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 AbstractScintigraphic evaluation of renal functional damage in volatile substance abusers    Next AbstractRapid determination of essential oils functional groups using compositional methods and VisNIR spectroscopy »

J Chromatogr A


Title:Substitution of carcinogenic solvent dichloromethane for the extraction of volatile compounds in a fat-free model food system
Author(s):Cayot N; Lafarge C; Bou-Maroun E; Cayot P;
Address:"Unite Procedes Alimentaires et Microbiologiques, UMR A 02.102, AgroSup Dijon/Universite de Bourgogne, 1 esplanade Erasme, F-21000 Dijon, France. Electronic address: nathalie.cayot@agrosupdijon.fr. Unite Procedes Alimentaires et Microbiologiques, UMR A 02.102, AgroSup Dijon/Universite de Bourgogne, 1 esplanade Erasme, F-21000 Dijon, France"
Journal Title:J Chromatogr A
Year:2016
Volume:20160616
Issue:
Page Number:77 - 88
DOI: 10.1016/j.chroma.2016.06.015
ISSN/ISBN:1873-3778 (Electronic) 0021-9673 (Linking)
Abstract:"Dichloromethane is known as a very efficient solvent, but, as other halogenated solvents, is recognized as a hazardous product (CMR substance). The objective of the present work is to propose substitution solvent for the extraction of volatile compounds. The most important physico-chemical parameters in the choice of an appropriate extraction solvent of volatile compounds are reviewed. Various solvents are selected on this basis and on their hazard characteristics. The selected solvents, safer than dichloromethane, are compared using the extraction efficiency of volatile compounds from a model food product able to interact with volatile compounds. Volatile compounds with different hydrophobicity are used. High extraction yields were positively correlated with high boiling points and high Log Kow values of volatile compounds. Mixtures of solvents such as azeotrope propan-2-one/cyclopentane, azeotrope ethyl acetate/ethanol, and mixture ethyl acetate/ethanol (3:1, v/v) gave higher extraction yields than those obtained with dichloromethane"
Keywords:"Acetates/chemistry Acetone/chemistry Carcinogens/*chemistry Chemistry, Physical Cyclopentanes/chemistry Ethanol/chemistry *Food Analysis Methylene Chloride/*chemistry Polysaccharides/chemistry Solubility Solvents/*chemistry Volatile Organic Compounds/*iso;"
Notes:"MedlineCayot, Nathalie Lafarge, Celine Bou-Maroun, Elias Cayot, Philippe eng Netherlands 2016/06/21 J Chromatogr A. 2016 Jul 22; 1456:77-88. doi: 10.1016/j.chroma.2016.06.015. Epub 2016 Jun 16"

 
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 02-11-2024