| Identification | Back Directory | [Name]
2,NAPHTHOL-3,6,8-TRISULFONIC ACID | [CAS]
6259-66-1 | [Synonyms]
Einecs 228-407-0
2,NAPHTHOL-3,6,8-TRISULFONIC ACID
7-Hydroxynaphthalin-1,3,6-trisulfonsure
7-Hydroxy-1,3,6-naphthalenedisulfonicacid
7-Hydroxy-1,3,6-naphthalenetrisulfonic acid
2-Hydroxynaphthalene-3,6,8-trisulfonic acid
7-hydroxynaphthalene-1,3-6-trisulfonic acid
7-hydroxynaphthalene-1,3,6-trisulphonic acid
1,3,6-Naphthalenetrisulfonic acid, 7-hydroxy- | [EINECS(EC#)]
228-407-0 | [Molecular Formula]
C10H8O10S3 | [MDL Number]
MFCD00035849 | [MOL File]
6259-66-1.mol | [Molecular Weight]
384.36 |
| Hazard Information | Back Directory | [Chemical Properties]
2-Hydroxynaphthalene-3,6,8-trisulfonic acid [6259-66-1]. (7-hydroxynaphthalene-1,3,6-trisulfonic acid), C10H8O10S3, Mr 384.3, and its alkali-metal salts are readily soluble in water; nevertheless, the sodium salt is obtainable by salting out. Amination at 240℃ gives 2-aminonaphthalene-3,6,8-trisulfonic acid. Alkali fusion gives a mixture of dihydroxynaphthalenedisulfonic acids and finally 4,6,7- trihydroxynaphthalene-2-sulfonic acid. Diazo coupling occurs slowly in the 1-position. | [Uses]
The acid is used as an azo coupling component in, e.g., C.I. Solvent Red 31. | [Production Methods]
2-Naphthol is heated with sulfuric acid monohydrate at 115℃ for 3 h. The reaction mixture is cooled and 65 % oleum is added, followed by heating at 115℃ for 12 h, after which it is poured into water. Salt is then added to the hot solution and the sodium salt of the product crystallizes. Further purification is effected by redissolving in water and salting out. |
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