35595
PCB No 14
analytical standard
Synonym(s):
3,5-Dichlorobiphenyl, 3,5-PCB
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About This Item
Empirical Formula (Hill Notation):
C12H8Cl2
CAS Number:
Molecular Weight:
223.10
Beilstein/REAXYS Number:
1944311
Ballschmiter Number:
14
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
Recommended Products
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
Clc1cc(Cl)cc(c1)-c2ccccc2
InChI
1S/C12H8Cl2/c13-11-6-10(7-12(14)8-11)9-4-2-1-3-5-9/h1-8H
InChI key
QHZSDTDMQZPUKC-UHFFFAOYSA-N
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 14 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.
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Nina P Gritsan et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 4(1), 23-32 (2004-12-24)
The dynamics of singlet 3,5-dichloro-2-biphenylnitrene and the products of its rearrangement were monitored by pico- and nanosecond laser flash photolysis and the results were consistent with the predictions of DFT and ab initio molecular orbital calculations.
J Havel et al.
Applied microbiology and biotechnology, 43(5), 914-919 (1995-10-01)
The influence of different forms of substrate administration (either through the vapour phase or the liquid phase) on growth of two bacterial strains on biphenyl, 2-chlorobiphenyl, and 3,5-dichlorobiphenyl has been investigated. During growth with all three compounds, the availability of
H A J Govers et al.
SAR and QSAR in environmental research, 13(2), 271-280 (2002-06-20)
Enthalpies of transfer at 300 K of various partitioning processes were calculated in order to study the suitability of 3D force fields for the calculation of partitioning constants. A 3D fulvic acid (FA) model of dissolved organic carbon (DOC) was
Metabolism of dichlorobiphenyls by hepatic microsomal cytochrome P-450.
M W Kennedy et al.
Biochemical pharmacology, 30(6), 577-588 (1981-03-15)
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