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35597

Supelco

PCB No 15

analytical standard

Synonym(s):

4,4′-Dichlorobiphenyl, 4,4′-PCB

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About This Item

Empirical Formula (Hill Notation):
C12H8Cl2
CAS Number:
2050-68-2
Molecular Weight:
223.10
Beilstein:
2044700
Ballschmiter Number:
15
EC Number:
218-095-4
MDL number:
MFCD00013641
UNSPSC Code:
41116107
PubChem Substance ID:
329755193
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

Clc1ccc(cc1)-c2ccc(Cl)cc2

InChI

1S/C12H8Cl2/c13-11-5-1-9(2-6-11)10-3-7-12(14)8-4-10/h1-8H

InChI key

YTBRNEUEFCNVHC-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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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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Certificates of Analysis (COA)

Lot/Batch Number
BCCD6884
BCCD4578
BCBV0152
SZBC340XV
SZB9315XV

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Uptake of 4-chlorobiphenyl and 4,4'-dichlorobiphenyl in six species of plant tissue cultures.
K Yamamoto et al.
Bulletin of environmental contamination and toxicology, 28(6), 728-732 (1982-06-01)
W Chu et al.
Water research, 36(9), 2187-2194 (2002-07-11)
Surfactant and organic solvents have individually been shown useful in assisting the solubilization of hydrophobic organics out of contaminated soil and promoting UV-induced photodecay at a succeeding treatment process. A newly proposed process is to use the mixtures of surfactant
R Mavoungou et al.
The Science of the total environment, 101(3), 263-268 (1991-01-15)
Anaerobic cultures containing 4,4'-dichlorobiphenyl (4,4'CB) were inoculated with various environmental samples. The degradation of the substrate was followed by gas chromatographic analysis. Three of the cultures tested showed an ability to dehalogenate the substrate, as judged by the presence of
L van Bree et al.
Toxicology, 42(2-3), 259-274 (1986-12-15)
Both 4,4'-dichlorobiphenyl (4,4'-DCB) and 3-methylcholanthrene (3-MC) caused a substantial increase of phenacetin-induced hepatic glutathione (GSH) depletion, whereas phenobarbital (PB) had no effect, suggesting that 4,4'-DCB possesses cytochrome P-448 inducing activity. The O-deethylation of phenacetin by liver microsomes from control and
C Edwin Garner et al.
Toxicology and applied pharmacology, 216(1), 157-167 (2006-06-21)
The fate of selected polychlorobiphenyls (PCBs) was investigated following single dermal administration (0.4 mg/kg) to determine the effects of chlorine content and position on the disposition of PCBs following dermal absorption. Single dermal doses of (14)C-labeled mono-, di-, tetra- and
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