Jérôme Ledauphin,¹ Naza Lahoutifard² and Andrew Gooley,^2
1 ERPCB — EA 3914, Université de Caen, France, ² SGE Analytical Science, Ringwood, Victoria, Australia.

Calvados is an apple-brandy of Normandy (France). Mashed apples are fermented to obtain cider and then distilled to give the young spirit.

Spirit aromas are a subtle balance of various volatile compounds belonging to different chemical classes, having different chemical functionalities and consequently various polarities. They may be acetals, aldehydes, alcohols, carboxylic acids, ketones and phenolic derivatives. In Calvados, esters with fruity descriptors are believed to improve the quality, while carboxylic acids with "rancid, sweat" notes are supposed to decrease the quality.

The GC analysis is typically performed using both a non-polar phase (such as 5% phenyl polysiloxane) and a polar phase (such as a polyethylene glycol) for the separation. In the work reported here, a medium polar phase [14% cyanopropylphenyl polysiloxane (BP10)] was used, as it was found to separate both volatile and semi-volatile compounds (such as a non-polar phase), and polar compounds of close molecular weights (such as a polar phase).

In this study, a detailed identification of the major volatile compounds present in young calvados was performed using GC–MS. Results were correlated to those obtained using GC–O (ODO–I, SGE Analytical Science) to evaluate the most odorant compounds.

Figure 1

The most represented chemical class was esters with powerful odorants such as ethyl 2-methylpropanoate (peak 5, fruity), ethyl butanoate (peak 8, fruity, alcohol) or 3-methylbutyl acetate (peak 12, banana). The majority of these esters, which are significant for the aroma characteristics of spirits, are produced during either the fermentation, or the distillation step. Some alcohols were also identified such as butan-2-ol (peak 1), butanol (peak 4), isopentanols (peak 7, plastic), hexanol (peak 13, green grass) and octanol (peak 18). These alcohols generally have a high perception threshold and, therefore, only the most concentrated ones could be detected by olfactometry.

The largest peak in the GC–MS chromatogram was recorded for isopentanols, which are known to be characteristic of brandies. Three phenolic derivatives were also detected in a relatively high amount. Of these, 4-ethylphenol (peak 26, animal) and 4-ethylguaiacol (peak 27, floral hyacinth) are considered to be responsible for organoleptic defects in red wines or brandies. Sensory evaluation tests were performed and revealed that the quality of the global aroma of the samples was not decreased by the presence of them. It appears that they need to reach a certain concentration before they cause a significant aromatic defect. Two acetals were also identified. 1,1-Diethoxyethane (peak 2, fruity) is considered as a marker of the presence of ethanal. The odour of 1,1,3-triethoxypropane (peak 16, floral, vegetal) was only perceived in samples with important aromatic defects. This compound is produced by the acetalization and Michael-type addition of acrolein in the presence of an excess of ethanol. This acetal is formed only when acrolein is present in high concentration in the cider prior to distillation. Hexanoic acid (peak 19, yeast-like, cider) was the sole carboxylic acid involved in the aromatic composition.