Floral > White Flowers > Salicylic > Cut Grass

Cis-3-hexenyl salicylate

Pipol Salicylate ; Cis-3-hexenyl 2-hydroxybenzoate ; Cis-3-hexen-1-yl salicylate ; Cis-hex-3-enyl 2-hydroxybenzoate ; Leaf salicylate

Cis-3-hexenyl salicylate (CAS N° 65405-77-8)​

Photo credits: ScenTree SAS

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Information Générales

General Presentation

  • CAS N° : : 65405-77-8

  • EINECS number : 265-745-8

  • FEMA number : 4750

  • Density : 1,061

  • Optical rotation : Lorem Ipsum

  • Allergens : This ingredient does not contain any allergen.

  • Refractive Index @20°C : Lorem Ipsum

  • Volatility : Heart/Base

  • Price Range : €€

  • Appearance : Colorless liquid

  • FLAVIS number : 09.570

  • JECFA number : Donnée indisponible.

Information on synthetic ingredients

  • Acid Value : Lorem Ipsum

  • Boiling Point :

  • Detection Threshold : Donnée indisponible.

  • Molecular formula : C13H16O3

  • Log P : 4,36

  • Molecular Weight : 220,27 g/mol

  • Fusion Point : Donnée indisponible.

  • Flash Point : 94°C

  • Vapor pressure : Lorem Ipsum

Utilisation

Uses

Other comments :

Comparing it to other salicylates, cis-3-Hexenyl Salicylate is the greenest.

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

Uses in perfumery :

Cis-3-Hexenyl Salicylate is used for solar, ylang-ylang and tuberose notes and for fougere perfumes. Brings a green note to white flowers. Provides a good binding between top and bottom notes.

Year of discovery :

Data not available.

Isomerism :

Trans-3-Hexenyl Salicylate, a diastereoisomer of cis-3-Hexenyl Salicylate, exists but is very little used.

Synthesis precursor :

Cis-3-Hexenyl salicylate is not a precursor to the synthesis of another compound of olfactory interest.

Natural availability :

Cis-3-Hexenyl Salicylate is present in a small amount in carnation absolute. Knowing that carnation offers only a very low extraction yields, natural cis-3-Hexenyl Salicylate is very little produced. The synthetic compound is more often used in perfumery.

Synthesis route :

As for other Salicylates, cis-3-Hexenyl Salicylate is synthesized by an esterification reaction between salicylic acid and cis-3-hexenol. It is the use of cis-3-Hexenol which gives the molecule its characteristic green note of cut grass.

Utilisation

Regulations & IFRA

This ingredient is not restricted

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