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2,2'-Dicarboxyhydrazobenzene, also known as 2,2'-azoisobutyronitrile (AIBN), is an organic compound widely used as a radical initiator in various chemical reactions, particularly in the polymerization process. It is a white crystalline solid with a molecular formula of C8H6N4O2 and a molecular weight of 194.16 g/mol. AIBN decomposes upon heating, producing free radicals that initiate the polymerization of monomers. It is commonly used in the synthesis of various polymers, such as polystyrene, polyvinyl chloride, and polyacrylates. Due to its sensitivity to heat and light, AIBN is typically stored in a cool, dark place and handled with care to prevent accidental decomposition.

612-44-2

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612-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 612-44-2 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 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 612-44:
(5*6)+(4*1)+(3*2)+(2*4)+(1*4)=52
52 % 10 = 2
So 612-44-2 is a valid CAS Registry Number.

612-44-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2'-dicarboxyhydrazobenzene

1.2 Other means of identification

Product number -
Other names N,N'-Bis-(2-carboxy-phenyl)-hydrazin

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:612-44-2 SDS

612-44-2Relevant academic research and scientific papers

Proton-coupled electron transfer in azobenzene/hydrazobenzene couples with pendant acid-base functions. Hydrogen-bonding and structural effects

Savéant, Jean-Michel,Tard, Cédric

, p. 8907 - 8910 (2014)

Electron transfer in azobenzene derivatives bearing two carboxylic acid groups is coupled with intramolecular proton transfer in a stepwise manner in the title 2e- + 2H+ redox couple. The presence of the pendant acid-base functions p

Immunochemical assay method

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, (2008/06/13)

Haptens and antigen derivatives are coupled, through an azo bond, to proteins to form a conjugated material. The conjugate is injected into laboratory animals to raise antibodies which are useful in immunochemically assaying for the original haptens and a

Radioimmune method of assaying quantitatively for a hapten

-

, (2008/06/13)

A radioimmune method of assaying quantitatively for a hapten comprising contacting an aqueous sample containing the hapten under assay, a known quantity of a radioactively labeled marker which incorporates a hapten homologous to the hapten under assay, an

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