Photo credits: ScenTree SAS
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General Presentation
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CAS N° : : 7492-67-3
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EINECS number : 231-324-2
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FEMA number : 2310
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Density : 0,97
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Optical rotation : Lorem Ipsum
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Allergens : This ingredient does not contain any allergen.
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Refractive Index @20°C : Lorem Ipsum
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Volatility : Head/Heart
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Price Range : Data not available.
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Appearance : Colorless liquid
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FLAVIS number : 05.079
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JECFA number : 593
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point :
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Detection Threshold : Donnée indisponible.
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Molecular formula : C12H22O2
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Log P : 3,26
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Molecular Weight : 198,31 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : >94°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Muguet Aldehyde has a molecular structure and a smell close to Citronellol. It has a more metallic and citric note, close to Geraniol. Most of the time, this ingredient is diluted at 50% in DEP to facilitate its usage and to limit its olfactive power. Also foundable diluated in TEC or in BB.
Stability :
This molecule may form Schiff bases by reacting with Methyl Anthranilate or Indole for example, forming another colored and differently smelling compound.
Uses in perfumery :
Muguet Aldehyde is used in floral-aldehydic and green notes of lily of the valley, to bring an aldehydic effect. It is over all used in functional perfumery.
Year of discovery :
Data not available.
Isomerism :
As Citronellol, Muguet Aldehyde has one asymetric carbon. A mixture of its two enantiomers is anyway used in perfumery. It also is a constitutional isomer of Citronellyl acetate, having a close structure, but being weigh fruitier.
Synthesis precursor :
Muguet Aldehyde is not a precursor for the synthesis of another compound of olfactive interest.
Natural availability :
Muguet Aldehyde is not found on a natural state.
Synthesis route :
Muguet Aldehyde is prepared by interaction between bromoacetals with sodium or potassium alcoholates.
Regulations & IFRA
This ingredient is not restricted
