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Key Documents

35601

Supelco

PCB No 28

analytical standard

Synonym(s):

2,4,4′-Trichlorobiphenyl, 2,4,4′-PCB

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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

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

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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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 28 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.

Recommended products

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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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number

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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
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)
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

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