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CAS 655249-87-9

1-Allyl-3-methylimidazolium Bis(trifluoromethanesulfonyl)imide TCI A3210

1-Allyl-3-methylimidazolium Bis(trifluoromethanesulfonyl)imide TCI A3210

Chemical Identity

CAS No.
655249-87-9
PubChem
CID 71310876·SID 354335682
Formula
C9H11F6N3O4S2
Molecular weight
403.3 g/mol
Purity
>98.0%(HPLC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
bis(trifluoromethylsulfonyl)azanide;1-methyl-3-prop-2-enylimidazol-1-ium
SMILES
C[N+]1=CN(C=C1)CC=C.C(F)(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F
InChIKey
DHMWATGUEVQTIY-UHFFFAOYSA-N
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1-Allyl-3-methylimidazolium Bis(trifluoromethanesulfonyl)imide is an ionic liquid widely used in complex chemical reactions within laboratory settings. As a unique ionic compound, it consists of the cation 1-allyl-3-methylimidazolium and the anion bis(trifluoromethanesulfonyl)imide. This material plays a crucial role in various synthetic processes due to its exceptional chemical stability and non-volatile nature. Its ability to remain in liquid form at high temperatures makes it ideal for reactions that require elevated thermal conditions.

The properties of this ionic liquid make it a preferred choice for advanced chemical applications. It is non-toxic, stable under a wide range of chemical conditions, and has low viscosity, which facilitates efficient mixing and reaction processes. Its solubility in various organic solvents enhances its utility in separation and purification techniques. These characteristics ensure that it remains a reliable and safe material for use in modern laboratory environments.

In Indonesian laboratories, this ionic liquid is commonly used in applied chemistry research, particularly in organic synthesis and electrochemistry. Its versatility supports the development of new technologies, including batteries and catalysts. Due to its unique properties, it is a valuable resource for academic and industrial research institutions in Indonesia.

Advantages (TCI brochure)

  • Bears allyl groups, reported as useful starting material for polymers with ionic liquid properties

TCI brochures (PDF)

  • Organic synthesis applications benefit from this ionic liquid due to its non-volatile nature and high thermal stability, allowing for prolonged reaction times without evaporation.
  • Electrochemical studies utilize this material because of its stable ionic environment and ability to support redox reactions under controlled conditions.
  • Solvent replacement in green chemistry is enhanced by its low toxicity and recyclability, making it a sustainable alternative to traditional volatile solvents.
  • Catalytic processes are supported by its ability to dissolve a wide range of substrates, improving reaction efficiency and product yield.
  • Battery development leverages its ionic conductivity and thermal stability, contributing to the performance and longevity of advanced energy storage systems.

From the TCI brochure

  • Polymeric electrolytes

Brand TCI
CAS number 655249-87-9
Molecular formula —
Purity —
Category Chemistry > Specialty Synthesis > Ionic Liquids
Pack sizes Available in various quantities as per supplier specifications
Physical form Liquid
Storage Store in a cool, dry place away from direct sunlight and incompatible materials

This ionic liquid should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use sealed, non-reactive containers such as glass or high-density polyethylene to prevent contamination and evaporation. As it is non-volatile, it does not require refrigeration but should be kept in a secure location to avoid accidental spills. In laboratory settings, proper personal protective equipment, including gloves and safety goggles, should be worn when handling. Regular inspection of storage containers is advised to ensure integrity and safety.

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