Identification | Back Directory | [Name]
DIHYDROXY-G-SALT | [CAS]
6357-93-3 | [Synonyms]
DioxyGsalt DIOXY G ACID Einecs 228-757-4 DIHYDROXY-G-SALT 4,6-Dihydroxy-2-naphthalenesulfonic acid 4,6-dihydroxynaphthalene-2-sulfonic acid 4,6-dihydroxynaphthalene-2-sulphonic acid 2,8-DIHYDROXY NAPHTHALENE-6-SULFONIC ACID 2,8-Dihydroxynaphthalene-6-sodiumsulfonate 2-Naphthalenesulfonic acid, 4,6-dihydroxy- 2,8-Dihydroxynaphthalene-6-sulfonate Sodium Salt 2,8-Dihydroxynaphthalene-6-sulfonic acid sodium salt 2-chloro-N-[2-[[2-oxo-2-(2,4,6-trimethylanilino)ethyl]thio]-1,3-benzothiazol-6-yl]benzamide | [EINECS(EC#)]
228-757-4 | [Molecular Formula]
C10H8O5S | [MDL Number]
MFCD00035845 | [MOL File]
6357-93-3.mol | [Molecular Weight]
240.23 |
Hazard Information | Back Directory | [Chemical Properties]
4,6-Dihydroxynaphthalene-2-sulfonic acid [6357-93-3]. (2,8-dihydroxynaphthalene6-sulfonic acid), dioxy G acid, C10H8O5S, Mr 240.2, is readily soluble in water, but the sodium salt is less so and can be salted out. | [Uses]
Dioxy G acid is used as an intermediate in the production of 2-amino-8-hydroxynaphthalene-6-sulfonic acid (g acid) and its Nsubstituted derivatives by means of the Bucherer reaction with ammonia or primary amines. It is also used as a coupling component for azo dyes such as C.I. Mordant Black 56. | [Production Methods]
The potassium salt of 2-hydroxynaphthalene-6,8-disulfonic acid is heated with 70 % caustic liquor for 3 h at 230℃ and then at 240℃ for completion of the reaction. The melt is diluted with water and poured into excess hydrochloric acid. After sulfur dioxide has been expelled, salt is added and the batch is cooled to precipitate the product, which is filtered off and washed with brine; the yield is 80 %. |
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