Photo credits: ScenTree SAS

Ambrinol

Animalic > Ambergris > Musky > Earthy

Ambrinol S ; Amber naphtalenol ; Ambrinol-alpha ; Alpha-ambrinol ; Ambrinol 95 ; 2-hydroxy-2,5,5-trimethyl-1,2,3,4,4a,5,6,7-octahydronaphtalene ; 1,2,3,4,4a,5,6,7-octahydro-2,5,5-trimethyl-2-naphtalenol ; 2,5,5-trimethyl-octahydro-2-naphtalenol

Photo credits: ScenTree SAS

Company	Ingredient Name	ID	Comments	Naturality	Certifications	MOQ	Purity
	AMBRINOL	908930	Visit website	Molecules		-	-
	AMBRINOL	AMBRI-1	Visit website	-		10 grs	-

AMBRINOL

ID : 908930

Certifications : Certifications : Biodegradable (Ultimately)

AMBRINOL

ID : AMBRI-1

Certifications :

General Presentation

CAS N° :
41199-19-3
EINECS number :
255-256-8
FEMA number :
Donnée indisponible.
FLAVIS number :
02.197

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

Physico-chemical properties

Appearance :
Colorless liquid
Density :
0,94
Refractive Index @20°C :
Donnée indisponible.
Optical rotation :
Donnée indisponible.
Vapor pressure :
0,003 mmHg @23°C
Flash Point :
>100°C (>212°F)

Molecular formula :
C₁₃H₂₂O
Molecular Weight :
194,32 g/mol
Log P :
4,2
Fusion Point :
Donnée indisponible.
Boiling Point :
Detection Threshold :
Donnée indisponible.

Chemistry & Uses

Uses in perfumery :

Ambrinol is used to reproduce the natural Ambergris smell, bringing an animalic, sensual and ambery note, with a fixative effect.

Year of discovery :

Data not available.

Natural availability :

Ambrinol is one of the components of Ambergris, previously used for its sensual and animalic notes, and extracted as a tincture in alcohol. Then, only synthetic Ambrinol is used for perfumery.

Isomerism :

Ambrinol frequently used in perfumes is Alpha-Ambrinol. Beta-Ambrinol also exists, but is much less used. On the other hand, Ambrinol has one asymmetric carbon, giving birth to two possible enantiomers for this molecule. It is anyway a mixture of these isomers that is used in perfumery. Eventually, Ambrinol also is a constitutional isomer of DihydroBeta-ionone, also prepared from Beta-Ionone.

Synthesis precursor :

Ambrinol is not a precursor for the synthesis of another material used in perfumery.

Synthesis route :

Ambrinol can be synthesized thanks to Beta-Ionone. This molecule can undergo thermolysis (chemical decomposition under the effect of heat), bringing dehydroambrinol. Hydrogenation in methanol, in the presence of Raney nickel catalysor leads to Ambrinol.

Stability :

Stable in perfumes and various functionnal bases.

Other comments :

Ambrinol can be compared with Ambrein or DihydroBeta-Ionone, as it is used to reproduce the smell of natural Ambergris.

Labelling

Allergens :

This ingredient does not contain any allergen.

IFRA

IFRA 51^th :

This ingredient is not restricted for the 51th amendment

Ambrinol

I buy this ingredient

I buy this ingredient

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 :