<\/p>\n
Structural formula<\/p>\n
Bromoform,<\/p>\n
Methyl tribromide,<\/p>\n
Tribromomethane,<\/p>\n
Formyltribromide,<\/p>\n
Aliphatic halogenated derivatives<\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n
CAS number:<\/b>75-25-2<\/p>\n
MDL number:<\/b>MFCD00000128<\/p>\n
EINECS number:<\/b>200-854-6<\/p>\n
RTECS number:<\/b>PB5600000<\/p>\n
BRN number:<\/b>1731048<\/p>\n
PubChem number:<\/b>24863014<\/p>\nPhysical property data<\/h2>\n
1. Properties: Colorless heavy liquid with a chloroform-like smell. [1]<\/sup><\/p>\n2. Melting point (\u00baC): 6~9[2]<\/sup><\/p>\n3. Boiling point (\u00baC) : 149.5[3]<\/sup><\/p>\n4. Relative density (water = 1): 2.89[4]<\/sup><\/p>\n5. Relative Vapor density (air=1): 8.7[5]<\/sup><\/p>\n6. Saturated vapor pressure (kPa): 0.75 (25\u00baC)[6]<\/sup><\/p>\n7. Critical pressure (MPa): 6.09[7]<\/sup><\/p>\n8. Octanol\/water partition coefficient: 2.38[8]<\/sup><\/p>\n9. Solubility: Slightly soluble in water, soluble in ethanol, ether, chloroform, benzene, etc. [9]<\/sup><\/p>\n10. Specific heat capacity (KJ\/(kg\u00b7K), 18~50\u00baC, constant pressure): 0.519<\/p>\n11. Electrical conductivity ( S\/m, 25\u00baC): <2\u00d710-8<\/sup><\/p>\n12. Vapor pressure (kPa, 22\u00baC): 0.67<\/p>\n13. Vapor pressure ( kPa, 48\u00baC): 2.67<\/p>\n14. Volume expansion coefficient (K-1<\/sup>): 0.00091<\/p>\n15. Refractive index at room temperature (n20 <\/sup>): 1.5976<\/p>\n16. Refractive index at room temperature (n25<\/sup>): 1.5956<\/p>\n17. Lennard-Jones parameter (A): 8.153 <\/p>\n18. Lennard-Jones parameter (K): 162.2<\/p>\n19. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup> sup>: 21.726<\/p>\n20. van der Waals area (cm2<\/sup>\u00b7mol-1<\/sup>): 6.810\u00d7109<\/sup><\/p>\n21. van der Waals volume (cm3<\/sup>\u00b7mol-1<\/sup>): 49.980<\/p>\n22. Gas phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 330.70<\/p>\n23. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 70.98<\/p>\n24. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K– 1<\/sup>): 129.9<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[10]<\/sup><\/strong><\/p>\nLD50: 933mg\/kg (rat oral); 414mg\/kg (rat intraperitoneal ); 1072mg\/kg (orally administered to mice)<\/p>\nLC50: 12100mg\/m3<\/sup> (inhaled to mice, 2h)<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
2. Melting point (\u00baC): 6~9[2]<\/sup><\/p>\n3. Boiling point (\u00baC) : 149.5[3]<\/sup><\/p>\n4. Relative density (water = 1): 2.89[4]<\/sup><\/p>\n5. Relative Vapor density (air=1): 8.7[5]<\/sup><\/p>\n6. Saturated vapor pressure (kPa): 0.75 (25\u00baC)[6]<\/sup><\/p>\n7. Critical pressure (MPa): 6.09[7]<\/sup><\/p>\n8. Octanol\/water partition coefficient: 2.38[8]<\/sup><\/p>\n9. Solubility: Slightly soluble in water, soluble in ethanol, ether, chloroform, benzene, etc. [9]<\/sup><\/p>\n10. Specific heat capacity (KJ\/(kg\u00b7K), 18~50\u00baC, constant pressure): 0.519<\/p>\n11. Electrical conductivity ( S\/m, 25\u00baC): <2\u00d710-8<\/sup><\/p>\n12. Vapor pressure (kPa, 22\u00baC): 0.67<\/p>\n13. Vapor pressure ( kPa, 48\u00baC): 2.67<\/p>\n14. Volume expansion coefficient (K-1<\/sup>): 0.00091<\/p>\n15. Refractive index at room temperature (n20 <\/sup>): 1.5976<\/p>\n16. Refractive index at room temperature (n25<\/sup>): 1.5956<\/p>\n17. Lennard-Jones parameter (A): 8.153 <\/p>\n18. Lennard-Jones parameter (K): 162.2<\/p>\n19. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup> sup>: 21.726<\/p>\n20. van der Waals area (cm2<\/sup>\u00b7mol-1<\/sup>): 6.810\u00d7109<\/sup><\/p>\n21. van der Waals volume (cm3<\/sup>\u00b7mol-1<\/sup>): 49.980<\/p>\n22. Gas phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 330.70<\/p>\n23. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 70.98<\/p>\n24. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K– 1<\/sup>): 129.9<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[10]<\/sup><\/strong><\/p>\nLD50: 933mg\/kg (rat oral); 414mg\/kg (rat intraperitoneal ); 1072mg\/kg (orally administered to mice)<\/p>\nLC50: 12100mg\/m3<\/sup> (inhaled to mice, 2h)<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3. Boiling point (\u00baC) : 149.5[3]<\/sup><\/p>\n4. Relative density (water = 1): 2.89[4]<\/sup><\/p>\n5. Relative Vapor density (air=1): 8.7[5]<\/sup><\/p>\n6. Saturated vapor pressure (kPa): 0.75 (25\u00baC)[6]<\/sup><\/p>\n7. Critical pressure (MPa): 6.09[7]<\/sup><\/p>\n8. Octanol\/water partition coefficient: 2.38[8]<\/sup><\/p>\n9. Solubility: Slightly soluble in water, soluble in ethanol, ether, chloroform, benzene, etc. [9]<\/sup><\/p>\n10. Specific heat capacity (KJ\/(kg\u00b7K), 18~50\u00baC, constant pressure): 0.519<\/p>\n11. Electrical conductivity ( S\/m, 25\u00baC): <2\u00d710-8<\/sup><\/p>\n12. Vapor pressure (kPa, 22\u00baC): 0.67<\/p>\n13. Vapor pressure ( kPa, 48\u00baC): 2.67<\/p>\n14. Volume expansion coefficient (K-1<\/sup>): 0.00091<\/p>\n15. Refractive index at room temperature (n20 <\/sup>): 1.5976<\/p>\n16. Refractive index at room temperature (n25<\/sup>): 1.5956<\/p>\n17. Lennard-Jones parameter (A): 8.153 <\/p>\n18. Lennard-Jones parameter (K): 162.2<\/p>\n19. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup> sup>: 21.726<\/p>\n20. van der Waals area (cm2<\/sup>\u00b7mol-1<\/sup>): 6.810\u00d7109<\/sup><\/p>\n21. van der Waals volume (cm3<\/sup>\u00b7mol-1<\/sup>): 49.980<\/p>\n22. Gas phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 330.70<\/p>\n23. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 70.98<\/p>\n24. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K– 1<\/sup>): 129.9<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[10]<\/sup><\/strong><\/p>\nLD50: 933mg\/kg (rat oral); 414mg\/kg (rat intraperitoneal ); 1072mg\/kg (orally administered to mice)<\/p>\nLC50: 12100mg\/m3<\/sup> (inhaled to mice, 2h)<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
4. Relative density (water = 1): 2.89[4]<\/sup><\/p>\n5. Relative Vapor density (air=1): 8.7[5]<\/sup><\/p>\n6. Saturated vapor pressure (kPa): 0.75 (25\u00baC)[6]<\/sup><\/p>\n7. Critical pressure (MPa): 6.09[7]<\/sup><\/p>\n8. Octanol\/water partition coefficient: 2.38[8]<\/sup><\/p>\n9. Solubility: Slightly soluble in water, soluble in ethanol, ether, chloroform, benzene, etc. [9]<\/sup><\/p>\n10. Specific heat capacity (KJ\/(kg\u00b7K), 18~50\u00baC, constant pressure): 0.519<\/p>\n11. Electrical conductivity ( S\/m, 25\u00baC): <2\u00d710-8<\/sup><\/p>\n12. Vapor pressure (kPa, 22\u00baC): 0.67<\/p>\n13. Vapor pressure ( kPa, 48\u00baC): 2.67<\/p>\n14. Volume expansion coefficient (K-1<\/sup>): 0.00091<\/p>\n15. Refractive index at room temperature (n20 <\/sup>): 1.5976<\/p>\n16. Refractive index at room temperature (n25<\/sup>): 1.5956<\/p>\n17. Lennard-Jones parameter (A): 8.153 <\/p>\n18. Lennard-Jones parameter (K): 162.2<\/p>\n19. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup> sup>: 21.726<\/p>\n20. van der Waals area (cm2<\/sup>\u00b7mol-1<\/sup>): 6.810\u00d7109<\/sup><\/p>\n21. van der Waals volume (cm3<\/sup>\u00b7mol-1<\/sup>): 49.980<\/p>\n22. Gas phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 330.70<\/p>\n23. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 70.98<\/p>\n24. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K– 1<\/sup>): 129.9<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[10]<\/sup><\/strong><\/p>\nLD50: 933mg\/kg (rat oral); 414mg\/kg (rat intraperitoneal ); 1072mg\/kg (orally administered to mice)<\/p>\nLC50: 12100mg\/m3<\/sup> (inhaled to mice, 2h)<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
5. Relative Vapor density (air=1): 8.7[5]<\/sup><\/p>\n6. Saturated vapor pressure (kPa): 0.75 (25\u00baC)[6]<\/sup><\/p>\n7. Critical pressure (MPa): 6.09[7]<\/sup><\/p>\n8. Octanol\/water partition coefficient: 2.38[8]<\/sup><\/p>\n9. Solubility: Slightly soluble in water, soluble in ethanol, ether, chloroform, benzene, etc. [9]<\/sup><\/p>\n10. Specific heat capacity (KJ\/(kg\u00b7K), 18~50\u00baC, constant pressure): 0.519<\/p>\n11. Electrical conductivity ( S\/m, 25\u00baC): <2\u00d710-8<\/sup><\/p>\n12. Vapor pressure (kPa, 22\u00baC): 0.67<\/p>\n13. Vapor pressure ( kPa, 48\u00baC): 2.67<\/p>\n14. Volume expansion coefficient (K-1<\/sup>): 0.00091<\/p>\n15. Refractive index at room temperature (n20 <\/sup>): 1.5976<\/p>\n16. Refractive index at room temperature (n25<\/sup>): 1.5956<\/p>\n17. Lennard-Jones parameter (A): 8.153 <\/p>\n18. Lennard-Jones parameter (K): 162.2<\/p>\n19. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup> sup>: 21.726<\/p>\n20. van der Waals area (cm2<\/sup>\u00b7mol-1<\/sup>): 6.810\u00d7109<\/sup><\/p>\n21. van der Waals volume (cm3<\/sup>\u00b7mol-1<\/sup>): 49.980<\/p>\n22. Gas phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 330.70<\/p>\n23. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 70.98<\/p>\n24. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K– 1<\/sup>): 129.9<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[10]<\/sup><\/strong><\/p>\nLD50: 933mg\/kg (rat oral); 414mg\/kg (rat intraperitoneal ); 1072mg\/kg (orally administered to mice)<\/p>\nLC50: 12100mg\/m3<\/sup> (inhaled to mice, 2h)<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
6. Saturated vapor pressure (kPa): 0.75 (25\u00baC)[6]<\/sup><\/p>\n7. Critical pressure (MPa): 6.09[7]<\/sup><\/p>\n8. Octanol\/water partition coefficient: 2.38[8]<\/sup><\/p>\n9. Solubility: Slightly soluble in water, soluble in ethanol, ether, chloroform, benzene, etc. [9]<\/sup><\/p>\n10. Specific heat capacity (KJ\/(kg\u00b7K), 18~50\u00baC, constant pressure): 0.519<\/p>\n11. Electrical conductivity ( S\/m, 25\u00baC): <2\u00d710-8<\/sup><\/p>\n12. Vapor pressure (kPa, 22\u00baC): 0.67<\/p>\n13. Vapor pressure ( kPa, 48\u00baC): 2.67<\/p>\n14. Volume expansion coefficient (K-1<\/sup>): 0.00091<\/p>\n15. Refractive index at room temperature (n20 <\/sup>): 1.5976<\/p>\n16. Refractive index at room temperature (n25<\/sup>): 1.5956<\/p>\n17. Lennard-Jones parameter (A): 8.153 <\/p>\n18. Lennard-Jones parameter (K): 162.2<\/p>\n19. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup> sup>: 21.726<\/p>\n20. van der Waals area (cm2<\/sup>\u00b7mol-1<\/sup>): 6.810\u00d7109<\/sup><\/p>\n21. van der Waals volume (cm3<\/sup>\u00b7mol-1<\/sup>): 49.980<\/p>\n22. Gas phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 330.70<\/p>\n23. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 70.98<\/p>\n24. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K– 1<\/sup>): 129.9<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[10]<\/sup><\/strong><\/p>\nLD50: 933mg\/kg (rat oral); 414mg\/kg (rat intraperitoneal ); 1072mg\/kg (orally administered to mice)<\/p>\nLC50: 12100mg\/m3<\/sup> (inhaled to mice, 2h)<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
7. Critical pressure (MPa): 6.09[7]<\/sup><\/p>\n8. Octanol\/water partition coefficient: 2.38[8]<\/sup><\/p>\n9. Solubility: Slightly soluble in water, soluble in ethanol, ether, chloroform, benzene, etc. [9]<\/sup><\/p>\n10. Specific heat capacity (KJ\/(kg\u00b7K), 18~50\u00baC, constant pressure): 0.519<\/p>\n11. Electrical conductivity ( S\/m, 25\u00baC): <2\u00d710-8<\/sup><\/p>\n12. Vapor pressure (kPa, 22\u00baC): 0.67<\/p>\n13. Vapor pressure ( kPa, 48\u00baC): 2.67<\/p>\n14. Volume expansion coefficient (K-1<\/sup>): 0.00091<\/p>\n15. Refractive index at room temperature (n20 <\/sup>): 1.5976<\/p>\n16. Refractive index at room temperature (n25<\/sup>): 1.5956<\/p>\n17. Lennard-Jones parameter (A): 8.153 <\/p>\n18. Lennard-Jones parameter (K): 162.2<\/p>\n19. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup> sup>: 21.726<\/p>\n20. van der Waals area (cm2<\/sup>\u00b7mol-1<\/sup>): 6.810\u00d7109<\/sup><\/p>\n21. van der Waals volume (cm3<\/sup>\u00b7mol-1<\/sup>): 49.980<\/p>\n22. Gas phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 330.70<\/p>\n23. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 70.98<\/p>\n24. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K– 1<\/sup>): 129.9<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[10]<\/sup><\/strong><\/p>\nLD50: 933mg\/kg (rat oral); 414mg\/kg (rat intraperitoneal ); 1072mg\/kg (orally administered to mice)<\/p>\nLC50: 12100mg\/m3<\/sup> (inhaled to mice, 2h)<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
8. Octanol\/water partition coefficient: 2.38[8]<\/sup><\/p>\n9. Solubility: Slightly soluble in water, soluble in ethanol, ether, chloroform, benzene, etc. [9]<\/sup><\/p>\n10. Specific heat capacity (KJ\/(kg\u00b7K), 18~50\u00baC, constant pressure): 0.519<\/p>\n11. Electrical conductivity ( S\/m, 25\u00baC): <2\u00d710-8<\/sup><\/p>\n12. Vapor pressure (kPa, 22\u00baC): 0.67<\/p>\n13. Vapor pressure ( kPa, 48\u00baC): 2.67<\/p>\n14. Volume expansion coefficient (K-1<\/sup>): 0.00091<\/p>\n15. Refractive index at room temperature (n20 <\/sup>): 1.5976<\/p>\n16. Refractive index at room temperature (n25<\/sup>): 1.5956<\/p>\n17. Lennard-Jones parameter (A): 8.153 <\/p>\n18. Lennard-Jones parameter (K): 162.2<\/p>\n19. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup> sup>: 21.726<\/p>\n20. van der Waals area (cm2<\/sup>\u00b7mol-1<\/sup>): 6.810\u00d7109<\/sup><\/p>\n21. van der Waals volume (cm3<\/sup>\u00b7mol-1<\/sup>): 49.980<\/p>\n22. Gas phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 330.70<\/p>\n23. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 70.98<\/p>\n24. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K– 1<\/sup>): 129.9<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[10]<\/sup><\/strong><\/p>\nLD50: 933mg\/kg (rat oral); 414mg\/kg (rat intraperitoneal ); 1072mg\/kg (orally administered to mice)<\/p>\nLC50: 12100mg\/m3<\/sup> (inhaled to mice, 2h)<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
9. Solubility: Slightly soluble in water, soluble in ethanol, ether, chloroform, benzene, etc. [9]<\/sup><\/p>\n10. Specific heat capacity (KJ\/(kg\u00b7K), 18~50\u00baC, constant pressure): 0.519<\/p>\n11. Electrical conductivity ( S\/m, 25\u00baC): <2\u00d710-8<\/sup><\/p>\n12. Vapor pressure (kPa, 22\u00baC): 0.67<\/p>\n13. Vapor pressure ( kPa, 48\u00baC): 2.67<\/p>\n14. Volume expansion coefficient (K-1<\/sup>): 0.00091<\/p>\n15. Refractive index at room temperature (n20 <\/sup>): 1.5976<\/p>\n16. Refractive index at room temperature (n25<\/sup>): 1.5956<\/p>\n17. Lennard-Jones parameter (A): 8.153 <\/p>\n18. Lennard-Jones parameter (K): 162.2<\/p>\n19. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup> sup>: 21.726<\/p>\n20. van der Waals area (cm2<\/sup>\u00b7mol-1<\/sup>): 6.810\u00d7109<\/sup><\/p>\n21. van der Waals volume (cm3<\/sup>\u00b7mol-1<\/sup>): 49.980<\/p>\n22. Gas phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 330.70<\/p>\n23. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 70.98<\/p>\n24. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K– 1<\/sup>): 129.9<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[10]<\/sup><\/strong><\/p>\nLD50: 933mg\/kg (rat oral); 414mg\/kg (rat intraperitoneal ); 1072mg\/kg (orally administered to mice)<\/p>\nLC50: 12100mg\/m3<\/sup> (inhaled to mice, 2h)<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
10. Specific heat capacity (KJ\/(kg\u00b7K), 18~50\u00baC, constant pressure): 0.519<\/p>\n
11. Electrical conductivity ( S\/m, 25\u00baC): <2\u00d710-8<\/sup><\/p>\n12. Vapor pressure (kPa, 22\u00baC): 0.67<\/p>\n13. Vapor pressure ( kPa, 48\u00baC): 2.67<\/p>\n14. Volume expansion coefficient (K-1<\/sup>): 0.00091<\/p>\n15. Refractive index at room temperature (n20 <\/sup>): 1.5976<\/p>\n16. Refractive index at room temperature (n25<\/sup>): 1.5956<\/p>\n17. Lennard-Jones parameter (A): 8.153 <\/p>\n18. Lennard-Jones parameter (K): 162.2<\/p>\n19. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup> sup>: 21.726<\/p>\n20. van der Waals area (cm2<\/sup>\u00b7mol-1<\/sup>): 6.810\u00d7109<\/sup><\/p>\n21. van der Waals volume (cm3<\/sup>\u00b7mol-1<\/sup>): 49.980<\/p>\n22. Gas phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 330.70<\/p>\n23. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 70.98<\/p>\n24. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K– 1<\/sup>): 129.9<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[10]<\/sup><\/strong><\/p>\nLD50: 933mg\/kg (rat oral); 414mg\/kg (rat intraperitoneal ); 1072mg\/kg (orally administered to mice)<\/p>\nLC50: 12100mg\/m3<\/sup> (inhaled to mice, 2h)<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
12. Vapor pressure (kPa, 22\u00baC): 0.67<\/p>\n
13. Vapor pressure ( kPa, 48\u00baC): 2.67<\/p>\n
14. Volume expansion coefficient (K-1<\/sup>): 0.00091<\/p>\n15. Refractive index at room temperature (n20 <\/sup>): 1.5976<\/p>\n16. Refractive index at room temperature (n25<\/sup>): 1.5956<\/p>\n17. Lennard-Jones parameter (A): 8.153 <\/p>\n18. Lennard-Jones parameter (K): 162.2<\/p>\n19. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup> sup>: 21.726<\/p>\n20. van der Waals area (cm2<\/sup>\u00b7mol-1<\/sup>): 6.810\u00d7109<\/sup><\/p>\n21. van der Waals volume (cm3<\/sup>\u00b7mol-1<\/sup>): 49.980<\/p>\n22. Gas phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 330.70<\/p>\n23. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 70.98<\/p>\n24. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K– 1<\/sup>): 129.9<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[10]<\/sup><\/strong><\/p>\nLD50: 933mg\/kg (rat oral); 414mg\/kg (rat intraperitoneal ); 1072mg\/kg (orally administered to mice)<\/p>\nLC50: 12100mg\/m3<\/sup> (inhaled to mice, 2h)<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
15. Refractive index at room temperature (n20 <\/sup>): 1.5976<\/p>\n16. Refractive index at room temperature (n25<\/sup>): 1.5956<\/p>\n17. Lennard-Jones parameter (A): 8.153 <\/p>\n18. Lennard-Jones parameter (K): 162.2<\/p>\n19. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup> sup>: 21.726<\/p>\n20. van der Waals area (cm2<\/sup>\u00b7mol-1<\/sup>): 6.810\u00d7109<\/sup><\/p>\n21. van der Waals volume (cm3<\/sup>\u00b7mol-1<\/sup>): 49.980<\/p>\n22. Gas phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 330.70<\/p>\n23. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 70.98<\/p>\n24. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K– 1<\/sup>): 129.9<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[10]<\/sup><\/strong><\/p>\nLD50: 933mg\/kg (rat oral); 414mg\/kg (rat intraperitoneal ); 1072mg\/kg (orally administered to mice)<\/p>\nLC50: 12100mg\/m3<\/sup> (inhaled to mice, 2h)<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
16. Refractive index at room temperature (n25<\/sup>): 1.5956<\/p>\n17. Lennard-Jones parameter (A): 8.153 <\/p>\n18. Lennard-Jones parameter (K): 162.2<\/p>\n19. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup> sup>: 21.726<\/p>\n20. van der Waals area (cm2<\/sup>\u00b7mol-1<\/sup>): 6.810\u00d7109<\/sup><\/p>\n21. van der Waals volume (cm3<\/sup>\u00b7mol-1<\/sup>): 49.980<\/p>\n22. Gas phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 330.70<\/p>\n23. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 70.98<\/p>\n24. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K– 1<\/sup>): 129.9<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[10]<\/sup><\/strong><\/p>\nLD50: 933mg\/kg (rat oral); 414mg\/kg (rat intraperitoneal ); 1072mg\/kg (orally administered to mice)<\/p>\nLC50: 12100mg\/m3<\/sup> (inhaled to mice, 2h)<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
17. Lennard-Jones parameter (A): 8.153 <\/p>\n
18. Lennard-Jones parameter (K): 162.2<\/p>\n
19. Solubility parameter (J\u00b7cm-3<\/sup>)0.5<\/sup> sup>: 21.726<\/p>\n20. van der Waals area (cm2<\/sup>\u00b7mol-1<\/sup>): 6.810\u00d7109<\/sup><\/p>\n21. van der Waals volume (cm3<\/sup>\u00b7mol-1<\/sup>): 49.980<\/p>\n22. Gas phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 330.70<\/p>\n23. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 70.98<\/p>\n24. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K– 1<\/sup>): 129.9<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[10]<\/sup><\/strong><\/p>\nLD50: 933mg\/kg (rat oral); 414mg\/kg (rat intraperitoneal ); 1072mg\/kg (orally administered to mice)<\/p>\nLC50: 12100mg\/m3<\/sup> (inhaled to mice, 2h)<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
20. van der Waals area (cm2<\/sup>\u00b7mol-1<\/sup>): 6.810\u00d7109<\/sup><\/p>\n21. van der Waals volume (cm3<\/sup>\u00b7mol-1<\/sup>): 49.980<\/p>\n22. Gas phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 330.70<\/p>\n23. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 70.98<\/p>\n24. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K– 1<\/sup>): 129.9<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[10]<\/sup><\/strong><\/p>\nLD50: 933mg\/kg (rat oral); 414mg\/kg (rat intraperitoneal ); 1072mg\/kg (orally administered to mice)<\/p>\nLC50: 12100mg\/m3<\/sup> (inhaled to mice, 2h)<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
21. van der Waals volume (cm3<\/sup>\u00b7mol-1<\/sup>): 49.980<\/p>\n22. Gas phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 330.70<\/p>\n23. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 70.98<\/p>\n24. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K– 1<\/sup>): 129.9<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[10]<\/sup><\/strong><\/p>\nLD50: 933mg\/kg (rat oral); 414mg\/kg (rat intraperitoneal ); 1072mg\/kg (orally administered to mice)<\/p>\nLC50: 12100mg\/m3<\/sup> (inhaled to mice, 2h)<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
22. Gas phase standard entropy (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 330.70<\/p>\n23. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 70.98<\/p>\n24. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K– 1<\/sup>): 129.9<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[10]<\/sup><\/strong><\/p>\nLD50: 933mg\/kg (rat oral); 414mg\/kg (rat intraperitoneal ); 1072mg\/kg (orally administered to mice)<\/p>\nLC50: 12100mg\/m3<\/sup> (inhaled to mice, 2h)<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
23. Gas phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K-1<\/sup>): 70.98<\/p>\n24. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K– 1<\/sup>): 129.9<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[10]<\/sup><\/strong><\/p>\nLD50: 933mg\/kg (rat oral); 414mg\/kg (rat intraperitoneal ); 1072mg\/kg (orally administered to mice)<\/p>\nLC50: 12100mg\/m3<\/sup> (inhaled to mice, 2h)<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
24. Liquid phase standard hot melt (J\u00b7mol-1<\/sup>\u00b7K– 1<\/sup>): 129.9<\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity[10]<\/sup><\/strong><\/p>\nLD50: 933mg\/kg (rat oral); 414mg\/kg (rat intraperitoneal ); 1072mg\/kg (orally administered to mice)<\/p>\nLC50: 12100mg\/m3<\/sup> (inhaled to mice, 2h)<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
1. Acute toxicity[10]<\/sup><\/strong><\/p>\nLD50: 933mg\/kg (rat oral); 414mg\/kg (rat intraperitoneal ); 1072mg\/kg (orally administered to mice)<\/p>\nLC50: 12100mg\/m3<\/sup> (inhaled to mice, 2h)<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
LD50: 933mg\/kg (rat oral); 414mg\/kg (rat intraperitoneal ); 1072mg\/kg (orally administered to mice)<\/p>\n
LC50: 12100mg\/m3<\/sup> (inhaled to mice, 2h)<\/p>\n2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
2. Irritation<\/strong> No data available<\/p>\n3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3. Subacute and chronic toxicity [11]<\/sup><\/strong> Rat inhalation 0.25mg\/L, 4 hours a day , 2 months later, abnormal liver and kidney function. <\/p>\n4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
4. Mutagenicity [12]<\/sup><\/strong> Microbial mutagenicity: Salmonella typhimurium 50\u03bcl\/dish. Sister chromatid exchange: human lymphocytes 80 \u03bcmol\/L. DNA damage: human lung 100 \u03bcmol\/L (3h). <\/p>\n5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
5. Teratogenicity[13]<\/sup> <\/strong>Mice were orally administered the lowest toxic dose (TDLo) 200mg\/kg for many generations, causing hepatobiliary and Developmental malformations of the genitourinary system. <\/p>\n6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
6. Carcinogenicity[14]<\/sup><\/strong> IARC Carcinogenicity Comment: G3, insufficient evidence of carcinogenicity to humans and animals. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
1. Ecotoxicity[15]<\/sup><\/strong> LC50: 40.4mg\/L (48h) (medaka)<\/p>\n2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
2. Biology Degradability[16]<\/sup><\/strong><\/p>\nAerobic biodegradation (h): 672~4320<\/p>\nAnaerobic biodegradation (h): 2688 ~17280<\/p>\n3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
Aerobic biodegradation (h): 672~4320<\/p>\n
Anaerobic biodegradation (h): 2688 ~17280<\/p>\n
3. Non-biodegradability[17]<\/sup><\/strong><\/p>\nPhotooxidation half-life in air (h): 1299~ 12989<\/p>\nFirst-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
Photooxidation half-life in air (h): 1299~ 12989<\/p>\n
First-order hydrolysis half-life (h): 6.02\u00d7106<\/sup><\/p>\n4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
4. Bioaccumulation [18]<\/sup><\/strong> BCF: 7.1~21 (carp, exposure concentration 100mg\/L, exposure time 6 weeks); 7.7~19 (carp, exposure concentration 10mg\/L, exposure time 6 weeks)<\/p>\n5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
5. Other harmful effects[19]<\/sup><\/strong> It decomposes when exposed to alkali, but it is a highly persistent compound in water and will not be biodegraded. Especially if it stays in drinking water for a long time, it will cause harm. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 29.83<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
1. Molar refractive index: 29.83<\/p>\n
2. Molar volume (cm3<\/sup>\/mol): 84.9<\/p>\n3. Isotonic specific volume (90.2K ): 225.7<\/p>\n4. Surface tension (dyne\/cm): 49.8<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3. Isotonic specific volume (90.2K ): 225.7<\/p>\n
4. Surface tension (dyne\/cm): 49.8<\/p>\n
5. Polarizability (10-24<\/sup>cm3<\/sup>): 11.82<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n2. Number of hydrogen bond donors: 0<\/p>\n3. Number of hydrogen bond acceptors: 0<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 0<\/p>\n7. Number of heavy atoms: 4<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 8<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
1. Reference value for hydrophobic parameter calculation (XlogP): 2.8<\/P><\/p>\n
2. Number of hydrogen bond donors: 0<\/p>\n
3. Number of hydrogen bond acceptors: 0<\/p>\n
4. Number of rotatable chemical bonds: 0<\/p>\n
5. Number of tautomers: none<\/p>\n
6. Topological molecule polar surface area 0<\/p>\n
7. Number of heavy atoms: 4<\/p>\n
8. Surface charge: 0<\/p>\n
9. Complexity: 8<\/p>\n
10. Number of isotope atoms: 0<\/p>\n
11. Determine the number of atomic stereocenters: 0<\/p>\n
12. Uncertain number of atomic stereocenters: 0<\/p>\n
13. Determine the number of chemical bond stereocenters: 0 <\/p>\n
14. Number of uncertain chemical bond stereocenters: 0<\/p>\n
15. Number of covalent bond units: 1<\/p>\n<\/p>\n
1. Stability[20]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
2. Incompatible substances[21]<\/sup> <\/strong> Strong oxidants, active metal powders<\/p>\n3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3. Conditions to avoid contact[22]<\/sup><\/strong> Light<\/p>\n4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
4.Polymerization hazard[23]<\/sup><\/strong> No polymerization<\/p>\n5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
5. Diversity products[24]<\/sup><\/strong> Bromine Hydrogen<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
Storage Precautions[25]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 32\u00b0C and the relative humidity does not exceed 80%. Keep container tightly sealed. They should be stored separately from oxidants, active metal powders, and food chemicals, and avoid mixed storage. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/span><\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\nPurpose<\/h2>\n1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
1. Under alkaline conditions, acetone reacts with sodium hypobromite to obtain tribromoacetone, which will continue to decompose under alkaline conditions to obtain crude product. After distillation, washing, filtering and drying, the finished product is obtained. <\/p>\n<\/p>\n
1. It can be used as dye intermediates, disinfectants, analgesics, anesthetics, refrigerants, mineral processing agents, precipitants, solvents and anti-explosion liquid components. <\/p>\n
2. Used as solvent, refractive index liquid and specific gravity liquid. <\/p>\n
3. Used as solvent and organic synthesis intermediate. [26]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
extended-reading:https:\/\/www.bdmaee.net\/nt-cat-a-240-catalyst-cas1739-84-0-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/38895<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-bl-13-niax-catalyst-a-133-niax-a-133\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1909<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/low-odor-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/808<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44944<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44658<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/30.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01JA Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":49341,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15448],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342"}],"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=49342"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/49342\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/49341"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=49342"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=49342"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=49342"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
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<\/p>\n<\/p>\n![\"\"](\"http:\/\/www.newtopchem.com\/wp-content\/uploads\/2024\/05\/201008311532028524.gif\")
<\/p>\n<\/p>\n![https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg<\/a><\/br>extended-reading:](\"https:\/\/www.bdmaee.net\/wp-content\/uploads\/2020\/06\/73.jpg\"){kind=link}
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