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Principaux documents

PS676

Methamidophos

analytical standard

Synonyme(s) :

O,S-Dimethyl phosphoramidothioate

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About This Item

Formule empirique (notation de Hill) :
C2H8NO2PS
Numéro CAS:
Poids moléculaire :
141.13
Beilstein:
8137714
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :

Qualité

analytical standard

Conditionnement

ampule of 100 mg

Fabricant/nom de marque

Chem Service, Inc. PS-676

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

neat

Chaîne SMILES 

COP(N)(=O)SC

InChI

1S/C2H8NO2PS/c1-5-6(3,4)7-2/h1-2H3,(H2,3,4)

Clé InChI

NNKVPIKMPCQWCG-UHFFFAOYSA-N

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Description générale

Methamidophos is a nonselective type of organophosphorus insecticide and a potent acetylcholinesterase inhibitor, which is commonly used in controlling a broad spectrum of pest insects such as chewing and sucking insects and spider mites on citrus fruits, ornamental plants, stone fruits and other intensive agricultural crops.[1]

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

413.6 °F - closed cup

Point d'éclair (°C)

212 °C - closed cup


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Certificats d'analyse (COA)

Lot/Batch Number

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Titanium dioxide mediated photocatalytic degradation of methamidophos in aqueous phase.
Wei L, et al.
Journal of Hazardous Materials, 164(1), 154-160 (2009)
Hongkun Li et al.
Talanta, 87, 93-99 (2011-11-22)
With citrate-coated Au nanoparticles as colorimetric probe, a novel visual method for rapid assay of organophosphorus pesticides has been developed. The assay principle is based on catalytic hydrolysis of acetylthiocholine into thiocholine by acetylcholinesterase, which induces the aggregation of Au
Guilherme L Emerick et al.
Environmental toxicology and chemistry, 31(2), 239-245 (2011-11-03)
Many chiral pesticides are introduced into the environment as racemates, although their pesticidal activity is usually the result of preferential reactivity of only one enantiomer, while the other enantiomer may have toxic effects against nontarget organisms. Methamidophos (O,S-dimethyl phosphoramidothioate), a
Zhong-Lan Shen et al.
Bioscience, biotechnology, and biochemistry, 75(3), 473-479 (2011-03-11)
An analytical methodology for the analysis of methamidophos in water and soil samples incorporating a molecularly imprinted solid-phase extraction process using methamidophos-imprinted polymer was developed. Binding study demonstrated that the polymer exhibited excellent affinity and high selectivity to the methamidophos.
Gabriella Xavier Maretto et al.
Ecotoxicology and environmental safety, 80, 203-207 (2012-04-03)
Poisoning by organophosphorus insecticides is often accompanied by cardiac complications which may be serious and even fatal. However, the effects of these compounds on the cardiovascular mechanisms involved in blood pressure regulation are not known. The aim of this study

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