Forensic Aspects of Designer LSD Analogs Identification by GC-MS (EI) and UV Spectroscopy.
Molecules (Basel, Switzerland) December 4, 2024 Kaja Tusiewicz, Olga Wachełko, Marcin Zawadzki et al. 5 citations
Lysergic acid diethylamide (LSD) analogs, synthesized to evade drug regulations, pose challenges for forensic identification, especially their isomeric forms. Gas chromatography-mass spectrometry (GC-MS) and UV spectroscopy analyzed 13 LSD analogs. Solvents like diethyl ether, tert-butyl methyl ether, dichloromethane, and acetone provided the best sensitivity and stability, while methanol caused alcoholysis of many analogs, potentially leading to false results. Effective chromatographic separation was achieved for isomers including LSD, MiPLA, LAMPA, 1P-LSD, 1P-MiPLA, 1cP-LSD, and 1cP-MiPLA. Key mass spectrometry ions (e.g.