Photo credits: ScenTree SAS
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General Presentation
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CAS N° : : 55066-48-3
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EINECS number : 259-461-3
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FEMA number : Donnée indisponible.
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Density : 0,96
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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 : C12H18O
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Log P : 2,7
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Molecular Weight : 178,27 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : 94°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
In comparision to other rosy and green notes of perfumery as Nerolidol or Rosacetol®, Phenoxanol® has a distinctive zesty facet.
Stability :
Most of the time, the occurrence of a benzenic cycle in a molecule causes a coloration of this molecule through time
Unstable in acid cleaners and very alkaline products.
Uses in perfumery :
Phenoxanol® is used in rose notes to replace some of the rose alcohols. Useful in geranium, lily of the valley, light floral and fruity notes.
Year of discovery :
1935
Isomerism :
This compound has an asymmetric carbon. Both enantiomers of the molecule have a similar smell. However, it is the racemic mixture of the two compounds that is used in perfumery. Moreover, Phenoxanol® is a constitutional isomer of Majantol®, although its smell is more aldehydic and aqueous.
Synthesis precursor :
Phenoxanol® is not a precursor to the synthesis of another compound of olfactory interest.
Natural availability :
Phenoxanol® is not available in its natural state.
Synthesis route :
The synthesis of Phenoxanol® is made from tetrahydro-4-methylene-5-phenylpyran (obtained by a cyclocondensation between benzaldehyde and 3-methyl-3-buten-1-ol, in the presence of para-toluenesulfonic acid), by a catalytic hydrogenation reaction.
Regulations & IFRA
This ingredient is not restricted
