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31139-42-1

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31139-42-1 Usage

Description

4,4'-BIPHENYLDISULFONIC ACID DISODIUM SALT is a chemical compound characterized by two benzene rings linked by sulfur atoms, with sulfonic acid groups that are associated with two sodium ions. It is recognized for its water solubility, lightfastness, and heat resistance, which contribute to its utility in various industrial applications.

Uses

Used in Textile Industry:
4,4'-BIPHENYLDISULFONIC ACID DISODIUM SALT is used as a fluorescent dye and optical brightener to enhance the color intensity and appearance of textiles, providing a durable and vibrant finish to fabrics.
Used in Paper Industry:
In the paper industry, 4,4'-BIPHENYLDISULFONIC ACID DISODIUM SALT serves as a brightening agent, improving the whiteness and visual appeal of paper products, while also contributing to their longevity due to its lightfastness.
Used in Detergent Industry:
4,4'-BIPHENYLDISULFONIC ACID DISODIUM SALT is utilized as a brightening agent in detergents to make fabrics appear cleaner and brighter, taking advantage of its ability to absorb and reflect ultraviolet light.
Used as a pH Buffer:
4,4'-BIPHENYLDISULFONIC ACID DISODIUM SALT is used as a pH buffer in various applications to maintain stable pH levels, which is crucial for processes sensitive to pH changes.
Used as a Corrosion Inhibitor:
Due to its capacity to form stable complexes with metal ions, 4,4'-BIPHENYLDISULFONIC ACID DISODIUM SALT is employed as a corrosion inhibitor in industrial settings to protect metal surfaces from degradation.
It is important to handle 4,4'-BIPHENYLDISULFONIC ACID DISODIUM SALT with care due to its potential irritant and corrosive properties, ensuring safety in its applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 31139-42-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,1,3 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 31139-42:
(7*3)+(6*1)+(5*1)+(4*3)+(3*9)+(2*4)+(1*2)=81
81 % 10 = 1
So 31139-42-1 is a valid CAS Registry Number.

31139-42-1SDS

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 sodium,4-(4-sulfophenyl)benzenesulfonic acid

1.2 Other means of identification

Product number -
Other names 4,4'-biphenyldisulfonic acid disodium salt

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:31139-42-1 SDS

31139-42-1Downstream Products

31139-42-1Relevant articles and documents

A Double Cation–π-Driven Strategy Enabling Two-Dimensional Supramolecular Polymers as Efficient Catalyst Carriers

Chen, Hongbo,Deng, Qiang,Dong, Xuxu,Ren, Dazhuo,Tian, Wei,Wang, Dapeng,Xiao, Xuedong

supporting information, p. 9534 - 9541 (2020/05/08)

The cation–π interaction is a strong non-covalent interaction that can be used to prepare high-strength, stable supramolecular materials. However, because the molecular plane of a cation-containing group and that of aromatic structure are usually perpendicular when forming a cation–π complex, it is difficult to exploit the cation–π interaction to prepare a 2D self-assembly in which the molecular plane of all the building blocks are parallel. Herein, a double cation–π-driven strategy is proposed to overcome this difficulty and have prepared 2D self-assemblies with long-range ordered molecular hollow hexagons. The double cation–π interaction makes the 2D self-assemblies stable. The 2D self-assemblies are to be an effective carrier that can eliminate metal-nanoparticle aggregation. Such 2D assembly/palladium nanoparticle hybrids are shown to exhibit recyclability and superior catalytic activity for a model reaction.

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