Photo credits: ScenTree SAS
Florol®
Florosa® ; 4-methyl-2-(2-methylpropyl)oxan-4-ol ; 2-isobutyl-4-hydroxy-4-methyltetrahydropyran ; Floral pyranol ; Floriffol ; Florosol ; Florotyl ; Flowerol ; Frescoflor ; Keflorol 90 ; Muguetol ; Pyranol ; Tetrahydro-4-methyl-2-(2-methylpropyl)pyran-4-ol
Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
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Florol - 30 Gr | - |
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- | - | - | - | - | - | |
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Pyranol | 30221242 |
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Molecule | - | - | - | - | - | |
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Pyranol BMBcert™ | 30770688 |
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Molecule | - | - | - | - | - |
Florol - 30 Gr
Certifications :
Pyranol
ID : 30221242
Certifications :
Pyranol BMBcert™
ID : 30770688
Certifications :
General Presentation
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CAS N° : 63500-71-0
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EINECS number : 405-040-6
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FEMA number : Donnée indisponible.
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FLAVIS number : Donnée indisponible.
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JECFA number : Donnée indisponible.
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Appearance : Colorless liquid
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Density : 0,952
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Volatility : Heart
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Price Range : €
Physico-chemical properties
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Molecular formula : C10H20O2
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Molecular Weight : 172,27 g/mol
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Log P : 2,22
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Fusion Point : <-100°C
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Boiling Point : 227°C
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Detection Threshold : Donnée indisponible.
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Optical rotation : Donnée indisponible
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Vapor pressure : Donnée indisponible
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Refractive Index @20°C : Donnée indisponible
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Acid Value : Donnée indisponible.
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Flash Point : >100°C (>212°F)
Uses
Uses in perfumery :
Florol® is used to replace Hydroxycitronnellal, for regulatory reasons, for lily of the valley or lilac accords in particular. However, it is less fresh and floral-lily of the valley than Hydroxycitronellal. Also used for its stability.
Year of discovery :
Discovered in 1986. ''Florol® '' tradename has been published and protected by Firmenich SA since 18/02/1988 (brand N°521114)
Natural availability :
Florol® is not available in its natural state.
Isomerism :
The molecule has an asymmetric carbon, but it is the racemic mixture of Florol® that is used in perfumery. Hydroxycitronellal is a constitutional isomer of Florol®. Moreover, these two molecules are used for the same purpose in perfumery: often for reproductions of lily of the valley notes. In compositions, Florol® tends to replace Hydroxycitronellal as it is not regulated.
Synthesis precursor :
Florol® is not a precursor to the synthesis of another compound of olfactory interest.
Synthesis route :
The synthesis of Florol® is made by cyclocondensation between 3-methyl-3-buten-1-ol and 3-methylbutanal, on silica gel and aluminum oxide, and in the presence of solvent.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment
