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.
General Presentation
-
CAS N° : : 166432-52-6
-
EINECS number : 417-840-2
-
FEMA number : --
-
Density : 0,845 - 0,855
-
Optical rotation : Lorem Ipsum
-
Allergens : This ingredient does not contain any allergen.
-
Refractive Index @20°C : Lorem Ipsum
-
Volatility : Head
-
Price Range : Data not available.
-
Appearance : Colorless to pale yellow liquid
-
FLAVIS number : Donnée indisponible.
-
JECFA number : Donnée indisponible.
Information on synthetic ingredients
-
Acid Value : Lorem Ipsum
-
Boiling Point :
-
Detection Threshold : 1,1 ng/l air
-
Molecular formula : C11H16
-
Log P : 5,11
-
Molecular Weight : 148,24 g/mol
-
Fusion Point : Donnée indisponible.
-
Flash Point : 77°C
-
Vapor pressure : Lorem Ipsum
Uses
Other comments :
The Violettyne is marketed while being diluted in the MIP, it is thus generally found under the name of ''Violettyne MIP ''. This dilution ensures its stability and allows a better use (very strong intensity)
Stability :
Stable
Uses in perfumery :
It can replace Methyl Octine or Methyl Heptine Carbonate, or be used as a new fresh green note.
A very stable and powerful green violet leaf note with a unique cucumber or bell pepper aspect.
Year of discovery :
1978 Brevet EP 0694604 registered in 1997 by Firmenich & CIE
Isomerism :
1,3-undecadien-5-yne (Violettyne) is present as either one of its (E) or (Z) configuration isomers or as a mixture of the two. In the case of a mixture, the (E) form has to takes the majority.
Synthesis precursor :
Violettyne is a synthesis intermediary for galbanolene (1,3,5-undecatriene) and its isomers.
Natural availability :
Violettyne is not available in its natural state
Synthesis route :
Full synthesis detailed here : https://doi.org/10.1002/hlca.19750580406
Regulations & IFRA
This ingredient is not restricted