1,3-Octenol (CAS N° 3391-86-4)​

Photo credits: ScenTree SAS

1,3-Octenol

Undergrowth > Mushroom

Amyl Vinyl Carbinol ; Morillol ; Oct-1en-3-ol ; 1-caprylene-3-alcohol ; Matsuica alcohol ; Matsuka alcohol ; Pentyl vinyl carbinol ; Vinyl hexanol ; Matsutake alcohol

1,3-Octenol (CAS N° 3391-86-4)​

Photo credits: ScenTree SAS



Company Ingredient Name Learn more Naturality Certifications MOQ Purity
PCW logo 1-OCTEN-3-OL
1O3O-1
Discover - 10 grs 98.0 - 100.0
Tilley Distribution logo 1-Octen-3-ol natural Discover Natural Aroma Chemicals - -
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1-OCTEN-3-OL

1O3O-1

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Tilley Distribution logo
1-Octen-3-ol natural
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General Presentation

General Presentation

  • CAS N° :

    3391-86-4
  • EINECS number :

    222-226-0
  • FEMA number :

    2805
  • FLAVIS number :

    2,023
  • JECFA number :

    1152
  • Volatility :

    Heart
  • Price Range :

    €€€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    0,83 - 0,85
  • Refractive Index @20°C :

    1,435 - 1,439
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    Donnée indisponible.
  • Flash Point :

    63°C (145,4°F)
  • Molecular formula :

    C8H16O
  • Molecular Weight :

    128,22 g/mol
  • Log P :

    2,7
  • Fusion Point :

    -49°C (-56,2°F)
  • Boiling Point :

    180°C (356°F)
  • Detection Threshold :

    Seuil de détection : 14 ppb (0,0000014%)
    Seuil de reconnaissance : 25 ppb (0,0000025%)
Chemistry & Uses

Chemistry & Uses

Uses in perfumery :

1,3-Octenol is used mainly in mushroom, lavender, woody and foody notes.

Year of discovery :

Data not available.

Natural availability :

The (R) enantiomer of 1,3-Octenol is present at 97% in the aromatic principle of mushrooms and 89% in the chanterelles aromatic principle. Nevertheless, 1,3-Octenol is not extracted in its natural state.

New
Ingredient % min % max
Genet absolute 3

Isomerism :

The (R) enantiomer of 1,3-Octenol is more powerful than the (S) enantiomer, which has a vegetable smell. In perfumery, the mixture both isomers is the most used.

Synthesis precursor :

1,3-Octenol is a precursor for the synthesis of esters obtained by reaction between this alcohol and a carboxylic acid.

Synthesis route :

1,3-Octenol can be obtained by a Grignard reaction reacting vinylmagnesium bromide with hexanal.

Stability :

Stable in acidic products, but not so much in alkaline bleaches or detergents.

Other comments :

Data not available.

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