Photo credits: ScenTree SAS
Do you sell any of the raw materials? Would you like to let our users know?
Send an email to fournisseurs@scentree.coto learn about our advertising opportunities.
General Presentation
-
CAS N° : : 122-63-4
-
EINECS number : 204-559-3
-
FEMA number : 2150
-
Density : 1,03
-
Optical rotation : Lorem Ipsum
-
Allergens : This ingredient does not contain any allergen.
-
Refractive Index @20°C : Lorem Ipsum
-
Volatility : Head/Heart
-
Price Range : €€
-
Appearance : Colorless liquid
-
FLAVIS number : 09.132
-
JECFA number : 842
Information on synthetic ingredients
-
Acid Value : Lorem Ipsum
-
Boiling Point : 222°C
-
Detection Threshold : Donnée indisponible.
-
Molecular formula : C10H12O2
-
Log P : -0,3
-
Molecular Weight : 164,2 g/mol
-
Fusion Point : Donnée indisponible.
-
Flash Point : 96°C
-
Vapor pressure : Lorem Ipsum
Uses
Other comments :
Benzyl Propionate can be compared to Isoamyl Propionate, as they both have a jasmine facet.
Stability :
May form propionic acid through time under the effect of heat.
Most of the time, the occurrence of a benzenic cycle in a molecule causes a coloration of this molecule through time
Uses in perfumery :
Benzyl Propionate is used in all types of perfumes, for the contribution of a fruity and tutti frutti effect (more used than benzyl acetate for this purpose). Used in yellow, exotic and red fruit, floral-jasmine and ambery notes.
Year of discovery :
Data not available.
Isomerism :
Phenyl Ethyl acetate and Styrallyl acetate are constitution isomers of Benzyl Propionate. Nevertheless, Phenyl Ethyl acetate is more rosy and honeyed, and Styrallyl acetate is greener and more fruity, reminiscent of rhubarb.
Synthesis precursor :
Benzyl Propionate is not a precursor to the synthesis of another compound of olfactory interest.
Natural availability :
Benzyl Propionate is present in trace amounts in Champaca Absolute or in melon for example, although it is not extracted in its natural state.
Synthesis route :
Benzyl Propionate is synthesized by an esterification between propanoic acid and Benzyl Alcohol. This reaction must be catalysed by a strong concentrated acid such as sulfuric acid.
Regulations & IFRA
This ingredient is not restricted