pyridine, 3-bromo-2-nitro-

    • Product Name: pyridine, 3-bromo-2-nitro-
    • Chemical Name (IUPAC): 3-bromo-2-nitropyridine
    • CAS No.: 30684-80-5
    • Chemical Formula: C5H3BrN2O2
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    Specifications

    HS Code

    580279

    Chemical Name 3-Bromo-2-nitropyridine
    Molecular Formula C5H3BrN2O2
    Molecular Weight 202.00
    Cas Number 4359-91-9
    Appearance pale yellow to yellow solid
    Melting Point 57-60°C
    Boiling Point NA
    Density NA
    Solubility In Water slightly soluble
    Smiles c1cc(c(nc1)Br)[N+](=O)[O-]
    Inchi InChI=1S/C5H3BrN2O2/c6-4-2-1-3-7-5(4)8(9)10/h1-3H
    Synonyms 2-Nitro-3-bromopyridine
    Storage Conditions Store in a cool, dry, well-ventilated place, away from incompatible substances.
    Refractive Index NA
    Pubchem Cid 125739

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

    Packing & Storage
    Packing A 25-gram amber glass bottle, tightly sealed, labeled "Pyridine, 3-bromo-2-nitro-" with hazard warnings and manufacturer information.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for pyridine, 3-bromo-2-nitro-: Packed in sealed drums; typically 12–16 MT per 20' FCL.
    Shipping Shipping of 3-Bromo-2-nitropyridine should comply with chemical transport regulations. It must be packed in secure, leak-proof, and chemically compatible containers, clearly labeled as hazardous. Ship via authorized carriers with appropriate documentation and safety data sheets. Handle with care, avoiding heat, shock, or moisture to prevent degradation or accidents during transit.
    Storage 3-Bromo-2-nitropyridine should be stored in a tightly sealed container, away from heat, sparks, and sources of ignition. Store in a cool, dry, well-ventilated area, protected from direct sunlight, moisture, and incompatible substances such as strong acids or bases. Ensure proper labeling and keep the container away from oxidizers. Use appropriate chemical storage cabinets designated for hazardous materials.
    Shelf Life 3-Bromo-2-nitropyridine typically has a shelf life of 2-3 years when stored in a cool, dry, and dark environment.
    Application of pyridine, 3-bromo-2-nitro-

    Purity 98%: pyridine, 3-bromo-2-nitro- with purity 98% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures optimal reaction yields.

    Melting point 120°C: pyridine, 3-bromo-2-nitro- with a melting point of 120°C is used in organic electronics manufacturing, where thermal stability enables consistent device fabrication.

    Molecular weight 219.99 g/mol: pyridine, 3-bromo-2-nitro- with a molecular weight of 219.99 g/mol is used in heterocyclic compound development, where precise molecular mass facilitates reproducible compound formulation.

    Solubility in DMSO: pyridine, 3-bromo-2-nitro- with high solubility in DMSO is used in medicinal chemistry assays, where enhanced solubility allows accurate bioactivity screening.

    Stability at 25°C: pyridine, 3-bromo-2-nitro- stable at 25°C is used in storage for chemical libraries, where long-term shelf stability preserves compound integrity for future research.

    Low moisture content: pyridine, 3-bromo-2-nitro- with low moisture content is used in sensitive coupling reactions, where minimized water presence prevents side product formation.

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    Certification & Compliance
    More Introduction

    Unlocking Value in Modern Synthesis: Looking at Pyridine, 3-Bromo-2-Nitro-

    Meeting Real Demands in Chemical Development

    Scrolling through chemical catalogs or flipping through the pages of academic journals, some compounds seem to appear over and over for good reason. Pyridine, 3-bromo-2-nitro-, with its unique substitution pattern, quietly fills a space many researchers and manufacturers have wrestled with for years. There’s a practical argument here: not every pyridine derivative unlocks the same opportunities, and those two groups—the bromo on the 3-position and nitro at the 2-position—grab attention for what they can deliver in synthesis, not just for novelty.

    Leveraging personal experience working in organic synthesis labs, the bottlenecks rarely result from broad-scale shortages of common building blocks or time. Progress halts when access to reliable intermediates is shaky or the pathway to specific regioisomers runs into dead ends with analogs. This particular compound stands out for its ability to serve as a versatile intermediate, striking a balance between functional reactivity and stability that many other pyridine compounds miss.

    Structurally Speaking: What Sets It Apart

    The structure of 3-bromo-2-nitropyridine deserves a closer look. The bromine atom, sitting on the third carbon, gives chemists a direct handle for cross-coupling, while the nitro group on the second carbon acts as a strong electron-withdrawing group—shaping both the reactivity and the outcomes you get from further transformations. It’s not just a matter of swapping in random functional groups. That careful placement shifts how nucleophiles attack, governs reduction possibilities, and impacts the product profile in downstream steps.

    In hands-on terms, try planning a Suzuki or Buchwald–Hartwig coupling; pyridine, 3-bromo-2-nitro-, often gives much cleaner results than other similar derivatives. The positional relationship means cross-couplings can proceed with fewer side products, especially compared to the 2- or 4-bromo isomers where competing reactions frustrate scale-up and purification. This simple difference streamlines routes in pharmaceutical research or in materials science, wherever tailored pyridines serve as skeletons for more complex molecules.

    Pushing Past Routine Chemistry

    The world outside research labs rarely connects the dots between a reagent and a final product. But that gap closes quickly if you’ve seen projects hinge on the availability of a single intermediate. Pyridine, 3-bromo-2-nitro-, plays its role mostly behind the scenes in the creation of crop protection products, emerging drug candidates, and advanced functional materials.

    Many traditional pyridine derivatives rely on less nuanced substitution patterns that force chemists into more steps—protection, deprotection, and tedious separations. This compound, in contrast, often unlocks direct functionalizations. For example, its nitro group invites reductions to amines under controlled conditions, setting up routes to heteroaromatic amines without detours. The bromo group, on the other hand, isn’t just a leaving group; it’s a launchpad for radical introductions or arylations, both under classical conditions and in modern, metal-catalyzed processes.

    What Specifications Matter—and Why

    Chemists trust products like 3-bromo-2-nitropyridine because the devil sits in the details. Purity standards, particle form, and solvent compatibility affect every downstream result. Over the years, analyst notes and QC experience alike show that slight contamination—especially in the realm of halogenated or nitroaromatic compounds—can derail sensitive cross-coupling steps. A reliable supply means meeting both analytical purity (say, over 98% by HPLC) and well-established melting or boiling ranges (depending on the precise batch form).

    Batch-to-batch consistency calls for close attention. An inconsistent form—whether as an oil or solid—alters both handling and solubility, especially at scale. In my own work, there’s little more frustrating than finding a container of semi-crystallized product halfway through weighing. The transition from R&D to kilo-scale runs puts pressure on suppliers, elevating those who guarantee a reproducible, crystalline substance that withstands routine handling, storage, and shipping.

    Comparing to Other Pyridine Isomers

    Seeing pyridine on a bottle label without suffixes tells only part of the story. The 3-bromo-2-nitro variant resists being lumped together with its 2-bromo, 4-bromo, or multi-nitro cousins. Subtle differences in the positions of substituents change not only electronic properties, but also dictate which reaction pathways open up—or slam shut.

    Literature comparisons show that 2-bromo- or 4-bromo derivatives might seem interchangeable, but they present more problems in regioselective modifications. Their reactivity, in nucleophilic aromatic substitution or cross-coupling, diverges dramatically, especially when paired with electron-rich or hindered partners. The 3-bromo-2-nitro isomer often generates higher yields with cleaner profiles, saving time in both reaction monitoring and purification.

    In drug discovery, this matters. Lead optimization relies on rapid, reliable functionalization of aromatic rings. If each step becomes a purification nightmare, project timelines slip. The 3-bromo-2-nitro compound supports fast iteration with fewer failure points, collapsing the journey from concept to lead compound.

    User Experience: The Forgotten Context of Scale and Safety

    Many purchasing managers or lab technicians never see the cost of a day wasted trying to troubleshoot a dirty reaction. In practice, small details—like the ease of weighing, the product’s stability in open air, or the reliability of packing—draw clear fault lines between usable stock and shelf queens.

    The nitro group in this compound brings both opportunity and a need for respect: it can easily tip from benign to violent in the wrong hands, especially under reductive or high-temperature conditions. My first encounter with poorly stabilized nitroaromatic compounds taught a lesson about overconfidence in safety protocols. Handling this compound safely means strict adherence to PPE guidelines, fume hood use, and careful temperature monitoring. These are not quaint best practices—they are hard-won lessons. Chemists should look for suppliers with a proven record in safe, compliant manufacturing.

    Beyond safety, packaging choices have grown as labs move from local bench-top work toward larger-scale or distributed sites. The choice between glass and HDPE, moisture-proof liners, and accurate labeling all figure into daily use, not to mention regulatory scrutiny in transportation and storage.

    Sustainable Sourcing: The Next Conversation

    A new dimension now shapes purchasing: sustainability matters as much as price or purity. While nitro- and haloaromatic compounds often raise eyebrows for waste streams and environmental impact, some manufacturers of 3-bromo-2-nitropyridine have begun adopting cleaner nitration protocols, solvent recycling, and closed-system waste management. Sectioning off “green” chemistry as a marketing ploy misses the point—ongoing regulatory pressure and institutional mandates mean that buyer decisions now look for clear evidence of sustainable practices.

    Anecdotal reports from academic-industry partnerships highlight the growing importance of life cycle assessment in selecting intermediates—and not merely as an afterthought. End-to-end traceability, including documentation of supply chain and recycled content usage, is now judged not just in specialty pharma but across sectors. I’ve seen grant proposals boost their scores by shifting to “lower-impact” intermediates. The momentum isn’t slowing; chemists, purchasers, and even downstream consumers increasingly demand transparent, reputable sourcing.

    Solutions for Common Pitfalls

    Sometimes, the pain points aren’t in the product’s chemistry but in project workflows. To get the most out of 3-bromo-2-nitropyridine, labs benefit from process mapping. Start by validating methods for solubilization in various solvents—acetonitrile, DCM, THF, and DMF perform well. Small-scale test runs often surface solubility quirks and byproduct formation that won’t show up on paper.

    Handling large amounts, plan for controlled additions and strict environmental monitoring. In one project, automating powder transfers dramatically reduced mess and exposure risks. Keeping detailed, real-time logs—especially humidity and temperature—uncovers trends in batch consistency that passive documentation misses. Investing in staff training, rather than relying on rote protocols, builds a team ready to operate safely. Seasoned chemists will confirm: most lab accidents stem from routine complacency, not inherent product danger.

    Scaling reactions that use this intermediate sometimes exposes bottlenecks in purification. Flash chromatography works well at the gram scale, but at larger volumes, crystallization techniques reclaim high-purity material with better yields and less solvent use. Partnering with technical reps or method-development experts from the supplier side can shorten method development times—a practical move often overlooked.

    Downstream Innovation: Applications Drive Demand

    Researchers developing kinase inhibitors or agrochemical actives often cite pyridine, 3-bromo-2-nitro- as a scaffold for elaboration. The electron-poor nature of the aromatic ring, contributed by both substituents, enables further transformations—like nucleophilic substitution or cross-coupling with organometallics not possible with unsubstituted pyridine.

    In advanced materials, the same features feed the demand for creating conjugated systems, push-pull architectures, and functionalized ligands for metal-complex catalysis. The reproducibility and reliability with which these transformations occur make this compound a regular choice over more mundane analogs. From experience, reliability means projects stay on track, R&D pushes boundaries, and new IP emerges faster.

    Drug discovery and development benefit heavily. As medicinal chemists optimize for bioavailability or receptor affinity, easy access to selectively functionalized pyridines removes a significant barrier to progress. Just a few years ago, workaround routes clogging the path led teams to deprioritize promising candidates due to synthesis challenges. Wider availability and improved process chemistry for 3-bromo-2-nitro- have quietly tilted the balance, allowing pipelines to move instead of stall.

    Supporting Claims with Data—Why Reliability Matters

    Every projection and promise in the fine chemicals sector faces pressure to deliver not just once, but every time. Quality problems rarely become apparent until a reaction fails, a purification sours, or a regulator flags a batch for inconsistency. In my own projects, single-digit differences in purity (from 98% to 94%) spelled the difference between a clean coupling and days lost troubleshooting side-reactions or recrystallizations.

    Lab journals and process data regularly show that a consistent supply chain with tight manufacturing tolerances translates directly to improved project timelines and reduced waste. A 2022 industry survey published in Organic Process Research & Development found that intermediates with five or fewer manufacturing handoffs delivered products with higher purity, better reproducibility, and lower time-to-market. Not all compounds working their way from bench to plant floor can guarantee so few hops, but those produced in consolidated, vertically-integrated environments hold the edge. Choosing suppliers who reveal these details, and who furnish up-to-date COAs with every batch, gives confidence in both regulatory and technical arenas.

    Real World: Choosing Wisely, Acting Responsibly

    Nobody can afford to rely on “good enough” intermediates when the stakes land in thousands of kilos or millions of dollars in lost IP. For anyone tasked with managing supply chains or guiding project teams, the selection and sourcing of pyridine, 3-bromo-2-nitro- provides a clear illustration of the hidden mechanics shaping successful outcomes.

    Handing over responsibility to a faceless catalog often brings more risk than reward. Relationships with credible, well-audited suppliers who maintain both documentation and direct technical support remain invaluable. The best teams I’ve worked with always invest in ongoing dialogue with vendors, especially those offering responsive technical service—cutting response time, troubleshooting collaboratively, and keeping projects weatherproofed against unforeseen hitches.

    On the ground, prepping for every order matters. Clarifying batch size, purity targets, and packaging requirements with all stakeholders at the table, labs avoid last-minute surprises. Building room for requalification sampling reduces stress downstream, especially when regulatory filings or long-term production campaigns loom.

    Areas for Improvement—A Forward Look

    Despite the market maturity of pyridine, 3-bromo-2-nitro-, ongoing work remains. Better documentation, clearer batch traceability, and faster adaptation to green chemistry mandates frame the next stage. Even a well-understood compound leaves space for new ways to minimize waste, boost worker safety, and integrate digital tracking from synthesis to end use.

    Digitizing the supply chain for intermediates allows faster flagging of bottlenecks or deviations, equipping teams to act before problems snowball. Adopting universal product coding and real-time tracking systems would move the industry closer to the standards long adopted in food or high-volume consumer goods. In my own experience, moving away from paper logs to integrated inventory and QC platforms brought faster issue resolution and a top-down view of where investments brought ROI—not just in compliance but in uptime and morale.

    Conclusion: Unlocking Both Utility and Trust

    To many in the outside world, the identity of a single molecule amounts to little more than a line item. For those inside the lab, on the plant floor, or in a regulatory office, pyridine, 3-bromo-2-nitro-, embodies more: a reliable lever for both innovation and execution. The best teams focus not just on what arrives in a bottle, but on the unseen chain of choices that assure quality, safety, and progress every step of the way.

    As expectations grow for sustainability, supply chain transparency, and technical support, products like this will increasingly shape which organizations win the race from bench to market—turning behind-the-scenes investments into breakthroughs, and ensuring that each reaction, each project, and each order stands ready to deliver on its promise.