Amyl salicylate (CAS N° 2050-08-0)​

Photo credits: ScenTree SAS

Floral > White Flowers > Salicylic > Leather

Amyl salicylate

Amyl Salicylate ; Pentyl 2-hydroxybenzoate ; Pentyl ortho-hydroxybenzoate ; Pentyl salicylate ; Rhodiaflor SoA

Amyl salicylate (CAS N° 2050-08-0)​

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 - Visit website Je me procure cet ingrédient - - - - - -

Salicylate d'Amyle - 30gr

Certifications :

Information Générales

General Presentation

  • CAS N° : 2050-08-0

  • EINECS number : 218-080-2

  • FEMA number : Donnée indisponible.

  • FLAVIS number : 09.762

  • JECFA number : Donnée indisponible.

  • Appearance : Colorless liquid

  • Density : 1,054

  • Volatility : Heart/Base

  • Price Range :

Physico-chemical properties

  • Molecular formula : C12H16O3

  • Molecular Weight : 208,26 g/mol

  • Log P : >4,4

  • Fusion Point : -12°C

  • Boiling Point : 282°C

  • Detection Threshold : Donnée indisponible.

  • Optical rotation : Donnée indisponible

  • Vapor pressure : Donnée indisponible

  • Refractive Index @20°C : Donnée indisponible

  • Acid Value : Donnée indisponible.

  • Flash Point : 126°C

Utilisation

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.

Utilisation

Regulations & IFRA

Allergens :

This ingredient does not contain any allergen.

IFRA 51th :

This ingredient is not restricted for the 51th amendment

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