Violiff® (CAS N° 87731-18-8)​

Photo credits: ScenTree SAS

Violiff®

Green > Fatty > Medicinal > Juicy Fruits

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

Company Ingredient Name ID Comments Naturality Certifications MOQ Purity
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VIOLIFF VIOF-2 Visit website Je me procure cet ingrédient - 10 grs -

VIOLIFF

ID : VIOF-2

Certifications :

Information Générales

General Presentation

  • CAS N° :

    87731-18-8
  • EINECS number :

    401-620-8
  • FEMA number :

    Donnée indisponible.
  • FLAVIS number :

    Donnée indisponible.
  • JECFA number :

    Donnée indisponible.
  • Volatility :

    Heart
  • Price Range :

    €€€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    Donnée indisponible.
  • Refractive Index @20°C :

    Donnée indisponible.
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    0,02307 mmHg @23°C
  • Flash Point :

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

    C10H16O3
  • Molecular Weight :

    184,24 g/mol
  • Log P :

    2,9
  • Fusion Point :

    Donnée indisponible.
  • Boiling Point :

  • Detection Threshold :

    1,9 ng/l air
Utilisation

Chemistry & Uses

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

Natural availability :

Violiff® is not available in its natural state.

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.

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.

Stability :

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

Other comments :

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

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