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33377

Supelco

δ-HCH

PESTANAL®, analytical standard

Sinónimos:

δ-1,2,3,4,5,6-Hexachlorocyclohexane

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About This Item

Fórmula empírica (notación de Hill):
C6H6Cl6
Número de CAS:
319-86-8
Peso molecular:
290.83
Beilstein:
1907334
Número CE:
206-272-9
Número MDL:
MFCD00135945
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
329754506
NACRES:
NA.24

grado

analytical standard

Nivel de calidad

100

Línea del producto

PESTANAL®

caducidad

limited shelf life, expiry date on the label

técnicas

HPLC: suitable
NMR: suitable
gas chromatography (GC): suitable

mp

136-140 °C

idoneidad

passes test for identity (NMR)

aplicaciones

agriculture
environmental

formato

neat

cadena SMILES

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-

Clave InChI

JLYXXMFPNIAWKQ-GPIVLXJGSA-N

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Aplicación

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Información legal

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

Palabra de señalización

Danger

Frases de peligro

H301,H312,H351,H410

Clasificaciones de peligro

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

Código de clase de almacenamiento

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

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

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

Choose from one of the most recent versions:

Certificados de análisis (COA)

Lot/Batch Number
BCCF4087
BCBS8734V
SZBD099XV
SZBA075XV
SZBA075X

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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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)
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
J H Kim et al.
Chemosphere, 43(2), 137-140 (2001-04-12)
Soil samples were collected from rice growing and industrial areas in South Korea and analysed for organochlorine pesticide content using gas chromatography with electron capture detection. The soils were monitored for the presence of 18 organochlorine pesticides. The main pesticides
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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