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CAS 65039-10-3

1-Allyl-3-methylimidazolium Chloride TCI A2084

1-Allyl-3-methylimidazolium Chloride TCI A2084

Chemical Identity

CAS No.
65039-10-3
PubChem
CID 11321106·SID 354334727
Formula
C7H11ClN2
Molecular weight
158.63 g/mol
Purity
>98.0%(HPLC)(T)
Reference databases
ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
1-methyl-3-prop-2-enylimidazol-1-ium chloride
SMILES
C[N+]1=CN(C=C1)CC=C.[Cl-]
InChIKey
QVRCRKLLQYOIKY-UHFFFAOYSA-M
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1-Allyl-3-methylimidazolium Chloride is an ionic liquid widely used in chemical and synthetic applications within laboratory settings. As a unique ionic compound, it consists of an imidazolium cation and a chloride anion, providing it with distinct chemical and physical properties. This material plays a crucial role in various experimental processes, serving as a solvent, reaction medium, or catalyst support in complex chemical syntheses. Its versatility makes it a valuable tool for researchers in both academic and industrial environments.

The compound is preferred due to its non-volatile nature, high boiling point, and excellent ionic conductivity. These properties make it ideal for reactions requiring stable and controlled conditions. Additionally, its non-flammable, colorless, and odorless characteristics contribute to its safety and efficiency in laboratory use. The absence of water and its resistance to evaporation further enhance its suitability for applications demanding high purity and chemical stability.

In Indonesian laboratories, 1-Allyl-3-methylimidazolium Chloride is commonly used in electrochemical studies, organic synthesis, and as a reaction medium for high-purity processes. Its ability to maintain chemical integrity under varying conditions makes it a reliable choice for researchers working on advanced chemical projects. The compound’s unique properties ensure it remains a key component in many experimental workflows.

Advantages (TCI brochure)

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

TCI brochures (PDF)

  • Electrochemical studies benefit from its high ionic conductivity, allowing efficient ion transfer in electrochemical cells.
  • Organic synthesis reactions often utilize this ionic liquid as a non-aqueous solvent due to its stability and inertness.
  • It serves as a reaction medium for high-purity chemical processes, ensuring minimal contamination from volatile solvents.
  • In catalytic reactions, its non-volatile nature helps maintain reaction conditions without the need for frequent solvent replacement.
  • It is used in green chemistry applications as an environmentally friendly alternative to traditional volatile organic solvents.

From the TCI brochure

  • Polymeric electrolytes
  • Polymer monolith

Brand TCI
CAS number 65039-10-3
Molecular formula —
Purity —
Category Chemistry > Specialty Synthesis > Ionic Liquids
Pack sizes Available in various quantities as per supplier listing
Physical form Liquid
Storage Store in a cool, dry place away from direct sunlight

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 containers made of materials compatible with its chemical nature, such as glass or high-density polyethylene. Due to its non-volatile properties, it does not require frequent replenishment, but regular checks for container integrity are advised. In laboratory settings, it should be handled with standard chemical safety precautions, including the use of appropriate personal protective equipment. Its non-flammable nature reduces fire hazards, but it should still be kept out of reach of children and unauthorized personnel. Proper labeling and storage practices ensure safe and effective use in research environments.

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