1,2-Dimethyl-3-propylimidazolium iodide, >98%
Price range: $81.84 through $3,521.76
Product Code: IL-0049-HPCAS NO: 218151-78-1
- Chemical Formula: C8H15IN2
- Synonyms: DMPIIm, DMPII, 1-Propyl-2,3-dimethyl-imidazolium iodide, PDiMIM I, C1C1C3Im I, Im113ย I
- Light sensitive
- Aromatic
SUM Formula: C8H15IN2
Molecular Weight: 266.12
Melting Point: 94ยฐC
Density: 1.383 g/cmยณ (25 ยฐC)
HMIS Key: NA
Purity: >98%
- SPECIFIC GRAVITY: NA
- SUM Formula: C8H15IN2
- Molecular Weight: 266.12
- Melting Point: 94ยฐC
- Density: 1.383 g/cmยณ (25 ยฐC)
- HMIS KEY: NA
1,2-Dimethyl-3-propyl imidazolium Iodide, CAS: 218151-78-1
Key Applications:
- RedoxโActive Electrolytes for DyeโSensitized Solar Cells (DSSCs)
- This iodideโbased ionic liquid is widely used as a nonโvolatile electrolyte component in DSSCs, where its high ionic conductivity and thermal stability support efficient Iโป/Iโโป redox cycling. Its low vapor pressure improves longโterm device durability compared to volatile organic solvents.
- Electrochemical Systems and ChargeโTransfer Media
- The iodide anion and imidazolium cation together provide a tunable medium for electronโtransfer reactions.ย
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- Its stable ionic environment supports reproducible electrochemical measurements.
- Precursor for Tailored Ionic Liquid Synthesis
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- Hydrophobic ionic liquids (via anion exchange to PFโโป, BFโโป, TFSIโป)
- Taskโspecific ionic liquids for catalysis, separations, and materials science
- Solvent and CoโSolvent in Organic Synthesis
- The compound functions as a polar, aprotic ionic medium.ย
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- Its thermal robustness and ionic character enable reaction conditions not accessible with conventional solvents.
- Template and StructureโDirecting Agent in Materials Chemistry
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- The cationโs steric profile and charge distribution influence pore formation and morphology.
- PhaseโTransfer and Extraction Applications
- The iodide counterion provides strong nucleophilicity, enabling the ionic liquid to act as a phaseโtransfer catalyst.
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