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HS Code |
602026 |
| Chemical Name | 1-Propyl-2,3-Dimethylimidazolium Hexafluorophosphate |
| Cas Number | 658444-85-4 |
| Molecular Formula | C8H16N2PF6 |
| Molecular Weight | 282.20 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Melting Point | -15 °C |
| Boiling Point | Decomposes before boiling |
| Density | 1.263 g/cm3 (at 25 °C) |
| Purity | Typically >98% |
| Solubility In Water | Slightly soluble |
| Storage Temperature | Room temperature, tightly sealed |
| Iupac Name | 1-propyl-2,3-dimethylimidazolium hexafluorophosphate |
As an accredited 1-Propyl-2,3-Dimethylimidazolium Hexafluorophosphate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100g, sealed with a PTFE-lined cap; chemical label lists "1-Propyl-2,3-Dimethylimidazolium Hexafluorophosphate," hazard symbols, and lot number. |
| Shipping | 1-Propyl-2,3-Dimethylimidazolium Hexafluorophosphate is shipped in tightly sealed containers, protected from moisture and heat. Appropriate labeling and documentation are provided. Handling complies with local and international regulations for chemicals, ensuring safety during transit. The product is typically shipped by ground or air, depending on destination and required delivery time. |
| Storage | Store 1-Propyl-2,3-dimethylimidazolium hexafluorophosphate in a tightly sealed container, away from moisture and incompatible substances such as strong oxidizers. Keep it in a cool, dry, well-ventilated area, protected from direct sunlight. Use non-reactive shelving and secondary containment. Ensure proper labeling and restrict access to trained personnel. Wear appropriate personal protective equipment when handling the chemical. |
Applications of 1-Propyl-2,3-Dimethylimidazolium Hexafluorophosphate in Industrial Manufacturing1-Propyl-2,3-dimethylimidazolium hexafluorophosphate is an advanced ionic liquid known for its chemical stability, negligible volatility, and unique solvation properties. As the original manufacturer, we supply this material for industries with strict process and compliance requirements, where its performance benefits are validated by real-world integration in high-value downstream manufacturing. The following application scenarios reflect its established roles in industrial and specialty chemical processes. 1. Electrolyte Additive in Supercapacitor and Lithium-Ion Battery ProductionOur supplied ionic liquid is actively used by manufacturers of high-performance energy storage devices to improve electrochemical stability and extend operational temperature ranges. The compound is blended into battery and supercapacitor electrolytes, supporting the development of safer and more durable electrical storage solutions, especially for automotive and grid-scale markets. Industry compliance standards
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2. Medium for Metal Electrodeposition and ElectroplatingElectroplating manufacturers utilize our ionic liquid as a non-aqueous medium for the deposition of metals such as aluminum and nickel, enabling smoother, defect-free coatings at lower environmental impact compared to cyanide or other conventional electrolyte systems. Its ionic conductivity supports controlled thickness and uniformity, particularly for precision electronic parts and aerospace components. Industry compliance standards
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3. Solvent in Cellulose Dissolution and Fiber Preparation for Specialty TextilesFiber producers leverage the solvating power of our ionic liquid to dissolve high molecular weight cellulose, enabling the direct spinning of regenerated cellulose fibers and films with reduced byproducts. The controllable solubility assists in producing uniform fibers for technical textiles and biomedical applications where process residue limitations are critical. Industry compliance standards
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4. Reaction Solvent and Phase Transfer Medium in Organic SynthesisSynthesis plants and fine chemical manufacturers select this ionic liquid as a reaction solvent and phase transfer medium for specialty organic transformations, particularly in nucleophilic substitutions where traditional solvents either limit conversion or pose greater handling risks. Its negligible vapor pressure contributes to contained processing and enhanced yield of target molecules. Industry compliance standards
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5. Lubrication Base for High-Temperature Engineering ApplicationsEquipment manufacturers and component OEMs use our ionic liquid as a synthetic lubricant base for bearings and moving interfaces operating under high thermal and oxidative stress, especially where mineral oil and standard synthetic bases degrade. The low volatility and ionic character enable reduced wear and extended maintenance intervals in production-line robotics and aerospace actuators. Industry compliance standards
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At our manufacturing facility, chemical performance is personal. We handle each batch of 1-Propyl-2,3-Dimethylimidazolium Hexafluorophosphate with the care one only finds where expertise and daily hands-on work meet. This material goes well beyond laboratory curiosity; it anchors benchwork and real process needs in high-value chemical industries. Its formula—updating the imidazolium backbone with two crucial methyl substitutions at the 2 and 3 positions, connected through a propyl chain, and partnered with the stable hexafluorophosphate anion—delivers a robust ionic liquid that answers industry’s call for clean, enduring solvents and safe electrolytes.
Over years, we’ve tracked exactly what makes an ionic liquid reliable. Not just with a spec sheet but in the flesh—clarity in the flask, a telltale lack of odor, reactivity firmly under control, and true, nail-down stability. After production, our teams run every order through actual working conditions to catch out any sign of water load, trace metal residues, or batch-to-batch drift in purity. Labs and industrial partners count on that honesty. If a solvent leaves even a hint of environmental or safety question marks, it ends up flagged, not boxed for delivery.
You see, most high-purity ionic liquids out there still fall into gray areas. Maybe the chloride content runs a tad high, maybe there’s lingering color, maybe the viscosity fights your process or post-run cleaning. But starting with 1-Propyl-2,3-Dimethylimidazolium Hexafluorophosphate means much less hands-on troubleshooting. The methyl groups cap the most reactive hot spots on the ring, lowering side reactivity—especially when paired with catalysts that would otherwise start chewing up classic imidazoliums. Synthetic chemists in our partner labs report more straightforward product isolation, sharper peaks in analysis, and far less chance of fouling or resinous build-up in flow reactors.
To offer a product right up to industrial and research standards, bulk lots come from a standardized route, free from ambiguous co-product overlays. Our typical production model (our own internal codename: IMPR-DM-HPF6) falls between 99.0% and 99.9% purity—an absolute floor, not an average. Product ships with documentation from in-house NMR and ion chromatography, not just paper specs from a catalog. Residual solvents, moisture (we keep this under 100 ppm), and acid numbers receive a critical eye, especially because just a hair too much water will wreck electrochemical reliability in real-world batteries or supercapacitor development.
Color matters, especially for users pushing photochemical work. We target a water-clear end product rather than “light yellow” allowances. In-house, this already cut out one round of post-filtration for many of our customers. Melting points tend to remain stable, but the biggest value comes from purification—fewer hidden species mean a lower risk of crystallization or phase separation during temperature cycling.
Researchers and engineers alike gravitate toward 1-Propyl-2,3-Dimethylimidazolium Hexafluorophosphate when old options clog up or demand lengthy pre-cleaning. Real-world electrolytic cells using this specific cation/anion blend run at wide electrochemical windows—over 4.5 volts in actual use, by our last round of cyclic voltammetry. Product developers in supercapacitors and energy storage reach for it because the combination of chemical stability and relatively high ionic mobility outperforms older alkylimidazolium salts. Our feedback comes straight from people building new lab-scale devices, hunting for both energy density and operational safety.
Catalytic processes with sensitive organometallics reveal another key difference. Our two methyl substitutions do more than tweak the viscosity; they shield the key ring positions from unexpected nucleophilic attack. This matters especially for long reaction runs in pharmaceutical and specialty chemical routes, where contamination or unplanned side reactions can burn through raw material and cost. The propyl chain increases fluid flexibility without crossing into “grease” territory. This means easier handling and faster mixing, especially at scale. Few suppliers can promise (or check for) salt stability over weeks, not just hours, but batches from our line consistently show zero detectable decomposition after weeks sealed in standard containers.
Ionic liquids all share certain broad claims, but we see major, ground-level differences every month between variants with different cation and anion pairs. In our tanks, a change from ethyl to propyl holds up through actual trials—propyl gives markedly improved solubility with many organics and less tendency to pick up water from the air. Compare it to standard 1-Butyl-3-methylimidazolium hexafluorophosphate: propyl-dimethyl closes down vulnerability to nucleophilic attack and slows down any hydrolysis of the PF6- anion. Way less hydrofluoric acid risk, way less headache. We watch our shelf-life data closely; the extra methyl groups add months of stability in ambient storage.
On a practical level, you notice the difference as soon as you work with aggressive or high-value reagents. Where traditional ionic liquids sometimes start browning or releasing strange smells after a few cycles, our 1-Propyl-2,3-dimethyl analog stands up to dozens of runs. The difference often shows up most for people recycling solvents—minimal buildup, less discoloration, and fewer fines clogging up inlets. Electrochemical users love the extra resistance to oxidation, pointing out the improved safety margin compared to basic tetraalkylammonium salts or older pyrrolidinium-based fluids.
We built up our process mostly listening to what industrial colleagues want out of a working ionic liquid. For supercapacitor developers, the window between electrode oxidation and reduction must be both broad and stable. Cell life and reproducibility matter even more than cost; our product’s record on those counts keeps customers coming back, often displacing less stable or more expensive salts.
Lab users working in catalysis need a solvent that won’t steal ligands or cause headaches with purification later. 1-Propyl-2,3-Dimethylimidazolium Hexafluorophosphate offers both a polar, aprotic medium with low enough viscosity to actually stir—and one that shrugs off both strong nucleophiles and basic washes. In the past twelve months alone, feedback on our product from carbon–carbon coupling reactions put it above both standard butyl and ethyl imidazolium options, especially when researchers worked at high concentration or recycled the solvent through several runs.
We’ve seen the biggest jump in demand from those using the product in extraction and separation, especially where the critic is trace water, base, or challenging recovery. Users report sharper phase boundaries and less formation of emulsions, shaving hours off process optimization. Waste minimization matters too: hexafluorophosphate as an anion offers a good line between conductivity and stability, with easier downstream waste treatment than some bulkier or more reactive anionic partners.
Unlike catalog sellers, we don’t just buy in stock and relabel it. Every decision going into our manufacturing line started with hands-on failures: early years taught us that sub-par purification, leftover metal from first-generation vessels, or minimal post-synthesis filtration all ramp up problems at the customer end. Only regular, specific upgrades—reactor material improvements, new ion-exchange steps, and careful control of drying parameters—turned this product into something reliable for sensitive applications.
Small tweaks matter: even a ten-degree drop or a few extra vacuum hours between synthesis steps cuts down on byproducts. We routinely throw out starting batches if they test above our moisture threshold or attract dust from poor cleanroom handling. This approach doesn’t make us fastest in shipping, but for those who need uncompromising results, it pays off with fewer bottlenecks down the line.
The biggest difference comes from in-house feedback channels. Our team brings in new data every week—trials of two pilot reactors last quarter let us shave another ten parts per million off the acid content. Changes don’t just come from the top; line technicians often spot early warning signs of drift in color or viscosity. By tuning procedures on the fly—and putting more weight on actual application feedback than on theoretical numbers—we've raised the floor on batch reliability for our flagship ionic liquid.
Handling ionic liquids safely demands experience that only comes from years on the job. We’ve learned to minimize both direct risks and environmental side issues by sticking to good process hygiene and honest reporting. Hexafluorophosphate systems inspire well-founded concern, mostly due to potential PF6– breakdown and trace HF formation in the presence of moisture or acid. Careful synthesis and drying let us shut down this risk to a point where workers face orders-of-magnitude lower exposure than with older, less stable analogs.
Our internal safety data backs this up—over a decade, not one batch flagged for HF, even under worst-case accelerated aging. We recommend all users maintain solid lab safety protocols, but our quality team tracks this by running acid strip tests and water quantitation on every drum released. Waste treatment after industrial use still needs attention: our waste stream integrates ion exchange and alkaline scrubbing to prevent PF6– escape or fluoride release.
On the environmental side, ionic liquids in general tend to outlast standard volatile organics—lower vapor pressure, lower flammability, minimal off-gassing. We take extra steps with each batch, pushing all fractions through waste separation until we’re satisfied nothing hits effluent over regulatory limits. This isn’t a theoretical result; it’s the net effect of a dozen small, real-world upgrades based on in-plant feedback and environmental audits. Anyone new to ionic liquid processes sees the impact fast: less solvent loss, safer air handling, and a traceable trail of compliance.
Distribution of high-stability ionic liquids throws up practical challenges. Trace contamination—you won’t always see it until something fails. We attack this by maintaining stringent purity controls, not just at the lab bench but all the way through shipping. Leakproof, water-free containers mean less stress for users—no one likes hunting for the source of a reaction gone wrong, only to find the culprit was a leaky cap or a poorly flushed transfer pipe.
On the industrial scale, any recurring differential between order-to-order batches means reworking protocols, running repeated checks, and slowing down production lines. Keeping their product steady batch to batch, our technicians live this reality: even a half-degree variance at the wrong spot in the distillation curve shows up weeks later, not in a glossy catalog but on a shop floor troubleshooting board. Only rigorous batch history and continuous monitoring let us spot these issues before customers ever get the product.
We also address end-of-life and waste. Disposal of spent ionic liquids stays under real scrutiny by regional and global organizations. Working with specialized partners, we design closed-loop routes for collection, purification, and safe breakdown of spent material. The same goes for user education—confusion about shelf life, storage, or compatibility can waste good solvent and slow research. That’s why we supply straightforward tips (not endless documentation): keep it cool, cap it tight, and avoid mixing with strong acids or alkali.
More than ever, new chemical products face demands for reliability, traceability, and performance under real-world stress. 1-Propyl-2,3-Dimethylimidazolium Hexafluorophosphate shines because it’s born from years of hard-won factory experience. Each bottle or drum packs months of thought, countless small improvements, and daily pride in putting out an honest, clean product.
The feedback we value most isn’t “it met spec,” but reports of new process records, easier solvent cycling, and real time or cost savings at the user end. We don’t chase fads or oversell speculative claims; our pride centers on those daily improvements that mean your reflux runs smoother, your electrochemical tests publish sooner, and your lines run with fewer unplanned stops. If something goes wrong, we don’t pass blame—we tear down process data, review logs, and invite direct lab-to-factory dialogue.
Those looking for the next edge in chemical process design weigh trade-offs: speed, safety, recyclability, long-term stability, and raw performance. By learning from thousands of batch notes, direct lab feedback, and real returns, we keep pushing our 1-Propyl-2,3-Dimethylimidazolium Hexafluorophosphate from a catalogue number into something sharper—an industrial, practical, truly reliable tool, shaped every day by those who work with it. If that feels direct, it’s because that’s how we operate: no shortcuts, no surprises.