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45449

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Dimethoate

PESTANAL®, analytical standard

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About This Item

Formule empirique (notation de Hill):
C5H12NO3PS2
Numéro CAS:
60-51-5
Poids moléculaire :
229.26
Numéro Beilstein :
1785339
Numéro CE :
200-480-3
Numéro MDL:
MFCD00053676
Code UNSPSC :
41116107
ID de substance PubChem :
329756743
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

CNC(CSP(OC)(OC)=S)=O

InChI

1S/C5H12NO3PS2/c1-6-5(7)4-12-10(11,8-2)9-3/h4H2,1-3H3,(H,6,7)

Clé InChI

MCWXGJITAZMZEV-UHFFFAOYSA-N

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Catégories apparentées

Application

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

Informations légales

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictogrammes

Skull and crossbonesEnvironment
GHS06,GHS09

Mention d'avertissement

Danger

Mentions de danger

H301 + H311,H411

Classification des risques

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 2

Code de la classe de stockage

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

224.6 °F - closed cup

Point d'éclair (°C)

107 °C - closed cup

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Choose from one of the most recent versions:

Certificats d'analyse (COA)

Lot/Batch Number
BCCF3993
BCBS9338
BCBS9338V
SZBG005XV
SZBC243XV

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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Nander Van Praet et al.
Aquatic toxicology (Amsterdam, Netherlands), 155, 236-243 (2014-07-27)
The combined effects of a pesticide and predation risk on sublethal endpoints in the midge Chironomus riparius were investigated using a combination of predator-release kairomones from common carp (Cyprinus carpio) and alarm substances from conspecifics together with the pesticide dimethoate.
Ruixin Guo et al.
Journal of hazardous materials, 237-238, 270-276 (2012-09-11)
This study analyzed the toxicity of organophosphorus pesticide, dimethoate on freshwater rotifer Brachionus calyciflorus, using swimming angular and linear speed alteration as the sub-lethal endpoints. Response surface methodology (RSM) was applied in experimental design and data analysis to consider two
Suguru Yoshida et al.
Journal of the American Chemical Society, 134(47), 19358-19361 (2012-11-16)
A novel nucleophilic substitution reaction at the nitrogen of arylsulfonamides by means of phosphide anions has been described. This reaction allows for the efficient transformation of arylsulfonamides into synthetically valuable phosphamides, amines, and a variety of protected amines.
Cecília M S Pereira et al.
The Science of the total environment, 443, 821-827 (2012-12-19)
The main mode of action of organophosphate insecticides is to inhibit acetylcholinesterase (AChE), which causes neuromuscular paralysis leading ultimately to death. The collembolan Folsomia candida is an important and standard test species in ecotoxicology, where effects on avoidance behaviour are
Sara C Novais et al.
PloS one, 7(4), e36068-e36068 (2012-05-05)
Molecular mechanisms of response to pesticides are scarce and information on such responses from soil invertebrates is almost inexistent. Enchytraeus albidus (Oligochaeta) is a standard soil ecotoxicology model species for which effects of many pesticides are known on survival, reproduction
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