/sup><\/p>\n7. Solubility: Slightly soluble in water, soluble in benzene, ether and acetone. [7]<\/sup><\/p>\n8. Crystal phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): 141.0<\/p>\n 9. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): 210.9<\/p>\n10. Gas phase standard entropy (J\u00b7mol-1<\/sup> \u00b7K-1<\/sup>): 355.62<\/p>\n11. Gas phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 178.0<\/p>\n12. Vapor phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 75.07<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[8]<\/sup><\/strong><\/p>\nLD50: 355mg\/kg (rat oral); 1184mg\/kg (rabbit dermal )<\/p>\nLC50: 2657mg\/m3<\/sup> (mouse inhalation, 7h)<\/p>\n2. Irritation<\/strong> No information available<\/p>\n3. Mutagenicity [9]<\/sup> <\/strong>Microbial mutagenicity: Salmonella typhimurium 67\u03bcg\/dish. Unprogrammed DNA synthesis and sister chromosome exchange in hamster embryos: 1mg\/L. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[10]<\/sup> <\/strong>LC50: 2.92mg\/L (96h) (fathead minnow, dynamic)<\/p>\n 2. Biodegradability <\/strong>No data yet<\/p>\n3. Non-biodegradability [11]<\/sup> <\/strong>In the air, when the concentration of hydroxyl radicals When the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 55d (theoretical). <\/strong><\/p>\n4. Other harmful effects [12]<\/sup> <\/strong>This substance is harmful to the environment and attention should be paid to atmospheric pollution. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 45.54<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 101.8<\/p>\n3. Isotonic specific volume (90.2K ): 291.2<\/p>\n4. Surface tension (dyne\/cm): 66.7<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
5. Relative Vapor density (air = 1): 13.0[5]<\/sup><\/p>\n6. Octanol\/water partition coefficient: 3.03[6]<\/sup><\/p>\n7. Solubility: Slightly soluble in water, soluble in benzene, ether and acetone. [7]<\/sup><\/p>\n8. Crystal phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): 141.0<\/p>\n 9. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): 210.9<\/p>\n10. Gas phase standard entropy (J\u00b7mol-1<\/sup> \u00b7K-1<\/sup>): 355.62<\/p>\n11. Gas phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 178.0<\/p>\n12. Vapor phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 75.07<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[8]<\/sup><\/strong><\/p>\nLD50: 355mg\/kg (rat oral); 1184mg\/kg (rabbit dermal )<\/p>\nLC50: 2657mg\/m3<\/sup> (mouse inhalation, 7h)<\/p>\n2. Irritation<\/strong> No information available<\/p>\n3. Mutagenicity [9]<\/sup> <\/strong>Microbial mutagenicity: Salmonella typhimurium 67\u03bcg\/dish. Unprogrammed DNA synthesis and sister chromosome exchange in hamster embryos: 1mg\/L. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[10]<\/sup> <\/strong>LC50: 2.92mg\/L (96h) (fathead minnow, dynamic)<\/p>\n 2. Biodegradability <\/strong>No data yet<\/p>\n3. Non-biodegradability [11]<\/sup> <\/strong>In the air, when the concentration of hydroxyl radicals When the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 55d (theoretical). <\/strong><\/p>\n4. Other harmful effects [12]<\/sup> <\/strong>This substance is harmful to the environment and attention should be paid to atmospheric pollution. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 45.54<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 101.8<\/p>\n3. Isotonic specific volume (90.2K ): 291.2<\/p>\n4. Surface tension (dyne\/cm): 66.7<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
6. Octanol\/water partition coefficient: 3.03[6]<\/sup><\/p>\n7. Solubility: Slightly soluble in water, soluble in benzene, ether and acetone. [7]<\/sup><\/p>\n8. Crystal phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): 141.0<\/p>\n 9. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): 210.9<\/p>\n10. Gas phase standard entropy (J\u00b7mol-1<\/sup> \u00b7K-1<\/sup>): 355.62<\/p>\n11. Gas phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 178.0<\/p>\n12. Vapor phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 75.07<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[8]<\/sup><\/strong><\/p>\nLD50: 355mg\/kg (rat oral); 1184mg\/kg (rabbit dermal )<\/p>\nLC50: 2657mg\/m3<\/sup> (mouse inhalation, 7h)<\/p>\n2. Irritation<\/strong> No information available<\/p>\n3. Mutagenicity [9]<\/sup> <\/strong>Microbial mutagenicity: Salmonella typhimurium 67\u03bcg\/dish. Unprogrammed DNA synthesis and sister chromosome exchange in hamster embryos: 1mg\/L. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[10]<\/sup> <\/strong>LC50: 2.92mg\/L (96h) (fathead minnow, dynamic)<\/p>\n 2. Biodegradability <\/strong>No data yet<\/p>\n3. Non-biodegradability [11]<\/sup> <\/strong>In the air, when the concentration of hydroxyl radicals When the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 55d (theoretical). <\/strong><\/p>\n4. Other harmful effects [12]<\/sup> <\/strong>This substance is harmful to the environment and attention should be paid to atmospheric pollution. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 45.54<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 101.8<\/p>\n3. Isotonic specific volume (90.2K ): 291.2<\/p>\n4. Surface tension (dyne\/cm): 66.7<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
7. Solubility: Slightly soluble in water, soluble in benzene, ether and acetone. [7]<\/sup><\/p>\n8. Crystal phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): 141.0<\/p>\n 9. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): 210.9<\/p>\n10. Gas phase standard entropy (J\u00b7mol-1<\/sup> \u00b7K-1<\/sup>): 355.62<\/p>\n11. Gas phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 178.0<\/p>\n12. Vapor phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 75.07<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[8]<\/sup><\/strong><\/p>\nLD50: 355mg\/kg (rat oral); 1184mg\/kg (rabbit dermal )<\/p>\nLC50: 2657mg\/m3<\/sup> (mouse inhalation, 7h)<\/p>\n2. Irritation<\/strong> No information available<\/p>\n3. Mutagenicity [9]<\/sup> <\/strong>Microbial mutagenicity: Salmonella typhimurium 67\u03bcg\/dish. Unprogrammed DNA synthesis and sister chromosome exchange in hamster embryos: 1mg\/L. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[10]<\/sup> <\/strong>LC50: 2.92mg\/L (96h) (fathead minnow, dynamic)<\/p>\n 2. Biodegradability <\/strong>No data yet<\/p>\n3. Non-biodegradability [11]<\/sup> <\/strong>In the air, when the concentration of hydroxyl radicals When the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 55d (theoretical). <\/strong><\/p>\n4. Other harmful effects [12]<\/sup> <\/strong>This substance is harmful to the environment and attention should be paid to atmospheric pollution. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 45.54<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 101.8<\/p>\n3. Isotonic specific volume (90.2K ): 291.2<\/p>\n4. Surface tension (dyne\/cm): 66.7<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
8. Crystal phase standard claims heat (enthalpy) (kJ\u00b7mol-1<\/sup>): 141.0<\/p>\n 9. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): 210.9<\/p>\n10. Gas phase standard entropy (J\u00b7mol-1<\/sup> \u00b7K-1<\/sup>): 355.62<\/p>\n11. Gas phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 178.0<\/p>\n12. Vapor phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 75.07<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[8]<\/sup><\/strong><\/p>\nLD50: 355mg\/kg (rat oral); 1184mg\/kg (rabbit dermal )<\/p>\nLC50: 2657mg\/m3<\/sup> (mouse inhalation, 7h)<\/p>\n2. Irritation<\/strong> No information available<\/p>\n3. Mutagenicity [9]<\/sup> <\/strong>Microbial mutagenicity: Salmonella typhimurium 67\u03bcg\/dish. Unprogrammed DNA synthesis and sister chromosome exchange in hamster embryos: 1mg\/L. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[10]<\/sup> <\/strong>LC50: 2.92mg\/L (96h) (fathead minnow, dynamic)<\/p>\n 2. Biodegradability <\/strong>No data yet<\/p>\n3. Non-biodegradability [11]<\/sup> <\/strong>In the air, when the concentration of hydroxyl radicals When the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 55d (theoretical). <\/strong><\/p>\n4. Other harmful effects [12]<\/sup> <\/strong>This substance is harmful to the environment and attention should be paid to atmospheric pollution. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 45.54<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 101.8<\/p>\n3. Isotonic specific volume (90.2K ): 291.2<\/p>\n4. Surface tension (dyne\/cm): 66.7<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
9. Gas phase standard claimed heat (enthalpy) (kJ\u00b7mol-1<\/sup>): 210.9<\/p>\n10. Gas phase standard entropy (J\u00b7mol-1<\/sup> \u00b7K-1<\/sup>): 355.62<\/p>\n11. Gas phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 178.0<\/p>\n12. Vapor phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 75.07<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[8]<\/sup><\/strong><\/p>\nLD50: 355mg\/kg (rat oral); 1184mg\/kg (rabbit dermal )<\/p>\nLC50: 2657mg\/m3<\/sup> (mouse inhalation, 7h)<\/p>\n2. Irritation<\/strong> No information available<\/p>\n3. Mutagenicity [9]<\/sup> <\/strong>Microbial mutagenicity: Salmonella typhimurium 67\u03bcg\/dish. Unprogrammed DNA synthesis and sister chromosome exchange in hamster embryos: 1mg\/L. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[10]<\/sup> <\/strong>LC50: 2.92mg\/L (96h) (fathead minnow, dynamic)<\/p>\n 2. Biodegradability <\/strong>No data yet<\/p>\n3. Non-biodegradability [11]<\/sup> <\/strong>In the air, when the concentration of hydroxyl radicals When the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 55d (theoretical). <\/strong><\/p>\n4. Other harmful effects [12]<\/sup> <\/strong>This substance is harmful to the environment and attention should be paid to atmospheric pollution. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 45.54<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 101.8<\/p>\n3. Isotonic specific volume (90.2K ): 291.2<\/p>\n4. Surface tension (dyne\/cm): 66.7<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
10. Gas phase standard entropy (J\u00b7mol-1<\/sup> \u00b7K-1<\/sup>): 355.62<\/p>\n11. Gas phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 178.0<\/p>\n12. Vapor phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 75.07<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[8]<\/sup><\/strong><\/p>\nLD50: 355mg\/kg (rat oral); 1184mg\/kg (rabbit dermal )<\/p>\nLC50: 2657mg\/m3<\/sup> (mouse inhalation, 7h)<\/p>\n2. Irritation<\/strong> No information available<\/p>\n3. Mutagenicity [9]<\/sup> <\/strong>Microbial mutagenicity: Salmonella typhimurium 67\u03bcg\/dish. Unprogrammed DNA synthesis and sister chromosome exchange in hamster embryos: 1mg\/L. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[10]<\/sup> <\/strong>LC50: 2.92mg\/L (96h) (fathead minnow, dynamic)<\/p>\n 2. Biodegradability <\/strong>No data yet<\/p>\n3. Non-biodegradability [11]<\/sup> <\/strong>In the air, when the concentration of hydroxyl radicals When the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 55d (theoretical). <\/strong><\/p>\n4. Other harmful effects [12]<\/sup> <\/strong>This substance is harmful to the environment and attention should be paid to atmospheric pollution. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 45.54<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 101.8<\/p>\n3. Isotonic specific volume (90.2K ): 291.2<\/p>\n4. Surface tension (dyne\/cm): 66.7<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
11. Gas phase standard free energy of formation (kJ\u00b7mol-1<\/sup>): 178.0<\/p>\n12. Vapor phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 75.07<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[8]<\/sup><\/strong><\/p>\nLD50: 355mg\/kg (rat oral); 1184mg\/kg (rabbit dermal )<\/p>\nLC50: 2657mg\/m3<\/sup> (mouse inhalation, 7h)<\/p>\n2. Irritation<\/strong> No information available<\/p>\n3. Mutagenicity [9]<\/sup> <\/strong>Microbial mutagenicity: Salmonella typhimurium 67\u03bcg\/dish. Unprogrammed DNA synthesis and sister chromosome exchange in hamster embryos: 1mg\/L. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[10]<\/sup> <\/strong>LC50: 2.92mg\/L (96h) (fathead minnow, dynamic)<\/p>\n 2. Biodegradability <\/strong>No data yet<\/p>\n3. Non-biodegradability [11]<\/sup> <\/strong>In the air, when the concentration of hydroxyl radicals When the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 55d (theoretical). <\/strong><\/p>\n4. Other harmful effects [12]<\/sup> <\/strong>This substance is harmful to the environment and attention should be paid to atmospheric pollution. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 45.54<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 101.8<\/p>\n3. Isotonic specific volume (90.2K ): 291.2<\/p>\n4. Surface tension (dyne\/cm): 66.7<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
12. Vapor phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 75.07<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[8]<\/sup><\/strong><\/p>\nLD50: 355mg\/kg (rat oral); 1184mg\/kg (rabbit dermal )<\/p>\nLC50: 2657mg\/m3<\/sup> (mouse inhalation, 7h)<\/p>\n2. Irritation<\/strong> No information available<\/p>\n3. Mutagenicity [9]<\/sup> <\/strong>Microbial mutagenicity: Salmonella typhimurium 67\u03bcg\/dish. Unprogrammed DNA synthesis and sister chromosome exchange in hamster embryos: 1mg\/L. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[10]<\/sup> <\/strong>LC50: 2.92mg\/L (96h) (fathead minnow, dynamic)<\/p>\n 2. Biodegradability <\/strong>No data yet<\/p>\n3. Non-biodegradability [11]<\/sup> <\/strong>In the air, when the concentration of hydroxyl radicals When the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 55d (theoretical). <\/strong><\/p>\n4. Other harmful effects [12]<\/sup> <\/strong>This substance is harmful to the environment and attention should be paid to atmospheric pollution. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 45.54<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 101.8<\/p>\n3. Isotonic specific volume (90.2K ): 291.2<\/p>\n4. Surface tension (dyne\/cm): 66.7<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
1. Acute toxicity[8]<\/sup><\/strong><\/p>\nLD50: 355mg\/kg (rat oral); 1184mg\/kg (rabbit dermal )<\/p>\nLC50: 2657mg\/m3<\/sup> (mouse inhalation, 7h)<\/p>\n2. Irritation<\/strong> No information available<\/p>\n3. Mutagenicity [9]<\/sup> <\/strong>Microbial mutagenicity: Salmonella typhimurium 67\u03bcg\/dish. Unprogrammed DNA synthesis and sister chromosome exchange in hamster embryos: 1mg\/L. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[10]<\/sup> <\/strong>LC50: 2.92mg\/L (96h) (fathead minnow, dynamic)<\/p>\n 2. Biodegradability <\/strong>No data yet<\/p>\n3. Non-biodegradability [11]<\/sup> <\/strong>In the air, when the concentration of hydroxyl radicals When the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 55d (theoretical). <\/strong><\/p>\n4. Other harmful effects [12]<\/sup> <\/strong>This substance is harmful to the environment and attention should be paid to atmospheric pollution. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 45.54<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 101.8<\/p>\n3. Isotonic specific volume (90.2K ): 291.2<\/p>\n4. Surface tension (dyne\/cm): 66.7<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
LD50: 355mg\/kg (rat oral); 1184mg\/kg (rabbit dermal )<\/p>\n
LC50: 2657mg\/m3<\/sup> (mouse inhalation, 7h)<\/p>\n2. Irritation<\/strong> No information available<\/p>\n3. Mutagenicity [9]<\/sup> <\/strong>Microbial mutagenicity: Salmonella typhimurium 67\u03bcg\/dish. Unprogrammed DNA synthesis and sister chromosome exchange in hamster embryos: 1mg\/L. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[10]<\/sup> <\/strong>LC50: 2.92mg\/L (96h) (fathead minnow, dynamic)<\/p>\n 2. Biodegradability <\/strong>No data yet<\/p>\n3. Non-biodegradability [11]<\/sup> <\/strong>In the air, when the concentration of hydroxyl radicals When the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 55d (theoretical). <\/strong><\/p>\n4. Other harmful effects [12]<\/sup> <\/strong>This substance is harmful to the environment and attention should be paid to atmospheric pollution. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 45.54<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 101.8<\/p>\n3. Isotonic specific volume (90.2K ): 291.2<\/p>\n4. Surface tension (dyne\/cm): 66.7<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
2. Irritation<\/strong> No information available<\/p>\n3. Mutagenicity [9]<\/sup> <\/strong>Microbial mutagenicity: Salmonella typhimurium 67\u03bcg\/dish. Unprogrammed DNA synthesis and sister chromosome exchange in hamster embryos: 1mg\/L. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[10]<\/sup> <\/strong>LC50: 2.92mg\/L (96h) (fathead minnow, dynamic)<\/p>\n 2. Biodegradability <\/strong>No data yet<\/p>\n3. Non-biodegradability [11]<\/sup> <\/strong>In the air, when the concentration of hydroxyl radicals When the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 55d (theoretical). <\/strong><\/p>\n4. Other harmful effects [12]<\/sup> <\/strong>This substance is harmful to the environment and attention should be paid to atmospheric pollution. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 45.54<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 101.8<\/p>\n3. Isotonic specific volume (90.2K ): 291.2<\/p>\n4. Surface tension (dyne\/cm): 66.7<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3. Mutagenicity [9]<\/sup> <\/strong>Microbial mutagenicity: Salmonella typhimurium 67\u03bcg\/dish. Unprogrammed DNA synthesis and sister chromosome exchange in hamster embryos: 1mg\/L. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[10]<\/sup> <\/strong>LC50: 2.92mg\/L (96h) (fathead minnow, dynamic)<\/p>\n 2. Biodegradability <\/strong>No data yet<\/p>\n3. Non-biodegradability [11]<\/sup> <\/strong>In the air, when the concentration of hydroxyl radicals When the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 55d (theoretical). <\/strong><\/p>\n4. Other harmful effects [12]<\/sup> <\/strong>This substance is harmful to the environment and attention should be paid to atmospheric pollution. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 45.54<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 101.8<\/p>\n3. Isotonic specific volume (90.2K ): 291.2<\/p>\n4. Surface tension (dyne\/cm): 66.7<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
1. Ecotoxicity[10]<\/sup> <\/strong>LC50: 2.92mg\/L (96h) (fathead minnow, dynamic)<\/p>\n 2. Biodegradability <\/strong>No data yet<\/p>\n3. Non-biodegradability [11]<\/sup> <\/strong>In the air, when the concentration of hydroxyl radicals When the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 55d (theoretical). <\/strong><\/p>\n4. Other harmful effects [12]<\/sup> <\/strong>This substance is harmful to the environment and attention should be paid to atmospheric pollution. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 45.54<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 101.8<\/p>\n3. Isotonic specific volume (90.2K ): 291.2<\/p>\n4. Surface tension (dyne\/cm): 66.7<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
2. Biodegradability <\/strong>No data yet<\/p>\n3. Non-biodegradability [11]<\/sup> <\/strong>In the air, when the concentration of hydroxyl radicals When the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 55d (theoretical). <\/strong><\/p>\n4. Other harmful effects [12]<\/sup> <\/strong>This substance is harmful to the environment and attention should be paid to atmospheric pollution. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 45.54<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 101.8<\/p>\n3. Isotonic specific volume (90.2K ): 291.2<\/p>\n4. Surface tension (dyne\/cm): 66.7<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3. Non-biodegradability [11]<\/sup> <\/strong>In the air, when the concentration of hydroxyl radicals When the concentration is 5.00\u00d7105<\/sup> pieces\/cm3<\/sup>, the degradation half-life is 55d (theoretical). <\/strong><\/p>\n4. Other harmful effects [12]<\/sup> <\/strong>This substance is harmful to the environment and attention should be paid to atmospheric pollution. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 45.54<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 101.8<\/p>\n3. Isotonic specific volume (90.2K ): 291.2<\/p>\n4. Surface tension (dyne\/cm): 66.7<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
4. Other harmful effects [12]<\/sup> <\/strong>This substance is harmful to the environment and attention should be paid to atmospheric pollution. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 45.54<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 101.8<\/p>\n3. Isotonic specific volume (90.2K ): 291.2<\/p>\n4. Surface tension (dyne\/cm): 66.7<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
1. Molar refractive index: 45.54<\/p>\n
2. Molar volume (cm3<\/sup>\/mol): 101.8<\/p>\n3. Isotonic specific volume (90.2K ): 291.2<\/p>\n4. Surface tension (dyne\/cm): 66.7<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3. Isotonic specific volume (90.2K ): 291.2<\/p>\n
4. Surface tension (dyne\/cm): 66.7<\/p>\n
5. Polarizability (10-24<\/sup>cm3<\/sup>): 18.05<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Hydrogen bond numberNumber of isomers: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: None<\/p>\n6. Topological molecular poles Surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n 10. Number of isotope atoms: 0<\/p>\n11. Number of determined atomic stereocenters: 0<\/p>\n12. Number of uncertain atomic stereocenters: 0<\/p>\n13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
1. Reference value for hydrophobic parameter calculation (XlogP): 2.7<\/P><\/p>\n
2. Number of hydrogen bond donors: 0<\/p>\n
3. Hydrogen bond numberNumber of isomers: 0<\/p>\n
4. Number of rotatable chemical bonds: 0<\/p>\n
5. Number of tautomers: None<\/p>\n
6. Topological molecular poles Surface area 0<\/p>\n
7. Number of heavy atoms: 4<\/p>\n
8. Surface charge: 0<\/p>\n
9. Complexity: 8<\/p>\n
10. Number of isotope atoms: 0<\/p>\n
11. Number of determined atomic stereocenters: 0<\/p>\n
12. Number of uncertain atomic stereocenters: 0<\/p>\n
13 .Determined number of stereocenters of chemical bonds: 0<\/p>\n
14. Uncertain number of stereocenters of chemical bonds: 0<\/p>\n
15. Number of covalent bond units: 1<\/p>\n<\/p>\n
1. Stability[13]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
2. Incompatible substances[14]<\/sup> <\/strong> Strong oxidants, strong bases, alkali metals, mercury and its compounds<\/p>\n3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3. Conditions to avoid contact[15]<\/sup><\/strong> Light, heat , friction, impact<\/p>\n4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
4. Polymerization hazard[16]<\/sup><\/strong> No polymerization<\/p>\n5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
5. Decomposition products[17]<\/sup><\/strong> Hydrogen iodide<\/p>\n<\/p>\nStorage method<\/h2>\n\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
\n Storage Precautions[18]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Avoid light. The packaging is sealed. They should be stored separately from oxidants, alkalis, alkali metals, and food chemicals, and avoid mixed storage. Suitable materials should be available in the storage area to contain spills.\n <\/p>\nSynthesis method<\/h2>\nIt is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
It is obtained by halogenation and hydrolysis of acetone (or ethanol). First add water, sodium iodide and acetone into the reaction pot, add ice and cool down to 10\u00b0C. Slowly add sodium hypochlorite while stirring until the end point is reached when no turbidity occurs, and control the temperature not to exceed 20\u00b0C. Let it stand for 1 hour, suck off the supernatant, take out the iodoform layer and filter. Wash the filter cake with water until it is neutral, and then wash it with distilled water until there is no chlorine radical. Then dry it at 35-40\u2103 to get the finished product. In addition, this product can also be prepared by reacting chloroform with methyl iodide. <\/p>\n<\/p>\n
1. Used as a preservative and disinfectant in medicine and biochemistry. <\/p>\n
2. Used as chemical intermediates and preservatives. [19]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
extended-reading:https:\/\/www.morpholine.org\/trimethylhydroxyethyl-bisaminoethyl-ether\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/catalyst-dabco-8154-acid-blocked-tertiary-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/u-cat-5003-catalyst-cas868077-29-6-sanyo-japan\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/strong-gel-amine-catalyst-bx405-low-odor-amine-catalyst-bx405\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44380<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/high-quality-246-trisdimethylaminomethylphenol-cas-90-72-2-dmp-30\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dabco-2040-low-odor-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44239<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/649<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-pt303-tertiary-amine-catalyst-dabco-pt303-catalyst-dabco-pt303\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
Structural formula Business number 01JM Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49486,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15485],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487"}],"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=49487"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49487\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49486"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49487"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49487"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49487"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
![\"Triiodomethane](\"http:\/\/www.newtopchem.com\/wp-content\/uploads\/2024\/06\/b3923cbb61264d96a1c6023d6b8b36bc.gif\")
<\/p>\n<\/p>\n