Valencene (CAS N° 4630-07-3)​

Photo credits: ScenTree SAS

Valencene

Aldehydes > Green

4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7-hexahydro-1H-naphthalene ; 4alpha,10alpha- dimethyl-6beta-isopropyl-delta1,9-octalin ; 5,6-dimethyl-8-(1-methylvinyl)bicyclo[4.4.0]dec-1-ene ; Eremophila-1(10),11-diene ; Octahydrodimethyl methyl vinyl naphthalene

Valencene (CAS N° 4630-07-3)​

Photo credits: ScenTree SAS



Company Ingredient Name Learn more Naturality Certifications MOQ Purity
BASF logo Valence 75 Discover Molecule - -
BASF logo Valencene 80 Discover Molecule - -
BASF logo
Valence 75
Discover
BASF logo
Valencene 80
Discover
General Presentation

General Presentation

  • CAS N° :

    4630-07-3
  • EINECS number :

    225-047-6
  • FEMA number :

    3443
  • FLAVIS number :

    1,017
  • JECFA number :

    1337
  • Volatility :

    Head
  • Price Range :

    €€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    0,92
  • Refractive Index @20°C :

    Donnée indisponible.
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    0,0109 mmHg @23°C
  • Flash Point :

    100°C (212°F)
  • Molecular formula :

    C15H24
  • Molecular Weight :

    204,36 g/mol
  • Log P :

    6,7
  • Fusion Point :

    Donnée indisponible.
  • Boiling Point :

    274°C (525,2°F)
  • Detection Threshold :

    Donnée indisponible.
Chemistry & Uses

Chemistry & Uses

Uses in perfumery :

Valencene is used for aldehydic and citrus notes in small quantities.

Year of discovery :

Data not available.

Natural availability :

Valencene in its natural state can be extracted from Clary Sage Absolute (up to 3%) or Sweet Orange EO.

Isomerism :

Caryophyllene, another sesquiterpene, is an isomer of Valencene. Its smell is less aldehydic and more spicy, close to Black Pepper EO.

Synthesis precursor :

Valencene is a precursor to the synthesis of Nootkatone by oxidation.

Synthesis route :

Valencene is more often synthesized biochemically using enzymes produced by fungi. The enzyme is called valencene synthase and the most used mushroom is the Schizophyllum commune.

Stability :

Terpenes tend to polymerize by oxydation.

Other comments :

Valencene is the only terpene with a powerful aldehydic note.

I am a chocolate hazelnut cookie. I come out of the oven. Impossible to refuse me.
This website is using cookies
Our website uses cookies for statistics, performance, and security. These anonymous data allow us to give you an optimal navigation experience. You can always disable cookies in your browser settings.