1-丁基磺酸-3-甲基咪唑硫酸氢盐
1-butylsulfonic-3-methylimidazolium hydrogensulfate
- 分子式:C8H16N2O7S2
- 分子量:316.35
- CAS编号:827320-59-2
- 纯度:98%
基本信息
产品名称: | 1-丁基磺酸-3-甲基咪唑硫酸氢盐 | ||
英文名称: | 1-butylsulfonic-3-methylimidazolium hydrogensulfate | ||
CAS编号: | 827320-59-2 | 简 写: | BSO3HMImHSO4 |
分 子 式 : | C8H16N2O7S2 | 分 子 量 : | 316.35 |
纯 度: | 98% | 产品编号: | CP0418 |
物性数据
项目 | 数据 | 测试条件 | 备注 | 数据来源 |
表面张力 mN/m | 45 | 20℃,101KPa | 2015 SCI论文 | |
玻璃化温度 ℃ | -34.7 | 2015 SCI论文 | ||
密度 g/mL | 1.4386 | 20℃,101KPa | 2015 SCI论文 | |
密度 g/mL | 1.4377 | 25℃,101KPa | 液体, Vibrating tube method | ILThermo |
溶解性 g/100mL | 不溶 | DMSO | 室温 | 实验实测 |
粘度 cP | 49850 | 20℃,101KPa | 2015 SCI论文 | |
粘度 cP | 1427 | 20℃,101KPa | 液体, Concentric cylinders viscometry | ILThermo |
折光率 | 1.5038 | 20℃,101KPa | 2015 SCI论文 | |
折光率 | 1.4973 | 21.4℃ | 实验实测 |
参考谱图
1-丁基磺酸-3-甲基咪唑硫酸氢盐,BSO3HMImHSO4,827320-59-2,1-butylsulfonic-3-methylimidazolium hydrogensulfate,核磁 NMR, H谱, 氘代DMSO
1-丁基磺酸-3-甲基咪唑硫酸氢盐,BSO3HMImHSO4,827320-59-2,1-butylsulfonic-3-methylimidazolium hydrogensulfate,NMR,H谱,D2O
Han, Feng; Organic & Biomolecular Chemistry, (2012), 10(2), 346-354, CAplus
1-丁基磺酸-3-甲基咪唑硫酸氢盐,BSO3HMImHSO4,827320-59-2,1-butylsulfonic-3-methylimidazolium hydrogensulfate,NMR,C谱,D2O
Han, Feng; Organic & Biomolecular Chemistry, (2012), 10(2), 346-354, CAplus
安全信息
Code |
Hazard Statement |
Source |
H318 |
Causes serious eye damage |
European Chemical Agency (ECHA) Classification&Labelling Inventory - Notified classification and labelling - most common notifications, European Chemical Agency (ECHA) Classification&Labelling Inventory - Notified classification and labelling - most serious notifications, European Chemical Agency (ECHA) Classification&Labelling Inventory - Notified classification and labelling according to CLP criteria |
H314 |
Causes severe skin burns and eye damage |
European Chemical Agency (ECHA) Classification&Labelling Inventory - Notified classification and labelling - most common notifications, European Chemical Agency (ECHA) Classification&Labelling Inventory - Notified classification and labelling - most serious notifications, European Chemical Agency (ECHA) Classification&Labelling Inventory - Notified classification and labelling according to CLP criteria |
H290 |
May be corrosive to metals |
European Chemical Agency (ECHA) Classification&Labelling Inventory - Notified classification and labelling - most common notifications, European Chemical Agency (ECHA) Classification&Labelling Inventory - Notified classification and labelling - most serious notifications, European Chemical Agency (ECHA) Classification&Labelling Inventory - Notified classification and labelling according to CLP criteria |
Other Names and Identifiers
Canonical SMILES
O=S(=O)([O-])O.O=S(=O)(O)CCCC[N+]=1C=CN(C1)C
InChI
InChI=1S/C8H14N2O3S.H2O4S/c1-9-5-6-10(8-9)4-2-3-7-14(11,12)13;1-5(2,3)4/h5-6,8H,2-4,7H2,1H3;(H2,1,2,3,4)
InChI Key
IEKJIBPFXKAASL-UHFFFAOYSA-N
4 Other Names for this Substance
- 1-(4-Sulfobutyl)-3-methylimidazolium sulfate
- 1-(4-Sulfobutyl)3-methylimidazolium hydrogen sulfate
- 1-Methyl-3-(4-sulfobutyl)imidazolium hydrogen sulfate
- 3-Methyl-1-(4-sulfobutyl)-1H-imidazol-3-ium hydrogensulfate
参考文献
Experimental Properties
Thermal
Experimental Spectra
1H-NMR
- (1) Calmanti, Roberto; Catalysts, (2019), 9(6), 534pp., CAplus
- (2) Li, Yu-Nong; Green Chemistry, (2012), 14(10), 2752-2758, CAplus
- (3) Garg, Bhaskar; Tetrahedron Letters, (2012), 53(42), 5674-5677, CAplus
- (4) Singh, Sandip Kumar; Catalysis Today, (2018), 309, 98-108, CAplus
- (5) Ullah, Zahoor; RSC Advances, (2015), 5(87), 71449-71461, CAplus
- (6) Teng, Junjiang; ACS Sustainable Chemistry & Engineering, (2016), 4(4), 2020-2026, CAplus
- (7) Muhammad, Nawshad; Journal of Chemical & Engineering Data, (2014), 59(3), 579-584, CAplus
- (8) Sun, Jiahan; RSC Advances, (2015), 5(106), 87200-87205, CAplus
- (9) Wu, Qin; RSC Advances, (2015), 5(71), 57968-57974, CAplus
- (10) Tao, Furong; Carbohydrate Research, (2011), 346(1), 58-63, CAplus
- (11) Tao, Furong; RSC Advances, (2011), 1(4), 672-676, CAplus
- (12) Wu, Qin; Industrial & Engineering Chemistry Research, (2014), 53(42), 16254-16260, CAplus
- (13) Tran, Phuong Hoang; RSC Advances, (2018), 8(63), 36392-36399, CAplus
- (14) Cao, Peng; New Journal of Chemistry, (2018), 42(5), 3909-3916, CAplus
- (15) Wang, Wen Juan; Chinese Science Bulletin, (2008), 53(17), 2612-2616, CAplus
- (16) Lu, Peng; Molecular Catalysis, (2017), 435, 24-32, CAplus
- (17) Song, Dayong; Synthetic Communications, (2018), 48(6), 692-698, CAplus
- (18) Senapak, W.; Organic & Biomolecular Chemistry, (2016), 14(4), 1302-1310, CAplus
- (19) Wu, Qin; Industrial & Engineering Chemistry Research, (2007), 46(24), 7955-7960, CAplus
- (20) Garcia-Suarez, Eduardo J.; Green Chemistry, (2014), 16(1), 161-166, CAplus
- (21) Rostamizadeh, Shahnaz; Chemistry of Heterocyclic Compounds (New York, NY, United States), (2015), 51(6), 526-530, CAplus
- (22) Song, Heyuan; Catalysis Letters, (2016), 146(7), 1264-1272, CAplus
- (23) Tejeswararao, D.; Journal of the Chilean Chemical Society, (2016), 61(1), 2843-2845, CAplus
- (24) Wu, Yajuan; Industrial & Engineering Chemistry Research, (2016), 55(7), 1859-1865, CAplus
- (25) Luo, Hui; Industrial & Engineering Chemistry Research, (2014), 53(29), 11653-11658, CAplus
- (26) Wu, Qin; Industrial & Engineering Chemistry Research, (2007), 46(24), 7955-7960, CAplus
- (27) Gui, Jianzhou; Journal of Molecular Catalysis A: Chemical, (2005), 225(1), 27-31, CAplus
- (28) Wang, Wenjuan; Catalysis Communications, (2007), 9(3), 337-341, CAplus
- (29) Wang, Wen Juan; Chinese Science Bulletin, (2008), 53(17), 2612-2616, CAplus
- (30) Xu, Dan-Qian; Green Chemistry, (2009), 11(8), 1239-1246, CAplus
- (31) Fang, Dong; Heteroatom Chemistry, (2010), 21(7), 546-550, CAplus
- (32) Turgis, Raphael; ChemSusChem, (2010), 3(12), 1403-1408, CAplus
- (33) Elavarasan, Pandian; Chemical Engineering Journal (Amsterdam, Netherlands), (2011), 166(1), 340-347, CAplus
- (34) Tavakoli-Hoseini, Niloofar; Bulletin of the Korean Chemical Society, (2011), 32(3), 787-792, CAplus
- (35) Tao, Furong; Bioresource Technology, (2011), 102(19), 9000-9006, CAplus
- (36) Salvi, P. P.; Comptes Rendus Chimie, (2011), 14(10), 883-886, CAplus
- (37) Xiao, Lin-Fei; Catalysis Letters, (2011), 141(12), 1838-1844, CAplus
13C-NMR
- (1) Calmanti, Roberto; Catalysts, (2019), 9(6), 534pp., CAplus
- (2) Garg, Bhaskar; Tetrahedron Letters, (2012), 53(42), 5674-5677, CAplus
- (3) Tao, Furong; RSC Advances, (2011), 1(4), 672-676, CAplus
- (4) Wu, Qin; Industrial & Engineering Chemistry Research, (2014), 53(42), 16254-16260, CAplus
- (5) Tran, Phuong Hoang; RSC Advances, (2018), 8(63), 36392-36399, CAplus
- (6) Cao, Peng; New Journal of Chemistry, (2018), 42(5), 3909-3916, CAplus
- (7) Song, Dayong; Synthetic Communications, (2018), 48(6), 692-698, CAplus
- (8) Senapak, W.; Organic & Biomolecular Chemistry, (2016), 14(4), 1302-1310, CAplus
- (9) Wu, Qin; Industrial & Engineering Chemistry Research, (2007), 46(24), 7955-7960, CAplus
- (10) Song, Heyuan; Catalysis Letters, (2016), 146(7), 1264-1272, CAplus
- (11) Tejeswararao, D.; Journal of the Chilean Chemical Society, (2016), 61(1), 2843-2845, CAplus
- (12) Wu, Yajuan; Industrial & Engineering Chemistry Research, (2016), 55(7), 1859-1865, CAplus
- (13) Wu, Qin; Industrial & Engineering Chemistry Research, (2007), 46(24), 7955-7960, CAplus
- (14) Gui, Jianzhou; Journal of Molecular Catalysis A: Chemical, (2005), 225(1), 27-31, CAplus
- (15) Elavarasan, Pandian; Chemical Engineering Journal (Amsterdam, Netherlands), (2011), 166(1), 340-347, CAplus
- (16) Tavakoli-Hoseini, Niloofar; Bulletin of the Korean Chemical Society, (2011), 32(3), 787-792, CAplus
- (17) Tao, Furong; Bioresource Technology, (2011), 102(19), 9000-9006, CAplus
- (18) Xiao, Lin-Fei; Catalysis Letters, (2011), 141(12), 1838-1844, CAplus
IR
- (1) Wu, Qin; Industrial & Engineering Chemistry Research, (2007), 46(24), 7955-7960, CAplus
- (2) Ai, Youhong; Analytica Chimica Acta, (2015), 880, 60-66, CAplus
- (3) Wang, Wen Juan; Chinese Science Bulletin, (2008), 53(17), 2612-2616, CAplus
- (4) Xiao, Lin-Fei; Catalysis Letters, (2011), 141(12), 1838-1844, CAplus