Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractTemporal and Longitudinal Characteristics of Volatile Organic Compound Emissions from Aeration Units of Publicly Owned Treatment Works    Next Abstract[Rapid determination of trace volatile organic compounds in ambient air by portable gas chromatography-mass spectrometry] »

J Agric Food Chem


Title:Ultrahigh performance liquid chromatography analysis of volatile carbonyl compounds in virgin olive oils
Author(s):Zhu H; Li X; Shoemaker CF; Wang SC;
Address:"Department of Food Science and Technology, University of California-Davis , Davis, California 95616, United States"
Journal Title:J Agric Food Chem
Year:2013
Volume:20131204
Issue:50
Page Number:12253 - 12259
DOI: 10.1021/jf404368m
ISSN/ISBN:1520-5118 (Electronic) 0021-8561 (Linking)
Abstract:"The enzymatic and chemical oxidation reaction in olive oil produces many volatile carbonyl compounds that contribute to the complex flavor of olive oil. A novel ultrahigh performance liquid chromatography (UHPLC) method with dynamic headspace sampling and 2,4-dinitrophenylhydrazine (DNPH) derivatization were established to determine the volatile carbonyls in virgin olive oil. Quantification of nine characteristic carbonyls (acetone, hexanal, E-2-hexenal, octanal, E-2-octenal, nonanal, E-2-nonenal, E,E-2,4-nonadienal, and E,E-2,4-decadienal) was achieved using cyclopentanal as an internal standard. This method provides comparable linearity (R(2) = 0.9917-1.0000) and repeatability (less than 7.6% relative standard deviations) with solid phase microextraction gas chromatography (SPME-GC). The relative standard deviations (%RSD) of all applied carbonyl standards were lower than 7.6%. The limits of detection (LOD) and quantification (LOQ) were in the ranges of 1.6-150.1 and 4.8-906.1 mug/kg. The recoveries obtained for olive oil samples were in the range of 81.0-115.3%. To show the potential of this method on the quantification of other volatile carbonyls that were not included in this study, GC-electron ionization mass spectrometry (GC-EI/MS) was employed to identify the derivatized carbonyls (carbonyl (2,4-DNPH) hydrazones) while peak assignments were made on the basis of elution sequences and peak areas. This method provided feasibility of using LC to determine volatile carbonyls in oil matrices, which can be applied to exam the degree of lipid oxidation and evaluate the sensory properties of VOO and other edible oils"
Keywords:"Aldehydes/*analysis/isolation & purification Chromatography, High Pressure Liquid/*methods Olive Oil Plant Oils/*analysis Solid Phase Microextraction Volatile Organic Compounds/*analysis/isolation & purification Volatilization;"
Notes:"MedlineZhu, Hanjiang Li, Xueqi Shoemaker, Charles F Wang, Selina C eng Evaluation Study 2013/11/28 J Agric Food Chem. 2013 Dec 18; 61(50):12253-9. doi: 10.1021/jf404368m. Epub 2013 Dec 4"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 22-11-2024