Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Naturality | Purity | Latin name | Treated part | Geographical origin | Certifications | Comments | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Stemone - 30 Gr | - | - | - | - | - | - | more | - |
General Presentation
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CAS N° : : 22457-23-4
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EINECS number : 245-010-8
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FEMA number : Donnée indisponible.
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Density : 0,888
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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 : Heart
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Price Range : €€
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Appearance : Colorless liquid
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FLAVIS number : Donnée indisponible.
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JECFA number : Donnée indisponible.
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point :
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Detection Threshold : Donnée indisponible.
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Molecular formula : C8H17NO
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Log P : 2,3
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Molecular Weight : 143,23 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : 95°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Stability :
Stable in perfumes and diverse functional bases, except bleach.
Uses in perfumery :
Stemone® is used in all types of fragrances, for notes of fig leaf, tomato leaf and blackcurrant. Brings a leafy and stem facet to floral notes in particular. Also brings a green facet to a violet. Gives a natural and modern effect.
Year of discovery :
1967
Isomerism :
Stemone® has an asymmetric carbon and a double bond that gives rise to four possible isomers. Nevertheless, it is the mixture of these isomers that is used in perfumery.
Synthesis precursor :
Stemone® is not a precursor to the synthesis of another compound of olfactory interest.
Natural availability :
Stemone® is not available in its natural state.
Synthesis route :
Stemone® is part of a family of molecules called oximes. It is therefore prepared by oximation of 5-methyl-3-heptanone. This reaction corresponds to the condensation of ketone with hydroxylamine.
Regulations & IFRA
This ingredient is not restricted
