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General Presentation
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CAS N° : 90-02-8
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EINECS number : 201-961-0
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FEMA number : 3004
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Density : 1,146
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Optical rotation : Donnée indisponible
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Allergens : This ingredient does not contain any allergen.
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Refractive Index @20°C : Donnée indisponible
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Volatility : Head/Heart
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Price Range : €€
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Appearance : Colorless liquid
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FLAVIS number : 05.055
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JECFA number : 897
Information on synthetic ingredients
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Acid Value : Donnée indisponible
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Boiling Point : 197°C
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Detection Threshold : 30 ppb (0,000003%)
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Molecular formula : C7H6O2
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Log P : 1,66
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Molecular Weight : 122,12 g/mol
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Fusion Point : 2°C
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Flash Point : 78°C
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Vapor pressure : Donnée indisponible
Uses
Other comments :
Salicylaldehyde is produced by certain insects.
Stability :
Aldehydes may form diethylacetals in alcoholic perfumes, with no real impact on their smell
Most of the time, the occurrence of a benzenic cycle in a molecule causes a coloration of this molecule through time
Uses in perfumery :
Salicylaldehyde is used in warm, almond and coumarinic notes.
Year of discovery :
Data not available.
Isomerism :
The ortho and meta positional isomers of Salicylaldehyde are little used in perfumery, although they also have a bitter almond, very hot, balsamic and sweet smell.
Synthesis precursor :
Salicylaldehyde is the main precursor to Coumarin synthesis by a Perkin reaction with acetic anhydride. It can also form a Schiff base by reaction with Methyl Anthranilate or Indole for example.
Natural availability :
Salicylaldehyde is found naturally in small quantities in Ceylon Cinnamon EO.
Synthesis route :
Salicylaldehyde is synthesized by a Reimer-Tiemann reaction, reacting phenol with potash and chloroform. Then, the aldehyde function implants in the ortho position with respect to the alcohol function.
Regulations & IFRA
This ingredient is not restricted