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化学名: | 1-ヨードブタン | 英語化学名: | 1-Iodobutane | 别名: | 1-Butyljodid;1-iodo-butan;1-Jodbutan;Butane,1-iodo-;Iodobutane;n-Butyliodid;n-C4H9I;1-IODOBUTANE , STABILIZED WITH COPPER | CAS番号: | 542-69-8 | 分子式: | C4H9I | 分子量: | 184.02 | EINECS: | 208-824-4 | カテゴリ情報: | Organics;Iodine Compounds | Mol File: | 542-69-8.mol | |
融点 | −103 °C(lit.) | 沸点 | 130-131 °C(lit.) | 比重(密度) | 1.617 g/mL at 25 °C(lit.) | 蒸気密度 | ~5 (vs air) | 蒸気圧 | 18.5 hPa (25 °C) | 屈折率 | n20/D 1.498(lit.) | 闪点 | 92 °F | 貯蔵温度 | Store below +30°C. | 溶解性 | alcohol: soluble | 外見 | Liquid | 色 | Clear colorless to pale yellow or light pink | 水溶解度 | Insoluble in water. | Sensitive | Light Sensitive | Merck | 14,1573 | BRN | 1420755 | Dielectric constant | 4.5(130℃) | 安定性: | Stable. Highly flammable. Incompatible with strong oxidizing agents. Light sensitive. | CAS データベース | 542-69-8(CAS DataBase Reference) | NISTの化学物質情報 | Butane, 1-iodo-(542-69-8) | EPAの化学物質情報 | Butane, 1-iodo- (542-69-8) |
| 1-ヨードブタン Usage And Synthesis |
外観 | 無色~うすい褐色, 澄明の液体 | 溶解性 | 水に難溶, エタノールに易溶。エタノール及びアセトンに極めて溶けやすく、水にほとんど溶けない。 | 化学的特性 | colorless liquid. Soluble in chloroform, miscible with ethanol and ether, insoluble in water, and will change color when exposed to light or left for a long time. | 使用 | 1-Iodobutane was used in the synthesis of S-alkylated 5-(2-,3- and 4-methoxyphenyl)-4H-1,2,4-triazole-3-thiol and 5-(2-,3- and 4-methoxyphenyl)-4-phenyl-4H-1,2,4-triazole-3-thiol. It is also used in wide range of medicals industrial applications as well as in human and animal nutrition products, pharmaceutical intermediates, polarizing films for Liquid Crystal Display (LCD) chemicals. | 製造方法 | 1-Iodobutane is obtained by reacting n-butanol with iodine in the presence of phosphorus. | Synthesis Reference(s) | The Journal of Organic Chemistry, 44, p. 2048, 1979 DOI: 10.1021/jo01326a042 Synthesis, p. 114, 1976 | 一般的な説明 | Thermal chemistry of 1-iodobutane has been investigated on clean and hydrogen- and deuterium-predosed Pt(111) single-crystal surfaces by temperature-programmed desorption and reflection-absorption infrared spectroscopy. | 純化方法 | Dry the iodide with MgSO4 or P2O5, fractionally distil it through a column packed with glass helices, taking the middle fraction and storing over calcium or mercury in the dark. Alternatively purify it by prior passage through activated alumina or by shaking with conc H2SO4 then washing with Na2SO3 solution. It has also been treated carefully with sodium to remove free HI and H2O, before distilling through a column containing copper turnings at the top. Another purification procedure consisted of treatment with bromine, followed by extraction of free halogen with Na2S2O3, washing with H2O, drying and fractionally distilling. [Beilstein 1 IV 271.] |
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