Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Naturality | Purity | Latin name | Treated part | Geographical origin | Certifications | Comments | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Salicylate d'Amyle - 30gr | - | - | - | - | - | - | more | - |
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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Density : 1,054
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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 : Colorless liquid
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FLAVIS number : 09.762
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JECFA number : Donnée indisponible.
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 282°C
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Detection Threshold : Donnée indisponible.
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Molecular formula : C12H16O3
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Log P : >4,4
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Molecular Weight : 208,26 g/mol
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Fusion Point : -12°C
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Flash Point : 126°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Isoamyl Salicylate has a more metallic and fruity aspect, while Amyl Salicylate has a pronounced jasmine note.
It is one of the most powerful salicylates.
Stability :
May form Salicylic acid through time.
Most of the time, the occurrence of a benzenic cycle in a molecule causes a coloration of this molecule through time.
Unstable in acidic products, except antiperspirants, and in bleach.
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.
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.
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.
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
This ingredient is not restricted
