1-Butyl-4-methylpyridinium bromide, >99%
Price range: $193.81 through $4,829.58
Product Code: IL-0082-HPCAS NO: 65350-59-6
- Chemical Formula: C10H16BrN
- Synonyms: Bu-4-Pic Br, Bu4Pic Br, 1-Butyl-4-picolinium bromide, N-Butyl-4-methylpyridinium bromide, N-Butyl-4-picolinium bromide, 4MBPBr
- Aromatic
SUM Formula: C10H16BrN
Molecular Weight: 230.15
Melting Point: 118 °C
Density: 1.556 g/cm³
Purity: >99%
- SUM Formula: C10H16BrN
- Molecular Weight: 230.15
- Melting Point: 118 °C
- Density: 1.556 g/cm³
1-Butyl-4-methylpyridinium bromide, CAS: 65350-59-6
Key Applications:
Electrochemistry & Energy Storage
- Employed as a supporting electrolyte in voltammetry, electrodeposition, and redox‑active systems due to its wide electrochemical window and stable cation framework.
- Used to study ion transport, charge mobility, and interfacial behavior in ionic‑liquid–based electrolytes for batteries and capacitors.
- Serves as a medium for metal ion stabilization and controlled electrodeposition.
Catalysis & Organic Synthesis
- Functions as a non‑volatile reaction solvent for nucleophilic substitutions, oxidations, and transition‑metal‑catalyzed transformations.
- Enhances catalyst dispersion and selectivity in biphasic and phase‑transfer systems.
- Supports green‑chemistry workflows by replacing volatile organic solvents.
Solvent Extraction & Separation Science
- Applied in liquid–liquid extraction of metal ions, dyes, and organic solutes, leveraging its tunable polarity and strong anion–cation interactions.
- Used in partitioning studies to model solvation dynamics and ion‑pairing behavior.
- Supports chromatographic method development as an ionic additive or mobile‑phase modifier.
Materials Science & Polymer Research
- Incorporated into polymer matrices to modify conductivity, thermal stability, and mechanical properties.
- Used as a templating or structure‑directing agent in the synthesis of porous materials and nanostructures.
- Serves as a plasticizer or ionic dopant in advanced functional materials.
Spectroscopy & Fundamental Studies
- Provides a controlled ionic environment for NMR, IR, and UV–Vis investigations of solvation, ion pairing, and molecular interactions.
- Used in benchmarking studies comparing pyridinium ionic liquids with imidazolium and ammonium analogues.
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