Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Naturality | Purity | Latin name | Treated part | Geographical origin | Certifications | Comments | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Oxane - 30gr | - | - | - | - | - | - | more | - |
General Presentation
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CAS N° : : 59323-76-1
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EINECS number : 261-699-8
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FEMA number : 3578
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Density : 1,05
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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 : 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 : C8H16OS
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Log P : Donnée indisponible.
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Molecular Weight : 160,28 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : 74°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Stability :
Stable in perfumes and diverse functional bases
Uses in perfumery :
Oxane is useful in fruity-exotic, blackcurrant, green and floral notes, as a top booster. Often used diluted.
Year of discovery :
1974
Isomerism :
Oxane is an enantiomerically pure molecule. Carbon 2 adopts an (R) conformation and carbon 4 conforms (S). These conformations are directly obtained during the synthesis of this compound. Other enantiomers are not used in perfumery.
Synthesis precursor :
Oxane is not a precursor to the synthesis of another compound of olfactory interest.
Natural availability :
Oxane is present in some fruits such as passion fruit, but Oxane used in perfumery is synthetic.
Synthesis route :
Oxane is synthesized by reaction between 3-mercaptohexanol and Acetaldehyde. This reaction causes a cyclization of the molecule, and therefore the sulfur compound Oxane.
Regulations & IFRA
This ingredient is not restricted
