35592
PCB No 2
analytical standard
Synonym(s):
3-Chlorobiphenyl, 3-PCB
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About This Item
Empirical Formula (Hill Notation):
C12H9Cl
CAS Number:
Molecular Weight:
188.65
Beilstein:
1863135
Ballschmiter Number:
2
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
grade
analytical standard
Quality Level
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
application(s)
environmental
format
neat
SMILES string
Clc1cccc(c1)-c2ccccc2
InChI
1S/C12H9Cl/c13-12-8-4-7-11(9-12)10-5-2-1-3-6-10/h1-9H
InChI key
NMWSKOLWZZWHPL-UHFFFAOYSA-N
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General description
Polychlorinated biphenyls (PCBs) are groups of chemical compounds which are persistent in the environment and are considered highly toxic to humans and animals. PCB No 2 may be used for environmental analysis and precise quality control of food and feed.
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Recommended products
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Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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M W Kennedy et al.
Biochemical pharmacology, 29(5), 727-736 (1980-03-01)
In vitro rat hepatic microsomal metabolism of the monochlorobiphenyls (MCBs) 2-, 3- and 4-chlorobiphenyl, has been investigated as a model for the metabolism of polychlorinated biphenyl pollutants. MCB metabolism was catalyzed by cytochrome P-450, as indicated by a dependence on
B P Maliwal et al.
Journal of lipid research, 23(3), 474-479 (1982-03-01)
The uptake, distribution, and exchange of chlorinated hydrocarbon insecticides (dieldrin and chlordecone) and biphenyls (2,4,5-2',4',5'-hexachlorobiphenyl and 3-chlorobiphenyl) among human lipoproteins was examined by fluorescence quenching, gel filtration, and ultrafiltration. The chlorinated hydrocarbons were rapidly taken up from solution or silica
F Fava et al.
Applied microbiology and biotechnology, 36(2), 240-245 (1991-11-01)
A mixed bacterial culture obtained from polychlorinated-biphenyl-contaminated river sediments proved capable of degrading 3-chlorobiphenyl (3-CB) under aerobic laboratory conditions. Almost total mineralization of 150 mg/l of 3-CB occurred when, after 3 days of incubation, the mineral medium was supplied with
Q Zhang et al.
Environmental science & technology, 35(24), 4933-4935 (2002-01-05)
Grinding a mixture of 3-chlorobiphenyl (BP-Cl) and CaO with or without the addition of quartz was conducted in air by a planetary ball mill to investigate the mechanochemical dechlorination of BP-Cl. The dechlorinating reaction proceeds with an increase in grinding
D Springael et al.
Microbiology (Reading, England), 142 ( Pt 11), 3283-3293 (1996-11-01)
Chromosomal DNA fragments encoding the ability to utilize biphenyl as sole carbon source (Bph+) were mobilized by means of plasmid RP4::Mu3A from strain JB1 (tentatively identified as Burkholderia sp.) to Alcaligenes eutrophus CH34 at a frequency of 10(-3) per transferred
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