Allyl Caproate
Naturelle - Synthétique
Fruity > Tropical Fruits > Butyric
Crédits photo: ScenTree SAS
Other names :
Allyl Hexanoate ; Prop-2-en-1-yl hexanoate ; Prop-2-en-1-yl caproate ; Prop-2-enyl hexanoate ; Prop-2-enyl caproate ; 2-propenyl hexanoate ; 2-propenyl caproate
Volatility :
Head
Uses in perfumery :
Allyl Caproate is used in pineapple and apple notes, for a ripe and sweet effect. Also used in exotic and yellow fruit notes.
Natural availability :
Allyl Caproate is present in pineapple and mushroom. There is also an Allyl Caproate of natural origin.
Year of discovery :
Data not available.
Other comments :
Data not available.
Price Range :
€
Stability :
May form caproic acid through time
Crédits photo: ScenTree SAS
- Molecular formula :
- C9H16O2
- Molecular Weight :
- 156,23 g/mol
- Density :
- 0,889
- Flash Point :
- 74°C
- Fusion Point :
- Donnée indisponible.
- Appearance :
- Colorless liquid
- Log P :
- 3,2
- Boiling Point :
- 190°C
- Detection Threshold :
- Donnée indisponible.
Synthesis route :
Allyl Caproate is prepared by esterification between Hexanoic acid and allylic alcohol (or prop-2-en-1-ol), by acid catalysis.
Synthesis precursor :
Allyl Caproate is not a precursor to the synthesis of another compound of olfactory interest.
Isomerism :
Isoamyl Butyrate and gamma-Nonalactone are constitutional isomers of Allyl Caproate. Isoamyl Butyrate also has a fruity and butyric smell, but gamma-Nonalactone has a very different note of peach and coconut.
- EINECS number :
- 204-642-4
- FEMA number :
- 2032
- JECFA number :
- 3
- FLAVIS number :
- 09.244
- Allergens :
- This ingredient does not contain any allergen.
- IFRA :
- This ingredient is not restricted
To learn more about IFRA's standards : https://ifrafragrance.org/safe-use/library
ScenTree is solely responsible for the information provided here.
Do you sell any of the raw materials? Would you like to let our users know?
Send an email to fournisseurs@scentree.co to learn about our advertising opportunities.
