Green > Fatty > Medicinal > Juicy Fruits

Violiff®

Violet T® ; Violet methyl carbonate ; [(4Z)-1-cyclooct-4-enyl] methyl carbonate ; Cyclooct-4-enyl methyl carbonate ; Violet ester

Violiff® (CAS N° 87731-18-8)​

Photo credits: ScenTree SAS

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Information Générales

General Presentation

  • CAS N° : : 87731-18-8

  • EINECS number : 401-620-8

  • FEMA number : Donnée indisponible.

  • Density : Donnée indisponible.

  • Optical rotation : Lorem Ipsum

  • Allergens : This ingredient does not contain any allergen.

  • Refractive Index @20°C : Lorem Ipsum

  • Volatility : Heart

  • Price Range : €€€

  • Appearance : Colorless liquid

  • FLAVIS number : Donnée indisponible.

  • JECFA number : Donnée indisponible.

Information on synthetic ingredients

  • Acid Value : Lorem Ipsum

  • Boiling Point :

  • Detection Threshold : 1,9 ng/l air

  • Molecular formula : C10H16O3

  • Log P : 2,9

  • Molecular Weight : 184,24 g/mol

  • Fusion Point : Donnée indisponible.

  • Flash Point : 110°C

  • Vapor pressure : Lorem Ipsum

Utilisation

Uses

Other comments :

Usually, Folione® among other molecules, is used in violet leaf reproductions, because Violiff® has a less characteristic smell.

Stability :

May form acidic compounds in stability, under the effect of heat.
Terpenes are subjected to polymerization under the effect of a strong oxydation.

Uses in perfumery :

Violiff® is used in violet leaf notes, to bring a fresh, heady and aromatic effect, and for a more medicinal note.

Year of discovery :

1981

Isomerism :

Violiff® has two asymmetric carbons. Nevertheless, the ingredient used in perfumery is a mix of those two enantiomers.

Synthesis precursor :

Violiff® is not a precursor to the synthesis of antoher compound of olfactory interest.

Natural availability :

Violiff® is not available in its natural state.

Synthesis route :

Violiff® can be synthesized by an esterification reaction between methanol and a racemic mixture of carbonic [(4Z)-1-cyclooct-4-ène] acid enantiomers. This reaction has to be catalyzed by the presence of a strong acid such as concentrated sulfuric acid.

Utilisation

Regulations & IFRA

This ingredient is not restricted

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