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Impurity profiling of methamphetamine synthesised from α-phenylacetoacetonitrile (APAAN).
- Source :
-
Drug testing and analysis [Drug Test Anal] 2022 Jan; Vol. 14 (1), pp. 56-71. Date of Electronic Publication: 2021 Aug 18. - Publication Year :
- 2022
-
Abstract
- The rise in popularity of 'designer' precursor compounds for the synthesis of amphetamine-type stimulants poses a significant challenge to law enforcement agencies. One such precursor is α-phenylacetoacetonitrile (APAAN). APAAN emerged in Europe in 2010 and quickly became one of the most popular precursors for amphetamine synthesis in that region. Previous literature has identified four APAAN-specific impurities formed in the synthesis of amphetamine; however, there is currently no research on the use of APAAN in the synthesis of methamphetamine, which is more likely to be employed in a non-European market. In this study methamphetamine was synthesised via three common clandestine methods: the Leuckart method and two reductive amination methods. We report the identification of five new impurities and two previously identified impurities characteristic for the use of APAAN in the synthesis of methamphetamine. The newly identified impurities were characterised by MS and NMR and determined to be (E)-3-(methylamino)-2-phenylbut-2-enenitrile, 3-(methylamino)-2-phenylbutanenitrile, 3-methyl-2,4-diphenylpentanedinitrile, 2-phenylbutyronitrile and 3-hydroxy-2-phenylbutanenitrile.<br /> (© 2021 John Wiley & Sons, Ltd.)
- Subjects :
- Drug Contamination
Magnetic Resonance Spectroscopy
Mass Spectrometry
Central Nervous System Stimulants analysis
Central Nervous System Stimulants chemical synthesis
Central Nervous System Stimulants chemistry
Illicit Drugs analysis
Illicit Drugs chemical synthesis
Illicit Drugs chemistry
Methamphetamine analysis
Methamphetamine chemical synthesis
Methamphetamine chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1942-7611
- Volume :
- 14
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Drug testing and analysis
- Publication Type :
- Academic Journal
- Accession number :
- 34355528
- Full Text :
- https://doi.org/10.1002/dta.3140