1,2-Dimethyl-3-propylimidazolium bis(trifluoromethylsulfonyl)imide, >99%
Price range: $179.73 through $9,858.65
Product Code: IL-0134-HPCAS NO: 169051-76-7
- Chemical Formula: C10H15F6N3O4S2
- Synonyms: DMPIIm, PDiMIM BTA, PDiMIM NTf2, PDiMIM TFSI, PDiMIM BTI, IM113ย BTA
- Weakly-coordinating anion
- Aromatic
- Hydrophobic
Conductivity: 1.95 mS/cm (25 ยฐC)
SUM Formula: C10H15F6N3O4S2
Molecular Weight: 419.36
Melting Point: 15 ยฐC
Density: 1.45 g/cmยณ (25 ยฐC)
ECW: 4.6 V
HMIS Key: NA
Purity: >99%
Viscosity: 107 cP (25 ยฐC)
- SPECIFIC GRAVITY: NA
- SUM Formula: C10H15F6N3O4S2
- Molecular Weight: 419.36
- Melting Point: 15 ยฐC
- Density: 1.45 g/cmยณ (25 ยฐC)
- ECW: 4.6 V
- HMIS KEY: NA
- TSCA: NA
- Viscosity: 107 cP (25 ยฐC)
1,2-Dimethyl-3-propylimidazolium bis(trifluoromethylsulfonyl)imide, CAS: 169051-76-7
Key Applications
Electrochemical Systems
- Serves as a highโstability ionic liquid electrolyte component for lithium, sodium, and multivalent metal batteries, benefiting from the TFSIโป anionโs wide electrochemical window and low coordinating character.
- Supports highโtemperature supercapacitor formulations where low volatility and strong thermal resilience are required.
- Functions as a conductive medium in redoxโflow and hybrid flow battery research, particularly where cation structure influences viscosity and ion mobility.
Catalysis and Synthesis
- Acts as a nonโvolatile reaction medium for transitionโmetalโcatalyzed transformations, including CโC and CโN coupling, hydrogenation, and selective oxidations.
- Provides a tunable solvent environment for organocatalysis, enabling enhanced selectivity and recyclability.
- Useful in biphasic catalysis where phase separation and catalyst retention are critical.
Materials Science and Polymer Processing
- Employed as a plasticizer or ionic additive in polymer electrolytes, ionogels, and highโperformance elastomers.
- Facilitates dispersion and stabilization of nanoparticles, carbon materials, and metal oxides due to its balanced polarity and low nucleophilicity.
- Supports surface modification and thinโfilm deposition processes where ionic liquids enable controlled morphology and reduced defect formation.
Separation Science and Extraction
- Functions as an extraction medium for metal ions, hydrophobic organics, and fluorinated species, leveraging the hydrophobic TFSIโป anion.
- Enables selective partitioning in liquidโliquid extraction systems, particularly for rareโearth and transitionโmetal separations.
- Useful in gas absorption studies, including COโ capture, where cation substitution patterns influence solubility and transport.
Thermal and Chemical Stability Applications
- Suitable for highโtemperature lubrication and tribological studies where nonโflammability and thermal endurance are required.
- Serves as a stable medium for studying reaction kinetics under elevated temperatures or inertโatmosphere conditions.
- Supports highโvacuum and highโtemperature environments where conventional solvents degrade or volatilize.
Analytical and Spectroscopic Uses
- Provides a lowโvolatility matrix for electrochemical impedance spectroscopy, NMR diffusion studies, and vibrational spectroscopy.
- Useful in calibrating ion transport models due to its wellโdefined cation structure and predictable physicochemical behavior.
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