Photo credits: ScenTree SAS
General Presentation
-
CAS N° : : 123-92-2
-
EINECS number : 204-662-3
-
FEMA number : 2055
-
Density : 0,876
-
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 : 09.024
-
JECFA number : 43
Information on synthetic ingredients
-
Acid Value : Lorem Ipsum
-
Boiling Point : 142°C
-
Detection Threshold : 2 à 43 ppb (0,0000043%)
-
Molecular formula : C7H14O2
-
Log P : 2,7
-
Molecular Weight : 130,19 g/mol
-
Fusion Point : -78°C
-
Flash Point : 25°C
-
Vapor pressure : Lorem Ipsum
Uses
Other comments :
For a jasmine facet, Isoamyl acetate is comparable to Benzyl Propionate.
Stability :
acetates may form acetic acid through time
Uses in perfumery :
Isoamyl acetate is used in banana notes. Enhances the head of a perfume, and gives a fruity-banana or pear nuance, especially in jasmine notes. However, it can make an accord become very artificial in the case of an overdose.
Year of discovery :
Data not available.
Isomerism :
Isoamyl acetate does not have any isomer used in perfumery.
Synthesis precursor :
Isoamyl acetate is not a precursor to the synthesis of another compound of olfactory interest.
Natural availability :
Isoamyl acetate can be extracted from Roman Chamomile EO, although it is present in very small quantities.
Synthesis route :
Isoamyl acetate is synthesized by an esterification reaction between acetic acid or acetic anhydride and Isoamyl alcohol, in the presence of an acid catalyst.
Regulations & IFRA
This ingredient is not restricted
