Photo credits: ScenTree SAS
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General Presentation
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CAS N° : : 57345-19-4
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EINECS number : 260-686-4
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FEMA number : Donnée indisponible.
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Density : 0,87 (dans le MIP)
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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 :
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Detection Threshold : Donnée indisponible.
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Molecular formula : C18H30O2
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Log P : 4,59
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Molecular Weight : 278,43 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : 102°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Most of the time, Amberketal® is diluted at around 10% in Isopropyl Myristate or Dipropylene Glycol for solubility and use reasons.
Stability :
Stable in perfumes and diverse functional bases, except very acid products and bleach.
Uses in perfumery :
According to its olfactive weakness, this woody and ambery molecule is less used than some others. Amberketal® can be used in woody-ambergris notes and especially in functionnal products thanks to its stability.
Year of discovery :
Discovered in 1953.
Isomerism :
Amberketal has got five asymmetric carbons, forming a few possible isomers. Nevertheless, only a mix of these isomers is used in perfumery.
Synthesis precursor :
Amberketal® is not a precursor to the synthesis of another compound of olfactory interest.
Natural availability :
Amberketal® is not available in its natural state.
Synthesis route :
Amberketal® is synthesized from manool, a natural component extracted from ''pink pine '' tree Halocarpus biformis, growing in New-Zealand. One of Manool's double bond is epoxidized, subsequent oxydative degradation of the allyl alcohol function into a ketone, and an intramolecular acetalization, giving birth to the final ketal function.
Regulations & IFRA
This ingredient is not restricted
