Cyclogalbanate®
Synthétique
Green > Crisp Green > Tropical Fruits
Crédits photo: ScenTree SAS
Other names :
Cyclogalbaniff® ; Isoananate® ; Prop-2-enyl 2-cyclohexyloxy acetate ; Allyl ananate ; Allyl (cyclohexyloxy)acetate ; Galbador CG ; Glycoflor ; Hexylix ; Langalbanate ; Prop-2-enyl 2-cyclohexyloxyacetate
Volatility :
Heart
Uses in perfumery :
Cyclogalbanate® is used in fruity notes to make them greener and give them power. Also gives a solar effect to a composition.
Natural availability :
Cyclogalbanate® is not available in its natural state.
Year of discovery :
Data not available.
Other comments :
Cyclogalbanate is frequently compared to Allyl Amyl Glycolate for its fruity and green note. It remains much greener than the later anyway.
Price Range :
€€
Stability :
Cyclogalabante may form its corresponding acid through time under heat.
Crédits photo: ScenTree SAS
- Molecular formula :
- C11H18O3
- Molecular Weight :
- 198,26 g/mol
- Density :
- 1,017
- Flash Point :
- 101°C
- Fusion Point :
- -20°C
- Appearance :
- Colorless liquid
- Log P :
- Donnée indisponible,
- Boiling Point :
- 259°C
- Detection Threshold :
- Donnée indisponible.
Synthesis route :
Cyclogalbanate® is synthesized by esterification of cyclohexyloxyacetic acid (prepared from phenoxyacetic acid) with allyl alcohol, catalysed by a strong acid.
Synthesis precursor :
Cyclogalbanate® is not a precursor to the synthesis of another compound of olfactory interest.
Isomerism :
Cyclogalbanate® does not have any isomer used in perfumery.
- EINECS number :
- 272-657-3
- FEMA number :
- Donnée indisponible.
- JECFA number :
- Donnée indisponible.
- FLAVIS number :
- Donnée indisponible.
- 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
ScenTree is solely responsible for the information provided here.
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