Trichloroacetic anhydride, technical grade, 95%

Code: 367710-25G D2-231

Application

Trichloroacetic anhydride may be used as derivatization reagent for the following studies:Simultaneous analysis of amphetamine, methamphetamine and 3,4-methylened...


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Your Price
€175.00 25G
€215.25 inc. VAT

Application

Trichloroacetic anhydride may be used as derivatization reagent for the following studies:Simultaneous analysis of amphetamine, methamphetamine and 3,4-methylenedioxymethamphetamine (MDMA or Ecstasy) in urine samples by solid-phase extraction, derivatization and gas chromatography/mass spectrometry.Analysis of halogenated amphetamines in brain tissue from rats by gas chromatography with electron-capture detection (GC-ECD).Quantitative determination of the metabolites of l-alpha-acetylmethadol (LAAM), such as noracetylmethadol, dinoracetylmethadol, methadol and normethadol by electron capture gas-liquid chromatography.

General description

Trichloroacetic anhydride is reported to be an efficient derivatization reagent, since it produces stable derivatives having both a higher mass fragmentation pattern and lesser volatility than derivatives of trifluoroacetic anhydride (TFAA) or heptafluorobutyric anhydride (HFBA). The interaction of thymidine 5′-phosphate with trichloroacetic anhydride in dimethylformamide and acetonitrile in the presence of tertiary amines hs been studied.

Packaging

25, 100 g in glass bottle

assay95%
bp139-141 °C/60 mmHg (lit.)
density1.69 g/mL at 25 °C (lit.)
formliquid
gradetechnical grade
InChI keyMEFKFJOEVLUFAY-UHFFFAOYSA-N
InChI1S/C4Cl6O3/c5-3(6,7)1(11)13-2(12)4(8,9)10
Quality Level100
refractive indexn20/D 1.484 (lit.)
SMILES stringClC(Cl)(Cl)C(=O)OC(=O)C(Cl)(Cl)Cl
Cas Number4124-31-6
Hazard Class8
Un Number3265
Pack GroupII
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