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Merck

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:
Molecular Weight:
291.99
PubChem Substance ID:
UNSPSC Code:
41116107
NACRES:
NA.24
MDL number:
Beilstein/REAXYS Number:
2053828
Ballschmiter Number:
52

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Product Name

2,2′,5,5′-Tetrachlorobiphenyl (IUPAC No. 52), BCR®, certified reference material

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

grade

certified reference material

agency

BCR®

manufacturer/tradename

JRC

format

neat

storage temp.

2-8°C

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1 of 4

This Item
BCR297BCR296BCR298
manufacturer/tradename

JRC

manufacturer/tradename

JRC

manufacturer/tradename

JRC

manufacturer/tradename

JRC

grade

certified reference material

grade

certified reference material

grade

certified reference material

grade

certified reference material

format

neat

format

neat

format

neat

format

neat

agency

BCR®

agency

BCR®

agency

BCR®

agency

BCR®

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

Analysis Note

For more information please see:
BCR293

Legal Information

BCR is a registered trademark of European Commission

pictograms

Health hazardEnvironment

signalword

Warning

hcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves


Certificates of Analysis (COA)

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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
Suleyman Sandal et al.
Mutation research, 654(1), 88-92 (2008-06-25)
Polychlorinated biphenyls (PCBs) are known to be carcinogenic, but the mechanisms of this action are uncertain. Most, but not all, studies have concluded that PCBs are not directly mutagenic, and that much if not all of the carcinogenic activity resides
Bayram Yilmaz et al.
Environmental toxicology, 27(3), 185-191 (2011-02-24)
Cultured porcine endothelial cells were used to determine the effects of several congeners of polychlorinated biphenyls (PCBs) on cell viability and changes induced by these congeners on levels of intracellular calcium and reactive oxygen species (ROS). Cultured endothelial cells were
Chiho Ohta et al.
Fukuoka igaku zasshi = Hukuoka acta medica, 100(5), 200-209 (2009-07-11)
Our preceding studies have reported that 2,2',5,5'-tetrachlorobiphenyl (tetraCB)(CB52) is mainly metabolized to 3-hydroxy (OH)-metabolite by phenobarbital (PB)-inducible cytochrome P450 (P450) isoforms such as CYP2B1 and CYP2B18. In this study, the metabolism of CB52 by liver microsomes of untreated and PB-treated
Marta Venier et al.
Environmental science & technology, 46(7), 3928-3934 (2012-03-22)
We analyzed the vapor phase atmospheric concentrations of representative persistent chemicals (i.e., α- and γ-hexachlorocyclohexane, phenanthrene, PCB-18 and PCB-52) in samples collected at a remote site near Eagle Harbor, Michigan, and at an urban site in Chicago, Illinois, using four

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