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1-(2’-hydroxylethyl)-3-methylimidazolium chloride

  • CAS No. 61755-34-8

  • Cat. No. CS-0158152
  • Purity≥98%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

1-(2’-hydroxylethyl)-3-methylimidazolium chloride|CS-0158152

Structure of 61755-34-8

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General Information

  • CAS No. 61755-34-8
  • Cat. No. CS-0158152
  • Purity ≥98%
  • MDL No. None
  • Storage Store at room temperature, keep dry and cool
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₁₁ClN₂O
  • Molecular Weight 162.62
  • Synonym(s) 1-(2-Hydroxyethyl)-3-methylimidazolium chloride
  • SMILES C[N+]1=CN(C=C1)CCO.[Cl-]

Description

This imidazolium salt features a hydroxylethyl side chain enabling hydrogen bonding and enhanced solubility in polar media. The chloride anion provides good ionic conductivity, while the methyl group at the 3-position stabilizes the cationic center. Designed for use in protic ionic liquids and electrochemical applications requiring tunable polarity and low volatility.

Application

1-(2’-Hydroxylethyl)-3-methylimidazolium chloride serves as a versatile ionic liquid precursor, enabling efficient synthesis of functionalized imidazolium salts with enhanced solubility and thermal stability. The hydroxylethyl side chain facilitates downstream derivatization through etherification or esterification, while the chloride counterion supports straightforward anion exchange. This compound functions effectively in catalytic systems, phase-transfer applications, and as a building block for bioactive heterocycles, offering bench-stable handling and compatibility with standard synthetic protocols.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H315-H319
Precautionary Statements : P264-P280-P302+P352-P362+P364

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Computational Chemistry Data

  • TPSA   29.04
  • LogP   -3.6911
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   2

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