367710
Trichloroacetic anhydride
technical grade, 95%
Synonyme(s) :
(2,2,2-Trichloroacetyl) 2,2,2-trichloroacetate, Trichloroacetic acid anhydride
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About This Item
Formule linéaire :
(Cl3CCO)2O
Numéro CAS:
Poids moléculaire :
308.76
Numéro Beilstein :
980355
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22
Produits recommandés
Qualité
technical grade
Niveau de qualité
Pureté
95%
Forme
liquid
Indice de réfraction
n20/D 1.484 (lit.)
Point d'ébullition
139-141 °C/60 mmHg (lit.)
Densité
1.69 g/mL at 25 °C (lit.)
Groupe fonctionnel
anhydride
chloro
ester
Chaîne SMILES
ClC(Cl)(Cl)C(=O)OC(=O)C(Cl)(Cl)Cl
InChI
1S/C4Cl6O3/c5-3(6,7)1(11)13-2(12)4(8,9)10
Clé InChI
MEFKFJOEVLUFAY-UHFFFAOYSA-N
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Catégories apparentées
Description générale
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.
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.
Mention d'avertissement
Danger
Mentions de danger
Classification des risques
Acute Tox. 4 Oral - Skin Corr. 1A
Code de la classe de stockage
8A - Combustible corrosive hazardous materials
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Les clients ont également consulté
M L Owen et al.
Journal of pharmacological methods, 25(2), 147-155 (1991-04-01)
p-Chloro-alpha-fluoromethylphenylethylamine (fluoro-p-chloroamphetamine) (FpCA) has been shown in acute studies to be a less potent depletor of the neurotransmitter amine 5-hydroxytryptamine (5-HT) in brain than is p-chloroamphetamine (pCA). Gas chromatographic assay procedures for FpCA and PCA have been developed in our
R J Czarny et al.
Journal of analytical toxicology, 13(5), 257-262 (1989-09-01)
An analytical procedure for methamphetamine and amphetamine has been developed using 4-carbethoxyhexafluorobutyryl chloride. This derivatizing reagent has all the previously reported advantages of trichloroacetic anhydride (TCAA) in that it produces stable derivatives having both a higher mass fragmentation pattern and
B K Gan et al.
Journal of forensic sciences, 36(5), 1331-1341 (1991-09-01)
A rapid and effective solid-phase extraction procedure using Bond Elute Certify bonded silica sorbent cartridges was adopted to extract amphetamine, methamphetamine, and 3,4-methylenedioxymethamphetamine (MDMA or Ecstasy) from urine samples. The extract was derivatized with trichloroacetic anhydride prior to gas chromatography/mass
D H Lau et al.
Journal of chromatography, 129, 329-338 (1976-12-22)
Six reagents-trichloroacetyl chloride, trichloroacetic anhydride, pentafluorobenzoyl chloride, heptafluorobutyryl chloride, heptafluorobutyric anhydride, and trifluoroacetic anhydride- were evaluated as potential derivatizing reagents for quantitating the metabolites of l-alpha-acetylmethadol (LAAM) -noracetylmethadol, dinoracetylmethadol, methadol, and normethadol-by electron capture gas-liquid chromatography. All of the reagents
V S Bogachev et al.
Bioorganicheskaia khimiia, 29(1), 64-74 (2003-03-28)
The interaction of thymidine 5'-phosphate with trichloroacetic anhydride, trichloroacetyl chloride, and tribromoacetyl bromide was studied in dimethylformamide and acetonitrile in the presence of tertiary amines. The first two reactions gave the mixed anhydride of trichloroacetic and thymidylic acids (acyl phosphate)
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