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.
General Presentation
-
CAS N° :
22629-49-8 -
EINECS number :
245-142-6 -
FEMA number :
Donnée indisponible. -
FLAVIS number :
Donnée indisponible.
-
JECFA number :
Donnée indisponible. -
Volatility :
Base -
Price Range :
€€€
Physico chemical properties
-
Appearance :
Pale yellow liquid -
Density :
0,84 -
Refractive Index @20°C :
Data not available. -
Optical rotation :
Data not available. -
Vapor pressure :
Data not available. -
Flash Point :
>93°C
-
Molecular formula :
C13H23N -
Molecular Weight :
193,33 g/mol -
Log P :
Donnée indisponible. -
Fusion Point :
Donnée indisponible. -
Boiling Point :
289°C -
Detection Threshold :
Donnée indisponible.
Chemistry & Uses
Year of discovery :
Data not available.
Natural availability :
Ozonil® is not reported as found in nature, and can thus not be extracted from any plant.
Isomerism :
Ozonil® has one double bond giving birth to two possible diastereoisomers. In perfumery, a mixture of these two isomers is used.
Synthesis precursor :
Ozonil® is not a precursor for the synthesis of another material used in perfumery.
Synthesis route :
Ozonil® is prepared by a Knoevenagel condensation between Aldehyde C-11 Undecylic and cyanoacetic acid. A decarboxylation reaction (use of high heat and decarboxylase enzym) is then carried out to form the alcene function of the final product, Ozonil®.
Stability :
Stable in perfumes and various functionnal bases.
Other comments :
Ozonil® is the only molecule combining a zesty smell of tangerine with a marine odor. It is a unique material.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment
