Literature DB >> 16620511

Chromatographic and mass spectral studies on methoxymethcathinones related to 3,4-methylenedioxymethamphetamine.

Tamer Awad1, C Randall Clark, Jack DeRuiter.   

Abstract

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. Differentiation 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.

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Year:  2006        PMID: 16620511     DOI: 10.1093/chromsci/44.3.155

Source DB:  PubMed          Journal:  J Chromatogr Sci        ISSN: 0021-9665            Impact factor:   1.618


  2 in total

1.  Systematic Structure-Activity Studies on Selected 2-, 3-, and 4-Monosubstituted Synthetic Methcathinone Analogs as Monoamine Transporter Releasing Agents.

Authors:  Donna Walther; Abdelrahman R Shalabi; Michael H Baumann; Richard A Glennon
Journal:  ACS Chem Neurosci       Date:  2018-11-07       Impact factor: 4.418

2.  Spectroscopic characterization and crystal structures of two cathinone derivatives: N-ethyl-2-amino-1-phenylpropan-1-one (ethcathinone) hydrochloride and N-ethyl-2-amino-1-(4-chlorophenyl)propan-1-one (4-CEC) hydrochloride.

Authors:  Piotr Kuś; Joachim Kusz; Maria Książek; Ewelina Pieprzyca; Marcin Rojkiewicz
Journal:  Forensic Toxicol       Date:  2016-10-31       Impact factor: 4.096

  2 in total

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