Name | Acid Yellow 127 |
Synonyms | Acid Yellow 127 Acid Brilliant Yellow 3GL Acid yellow 127 (C.I. 18888) Sodium 4-((4-chloro-6-(methylanilino)-1,3,5-triazin-2-yl)amino)-2-((1-(2-chlorophenyl)-4,5-dihydro-3-methyl-5-oxo-1H-pyrazol-4-yl)azo)benzenesulphonate sodium 4-({4-chloro-6-[methyl(phenyl)amino]-1,3,5-triazin-2-yl}amino)-2-{(E)-[1-(2-chlorophenyl)-3-methyl-5-oxo-4,5-dihydro-1H-pyrazol-4-yl]diazenyl}benzenesulfonate Benzenesulfonic acid, 4-[[4-chloro-6-(methylphenylamino)-1, 3, 5-triazin-2-yl]amino]-2-[[1-(2-chlorophenyl)-4, 5-dihydro-3-methyl-5-oxo-1H-pyrazol-4-yl]azo], monosodium salt |
CAS | 73384-78-8 |
EINECS | 277-419-2 |
InChI | InChI=1/C26H21Cl2N9O4S.Na/c1-15-22(23(38)37(35-15)20-11-7-6-10-18(20)27)34-33-19-14-16(12-13-21(19)42(39,40)41)29-25-30-24(28)31-26(32-25)36(2)17-8-4-3-5-9-17;/h3-14,22H,1-2H3,(H,39,40,41)(H,29,30,31,32);/q;+1/p-1/b34-33+ |
Molecular Formula | C26H20Cl2N9NaO4S |
Molar Mass | 648.45567 |
Physical and Chemical Properties | Yellow powder. Soluble in water. The aqueous solution was green and light yellow, and a clear solution was obtained by dissolving in boiling water or boiling for a moment. Yellow in concentrated sulfuric acid, diluted yellow solution, accompanied by precipitation. It is yellow in concentrated nitric acid, and it is a bright yellow solution after dilution, accompanied by precipitation. Yellow in concentrated sodium hydroxide solution, diluted bright yellow solution, accompanied by precipitation. |
Use | neutral brilliant yellow 3GL is mainly used for dyeing hair and wool fabrics, mostly used for color matching, and also used for dyeing silk and nylon. In wool, silk, nylon fabric directly printed bright yellow, and suitable for discharge printing with color. Can also be used for leather coloring. |
production method | with 2, 4-diaminobenzenesulfonic acid, cyanuric chloride, N-methylaniline, 1-(o-chlorophenyl)-3-methyl-5-pyrazolone as raw material, cyanuric chloride first with 2, 4-diaminobenzenesulfonic acid condensation, and then with N-methylaniline for the second condensation, and then the condensation product diazotization, the product is obtained by coupling with 1-(o-chlorophenyl)-3-methyl-5-pyrazolone. The final product was obtained by filtration and drying.. |