A qualitative GC/MS proΓle was obtained and its mass spectrometric features characterized for the analysis of the enantiomers of (RS)-3,4-methylenedioxymethamphetamine (MDMA) and its metabolites (RS)-3,4methylenedioxyamphetamine (MDA), (RS)-4-hydroxy-3-methoxymethamphetamine (HMMA) and (RS)-4hydroxy
β¦ LIBER β¦
Stereospecific gas chromatographic/mass spectrometric assay of the chiral labetalol metabolite 3-amino-1-phenylbutane
β Scribed by A. Changchit; J. Gal; J. A. Zirrolli
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 638 KB
- Volume
- 20
- Category
- Article
- ISSN
- 1076-5174
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The gas chromatographic and mass spectrometric behavior of 2-amino-1-iodo-3-phenylpropane (iodoamphetamine) was investigated. It was determined that the compound is unstable under the gas chromatographic mass spectrometric conditions used, undergoing a number of reactions and rearrangements. When io