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Benzene, 1,2,3,4-tetrachloro-5,6-bis(chloromethyl)-, also known as Hexachloro-1,3-butadiene or Perchlorobutadiene, is a chlorinated organic compound with the chemical formula C4Cl6. It is a colorless, oily liquid with a pungent odor. Benzene, 1,2,3,4-tetrachloro-5,6-bis(chloromethyl)- is formed by the addition of two chloromethyl groups to the 1,3-butadiene molecule, which is already substituted with four chlorine atoms. Due to its highly chlorinated nature, it is considered a persistent and potentially hazardous chemical. It has been used in the past as a chemical intermediate in the production of pesticides and other chemicals, but its use has been restricted or banned in many countries due to its toxicity and environmental persistence.

1079-15-8

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1079-15-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1079-15-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1079-15:
(6*1)+(5*0)+(4*7)+(3*9)+(2*1)+(1*5)=68
68 % 10 = 8
So 1079-15-8 is a valid CAS Registry Number.

1079-15-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4-tetrachloro-5,6-bis(chloromethyl)benzene

1.2 Other means of identification

Product number -
Other names 1,2,3,4-Tetrachlor-5,6-bis-chlormethyl-benzol

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:1079-15-8 SDS

1079-15-8Relevant academic research and scientific papers

Polyhalobenzylic disulfooxonium compounds

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, (2008/06/13)

Polyhalobenzylic disulfooxonium compounds are produced by the reaction of aromatic methyl, halomethyl or hydroxymethyl substituents with sulfur trioxide. The disulfooxonium salts are readily converted to alcohols by hydrolysis to provide monomers for the production of fire resistant polymers and additives for polymers. Likewise, the disulfooxonium compounds of this invention present chemical intermediates for a wide range of useful products such as halogenated pesticides.

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