Vetyvenal®
Synthétique
Woody > Warm Woods > Vetiver > Sandalwood > Buttery
Crédits photo: ScenTree SAS
Other names :
Caryoketone® ; Caryophyllene Alcohol acetate ; (3Z)-4,11,11-trimethyl-8-methylidene-5-bicyclo[7.2.0]undec-3-enyl acetate ; Acetyl caryophyllene ; Caryophyllene acetate
Volatility :
Base
Uses in perfumery :
Vetyvenal® is used in vetiver reconstitutions, sandalwood notes and woody perfumes. Gives a milky and sandalwood side to an accord.
Natural availability :
Vetyvenal® is a compound present in trace amounts in Clove Bud EO, although it is not extracted. It is therefore the synthetic compound that is used in perfumery.
Year of discovery :
Data not available.
Other comments :
Data not available.
Price Range :
€€€
Stability :
Stable in perfumes and diverse functional bases
Crédits photo: ScenTree SAS
- Molecular formula :
- C17H26O2
- Molecular Weight :
- 262,39 g/mol
- Density :
- 1,003
- Flash Point :
- 144°C
- Fusion Point :
- Donnée indisponible.
- Appearance :
- Colorless viscous liquid
- Log P :
- Donnée indisponible,
- Boiling Point :
- 152°C (à 10 mmHg)
- Detection Threshold :
- Donnée indisponible.
Synthesis route :
Vetyvenal® is synthesized from an alcohol derived from Caryophyllene, reacting with acetic anhydride in an esterification reaction, in an acid medium.
Synthesis precursor :
Vetyvenal® is not a precursor to the synthesis of another compound of olfactory interest.
Isomerism :
Vetiveryl acetate is a constitutional isomer of Vetyvenal®. Both can be used in vetiver note reconstructions.
- EINECS number :
- 250-960-1
- 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
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