3,5-Dibromo-4-methoxypyridine

    • Product Name: 3,5-Dibromo-4-methoxypyridine
    • Chemical Name (IUPAC): 3,5-dibromo-4-methoxypyridine
    • CAS No.: 3430-18-0
    • Chemical Formula: C6H5Br2NO
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    962826

    Chemical Name 3,5-Dibromo-4-methoxypyridine
    Cas Number 72934-15-5
    Molecular Formula C6H5Br2NO
    Molecular Weight 266.92
    Appearance White to off-white solid
    Melting Point 91-94°C
    Solubility Soluble in organic solvents such as DMSO and methanol
    Smiles COC1=C(C=C(N=C1)Br)Br
    Inchi InChI=1S/C6H5Br2NO/c1-10-6-4(7)2-5(8)9-3-6/h2-3H,1H3
    Storage Conditions Store at room temperature, in a tightly closed container, away from light and moisture

    As an accredited 3,5-Dibromo-4-methoxypyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 5-gram amber glass bottle with a secure screw cap, labeled "3,5-Dibromo-4-methoxypyridine, 98%," safety instructions included.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 3,5-Dibromo-4-methoxypyridine: 7–10 metric tons, packed in 25 kg fiber drums or bags, safely palletized.
    Shipping 3,5-Dibromo-4-methoxypyridine is shipped in tightly sealed containers, protected from moisture and light, and compliant with chemical transport regulations. Packaging ensures safe handling during transit, typically requiring labeling for hazardous materials. It is transported at ambient temperature unless otherwise specified, with documentation provided for regulatory and safety compliance.
    Storage Store **3,5-Dibromo-4-methoxypyridine** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, heat, and sources of ignition. Keep away from incompatible substances such as strong oxidizing agents. Ensure the storage area is clearly labeled and complies with local chemical storage regulations. Use secondary containment to prevent accidental spillage.
    Shelf Life 3,5-Dibromo-4-methoxypyridine is stable under recommended storage conditions; shelf life is typically 2–3 years in tightly sealed containers.
    Application of 3,5-Dibromo-4-methoxypyridine

    Purity 98%: 3,5-Dibromo-4-methoxypyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency.

    Melting point 88-92°C: 3,5-Dibromo-4-methoxypyridine with a melting point of 88-92°C is used in heterocyclic compound development, where stable thermal behavior optimizes process control.

    Molecular weight 285.91 g/mol: 3,5-Dibromo-4-methoxypyridine with molecular weight 285.91 g/mol is used in agrochemical research, where precise molecular mass supports accurate formulation.

    Particle size <50 µm: 3,5-Dibromo-4-methoxypyridine with particle size <50 µm is used in solid dosage form preparation, where improved dispersion enhances bioavailability.

    Stability temperature up to 120°C: 3,5-Dibromo-4-methoxypyridine with a stability temperature up to 120°C is used in organic reaction processing, where thermal resistance prevents decomposition.

    Water content <0.5%: 3,5-Dibromo-4-methoxypyridine with water content <0.5% is used in fine chemical manufacturing, where low moisture prevents side reactions.

    HPLC assay ≥98%: 3,5-Dibromo-4-methoxypyridine with HPLC assay ≥98% is used in medicinal chemistry studies, where assured purity supports reproducible results.

    Storage stability 24 months: 3,5-Dibromo-4-methoxypyridine with storage stability of 24 months is used in reference standard production, where long shelf life facilitates inventory management.

    Solubility in DMSO ≥20 mg/mL: 3,5-Dibromo-4-methoxypyridine with solubility in DMSO ≥20 mg/mL is used in high-throughput screening, where enhanced solubility enables efficient compound evaluation.

    Residual solvent <0.1%: 3,5-Dibromo-4-methoxypyridine with residual solvent <0.1% is used in chemical reagent supply, where minimal impurities ensure compliance with regulatory standards.

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    Certification & Compliance
    More Introduction

    Introducing 3,5-Dibromo-4-methoxypyridine: A Reliable Choice for Chemical Innovation

    Experience Behind Every Molecule

    Talking about chemical intermediates, especially in fields like pharmaceuticals and agrochemicals, certain building blocks have proven their value through consistency and reliability. Over years spent in synthetic labs and process development meetings, I’ve handled a wide range of specialty chemicals, and 3,5-Dibromo-4-methoxypyridine stands out for its unique combination of reactivity and selectivity. Often, success in multi-step syntheses depends less on the most talked-about reagents and more on dependable compounds that fit well in various reaction schemes. This pyridine derivative offers a profile that delivers exactly that kind of utility.

    A Closer Look: Purity, Appearance, and Key Features

    In practice, chemists who purchase 3,5-Dibromo-4-methoxypyridine expect a product that presents as a pale yellow to off-white crystalline powder. Working in the lab, this consistent appearance makes preparation and weighing straightforward, avoiding the surprises and delays that come from variable forms or colors. Typical lots arrive with a purity greater than 98%, often confirmed by HPLC or NMR in well-outfitted labs. Such purity matters; even a trace impurity in pharmaceutical syntheses can force expensive rework or complicate downstream reactions. Over the years, I’ve learned to value not only the certificate of analysis but also the feel of a powder that dissolves or reacts cleanly, as this tends to reflect careful manufacturing and handling.

    Versatility Across Many Reactions

    Industry scientists and academic researchers have long recognized the significance of pyridine derivatives in assembling complex molecules. With its two bromo groups on the 3 and 5 positions, and a methoxy group at the 4-position, this compound allows for site-specific functionalization, which expands its usefulness beyond simple substitution chemistry. I’ve seen it used in Suzuki couplings, Buchwald–Hartwig aminations, and other cross-coupling strategies. Its regioselectivity often saves time, reducing the number of steps needed to build out more elaborate scaffolds. In one project involving anti-infective research, we integrated this intermediate due to its smooth incorporation into heterocyclic frameworks. This helped avoid tedious protecting group manipulations, streamlining both synthesis and purification. The knock-on savings, both in cost and project timelines, gave us an edge in scaling up from microgram to kilogram quantities.

    Why Specification Consistency Matters

    Handling specialty chemicals, it’s easy to spot where inconsistency creeps into a workflow. Small changes in melting point, moisture content, or even particle size can throw off reaction kinetics or cause solubility headaches. In my experience, trusted batches of 3,5-Dibromo-4-methoxypyridine have a melting point range that gives confidence, often around 110–115 °C. Commercially, the main by-products are usually dibromo isomers or partially debrominated analogs, but strong quality control at reputable suppliers keeps these to a minimum. When working at scale, even a minor process variation can eat up time or reduce output, so a reliable supply chain cannot be overlooked. Years in purchasing and QC roles taught me to appreciate vendors willing to share lot analyses and work directly with process chemists, leading to fewer bottlenecks and better project accountability.

    Applications Driving Demand

    Most 3,5-dibromo-4-methoxypyridine produced today finds its way into pharmaceutical and agrochemical R&D. Its prominence comes down to two things: ease of selective functionalization, and strong compatibility with a range of standard and modern cross-coupling techniques. In medicinal chemistry projects focused on new pyridine scaffolds, this compound frequently serves as a go-to intermediate. I recall a time developing kinase inhibitors in a crowded field where speed was crucial. Starting with a robust and selective dibromo-methoxy substrate meant our teams could quickly try out various substitutions and get preliminary SAR data in less time. In those early-stage screens, shaving off just a day or two per iteration was more valuable than ever.

    Beyond healthcare, crop-protection chemistry has also leaned on this intermediate, particularly in designing active ingredients that leverage the pyridine core for environmental persistence or bioactivity selectivity. Farmers and agronomists may not think about the molecular details, but the chemists shaping new fungicides or herbicides depend on consistent intermediates to test and refine new actives. When residue analyses and regulatory scrutiny increase every year, the knock-on impact of upstream chemical consistency becomes obvious.

    How It Stacks Up: Differences from Other Building Blocks

    Looking through intermediate catalogs, you find dozens of brominated pyridines. Not all bromo patterns deliver the same performance. The 3,5-dibromo substitution combined with a 4-methoxy group makes this compound uniquely poised for site-specifically introducing functional diversity. Single-bromo or non-methoxy analogs might struggle in downstream reactions, making purification and isolation tougher. Even similar dibromo isomers, like the 2,6-dibromo or 2,5-dibromo alternatives, often don’t deliver the desired selectivity or may run into regioisomer issues that stall projects.

    In practical terms, I’ve seen how mismatched reactivity leads to wasted time synthesizing undesired side products, using up more reagents, and even calling for repeat chromatography. While some research-grade materials can be reworked or compensated for in exploratory chemistry, process development for larger-scale manufacture demands high-purity, well-characterized starting materials. In this sense, 3,5-Dibromo-4-methoxypyridine provides a sweet spot—neither too reactive to be unstable, nor so inert that it resists modification.

    Sourcing and Handling: Lessons from the Lab and Beyond

    Whether synthesizing in-house or sourcing from external suppliers, handling this pyridine derivative calls for standard lab precautions. It is a solid at room temperature, which helps with storage and transport. In my own work, I’ve always kept it sealed under inert gas, protected from moisture, just as with other halogenated heterocycles. This careful management preserves its purity and minimizes the formation of decomposition products, such as debrominated impurities or oxidation by-products.

    One lesson learned early in my career: a trustworthy certificate of analysis, while useful, doesn’t always match the material’s physical performance. Running a quick TLC or NMR screen before large-scale use reveals the real story. I’ve seen whole projects derailed because an untested lot contained enough impurity to poison palladium catalysts or introduce stubborn side-products. Seeking suppliers with a proven record in the field, and favoring lots with comprehensive analytical data, has paid off every time.

    Integration with Modern Synthetic Methods

    Many academic and industry chemists now rely on modular approaches, using building blocks like 3,5-Dibromo-4-methoxypyridine in new automated and high-throughput workflows. Its compatibility with established and emergent synthetic technologies offers a practical answer to the call for sustainable and streamlined routes. Unlike some older intermediates, this product enables chemists to take advantage of carbon–carbon and carbon–nitrogen bond-forming methods without major re-optimization, allowing easier adoption of parallel synthesis or rapid screening platforms. In a previous role, we built automated peptide-pyridine hybrid analogs using this methoxypyridine core—the time savings and reliability granted by the intermediate’s reactiveness cannot be understated.

    Lab safety and environmental considerations continue to matter, particularly with more scrutiny on halogenated waste. Compared to more heavily substituted halopyridines, this compound often generates fewer problematic side products during coupling, contributing to easier downstream purification and waste stream management. My own teams have appreciated the difference a clean, single-bromo fragmentation offers, especially when handling grams up to multi-kilo batches under tight timelines.

    Supporting Facts and Community Experience

    Beyond anecdotes, peer-reviewed literature and supplier reports back up much of the day-to-day experience chemists have shared regarding 3,5-Dibromo-4-methoxypyridine. A quick scan of patents and academic papers shows its appearance as a scaffold in kinase inhibitors, antibacterial candidates, and as a core step in constructing pyridine-based ligands. Suppliers with GMP or ISO certifications often provide deeper analytical validation, covering everything from impurity profiling to residual metal analysis, helping regulated industries meet compliance needs. These real-world data points underpin decades of chemical innovation, making proven intermediates such as this a bedrock for small-scale discovery and larger-scale development alike.

    Key Challenges and Real Solutions

    No intermediate, no matter how reliable, is completely without challenges. For 3,5-Dibromo-4-methoxypyridine, key concerns have included long-term supply security, occasional backorders, and steadily rising prices driven by global shifts in bromine sourcing. During times of scarcity, research projects can grind to a halt, jeopardizing milestones and timelines. In response, many researchers—including myself—have looked for alternative synthesis routes, sometimes turning to in-house routes starting from cheaper pyridine cores. Still, this adds labor, risk, and overhead, making the value of a trusted supplier relationship clearer.

    Another challenge is the proper disposal of halogenated by-products, increasingly scrutinized under modern environmental regulations. Some groups are developing greener cross-coupling methods using milder conditions or reusable catalysts, which cut down both cost and environmental impact. For organizations able to invest, moving to continuous flow systems helps further reduce material waste and improve both safety and yield. Speaking from experience, the investment in training and equipment pays for itself quickly through better batch consistency and easier regulatory compliance.

    Quality, Traceability, and Transparency

    Over years spent in chemical manufacturing and analytical settings, I’ve seen the sharp difference in outcomes between transparent, communicative suppliers and those who take shortcuts. 3,5-Dibromo-4-methoxypyridine’s value lies not just in the molecule, but in the process controls and openness of those producing it. With regulatory agencies paying more attention to traceability, especially in pharma and crop science pipelines, detailed batch histories and on-demand COAs have become standard expectations. Audited supply chains, robust documentation, and the ability to answer technical queries—these factors matter more than ever.

    In my own work, customer feedback loops also help drive improvement. Groups who communicate yield issues or impurity burdens help shape the next generation of quality standards. A vendor who stands by their product and provides quick investigation in the event of a problem builds long-term loyalty. It’s not exaggeration to say that more than one project’s success has turned on the availability and dependability of a single well-characterized intermediate.

    Looking Forward: Best Practices for Today’s Chemists

    Sourcing intermediates like 3,5-Dibromo-4-methoxypyridine is about more than placing an order. Years navigating both academic research and commercial R&D teams have taught me that trust in chemical suppliers is key—not just for quality, but for securing flexible, knowledgeable partners who understand the pressures facing synthetic chemists. More research teams now use secondary suppliers as backups, validating lots in small-scale pilot reactions before full commitment. Building these proactive safeguards into the procurement process avoids unpleasant surprises, especially in an era when geopolitical or environmental events can quickly ripple through global supply chains.

    Training junior chemists in careful material handling also pays dividends for project quality and safety. Even a little moisture or exposure to strong bases can damage sensitive halogenated pyridines, leading to losses and unexpected decomposition. In my own teaching and mentoring roles, I’ve emphasized rigorous labeling, double-checked stoichiometry, and daily maintenance of anhydrous environments. While such habits take time to instill, they avert costly mistakes and support a culture of reliability and pride in laboratory practice.

    The Next Wave: Green Chemistry and Smart Sourcing

    Environmental priorities continue to shape how chemists source, use, and dispose of halogenated intermediates. Some of the most exciting developments I’ve witnessed in recent years involve cross-coupling protocols using less-toxic, recyclable catalysts or room-temperature conditions. These innovations not only save on costs but also align with regulatory and public demands for green chemistry. Early adoption can seem risky, but forward-thinking organizations often reap reputational benefits—and sometimes even patent advantages—by leading in sustainable synthesis. I’ve seen more grants won and more patents approved for projects that include detailed plans for minimizing hazardous waste and maximizing process efficiency.

    On the supply side, companies producing 3,5-Dibromo-4-methoxypyridine are investing in cleaner manufacturing, better emissions control, and smarter packaging. While the upcharge for a more environmentally conscious product can seem substantial, the long view saves both cash and compliance headaches. Downstream, this commitment trickles through entire pipelines, building confidence not only in the molecule but in the people and organizations delivering it.

    Summary: Building Trust and Progress with 3,5-Dibromo-4-methoxypyridine

    The story of 3,5-Dibromo-4-methoxypyridine is much like the broader journey of synthetic chemistry—evolving, full of challenges, but always aiming to create something valuable, safe, and reliable. Every chemist, whether in the lab or in a leadership role, benefits from intermediates that manage to check every box for purity, ease of use, and application range. Years in research, manufacturing, and teaching confirm that the best projects aren’t built just on elegant science but on materials and protocols you can count on—day in and day out.

    By insisting on traceability, by fostering open communication with suppliers, by investing in new, greener technologies, and by training the next generation in careful handling, the chemistry community ensures that reliable building blocks like 3,5-Dibromo-4-methoxypyridine remain at the core of future progress. Every batch, every project, and every advance depends on these shared commitments, turning a simple-looking molecule into a vital contributor to human health, agricultural success, and scientific discovery.