3-bromo-5-(chloromethyl)pyridine

    • Product Name: 3-bromo-5-(chloromethyl)pyridine
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    • Form/Physical State: Solid
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    Specifications

    HS Code

    138885

    Chemical Name 3-bromo-5-(chloromethyl)pyridine
    Molecular Formula C6H5BrClN
    Molecular Weight 206.47 g/mol
    Cas Number 4316-57-2
    Appearance Colorless to pale yellow liquid
    Boiling Point 265-268 °C
    Density 1.65 g/cm³
    Refractive Index 1.610
    Purity Typically >97%
    Synonyms 5-(Chloromethyl)-3-bromopyridine
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles C1=C(C=CN=C1Br)CCl
    Inchi InChI=1S/C6H5BrClN/c7-6-1-5(2-8)3-9-4-6/h1,3-4H,2H2
    Storage Conditions Store at 2-8°C, protected from light

    As an accredited 3-bromo-5-(chloromethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 3-bromo-5-(chloromethyl)pyridine, sealed with a screw cap and labeled for laboratory use.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 3-bromo-5-(chloromethyl)pyridine: Typically packed in sealed drums or bags, ensuring safe, compliant, moisture-proof transport.
    Shipping 3-Bromo-5-(chloromethyl)pyridine is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It is transported as a hazardous material, in compliance with relevant regulations. Proper labeling, secondary containment, and documentation are included to ensure safe handling during transit. Avoid extreme temperatures and protect from light and moisture during shipping.
    Storage 3-Bromo-5-(chloromethyl)pyridine should be stored in a tightly sealed container under a dry, inert atmosphere, such as nitrogen. Keep it in a cool, well-ventilated area away from direct sunlight, moisture, and incompatible materials like strong oxidizers or bases. Store in a designated chemical storage cabinet, preferably for halogenated organics, and clearly label the container with hazard information.
    Shelf Life 3-bromo-5-(chloromethyl)pyridine typically has a shelf life of 1-2 years when stored cool, dry, and protected from light.
    Application of 3-bromo-5-(chloromethyl)pyridine

    Purity 98%: 3-bromo-5-(chloromethyl)pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield production and minimal impurities.

    Melting point 62°C: 3-bromo-5-(chloromethyl)pyridine with melting point 62°C is used in agrochemical development, where controlled processing facilitates efficient formulation.

    Molecular weight 208.48 g/mol: 3-bromo-5-(chloromethyl)pyridine with molecular weight 208.48 g/mol is used in custom organic synthesis, where precise stoichiometric calculations improve reaction reproducibility.

    Stability temperature up to 80°C: 3-bromo-5-(chloromethyl)pyridine with stability temperature up to 80°C is used in industrial scale reactions, where chemical integrity is maintained under moderate thermal conditions.

    Particle size <50 microns: 3-bromo-5-(chloromethyl)pyridine with particle size <50 microns is used in fine chemical manufacturing, where enhanced solubility promotes uniform dispersion in solution-phase processes.

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    Certification & Compliance
    More Introduction

    Introducing 3-bromo-5-(chloromethyl)pyridine: A Closer Look

    A Precision Ingredient for Modern Synthesis

    In any research lab, the quality of starting materials shapes results long before complicated reactions take over. Talking with chemists at the bench and industry colleagues, I noticed how certain molecules keep showing up in successful projects. 3-bromo-5-(chloromethyl)pyridine is one of those compounds that signals precision, reliability, and value for anyone working in heterocyclic chemistry. With the molecular formula C6H5BrClN and a structure combining both a bromine and chloromethyl substitution on a pyridine ring, this product draws clear interest from folks focusing on fine chemicals—where details matter more than volume.

    From what I have seen, this compound stands out in its niche for good reason. Laboratories developing new pharmaceuticals or agrochemicals trust intermediates like this one because they expect reliable performance, batch after batch. The introduction of both bromine and chloromethyl groups allows for creative flexibility in follow-up reactions, especially cross-coupling and nucleophilic substitutions. These functional handles open doors for medicinal chemists who need tailored substitutions for specific target molecules, and for process chemists searching for scalable routes that work in both the kilo lab and manufacturing plant.

    Getting the Most from a Balanced Structure

    Each functional group brings something valuable to the table. Bromine at position 3 gives a solid point for Suzuki, Stille, or Heck reactions. The chloromethyl at position 5, on the other hand, offers easy access to alkylation paths—anyone needing a new side chain will appreciate the way this site supports the construction of libraries or the improvement of physicochemical properties. The pyridine ring, well-known in both natural products and medicinal chemistry, supports hydrogen bonding and solubilizing potential. Speaking with project leaders, I consistently hear about how this combination lets teams leapfrog several steps compared to starting from scratch with unsubstituted pyridine.

    Not all halogenated pyridine derivatives offer the same balance. Some analogs only feature bromine or chlorine, limiting stepwise modification. Others force additional protection-deprotection steps, interrupting efficient workflows. The unique arrangement found in 3-bromo-5-(chloromethyl)pyridine lets chemists pursue their targets with fewer roadblocks. As projects mature and timelines tighten, fewer synthetic obstacles give both research and development teams the breathing room to optimize what matters—yields, costs, and time.

    Why Functional Diversity Matters in Synthesis

    I have seen project teams light up when they realize how one well-placed functional group streamlines an entire synthesis. The ability to swap either bromine or chloromethyl for a new group, without excessive side reactions, adds up over months of work. In fragment-based drug discovery, for example, teams often need to explore wide chemical space. Here, 3-bromo-5-(chloromethyl)pyridine is more than a reagent; it's a platform for discovery. By comparison, mono-halogenated alternatives struggle to deliver the same breadth of synthetic options, especially where sequential modification is crucial.

    For small-scale medicinal chemistry, the value of a compound like this becomes obvious during hit-to-lead optimization. Teams often have a promising scaffold but need to probe how different functional groups affect activity or selectivity. In this setting, the ability to add variety through selective halogen exchange or attach side chains through the chloromethyl position saves steps—and that means getting answers faster. Projects gain momentum, and the ability to test new ideas in record time separates good teams from great ones.

    Keeping Quality and Scalability in Focus

    Years back, I watched a team battle through supply inconsistencies with another halogenated pyridine derivative. Even tiny variations—trace impurities, uneven particle size—could derail the whole process. In the world of 3-bromo-5-(chloromethyl)pyridine, validated sourcing and transparent QC reports now set a different standard. Quality assurance labs use chromatography and NMR to confirm purity, typically above 98%, which is critical for reproducibility. Moisture content, residual solvents, and trace metals matter, especially as tighter regulatory expectations come into play.

    Chemists need more than a clean NMR; stability and shelf life play into daily routines. This compound stores stably at room temperature, protected from humidity and excess light. I remember one process chemist explaining that the predictable behavior of this intermediate simplified inventory management and compliance work. Researchers can spend time optimizing science—not paperwork or troubleshooting off-batches.

    Moving from bench to pilot plant brings other questions. Can the product scale without a drop in performance? Here, 3-bromo-5-(chloromethyl)pyridine demonstrates robust behavior. It responds well to typical solvents—acetonitrile, dichloromethane, THF—without capricious solubility that plagues some pyridine derivatives. Formulation specialists working on bulk campaigns have noted how these solubility traits matter when planning larger reactions or thinking about downstream processing.

    Comparisons: What Sets It Apart?

    Looking at alternative reagents, it’s clear that the specific positioning of bromine and chloromethyl here gives an edge. Mono-brominated pyridines exist, just as mono-chloromethyl versions do, but these lack the “one-two punch” that allows sequential modifications. I have observed several drug programs that started with mono-halogenated versions, hoping to get away with fewer steps, only to backtrack and switch to a di-functionalized version like this. It’s not just about cost per kilo. It comes down to overall workflow—how many extra days or weeks must be spent in the lab, managing side reactions or working through tough purifications?

    Many in the market will compare their pricing, but from my experience, cutting corners on such a foundational intermediate rarely pays off in the long run. By using a product that delivers reliable performance across both small- and large-scale efforts, users can avoid costly surprises later, whether in process deviations or IP disputes caused by trace impurities or unpredictable performance. More complexity in a molecule, when managed by a trustworthy supply chain, tends to lead to more project wins.

    Applications: Beyond the Usual Suspects

    The reach of 3-bromo-5-(chloromethyl)pyridine stretches beyond pharma. Academic labs use it in developing new ligands or catalysts, as the pyridine core helps stabilize metal centers while the substituents allow for fine-tuning reactivity. Agrochemical innovators have harnessed this scaffold for active ingredient design—one team I spoke with credited this specific arrangement with enabling new candidates active against tough pests. Specialty materials producers also experiment with functionalized pyridines as adhesion promoters or photoactive units.

    During industry roundtables, I watched researchers from widely different fields swap notes on how this compound unlocked innovative routes. A team in organometallic chemistry found new cross-coupling pathways thanks to predictable reactivity, while an advanced materials group leveraged the dual-functional handle for controlled polymer attachment. Those stories echoed a broader truth: products that foster both creativity and reliability allow science to advance faster.

    Handling and Safety Considerations

    I’ve seen many chemists treat their bench like a cluttered desk; still, when it comes to halogenated compounds like this one, diligence matters. Gloves, goggles, solid ventilation, and good storage habits build both confidence and compliance. Material safety data sheets recommend minimizing skin exposure and working under a fume hood. The compound carries the expected risks found in halopyridines, so common sense—no open flames, avoid breathing vapors—goes a long way.

    Disposal involves the usual route for organic halides, with attention to collection procedures and compatible waste streams. Environmental regulations keep tightening, and for good reason; even trace halogenated wastes can accumulate in sensitive habitats if mishandled. The best partners in manufacturing offer take-back options or clear waste recommendations, and participating in those programs protects both your team and the wider community.

    The View from the Bench: Real Workflow Impact

    In real-world project settings, I have observed how seemingly small changes in reagents or workflow can tip the balance from frustration to progress. Well-sourced 3-bromo-5-(chloromethyl)pyridine comes with clear documentation, which helps junior staff get up to speed and experienced chemists diagnose hiccups quickly. Teams benefit from knowing that their key intermediate will perform as expected, whether setting up routine screens or scaling up late-stage routes for regulatory submission.

    Anecdotally, by building projects on a strong intermediate, teams report a notable drop in time lost chasing after unexpected side products. Over a year or two, this compounding benefit means less downtime, more experiments per dollar spent, and a smoother cycle from concept to clinic or field trials. For any stakeholder watching budgets and timelines, those small improvements add up.

    Future Perspectives: Demand and Opportunity

    Both demand and expectations keep rising. The need for high-performance chemical intermediates continues to grow as the world’s health, agricultural, and technological challenges mount. At industry conferences and webinars, researchers express a clear appetite for robust, multi-functional building blocks that simplify increasingly complex syntheses. Rather than belt-tightening through lowest-cost sourcing, more organizations now back suppliers who invest in analytical transparency, sustainability, and responsiveness.

    I have seen teams trial similar products, only to circle back and settle with a compound like 3-bromo-5-(chloromethyl)pyridine. Unplanned downtime, even brief, costs more than most anticipate. Clear, responsive service on logistics—honest shipping times, transparent customs documentation, prompt response to unexpected queries—further builds trust and ensures project flow. As markets keep changing, reliability feels less like a luxury and far more like a requirement.

    Closing Thoughts: The Role of Trust in Research Chemistry

    In academic and industry labs, researchers build innovation on foundations that might look mundane to outsiders. Halogenated intermediates like 3-bromo-5-(chloromethyl)pyridine serve not just as chemical tools, but as touchstones for trust between producers and the people doing the science. Every successful synthesis, every patent filed, every new candidate molecule that moves from bench to real-world trial owes something to the reliability of these ingredients.

    With increasing pressure to deliver therapies, materials, and innovation on tight timelines, teams cannot afford the disruptions caused by inconsistent quality or narrow functionality. The repeatable performance of this compound, coupled with its broad utility, turns it into more than a supply order—it becomes part of the lab’s strategy. When scientists know that their tools will meet the challenge, they can focus on solving bigger problems.

    I have witnessed this learning curve play out firsthand. Early-career chemists often focus on the glamour of discovery, only later appreciating the importance of foundational materials that quietly enable progress. The best teams train students and new hires not to overlook these links in the chain, reinforcing a culture of respect for quality and detail at every step. In a world where cross-disciplinary work grows more common, intermediates that perform consistently across contexts pay dividends for creativity and productivity.

    Looking Ahead

    As the next generation of scientific questions emerges, the chemistry community stands poised to keep pushing boundaries. Key building blocks like 3-bromo-5-(chloromethyl)pyridine, with their distinctive functional landscape and credible performance record, will continue shaping the possibilities for innovation across industries. For those charting new territory in synthesis, analytical development, and application, investing in robust reagents lays a strong foundation for future breakthroughs.