|
HS Code |
952801 |
| Cas Number | 93398-86-0 |
| Molecular Formula | C7H16BrN |
| Molecular Weight | 194.12 |
| Iupac Name | 1-methyl-1-ethylpyrrolidinium bromide |
| Appearance | White to off-white solid |
| Melting Point | Approx. 170-175°C (decomposes) |
| Solubility In Water | Highly soluble |
| Purity | Typically >98% |
| Synonyms | 1-Ethyl-1-methylpyrrolidinium bromide |
| Density | 1.23 g/cm3 (approximate, solid state) |
| Storage Conditions | Store in a cool, dry place, tightly closed |
| Chemical Structure | Quaternary ammonium salt with a pyrrolidinium ring |
As an accredited 1-Methyl-ethylpyrrolidinium Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 50g of 1-Methyl-ethylpyrrolidinium Bromide is packaged in a tightly sealed amber glass bottle with a tamper-evident cap. |
| Shipping | **Shipping Description for 1-Methyl-ethylpyrrolidinium Bromide:** This chemical is shipped in tightly sealed, chemically resistant containers, compliant with safety regulations for corrosive and hygroscopic materials. Shipping must include appropriate labeling, protective packaging, and accompanying safety documentation. Handle as a potentially hazardous substance, avoiding exposure to moisture and extreme temperatures during transportation. Suitable for ground or air freight as regulated. |
| Storage | 1-Methyl-ethylpyrrolidinium bromide should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture and incompatible substances such as strong oxidizers. Keep the chemical away from sources of ignition and direct sunlight. Always use appropriate personal protective equipment (PPE) when handling, and follow relevant safety protocols and regulations for storage and disposal. |
|
Purity 99%: 1-Methyl-ethylpyrrolidinium Bromide with a purity of 99% is used in pharmaceutical synthesis, where it ensures high yield and product consistency. Melting Point 180°C: 1-Methyl-ethylpyrrolidinium Bromide with a melting point of 180°C is used in ionic liquid formulations, where it provides reliable thermal stability. Viscosity Grade Low: 1-Methyl-ethylpyrrolidinium Bromide of low viscosity grade is used in electrochemical devices, where it enables rapid ion transport. Water Solubility High: 1-Methyl-ethylpyrrolidinium Bromide with high water solubility is used in catalyst preparation, where it allows homogeneous reaction mixtures. Particle Size <50 µm: 1-Methyl-ethylpyrrolidinium Bromide with particle size below 50 µm is used in advanced material synthesis, where it improves mixing efficiency. Thermal Stability 200°C: 1-Methyl-ethylpyrrolidinium Bromide with thermal stability up to 200°C is used in polymer electrolyte membranes, where it maintains conductivity at elevated temperatures. Molecular Weight 208.09 g/mol: 1-Methyl-ethylpyrrolidinium Bromide with a molecular weight of 208.09 g/mol is used in chemical research, where it provides precise stoichiometric calculations. Hydrophobicity Moderate: 1-Methyl-ethylpyrrolidinium Bromide with moderate hydrophobicity is used in phase transfer catalysis, where it enhances reactant partitioning. Shelf Life 24 Months: 1-Methyl-ethylpyrrolidinium Bromide with a shelf life of 24 months is used in laboratory reagent storage, where it ensures reliable long-term usability. Electrochemical Stability Window 4V: 1-Methyl-ethylpyrrolidinium Bromide with an electrochemical stability window of 4V is used in supercapacitor electrolytes, where it provides improved energy storage performance. |
Competitive 1-Methyl-ethylpyrrolidinium Bromide prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
In research and industry, certain chemicals make things easier despite their complex names and origins. 1-Methyl-ethylpyrrolidinium Bromide stands out for anyone pursuing reliable ionic liquids or looking to fine-tune solvent systems. At first glance, it's easy to underestimate a salt with such a technical name, but this compound quietly fuels advances in everything from electrochemistry to analytical separation.
Every time I work with the model EMPyBr, I'm reminded of its roots: crafted with a pyrrolidinium core swapped with methyl and ethyl groups, then paired with bromide for steady performance. This structure keeps the compound stable across a broad range of temperatures and compatible with a wide set of organic and inorganic systems. Purity regularly lands above 98%, which simply means fewer headaches in tasks demanding reproducibility. White to off-white and solid at room temperature, it dissolves well in water and polar organic solvents, a trait chemists crave for quick application or smooth reactions.
Few compounds provide the flexibility that comes with 1-Methyl-ethylpyrrolidinium Bromide. Its unique ionic character, slight bulkiness, and even the quirky way it interacts with different anions make it ideal for ionic liquid preparation. Over the years, ionic liquids based on pyrrolidinium salts have allowed me to set up stable batteries and electrochemical cells, not least because they don't break down under voltage or intense light. With its bromide anion, this one maintains a low vapor pressure that helps in processes where minimizing volatility can make the difference between a failed and a successful trial. Another plus comes during phase-transfer catalysis, where salts like EMPyBr bridge gaps between otherwise stubborn reactants.
Whenever industry talks about environmentally friendly solvents, this compound slips into the discussion. Traditional organic solvents often evaporate or ignite too quickly, taking pollution concerns with them. Swapping them out for ionic liquids designed from 1-Methyl-ethylpyrrolidinium Bromide means cleaner working spaces and less flammable risk. While 'green chemistry' sounds like a slogan, for chemists working with sensitive compounds or large-scale synthesis, minimizing exposure and hazards ranks higher than any abstract mission statement. My own time working in synthetic labs showed me how ionic liquids free from volatile organics reduce headaches from lengthy ventilation protocols and costly spill cleanups.
It takes more than a fresh label to make a useful salt. Comparing this pyrrolidinium compound to run-of-the-mill alkylammonium or imidazolium salts, users notice a few sharp differences. Most imidazolium alternatives work well until high voltages or low temperatures creep in; their aromatic rings slip into side reactions under extreme conditions. Pyrrolidinium salts bring in a saturated five-membered ring, so their stability under tough conditions beats out the rest, especially where lasting ionic strength matters.
Switching out the anion changes things too. With bromide, EMPyBr falls right into a useful niche. Chloride and tetrafluoroborate anions dominate cheaper products, but bromide improves compatibility with transition metals during catalysis or electrodeposition. When designing metal-organic frameworks or prepping electroplating baths, I often see folks turn to bromide salts to tune solubility without driving up costs or introducing side products. Sometimes it's the ability to dissolve in both water and nonaqueous solvents that wins over the crowd. 1-Methyl-ethylpyrrolidinium Bromide plays both sides effectively, which I've seen help both in small-scale analytical setups and larger production demands.
Working with 1-Methyl-ethylpyrrolidinium Bromide, the melting point, solubility, and stability always serve as concrete advantages. Its melting point typically falls well above room temperature, but not so high as to slow preparation of ionic liquid solutions. For those mixing new electrolytes on a regular basis, that means less time fiddling with heating or specialized glassware.
The moisture content usually remains below 0.5%, which sounds minor unless you've ever watched a supposedly pure salt generate haze or fizz in sensitive reactions. In my experience, this translates into less prep time before every use, letting researchers skip endless drying steps and get right to the test. A salt with this level of purity and thermal stability stands out, especially when alternatives need constant monitoring or tend to pick up impurities from the air.
Storing it, I’ve rarely run into caking or clumping. Whether in a busy university stockroom or at a small startup, a stable powdered product means fewer worries about batch variations and dosing errors. These little practical notes make all the difference on the production floor or in academic labs, where standardizing experiments and getting repeatable results matter more than buzzwords.
There's a growing drive toward replacing traditional organic solvents across the board. In battery research, 1-Methyl-ethylpyrrolidinium Bromide shows up as an easy-to-handle building block for high-energy capacitors and lithium-ion batteries. Its resilience to electrochemical degradation provides an edge over older salts, offering longer device lifetimes and fewer disposal headaches. During the rise of green energy labs, teams looking to improve battery safety without compromising performance seem to reach for these sorts of pyrrolidinium-based materials.
In chromatography, the demands for selectivity and cleanliness often put common salts on the back foot. Bromide-based pyrrolidinium salts provide better separation power for both small molecules and peptides. When working in pharmaceutical analytics or environmental monitoring, switching to 1-Methyl-ethylpyrrolidinium Bromide means fewer ghost peaks and more reliable calibration.
In catalysis, users note easier phase transfer between water and organic layers. Catalysts that typically choke on conventional counterions manage better yields and cleaner isolations. Whenever scale-up for industrial synthesis comes up, the ability to recycle and recover ionic liquids based on this compound cuts waste and cost. Those aren't just boardroom statistics—they save time for R&D teams and reduce headaches in compliance and reporting.
As someone familiar with both academic research and industrial practice, the headway made by 1-Methyl-ethylpyrrolidinium Bromide in safety and environment can’t be overstated. Unlike legacy solvents, it has almost no vapor pressure at room temperature, which means fewer emissions and a safer work environment. Exposure by inhalation, always a concern with volatile organic compounds, drops off the radar. While every lab follows safety protocols, knowing a compound is less likely to escape into the air brings real relief to everyone.
Wastewater problems ease up, too. Disposal of solvent-laden water remains the bane of modern chemistry, both in cost and compliance risk. Salts based on pyrrolidinium and bromide remain relatively unchanged in the waste stream, with less risk of forming harmful byproducts. I’ve seen companies accelerate permitting and reduce insurance loads after making the switch away from organic solvents. While regulations keep tightening, products like this help labs and plants get ahead of legal headaches.
Still, no chemical solves every problem outright. Each facility ought to weigh risks according to its workflow. Yet for scientists and engineers frustrated with mounting safety paperwork and endless exhaust upgrades, using ionic liquids based on 1-Methyl-ethylpyrrolidinium Bromide opens the path to safer handling and cleaner records.
There’s no shortage of hype around ionic liquids, but that doesn’t mean every salt fits every purpose. Costs can run higher than bulk organic or inorganic salts, especially for very pure batches. Some customers struggle with supply chain snags, as less common compounds depend on specialty chemical suppliers. For my own projects, sourcing has required a bit more planning and the occasional swap for close analogs when stocks run dry.
Thanks to rising demand across electronics and pharmaceuticals, prices trend upward year by year. Some labs resort to recapturing and recycling spent ionic liquid in-house which brings its own set of challenges: separation, cleaning, and verifying purity. For smaller outfits, this gets resource-intensive, requiring more specialized equipment and careful record-keeping. I know colleagues who, after the initial spike in productivity, had to reinvest in purification columns and analytical kits just to keep the cycle viable.
Technical training presents another challenge. Old habits die hard. Many staff learned solvent usage with legacy chemicals, and switching to an unfamiliar format like a hygroscopic salt means dealing with spills, learning new drying protocols, and updating storage guidelines. Any real gains depend on smart, ongoing staff training and commitment from management to follow through on those changes.
Experience largely shapes which chemicals stay in rotation. For years, chemists fell back on imidazolium-based ionic liquids, given their market saturation and decent overall profile. Yet pyrrolidinium derivatives—especially 1-Methyl-ethylpyrrolidinium Bromide—carve out niches where thermal and electrochemical stability can’t be sacrificed. Its solid, non-aromatic backbone shields it from radical breakdown, while the bromide brings solution flexibility.
Handling over time shows more subtle strengths. Glassware stays clearer, residue formation drops, and fewer clean-up cycles pop up after high-heat reactions. In devices like supercapacitors, where lifespan and stability mean financial returns, this translates into actual performance results—something not lost on industry managers balancing budgets and long-term projections.
Compared to cheap trialkylammonium salts, the performance gap widens. While others degrade or lose potency at scale, EMPyBr sticks to its job. Even under routine transfer, from bench to pilot scale, it holds up better, requiring less downtime for troubleshooting and delivering results with fewer surprises. This repeatability, more than any single analytical stat, wins loyalty from labs and tech developers.
Surging demand in renewable energy storage and advanced material production puts 1-Methyl-ethylpyrrolidinium Bromide in the spotlight. Universities and private labs keep reporting gains in capacitor performance and synthesis efficiency using pyrrolidinium intermediates. Growing pressure to meet green goals at state and federal levels has made incremental improvements in chemical sustainability real priorities. For those of us who follow policy as closely as the latest technical trends, this means compounds that blend safety, recyclability, and performance edge out riskier, outdated choices.
Research teams constantly hunt for new alloy combinations in batteries or ways to make chemical separations both cleaner and cheaper. Discussions with industry partners always come around to one issue: keeping up with regulations while staying competitive. Knowing that 1-Methyl-ethylpyrrolidinium Bromide lets teams meet both sets of requirements matters. In return, suppliers have responded with more transparent sourcing, better purity guarantees, and tighter documentation to help users verify quality for traceability.
There’s plenty of room to expand applications. In biochemistry, for example, enzymes tolerate pyrrolidinium ionic liquids better than many others. New approaches in protein crystallization and drug delivery benefit, since the bromide counterion can often prevent unwanted side reactions. Teams in these fields appreciate additives that don’t derail results or create batch-to-batch variation; seeing a steady uptick in related studies makes it clear that the market isn’t near saturation.
For all its strengths, cost and recovery remain pain points. Based on my years in both corporate and academic settings, pooling resources through shared purification units and recycling protocols pays dividends. Consortia arrangements, where universities and small companies share recovery gear or batch purification, help offset up-front investment burdens and keep material costs in check.
On the education side, developing short training modules focused on storage, handling, and recycling empowers staff while ensuring protocols get followed. I’ve helped run workshops that use straightforward demos, linking hands-on practice to written safety steps, and the result shows up in fewer accidents and more confident staff.
Product improvement runs in tandem with demand. As new variants hit the market, including alternative anions or functional groups aimed at better solubility or biological compatibility, end-users gain choice. The broader chemical community often shapes these tweaks, by reporting back on practical snags that come up during routine work. Companies open to those back-and-forth conversations roll out improved versions that fit new needs. It’s these cycles of honest feedback and responsive formulation that keep real progress rolling.
Looking ahead, it’s not just the technical credentials or a shiny spec sheet that keep 1-Methyl-ethylpyrrolidinium Bromide relevant. Instead, it’s the quiet accumulation of trust—earned through every project that runs smoother, every process that gets a little safer, and each year end-users can keep to stricter budgets without sacrificing performance. Having worked on both sides, as bench chemist and process manager, I’ve seen how a reliable building block makes complex work feel just a little less daunting.
The next generation of batteries, electrochemical cells, and advanced chemical syntheses continue to look to salts like EMPyBr for their combination of toughness and adaptability. For anyone invested in smooth workflows, regulatory compliance, and actual bottom-line results, this pyrrolidinium salt delivers—quietly, persistently, and without the usual drama. As new challenges emerge, the adaptability and solid record of use may carry 1-Methyl-ethylpyrrolidinium Bromide into even broader fields, fueling both innovation and responsible practice for years to come.