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Sodium o-aminobenzenesulfonate, also known as sodium 2-aminobenzenesulfonate, is a chemical compound characterized by its molecular formula C6H7NNaO3S. It is a white to off-white, crystalline powder that exhibits solubility in water. Sodium o-aminobenzenesulfonate is recognized for its good stability and water solubility, attributes that stem from its sulfonate group, making it a versatile and widely used chemical in a range of industries.

13846-13-4

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13846-13-4 Usage

Uses

Used in Dye and Pigment Manufacturing:
Sodium o-aminobenzenesulfonate is utilized as a key intermediate in the production of dyes and pigments. Its chemical properties allow for the creation of a variety of colorants used across different applications.
Used in Pharmaceutical Products:
In the pharmaceutical industry, sodium o-aminobenzenesulfonate serves as an important component in the formulation of certain medications. Its solubility and stability contribute to the effectiveness and safety of these products.
Used in Cosmetic Products:
Sodium o-aminobenzenesulfonate is also incorporated into cosmetic products, where it plays a role in enhancing their performance and quality, leveraging its solubility and chemical characteristics.
Used in Water Treatment as a Corrosion Inhibitor:
In the water treatment sector, sodium o-aminobenzenesulfonate is applied as a corrosion inhibitor. Its ability to prevent the corrosion of metal surfaces in water systems is valuable for maintaining the integrity and longevity of water infrastructure.

Check Digit Verification of cas no

The CAS Registry Mumber 13846-13-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,4 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13846-13:
(7*1)+(6*3)+(5*8)+(4*4)+(3*6)+(2*1)+(1*3)=104
104 % 10 = 4
So 13846-13-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H7NO3S.Na/c7-10-11(8,9)6-4-2-1-3-5-6;/h1-5H,7H2;/q;+1

13846-13-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,2-aminobenzenesulfonate

1.2 Other means of identification

Product number -
Other names sodium 2-aminobenzenesulfonate

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:13846-13-4 SDS

13846-13-4Relevant articles and documents

A porous trimetallic Au@Pd@Ru nanoparticle system: Synthesis, characterisation and efficient dye degradation and removal

Sahoo, Anupam,Tripathy, Suman Kumar,Dehury, Niranjan,Patra, Srikanta

, p. 19376 - 19383 (2015)

A facile room temperature one-pot synthesis of trimetallic porous Au@Pd@Ru nanoparticles (Au@Pd@RuNPs) has been developed. The trimetallic nanoparticles have been prepared by the successive sacrificial oxidation of cobalt nanoparticles (CoNPs). The average particle size of Au@Pd@RuNPs is 110 nm. The porous nature and the presence of Au, Pd and Ru have been confirmed via TEM, FE-SEM and EDS analyses. The trimetallic nanoparticles have shown excellent catalytic activity towards the reduction of p-nitrophenol and efficient degradation of various azo dyes. This has been further extended towards the removal of colour from waste water via the catalytic degradation of azo dyes. Moreover, the produced amine can be eliminated from the waste water via its sorption on an industrial solid waste dolochar.

Hydrogenation of ortho-substituted nitrobenzenes over palladium catalysts

Klyuev,Volkova,Abdullaev

, p. 30 - 33 (2007/10/03)

Hydrogenation of o-nitrobenzenes, under mild conditions (1 atm of hydrogen, 20-40°C, organic solvents) over a Pd/C catalyst and the palladium-containing anion exchangers AN-1 and AV-17-8 proceeds without the formation of intermediate products. The yield of primary amines varies from 25 to 100%. It was shown that the palladium-containing anion exchangers are superior to Pd/C in selectivity and stability in the hydrogenation of o-nitrobenzenes. Based on quantum-chemical calculations of substrate molecules, a two-parameter correlation was proposed to describe the electronic and steric effects of the substituent on the hydrogenation rate.

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