35596
PCB No 3
analytical standard
Synonym(s):
4-Chlorobiphenyl, 4-PCB
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About This Item
Empirical Formula (Hill Notation):
C12H9Cl
CAS Number:
Molecular Weight:
188.65
EC Number:
218-127-7
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
774966
Ballschmiter Number:
3
Product Name
PCB No 3, analytical standard
InChI key
FPWNLURCHDRMHC-UHFFFAOYSA-N
InChI
1S/C12H9Cl/c13-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9H
SMILES string
Clc1ccc(cc1)-c2ccccc2
grade
analytical standard
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
application(s)
environmental
format
neat
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Application
PCB No 3 may be used as an analytical reference standard for the quantification of the analyte in aqueous solution in the presence of dissolved organic carbon using high-performance liquid chromatography technique.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
General description
Polychlorinated biphenyls (PCBs) belong to the class of highly toxic pollutants commonly found in various environmental matrices and food products. They find a variety of applications as flame retardants, plasticizers, dielectric and heat transfer fluids, etc.
Other Notes
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
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
dust mask type N95 (US), Eyeshields, Gloves
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Direct determination of hydrophobic organic compounds in aqueous solution in the presence of dissolved organic carbon by high-performance liquid chromatography
Schulze M, et al.
Chemosphere, 39(13), 2365-2374 (1999)
Anna Ptak et al.
Toxicology letters, 164(2), 113-122 (2006-01-18)
The present study was undertaken to investigate the endocrine disrupting activity of PCB3 and its hydroxylated metabolites 4-OH-PCB3 and 3,4-diOH-PCB3 in ovarian follicle cells derived from prepubertal animals with special emphasis on cytochrome P-450-dependent aromatase (CYP19). Aromatase activity was assayed
Donna L Bedard et al.
Environmental science & technology, 39(17), 6831-6838 (2005-09-30)
We have characterized the substrate range of Process LP, a PCB dechlorination activity mediated by anaerobic bacteria, in Housatonic River sediment (Lenox, MA). Process LP has the rare ability to remove unflanked para chlorines from polychlorinated biphenyls (PCBs). We used
G Luthe et al.
Acta crystallographica. Section B, Structural science, 63(Pt 2), 319-327 (2007-03-22)
Accurate structure determinations by X-ray crystal analysis and computation using semi-empirical self-consistent field molecular orbital calculations are described and compared for five monofluorinated analogues of 4-chlorobiphenyl, i.e. 2-fluoro-4-chlorobiphenyl, 2'-fluoro-4-chlorobiphenyl, 3-fluoro-4-chlorobiphenyl, 3'-fluoro-4-chlorobiphenyl and 4'-fluoro-4-chlorobiphenyl. Intermolecular interactions for all monofluorinated isomers are
Parvaneh Espandiari et al.
Toxicological sciences : an official journal of the Society of Toxicology, 79(1), 41-46 (2004-02-21)
We recently reported that several mono- to tetrachlorinated biphenyls have initiating activity in the livers of Fischer 344 rats. In the present study, we investigated the metabolic activation of one of those compounds, 4-chlorobiphenyl (PCB 3). Monohydroxy (400 micromol/kg), dihydroxy
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