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40111

Supelco

Toxaphene solution

certified reference material, 5000 μg/mL in methanol

Synonym(s):

Camphechlor solution

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About This Item

CAS Number:
8001-35-2
UNSPSC Code:
41116105

grade

certified reference material
TraceCERT®

Quality Level

100

Agency

EPA 505,508,608,625,1311

feature

standard type calibration

packaging

ampule of 1 mL

concentration

5000 μg/mL in methanol

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

single component solution

storage temp.

2-8°C

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.

Other Notes

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Legal Information

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Flam. Liq. 2 - STOT SE 1

Target Organs

Eyes,Central nervous system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

49.5 °F - closed cup - Solvent

Flash Point(C)

9.7 °C - closed cup - Solvent

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

EU REACH Annex XVII (Restriction List)

CAS No.

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Certificates of Analysis (COA)

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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
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
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
Erin L Pulster et al.
Environmental toxicology and chemistry, 28(7), 1390-1399 (2009-02-11)
Although the Turtle/Brunswick River Estuary (TBRE) in coastal Georgia (USA) is severely contaminated by persistent organochlorine pollutants (POPs), little information regarding POPs in higher-trophic-level biota in this system is available. In the present study, polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs;
Xiaoyan Xia et al.
Analytical and bioanalytical chemistry, 395(2), 457-463 (2009-07-31)
Toxaphene is considered to be a problematic organochlorine pollutant because of its bioaccumulation potential and persistence in aquatic environments. In this study, whole lake trout and walleye composites were used to evaluate two analytical techniques for total toxaphene and selected
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