1-Butyl-3-methylimidazolium methylcarbonate, >97%, 30% in MeOH

Price range: $39.60 through $432.00

Product Code: IN-0028-SG

CAS NO: 916850-37-8

  • Chemical Formula: C10H18N2O3
  • Synonyms: BMIM MeCO3, C1C4Im MeCO3, Im14 MeCO3
  • Hydrophilic

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SUM Formula: C10H18N2O3

Molecular Weight: 214.13

Purity: >97%

  • SUM Formula: C10H18N2O3
  • Molecular Weight: 214.13

1-Butyl-3-methylimidazolium methylcarbonate, CAS: 916850-37-8

Key Applications:

Solvent and Medium for Organic Synthesis

  • Functions as a polar, nonโ€‘volatile reaction medium for nucleophilic substitutions, condensations, and baseโ€‘sensitive transformations.
  • Supports homogeneous catalysis and transitionโ€‘metalโ€“mediated coupling reactions by stabilizing reactive intermediates.
  • The methylcarbonate anion provides mild basicity, enabling selective deprotonation without the harshness of inorganic bases.

COโ‚‚โ€‘Responsive and Carbonateโ€‘Based Chemistry

  • Useful in COโ‚‚โ€‘capture and COโ‚‚โ€‘activation studies due to the reversible nature of the methylcarbonate anion.
  • Serves as a model ionic liquid for probing carbonate equilibria, anion exchange, and COโ‚‚โ€‘triggered speciation changes.
  • Employed in developing reversible COโ‚‚โ€‘binding solvents and switchable polarity systems.

Polymer Processing and Functional Material Development

  • Acts as a processing aid for cellulose, chitosan, and other biopolymers that require strong hydrogenโ€‘bond disruption.
  • Supports the preparation of carbonateโ€‘functionalized polymers and polymer electrolytes.
  • Enables dissolution and regeneration workflows for sustainable materials research.

Electrochemical and Energyโ€‘Related Applications

  • Provides a stable ionic environment for electrochemical studies, including electrodeposition and redoxโ€‘active species stabilization.
  • Investigated as a component in electrolyte formulations for lowโ€‘volatility, nonโ€‘flammable systems.
  • The carbonate anion contributes to SEIโ€‘relevant decomposition pathways, making it useful in mechanistic battery research.

Catalysis and Reaction Engineering

  • Enhances catalytic turnover in baseโ€‘assisted reactions due to its intrinsic anion basicity.
  • Supports organocatalytic transformations where carbonate species participate in proton shuttling or transient activation.
  • Compatible with biphasic catalysis and catalyst recycling strategies.

Separation Science and Extraction

  • Applied in liquidโ€“liquid extraction of metal ions, organic acids, and polar organics.
  • The carbonate anion modulates extraction selectivity through tunable hydrogenโ€‘bonding and acidโ€“base interactions.
  • Useful in designing greener extraction systems with reduced volatility and improved recyclability.

Analytical and Spectroscopic Studies

  • Serves as a reference ionic liquid for studying carbonate speciation, ion pairing, and solventโ€“solute interactions.
  • Suitable for NMR, IR, and conductivity studies due to its wellโ€‘defined structure and high purity.
  • The methanol solution format (30% in MeOH) improves handling and facilitates direct injection into analytical workflows.

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Additional information

Weight 0.025 g
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