Woody > Ambery Woods > Ambergris > Dry Woods > Green

Timberol®

Norlimbanol® ; Karmawood® ; 1-(2,2,6-trimethylcyclohexyl)hexan-3-ol ; Dextramber ; Fine timber ; Nimberlan ; Nimberol ; Nirlimberol ; Timber forte ; Timber propanol ; Timber touch ; Timberone ; Trimethyl propyl cyclohexane propanol ; Woodamber

Timberol® (CAS N° 70788-30-6)​

Photo credits: ScenTree SAS

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Information Générales

General Presentation

  • CAS N° : : 70788-30-6

  • EINECS number : 274-892-7

  • FEMA number : Donnée indisponible.

  • Density : 0,9

  • 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 : 5,8 ng/l air

  • Molecular formula : C15H30O

  • Log P : 5,9

  • Molecular Weight : 226,4 g/mol

  • Fusion Point : Donnée indisponible.

  • Flash Point : 122°C

  • Vapor pressure : Lorem Ipsum

Utilisation

Uses

Other comments :

In comparision to other ambergris and woody notes as Ambermax 50® and Boisambrene Forte®, Timberol® has a distinctive green note.

Stability :

Stable in perfumes and diverse functional bases

Uses in perfumery :

Timberol® is used in masculine, woody, ambery, leather, fougere and citrus notes. Often used in detergents and other alkaline bases because it is very stable.

Year of discovery :

Discovered in 1978.

Isomerism :

Timberol® does not have any isomer used in perfumery.

Synthesis precursor :

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

Natural availability :

Timberol® is not available in its natural state.

Synthesis route :

The synthesis of Timberol® consists of several stages. The first is an aldolization reaction between Citral and 2-pentanone (in the presence of a basic substance), followed by a cyclization of the aldol obtained by a phosphoric acid, and then a hydrogenation of the compound obtained with a Raney nickel catalysis.

Utilisation

Regulations & IFRA

  • IFRA 51th : This ingredient is restricted by IFRA

  • This ingredient is not restricted for the 49th amendment

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