Wine Chemistry and Biochemistry

(Steven Felgate) #1

278 D. Dubourdieu and T. Tominaga


Ta b l e 8 B. 1 (continued)


XII: 2-Methyl-3-sulfanylbutan-1-ol 1745
onion
OH

SH
XIII: Benzenemethanethiol n.d. Smoky
SH

XIV: 3-Sulfanylpentan-1-ol 1772 Grapefruit OH

SH
XV: 2-Methyl-3-sulfanylpentan-1-ol 1833 Raw
onion
OH

SH
XVI: 3-Sulfanyl-hexyl acetate n.d. Box-tree O

SH O
XVII: 3-Sulfanylhexan-1-ol 1857 Passion
fruit
Grapefruit

OH

SH
XVIII: 3-Sulfanylheptan-1-ol 1956 Grapefruit OH

SH

Raw

These volatile thiols are also present in wines made from otherVitis vinifera


grape varieties (Tominaga et al. 2000a). Concentrations of 4MSPOH and 3SH
are particularly high in white Muscat d’Alsace and Gew`‘urztraminer from Alsace,


respectively (Fig. 8B.1) (Tominaga et al. 2001). Thus, 4MSPOH gives Muscat wines


their “Sauvignon blanc” aroma, while 3SH, with its hints of grapefruit and tropical


fruit, makes a significant contribution to Gew ̈urztraminer aromas.


Ta b l e 8 B. 2Assay of volatile thiols (ng/L) in fourwhite Bordeaux wines made from Sauvignon
blanc 1996 vintage (Tominaga et al. 1998a)


Compounds Samples
12 34


4-Methyl-4-sulfanylpentan-2-one 5(6) 4(5) 10(13) 4(5)
4-Methyl-4-sulfanylpentan-2-ol 18(0.3) 20(0.4) 22(0.4) 20(0.4)
3-Sulfanylhexan-1-ol 8402(140) 12822(214) 7465(123) 3736(63)
3-Sulfanylhexyl acetate 724(181) 451(113) 451(113) 275(69)
Entries in parentheses are the aromatic index of each compound: concentration/perception
threshold

Free download pdf