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1-Butylpyridinium Hydrobromide

    • Product Name 1-Butylpyridinium Hydrobromide
    • Alias 1-Butylpyridinium bromide
    • Einecs 637-584-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
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    Specifications

    HS Code

    369288

    Product Name 1-Butylpyridinium Hydrobromide
    Chemical Formula C9H14BrN
    Molecular Weight 216.12 g/mol
    Cas Number 374089-54-2
    Appearance White to off-white crystalline powder
    Solubility Soluble in water
    Melting Point 110-115°C
    Density 1.33 g/cm³
    Storage Temperature Room temperature (15-25°C)
    Purity Typically ≥98%

    As an accredited 1-Butylpyridinium Hydrobromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1-Butylpyridinium Hydrobromide is supplied in a 25g amber glass bottle, sealed with a screw cap and labeled for laboratory use.
    Shipping 1-Butylpyridinium Hydrobromide is shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. It is transported under ambient conditions with proper labeling according to hazardous material regulations. Appropriate documentation and safety data sheets accompany the shipment to ensure compliance and safe handling during transit and upon delivery.
    Storage 1-Butylpyridinium Hydrobromide should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition. Protect from moisture, direct sunlight, and incompatible substances such as strong oxidizers. Avoid prolonged exposure to air. Ensure proper labeling and keep out of reach of unauthorized personnel. Follow standard chemical storage regulations and safety protocols.
    Application of 1-Butylpyridinium Hydrobromide

    Purity 99%: 1-Butylpyridinium Hydrobromide with 99% purity is used in ionic liquid synthesis, where it ensures high ionic conductivity in electrochemical devices.

    Melting Point 180°C: 1-Butylpyridinium Hydrobromide with a melting point of 180°C is used in advanced material research, where it provides stable phase behavior under elevated temperatures.

    Molecular Weight 216.1 g/mol: 1-Butylpyridinium Hydrobromide at 216.1 g/mol is used in pharmaceutical intermediate formulations, where it guarantees precise molecular integration during synthesis.

    Viscosity Grade Low: 1-Butylpyridinium Hydrobromide of low viscosity grade is used in catalyst systems, where it facilitates efficient mass transfer and reaction rates.

    Water Solubility High: 1-Butylpyridinium Hydrobromide with high water solubility is used in aqueous two-phase extraction processes, where it improves separation efficiency for biomolecules.

    Thermal Stability up to 200°C: 1-Butylpyridinium Hydrobromide with thermal stability up to 200°C is used in high-temperature battery electrolytes, where it maintains structural integrity and low decomposition.

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    Certification & Compliance
    More Introduction

    1-Butylpyridinium Hydrobromide: A Closer Look at an Innovative Compound

    Rethinking Chemical Tools: The Role of 1-Butylpyridinium Hydrobromide

    Daily life seldom calls for conversations about ionic liquids, but in the realm of research and industry, substances like 1-Butylpyridinium Hydrobromide can make a real difference. The name itself might sound complex, yet as I have seen in university labs and specialty manufacturing plants, its value becomes clear once you grasp its performance and versatility. Over the years, with more demand in pharmaceuticals, catalysis, and organic synthesis, interest in innovative ionic liquids keeps rising.

    1-Butylpyridinium Hydrobromide, often identified with the model code BPy·HBr, offers researchers a fresh take on ionic liquids. Its composition—basically a combination of butyl-substituted pyridinium and hydrobromic acid—gives it unique features compared to many salts and organic compounds. The butyl group latches onto the nitrogen atom of the pyridine ring, producing a quaternary ammonium salt that stands out for its stability and flexibility in a variety of environments. In a chemical landscape where subtle molecular tweaks can result in profound performance changes, compounds like this one are worth knowing.

    Digging Deeper: Understanding the Specifications

    Let’s break things down from a practical perspective. 1-Butylpyridinium Hydrobromide typically appears as a solid with crystalline structure, usually white or off-white. Its purity as offered by leading chemical suppliers typically exceeds 98%, based on methods such as NMR or HPLC. The compound carries a molecular formula of C9H14BrN, and the molecular weight lands around 216.1 g/mol. This sort of specification matters for researchers who care about consistency, reaction yields, and contamination risk. I’ve had colleagues lament lost time and money over sloppy impurity controls in similar compounds—a risk you don’t want to take in high-stakes projects.

    Hydroscopicity, or the ability to absorb water from the air, is a practical concern. If you leave the cap off the jar too long, the material tends to clump or convert into a sticky mass. So, its handling requires some care: researchers often store it in tightly sealed and desiccated conditions. Working with this material in typical lab settings has taught me that while it’s more robust than some specialty salts, it still needs respect to maintain performance, especially before entering sensitive reaction vessels or analytical setups.

    Where 1-Butylpyridinium Hydrobromide Truly Applies

    My own experience in synthetic laboratories has highlighted the range of tasks 1-Butylpyridinium Hydrobromide can tackle. It serves as a go-to agent in ion-exchange and phase-transfer scenarios. For reaction developers, this means it can help facilitate processes that would otherwise crawl along or sputter to a halt due to solubility limitations. Many colleagues have praised its effectiveness as a supporting electrolyte in electrochemical experiments, particularly where traditional salts like sodium or potassium bromide introduce unwanted variables.

    Catalysis is another critical area. In organic synthesis, chemists have long sought alternatives to volatile organic solvents. The structure of 1-Butylpyridinium Hydrobromide allows it to function as an ionic liquid in some contexts, fostering easier separation and purification down the line. I remember working on a green chemistry project where replacing a commonly used, hazardous solvent with an ionic liquid led to cleaner products and fewer headaches for all involved. The butyl chain and pyridine ring of this molecule create an environment that stabilizes reactive intermediates, making tough conversions more manageable.

    Comparisons to Other Common Ionic Liquids

    Plenty of professionals find themselves stuck between choosing the right ionic liquid for a particular challenge. The most common alternatives usually include imidazolium- and ammonium-derived compounds. One clear upside with 1-Butylpyridinium Hydrobromide comes from the pyridinium ring: compared to imidazolium salts, pyridinium-based compounds sometimes demonstrate improved stability toward nucleophilic attack, especially when exposed to strong bases or nucleophiles. This extra measure of resistance protects experiments from side reactions that are costly and time-consuming.

    Another difference surfaces in phase behavior and melting points. Imidazolium salts often show low melting points and form liquids at room temperature, which appeals for certain applications. 1-Butylpyridinium Hydrobromide has a higher melting point, usually placing it in a solid or semi-solid state under ambient conditions. Whether this property helps or hinders depends entirely on the circumstances. Electrochemists sometimes prefer a solid that can be easily dosed, while reaction chemists targeting room-temperature ionic liquids might want the fluidity of imidazolium types.

    The hydrobromide anion, meanwhile, separates this product from competitors relying on halides like chloride or iodide or more exotic counterions such as PF6 or BF4. Chemical reactivity and handling safety diverge significantly depending on the anion present. With bromide in hand, researchers can perform bromination reactions more efficiently, or, in my case, ensure that side products from halogen exchange stay manageable. Some ionic liquids release strong odors or pose disposal issues due to toxicity; hydrobromide salts skirt many of these complications, making the workbench life a bit less stressful.

    Performance and Reliability: Real-World Impact

    Quality assurance depends less on glossy brochures and more on repeated hands-on success. My own attempts to push a Suzuki coupling reaction forward underscored the value of working with tightly controlled, pure ionic liquids. Impurities bring unpredictability and rate suppression—two things nobody wants in a time-sensitive, resource-limited environment. The track record for 1-Butylpyridinium Hydrobromide in performing these tough jobs speaks volumes. Colleagues in industrial process optimization usually return to this compound for its reliable nature, often confirming through NMR spectra and repeated batch-testing.

    Its thermal stability also draws attention. Many ionic liquids decompose or discolor above moderate temperatures, but in well-run synthesis campaigns I’ve taken part in, neat 1-Butylpyridinium Hydrobromide withstands moderate heat. This makes it more than a one-trick pony: besides catalysis, it assists in extraction, phase-transfer catalysis, and even as a medium for crystallization in academic research setups.

    Addressing Safety and Environmental Impact

    Handling safety should always sit near the top of any user’s list. One benefit I have seen in 1-Butylpyridinium Hydrobromide lies in its relatively straightforward safety profile. Unlike some ionic liquids that introduce persistent environmental worries, this compound allows for a bit more flexibility. Hydrobromide-based materials definitely require gloves and basic lab safety, but compared to volatile organic solvents they present fewer inhalation or long-term health risks. Disposal still demands attention, since bromide-containing waste enters regulated streams, but this challenge feels more sensible than wrangling with fluorinated by-products or persistent halogenated solvents.

    Across multiple organizations, I have noticed a mounting push toward “greener” approaches. 1-Butylpyridinium Hydrobromide isn’t free from criticism—some stakeholders find the energy and material costs associated with ionic liquid production substantial. Fact remains, though, that reducing reliance on petroleum-derived solvents marks progress for many labs and pilot plants. In teaching labs and scale-up settings, swapping out flammable hydrocarbon solvents for a stable, non-volatile ionic liquid has lowered incidents and eased compliance reporting. These experiences don’t erase the product’s environmental footprint, but they certainly point to viable trade-offs in real-world conditions.

    Challenges in Use and Solutions Moving Forward

    No chemical compound solves every problem. I’ve watched new researchers wrestle with the downsides of ionic liquid work, especially issues around cost and recovery. 1-Butylpyridinium Hydrobromide, due to its specialty nature and purity standards, often commands a premium price. Some research budgets bend under the cost of stocking enough material for all possible experiments. As a result, many teams now focus on developing effective recovery and reuse protocols. Simple distillation techniques, extraction, or back-exchange strategies help stretch supplies.

    Another sticking point involves solubility with certain organic substrates. While it dissolves well in polar solvents and supports many reactions, big or highly aromatic molecules sometimes pose trouble. Some colleagues in medicinal chemistry have reported slower dissolving rates when trying to perform multi-step syntheses. This forces a kind of adaptability among researchers. Layering in co-solvents, carefully warming solutions, or pre-dissolving reactants offer partial workarounds. The difference from other products, in my view, is not so much about any magical property, but about developing consistent lab skills and knowing how to coax the maximum result from what’s available.

    Quality, Supply, and Reliability: The Human Element

    It’s easy to overlook human stories in the talk of chemical performance. Those of us working in research or production know that the success or failure of an experiment often comes down to how well a supplier follows purity standards or how carefully the compound is handled at each step. I have worked with teams where an unexpected change in source led to a cascade of minor issues: strange colorations, altered melting point, unpredictable yields. With 1-Butylpyridinium Hydrobromide, maintaining a relationship with suppliers who publish transparent data—showing actual spectra and batch histories—builds trust and saves time. No scientist likes rerunning purification steps due to hidden impurities.

    I’ve developed the habit, shared among many colleagues, of always verifying incoming lots. Reference NMR spectra, simple melting point checks, and even basic IR scans reveal a lot about product consistency. These measures pay for themselves by preventing wasted batches or compromised safety down the line. In the ever-hurried world of research, a reliable product makes for reliable results—a lesson learned by many, sometimes the hard way.

    Expanding Boundaries: 1-Butylpyridinium Hydrobromide and Innovation

    Beyond its staple roles, some frontier research seeks to harness 1-Butylpyridinium Hydrobromide in less conventional scenarios. Researchers exploring recyclable solvents for capture of atmospheric CO2 or energy storage often choose ionic liquids for their fine-tuned interactions with gases and ions. Here, the pyridinium-based structure sometimes reveals unique selectivity or physical stability. In some journals, teams showcase its use in batteries or supercapacitors, where traditional electrolytes fall short.

    I’ve observed that even in analytical chemistry, where high sensitivity matters, people turn to this compound to improve extraction techniques or solubilize challenging analytes. Its predictable response to an external potential in electrochemical set-ups allows for more precise measurement—an advantage over less stable or more hydrophobic species. Each of these small wins stacks up to reshape what’s possible, whether in energy, drug development, or materials science.

    The Real-World Payoff: Practical Value Over Hype

    There’s a temptation in the specialty chemicals market to oversell breakthrough properties and ignore the nuanced work backing true advances. From hands-on experience, I appreciate 1-Butylpyridinium Hydrobromide for its practical impact. It doesn’t promise to overhaul entire industries overnight, but in informed hands it solves concrete problems—helping edge forward a little faster, safer, or smarter. Labs aiming to refine reactions, cut down on hazardous solvent usage, and nail reliable batch results have plenty to appreciate here.

    Long hours in the lab reinforce the difference between what sounds exciting and what quietly delivers, experiment after experiment. Over the past few years, I’ve been lucky to work alongside researchers who employ this compound both for painstaking method development and practical scale-up. The lessons learned—mind storage, double-check purity, talk openly with suppliers, and share tips for recovery—form the real value chain in specialty chemical use. 1-Butylpyridinium Hydrobromide earns its place by meeting those everyday demands with a balance of reliability and modern chemical performance.

    Looking Ahead: Future of Pyridinium-Based Compounds

    For those charting the next decade of green chemistry or electrochemical synthesis, the continued development and application of pyridinium compounds like 1-Butylpyridinium Hydrobromide represent cause for optimism. Many believe, based on published data and field experience, that expanding the selection of ionic liquids with tunable structural features promises new breakthroughs. Applying lived lessons from handling, cost management, and green disposal methods will help ensure these compounds fulfill their promise.

    Those in academia and industry should continue scrutinizing performance gains and environmental trade-offs. Standardizing reporting on impurity levels, expanding training for new users, and fostering better supplier transparency can all raise the baseline for successful application. While markets evolve, and as regulatory standards increase, a commitment to practical, evidence-driven practices keeps compounds like 1-Butylpyridinium Hydrobromide relevant, usable, and impactful.

    Final Thoughts

    Standing out in the world of specialty chemicals requires more than just novel composition. The best products, like 1-Butylpyridinium Hydrobromide, win favor through steady, real-world performance. Each challenge in synthesis, catalysis, or electrochemistry that finds a solution with this compound contributes to a broader picture: research doesn’t just live inside the lab, but translates to safer, cleaner, and more efficient processes. People who demand better results and fewer headaches know the difference earned experience brings. In that work, this compound proves its merit day after day.