Fructone® (CAS N° 6413-10-1)​

Photo credits: ScenTree SAS

Fructone®

Fruity > Green Fruits > Butyric > Tropical Fruits

Jasmaprunate® ; Aplifine® ; Frutimety® ; Methyl Dioxolan ; Applinal® ; Ethyl 2-(2-methyl-1,3-dioxolan-2-yl) acetate ; Apple ketal ; Applinal ; Applitone ; Ethyl aceto acetate EG acetal ; Ethyl acetoacetate ethylene glycol ketal ; Ethyl-2-methyl-1,3-dioxolane-2-acetate ; Fragolan ; Frutinal ; Ketopommal ; Methyldioxolan

Fructone® (CAS N° 6413-10-1)​

Photo credits: ScenTree SAS



Company Ingredient Name Learn more Naturality Certifications MOQ Purity
PCW logo FRUCTONE
FRUC-1
Discover - 10 grs 98.0 - 100.0
Quosentis logo Fructone® - 30gr Discover - 30grs -
Tilley Distribution logo Fructone Discover Synthetic Aroma Chemicals - -
PCW logo
FRUCTONE

FRUC-1

Discover
Quosentis logo
Fructone® - 30gr
Discover
Tilley Distribution logo
Fructone
Discover
General Presentation

General Presentation

  • CAS N° :

    6413-10-1
  • EINECS number :

    229-114-0
  • FEMA number :

    4477
  • FLAVIS number :

    Donnée indisponible.
  • JECFA number :

    1969
  • Volatility :

    Head/Heart
  • Price Range :

Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    1,085
  • Refractive Index @20°C :

    1,431 – 1,435
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    0,0477 mmHg @23°C
  • Flash Point :

    94°C (201,2°F)
  • Molecular formula :

    C8H14O4
  • Molecular Weight :

    174,2 g/mol
  • Log P :

    0,98
  • Fusion Point :

    Donnée indisponible.
  • Boiling Point :

    95°C (203°F)
  • Detection Threshold :

    Donnée indisponible.
Chemistry & Uses

Chemistry & Uses

Uses in perfumery :

Fructone® is used in fruity notes for all types of fruit. Useful in rose notes for a fruity nuance, in green, aromatic and marine notes. if overdosed, addition of a fermented facet.

Year of discovery :

1938

Natural availability :

Fructone® is not available in its natural state.

Isomerism :

Fructone® does not have an isomer used in perfumery.

Synthesis precursor :

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

Synthesis route :

Fructone® and an acetal of Ethyl Acetoacetate (synthesis from formic acid and acetone in its enol form), obtained by reaction between this reagent and ethylene glycol.

Stability :

Stable in perfumes and diverse functional bases

Other comments :

Data not available.

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