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Merck
CN

BCR291

2,4,4′-三氯联苯

BCR®, certified reference material

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经验公式(希尔记法):
C12H7Cl3
化学文摘社编号:
分子量:
257.54
EC Number:
230-293-2
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1956846
Ballschmiter Number:
28
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InChI key

BZTYNSQSZHARAZ-UHFFFAOYSA-N

InChI

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

SMILES string

Clc1ccc(cc1)-c2ccc(Cl)cc2Cl

grade

certified reference material

agency

BCR®

manufacturer/tradename

JRC

format

neat

storage temp.

2-8°C

Analysis Note

For more information please see:
BCR291

Legal Information

BCR is a registered trademark of European Commission

pictograms

Health hazardEnvironment

signalword

Warning

hcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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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
Xiang-Hui Sun et al.
Huan jing ke xue= Huanjing kexue, 31(10), 2327-2330 (2011-01-15)
Sorption behaviors of PCB28 to phosphatidylcholine (PC)and triglyceride (TG) were studied. Results showed that sorption equilibrium could be achieved in 8 h for PCB28, and the sorption amount on PC was higher than that of TG when the initial PCB28
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
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)
Chen Tu et al.
Journal of hazardous materials, 186(2-3), 1438-1444 (2011-01-05)
Resting cell assay and soil microcosms were set up to investigate the biodegradation capability and metabolic intermediate of polychlorinated biphenyls (PCBs) by a rhizobial strain Sinorhizobium meliloti. Biodegradation was observed immediately after 2,4,4'-TCB was supplied as a sole source of

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