Trichome

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[[Category:Carboxylate esters]]
[[Category:Carboxylate esters]]
[[Category:Alkenes]]


[[ja:カプロン酸アリル]]
[[ja:カプロン酸アリル]]

Revision as of 23:47, 27 March 2011

Allyl hexanoate
Names
IUPAC name
prop-2-enyl hexanoate
Other names
Allyl caproate; Allyl n-caproate; 2-Propenyl n-hexanoate; Hexanoic acid, 2-propenyl ester
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.004.222 Edit this at Wikidata
EC Number
  • 204-642-4
  • InChI=1S/C9H16O2/c1-3-5-6-7-9(10)11-8-4-2/h4H,2-3,5-8H2,1H3 checkY
    Key: RCSBILYQLVXLJG-UHFFFAOYSA-N checkY
  • InChI=1/C9H16O2/c1-3-5-6-7-9(10)11-8-4-2/h4H,2-3,5-8H2,1H3
    Key: RCSBILYQLVXLJG-UHFFFAOYAX
  • CCCCCC(OCC=C)=O
  • O=C(OCC=C)CCCCC
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 190-191 °C[1]
75-76 °C (15 mmHg)[2]
Insoluble[1]
Hazards
Flash point 66 °C[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

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.

References

  1. ^ a b c d e f Allyl hexanoate at The Good Scents Company
  2. ^ a b Allyl caproate at Sigma-Aldrich

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