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Merck

35596

PCB No 3

analytical standard

Sinónimos:

4-Chlorobiphenyl

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Acerca de este artículo

Fórmula empírica (notación de Hill):
C12H9Cl
Número CAS:
Peso molecular:
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
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Nombre del producto

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.

pictograms

Health hazardEnvironment

signalword

Warning

hcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Clase de almacenamiento

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)
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
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
Guangshu Zhai et al.
Environmental science & technology, 47(1), 557-562 (2012-12-12)
4-Monochlorobiphenyl (PCB3) has been proven to be transformed into hydroxylated metabolites of PCB3 (OH-PCB3s) in whole poplar plants in our previous work. However, hydroxylated metabolites of PCBs, including OH-PCB3s, as the substrates of sulfotransferases have not been studied in many
Markus Alexander Zettner et al.
Toxicological sciences : an official journal of the Society of Toxicology, 100(1), 88-98 (2007-08-10)
4-Monochlorobiphenyl (PCB3) is a component of commercial polychlorinated biphenyl (PCB) products and is an airborne environmental pollutant. Our recent study with transgenic Fischer 344 rats revealed the mutagenic potential of PCB3 in the livers of male rats. PCB3 is converted

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