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80814

Supelco

Tembotrione-(methyl-d3)

PESTANAL®, analytical standard

Synonym(s):

2-{2-Chloro-4-(methyl-d3-sulfonyl)-3-[(2,2,2-trifluoroethoxy)methyl]benzoyl}-1,3-cyclohexanedione, 2-{2-Chloro-4-mesyl-d3-3-[(2,2,2-trifluoroethoxy)methyl]benzoyl}cyclohexane-1,3-dione, Tembotrione-d3

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About This Item

Empirical Formula (Hill Notation):
C17D3H13ClF3O6S
Molecular Weight:
443.84
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

Assay

≥98.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

application(s)

agriculture

format

neat

storage temp.

2-8°C

General description

Tembotrione-(methyl-d3) is an isotope-labeled analog of triketone herbicide tembotrione, wherein S-methyl protons are substituted by deuterium.

Application

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.

Legal Information

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

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 2 - Skin Sens. 1 - STOT RE 2

Target Organs

Eyes,Liver,Kidney

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Chlorination of the beta-triketone herbicides tembotrione and sulcotrione: kinetic and mechanistic study, transformation products identification and toxicity
Tawk A, et al.
Water Research, 76, 132-142 (2015)
Photolysis of tembotrione and its main by-products under extreme artificial conditions:: Comparison with another β-triketone herbicide
Calvayrac C, et al.
The Science of the Total Environment, 452, 227-232 (2013)

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