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Abstract

Methylhexaneamine (MHA) is a stimulant that is added to dietary supplements and its safety is an on-going debate, prompting the World Anti-Doping Agency to add it to the 2010 prohibited list. Gas chromatography-low resolution mass spectrometry (GC-MS) with electron ionization (EI) requires derivatization to convert MHA into a less volatile compound, and a 2-3min solvent delay to prevent filament damage. Without derivatization, the EI mass spectrum of MHA, which exhibits an abundant immonium ion atm/z44 and no other fragment ions with relative intensity >10%, is very similar to the EI mass spectra of 2-aminoheptane, 1,4-dimethylamylamine, andn-hexylmethylamine. When using derivatization with trifluoroacetic anhydride (TFAA) and GC-high resolution time-of-flight mass spectrometry with soft ionization, the derivatized MHA diastereoisomers can be distinguished from the trifluoroacetyl-derivatives of 1-aminoheptane, 2-aminoheptane, 1,4-dimethylamylamine (1,4-DMAA) andn-hexylmethylamine. Several nutritional supplements were analysed for MHA by this technique and the results of the measurements are presented here.Keywords: GC high-resolution TOFMS; Soft-ionization; Methylhexaneamine; Nutritional supplements

Details

Title
Identification of methylhexaneamine by GC high-resolution TOFMS and soft ionization
Author
Lopez-Avila, Viorica; Zorio, Mirela
Pages
113-9
Publication year
2013
Publication date
Sep 10, 2013
Publisher
Elsevier Limited
e-ISSN
18726283
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
1412582202
Copyright
Copyright Elsevier Limited Sep 10, 2013