Photo credits: ScenTree SAS

Timberol®

Woody > Ambery Woods > Ambergris > Dry Woods > Green

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

Ingredient Name	ID	Comments	Naturality	MOQ	Purity
NORLIMBANOL®	967412	Visit website	Molecules	-	-
NORLIMBANOL® DEXTRO	967406	Visit website	Molecules	-	-
LIMBEROL	NIM-1	Visit website	-	10 grs	-
TIMBER SOFT	TIM-1	Visit website	-	10 grs	-

NORLIMBANOL®

ID : 967412

Certifications : Certifications : Biodegradable (Readily)

NORLIMBANOL® DEXTRO

ID : 967406

Certifications : Certifications : Biodegradable (Readily) Certifications : Upcycled

LIMBEROL

ID : NIM-1

Certifications :

TIMBER SOFT

ID : TIM-1

Allemagne

Certifications :

General Presentation

CAS N° :
70788-30-6
EINECS number :
274-892-7
FEMA number :
Donnée indisponible.
FLAVIS number :
Donnée indisponible.

JECFA number :
Donnée indisponible.
Volatility :
Base
Price Range :
€€

Physico-chemical properties

Appearance :
Colorless liquid
Density :
0,9
Refractive Index @20°C :
Donnée indisponible.
Optical rotation :
Donnée indisponible.
Vapor pressure :
0,00051 mmHg @25°C
Flash Point :
122°C (251,6°F)

Molecular formula :
C₁₅H₃₀O
Molecular Weight :
226,4 g/mol
Log P :
5,9
Fusion Point :
Donnée indisponible.
Boiling Point :
Detection Threshold :
5,8 ng/l air

Chemistry & Uses

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.

Natural availability :

Timberol® is not available in its natural state.

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.

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.

Stability :

Stable in perfumes and diverse functional bases

Other comments :

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

Labelling

Allergens :

This ingredient does not contain any allergen.

IFRA

IFRA 51^th :

This ingredient is restricted by the 51th amendment

Restriction type :

RESTRICTION

Cause of restriction :

DERMAL SENSITIZATION AND SYSTEMIC TOXICITY

Amendment :

Quantitative limit on the use :

Cat.1	Cat.2	Cat.3	Cat.4	Cat.5 A B C D		Cat.6
0,17 %	0,071 %	0,51 %	1,3 %	0,34 % 0,34 % 0,34 % 0,11 %		0,17 %
Cat.5 A B C D			Cat.6
0,34 % 0,34 % 0,34 % 0,11 %			0,17 %
Cat.7 A B		Cat.8	Cat.9	Cat.10 A B	Cat.11 A B	Cat.12
0,51 % 0,51 %		0,11 %	2,6 %	0,68 % 4,7 %	0,11 % 0,11 %	No restriction
Cat.10 A B	Cat.11 A B	Cat.12
0,68 % 4,7 %	0,11 % 0,11 %	No restriction

Timberol®

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General Presentation

CAS N° :

EINECS number :

FEMA number :

FLAVIS number :

JECFA number :

Volatility :

Price Range :

Physico-chemical properties

Appearance :

Density :

Refractive Index @20°C :

Optical rotation :

Vapor pressure :

Flash Point :

Molecular formula :

Molecular Weight :

Log P :

Fusion Point :

Boiling Point :

Detection Threshold :