Galbanolene (CAS N° 16356-11-9)​

Photo credits: ScenTree SAS

Galbanolene

Green > Crisp Green > Tropical Fruits

1,3,5-Undecatriene ; Undecatriene ; Undecatriene-10 ; Galbanolène SUPER ; Cis-galbanolene ; galbanum decatriene

Galbanolene (CAS N° 16356-11-9)​

Photo credits: ScenTree SAS



Company Ingredient Name Learn more Naturality Certifications MOQ Purity
PCW logo UNDECATRIENE
UND-1
Discover - 10 grs -
dsm-firmenich logo GALBANOLENE 10 TEC
944252
Discover Molecules Certifications : Biodegradable (Ultimately) - -
PCW logo
UNDECATRIENE

UND-1

Discover
dsm-firmenich logo
GALBANOLENE 10 TEC

944252

Discover
General Presentation

General Presentation

  • CAS N° :

    16356-11-9
  • EINECS number :

    240-416-1
  • FEMA number :

    3795
  • FLAVIS number :

    1,061
  • JECFA number :

    1341
  • Volatility :

    Head
  • Price Range :

    €€€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    1,08 - 1,09 @20°C (@10% TEC) 0,788 - 0,796 @20°C (pur)
  • Refractive Index @20°C :

    1,449 - 1,453
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    0,421 mmHg @20°C
  • Flash Point :

    89°C (192,2°F)
  • Molecular formula :

    C11H18
  • Molecular Weight :

    150,27 g/mol
  • Log P :

    5,68
  • Fusion Point :

    Donnée indisponible.
  • Boiling Point :

  • Detection Threshold :

    Donnée indisponible.
Chemistry & Uses

Chemistry & Uses

Uses in perfumery :

Galbanolene is a synthetic green galbanum note. Extremely powerful, its usage is usually done with a 10% solution. It brings character and lift to a green note. Interesting to play on the naturalness degree of a fruit, for the stem side of a flower, in lilies of the valley or for reconstitutions of Galbanum EO or Neroli EO.

Year of discovery :

Patent EP0203615A1 (1985) reports an earlier synthesis dating from 1967.

Natural availability :

It occurs in trace amounts in Celery Seed EO as well as in Galbanum EO

New
Ingredient % min % max
Galbanum oil 0.40 2

Isomerism :

Occurs as a mixture of two diastereomers. 1,3(E),5(Z) and 1,3(E),5(E) The ratio of these two molecules may vary from one supplier to another

Synthesis precursor :

Data not available.

Synthesis route :

See Patent EP0203615A1 (1985)

Stability :

Data not available.

Other comments :

Data not available.

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.