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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 80708Generated: November 3, 2026

1,7-Naphthalenedisulfonic acid, 4-(benzoylamino)-5-hydroxy-

Einecs 228-838-4 · 4-Benzamido-5-hydroxy-1,7-naphthalenedisulfonic acid · 4-benzamido-5-hydroxynaphthalene-1,7-disulfonic acid · 4-Benzoylamino-5-hydroxy-1,7-naphthalenedisulfonic acid · 5-Hydroxy-4-(benzoylamino)-1,7-naphthalenedisulfonic acid · 4-(Benzoylamino)-5-hydroxy-1,7-naphthalenedisulfonic acid · 4-(benzoylamino)-5-hydroxynaphthalene-1,7-disulphonic acid · 1,7-Naphthalenedisulfonic acid, 4-(benzoylamino)-5-hydroxy-

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1,7-Naphthalenedisulfonic acid, 4-(benzoylamino)-5-hydroxy- molecular structure

Identifiers & Physical Properties

CAS No.6361-49-5
Molecular formulaC17H13NO8S2
Average molar mass423.4 g/mol
Monoisotopic mass423.00825872 g/mol
SMILESO=C(Nc1ccc(S(=O)(=O)O)c2cc(S(=O)(=O)O)cc(O)c12)c1ccccc1
InChIKeyBUVOCOQOYNGMCO-UHFFFAOYSA-N
PubChem CID80708
EC No.228-838-4
DTXSIDDTXSID50884276

Chemical & Physical Properties

XLogP1.7
Topological polar surface area175
Hydrogen bond donors4
Hydrogen bond acceptors8
Rotatable bonds4
Heavy atoms28
Formal charge0
Complexity779
EPA Substance Registry System1,7-Naphthalenedisulfonic acid, 4-(benzoylamino)-5-hydroxy- (6361-49-5)
TSCA inventory statusTSCA listed

Safety & Regulations

TSCA inventory statusTSCA listed

Applications & Uses

Uses

4-Benzamido-5-hydroxynaphthalene-1,7-disulfonic acid [6361-49-5], N-benzoyl K acid, is produced by reacting purified K acid with benzoyl chloride in aqueous alkaline sodium carbonate solution at 35 – 40 ℃ for 18 h, followed by heating for 1 h at 90℃ to hydrolyze the O-benzoyl derivative (yield 80 %). It is used to produce C.I. Acid Red 133, C.I. Acid Red 157, and C.I. Mordant Red 21.