1-Butyl-2,3-dimethylimidazolium chloride, >99%
Price range: $137.20 through $5,851.45
Product Code: IL-0056-HPCAS NO: 98892-75-2
- Chemical Formula: C9H17ClN2
- Synonyms: BDiMIM Cl, Im114 cl
- Hydrophobic
- Aromatic
SUM Formula: C9H17ClN2
Molecular Weight: 188.70
Melting Point: 100 °C
Density: 1.259 g/cm³
Purity: >99%
- SUM Formula: C9H17ClN2
- Molecular Weight: 188.70
- Melting Point: 100 °C
- Density: 1.259 g/cm³
1-Butyl-2,3-dimethylimidazolium chloride, CAS: 98892-75-2
Key Applications:
Solvent and Reaction Medium
- Functions as a stable, low‑volatility ionic liquid for organic synthesis where enhanced cation steric bulk is beneficial.
- Supports transition‑metal‑catalyzed transformations, including cross‑coupling and hydrogenation, by providing a polar, non‑coordinating environment.
- Useful in acid‑sensitive or moisture‑sensitive systems due to its thermal robustness and low vapor pressure.
Electrochemical and Materials Applications
- Serves as an electrolyte component or ionic additive in electrochemical cells, benefiting from its wide electrochemical window and high ionic conductivity.
- Employed in electrodeposition studies where chloride coordination influences metal nucleation and morphology.
- Acts as a structuring agent in polymer–ionic liquid composites, improving ion transport and mechanical stability.
Extraction and Separation Processes
- Effective in biphasic extraction systems for metal ions, organic molecules, and catalytic species, leveraging its tunable polarity and chloride‑based coordination behavior.
- Supports liquid–liquid extraction workflows in analytical chemistry and process development.
Catalysis and Phase‑Transfer Systems
- Functions as a phase‑transfer medium for reactions requiring chloride availability or enhanced solvation of polar intermediates.
- Can be incorporated into supported ionic liquid phases (SILPs) for heterogeneous catalysis, improving catalyst dispersion and recyclability.
Thermal and Process Engineering Uses
- Suitable as a heat‑transfer or thermal‑stabilizing component in high‑temperature process environments where conventional solvents degrade.
- Utilized in studies of ionic‑liquid structure–property relationships, particularly those involving steric modification of imidazolium cations.
Research and Method Development
- Applied in spectroscopic and mechanistic investigations of ionic‑liquid microenvironments, ion pairing, and solvation dynamics.
- Supports formulation screening in materials science, electrochemistry, and catalysis where chloride‑based ionic liquids serve as benchmarks or tuning agents.
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