Characterization of Phenolic and Secoiridoid Aglycons Present in Virgin Olive Oil by GC-CI-MS
Articolo
Data di Pubblicazione:
1996
Abstract:
Olive oil phenolic and secoiridoid compound derivatives were detected by mass spectrometry. Chemical ionization (Cl) allowed us to obtain parent ions, that were not detectable in the electron impact mode. CI experiments were performed using either CH4 or NH3 as the reactant gas. Unlike CH4-CI, which fails to give molecular mass information, NH3-CI provided, in all the cases explored, an adduct ion [M+18] + that was sufficiently stable to be detected and recorded. Information about molecular masses was very useful for the complete characterization of aglycons from glycosides occurring in virgin olive
oils. Aglycons of ligstroside, of decarbomethoxyoleuropein and of oleuropein were detected. Each aglycon, because of several tautomeric equilibria involving the ring opening of secoiridoid, showed up as compounds with four main structures after derivatization with bis(trimethylsilyl)trifluoracetamide.
oils. Aglycons of ligstroside, of decarbomethoxyoleuropein and of oleuropein were detected. Each aglycon, because of several tautomeric equilibria involving the ring opening of secoiridoid, showed up as compounds with four main structures after derivatization with bis(trimethylsilyl)trifluoracetamide.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Olive oil; Food analysis; Aglycons; Glycosides; Secoiridoid; Phenolic compounds; Oleuropeins; Ligstroside;
Hydroxytyrosol; Tyrosol
Elenco autori:
Angerosa, F; D'Alessandro, N; Corana, F; Mellerio, G.
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