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2,4,5,6-TETRACHLORO-M-XYLENE-A,A'-DIOL, also known as TCX, is a synthetic organic compound belonging to the chlorinated m-xylene family. It serves as a precursor in the production of specific polymers and resins, characterized by its potential toxicity and environmental impact.

39568-89-3

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39568-89-3 Usage

Uses

Used in Polymer and Resin Production:
2,4,5,6-TETRACHLORO-M-XYLENE-A,A'-DIOL is used as a precursor in the chemical industry for the synthesis of certain polymers and resins. Its application is crucial for creating materials with specific properties required in various industrial applications.
Used in Chemical Synthesis:
In the chemical synthesis industry, 2,4,5,6-TETRACHLORO-M-XYLENE-A,A'-DIOL is utilized as an intermediate in the production of other chemical compounds. Its unique structure allows for further reactions to yield desired end products.

Check Digit Verification of cas no

The CAS Registry Mumber 39568-89-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,5,6 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 39568-89:
(7*3)+(6*9)+(5*5)+(4*6)+(3*8)+(2*8)+(1*9)=173
173 % 10 = 3
So 39568-89-3 is a valid CAS Registry Number.

39568-89-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [2,3,4,6-tetrachloro-5-(hydroxymethyl)phenyl]methanol

1.2 Other means of identification

Product number -
Other names 2,4,5,6-Tetrachlorobenzene-l,3-dimethanol

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:39568-89-3 SDS

39568-89-3Upstream product

39568-89-3Downstream Products

39568-89-3Relevant 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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