Methyl heptyl ketone (CAS N° 821-55-6)​

Photo credits: ScenTree SAS

Methyl heptyl ketone

Fruity > Green Fruits > Butyric > Fatty > Etheric Solvent

2-Nonanone

Methyl heptyl ketone (CAS N° 821-55-6)​

Photo credits: ScenTree SAS



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Tilley Distribution logo 2-Nonanone natural/Methyl Heptyl Ketone natural Discover Natural Aroma Chemicals - -
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2-Nonanone natural/Methyl Heptyl Ketone natural
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Methyl Heptyl Ketone/2-Nonanone
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General Presentation

General Presentation

  • CAS N° :

    821-55-6
  • EINECS number :

    212-480-0
  • FEMA number :

    2785
  • FLAVIS number :

    7,02
  • JECFA number :

    292
  • Volatility :

    Heart/Base
  • Price Range :

    €€€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    0,82
  • Refractive Index @20°C :

    1,418 – 1,423
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    Donnée indisponible.
  • Flash Point :

    79°C (174,2°F)
  • Molecular formula :

    C9H18O   
  • Molecular Weight :

    142,24 g/mol
  • Log P :

    2,71
  • Fusion Point :

    -21°C (-5,8°F)
  • Boiling Point :

    193°C (379,4°F)
  • Detection Threshold :

    Donnée indisponible.
Chemistry & Uses

Chemistry & Uses

Uses in perfumery :

Year of discovery :

Data not available.

Natural availability :

Methyl Heptyl Ketone is present in fruits and spice such as banana, ginger, clove, coconut, tomato, corn, cheese, wine.. Thus, natural qualities are available

Isomerism :

Methyl Heptyl Ketone is the constitutional isomer of Cinnamaldehyde, although these two molecules do not smell the same.

Synthesis precursor :

A condensation of this ketone with another ketone may form the desired alkene. Hydrogenation of Methyl Heptyl Ketone can form 2-nonanol, also relevant in perfumery.

Synthesis route :

Methyl Heptyl Ketone can be synthesized by dry distillation of Barium Caprylate and Barium acetate at very low pressure (0.5 to 2 mmHg). Another method for synthesizing this compound is to use chromic acid, reacting with methyl heptyl carbinol at room temperature, to oxidize the latter.

Stability :

Stable in perfumes and in diverse bases.

Other comments :

Data not available.

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