Hyacinth Acetal
Synthétique
Floral > Rosy > Honeyed > Green
Crédits photo: ScenTree SAS
Other names :
Hyacinth Acetal ; Acetal CD® ; 2-(phenylmethyl)-1,3-dioxan-5-ol ; Benzene acetaldehyde cyclic acetals with glycerol ; Phenyl acetaldehyde glyceryl acetals ; Phenyl acetaldehyde glycerine acetals
Volatility :
Head/Heart
Uses in perfumery :
Hyacinth Acetal is used in floral-lily of the valley, rosy, spicy and marine notes in small quantities. Used in all types of perfumes.
Natural availability :
Hyacinth Acetal is not available in its natural state.
Year of discovery :
Data not available.
Other comments :
Hyacinth Acetal derivating from Phenyl Acetaldehyde, its smell remains close to it, but has a cinnamic undernote.
Price Range :
€€€
Stability :
Stable in perfumes and diverse functional bases, except very alkaline detergents and bleaches.
Crédits photo: ScenTree SAS
- Molecular formula :
- C11H14O3
- Molecular Weight :
- 194,23 g/mol
- Density :
- 1,162
- Flash Point :
- 100°C
- Fusion Point :
- Donnée indisponible.
- Appearance :
- Colorless liquid
- Log P :
- 0,8 (très bas comparé à la moyenne)
- Boiling Point :
- 358°C
- Detection Threshold :
- Donnée indisponible.
Synthesis route :
Hyacinth Acetal is synthesized by acetalization of Phenyl Acetaldehyde, by reaction of this molecule with glycerine. Hyacinth Acetal has a fruty and slightly less rosy smell than its starting reagent.
Synthesis precursor :
Hyacinth Acetal is not a precursor to the synthesis of another compound of olfactory interest.
Isomerism :
Hyacinth Acetal has an asymmetric carbon, but it is its racemic mixture that is used in perfumery.
- EINECS number :
- 249-934-2
- FEMA number :
- 2877
- JECFA number :
- 1004
- FLAVIS number :
- 06.007
- Allergens :
- This ingredient does not contain any allergen.
- IFRA :
- This ingredient is not restricted
To learn more about IFRA's standards : https://ifrafragrance.org/safe-use/library
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