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Effect of Fluorination on Skin Sensitization Potential and Fragrant Properties of Cinnamyl Compounds
Authors:Julie Charpentier  Roger Emter  Heinz Koch  Dominique Lelièvre  Xavier Pannecoucke  Samuel Couve‐Bonnaire  Andreas Natsch  Agnes Bombrun
Institution:1. Ingredients Research, Givaudan International SA, Dübendorf, Switzerland;2. Normandie Université, COBRA, UMR 6014 et FR 3038, Université Rouen, INSA Rouen, CNRS, Mont Saint‐Aignan Cedex, France
Abstract:A series of three α‐ and three β‐fluorinated representatives of the family of cinnamate‐derived odorants (cinnamaldehyde ( 1 ), cinnamyl alcohol ( 2 ), and ethyl cinnamate ( 3 )) as used as fragrance ingredients is described. Olfactive evaluation shows that the fluorinated compounds exhibit a similar odor profile to their parent compounds, but the olfactive detection thresholds are clearly higher. In vitro evaluation of the skin sensitizing properties with three different assays indicates that α‐fluorination of Michael acceptor systems 1 and 3 slightly improves the skin sensitization profile. α‐Fluorocinnamyl alcohol 2b is a weaker skin sensitizer than cinnamyl alcohol 2a by in vitro tests and the fluorinated product drops below the sensitization threshold of the KeratinoSens® assay. On the other hand, β‐fluorination of compounds 1  –  3 results in highly reactive products which display a worsened in vitro skin sensitization profile.
Keywords:cinnamyl derivatives  fluoroalkenes  fragrance ingredients  skin sensitization     KeratinoSens   ®     
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