6-Amino-2,3-dibromopyridine

    • Product Name: 6-Amino-2,3-dibromopyridine
    • Chemical Name (IUPAC): 6-amino-2,3-dibromopyridine
    • CAS No.: 50839-99-5
    • Chemical Formula: C5H4Br2N2
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    585566

    Productname 6-Amino-2,3-dibromopyridine
    Casnumber 19798-79-3
    Molecularformula C5H4Br2N2
    Molecularweight 267.91
    Appearance Light yellow to beige powder
    Meltingpoint 163-167°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water
    Smiles Nc1ccc(Br)n1Br
    Inchi InChI=1S/C5H4Br2N2/c6-3-1-2-4(8)9-5(3)7/h1-2H,8H2
    Synonyms 2,3-Dibromo-6-aminopyridine
    Storagetemperature Store at 2-8°C

    As an accredited 6-Amino-2,3-dibromopyridine 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 sealed with a screw cap, labeled "6-Amino-2,3-dibromopyridine, 98%," featuring standard hazard warnings.
    Container Loading (20′ FCL) 20′ FCL loads approximately 10–12 metric tons of 6-Amino-2,3-dibromopyridine, packaged in sealed HDPE drums or cartons.
    Shipping 6-Amino-2,3-dibromopyridine is shipped in tightly sealed containers, protected from moisture, heat, and light. The chemical is classified as hazardous, requiring appropriate labeling and documentation in compliance with local and international regulations. Handling precautions and safety data sheets accompany the shipment to ensure safe transportation and storage conditions.
    Storage 6-Amino-2,3-dibromopyridine should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. The container must be tightly sealed to prevent moisture ingress. Store at room temperature and keep away from heat sources. Proper labeling and containment are necessary to prevent accidental exposure or contamination.
    Shelf Life **Shelf life:** 6-Amino-2,3-dibromopyridine is stable for at least 2 years when stored in a cool, dry place, away from light.
    Application of 6-Amino-2,3-dibromopyridine

    Purity 98%: 6-Amino-2,3-dibromopyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product consistency.

    Melting point 204°C: 6-Amino-2,3-dibromopyridine with a melting point of 204°C is used in organic electronics research, where it enables stable solid-state device fabrication.

    Molecular weight 254.90 g/mol: 6-Amino-2,3-dibromopyridine with molecular weight 254.90 g/mol is used in heterocyclic compound development, where it allows accurate stoichiometric control in reactions.

    Particle size <50 μm: 6-Amino-2,3-dibromopyridine with particle size less than 50 μm is used in fine chemical manufacturing, where it improves dispersion and processing efficiency.

    Stability temperature up to 150°C: 6-Amino-2,3-dibromopyridine with stability temperature up to 150°C is used in polymer additive formulation, where it maintains chemical integrity during processing.

    Moisture content <0.5%: 6-Amino-2,3-dibromopyridine with moisture content below 0.5% is used in agrochemical intermediate production, where it prevents hydrolysis and degradation during storage.

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    Certification & Compliance
    More Introduction

    Digging Into 6-Amino-2,3-dibromopyridine: A Practical Compound for Modern Chemistry

    There’s something satisfying about working with a chemical that behaves the way you expect. From my time in the lab, I’ve learned how small tweaks to a molecule can shape whole research projects and drive real progress. 6-Amino-2,3-dibromopyridine, an aromatic compound with two bromine atoms and one amine group attached to a pyridine ring, stands out for this very reason. It doesn’t make headlines outside chemistry circles, but anyone who’s spent hours refining synthetic routes knows compounds like this keep projects moving forward.

    Getting to Know the Structure and Model

    Let’s walk through what makes this molecule tick. 6-Amino-2,3-dibromopyridine features a six-membered pyridine ring with a nitrogen atom offering unique electronic properties, setting it apart from similar benzene-based structures. The amine group sits at position six, while bromine atoms occupy the two and three positions. This arrangement opens up specific opportunities for substitution reactions and coupling processes, which anyone fine-tuning building blocks for pharmaceuticals or advanced materials knows to be a game-changer. Having both an electron-donating amino group and electron-withdrawing bromine atoms means researchers gain remarkable flexibility in planning their reactions.

    Most of the 6-Amino-2,3-dibromopyridine on the market appears as an off-white to pale yellow crystalline powder, a state that helps avoid unnecessary fuss with purification steps. Its melting point typically falls within a stable range, giving those who handle it some predictability during heating or solvent evaporation. Purity plays a huge role, especially in demanding applications; experienced suppliers test batches by HPLC and NMR, ensuring impurity profiles stay below levels that would cause headaches later in synthesis. That kind of rigor isn’t just for academics—industrial scale-ups and pilot processes run smoother when the starting blocks don’t throw curveballs.

    What Sets This Compound Apart?

    Plenty of pyridine derivatives exist, but 6-Amino-2,3-dibromopyridine distinguishes itself with its directness. The spatial setup of its functional groups makes it highly sought after for certain cross-coupling reactions, especially those relying on palladium or copper catalysts. Researchers looking at Suzuki, Sonogashira, or Buchwald–Hartwig couplings often prefer starting materials that balance reactivity with a manageable side-reaction profile. Fewer byproducts mean less time chasing impurities down the line, saving both reagents and patience.

    Compared to closely related compounds like 2,3,6-tribromopyridine or 2,3-dibromo-6-nitropyridine, adding an amine at position six rather than a nitro or third bromine changes how the compound sits in solution and how it reacts. Substituting an amino group introduces new hydrogen bonding possibilities, which some catalysts grasp onto, boosting selectivity or increasing yield. It’s a detail that only becomes obvious after banging your head against frustrating purification problems. Over the years, I’ve watched research groups waste months on knockoff compounds with less predictable reactivity, only to switch to 6-Amino-2,3-dibromopyridine and see the bottleneck disappear.

    How 6-Amino-2,3-dibromopyridine Fuels Innovation

    Step into any medicinal chemistry lab and you’ll spot 6-Amino-2,3-dibromopyridine somewhere on a shelf, its label curling with age. That’s because its combination of bromines and amine allows for rapid construction of more complicated molecules. Anyone designing kinase inhibitors, ion channel ligands, or new anti-infective scaffolds soon realizes how crucial robust starting points can be. The electron-rich nature of the amino group helps anchor the core, while the bromines serve as springboards for further modifications, including arylations, alkynylations, or even heterocycle formations. That versatility saves budgets and trims weeks from project timelines.

    Beyond pharmaceuticals, folks building OLED emitters, specialty polymers, or liquid crystalline materials reach for this compound for similar reasons. The bromines act as gateways to install larger, more exotic fragments, giving rise to new properties—whether that means better luminescence, altered conductivity, or new binding pockets for metal complexes. Some materials science teams see a clear path forward by swapping in only one or two key building blocks early, and 6-Amino-2,3-dibromopyridine meets that need by supporting focused diversification.

    In my experience, the confidence in a starting material counts as much as the cleverness of your design. If you trust its performance across runs and suppliers, you spend more time testing out creative ideas and less on fixing mistakes that show up only after scale-up. That’s part of the know-how passed down from senior researchers: use materials with a reputation for reliability, not just the cheapest or most convenient derivative.

    Challenges and Value in Supply Chains

    Anyone buying specialty chemicals knows supply can make or break timelines. 6-Amino-2,3-dibromopyridine doesn’t always enjoy blockbuster demand, so procuring consistent lots from reputable makers matters. Trusted suppliers usually confirm each batch using spectra, and labs often re-check samples before launching key experiments. Over time, I’ve noticed that cutting corners here slows whole teams, while investing in proven sources pays back in overlooked ways—fewer delays, fewer lost experiments, and less paperwork chasing replacements.

    Price inevitably weighs on project budgets. The synthesis requires careful handling of brominating agents and skilled workers to ensure regioselectivity, which bumps up costs compared to more straightforward pyridine analogs. Some procurement managers push back against the price, but chemists in the trenches know the downstream value. Poor consistency or off-spec intermediates can waste months and throw off large investments, as anyone who’s sorted through box after box of failed syntheses will attest. It’s not hype—real results follow from starting strong.

    Potential for Substitution and Upgrade

    Debates often crop up in development teams about whether to swap in similar compounds—perhaps to trim costs or dodge shipping delays. Sometimes switching pays off, especially if the target reaction doesn’t depend too heavily on the subtle properties of the amine or bromine positions. Other times, the fine-tuned reactivity window matters more than price per kilogram. For those chasing the next generation of complex drug candidates or optoelectronic components, getting the right functional group in the right place early speeds up the rest of the process. Over my career, the incremental cost of a better intermediate nearly always pays back in fewer headaches down the line.

    Green chemistry considerations keep gaining ground. Some synthetic methods for creating 6-Amino-2,3-dibromopyridine do produce halogenated waste that needs responsible handling, adding a layer of complexity. Labs serious about minimizing their environmental impact look for sources that follow accepted waste treatment and recycling practices, and I’ve seen a move toward greener bromination methods entering the market. While it’s tempting to focus only on yield and price, research directors who take the long view keep sustainability in focus—they know the future of their programs depends on more than just short-term gains.

    Day-to-Day Reliability: Purity, Handling, and Storage

    Lab benches can devolve into chaos during crunch time, so a stable, reliable intermediate means more than just a number on a data sheet. 6-Amino-2,3-dibromopyridine resists dramatic degradation under typical storage conditions, so it rarely gives unexpected surprises after a few months in a tightly sealed bottle. Sensitivity to air and moisture stays low, though precautions help when long-term storage is planned—using tight closures or inert atmospheres protects valuable stockrooms. Those charged with preparing solutions or weighing daily batches won’t run into sudden color changes or runaway decomposition, a trait that helps newer staff avoid costly errors.

    Safety always looms in the background. Like most halogenated aromatics, the compound demands care during weighing and transfer, and experienced hands work under fume hoods with gloves and goggles. Training new staff to respect these risks makes a difference. In my own teaching days, emphasizing basic eye and skin protection felt tedious at times, but the safety culture in research labs improves outcomes in ways that can’t always be tracked on a spreadsheet. Professionals know: staying safe isn’t just about rules—it protects everyone’s investment in months of careful work.

    Continued Research and the Search for Efficiency

    It’s remarkable how much research effort targets that crucial “middle” of synthetic workflows—pieces like 6-Amino-2,3-dibromopyridine that let you jump from simple precursors to intricate final products. Teams spend hours screening reaction conditions, looking for solvent or catalyst tweaks that bump up yields. NMR and LCMS studies pick apart each slot on the ring, showing which positions tolerate modification and which fall apart too quickly. For every successful synthesis, stories unfold about trying lesser-known analogs before coming back to this well-characterized, reliable backbone.

    Improvements keep arriving, especially on the process chemistry side. Teams working with continuous flow or automated parallel reactors speed up their optimization cycles, trying dozens of variants in a fraction of the time older methods required. 6-Amino-2,3-dibromopyridine’s predictable personality makes it easier to transfer discoveries from bench to kilo-lab, a trait project managers appreciate when they review timelines and risk profiles. Innovation springs not only from the “eureka” moments, but from dependable, hard-working intermediates like this—bridging academic curiosity and real-world solutions.

    Real Impact: Beyond the Chemical Bench

    For all its technical features, the most powerful stories come from people who depend on chemistry making a difference. Pharmaceutical breakthroughs become household names, but their roots start with compounds like this: versatile, behind-the-scenes molecules that let scientists test hypotheses and refine designs. Whether helping uncover a new therapy or creating materials for sustainable energy, it’s these understated building blocks that underpin decades of incremental progress.

    Discussions at industry conferences and graduate seminars often circle back to the same questions: How can we boost reliability? Where do new materials come from? How much does a robust supply chain matter? In these conversations, examples like 6-Amino-2,3-dibromopyridine come up, not because they’re flashy, but because they reflect decades of accumulated wisdom. Teams want something that supports ambitious targets, fills gaps in toolkits, and doesn’t introduce trouble. As new fields open—think artificial intelligence in chemical synthesis or programmable materials—reliable core molecules will matter even more.

    Looking Toward Continued Progress

    Over the span of a career, it’s easy to lose track of all the individual compounds handled or debated during planning meetings. Yet 6-Amino-2,3-dibromopyridine stands out for its blend of flexibility, reliability, and distinct reactivity. Each batch moves projects a little further, builds confidence in data, and frees up teams to focus on higher-order problems instead of fixing basics. Whether you’re launching a new medicinal chemistry program, advancing functional material pipelines, or seeking to optimize every rung of the synthesis ladder, the value of smart starting materials sticks with you long after the bottles run dry.

    Every successful project sits atop the hard work of unsung molecules and the professionals who know how to use them well. 6-Amino-2,3-dibromopyridine won’t wind up in glossy ads or splashy corporate brochures, but it helps power the quiet progress that defines modern science. In the race for the next breakthrough, it pays to keep trusted allies on hand—a lesson repeated everywhere real work gets done.