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
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2
存储类别
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
法规信息
监管及禁止进口产品
此项目有
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)
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)
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
Zhaojie Cui et al.
Journal of bioscience and bioengineering, 113(6), 765-770 (2012-02-14)
The reductive biotransformation of α-, β-, γ-, and δ-hexachlorocyclohexane isomers was investigated using five alternative electron donors (i.e., glucose plus methanol, glucose only, methanol only, acetate, and ethanol) in a batch assay of an HCH-dechlorinating anaerobic culture. In addition, a
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