Isotopic methods for control of natural flavours authenticity

The use of natural flavours or essential oils often brings a clear marketing advantage in certain products (ice creams, soft drinks, sweets, etc.). The cost of natural flavours, however, is often a factor of 10 or more higher than the price of synthetic copies. Owing to this price advantage and to the difficulty of differentiating natural flavours from the same molecules made by chemical synthesis, it has been reported that synthetic flavours are sometimes sold as natural ones. Isotopic mass spectrometry (carbon-13 and deuterium) have in the past made it possible in many cases to differentiate natural and synthetic molecules. Unfortunately, the possibility of isotopic marking or 13C enrichment, more recently reported, renders, in some cases (such as vanilla), isotopic mass spectrometry of less interest nowadays. The SNIF–NMRTM method (site-specific natural isotope fractionation measured by nuclear magnetic resonance) makes possible the measurement of the D/H ratios in several sites in the molecule (five in the case of vanillin). This isotopic fingerprint is very much correlated with the origin of the molecule (type of plant, biotechnology, synthesis) and therefore makes possible a real guarantee of the natural origin of many flavours.

[1]  C. Guillou,et al.  A coupled NMR and MS isotopic method for the authentication of natural vinegars , 1992 .

[2]  Gerard J. Martin,et al.  Authentication of essential oils containing linalool and linalyl acetate by isotopic methods , 1992 .

[3]  C. Guillou,et al.  A site-specific and multi-element isotopic approach to origin inference of sugars in foods and beverages , 1991 .

[4]  C. Guérin,et al.  Détermination de l'origine de la vanilline par analyse multidimensionnelle du fractionnement isotopique naturel spécifique de l'hydrogène , 1988 .

[5]  G. Martin,et al.  Deuterium transfer in the bioconversion of glucose to ethanol studied by specific isotope labeling at the natural abundance level , 1986 .

[6]  M. J. Deniro,et al.  Carbon, hydrogen, and oxygen isotope ratios of cellulose from plants having intermediary photosynthetic modes. , 1984, Plant physiology.

[7]  G. .. Martin,et al.  Détermination par résonance magnétique nucléaire du deutérium du fractionnement isotopique spécifique naturel. Application à la détection de la chaptalisation des vins , 1983 .

[8]  John Dunbar,et al.  A study of the factors affecting the 180/160 ratio of the water of wine , 1982 .

[9]  H. Krueger,et al.  Carbon isotope analyses in food technology , 1982 .

[10]  G. Martin,et al.  A new method for the identification of the origin of natural products. Quantitative deuterium NMR at the natural abundance level applied to the characterization of anetholes , 1982 .

[11]  C. Hutchinson The use of isotopic hydrogen and nuclear magnetic resonance spectroscopic techniques for the analysis of biosynthetic pathways , 1982 .

[12]  G. Martin,et al.  Deuterium labelling at the natural abundance level as studied by high field quantitative 2H NMR , 1981 .

[13]  J. Hayes,et al.  Biosynthetic control of the natural abundance of carbon 13 at specific positions within fatty acids in Escherichia coli. Evidence regarding the coupling of fatty acid and phospholipid synthesis. , 1980, The Journal of biological chemistry.

[14]  M. Estep,et al.  Biogeochemistry of the stable hydrogen isotopes , 1980 .

[15]  M. Garson,et al.  Some new n.m.r. methods for tracing the fate of hydrogen in biosynthesis , 1979 .

[16]  R. GONFIANTINI,et al.  Standards for stable isotope measurements in natural compounds , 1978, Nature.

[17]  T. J. Simpson Carbon-13 nuclear magnetic resonance in biosynthetic studies , 1975 .

[18]  H. Simon,et al.  [Studies of carbohydrate metabolism with hydrogen-labelling, V. Measurement of T-fixation in ethanol following yeast fermentation in H2O-HOT or with different T-labelled sugars]. , 1968, Zeitschrift fur Naturforschung. Teil B, Chemie, Biochemie, Biophysik, Biologie und verwandte Gebiete.

[19]  S. Epstein,et al.  Carbon isotope fractionation during photosynthesis , 1960 .

[20]  F. E. Wickman,et al.  Variations in the Relative Abundance of the Carbon Isotopes in Plants , 1952, Nature.