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88-52-8

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88-52-8 Usage

Description

4,6-DiaminoToluene-3-Sulphonic Acid, also known as DPTS, is a chemical compound that features a benzene ring with an amino group and a sulfonic acid group attached at different positions. It is characterized by its white to off-white solid appearance at room temperature and exhibits strong acidic properties due to the presence of the sulfonic acid group.

Uses

Used in Dye Production:
4,6-DiaminoToluene-3-Sulphonic Acid is used as a diazo component in the production of dyes, particularly azo dyes. Its chemical structure allows it to react with other compounds to form a wide range of colored dyes, making it a valuable ingredient in the dye manufacturing process.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 4,6-DiaminoToluene-3-Sulphonic Acid serves as an intermediate in the synthesis of various drugs. Its unique chemical properties enable it to be incorporated into the molecular structures of different pharmaceuticals, contributing to their development and effectiveness.
Used in Agrochemical Production:
4,6-DiaminoToluene-3-Sulphonic Acid is also utilized as an intermediate in the synthesis of agrochemicals. Its role in creating these compounds helps to enhance crop protection and contribute to the overall efficiency of agricultural practices.

Check Digit Verification of cas no

The CAS Registry Mumber 88-52-8 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88-52:
(4*8)+(3*8)+(2*5)+(1*2)=68
68 % 10 = 8
So 88-52-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H10N2O3S/c1-4-2-7(13(10,11)12)6(9)3-5(4)8/h2-3H,8-9H2,1H3,(H,10,11,12)

88-52-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-Diamino-5-methylbenzenesulfonic acid

1.2 Other means of identification

Product number -
Other names 2,4-Tolylenediamine-5-sulfonic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:88-52-8 SDS

88-52-8Downstream Products

88-52-8Relevant articles and documents

Triazinyl reactive dyestuffs in which triazinyl group is further substituted with a beta-chloroethylsulfonyl- or vinylsulfonylbutyrylamino moiety

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, (2008/06/13)

Reactive dyes of the formula STR1 in which D is the radical of an organic dye of the monoazo, polyazo, metal complex azo, anthraquinone, phthalocyanine, formazan, azomethine, dioxazine, phenazine, stilbene, triphenylmethane, xanthene, thioxanthrone, nitroaryl, naphthoquinone, pyrenequinone or perylenetetracarbimide series, R is hydrogen or substituted or unsubstituted C1-4 -alkyl, X is a substituent which is detachable as an anion, B is a radical of the formula STR2 R1 and R2, independently of each other, are hydrogen or substituted or unsubstituted C1-4 -alkyl or phenyl, A is a substituted or unsubstituted aliphatic or aromatic bridge member, Y is a --CO--Z or --SO2 --Z radical, Z is an aliphatic, aromatic or heterocyclic reactive radical, and n is 1 or 2, are suitable for dyeing or printing cellulose-containing and nitrogen-containing materials and in high dyeing yield produce dyeings and prints having good fastness properties.

Reactive dyestuffs, their manufacture and use

-

, (2008/06/13)

Dyestuffs of the formula STR1 wherein R1 is hydrogen or a low-molecular alkyl group, R2 is hydrogen, a low-molecular alkyl group, an aryl radical or the radical of an organic dyestuff containing sulpho groups, and R1 and R2 together with the nitrogen atom can form a ring, X1 and X2 are hydrogen, a sulpho group or the --N=N--K radical, wherein K is the radical of a coupling component and, if one X is the --N=N--K radical, the other X is a sulpho group, and the benzene ring A can contain further substituents.

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