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Trichloroacetic anhydride

ALDRICH/367710 - technical grade, 95%

Synonym: (2,2,2-Trichloroacetyl) 2,2,2-trichloroacetate; Trichloroacetic acid anhydride

CAS Number: 4124-31-6
Empirical Formula (Hill Notation): C4Cl6O3
Molecular Weight: 308.76
EC Number: 223-925-3
MDL Number: MFCD00000793
Linear Formula: (Cl3CCO)2O
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-367710-25G 25 g
$179.00
1/EA
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45-367710-100G 100 g
$379.00
1/EA
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assay 95%
bp 139-141 °C/60 mmHg (lit.)
density 1.69 g/mL at 25 °C (lit.)
form liquid
grade technical grade
InChI 1S/C4Cl6O3/c5-3(6,7)1(11)13-2(12)4(8,9)10
InChI key MEFKFJOEVLUFAY-UHFFFAOYSA-N
refractive index n20/D 1.484 (lit.)
SMILES string ClC(Cl)(Cl)C(=O)OC(=O)C(Cl)(Cl)Cl
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
Purity 95%
bp 139-141 °C/60 mmHg (lit.)
Density 1.69 g/mL at 25 °C (lit.)
Refractive Index n20/D 1.484 (lit.)
UNSPSC 12352100

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