Phenylethyl cinnamate (CAS N° 103-53-7)​

Photo credits: ScenTree SAS

Floral > Rosy > Cinnamic

Phenylethyl cinnamate

Benzyl carbinyl 3-phenylpropenoate ; Benzyl carbinyl cinnamate ; Beta-phenylethyl-beta-phenylacrylate ; 2-phenylethyl 3-phenylpropenoate ; Phenylethyl cinnamate ; 3-phenyl-2-propenoate de phenylethyl ; 3-phenylprop-2-enoate de phenylethyl

Phenylethyl cinnamate (CAS N° 103-53-7)​

Photo credits: ScenTree SAS

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Information Générales

General Presentation

  • CAS N° : 103-53-7

  • EINECS number : 203-120-3

  • FEMA number : 2863

  • FLAVIS number : 09.743

  • JECFA number : 671

  • Appearance : White crystals

  • Density : Donnée indisponible.

  • Volatility : Base

  • Price Range : €€

Physico-chemical properties

  • Molecular formula : C17H16O2

  • Molecular Weight : 252,31 g/mol

  • Log P : 4,6

  • Fusion Point : 54°C

  • Boiling Point : 195°C (à 2,6 mbar)

  • Detection Threshold : Donnée indisponible.

  • Optical rotation : Donnée indisponible

  • Vapor pressure : Donnée indisponible

  • Refractive Index @20°C : Donnée indisponible

  • Acid Value : Donnée indisponible.

  • Flash Point : 113°C

Utilisation

Uses

Uses in perfumery :

Phenyl Ethyl Cinnamate is used to bring volume and as a fixative in perfumes. It enlarges the perfume and brings tenacity, especially for rosy notes.

Year of discovery :

Data not available.

Natural availability :

Phenyl Ethyl Cinnamate can be extracted from Populus balsamifera bud extract. Nevertheless, the synthetic molecule is used most of the time in perfumery.

Isomerism :

Phenyl Ethyl Cinnamate used in perfumery corresponds to the trans isomer of this molecule. The cis isomer has a relatively similar smell.

Synthesis precursor :

Phenyl Ethyl Cinnamate is not a precursor for the synthesis of another compound of olfactive interest.

Synthesis route :

Phenyl Ethyl Cinnamate is synthesized by an esterification reaction involving cinnamic acid and Phenyl Ethyl Alcohol. This reaction uses a small quantity of catalysor as concentrated sulfuric acid. A better synthesis yield can result from this reaction by using chlorocinnamic acid or cinnamic anhydride, more costly. This synthesis involves the use of the trans isomer of cinnamic acid.

Utilisation

Regulations & IFRA

Allergens :

This ingredient does not contain any allergen.

IFRA 51th :

This ingredient is not restricted for the 51th amendment

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