Effects of distillation cut on the distribution of higher alcohols and esters in brandy produced from three plum varieties

The purpose of this investigation was to determinate effects of distillation cuts on the distributions of higher alcohols (1‐propanol, 2‐methyl‐1‐propanol, 3‐methyl‐1‐butanol, 2‐methyl‐1‐butanol, 1‐butanol, 2‐butanol, 1‐hexanol and 1‐pentanol) and esters (ethyl acetate, isopentyl acetate + ethyl lactate, isobutyl acetate, ethyl propionate and ethyl butyrate) in plum brandy. The volatiles were determined by gas chromatography–flame ionization detection. The three most popular plum varieties used in plum brandy (Sljivovica) production, Stanley, Pozegaca and Bilska rana (Buhler), were distilled using a traditional distilling pot and fraction distillation. Three distillation cuts were considered. After separating the head fraction, in the amount of 1.7% of the distilling pot volume, heart fractions were cut at 40, 45 and 50% (v/v) ethanol and tail fractions, analogous to the heart fraction, were collected up to 10% (v/v) ethanol. The ratio of the content of 2‐methyl‐1‐propanol and 3‐methyl‐1‐butanol was 1:1 in the plum brandy produced from Stanley and Pozegaca and the ratio was 2:1 in the plum brandy produced from Bilska rana. This ratio can be used as a ‘mark’ of variety recognition in plum brandy production. The main differences in the heart fraction were accounted for by the content of the higher alcohols and esters for the distilling cut at 40 and 50% (v/v) ethanol. Copyright © 2013 The Institute of Brewing & Distilling.     

Behaviour of some volatile compounds during distillation of fermented marc exposed to the smoking process

Fermented marc was exposed to a controlled smoking process for 120, 240 and 460 min before distillation. To improve insight into the behaviour of ethanol and the partitioning of some volatile compounds, each distillate was collected in fractions (ethanol content from 24 to 59% vol) and analysed for the higher alcohols (2‐butanol, n‐butanol, n‐propanol, isoamyl alcohols, n‐hexanol) ethyl esters (ethyl acetate, ethyl lactate, ethyl caproate, ethyl caprylate, ethyl caprate, ethyl myristate and ethyl laurate) and volatile phenols (guaiacol, methyl guaiacol, ethyl guaiacol, propyl guaiacol, eugenol and isoeugenol). The results obtained showed that the behaviour of ethanol was not regular and the alcohol strength was lower when the smoking process was applied to fermented marc. The volatile phenols highlighted a distillation behaviour characterised by an increase in concentration at the end of the distillation process when ethanol decreased. Long time exposure of the marc to the smoking process resulted in higher reduction of ethanol, higher alcohols and ethyl esters. Instead, the volatile phenols increased with the duration of the smoking process.     

Multivariate analysis of maturity stages,including quality and aroma,in ‘Royal Glory’ peaches and ‘Big Top’ nectarines

Ethylene production, quality attributes and aroma compounds were analysed to determine the maturity evolution of ‘Big Top’ nectarines and ‘Royal Glory’ peaches at harvest dates ranging from 89 to 116 days after full bloom (DAFB) for nectarines and from 85 to 112 DAFB for peaches. These cultivars are highly coloured even in the early stages of maturity. However, the two cultivars had different patterns of ethylene production, this being slower in nectarines than in peaches. Principal component analysis (PCA) was used to provide partial visualisation of the complete data set in a reduced dimension plot. Separation of the two cultivars can be shown by means of a two‐dimensional plot of the samples. Although only some aroma compounds are slightly correlated with quality parameters, when aroma volatiles were included in the PCA, the aroma compound set allowed both cultivars to be classified into three stages of maturity: immature, intermediate and fully mature. Compounds such as propanol, hexyl acetate, 2‐methylpropyl acetate, limonene, butanol, (Z)‐3‐hexenyl acetate, buthyl acetate, linalool, ethanol, propyl acetate and ethyl acetate are the most important volatiles for ‘Big Top’ nectarines. It is suggested that the presence of these compounds can be used to indicate when the fruit should be harvested. The presence of γ‐decalactone, δ‐octalactone, γ‐octalactone, ethyl butyrate, hexanal and (E)‐2‐hexenol can be used to indicate the harvesting maturity stage for ‘Royal Glory’ peaches. The optimum maturity date for harvest would be 105–107 DAFB for ‘Big Top’ nectarines and 93–95 DAFB for ‘Royal Glory’ peaches. © 2002 Society of Chemical Industry     

Influence of composition and structure of oil‐in‐water emulsions on retention of aroma compounds

The influence of the composition and structure of oil‐in‐water emulsions on aroma retention was examined for 20 volatile compounds. Compositional and structural parameters included the fraction of emulsifier phase, the fraction of lipid phase and the particle size distribution of the dispersed lipid phase in the emulsion. Air/liquid partition coefficients of dimethyl sulphide, 1‐propanol, diacetyl, 2‐butanone, ethyl acetate, 1‐butanol, 2‐pentanol, propyl acetate, 3‐methyl‐1‐butanol, ethyl butyrate, hexanal, butyl acetate, 1‐hexanol, 2‐heptanone, heptanal, α‐pinene, 2‐octanone, octanal, 2‐nonanol and 2‐decanone were determined by static headspace gas chromatography. The hydrophobicity of the compounds determined the influence of the compositional and structural parameters of the emulsions on air/liquid partitioning. Increase of the emulsifier fraction increased the retention of mainly hydrophilic aroma compounds and decreased the retention of hydrophobic compounds. Higher lipid levels led to increased retention of hydrophobic compounds and release of hydrophilic compounds. Emulsions with larger particles showed increased aroma retention, which was independent of the lipid fraction and the polarity of the aroma compounds. The data demonstrated a profound effect of both composition and structure of oil‐in‐water emulsions on the air/liquid partitioning of the 20 aroma compounds under equilibrium conditions. © 2002 Society of Chemical Industry     

Influence of yeast on the yield of fermentation and volatile profile of ‘Węgierka Zwykła’ plum distillates

The character of plum brandies depends on a unique aroma profile of the plum and the microbiota present on the surface of the fruits, as well as yeast used for fermentation. In this study, an evaluation of the effect of microorganisms applied for the fermentation of W?gierka Zwyk?a var. plum mashes and processing temperature (18 °C, 30 °C) on its efficiency and volatile profile, as well as taste and flavour of distillates obtained was performed. An estimation of the odour activity values (OAVs) of the volatile compounds was also conducted. Regardless of whether the fermentation was carried out using Saccharomyces bayanus wine yeast or by native microflora present on plums as well as raisins, the efficiency of this process was high and ranged between 91.7 and 96.7% of the theoretical efficiency. Especially rich in esters (among others ethyl acetate and isoamyl acetate) was the distillate derived after fermentation with the microflora of plums and raisins, at 18 °C. An evaluation of the individual aromatic effect of chemical compounds present in tested distillates, in terms of their OAVs, revealed that the highest OAVs were reached with isovaleraldehyde. Other compounds that showed aroma values >1 and possibly had an effect on the overall aroma of tested plum distillates were the following: hexanal, benzaldehyde, ethyl acetate, isoamyl acetate, ethyl benzoate, ethyl hexanoate, 1‐propanol, 2‐methyl‐1‐butanol, 3‐methyl‐1‐butanol and 1‐hexanol. The performed sensory ranking showed that the best rated distillate was the one obtained after fermentation with the indigenous microflora of plums and raisins, at 18 °C. Copyright © 2016 The Institute of Brewing & Distilling     

Identification of aroma‐active compounds in fresh and stored ‘Mor’ mandarins

In this study, gas chromatography–olfactometry (GC‐O) (sniffing) combined with gas chromatography–mass spectrometry (GC‐MS) analysis was applied to identify volatile aroma‐active compounds in homogenised segments of fresh and stored ‘Mor’ mandarins. The GC‐O nasal impact frequency method was used to identify Twenty‐three aroma‐active compounds, of which seventeen odorants were identified by GC‐MS. The aroma of fresh ‘Mor’ mandarins derived from a mixture of eleven odorants that contribute ‘green’ [(E)‐3‐hexenol and hexanal], ‘fresh’ [(E)‐carveol], ‘fruity’ (ethyl 2‐methylbutanoate), ‘citrus’ (limonene), ‘floral’ (linalool), ‘musty’ (β‐myrecene and γ‐terpinene), ‘potato’ (α‐terpinene), ‘mushroom’ (unknown 2) and ‘cabbage’ (α‐cubebene) odours. During postharvest, storage losses were observed in ‘green’ [(E)‐3‐hexenol] and ‘fresh’ [(E)‐carveol] odours, accompanied by increases in ‘fruity’ (ethyl propanoate) and several unpleasant aromas, such as ‘alcohol’ (ethanol), ‘musty’ [α‐pinene, (E)‐2‐nonenal and 1‐terpinen‐4‐ol] and ‘fatty’ (octyl acetate and δ‐cadinene) odours, all of which possibly account for the observed decrease in sensory acceptability after harvest.     

Evolution of aroma compounds of murtilla fruits (Ugni molinae Turcz) during storage

BACKGROUND: ‘Murtilla’, ‘mutilla’ or ‘murta’ (Ugni molinae Turcz) is a native Chilean species that produces a small berry fruit with a special aroma, whose volatile compounds have not yet been identified. The fruit may be consumed raw and also as jams, juice, canned products, confections and liquor. RESULTS: At the beginning and end of the storage, 24 volatile compounds were identified in murtilla fruit aroma and the concentration of these compounds in murtilla fruit ranged from 1.2 to 250.5 µg kg^?1 fresh weight. Methyl 2‐methyl butanoate, ethyl butanoate, ethyl 2‐methyl butanoate, methyl hexanoate, ethyl hexanoate, methyl benzoate and ethyl benzoate were the major components, all of which have been reported as potent odors in other aromatic fruits. Based on estimated odor activity value, the most potent compound in the murtilla fruit aroma were ethyl hexanoate and 4‐methoxy‐2,5‐dimethyl‐furan‐3‐one. The statistical analysis showed that the storage produced a distinct effect on the same volatile compounds released from the murtilla ecotypes. CONCLUSION: The volatile compounds identified in murtilla fruit aroma, which may be described as fruity, sweet and floral, have been found in other aromatic fruits. Concerning the aroma, the murtilla fruit from ecotype 19‐1 was shown to be the best in cooled storage. Copyright © 2007 Society of Chemical Industry     

Influence of fast and slow distillation on ethyl carbamate content and on coefficient of non‐alcohol components in Brazilian sugarcane spirits

Ethyl carbamate is an impurity present in distilled beverages. Given the risk of it being a carcinogenic substance, Brazilian legislation has determined that its presence in distilled beverages, such as ‘aguardente’ and ‘cachaça’ (two types of sugarcane spirits), should be limited to a maximum of 150 µg/L. Ordinary spirits usually contain variable amounts of ethyl carbamate, although in lower concentrations than the maximum determined by law. The finding that commercial spirits had a much lower concentration of this impurity (around 50 µg/L) led the authors to research the reasons for the differences, and these are explored in this paper, with a focus on the speed of the distillation process and its influence on the spirit's composition. The team conducted research in a sugarcane distillery producing ‘aguardente’ using a simple pot still and measured the influence of fast and slow distillation on the presence of ethyl carbamate and non‐alcohol components in the process. The results demonstrated that the speed of distillation was proportionally related to the concentration of ethyl carbamate and secondary components in the beverage's composition. Copyright © 2012 The Institute of Brewing & Distilling     

Olfactory and quantitative analysis of volatiles in elderberry (Sambucus nigra L) juice processed from seven cultivars

Aroma compounds emitted from elderberry juices processed from seven cultivars were collected by the dynamic headspace technique and analysed by GC–FID and GC–MS. Forty aroma compounds were identified and quantified, including nine compounds which had not previously been detected in elderberry juice. Significant differences were found among cultivars in the concentration levels of 30 compounds. The sensory characteristics of the individual aroma compounds in elderberry juice were determined by a GC‐sniffing technique, and the compounds were grouped according to their odour. The characteristic elderberry odour is due to dihydroedulan and β‐damascenone, of which the former occurs in relatively high concentrations in the headspace of elderberry juice. The fruity group consisted of aliphatic alcohols and aldehydes and aromatic esters, of which 1‐pentanal, 2‐methyl‐1‐propanol, 2‐ and 3‐methyl‐1‐butanol, 1‐octanal, 1‐octanol and methyl and ethyl benzoate contributed with fruity notes. In the flowery group, 1‐nonanal, nerol oxide and (Z)‐ and (E)‐rose oxide contributed with characteristic elder flower odour, whereas other flowery notes were associated with hotrienol, linalool and α‐terpineol. Fresh and grassy odours were correlated with 1‐hexanal, (E)‐2‐hexen‐1‐al, (Z)‐3‐hexen‐1‐ol, (E)‐2‐hexen‐1‐ol and (E)‐2‐octen‐1‐al of the grassy group, whereas 1‐octen‐3‐ol and 1‐octen‐3‐one of the agrestic group contributed significantly with the characteristic aroma of mushrooms. © 2000 Society of Chemical Industry     

Membrane processing of the Brazilian spirit Cachaça

As an alternative technology for the production of cachaça, fermented sugar cane must was clarified by ceramic α‐alumina membranes, followed by water removal by pervaporation using a silk sericin/polyvinylalcohol (PVA) non‐porous membrane. The high solute content in the fermented must resulted in fouling and concentration polarisation in both microfiltration and pervaporation. The hydrophilicity of the sericin/PVA blends was exploited in ethanol and aroma concentration, at an optimal temperature of 20°C, resulting in a separation factor and permeation flux of 3.7 and 958.3 g/m² h. An aroma profile was performed using GC SPME/headspace and GC‐MS, analysing the content of ethanol, 3‐methyl‐1‐butanol, 2‐methyl‐1‐butanol, ethyl lactate, isoamyl acetate, ethyl octanoate and ethyl laurate. The results show that the volatiles present in the fermented sugar cane must were concentrated, with recoveries of 93.9 and 94.3% of the principal aromatic compounds. © 2019 The Institute of Brewing & Distilling     

Chemical and microbiological quality of sugar cane juice influences the concentration of ethyl carbamate and volatile congeners in cachaça

The aim of this study was to assess the influence of heat treatment of sugar cane juice, supplementation with urea and double distillation on the concentration of volatile congeners (acetic aldehyde, ethyl acetate, n‐propyl, isobutyl and isoamyl alcohols and acetic acid) and contaminants (methanol, 1‐propyl and 2‐butyl alcohols, copper, and ethyl carbamate) in cachaça. Samples of fresh sugar cane juice, sugar cane juice submitted to heat treatment and contaminated sugar cane juice were supplemented (or not) with urea and fermented. The washes so obtained underwent single and double distillation. Supplementation with urea stimulated ethyl carbamate formation. The distilled products that originated from contaminated worts presented higher concentration of acetic acid and ethyl carbamate. Double distillation reduced the concentration of contaminants. The best quality pot still cachaça was obtained employing heat treatment of sugar cane juice, nonsupplementation with urea and double distillation. Copyright © 2015 The Institute of Brewing & Distilling     

Aroma compounds in barrel aged apple distillates from two different distillation techniques

The major fermentation and maturation related congeners in apple distillates from two different distillation techniques (alembic and column), matured in oak for 18 months, were measured by GC‐MS and HPLC. Together with a higher ethanol content, column distillates had higher ethyl acetate, methanol and n‐propanol levels compared with alembic distillates. A higher content of acetaldehyde was characteristic of the alembic distillates. The concentrations of i‐butanol, n‐butanol, amyl alcohols and n‐hexanol were not affected by the distillation technique used. Increasing the ageing time of distillates in oak resulted in an increase in the contents of acetaldehyde, ethyl acetate and amyl alcohols while the content of methanol decreased during ageing. Throughout ageing, there were no significant changes in the concentrations of n‐propanol, i‐butanol, n‐butanol and n‐hexanol. Among the maturation related compounds, gallic acid, ellagic acid, vanillin and syringaldehyde were determined in apple distillates with ellagic acid being the most abundant. The contents of gallic acid and ellagic acid increased during ageing whereas vanillin and syringaldehyde slightly increased throughout the 18 months of maturation. © 2019 The Institute of Brewing & Distilling     

Impact of fining agents on the volatile composition of sparkling mead

Sparkling mead is obtained by secondary fermentation of the mead involving the addition of starter yeast culture, sucrose, nutrients and fining agents. The aim of this study was to evaluate the effect of different fining agents (tannins vs combined fining agents) on the volatile composition of sparkling mead. Sparkling mead was produced from a base mead using a commercial yeast strain (Saccharomyces bayanus) and the volatile compounds were determined by gas chromatography–flame ionisation detection and gas chromatography–mass spectrometry. Thirty six volatile compounds were quantified and the major groups were alcohols (73.2%), acetates (19.1%), carbonyl compounds (5.5%) and ethyl esters (1.2%), represented by 3‐methyl‐1‐butanol, ethyl acetate, acetaldehyde and monoethyl succinate, respectively. The remaining compounds were present at <1%. Eleven volatile compounds exhibited odour activity values >1, with ethyl octanoate and ethyl hexanoate contributing to the aroma of sparkling mead, with fruity, strawberry and sweet notes. The combined fining agents caused a marked decrease in the concentration of volatile compounds compared with tannins. In general, 3‐ethoxy‐1‐propanol, ethyl lactate, ethyl octanoate, diethyl succinate, diethyl malate, monoethyl succinate, 2‐methylpropanoic acid, hexanoic acid, octanoic acid, acetaldehyde, acetoin, furfural, benzaldehyde, 5‐hydroxymethylfurfural, trans‐furan linalool oxide, cis‐furan linalool oxide and 4‐oxo‐isophorone decreased in concentration. Conversely, 1‐propanol and 2‐methylpropanoic acid (tannins) and ethyl butyrate (combined fining agents) increased in concentration. The remaining volatile compounds were not affected. Significant differences (p < 0.05) were found for 19 volatile compounds independently of the type of fining agents used. © 2018 The Institute of Brewing & Distilling     

APC values and volatile compounds formed in commercially processed,raw chicken parts during storage at 4 and 13 °C and under simulated temperature abuse conditions

Skinless chicken breast fillets, thighs, wings and boneless breast with skin were selected from the production line of a commercial processor. Samples were evaluated over time in storage at 4 and 13 °C and under temperature abuse conditions for microbial proliferation and production of volatile compounds (VCs). Aerobic plate counts (APCs) were enumerated and VCs quantitated at 24 h storage intervals; however, APC increases were not reflected by significant correlations with headspace VCs. Compounds isolated from sample headspaces by solid phase microextraction (SPME) and direct headspace sampling and then analysed by gas chromatography (GC), gas chromatography/mass spectrometry (GC/MS) and gas chromatography/chemiluminescence detection (GC/SCD) were hydrogen sulphide, methanethiol, ethanol, acetone, C5, C6 and C7 hydrocarbons, dimethyl sulphide, methyl ethyl ketone, carbon disulphide, 1‐propanol, ethyl acetate, 1‐butanol, S‐methyl thioacetate, 3‐methyl‐1‐butanol, dimethyl disulphide and dimethyl trisulphide. Compounds appearing in the samples with any degree of consistency and therefore considered pertinent for these analyses were ethanol, acetone, methyl ethyl ketone, ethyl acetate, hydrogen sulfide, dimethyl sulphide and carbon disulphide. Elevated APCs and VC diversity occurred more prevalently in those samples from higher‐temperature storage. Published in 2000 for SCI by John Wiley & Sons, Ltd.     

A Study on Characteristic Flavor Compounds in Traditional Chinese Rice Wine — Guyue Longshan Rice Wine

The objective of the study was to systematically investigate flavor compounds in Chinese rice wine (CRW) using chromatography technology. In twelve CRW samples, 93 different flavor compounds were detected and identified including 16 alcohols in addition to ethanol, 29 esters, 9 aldehydes, 9 organic acids, 19 amino acids and 11 fatty acids. Statistical analysis by principal component analysis (PCA) indicated that seventeen flavor compounds in Guyue Longshan rice wine made a large contribution to its special flavor. These compounds were benzaldehyde, acetaldehyde, ethyl 2‐hydroxy‐4‐methylvalerate, ethyl butyrate, phenyl ethyl isobutyrate, ethyl benzoate, ethyl phenyl‐acetate, methyl dodecanoate, methyl oleate, ethyl dedecanoate, 1‐butanol, 3‐ethoxyl‐1‐propanol, 1‐enanthol, dodecanol, lactic acid, fumaric acid and lauric acid.     

Sherry wine vinegar: physicochemical changes during the acetification process

The quality of a wine vinegar is determined by the raw wine substrate and the acetification process employed in its production. Attempts to characterise vinegars have been based on these two features, along with variables such as total extract, glycerol, organic acids, volatile compounds and phenolic composition. When the final products are analysed, it is difficult to evaluate to what extent quality differences are due to the raw material or to differences in production methods, so it is necessary to determine the influence of each feature separately. The present work focuses on monitoring physicochemical changes during the acetification of sherry wine by submerged culture. ANOVA showed significant differences for ethanol, acetic and lactic acids and some volatile compounds (methanol, 1‐propanol, 2‐methyl‐1‐propanol, 2‐methyl‐1‐butanol, 3‐methyl‐1‐butanol, acetoin, acetaldehyde, ethyl acetate and ethyl lactate). However, no statistical changes were found for phenolic compounds during acetification. The phenolic composition of the final product was determined by the substrate employed. In addition, the influence of cycle duration on the chemical composition was studied; the only compound affected by this factor was 2‐methyl‐1‐butanol. © 2001 Society of Chemical Industry     

Odour‐active compounds in pineapple (Ananas comosus [L.] Merril cv. Red Spanish)

Application of solid‐phase microextraction, simultaneous distillation–extraction and liquid–liquid extraction combined with GC‐FID, GC‐MS, aroma extract dilution analysis, and odour activity value was used to analyse volatile compounds from pineapple (Ananas comosus [L.] Merril cv. Red Spanish) and to estimate the most odour‐active compounds. The analyses led to the identification of ninety‐four compounds, seventy‐two of them were positively identified. Twenty odorants were considered as odour‐active compounds, from which ethyl 2‐methylbutanoate, 2,5‐dimethyl‐4‐hydroxy‐3(2H)‐furanone, 1‐(E,Z,Z)‐3,5,8‐undecatetraene, ethyl 3‐(methylthio)propanoate, 1‐(E,Z)‐3,5‐undecatriene, ethyl hexanoate and methyl hexanoate were the most odour contributors and contribute to the typical pineapple aroma, while the others are responsible for fruity and sweet odour notes.     

Variations in volatile compounds and flavour in Idiazabal cheese manufactured from ewe's milk in farmhouse and factory

Stage of lactation, use of bulk milk or milk from individual flocks, and cheese‐making in farmhouse or industrial factory are important factors affecting the production and quality of Idiazabal cheese. The volatile composition of cheese samples made from raw ewe's milk in farmhouses or industrial plants at two different times of the year and aged for 90 and 180 days was analysed by dynamic headspace coupled to GC‐MS. Short‐chain fatty acids, primary and secondary alcohols, methyl ketones and ethyl esters were the most abundant compounds in the aroma of Idiazabal cheese samples. Differences in the volatile composition were found between farmhouse and industrial cheeses made at different times of the year and ripened for 90 or 180 days. Likewise, the sensory profiles of the farmhouse and industrial cheeses were significantly different, regardless of the time of the year and ripening time. The results for the principal component analysis (PCA) performed on the sensory attributes of the cheese samples showed two PCs defined as ‘farmhouse flavour factor’ and ‘industrial flavour factor’. Farmhouse cheeses showed high scores for buttery, milky and toasty odours, and buttery and nutty flavours, whereas industrial cheeses showed high scores for sharp, rennet and brine odours, and rennet and rancid flavours. The percentages of methyl ketones such as 3‐hydroxy‐2‐butanone, 2‐butanone, 2‐pentanone and 2‐heptanone, and acids such as n‐propanoic, 2‐methylpropanoic and 3‐methylbutanoic acids were higher in farmhouse cheeses than in industrial cheeses. On the other hand, the percentages of esters such as ethyl butanoate and ethyl hexanoate, and alcohols such as 3‐methyl‐1‐butanol, and acids like n‐hexanoic acid were higher in industrial cheeses than in farmhouse cheeses. Relationships between sensory attributes and volatile compounds were studied on the basis of the differences found in sensory profile and volatile composition between farmhouse and industrial cheeses. Copyright © 2005 Society of Chemical Industry     

Odour‐active compounds in mango (Mangifera indica L. cv. Corazón)

Simultaneous distillation–extraction combined with GC‐FID and GC‐MS were used to analyse volatile compounds from mango (Mangifera indica L. cv. Corazón) and to estimate the most odour‐active compounds in the fruit. The analyses led to the identification of 167 components, from which 128 were positively identified. The aroma‐active areas in the gas chromatogram were screened by the application of the aroma extract dilution analysis and by odour activity values. Eighteen odorants were considered as the most odour‐active compounds: (E)‐β‐damascenone, ethyl butanoate, (E,Z)‐nonadienal, ethyl 2‐methylpropanoate, (E)‐2‐nonenal, (E)‐β‐ionone, terpinolene, δ‐3‐carene, β‐caryophyllene, ethyl 2‐methylbutanoate, limonene, myrcene, linalool, γ‐octalactone, nonanal, methyl benzoate, 2,5‐dimethyl‐4‐methoxy‐3(2H)‐furanone and hexanal.