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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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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;
R G Schnellmann et al.
Biochemical pharmacology, 33(21), 3503-3509 (1984-11-01)
Since chlorine placement and the degree of chlorination of the biphenyl nucleus play an important role in the metabolism and ultimate elimination of polychlorinated biphenyls (PCBs), we have studied the metabolism of 4,4'-dichlorobiphenyl (4-DCB) by human hepatic microsomes. This low
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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