Vat Green 3
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Vat Green 3
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CAS No:
3271-76-9
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Formula:
C31H15NO3
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Chemical Name:
Vat Green 3
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Synonyms:
Anthra[2,1,9-mna]naphth[2,3-h]acridine-5,10,15(16H)-trione;C.I. 69500;Ahcovat Olive Green BL-F;Ahcovat Olive Green BL;Ahcovat Olive Green BLD;Ahcovat Printing Olive Green BL;Amanthrene Olive Green B;Amanthrene Supra Olive Green B;Arlanthrene Olive Green B;Atic Vat Olive Green B;Belanthrene Olive Green B;Benzadone Olive Green B;Calcoloid Olive Green BDC;Calcoloid Olive Green BD;Calcoloid Olive Green BDL;Calcoloid Olive Green BN;Calcoloid Olive Green BNC;Caledon Olive Green B;Caledon Printing Olive Green B;Carbanthrene Olive Green B;Cibanone Olive 2B;Cibanone Olive FB;Cibanone Olive 2BD;C.I. Vat Green 3;Fenanthren Olive Green B;Helanthrene Olive Green B;Indanthrene Olive Green B;Indanthrene Olive Green BA;Indanthren Olive Green B;Mayvat Olive Green B;Mikethrene Olive Green B;Nihonthrene Olive Green B;Nihonthrene Olive Green B Disperse Powder;Nyanthrene Olive Green B;Ostanthren Olive Green B;Palanthrene Olive Green B;Pernithrene Olive Green B;Ponsol Green 2BL;Ponsol Green 2BLD;Romantrene Olive Green FB;Solanthrene Dark Green J;Tinon Olive B;Tinon Olive BM;Tyrian Olive Green I-B;Vat Olive Green B;Vat Green 3;Solanthrene Dark Green F-J;C.I. 70311;Cibanone Olive B;Sandothrene Olive N 2B;Novatic Olive Green B;1328-45-6
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CAS No:
Safety Information
P273, P501
H412
Not Classified|H412 (100%): Harmful to aquatic life with long lasting effects [Hazardous to the aquatic environment, long-term hazard]|P273, and P501|Aggregated GHS information provided by 3 companies from 2 notifications to the ECHA C&L Inventory.
Vat Green 3 Use and Manufacturing
Using benzoxanthone and 1-aminoanthraquinone as raw materials, the benzoxanthone is first brominated, and then condensed with 1-aminoanthraquinone, alkali fusion, and ring closure to obtain the product. After filtering, neutralizing, washing, drying and crushing, the finished product is obtained. . Add 300-400L of water, 50kg of hydrochloric acid (30%), 90kg of benzoxanthone, 2kg of chlorobenzene, 35kg of bromine into the reaction pot, raise the temperature to 70-75℃, keep it for 1.5h, and then slowly add 10% sodium hypochlorite solution. 100% 130kg), about 1.5-2h after adding, continue to stir for 1h. After reaching the end of the reaction, add sodium bisulfite solution to decompose unreacted bromine. Cool, filter, wash with water to neutrality, and dry to obtain about 118kg of bromobenzopyranthrone. Add 232.5kg of bromophenanthrone, 160kg of 1-aminoanthraquinone, 50kg of sodium carbonate, and 4.5kg of copper oxide into the condensation pot, mix for 1h, slowly raise the temperature to 200℃, keep the temperature for 2h, and cool and smash when it reaches the end. A mixture of imines. Add 1000kg of butanol and 200kg of potassium hydroxide into the caustic pot, raise the temperature to 100-120°C to dissolve all, then lower the temperature to 90°C, add 240kg of imine mixture, and then raise the temperature to 110°C for 6h. Then, the butanol is evaporated with water vapor, filtered, washed, ground and dried to obtain the finished product.
Mainly used for dyeing and printing of cotton fabrics, but also for dyeing of Victorian/cotton blended fabrics
Anthra[2,1,9-mna]naphth[2,3-h]acridine-5,10,15(16H)-trione: ACTIVE
Computed Properties
Molecular Weight:449.5
XLogP3:7.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Exact Mass:449.10519334
Monoisotopic Mass:449.10519334
Topological Polar Surface Area:67.3
Heavy Atom Count:35
Complexity:902
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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