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| 融点 | 94-96 °C(lit.) | | 沸点 | 278-280 °C(lit.) | | 比重(密度) | 1.224 | | 蒸気密度 | 4.5 (120 °C, vs air) | | 蒸気圧 | 1 mm Hg ( 94 °C) | | 屈折率 | 1.6224 | | 闪点 | 125 °C | | 貯蔵温度 | Store below +30°C. | | 溶解性 | Soluble in benzene, chloroform, ether and ethanol. | | 酸解離定数(Pka) | 9.34(at 25℃) | | 外見 | Crystalline Flakes | | 色 | white to off-white | | 臭い (Odor) | Slight phenolic odor | | 爆発限界(explosive limit) | 5% | | 水溶解度 | 436.7mg/L(25 ºC) | | 極大吸収波長 (λmax) | 324nm(MeOH)(lit.) | | Sensitive | Air & Light Sensitive | | Merck | 14,6383 | | BRN | 1817321 | | 安定性： | Stable, but air and light sensitive - store under inert gas. Incompatible with strong bases, strong oxidizing agents. | | InChIKey | KJCVRFUGPWSIIH-UHFFFAOYSA-N | | LogP | 2.84 at 25℃ | | CAS データベース | 90-15-3(CAS DataBase Reference) | | NISTの化学物質情報 | 1-Naphthalenol(90-15-3) | | EPAの化学物質情報 | 1-Naphthol (90-15-3) |
| | 1-ナフトール Usage And Synthesis |
| 外観 | 白色～うすい褐色又はうすい灰赤色、結晶～結晶性粉末又はフレーク | | 溶解性 | エタノール及びジエチルエーテルに極めて溶けやすく、水に溶けにくい。 | | 用途 | 有機合成原料(染料等)。 | | 用途 | 染料合成中間体、医薬原料 | | 使用上の注意 | 空気中で次第に着色する。 | | 説明 | 1-Naphthol, or α-naphthol, is a fluorescent organic compound with the formula C10H7OH. It is a white solid. It is an isomer of 2-naphthol differing by the location of the hydroxyl group on the naphthalene ring. The naphthols are naphthalene homologues of phenol, with the hydroxyl group being more reactive than in the phenols. Both isomers are soluble in simple alcohols, ethers, and chloroform. They are precursors to a variety of useful compounds. Naphthols (both 1 and 2 isomers) are used as biomarkers for livestock and humans exposed to polycyclic aromatic hydrocarbons.
α-naphtol, combined with epichlorhydrine and sodium hydroxide to form alpha-naphtyl glycidyl ether, caused sensitization in one of three workers in a chemical plant. | | 化学的特性 | Pale grey to brown solid with an unpleasant phenol odour. Darkens in the presence of light. Evaporates with water vapour. Soluble in ethanol, ether, benzene, chloroform and alkali solutions, insoluble in water. Precipitates violet when exposed to ferric chloride. 1-Naphthol [90-15-3] a-naphthol, 1- naphthalenol, 1-hydroxynaphthalene, C10H8O, Mr 144.16, forms colorless prisms (from toluene) which darken on exposure to air or light. The compound is steam volatile and sublimable. 1-Naphthol is reduced by sodium in liquid ammonia to give 5,6,7,8-tetrahydro-1-naphthol and is oxidized by NaOCl – FeCl3 or I2–KI to give a violet color. It is chlorinated by phosphorus pentachloride at 150℃ to give 1-chloronaphthalene, by sulfuryl chloride to give 4- chloro-1-naphthol, or by Cl2–CH3COOH to give 2,4-dichloro-1-naphthol. Similarly bromine forms 2,4-dibromo-1-naphthol, and this reaction may be used quantitatively for titration. Nitration of 1-naphthol gives complex mixtures. The crude 2,4-dinitro derivative was used in the mid-1800s as an acid yellow dye comparable to picric acid. Sulfonation at 50℃ readily yields 1-naphthol-2,4-disulfonic acid. Nitrous acid gives mainly the 2-nitroso derivative, contaminated with the 4-nitroso isomer. | | 使用 | 1-Naphthol is used as a precursor in the manufacturing of various azo dyes and pharmaceuticals such as nadolol. It is used as biomarkers. It is used in analytical chemistry as Molisch's reagent (1-naphthol dissolved in ethanol) for checking the presence of carbohydrates. It plays an essential role with sodium hypobromite to detect the presence of arginine in proteins, which is called as Sakaguchi test. | | 製造方法 | 2-Isopropylnaphthalene can be used to synthesize 1-naphthol by oxidation via the hydroperoxide (Hock synthesis).
Historically 1-naphthol was produced via caustic fusion of naphthalene-1-sulfonic acid, but this was superseded by the I.G. Farbenindustrie process involving hydrolysis of 1-naphthylamine with aqueous 22 % sulfuric acid at 200°C under pressure in a lead-lined autoclave. To obtain a purer product, Union Carbide developed a process based on catalytic oxidation of tetralin to 1-tetralol and 1-tetralone followed by dehydrogenation. The two-stage catalytic process is claimed to give an overall yield of 72% 1-naphthol, with an overall efficiency of 97%. | | 主な応用 | 1-Naphthol is a hydroxyl-aromatic compound. It has been used as a prooxidant to analyze its ability to induce hemolysis in a zebrafish G6PD (glucose-6-phosphate dehydrogenase) deficiency model. | | 定義 | ChEBI: 1-naphthol is a naphthol carrying a hydroxy group at position 1. It has a role as a genotoxin and a human xenobiotic metabolite. | | Synthesis Reference(s) | Synthetic Communications, 21, p. 379, 1991 DOI: 10.1080/00397919108016759
Journal of the American Chemical Society, 107, p. 493, 1985 DOI: 10.1021/ja00288a037 | | 一般的な説明 | 1-Naphthol, a metabolite of carbaryl and naphthanlene. It is formed by spontaneous reaction from (1R, 2S)-Naphthalene epoxide followed to form 1, 4-Dihydroxynaphthalene. | | 危険性 | Toxic by ingestion and skin absorption. | | 燃焼性と爆発性 | Not classified | | 接触アレルゲン | 1-Naphthol can be used in dye manufacture and is
classified as a hair dye. Combined with epichlorhydrin
and NaOH to form alpha-naphthyl glycidyl ether, it caused
sensitization in one of three workers in a chemical plant. | | 安全性プロファイル | Poison by ingestion and
intraperitoneal routes. Moderately toxic by
skin contact. An experimental teratogen.
Experimental reproductive effects. A severe
eye and skin irritant. Mutation data reported.
Ingestion of large amounts can cause
nephritis, vomiting, diarrhea, circulatory
collapse, anemia, convulsions, and death.
Can cause kidney irritation and injury to
cornea and lens of the eye. Combustible
when exposed to heat or flame. When
heated to decomposition it emits acrid
smoke and irritating fumes. | | 合成 | To a 10 mL pressure vessel, aryl halide (1.00 mmol), copper (I) oxide (0.05 mol), ligand (0.05 mol), 3 M sodium hydroxide (2 mL), and organic solvent (2 mL) were added. The reaction mixture was irradiated at 160 °C for 10 min with strong stirring. The reaction mixture was allowed to cool to room temperature. The reaction mixture was filtered through a plug of celite in a fritted filter funnel and washed with ethyl acetate. The product was extracted using 30 mL of ethyl acetate for three times. The organic extract is washed three times with 10 mL water and two times with 10 mL of brine. The combined organic phases were dried over anhydrous MgSO4 and the solvent was removed under reduced pressure to afford 1-naphthol. | | 概要 | ナフタレンの水素を1個、ヒドロキシ基に置換した化合物で、フェノール類に分類される芳香族化合物。ヒドロキシ基の置換位置が異なる異性体、2-ナフトールが存在する。化学工業ではα-ナフトールと呼ばれている。 | | 純化方法 | Sublime 1-naphthol, then crystallise it from aqueous MeOH (charcoal), aqueous 25% or 50% EtOH, *C6H6, cyclohexane, heptane, CCl4 or H2O. Dry it over P2O5 in vacuo. The 4-nitrobenzoate has m 143o (from EtOH). [Shizuka et al. J Am Chem Soc 107 7816 1985, Beilstein 8 H 596, 6 IV 4208.] |
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