Habanolide® (CAS N° 111879-80-2)​

Photo credits: ScenTree SAS

Habanolide®

Musky > Berries > Orange Blossom

(12E)-1-oxacyclohexadec-12-en-2-one

Habanolide® (CAS N° 111879-80-2)​

Photo credits: ScenTree SAS



Company Ingredient Name Learn more Naturality Certifications MOQ Purity
PCW logo GLOBALIDE 100% (SYMRISE)
HAB-2
Discover - 10 grs -
dsm-firmenich logo HABANOLIDE®
947303
Discover Molecules Certifications : Biodegradable (Readily) - -
Quosentis logo Habanolide® - 30gr Discover - 30grs -
Tilley Distribution logo Habanolide Discover Synthetic Aroma Chemicals - -
PCW logo
GLOBALIDE 100% (SYMRISE)

HAB-2

Discover
dsm-firmenich logo
HABANOLIDE®

947303

Discover
Quosentis logo
Habanolide® - 30gr
Discover
Tilley Distribution logo
Habanolide
Discover
General Presentation

General Presentation

  • CAS N° :

    111879-80-2
  • EINECS number :

    422-320-3
  • FEMA number :

    Donnée indisponible.
  • FLAVIS number :

    Donnée indisponible.
  • JECFA number :

    Donnée indisponible.
  • Volatility :

    Base
  • Price Range :

    €€€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    0,964
  • Refractive Index @20°C :

    Donnée indisponible.
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    0,00003 mmHg @20°C
  • Flash Point :

    >100°C (>212°F)
  • Molecular formula :

    C15H26O2
  • Molecular Weight :

    238,37 g/mol
  • Log P :

    6,2
  • Fusion Point :

    -33°C (-27,4°F)
  • Boiling Point :

    307°C (584,6°F)
  • Detection Threshold :

    0,5 ng/l air
Chemistry & Uses

Chemistry & Uses

Uses in perfumery :

Habanolide® is used in white floral notes, orange blossom and woody notes. Useful in marine and amber notes.
Used only in fine fragrance, especially for colognes.

Year of discovery :

Discovered in 1969. "Habanolide®" tradename has been published and protected by Firmenich SA since 05/03/1992 (brand N°584055)

Natural availability :

Habanolide® is not available in its natural state.

Isomerism :

Two diastereoisomers of Habanolide® exist. The molecule called Habanolide® is the (E) (trans) diastereoisomer of the molecule. The diastereoisomer (Z) is less used, but has a similar smell. The mixture of the two isomers is also widely used.

Synthesis precursor :

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

Synthesis route :

Habanolide® is a macrocyclic musk, close to Exaltolide®. Therefore, it can be synthesized in a similar way, by enlarging the Cyclododecenone cycle.

Stability :

Musks are very stable, as in alcoholic and in functional fragrances

Other comments :

In comparision to other musks, Habanolide® has an orange blossom note making the difference with other ones. This facet is only percievable when the molecule macerates a few weeks in its base.

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