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Safety Information

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
Beilstein:
2053828
Ballschmiter Number:
52
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
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

Signal Word

Warning

Hazard Statements

Precautionary Statements

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

PRTR

Specified Class I Designated Chemical Substances

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

BCR293-25MG:


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
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
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
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

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