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preferred IUPAC name (PIN) according to ''Nomenclature of Organic Chemistry – IUPAC Recommendations and Preferred Names 2013 (Blue Book)'' |
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| ImageFile = Prop-2-enyl hexanoate.svg |
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| PIN = Prop-2-en-1-yl hexanoate |
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| OtherNames = Allyl caproate |
| OtherNames = Prop-2-enyl hexanoate<br />Allyl hexanoate<br />Allyl caproate<br />Allyl ''n''-caproate<br />2-Propenyl ''n''-hexanoate<br />Hexanoic acid 2-propenyl ester |
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Revision as of 21:27, 12 September 2016
Names | |
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Preferred IUPAC name
Prop-2-en-1-yl hexanoate | |
Other names
Prop-2-enyl hexanoate
Allyl hexanoate Allyl caproate Allyl n-caproate 2-Propenyl n-hexanoate Hexanoic acid 2-propenyl ester | |
Identifiers | |
3D model (JSmol)
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ChemSpider | |
ECHA InfoCard | 100.004.222 |
EC Number |
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PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C9H16O2 | |
Molar mass | 156.225 g·mol−1 |
Appearance | Colorless to pale yellow clear liquid[1] |
Density | 0.887 g/mL[2] 0.884-0.892 g/mL[1] |
Boiling point | 190 to 191 °C (374 to 376 °F; 463 to 464 K)[1] 75-76 °C (15 mmHg)[2] |
Insoluble[1] | |
Hazards | |
Flash point | 66 °C (151 °F; 339 K) [1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Allyl hexanoate is a colorless to pale yellow clear liquid.
Uses
Allyl hexanoate is employed principally in the formulation of pineapple flavors but it can also be used for peach and apricot essences and for apple blossom, peach blossom, and wisteria perfume compositions.[1] Allyl caproate is an ingredient of some lipstick perfumes. It also adds a sweet juicy note to citrus flavors. It is also used as an additive to cigarettes.
References
- ^ a b c d e f Allyl hexanoate at The Good Scents Company
- ^ a b Allyl caproate at Sigma-Aldrich