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36666

Supelco

Aldrin

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C12H8Cl6
CAS Number:
Molecular Weight:
364.91
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

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(C=C4)C3C1(Cl)C2(Cl)Cl

InChI

1S/C12H8Cl6/c13-8-9(14)11(16)7-5-2-1-4(3-5)6(7)10(8,15)12(11,17)18/h1-2,4-7H,3H2/t4-,5+,6+,7-,10+,11-

InChI key

QBYJBZPUGVGKQQ-SJJAEHHWSA-N

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General description

Aldrin is a chlorinated cyclodiene, which is a synthetically produced pyrethroid insecticide.

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

Signal Word

Danger

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - STOT RE 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)

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Organochlorine insecticide residues in drinking and ground water in and around Delhi
Mukherjee I and Gopal M
Environmental Monitoring and Assessment, 76, 185-193 (2002)
Long-term health effects of aldrin and dieldrin: a study of exposure, health effects and mortality of workers engaged in the manufacture and formulation of the insecticides aldrin and dieldrin
Jong DC
Toxicology Letters, 1-206 (1991)
paper-based thioglycolic acid (TGA)-capped CdTe QD device for rapid screening of organophosphorus and carbamate insecticides
Apilux.A, et al.
Analytical Methods : Advancing Methods and Applications, 9, 519-527 (2017)
Hans Ragnar Norli et al.
Journal of chromatography. A, 1218(41), 7234-7241 (2011-09-09)
The QuEChERS method developed for 22 organochlorine pesticides (OCPs) and 7-polychlorinated biphenyls (PCBs) in fish tissue involves a simple and efficient freezing technique for removal of lipids. The equipment developed consists of disposable syringes and a freezing block constructed from
Xiao-Yuan Tao et al.
Molecular ecology, 21(17), 4371-4385 (2012-04-21)
Cotton plants accumulate phytotoxins, including gossypol and related sesquiterpene aldehydes, to resist insect herbivores and pathogens. To counteract these defensive plant secondary metabolites, cotton bollworms (Helicoverpa armigera) elevate their production of detoxification enzymes, including cytochrome P450 monooxygenases (P450s). Besides their

Protocols

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

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