Chiral Evaluation of Aroma-active Compounds in Real Complex Samples

ABSTRACT The enantiomeric distribution of aroma‐active compounds resulting from stereospecific biosyn‐thetic pathways was established using a multidimensional chromatographic system, which involves the on‐line coupling of reversed‐phase liquid chromatography and gas chromatography (RPLC‐GC). The pro...

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Bibliographic Details
Published inJournal of food science Vol. 68; no. 3; pp. 770 - 774
Main Authors Ruiz del Castillo, M.L., Caja, M.M., Blanch, G.P., Herraiz, M.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.04.2003
Wiley Subscription Services, Inc
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Summary:ABSTRACT The enantiomeric distribution of aroma‐active compounds resulting from stereospecific biosyn‐thetic pathways was established using a multidimensional chromatographic system, which involves the on‐line coupling of reversed‐phase liquid chromatography and gas chromatography (RPLC‐GC). The proposed approach allowed the rapid determination of the enantiomeric composition of chiral terpenes such as α‐pinene, limonene, linalool and α‐terpineol in different products (that is, orange aroma, orange essential oils, and fruit beverage) without requiring the previous concentration of the sample. Relative standard deviation values lower than 7.5% were obtained for the investigated compounds. Applications to the authentication of fruit products based on both the R‐ and S‐form contents of chiral terpenes were considered.
Bibliography:ArticleID:JFDS770
istex:00937CC18DCD853A9A2F9D8B853F65CF5FAA858F
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Financial support for this work by CICYT (Project AL199‐1188) is gratefully acknowledged.
ObjectType-Article-2
SourceType-Scholarly Journals-1
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ISSN:0022-1147
1750-3841
DOI:10.1111/j.1365-2621.2003.tb08240.x