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, Im114ย cl
- Hydrophobic
- Aromatic
SUM Formula: C9H17ClN2
Molecular Weight: 188.70
Melting Point: 100 ยฐC
Density: 1.259 g/cmยณ
Purity: >99%
- SUM Formula: C9H17ClN2
- Molecular Weight: 188.70
- Melting Point: 100 ยฐC
- Density: 1.259 g/cmยณ
1-Butyl-2,3-dimethylimidazolium chloride, CAS: 98892-75-2
Key Applications:
Solvent and Reaction Medium
- Functions as a stable, lowโvolatility ionic liquid for organic synthesis where enhanced cation steric bulk is beneficial.
- Supports transitionโmetalโcatalyzed transformations, including crossโcoupling and hydrogenation, by providing a polar, nonโcoordinating environment.
- Useful in acidโsensitive or moistureโsensitive 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 polymerโionic 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 chlorideโbased coordination behavior.
- Supports liquidโliquid extraction workflows in analytical chemistry and process development.
Catalysis and PhaseโTransfer Systems
- Functions as a phaseโtransfer 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 heatโtransfer or thermalโstabilizing component in highโtemperature process environments where conventional solvents degrade.
- Utilized in studies of ionicโliquid structureโproperty relationships, particularly those involving steric modification of imidazolium cations.
Research and Method Development
- Applied in spectroscopic and mechanistic investigations of ionicโliquid microenvironments, ion pairing, and solvation dynamics.
- Supports formulation screening in materials science, electrochemistry, and catalysis where chlorideโbased ionic liquids serve as benchmarks or tuning agents.
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