Literature DB >> 26267375

Impurities in Illicit Drug Preparations: 3,4-(Methylenedioxy)amphetamine and 3,4-(Methylenedioxy)methylamphetamine.

A M Verweij1.   

Abstract

Attention is given here to the mass spectral data of impurities present in illicit drug preparations of 3,4-(methylenedioxy)amphetamine and 3,4-(methylenedioxy)methylamphetamine. These "designer" drugs, having emphatic properties, were synthesized following well-known procedures such as the reductive amination route, the Leuckart reaction, and the nitropropene and the bromopropane routes. Based on the structure elucidation of impurities - especially those so-called "route specific" ones - present in these illicit drug preparations conclusions can be drawn about the method of preparation of a drug sample. Furthermore, on the basis of this kind of information methods can be developed for the comparison of drug samples, by which questions about the origin of drug samples can be solved (commonly known as the signature method).
Copyright © 1992 Central Police University.

Entities:  

Keywords:  Designer drugs; dioxyamphetamine; impurities; mass spectrometry; synthesis

Year:  1992        PMID: 26267375

Source DB:  PubMed          Journal:  Forensic Sci Rev        ISSN: 1042-7201


  2 in total

1.  Adulterants and altruism: A qualitative investigation of "drug checkers" in North America.

Authors:  Joseph J Palamar; Patricia Acosta; Rachel Sutherland; Michele G Shedlin; Monica J Barratt
Journal:  Int J Drug Policy       Date:  2019-10-11

2.  A convenient route to symmetrically and unsymmetrically substituted 3,5-diaryl-2,4,6-trimethylpyridines via Suzuki-Miyaura cross-coupling reaction.

Authors:  Dariusz Błachut; Joanna Szawkało; Zbigniew Czarnocki
Journal:  Beilstein J Org Chem       Date:  2016-04-28       Impact factor: 2.883

  2 in total

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