Octahydrocoumarin (CAS N° 4430-31-3)​

Photo credits: ScenTree SAS

Octahydrocoumarin

Balsamic Ambery > Coumarinic > Tropical Fruits

Bicyclononalactone ; 3,4,4a,5,6,7,8,8a-octahydrochromen-2-one ; Octahydro-2H-1-benzopyran-2-one ; Cyclohexyl lactone ; Octahydro-1-benzopyran-2-one ; Octahydrochromen-2-one

Octahydrocoumarin (CAS N° 4430-31-3)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Comments Naturality Certifications MOQ Purity
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OCTAHYDROCOUMARIN OC-1 Visit website Je me procure cet ingrédient - 10 grs 90 - 100

OCTAHYDROCOUMARIN

ID : OC-1

Certifications :

Information Générales

General Presentation

  • CAS N° :

    4430-31-3
  • EINECS number :

    224-623-4
  • FEMA number :

    3791
  • FLAVIS number :

    13.161
  • JECFA number :

    1166
  • Volatility :

    Base
  • Price Range :

    €€€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    1,09
  • Refractive Index @20°C :

    Donnée indisponible.
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    0,001558 mmHg @23°C
  • Flash Point :

    113°C (235,4°F)
  • Molecular formula :

    C9H14O2
  • Molecular Weight :

    154,21 g/mol
  • Log P :

    2,52
  • Fusion Point :

    Donnée indisponible.
  • Boiling Point :

  • Detection Threshold :

    Donnée indisponible.
Utilisation

Chemistry & Uses

Uses in perfumery :

Octahydrocoumarin is used in fine fragrance in fougere fragrances. Allows to work on fig, coconut, white and heady flowers, vanillic, ambery and spicy-cinnamon notes.

Year of discovery :

Data not available.

Natural availability :

Octahydrocoumarin is not available in its natural state.

Isomerism :

Folione® is a constitutional isomer of Octahydrocoumarin, even if these two ingredient do not have the same smell at all.

Synthesis precursor :

Octahydrocoumarin is not a precursor to the synthesis of another compound of olfactory interest.

Synthesis route :

Octahydrocoumarin is synthesized from Coumarin by a catalytic hydrogenation reaction carried at a high temperature which must reach 392 to 482°F to synthesize this compound. Another synthetic route is an intramolecular esterification of 3-(2-hydroxycyclohexyl)propanoic acid.

Stability :

Stable in perfumes and diverse functional bases

Other comments :

Octahydrocoumarin has a much more fruity and lactonic smell than other coumarin derivatives.

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