89953
Dimethomorph-(dimethoxy-d6)
PESTANAL®, analytical standard
Sinónimos:
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
Fórmula empírica (notación de Hill):
C21D6H16ClNO4
Peso molecular:
393.89
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
NACRES:
NA.24
Productos recomendados
grado
analytical standard
Nivel de calidad
Línea del producto
PESTANAL®
Análisis
≥98.0% (HPLC)
caducidad
limited shelf life, expiry date on the label
aplicaciones
agriculture
formato
neat
temp. de almacenamiento
2-8°C
Categorías relacionadas
Descripción general
Dimethomorph-(dimethoxy-d6) is an isotope-labeled analog of the systemic morpholine fungicide dimethomorph, wherein the dimethoxy protons are replaced by deuterium.
Aplicación
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.
Información legal
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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