Aroma fruity

The addition of exogenous glycosidases enhance greatly aromas in wines in relation with the aromatic potential of grape varieties. Tastings confirm that the improvement is obvious for red and for white wines. Wines are always judged more fruity and more intense. 

Example 5.4 Benzyl acetate is used in perfumes, soaps, cosmetics and household items where it produces a fruity, jasminelike aroma, and it is used to a minor extent as a flavor. It can be manufactured by the reaction between benzyl chloride and sodium acetate in a solution of xylene in the presence of triethylamine as catalyst9. 

Possible differences are also well illustrated by 3-thio- and 3-methyl-thiohex-anols and their esters (Table 1). Among these compounds, there is a tendency for the (R) enantiomers to have a typical, fruity aroma. However, for 3-methylthiohexanol (an aroma component of yellow passion fruit) this situation is reversed the (S) enantiomer had the characteristic fruity aroma ( exotisch, fruchtig ).52 For the separation of enantiomers of odorous compounds, enan-tioselective GLC with chiral stationary phases, and MGDC techniques using a conventional capillary column and an enantioselective column are commonly used.53... 

In an initial survey at the University of Auckland in 2004 on Cabernet Sauvignon, Merlot and Malbec wines, subject to MOX in 2000-L tanks at 4-8 mg/L/month for 12 weeks post-MLF, no changes were seen in the aroma profiles of the wines (vs. controls) for a wide range of aroma compounds, including herbaceous methoxypyrazines and C6 alcohols, floral terpenes and (3-ionone, or for fruity esters and higher alcohols (Rowdon, 2005). Likewise, the concentrations of the varietal thiol 3MH,... 

In the case of the esters, considered responsible for the fruity aromas of yoimg wines, there was no consistent difference brought about by the oxygenation procedure between the MOX (dotted lines) and control (solid... 

CH3CH2CH2CH = CHCH20H, C6H12O, M, 100.16, Z>i ioi.3kPa 155 °C, df 0.8459, 1.4382, occurs in many fruits and has a fruity, green odor, which is sweeter than that of the isomeric ci5-3-hexen-l-ol and is, therefore, preferred in aroma compositions. 

Straight-chain, saturated aliphatic acids are found in many essential oils and foods. These acids contribute to aromas, but are not important as fragrance substances. In flavor compositions, aliphatic acids up to Cio are used to accentuate certain aroma characteristics (C3-C8 for fruity notes C4, C6-C12 for cheese flavors). However, straight-chain and some branched-chain aliphatic acids are of... 

Wp 1.4017, is a strongly fruity smelling liquid and has been identified in many fruit aromas. It is the main component of banana aroma and is, therefore, also used in banana flavors. 

CH3COO(CH2)sCH3, C8H.602, Mr 144.21, p,oi.3kPa 171.5°C, < 0.8779, < 1.4092, is a liquid with a sweet-fruity, pearlike odor. It is present in a number of fruits and alcoholic beverages, and is used in fruit aroma compositions. 

Methyl cinnamate is a colorless crystalline solid mp 36.5 °C) with a fruity, sweet-balsamic odor. In addition to the common esterification methods, it can be prepared by Claisen condensation of benzaldehyde and methyl acetate in the presence of sodium. Methyl cinnamate is used in soap perfumes, as well as in blossom and oriental perfumes, and is sometimes added to aromas. 

It is used in accentuated flowery fragrances and in aroma compositions to achieve fruity effects. FCT 1982 (20) 829 [8016-84-0], [91770-75-1]. 

Ethyl 2-methylbutanoate, 2-methylbutyl acetate and hexyl acetate contribute most to the characteristic aroma of Fuji apples [49]. In Red Delicious apples, ethyl butanoate, ethyl 2-methylbutanoate, propyl 2-methylbutanoate and hexyl acetate contribute to the characteristic aroma as determined by Charm-Analysis and/or AEDA [50, 51]. In a comparative study of 40 apple cultivars, the highest odour potency or Charm value was found for -damascenone [52]. This compound usually occurs in a glycosidically bound form and is present primarily in processed products owing to hydrolysis of the glycoside bond after crushing fruit cells [53]. -Damascenone has a very low odour threshold with a sweet, fruity, perfumery odour and is not typical of apple aroma in gen-... 

Sugars, acids and aroma compounds contribute to the characteristic strawberry flavour [85]. Over 360 different volatile compounds have been identified in strawberry fruit [35]. Strawberry aroma is composed predominately of esters (25-90% of the total volatile mass in ripe strawberry fruit) with alcohols, ketones, lactones and aldehydes being present in smaller quantities [85]. Esters provide a fruity and floral characteristic to the aroma [35,86], but aldehydes and furanones also contribute to the strawberry aroma [85, 87]. Terpenoids and sulfur compounds may also have a significant impact on the characteristic strawberry fruit aroma although they normally only make up a small portion of the strawberry volatile compounds [88, 89]. Sulfur compounds, e.g. methanethiol. 

Important aroma compounds of black currant berries have been identified mainly by GC-O techniques by Latrasse et al. [119], Mikkelsen and Poll [115] and Varming et al. [7] and those of black currant nectar and juice by Iversen et al. [113]. The most important volatile compounds for black currant berry and juice aroma include esters such as 2-methylbutyl acetate, methyl butanoate, ethyl butanoate and ethyl hexanoate with fruity and sweet notes, nonanal, /I-damascenone and several monoterpenes (a-pinene, 1,8-cineole, linalool, ter-pinen-4-ol and a-terpineol) as well as aliphatic ketones (e.g. l-octen-3-one) and sulfur compounds such as 4-methoxy-2-methyl-butanethiol (Table 7.3, Figs. 7.3, 7.4, 7.6). 4-Methoxy-2-methylbutanethiol has a characteristic catty note and is very important to blackcurrant flavour [119]. 

The kiwi fruit is a cultivar group of the species Actinidia deliciosa. More than 80 compounds have been identified in fresh and processed kiwi [137]. Methyl acetate, methyl butanoate, ethyl butanoate, methyl hexanoate and ( )-2-hexenal have the most prominent effect on consumer acceptability of kiwi fruit flavour [137-140]. The volatile composition of kiwi fruit is very sensitive to ripeness, maturity and storage period [138, 139]. Bartley and Schwede [140] found that ( )-2-hexenal was the major aroma compound in mature kiwi fruits, but on further ripening ethyl butanoate began to dominate. Ripe fruits had sweet and fruity flavours, which were attributed to butanoate esters, while unripe fruits had a green grassy note due to ( )-2-hexenal [140]. The most important character-impact compounds of kiwi fruits are summarised in Table 7.4. 

Twenty-nine odour-active compounds were detected by using aroma extract dilution analysis (AEDA) [60]. The results of AEDA together with GC-MS analysis showed ethyl 2-methylbutanoate (described as fruity flavour), followed by methyl 2-methylbutanoate and 3-methylbutanoate (fruity, apple-like), 4-hydroxy-2,5-dimethyl-3(2H)-furanone (sweet, pineapple-like, caramel-like), d-decalactone (sweet, coconut-like), l-( ,Z)-3,5-undecatriene (fresh, pineapple-like), and a unknown compound (fruity, pineapple-like) as the most odour-active compounds. 

More recently, several aroma compounds were isolated from cupuacu pulp by vacuum distillation, solid-phase extraction, and simultaneous steam distil-lation-extarction and were analysed by GC, GC-MS, and GG-O [8]. The olfaction of the extracts obtained by solid-phase extraction indicated linalool, a-ter-pineol, 2-phenylethanol, myrcene, and limonene as contributors of the pleasant floral flavour. In this study, the esters ethyl 2-methylbutanoate, ethyl hexanoate, and butyl butanoate were involved in the typical fruity characteristics. 

In the case of pineapples, the 12 odorants listed in Table 16.7 were dissolved in water in concentrations equal to those determined in the fruit [50]. Then the odour profile of this aroma model was evaluated by a sensory panel in comparison to fresh pineapple juice. The result was a high agreement in the two odour profiles. Fresh, fruity and pineapple-like odour notes scored almost the same intensities in the model as in the juice. Only the sweet aroma note was more intense in the model than in the original sample [50]. In further experiments, the contributions of the six odorants showing the highest OAV (Table 16.7) were evaluated by means of omission tests [9]. The results presented in Table 16.8 show that the omission of 4-hydroxy-2,5-dimethyl-3(2H)-furanone, ethyl 2-methylbutanoate or ethyl 2-methylpropanoate changed the odour so clearly that more than half of the assessors were able to perceive an odour difference between the reduced and the complete aroma model. Therefore, it was concluded that these compounds are the character-impact odorants of fresh pineapple juice. 

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