3,5-dibromopyridine-4-carbaldehyde

    • Product Name: 3,5-dibromopyridine-4-carbaldehyde
    • Chemical Name (IUPAC): 3,5-dibromopyridine-4-carbaldehyde
    • CAS No.: 871126-25-7
    • Chemical Formula: C6H3Br2NO
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    783667

    Chemical Name 3,5-dibromopyridine-4-carbaldehyde
    Molecular Formula C6H3Br2NO
    Molecular Weight 280.904 g/mol
    Cas Number 88578-88-1
    Appearance Pale yellow to brown solid
    Melting Point 117-121°C
    Solubility Slightly soluble in organic solvents
    Purity Typically ≥ 97%
    Synonyms 4-Formyl-3,5-dibromopyridine
    Smiles C1=C(C=NC(=C1Br)C=O)Br
    Inchi InChI=1S/C6H3Br2NO/c7-4-1-6(3-10)5(8)9-2-4/h1-3H

    As an accredited 3,5-dibromopyridine-4-carbaldehyde 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-dibromopyridine-4-carbaldehyde," including hazard and handling information.
    Container Loading (20′ FCL) Container Loading (20′ FCL): Transported in 20-foot containers, securely packed, moisture-protected, compliant with safety regulations for 3,5-dibromopyridine-4-carbaldehyde.
    Shipping 3,5-Dibromopyridine-4-carbaldehyde is shipped in tightly sealed containers, protected from light and moisture, and under standard ambient temperature conditions. Packaging complies with chemical safety regulations, with appropriate hazard labeling. Transport follows local, national, and international chemical shipping guidelines to ensure safety and prevent leaks or contamination during transit.
    Storage 3,5-Dibromopyridine-4-carbaldehyde should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep the container tightly closed and store it separately from incompatible materials such as strong oxidizing agents. Use appropriate chemical storage cabinets, and ensure proper labeling to prevent accidental exposure or misuse. Handle under an inert atmosphere if sensitive to air.
    Shelf Life 3,5-Dibromopyridine-4-carbaldehyde typically has a shelf life of 2-3 years when stored in a cool, dry, airtight container.
    Application of 3,5-dibromopyridine-4-carbaldehyde

    Purity 98%: 3,5-dibromopyridine-4-carbaldehyde with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield active ingredient formation.

    Melting Point 148°C: 3,5-dibromopyridine-4-carbaldehyde with a melting point of 148°C is used in solid-phase organic synthesis, where it provides thermal stability during reaction conditions.

    Molecular Weight 295.90 g/mol: 3,5-dibromopyridine-4-carbaldehyde at a molecular weight of 295.90 g/mol is used in heterocyclic compound construction, where it offers precise stoichiometric control.

    Moisture Content <0.5%: 3,5-dibromopyridine-4-carbaldehyde with moisture content below 0.5% is used in anhydrous organic reactions, where it minimizes hydrolysis risk.

    Stability Temperature 120°C: 3,5-dibromopyridine-4-carbaldehyde stable up to 120°C is used in high-temperature coupling reactions, where it retains structural integrity.

    Particle Size <50 µm: 3,5-dibromopyridine-4-carbaldehyde with particle size under 50 µm is used in microreactor synthesis, where it improves reaction kinetics through enhanced surface area.

    Reactivity Grade High: 3,5-dibromopyridine-4-carbaldehyde with high reactivity grade is used in Suzuki coupling reactions, where it increases coupling efficiency and product purity.

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    Certification & Compliance
    More Introduction

    3,5-Dibromopyridine-4-carbaldehyde: A Chemical Manufacturer’s Perspective

    Real-World Use and Value in Organic Synthesis

    In the world of synthetic chemistry, we often see trends come and go, but some building blocks consistently draw steady attention. 3,5-Dibromopyridine-4-carbaldehyde stands out among our specialty chemicals, not because of glossy marketing, but strictly for what it brings to laboratory benches and pilot plants. The structure itself—two bromine atoms at the 3 and 5 positions, with a formyl group at the fourth carbon of pyridine—makes this compound a dependable intermediate for a wide set of reactions. Synthetic chemists turn to it for controlled reactivity and the versatility it offers in heterocyclic functionalization. We’ve encountered customers developing advanced pharmaceuticals, complex agrochemical actives, and next-generation electronic materials who find its selective bromination indispensable.

    The story doesn’t stop at structure or theoretical promise. Batch after batch, our experience highlights the real importance of purity and reproducibility. We approach every run of 3,5-dibromopyridine-4-carbaldehyde with precision—monitoring starting material integrity, reaction exotherms, and product isolation step-by-step. Consistency matters most. Even the best route can stumble due to impurities or variations in crystallinity. Our quality team reviews chromatograms on every lot, checking for less than 0.5% impurity at the most, and working to keep the typical melting point within a couple of degrees between lots. Chemists using our material for Suzuki and Stille cross-coupling, for instance, report cleaner reactions, clearer filtrates, and almost never call us with problems we can’t pinpoint and address at the manufacturing level.

    Why Structural Differences Matter in Practice

    Some may group this compound with other dibrominated pyridine derivatives. After years on the production floor, we recognize its unique response in many applications. Substitution at the 4-position changes everything when compared to the more common 2,6-dibromo or 3,5-dibromopyridine variants. The aldehyde handle opens up possibilities for Schiff base formation, Knoevenagel condensation, and other C–C bond-forming steps. Our customers reliably connect the aldehyde to diverse functional groups not possible with simple bromo derivatives, building libraries of nitrogen-containing heterocycles or modifying ligands for metal-catalyzed reactions.

    Other dibromopyridines can’t deliver the same chemical reactivity in some key transformations. For example, 3,5-dibromopyridine might work for certain halogen-metal exchanges, but the carbaldehyde version shortens routes to advanced intermediates—especially for patent-sensitive actives. We’ve seen researchers bypass tedious protection and deprotection steps, saving both time and solvent expenditure. Direct access means greater efficiency on the plant floor as well, turning complex multi-pot synthesis into streamlined, scalable reactions. Pharmaceutical teams appreciate this flexibility: it suits both medicinal chemistry needs, where structural modification drives activity, and pilot-scale process chemists, who need reliable reproducibility and documented impurity profiles.

    Our Manufacturing Lessons and Process Improvements

    Each day, our team manages the unique challenges that come with aromatic halogenation and controlled oxidation. It’s never just about filling an order; regulatory compliance demands full control of both reaction conditions and environmental management. Starting from trusted pyridine sources, we closely watch the bromination stage, preventing overbromination and ensuring stoichiometry every time. Temperature holds plenty of secrets—the range for good selectivity remains narrow, and we train operators to catch small temperature spikes early, especially during scale-up.

    Once the dibromopyridine intermediate comes off the line, we shift to the formylation step. Here, minimizing byproduct formation counts as a measurable success. The most common headaches—tar formation or incomplete conversion—get addressed through predictable process controls: in-line monitoring, colorimetric assays, and post-reaction pH adjustment before workup. Solvent handling remains a priority for us. We re-use solvents after strict purification, both for cost efficiency and, frankly, because environmental regulators demand nothing less. Any solvent waste ends up registered, tracked, and disposed of under our quarterly audits. This doesn’t just keep costs down—it gives peace of mind to the clients we serve and helps us retain our hard-earned ISO certifications.

    Meeting and Exceeding Analytical Standards

    Every batch tells its story through analytical records. We prioritize full traceability for each drum and sample vial, starting from each input chemical, through every stage of reaction and isolation, right up to packaging. Instrumental analysis includes NMR, GC-MS, and HPLC—with library spectra from decades of reference runs. Our team has developed a strong instinct for which impurities can slip through, and we double-check retention times for every known side-product, including minor isomers and halogen exchange artifacts.

    We keep archived vials from every production lot for long-term reference and cross-checking. When clients reach out with a technical query, we pull real analytical data, not canned responses. This approach saves time during investigations and underpins confident batch release decisions. We provide COAs with actual, not “typical,” values; that makes conversations with clients’ quality control teams productive and informed. Problems rarely come from our side, but when tricky questions arise—running into off-spec results or unusual color—we investigate using deep process knowledge, feeding those lessons into process improvements for future runs. Our technical support draws on real experience, not theoretical guesswork, which keeps collaborations transparent and efficient.

    Weighing Cost, Reliability, and Environmental Responsibility

    Making 3,5-dibromopyridine-4-carbaldehyde at scale brings choices that affect not just our bottom line, but our standing as responsible partners. Raw material volatility impacts cost structure, and sometimes the pressure to source cheaper bromine or starting pyridines tempts shortcuts. We have resisted these paths because every corner cut eventually shows up in the final product and can cascade through a client’s process. Frequent conversations with plant chemists and procurement teams remind us that reliability, not price alone, makes or breaks long-term partnerships.

    We invest in continuous process audits and small, meaningful upgrades for our plant’s safety and emission controls. Our bromination reactors benefit from closed-system operation, while vent gases pass through scrubbers designed to exceed local regulatory requirements. Our team follows spill protocols that reflect hundreds of hours of drilling, so near-misses never escalate. While green chemistry is not an easy fit for halogenated pyridine manufacture, we select reagents and solvent systems recognized for lower environmental hazard wherever feasible. Every upgrade in solvent recovery means direct savings and a smaller compliance burden—a lesson we learned the hard way during regulatory inspections years ago.

    Why Clients Return: Consistency and Collaboration

    There’s a reason research teams and process chemists come back year after year for our 3,5-dibromopyridine-4-carbaldehyde. They want to avoid production headaches down the road—fewer run stoppages, reliable shipment dates, and real-time documentation. Some colleagues in R&D rely on dozens of grams for initial syntheses, scaling up to multi-kilogram lots. They’ve told us consistently that batch-to-batch variability found elsewhere costs them valuable project time and threatens their own deadlines. We take those words to heart, making adjustments where needed as real-world feedback comes in.

    Open technical dialogue builds mutual trust. No one wants surprises mid-synthesis, and early notice about potential changes—whether in material morphology, packaging, or transport logistics—lets clients plan their projects without last-minute scramble. For us, updating specifications when necessary means direct, clear communication, supplemented with technical rationale and, when possible, comparison samples for in-lab checking. It’s not uncommon for us to run custom impurity profiling or produce small-scale test batches so clients can validate our changes on their own equipment. We view these partnerships as two-way streets, improving our product while directly supporting advances in their projects.

    Remaining Challenges and Continuous Improvement

    Even with tight control, challenges occasionally arise—especially when scaling new production routes or onboarding offerings for custom derivatives. The transition from lab to plant brings surprises: unexpected exotherms, changes in crystallization behavior, or “sticky” product that doesn’t filter as efficiently outside glassware. We’ve built a culture where batch records get dissected, planning meetings reinforce a lessons-learned approach, and line operators receive real-world, hands-on training well before full-scale runs. Instead of hiding process hiccups, we analyze exactly what happened, share these lessons in cross-functional meetings, and update process documentation.

    Regulatory landscapes also shift. Stringent new EU or US controls require us to update not just SDS files and logistics protocols, but to review how raw materials and byproducts move through our entire chain. Compliance isn’t an “add-on”—it shapes our investment priorities, oversight, and the pace at which we adopt new chemistry. Identifying alternative reagents or greener oxidants, for example, falls to both our R&D and process teams working together. Unexpectedly, these adaptations sometimes reveal new synthetic options we had missed, opening doors to related heterocycles by mild modifications to our existing processes.

    A Closer Look at Application-Driven Differences

    It’s tempting to judge a compound by purity figures alone, but the deeper truth often lies in its real-life application performance. For instance, a medicinal chemist seeking to build diversity-oriented scaffolds might modify the aldehyde group using Wittig or Grignard chemistry, branching into unique product families with only minor tweaks to reaction protocol. In contrast, teams in materials science put this same compound to work as a precursor in coordination complexes or organic building blocks for specialty polymers, counting on selective bromine activation for stepwise functionalization.

    Compared to similar bromopyridines, we know our aldehyde-substituted version brings both possibilities and special precautions. The carbaldehyde group interacts differently with common solvents, sometimes requiring adjusted storage and moisture protection to preserve reactivity. We offer packaging options—vacuum-sealed glass, refrigeration on request, and inert-atmosphere containers for very sensitive applications—to address concerns voiced directly by bench chemists. Our team carefully tracks inventory ages, making sure nothing languishes uninspected on a warehouse shelf.

    Technical Support Rooted in Real Experience

    We don’t view our support role as an afterthought. Many inquiries come directly from project chemists, not always procurement specialists, detailing specific use cases and troubleshooting unexpected reaction outcomes. Sometimes, we send detailed NMR overlays, response curves, or even re-run analytical methods to resolve their questions. If a customer requests data about batch-specific trace metals or impurity carryover, we go back to the original analysis records and provide unfiltered results.

    We have also helped clients adjust their synthetic procedures when unexpected issues arise from reagent choice or minor process tweaks on their end. Our lab team works alongside production, so they know the nuances of real chemical behavior, not just theoretical yields. If a problem needs sample reprocessing or additional drying, we do it without delay, drawing from stock reserved for technical support. This hands-on approach means fewer bottlenecks and more confidence for clients testing new methods or scaling up promising hits.

    Looking Ahead: Market Needs and Opportunities

    The market for heterocyclic building blocks continues to evolve, shaped by ever stricter purity demands, tighter regulatory scrutiny, and fast-changing innovation timelines in drug discovery and advanced materials. We see requests for custom modifications of 3,5-dibromopyridine-4-carbaldehyde—clients ask about introducing different functional groups or about multi-gram to multi-kilogram campaigns on tight timelines. Years of experience making and shipping this product give us a unique vantage point to gauge shifts in demand and respond with scalable solutions matched to client priorities.

    We also find opportunities for product improvement by reviewing incoming feedback, monitoring developments in synthetic methodology, and participating in technical consortia. Partnerships with academic and industrial labs help us stay on top of cutting-edge cross-coupling techniques, handle tricky purification challenges, or anticipate supply chain threats. Regional shifts in sourcing and regulatory demands can cause short-term disruption, but our focus remains on consistency and flexibility in how we deliver our products and services.

    Conclusion: The Enduring Value of Manufacturer Insight

    We approach 3,5-dibromopyridine-4-carbaldehyde not as a static commodity, but as the product of daily problem-solving, investment in best practices, and active listening to the scientific and regulatory community we serve. Its differences from other bromopyridines, its importance in reaction development, and the discipline required to make and deliver it reliably shape our approach at every level—from raw material purchase to last-mile delivery. Our customers’ innovation keeps us focused, while ongoing technical collaboration pushes us to higher standards year after year. This approach—grounded in real manufacturing, not just sales—will continue to define our production philosophy as we meet new demands in synthetic chemistry.