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BCR298

2,2′,3,4,4′,5,5′-Heptachlorobiphenyl (IUPAC No. 180)

BCR®, certified reference material

Synonym(s):

2,2′,3,4,4′,5,5′-Heptachlorobiphenyl

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About This Item

Empirical Formula (Hill Notation):
C12H3Cl7
CAS Number:
Molecular Weight:
395.32
PubChem Substance ID:
UNSPSC Code:
41116107
NACRES:
NA.21
MDL number:
Beilstein/REAXYS Number:
2509255
Ballschmiter Number:
180
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grade

certified reference material

agency

BCR®

manufacturer/tradename

JRC

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

SMILES string

Clc1cc(Cl)c(cc1Cl)-c2cc(Cl)c(Cl)c(Cl)c2Cl

InChI

1S/C12H3Cl7/c13-6-3-8(15)7(14)1-4(6)5-2-9(16)11(18)12(19)10(5)17/h1-3H

InChI key

WBHQEUPUMONIKF-UHFFFAOYSA-N

Analysis Note

For more information please see:
BCR298

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

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves



Certificates of Analysis (COA)

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Robert Roos et al.
Toxicology, 284(1-3), 42-53 (2011-04-05)
PCB 180 (2,2',3,4,4',5,5'-heptachlorobiphenyl) is a persistent and accumulating polychlorinated biphenyl abundantly present in food and the environment. In this study, we used highly purified PCB 180 (dioxinlike impurities: 2.7 ng TEQ(WHO)/g PCB 180) in a 28-day toxicity study in young
Roshan Tofighi et al.
Toxicological sciences : an official journal of the Society of Toxicology, 124(1), 192-201 (2011-09-13)
Developmental exposure to food contaminants, such as polychlorinated biphenyls (PCBs), has been considered as a possible cause of neurodevelopmental disorders. We have investigated the effects of noncytotoxic concentrations of PCBs 153 and 180 on spontaneous differentiation of rat embryonic neural
Elsa C Antunes-Fernandes et al.
Toxicology letters, 206(2), 158-165 (2011-07-26)
Traditional risk assessment of potential endocrine-disruptive pollutants, including PCBs, focus mainly on the effects of parent compounds. Still, biotransformation results in systemic exposure to PCBs and their bioactive metabolites. In the present paper, the effects of twenty ultra-pure non-dioxin-like (NDL)