4.5 Article

GC-IRD methods for the identification of isomeric ethoxyphenethylamines and methoxymethcathinones

期刊

FORENSIC SCIENCE INTERNATIONAL
卷 184, 期 1-3, 页码 54-63

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.forsciint.2008.12.003

关键词

GC-IRD; Ethoxyphenethylamines; Methoxymethcathinones; Regioisomers; Isobaric substances

资金

  1. U.S. Department of Justice [2006-DN-BX-K016]
  2. Office of Justice Programs
  3. National Institute of Justice

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A series of 12 isomeric phenethylamines were evaluated by gas chromatography using vapor phase infrared spectrophotometric detection. The major mass spectral fragments for each of these unique isomers occur at equivalent mass and all have equal molecular weight. The infrared spectra for these compounds allow for identification of any one of these amines to the exclusion of all other isomers. This differentiation is accomplished without the need for chemical derivatization. The methoxymethcathinones show unique infrared absorption bands in the 1690-1700 cm(-1) range for the carbonyl group and the ring substitution pattern in the ethoxymethamphetamines can be differentiated by several bands in the 700-1610 cm(-1) region. Side chain and degree of nitrogen substitution can be evaluated in the 2770-3000 cm(-1) region of the infrared range. All the studied regioisomers could be differentiated from 3,4-MDMA via their vapor phase 1R spectra. Capillary gas chromatography on an Rxi-50 stationary phase successfully resolved the side chain regioisomers, the substituted methamphetamines and the methoxymethcathinones. (c) 2009 Published by Elsevier Ireland Ltd.

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