1-Methyl-1-propylpyrrolidinium iodide, >98%
Price range: $164.15 through $1,847.10
Product Code: IL-0161-HPCAS NO: 56511-19-4
- Chemical Formula: C8H18IN
- Synonyms: PMPyrr I, PYR13 I, PY13 I, N-Methyl-N-propylpyrrolidinium iodide
- Light sensitive
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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