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Key Documents

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:
Molecular Weight:
223.10
Beilstein:
2044700
Ballschmiter Number:
15
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

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

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

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Accumulation and excretion of isopropylchlorobiphenyls in mouse and fish.
K Sugiura et al.
Bulletin of environmental contamination and toxicology, 26(1), 46-53 (1981-01-01)
Ichiro Kamei et al.
Applied microbiology and biotechnology, 72(3), 566-575 (2006-03-11)
Degradation experiment of model polychlorinated biphenyl (PCB) compound 4,4'-dichlorobiphenyl (4,4'-DCB) and its metabolites by the white-rot fungus Phanerochaete chrysosporium and newly isolated 4,4'-DCB-degrading white-rot fungus strain MZ142 was carried out. Although P. chrysosporium showed higher degradation of 4,4'-DCB in low-nitrogen
W Chu et al.
Water research, 37(10), 2442-2448 (2003-05-03)
The system design based on the photodegradation kinetics of 4,4'-dichlorobiphenyl (4,4'-DCB) in surfactant solution with the aid of solvents (acetone and/or squalane) has been studied. Organic solvents acetone and squalane were added as a photosensitizer and a hydrogen source, respectively
T A Marks et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 13(4), 681-693 (1989-11-01)
Outbred albino (CD-1) mice were given the following biphenyl isomers by gavage in cottonseed oil on Days 6-15 of gestation: 4,4'-dichlorobiphenyl (DCB) at 16, 32, and 64 mg/kg/day; 3,3',4,4'-tetrachlorobiphenyl (3,4-TCB) at 1,2,4,8,16,32, and 64 mg/kg/day; 3,3',5,5'-tetrachlorobiphenyl (3,5-TCB) at 64 mg/kg/day;
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)

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