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BCR293

2,2′,5,5′-Tetrachlorobiphenyl (IUPAC No. 52)

BCR®, certified reference material

Synonym(s):

2,2′,5,5′-Tetrachlorobiphenyl

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About This Item

Empirical Formula (Hill Notation):
C12H6Cl4
CAS Number:
35693-99-3
Molecular Weight:
291.99
Beilstein:
2053828
Ballschmiter Number:
52
MDL number:
MFCD00055544
UNSPSC Code:
41116107
PubChem Substance ID:
329773809
NACRES:
NA.24

grade

certified reference material

Agency

BCR®

manufacturer/tradename

JRC

format

neat

storage temp.

2-8°C

SMILES string

Clc1ccc(Cl)c(c1)-c2cc(Cl)ccc2Cl

InChI

1S/C12H6Cl4/c13-7-1-3-11(15)9(5-7)10-6-8(14)2-4-12(10)16/h1-6H

InChI key

HCWZEPKLWVAEOV-UHFFFAOYSA-N

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Analysis Note

For more information please see:
BCR293

Legal Information

BCR is a registered trademark of European Commission

Pictograms

Health hazardEnvironment
GHS08,GHS09

Signal Word

Warning

Hazard Statements

H373,H410

Precautionary Statements

P260 - P273 - P314 - P391 - P501

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Patrick Schäfer et al.
Archives of biochemistry and biophysics, 488(1), 60-68 (2009-07-01)
There are 75 full length cytochrome P450 (CYP) genes known in the genome of the nematode Caenorhabditis elegans. The individual biological functions of the vast majority are mostly as yet unknown. Here the impact of cytochrome P450 isoforms on the
Ze-Yu Yang et al.
Chemosphere, 72(10), 1435-1440 (2008-07-04)
To verify a theoretical mass balance and multiple compartment partitioning model developed to predict freely dissolved concentrations (FDCs) of hydrophobic organic chemicals (HOCs) using negligible depletion-solid phase microextraction (nd-SPME), a series of sediment slurry experiments were performed using disposable poly(dimethyl)siloxane
R J Jandacek et al.
Environment international, 36(8), 880-883 (2009-07-21)
Mice were gavaged with either (14)C-labeled 2,2'5,5' tetrachlorobiphenyl; 3,3',4,4' tetrachlorobiphenyl; or perfluorooctanoic acid. Absorption of these compounds was determined by assay of feces collected for 48 h after the gavage. Part of the animals received test diets containing olestra during
Chia-Hua Lin et al.
Toxicology letters, 188(1), 11-19 (2009-05-13)
Polychlorinated biphenyls (PCBs) are ubiquitous environmental contaminants. Much of the research has focused on the carcinogenic potential of higher chlorinated PCBs, but accumulative evidence has shown that lower chlorinated PCB congeners have initiating and promoting activities. The goal of this
Kristine L Richardson et al.
Chemical research in toxicology, 24(5), 718-725 (2011-04-13)
The rates of oxidative metabolism of two tetrachlorobiphenyl congeners were determined in hepatic microsomes from four species of sea turtles, green (Chelonia mydas), olive ridley (Lepidochelys olivacea), loggerhead (Caretta caretta), and hawksbill (Eretmochelys imbricata). Hydroxylation of 3,3',4,4'-tetrachlorobiphenyl (PCB 77), an
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