Javanol® (CAS N° 198404-98-7)​

Photo credits: ScenTree SAS

Woody > Sandalwood > Milky > Fatty > Rosy

Javanol®

[(1R,2S)-1-methyl-2-[[(1R,3S,5S)-1,2,2-trimethyl-3-bicyclo[3.1.0]hexanyl]methyl]cyclopropyl]methanol ; 1-methyl-2-[(1,2,2-trimethylbicyclo[3.1.0]hex-3-yl)methyl]-cyclopropanemethanol

Javanol® (CAS N° 198404-98-7)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Comments Naturality Certifications Purity Latin name Treated part Geographical origin MOQ
Quosentis logo
Javanol® - 30gr - Visit website Je me procure cet ingrédient - - - - - -

Javanol® - 30gr

Certifications :

Information Générales

General Presentation

  • CAS N° : 198404-98-7

  • EINECS number : 427-900-1

  • FEMA number : 4776

  • FLAVIS number : Donnée indisponible.

  • JECFA number : 2254

  • Appearance : Colorless viscous liquid

  • Density : 0,947

  • Volatility : Base

  • Price Range : €€€€

Physico-chemical properties

  • Molecular formula : C15H26O

  • Molecular Weight : 222,37 g/mol

  • Log P : 4,8

  • Fusion Point : Donnée indisponible.

  • Boiling Point : 271°C

  • Detection Threshold : Donnée indisponible.

  • Optical rotation : Donnée indisponible

  • Vapor pressure : Donnée indisponible

  • Refractive Index @20°C : Donnée indisponible

  • Acid Value : Donnée indisponible.

  • Flash Point : >93°C

Utilisation

Uses

Uses in perfumery :

Javanol® is used for the same reasons as Bacdanol®, and for its aromatic facet, similar to thyme. Often used in small quantities as it is a very powerful and effective ingredient.

Year of discovery :

1996

Natural availability :

Javanol® is not available in its natural state.

Isomerism :

Javanol® has several asymmetric carbons that give rise to several possible isomers. Nevertheless, it is a mixture of isomers that is used in perfumery. In addition, Javanol® is a constitutional isomer of Polysantol®. These two compounds have a similar structure, and are used for similar reasons in perfumes. Javanol® still has a less milky note than Polysantol®, but is more powerful.

Synthesis precursor :

Javanol® is not involved in the synthesis of another compound of olfactory interest.

Synthesis route :

Javanol® is synthesized by a Simmons-Smith double reaction, consisting in cyclopropanation from 2-methyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)-2-buten-1-ol. This reaction involves a catalysis with Zinc and Copper, as well as diodomethane, to convert a double bond into a cyclopropane group.

Utilisation

Regulations & IFRA

Allergens :

This ingredient does not contain any allergen.

IFRA 51th :

This ingredient is not restricted for the 51th amendment

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.