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Merck

33377

Supelco

δ-HCH

PESTANAL®, analytical standard

Synonym(e):

δ-1,2,3,4,5,6-Hexachlorcyclohexan

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About This Item

Empirische Formel (Hill-System):
C6H6Cl6
CAS-Nummer:
Molekulargewicht:
290.83
Beilstein:
1907334
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

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

mp (Schmelzpunkt)

136-140 °C

Eignung

passes test for identity (NMR)

Anwendung(en)

agriculture
environmental

Format

neat

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-

InChIKey

JLYXXMFPNIAWKQ-GPIVLXJGSA-N

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Anwendung

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

Rechtliche Hinweise

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

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

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

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

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


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Analysenzertifikate (COA)

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1 of 3

Endrin PESTANAL®, analytical standard

Supelco

32014

Endrin

P Popp et al.
Chemosphere, 41(6), 849-855 (2000-06-23)
Concentrations of tetrachlorobenzenes, pentachlorobenzene, hexachlorobenzene and alpha-, beta-, gamma- and delta-HCH in air and deposition were measured at three different contaminated sites in Greppin, Roitzsch (both near Bitterfeld) and Leipzig during five time intervals of 14 days in the summer
Poonam Sharma et al.
Applied and environmental microbiology, 72(9), 5720-5727 (2006-09-08)
Incubation of resting cells of Sphingobium indicum B90A, Sphingobium japonicum UT26, and Sphingobium francense Sp+ showed that they were able to transform beta- and delta-hexachlorocyclohexane (beta- and delta-HCH, respectively), the most recalcitrant hexachlorocyclohexane isomers, to pentachlorocyclohexanols, but only resting cells
R Calvelo Pereira et al.
Environmental pollution (Barking, Essex : 1987), 155(2), 350-358 (2007-12-26)
This study focuses on the main routes of distribution and accumulation of different hexachlorocyclohexane (HCH) isomers (mainly alpha-, beta-, gamma- and delta-HCH) in a soil-plant-air system. A field assay was carried out with two plant species, Cynara scolymus L. and
E D Buck et al.
The Journal of pharmacology and experimental therapeutics, 289(1), 477-485 (1999-03-23)
Several isomers of hexachlorocyclohexanes (HCHs) have been shown to be toxic to mammals. Previous studies have revealed that the delta isomer (delta-HCH) was particularly potent toward disrupting Ca2+ homeostasis in a variety of excitable and nonexcitable cells and altering contractility
Yong Qian et al.
Environmental monitoring and assessment, 116(1-3), 157-167 (2006-06-17)
The contamination of organochlorine pesticides hexachlorocyclohexane (HCH) and Dichlorodiphenyltrichloroethane (DDT) and their eco-environmental assessment in surface sediments from Lake Dongting, the second-largest freshwater lake in China, were studied. Concentrations of summation HCH (=alpha-HCH + beta-HCH + gamma-HCH +delta-HCH) were 0.21-9.59

Protokolle

US EPA Method 8081: GC Analysis of Organochlorine Pesticides on Equity®-5

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