Ambrinol (CAS N° 41199-19-3)​

Photo credits: ScenTree SAS

Animalic > Ambergris > Musky > Earthy

Ambrinol

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

Ambrinol (CAS N° 41199-19-3)​

Photo credits: ScenTree SAS

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Information Générales

General Presentation

  • CAS N° : 41199-19-3

  • EINECS number : 255-256-8

  • FEMA number : Donnée indisponible.

  • FLAVIS number : 02.197

  • JECFA number : Donnée indisponible.

  • Appearance : Colorless liquid

  • Density : 0,94

  • Volatility : Base

  • Price Range : €€€€

Physico-chemical properties

  • Molecular formula : C13H22O

  • Molecular Weight : 194,32 g/mol

  • Log P : 4,2

  • Fusion Point : Donnée indisponible.

  • Boiling Point :

  • Detection Threshold : Donnée indisponible.

  • Optical rotation : Donnée indisponible

  • Vapor pressure : Donnée indisponible

  • Refractive Index @20°C : Donnée indisponible

  • Acid Value : Donnée indisponible.

  • Flash Point : >100°C (>212°F)

Utilisation

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.

Utilisation

Regulations & IFRA

Allergens :

This ingredient does not contain any allergen.

IFRA 51th :

This ingredient is not restricted for the 51th amendment

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