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・ 4-methoxybenzoate monooxygenase (O-demethylating)
・ 4-Methoxycinnamaldehyde
・ 4-Methoxyresveratrol
・ 4-Methyl-1-pentanol
・ 4-Methyl-1-pentene
・ 4-Methyl-2,4-bis(4-hydroxyphenyl)pent-1-ene
・ 4-Methyl-2,5-methoxyphenylcyclopropylamine
・ 4-Methyl-2-pentanol
・ 4-Methyl-3-thiosemicarbazide
・ 4-Methyl-α-ethyltryptamine
・ 4-Methylaminobutanoate oxidase (formaldehyde-forming)
・ 4-Methylaminobutanoate oxidase (methylamine-forming)
・ 4-Methylaminorex
・ 4-Methylamphetamine
・ 4-Methylbenzaldehyde
4-Methylbenzylidene camphor
・ 4-Methylbuphedrone
・ 4-Methylcatechol
・ 4-Methylcathinone
・ 4-Methylcyclohexanemethanol
・ 4-Methyldiphenhydramine
・ 4-methyleneglutamate—ammonia ligase
・ 4-methyleneglutaminase
・ 4-Methylethcathinone
・ 4-Methylhistamine
・ 4-Methylimidazole
・ 4-Methylmethamphetamine
・ 4-Methylmethylphenidate
・ 4-methyloxaloacetate esterase
・ 4-Methylpentanoic acid


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4-Methylbenzylidene camphor : ウィキペディア英語版
4-Methylbenzylidene camphor

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4-Methylbenzylidene camphor (4-MBC, enzacamene) is an organic camphor derivative that is used in the cosmetic industry for its ability to protect the skin against UV, specifically UV B radiation. As such it is used in sunscreen lotions and other skincare products claiming a SPF value. Its tradenames include Eusolex 6300 (Merck) and Parsol 5000 (DSM).
==Mechanism==
All the camphor sunscreens are supposed to dissipate the photon energy by cis-trans isomerisation. But for 4-MBC the quantum yield for this isomerisation is reported to be only between 0.13 - 0.3. This low quantum yield means that other photochemical processes are occurring.〔''Sun Protection in Man''. Chapter 26: Cantrell, Ann; McGarvey, David J.; Truscott, T. George. Photochemical and photophysical properties of sunscreens.〕

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