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90039

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Fenthion oxon sulfone-(S-methyl-d3)

PESTANAL®, analytical standard

Synonym(s):

Dimethyl 3-methyl-4-(methyl-d3-sulfonyl)phenyl phosphate, Fenoxon sulfone-(S-methyl-d3)

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About This Item

Empirical Formula (Hill Notation):
C10D3H12O6PS
Molecular Weight:
297.28
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

Assay

≥98.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

mp

40-46 °C

application(s)

agriculture

format

neat

storage temp.

2-8°C

SMILES string

O=P(OC)(OC)OC1=CC(C)=C(S(=O)(C([2H])([2H])[2H])=O)C=C1

General description

Fenthion oxon sulfone-(S-methyl-d3) is a deuterated isotope analog of fenthion oxon sulfone-(S-methyl), a derivative of organophosphorus insecticide fenthion, wherein S-methyl protons are replaced by deuterium.

Application

Isotope-labeled compounds are increasingly used in isotope dilution mass spectrometry (IDMS) for the quantitative analysis of pesticides. The major advantage of using this technique is that the isotope-labeled compounds have nearly the same physical properties as their non-labeled counterpart analogs, and thus show identical behavior during the workup and sample preparation process. This helps in overcoming the problems of matrix effects generally encountered in the usual LC-MS/GC-MS analysis potentially resulting in biased results. By spiking the sample before workup with its isotope labeled analog, the loss of analyte that leads to matrix effects can be determined and compensated.

Legal Information

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

Pictograms

Skull and crossbones

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 2 Oral

Storage Class Code

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

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Simultaneous Analysis of Fenthion and Its Five Metabolites in Produce Using Ultra-High Performance Liquid Chromatography-Tandem Mass Spectrometry
Lee J and Kim J-H
Molecules (Basel), 25(8), 1938-1938 (2020)
Kuniyo Sugitate et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 28(7), 669-673 (2012-07-14)
Fenthion, fenthion sulfoxide, fenthion oxon sulfoxide and fensulfothion showed two different mass spectra in GC/MS, depending on their concentrations. The base peaks shifted to lower levels by 1 m/z at lower concentration, and no retention time shifts were observed.

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