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13209-20-6

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13209-20-6 Usage

General Description

ALPHA,ALPHA,ALPHA',ALPHA',4,5-HEXABROMO-O-XYLENE, also known as HBCD, is a highly brominated flame retardant used in a variety of industries, including the production of polystyrene foam insulation, textiles, and electronics. It is a persistent organic pollutant that can build up in the environment and bioaccumulate in organisms. HBCD has been found to have toxic effects on aquatic organisms and may also pose human health risks. Due to its persistence and potential for harm, HBCD has been banned or restricted in several countries and is classified as a substance of very high concern by the European Chemicals Agency. Efforts to find safer alternatives to HBCD are ongoing in order to minimize its environmental and health impacts.

Check Digit Verification of cas no

The CAS Registry Mumber 13209-20-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,0 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13209-20:
(7*1)+(6*3)+(5*2)+(4*0)+(3*9)+(2*2)+(1*0)=66
66 % 10 = 6
So 13209-20-6 is a valid CAS Registry Number.

13209-20-6SDS

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 1,2-dibromo-4,5-bis(dibromomethyl)benzene

1.2 Other means of identification

Product number -
Other names H0831

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:13209-20-6 SDS

13209-20-6Relevant articles and documents

Synthesis and investigation of spectral and electrochemical properties of alkyl-substituted planar binuclear phthalocyanine complexes sharing a common naphthalene ring

Dubinina, Tatiana V.,Ivanov, Aleksey V.,Borisova, Natalia E.,Trashin, Stanislav A.,Gurskiy, Stanislav I.,Tomilova, Larisa G.,Zefirov, Nikolay S.

, p. 1869 - 1878 (2010)

Hexa-tert-butyl and dodeca-n-butyl-substituted planar binuclear phthalocyanines sharing a common naphthalene ring with Mg as a central metal were synthesized with high yields and characterized by UV/Vis spectra, luminescence spectra, NMR, electrochemical,

On-Surface Cyclization of ortho-Dihalotetracenes to Four- and Six-Membered Rings

Sánchez-Sánchez, Carlos,Nicola?, Adrien,Rossel, Frédéric,Cai, Jinming,Liu, Junzhi,Feng, Xinliang,Müllen, Klaus,Ruffieux, Pascal,Fasel, Roman,Meunier, Vincent

, p. 17617 - 17623 (2017)

We report on the surface-catalyzed formal [2+2] and [2+2+2] cycloadditions of ortho-activated tetracene species on a Ag(111) substrate under ultrahigh vacuum conditions. Three different products are obtained: tetracene dimers, trimers, and tetramers. The

Enhanced optical limiting performance of substituted metallo- naphthalocyanines with wide optical limiting window

Xu, Jian,Chen, Jun,Chen, Li,Hu, Rui,Wang, Shuangqing,Li, Shayu,Ma, Jin Shi,Yang, Guoqiang

, p. 144 - 150 (2014/06/23)

Octa-(4-tert-butylphenoxy) substituted naphthalocyanines coordinated with different central metals (Ga, In) were synthesized and their photophysical and optical limiting properties were investigated. The naphthalocyanines substituted peripherally with bul

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