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47616-U

Supelco

Toxaphene solution

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

Synonym(s):

Camphechlor solution

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About This Item

CAS Number:
UNSPSC Code:
77101502
NACRES:
NA.24

grade

analytical standard

feature

calibration

packaging

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

storage temp.

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

InChI key

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.

signalword

Danger

Hazard Classifications

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

target_organs

Central nervous system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

10.4 °F

flash_point_c

-12 °C


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J I Goodman et al.
Toxicological sciences : an official journal of the Society of Toxicology, 55(1), 3-16 (2000-05-02)
This reevaluation of the current U.S. EPA cancer potency factor for toxaphene is based upon a review of toxaphene carcinogenesis bioassays in mice conducted by Litton Bionetics (unpublished report, 1978) and the National Cancer Institute (NCI) (Technical Report Series No.
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
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

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