| Identification | More | [Name]
1-Butyl-3-methylimidazolium trifluoromethansulfonate | [CAS]
174899-66-2 | [Synonyms]
1-BUTYL-3-ETHYLIMIDAZOLIUM TRIFLUOROMETHANESULFONATE
1-BUTYL-3-METHYL-IMIDAZOLIUM TRIFLUORMETHANSULFONATE
1-BUTYL-3-METHYLIMIDAZOLIUM TRIFLUOROMETHANESULFONATE
1-BUTYL-3-METHYL-IMIDAZOLIUM TRIFLUOROMETHANSULFONATE
1-BUTYL-3-METHYLIMIDAZOLIUM TRIFLUOROMETHYLSULFONATE
1-N-BUTYL-3-METHYLIMIDAZOLIUM TRIFLUOROMETHANESULFONATE
1-n-Butyl-3-methylimidazoliumtriflate
1-BUTYL-3-METHYLIMIDAZOLIUM TRIFLUOROMETHANE SULFONATE 98+%
1-n-Butyl-3-methylimidazolium trifluoromethanesulfonate, 98+%
BMIM Otf | [EINECS(EC#)]
200-145-6 | [Molecular Formula]
C9H15F3N2O3S | [MDL Number]
MFCD03427620 | [Molecular Weight]
288.29 | [MOL File]
174899-66-2.mol |
| Chemical Properties | Back Directory | [Appearance]
Clear pale yellow to yellow liquid | [Melting point ]
16°C | [density ]
1.292 g/mL at 20 °C(lit.) | [refractive index ]
1.434 | [Fp ]
>100°C | [storage temp. ]
Store below +30°C. | [form ]
clear liquid | [color ]
Colorless to Yellow to Green | [PH]
7-8 (200g/l, H2O, 20℃) | [Sensitive ]
Hygroscopic | [InChI]
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 | [InChIKey]
FRZPYEHDSAQGAS-UHFFFAOYSA-M | [SMILES]
N1(CCCC)C=C[N+](C)=C1.C(F)(F)(F)S([O-])(=O)=O | [CAS DataBase Reference]
174899-66-2(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin .
R21/22:Harmful in contact with skin and if swallowed . | [Safety Statements ]
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [RIDADR ]
3265 | [WGK Germany ]
3 | [HS Code ]
29332900 |
| Hazard Information | Back Directory | [Chemical Properties]
Clear pale yellow to yellow liquid | [Uses]
[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.
| [Uses]
1-Butyl-3-methylimidazolium trifluoromethanesulfonate can be used as an alternative to lithium perchlorate-diethyl ether mixture in the Diels-Alder reaction. | [General Description]
1-Butyl-3-methylimidazolium trifluoromethanesulfonate [bmim][OTf] is a versatile ionic liquid commonly used in synthetic chemistry. |
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