1-(2-Hydroxyethyl)-3-methylimidazolium tetrafluoroborate, >98%

Price range: $128.80 through $1,163.41

Product Code: IL-0038-HP

CAS NO: 374564-83-7

  • Chemical Formula: C6H11BF4N2O
  • Synonyms: HO-EMIM BF4
  • Anion decomposes slowly in the presence of water
  • Hydrophilic
  • Aromatic
Clear

Conductivity: 3.42 mS/cm (20 ยฐC)

SUM Formula: C6H11BF4N2O

Molecular Weight: 213.97

Melting Point: -44 ยฐC

Density: 1.34 g/cmยณ (22 ยฐC)

Purity: >98%

Viscosity: 137 cP (20 ยฐC)

  • SPECIFIC GRAVITY: NA
  • SUM Formula: C6H11BF4N2O
  • Molecular Weight: 213.97
  • Melting Point: -44 ยฐC
  • Density: 1.34 g/cmยณ (22 ยฐC)
  • TSCA: NA
  • Viscosity: 137 cP (20 ยฐC)

1- (2-Hydroxyethyl)-3-methylimidazolium Tetrafluoroborate, CAS: 374564-83-7

Key Applications:

1. Solvent and Coโ€‘solvent in Organic Synthesis

  • Supports acidโ€‘catalyzed and metalโ€‘catalyzed transformations due to its polar, mildly coordinating environment.
  • Hydroxyl group enhances miscibility with water and alcohols, enabling biphasic or monophasic reaction tuning.
  • Useful in nucleophilic substitution, esterification, and condensation reactions where controlled polarity is beneficial.

2. Medium for Biocatalysis

  • Hydroxyl-functionalized ionic liquids often improve enzyme stability and activity relative to non-functionalized ILs.
  • Suitable for lipaseโ€‘catalyzed esterifications, transesterifications, and kinetic resolutions.
  • BFโ‚„โป salts with hydroxyethyl cations can modulate water activity, improving selectivity in biotransformations.

3. Electrochemical Applications

  • Serves as a conductive electrolyte or electrolyte additive in systems requiring high ionic strength and low volatility.
  • Hydroxyl group increases hydrogenโ€‘bonding networks, influencing viscosity and ionic mobility.
  • Applicable in supercapacitors, electrochemical sensors, and electrodeposition environments where protic ILs improve interface behavior.

4. Gas Absorption and Separation

  • Hydroxyethyl-functionalized ILs show enhanced COโ‚‚ solubility via physical absorption and weak chemisorption.
  • Can be used in COโ‚‚ capture, acid gas scrubbing, and gasโ€“liquid separation studies.
  • BFโ‚„โป anion provides relatively low viscosity compared to more strongly coordinating anions, improving mass transfer.

5. Catalytic Support and Reaction Medium for Green Chemistry

  • Acts as a recyclable reaction medium for catalytic systems (e.g., Pd, Cu, Brรธnsted acids).
  • Hydroxyl group can participate in secondary interactions that stabilize catalytic intermediates.
  • Useful in microwaveโ€‘assisted and solventโ€‘free reaction protocols.

6. Polymer and Material Processing

  • Functions as a plasticizer or processing aid for polar polymers such as PVA, cellulose derivatives, and polyamides.
  • Hydroxyl-functionalized ILs can dissolve or swell biopolymers, enabling film formation, fiber spinning, or composite preparation.
  • BFโ‚„โป salts are often used in ion-conductive polymer blends.

7. Extraction and Separation Processes

  • Effective in liquidโ€“liquid extraction of metal ions, dyes, and polar organics due to tunable polarity.
  • Hydroxyl group enhances selectivity for hydrogenโ€‘bonding solutes.
  • Useful in aqueous biphasic systems (ABS) when paired with salts or polymers.

8. Thermal Fluids and Heatโ€‘Transfer Media

  • High thermal stability and negligible vapor pressure make it suitable for heatโ€‘transfer and thermal storage studies.
  • Hydroxyl functionality can modulate heat capacity and viscosity relative to alkyl-only ILs.

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Additional information

Weight 0.025 g
Qty

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