Photo credits: ScenTree SAS

Floral > Light Flowers > Aldehydes > Juicy Fruits > Ozonic

Florhydral®

3-(3-Isopropylphenyl)butanal ; Floral butanal ; 3-(3-(1-methylethyl)phenyl)benzene propanal ; 3-(3-propan-2-ylphenyl)butanal ; Isopropyl phenyl butanal ; Isopropylmethylbenzene propanal

Photo credits: ScenTree SAS

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General Presentation

CAS N° :
125109-85-5
EINECS number :
412-050-4
FEMA number :
Donnée indisponible.
FLAVIS number :
Donnée indisponible.

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

Physico chemical properties

Appearance :
Colorless liquid
Density :
0,95
Refractive Index @20°C :
Data not available.
Optical rotation :
Data not available.
Vapor pressure :
Data not available.
Flash Point :
68°C

Molecular formula :
C₁₃H₁₈O
Molecular Weight :
190,29 g/mol
Log P :
3,8
Fusion Point :
Donnée indisponible.
Boiling Point :
257°C
Detection Threshold :
0,07 ng/l air

Chemistry & Uses

Uses in perfumery :

Florhydral® is generally used to create lily of the valley or hyacinth notes. It is especially used for reformulating Lilial®-containing perfumes. Its notes give it a good synergy with citrus notes. Used in all kinds of perfumes.

Year of discovery :

Patent N°4,910,346 (US) published on Nov. 10, 1988 by Chalk.A for Givaudan Corp.

Natural availability :

Florhydral® does not exist on a natural state. Thus, it can't be used as extracted from a plant.

Isomerism :

Florhydral® has an asymmetric carbon, giving birth to two possible enantiomers. It is anyway a blend of these two isomers that is used in perfumery. Florhydral® also is a positional isomer of Cyclamen Aldehyde, which has a relatively close smell, although more marine.

Synthesis precursor :

Florhydral® is not used for the synthesis of another molecule of olfactive interest.

Synthesis route :

Florhydral® can be synthesized by a hydroformylation reaction of 1,3-diisopropenylbenzene, using carbon monoxide and hydrogen to form an aldehydic group, starting from an alcene group.

Stability :

Stable in perfumes and in diverse functional bases, except in very acidic bases (detergents) and strong alkaline bases (liquid bleach).

Other comments :

Good synergy with Ultrazur®, with a 4:1 ratio to create beautiful ozonic and aquatic notes.

Florhydral®

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 :

Florhydral®

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 :