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Safety Information

300683

Sigma-Aldrich

α-1,2,3,4,5,6-Hexachlorocyclohexane

99%

Synonym(s):

α-BHC

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About This Item

Empirical Formula (Hill Notation):
C6H6Cl6
CAS Number:
Molecular Weight:
290.83
Beilstein:
7073451
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

Assay

99%

form

solid

mp

156-161 °C (lit.)

SMILES string

Cl[C@@H]1[C@H](Cl)[C@@H](Cl)[C@H](Cl)[C@@H](Cl)[C@H]1Cl

InChI

1S/C6H6Cl6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-6H/t1-,2-,3-,4-,5+,6+/m1/s1

InChI key

JLYXXMFPNIAWKQ-SHFUYGGZSA-N

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General description

α-1,2,3,4,5,6-Hexachlorocyclohexane is a racemic compound with anticonvulsant and tremorogenic activities and its accumulation in cerebral white over grey matter in rats was confirmed. Administration of α -1,2,3,4,5,6-hexachlorocyclohexane (α-HCH) to rats decreased the utilization of [2-14C]orotic acid for the synthesis of liver cytidine nucleotides.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

监管及禁止进口产品

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J Seifert et al.
Toxicology, 7(2), 155-161 (1977-04-01)
Administration of alpha-1,2,3,4,5,6-hexachlorocyclohexane (alpha-HCH) to rats decreased the utilization of [2-14C]orotic acid for the synthesis of liver cytidine nucleotides. The specific radioactivities of uridine components of the acid-soluble pool and rRNA increased during the first hours of treatment with the
J Portig et al.
Xenobiotica; the fate of foreign compounds in biological systems, 19(1), 123-130 (1989-01-01)
1. Whole-body autoradiographic evidence that alpha-1,2,3,4,5,6-hexachlorocyclohexane (alpha-HCH), a racemic compound with anticonvulsant and tremorogenic activities, accumulates in cerebral white over grey matter was confirmed in rats using unlabelled compound and g.l.c. determination in tissue samples. 2. Accumulation in, and retention
Pernilla Carlsson et al.
Journal of environmental monitoring : JEM, 14(5), 1437-1443 (2012-04-07)
A pilot study is presented evaluating selected chlorinated pesticides as chemical tracers for water masses in a sub-Arctic fjord system (Godthåbsfjord, western Greenland). Polyoxymethylene (POM) based passive water samplers were deployed during summer-autumn 2010. The levels of the analysed chlorinated
Sung-Deuk Choi et al.
Environmental science & technology, 45(20), 8834-8841 (2011-09-13)
An understanding of the factors that control the time trends of persistent organic pollutants (POPs) in the environment is required to evaluate the effectiveness of emission reductions and to predict future exposure. Using a regional contaminant fate model, CoZMo-POP 2
Gaoxin Zhou et al.
Chirality, 24(8), 615-620 (2012-06-08)
The enantioselective bioaccumulation and elimination behaviors of α-hexachlorocyclohexane (α-HCH) enantiomers in earthworm and soil were investigated by chiral gas chromatography. Enantiomer fraction values were calculated as indicators of the enantioselectivity. The mature earthworms were exposed to 0.10 µg g(-1)(wwt) (0.14

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