C.I. Sulphur Blue 7
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C.I. Sulphur Blue 7
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CAS No:
1327-57-7
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Chemical Name:
C.I. Sulphur Blue 7
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Synonyms:
C.I. Sulphur Blue 7;C.I. 53440;Acco Sulfur Blue B-CF;Acco Sulfur Blue R-CF;Acco Sulfur Blue 2R-CF;Acco Sulfur Blue 4R-CF;Acco Sulfur Blue 6R-CF;Acco Sulfur Blue GLP-CF;Acco Sulfur Blue GLR-CF;Atul Sulfur Navy Blue;Calcogene Blue 2B-CF;Calcogene Blue 2R-CF;Calcogene Navy Blue 2GS-CF;Calcogene Blue 6R-CF;Diresul Blue 8RS;Diresul Navy Blue GIS;Diresul Blue 9RS;Eclipse Dark Blue B;Fenoxyl Blue L;Fenoxyl Blue 9R;Fenoxyl Blue LC;Fenoxyl Blue LCR;Immedial Indone RR;Immedial Indone Violet B;Katigen Blue BC 3R Conc. CF;Katigen Blue BC 8R Conc. CF;Katigen Blue BCR Conc. CF;Kayaku Indone Violet BC;Kayaku Sulphur Blue 4R;Kayaku Sulphur Blue BK;Kayaku Sulphur Blue BN;Kayaku Sulphur Blue BP;Kayaku Sulphur Blue FBB;Kayaku Sulphur Blue RC;Kayaku Sulphur Blue RN;Kayaku Sulphur Blue RS;Kayaku Sulphur Blue TFB;Kayaku Sulphur Blue TFR;Kayaku Sulphur Indone Violet;Mitsui Sulphur Blue R;Mitsui Sulphur Blue 3BN;Mitsui Sulphur Blue 4R;Mitsui Sulphur Blue BC;Mitsui Sulphur Blue FB;Mitsui Sulphur Blue LC;Mitsui Sulphur Blue LCR;Mitsui Sulphur Blue RC;Mitsui Sulphur Blue RCP;Mitsui Sulphur Blue TFA;Mitsui Sulphur Blue TFB;Mitsui Sulphur Blue TFBP;Nissen Brilliant Violet B;Pyrogene Deep Blue B;Sodyeco Sulphur Blue 8RL;Sodyeco Sulphur Blue 8RP;Sodyesul Blue GW;Sodyesul Blue RW;Sodyesul Brilliant Blue RN;Sodyesul Navy Blue G 2CF;Sodyesul Navy Blue 6RCF;Sodyesul Navy Blue BCF;Sulfanol Brilliant Blue R;56730-67-7;61814-33-3;85586-03-4
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CAS No:
Characteristics
58.3
1.60
4-amino-4'-hydroxy-3-methyldiphenylamine is a black crystalline solid. (NTP, 1992)
1.2±0.1 g/cm3
320° F (NTP, 1992)
388.2±27.0 °C at 760 mmHg
188.6±23.7 °C
1.699
less than 1 mg/mL at 68.9° F (NTP, 1992)
Safety Information
P264, P270, P273, P280, P301+P312, P302+P352, P305+P351+P338, P321, P330, P332+P313, P337+P313, P362, P501
H302
C.I. Sulphur Blue 7 Use and Manufacturing
Using o-toluidine and phenol as raw materials, firstly nitrosate phenol, then dissolve o-toluidine in sulfuric acid and condense with p-nitrosophenol to obtain intermediate 3-methyl-4-amino-4'-hydroxydiphenylamine (I), then vulcanize (I) with sodium polysulfide, oxidize, filter, and dry to obtain the finished product (II). 1 part of phenol, 1.36 parts of sodium nitrite, 0.86 parts of sulfuric acid, and 4.5t of water are subjected to nitrosation reaction at 12°C to obtain p-nitrosophenol. Dissolve 1 part of o-toluidine in 4.3675 parts of sulfuric acid, then add 1.0149 parts of p-nitrosophenol, heat up to 30°C, condense for 1h to obtain intermediate (I). Heat the above-mentioned intermediate (I) with 1 part of sodium sulfide, 2.75 parts of sulfur, and water to 110-111°C for 30 hours to carry out vulcanization. Then add water to dilute, heat up to 88-90℃, oxidize with air for 14h to obtain the product (different proportion of sulfur content in sodium polysulfide, different curing temperature, different color and light of the obtained product. The proportion of sulfur content increases, the temperature rises, and the product color is better Red and bright, so there are different trade names. For example, sulfur blue BN with cyan light, sulfur blue BRN with cyan red light, sulfur blue RN with red light, etc.).
Sulfide blue BRN is mainly used for dyeing cotton, hemp, viscose fiber, vinylon and its fabrics. It is the main color dye for navy blue and has a bright color. It can also be dyed with yellow dye in dark gray.
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