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| Company | Ingredient Name | ID | Comments | Naturality | Certifications | MOQ | Purity |
|---|---|---|---|---|---|---|---|
|
FLOROPAL | - |
Visit website
|
- | 10 grs | - |
General Presentation
-
CAS N° :
5182-36-5 -
EINECS number :
225-963-6 -
FEMA number :
Donnée indisponible. -
FLAVIS number :
Donnée indisponible.
-
JECFA number :
Donnée indisponible. -
Volatility :
Head/Heart -
Price Range :
€€
Physico-chemical properties
-
Appearance :
Colorless liquid -
Density :
1,02 -
Refractive Index @20°C :
1.501 - 1.506 -
Optical rotation :
Data not available. -
Vapor pressure :
0.0075 mmHg @20°C -
Flash Point :
114°C (237,2°F)
-
Molecular formula :
C13H18O2 -
Molecular Weight :
206,28 g/mol -
Log P :
2,8 -
Fusion Point :
Donnée indisponible. -
Boiling Point :
93°C (199,4°F) -
Detection Threshold :
Donnée indisponible.
Chemistry & Uses
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
Natural availability :
Floropal® is not available in its natural state.
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.
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.
Stability :
Stable in perfumes and diverse functional bases
Other comments :
Comparing it to Styrallyl acetate and Rhubafuran® for example, Floropal® has a much less green note than these two components.
IFRA
IFRA 51th :
This ingredient is not restricted for the 51th amendment
