Fraistone® (CAS N° 6290-17-1)​

Photo credits: ScenTree SAS

Fraistone®

Fruity > Green Fruits > Anisic > Green

Fragolane® ; Dimethyl Dioxolan ; Fraisberry® ; Ethyl 2-(2,4-dimethyl-1,3-dioxolan-2-yl) acetate ; 2,4-dimethyl-1,3-dioxolane-2-ethyl acetate ; Dimethyldioxolan ; Ethyl 2-(2,4-dimethyl-1,3-dioxolan-2-yl)acetate ; Ethyl aceto acetate PG acetal ; Ethyl acetoacetate propylene glycol ketal ; Fructone B ; Fruity ketal ; Propyl fruitat ; Strawberry ketal

Fraistone® (CAS N° 6290-17-1)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Comments Naturality Certifications MOQ Purity
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FRAISTONE FRASTN-1 Visit website Je me procure cet ingrédient - 10 grs 97 - 100

FRAISTONE

ID : FRASTN-1

Certifications :

Information Générales

General Presentation

  • CAS N° :

    6290-17-1
  • EINECS number :

    228-536-2
  • FEMA number :

    4294
  • FLAVIS number :

    06.087
  • JECFA number :

    1715
  • Volatility :

    Head/Heart
  • Price Range :

    €€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    1,042
  • Refractive Index @20°C :

    1,422 – 1,432
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    0,0589 mmHg @23°C
  • Flash Point :

    91°C (195,8°F)
  • Molecular formula :

    C9H16O4
  • Molecular Weight :

    188,22 g/mol
  • Log P :

    1,5
  • Fusion Point :

    -68°C (-90,4°F)
  • Boiling Point :

    85°C (185°F)
  • Detection Threshold :

    Donnée indisponible.
Utilisation

Chemistry & Uses

Uses in perfumery :

Fraistone® is used in fruity and floral notes of fruity rose, tuberose, jasmine, orange blossom and syringua.

Year of discovery :

1937

Natural availability :

Fraistone® is not available in its natural state.

Isomerism :

Fraistone® has two asymmetric carbons. It is however a mixture of isomers that is used in perfumery.

Synthesis precursor :

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

Synthesis route :

Fraistone® is an acetal of Ethyl Acetoacetate (a synthesis based on formic acid and acetone in its enolic form). It is obtained by reaction between this reagent and propan-1,2-diol.

Stability :

Stable in perfumes and diverse functional bases

Other comments :

Data not available.

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