Galbanolene
Synthétique
Green > Crisp Green > Tropical Fruits
Crédits photo: ScenTree SAS
Other names :
1,3,5-Undecatriene ; Undecatriene ; Undecatriene-10 ; Galbanolène SUPER ; Cis-galbanolene ; galbanum decatriene
Volatility :
Head
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.
Natural availability :
It occurs in trace amounts in Celery Seed EO as well as in Galbanum EO
Year of discovery :
Patent EP0203615A1 (1985) reports an earlier synthesis dating from 1967.
Other comments :
Data not available.
Price Range :
€€€
Stability :
Data not available.
Crédits photo: ScenTree SAS
- Molecular formula :
- C11H18
- Molecular Weight :
- 150,27 g/mol
- Density :
- 1,08 - 1,09 @20°C (@10% TEC) 0,788 - 0,796 @20°C (pur)
- Flash Point :
- 89°C (192°F)
- Fusion Point :
- Donnée indisponible.
- Appearance :
- Colorless liquid
- Log P :
- 5,68
- Boiling Point :
- Donnée indisponible.
- Detection Threshold :
- Donnée indisponible.
Synthesis route :
See Patent EP0203615A1 (1985)
Synthesis precursor :
Data not available.
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
- EINECS number :
- 240-416-1
- FEMA number :
- 3795
- JECFA number :
- 1341
- FLAVIS number :
- 01.061
- Allergens :
- This ingredient does not contain any allergen.
- IFRA :
- This ingredient is not restricted
To learn more about IFRA's standards : https://ifrafragrance.org/safe-use/library
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