Fructone®
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
Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Naturality | Purity | Latin name | Treated part | Geographical origin | Certifications | Comments | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Fructone® - 30gr | - | - | - | - | - | - | more | - |
General Presentation
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CAS N° : : 6413-10-1
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EINECS number : 229-114-0
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FEMA number : 4477
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Density : 1,085
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Optical rotation : Lorem Ipsum
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Allergens : This ingredient does not contain any allergen.
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Refractive Index @20°C : Lorem Ipsum
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Volatility : Head/Heart
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Price Range : €
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Appearance : Colorless liquid
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FLAVIS number : Donnée indisponible.
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JECFA number : 1969
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 95°C
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Detection Threshold : Donnée indisponible.
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Molecular formula : C8H14O4
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Log P : 0,98
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Molecular Weight : 174,2 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : 94°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Stability :
Stable in perfumes and diverse functional bases
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
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.
Natural availability :
Fructone® is not available in its natural state.
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.
Regulations & IFRA
This ingredient is not restricted
