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36143

Supelco

Malathion

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C10H19O6PS2
CAS Number:
Molecular Weight:
330.36
Beilstein:
1804525
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
environmental

format

neat

storage temp.

2-8°C

SMILES string

CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC

InChI

1S/C10H19O6PS2/c1-5-15-9(11)7-8(10(12)16-6-2)19-17(18,13-3)14-4/h8H,5-7H2,1-4H3

InChI key

JXSJBGJIGXNWCI-UHFFFAOYSA-N

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General description

Malathion is a commonly used organophosphate pesticide, which is generally sprayed on aquatic habitats in order to have a control over mosquitoes that carry malaria and the west nile virus.

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

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1

Storage Class Code

10 - Combustible liquids

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

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Removal of lindane and malathion from wastewater using bagasse fly ash?a sugar industry waste
Gupta.KV, et al.
Water Research, 36, 2483-2490 (2002)
Synergistic impacts of malathion and predatory stress on six species of North American tadpoles
Relyea.AR
Environmental Toxicology and Chemistry / Setac, 23, 1080-1084 (2004)
Oxidative stress and cholinesterase inhibition in saliva and plasma of rats following subchronic exposure to malathion
Abdollahi M, et al.
Comparative Biochemistry and Physiology. Toxicology & Pharmacology : CBP, 137, 29-34 (2004)
Hu Zhang et al.
Journal of agricultural and food chemistry, 60(41), 10188-10195 (2012-09-27)
An enantioselective method is presented for the determination of isocarbophos in soil by liquid chromatography coupled with tandem mass spectrometry. The pesticide residues in soil samples were extracted with acetonitrile, and complete enantioseparation was obtained on an amylose tris(3,5-dimethylphenylcarbamate) chiral
Maya L Groner et al.
Ecological applications : a publication of the Ecological Society of America, 23(6), 1443-1454 (2013-10-24)
For the past several decades, amphibian populations have been decreasing around the globe at an unprecedented rate. Batrachochytrium dendrobatidis (Bd), the fungal pathogen that causes chytridiomycosis in amphibians, is contributing to amphibian declines. Natural and anthropogenic environmental factors are hypothesized

Protocols

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