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35601

Supelco

PCB No 28

analytical standard

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Synonym(s):
2,4,4′-Trichlorobiphenyl, 2,4,4′-PCB
Empirical Formula (Hill Notation):
C12H7Cl3
CAS Number:
Molecular Weight:
257.54
Beilstein/REAXYS Number:
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

signalword

Warning

hcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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)
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
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

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