Musky > Berries > Orange Blossom

Habanolide®

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

Habanolide® (CAS N° 111879-80-2)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Naturality Purity Latin name Treated part Geographical origin Certifications Comments MOQ
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Habanolide® - 30gr - - - - - - more -
Information Générales

General Presentation

  • CAS N° : : 111879-80-2

  • EINECS number : 422-320-3

  • FEMA number : Donnée indisponible.

  • Density : 0,964

  • Optical rotation : Lorem Ipsum

  • Allergens : This ingredient does not contain any allergen.

  • Refractive Index @20°C : Lorem Ipsum

  • Volatility : Base

  • Price Range : €€€

  • Appearance : Colorless liquid

  • FLAVIS number : Donnée indisponible.

  • JECFA number : Donnée indisponible.

Information on synthetic ingredients

  • Acid Value : Lorem Ipsum

  • Boiling Point : 307°C

  • Detection Threshold : 0,5 ng/l air

  • Molecular formula : C15H26O2

  • Log P : 6,2

  • Molecular Weight : 238,37 g/mol

  • Fusion Point : -33°C

  • Flash Point : >100°C (>212°F)

  • Vapor pressure : Lorem Ipsum

Utilisation

Uses

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.

Stability :

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

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)

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.

Natural availability :

Habanolide® is not available in its natural state.

Synthesis route :

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

Utilisation

Regulations & IFRA

This ingredient is not restricted

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