1-Butyl-4-methylpyridinium iodide, >98%
Price range: $236.34 through $1,868.36
Product Code: IL-0185-HPCAS 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
SUM Formula: C10H16IN
Molecular Weight: 277.15
Melting Point: 60ยฐC
Density: 1.404 g/cmยณ (24 ยฐC)
Purity: >98%
- SUM Formula: C10H16IN
- Molecular Weight: 277.15
- Melting Point: 60ยฐC
- Density: 1.404 g/cmยณ (24 ยฐC)
1-Butyl-4-methylpyridinium iodide, CAS: 32353-64-3
Key Applications:
Electrochemical Systems
- Serves as a supporting electrolyte in nonโaqueous electrochemical studies where high ionic strength and wide electrochemical windows are required.
- Used in redoxโactive 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 phaseโtransferโactive ionic medium for halideโdriven 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 ThinโFilm Research
- Incorporated into precursor formulations for halideโcontaining thin films, where the iodide counterion can influence crystallization pathways.
- Explored as a structureโdirecting ionic component in polymerโionic liquid composites, improving ion transport and mechanical stability.
- Utilized in studies of ionic liquidโmodified surfaces to adjust wettability, charge distribution, and interfacial behavior.
Solvent Extraction and Separation Processes
- Acts as an iodideโrich 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 halideโcation interactions.
- Serves as a reference ionic liquid for comparative studies across positional isomers (e.g., 2โmethyl, 3โmethyl, 4โmethyl pyridinium salts).
- Supports NMR and IR investigations into cationโanion structuring and hydrogenโbonding environments.
Research and Development
- Suitable for formulation screening in ionic liquid design, enabling structureโproperty comparisons across pyridinium families.
- Used in fundamental studies of halideโdependent 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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