This paper discusses chromatographic and mass spectral studies on methoxymethcathinones.
This study found that differentiation of methoxymethcathinones by mass spectrometry was only possible after formation of the perfluoroacyl derivatives, pentafluoropropionylamides (PFPA), and heptafluorobutrylamides (HFBA). Gas chromatographic separation on nonpolar stationary phases successfully resolved the three methcathinones from 2,3- and 3,4-MDMA as the PFPA and HFBA derivatives. The methoxymethcathinones are uniquely regioisomeric with the controlled drug substance 3,4-methylenedioxymethamphetamine (3,4-MDMA) or Ecstacy. The various isomeric forms of the methoxymethcathinones have mass spectra essentially equivalent to 3,4-MDMA. They all have a molecular weight of 193 and major fragment ions in their electron ionization mass spectra at m/z 58 and 135/136. (Published Abstract Provided)
Downloads
Similar Publications
- Comparative Evaluation of Genotyping Technologies for Investigative Genetic Genealogy in Sexual Assault Casework
- Enhancing Our Genetic Knowledge of Human Iris Pigmentation and Facial Morphology
- The Collection, Preservation, and Processing of DNA Samples from Decomposing Human Remains for More Direct Disaster Victim Identification (DVI)