2-Hydroxymethyl-5-bromopyridine

    • Product Name: 2-Hydroxymethyl-5-bromopyridine
    • Chemical Name (IUPAC): 5-Bromo-2-(hydroxymethyl)pyridine
    • CAS No.: 3430-18-0
    • Chemical Formula: C6H6BrNO
    • Form/Physical State: Crystalline Powder
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    552295

    Chemical Name 2-Hydroxymethyl-5-bromopyridine
    Cas Number 3430-18-0
    Molecular Formula C6H6BrNO
    Molecular Weight 188.03 g/mol
    Appearance White to off-white solid
    Purity Typically >98%
    Melting Point 90-94°C
    Solubility Soluble in common organic solvents
    Smiles C(O)Cn1ccc(Br)cc1
    Inchi InChI=1S/C6H6BrNO/c7-5-1-2-8-6(3-5)4-9/h1-3,9H,4H2
    Storage Conditions Store at 2-8°C, tightly closed
    Synonyms 5-Bromo-2-(hydroxymethyl)pyridine

    As an accredited 2-Hydroxymethyl-5-bromopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2-Hydroxymethyl-5-bromopyridine is packaged in a 10 g amber glass bottle with a tamper-evident cap and labeling.
    Container Loading (20′ FCL) Container Loading (20′ FCL): Securely packed in drums, 2-Hydroxymethyl-5-bromopyridine efficiently loaded, ensuring safe chemical transport and minimal contamination.
    Shipping 2-Hydroxymethyl-5-bromopyridine is shipped in sealed containers to prevent moisture exposure and contamination. It must be handled as a potentially hazardous chemical, following appropriate safety protocols. Transport complies with local regulations for chemical substances, ensuring secure, labeled packaging and shipment via certified carriers specializing in chemical materials.
    Storage 2-Hydroxymethyl-5-bromopyridine should be stored in a tightly sealed container, away from moisture and incompatible materials such as strong oxidizing agents. Store the chemical in a cool, dry, well-ventilated area, ideally under inert atmosphere like nitrogen or argon if long-term storage is required. Protect from direct light and heat to maintain stability and prevent decomposition.
    Shelf Life 2-Hydroxymethyl-5-bromopyridine is stable under recommended storage conditions, typically giving a shelf life of 2-3 years.
    Application of 2-Hydroxymethyl-5-bromopyridine

    Purity 98%: 2-Hydroxymethyl-5-bromopyridine with 98% purity is used in pharmaceutical intermediate synthesis, where high purity ensures efficient yield and reduced impurities in final compounds.

    Melting point 80–84°C: 2-Hydroxymethyl-5-bromopyridine with melting point 80–84°C is used in chemical research reactions, where controlled melting point supports reproducible phase-transition behavior during compound preparation.

    Molecular weight 188.03 g/mol: 2-Hydroxymethyl-5-bromopyridine with molecular weight 188.03 g/mol is used in medicinal chemistry, where precise molecular weight facilitates accurate stoichiometric calculations in drug design.

    Particle size <100 µm: 2-Hydroxymethyl-5-bromopyridine with particle size below 100 µm is used in catalyst development, where fine particle size improves dissolution and reaction rates.

    Storage stability at 25°C: 2-Hydroxymethyl-5-bromopyridine with storage stability at 25°C is used in organic synthesis labs, where thermal stability ensures long-term material integrity and reliability.

    Assay ≥97%: 2-Hydroxymethyl-5-bromopyridine with assay value ≥97% is used in agrochemical API manufacturing, where high assay guarantees consistent active ingredient concentration in formulations.

    Water content <0.5%: 2-Hydroxymethyl-5-bromopyridine with water content below 0.5% is used in moisture-sensitive syntheses, where low water content prevents hydrolysis and preserves chemical reactivity.

    Residual solvent <200 ppm: 2-Hydroxymethyl-5-bromopyridine with residual solvent under 200 ppm is used in material science applications, where minimized solvent content enhances material purity and product performance.

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    Certification & Compliance
    More Introduction

    Unlocking the Value of 2-Hydroxymethyl-5-bromopyridine in Modern Chemistry

    Understanding the Backbone of Laboratories: What Sets 2-Hydroxymethyl-5-bromopyridine Apart

    2-Hydroxymethyl-5-bromopyridine has quietly become one of those chemical compounds that just makes life easier in the lab. Chemists who’ve spent years puzzling over the best intermediates for building more complex molecules often end up relying on this compound. With a molecular structure that puts both a bromine atom and a hydroxymethyl group onto a pyridine ring, you get a rare combination of reactivity and selectivity. Unlike alternative pyridine derivatives, this particular molecule delivers more flexible reaction positions, which expands the toolkit for professionals dealing with heterocyclic synthesis.

    I’ve seen first-hand how it’s used during pharmaceutical research, especially in the run-up to developing new candidates for clinical trials. Its role pops up most clearly in cross-coupling reactions, those bread-and-butter steps that join organic building blocks together. If your job revolves around building custom scaffolds or slotting new side-chains onto a pyridine ring, the bromine at the 5-position really comes into play, helping chemists direct substitutions wherever they want them.

    Other pyridine building blocks might look similar at first glance, but they just don’t bring the same adaptability. Unsubstituted pyridines lack both handles for easy functionalization, so researchers often struggle with extra steps or more complicated protection and deprotection sequences. 2-Hydroxymethyl-5-bromopyridine, by contrast, comes ready for action—just dissolve it in your solvent of choice and the chemistry flows with fewer roadblocks and far fewer byproducts.

    Specifications That Matter in the Real World

    Lab workers care about purity, and for good reason. Impurities at the trace level can sink a whole week’s worth of work, sometimes in ways that only show up when it’s too late to salvage results. Reputable suppliers typically deliver 2-Hydroxymethyl-5-bromopyridine at a purity north of 98 percent, with moisture and heavy metal levels carefully controlled. While it’s a white to off-white crystalline solid, the real test comes in its reliability, batch after batch. I’ve pulled powders that are consistent in texture and easy to weigh out without the clumping or sticking that plagues so many similar products.

    Storage also favors those who plan ahead—this compound stands up well in a dry, cool environment, shielded from direct sunlight. It holds its character and doesn’t yellow or degrade quickly. The stability extends shelf life, giving procurement officers a break from the constant pressure to rotate stock.

    Solubility marks another step up for this compound. Dissolving in common solvents like ethanol, methanol, or slightly polar organics is straightforward, which means you spend less time coaxing it into solution and more time generating actionable data. This simple fact has saved me headache after headache over the years, especially when running late-stage functionalizations or combinatorial chemistry runs where throughput matters.

    Applications in Research and Industry: Why Chemists Keep Coming Back

    Applications for 2-Hydroxymethyl-5-bromopyridine are anything but limited. In my experience, the most common use comes in preparing key intermediates for pharmaceutical synthesis. Its unique structure, blending nucleophilic and electrophilic sites, opens the door for Suzuki-Miyaura and Buchwald-Hartwig cross-coupling reactions. Medicinal chemists looking to introduce new functionalities onto aromatic systems routinely turn to this compound because the bromine is reactive enough for classic palladium-catalyzed couplings, but not so reactive that you lose control over side reactions.

    On top of this, the hydroxymethyl group at the 2-position lets researchers protect, deprotect, or transform the molecule in countless ways. Need a masked alcohol for downstream coupling or oxidation? Here, the chemistry adapts. Want to create a fluorinated analog for positron emission tomography (PET) imaging agents? The scaffold works. The value multiplies when working on drug metabolism and pharmacokinetics, since pyridine rings appear often in the structure of both approved drugs and advanced candidates.

    Beyond the pharmaceutical realm, the compound shines in agrochemical development and advanced material research. Formulators who want robust, heteroaromatic spacers in their molecular designs have fewer headaches when their starting material comes with well-defined functional groups right off the shelf. I've worked alongside teams optimizing crop protection agents, and the ability to introduce substituents under mild conditions can streamline months of synthetic troubleshooting down to a few days—sometimes saving projects that might otherwise stall out due to synthetic intractability.

    Direct Comparison with Other Pyridine Derivatives

    Pyridine chemistry looks crowded at first—dozens of ring substitutions and functional group arrangements, some with promising properties on paper. In practice, many compounds trade useful reactivity for challenging handling or poor selectivity. Take plain 2-bromopyridine as a comparison. The lack of an extra functional group narrows your options, often forcing researchers to rely on riskier reagents or expensive catalysts, just to eke out a single useful transformation.

    On the flip side, try using 2-hydroxymethylpyridine without the halide; functionalizing the ring becomes much less predictable, and you rapidly run into dead-ends during side-chain manipulation. By combining both features—bromine at the para position, hydroxymethyl at the ortho—2-Hydroxymethyl-5-bromopyridine sidesteps these trade-offs. The synthetic routes become shorter and more robust, letting project teams rapidly explore new chemical space without as many unplanned diversions or purification headaches.

    I’ve seen teams cut out whole stages of chromatography just because the building block they switched to required fewer protection and deprotection cycles. Each cleaned-up process shaves labor hours and waste generation, delivering not just savings, but tighter scalability as projects ramp up.

    The Bigger Picture: Supporting Innovation Through Reliable Intermediates

    Every chemist knows the frustration of working with unreliable building blocks. Wasted effort adds up quickly with flawed reagents. With 2-Hydroxymethyl-5-bromopyridine, I’ve seen greater project confidence from early-stage research through to process optimization. It doesn’t just react in textbook fashion; it performs predictably in real lab environments, even as conditions inevitably diverge from idealized procedures.

    Patents published in the last decade confirm its growing use in blockbuster small-molecule drugs and specialty chemicals. In terms of output, this single compound keeps finding new applications as molecular architects target more challenging chemical motifs. For young researchers starting out, working with a well-behaved intermediate like this one builds morale, since experiments unfold more like designed and less like an unpredictable series of compromises.

    The utility extends even into analytical chemistry. If you need reference materials for chromatography or NMR calibration, a compound with clean spectral features, sharp melting points, and robust linearity across concentration ranges helps anchor entire methods sections. Accuracy improves, instrument drift decreases, and audits become less stressful when your reference materials act predictably.

    Supporting Data and Regulatory Considerations

    Published studies show how closely impurities track with process scale and storage conditions. Analytical chemists depend on products like 2-Hydroxymethyl-5-bromopyridine as anchor points, setting baselines for purity and repeatability in results. In regulated labs, such as those working under Good Manufacturing Practice, traceability and batch consistency come under the microscope. I’ve worked under these conditions, where every deviation prompts a cascade of documentation and review, underscoring the importance of intermediates that behave as advertised.

    Analytical protocols typically cover identification by NMR and HPLC, with confirmation against published spectra and retention times. For scale-up specialists, the inherent stability and low reactivity of this compound under ambient storage puts fewer demands on cold storage or inert atmosphere precautions, helping streamline compliance with inventory and transport rules.

    Addressing Safety and Environmental Footprint

    Every laboratory product brings its own safety and disposal considerations. 2-Hydroxymethyl-5-bromopyridine, with its moderate handling requirements, strikes a good balance. Standard best practices—wearing gloves, eye protection, and working in a well-ventilated hood—cover most scenarios. I haven’t experienced the acute hazards or environmental headaches associated with some more volatile or reactive building blocks.

    Disposal follows the principles familiar to chemists working with organic halides. Waste is collected and processed with attention to regulatory guidelines around brominated compounds. Any solution that includes this intermediate can typically be treated at standard chemical waste facilities, avoiding exotic destruction routes or special high-temperature incineration. Environmental, health, and safety teams appreciate intermediates that play nice with established routines, as tracking and disposal processes become simpler to standardize.

    On a wider scale, responsible sourcing and lifecycle considerations for synthetic intermediates are coming to the forefront. Companies selecting this compound as a core intermediate benefit from the global supply chain’s gradual push toward greener, less energy-intensive manufacturing steps. While the chemistry itself still carries the mark of core synthetic organohalide transformations, cleaner production routes and investments in solvent recycling help shrink the overall footprint.

    Solutions to Challenges in Supply, Complexity, and Cost

    Availability sometimes throws a wrench into research timelines. With more demand from pharma and biotech, lead times may stretch during high-volume periods. I’ve learned to manage research supply chains by ordering critical intermediates like 2-Hydroxymethyl-5-bromopyridine in advance and developing contacts with multiple suppliers. Communication across departments helps, keeping everyone looped into stock levels and changes in delivery schedules.

    On the complexity front, the biggest wins come from clear communication between synthetic chemists and suppliers. Sharing application details can prompt manufacturers to fine-tune their purification and packaging methods, minimizing mishaps like caked product or unexpected trace contaminants. Whenever I’ve seen buyers reach out proactively, the result is improved quality and fewer last-minute surprises in the lab.

    Cost always looms large in industrial and research settings alike. Single gram samples for research rarely trigger scrutiny. Once projects move to scale, cost per mole can eat up budgets unexpectedly—especially if yield drops or rework becomes necessary. By switching to an intermediate like 2-Hydroxymethyl-5-bromopyridine that streamlines synthetic steps, I’ve watched entire process mass intensity calculations swing in favor of greener, more affordable routes. The up-front expense quickly recoups through simpler workups, leaner purification, and fewer reruns.

    Potential Solutions and Industry Best Practices

    To keep the supply chain healthy, partnerships between research labs and raw material distributors will play a key role. Transparent dialogue on future demand signals allows for timely scale-up in production, avoiding shortages that punish both science and business. On-site inventory tracking systems have helped me stay ahead of abrupt shortages, smoothing out batch planning and reducing stress for research teams.

    For those struggling with process bottlenecks, investing in automation around weighing, mixing, and dosing cuts down on both waste and inconsistency. I’ve worked with setups allowing operators to track weight, humidity, and temperature—in effect, wringing every last drop of value from each batch of high-value intermediates. Process improvements like this give research organizations the edge, freeing chemists to focus on discovery.

    Environmental impact, while complex, often improves through simple substitution. Where possible, using less hazardous solvents during reactions involving this intermediate reduces both direct costs and headaches during downstream waste handling. Further gains stem from partnering with vendors committed to responsible production, verified through third-party certifications. Every step toward green chemistry inches the enterprise in the right direction.

    Looking Ahead: The Case for Trustworthy Intermediates in Tomorrow’s Molecules

    Research across the sciences only advances as quickly as its foundation—the reagents that power each stage from discovery to scale-up. 2-Hydroxymethyl-5-bromopyridine strengthens that foundation. It’s the rare example of a compound that moves smoothly from benchtop experiment to kilo lab, supporting both rapid prototyping and rigorous manufacturing. Anyone who’s run late-night reactions or juggled parallel syntheses can appreciate the peace of mind that comes from reliable, well-understood intermediates.

    In pharmaceutical innovation, the pressure to move from discovery to clinic never lets up. A single setback, whether through inconsistency in reaction outcomes or unpredictable impurity profiles, can derail projects and shroud months of effort in uncertainty. I’ve watched seasoned scientists lean into intermediates like this, not because they’re trendy, but because they’ve proven themselves useful hundreds of times over.

    Collaboration only works when each team, from early research to scale-up and quality assurance, pulls from the same toolbox. Compounds like 2-Hydroxymethyl-5-bromopyridine—stable, accessible, and dependable—let researchers pull off ambitious chemistry without last-minute substitutions or back-up plans. In my work, every successful experiment using this intermediate builds confidence that the next big breakthrough might really be within reach.

    Final Thoughts on Innovation, Reliability, and Real-World Lab Work

    Having spent many years in both academic and industry labs, I appreciate compounds that quietly do their job well. While the high-profile targets may steal the spotlight, much of modern chemical progress relies on versatile intermediates that let scientists push boundaries instead of wrestling with their materials. 2-Hydroxymethyl-5-bromopyridine proves, day after day, why thoughtful molecular design and attention to usability matter. Anyone involved in the business of invention—be it medicines, new materials, or agricultural solutions—should keep an eye on the building blocks shaping the landscape. In my experience, practical solutions begin with practical chemistry, and for that, high-quality pyridine derivatives like this one belong on every lab’s shelf.