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45449

Supelco

Dimethoate

PESTANAL®, analytical standard

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Wszystkie zdjęcia(2)

About This Item

Wzór empiryczny (zapis Hilla):
C5H12NO3PS2
Numer CAS:
60-51-5
Masa cząsteczkowa:
229.26
Beilstein:
1785339
Numer WE:
200-480-3
Numer MDL:
MFCD00053676
Kod UNSPSC:
41116107
Identyfikator substancji w PubChem:
329756743
NACRES:
NA.24

klasa czystości

analytical standard

Poziom jakości

100

linia produktu

PESTANAL®

okres trwałości

limited shelf life, expiry date on the label

metody

HPLC: suitable
gas chromatography (GC): suitable

Zastosowanie

agriculture
environmental

format

neat

temp. przechowywania

2-8°C

ciąg 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)

Klucz InChI

MCWXGJITAZMZEV-UHFFFAOYSA-N

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Zastosowanie

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

Informacje prawne

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
This page may contain text that has been machine translated.

Piktogramy

Skull and crossbonesEnvironment
GHS06,GHS09

Hasło ostrzegawcze

Danger

Zwroty wskazujące rodzaj zagrożenia

H301 + H311,H411

Klasyfikacja zagrożeń

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

Kod klasy składowania

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

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

224.6 °F - closed cup

Temperatura zapłonu (°C)

107 °C - closed cup

Środki ochrony indywidualnej

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

Choose from one of the most recent versions:

Certyfikaty analizy (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.
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
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.
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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