Photo credits: ScenTree SAS

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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

Ingredient Name	ID	Comments	Naturality	MOQ	Purity
Florol - 30 Gr	-	Visit website	-	-	-
Pyranol	30221242	Visit website	Molecule	-	-
Pyranol BMBcert™	30770688	Visit website	Molecule	-	-

Florol - 30 Gr

Certifications :

Pyranol

ID : 30221242

Certifications :

Pyranol BMBcert™

ID : 30770688

Certifications :

General Presentation

CAS N° :
63500-71-0
EINECS number :
405-040-6
FEMA number :
Donnée indisponible.
FLAVIS number :
Donnée indisponible.

JECFA number :
Donnée indisponible.
Volatility :
Heart
Price Range :
€

Physico chemical properties

Appearance :
Colorless liquid
Density :
0,952
Refractive Index @20°C :
1,455 – 1,460
Optical rotation :
Data not available.
Vapor pressure :
0,0486 hPa @20°C
Flash Point :
>100°C (>212°F)

Molecular formula :
C₁₀H₂₀O₂
Molecular Weight :
172,27 g/mol
Log P :
2,22
Fusion Point :
<-100°C
Boiling Point :
227°C
Detection Threshold :
Donnée indisponible.

Chemistry & 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.

Stability :

Unstable in acidic products, except in fabric conditioners, and in alkaline products, except powder detergents.

Other comments :

Unlike Hydroxycitronellal, Florol® is not regulated or allergenic.

Florol®

I buy this ingredient

General Presentation

CAS N° :

EINECS number :

FEMA number :

FLAVIS number :

JECFA number :

Volatility :

Price Range :

Physico chemical properties

Appearance :

Density :

Refractive Index @20°C :

Optical rotation :

Vapor pressure :

Flash Point :

Molecular formula :

Molecular Weight :

Log P :

Fusion Point :

Boiling Point :

Detection Threshold :

Chemistry & Uses

Uses in perfumery :

Year of discovery :

Natural availability :

Isomerism :

Synthesis precursor :

Synthesis route :

Stability :

Other comments :

Regulations & IFRA

Allergens :

IFRA 51^th :

Florol®

I buy this ingredient

I buy this ingredient

General Presentation

CAS N° :

EINECS number :

FEMA number :

FLAVIS number :

JECFA number :

Volatility :

Price Range :

Physico chemical properties

Appearance :

Density :

Refractive Index @20°C :

Optical rotation :

Vapor pressure :

Flash Point :

Molecular formula :

Molecular Weight :

Log P :

Fusion Point :

Boiling Point :

Detection Threshold :

Chemistry & Uses

Uses in perfumery :

Year of discovery :

Natural availability :

Isomerism :

Synthesis precursor :

Synthesis route :

Stability :

Other comments :

Regulations & IFRA

Allergens :

IFRA 51th :

IFRA 51^th :