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Merck

40051

Supelco

Hexachlorocyclopentadiene solution

certified reference material, 5000 μg/mL in methanol

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About This Item

Número de CAS:
UNSPSC Code:
41116105

grade

certified reference material
TraceCERT®

agency

EPA 508

product line

TraceCERT®

feature

standard type calibration

packaging

ampule of 1 mg

concentration

5000 μg/mL in methanol

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

environmental

format

single component solution

storage temp.

2-8°C

InChI

1S/C5Cl6/c6-1-2(7)4(9)5(10,11)3(1)8

InChI key

VUNCWTMEJYMOOR-UHFFFAOYSA-N

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General description

Hexachlorocyclopentadiene is an organochlorine compound, which may be used, in the manufacture of some pesticides.

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

signalword

Danger

Hazard Classifications

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

target_organs

Eyes,Central nervous system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

51.8 °F - closed cup

flash_point_c

11.0 °C - closed cup


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Visite la Librería de documentos

Sublethal effects of the flame retardant intermediate hexachlorocyclopentadiene (HCCPD) on the gene transcription and protein activity of Daphnia magna
Houde M, et al.
Aquatic Toxicology (Amsterdam, Netherlands), 140, 213-219 (2013)
Retention and fate of inhaled hexachlorocyclopentadiene in the rat.
L J Lawrence et al.
Bulletin of environmental contamination and toxicology, 26(5), 663-668 (1981-05-01)
Teratogenic potential of hexachlorocyclopentadiene in mice and rabbits.
F J Murray et al.
Toxicology and applied pharmacology, 53(3), 497-500 (1980-05-01)
J G Garcia et al.
Acta crystallographica. Section C, Crystal structure communications, 54 ( Pt 5), 645-647 (1998-06-24)
There are two independent molecules of endo-endo-anti-1,7,8,9,10,16,17,18,19,19,20,20-dodecachloro-4,13- dioxapentacyclo[14.2.1.1(7,10).0(2,15).0(6,11)]icosa-8,17-di ene, C18H12Cl12O2, in the unit cell with different conformations. In one, the ten-membered ring adopts a chair-chair conformation, and in the other, it adopts a distorted chair-chair conformation. There are near-zero torsion
K M Abdo et al.
Journal of applied toxicology : JAT, 4(2), 75-81 (1984-04-01)
A 13-week subchronic study was conducted by administering hexachlorocyclopentadiene ( HCCP ) in corn oil by gavage to groups of ten male and ten female F344 rats at doses of 150, 75, 38, 19, 10 or 0 mg kg-1, and

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