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Aromatic compounds profile of DOC Piedmontese wines by HS-SPME-GC-MS

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Aromatic compounds profile of DOC Piedmontese wines by HS-SPME-GC-MS

E. Bonometti, G. Cerrato, E. Diana, L. Operti, F. Turco, E. Priola, A. Giordana*, R. Rabezzana

(1) Deparment of Chemistry - University of Turin - Via P. Giuria 7 – 10125

(2) CrisDi – Interdepartmental Center for Crystallography, Via Pietro Giuria 7, 10125-Torino, Italy Mail to: alessia.giordana@unito.it

Purpose of the work: determination of aromatic profile of wines

Wine aroma is the result of hundreds of volatile compounds already present in grapes and originating from fermentation and wine aging. Wine aroma is crucial in determining organoleptic features and quality of wine. Determination of the aromatic profile of wines gives the producers the opportunity to control the production in order to obtain a great varietal tipicity and quality. Moreover, it enables wine characterization and differentation, which is fundamental for wine authenticity control and to prevent frauds.

Experimental method: HS SPME GC-MS

By hyphenated GC-MS technique (Focus GC DSQ Thermo corporation-single quadrupole) we determined the aromatic profile of some typical Piedmontese hillock wines. Volatile molecules were extracted by means of

headspace microextraction with a triphasic fiber (CAR/PDMS/DVB

30/50µm). This is a fast, efficient and economic extraction technique [2]. In

SPME, equilibria are achieved among analytes, sample, headspace and fiber. Low detection limits are gained although with an high resolution. SPME

provides linear responses even with high concentrations [3].

Coming soon……..

Experimental results will be processed by high-quality chemometric techniques in order to achieve wine differentiation based on varietal origin and harvest year. At the beginning research will be focused on some typical Piedmontese wines [4]. Results will represent an identity card of products very useful for traceability and hopefully to prevent food frauds.

Ethyl hexanoate

neroloxide limonene

Bibliografy:

[1] G. Antalick, M.C. Perello, G. De Revel, Food Chemistry, 121 (2010) 1236-1245;

[2] R.M. Peña, J. Barciela, C. Herrero, S. Garcia-Martin, J. Sci Food Agric. 85 (2005) 1227-1234;

[3] J.S. Camara, M. Arminda Alves, J.C. Marques, Anal. Chem. Acta, 555 (2006) 191-200; [4] E. Marengo, M. Aceto, V. Maurino, J. Chromatogr. A, 943 (2001) 123-137

Bitter almond Benzoic aldehyde Secondary aroma

Pineapple Ethyl and Isoamyl butirrate Secondary aroma

Anise Anetole Tertiary aroma

Howthorn Anisic aldehyde Tertiary aroma

Banana Isoamyl acetate Secondary aroma

Butter, Nut Diacetyl Tertiary aroma

Cinnamom Cinnamic aldehyde e Tertiary aroma

Caramel Furfurole Tertiary aroma

Lemon Limonene, Citronellale, Citrale Primary aroma

Civet Civetone Tertiary aroma

Fern Filmarone Tertiary aroma

Strawberry Exadecilic aldehyde Secondary aroma

Hay Cumarine Tertiary aroma

Geranium Geraniole Primary aroma

Carnation Eugenole, Isoeugenole Tertiary aroma

Muscat Linalole Primary aroma

Mint Mentol Primary aroma

Honey Chinoline, Phenylacetic acid Secondary aroma

Misky Muscone Tertiary aroma

Walnut Acetaldehyde Secondary aroma

Orange Limonene Primary aroma

Peony Fenilethanole Tertiary aroma

Pine Bornyl acetate Tertiary aroma

Pear Butyl and Etyl acetate Secondary aroma

Green pepper 2,metoxy-3 isobutylpyrazine Primary aroma

Apple Ethyl caproate, Ethyl malate Secondary aroma

Plum Phenyl ethyl acetate Secondary aroma

Rose Phenylethylic alchol, farnesole, Alfa-Ionone

Primary aroma

Vanilla Vanilla aldheyde Tertiary aroma

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