Photo credits: ScenTree SAS
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General Presentation
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CAS N° : : 102-20-5
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EINECS number : 203-013-1
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FEMA number : 2866
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Density : 1,082
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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 : Base
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Price Range : €
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Appearance : White solid
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FLAVIS number : 09.707
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JECFA number : 999
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 325°C
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Detection Threshold : Donnée indisponible.
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Molecular formula : C16H16O2
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Log P : 3,93
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Molecular Weight : 240,3 g/mol
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Fusion Point : 28°C
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Flash Point : 113°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
In comparision with other typical rosy notes as Phenyl Ethyl Alcohol and Phenyl Ethyl acetate, Phenyl Ethyl Phenyl acetate has a distinctive green smell.
Stability :
May form Phenylacetic acid through time under the effect of heat.
Most of the time, the occurrence of a benzenic cycle in a molecule causes a coloration of this molecule through time
Uses in perfumery :
Phenyl Ethyl Phenyl acetate is used in all types of perfumery for rosy or white floral notes. Allows to bring tenacity and a natural effect to the note.
Year of discovery :
Data not available.
Isomerism :
Phenyl Ethyl Phenyl acetate does not have any isomer used in perfumery.
Synthesis precursor :
Phenyl Ethyl Phenyl acetate is not a precursor to the synthesis of another compound of olfactory interest.
Natural availability :
Phenyl Ethyl Phenyl acetate is present in Champaca Absolute and can be extracted in its natural state but at a very high cost. Therefore, Phenyl Ethyl Phenyl acetate is greatly produced by organic synthesis.
Synthesis route :
Phenyl Ethyl Phenyl acetate is synthesized by an esterification reaction between Phenylacetic Acid (obtained from benzyl chloride and sodium cyanide) and Phenyl Ethyl Alcohol (obtained by a Friedel-Craft reaction between benzene and ethylene chloride). This reaction is catalysed by a concentrated sulfuric acid.
Regulations & IFRA
This ingredient is not restricted