Photo credits: ScenTree SAS
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General Presentation
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CAS N° : : 22629-49-8
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EINECS number : 245-142-6
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FEMA number : Donnée indisponible.
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Density : 0,84
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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 : Base
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Price Range : €€€
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Appearance : Pale yellow 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 : 289°C
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Detection Threshold : Donnée indisponible.
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Molecular formula : C13H23N
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Log P : Donnée indisponible.
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Molecular Weight : 193,33 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : >93°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Ozonil® is the only molecule combining a zesty smell of tangerine with a marine odor. It is a unique material.
Stability :
Stable in perfumes and various functionnal bases.
Uses in perfumery :
Ozonil® is used in zesty notes, to bring an aldehidic top note and a marine, ozonic and voluminous base. It is also used to bring a zesty nuance to marine notes.
Year of discovery :
Data not available.
Isomerism :
Ozonil® has one double bond giving birth to two possible diastereoisomers. In perfumery, a mixture of these two isomers is used.
Synthesis precursor :
Ozonil® is not a precursor for the synthesis of another material used in perfumery.
Natural availability :
Ozonil® is not reported as found in nature, and can thus not be extracted from any plant.
Synthesis route :
Ozonil® is prepared by a Knoevenagel condensation between Aldehyde C-11 Undecylic and cyanoacetic acid. A decarboxylation reaction (use of high heat and decarboxylase enzym) is then carried out to form the alcene function of the final product, Ozonil®.
Regulations & IFRA
This ingredient is not restricted
