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BCR291

2,4,4′-Trichlorobiphenyl

BCR®, certified reference material

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About This Item

Empirical Formula (Hill Notation):
C12H7Cl3
CAS Number:
7012-37-5
Molecular Weight:
257.54
Beilstein:
1956846
Ballschmiter Number:
28
EC Number:
230-293-2
MDL number:
MFCD00055554
UNSPSC Code:
41116107
PubChem Substance ID:
329773808
NACRES:
NA.24

grade

certified reference material

Agency

BCR®

manufacturer/tradename

JRC

format

neat

storage temp.

2-8°C

SMILES string

Clc1ccc(cc1)-c2ccc(Cl)cc2Cl

InChI

1S/C12H7Cl3/c13-9-3-1-8(2-4-9)11-6-5-10(14)7-12(11)15/h1-7H

InChI key

BZTYNSQSZHARAZ-UHFFFAOYSA-N

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Analysis Note

For more information please see:
BCR291

Legal Information

BCR is a registered trademark of European Commission

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

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Shui-Ping Wu et al.
Huan jing ke xue= Huanjing kexue, 32(11), 3277-3283 (2012-02-03)
The levels and congener patterns of 28 PCBs compounds were investigated in soil and dust fallout collected in a capacitor storage site and an industrial brownfield, respectively in Sichuan Ziyang Locomotive Factory. The highest concentration of the total PCBs(sigma PCBs
A J Lambo et al.
Journal of applied microbiology, 102(5), 1318-1329 (2007-04-24)
To determine the extent and pattern of degradation of polychlorinated biphenyls (PCBs) in Aroclor 1232 at 5 degrees C by a psychrotolerant bacterium, and to confirm the formation of intermediates of PCB metabolism at low temperature using 2,4,4'-trichlorobiphenyl (2,4,4'-TCB). 10
Yu Wang et al.
Environmental science and pollution research international, 19(2), 448-457 (2011-08-09)
Dechlorination of polychlorinated biphenyls (PCBs) by nanoscale zerovalent iron (NZVI) is often strongly hindered by increased pH because large amounts of H(+) ions were consumed during the surface reaction. The main objective of this work was to evaluate the effect
Leticia Gómez-Gil et al.
Journal of bacteriology, 189(15), 5705-5715 (2007-05-29)
Biphenyl dioxygenase (BPDO) catalyzes the aerobic transformation of biphenyl and various polychlorinated biphenyls (PCBs). In three different assays, BPDO(B356) from Pandoraea pnomenusa B-356 was a more potent PCB-degrading enzyme than BPDO(LB400) from Burkholderia xenovorans LB400 (75% amino acid sequence identity)
Li Xu et al.
Huan jing ke xue= Huanjing kexue, 31(1), 255-259 (2010-03-25)
The capability of Rhizobium meliloti on degrading 2,4,4'-trichlorobiphenyl and 18 kinds of polychlorinated biphenyl congener mixtures was studied by shaking flask experiment. The results showed that the degradation capability of Rhizobium meliloti to 2, 4, 4'-trichlorobiphenyl increased gradually with the
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