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===Furaneol acetate=== | |||
The acetate of Furaneol also known as Caramel acetate and Strawberry Acetate is also popular with Flavorists to achieve a fatty toffee taste and it's used in traces in perfumery to add a Sweet Gourmand note. <ref>https://www.thegoodscentscompany.com/data/rw1106051.html</ref> | |||
==Stereoisomerism== | ==Stereoisomerism== |
Revision as of 04:45, 14 September 2024
Names | |
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IUPAC name 4-Hydroxy-2,5-dimethyl-3-furanone | |
Other names
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Identifiers | |
CAS Number |
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3D model (JSmol) | |
Abbreviations | DMHF |
ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.020.826 |
PubChem CID | |
UNII | |
CompTox Dashboard (EPA) | |
InChI
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SMILES
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Properties | |
Chemical formula | C6H8O3 |
Molar mass | 128.127 g·mol |
Melting point | 73 to 77 °C (163 to 171 °F; 346 to 350 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). N verify (what is ?) Infobox references |
Furaneol, or strawberry furanone, is an organic compound used in the flavor and perfume industry. It is formally a derivative of furan. It is a white or colorless solid that is soluble in water and organic solvents.
Odor and occurrence
Although malodorous at high concentrations, it exhibits a sweet strawberry aroma when dilute. It is found in strawberries and a variety of other fruits and it is partly responsible for the smell of fresh pineapple. It is also an important component of the odours of buckwheat, and tomato. Furaneol accumulation during ripening has been observed in strawberries and can reach a high concentration of 37 μg/g.
Furaneol acetate
The acetate of Furaneol also known as Caramel acetate and Strawberry Acetate is also popular with Flavorists to achieve a fatty toffee taste and it's used in traces in perfumery to add a Sweet Gourmand note.
Stereoisomerism
Furaneol has two enantiomers, (R)-(+)-furaneol and (S)-(−)-furaneol. The (R)-form is mainly responsible for the smell.
(S)-configuration |
(R)-configuration |
Biosynthesis
It is one of several products from the dehydration of glucose. Its immediate biosynthetic precursor is the glucoside, derived from dehydration of sucrose.
References
- 4-Hydroxy-2,5-dimethyl-3(2H)-furanone at Sigma-Aldrich
- ^ Zabetakis, I.; Gramshaw, J. W.; Robinson, D. S. (1999). "2,5-Dimethyl-4-hydroxy-2H-furan-3-one and its derivatives: analysis, synthesis and biosynthesis - a review". Food Chemistry. 65: 139–151. doi:10.1016/S0308-8146(98)00203-9.
- Ulrich, D.; Hoberg, Edelgard; Rapp, Adolf; Kecke, Steffen (1997). "Analysis of strawberry flavour – discrimination of aroma types by quantification of volatile compounds". Zeitschrift für Lebensmittel-Untersuchung und -Forschung A. 205 (3): 218–223. doi:10.1007/s002170050154. S2CID 96680333.
- Tokitomo Y, Steinhaus M, Büttner A, Schieberle P (2005). "Odor-active constituents in fresh pineapple (Ananas comosus [L.] Merr.) by quantitative and sensory evaluation". Biosci. Biotechnol. Biochem. 69 (7): 1323–30. doi:10.1271/bbb.69.1323. PMID 16041138.
- Janes D, Kantar D, Kreft S, Prosen H (2008). "Identification of buckwheat (Fagopyrum esculentum Moench) aroma compounds with GC-MS". Food Chemistry. 112: 120–124. doi:10.1016/j.foodchem.2008.05.048.
- Buttery, Ron G.; Takeoka, Gary R.; Naim, Michael; Rabinowitch, Haim; Nam, Youngla (2001). "Analysis of Furaneol in Tomato Using Dynamic Headspace Sampling with Sodium Sulfate". Journal of Agricultural and Food Chemistry. 49 (9): 4349–4351. doi:10.1021/jf0105236. PMID 11559136.
- Pérez, A. G. (2008). Fruit and Vegetable Flavour. Woodhead Publishing. ISBN 978-1-84569-183-7.
- https://www.thegoodscentscompany.com/data/rw1106051.html
- Leffingwell,:John C. Chirality & Odour Perception – The Furaneols.