Photo credits: ScenTree SAS
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General Presentation
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CAS N° : : 65405-77-8
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EINECS number : 265-745-8
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FEMA number : 4750
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Density : 1,061
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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 : 09.570
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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 :
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Detection Threshold : Donnée indisponible.
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Molecular formula : C13H16O3
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Log P : 4,36
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Molecular Weight : 220,27 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : 94°C
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Vapor pressure : Lorem Ipsum
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.
Regulations & IFRA
This ingredient is not restricted