Photo credits: ScenTree SAS
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General Presentation
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CAS N° : : 5182-36-5
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EINECS number : 225-963-6
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FEMA number : Donnée indisponible.
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Density : 1,02
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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 : Donnée indisponible.
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 93°C (à 3 mbar)
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Detection Threshold : Donnée indisponible.
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Molecular formula : C13H18O2
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Log P : 2,8
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Molecular Weight : 206,28 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : 114°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Comparing it to Styrallyl acetate and Rhubafuran® for example, Floropal® has a much less green note than these two components.
Stability :
Stable in perfumes and diverse functional bases
Uses in perfumery :
Floropal® is used in all types of perfumes, in rhubarb, grapefruit, blackcurrant, raspberry, green and tomato leaf notes.
Year of discovery :
1966
Isomerism :
Floropal® contains two asymmetric carbons. One of the most powerful isomers is present at around 60% in marketed Floropal®. A distillation allows to increase the proportion and the obtained product is called Floropal® Heart. IsoAmyl Phenyl acetate is a constitutional isomer of Floropal®. However, they do not share the same smell, rosy and gourmand in the case of IsoAmyl Phenyl acetate.
Synthesis precursor :
Floropal® is not a precursor to the synthesis of another compound of olfactory interest.
Natural availability :
Floropal® is not available in its natural state.
Synthesis route :
Floropal® is synthesized by a Prins reaction, reacting acetaldehyde with alpha-methylstyrene, in an acid medium. The synthesis is done in one step.
Regulations & IFRA
This ingredient is not restricted
