Photo credits: ScenTree SAS
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
Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
PHENYLETHYL SALICYLATE | 368 |
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|
Molecule | - | - | - | - | - |
PHENYLETHYL SALICYLATE
ID : 368
Certifications :
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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FLAVIS number : 09.753
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JECFA number : 905
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Appearance : White solid
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Density : 1,15
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Volatility : Heart/Base
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Price Range : €€
Physico-chemical properties
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Molecular formula : C15H14O3
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Molecular Weight : 242,27 g/mol
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Log P : Donnée indisponible.
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Fusion Point : 41°C
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Boiling Point : 370°C
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Detection Threshold : Donnée indisponible.
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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 : 113°C
Uses
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.
Natural availability :
No natural extract include Phenyl Ethyl Salicylate among their major components.
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.
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
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment
