Photo credits: ScenTree SAS
Company | Ingredient Name | ID | Naturality | Purity | Latin name | Treated part | Geographical origin | Certifications | Comments | MOQ |
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Kephalis® - 30gr | - | - | - | - | - | - | more | - |
General Presentation
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CAS N° : : 36306-87-3
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EINECS number : 252-961-2
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FEMA number : Donnée indisponible.
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Density : 0,947
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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/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 : 272°C
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Detection Threshold : 3,9547 ng/l air
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Molecular formula : C14H24O2
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Log P : 4,3
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Molecular Weight : 224,34 g/mol
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Fusion Point : -80°C
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Flash Point : 120°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
In comparision to other woody-ambergris notes also having a violet flower undernote, Iso E Super® is more reminiscent of Cedarwood Virginia EO than Vetiver Haiti EO, in the case of Kephalis®.
Stability :
Unstable in acidic products, except fabric conditioners, and in very alkaline detergents.
Uses in perfumery :
Kephalis® is used in woody, ambery, masculine fragrances, leather, suede, spicy and floral notes. Gives a leather and woody appearance from the head to the base.
Year of discovery :
Data not available.
Isomerism :
Kephalis® does not have any isomer used in perfumery.
Synthesis precursor :
Kephalis® is not a precursor to the synthesis of another compound of olfactory interest.
Natural availability :
Kephalis® is not available in its natural state.
Synthesis route :
Kephalis® is one of two compounds synthesized by a cyclodimerization reaction of mesityl oxide (or 4-methylpent-3-en-2-one), in the presence of boron trifluoride etherate, by reaction with ethyl orthoformate. The other compound formed during this reaction has no olfactory interest.
Regulations & IFRA
This ingredient is not restricted