Photo credits: ScenTree SAS
Company | Ingredient Name | ID | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
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Cis-Jasmone - 30gr | - |
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JASMONE CIS | 85035 |
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Molecule | - | - | - | - | - |
General Presentation
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CAS N° : 488-10-8
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EINECS number : 207-668-4
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FEMA number : 3196
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FLAVIS number : 07.094
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JECFA number : 1114
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Appearance : Colorless liquid
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Density : 0,941
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Volatility : Heart/Base
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Price Range : €€€
Physico-chemical properties
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Molecular formula : C11H16O
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Molecular Weight : 164,25 g/mol
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Log P : 2,8
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Fusion Point : Donnée indisponible.
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Boiling Point : 86°C
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Detection Threshold : 2,9302 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 : 121°C
Uses
Uses in perfumery :
Cis-jasmone is used in floral notes (tuberose, jasmine, gardenia) and ambery notes. Supports Hedione® and brings depth and power to jasmine notes.
Year of discovery :
Data not available.
Natural availability :
Cis-jasmone is found in Grandiflorum Jasmine Absolute (and other origins), Daffodil Absolute and Champaca Absolute. It can be extracted in its natural state from Grandiflorum Jasmine Absolute.
Isomerism :
The double bond guiding this cis-Jasmone conformation could also give rise to a trans conformation, depending on the synthesis conditions. The resulting smell would be much more earthy and close to mushroom.
Synthesis precursor :
Cis-jasmone is not a precursor to the synthesis of another compound of olfactory interest.
Synthesis route :
A synthetic route of cis-Jasmone consists of a nucleophilic substitution reaction between 3-methyl-2-cyclopenten-1-one and cis-2-pentenyl chloride, in the presence of sodium hydroxide.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment