추천 제품
Quality Level
분석
97%
형태
liquid
불순물
≤0.5% water
refractive index
n20/D 1.434
density
1.292 g/mL at 20 °C (lit.)
작용기
fluoro
triflate
SMILES string
[O-]S(=O)(=O)C(F)(F)F.CCCCn1cc[n+](C)c1
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
InChI key
FRZPYEHDSAQGAS-UHFFFAOYSA-M
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일반 설명
1-Butyl-3-methylimidazolium trifluoromethanesulfonate [bmim][OTf] is a versatile ionic liquid commonly used in synthetic chemistry.
애플리케이션
[bmim][OTf] can be used as:
- A glycosylation promoter in the synthesis of oligosaccharides from thiophenyl and trichloroacetimidate glycoside donors.
- A solvent for the extraction of sulfur and nitrogen containing aromatic organic compounds from aliphatic hydrocarbons.
- A reagent in the preparation of ion-conductive polymeric membranes.
- A dopant in the synthesis of poly (ethyl methacrylate) based polymer electrolytes to increase the ionic conductivity.
- A reaction medium to synthesize aryl ketones by Friedel–Crafts benzoylation of aryl compounds by using bismuth triflate as a catalyst.
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
>212.0 °F
Flash Point (°C)
> 100 °C
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
A new application of Baylis?Hillman alcohols to a diastereoselective synthesis of 3-nitrothietanes.
Tetrahedron, 68(11), 2459-2464 (2012)
Efficient Air?Stable Organometallic Low?Molecular?Mass Gelators for Ionic Liquids: Synthesis, Aggregation and Application of Pyridine?Bridged Bis (benzimidazolylidene)?Palladium Complexes.
Chemistry?A European Journal , 15(8), 1853-1861 (2009)
Selective Quenching of 2-Naphtholate Fluorescence by Imidazolium Ionic Liquids.
The Journal of Physical Chemistry B, 116(39), 12030-12037 (2012)
Preparation and characterization of poly (ethyl methacrylate) based polymer electrolytes doped with 1-butyl-3-methylimidazolium trifluoromethanesulfonate
MEASUREMENT, 48, 263-273 (2014)
Ion-conductive polymer membranes containing 1-butyl-3-methylimidazolium trifluoromethanesulfonate and 1-ethylimidazolium trifluoromethanesulfonate
Journal of Membrane Science , 367(1-2), 332-339 (2011)
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