Allyl hexanoate

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Allyl hexanoate
Prop-2-enyl hexanoate.svg
Names
IUPAC name
prop-2-enyl hexanoate
Other names
Allyl caproate; Allyl n-caproate; 2-Propenyl n-hexanoate; Hexanoic acid, 2-propenyl ester
Identifiers
123-68-2 N=
ChemSpider 29006 YesY
EC number 204-642-4
Jmol-3D images Image
Image
PubChem 31266
Properties
C9H16O2
Molar mass 156.22 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
R-phrases R22 R24 R51/53
S-phrases (S2) S26 S36/37/39 S45 S61
Flash point 66 °C (151 °F; 339 K) [1]
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
 N verify (what isYesY/N?)
Infobox references

Allyl hexanoate is a colorless to pale yellow clear liquid.

Uses[edit]

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[edit]

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