20.2 Wine 925
Fig. 20.7.Monoterpenes in wines from the grape cultivar “White Riesling” and in wines from other grape cultivars
which are also sold as “Riesling” (according toRappet al., 1985). A: White Riesling (Rheinpfalz), B: White
Riesling (France), C: Welschriesling (Austria), D: Welschriesling (Italy), E: Laski Rizling (Yugoslavia), F: Hunter
Valley Riesling (Australia), G: Emerald Riesling (USA). Monoterpenes: 1 trans-furan linalool oxide, 2 cis-furan
linalool oxide, 3 neroloxide, 4 linalool, 5 hotrienol, 6 α-terpineol, 7 not identified, 8 trans-pyran linalool oxide,
9 cis-pyran linalool oxide, 10 3,7-dimethylocta-1,5-trans-dien-3,7-diol, 11 3,7-dimethyl-1-octen-3,7-diol
Table 20.24.Aroma defects in wine
Aroma defect Key aroma substances Cause
Mousy note 2-Ethyl-3,4,5,6-tetrahydropyridine,
2-acetyl-3,4,5,6-tetrahydropyridine,
2-acetyl-1,2,5,6-tetrahydropyridine
Lactic acid bacteria in combination
with yeasts
of the genusBrettanomyces
Strawberry note 4-Hydroxy-2,5-dimethyl-3(2H)-furanone
(HD3F):>1500 μg/l
Characteristic of the cultivar
Medicine note 4-Vinylphenol +
4-vinylguaiacol:>800 μg/l
Climate, microbiological processes
Medicinal, woody,
smoky, horse sweat
4-Ethylphenol +
4-ethylguaiacol:>400 μg/l
Climate, microbiological processes
Kerosine/petrol note 1,1,6-Trimethyl-1,2-dihydro-naphthaline
(TDN):>300 μg/l
Southern climate, excessively high
carotinoid concentration in Riesling
“Boeckser” Hydrogen sulfide Fermentation
Cork taste/musty note 2,4,6-Trichloroanisole, geosmin,
2-methylisoborneol, 1-octen-3-one,
4,5-dichloroguaiacol, chlorovanillin
Contamination during wine storage
Untypical aging note
(naphthaline note, fox
note, hybrid note)
2-Aminoacetophenone:> 0 .5μg/l Stress reaction of the vine
The so-called “boeckser” is caused by the smell
of hydrogen sulfide. The very unpleasant, rot-
ten and yeasty “boeckser” (= mercaptan) odor is
most objectionable and lingers for a long time.
It is due to ethylthiol, which can be removed
by activated charcoal. The volatile sulfur com-
pounds originate from sulfite which is reduced
to H 2 S by yeast, later reacting with ethanol to
form ethylthiol. Additional wine taste defects are
the odd and disagreeable cork tastes which is
due to the formation of the odorants listed in Ta-
ble 20.24 and 2,4,6-trichloroanisole. Above con-