Tetrahydrofurfuryl acetate
| Names | |
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| Preferred IUPAC name
(Oxolan-2-yl)methyl acetate | |
| Other names
Tetrahydro-2-furanylmethyl acetate
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| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.010.270 |
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PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| CH 3CO 2CH 2C 4H 7O | |
| Molar mass | 144.170 g·mol−1 |
| Appearance | clear liquid |
| Density | 1.061 g/cm3 (20 °C) |
| Boiling point | 194 °C (381 °F; 467 K) |
| Miscible | |
| Solubility in alcohol, chloroform, ether | Soluble |
| log P | 0.349 |
Refractive index (nD)
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1.4475 (liquid 20°) |
| Hazards | |
| GHS labelling:[1] | |
| Warning | |
| H302 | |
| P264, P270, P301+P317, P330, P501 | |
| NFPA 704 (fire diamond) | |
| Flash point | 83 °C (181 °F; 356 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
(what is ?)
Infobox references
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Tetrahydrofurfuryl acetate is an organic chemical compound used for food flavouring and cosmetics. It has a fruity ethereal flavour, also described as honey, maple, or bread-like.
It is generally accepted as safe in the USA. Typical levels of use are 2 ppm in drinks, 8 ppm in ice cream, and 20 ppm in baked products and confectionery.
Classified as a heterocyclic ester, it is made by reacting tetrahydrofurfuryl alcohol with acetic anhydride.
Related flavouring compounds are tetrahydrofurfuryl butyrate, tetrahydrofurfuryl cinnamate, tetrahydrofurfuryl alcohol, and tetrahydrofurfuryl propionate.