Photo credits: ScenTree SAS
Do you sell any of the raw materials? Would you like to let our users know?
Send an email to fournisseurs@scentree.coto learn about our advertising opportunities.
General Presentation
-
CAS N° : : 29895-73-6
-
EINECS number : 249-934-2
-
FEMA number : 2877
-
Density : 1,162
-
Optical rotation : Lorem Ipsum
-
Allergens : This ingredient does not contain any allergen.
-
Refractive Index @20°C : Lorem Ipsum
-
Volatility : Head/Heart
-
Price Range : €€€
-
Appearance : Colorless liquid
-
FLAVIS number : 06.007
-
JECFA number : 1004
Information on synthetic ingredients
-
Acid Value : Lorem Ipsum
-
Boiling Point : 358°C
-
Detection Threshold : Donnée indisponible.
-
Molecular formula : C11H14O3
-
Log P : 0,8 (très bas comparé à la moyenne)
-
Molecular Weight : 194,23 g/mol
-
Fusion Point : Donnée indisponible.
-
Flash Point : 100°C
-
Vapor pressure : Lorem Ipsum
Uses
Other comments :
Hyacinth Acetal derivating from Phenyl Acetaldehyde, its smell remains close to it, but has a cinnamic undernote.
Stability :
Stable in perfumes and diverse functional bases, except very alkaline detergents and bleaches.
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.
Year of discovery :
Data not available.
Isomerism :
Hyacinth Acetal has an asymmetric carbon, but it is its racemic mixture that is used in perfumery.
Synthesis precursor :
Hyacinth Acetal is not a precursor to the synthesis of another compound of olfactory interest.
Natural availability :
Hyacinth Acetal is not available in its natural state.
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.
Regulations & IFRA
This ingredient is not restricted
