|
HS Code |
733672 |
| Iupac Name | 3-Bromopyridine 1-oxide |
| Cas Number | 13532-98-2 |
| Molecular Formula | C5H4BrNO |
| Molar Mass | 173.998 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 93-95 °C |
| Density | 1.77 g/cm³ (estimated) |
| Solubility In Water | Slightly soluble |
| Smiles | c1cc(Br)cn[n+]1[O-] |
| Inchi | InChI=1S/C5H4BrNO/c6-5-2-1-3-7(8)4-5/h1-4H |
| Pubchem Cid | 154139 |
| Storage Conditions | Store at room temperature, away from light and moisture |
| Synonyms | 3-Bromopyridine N-oxide |
As an accredited Pyridine, 3-bromo-, 1-oxide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of Pyridine, 3-bromo-, 1-oxide is supplied in a tightly sealed amber glass bottle with hazard labeling and safety instructions. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for Pyridine, 3-bromo-, 1-oxide: Typically loaded in secure, drum or bag packaging, maximizing safety and stability. |
| Shipping | Pyridine, 3-bromo-, 1-oxide should be shipped in tightly sealed containers under cool, dry, and well-ventilated conditions. It must comply with all applicable regulations for hazardous chemicals, including appropriate labeling and documentation. Avoid exposure to heat, sunlight, and incompatible substances. Ensure secure packaging to prevent leaks or spills during transportation. |
| Storage | Store Pyridine, 3-bromo-, 1-oxide in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers and acids. Ensure the storage area is equipped with appropriate spill containment. Clearly label containers, and restrict access to trained personnel. Follow all local, state, and federal chemical storage regulations. |
| Shelf Life | **Shelf Life:** Pyridine, 3-bromo-, 1-oxide is stable for at least 2 years when stored in a cool, dry, and dark place. |
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Purity 98%: Pyridine, 3-bromo-, 1-oxide with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and consistent batch quality. Molecular weight 174.01 g/mol: Pyridine, 3-bromo-, 1-oxide with molecular weight 174.01 g/mol is used in organic synthesis, where precise stoichiometric calculations improve reaction efficiency. Melting point 110°C: Pyridine, 3-bromo-, 1-oxide with melting point 110°C is used in high-temperature catalytic reactions, where thermal stability enhances product safety and purity. Particle size ≤50 µm: Pyridine, 3-bromo-, 1-oxide with particle size ≤50 µm is used in solid-phase synthesis, where increased surface area promotes faster reaction rates. Stability temperature up to 120°C: Pyridine, 3-bromo-, 1-oxide with stability temperature up to 120°C is used in heated chemical processing, where it minimizes decomposition risks and contamination. Assay ≥99.0%: Pyridine, 3-bromo-, 1-oxide with assay ≥99.0% is used in fine chemical manufacturing, where high assay guarantees reproducibility in final product properties. |
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Some chemicals don’t get much fanfare, but in a laboratory, their name means progress. Pyridine, 3-bromo-, 1-oxide is that kind of compound. With its systematic name and single bromine atom attached at the third position, it might look simple at first glance, but this molecule regularly plays a crucial role in contemporary research and industrial applications. Whether you find yourself in a university synthetic chemistry lab or are managing a production facility with rigorous standards, the difference this compound makes can be measured in time saved and results enhanced.
Plenty of pyridine derivatives compete for attention, yet adding bromine at the 3-position and oxidizing pyridine opens unexpected doors. The N-oxide group influences both the reactivity and stability of the core structure. Compared to other halogenated pyridines, this change nudges the electronic properties just enough to invite novel reaction pathways while offering increased resistance to unwanted side reactions. The 1-oxide modification is more than a technicality; it’s the reason why this molecule so often lands on the workbench of chemists who need precision.
Many researchers go through countless substitutions while designing synthetic routes. When stacking up 3-bromo-pyridine without an oxide against the N-oxide version, there’s a notable difference in the way they behave in reactions like nucleophilic substitution or cross-coupling. Oxidation at the nitrogen atom makes this particular molecule both more electron-withdrawing and a little less prone to certain kinds of radical scavenging. It lends itself to selective transformations that unmodified pyridines simply can’t match. Ask a practicing synthetic chemist—these differences are not just esoteric theoretical points but real-world solutions to tough reaction challenges.
A quick glance at the datasheet shows purity levels better than 98 percent, a boiling point distinct from common isomers, and a tendency to stay shelf-stable with proper care. That might not sound thrilling on its own, but dig into the details and it becomes clear why this matters. In high-throughput labs, even minor impurities in starting materials throw off entire batch runs or introduce intractable purification problems. Sourcing a reliable grade of Pyridine, 3-bromo-, 1-oxide means fewer headaches later.
With the ongoing push for greener processes, suppliers have also started paying closer attention to how they handle, store, and distribute specialty chemicals like this one. From tamper-evident seal packaging to analytical certificates confirming identity and purity, these changes put practitioners in a stronger position to meet both safety expectations and performance goals.
My own lab experience working with oxidized pyridines confirmed just how valuable this molecule can be for medicinal chemistry. In lead optimization projects, the smallest structural tweaks sometimes spell the difference between a promising hit and an unworkable dead end. We once replaced a standard pyridine moiety with 3-bromo-pyridine N-oxide and saw a change in binding affinity thanks to subtle shifts in hydrogen bond acceptor characteristics and molecular orientation. This isn’t an isolated case. Across the industry, researchers use such functionalized heterocycles to build up molecular libraries that would be impossible to access otherwise.
Handling larger quantities is a different challenge. Scale-up teams focus on robustness and reproducibility, and any variation in input materials gets magnified in a pilot plant. The crystalline nature and thermal profile of this compound, with its marked melting and boiling points, lets process engineers predict risks better and adapt purification protocols. There’s less guesswork about volatility losses or decomposition compared to some other halogenated aromatics, which helps keep projects on schedule.
Any discussion about organic building blocks should highlight traceability and analytical assurances. For leading research institutes and pharmaceutical partners, compliance is just as important as innovation. Analytical validation takes on special urgency here. The ability to supply a batch’s complete impurity profile and origins gives downstream users peace of mind. Trace-level brominated contaminants or unknown residual solvents can jeopardize multi-million-dollar campaigns in regulated settings. That’s why the producers behind leading samples of Pyridine, 3-bromo-, 1-oxide invest in thorough batch records and up-to-date analytical instrumentation to back every shipment.
There’s another layer here. Chemical suppliers are under increasing scrutiny from regulators and clients alike, with everyone from drug developers to material scientists demanding low environmental impact, non-conflict sourcing of raw materials, and assurance that products live up to label claims. Trust builds not only on purity specifications but on open communication about the supply chain. When those standards come together, research outcomes improve—and waste diminishes.
For organic chemists, synthesizing new ligands for catalysis would drift into the slow lane without specialty compounds. Pyridine, 3-bromo-, 1-oxide finds a niche in Suzuki-Miyaura and Buchwald-Hartwig coupling reactions that underpin everything from advanced agrochemicals to active pharmaceutical ingredients. Researchers use it for introducing bromo-functionalized scaffolds where selective oxidation unlocks new rearrangements or activation positions. In my hands, the predictability of this compound’s reactivity—its favorable leaving ability and fine-tuned electron structure—has sped up optimization cycles.
Beyond traditional chemistry, the electronics and materials sectors have started eyeing modified pyridines for specialized coatings, sensors, and as interfacial agents that resist degradation under demanding conditions. Adding an N-oxide feature not only improves polarity, but creates new routes for functionalization that weren’t previously accessible. The results show in the durability and performance of final products, whether you’re talking sensors that monitor industrial emissions or layered materials for novel applications.
Some scientists push this compound even further, using it in late-stage functionalization of bioactive molecules. Substituting with a brominated, oxidized pyridine changes a drug molecule’s solubility, metabolic profile, and binding characteristics. This gives researchers better odds at discovering hits that stick when they enter clinical trials. These are breakthroughs you don’t forget—they shift how whole classes of pharmaceuticals get designed and produced.
Plenty of alternatives crowd the catalog: simple pyridines, other bromo isomers, unoxidized forms, and derivatives bearing different functional handles. In product meetings, the usual question revolves around balancing cost, reactivity, and safety. The unoxidized 3-bromo-pyridine works well for a handful of legacy transformations, but its reactivity profile often limits chemselectivity, especially when working under milder conditions. Substituting N-oxide gives chemists more control over selectivity, and is less prone to environmental and handling issues that crop up with less stable analogs.
Even in high-stakes syntheses—where losing yield or introducing byproducts can stall months of progress—this compound consistently earns its spot. The ability to incorporate it in late-stage routes, or to use it as a strategic intermediate for further elaboration, unlocks new synthetic routes. In my own projects, choosing the oxidized form has meant fewer purification headaches and smoother scale-up, again and again. This isn’t just chemical theory; it’s a reality that saves time and cuts down on wasted resources.
Lab veterans know the ripple effect poor storage practices have on sensitive building blocks. Pyridine, 3-bromo-, 1-oxide maintains stability in cool, dry conditions and proves less volatile than some homologs. Still, responsible practice means checking every container for signs of moisture ingress or degradation, since even minor exposure undermines performance in precise applications.
For this compound, standard PPE—gloves, eye protection, and well-ventilated workspaces—are sensible and expected. Respected sources ensure up-to-date safety information remains available, allowing users to stay current on evolving best practices and regulatory requirements. You don’t want surprises in a scaled-up reaction, and handling protocols reflect this practical perspective. With the right approach, risks diminish and productivity rises.
Sustainable chemistry no longer sits on the sidelines. More teams now evaluate not just the technical suitability of a compound, but also the environmental and social legacy that comes with it. Sourcing bromo intermediates historically posed problems, from questionable supply chains to inconsistent environmental controls at various production sites. Today’s leading suppliers focus on green chemistry principles, with minimized waste streams and controlled emissions.
This scrutiny follows each drum, bottle, and shipment. Transparent traceability records and clear sustainability reporting separate the most trusted suppliers. In my experience, choosing a product with strong environmental credentials boosts not only compliance but morale—people like knowing the tools they use came from responsible processes.
Textbook chemistry might seem detached from the day-to-day pressure of deadline-driven research, but that’s often where the true character of a chemical shines through. In pressure-cooker projects—short timelines, limited budgets, and little room for error—having access to a specialty building block that consistently performs can mean the difference between project success and costly failure.
When troubleshooting, personal networks and user stories count as much as published specifications. The handful of colleagues who use Pyridine, 3-bromo-, 1-oxide will often swap tips about solvent choices, storage tweaks, or minor modifications to reaction protocols that squeeze out better yields. Over the years, these ground-level insights add up, creating a living body of knowledge that rarely makes it into published methods sections but makes all the difference in operational efficiency.
Academic labs put a premium on hands-on education. Compounds that perform predictably help teach the next wave of scientists about structure-reactivity relationships, chromatography, and purification challenges in real time. In the synthesis workshop courses I’ve taught, giving students access to thoughtfully chosen reagents like Pyridine, 3-bromo-, 1-oxide has led to more productive learning—not just rote repetition but meaningful exploration and problem-solving.
Building chemical intuition early matters. When students can see and feel the tangible impact of selecting the right substrate, they grow into professionals who think creatively and troubleshoot confidently. Over time, nurturing this expertise strengthens the scientific community and accelerates discovery.
Chemical research is rarely linear. It stretches across continents, disciplines, and goals—sometimes breaking new ground, other times solving old problems in fresh ways. Through it all, reliable compounds like Pyridine, 3-bromo-, 1-oxide provide a foundation for progress. Whether you’re scaling a new synthesis, teaching eager students, or balancing safety with performance, trusted building blocks change what’s possible in a lab or plant.
The drive for transparency, purity, and sustainability guides both suppliers and end users toward better partnerships. Each purchase, each chosen bottle on the shelf, represents not just a transaction but an investment in shared standards and aspirations. In my career, sticking with dependable reagents has smoothed plenty of obstacles. As new applications and challenges emerge, products like Pyridine, 3-bromo-, 1-oxide remind us that real chemistry is shaped by the tools we trust—and by the hands and minds that put them to work.