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Violettyne

1,3-Undecadien-5-yne ; (3Z)-undeca-1,3-dien-5-yne

Violettyne (CAS N° 166432-52-6)​

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Information Générales

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

Utilisation

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

Utilisation

Regulations & IFRA

This ingredient is not restricted

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