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

Photo credits: ScenTree SAS

Methyl octine carbonate

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 - Learn more Je me procure cet ingrédient - 10 grs -

METHYL OCTINE CARBONATE

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 :

    Data not available.
  • Optical rotation :

    Data not available.
  • Vapor pressure :

    Data not available.
  • 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.

Utilisation

IFRA

IFRA 51th :

This ingredient is restricted by the 51th amendment

    IFRA's logo
  • Restriction type :

    RESTRICTION
  • Cause of restriction :

    DERMAL SENSITIZATION
  • Amendment :

    49
Quantitative limit on the use :
Cat.1 Cat.2 Cat.3 Cat.4
Cat.5
A B C D
Cat.6
0,0018 % 0,00055 % 0,011 % 0,01 %
0,0026 % 0,0026 % 0,0026 % 0,0026 %
0,0061 %
Cat.5
A B C D
Cat.6
0,0026 % 0,0026 % 0,0026 % 0,0026 %
0,0061 %
Cat.7
A B
Cat.8 Cat.9
Cat.10
A B
Cat.11
A B
Cat.12
0,021 % 0,021 %
0,0011 % 0,02 %
0,072 % 0,072 %
0,04 % 0,04 %
No Restriction
Cat.10
A B
Cat.11
A B
Cat.12
0,072 % 0,072 %
0,04 % 0,04 %
No Restriction
  • Restricted ingredients: notes
    When used in the same fragrance compound within a specific QRA category, the sum total of and Methyl heptine carbonate (MHC, CAS number 111-12-6) and Methyl octine carbonate (MOC, CAS number 111-80-8) contributions must not exceed the maximum permitted level for MHC. At the same time, the contribution from MOC should always respect the maximum levels permitted as listed in the table above.
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