Skip to Content
Merck
All Photos(1)

Documents

BCR291

2,4,4′-Trichlorobiphenyl

BCR®, certified reference material

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C12H7Cl3
CAS Number:
Molecular Weight:
257.54
Beilstein:
1956846
Ballschmiter Number:
28
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
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

Looking for similar products? Visit Product Comparison Guide

Analysis Note

For more information please see:
BCR291

Legal Information

BCR is a registered trademark of European Commission

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


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Sorry, we don't have COAs for this product available online at this time.

If you need assistance, please contact Customer Support.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
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
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
Theodora E M ten Hulscher et al.
Environmental toxicology and chemistry, 24(9), 2154-2159 (2005-10-01)
The desorption kinetics of hexachlorobenzene (HCB) and 2,4,4'-trichlororbiphenyl (PCB 28) spiked to a field sediment were studied using a gas-purge technique. A contact time of up to 1,461 d was used to assess long-term changes in desorption kinetics. Purge-induced desorption

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service