Electron ionization mass spectral fragmentation of deoxynivalenol and related tricothecenes

Careful analysis of the electron impact (EI) mass spectral data obtained for the trimethylsilyl (TMS) ethers of known trichothecene mycotoxins of the deoxynivalenol group permitted the construction of a database useful for the identification of these mycotoxins directly from a gas chromatography/mas...

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Bibliographic Details
Published in:Rapid communications in mass spectrometry Vol. 16; no. 19; pp. 1827 - 1835
Main Authors: Rodrigues-Fo, Edson, Mirocha, C. J., Xie, Weiping, Krick, Thomas P., Martinelli, J. A.
Format: Journal Article
Language:English
Published: Chichester, UK John Wiley & Sons, Ltd 01-01-2002
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Summary:Careful analysis of the electron impact (EI) mass spectral data obtained for the trimethylsilyl (TMS) ethers of known trichothecene mycotoxins of the deoxynivalenol group permitted the construction of a database useful for the identification of these mycotoxins directly from a gas chromatography/mass spectrometry (GC/MS) run. Structures of the ions at m/z 103, 117, 147 and 191 were elucidated by high‐resolution mass spectrometry (HRMS) and a fragmentation scheme was suggested. The relative abundances of these ions in the mass spectra of the trichothecenes allowed a fast structural diagnosis during analysis of biological matrices. A new mycotoxin of this group, 3‐acetylnivalenol, was tentatively identified by using MS data interpretation only. Copyright © 2002 John Wiley & Sons, Ltd.
Bibliography:istex:F254D6681EECD4B9BAE038A24EF4281BE89D1079
ark:/67375/WNG-VGD0B1GQ-X
ArticleID:RCM796
ISSN:0951-4198
1097-0231
DOI:10.1002/rcm.796