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47616-U

Supelco

Camphechlor solution

analytical standard, 200 μg/mL in isooctane, ampule of 1 mL

Synonyme(s) :

Camphechlor solution

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About This Item

Numéro CAS:
8001-35-2
Code UNSPSC :
77101502
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Caractéristiques

calibration

Conditionnement

ampule of 1 mL

Concentration

200 μg/mL in isooctane

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

environmental

Format

single component solution

Température de stockage

room temp

InChI

1S/C10H8Cl8/c1-4-7(2-11,3-12)9(16)6(14)5(13)8(4,15)10(9,17)18/h5-6H,1-3H2

Clé InChI

OEJNXTAZZBRGDN-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Mention d'avertissement

Danger

Mentions de danger

H225,H304,H315,H336,H410

Classification des risques

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

Organes cibles

Central nervous system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

10.4 °F

Point d'éclair (°C)

-12 °C

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Certificats d'analyse (COA)

Lot/Batch Number
LC20889V
LC02537
LB82293
LB61006
LB51973

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Consulter la Bibliothèque de documents

Toxaphene (polychlorinated camphenes).
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 20, 327-348 (1979-10-01)
M A Saleh
Reviews of environmental contamination and toxicology, 118, 1-85 (1991-01-01)
The chemistry of toxaphene is now well developed; 20 isomers have been isolated and identified. The molecular weight and molecular formula are known for the remaining major components. The major metabolic degradation mechanisms for toxaphene in all organisms from bacteria
Toxaphene.
Reviews of environmental contamination and toxicology, 104, 203-213 (1988-01-01)
M D Reuber
Journal of toxicology and environmental health, 5(4), 729-748 (1979-07-01)
Toxaphene is highly carcinogenic in rats and mice. Toxaphene induced malignant neoplasms of the liver in rats. Neoplasms at all sites, as well as malignant neoplasms, were increased in male and female rats ingesting toxaphene. Sarcomas were found more often
John R Kucklick et al.
Analytical and bioanalytical chemistry, 386(4), 819-836 (2006-10-05)
Recent advances in the analysis of the chlorinated environmental pollutants polychlorinated naphthalenes (PCNs) and toxaphene are highlighted in this review. Method improvements have been realized for PCNs over the past decade in isomer-specific quantification, peak resolution, and the availability of
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