Photo credits: ScenTree SAS
Company | Ingredient Name | ID | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
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Salicylate d'Amyle - 30gr | - |
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General Presentation
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CAS N° : 2050-08-0
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EINECS number : 218-080-2
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FEMA number : Donnée indisponible.
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FLAVIS number : 09.762
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JECFA number : Donnée indisponible.
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Appearance : Colorless liquid
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Density : 1,054
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Volatility : Heart/Base
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Price Range : €
Physico-chemical properties
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Molecular formula : C12H16O3
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Molecular Weight : 208,26 g/mol
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Log P : >4,4
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Fusion Point : -12°C
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Boiling Point : 282°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 : 126°C
Uses
Uses in perfumery :
Amyl Salicylate is used in white flowers, carnation, fougere, ambery and vanillic notes.
Year of discovery :
Initially marketed under the name Trefol, Amyl Salicylate was first used in the perfume Trèfle Incarnat - L.T. Pivert (1898) First synthesized in 1854 by reaction of salycile chloride with amyl alcohol by Drion et al.
Natural availability :
Amyl Salicylate is present in trace amounts in Osmanthus Absolute. It can therefore be extracted, but it is mostly the synthetic compound that is used in perfumery.
Isomerism :
PhenoxyEthyl IsoButyrate is a constitutional isomer of Amyl Salicylate. It smell is closer to rose than jasmine, and is not solar.
Synthesis precursor :
Amyl Salicylate is not a precursor to the synthesis of another compound of olfactory interest.
Synthesis route :
Like other Salicylates, Amyl Salicylate is synthesized by an esterification reaction between salicylic acid and amyl alcohol (or pentenol). This reaction is catalysed by the presence of a strong concentrated acid such as sulfuric acid in the reaction medium.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment