89953
Dimethomorph-(dimethoxy-d6)
PESTANAL®, analytical standard
Sinonimo/i:
3-(4-Chlorophenyl)-3-[3,4-di(methoxy-d3)phenyl]-1-(4-morpholinyl)-2-propen-1-one, Dimethomorph-d6
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5 MG
CHF 278.00
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5 MG
CHF 278.00
About This Item
Formula empirica (notazione di Hill):
C21D6H16ClNO4
Peso molecolare:
393.89
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24
Prodotti consigliati
Grado
analytical standard
Livello qualitativo
Nome Commerciale
PESTANAL®
Saggio
≥98.0% (HPLC)
Durata
limited shelf life, expiry date on the label
applicazioni
agriculture
Formato
neat
Temperatura di conservazione
2-8°C
Categorie correlate
Descrizione generale
Dimethomorph-(dimethoxy-d6) is an isotope-labeled analog of the systemic morpholine fungicide dimethomorph, wherein the dimethoxy protons are replaced by deuterium.[1]
Applicazioni
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.[2]
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.
Note legali
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
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I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.
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)
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)
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