T König, B Gutsche, M Hartl, R Hübscher, P Schreier, W Schwab
Index: J. Agric. Food Chem. 47(8) , 3288-91, (1999)
Full Text: HTML
Gas chromatography/olfactometry (GCO) and gas chromatography-mass spectrometry (HRGC-MS) revealed 3-hydroxy-4, 5-dimethyl-2(5H)-furanone (sotolon) to be responsible for the "burnt" and "spicy" off-flavor observed in citrus soft drinks during storage. Among the ingredients of citrus soft drinks, ethanol and ascorbic acid were identified as the essential precursors of sotolon. Two formation pathways were postulated by studies using (2)H (D)- and (13)C-labeled ethanol and ascorbic acid; i.e., sotolon is formed from two molecules of ethanol and carbons 2 and 3 of ascorbic acid (pathway 1), or it is generated from one molecule of ethanol and carbons 3-6 of ascorbic acid (pathway 2).
Structure | Name/CAS No. | Molecular Formula | Articles |
---|---|---|---|
![]() |
Sotolon
CAS:28664-35-9 |
C6H8O3 |
Prooxidant action of furanone compounds: implication of reac...
2007-07-01 [Food Chem. Toxicol. 45(7) , 1258-62, (2007)] |
Quantitative determination of sotolon, maltol and free furan...
2003-08-22 [J. Chromatogr. A. 1010(1) , 95-103, (2003)] |
French Jura flor yeasts: genotype and technological diversit...
2009-03-01 [Antonie van Leeuwenhoek 95(3) , 263-73, (2009)] |
4,5-dimethyl-3-hydroxy-2[5H]-furanone (sotolone)--the odour ...
1999-04-01 [J. Inherit. Metab. Dis. 22(2) , 107-14, (1999)] |
Instrumental and sensory approaches for the characterization...
2008-06-01 [Chem. Biodivers. 5(6) , 1170-83, (2008)] |
Home | MSDS/SDS Database Search | Journals | Product Classification | Biologically Active Compounds | Selling Leads | About Us | Disclaimer
Copyright © 2024 ChemSrc All Rights Reserved