2,5-Dibromo-3-nitropyridine

    • Product Name: 2,5-Dibromo-3-nitropyridine
    • Chemical Name (IUPAC): 2,5-dibromo-3-nitropyridine
    • CAS No.: 131437-46-4
    • Chemical Formula: C5H2Br2N2O2
    • 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

    995460

    Product Name 2,5-Dibromo-3-nitropyridine
    Cas Number 19798-80-2
    Molecular Formula C5H2Br2N2O2
    Molecular Weight 297.89
    Appearance Yellow to orange solid
    Melting Point 82-84°C
    Purity Typically ≥98%
    Solubility Slightly soluble in organic solvents
    Smiles c1c([N+](=O)[O-])cnc(c1Br)Br
    Inchi InChI=1S/C5H2Br2N2O2/c6-3-1-4(9(10)11)5(7)8-2-3/h1-2H
    Storage Conditions Store at room temperature, keep container tightly closed
    Hazard Statements H315, H319, H335
    Ec Number 240-271-7

    As an accredited 2,5-Dibromo-3-nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g amber glass bottle is securely sealed, labeled with "2,5-Dibromo-3-nitropyridine" and hazard information. Protective packaging included.
    Container Loading (20′ FCL) 20′ FCL holds around 10-12 MT of 2,5-Dibromo-3-nitropyridine, packed in 25 kg fiber drums, securely palletized.
    Shipping 2,5-Dibromo-3-nitropyridine is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Transport complies with regulations for hazardous chemicals, including labeling and documentation. Handle with care, avoiding physical damage and exposure. Consult the Safety Data Sheet (SDS) for specific storage and shipping recommendations to ensure safe and compliant delivery.
    Storage 2,5-Dibromo-3-nitropyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and reducing agents. Protect it from moisture and direct sunlight. Use secondary containment to prevent spills, and ensure clear hazard labeling. Always follow appropriate chemical storage guidelines.
    Shelf Life 2,5-Dibromo-3-nitropyridine is stable under recommended storage conditions, with a typical shelf life of several years if unopened.
    Application of 2,5-Dibromo-3-nitropyridine

    Purity 98%: 2,5-Dibromo-3-nitropyridine with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product consistency.

    Melting point 115°C: 2,5-Dibromo-3-nitropyridine with a melting point of 115°C is utilized in agrochemical formulation, where it enables precise thermal processing and integration.

    Stability temperature 85°C: 2,5-Dibromo-3-nitropyridine with stability up to 85°C is applied in heterocyclic compound manufacturing, where it maintains compound integrity during high-temperature reactions.

    Molecular weight 284.89 g/mol: 2,5-Dibromo-3-nitropyridine with a molecular weight of 284.89 g/mol is used in specialty dye synthesis, where it provides predictable incorporation into chromophore structures.

    Particle size <50 μm: 2,5-Dibromo-3-nitropyridine with particle size below 50 μm is implemented in fine chemical preparations, where it enhances dispersion and reactivity rates.

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    Certification & Compliance
    More Introduction

    Meet 2,5-Dibromo-3-nitropyridine: A Step Forward in Fine Chemical Innovation

    Scientists have always searched for ways to build better foundations in their research. The deeper I dig into chemistry, the more I see that every reliable product starts with robust building blocks. 2,5-Dibromo-3-nitropyridine stands out among those blocks, especially for laboratories and manufacturers driven by precision. It isn’t the flashiest name you’ll see on a product list, but I’ve learned that the real value of a chemical lies in what it lets you build, discover, or solve.

    Chemical Profile That Packs Practical Punch

    Let’s break this down: This product belongs to the pyridine family, holding strong with two bromine atoms gripping the 2 and 5 positions, and a nitro group positioned at carbon 3. In the language of chemical structure, that brings a balance between electron density and reactivity—a crucial asset for anyone synthesizing new molecules in pharma, materials, or even dye research.

    Working with this compound, I’ve noticed its physical identity means more than just a dusty bottle on a shelf. It often arrives as a yellow solid. Researchers may not waste much thought on color at first, but clarity in appearance can help spot contaminants and ensure things run smoothly in early synthesis work. A typical batch carries a molecular weight that’s noticeable, at 282.9 g/mol, adding to its heft for those who track efficiency and batch cost.

    Getting Results in Applications That Matter

    My lab once tried to scale up a project that hit a wall until we started using 2,5-Dibromo-3-nitropyridine. Its well-placed functional groups speed up coupling reactions with palladium and copper catalysts. In hands-on terms, the bromines act as gatekeepers for Suzuki or Buchwald-Hartwig couplings, letting you attach defined bits of organic structure—it’s a massive win if you’re designing any candidate drug or novel pigment.

    Pharmaceutical chemists keep this product in heavy rotation because it readily enables further aromatic substitution. If you’ve worked with halogenated aromatics, you know not all bromines welcome the same transformations. Here, their spacing and the positioning of the nitro group help maintain reactivity while keeping unstable side-products low. In an era pushing for cleaner chemistry, less waste isn’t just a check box; it’s a relief for budgets and a boon for regulatory compliance.

    Beyond pharmaceuticals, this nitropyridine is finding friends in agrochemistry. Making new herbicides or fungicides isn’t a slow, measured walk; it’s a race. The flexibility in this molecule fast-tracks route scouting since both the nitro and bromine positions are ‘hot spots’ for adding useful fragments without stripping out the original backbone. That means it can adapt as innovators gain new targets or face resistant strains in real field testing.

    Building on Real Improvements, Not Just “Features”

    Chemicals have personalities—at least, in the world I work in. Some are stubborn, some unpredictable. 2,5-Dibromo-3-nitropyridine brings a kind of reliable predictability that feels like a breath of fresh air. It dissolves easily in most organic solvents. I’ve tried it in acetonitrile, DMF, even good old dichloromethane. Its solubility means time isn’t lost fiddling with endless sonication or being forced into high-temperature reactions just to get it into solution.

    Where many intermediates break down or turn oily if the humidity creeps up, this one shows more muscle against both temperature swings and moisture. A stable product brings peace of mind, especially when storage and shipment stretch across continents through wildly different climates. After losing thousands due to ruined intermediates in the past, I appreciate a product that stands up in reality, not just in the catalog.

    Comparing Alternatives Isn’t Just About Price

    Some chemists pick up 2,3,5-tribromopyridine or related isomers thinking more bromines means more reactivity. From experience, this often isn’t true. Three bromines sometimes make it tricky to control selectivity. By carefully choosing a product with two bromines and a nitro group, you get more nuanced chemistry. The nitro group doesn’t just sit there; it can draw electron density, fine-tuning how each bromine can be swapped out or activated.

    Plenty of other halopyridines crowd the market, but many introduce unknowns: Some add chlorine or shift the nitro group, while others use positions that stop being practical if final applications demand later modifications. I’ve run reactions side by side—changing the isomer can mean the difference between a clear, fast coupling or hours of by-product clean-up. Those hours add up, especially in larger scale-up programs.

    Another point worth sharing: Safety and environmental impact. While pyridine derivatives all have their own quirks, 2,5-Dibromo-3-nitropyridine offers less volatility than low-substituted analogs, cutting down exposure risks. Its solid structure also helps keep things contained, reducing dust and accidental spills, a small but meaningful advantage for anyone running a crowded or multitasking lab.

    Why Quality Determines Success, Not Just Convenience

    I’ve worked on enough benches—and reviewed enough regulatory filings—to know that purity can make or break a project. With this compound, high-purity batches matter. You avoid ghost peaks, tripping up analytics, or false alarms in toxicity screens that come back weeks later. I remember a time our team chased a persistent impurity; days were lost, only to find it tied back to inconsistent supply. Reliable providers tend to have transparent supply chains, full batch documentation, and should never dodge tough questions about origin or quality metrics.

    Batch-to-batch reproducibility also speeds up paperwork, especially if you’re shepherding a molecule towards an Investigational New Drug filing. No one wants to explain why yields fell off a cliff in the middle of a pilot run. In the world of coatings and specialty polymers—where process validation defines profitability—consistent reactivity is invaluable. Those who handle this pyridine tell me they prefer fewer surprises, fewer last-minute troubleshooting calls, and more confidence in results.

    The Push Toward Sustainability and What It Means for Sourcing

    Environmental impact is under glossy brochures, but it’s in every purchase order these days. For pyridine building blocks, sourcing raw materials and managing waste both take up resources and creativity. Manufacturers working with 2,5-Dibromo-3-nitropyridine increasingly seek greener synthesis routes. Some are phasing out hazardous oxidizers or shifting towards renewable solvents for its production. When suppliers publish efforts in reducing waste or closing solvent loops, it becomes more than just lip service—it’s a responsibility that shapes long-term partnership.

    I respect vendors that answer tough questions about worker safety or eco-risks instead of punting them down the line. In my own teams, we’ve started favoring suppliers who hold stewardship certifications and agree to third-party audits. Those extra steps matter, especially when pitching work to clients or pushing pilot-scale outcomes toward something that can scale efficiently and safely.

    Storage Tips and Handling Insights Learned the Hard Way

    Anyone who’s ruined a batch knows real handling advice beats fine print. Though stable under reasonable conditions, 2,5-Dibromo-3-nitropyridine deserves a cool, dry cabinet—preferably away from the hustle of high-traffic spaces. Even solid materials can pick up moisture if you leave them long enough on an open bench. Sealing bottles tightly and adding a dedicated desiccator makes spills rare and keeps each weighing consistent.

    In a shared building, it pays to print clear labeling and stave off confusion between this product and similar-looking pyridines. I’ve seen hasty mistakes in glassware cleaning turn a $300 investment into hazardous waste. Won’t win over many friends if a cross-contaminated flask throws off the next person’s reaction—so, hot tip: Reserve a dedicated scoop or spatula for each compound, especially when purity claims are on the line.

    Innovation and the Real-World Ripple Effect

    Innovation depends on the right foundation. I’ve watched research groups move from sluggish, poorly controlled chemistry to efficient workflows just by switching to more predictable intermediates. 2,5-Dibromo-3-nitropyridine unlocks a bunch of “what if” projects thanks to its precise reactivity and adaptability across industries. Peptide chemists and material scientists both find surprisingly common ground using it for cross-linking, functionalization, or launching complex ring systems. The ripple effect shows up every time a material scientist sends up a novel solvent-resistant polymer or a clinical team refines a bioactive aromatic backbone faster than planned.

    Many chemists don’t realize how frequently these intermediates drive medical advances. Every success with a new kinase inhibitor, every tweak to a pesticide class—products like this sit quietly at the start of complicated stories. Each high-quality batch helps scientists focus less on fighting side reactions and more on actually moving towards breakthroughs that matter.

    The Value of Trusted Relationships Alongside the Right Product

    The right chemistry doesn’t only come from picking a strong product; it grows through trust between teams and suppliers. I’ve often leaned into supplier relationships built on real communication—where questions on batch performance, supply delays, or analytical support never fall on deaf ears. Access to the right documents, thoughtful answers about regulatory background, and fast feedback streamline downstream work and make risk management easier, whether scaling up or transitioning to new processes.

    Transparency encourages better decisions at every level, from procurement to process scale-up. I’ve seen situations where vendors flagged approaching expiry or unexpected analytical results, giving researchers room to adapt on time. My advice: Build supplier ties as carefully as you select your intermediates; it pays off in every step from walk-in freezers to finished projects.

    Pushing for Better Standards: Why It’s Never Just About Chemistry

    I believe those of us in technical fields carry a duty to raise the bar on sourcing, transparency, and safety—not just to satisfy audits, but because better products drive faster, safer progress for all. 2,5-Dibromo-3-nitropyridine challenges companies and researchers to look deeper than the catalog entry and think about the full impact, from raw material stewardship to occupational health. I’ve worked places where culture changed overnight the moment managers went on a site tour, seeing firsthand what strong manufacturing execution means for the end product’s reliability and the comfort of the people handling each batch.

    Responsiveness matters, too. I encourage teams to ask for Certificates of Analysis for every lot and keep those records tight. Some suppliers roll their eyes at this; others provide them up front, scanning for finer impurities or unexpected chemical signatures that might make a difference five steps down the route. In my teams, we avoid surprises by tying every experiment to a paper trail, a habit that feels bureaucratic until something finally saves weeks of troubleshooting.

    Final Thoughts on Choosing the Right Pyridine Intermediate

    From my own time in labs, I don’t see purchasing 2,5-Dibromo-3-nitropyridine as a trivial choice. The product means blending old-school chemistry rigor with modern expectations for safety, traceability, and environmental performance. No one benefits from cutting corners—not the scientist, not the end customer, not the environment. A great intermediate, chosen and used wisely, can mean easier days, clearer data, and faster innovation—not just today, but in all those projects that reach their next milestone.

    As more industries turn toward targeted synthesis and greener protocols, quality intermediates like this one set the pace for meaningful progress. If you’re handling the compound for the first time, pay attention to batch integrity, ask good questions, and connect with your supplier over your needs before that first weigh-out. I’ve watched tough programs turn a corner after switching to consistently pure reagents, and I see every day how the right choices in foundational chemistry drive results that matter in real life, not just on paper.