<\/p>\n
Structural formula<\/p>\n
1-Aminoanthraquinone,<\/p>\n
\u03b1-Aminoanthraquinone,<\/p>\n
1-Amino-9,10-anthracenedione,<\/p>\n
Aromatic nitrogen-containing compounds and their derivatives<\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n
CAS number:<\/b>82-45-1<\/p>\n
MDL number:<\/b>MFCD00001213<\/p>\n
EINECS number:<\/b>201-423-5<\/p>\n
RTECS number:<\/b>CB5075000<\/p>\n
BRN number:<\/b>396360<\/p>\n
PubChem number:<\/b>24890825<\/p>\nPhysical property data<\/h2>\n
1. Properties: ruby \u200b\u200bred crystal. <\/p>\n
2. Density (g\/mL, 25\/4\u2103): Undetermined<\/p>\n
3. Relative vapor density (g\/mL, air=1): Undetermined<\/p>\n
4. Melting point (\u00baC): 253~254<\/p>\n
5. Boiling point (\u00baC, normal pressure): Undetermined<\/p>\n
6. Boiling point (\u00baC, 5.2kPa): Undetermined<\/p>\n
7. Refractive index: Undetermined<\/p>\n
8. Flash point (\u00baC): Undetermined<\/p>\n
9. Specific rotation (\u00ba): Undetermined Determined<\/p>\n
10. Autoignition point or ignition temperature (\u00baC): Not determined<\/p>\n
11. Vapor pressure (kPa, 25\u00baC): Not determined<\/p>\n
12. Saturated vapor pressure (kPa, 60\u00baC): Undetermined<\/p>\n
13. Heat of combustion (KJ\/mol): Undetermined<\/p>\n
14. Critical temperature (\u00baC): Undetermined<\/p>\n
15. Critical pressure (KPa): Undetermined<\/p>\n
16. Log value of oil-water (octanol\/water) partition coefficient: Undetermined<\/p>\n
17. Explosion upper limit ( %, V\/V): Undetermined<\/p>\n
18. Lower explosion limit (%, V\/V): Undetermined<\/p>\n
19. Solubility: Easily soluble in ethanol, benzene, and chloroform , ether, glacial acetic acid, hot nitrobenzene and hydrochloric acid, almost insoluble in water. Slightly soluble in ethanol. <\/p>\n<\/p>\n
1. Acute toxicity:<\/p>\n
Rat abdominal LD50: 1500 mg\/kg; Rat LDL0: 600 mg\/kg;<\/p>\n
Mouse caliber LD: >10 gm\/ kg; rat abdominal cavity LD50: 6020mg\/kg; <\/p>\n
2. Oncogenicity: rat caliber TDL0: 2400 mg\/kg\/60W-I; rat caliber TD: 3000 mg\/kg\/60W-I ;<\/p>\n
3. Teratogenicity: mice: 250 mg\/kg<\/p>\n<\/p>\n
\n None\n <\/p>\n
5. Molecular property data:<\/p>\n
1. Molar refractive index: 62.90<\/p>\n
2. Molar volume (cm3<\/sup>\/mol): 161.3<\/p>\n3. Isotonic specific volume (90.2K): 462.7<\/p>\n4. Surface tension (dyne\/cm): 67.6<\/p>\n5. Polarizability (10-24<\/sup>cm3<\/sup>): 24.93<\/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: 3<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: 5<\/p>\n6. Topological molecule polar surface area 60.2<\/p>\n7. Number of heavy atoms: 17<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 352<\/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. It is more toxic and irritating than anthraquinone. Can cause skin allergies and cause eczema. The production workshop should be well ventilated and the equipment should be sealed. Protective equipment should be worn during operation. <\/span><\/p>\n2. Avoid inhaling the dust of this product and avoid contact with eyes and skin. \u3000<\/span><\/p>\n<\/p>\nStorage method<\/h2>\n Store in a sealed, cool place away from light. <\/p>\nPackaged in iron drums lined with plastic bags. Net weight per barrel is 25kg or 50kg. Store in a cool, ventilated place. Moisture-proof and sun-proof. Store and transport according to regulations on toxic chemicals. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Nitrification reduction method: Anthraquinone is nitrated with mixed acid to obtain nitroanthraquinone. The reaction product is filtered and washed with hot water until neutral, and then refined with sodium sulfite. Among them, 2-nitroanthraquinone and sodium sulfite generate anthraquinone-2-sodium sulfonate that is easily soluble in water, which is removed by filtering and washing. The obtained 1-nitroanthraquinone is reduced with sodium sulfide to obtain crude 1-aminoanthraquinone, which is refined by adding alkali solution and insurance powder to remove the diaminoanthraquinone, and then oxidized with oxygen, filtered, and dried to obtain the finished product. <\/span><\/p>\n<\/p>\n2. Anthraquinone sulfonate ammonolysis method: Anthraquinone reacts with fuming sulfuric acid in the presence of mercury sulfate to generate anthraquinone-1-sulfonic acid, which is neutralized with ammonia and then replaced with sodium salt, and then catalyzed by sodium m-nitrobenzene sulfonate Under ammonolysis, 1-aminoanthraquinone is generated, and the finished product is obtained after refining. <\/span><\/span><\/p>\n<\/span><\/p>\n<\/span><\/p>\n<\/p>\nPurpose<\/h2>\n\n 1. Determine nitrite. Dyes and pharmaceutical intermediates. Organic Synthesis. 2. Important dye intermediates. It can be used to produce reduced khaki 2G, reduced red brown R, reduced olive green B, olive T, olive R, reduced gray M, dispersed red 3B, as well as reactive brilliant blue KN-R and reactive brilliant blue M-BR. \u200b\n <\/p>\n extended-reading:https:\/\/www.bdmaee.net\/fascat4233-catalyst-butyl-tin-mercaptan-fascat-4233\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-bdmaee-catalyst-cas3033-62-3-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-ea-104-catalyst-cas10027-41-9-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-pc520-catalyst-cas10294-43-5-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/979<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/87<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44478<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-33-lsi-dabco-33lsi\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/40325<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45212<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01SY Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48065,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15102],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48066"}],"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=48066"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48066\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48065"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48066"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48066"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48066"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3. Isotonic specific volume (90.2K): 462.7<\/p>\n
4. Surface tension (dyne\/cm): 67.6<\/p>\n
5. Polarizability (10-24<\/sup>cm3<\/sup>): 24.93<\/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: 3<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: 5<\/p>\n6. Topological molecule polar surface area 60.2<\/p>\n7. Number of heavy atoms: 17<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 352<\/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. It is more toxic and irritating than anthraquinone. Can cause skin allergies and cause eczema. The production workshop should be well ventilated and the equipment should be sealed. Protective equipment should be worn during operation. <\/span><\/p>\n2. Avoid inhaling the dust of this product and avoid contact with eyes and skin. \u3000<\/span><\/p>\n<\/p>\nStorage method<\/h2>\n Store in a sealed, cool place away from light. <\/p>\nPackaged in iron drums lined with plastic bags. Net weight per barrel is 25kg or 50kg. Store in a cool, ventilated place. Moisture-proof and sun-proof. Store and transport according to regulations on toxic chemicals. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Nitrification reduction method: Anthraquinone is nitrated with mixed acid to obtain nitroanthraquinone. The reaction product is filtered and washed with hot water until neutral, and then refined with sodium sulfite. Among them, 2-nitroanthraquinone and sodium sulfite generate anthraquinone-2-sodium sulfonate that is easily soluble in water, which is removed by filtering and washing. The obtained 1-nitroanthraquinone is reduced with sodium sulfide to obtain crude 1-aminoanthraquinone, which is refined by adding alkali solution and insurance powder to remove the diaminoanthraquinone, and then oxidized with oxygen, filtered, and dried to obtain the finished product. <\/span><\/p>\n<\/p>\n2. Anthraquinone sulfonate ammonolysis method: Anthraquinone reacts with fuming sulfuric acid in the presence of mercury sulfate to generate anthraquinone-1-sulfonic acid, which is neutralized with ammonia and then replaced with sodium salt, and then catalyzed by sodium m-nitrobenzene sulfonate Under ammonolysis, 1-aminoanthraquinone is generated, and the finished product is obtained after refining. <\/span><\/span><\/p>\n<\/span><\/p>\n<\/span><\/p>\n<\/p>\nPurpose<\/h2>\n\n 1. Determine nitrite. Dyes and pharmaceutical intermediates. Organic Synthesis. 2. Important dye intermediates. It can be used to produce reduced khaki 2G, reduced red brown R, reduced olive green B, olive T, olive R, reduced gray M, dispersed red 3B, as well as reactive brilliant blue KN-R and reactive brilliant blue M-BR. \u200b\n <\/p>\n extended-reading:https:\/\/www.bdmaee.net\/fascat4233-catalyst-butyl-tin-mercaptan-fascat-4233\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-bdmaee-catalyst-cas3033-62-3-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-ea-104-catalyst-cas10027-41-9-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-pc520-catalyst-cas10294-43-5-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/979<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/87<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44478<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-33-lsi-dabco-33lsi\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/40325<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45212<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01SY Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48065,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15102],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48066"}],"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=48066"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48066\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48065"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48066"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48066"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48066"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
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: 3<\/p>\n
4. Number of rotatable chemical bonds: 0<\/p>\n
5. Number of tautomers: 5<\/p>\n
6. Topological molecule polar surface area 60.2<\/p>\n
7. Number of heavy atoms: 17<\/p>\n
8. Surface charge: 0<\/p>\n
9. Complexity: 352<\/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. It is more toxic and irritating than anthraquinone. Can cause skin allergies and cause eczema. The production workshop should be well ventilated and the equipment should be sealed. Protective equipment should be worn during operation. <\/span><\/p>\n2. Avoid inhaling the dust of this product and avoid contact with eyes and skin. \u3000<\/span><\/p>\n<\/p>\nStorage method<\/h2>\n Store in a sealed, cool place away from light. <\/p>\nPackaged in iron drums lined with plastic bags. Net weight per barrel is 25kg or 50kg. Store in a cool, ventilated place. Moisture-proof and sun-proof. Store and transport according to regulations on toxic chemicals. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Nitrification reduction method: Anthraquinone is nitrated with mixed acid to obtain nitroanthraquinone. The reaction product is filtered and washed with hot water until neutral, and then refined with sodium sulfite. Among them, 2-nitroanthraquinone and sodium sulfite generate anthraquinone-2-sodium sulfonate that is easily soluble in water, which is removed by filtering and washing. The obtained 1-nitroanthraquinone is reduced with sodium sulfide to obtain crude 1-aminoanthraquinone, which is refined by adding alkali solution and insurance powder to remove the diaminoanthraquinone, and then oxidized with oxygen, filtered, and dried to obtain the finished product. <\/span><\/p>\n<\/p>\n2. Anthraquinone sulfonate ammonolysis method: Anthraquinone reacts with fuming sulfuric acid in the presence of mercury sulfate to generate anthraquinone-1-sulfonic acid, which is neutralized with ammonia and then replaced with sodium salt, and then catalyzed by sodium m-nitrobenzene sulfonate Under ammonolysis, 1-aminoanthraquinone is generated, and the finished product is obtained after refining. <\/span><\/span><\/p>\n<\/span><\/p>\n<\/span><\/p>\n<\/p>\nPurpose<\/h2>\n\n 1. Determine nitrite. Dyes and pharmaceutical intermediates. Organic Synthesis. 2. Important dye intermediates. It can be used to produce reduced khaki 2G, reduced red brown R, reduced olive green B, olive T, olive R, reduced gray M, dispersed red 3B, as well as reactive brilliant blue KN-R and reactive brilliant blue M-BR. \u200b\n <\/p>\n extended-reading:https:\/\/www.bdmaee.net\/fascat4233-catalyst-butyl-tin-mercaptan-fascat-4233\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-bdmaee-catalyst-cas3033-62-3-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-ea-104-catalyst-cas10027-41-9-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-pc520-catalyst-cas10294-43-5-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/979<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/87<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44478<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-33-lsi-dabco-33lsi\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/40325<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45212<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01SY Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48065,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15102],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48066"}],"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=48066"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48066\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48065"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48066"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48066"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48066"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
2. Avoid inhaling the dust of this product and avoid contact with eyes and skin. \u3000<\/span><\/p>\n<\/p>\nStorage method<\/h2>\n Store in a sealed, cool place away from light. <\/p>\nPackaged in iron drums lined with plastic bags. Net weight per barrel is 25kg or 50kg. Store in a cool, ventilated place. Moisture-proof and sun-proof. Store and transport according to regulations on toxic chemicals. <\/p>\n<\/p>\nSynthesis method<\/h2>\n1. Nitrification reduction method: Anthraquinone is nitrated with mixed acid to obtain nitroanthraquinone. The reaction product is filtered and washed with hot water until neutral, and then refined with sodium sulfite. Among them, 2-nitroanthraquinone and sodium sulfite generate anthraquinone-2-sodium sulfonate that is easily soluble in water, which is removed by filtering and washing. The obtained 1-nitroanthraquinone is reduced with sodium sulfide to obtain crude 1-aminoanthraquinone, which is refined by adding alkali solution and insurance powder to remove the diaminoanthraquinone, and then oxidized with oxygen, filtered, and dried to obtain the finished product. <\/span><\/p>\n<\/p>\n2. Anthraquinone sulfonate ammonolysis method: Anthraquinone reacts with fuming sulfuric acid in the presence of mercury sulfate to generate anthraquinone-1-sulfonic acid, which is neutralized with ammonia and then replaced with sodium salt, and then catalyzed by sodium m-nitrobenzene sulfonate Under ammonolysis, 1-aminoanthraquinone is generated, and the finished product is obtained after refining. <\/span><\/span><\/p>\n<\/span><\/p>\n<\/span><\/p>\n<\/p>\nPurpose<\/h2>\n\n 1. Determine nitrite. Dyes and pharmaceutical intermediates. Organic Synthesis. 2. Important dye intermediates. It can be used to produce reduced khaki 2G, reduced red brown R, reduced olive green B, olive T, olive R, reduced gray M, dispersed red 3B, as well as reactive brilliant blue KN-R and reactive brilliant blue M-BR. \u200b\n <\/p>\n extended-reading:https:\/\/www.bdmaee.net\/fascat4233-catalyst-butyl-tin-mercaptan-fascat-4233\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-bdmaee-catalyst-cas3033-62-3-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-ea-104-catalyst-cas10027-41-9-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-pc520-catalyst-cas10294-43-5-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/979<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/87<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44478<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-33-lsi-dabco-33lsi\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/40325<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45212<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01SY Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48065,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15102],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48066"}],"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=48066"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48066\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48065"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48066"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48066"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48066"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
Store in a sealed, cool place away from light. <\/p>\n
Packaged in iron drums lined with plastic bags. Net weight per barrel is 25kg or 50kg. Store in a cool, ventilated place. Moisture-proof and sun-proof. Store and transport according to regulations on toxic chemicals. <\/p>\n<\/p>\n
1. Nitrification reduction method: Anthraquinone is nitrated with mixed acid to obtain nitroanthraquinone. The reaction product is filtered and washed with hot water until neutral, and then refined with sodium sulfite. Among them, 2-nitroanthraquinone and sodium sulfite generate anthraquinone-2-sodium sulfonate that is easily soluble in water, which is removed by filtering and washing. The obtained 1-nitroanthraquinone is reduced with sodium sulfide to obtain crude 1-aminoanthraquinone, which is refined by adding alkali solution and insurance powder to remove the diaminoanthraquinone, and then oxidized with oxygen, filtered, and dried to obtain the finished product. <\/span><\/p>\n<\/p>\n2. Anthraquinone sulfonate ammonolysis method: Anthraquinone reacts with fuming sulfuric acid in the presence of mercury sulfate to generate anthraquinone-1-sulfonic acid, which is neutralized with ammonia and then replaced with sodium salt, and then catalyzed by sodium m-nitrobenzene sulfonate Under ammonolysis, 1-aminoanthraquinone is generated, and the finished product is obtained after refining. <\/span><\/span><\/p>\n<\/span><\/p>\n<\/span><\/p>\n<\/p>\nPurpose<\/h2>\n\n 1. Determine nitrite. Dyes and pharmaceutical intermediates. Organic Synthesis. 2. Important dye intermediates. It can be used to produce reduced khaki 2G, reduced red brown R, reduced olive green B, olive T, olive R, reduced gray M, dispersed red 3B, as well as reactive brilliant blue KN-R and reactive brilliant blue M-BR. \u200b\n <\/p>\n extended-reading:https:\/\/www.bdmaee.net\/fascat4233-catalyst-butyl-tin-mercaptan-fascat-4233\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-bdmaee-catalyst-cas3033-62-3-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-ea-104-catalyst-cas10027-41-9-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-pc520-catalyst-cas10294-43-5-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/979<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/87<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44478<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-33-lsi-dabco-33lsi\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/40325<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45212<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01SY Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48065,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15102],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48066"}],"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=48066"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48066\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48065"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48066"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48066"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48066"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
2. Anthraquinone sulfonate ammonolysis method: Anthraquinone reacts with fuming sulfuric acid in the presence of mercury sulfate to generate anthraquinone-1-sulfonic acid, which is neutralized with ammonia and then replaced with sodium salt, and then catalyzed by sodium m-nitrobenzene sulfonate Under ammonolysis, 1-aminoanthraquinone is generated, and the finished product is obtained after refining. <\/span><\/span><\/p>\n<\/span><\/p>\n<\/span><\/p>\n<\/p>\nPurpose<\/h2>\n\n 1. Determine nitrite. Dyes and pharmaceutical intermediates. Organic Synthesis. 2. Important dye intermediates. It can be used to produce reduced khaki 2G, reduced red brown R, reduced olive green B, olive T, olive R, reduced gray M, dispersed red 3B, as well as reactive brilliant blue KN-R and reactive brilliant blue M-BR. \u200b\n <\/p>\n extended-reading:https:\/\/www.bdmaee.net\/fascat4233-catalyst-butyl-tin-mercaptan-fascat-4233\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-bdmaee-catalyst-cas3033-62-3-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-ea-104-catalyst-cas10027-41-9-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-pc520-catalyst-cas10294-43-5-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/979<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/87<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44478<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-33-lsi-dabco-33lsi\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/40325<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45212<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01SY Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48065,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15102],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48066"}],"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=48066"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48066\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48065"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48066"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48066"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48066"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
<\/span><\/p>\n<\/span><\/p>\n<\/p>\nPurpose<\/h2>\n\n 1. Determine nitrite. Dyes and pharmaceutical intermediates. Organic Synthesis. 2. Important dye intermediates. It can be used to produce reduced khaki 2G, reduced red brown R, reduced olive green B, olive T, olive R, reduced gray M, dispersed red 3B, as well as reactive brilliant blue KN-R and reactive brilliant blue M-BR. \u200b\n <\/p>\n extended-reading:https:\/\/www.bdmaee.net\/fascat4233-catalyst-butyl-tin-mercaptan-fascat-4233\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-bdmaee-catalyst-cas3033-62-3-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-ea-104-catalyst-cas10027-41-9-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-pc520-catalyst-cas10294-43-5-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/979<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/87<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44478<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-33-lsi-dabco-33lsi\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/40325<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45212<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01SY Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48065,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15102],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48066"}],"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=48066"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48066\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48065"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48066"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48066"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48066"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
<\/span><\/p>\n<\/p>\nPurpose<\/h2>\n\n 1. Determine nitrite. Dyes and pharmaceutical intermediates. Organic Synthesis. 2. Important dye intermediates. It can be used to produce reduced khaki 2G, reduced red brown R, reduced olive green B, olive T, olive R, reduced gray M, dispersed red 3B, as well as reactive brilliant blue KN-R and reactive brilliant blue M-BR. \u200b\n <\/p>\n extended-reading:https:\/\/www.bdmaee.net\/fascat4233-catalyst-butyl-tin-mercaptan-fascat-4233\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-bdmaee-catalyst-cas3033-62-3-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-ea-104-catalyst-cas10027-41-9-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-pc520-catalyst-cas10294-43-5-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/979<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/87<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44478<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-33-lsi-dabco-33lsi\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/40325<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45212<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01SY Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48065,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15102],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48066"}],"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=48066"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48066\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48065"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48066"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48066"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48066"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
\n 1. Determine nitrite. Dyes and pharmaceutical intermediates. Organic Synthesis. 2. Important dye intermediates. It can be used to produce reduced khaki 2G, reduced red brown R, reduced olive green B, olive T, olive R, reduced gray M, dispersed red 3B, as well as reactive brilliant blue KN-R and reactive brilliant blue M-BR. \u200b\n <\/p>\n
extended-reading:https:\/\/www.bdmaee.net\/fascat4233-catalyst-butyl-tin-mercaptan-fascat-4233\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-bdmaee-catalyst-cas3033-62-3-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-ea-104-catalyst-cas10027-41-9-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/nt-cat-pc520-catalyst-cas10294-43-5-newtopchem\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/979<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/87<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44478<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/dabco-33-lsi-dabco-33lsi\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/40325<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/45212<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 01SY Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48065,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15102],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48066"}],"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=48066"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48066\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48065"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48066"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48066"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48066"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
Structural formula Business number 01SY Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48065,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[15102],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48066"}],"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=48066"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48066\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48065"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48066"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48066"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48066"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
![\"1-Aminoanthraquinone](\"http:\/\/www.newtopchem.com\/wp-content\/uploads\/2024\/04\/ddb6aab8eb174d71b8d881afa381bc7d.gif\")
<\/p>\n<\/p>\n![\"\"](\"http:\/\/www.newtopchem.com\/wp-content\/uploads\/2024\/04\/201009271429378798.gif\")
<\/p>\n![\"\"](\"http:\/\/www.newtopchem.com\/wp-content\/uploads\/2024\/04\/201009271429521222.gif\")
<\/span><\/p>\n![\"\"](\"http:\/\/www.newtopchem.com\/wp-content\/uploads\/2024\/04\/201009271430016094.gif\")