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Supelco

Endosulfan

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C9H6Cl6O3S
CAS Number:
115-29-7
Molecular Weight:
406.93
Beilstein:
2062338
EC Number:
204-079-4
MDL number:
MFCD00137651
UNSPSC Code:
41116107
PubChem Substance ID:
329753961
NACRES:
NA.24

grade

analytical standard

Quality Level

100

description

(α + β ~ 2 + 1)

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

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?

InChI key

RDYMFSUJUZBWLH-QTSFFCDASA-N

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General description

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.

Application

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

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

Danger

Hazard Statements

H300 + H310 + H330,H410

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG1926
BCBT1374
SZBC166XV
SZB8163XV
4345X

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Vedant Singh et al.
International journal of occupational safety and ergonomics : JOSE, 1-26 (2018-06-02)
This article reviews 60 studies examining safety climates related to manufacturing. The study identifies several conceptual and methodological limitations associated with developing safety climate measurements, such as lack of a rigorous validation process, problematic sample sizes and composition. Within the
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
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
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
Edebi N Vaikosen et al.
European journal of mass spectrometry (Chichester, England), 25(4), 362-371 (2018-12-19)
Most environmental analytical methods for the determination of organochlorine pesticides (OCPs) are multi-residual with other organic compounds co-extracted and co-eluted. This has been observed in GC spectra using classical detectors like electron-capture detector (ECD) even after appropriate clean-up. This limitation
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