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36181

Supelco

Omethoate

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C5H12NO4PS
CAS Number:
1113-02-6
Molecular Weight:
213.19
Beilstein:
1785256
EC Number:
214-197-8
MDL number:
MFCD00055441
UNSPSC Code:
41116107
PubChem Substance ID:
329755323
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

storage temp.

2-8°C

SMILES string

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

InChI

1S/C5H12NO4PS/c1-6-5(7)4-12-11(8,9-2)10-3/h4H2,1-3H3,(H,6,7)

InChI key

PZXOQEXFMJCDPG-UHFFFAOYSA-N

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Application

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

Legal Information

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

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

Danger

Hazard Statements

H300,H311,H400

Hazard Classifications

Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Aquatic Acute 1

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

212.0 °F - closed cup

Flash Point(C)

100 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCL9589
BCCB7743
BCBZ2933
SZBD332XV
SZB9125XV

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Yiou Pan et al.
Chemico-biological interactions, 188(3), 553-557 (2010-08-10)
The degree of insecticide resistance, acetylcholinesterase (AChE) activity kinetics, AChE gene expression and the cDNA sequence of AChE gene were investigated in resistant and relatively susceptible strains of the cotton aphids, Aphis gossypii (Glover). The resistant strain (ORR) exhibited 53.28-fold
F A Tarbah et al.
Forensic science international, 170(2-3), 129-132 (2007-07-24)
Many organophosphate pesticides (OPs) such as dimethoate are used to eradicate household pests, and those occurring in agriculture and forestry sectors. Combinations of two or more different insecticides have been manufactured to increase their effectiveness. A case of death is
Yanhong Bai et al.
Journal of agricultural and food chemistry, 57(14), 6238-6245 (2009-06-19)
A practical, inexpensive, and green chemical process is greatly needed for degrading pesticides in food and environmental water. In this work, the impact of O(2) plasma treatment on reduction of dichlorvos (DDVP) and omethoate in maize was determined by gas
Musa Isnas et al.
Toxicology and industrial health, 28(1), 27-34 (2011-10-26)
The study aimed mainly to assess effects of omethoate on certain oxidative stress biomarkers in various tissues of frogs (Rana ridibunda). Biomarkers selected for stress monitoring were malondialdehyde (MDA) and antioxidant defense system (ADS) constituent such as reduced glutathione (GSH)
Ozden Tacal et al.
Journal of applied toxicology : JAT, 30(5), 469-475 (2010-03-17)
Organophosphorus pesticides used most commonly in Turkey include methamidophos, dichlorvos, O-methoate and diazinon. These toxic chemicals or their metabolites make a covalent bond with the active site serine of butyrylcholinesterase. Our goal was to identify the adducts that result from
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