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HS Code |
680404 |
| Cas Number | 36052-48-1 |
| Molecular Formula | C7H10BrN |
| Molecular Weight | 188.07 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 150-155°C |
| Density | 1.39 g/cm³ |
| Solubility In Water | Soluble |
| Purity | Typically >98% |
| Chemical Structure | Ethyl group attached to nitrogen of pyridinium ring with bromide counterion |
| Iupac Name | 1-ethylpyridin-1-ium bromide |
As an accredited 1-Ethylpyridinium Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1-Ethylpyridinium Bromide is supplied in a sealed, amber glass bottle containing 25 grams, clearly labeled with hazard and product information. |
| Shipping | 1-Ethylpyridinium Bromide is shipped in tightly sealed containers, compliant with chemical safety regulations. It is protected from moisture and incompatible substances, with clear labeling indicating hazardous material. Handling and transport follow standard protocols for corrosive or toxic chemicals, ensuring safety during transit. Shipping documentation includes material safety and hazard information. |
| Storage | 1-Ethylpyridinium Bromide should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Keep it out of direct sunlight and sources of heat and moisture. Properly label the container, and store it at room temperature to maintain stability and minimize decomposition or degradation. |
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Purity 99%: 1-Ethylpyridinium Bromide with 99% purity is used in organic synthesis reactions, where it ensures high product yield and minimal side reactions. Melting point 200°C: 1-Ethylpyridinium Bromide with a melting point of 200°C is used in thermal processing applications, where it provides stable phase properties under elevated temperatures. Particle size <50 μm: 1-Ethylpyridinium Bromide with particle size less than 50 μm is used in catalytic systems, where fine dispersion enhances reaction kinetics. Moisture content <0.1%: 1-Ethylpyridinium Bromide with moisture content below 0.1% is used in pharmaceutical formulations, where low water content prevents degradation and improves shelf-life. Stability temperature up to 150°C: 1-Ethylpyridinium Bromide stable up to 150°C is used in ionic liquid electrolyte preparation, where thermal stability maintains consistent ionic conductivity. Viscosity grade low: 1-Ethylpyridinium Bromide of low viscosity grade is used in polymer electrolytes, where reduced viscosity optimizes processing and ionic mobility. Molecular weight 186.07 g/mol: 1-Ethylpyridinium Bromide with a molecular weight of 186.07 g/mol is used in analytical chemistry standards, where precise molecular characteristics support accurate calibration. |
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Many of us who have spent years in a lab know the satisfaction of finding a chemical that does its job—no headaches, no surprises. 1-Ethylpyridinium Bromide, often abbreviated by some as EPyBr, fills this role when researchers and process developers want a trustworthy ionic compound for synthesis or catalysis. With a chemistry industry always searching for new tools, this salt stands out because of its stability and functionality across organic and materials science fields.
Known structurally as a pyridinium-based ionic compound carrying a single ethyl group, this salt features a quaternary nitrogen bound to an ethyl moiety and paired with a bromide ion. Its chemical structure gives it a few notable traits, not least predictable solubility in water and some organic solvents. In everyday terms, you measure its purity above 98 percent in most research and development supply chains, while the physical characteristics—fine crystalline powder with a pale off-white hue—signal a quality that skilled technicians appreciate.
The melting point generally sits above room temperature, often in the range of 180 to 200 degrees Celsius. This thermal profile provides an edge for processes requiring heat without compound breakdown, whether in solubilizing agents, ionic liquid formation, or catalysis. The specific molecular formula (C7H10BrN) reflects an economy of atoms that helps avoid extra baggage in downstream processes. As a chemist, I often look for products that "just work," and EPyBr delivers on that front with minimal impurities.
In discussions with colleagues, the value of 1-Ethylpyridinium Bromide repeatedly comes up in the context of making ionic liquids. The trend toward ionic liquids is easy to understand—these salts open up a world of tunable solvents, non-volatile reaction media, and green chemistry options. EPyBr offers a consistent building block for crafting such ionic liquids with tailored cations.
Beyond this, it offers utility as a phase-transfer catalyst. Typical halide transfer reactions pick up speed and reliability because the bromide ion moves between organic and aqueous layers with little fuss. This saves time and reduces excess waste, something every lab director watches closely as budgets tighten and green metrics come under scrutiny.
In synthesis settings, I have seen EPyBr chosen during alkylation, nucleophilic substitution reactions, and as a bromide source for more specialized organic transformations. Its ionic nature helps dissolve diverse starting materials, making previously “difficult” reactions smoother and more predictable.
Some material scientists also use 1-Ethylpyridinium Bromide to modify electrode surfaces or prepare new polymers. Its predictable behavior often improves conductivity or alters solubility in composite materials. In my own work, I have seen how easy it is to get reproducible results—something that speaks to the real-world value of the compound more than any marketing sheet could.
Chemists have a habit of asking, “What makes this salt different?” In the case of 1-Ethylpyridinium Bromide, the answer comes from the short, simple ethyl group. Some might try using longer alkyl chains, but those often bring undesirable viscosity or decrease water solubility.
Take, for example, the comparison with 1-Butylpyridinium Bromide. As the chain grows from ethyl to butyl, the salt shifts toward higher viscosity and lower polarity. The differences start to show in solvent compatibility and how quickly reactions proceed. For those of us who want reliable phase-transfer capacity or wish to avoid clogging fine equipment, the smaller ethyl group proves more manageable.
1-Methylpyridinium Bromide, while close in composition, sometimes shows less chemical flexibility. Ethyl substitution strikes a sweet spot between hydrophilicity and organic solubility. This balance means wider compatibility with both aqueous and non-aqueous systems, translating into less troubleshooting and more actual science.
Throughout my industry career, I have lost track of the times a “standard” salt batch ruined experimental results with inconsistent hydration levels or lingering contaminants. High-purity 1-Ethylpyridinium Bromide rarely gives this trouble. Reliable vendors maintain quality through robust synthesis and purification routes, generally avoiding batch-to-batch surprises.
This level of consistency saves time and helps researchers experiment freely, without constantly checking for unexpected impurity peaks in NMR or mass spectrometry. I believe this predictability separates top compounds from merely serviceable ones—it lets scientists innovate, rather than troubleshoot all day.
Any chemist who has carried bags of hygroscopic solids across a busy teaching lab knows the headaches they create. EPyBr holds up well under typical lab environments. It resists rapid moisture uptake and stays free-flowing in closed containers. Ordinary chemical shelving or dryboxes provide enough protection, though as with most salts, wet storage never ends well.
Because the compound contains bromide, some care is due to avoid unwanted exposure, especially during weighing or sample transfer. Most users report stable odorless handling, unlike volatile amines or halides that need fumehoods for every step. Proper labeling and prudent practice stay important, yet the risk profile remains on the lower side compared to more hazardous salts.
The evolving conversation around green chemistry inspires a closer look at reagents like EPyBr. Many technologists are seeking ways to cut back on waste and boost process safety. 1-Ethylpyridinium Bromide’s stability and recyclability matter here, since it helps support ionic liquid-based syntheses that avoid aggressive acids or bases. In the right contexts, it allows for solvent systems with sharply reduced emissions and less environmental impact.
Some syntheses exploit the ability to recover and reuse the bromide salt after use, with simple precipitation or filtration methods. Compared to volatile organic compounds that evaporate into the air, working with salts feels like a win from a sustainability perspective. From my point of view, this bridges the gap between research-scale feasibility and real world, scalable green processes.
Across the past decade, more labs and manufacturers have integrated ionic salts into their workflows. 1-Ethylpyridinium Bromide moved from a niche specialty item to a common sight in academic and industrial catalogs. What signals practical trust in a product is not just its availability, but consistent repeat business—and this compound pops up on those reorder forms steadily.
I have noticed more vendors carrying higher grade material, with greater transparency in documentation—batch-specific NMR, IR, and purity data come standard. This transparency lets buyers make informed choices and boosts research reproducibility. Given the increased regulatory focus on chemical tracking, ready access to quality data protects lab interests and makes future audits much smoother.
Like any synthetic compound, EPyBr brings its own set of issues. Over the years, I have seen a few recurring hurdles. Some syntheses produce excess bromide waste, which if neglected, builds up and presents disposal challenges. The best approach here is to set up efficient capture and neutralization, taking cues from standard halide disposal protocols. In mid- to large-scale settings, on-site treatment systems proved highly effective at rendering bromide concentrations compliant before wastewater discharge.
Cost also comes up, especially for researchers running pilot batches or scaling to production. While not prohibitively expensive, EPyBr commands a slightly higher price due to processing and purity standards. In practice, many labs offset the cost by reusing the compound in closed-loop setups—aligning with the broader push for process intensification and cost control. Vendors who offer bulk purchase discounts or supply chain guarantees make long-term adoption more comfortable for institutions large and small.
Modern chemists enjoy access to more efficient methods for preparing ionic compounds like 1-Ethylpyridinium Bromide. Some laboratories draw on improved routes that cut down on precursor waste, shorten reaction times, or boost yields per batch. Advances in catalysis and continuous flow systems also minimize exposure risks for workers, without sacrificing quality.
On the analytical side, high-resolution spectroscopy data sets—NMR, FTIR, and even X-ray crystallography—give researchers confidence in what they have. The routine availability of such data reflects the collective push by both producers and users to prove E-E-A-T principles: experience and expertise in synthesis, authoritative characterization, and trust as shown by peer-reviewed literature and returned experiments.
Undergraduate and graduate teaching labs now draw on a wider toolkit of specialty salts than twenty years ago. 1-Ethylpyridinium Bromide enters countless curricula as students practice phase-transfer catalysis, explore ionic liquids, or simulate industrial-scale processes. The salt’s balance between challenge and reliability makes it an excellent teaching tool. Students discover the link between structure and reactivity, learning first-hand how variations in alkyl chain length or counterion shape drive physical properties.
Instructors tell me that including such ionic salts in coursework spurs better engagement. Students see theory convert into action, and they pick up the practical skills—measuring, transferring, weighting—without the pitfalls of excessive risk. Having witnessed a few classroom spills and mishandled volatile reagents, I appreciate how certain stable salts keep curriculum practical and safe.
Industries specializing in pharmaceuticals, advanced materials, and analytical chemistry prize reagents that stand up to downstream scrutiny. In synthesis, every intermediate and catalyst eventually passes through layers of purification and registration. 1-Ethylpyridinium Bromide’s straightforward structure minimizes red flags on impurity checks or regulatory filings. The salt operates in strict, high-purity environments without generating problematic byproducts.
Multiple process engineers report that, with EPyBr, they bypass certain workups or purification steps required by other pyridinium salts, freeing up time and equipment. In sectors where time means money—drug discovery, contract manufacturing—these advantages carry real business value.
Over decades, the chemical industry has seen fads come and go. Products that thrive long-term usually embody reliability. By this standard, 1-Ethylpyridinium Bromide stands tall. Its established synthesis, repeatable behavior in the lab, and broad literature base all support further work.
New projects in electrochemistry and nanotechnology have begun to incorporate this pyridinium salt in applications where electrical performance and predictable charge transport matter. As research broadens into batteries and conductive composites, ionic salts that provide both mobility and process control rise in value. I see collaborators return to EPyBr in these contexts, citing its track record.
Precise analytical work underpins good chemistry. 1-Ethylpyridinium Bromide responds well to standard detection techniques, showing clear peaks in NMR and infra-red spectrometry. Its purity lends clarity to mass spectrometry runs with little signal interference. This integrity matter especially in pharma or biotech, where analytical sign-off determines whether a compound or process moves forward.
In environmental testing labs, the salt can serve as both an internal standard and as a chemical modifier, helping drive selectivity in ion chromatography or improving extraction protocols. Such specific roles only work when the salt plays cleanly with existing workflows—a pattern I have observed across numerous analyst teams.
No matter how much automation comes into the lab, chemicals ultimately rely on humans for ordering, handling, and decision-making. In my experience, teams stick longer with products that earn their trust—salts that never cake up, bottles that always arrive correctly sealed. Feedback loops between chemists and suppliers make all the difference. In platforms where I participate, honest product reviews and side-by-side testing often highlight EPyBr as a preferred choice, especially for new project launches where the room for error is slim.
Reliable products encourage experimentation and risk-taking in the right way—enabling scientists to innovate without the distraction of unreliable stock. This comfort trickles down to better work, happier teams, and long-term lab efficiency.
The role of 1-Ethylpyridinium Bromide in modern chemistry shows no sign of fading. As labs aim for greener processes, more efficient catalysis, and smarter analytical work, this salt brings flexibility and control. With sustained effort from researchers, industry partners, and quality suppliers, its use continues to expand across chemistry’s many frontiers.
For those seeking a dependable, accessible, and proven ionic compound, EPyBr—shaped by experience and constant vetting—delivers not just as a reagent but as a reliable partner in discovery. In every well-run lab, these quiet performers enable bigger breakthroughs by making the basics reliable, day in and day out.