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Naphtalene-1,3,6-trisulfonic Acid

CAS No.
86-66-8
Chemical Name:
Naphtalene-1,3,6-trisulfonic Acid
Synonyms
2,5,7-Naphthalenetrisulfonic acid;naphthalene-1,3,6-trisulphonic acid
CBNumber:
CB8875761
Molecular Formula:
C10H8O9S3
Molecular Weight:
368.36
MDL Number:
MFCD00128840
MOL File:
86-66-8.mol
MSDS File:
SDS
Last updated:2023-10-30 17:15:29

Naphtalene-1,3,6-trisulfonic Acid Properties

Density 1.919±0.06 g/cm3(Predicted)
pka -0.76±0.40(Predicted)
FDA UNII 66WF59G54Q
EPA Substance Registry System 1,3,6-Naphthalenetrisulfonic acid (86-66-8)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS05
Signal word  Danger
Hazard statements  H314
Precautionary statements  P310-P260-P280
HS Code  2904100090

Naphtalene-1,3,6-trisulfonic Acid price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
AK Scientific 3611AC Naphthalene-1,3,6-trisulfonicacid 86-66-8 250mg $1051 2021-12-16 Buy
American Custom Chemicals Corporation CHM0117473 1,3,6-NAPHTHALENE TRISULFONIC ACID 95.00% 86-66-8 5G $1334.03 2021-12-16 Buy
Alichem 86668 Naphthalene-1,3,6-trisulfonicacid 86-66-8 1g $615.44 2021-12-16 Buy
Chemenu CM140026 Naphthalene-1,3,6-trisulfonicacid 95% 86-66-8 1g $729 2021-12-16 Buy
Product number Packaging Price Buy
3611AC 250mg $1051 Buy
CHM0117473 5G $1334.03 Buy
86668 1g $615.44 Buy
CM140026 1g $729 Buy

Naphtalene-1,3,6-trisulfonic Acid Chemical Properties,Uses,Production

Uses

The total reaction mixture is nitrated, and the resulting 8-nitro derivative is reduced to give 1-aminonaphthalene-3,6,8-trisulfonic acid (Koch acid), the key intermediate in the production of the important H acid. The crude trisodium salt may be precipitated from the quenched mixture after dilution to 75 % acid strength to give a product (Azoguard) used as a diazo stabilizer.

Definition

ChEBI: Naphthalene-1,3,6-trisulfonic acid is a naphthalenesulfonic acid.

Production Methods

Naphthalene is initially sulfonated with sulfuric acid monohydrate under programmed temperature control between 80 and 145℃. Then, 65 % oleum is added gradually at 40℃ and heating is continued for 2.5 h at 145℃. Trisulfonation is complete after the further addition of 65 % oleum and heating for 3 h at 150℃. This complex procedure maximizes the formation of Naphtalene-1,3,6-trisulfonic Acid with a conversion of up to 75 %.

Naphtalene-1,3,6-trisulfonic Acid Preparation Products And Raw materials

Raw materials

Preparation Products

Naphtalene-1,3,6-trisulfonic Acid Suppliers

Global( 10)Suppliers
Supplier Tel Email Country ProdList Advantage
Hu Bei Jiutian Bio-medical Technology CO.,Ltd
027-88013699 17354350817 Ryan@jiutian-bio.com China 7433 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131981 58
Aikon International Limited 025-66113011 13155353615 qzhang@aikonchem.com China 15396 58
Yangzhou modier Electronic Materials Co., Ltd 0514-82098883; 13761402923 market@modeltemol.com China 876 58
Baoji Didu Pharmaceutical and Chemical Co., Ltd 029-61856358 15829046862 1035@dideu.com China 10011 58

Naphtalene-1,3,6-trisulfonic Acid Spectrum

naphthalene-1,3,6-trisulphonic acid 2,5,7-Naphthalenetrisulfonic acid 86-66-8