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CAS number : 12227-50-8
molecular formula : C54H32N4O6
EINECS : 235-436-2
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CAS number:12227-50-8
molecular formula:C54H32N4O6
molecular weight:832.86
EINECS number:235-436-2
vat yellow 33;4',4'''-azobis[n-(9,10-dihydro-9,10-dioxo-1-anthryl)]-[1,1'-biphenyl]-4-carboxamide;C.I. 65429;Vat yellow 33 (C.I. 65429);[1,1'-Biphenyl]-4-carboxamide, 4',4'''-azobis[N-(9,10-dihydro- 9,10-dioxo-1-anthracenyl)-;Cibanone Yellow 2GN;Indanthren Yellow F3GC;Nihonthrene Yellow 3GC
Dyes; Vat Dyes; Dyes and Pigments; Organics
Density | 1.35 |
Yellow powder. It is brown-red in concentrated sulfuric acid, yellow in hydrosulfite acid solution, and purplish red in hydrosulfite alkaline solution.
● Vat Yellow F3GC is used for dyeing cotton fabrics and is a brilliant yellow light red. High directness to cotton fibers and good levelness. Anti-dyeing and discharge printing can be carried out.
Production method
● Using 4'-nitro-4-bibenzoic acid and 1-aminoanthraquinone as raw materials, firstly reduce 4'-nitro-4-bibenzoic acid and glucose under alkaline conditions to obtain azo compounds, and then use chlorine Sulfoxide (SOCl2) for acyl chlorination, and finally condensed with 1-aminoanthraquinone to obtain the product. .
CAS number:12227-50-8
molecular formula:C54H32N4O6
molecular weight:832.86
EINECS number:235-436-2
vat yellow 33;4',4'''-azobis[n-(9,10-dihydro-9,10-dioxo-1-anthryl)]-[1,1'-biphenyl]-4-carboxamide;C.I. 65429;Vat yellow 33 (C.I. 65429);[1,1'-Biphenyl]-4-carboxamide, 4',4'''-azobis[N-(9,10-dihydro- 9,10-dioxo-1-anthracenyl)-;Cibanone Yellow 2GN;Indanthren Yellow F3GC;Nihonthrene Yellow 3GC
Dyes; Vat Dyes; Dyes and Pigments; Organics
Density | 1.35 |
Yellow powder. It is brown-red in concentrated sulfuric acid, yellow in hydrosulfite acid solution, and purplish red in hydrosulfite alkaline solution.
● Vat Yellow F3GC is used for dyeing cotton fabrics and is a brilliant yellow light red. High directness to cotton fibers and good levelness. Anti-dyeing and discharge printing can be carried out.
Production method
● Using 4'-nitro-4-bibenzoic acid and 1-aminoanthraquinone as raw materials, firstly reduce 4'-nitro-4-bibenzoic acid and glucose under alkaline conditions to obtain azo compounds, and then use chlorine Sulfoxide (SOCl2) for acyl chlorination, and finally condensed with 1-aminoanthraquinone to obtain the product. .