1,2-Dimethyl-3-propylimidazolium iodide, >98%
Price range: $87.76 through $3,776.41
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, Im113 I
- Light sensitive
- Aromatic
SUM Formula: C8H15IN2
Molecular Weight: 266.12
Melting Point: 94°C
Density: 1.383 g/cm³ (25 °C)
HMIS Key: NA
Purity: >98%
- SPECIFIC GRAVITY: NA
- SUM Formula: C8H15IN2
- Molecular Weight: 266.12
- Melting Point: 94°C
- Density: 1.383 g/cm³ (25 °C)
- HMIS KEY: NA
1,2-Dimethyl-3-propyl imidazolium Iodide, CAS: 218151-78-1
Key Applications:
- Redox‑Active Electrolytes for Dye‑Sensitized Solar Cells (DSSCs)
- This iodide‑based ionic liquid is widely used as a non‑volatile electrolyte component in DSSCs, where its high ionic conductivity and thermal stability support efficient I⁻/I₃⁻ redox cycling. Its low vapor pressure improves long‑term device durability compared to volatile organic solvents.
- Electrochemical Systems and Charge‑Transfer Media
- The iodide anion and imidazolium cation together provide a tunable medium for electron‑transfer reactions.
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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 PF₆⁻, BF₄⁻, TFSI⁻)
- Task‑specific ionic liquids for catalysis, separations, and materials science
- Solvent and Co‑Solvent in Organic Synthesis
- The compound functions as a polar, aprotic ionic medium.
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- Its thermal robustness and ionic character enable reaction conditions not accessible with conventional solvents.
- Template and Structure‑Directing Agent in Materials Chemistry
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- The cation’s steric profile and charge distribution influence pore formation and morphology.
- Phase‑Transfer and Extraction Applications
- The iodide counterion provides strong nucleophilicity, enabling the ionic liquid to act as a phase‑transfer catalyst.
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