Photo credits: ScenTree SAS
Aurantiol (Schiff Base)
Floxyl® ; Auralva® ; Methyl 2-[(7-hydroxy-3,7-dimethyloctylidene)amino] Benzoate ; Auranthesin ; Aurantha ; Aurantia ; Aurantine ; Aurantion ; Aurantium ; Methyl anthranilate / hydroxycitronellal schiff base ; Methyl N-3,7-dimethyl-7-hydroxyoctylideneanthranilate ; Orangeol ; Orantha-L-super
Photo credits: ScenTree SAS
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General Presentation
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CAS N° : 89-43-0
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EINECS number : 201-908-1
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FEMA number : Donnée indisponible.
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FLAVIS number : Donnée indisponible.
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JECFA number : Donnée indisponible.
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Appearance : Orange liquid
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Density : 0,9
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Volatility : Base
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Price Range : €€
Physico-chemical properties
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Molecular formula : C18H27NO3
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Molecular Weight : 305,42 g/mol
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Log P : 4,8
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Fusion Point : Donnée indisponible.
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Boiling Point : 162°C
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Detection Threshold : 0,2305 ng/l air
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Optical rotation : Donnée indisponible
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Vapor pressure : Donnée indisponible
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Refractive Index @20°C : Donnée indisponible
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Acid Value : Donnée indisponible.
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Flash Point : 140°C
Uses
Uses in perfumery :
Aurantiol (Schiff Base) is used in all types of perfumes, for notes of orange blossom, neroli, lime, mimosa, tuberose. Brings tenacity and boosts the head of eaux fraiches and colognes. Brings an oriental facet to chypre and oriental notes.
Year of discovery :
Data not available.
Natural availability :
Aurantiol (Schiff Base) is not available in its natural state.
Isomerism :
Aurantiol (Schiff Base) has an asymmetric carbon. The raw material used in perfumery is a racemic mixture of the two enantiomers.
Synthesis precursor :
Aurantiol (Schiff Base) is not a precursor to the synthesis of another compound of olfactory interest.
Synthesis route :
Aurantiol (Schiff Base) is a Schiff base between Hydroxycitronellal and Methyl Anthranilate. Its synthesis is made by reaction between these two compounds. The result is an orange to red coloured product.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment
