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Merck

89947

Supelco

三唑醇-D4

PESTANAL®, analytical standard

别名:

α-tert-Butyl-β-(4-chlorophenoxy-d4)-1H-1,2,4-triazole-1-ethanol, Triadimenol-d4

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About This Item

经验公式(希尔记法):
C14D4H14ClN3O2
分子量:
299.79
MDL编号:
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®

方案

≥98.0% (HPLC)

保质期

limited shelf life, expiry date on the label

应用

agriculture

包装形式

neat

储存温度

2-8°C

SMILES字符串

ClC1=C([2H])C([2H])=C(OC(N2N=CN=C2)C(C(C)(C)C)O)C([2H])=C1[2H]

InChI

1S/C14H18ClN3O2/c1-14(2,3)12(19)13(18-9-16-8-17-18)20-11-6-4-10(15)5-7-11/h4-9,12-13,19H,1-3H3/i4D,5D,6D,7D

InChI key

BAZVSMNPJJMILC-UGWFXTGHSA-N

一般描述

Triadimenol-(4-chlorophenoxy-d4) is an isotope-labeled analog of the systemic fungicide triadimenol, wherein the 4-chlorophenoxy protons are replaced by deuterium.[1][2]

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

警示用语:

Danger

危险分类

Acute Tox. 4 Oral - Aquatic Chronic 2 - Lact. - Repr. 1B

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Aqueous photochemistry of pesticides triadimefon and triadimenol
Da Silva JP, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 154(2-3), 293-298 (2003)
Photophysics and photochemistry of azole fungicides: triadimefon and triadimenol
Da Silva JP, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 142(1), 31-37 (2001)

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