Caroline Thomas, Frédéric Mercier, Pascal Tournayre, Jean-Luc Martin, Jean-Louis Berdagué
Index: Food Chem. 173 , 790-5, (2015)
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This study shows that thiamine plays a major role in the formation of three key odorants of cooked ham: 2-methyl-3-furanthiol, 2-methyl-3-methyldithiofuran, and bis(2-methyl-3-furyl)disulphide. Analyses revealed that under identical cooking conditions, the productions of these three aroma compounds increase in a closely intercorrelated way when the dose of thiamine increases. Using a specific 2-methyl-3-furanthiol extraction-quantification method, it was possible to relate the amounts of thiamine added in model cooked hams to the amounts of 2-methyl-3-furanthiol produced in the cooking process. Sensory analyses highlighted the role of thiamine as a precursor of cooked ham aroma. Copyright © 2014 Elsevier Ltd. All rights reserved.
| Structure | Name/CAS No. | Molecular Formula | Articles |
|---|---|---|---|
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2-Methyl-3-furanthiol
CAS:28588-74-1 |
C5H6OS |
|
2-Methyl-3-furanthiol and methional are possible off-flavors...
2001-11-01 [J. Agric. Food Chem. 49(11) , 5425-32, (2001)] |
|
Identification and origin of odorous sulfur compounds in coo...
2014-07-15 [Food Chem. 155 , 207-13, (2014)] |
|
Quantification of 2-methyl-3-furanthiol, 2-furfurylthiol, 3-...
[J. Agric. Food Chem. 46(5) , 1954-58, (1998)] |
|
Identification of 2-Methyl-3-Furanthiol in the Steam Distill...
[J. Food Sci. 53(2) , 658, (1988)] |
|
Mosciano, G.
[Perfum. Flavor. 3rd ed., 21 , 53, (1996)] |
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