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HS Code |
617268 |
| Productname | 1-Methyl-1-Butylpyrrolidinium Trifluoromethanesulfonate |
| Casnumber | 928790-03-0 |
| Chemicalformula | C10H20F3NO3S |
| Molecularweight | 307.33 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Meltingpoint | -30°C (approximate) |
| Boilingpoint | Decomposes before boiling |
| Solubility | Miscible with water and polar solvents |
| Density | 1.18 g/cm³ (at 25°C) |
| Purity | Typically ≥99% |
| Conductivity | High ionic conductivity |
| Storagetemperature | Store at room temperature, tightly closed |
| Refractiveindex | 1.425 (at 20°C) |
| Synonyms | BMPy OTf; [BMpy][OTf] |
As an accredited 1-Methyl-1-Butylpyrrolidinium Trifluoromethanesulfonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100g, with tamper-evident screw cap, labeled with chemical name, purity, hazard symbols, and batch information. |
| Shipping | 1-Methyl-1-Butylpyrrolidinium Trifluoromethanesulfonate is shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. It should be handled in accordance with standard chemical transport regulations, away from incompatible substances. Temperature control may be recommended. Appropriate labeling and documentation are required for safe handling during shipping. |
| Storage | Store **1-Methyl-1-butylpyrrolidinium trifluoromethanesulfonate** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong oxidizers and strong acids. Protect from heat and direct sunlight. Ensure appropriate labeling and secure storage to prevent unauthorized access. Use suitable materials such as glass or compatible plastics for containment. |
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Purity 99%: 1-Methyl-1-Butylpyrrolidinium Trifluoromethanesulfonate with a purity of 99% is used in electrochemical capacitors, where it ensures high ionic conductivity and low electronic leakage. Viscosity grade 34 cP: 1-Methyl-1-Butylpyrrolidinium Trifluoromethanesulfonate of viscosity grade 34 cP is used in lithium-ion batteries, where it provides enhanced ion mobility and improved cycle durability. Melting point -12°C: 1-Methyl-1-Butylpyrrolidinium Trifluoromethanesulfonate with a melting point of -12°C is used in low-temperature supercapacitors, where it enables reliable operation at subzero conditions. Stability temperature 220°C: 1-Methyl-1-Butylpyrrolidinium Trifluoromethanesulfonate with stability up to 220°C is used in high-temperature fuel cells, where it offers sustained electrochemical performance under thermal stress. Ionic conductivity 8.1 mS/cm: 1-Methyl-1-Butylpyrrolidinium Trifluoromethanesulfonate with an ionic conductivity of 8.1 mS/cm is used in solid-state electrolytes, where it facilitates rapid ion transfer for enhanced device efficiency. Water content <0.01%: 1-Methyl-1-Butylpyrrolidinium Trifluoromethanesulfonate with water content below 0.01% is used in moisture-sensitive synthesis, where it prevents side reactions and improves product yields. |
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Trying something out of the ordinary can change the way a lab or factory works. That often means picking a material that steps outside the common playbook. 1-Methyl-1-butylpyrrolidinium trifluoromethanesulfonate belongs in that category. As an ionic liquid, this compound has turned heads for engineers and researchers looking to push boundaries in electrochemical applications, catalysis, and separation processes. People talk a lot about the quirks of pyrrolidinium-based ionic liquids. Plenty of attention goes toward their low vapor pressure and their ability to stay liquid across a broad temperature range. It’s these traits that can make a real difference even when research moves from the benchtop to scale-up.
You find this ionic liquid under different product codes, but in the end, the backbone stays the same: a pyrrolidinium ring with a 1-butyl and 1-methyl group, paired with a trifluoromethanesulfonate (triflate) anion. This molecular pairing brings out a mix of chemical stability and physical resilience. Most suppliers will report a water-like viscosity, strong oxidative stability, and thermal resistance that outlasts many other organic solutions. Unlike imidazolium relatives, which can degrade in harsh alkali, the pyrrolidinium structure keeps its shape even around strong bases and under higher voltages.
On paper, it can look a lot like other ionic liquids. But the switch from imidazolium to pyrrolidinium matters. Triflate, as an anion, puts a different spin on things compared to PF6, BF4, or TFSI. That’s not just chemistry jargon: anyone working with lithium batteries or specialty electrolytes will notice the reduced corrosiveness and lower risk of hazardous by-products. Triflate-based salts keep hydrolysis at bay and don’t give off the toxic or corrosive gases that worry so many folks working with hexafluorophosphate or tetrafluoroborate. Tuning the length of the butyl chain changes the viscosity and conductivity, but this particular combination balances fluid movement and charge transport.
I’ve seen people look for solvents that don’t burst into flames or evaporate away as soon as things heat up. In battery labs, you hear constant talk about finding a liquid that stands up to high voltages but doesn’t fall apart chemically. This compound gets a nod for that reason alone. Its high ionic conductivity ushers charges along in supercapacitors and next-gen lithium-ion batteries. It beats out common carbonate mixtures on safety, especially since its volatility can’t compare. Folks working in catalysis reach for it when they want an inert medium that doesn’t bind or poison their precious metal catalysts—something not every salt can promise.
In separation technology, especially gas capture (like CO2 or SO2 scrubbing), researchers like this ionic liquid’s ability to stay in one phase and let target gases dissolve without decomposing under cycling. That’s a big deal for reducing solvent loss and cutting replacement costs. Its distinct combination of hydrophobicity and ion mobility means it straddles the world of organic and inorganic chemistry, much to the delight (or bane) of chemists who must tune separation columns day after day.
Anyone who’s tried to switch out a familiar solvent with something greener or safer knows the litany of complaints that usually follows: poor solubility, slow reactions, fouling of sensors, or metal component corrosion. This pyrrolidinium triflate addresses several of these issues in one shot. It doesn’t clog the system or promote corrosion in stainless pipes the way some halide-based salts do. Clean-up gets easier, too, since it resists forming the sticky residues typical of phosphonium-based alternatives.
If voltammetry data matter, people have seen electrochemical windows stretch up to 5 volts or more, which opens up work with metal-air batteries and some fuel cells. Its viscosity sits higher than water but well below many other ionic liquids, making it workable without diluting with volatile organics. Chemists and engineers get to tinker with concentrations and additives, knowing this base liquid stays put and doesn’t sabotage the rest of the process.
It’s not all smooth sailing. Price gets in the way for a lot of groups trying to move out of the research zone and into pilot plants. Raw material costs for triflate anions and the multi-step syntheses required tend to keep the price tag high. Disposal is safer than a lot of alternatives, but local regulations about ionic liquids change from region to region. Many buyers end up second-guessing their solvent choices based on disposal requirements alone. Material compatibility remains a hurdle, too. Not every seal or gasket stands up to ionic liquids, and switching out common elastomers for specialized ones bumps up costs on a project.
Purity can turn into a sticking point on sensitive equipment. Trace halides or unreacted starting materials skew analytical results and sometimes sulfur builds up in downstream analytics. Quality verification ends up taking more time than it should, forcing folks to trust only select vendors or turn to custom synthesis for high-stakes experiments.
Manufacturers keep introducing new salts with taglines about safety or “green” appeal, but too many fail to deliver in real-world conditions. 1-Methyl-1-butylpyrrolidinium trifluoromethanesulfonate doesn’t bleed toxic HF or break down in open air. Its thermal range covers everything up to most industrial heating scenarios, and its chemical backbone doesn’t scavenge water from the air, so it stores well. Battery engineers often search for a happy medium between low volatility and high mobility. With this compound, they get a solvent and electrolyte that doesn’t pit their electrodes and doesn’t fall apart after months of cycling.
Industrial electroplating, supercapacitor design, and analytical separations all benefit because a little fine-tuning of additives or electrode material brings better performance without constant troubleshooting. The liquid’s resilience makes it attractive not only for research but for businesses looking to standardize processes and reduce hazardous waste.
Plenty of researchers are wary of new materials, especially if the hype doesn’t match reality. Over time, word gets around when a compound actually delivers. One strong point here is long-term reliability. Devices running at higher voltages or under thermal stress don’t show the same slow performance degradation as you’d see using older, less stable ionic liquids. Equipment operators, who’ve burned through countless seals and O-rings due to reactive fluorinated anions in the past, end up staying put with the triflate version once it proves itself.
If a process runs around the clock, avoiding solvent batch changes brings savings in labor and downtime. Many users highlight the reduction in by-product formation, fewer maintenance issues with analytic equipment, and the drop in raw material cycling costs over the year. In labs, the higher cost of entry pays off through more robust results and fewer analytical corrections down the line.
A solution to high costs hasn’t emerged across the board, but greater scale and pull-through by end-use industries could help. Collaborative partnerships between academic labs and manufacturers hold some promise, letting groups test re-purified solvent batches and share data on real-world use. Instead of relying strictly on fresh synthesis, labs sometimes recover and recondition spent ionic liquid, stretching budgets and reducing waste.
To offset compatibility snags, industrial users often run short-term trials with new equipment parts, taking careful records of material interactions. Newer fluoropolymer and PTFE gaskets show good promise but need consistent documentation to reach industry-wide adoption. Some companies pursuing battery recycling and solvent recovery push for closed-loop systems, ensuring the solvent stays out of waste streams, further lowering environmental load.
From a chemist’s perspective, few ionic liquids hit the sweet spot between chemical stability and user safety. I’ve seen groups choose this compound after long vetting processes, weighing the tradeoffs between price and performance. In analytical work, it’s gratifying to see spectra and chromatograms without the suspected background noise that comes from breakdown products. Launching new electrochemical setups always brings risk, but the reliability of this salt supports experiments involving rare or expensive materials, reducing the chance of losing costly samples.
On the production side, repeatable performance becomes a selling point by itself. Plant operators can rely on consistent viscosity and conductivity numbers lot-to-lot, which means process adjustments become less frequent. The impact on health and safety meetings also turns positive, with fewer incidents or close calls due to volatility or reactivity compared to older liquid electrolytes.
Nothing in specialty chemistry stays still for long. As more industries chase lower emissions, longer battery life, and smarter process design, the demand for rugged, stable solvents grows. 1-Methyl-1-butylpyrrolidinium trifluoromethanesulfonate stands out for its blend of practical properties. It offers users a material that adapts to cutting-edge research while meeting reliability and safety standards. The roadblocks—cost, compatibility, disposal—invite continuous improvement. Collaboration, smarter purification strategies, and new manufacturing techniques hold promise for making this compound easier and cheaper to use.
Market pressures can push both suppliers and users to find more sustainable production routes. Some experts predict biobased synthesis of pyrrolidinium precursors will expand, lowering both the environmental footprint and cost. Greater cross-talk between the clean energy sector, manufacturers, and applied research could help steer this compound’s place as a workhorse rather than a specialty. If pilot studies in grid storage pay off, the jump to wider adoption in automotive, portable electronics, and chemical plants could follow.
People in the field keep searching for answers to perennial questions: Will this solvent last through a thousand charge cycles? Does it keep impurities at bay in sensitive detection systems? Can it survive constant heating and cooling without warping results? For many, 1-methyl-1-butylpyrrolidinium trifluoromethanesulfonate delivers, if not every answer, at least a measurable improvement over what came before.
Trust in a material builds over time. Users tend to talk more about what it doesn’t do—cause safety incidents, go out of spec, produce hazardous decomposition—than about a miracle cure-all. For labs, plants, and R&D teams looking not just for something new but something reliable, this ionic liquid becomes a serious contender. The details matter in chemistry, and practical experience keeps showing that this salt brings enough advantages to outweigh its few downsides. That’s a story researchers, engineers, and operators directly shape, with each project, battery, or analysis that puts this compound to work.