Heterocyclic acetals from glycerol and acetaldehyde in port wines: Evolution with aging

Antonio Cesar Da Silva Ferreira*, Jean Christophe Barbe, Alain Bertrand

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

104 Citations (Scopus)

Abstract

In Port wine, isomers of glycerol and acetaldehyde acetals have been found at total contents ranging from 9.4 to 175.3 mg/L. During oxidative aging, the concentrations of the 5-hydroxy-2-methyl-1,3-ioxane and 4-hydroxymethyl-2-methyl-1,3-dioxolane isomers increased with time showing a linear correlation (r > 0.95). The flavor threshold for the mixture of the four isomers was evaluated in wine at 100 mg/L. Thus, it is expected that they contribute to "old Port wine" aroma in wines older than 30 years. Experiments with model solutions and wine clearly demonstrated that SO2 combines with acetaldehyde and blocks the acetalization reaction.

Original languageEnglish
Pages (from-to)2560-2564
Number of pages5
JournalJournal of Agricultural and Food Chemistry
Volume50
Issue number9
DOIs
Publication statusPublished - 24 Apr 2002

Keywords

  • 1,3-Dioxanes
  • 1,3-dioxolanes
  • Acetalization
  • Oxidative wine-aging

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