Methyl octine carbonate (CAS N° 111-80-8)​

Photo credits: ScenTree SAS

Methyl octine carbonate

Green > Fatty > Mushroom > Juicy Fruits

MOC ; Methyl non-2-ynoate ; Methyl 2-nonynoate ; Methyl octyne carbonate ; 2-nonynoic acid methyl ester

Methyl octine carbonate (CAS N° 111-80-8)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Comments Naturality Certifications MOQ Purity
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METHYL OCTINE CARBONATE OCM-1 Visit website Je me procure cet ingrédient - 10 grs -

METHYL OCTINE CARBONATE

ID : OCM-1

Certifications :

Information Générales

General Presentation

  • CAS N° :

    111-80-8
  • EINECS number :

    203-909-2
  • FEMA number :

    2726
  • FLAVIS number :

    09.156
  • JECFA number :

    1356
  • Volatility :

    Heart
  • Price Range :

    €€€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    0,921
  • Refractive Index @20°C :

    Donnée indisponible.
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    Donnée indisponible.
  • Flash Point :

    101°C (213,8°F)
  • Molecular formula :

    C10H16O2
  • Molecular Weight :

    168,24 g/mol
  • Log P :

    4
  • Fusion Point :

    Donnée indisponible.
  • Boiling Point :

    122°C (251,6°F)
  • Detection Threshold :

    Donnée indisponible.
Utilisation

Chemistry & Uses

Uses in perfumery :

Methyl Octine Carbonate is used in notes of violet flower, tuberose, linden and mimosa. A green facet with fruity notes. Used in combination with green notes and ionones.

Year of discovery :

1903

Natural availability :

Methyl Octine Carbonate is not available in its natural state.

Isomerism :

Jasmolactone is a constitutional isomer of Methyl Octine Carbonate. Its smell is however very different, as it is reminiscent of peach and jasmine.

Synthesis precursor :

Methyl Octine Carbonate is not a precursor to the synthesis of another compound of olfactory interest.

Synthesis route :

Methyl Octine Carbonate is synthesized by an esterification reaction between non-2-ynoic acid and methanol. This reaction is catalysed by the presence of a strong concentrated acid such as sulfuric acid.

Stability :

May form octine carbonic acid through time, under the effect of heat.
Unstable in acidic products, except antiperspirants, and very alkaline products

Other comments :

In comparision to other green notes of Violet Leaf Absolute as Folione® or Violiff®, Methyl Octine Carbonate has a clear mushroom note.

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