89953
Dimethomorph-(dimethoxy-d6)
PESTANAL®, analytical standard
Synonyme(s) :
3-(4-Chlorophenyl)-3-[3,4-di(methoxy-d3)phenyl]-1-(4-morpholinyl)-2-propen-1-one, Dimethomorph-d6
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About This Item
Formule empirique (notation de Hill):
C21D6H16ClNO4
Poids moléculaire :
393.89
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24
Produits recommandés
Qualité
analytical standard
Niveau de qualité
Gamme de produits
PESTANAL®
Pureté
≥98.0% (HPLC)
Durée de conservation
limited shelf life, expiry date on the label
Application(s)
agriculture
Format
neat
Température de stockage
2-8°C
Catégories apparentées
Description générale
Dimethomorph-(dimethoxy-d6) is an isotope-labeled analog of the systemic morpholine fungicide dimethomorph, wherein the dimethoxy protons are replaced by deuterium.
Application
Dimethomorph-(dimethoxy-d6) may be used as a deuterated internal standard to quantify the analyte in dairy milk by liquid chromatography-tandem mass spectrometry (LC-MS/MS) technique.
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.
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.
Informations légales
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
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Responses of indigenous microorganisms to a fungicidal mixture of mancozeb and dimethomorph added to sandy soils
Cycon M, et al.
International Biodeterioration & Biodegradation, 64(4), 316-323 (2010)
Human pharmaceutical and pesticide residues in Israeli dairy milk in association with dietary risk assessment
Bommuraj V, et al.
Food additives & contaminants. Part B, Surveillance, 64(4), 1-11 (2020)
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