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45449

Supelco

Dimethoat

PESTANAL®, analytical standard

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About This Item

Empirische Formel (Hill-System):
C5H12NO3PS2
CAS-Nummer:
60-51-5
Molekulargewicht:
229.26
Beilstein:
1785339
EG-Nummer:
200-480-3
MDL-Nummer:
MFCD00053676
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329756743
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

agriculture
environmental

Format

neat

Lagertemp.

2-8°C

SMILES String

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)

InChIKey

MCWXGJITAZMZEV-UHFFFAOYSA-N

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Anwendung

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

Rechtliche Hinweise

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

Piktogramme

Skull and crossbonesEnvironment
GHS06,GHS09

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

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

WGK

WGK 3

Flammpunkt (°F)

224.6 °F - closed cup

Flammpunkt (°C)

107 °C - closed cup

Persönliche Schutzausrüstung

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

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (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.
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
Mariana Astiz et al.
Toxicology and applied pharmacology, 272(2), 263-271 (2013-07-31)
Dimethoate is an organophosphorus insecticide extensively used in horticulture. Previous studies have shown that the administration of dimethoate to male rats, at a very low dose and during a sub-chronic period, increases the oxidation of lipids and proteins, reduces the
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Protokolle

US EPA Method 8141: GC Analysis of Organophosphorus Pesticides (OP-Pest) on Equity®-5, NPD Detection

analytical standard; Tokuthion, technical grade, pkg of 50 mg; Crotoxyphos; Phorate; Azinphos-ethyl; Diazinon; Azinphos-methyl; Demeton-O; Dimethoate; Chlorpyrifos-methyl

Testing Food for Fipronil Contamination

Test your food for fipronil contamination using our analytical standards, certified reference materials, solvents, and columns for analysis.

US EPA Method 8270 (Appendix IX): GC Analysis of Semivolatiles on Equity®-5 (30 m x 0.25 mm I.D., 0.50 μm)

US EPA Method 8270 (Appendix IX): GC Analysis of Semivolatiles on Equity®-5 (30 m x 0.25 mm I.D., 0.50 μm)

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