Orivone® (CAS N° 16587-71-6)​

Photo credits: ScenTree SAS

Woody > Dry Woods > Orris Root > Earthy > Nutty

Orivone®

Iris Hexanone ; Orris Hexanone ; 4-(2-methylbutan-2-yl)cyclohexan-1-one ; 4-tert-amyl cyclohexanone ; 4-tert-pentyl cyclohexanone ; 4-(1,1-dimethylpropyl)cyclohexanone ; Orris hexanone

Orivone® (CAS N° 16587-71-6)​

Photo credits: ScenTree SAS

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Information Générales

General Presentation

  • CAS N° : 16587-71-6

  • EINECS number : 240-642-0

  • FEMA number : Donnée indisponible.

  • FLAVIS number : Donnée indisponible.

  • JECFA number : Donnée indisponible.

  • Appearance : Colorless liquid

  • Density : 0,92

  • Volatility : Heart

  • Price Range : €€€€

Physico-chemical properties

  • Molecular formula : C11H20O

  • Molecular Weight : 168,28 g/mol

  • Log P : 3,4

  • 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 : 104°C

Utilisation

Uses

Uses in perfumery :

Orivone® is used in majority in orris root accords. It can also be used in nutty, dry woods and leather accords, to bring a dry effect and an orris root and powdery note in small quantity.

Year of discovery :

1950

Natural availability :

Orivone® is not found in nature.

Isomerism :

Orivone® is a constitutional isomer of Ethyl Linalool and so called Aldehyde C11 Lenic, but has no common facet with these two molecules.

Synthesis precursor :

Orivone® is not a precursor to the synthesis of any other molecule used in perfumery.

Synthesis route :

Orivone® can be synthesized in one step from 4-tert-amylphenol, by a selective hydrogenation reaction, catalyzed by a heterogeneous catalysor such as palladium on alumina. 4-tert-amylphenol can be taken as a starting reagent, but it can also be synthesized first by an selective alkylation reaction from phenol, on a para position, reacting with amyl chloride, with a Lewis acid catalysor.

Utilisation

Regulations & IFRA

Allergens :

This ingredient does not contain any allergen.

IFRA 51th :

This ingredient is restricted by the 51th amendment

    IFRA's logo
  • Restriction type : RESTRICTION

  • Cause of restriction : DERMAL SENSITIZATION AND SYSTEMIC TOXICITY

  • Amendment : 51

Quantitative limit on the use :
Cat.1 Cat.2 Cat.3 Cat.4
Cat.5
A B C D
Cat.6
0,027 % 0,0080 % 0,16 % 0,15 %
0,038 % 0,038 % 0,038 % 0,013 %
0,061 %
Cat.5
A B C D
Cat.6
0,038 % 0,038 % 0,038 % 0,013 %
0,061 %
Cat.7
A B
Cat.8 Cat.9
Cat.10
A B
Cat.11
A B
Cat.12
0,24 % 0,24 %
0,013 % 0,29 %
0,061 % 1,1 %
0,013 % 0,013 %
61 %
Cat.10
A B
Cat.11
A B
Cat.12
0,061 % 1,1 %
0,013 % 0,013 %
61 %
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