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MilliporeSigma

48495

δ-BHC

PESTANAL®, analytical standard

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About This Item

CAS Number:
UNSPSC Code:
12352200
PubChem Substance ID:
EC Number:
206-272-9
MDL number:
NACRES:
NA.24
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InChI key

JLYXXMFPNIAWKQ-GPIVLXJGSA-N

InChI

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

SMILES string

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

grade

analytical standard

product line

PESTANAL®

CofA

current certificate can be downloaded

packaging

ampule of 50 mg

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

storage temp.

2-30°C

Application

δ-BHC may be used as a standard in determining the concentration of δ-BHC in plant extracts used in traditional chinese medicines using gas chromatography method coupled with electron capture detector (GC-ECD) or quick easy cheap effective rugged and safe multi-residue method (QuEChERS) in combination with gas chromatography coupled with electron capture detector (GC-ECD).
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

signalword

Danger

Hazard Classifications

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

Storage Class

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

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Analysis of pesticide residues using the Quick Easy Cheap Effective Rugged and Safe (QuEChERS) pesticide multiresidue method in traditional Chinese medicine by gas chromatography with electron capture detection
Chemosphere, 84(7), 908-912 (2011)
Residues of 18 organochlorine pesticides in 30 traditional Chinese medicines
Xue J, et al.
Chemosphere, 71(6), 1051-1055 (2008)
Vishakha Raina et al.
Environmental science & technology, 41(12), 4292-4298 (2007-07-14)
Although the use of hexachlorocyclohexane (HCH), one of the most popular insecticides after the Second World War, has been discontinued in many countries, problems remain from former production and waste sites. Despite the widespread occurrence of HCHs, the environmental fate
S N Wu et al.
Molecular pharmacology, 57(5), 865-874 (2000-04-25)
delta-Hexachlorocyclohexane (delta-HCH), a lipophilic neurodepressant agent, has been shown to inhibit neurotransmitter release and stimulate ryanodine-sensitive Ca(2+) channels. However, the effect of delta-HCH on neuronal activity remains unclear, although it may enhance the gamma-aminobutyric acid-induced current. Its effects on ionic
D Belelli et al.
British journal of pharmacology, 127(3), 601-604 (1999-07-13)
Many structurally diverse general anaesthetics enhance inhibitory neurotransmission in the central nervous system by interacting with the GABAA receptor. By contrast, GABA receptors composed of the rho 1 subunit are anaesthetic-insensitive. Here, we demonstrate that both delta-hexachlorocyclohexane (delta-HCH; 1-100 microM)

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