Fruity > Tropical Fruits > Butyric

Allyl caproate

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

Allyl caproate (CAS N° 123-68-2)​

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Information Générales

General Presentation

  • CAS N° : : 123-68-2

  • EINECS number : 204-642-4

  • FEMA number : 2032

  • Density : 0,889

  • Optical rotation : Lorem Ipsum

  • Allergens : This ingredient does not contain any allergen.

  • Refractive Index @20°C : Lorem Ipsum

  • Volatility : Head

  • Price Range :

  • Appearance : Colorless liquid

  • FLAVIS number : 09.244

  • JECFA number : 3

Information on synthetic ingredients

  • Acid Value : Lorem Ipsum

  • Boiling Point : 190°C

  • Detection Threshold : Donnée indisponible.

  • Molecular formula : C9H16O2

  • Log P : 3,2

  • Molecular Weight : 156,23 g/mol

  • Fusion Point : Donnée indisponible.

  • Flash Point : 74°C

  • Vapor pressure : Lorem Ipsum

Utilisation

Uses

Other comments :

Stability :

May form caproic acid through time

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.

Year of discovery :

Data not available.

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.

Synthesis precursor :

Allyl Caproate is not a precursor to the synthesis of another compound of olfactory interest.

Natural availability :

Allyl Caproate is present in pineapple and mushroom. There is also an Allyl Caproate of natural origin.

Synthesis route :

Allyl Caproate is prepared by esterification between Hexanoic acid and allylic alcohol (or prop-2-en-1-ol), by acid catalysis.

Utilisation

Regulations & IFRA

This ingredient is not restricted

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