| Identification | Back Directory | [Name]
1-ETHYL-1-METHYLPYRROLIDINIUM BROMIDE | [CAS]
69227-51-6 | [Synonyms]
[EMPyrr]Br
N-Ethyl,methylpyrrolidinium
MethylEthylPyrollidiumBromide
N-ethyl,methylpyrrolidinium bromide
1-ETHYL-METHYL-PYRROLIDINIUM BROMIDE
1-ETHYL-1-METHYLPYRROLIDINIUM BROMIDE
N-ETHYL-N-METHYLPYRROLIDINIUM BROMIDE
1-Ethyl-1-MethylpyrrolidiniuM broMinde
1-ethyl-1-Methylpyrrolidin-1-iuM broMide
1-Ethyl-1-methylpyrrolidinium bromide 99% | [EINECS(EC#)]
418-200-5 | [Molecular Formula]
C7H16BrN | [MDL Number]
MFCD03095384 | [MOL File]
69227-51-6.mol | [Molecular Weight]
194.11 |
| Hazard Information | Back Directory | [Chemical Properties]
Off-white crystalline | [Uses]
1-Ethyl-1-methylpyrrolidinium bromide may be used in the preparation of 1-ethyl-1-methylpyrrolidinium lactate, a potential solvent for the separation of hexan-1-ene from hexane. It can also be used to prepare 1-ethyl-1-methylpyrrolidinium tribromide. It can be used as a co-catalyst during the cycloaddition of CO2 with different epoxides to form cyclic carbonates in the presence of a nona-vacant Keggin-type tricarbonyl rhenium derivative catalyst. | [Uses]
1-Ethyl-1-methylpyrrolidinium bromide s an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff. | [General Description]
1-Ethyl-1-methylpyrrolidinium bromide is an ionic liquid that can be prepared by reacting N-methylpyrrolidine with bromoethane. it is conventionally used as a bromine-sequestering agent (BSA) in zinc/bromine redox flow batteries. | [Synthesis]
A process for synthesizing quaternary ammonium salt, including the following steps: S1, replace nitrogen in the whole system in advance, open the metering valves for raw materials and solvent respectively, and add raw material A, raw material B a |
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