Phenylethyl salicylate
Benzoate de 2-hydroxy-2-phenylethyl ; 2-hydroxy-2-phenylethyl benzoate ; 2-hydroxybenzoate de benzylcarbinyl ; Benzylcarbinyl 2-hydroxybenzoate ; Benzyl carbinyl salicylate ; Salicylate de benzylcarbinyl ; Salicylate de phenethyl ; Phenethyl salicylate ; Diethyl-1,2-dihydroxy-1,2-ethanedicarboxylate ; 1,2-dihydroxy-1,2-ethanedicarboxylate de diethyl
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General Presentation
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CAS N° : : 87-22-9
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EINECS number : 201-732-5
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FEMA number : 2868
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Density : 1,15
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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 : Heart/Base
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Price Range : €€
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Appearance : White solid
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FLAVIS number : 09.753
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JECFA number : 905
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 370°C
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Detection Threshold : Donnée indisponible.
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Molecular formula : C15H14O3
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Log P : Donnée indisponible.
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Molecular Weight : 242,27 g/mol
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Fusion Point : 41°C
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Flash Point : 113°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Phenyl Ethyl Salicylate is the only solid compound among other salicylates used in perfumes. On the other hand, it is the most rosy one. In comparision, Cis-3-Hexenyl Salicylate is used in green white flowers notes, and Benzyl Salicylate is used in jasmine notes for example.
Stability :
My form Salicylic acid in stability.
Most of the time, the presence of an aromatic cycle in the molecule brings coloration through time.
Unstable in acidic products, except antiperspirants, and in very alkaline products.
Uses in perfumery :
Phenyl Ethyl Salicylate is sometimes used as a base note in floral bouquets, spicy-floral and balsamic perfumes, to make the link between a white flower and a rosy note for example. It brings volume, tenacity and a balsamic effect to a composition.
Year of discovery :
Data not available.
Isomerism :
Phenyl Ethyl Salicylate does not have any isomer used in perfumery.
Synthesis precursor :
Phenyl Ethyl Salicylate is not used for the synthesis of another compound used in perfumes.
Natural availability :
No natural extract include Phenyl Ethyl Salicylate among their major components.
Synthesis route :
Phenyl Ethyl Salicylate can be synthesized in two ways. The first one is an interchange reaction involving Phenyl Ethyl Alcohol and Methyl Salicylate. The second synthetic route is an esterification reaction between Salicylic Acid and Phenyl Ethyl Alcohol. This reaction involves an acidic catalysis to raise its yield.
Regulations & IFRA
This ingredient is not restricted
