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45449

Supelco

Dimethoate

PESTANAL®, analytical standard

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About This Item

Formula empirica (notazione di Hill):
C5H12NO3PS2
Numero CAS:
60-51-5
Peso molecolare:
229.26
Beilstein:
1785339
Numero CE:
200-480-3
Numero MDL:
MFCD00053676
Codice UNSPSC:
41116107
ID PubChem:
329756743
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

agriculture
environmental

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

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)
MCWXGJITAZMZEV-UHFFFAOYSA-N

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Applicazioni

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

Note legali

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

Pittogrammi

Skull and crossbonesEnvironment
GHS06,GHS09

Avvertenze

Danger

Indicazioni di pericolo

H301 + H311,H411

Classi di pericolo

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

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

224.6 °F - closed cup

Punto d’infiammabilità (°C)

107 °C - closed cup

Dispositivi di protezione individuale

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

Choose from one of the most recent versions:

Certificati d'analisi (COA)

Lot/Batch Number
BCCF3993
BCBS9338
BCBS9338V
SZBG005XV
SZBC243XV

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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.
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
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
Mirna Velki et al.
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP, 156(2), 104-112 (2012-05-23)
Earthworms ingest large amounts of soil and therefore are continuously exposed to contaminants through their alimentary surfaces. Additionally, several studies have shown that earthworm skin is a significant route of contaminant uptake as well. In order to determine effects of
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