1-Ethyl-1-methylpyrrolidinium iodide, >98%

Price range: $220.44 through $2,424.84

Product Code: IL-0164-HP

CAS NO: 4186-68-9

  • Chemical Formula: C7H16IN
  • Synonyms: EMPyrr I, PYR12ย I, PY12ย I,ย N-Ethyl-N-methylpyrrolidinium iodide
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SUM Formula: C7H16IN

Molecular Weight: 241.11

Melting Point: >300 ยฐC

Density: 1.470 g/cmยณ (25 ยฐC)

Purity: >98%

  • SUM Formula: C7H16IN
  • Molecular Weight: 241.11
  • Melting Point: >300 ยฐC
  • Density: 1.470 g/cmยณ (25 ยฐC)

1-Ethyl-1-methylpyrrolidinium iodide, CAS: 4186-68-9

Key Applications:

Electrochemical Systems

  • Serves as a quaternary ammonium iodide salt for use in electrolyte formulation, particularly where iodide anions support redox mediation or halide exchange.
  • Utilized in reference electrolyte studies to evaluate cationโ€“anion interactions, ionic mobility, and conductivity trends within pyrrolidinium-based salts.
  • Supports electrode interface investigations, including adsorption behavior and halide-driven surface modification.

Materials Science and Ion Transport Studies

  • Employed as a model ionic species in transport, viscosity, and ion-pairing research, enabling comparison across pyrrolidinium iodide derivatives.
  • Useful in solidโ€“liquid interface studies, including polymerโ€“salt compatibility, ion dissociation behavior, and dielectric response mapping.
  • Incorporated into polymer electrolyte matrices to probe mechanical and conductive properties influenced by bulky organic cations.

Catalysis and Synthesis

  • Functions as a phase-transfer catalyst or halide source in organic transformations requiring iodide-mediated nucleophilicity.
  • Supports halide exchange reactions, enabling controlled introduction of iodide into organometallic or coordination complexes.
  • Applied in ionic-liquid-assisted synthesis, where the cation structure provides tunable solvation and microenvironment effects.

Photochemical and Redox Applications

  • Utilized in iodide/triiodide redox couple studies, including dye-sensitized solar cell research and photoredox benchmarking.
  • Suitable for charge-transfer investigations, where iodideโ€™s redox activity and the pyrrolidinium cationโ€™s stability enable reproducible measurements.

Analytical and Spectroscopic Uses

  • Serves as a reference iodide salt for calibration, ion-pairing studies, and comparative NMR, FTIR, or Raman analyses.
  • Supports solvation and ion-association research, particularly in mixed-solvent systems where cation structure influences iodide behavior.

General Research Utility

  • Provides a stable, non-volatile iodide source for halide chemistry, ionic liquid precursor studies, and structureโ€“property mapping across quaternary ammonium salts.
  • Suitable for method development in electrochemical, spectroscopic, and materials characterization workflows.

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Additional information

Weight 25 g
Qty

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