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° : : 27606-09-3
-
EINECS number : 248-561-2
-
FEMA number : Donnée indisponible.
-
Density : 1,088
-
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 : Donnée indisponible.
-
JECFA number : Donnée indisponible.
Information on synthetic ingredients
-
Acid Value : Lorem Ipsum
-
Boiling Point : 258°C
-
Detection Threshold : Donnée indisponible.
-
Molecular formula : C13H16O2
-
Log P : 2,7
-
Molecular Weight : 204,27 g/mol
-
Fusion Point : -40°C
-
Flash Point : 136°C
-
Vapor pressure : Lorem Ipsum
Uses
Other comments :
Magnolan® takes its name from its smell, evoking magnolia flower. It is often used for representing this flower in perfumes.
Stability :
Stable in perfumes and in diverse functional bases
Uses in perfumery :
Magnolan® is used for rhubarb and exotic fruits (mango) accords, floral (magnolia, geranium), citrus (grapefruit) notes, usually associated with woody and green notes. It brings modernity and roundness to citrus notes.
Year of discovery :
1967
Isomerism :
Magnolan® has four asymmetric carbons. Nevertheless, a mixture of its diastereoisomers is used in perfumery. Cis-3-Hexenyl Benzoate is a constitutional isomer of Magnolan®. Although, these two compounds don't have the same smell.
Synthesis precursor :
Magnolan® is not a precursor for the synthesis of another compound of olfactive interest.
Natural availability :
Magnolan® can't be found in nature. It can't be used as a plant extract.
Synthesis route :
Magnolan® can be synthesized by reacting Indene with Acetaldehyde.
Regulations & IFRA
This ingredient is not restricted
