Literature DB >> 18508067

Enantiomer identification in the flavour and fragrance fields by "interactive" combination of linear retention indices from enantioselective gas chromatography and mass spectrometry.

Erica Liberto1, Cecilia Cagliero, Barbara Sgorbini, Carlo Bicchi, Danilo Sciarrone, Barbara D'Acampora Zellner, Luigi Mondello, Patrizia Rubiolo.   

Abstract

This study describes the development of a gas chromatography-mass spectrometry (GC-MS) library to identify optically active compounds in the flavour and fragrance field using enantioselective GC with cyclodextrin derivatives (CDs) as chiral selectors in combination with MS. The library operates on the "interactive" combination of linear retention indices (I(T) values) in parallel to MS spectra, so as to identify enantiomers reliably and to measure EE and/or ER unequivocally. Since MS is not a selective probe to discriminate optical isomers, mass spectra (or diagnostic ions in SIM mode) are used to locate the enantiomer(s) in the chromatogram, and I(T) values to identify it(them) safely and reliably in particular in complex mixtures. The library has been built up through the following steps: Some applications of the library are also reported. (a) Selection of CD derivatives able to cover a wide range of racemate separations. Four cyclodextrin derivatives were used: 2,6-di-O-methyl-3-O-pentyl-beta-CD, 2,3-di-O-methyl-6-O-tert-butyldimethylsilyl-beta-CD, 2,3-di-O-ethyl-6-AO-tert-butyldimethylsilyl-beta-CD, and 2,3-di-O-acetyl-6-O-tert-butyldimethylsilyl-beta-CD. (b) Determination of the analytes' I(T) values and evaluation of their stability and reliability at both intra- and inter-laboratory level. (c) Determination of the range within which the I(T) of an enantiomer has to be correctly identified, i.e. determination of a common retention index allowance (RIA). (d) Construction of the library, at the moment comprising the enantiomers of 134 racemates. A record has been attributed to each enantiomer including I(T) values determined on the four CD coated columns, mass spectrum, IUPAC chemical names, CAS numbers, molecular weight, and, when separated, racemate enantiomer resolution on the CD investigated. Some applications of the library are also reported.

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Year:  2008        PMID: 18508067     DOI: 10.1016/j.chroma.2008.04.045

Source DB:  PubMed          Journal:  J Chromatogr A        ISSN: 0021-9673            Impact factor:   4.759


  4 in total

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Journal:  Front Plant Sci       Date:  2022-04-25       Impact factor: 6.627

2.  Chemical, Enantioselective, and Sensory Analysis of a Cholinesterase Inhibitor Essential Oil from Coreopsis triloba S.F. Blake (Asteraceae).

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3.  Chemical Composition, Enantiomeric Distribution, and Sensory Evaluation of the Essential Oils Distilled from the Ecuadorian Species Myrcianthes myrsinoides (Kunth) Grifo and Myrcia mollis (Kunth) DC. (Myrtaceae).

Authors:  Mayra Montalván; Manuel Alejandro Peñafiel; Jorge Ramírez; Nixon Cumbicus; Nicole Bec; Christian Larroque; Carlo Bicchi; Gianluca Gilardoni
Journal:  Plants (Basel)       Date:  2019-11-15

4.  A Novel Chemical Profile of a Selective In Vitro Cholinergic Essential Oil from Clinopodium taxifolium (Kunth) Govaerts (Lamiaceae), a Native Andean Species of Ecuador.

Authors:  Sandra Espinosa; Nicole Bec; Christian Larroque; Jorge Ramírez; Barbara Sgorbini; Carlo Bicchi; Nixon Cumbicus; Gianluca Gilardoni
Journal:  Molecules       Date:  2020-12-23       Impact factor: 4.411

  4 in total

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