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

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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

Company Ingredient Name ID Comments Naturality Certifications MOQ Purity
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CIS 3 HEXENYL SALICYLATE - Learn more Je me procure cet ingrédient - 10 grs -

CIS 3 HEXENYL SALICYLATE

Certifications :

Information Générales

General Presentation

  • CAS N° :

    65405-77-8
  • EINECS number :

    265-745-8
  • FEMA number :

    4750
  • FLAVIS number :

    09.570
  • JECFA number :

    Donnée indisponible.
  • Volatility :

    Heart/Base
  • Price Range :

    €€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    1,061
  • Refractive Index @20°C :

    Data not available.
  • Optical rotation :

    Data not available.
  • Vapor pressure :

    0.00033 mmHg @23°C
  • Flash Point :

    94°C (201,2°F)
  • Molecular formula :

    C13H16O3
  • Molecular Weight :

    220,27 g/mol
  • Log P :

    4,36
  • Fusion Point :

    Donnée indisponible.
  • Boiling Point :

  • Detection Threshold :

    Donnée indisponible.
Utilisation

Chemistry & Uses

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.

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.

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.

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.

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

Other comments :

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

Utilisation

IFRA

IFRA 51th :

This ingredient is not restricted for the 51th amendment

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