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
Photo credits: ScenTree SAS
Do you sell any of the raw materials? Would you like to let our users know?
Send an email to fournisseurs@scentree.coto learn about our advertising opportunities.
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
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.
Regulations & IFRA
-
IFRA 51th : This ingredient is restricted by IFRA
This ingredient is not restricted for the 49th amendment