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Supelco

Endrin

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C12H8Cl6O
CAS Number:
72-20-8
Molecular Weight:
380.91
EC Number:
200-775-7
MDL number:
MFCD00151158
UNSPSC Code:
41116107
PubChem Substance ID:
329753958
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

ClC1=C(Cl)C2(Cl)C3C4CC(C5OC45)C3C1(Cl)C2(Cl)Cl

InChI

1S/C12H8Cl6O/c13-8-9(14)11(16)5-3-1-2(6-7(3)19-6)4(5)10(8,15)12(11,17)18/h2-7H,1H2/t2-,3-,4-,5-,6-,7+,10+,11+/m1/s1

InChI key

DFBKLUNHFCTMDC-SPJPLABQSA-N

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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,H410

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 1 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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCF0215
BCBR7539V
SZBD149XV
SZBD119XV
SZBB2790V

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M J Moreno-Aliaga et al.
Molecular pharmacology, 56(1), 91-101 (1999-07-01)
The effects of selected chlorinated cyclodiene pesticides on the adipocyte differentiation process were examined using the 3T3-L1 adipocyte model in vitro. Endrin was found to cause a dose-dependent inhibition of adipocyte differentiation in 3T3-L1 cells. Aldrin and dieldrin were less
Debasis Bagchi et al.
Toxicology, 175(1-3), 73-82 (2002-06-07)
The mechanism of toxicity of structurally diverse environmental toxicants including heavy metals and polyhalogenated and polycyclic hydrocarbons may involve a common cascade of events which entails an oxidative stress and production of reactive oxygen species. We have determined the comparative
D B Tully et al.
Reproductive toxicology (Elmsford, N.Y.), 14(2), 95-102 (2000-05-29)
There have been increasing concerns that environmental chemicals may adversely affect the health of humans and wildlife by acting as endocrine modulators. These concerns have been augmented by the realization that human exposure occurs not just to single chemical agents
E Concha-Graña et al.
Talanta, 78(3), 764-771 (2009-03-10)
In this work, a large-volume on-column injection method for the analysis of 21 organochlorine pesticides, including HCH isomers, DDT derivatives and cyclodiene derivatives, was optimized. The solvent selected to carry out the study was ethyl acetate and the injection volume
Xianjia Peng et al.
Journal of hazardous materials, 168(1), 210-214 (2009-03-10)
It has been discovered previously that clay minerals may have a greater potential for sorption of pesticides. In this paper, the sorption of endrin, a nonionic persistent organochlorine pesticide, to montmorillonite and kaolinite was investigated. The effect of pH, ionic
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