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34309

Supelco

Heptachlor exo-epoxide

PESTANAL®, analytical standard, isomer B

Synonym(s):

cis-Heptachlor epoxide, exo-1,4,5,6,7,8,8-Heptachloro-2,3-epoxy-4,7-methano-3a,4,7,7a-tetrahydroindane, HCE

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About This Item

Empirical Formula (Hill Notation):
C10H5Cl7O
CAS Number:
1024-57-3
Molecular Weight:
389.32
EC Number:
213-831-0
MDL number:
MFCD01311793
UNSPSC Code:
41116107
PubChem Substance ID:
329754937
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

Cl[C@H]1[C@H]2O[C@H]2[C@H]3[C@@H]1C4(Cl)C(Cl)=C(Cl)C3(Cl)C4(Cl)Cl

InChI

1S/C10H5Cl7O/c11-3-1-2(4-5(3)18-4)9(15)7(13)6(12)8(1,14)10(9,16)17/h1-5H/t1-,2+,3+,4-,5+,8?,9?/m0/s1

InChI key

ZXFXBSWRVIQKOD-TTWWGNBVSA-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.

Legal Information

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

Signal Word

Danger

Hazard Statements

H300,H351,H373,H410

Hazard Classifications

Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - STOT RE 2

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM4040
BCCH4154
BCCG7448
BCBV9995
BCBV3043

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Guadalupe Prado et al.
Mutation research, 673(2), 87-91 (2009-01-17)
The genotoxic potential of the organochlorine insecticides heptachlor (HC) and its metabolite heptachlor epoxide (HCE) has been evaluated in TK6 cells, a well-established human lymphoblastoid cell line. Genotoxicity has been determined by scoring the induction of DNA breaks in the
Wim J M Hegeman et al.
Reviews of environmental contamination and toxicology, 173, 85-116 (2002-01-05)
Enantiomer fractions (EFs) of chiral compounds have been used to explain the mechanisms of enantiomer enrichment in air, soil, water, and biota. The EFs were calculated from enantiomeric ratios (ERs) of chiral compounds measured by researchers during the past 10
Jijun Gao et al.
Environment international, 34(8), 1097-1103 (2008-05-30)
Persistent organochlorine pesticides pollutants (OCPs) have been reported to occur at relatively high concentrations in some Chinese waters. In order to map the distribution of organochlorine pesticides in the surface water throughout China, samples were collected from over 600 sites
M Grynkiewicz et al.
Chemosphere, 43(3), 303-312 (2001-04-17)
Selected organonitrogen, organophosphorus and organochlorine pesticides have been determined in precipitation samples collected at 10 sites in the Gdańsk region (northern Poland) over a period of one year (1998). Compounds which were detected most often included simazine (0.11-5.80 ng/l), fenitrothion
Frank H Pierik et al.
Environmental research, 105(3), 364-369 (2007-05-29)
Prenatal exposure to environmental endocrine disrupters has been postulated to cause adverse effects on male reproductive health. Exposure to organochlorine pesticides with anti-androgenic and estrogenic potency has been shown to interfere with the sex-hormone-dependent process of testicular descent in animal
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