The mass spectra of the 4,4-dimethyloxazoline derivatives of some conjugated hydroxy ene-yne C17 and C18 fatty acids

  • Volker Spitzer
Article

Abstract

The mass spectra of the 4,4-dimethyloxazoline derivatives from various fatty acids with a hydroxy group in conjugation with conjugated double-triple bonds (7-hydroxy-trans-10-heptadecene-8-ynoic acid; 7-hydroxy-trans-10, 16-heptadecadiene-8-ynoic acid; 8-hydroxy-rans-11-octadecene-9-ynoic acid; 8-hydroxy-trans-11, 17-octadecadiene-9-ynoic acid) have been examined and compared with their analogous nonhydroxy derivatives. The position of the hydroxy group was unequivocally proven by characteristic odd-numbered fragment peaks, explainable by α-cleavage at the hydroxy group at the oxazoline end of the molecule. The weak ions produced by α-cleavage at the other side of the hydroxy group indicated that the hydroxy group must be in conjugation with the ene-yne system. Fragments that allow one to distinguish between ene-yne or yne-ene systems were absent. In conjunction, the weak molecular ion and the more intense M-18 ion could confirm the molecular weight of each fatty acid.

Key Words

Acetylenic fatty acids 4,4-dimethyloxazoline derivatives GC/MS hydroxy fatty acids 

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Copyright information

© AOCS Press 1996

Authors and Affiliations

  • Volker Spitzer
    • 1
  1. 1.Faculdade de Farmácia, Curso de Pós-GraduaçãoUniversidade Federal do Rio Grande do SulPorto AlegreBrazil

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