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Merck
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34234

Supelco

Demeton-S-methyl solution

100 μg/mL in acetonitrile, PESTANAL®, analytical standard

Sinónimos:

S-[2-(Ethylthio)ethyl] O,O-dimethyl phosphorothioate, Methyldemetone

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About This Item

Fórmula empírica (notación de Hill):
C6H15O3PS2
Número de CAS:
919-86-8
Peso molecular:
230.29
MDL number:
MFCD00055464
UNSPSC Code:
41116107
PubChem Substance ID:
329754918
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

concentration

100 μg/mL in acetonitrile

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture

format

single component solution

storage temp.

2-8°C

SMILES string

CCSCCSP(=O)(OC)OC

InChI

1S/C6H15O3PS2/c1-4-11-5-6-12-10(7,8-2)9-3/h4-6H2,1-3H3

InChI key

WEBQKRLKWNIYKK-UHFFFAOYSA-N

General description

Demeton-S-methyl is a metabolite of the pesticide thiometon, used for food, environmental, and toxicology analyses.

Application

Demeton-S-methyl may be used as an analytical reference standard for the determination of the analyte in rice, wines and baby food products by various chromatography techniques.
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

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

35.6 °F

flash_point_c

2 °C

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análisis (COA)

Lot/Batch Number
BCCL8151
BCCH1297
BCCB4805
BCBZ8745
BCBS0430V

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Young-Su Jeong et al.
Biochemical and biophysical research communications, 449(3), 263-267 (2014-05-16)
V-type nerve agents, known as VX, are organophosphate (OP) compounds, and show extremely toxic effects on human and animals by causing cholinergic overstimulation of synapses. The bacterial organophosphorus hydrolase (OPH) has attracted much attention for detoxifying V-type agents through hydrolysis
Simo O Pehkonen et al.
Environmental science & technology, 39(8), 2586-2591 (2005-05-12)
The chemical fate of organophosphorus pesticides (OPs) has been proven to depend strongly on the chemistry of their aquatic environment. In particular, metal ions (and metal oxide surfaces) have been known to play an important role in the hydrolytic fate
V Vallet et al.
Toxicology in vitro : an international journal published in association with BIBRA, 21(6), 1182-1190 (2007-05-08)
Organophosphorus compounds (OPs), such as pesticides and chemical warfare agents like sarin (GB), soman (GD) and VX, are highly toxic compounds. The OP vapours and their liquid forms are readily absorbed through the skin, therefore, protecting the skin of people
Organophosphorus poisoning at a chemical packaging company.
R D Jones
British journal of industrial medicine, 39(4), 377-381 (1982-11-01)
L Girbal et al.
Applied and environmental microbiology, 66(3), 1202-1204 (2000-03-04)
Corynebacterium glutamicum is able to biotransform demeton-S-methyl, an organophosphorus compound, during cometabolism with more readily metabolizable substrates. Among the cosubstrates used, fructose is the growth substrate that is most favorable for demeton-S-methyl biotransformation. The reaction mechanism of demeton-S-methyl biotransformation involves
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