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32015

Supelco

Endosulfan

PESTANAL®, analytical standard

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About This Item

Formula empirica (notazione di Hill):
C9H6Cl6O3S
Numero CAS:
115-29-7
Peso molecolare:
406.93
Beilstein:
2062338
Numero CE:
204-079-4
Numero MDL:
MFCD00137651
Codice UNSPSC:
41116107
ID PubChem:
329753961
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Descrizione

(α + β ~ 2 + 1)

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

ClC1=C(Cl)[C@]2(Cl)C3COS(=O)OCC3[C@@]1(Cl)C2(Cl)Cl

InChI

1S/C9H6Cl6O3S/c10-5-6(11)8(13)4-2-18-19(16)17-1-3(4)7(5,12)9(8,14)15/h3-4H,1-2H2/t3?,4?,7-,8+,19?
RDYMFSUJUZBWLH-QTSFFCDASA-N

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Categorie correlate

Descrizione generale

Endosulfan, a broad spectrum insecticide, is mostly used to control insects and pest in crops. It consists of two stereochemical isomers namely α-endosulfan and β-endosulfan.

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

Pittogrammi

Skull and crossbonesEnvironment
GHS06,GHS09

Avvertenze

Danger

Indicazioni di pericolo

H300 + H310 + H330,H410

Classi di pericolo

Acute Tox. 2 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Codice della classe di stoccaggio

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

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 N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
BCCG1926
BCBT1374
SZBC166XV
SZB8163XV
4345X

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M Guest et al.
Pesticide biochemistry and physiology, 158, 32-39 (2019-08-06)
Mutations in the GABA-gated chloride channel are associated with resistance to cyclodiene organochlorine and phenyl pyrazole insecticides. The best characterised of these is A301S, which was initially identified in a Dieldrin resistant strain of Drosophila melanogaster. The orthologous mutation has
Kgotla K Masibi et al.
Materials (Basel, Switzerland), 14(4) (2021-02-10)
This report narrates the successful application of a fabricated novel sensor for the trace detection of endosulfan (EDS). The sensor was made by modifying a glassy-carbon electrode (GCE) with polyaniline (PANI), chemically synthesized antimony oxide nanoparticles (AONPs), acid-functionalized, single-walled carbon
Anke M Tukker et al.
Neurotoxicology, 67, 215-225 (2018-06-18)
Neurotoxicity testing still relies on ethically debated, expensive and time consuming in vivo experiments, which are unsuitable for high-throughput toxicity screening. There is thus a clear need for a rapid in vitro screening strategy that is preferably based on human-derived
Effect of endosulfan on male reproductive development.
Saiyed H
Environmental Health Perspectives, 111(16), 1958-1962 (2003)
Ashfaq Ahmad et al.
Environmental science and pollution research international, 26(20), 20079-20091 (2018-09-20)
This study is based on self-reported information collected from selected farmers of Vehari District, Punjab, Pakistan, to determine their technical knowledge and awareness about pesticide use and associated environmental and health risks. Moreover, soil contamination by routinely used persistent organochlorine
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