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・ 2-hydroxyquinoline 8-monooxygenase
・ 2-Imidazoline
・ 2-iminoacetate synthase
・ 2-Iminothiolane
・ 2-in-1 PC
・ 2-inch Medium Mortar
・ 2-inch mortar
・ 2-Iodobenzoic acid
・ 2-Iodoxybenzoic acid
・ 2-Isopropyl-5-methyl-1-(2,6-dihydroxy-4-nonylphenyl)cyclohex-1-ene
・ 2-isopropylmalate synthase
・ 2-Ketoarginine methyltransferase
・ 2-lane expressway
・ 2-MDP
・ 2-Me-DET
2-Mercaptoethanol
・ 2-Mercaptoindole
・ 2-Mercaptopyridine
・ 2-meter band
・ 2-Methoxy-4-vinylphenol
・ 2-Methoxy-6-polyprenyl-1,4-benzoquinol methylase
・ 2-Methoxyamphetamine
・ 2-Methoxyestradiol
・ 2-Methoxyethanol
・ 2-Methoxyethyl-18-methoxycoronaridinate
・ 2-Methoxypropene
・ 2-Methyl-1-butanol
・ 2-Methyl-1-pentanol
・ 2-Methyl-2,4-pentanediol
・ 2-Methyl-2-butene


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2-Mercaptoethanol : ウィキペディア英語版
2-Mercaptoethanol

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2-Mercaptoethanol (also β-mercaptoethanol, BME, 2BME, 2-ME or β-met) is the chemical compound with the formula HOCH2CH2SH. ME or βME, as it is commonly abbreviated, is used to reduce disulfide bonds and can act as a biological antioxidant by scavenging hydroxyl radicals (amongst others). It is widely used because the hydroxyl group confers solubility in water and lowers the volatility. Due to its diminished vapor pressure, its odor, while unpleasant, is less objectionable than related thiols.
==Preparation==
2-Mercaptoethanol may be prepared by the action of hydrogen sulfide on ethylene oxide:〔Knight, J. J. (2004) "2-Mercaptoethanol" in ''Encyclopedia of Reagents for Organic Synthesis'' (Ed: L. Paquette), J. Wiley & Sons, New York. .〕
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