Osyrol® (CAS N° 41890-92-0)​

Photo credits: ScenTree SAS

Woody > Sandalwood > Milky

Osyrol®

Acsantol ; Dihydromethoxyelgenol ; 3,7-dimethyl-7-methoxy-2-octanol ; 3,7-dimethyl-7-methoxyoctan-2-ol ; Elesant ; 7-methoxy-3,7-dimethyloctan-2-ol ; Methoxyelgenol ; Methoxytrimethylheptanol ; Osirol ; Sandal octanol

Osyrol® (CAS N° 41890-92-0)​

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.

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.

Information Générales

General Presentation

  • CAS N° :

    41890-92-0
  • EINECS number :

    255-574-7
  • FEMA number :

    Donnée indisponible.
  • FLAVIS number :

    Donnée indisponible.
  • JECFA number :

    Donnée indisponible.
  • Volatility :

    Base
  • Price Range :

    €€
Physico-chemical properties

Physico chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    0,9
  • Refractive Index @20°C :

    Data not available.
  • Optical rotation :

    Data not available.
  • Vapor pressure :

    Data not available.
  • Flash Point :

    >110°C (>230°F)
  • Molecular formula :

    C11H24O2
  • Molecular Weight :

    188,31 g/mol
  • Log P :

    2,76
  • Fusion Point :

    8°C
  • Boiling Point :

    230°C
  • Detection Threshold :

    Donnée indisponible.
Utilisation

Chemistry & Uses

Year of discovery :

1972

Natural availability :

Osyrol® is not reported as found in nature, and can thus not be extracted from any plant.

Isomerism :

Osyrol® has two asymmetric carbons. This gives birth to four possible isomers for this molecule. A mixture of these isomers is used in perfumery.

Synthesis precursor :

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

Synthesis route :

Osyrol® synthesis is done starting from Dihydromyrcene, reacting it with hydrochloric acid during a hydrochlorination reaction. The obtained chlorinated compound undergoes methoxylation using methyl iodide, in the presence of lithium carbonate for example. Subsequently, an epoxidation reaction is carried out, reacting the remaining alcene function with a peracid, forming the epoxide. This epoxide can be hydrogenated in the presence of Raney nickel and trimethylamine, to obtain final Osyrol®.

Stability :

Stable in perfumes and various functionnal bases.

Other comments :

Osyrol® is a milky sandalwood note that does not have a real distinctive undernote, as Javanol® and Sandalore® for example.

Utilisation

Regulations & IFRA

Allergens :

This ingredient does not contain any allergen.

IFRA 51th :

This ingredient is not restricted for the 51th amendment

I am a chocolate hazelnut cookie. I come out of the oven. Impossible to refuse me.
This website is using cookies
Our website uses cookies for statistics, performance, and security. These anonymous data allow us to give you an optimal navigation experience. You can always disable cookies in your browser settings.