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Merck
CN

90039

Supelco

Fenthion oxon sulfone-(S-methyl-d3)

PESTANAL®, analytical standard

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别名:
Dimethyl 3-methyl-4-(methyl-d3-sulfonyl)phenyl phosphate, Fenoxon sulfone-(S-methyl-d3)
经验公式(希尔记法):
C10D3H12O6PS
分子量:
297.28
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24

等级

analytical standard

质量水平

产品线

PESTANAL®

检测方案

≥98.0% (HPLC)

保质期

limited shelf life, expiry date on the label

mp

40-46 °C

应用

agriculture

格式

neat

储存温度

2-8°C

SMILES字符串

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

相关类别

一般描述

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.

应用

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.

法律信息

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

象形图

Skull and crossbones

警示用语:

Danger

危险声明

预防措施声明

危险分类

Acute Tox. 2 Oral

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°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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