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filingDate 2010-07-16^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2012-12-27^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2012533520-A
titleOfInvention Photostabilization of retinoids by alkoxycrylene compounds
abstract The electronically excited state energy (especially the singlet state energy from the retinoid compound) to be photostabilized is an alkoxy radical in the 4 (para) coordination of one of the phenyl rings having the chemical formula (I) (herein It has been found that it readily migrates to (accepts to) α-cyanodiphenyl acrylate compounds having a medium or less “alkoxychryrene”). Where one of R 1 and R 2 is a linear or branched C 1 -C 30 alkoxy radical, preferably C 1 -C 8 , more preferably methoxy, non-alkoxy The radical R 1 or R 2 is hydrogen and R 3 is a linear or branched C 1 -C 30 alkyl radical, preferably C 2 -C 20 . The alkoxycrylene compound of formula (I) significantly increases the light stability of the retinoid compound in the composition by at least 3 times and even 10 times or more. Since the ability of the alkoxycrylene compound to stabilize the retinoid compound is concentration-dependent, the amount of retinoid light stabilizing action increases with the concentration of the alkoxycrylene compound.
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