1-Butyl-1-methylpiperidinium bromide, >99%
Price range: $151.42 through $3,466.39
Product Code: IL-0153-HPCAS NO: 94280-72-5
- Chemical Formula: C10H22BrN
- Synonyms: N-Butyl-N-methylpiperidinium bromide, BMPip Br, PIP14 Br
SUM Formula: C10H22BrN
Molecular Weight: 236.19
Melting Point: 231 °C
Density: 1.053 g/cm³
Purity: >99%
- SUM Formula: C10H22BrN
- Molecular Weight: 236.19
- Melting Point: 231 °C
- Density: 1.053 g/cm³
1-Butyl-1-methylpiperidinium bromide, CAS: 94280-72-5
Key Applications:
Electrochemical Systems
- Employed as a supporting electrolyte in cyclic voltammetry, electrodeposition, and redox‑active materials research.
- Used in ionic‑liquid‑based electrolytes for batteries, supercapacitors, and ion‑transport studies where low volatility and stable ion pairing are required.
- Supports metal‑ion solvation and controlled electrode interfaces in fundamental electrochemistry.
Catalysis & Reaction Media
- Functions as a non‑volatile solvent or co‑solvent for transition‑metal catalysis, phase‑transfer catalysis, and nucleophilic substitution reactions.
- Provides a tunable ionic environment that enhances reaction rates, selectivity, and catalyst recyclability.
- Suitable for green‑chemistry workflows due to low vapor pressure and reusability.
Materials Science & Polymer Processing
- Serves as a plasticizing ionic additive in polymer electrolytes, ionogels, and conductive films.
- Used in nanomaterial dispersion, including carbon nanostructures and metal nanoparticles, where ionic stabilization is beneficial.
- Supports thin‑film fabrication and surface modification studies requiring controlled ionic interfaces.
Separation Science & Extraction
- Applied in liquid–liquid extraction systems for metal ions, organic molecules, and environmental analytes.
- Enables selective partitioning due to its structured ionic environment and tunable solvation behavior.
Spectroscopy & Fundamental Research
- Utilized as a model ionic medium for studying ion pairing, solvation dynamics, and transport phenomena.
- Compatible with NMR, FTIR, Raman, and conductivity studies requiring stable, non‑volatile ionic matrices.
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