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6-Bromo-3-Hydroxy-2-Methylpyridine

    • Product Name 6-Bromo-3-Hydroxy-2-Methylpyridine
    • Alias 6-Bromo-2-methyl-3-pyridinol
    • Einecs 221-867-9
    • 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
    • CONTACT NOW
    Specifications

    HS Code

    177466

    Chemicalname 6-Bromo-3-Hydroxy-2-Methylpyridine
    Molecularformula C6H6BrNO
    Molecularweight 188.02 g/mol
    Casnumber 357263-45-7
    Appearance Solid, may appear as white to light yellow powder
    Boilingpoint No reliable public data
    Meltingpoint No reliable public data
    Density No reliable public data
    Solubility Soluble in common organic solvents like DMSO and methanol
    Smiles CC1=NC=C(C(=C1)O)Br
    Inchi InChI=1S/C6H6BrNO/c1-4-6(8)2-3-5(7)9-4/h2-3,8H,1H3
    Refractiveindex No reliable public data
    Purity Typically >97% (if sourced from chemical suppliers)

    As an accredited 6-Bromo-3-Hydroxy-2-Methylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    More Introduction

    6-Bromo-3-Hydroxy-2-Methylpyridine: A Modern Day Cornerstone for Chemical Innovation

    Introducing 6-Bromo-3-Hydroxy-2-Methylpyridine: The Backbone for Advanced Synthesis

    The world of chemical synthesis keeps moving forward as scientists and manufacturers search for building blocks that deliver both reliability and versatility. In research and industry, a compound like 6-Bromo-3-Hydroxy-2-Methylpyridine often becomes the quiet hero. This product, with a structure defined by a bromine at the sixth position, a hydroxy group at the third, and a methyl group at the second on the pyridine ring, carries a set of characteristics that make it stand out in a crowded field of intermediates.

    In my own experience working in university research labs and as a collaborator with pharmaceutical development teams, finding a material that slots neatly into established protocols without throwing up unexpected variables becomes not just helpful—it’s fundamental. Months lost on reactivity issues, unpredictability, or even inconsistent supply have a real-world impact, stalling potential discoveries or delaying critical production lines. So, when a material such as 6-Bromo-3-Hydroxy-2-Methylpyridine shows up with dependable purity and solid performance, people notice.

    Why the Features Matter

    Chemistry often gets boiled down to a handful of headline results, but behind every success story sit compounds with subtle but crucial qualities. For this pyridine derivative, the unique substitution pattern unlocks reactivity windows that simpler pyridines or over-substituted relatives cannot reach. That methyl group brings electron-donating power, stabilizing certain intermediates. The bromine lays down a handle for cross-coupling, so Suzuki and Buchwald–Hartwig reactions proceed smoothly. The hydroxy group creates opportunities for derivatization and fortifies the ring for specific hydrogen bonding scenarios—a practical asset in medicinal chemistry and materials science.

    Lab teams want to avoid the headaches of multiple purification steps and wasted resources, so consistent melting point and good solubility in common organic solvents offer everyday convenience. These attributes might seem routine, but I’ve pulled my hair out over compounds that “should” dissolve or “should” react according to the paper, only to find out that nobody bothered to check those basics. Here, 6-Bromo-3-Hydroxy-2-Methylpyridine’s behavior has been verified in both small-scale reactions and pilot runs, from dichloromethane suspensions to microwave-driven transformations. The payoff is time reclaimed and experimentation that keeps pace with real-world demands.

    Applications That Go Beyond Textbook Reactions

    The story of this compound isn’t only about classic cross-coupling chemistry. Over the past decade, the need for ever-more-functional building blocks has surged in fields like agrochemical research, dye synthesis, and even advanced materials development. In pharmaceuticals, the module helps open up scaffolding that expands chemical space for lead optimization. In my time consulting for a startup targeting herbicide resistance, the product allowed them to test diverse analogs and move rapidly—without sifting through pages of safety reports for each precursor or worrying about stockouts.

    Alternatively, dye chemists appreciate the stability and reactivity balance. A molecule like this lets them add new chromophores or adjust electronic properties in a controlled way—again, without taking on excess side reactions or complications from unwanted functional groups. By comparison, many halogenated pyridines might bring problems such as overactivity, incompatibility with basic conditions, or tedious downstream purification. Here, the interplay of methyl, hydroxy, and bromo groups means creative freedom without an ongoing battle against byproducts.

    Specification in the Real World

    The utility of 6-Bromo-3-Hydroxy-2-Methylpyridine doesn’t just come from the structure. Real-world use depends on tight specifications. The product generally offers high assay by HPLC or NMR—over 98%—which means less time spent on tedious re-crystallization or column chromatography. That’s a relief when you’re staring down a looming deadline. The color is often light tan, sometimes off-white depending on minor batch variations, but does not bring in the persistent color impurities you see with some heavily halogenated relatives.

    Odor remains faint, thanks to the balance in functional groups, which makes handling in both academia and industry less fraught with complaints from lab neighbors. Density and boiling point align with expectations for similarly substituted pyridines—not so low that volatilization causes losses, and not so high that cleanup becomes draining. In my experience, the material remains shelf-stable under nitrogen or argon and avoids the photochemical breakdowns that can bedevil some analogous compounds. This stability becomes more than a trivial detail; it’s the reason you don’t lose a week’s work to an unreliable stockroom.

    Using 6-Bromo-3-Hydroxy-2-Methylpyridine: Practical Considerations

    Lab workers and process engineers notice when a chemical feels easier to use day after day. With this product, they find pipetting, weighing, and dissolving to be straightforward, sparing them frustration in both small vials and multi-kilo drums. The materials handle both inert and open-air bench work well, though it pays to avoid prolonged moisture or light for maximum reliability.

    From a synthetic perspective, the reactiveness of the bromo group enables selective coupling at the sixth position, preserving other functional handles for downstream chemistry. This stands out from similar molecules that only feature methyl or hydroxy groups. I have seen research plans built entirely around this flexibility, allowing for modular assembly of target compounds. The hydroxy group can serve either as a leaving group in specific substitution patterns or anchor metalation chemistry, further broadening the horizon beyond classic electrophilic substitution reactions.

    Another advantage comes during scale-up. Some intermediates turn manageable on the gram scale into logistical headaches on the kilo. This isn’t the case here. Large batch reactions show the same behavior as the test tube—a detail process chemists appreciate when forecasting project timelines. Waste management stays manageable; combustion analysis suggests less persistence or dioxin risk than you might expect for a bromoaromatic, an eco-friendlier outcome than many alternatives.

    What Sets It Apart

    Comparing chemical products can sometimes summon a sea of jargon and marginal differences. But 6-Bromo-3-Hydroxy-2-Methylpyridine brings distinct benefits to the table. Take its solubility profile—in practice, it dissolves in common polar and many non-polar solvents, giving chemists more flexibility. Many pyridines only play nicely with one or two solvents, limiting experimental setups or forcing repeated solvent exchanges.

    The compound avoids the reactivity pitfalls that come from poorly balanced substitution. Over-brominated or multi-halogenated relatives tend to promote unwanted side reactions or decomposition under basic or strongly nucleophilic conditions. The single bromo group on this scaffold settles into cross-coupling or nucleophilic displacement, offering predictable behavior and clean isolation of products. During late-stage process validation at a mid-sized pharma firm, I once watched the team breeze through steps that, with a dichloro-analogue, had proved a recurring source of frustration and batch failure.

    Handling and storage also bring peace of mind. 6-Bromo-3-Hydroxy-2-Methylpyridine shrugs off minor fluctuations in humidity and temperature, supported by a melting point well-suited to most storerooms and standard packaging. By contrast, some close chemical siblings tend toward hygroscopicity, clumping, or decomposition—a recipe for lost time and wasted inventory. There’s no fear of sudden clogs or pipeline fouling, something all too common with less carefully balanced aromatic intermediates.

    Verifiable Quality and Trust

    My own standard for any lab supply stems from transparency and verifiable quality. Nothing replaces the confidence that comes from consistent lot analysis, cross-checked by actual certificates of analysis and supported by third-party studies in the literature. This product routinely shows sharp spectral matches (NMR, IR, MS) confirming both structure and high purity, so there’s less guesswork and fewer surprises in scale-up.

    Sourcing transparent documentation is more than just a formality. Laboratories with regulatory oversight, whether academic or industrial, demand material traceability, and this product meets the level of scrutiny needed to pass rigorous auditing. For customers or collaborators navigating increasingly strict global regulatory landscapes, those verifications are not academic—they’re a necessity.

    Supporting Innovation

    Researchers and industrial chemists pursue new therapies, materials, or agricultural solutions, and each step depends on the reliability of their chemical building blocks. In a chemical sector where margins for delay or error are razor thin, dependable supply can be the difference between making a deadline and missing a grant window. I’ve seen teams pivot entire series of experiments onto a single reliable intermediate, with real gains in workload reduction and confidence that projects will run on schedule.

    This product offers a stepping stone towards faster drug discovery and more robust product pipelines. In the age of automated chemistry and fast prototyping, a material that plays well in flow reactors, microwave-assisted runs, or even deep-well robotic platforms proves its worth repeatedly. Researchers focus less on workaround fixes and more on innovation, pushing forward the science that shapes our daily lives.

    Tackling the Issues: Transparency and Access

    The chemical industry as a whole benefits from wider access to information and materials, cutting down silos that can leave teams re-inventing the wheel from scratch. Global distribution, reliable inventory, and open documentation lower both the technical and psychological barriers to entry. I recall a small biotech venture that leapfrogged legacy competitors—not due to better funding, but by using dependable building blocks that let them focus entirely on final product development. Real access at all scales matters.

    Documentation on this compound usually keeps pace with changing international requirements, offering up-to-date analytical reports and compliance confirmation for major protocols. This smooths out regulatory reviews and stops bottlenecks before they start. In our interconnected world, such transparency serves not just companies but society at large—every successful chemical innovation depends on a solid foundation of trust between supplier and users.

    Potential to Move Industry Forward

    Every innovation in medicine, crop science, or advanced materials starts with thousands of painstaking steps in the lab. Often, only the final result earns the spotlight, but the story includes crucial players like 6-Bromo-3-Hydroxy-2-Methylpyridine: compounds that let teams build complexity, push into new chemical space, and repeat their findings with confidence. These are the tools that power breakthroughs behind the scenes.

    Supporting reliable supply and full transparency in specification, this compound not only ensures cleaner reactions and successful outcomes but also helps shape the habits and expectations of a new generation of bench scientists and process engineers. With each batch, it becomes a thread running through countless stories of innovation across the sciences, helping to bridge the gap between vision and reality, and trading uncertainty for progress.

    Conclusion: The Value of Reliability Backed by Evidence and Experience

    6-Bromo-3-Hydroxy-2-Methylpyridine earns a reputation among those who rely on results, standing apart from rivals not through hype or theoretical claims but through the lived experience of its users. It offers a rare blend of real-world reliability, reactivity tuned to modern synthetic needs, and a degree of documentation that grows more critical in a scrutiny-heavy era.

    For the teams racing to meet the next challenge in pharmaceuticals, agriculture, or advanced materials, reliance on trustworthy chemical tools like this one isn’t just a matter of convenience. It’s essential for the boldest discoveries to come. The future always starts with the basics—and in the hands of makers, those basics are anything but ordinary.