Musky > Tea

Muscenone®

(5E)-3-methylcyclopentadec-5-en-1-one ; 3-methyl cyclopentadecenone ; 3-methyl-5-cyclopentadecen-1-one ; Muscanona ; 3-methyl-5-cyclopentadecen-1-one ; Muscemor® ; Muskeynone

Muscenone® (CAS N° 82356-51-2)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Naturality Purity Latin name Treated part Geographical origin Certifications Comments MOQ
Quosentis logo
Muscenone - 30 Gr - - - - - - more -
Information Générales

General Presentation

  • CAS N° : : 82356-51-2

  • EINECS number : 429-900-5

  • FEMA number : Donnée indisponible.

  • Density : 0,93

  • 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 :

  • Detection Threshold : Donnée indisponible.

  • Molecular formula : C16H28O

  • Log P : 4,88

  • Molecular Weight : 236,39 g/mol

  • Fusion Point : Donnée indisponible.

  • Flash Point : >100°C (>212°F)

  • Vapor pressure : Lorem Ipsum

Utilisation

Uses

Other comments :

Muscenone® is slightly more powerful than Muscone®, with a similar structure.

Stability :

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

Uses in perfumery :

Muscenone® is used only in fine fragrance for all types of accords, especially musky, leather, chypre, fairly heavy and warm notes.
Gives volume when mixed with other musks.

Year of discovery :

Discovered in 1967. 'Muscenone®' trademark has been published and protected by Firmenich SA since 28/01/2011 (brand N°1069869)

Isomerism :

The molecule has a double bond that gives rise to two possible diastereoisomers with similar smells. It is the mixture of the two isomers that is used in perfumery. Sandela®, Cedramber® and Ambroxan® are constitutional isomers of Muscenone®. Their smell is however very different, as it is woody and ambery, instead of musky. Velvione®, on the other hand, has a structure that is relatively similar to Muscenone® and is its constitutional isomer. This explains the musky aspect shared by both molecules.

Synthesis precursor :

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

Natural availability :

Muscenone® is not available in its natural state.

Synthesis route :

Muscenone® is a macrocyclic musk synthesized from cyclododecanone. A synthesis in several steps allows to synthesize 14-methyl-16-oxabicyclo [10.3.1] hexadec-1(15)-ene. This compound can finally be isomerized in the presence of phosphoric acid to give the racemic mixture of Muscenone®.

Utilisation

Regulations & IFRA

This ingredient is not restricted

I am a chocolate hazelnut cookie. I come out of the oven. Impossible to refuse me.
This website is using cookies
Our website uses cookies for statistics, performance, and security. These anonymous data allow us to give you an optimal navigation experience. You can always disable cookies in your browser settings.