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33377

Supelco

δ-HCH

PESTANAL®, analytical standard

Sinonimo/i:

δ-1,2,3,4,5,6-Hexachlorocyclohexane

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About This Item

Formula empirica (notazione di Hill):
C6H6Cl6
Numero CAS:
319-86-8
Peso molecolare:
290.83
Beilstein:
1907334
Numero CE:
206-272-9
Numero MDL:
MFCD00135945
Codice UNSPSC:
41116107
ID PubChem:
329754506
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

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

Punto di fusione

136-140 °C

Compatibilità

passes test for identity (NMR)

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

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-
JLYXXMFPNIAWKQ-GPIVLXJGSA-N

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Applicazioni

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

Note legali

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

Avvertenze

Danger

Indicazioni di pericolo

H301,H312,H351,H410

Classi di pericolo

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

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

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

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number
BCCF4087
BCBS8734V
SZBD099XV
SZBA075XV
SZBA075X

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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
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