<\/p>\n
Structural formula<\/p>\n
m-dimethylaniline,<\/p>\n
2,4-Dimethyl-Benzenemine,<\/p>\n
2,4-Dimethylaniline,<\/p>\n
m-Xylidine<\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n
CAS number:<\/b>95-68-1<\/p>\n
MDL number:<\/b>MFCD00007738<\/p>\n
EINECS number:<\/b>202-440-0<\/p>\n
RTECS number:<\/b>ZE8925000<\/p>\n
BRN number:<\/b>636243<\/p>\n
PubChem number:<\/b>24854443<\/p>\nPhysical property data<\/h2>\n
1. Properties: colorless oily liquid [1]<\/sup><\/p>\n2. Melting point (\u2103): -14.3[2] <\/sup><\/p>\n3. Boiling point (\u2103): 214[3]<\/sup><\/p>\n4. Relative density (water=1): 0.97 [4]<\/sup><\/p>\n5. Relative vapor density (air=1): 4.18[5]<\/sup><\/p>\n6. Saturated vapor pressure (kPa ): 0.05 (38\u2103)[6]<\/sup><\/p>\n7. Octanol\/water partition coefficient: 1.68[7]<\/sup><\/p>\n8. Flash point (\u2103): 90.56[8]<\/sup><\/p>\n9. Ignition temperature (\u2103): 460[9]<\/sup><\/p>\n10. Explosion upper limit (%): 7.0[10]<\/sup><\/p>\n11. Explosion lower limit (%): 1.1[11]<\/sup><\/p>\n12. Solubility: Slightly soluble in water, soluble in ethanol, ether, benzene and other organic solvents. [12]<\/sup><\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity:<\/p>\nOral LD50 in rats: 467mg\/kg; Oral LD50 in mice: 250mg\/kg; Inhalation LC50 in mice: 149ppm\/7H; <\/p>\n2. Other multiple dose toxicity: rat oral TDLo: 1170mg\/kg\/10D-C; rat oral TDLo: 13300mg\/kg\/4W-I;<\/p>\n3. Mutagenicity<\/p>\nMutation of microbial Salmonella typhimurium: 1\u03bcmol\/plate;<\/p>\nDNA synthesis in rat liver: 1\u03bcmol\/L;<\/p>\nTransperitoneal DNA damage in mice: 200mg \/kg;<\/p>\nOral DNA inhibition in mice: 200mg\/kg;<\/p>\n4. Acute toxicity[13]<\/sup> <\/strong> <\/p>\nLD50: 467mg\/kg (rat oral)<\/p>\nLC50: 149ppm (mouse inhalation, 7h)<\/p>\n5. Irritation<\/strong> No data yet<\/p>\n6. Subacute and chronic toxicity [14]<\/sup><\/strong> Rat intragastric doses are 25, 50, 100 and 250mg \/kg for 7 consecutive days, liver weight increased. The dose is 400mg\/kg, 7 days, and the liver weight is seriously damaged. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[15]<\/sup> <\/strong>In air, when the concentration of hydroxyl radicals is 5.00\u00d7105<\/sup>\/cm3<\/sup> When, the degradation half-life is 2h (theoretical). <\/p>\n4. Other harmful effects [16]<\/sup><\/strong> This substance is harmful to the environment, and special attention should be paid to the pollution of water bodies. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 40.13<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 124.2<\/p>\n3. Isotonic specific volume (90.2K ): 308.3<\/p>\n4. Surface tension (dyne\/cm): 37.9<\/p>\n5. Polarizability (10-24cm3): 15.91<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 1<\/p>\n3. Number of hydrogen bond acceptors: 1<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 26<\/p>\n7. Number of heavy atoms: 9<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 90.6<\/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[17]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
2. Melting point (\u2103): -14.3[2] <\/sup><\/p>\n3. Boiling point (\u2103): 214[3]<\/sup><\/p>\n4. Relative density (water=1): 0.97 [4]<\/sup><\/p>\n5. Relative vapor density (air=1): 4.18[5]<\/sup><\/p>\n6. Saturated vapor pressure (kPa ): 0.05 (38\u2103)[6]<\/sup><\/p>\n7. Octanol\/water partition coefficient: 1.68[7]<\/sup><\/p>\n8. Flash point (\u2103): 90.56[8]<\/sup><\/p>\n9. Ignition temperature (\u2103): 460[9]<\/sup><\/p>\n10. Explosion upper limit (%): 7.0[10]<\/sup><\/p>\n11. Explosion lower limit (%): 1.1[11]<\/sup><\/p>\n12. Solubility: Slightly soluble in water, soluble in ethanol, ether, benzene and other organic solvents. [12]<\/sup><\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity:<\/p>\nOral LD50 in rats: 467mg\/kg; Oral LD50 in mice: 250mg\/kg; Inhalation LC50 in mice: 149ppm\/7H; <\/p>\n2. Other multiple dose toxicity: rat oral TDLo: 1170mg\/kg\/10D-C; rat oral TDLo: 13300mg\/kg\/4W-I;<\/p>\n3. Mutagenicity<\/p>\nMutation of microbial Salmonella typhimurium: 1\u03bcmol\/plate;<\/p>\nDNA synthesis in rat liver: 1\u03bcmol\/L;<\/p>\nTransperitoneal DNA damage in mice: 200mg \/kg;<\/p>\nOral DNA inhibition in mice: 200mg\/kg;<\/p>\n4. Acute toxicity[13]<\/sup> <\/strong> <\/p>\nLD50: 467mg\/kg (rat oral)<\/p>\nLC50: 149ppm (mouse inhalation, 7h)<\/p>\n5. Irritation<\/strong> No data yet<\/p>\n6. Subacute and chronic toxicity [14]<\/sup><\/strong> Rat intragastric doses are 25, 50, 100 and 250mg \/kg for 7 consecutive days, liver weight increased. The dose is 400mg\/kg, 7 days, and the liver weight is seriously damaged. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[15]<\/sup> <\/strong>In air, when the concentration of hydroxyl radicals is 5.00\u00d7105<\/sup>\/cm3<\/sup> When, the degradation half-life is 2h (theoretical). <\/p>\n4. Other harmful effects [16]<\/sup><\/strong> This substance is harmful to the environment, and special attention should be paid to the pollution of water bodies. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 40.13<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 124.2<\/p>\n3. Isotonic specific volume (90.2K ): 308.3<\/p>\n4. Surface tension (dyne\/cm): 37.9<\/p>\n5. Polarizability (10-24cm3): 15.91<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 1<\/p>\n3. Number of hydrogen bond acceptors: 1<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 26<\/p>\n7. Number of heavy atoms: 9<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 90.6<\/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[17]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3. Boiling point (\u2103): 214[3]<\/sup><\/p>\n4. Relative density (water=1): 0.97 [4]<\/sup><\/p>\n5. Relative vapor density (air=1): 4.18[5]<\/sup><\/p>\n6. Saturated vapor pressure (kPa ): 0.05 (38\u2103)[6]<\/sup><\/p>\n7. Octanol\/water partition coefficient: 1.68[7]<\/sup><\/p>\n8. Flash point (\u2103): 90.56[8]<\/sup><\/p>\n9. Ignition temperature (\u2103): 460[9]<\/sup><\/p>\n10. Explosion upper limit (%): 7.0[10]<\/sup><\/p>\n11. Explosion lower limit (%): 1.1[11]<\/sup><\/p>\n12. Solubility: Slightly soluble in water, soluble in ethanol, ether, benzene and other organic solvents. [12]<\/sup><\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity:<\/p>\nOral LD50 in rats: 467mg\/kg; Oral LD50 in mice: 250mg\/kg; Inhalation LC50 in mice: 149ppm\/7H; <\/p>\n2. Other multiple dose toxicity: rat oral TDLo: 1170mg\/kg\/10D-C; rat oral TDLo: 13300mg\/kg\/4W-I;<\/p>\n3. Mutagenicity<\/p>\nMutation of microbial Salmonella typhimurium: 1\u03bcmol\/plate;<\/p>\nDNA synthesis in rat liver: 1\u03bcmol\/L;<\/p>\nTransperitoneal DNA damage in mice: 200mg \/kg;<\/p>\nOral DNA inhibition in mice: 200mg\/kg;<\/p>\n4. Acute toxicity[13]<\/sup> <\/strong> <\/p>\nLD50: 467mg\/kg (rat oral)<\/p>\nLC50: 149ppm (mouse inhalation, 7h)<\/p>\n5. Irritation<\/strong> No data yet<\/p>\n6. Subacute and chronic toxicity [14]<\/sup><\/strong> Rat intragastric doses are 25, 50, 100 and 250mg \/kg for 7 consecutive days, liver weight increased. The dose is 400mg\/kg, 7 days, and the liver weight is seriously damaged. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[15]<\/sup> <\/strong>In air, when the concentration of hydroxyl radicals is 5.00\u00d7105<\/sup>\/cm3<\/sup> When, the degradation half-life is 2h (theoretical). <\/p>\n4. Other harmful effects [16]<\/sup><\/strong> This substance is harmful to the environment, and special attention should be paid to the pollution of water bodies. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 40.13<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 124.2<\/p>\n3. Isotonic specific volume (90.2K ): 308.3<\/p>\n4. Surface tension (dyne\/cm): 37.9<\/p>\n5. Polarizability (10-24cm3): 15.91<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 1<\/p>\n3. Number of hydrogen bond acceptors: 1<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 26<\/p>\n7. Number of heavy atoms: 9<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 90.6<\/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[17]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
4. Relative density (water=1): 0.97 [4]<\/sup><\/p>\n5. Relative vapor density (air=1): 4.18[5]<\/sup><\/p>\n6. Saturated vapor pressure (kPa ): 0.05 (38\u2103)[6]<\/sup><\/p>\n7. Octanol\/water partition coefficient: 1.68[7]<\/sup><\/p>\n8. Flash point (\u2103): 90.56[8]<\/sup><\/p>\n9. Ignition temperature (\u2103): 460[9]<\/sup><\/p>\n10. Explosion upper limit (%): 7.0[10]<\/sup><\/p>\n11. Explosion lower limit (%): 1.1[11]<\/sup><\/p>\n12. Solubility: Slightly soluble in water, soluble in ethanol, ether, benzene and other organic solvents. [12]<\/sup><\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity:<\/p>\nOral LD50 in rats: 467mg\/kg; Oral LD50 in mice: 250mg\/kg; Inhalation LC50 in mice: 149ppm\/7H; <\/p>\n2. Other multiple dose toxicity: rat oral TDLo: 1170mg\/kg\/10D-C; rat oral TDLo: 13300mg\/kg\/4W-I;<\/p>\n3. Mutagenicity<\/p>\nMutation of microbial Salmonella typhimurium: 1\u03bcmol\/plate;<\/p>\nDNA synthesis in rat liver: 1\u03bcmol\/L;<\/p>\nTransperitoneal DNA damage in mice: 200mg \/kg;<\/p>\nOral DNA inhibition in mice: 200mg\/kg;<\/p>\n4. Acute toxicity[13]<\/sup> <\/strong> <\/p>\nLD50: 467mg\/kg (rat oral)<\/p>\nLC50: 149ppm (mouse inhalation, 7h)<\/p>\n5. Irritation<\/strong> No data yet<\/p>\n6. Subacute and chronic toxicity [14]<\/sup><\/strong> Rat intragastric doses are 25, 50, 100 and 250mg \/kg for 7 consecutive days, liver weight increased. The dose is 400mg\/kg, 7 days, and the liver weight is seriously damaged. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[15]<\/sup> <\/strong>In air, when the concentration of hydroxyl radicals is 5.00\u00d7105<\/sup>\/cm3<\/sup> When, the degradation half-life is 2h (theoretical). <\/p>\n4. Other harmful effects [16]<\/sup><\/strong> This substance is harmful to the environment, and special attention should be paid to the pollution of water bodies. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 40.13<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 124.2<\/p>\n3. Isotonic specific volume (90.2K ): 308.3<\/p>\n4. Surface tension (dyne\/cm): 37.9<\/p>\n5. Polarizability (10-24cm3): 15.91<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 1<\/p>\n3. Number of hydrogen bond acceptors: 1<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 26<\/p>\n7. Number of heavy atoms: 9<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 90.6<\/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[17]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
5. Relative vapor density (air=1): 4.18[5]<\/sup><\/p>\n6. Saturated vapor pressure (kPa ): 0.05 (38\u2103)[6]<\/sup><\/p>\n7. Octanol\/water partition coefficient: 1.68[7]<\/sup><\/p>\n8. Flash point (\u2103): 90.56[8]<\/sup><\/p>\n9. Ignition temperature (\u2103): 460[9]<\/sup><\/p>\n10. Explosion upper limit (%): 7.0[10]<\/sup><\/p>\n11. Explosion lower limit (%): 1.1[11]<\/sup><\/p>\n12. Solubility: Slightly soluble in water, soluble in ethanol, ether, benzene and other organic solvents. [12]<\/sup><\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity:<\/p>\nOral LD50 in rats: 467mg\/kg; Oral LD50 in mice: 250mg\/kg; Inhalation LC50 in mice: 149ppm\/7H; <\/p>\n2. Other multiple dose toxicity: rat oral TDLo: 1170mg\/kg\/10D-C; rat oral TDLo: 13300mg\/kg\/4W-I;<\/p>\n3. Mutagenicity<\/p>\nMutation of microbial Salmonella typhimurium: 1\u03bcmol\/plate;<\/p>\nDNA synthesis in rat liver: 1\u03bcmol\/L;<\/p>\nTransperitoneal DNA damage in mice: 200mg \/kg;<\/p>\nOral DNA inhibition in mice: 200mg\/kg;<\/p>\n4. Acute toxicity[13]<\/sup> <\/strong> <\/p>\nLD50: 467mg\/kg (rat oral)<\/p>\nLC50: 149ppm (mouse inhalation, 7h)<\/p>\n5. Irritation<\/strong> No data yet<\/p>\n6. Subacute and chronic toxicity [14]<\/sup><\/strong> Rat intragastric doses are 25, 50, 100 and 250mg \/kg for 7 consecutive days, liver weight increased. The dose is 400mg\/kg, 7 days, and the liver weight is seriously damaged. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[15]<\/sup> <\/strong>In air, when the concentration of hydroxyl radicals is 5.00\u00d7105<\/sup>\/cm3<\/sup> When, the degradation half-life is 2h (theoretical). <\/p>\n4. Other harmful effects [16]<\/sup><\/strong> This substance is harmful to the environment, and special attention should be paid to the pollution of water bodies. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 40.13<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 124.2<\/p>\n3. Isotonic specific volume (90.2K ): 308.3<\/p>\n4. Surface tension (dyne\/cm): 37.9<\/p>\n5. Polarizability (10-24cm3): 15.91<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 1<\/p>\n3. Number of hydrogen bond acceptors: 1<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 26<\/p>\n7. Number of heavy atoms: 9<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 90.6<\/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[17]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
6. Saturated vapor pressure (kPa ): 0.05 (38\u2103)[6]<\/sup><\/p>\n7. Octanol\/water partition coefficient: 1.68[7]<\/sup><\/p>\n8. Flash point (\u2103): 90.56[8]<\/sup><\/p>\n9. Ignition temperature (\u2103): 460[9]<\/sup><\/p>\n10. Explosion upper limit (%): 7.0[10]<\/sup><\/p>\n11. Explosion lower limit (%): 1.1[11]<\/sup><\/p>\n12. Solubility: Slightly soluble in water, soluble in ethanol, ether, benzene and other organic solvents. [12]<\/sup><\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity:<\/p>\nOral LD50 in rats: 467mg\/kg; Oral LD50 in mice: 250mg\/kg; Inhalation LC50 in mice: 149ppm\/7H; <\/p>\n2. Other multiple dose toxicity: rat oral TDLo: 1170mg\/kg\/10D-C; rat oral TDLo: 13300mg\/kg\/4W-I;<\/p>\n3. Mutagenicity<\/p>\nMutation of microbial Salmonella typhimurium: 1\u03bcmol\/plate;<\/p>\nDNA synthesis in rat liver: 1\u03bcmol\/L;<\/p>\nTransperitoneal DNA damage in mice: 200mg \/kg;<\/p>\nOral DNA inhibition in mice: 200mg\/kg;<\/p>\n4. Acute toxicity[13]<\/sup> <\/strong> <\/p>\nLD50: 467mg\/kg (rat oral)<\/p>\nLC50: 149ppm (mouse inhalation, 7h)<\/p>\n5. Irritation<\/strong> No data yet<\/p>\n6. Subacute and chronic toxicity [14]<\/sup><\/strong> Rat intragastric doses are 25, 50, 100 and 250mg \/kg for 7 consecutive days, liver weight increased. The dose is 400mg\/kg, 7 days, and the liver weight is seriously damaged. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[15]<\/sup> <\/strong>In air, when the concentration of hydroxyl radicals is 5.00\u00d7105<\/sup>\/cm3<\/sup> When, the degradation half-life is 2h (theoretical). <\/p>\n4. Other harmful effects [16]<\/sup><\/strong> This substance is harmful to the environment, and special attention should be paid to the pollution of water bodies. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 40.13<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 124.2<\/p>\n3. Isotonic specific volume (90.2K ): 308.3<\/p>\n4. Surface tension (dyne\/cm): 37.9<\/p>\n5. Polarizability (10-24cm3): 15.91<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 1<\/p>\n3. Number of hydrogen bond acceptors: 1<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 26<\/p>\n7. Number of heavy atoms: 9<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 90.6<\/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[17]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
7. Octanol\/water partition coefficient: 1.68[7]<\/sup><\/p>\n8. Flash point (\u2103): 90.56[8]<\/sup><\/p>\n9. Ignition temperature (\u2103): 460[9]<\/sup><\/p>\n10. Explosion upper limit (%): 7.0[10]<\/sup><\/p>\n11. Explosion lower limit (%): 1.1[11]<\/sup><\/p>\n12. Solubility: Slightly soluble in water, soluble in ethanol, ether, benzene and other organic solvents. [12]<\/sup><\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity:<\/p>\nOral LD50 in rats: 467mg\/kg; Oral LD50 in mice: 250mg\/kg; Inhalation LC50 in mice: 149ppm\/7H; <\/p>\n2. Other multiple dose toxicity: rat oral TDLo: 1170mg\/kg\/10D-C; rat oral TDLo: 13300mg\/kg\/4W-I;<\/p>\n3. Mutagenicity<\/p>\nMutation of microbial Salmonella typhimurium: 1\u03bcmol\/plate;<\/p>\nDNA synthesis in rat liver: 1\u03bcmol\/L;<\/p>\nTransperitoneal DNA damage in mice: 200mg \/kg;<\/p>\nOral DNA inhibition in mice: 200mg\/kg;<\/p>\n4. Acute toxicity[13]<\/sup> <\/strong> <\/p>\nLD50: 467mg\/kg (rat oral)<\/p>\nLC50: 149ppm (mouse inhalation, 7h)<\/p>\n5. Irritation<\/strong> No data yet<\/p>\n6. Subacute and chronic toxicity [14]<\/sup><\/strong> Rat intragastric doses are 25, 50, 100 and 250mg \/kg for 7 consecutive days, liver weight increased. The dose is 400mg\/kg, 7 days, and the liver weight is seriously damaged. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[15]<\/sup> <\/strong>In air, when the concentration of hydroxyl radicals is 5.00\u00d7105<\/sup>\/cm3<\/sup> When, the degradation half-life is 2h (theoretical). <\/p>\n4. Other harmful effects [16]<\/sup><\/strong> This substance is harmful to the environment, and special attention should be paid to the pollution of water bodies. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 40.13<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 124.2<\/p>\n3. Isotonic specific volume (90.2K ): 308.3<\/p>\n4. Surface tension (dyne\/cm): 37.9<\/p>\n5. Polarizability (10-24cm3): 15.91<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 1<\/p>\n3. Number of hydrogen bond acceptors: 1<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 26<\/p>\n7. Number of heavy atoms: 9<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 90.6<\/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[17]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
8. Flash point (\u2103): 90.56[8]<\/sup><\/p>\n9. Ignition temperature (\u2103): 460[9]<\/sup><\/p>\n10. Explosion upper limit (%): 7.0[10]<\/sup><\/p>\n11. Explosion lower limit (%): 1.1[11]<\/sup><\/p>\n12. Solubility: Slightly soluble in water, soluble in ethanol, ether, benzene and other organic solvents. [12]<\/sup><\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity:<\/p>\nOral LD50 in rats: 467mg\/kg; Oral LD50 in mice: 250mg\/kg; Inhalation LC50 in mice: 149ppm\/7H; <\/p>\n2. Other multiple dose toxicity: rat oral TDLo: 1170mg\/kg\/10D-C; rat oral TDLo: 13300mg\/kg\/4W-I;<\/p>\n3. Mutagenicity<\/p>\nMutation of microbial Salmonella typhimurium: 1\u03bcmol\/plate;<\/p>\nDNA synthesis in rat liver: 1\u03bcmol\/L;<\/p>\nTransperitoneal DNA damage in mice: 200mg \/kg;<\/p>\nOral DNA inhibition in mice: 200mg\/kg;<\/p>\n4. Acute toxicity[13]<\/sup> <\/strong> <\/p>\nLD50: 467mg\/kg (rat oral)<\/p>\nLC50: 149ppm (mouse inhalation, 7h)<\/p>\n5. Irritation<\/strong> No data yet<\/p>\n6. Subacute and chronic toxicity [14]<\/sup><\/strong> Rat intragastric doses are 25, 50, 100 and 250mg \/kg for 7 consecutive days, liver weight increased. The dose is 400mg\/kg, 7 days, and the liver weight is seriously damaged. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[15]<\/sup> <\/strong>In air, when the concentration of hydroxyl radicals is 5.00\u00d7105<\/sup>\/cm3<\/sup> When, the degradation half-life is 2h (theoretical). <\/p>\n4. Other harmful effects [16]<\/sup><\/strong> This substance is harmful to the environment, and special attention should be paid to the pollution of water bodies. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 40.13<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 124.2<\/p>\n3. Isotonic specific volume (90.2K ): 308.3<\/p>\n4. Surface tension (dyne\/cm): 37.9<\/p>\n5. Polarizability (10-24cm3): 15.91<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 1<\/p>\n3. Number of hydrogen bond acceptors: 1<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 26<\/p>\n7. Number of heavy atoms: 9<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 90.6<\/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[17]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
9. Ignition temperature (\u2103): 460[9]<\/sup><\/p>\n10. Explosion upper limit (%): 7.0[10]<\/sup><\/p>\n11. Explosion lower limit (%): 1.1[11]<\/sup><\/p>\n12. Solubility: Slightly soluble in water, soluble in ethanol, ether, benzene and other organic solvents. [12]<\/sup><\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity:<\/p>\nOral LD50 in rats: 467mg\/kg; Oral LD50 in mice: 250mg\/kg; Inhalation LC50 in mice: 149ppm\/7H; <\/p>\n2. Other multiple dose toxicity: rat oral TDLo: 1170mg\/kg\/10D-C; rat oral TDLo: 13300mg\/kg\/4W-I;<\/p>\n3. Mutagenicity<\/p>\nMutation of microbial Salmonella typhimurium: 1\u03bcmol\/plate;<\/p>\nDNA synthesis in rat liver: 1\u03bcmol\/L;<\/p>\nTransperitoneal DNA damage in mice: 200mg \/kg;<\/p>\nOral DNA inhibition in mice: 200mg\/kg;<\/p>\n4. Acute toxicity[13]<\/sup> <\/strong> <\/p>\nLD50: 467mg\/kg (rat oral)<\/p>\nLC50: 149ppm (mouse inhalation, 7h)<\/p>\n5. Irritation<\/strong> No data yet<\/p>\n6. Subacute and chronic toxicity [14]<\/sup><\/strong> Rat intragastric doses are 25, 50, 100 and 250mg \/kg for 7 consecutive days, liver weight increased. The dose is 400mg\/kg, 7 days, and the liver weight is seriously damaged. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[15]<\/sup> <\/strong>In air, when the concentration of hydroxyl radicals is 5.00\u00d7105<\/sup>\/cm3<\/sup> When, the degradation half-life is 2h (theoretical). <\/p>\n4. Other harmful effects [16]<\/sup><\/strong> This substance is harmful to the environment, and special attention should be paid to the pollution of water bodies. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 40.13<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 124.2<\/p>\n3. Isotonic specific volume (90.2K ): 308.3<\/p>\n4. Surface tension (dyne\/cm): 37.9<\/p>\n5. Polarizability (10-24cm3): 15.91<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 1<\/p>\n3. Number of hydrogen bond acceptors: 1<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 26<\/p>\n7. Number of heavy atoms: 9<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 90.6<\/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[17]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
10. Explosion upper limit (%): 7.0[10]<\/sup><\/p>\n11. Explosion lower limit (%): 1.1[11]<\/sup><\/p>\n12. Solubility: Slightly soluble in water, soluble in ethanol, ether, benzene and other organic solvents. [12]<\/sup><\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity:<\/p>\nOral LD50 in rats: 467mg\/kg; Oral LD50 in mice: 250mg\/kg; Inhalation LC50 in mice: 149ppm\/7H; <\/p>\n2. Other multiple dose toxicity: rat oral TDLo: 1170mg\/kg\/10D-C; rat oral TDLo: 13300mg\/kg\/4W-I;<\/p>\n3. Mutagenicity<\/p>\nMutation of microbial Salmonella typhimurium: 1\u03bcmol\/plate;<\/p>\nDNA synthesis in rat liver: 1\u03bcmol\/L;<\/p>\nTransperitoneal DNA damage in mice: 200mg \/kg;<\/p>\nOral DNA inhibition in mice: 200mg\/kg;<\/p>\n4. Acute toxicity[13]<\/sup> <\/strong> <\/p>\nLD50: 467mg\/kg (rat oral)<\/p>\nLC50: 149ppm (mouse inhalation, 7h)<\/p>\n5. Irritation<\/strong> No data yet<\/p>\n6. Subacute and chronic toxicity [14]<\/sup><\/strong> Rat intragastric doses are 25, 50, 100 and 250mg \/kg for 7 consecutive days, liver weight increased. The dose is 400mg\/kg, 7 days, and the liver weight is seriously damaged. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[15]<\/sup> <\/strong>In air, when the concentration of hydroxyl radicals is 5.00\u00d7105<\/sup>\/cm3<\/sup> When, the degradation half-life is 2h (theoretical). <\/p>\n4. Other harmful effects [16]<\/sup><\/strong> This substance is harmful to the environment, and special attention should be paid to the pollution of water bodies. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 40.13<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 124.2<\/p>\n3. Isotonic specific volume (90.2K ): 308.3<\/p>\n4. Surface tension (dyne\/cm): 37.9<\/p>\n5. Polarizability (10-24cm3): 15.91<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 1<\/p>\n3. Number of hydrogen bond acceptors: 1<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 26<\/p>\n7. Number of heavy atoms: 9<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 90.6<\/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[17]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
11. Explosion lower limit (%): 1.1[11]<\/sup><\/p>\n12. Solubility: Slightly soluble in water, soluble in ethanol, ether, benzene and other organic solvents. [12]<\/sup><\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity:<\/p>\nOral LD50 in rats: 467mg\/kg; Oral LD50 in mice: 250mg\/kg; Inhalation LC50 in mice: 149ppm\/7H; <\/p>\n2. Other multiple dose toxicity: rat oral TDLo: 1170mg\/kg\/10D-C; rat oral TDLo: 13300mg\/kg\/4W-I;<\/p>\n3. Mutagenicity<\/p>\nMutation of microbial Salmonella typhimurium: 1\u03bcmol\/plate;<\/p>\nDNA synthesis in rat liver: 1\u03bcmol\/L;<\/p>\nTransperitoneal DNA damage in mice: 200mg \/kg;<\/p>\nOral DNA inhibition in mice: 200mg\/kg;<\/p>\n4. Acute toxicity[13]<\/sup> <\/strong> <\/p>\nLD50: 467mg\/kg (rat oral)<\/p>\nLC50: 149ppm (mouse inhalation, 7h)<\/p>\n5. Irritation<\/strong> No data yet<\/p>\n6. Subacute and chronic toxicity [14]<\/sup><\/strong> Rat intragastric doses are 25, 50, 100 and 250mg \/kg for 7 consecutive days, liver weight increased. The dose is 400mg\/kg, 7 days, and the liver weight is seriously damaged. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[15]<\/sup> <\/strong>In air, when the concentration of hydroxyl radicals is 5.00\u00d7105<\/sup>\/cm3<\/sup> When, the degradation half-life is 2h (theoretical). <\/p>\n4. Other harmful effects [16]<\/sup><\/strong> This substance is harmful to the environment, and special attention should be paid to the pollution of water bodies. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 40.13<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 124.2<\/p>\n3. Isotonic specific volume (90.2K ): 308.3<\/p>\n4. Surface tension (dyne\/cm): 37.9<\/p>\n5. Polarizability (10-24cm3): 15.91<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 1<\/p>\n3. Number of hydrogen bond acceptors: 1<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 26<\/p>\n7. Number of heavy atoms: 9<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 90.6<\/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[17]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
12. Solubility: Slightly soluble in water, soluble in ethanol, ether, benzene and other organic solvents. [12]<\/sup><\/p>\n<\/p>\nToxicological data<\/h2>\n1. Acute toxicity:<\/p>\nOral LD50 in rats: 467mg\/kg; Oral LD50 in mice: 250mg\/kg; Inhalation LC50 in mice: 149ppm\/7H; <\/p>\n2. Other multiple dose toxicity: rat oral TDLo: 1170mg\/kg\/10D-C; rat oral TDLo: 13300mg\/kg\/4W-I;<\/p>\n3. Mutagenicity<\/p>\nMutation of microbial Salmonella typhimurium: 1\u03bcmol\/plate;<\/p>\nDNA synthesis in rat liver: 1\u03bcmol\/L;<\/p>\nTransperitoneal DNA damage in mice: 200mg \/kg;<\/p>\nOral DNA inhibition in mice: 200mg\/kg;<\/p>\n4. Acute toxicity[13]<\/sup> <\/strong> <\/p>\nLD50: 467mg\/kg (rat oral)<\/p>\nLC50: 149ppm (mouse inhalation, 7h)<\/p>\n5. Irritation<\/strong> No data yet<\/p>\n6. Subacute and chronic toxicity [14]<\/sup><\/strong> Rat intragastric doses are 25, 50, 100 and 250mg \/kg for 7 consecutive days, liver weight increased. The dose is 400mg\/kg, 7 days, and the liver weight is seriously damaged. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[15]<\/sup> <\/strong>In air, when the concentration of hydroxyl radicals is 5.00\u00d7105<\/sup>\/cm3<\/sup> When, the degradation half-life is 2h (theoretical). <\/p>\n4. Other harmful effects [16]<\/sup><\/strong> This substance is harmful to the environment, and special attention should be paid to the pollution of water bodies. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 40.13<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 124.2<\/p>\n3. Isotonic specific volume (90.2K ): 308.3<\/p>\n4. Surface tension (dyne\/cm): 37.9<\/p>\n5. Polarizability (10-24cm3): 15.91<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 1<\/p>\n3. Number of hydrogen bond acceptors: 1<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 26<\/p>\n7. Number of heavy atoms: 9<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 90.6<\/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[17]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
1. Acute toxicity:<\/p>\n
Oral LD50 in rats: 467mg\/kg; Oral LD50 in mice: 250mg\/kg; Inhalation LC50 in mice: 149ppm\/7H; <\/p>\n
2. Other multiple dose toxicity: rat oral TDLo: 1170mg\/kg\/10D-C; rat oral TDLo: 13300mg\/kg\/4W-I;<\/p>\n
3. Mutagenicity<\/p>\n
Mutation of microbial Salmonella typhimurium: 1\u03bcmol\/plate;<\/p>\n
DNA synthesis in rat liver: 1\u03bcmol\/L;<\/p>\n
Transperitoneal DNA damage in mice: 200mg \/kg;<\/p>\n
Oral DNA inhibition in mice: 200mg\/kg;<\/p>\n
4. Acute toxicity[13]<\/sup> <\/strong> <\/p>\nLD50: 467mg\/kg (rat oral)<\/p>\nLC50: 149ppm (mouse inhalation, 7h)<\/p>\n5. Irritation<\/strong> No data yet<\/p>\n6. Subacute and chronic toxicity [14]<\/sup><\/strong> Rat intragastric doses are 25, 50, 100 and 250mg \/kg for 7 consecutive days, liver weight increased. The dose is 400mg\/kg, 7 days, and the liver weight is seriously damaged. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[15]<\/sup> <\/strong>In air, when the concentration of hydroxyl radicals is 5.00\u00d7105<\/sup>\/cm3<\/sup> When, the degradation half-life is 2h (theoretical). <\/p>\n4. Other harmful effects [16]<\/sup><\/strong> This substance is harmful to the environment, and special attention should be paid to the pollution of water bodies. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 40.13<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 124.2<\/p>\n3. Isotonic specific volume (90.2K ): 308.3<\/p>\n4. Surface tension (dyne\/cm): 37.9<\/p>\n5. Polarizability (10-24cm3): 15.91<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 1<\/p>\n3. Number of hydrogen bond acceptors: 1<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 26<\/p>\n7. Number of heavy atoms: 9<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 90.6<\/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[17]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
LD50: 467mg\/kg (rat oral)<\/p>\n
LC50: 149ppm (mouse inhalation, 7h)<\/p>\n
5. Irritation<\/strong> No data yet<\/p>\n6. Subacute and chronic toxicity [14]<\/sup><\/strong> Rat intragastric doses are 25, 50, 100 and 250mg \/kg for 7 consecutive days, liver weight increased. The dose is 400mg\/kg, 7 days, and the liver weight is seriously damaged. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[15]<\/sup> <\/strong>In air, when the concentration of hydroxyl radicals is 5.00\u00d7105<\/sup>\/cm3<\/sup> When, the degradation half-life is 2h (theoretical). <\/p>\n4. Other harmful effects [16]<\/sup><\/strong> This substance is harmful to the environment, and special attention should be paid to the pollution of water bodies. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 40.13<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 124.2<\/p>\n3. Isotonic specific volume (90.2K ): 308.3<\/p>\n4. Surface tension (dyne\/cm): 37.9<\/p>\n5. Polarizability (10-24cm3): 15.91<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 1<\/p>\n3. Number of hydrogen bond acceptors: 1<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 26<\/p>\n7. Number of heavy atoms: 9<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 90.6<\/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[17]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
6. Subacute and chronic toxicity [14]<\/sup><\/strong> Rat intragastric doses are 25, 50, 100 and 250mg \/kg for 7 consecutive days, liver weight increased. The dose is 400mg\/kg, 7 days, and the liver weight is seriously damaged. <\/p>\n<\/p>\nEcological data<\/h2>\n1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[15]<\/sup> <\/strong>In air, when the concentration of hydroxyl radicals is 5.00\u00d7105<\/sup>\/cm3<\/sup> When, the degradation half-life is 2h (theoretical). <\/p>\n4. Other harmful effects [16]<\/sup><\/strong> This substance is harmful to the environment, and special attention should be paid to the pollution of water bodies. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 40.13<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 124.2<\/p>\n3. Isotonic specific volume (90.2K ): 308.3<\/p>\n4. Surface tension (dyne\/cm): 37.9<\/p>\n5. Polarizability (10-24cm3): 15.91<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 1<\/p>\n3. Number of hydrogen bond acceptors: 1<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 26<\/p>\n7. Number of heavy atoms: 9<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 90.6<\/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[17]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
1. Ecotoxicity<\/strong> No data available<\/p>\n2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[15]<\/sup> <\/strong>In air, when the concentration of hydroxyl radicals is 5.00\u00d7105<\/sup>\/cm3<\/sup> When, the degradation half-life is 2h (theoretical). <\/p>\n4. Other harmful effects [16]<\/sup><\/strong> This substance is harmful to the environment, and special attention should be paid to the pollution of water bodies. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 40.13<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 124.2<\/p>\n3. Isotonic specific volume (90.2K ): 308.3<\/p>\n4. Surface tension (dyne\/cm): 37.9<\/p>\n5. Polarizability (10-24cm3): 15.91<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 1<\/p>\n3. Number of hydrogen bond acceptors: 1<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 26<\/p>\n7. Number of heavy atoms: 9<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 90.6<\/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[17]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
2. Biodegradability<\/strong> No data available<\/p>\n3 .Non-biodegradability[15]<\/sup> <\/strong>In air, when the concentration of hydroxyl radicals is 5.00\u00d7105<\/sup>\/cm3<\/sup> When, the degradation half-life is 2h (theoretical). <\/p>\n4. Other harmful effects [16]<\/sup><\/strong> This substance is harmful to the environment, and special attention should be paid to the pollution of water bodies. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 40.13<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 124.2<\/p>\n3. Isotonic specific volume (90.2K ): 308.3<\/p>\n4. Surface tension (dyne\/cm): 37.9<\/p>\n5. Polarizability (10-24cm3): 15.91<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 1<\/p>\n3. Number of hydrogen bond acceptors: 1<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 26<\/p>\n7. Number of heavy atoms: 9<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 90.6<\/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[17]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3 .Non-biodegradability[15]<\/sup> <\/strong>In air, when the concentration of hydroxyl radicals is 5.00\u00d7105<\/sup>\/cm3<\/sup> When, the degradation half-life is 2h (theoretical). <\/p>\n4. Other harmful effects [16]<\/sup><\/strong> This substance is harmful to the environment, and special attention should be paid to the pollution of water bodies. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 40.13<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 124.2<\/p>\n3. Isotonic specific volume (90.2K ): 308.3<\/p>\n4. Surface tension (dyne\/cm): 37.9<\/p>\n5. Polarizability (10-24cm3): 15.91<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 1<\/p>\n3. Number of hydrogen bond acceptors: 1<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 26<\/p>\n7. Number of heavy atoms: 9<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 90.6<\/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[17]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
4. Other harmful effects [16]<\/sup><\/strong> This substance is harmful to the environment, and special attention should be paid to the pollution of water bodies. <\/p>\n<\/p>\nMolecular structure data<\/h2>\n1. Molar refractive index: 40.13<\/p>\n2. Molar volume (cm3<\/sup>\/mol): 124.2<\/p>\n3. Isotonic specific volume (90.2K ): 308.3<\/p>\n4. Surface tension (dyne\/cm): 37.9<\/p>\n5. Polarizability (10-24cm3): 15.91<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 1<\/p>\n3. Number of hydrogen bond acceptors: 1<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 26<\/p>\n7. Number of heavy atoms: 9<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 90.6<\/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[17]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
1. Molar refractive index: 40.13<\/p>\n
2. Molar volume (cm3<\/sup>\/mol): 124.2<\/p>\n3. Isotonic specific volume (90.2K ): 308.3<\/p>\n4. Surface tension (dyne\/cm): 37.9<\/p>\n5. Polarizability (10-24cm3): 15.91<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 1<\/p>\n3. Number of hydrogen bond acceptors: 1<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: none<\/p>\n6. Topological molecule polar surface area 26<\/p>\n7. Number of heavy atoms: 9<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 90.6<\/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[17]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3. Isotonic specific volume (90.2K ): 308.3<\/p>\n
4. Surface tension (dyne\/cm): 37.9<\/p>\n
5. Polarizability (10-24cm3): 15.91<\/p>\n<\/p>\n
1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n
2. Number of hydrogen bond donors: 1<\/p>\n
3. Number of hydrogen bond acceptors: 1<\/p>\n
4. Number of rotatable chemical bonds: 0<\/p>\n
5. Number of tautomers: none<\/p>\n
6. Topological molecule polar surface area 26<\/p>\n
7. Number of heavy atoms: 9<\/p>\n
8. Surface charge: 0<\/p>\n
9. Complexity: 90.6<\/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[17]<\/sup><\/strong> Stable<\/p>\n2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
2. Incompatible substances[18]<\/sup> <\/strong> Acids, acid chlorides, acid anhydrides, strong oxidants, chloroform, halogens<\/p>\n3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3. Conditions to avoid contact[19]<\/sup><\/strong> Heating<\/p>\n4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
4. Hazards of aggregation[20]<\/sup><\/strong> No aggregation<\/p>\n<\/p>\nStorage method<\/h2>\nStorage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
Storage Precautions[21]<\/sup><\/strong> Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Keep container tightly sealed. They should be stored separately from oxidants, acids, halogens, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\nPurpose<\/h2>\n1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
1. Prepared from m-xylene through nitration and reduction. <\/p>\n<\/p>\n
1. Used as analytical reagents to produce dyes. [22]<\/sup><\/p>\n<\/p>\n extended-reading:https:\/\/www.cyclohexylamine.net\/category\/product\/page\/18\/<\/a><\/br>extended-reading:https:\/\/www.cyclohexylamine.net\/dibutyl-stannane-diacetate-bis-acetoxy-dibutyl-stannane\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/152<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/22.jpg<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/5392\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/high-rebound-delayed-catalyst-c-225\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/high-efficiency-amine-catalyst-dabco-amine-catalyst\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/-17-PC-Amine-MA-190-amine-balance-catalyst.pdf<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/1845<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/cas-870-08-6\/<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 029K Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48470,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,11324],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471"}],"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=48471"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48471\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48470"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48471"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48471"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48471"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
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