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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
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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.

Signal Word

Danger

Hazard Statements

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 Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

10.4 °F

Flash Point(C)

-12 °C


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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 composition and metabolism in rats.
J E Casida et al.
Environmental quality and safety. Supplement, 3, 346-349 (1975-01-01)
H J de Geus et al.
Journal of environmental monitoring : JEM, 2(5), 503-511 (2001-03-20)
The analysis of toxaphene, a highly complex mixture of chlorinated bornanes, bornenes and camphenes, is a challenging problem, especially as individual congeners are present at trace levels in biota and other relevant samples. The complicated nomenclature of the compounds of
H J de Geus et al.
Environmental health perspectives, 107 Suppl 1, 115-144 (1999-05-07)
Toxaphene production, in quantities similar to those of polychlorinated biphenyls, has resulted in high toxaphene levels in fish from the Great Lakes and in Arctic marine mammals (up to 10 and 16 microg g-1 lipid). Because of the large variabiliity

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