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89136

Supelco

Fenamiphos-(S-methyl-d3)

PESTANAL®, analytical standard

Synonym(s):

Fenamiphos-d3, Phenamiphos-d3

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About This Item

Empirical Formula (Hill Notation):
C13D3H19NO3PS
Molecular Weight:
306.38
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

Assay

≥98.0% (GC)

shelf life

limited shelf life, expiry date on the label

application(s)

agriculture

format

neat

storage temp.

2-8°C

SMILES string

O=P(NC(C)C)(OC1=CC(C)=C(SC([2H])([2H])[2H])C=C1)OCC

General description

Fenamiphos-(S-methyl-d3) is a deuterated isotope analog of fenamiphos-(S-methyl), a derivative of the broad-spectrum, non-volatile organophosphorus nematicide fenamiphos, 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 crossbonesEnvironment

Signal Word

Danger

Hazard Classifications

Acute Tox. 2 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Bioremedial potential of fenamiphos and chlorpyrifos degrading isolates: influence of different environmental conditions
Singh BK, et al.
Soil Biology and Biochemistry, 38(9), 2682-2693 (2006)
Land use effects on sorption of pesticides and their metabolites in sandy soils. I. Fenamiphos and two metabolites, fenamiphos sulfoxide and fenamiphos sulfone, and fenarimol and azinphos methyl
Oliver DP, et al.
Australian Journal of Soil Research, 41(5), 847-860 (2003)

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