Kephalis® (CAS N° 36306-87-3)​

Photo credits: ScenTree SAS

Kephalis®

Woody > Vetiver > Ambergris > Violet Flower > Spicy

4-(1-ethoxyethenyl)-3,3,5,5-tetramethylcyclohexan-1-one ; Kephalan ; Kephalor ; Tetrambrone ; 3,3,5,5-tetramethyl-4-(1-ethoxyvinyl) cyclohexanone ; Woody cyclohexanone

Kephalis® (CAS N° 36306-87-3)​

Photo credits: ScenTree SAS



Company Ingredient Name Learn more Naturality Certifications MOQ Purity
PCW logo KEPHALIS
KE-1
Discover - 10 grs -
Quosentis logo Kephalis® - 30gr Discover - 30grs -
Tilley Distribution logo Kephalis Discover Synthetic Aroma Chemicals - -
PCW logo
KEPHALIS

KE-1

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Quosentis logo
Kephalis® - 30gr
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Tilley Distribution logo
Kephalis
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General Presentation

General Presentation

  • CAS N° :

    36306-87-3
  • EINECS number :

    252-961-2
  • FEMA number :

    Donnée indisponible.
  • FLAVIS number :

    Donnée indisponible.
  • JECFA number :

    Donnée indisponible.
  • Volatility :

    Head/Heart
  • Price Range :

    €€€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    0,947
  • Refractive Index @20°C :

    1,475 - 1,480
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    0,0034 mmHg @20°C 0,0065 mmHg @25°C
  • Flash Point :

    120°C (248°F)
  • Molecular formula :

    C14H24O2
  • Molecular Weight :

    224,34 g/mol
  • Log P :

    4,3
  • Fusion Point :

    -80°C (-112°F)
  • Boiling Point :

    272°C (521,6°F)
  • Detection Threshold :

    3,9547 ng/l air
Chemistry & Uses

Chemistry & Uses

Uses in perfumery :

Kephalis® is used in woody, ambery, masculine fragrances, leather, suede, spicy and floral notes. Gives a leather and woody appearance from the head to the base.

Year of discovery :

Data not available.

Natural availability :

Kephalis® is not available in its natural state.

Isomerism :

Kephalis® does not have any isomer used in perfumery.

Synthesis precursor :

Kephalis® is not a precursor to the synthesis of another compound of olfactory interest.

Synthesis route :

Kephalis® is one of two compounds synthesized by a cyclodimerization reaction of mesityl oxide (or 4-methylpent-3-en-2-one), in the presence of boron trifluoride etherate, by reaction with ethyl orthoformate. The other compound formed during this reaction has no olfactory interest.

Stability :

Unstable in acidic products, except fabric conditioners, and in very alkaline detergents.

Other comments :

In comparision to other woody-ambergris notes also having a violet flower undernote, Iso E Super® is more reminiscent of Cedarwood Virginia EO than Vetiver Haiti EO, in the case of Kephalis®.

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