Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Comments | Naturality | Certifications | MOQ | Purity |
|---|---|---|---|---|---|---|---|
|
MAGNOLAN | MAG-1 |
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|
- | 10 grs | - |
General Presentation
-
CAS N° :
27606-09-3 -
EINECS number :
248-561-2 -
FEMA number :
Donnée indisponible. -
FLAVIS number :
Donnée indisponible.
-
JECFA number :
Donnée indisponible. -
Volatility :
Head/Heart -
Price Range :
€€
Physico-chemical properties
-
Appearance :
Colorless liquid -
Density :
1,088 -
Refractive Index @20°C :
Donnée indisponible. -
Optical rotation :
Donnée indisponible. -
Vapor pressure :
Donnée indisponible. -
Flash Point :
136°C (276,8°F)
-
Molecular formula :
C13H16O2 -
Molecular Weight :
204,27 g/mol -
Log P :
2,7 -
Fusion Point :
-40°C (-40°F) -
Boiling Point :
258°C (496,4°F) -
Detection Threshold :
Donnée indisponible.
Chemistry & Uses
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
Natural availability :
Magnolan® can't be found in nature. It can't be used as a plant extract.
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.
Synthesis route :
Magnolan® can be synthesized by reacting Indene with Acetaldehyde.
Stability :
Stable in perfumes and in diverse functional bases
Other comments :
Magnolan® takes its name from its smell, evoking magnolia flower. It is often used for representing this flower in perfumes.
Labelling
Allergens :
This ingredient does not contain any allergen.
IFRA
IFRA 51th :
This ingredient is not restricted for the 51th amendment
