|
HS Code |
219043 |
| Productname | 4-Bromo-3-Nitropyridine |
| Casnumber | 23056-43-9 |
| Molecularformula | C5H3BrN2O2 |
| Molecularweight | 202.99 |
| Appearance | Yellow crystalline solid |
| Meltingpoint | 96-99°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents (e.g., DMSO, dichloromethane) |
| Storagetemperature | Store at 2-8°C |
| Smiles | c1cncc(c1Br)[N+](=O)[O-] |
As an accredited 4-Bromo-3-Nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | |
| Shipping | |
| Storage |
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Science often demands more than just a good theory or a fancy lab. It expects reliability from simple things—like accuracy in the chemical building blocks we use every day. 4-Bromo-3-nitropyridine stands out here. This compound, set apart by a bromine and a nitro group on the pyridine ring, keeps showing up in research circles, process development, and the manufacturing of specialty compounds.
Having spent years navigating between academic labs and industrial research spaces, it's clear that refining these seemingly ordinary ingredients keeps innovation moving forward. I've seen how the right intermediate saves scientists weeks of troubleshooting, and on the factory floor, it means the difference between predictable yields and mysterious bottlenecks. That’s where the conversation about 4-bromo-3-nitropyridine gets real. It’s not a headline-grabbing celebrity, but it quietly supports work in areas like pharmaceutical design, agricultural chemicals, and advanced materials.
This compound, with its CAS number 39446-47-4, adds a bromine at the fourth carbon of the pyridine ring and a nitro at the third. Chemists recognize this pattern right away—not just because it looks good on paper, but because it reacts in predictable, strategic ways. Molecularly, it weighs in at 203.99 g/mol, giving it the heft needed for cross-coupling and substitution reactions. Its melting point frequently lands between 67–70°C, and experience tells me that this kind of thermal behavior offers flexibility in planning reaction conditions.
Talk to any synthetic chemist who deals with heterocycles, and one point comes up. You want a consistent, pure compound, free of the odd contaminant that can ruin an experiment. Analytical reports for 4-bromo-3-nitropyridine usually show a purity above 98%, confirmed with techniques like HPLC and NMR. This is not just a number for a spec sheet—repeatable, high purity lets researchers trust their results. I recall a project where a batch with inconsistent purity derailed a whole series of steps. Clean compounds prevent that sort of setback.
It’s tempting to get bogged down in catalog numbers or stockroom labels. But the real significance of 4-bromo-3-nitropyridine comes from the opportunities it opens up, not the bottle it arrives in. I remember helping a colleague troubleshoot a stalled synthesis. After days of frustration, the answer was a simple swap: switching to this particular compound provided a better leaving group and took the reaction over the finish line. Seemingly minor changes in structure, especially the placement of reactive groups, drive big differences in how these molecules perform.
This nitro-brominated pyridine earns its place mostly as a versatile intermediate. It participates in Suzuki and Buchwald-Hartwig reactions, helping build complex molecules for pharmaceutical leads, agrochemical research, and even performance polymers. The presence of both the bromine and the nitro group offers chemists a dual handle; you can swap out the bromine for a broad range of partners, while the electron-withdrawing nitro group controls reactivity and orientation, sometimes even protecting the molecule from unwanted side reactions.
Among the many pyridine derivatives on the market, this one fills a unique niche. Compare it to something like 3-bromopyridine or 4-nitropyridine, and its value becomes clearer. The combination of substituents means you’re not just getting another chemical—you're picking a modular piece that unlocks select avenues in synthesis.
3-bromopyridine, for instance, lacks the electronic balance that the nitro group brings. Without it, certain coupling reactions can run into trouble or deliver poor yields. On the other hand, 4-nitropyridine doesn’t offer the bromine as a suitable leaving group for many cross-coupling strategies. It’s the meeting of these two groups in one molecule that lets chemists push into new territory, particularly for challenging multi-step syntheses.
In experience, these distinctions are most obvious during route scouting. Faced with a demanding synthesis, you start to notice which reagents tolerate diverse conditions and resist decomposing under pressure. 4-bromo-3-nitropyridine rarely disappoints. Its inherent reactivity often allows milder reaction conditions, something I’ve appreciated during scale-up when harsher settings could mean higher costs or more byproduct headaches.
People often talk about the “invisible infrastructure” behind modern research. Here, 4-bromo-3-nitropyridine fits right in. Take pharmaceutical R&D. Early-stage drug discovery can rise or fall on the speed of synthesizing novel scaffolds. Efficient and reliable intermediates quickly take on outsized importance. On one project, a new kinase inhibitor candidate emerged—its synthesis hinged on accessing a specific heterocyclic scaffold, for which this compound provided the logical starting point. Sourcing a consistently pure batch meant researchers focused on optimizing biological activity, rather than hacking through unnecessary purification steps.
In agrochemicals, time often runs short because of seasonal deadlines. Missing a planting window can mean another year of delays. I’ve seen teams favor flexible intermediates like 4-bromo-3-nitropyridine, since their robust behavior in both early research and late-stage optimization simplifies the path from the bench to the greenhouse. A good intermediate, in this context, isn’t just a piece of a puzzle, it’s a time-saver and a risk reducer.
The same thinking extends to electronics or functional materials. Performance polymers demand customization, where fine control over backbone construction makes or breaks the process. Chemists turn to functionalized heterocycles like this one for their twin assets—broad reactivity and chemical reliability.
Working with halogenated nitropyridines raises familiar issues in both lab and factory settings. Safety concerns are never far from mind. Nitrated compounds, depending on their context, might present additional handling risks. Good ventilation, careful temperature management, and clear training keep operation smooth.
The environmental angle matters, too. With growing attention on green chemistry, the sourcing, use, and disposal of brominated nitropyridines now receive extra scrutiny. Early in my career, waste was just something to deal with later. Attitudes have shifted. More companies now design processes that limit halogenated waste or allow for cleaner separations and recycling. Catalysts, especially those based on palladium, have become more efficient, driving down both costs and environmental mess.
From a procurement angle, ensuring stable supply occasionally proves tricky. Global supply chains don’t offer guarantees. Unpredictable disruptions, prompted by regulatory hurdles or shipping problems, can derail project timelines. To address these realities, many labs and manufacturers work with dual sourcing or build up local supply agreements, rather than risking all-or-nothing contracts. Greater transparency from vendors—detailed certificates of analysis, batch tracking, and open channels for troubleshooting—goes a long way toward partnership and trust.
Even at the earliest stages of development, product reliability counts for more than most people realize. An unreliable batch means lost days, inconclusive data, sometimes worse. In discussions with quality control teams, I hear the same refrain: “We can fix process issues, but unpredictable raw materials are real headaches.” Having 4-bromo-3-nitropyridine supplied to a well-defined, repeatable standard makes QA’s job routine rather than reactive.
Working on several cross-border collaborations, the point drives home: researchers from different continents, with different equipment, all rely on tight product specs. NMR, GC-MS, TLC—the techniques might vary, but the mantra stays the same. Well-labeled, consistently packaged, safely transported chemicals like this one lay the groundwork for all the rest.
Thinking ahead, the chemical industry faces pressures from both sides: faster innovation cycles and heavier regulatory oversight. This context makes robust intermediates like 4-bromo-3-nitropyridine even more valuable. Their broad utility lowers barriers to entry for new research topics, while their reliability assists regulatory compliance and documentation. Products that meet tough standards for impurities, trace metals, and documentation already put teams on the right side of compliance—and make audits less stressful.
I’ve seen creative sourcing agreements and direct R&D partnerships with suppliers reshape the terrain. This isn’t just about logistics. Close cooperation between manufacturers and research programs brings mutual benefit. Real-time feedback leads to tighter specs and faster troubleshooting. Shared knowledge about process improvements or application notes spreads good practices across the industry. It’s a virtuous circle where one side’s reliability feeds the other’s innovation.
Much of what gets classified as “supporting work” in chemistry is anything but optional. Reliable intermediates matter, and the best ones make advanced research possible. In conversations over coffee, colleagues often circle back to the same conclusion: When progress stalls, the answer isn’t always a new high-throughput robot or fancy computational model, but a better way to make or acquire a vital building block.
4-bromo-3-nitropyridine, despite its unassuming label, keeps surfacing not just for its chemical attributes but because it solves real problems. If the goal is innovation—new medicines, smarter crop protection, improved materials—you need products that won’t let you down. Looking at it from the perspective of someone who’s had to troubleshoot more lab headaches than I want to remember, this is the kind of intermediate worth making room for on the shelves.
Value in chemistry does not emerge from isolation. Expertise gets shared, best practices evolve, and the best teams pull together knowledge that spans domains. I’ve learned the hard way that even a proven molecule like this one shows its full potential only with strong communication up and down the value chain. Regular communication between suppliers, buyers, researchers, and even logistics professionals keeps the process flowing smoothly.
When new regulations drop or global markets shift, resilient partnerships—underpinned by transparency and prompt feedback—prove their worth. Quick responses to technical questions, accessible product data, and willingness to customize batches mean better outcomes and less frustration. The best outcomes never happen by accident, and a well-supported intermediate quickly becomes a foundation that creative teams rely on.
Having mentored students and new industrial hires, something stands out. People remember the allure of “big science,” but it’s painstaking work with foundational reagents that turns ideas into reality. Part of preparing new chemists for challenging careers lies in showing them the significance of intermediate chemicals and the detail-oriented care that goes into their selection and use.
It helps to reinforce that technical data only tells part of the story. Factors like source reliability, batch-to-batch repeatability, and responsive documentation don’t just keep projects on track; they build habits that serve a career. Working with solid intermediates, like 4-bromo-3-nitropyridine, gives those learning the ropes a firm footing in both lab safety and successful synthesis.
Every field sees star players and unsung workers. In the world of chemistry, smart building blocks power the breakthroughs dressed up in company press releases or journal splash pages. 4-bromo-3-nitropyridine earns respect not from marketing, but from a real-world track record. From small-batch benchtop experiments to scaled-out production, it keeps important projects moving. As research grows even more demanding and regulatory scrutiny deepens, securing robust, high-purity, and trusted intermediates lays the groundwork for steady progress.
Having relied on this compound for projects small and large, the takeaway stays the same: trustworthy chemicals do more than prop up daily routines—they clear the way for tomorrow’s responses to health, food, and technology challenges. Behind every elegant synthesis, every hard-won patent application, and every new product rollout, you’ll likely find intermediates like 4-bromo-3-nitropyridine making the difference between talk and real accomplishment.