Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Naturality | Purity | Latin name | Treated part | Geographical origin | Certifications | Comments | MOQ |
|---|
General Presentation
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CAS N° : : 4630-07-3
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EINECS number : 225-047-6
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FEMA number : 3443
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Density : 0,92
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Optical rotation : Lorem Ipsum
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Allergens : This ingredient does not contain any allergen.
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Refractive Index @20°C : Lorem Ipsum
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Volatility : Head
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Price Range : €€
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Appearance : Colorless liquid
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FLAVIS number : 01.017
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JECFA number : 1337
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 274°C
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Detection Threshold : Donnée indisponible.
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Molecular formula : C15H24
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Log P : 6,7
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Molecular Weight : 204,36 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : 100°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Valencene is the only terpene with a powerful aldehydic note.
Stability :
Terpenes tend to polymerize by oxydation.
Uses in perfumery :
Valencene is used for aldehydic and citrus notes in small quantities.
Year of discovery :
Data not available.
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.
Natural availability :
Valencene in its natural state can be extracted from Clary Sage Absolute (up to 3%) or Sweet Orange EO.
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.
Regulations & IFRA
This ingredient is not restricted
