1-(2-Hydroxyethyl)-3-methylimidazolium chloride, >99%

Price range: $107.54 through $3,497.54

Product Code: IL-0039-HP

CAS NO: 61755-34-8

  • Chemical Formula: C6H11ClN2O
  • Synonyms: HO-EMIM Cl
  • Hydrophilic
  • Aromatic
Clear

SUM Formula: C6H11ClN2O

Molecular Weight: 162.62

Melting Point: 83 ยฐC

Density: 1.300 g/cmยณ (26 ยฐC)

Purity: >99%

  • SPECIFIC GRAVITY: NA
  • SUM Formula: C6H11ClN2O
  • Molecular Weight: 162.62
  • Melting Point: 83 ยฐC
  • Density: 1.300 g/cmยณ (26 ยฐC)
  • TSCA: NA

1-(2-Hydroxyethyl)-3-methylimidazolium chloride, CAS: 61755-34-8

Key Applications:

1. Solvent and Coโ€‘solvent in Catalysis

  • Enhances solubility of polar substrates and metal catalysts.
  • Hydroxyl group improves coordination with transitionโ€‘metal centers, supporting homogeneous catalysis.
  • Used in acidโ€‘catalyzed esterifications, dehydration reactions, and biomassโ€‘derived platform molecule upgrading.

2. Biomass Processing and Carbohydrate Chemistry

  • Effective for dissolving cellulose, hemicellulose, and lignin fragments due to strong hydrogenโ€‘bonding capability.
  • Supports pretreatment of lignocellulosic feedstocks for biofuel and biochemical production.
  • Facilitates selective hydrolysis and derivatization of polysaccharides.

3. Electrolytes for Electrochemical Systems

  • High ionic conductivity and strong hydrophilicity make it suitable for aqueous and mixedโ€‘solvent electrolytes.
  • Applied in supercapacitors, electrochemical sensors, and electrodeposition baths.
  • Chloride anion supports metalโ€‘ion complexation in electrodeposition of Cu, Ni, and Co.

4. Extraction and Separation Processes

  • Used in aqueous biphasic systems (ABS) for protein, enzyme, and metalโ€‘ion partitioning.
  • Hydroxyl functionality improves phase behavior and selectivity in ABS formulations.
  • Supports separation of rareโ€‘earth ions and transition metals in hydrometallurgical workflows.

5. Stabilization of Enzymes and Biocatalysis

  • Enhances enzyme solubility and stability in nontraditional media.
  • Applied in lipaseโ€‘catalyzed esterifications, oxidations, and kinetic resolutions.
  • Hydroxyl group reduces denaturing effects compared to more hydrophobic imidazolium salts.

6. Polymer Synthesis and Processing

  • Acts as a reaction medium for ringโ€‘opening polymerization and controlled radical polymerization.
  • Useful as a plasticizer or ionic additive in hydrophilic polymer matrices (e.g., PVA, PEG).
  • Supports fabrication of ionโ€‘conducting polymer films and hydrogels.

7. Corrosion Inhibition

  • Adsorbs strongly onto steel and copper surfaces through imidazolium ring and hydroxyl group.
  • Demonstrates inhibition performance in acidic chloride environments.
  • Used in pickling, pipeline protection, and industrial water systems.

8. COโ‚‚ Capture and Gas Absorption

  • Hydroxyl group enhances chemisorption and physisorption interactions with COโ‚‚.
  • Applied in aqueous IL blends for postโ€‘combustion capture and gasโ€‘scrubbing research.

9. Nanomaterials and Surface Modification

  • Serves as a templating or stabilizing agent for nanoparticles (Au, Ag, Feโ‚ƒOโ‚„).
  • Supports controlled growth of nanostructures due to hydrogenโ€‘bonding and ionic interactions.
  • Used in surface functionalization of silica, graphene oxide, and metal oxides.

10. Organic Synthesis Medium

  • Promotes SN1/SN2 reactions, cyclizations, and nucleophilic substitutions.
  • Hydroxyl functionality modulates polarity and reduces volatility, enabling greener reaction conditions.

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Additional information

Weight 0.025 g
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