1-Methyl-1-propylpyrrolidinium iodide, >98%

Price range: $164.15 through $1,847.10

Product Code: IL-0161-HP

CAS NO: 56511-19-4

  • Chemical Formula: C8H18IN
  • Synonyms: PMPyrr I, PYR13 I, PY13 I, N-Methyl-N-propylpyrrolidinium iodide
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SUM Formula: C8H18IN

Molecular Weight: 255.14

Melting Point: 120 °C

Purity: >98%

  • SUM Formula: C8H18IN
  • Molecular Weight: 255.14
  • Melting Point: 120 °C

1-Methyl-1-propylpyrrolidinium iodide, CAS: 56511-19-4

Key Applications:

Electrochemical Systems

  • Serves as a halide‑based ionic liquid component for studying ion transport, conductivity behavior, and electrode–electrolyte interfaces.
  • Useful in evaluating iodide-containing electrolytes for redox‑active systems, including early‑stage dye‑sensitized solar cell research where iodide mobility and stability are key variables.
  • Supports development of reference electrolytes for benchmarking cation–anion pairing effects in electrochemical devices.

Materials Science and Thin‑Film Processing

  • Employed as a structure‑directing additive or templating agent in the formation of hybrid organic–inorganic materials.
  • Investigated for its role in modulating crystallization, morphology, and surface charge in thin‑film deposition studies.
  • Enables comparative studies on iodide vs. non‑halide pyrrolidinium salts in polymer matrices and composite materials.

Ion Transport and Solvation Studies

  • Used in fundamental research on cation–anion interactions, solvation structure, and phase behavior of pyrrolidinium iodide systems.
  • Supports NMR, Raman, and impedance spectroscopy investigations into ion pairing, viscosity effects, and temperature‑dependent transport.
  • Provides a model system for understanding how alkyl chain length and halide identity influence ionic liquid physicochemical properties.

Catalysis and Reaction Media

  • Functions as a non‑volatile, high‑ionic‑strength medium for halide‑assisted catalytic transformations.
  • Suitable for exploring iodide‑driven nucleophilic substitution, phase‑transfer catalysis, and halide exchange reactions.
  • Enables comparative studies of reaction kinetics in iodide‑rich ionic environments.

Analytical and Separation Science

  • Utilized as an additive in chromatographic and electrophoretic method development to tune selectivity, retention, and ion–analyte interactions.
  • Supports extraction and partitioning studies where iodide activity or halide‑specific interactions are variables of interest.

Reference Material for Structure–Property Mapping

  • Provides a benchmark iodide salt for systematic comparison across pyrrolidinium cations with varying alkyl substituents.
  • Useful in computational and experimental datasets mapping viscosity, conductivity, density, and thermal stability trends.

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Additional information

Weight 25 g
Qty

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