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1,8-Dihydroxynaphthylene-3,6-disulfonic acid

1,8-Dihydroxynaphthylene-3,6-disulfonic acid Structure
CAS No.
148-25-4
Chemical Name:
1,8-Dihydroxynaphthylene-3,6-disulfonic acid
Synonyms
CHROMOTROPIC ACID;CHROMOGEN;Aids000369;Aids-000369;Chrmotropicacid;chromotropicaci;Chromotopic acid;Chromotrophic Acid;TIMTEC-BB SBB001312;1,8-Dihydroxynaphthy
CBNumber:
CB7196825
Molecular Formula:
C10H8O8S2
Molecular Weight:
320.3
MOL File:
148-25-4.mol
Modify Date:
2024/6/6 17:55:34

1,8-Dihydroxynaphthylene-3,6-disulfonic acid Properties

Boiling point 429.2°C (rough estimate)
Density 1.7929 (rough estimate)
refractive index 1.6000 (estimate)
storage temp. Inert atmosphere,Room Temperature
pka -0.51±0.40(Predicted)
CAS DataBase Reference 148-25-4(CAS DataBase Reference)
EPA Substance Registry System 2,7-Naphthalenedisulfonic acid, 4,5-dihydroxy- (148-25-4)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H335-H315-H319
Precautionary statements  P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
HS Code  29089990

1,8-Dihydroxynaphthylene-3,6-disulfonic acid Chemical Properties,Uses,Production

Chemical Properties

4,5-Dihydroxynaphthalene-2,7-disulfonic acid [148-25-4]. (1,8-dihydroxynaphthalene-3,6-disulfonic acid), chromotropic acid, C10H8O8S2, Mr 320.3: the disodium salt is readily soluble in water. Alkali fusion yields 1,3,8-trihydroxynaphthalene-6-sulfonic acid. Diazo coupling occurs in the 3- and 6-positions.

Uses

Chromotropic acid is used as an analytical reagent and as a coupling component for a wide range of azo dyes, e.g., C.I. Acid Violet 6, C. I. Mordant Blue 13, and C.I. Direct Blue 84.

Definition

ChEBI: A naphthalenesulfonic acid that is naphthalene-2,7-disulfonic acid substituted by hydroxy groups at positions 4 and 5.

Production Methods

2-Hydroxynaphthalene-3,6,8- trisulfonic acid total liquor is concentrated and heated with caustic soda liquor to 158℃ for 20 – 30 h . The melt is diluted with water and poured into excess hydrochloric acid. Salt is added, sulfur dioxide expelled, and the mixture cooled to precipitate the product as the disodium salt in 88 % yield.
An alternative process is based on direct fusion (caustic liquor at 228℃ under pressure) of 1-aminonaphthalene-3,6,8-trisulfonic acid to chromotropic acid without isolating the intermediate oxy Koch acid.

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4,5-dihydroxy-7-naphthalenedisulfonicacid 7-Naphthalenedisulfonicacid,4,5-dihydroxy-2 Chrmotropicacid 4,5-Dihydroxy-2,7-naphthalene disulfonic acid 1,8-Dihydroxynaph-thalene-3,6-disulfonic acid 4,5-DIHYDROXY-2,7-NAPHTHALENEDISULFONIC ACID 4,5-dihydroxynaphthalene-2,7-disulphonic acid 1,8-DIHYDROXYNAPHTHALENE-3,6-DISULFONIC ACID 1,8-DIHYDROXYNAPHTHYLENE-3,6-DISULFONIC ACID TIMTEC-BB SBB001312 4,5-dihydroxynaphthalene-2,7-disulfonic acid Chromotopic acid 2,7-Naphthalenedisulfonic acid, 4,5-dihydroxy- 1,8-Dihydroxynaphthy Aids000369 Aids-000369 CHROMOTROPIC ACID(1,8-DIHYDROXYNAPHTHALENE-3,6-DISULFONIC ACID) 8-Dihydroxynaphthylene-3 Chromotropic acid, AR Chromotropic acid, ACS,99% chromotropicaci 4,5-Dihydroxynaphthalene-2,7-disulfonic Acid DISCONTINUED. Please see D494918 CHROMOGEN CHROMOTROPIC ACID Chromotrophic Acid 148-25-4 C10H4SO3H2OH2 C10H4OH2SO3H2 C10H8O8S2 Intermediates of Dyes and Pigments