Benzyl cinnamate (CAS N° 103-41-3)​

Photo credits: ScenTree SAS

Benzyl cinnamate

Benzyl 3-Phenylprop-2-enoate ; Benzyl 3-phenyl propenoate ; Benzyl alcohol cinnamate ; Benzyl gamma-phenyl acrylate ; Benzyl-3-phenyl propenoate ; Cinnamein ; Phenyl methyl 3-phenyl-2-propenoate ; Phenylmethyl 3-phenylprop-2-enoate

Benzyl cinnamate (CAS N° 103-41-3)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Comments Naturality Certifications MOQ Purity
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BENZYL CINNAMATE - Visit website Je me procure cet ingrédient - 10 grs -

BENZYL CINNAMATE

Certifications :

Information Générales

General Presentation

  • CAS N° :

    103-41-3
  • EINECS number :

    203-109-3
  • FEMA number :

    2142
  • FLAVIS number :

    09.738
  • JECFA number :

    670
  • Volatility :

    Heart/Base
  • Price Range :

    €€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    White to pale yellow solid
  • Density :

    1,1
  • Refractive Index @20°C :

    Data not available.
  • Optical rotation :

    Data not available.
  • Vapor pressure :

    < 0.075 mmHg @20°C
  • Flash Point :

    180°C (356°F)
  • Molecular formula :

    C16H14O2
  • Molecular Weight :

    238,29 g/mol
  • Log P :

    4,1
  • Fusion Point :

    34°C (93,2°F)
  • Boiling Point :

    350°C (662°F)
  • Detection Threshold :

    Donnée indisponible.
Utilisation

Chemistry & Uses

Uses in perfumery :

Benzyl Cinnamate is used mainly in oriental perfumes as a fixative note. Used in heavy fragrances, reproducing notes of vanillic tree resin.

Year of discovery :

Data not available.

Natural availability :

Benzyl Cinnamate is found in Peru Balsam Resinoid and in Tolu Balsam Resinoid as well as in Copahu EO or Cabreuva EO, among others. Therefore, natural Benzyl Cinnamate can be extracted from these balsams and essential oils.

Isomerism :

Benzyl Cinnamate has a double bond allowing the existence of two diastereoisomers (Z) and (E) which have a similar smell.

Synthesis precursor :

Benzyl CInnamate is not a precursor to the synthesis of another compound of olfactory interest.

Synthesis route :

Benzyl Cinnamate is synthesized by an esterification reaction, using Cinnamic Acid, Benzyl Alcohol and an acidic catalyst such as sulfuric acid.

Stability :

May form Cinnamic Acid through time.
Tends to get a yellow color through time.

Other comments :

Benzyl Cinnamate is one of the 26 allergens in perfumery.

Utilisation

IFRA

IFRA 51th :

This ingredient is restricted by the 51th amendment

  • Restriction type :

    RESTRICTION
  • Cause of restriction :

    DERMAL SENSITIZATION AND SYSTEMIC TOXICITY
  • Amendment :

    49
Quantitative limit on the use :
Cat.1 Cat.2 Cat.3 Cat.4
Cat.5
A B C D
Cat.6
0,36 % 0,11 % 1,2 % 2 %
0,51 % 0,51 % 0,51 % 0,17 %
1,2 %
Cat.5
A B C D
Cat.6
0,51 % 0,51 % 0,51 % 0,17 %
1,2 %
Cat.7
A B
Cat.8 Cat.9
Cat.10
A B
Cat.11
A B
Cat.12
2,4 % 2,4 %
0,17 % 3,9 %
3,9 % 14 %
0,17 % 0,17 %
No Restriction
Cat.10
A B
Cat.11
A B
Cat.12
3,9 % 14 %
0,17 % 0,17 %
No Restriction
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