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617-97-0

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617-97-0 Usage

Uses

3-?Methylbenzenesulfoni?c Acid was one of the major biodegradation product from azo dyes in fungal degradation by capillary electrophoresis.

Check Digit Verification of cas no

The CAS Registry Mumber 617-97-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 617-97:
(5*6)+(4*1)+(3*7)+(2*9)+(1*7)=80
80 % 10 = 0
So 617-97-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H8O3S/c1-6-3-2-4-7(5-6)11(8,9)10/h2-5H,1H3,(H,8,9,10)

617-97-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylbenzenesulfonic acid

1.2 Other means of identification

Product number -
Other names -

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:617-97-0 SDS

617-97-0Relevant articles and documents

Textile dye degradation potential of plant laccase significantly enhances upon augmentation with redox mediators

Kagalkar, Anuradha N.,Khandare, Rahul V.,Govindwar, Sanjay P.

, p. 80505 - 80517 (2015)

Cell suspension cultures of Blumea malcolmii Hook. exhibited 98% decolorization of a textile dye Brilliant Blue R (BBR) at a concentration of 40 mg L-1 within 24 h. A significant induction in the intracellular laccase activity (607%) was observ

Tetrakis(pyridine)silver(II) Peroxodisulfate, S2O8, a Reagent for the Oxidative Transformations

Firouzabadi, Habib,Salehi, Peyman,Mohammadpour-Baltork, Iraj

, p. 2878 - 2880 (2007/10/02)

Tetrakis(pyridine)silver(II) peroxodisulfate oxidizes aromatic aldehydes to carboxylic acids, benzylic alcohols to carbonyl compounds, aromatic thiols, and allylaryl thioethers to arylsulfonic acids and benzylic carbon-hydrogen bonds to carbonyl groups. α-Hydroxycarboxylic acids and phenylacetic acids are decarboxylated to produce carbonyl compounds.Dibenzyl ether and its sulfur analogue are converted to their corresponding ester and the thioester, respectively.

EFFECT OF STRUCTURE ON THE KINETICS AND MECHANISM OF THE ACID-CATALYZED DECOMPOSITION OF N-ALKYL-N-NITROBENZENESULFONAMIDES

Drozdova, O. A.,Astrat'ev, A. A.,Kuznetsov, L. L.,Selivanov, V. F.

, p. 671 - 675 (2007/10/02)

The decomposition rate of a series of meta- and para-substituted N-alkyl-N-nitrobenzenesufonamides was determined by a spectrophotometric method in aqueous sulfuric acid.It was shown that the decomposition of the compounds takes place both by denitration and by cleavage of the N-S bond with the formation fo primary aliphatic N-nitrosamines.Electron-withdrawing substituents in the aromatic ring shift the process toward denitration.

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