Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Habanolide® - 30gr | - |
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|
- | - | - | - | - | - |
Habanolide® - 30gr
Certifications :
General Presentation
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CAS N° : 111879-80-2
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EINECS number : 422-320-3
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FEMA number : Donnée indisponible.
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FLAVIS number : Donnée indisponible.
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JECFA number : Donnée indisponible.
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Appearance : Colorless liquid
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Density : 0,964
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Volatility : Base
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Price Range : €€€
Physico-chemical properties
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Molecular formula : C15H26O2
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Molecular Weight : 238,37 g/mol
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Log P : 6,2
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Fusion Point : -33°C
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Boiling Point : 307°C
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Detection Threshold : 0,5 ng/l air
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Optical rotation : Donnée indisponible
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Vapor pressure : Donnée indisponible
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Refractive Index @20°C : Donnée indisponible
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Acid Value : Donnée indisponible.
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Flash Point : >100°C (>212°F)
Uses
Uses in perfumery :
Habanolide® is used in white floral notes, orange blossom and woody notes. Useful in marine and amber notes.
Used only in fine fragrance, especially for colognes.
Year of discovery :
Discovered in 1969. ''Habanolide® '' tradename has been published and protected by Firmenich SA since 05/03/1992 (brand N°584055)
Natural availability :
Habanolide® is not available in its natural state.
Isomerism :
Two diastereoisomers of Habanolide® exist. The molecule called Habanolide® is the (E) (trans) diastereoisomer of the molecule. The diastereoisomer (Z) is less used, but has a similar smell. The mixture of the two isomers is also widely used.
Synthesis precursor :
Habanolide® is not a precursor to the synthesis of another compound of olfactory interest.
Synthesis route :
Habanolide® is a macrocyclic musk, close to Exaltolide®. Therefore, it can be synthesized in a similar way, by enlarging the Cyclododecenone cycle.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment
