1-Butyl-4-methylpyridinium iodide, >98%

Price range: $236.34 through $1,868.36

Product Code: IL-0185-HP

CAS NO: 32353-64-3

  • Chemical Formula: C10H16IN
  • Synonyms: Bu-4-Pic I, Bu4Pic I, 1-Butyl-4-picolinium iodide, N-Butyl-4-methylpyridinium iodide, N-Butyl-4-picolinium iodide
  • Light sensitive
  • Aromatic
Clear

SUM Formula: C10H16IN

Molecular Weight: 277.15

Melting Point: 60°C

Density: 1.404 g/cm³ (24 °C)

Purity: >98%

  • SUM Formula: C10H16IN
  • Molecular Weight: 277.15
  • Melting Point: 60°C
  • Density: 1.404 g/cm³ (24 °C)

1-Butyl-4-methylpyridinium iodide, CAS: 32353-64-3

Key Applications:

Electrochemical Systems

  • Serves as a supporting electrolyte in non‑aqueous electrochemical studies where high ionic strength and wide electrochemical windows are required.
  • Used in redox‑active systems to stabilize charged intermediates and improve conductivity in organic media.
  • Investigated in electrodeposition research, particularly where halide coordination influences metal nucleation behavior.

Catalysis and Organic Synthesis

  • Functions as a phase‑transfer‑active ionic medium for halide‑driven transformations, including nucleophilic substitution and alkylation reactions.
  • Employed as a tunable ionic additive to influence reaction selectivity, solvation environment, and reagent dispersion in homogeneous catalysis.
  • Useful in mechanistic studies examining how pyridinium cations modulate halide availability and reaction kinetics.

Materials Science and Thin‑Film Research

  • Incorporated into precursor formulations for halide‑containing thin films, where the iodide counterion can influence crystallization pathways.
  • Explored as a structure‑directing ionic component in polymer–ionic liquid composites, improving ion transport and mechanical stability.
  • Utilized in studies of ionic liquid–modified surfaces to adjust wettability, charge distribution, and interfacial behavior.

Solvent Extraction and Separation Processes

  • Acts as an iodide‑rich ionic phase for selective extraction of metal ions that form stable iodide complexes.
  • Supports biphasic separation systems where hydrophobic cation/halide combinations enhance partitioning efficiency.
  • Applied in analytical extraction workflows requiring controlled halide activity.

Spectroscopy and Analytical Chemistry

  • Used as a calibration or matrix component in spectroscopic studies probing ion pairing, solvation, and halide–cation interactions.
  • Serves as a reference ionic liquid for comparative studies across positional isomers (e.g., 2‑methyl, 3‑methyl, 4‑methyl pyridinium salts).
  • Supports NMR and IR investigations into cation–anion structuring and hydrogen‑bonding environments.

Research and Development

  • Suitable for formulation screening in ionic liquid design, enabling structure–property comparisons across pyridinium families.
  • Used in fundamental studies of halide‑dependent reactivity, ion mobility, and thermal behavior.
  • Supports development of custom electrolytes, catalytic media, and separation systems where iodide activity is a key variable.

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Additional information

Weight 25 g
Qty

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