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General Presentation
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CAS N° : : 125109-85-5
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EINECS number : 412-050-4
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FEMA number : Donnée indisponible.
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Density : 0,95
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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 : 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 : 257°C
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Detection Threshold : 0,07 ng/l air
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Molecular formula : C13H18O
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Log P : 3,8
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Molecular Weight : 190,29 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : 68°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Good synergy with Ultrazur®, with a 4:1 ratio to create beautiful ozonic and aquatic notes.
Stability :
Stable in perfumes and in diverse functional bases, except in very acidic bases (detergents) and strong alkaline bases (liquid bleach).
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.
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.
Natural availability :
Florhydral® does not exist on a natural state. Thus, it can't be used as extracted from a plant.
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.
Regulations & IFRA
This ingredient is not restricted
