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1,3-Butadiene-1,4-dicarbonitrile, also known as Pandion, is a synthetic organic compound characterized by its colorless liquid form and a pungent odor. It is highly flammable and classified as a hazardous chemical, with its potential carcinogenic properties posing significant health risks to humans. Exposure to this chemical can occur through various routes, including inhalation, ingestion, or skin contact, necessitating strict handling and disposal protocols to mitigate its negative environmental and health impacts.

821-60-3

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821-60-3 Usage

Uses

Used in Chemical Industry:
1,3-Butadiene-1,4-dicarbonitrile is used as a crosslinking agent for the production of acrylic resins. Its ability to form crosslinks enhances the properties of the resulting resins, such as their stability, durability, and resistance to various environmental factors.
Used in Manufacturing of Acrylic Resins:
In the manufacturing process of acrylic resins, 1,3-Butadiene-1,4-dicarbonitrile serves as a crucial component that improves the structural integrity and performance of the final product. Its crosslinking capabilities contribute to the development of resins with enhanced mechanical strength, thermal stability, and chemical resistance, making them suitable for a wide range of applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 821-60-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 821-60:
(5*8)+(4*2)+(3*1)+(2*6)+(1*0)=63
63 % 10 = 3
So 821-60-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H4N2/c7-5-3-1-2-4-6-8/h1-4H

821-60-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-Hexadienedinitrile

1.2 Other means of identification

Product number -
Other names 1,4-Dicyano-1,3-butadien

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:821-60-3 SDS

821-60-3Downstream Products

821-60-3Relevant academic research and scientific papers

Improvement of catalyst activity in the Ru-catalyzed dimerization of acrylonitrile by using diphenyl ether as a solvent

Kashiwagi, Kohichi,Sugise, Ryoji,Shimakawa, Toshihiro,Matuura, Tunao

, p. 1384 - 1385 (2008/03/18)

For the catalyst system of ruthenium and carboxylic acid, which is useful for the efficient tail-to-tail dimerization of acrylonitrile, the TON increases as the ruthenium catalyst concentration is decreased. Furthermore, the addition of aromatic solvents of equal volume to that of acrylonitrile improves the catalyst activity. Especially, the use of diphenyl ether leads to a 1.7 time improvement of the TON. Copyright

Linear relationship between activity of a new Ru-catalyst and acidity of substituted benzoic acids in the dimerization of acrylonitrile

Kashiwagi, Kohichi,Sugise, Ryoji,Shimakawa, Toshihiro,Matuura, Tunao,Shirai, Masashi

, p. 186 - 187 (2007/10/03)

A new type of catalyst system using ruthenium and carboxylic acid is useful for the tail-to-tail dimerization of acrylonitrile, proceeding without the formation of undesired by-product propionitrile. Carboxylic acids having pK a 3.5-5 are suitable as co-catalysts for the dimerization of acrylonitrile. The relationship between the logarithm of the relative rate in the dimer formation and the pKa of m- and p-substituted benzoic acids (Bronsted plot) was linear (R2 = 0.946) with a slope of -0.199. The role of the carboxylic acids can be considered to be effective protonation in the protonolysis of the carbon-ruthenium bond of an intermediate Ru complex. Copyright

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