Photo credits: ScenTree SAS
Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Comments | Naturality | Certifications | MOQ | Purity |
|---|---|---|---|---|---|---|---|
|
Valence 75 | - |
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|
Molecule | - | - | |
|
|
Valencene 80 | - |
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|
Molecule | - | - | |
|
VALENCENE NATURAL | 2311123510 |
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|
Natural Aroma Chemicals |
|
- | - |
General Presentation
-
CAS N° :
4630-07-3 -
EINECS number :
225-047-6 -
FEMA number :
3443 -
FLAVIS number :
01.017
-
JECFA number :
1337 -
Volatility :
Head -
Price Range :
€€
Physico-chemical properties
-
Appearance :
Colorless liquid -
Density :
0,92 -
Refractive Index @20°C :
Data not available. -
Optical rotation :
Data not available. -
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
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.
IFRA
IFRA 51th :
This ingredient is not restricted for the 51th amendment
