Phenoxanol® (CAS N° 55066-48-3)​

Photo credits: ScenTree SAS

Phenoxanol®

Floral > Rosy > Green > Zesty

Phenylhexanol ; Mefrosol® ; 3-methyl-5-phenylpentan-1-ol ; Gamma-methyl benzene pentanol ; 3-methyl-5-phenyl pentanol ; Phenyl hexanol ; Phenyl isohexanol ; Phenyxol ; Rose absolute pentanol

Phenoxanol® (CAS N° 55066-48-3)​

Photo credits: ScenTree SAS



Company Ingredient Name Learn more Naturality Certifications MOQ Purity
PCW logo PHENYL HEXANOL
PHEX-1
Discover - 10 grs 97
dsm-firmenich logo PHENYLHEXANOL
973080
Discover Molecules Certifications : Biodegradable (Readily) - -
Tilley Distribution logo Phenyl Hexanol Discover Synthetic Aroma Chemicals - -
PCW logo
PHENYL HEXANOL

PHEX-1

Discover
dsm-firmenich logo
PHENYLHEXANOL

973080

Discover
Tilley Distribution logo
Phenyl Hexanol
Discover
General Presentation

General Presentation

  • CAS N° :

    55066-48-3
  • EINECS number :

    259-461-3
  • FEMA number :

    Donnée indisponible.
  • FLAVIS number :

    Donnée indisponible.
  • JECFA number :

    Donnée indisponible.
  • Volatility :

    Heart
  • Price Range :

    €€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    0,96
  • Refractive Index @20°C :

    Donnée indisponible.
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    0,000311 mmHg @23°C
  • Flash Point :

    94°C (201,2°F)
  • Molecular formula :

    C12H18O
  • Molecular Weight :

    178,27 g/mol
  • Log P :

    2,7
  • Fusion Point :

    Donnée indisponible.
  • Boiling Point :

  • Detection Threshold :

    Donnée indisponible.
Chemistry & Uses

Chemistry & Uses

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

Natural availability :

Phenoxanol® is not available in its natural state.

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.

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.

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.

Other comments :

In comparision to other rosy and green notes of perfumery as Nerolidol or Rosacetol®, Phenoxanol® has a distinctive zesty facet.

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