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・ 4-Methylpentedrone
・ 4-Methylphenethylamine
・ 4-Methylphenylisobutylamine
・ 4-Methylpregabalin
・ 4-Methylpyridine
・ 4-Methylsalicylic acid
・ 4-Methylthioamphetamine
・ 4-millimeter band
・ 4-MMA
・ 4-NEMD
・ 4-Nitroaniline
・ 4-Nitrobenzaldehyde
・ 4-Nitrobenzoic acid
・ 4-Nitrocatechol 4-monooxygenase
・ 4-Nitrochlorobenzene
4-Nitrophenol
・ 4-nitrophenol 2-monooxygenase
・ 4-Nitrophenol 4-monooxygenase
・ 4-nitrophenylphosphatase
・ 4-Nitropyridine-N-oxide
・ 4-Nitroquinoline 1-oxide
・ 4-Nitrotoluene
・ 4-Nonanoylmorpholine
・ 4-Nonylphenylboronic acid
・ 4-O-beta-D-mannosyl-D-glucose phosphorylase
・ 4-O-Methylhonokiol
・ 4-oxalmesaconate hydratase
・ 4-oxalocrotonate decarboxylase
・ 4-Oxalocrotonate tautomerase
・ 4-oxalomesaconate tautomerase


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

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4-Nitrophenol (also called ''p''-nitrophenol or 4-hydroxynitrobenzene) is a phenolic compound that has a nitro group at the opposite position of hydroxyl group on the benzene ring.
==Properties==
4-Nitrophenol shows two polymorphs in the crystalline state. The alpha-form is colorless pillars, unstable at room temperature, and stable toward sunlight. The beta-form is yellow pillars, stable at room temperature, and gradually turns red upon irradiation of sunlight. Usually 4-nitrophenol exists as a mixture of these two forms.
In solution, 4-nitrophenol has a dissociation constant (p''K''a) of 7.16 at 22 °C. Solution of 4-nitrophenol alone appears colorless or pale yellow, whereas its phenolic salts tend to develop a bright yellow color. This color-changing property makes this compound useful as a pH indicator.

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