1-ブチル-3-メチルイミダゾリウムヘキサフルオロホスファート

危険有害性情報のコード(GHS)

• 絵表示(GHS)

  

• 注意喚起語

  Warning

• 危険有害性情報

  H315：皮膚刺激

  H319：強い眼刺激

• 注意書き

  P264：取扱い後は皮膚をよく洗うこと。

  P264：取扱い後は手や顔をよく洗うこと。

  P280：保護手袋/保護衣/保護眼鏡/保護面を着用するこ と。

  P302+P352：皮膚に付着した場合：多量の水と石鹸で洗うこと。

  P305+P351+P338：眼に入った場合：水で数分間注意深く洗うこと。次にコ ンタクトレンズを着用していて容易に外せる場合は外す こと。その後も洗浄を続けること。

  P332+P313：皮膚刺激が生じた場合：医師の診断/手当てを受けるこ と。

  P337+P313：眼の刺激が続く場合：医師の診断/手当てを受けること。

1-ブチル-3-メチルイミダゾリウムヘキサフルオロホスファート 価格

1-ブチル-3-メチルイミダゾリウムヘキサフルオロホスファート 化学特性,用途語,生産方法

• 外観

  無色～黄色、液体

• 用途

  テトラフルオロホウ酸1-ブチル-3-メチルイミダゾリウム(BMIM-BF4)とともに最も広く研究されているイオン液体の一つで。

• 使用上の注意

  アルゴン封入

• 化学的特性

  Clear pale yellow oil

• 使用

  those consisting of tetrafluoroborate, alkylsulfate, alkylsulfonate, carboxylate, or phosphate anions are hydrophilic and are completely dissolved in water. Dupont and coworkers first reported stable hydrophobic imidazolium salt, 1-butyl-3-methylimidazolium hexafluorophosphate ([C4mim][PF6]) in 1996. Since then, this salt has been used as a typical hydrophobic IL in many chemical reactions because its mixture with water forms a biphasic layer. Furthermore, this IL shows poor solubility in hexane or ether, which allows realization of an easy work-up process. However, [C4mim][PF6] was reported to be sensitive to the moisture at high temperature and produced hazardous hydrogen fluoride as it decomposed. Therefore, bis(trifluoromethanesulfonyl)amide (NTf2) salts are now recommended as the anion for preparing hydrophobic ILs.

• 一般的な説明

  1-Butyl-3-methylimidazolium hexafluorophosphate is an imidazolium-based, hydrophobic, room temperature ionic liquid (RTIL). It can be prepared by reacting 1-methylimidazole with chlorobutane. Gaseous hydrofluorocarbons (HFCs) such as fluoromethane, fluoroethane and 1,1,2,2-tetrafluoroethane are soluble in BMIMPF₆.

• 合成

  81.89 g (1.0 mol) of 1-methylimidazole, 128.95 g (1.0 mol) of and 92.0 g (1.0 mol) of potassium hexafluorophosphate in a 500 ml three-necked round bottom flask with a reflux condenser at 80 °C for 12 h. 1-bromobutane De-ionized water (100 ml) was added and a bi-phase was formed. The immiscible ionic liquid layer was separated from the water phase with a separating funnel. The ionic liquid was washed with de-ionized water (2 × 50 ml) until the water phase did not react with 0.001 M aqueous silver nitrate (AgNO3). Diethyl ether(2 × 30ml) was added to the ionic liquid and separated in a separating funnel. The ionic liquid 1-Butyl-3-methylimidazolium hexafluorophosphate was dried in a vacuum for 2 h. A colourless liquid was obtained Yield (86 per cent). 1H NMRof the ionic liquid sample (300MHz, DMSO) contains peaks at δ: 9.05 (s, 1H-imidazole), 7.77 (s, 1H-imidazole), 7.65 (s, 1H-imidazole),4.16 (s, N–CH3), 3.8 (s, N–methyl), 1.8 (s, CH2), 1.30 (s, CH2), and 0.92(t, methyl).

• 参考文献

  [1] Shaukat Ali Mazari . “Prediction of thermo-physical properties of 1-Butyl-3-methylimidazolium hexafluorophosphate for CO2 capture using machine learning models.” Journal of Molecular Liquids 327 (2021): Article 114785.

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