76420
1-丁基-3-甲基咪唑鎓三氟甲磺酸盐
≥95.0% (H-NMR)
别名:
BMIM Otf
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关于此项目
经验公式（希尔记法）:
C9H15F3N2O3S
化学文摘社编号:
分子量:
288.29
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
产品名称
1-丁基-3-甲基咪唑鎓三氟甲磺酸盐, ≥95.0% (H-NMR)
form
liquid
InChI
1S/C8H15N2.CHF3O3S/c1-3-4-5-10-7-6-9(2)8-10;2-1(3,4)8(5,6)7/h6-8H,3-5H2,1-2H3;(H,5,6,7)/q+1;/p-1
SMILES string
[O-]S(=O)(=O)C(F)(F)F.CCCCn1cc[n+](C)c1
InChI key
FRZPYEHDSAQGAS-UHFFFAOYSA-M
assay
≥95.0% (H-NMR)
refractive index
n20/D 1.434
density
1.292 g/mL at 20 °C (lit.)
functional group
fluoro
triflate
Quality Level
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Application
在Diels-Alder反应中，1-丁基-3-甲基咪唑三氟甲磺酸酯可以用作高氯酸锂-乙醚混合物的替代品。
General description
1-丁基-3-甲基咪唑三氟甲磺酸酯是一种非质子 中性离子液体。
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
>212.0 °F
flash_point_c
> 100 °C
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Activity coefficients at infinite dilution of alkanes, alkenes, and alkyl benzenes in 1-butyl-3-methylimidazolium trifluoromethanesulfonate using gas? liquid chromatography
Ge, Ming-Lan, et al.
Journal of Chemical and Engineering Data, 52.6, 2257-2260 (2007)
tert-Amyl ethyl ether separation from its mixtures with ethanol using the 1-butyl-3-methylimidazolium trifluoromethanesulfonate ionic liquid: Liquid? liquid equilibrium
Arce, Alberto, Oscar Rodriguez, and Ana Soto
Industrial & Engineering Chemistry Research, 43.26, 8323-8327 (2004)
Ion-conductive polymer membranes containing 1-butyl-3-methylimidazolium trifluoromethanesulfonate and 1-ethylimidazolium trifluoromethanesulfonate.
Schauer J, et al.
Journal of Membrane Science, 367(1), 332-339 (2011)
Activity coefficients at infinite dilution measurements for organic solutes and water in the ionic liquid 1-butyl-3-methylimidazolium trifluoromethanesulfonate
Doman?ska, Urszula, and Andrzej Marciniak
The Journal of Physical Chemistry B, 112.35, 11100-11105 (2008)
Deep fuels desulfurization and denitrogenation using 1-butyl-3-methylimidazolium trifluoromethanesulfonate
Ke?dra-Krolik, Karolina, et al.
Energy and Fuels, 25.4, 1559-1565 (2011)
商品
Functionalized imidazolium cations with thioether, urea, or thiourea derivatized side chains act as metal-ligating moieties, whereas the PF6– anions provide the desired water immiscibility.
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