2-Amino-5-bromo-4-pyridinecarboxylic acid

    • Product Name: 2-Amino-5-bromo-4-pyridinecarboxylic acid
    • Chemical Name (IUPAC): 2-amino-5-bromopyridine-4-carboxylic acid
    • CAS No.: 38534-97-5
    • Chemical Formula: C6H5BrN2O2
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    112450

    Productname 2-Amino-5-bromo-4-pyridinecarboxylic acid
    Molecularformula C6H5BrN2O2
    Molecularweight 217.02 g/mol
    Casnumber 351003-22-6
    Appearance White to off-white solid
    Solubility Slightly soluble in water
    Purity Typically >98%
    Smiles C1=CN=C(C(=C1Br)C(=O)O)N
    Synonyms 5-Bromo-2-aminoisonicotinic acid
    Storageconditions Store at 2-8°C, protected from light and moisture
    Inchi InChI=1S/C6H5BrN2O2/c7-3-1-4(8)9-2-5(3)6(10)11/h1-2H,(H2,8,9)(H,10,11)

    As an accredited 2-Amino-5-bromo-4-pyridinecarboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 10g package of 2-Amino-5-bromo-4-pyridinecarboxylic acid arrives in a sealed amber glass bottle with hazard labeling.
    Container Loading (20′ FCL) 20′ FCL container: Securely packed 2-Amino-5-bromo-4-pyridinecarboxylic acid in durable drums or bags, ensuring safety during transit.
    Shipping 2-Amino-5-bromo-4-pyridinecarboxylic acid is typically shipped in tightly sealed containers to prevent moisture absorption and contamination. It should be clearly labeled and handled according to standard chemical safety regulations, including transport under ambient conditions, away from incompatible substances, and in compliance with relevant local, national, and international shipping regulations.
    Storage 2-Amino-5-bromo-4-pyridinecarboxylic acid should be stored in a tightly sealed container, protected from light and moisture. Keep it at room temperature (15–25°C) in a dry, cool, and well-ventilated area, away from incompatible substances such as strong oxidizers. Label the container clearly and store it in a chemical storage cabinet designed for non-volatile organics.
    Shelf Life 2-Amino-5-bromo-4-pyridinecarboxylic acid is stable at room temperature; store in a cool, dry place, tightly sealed.
    Application of 2-Amino-5-bromo-4-pyridinecarboxylic acid

    Purity 98%: 2-Amino-5-bromo-4-pyridinecarboxylic acid with 98% purity is used in pharmaceutical intermediate synthesis, where high yield and reduced impurity profile are achieved.

    Melting point 250°C: 2-Amino-5-bromo-4-pyridinecarboxylic acid with a melting point of 250°C is used in high-temperature reactions, where solid-state stability during process operations is ensured.

    Molecular weight 219.01 g/mol: 2-Amino-5-bromo-4-pyridinecarboxylic acid with a molecular weight of 219.01 g/mol is used in analytical method development, where precise stoichiometry and reproducible standardization are required.

    Particle size <50 µm: 2-Amino-5-bromo-4-pyridinecarboxylic acid with particle size below 50 µm is used in formulation blending, where enhanced dispersion and uniformity are obtained.

    Stability at pH 7: 2-Amino-5-bromo-4-pyridinecarboxylic acid stable at pH 7 is used in biochemical assay preparation, where consistent activity and prolonged reagent life are provided.

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    Certification & Compliance
    More Introduction

    Introducing 2-Amino-5-bromo-4-pyridinecarboxylic Acid: A Manufacturer’s Perspective

    Many industries rely on specialty pyridine derivatives, and 2-Amino-5-bromo-4-pyridinecarboxylic acid stands out among these for a few practical reasons. In our facility, every batch is born out of years of experience working with nitrogen- and halogen-containing heterocycles. Our chemists see firsthand where meticulous control over synthesis leads to better downstream results. Compared to generic intermediates, this compound brings a unique combination of chemical handles—the amine, carboxylic acid, and bromine—right onto the pyridine core, which opens up a set of functionalization options that’s tough to match with more traditional building blocks.

    Dedicated Production Processes

    Our process engineers have wrestled with bromopyridines long enough to appreciate their temperament. During production, we avoid shortcuts, because those tend to creep up later, damaging yields or purity in customers’ steps. Yields are only half the story, though. Purity profiles make all the difference in medicinal and agrochemical research, and small amounts of isomers or residuals can sideline an entire project. Rigorous in-process analysis informs every step—starting from the choice of starting materials, monitored reaction kinetics, and purification methods tailored for heteroaromatics. This is where experience in scale-up separates lab curiosity from an industrially reliable intermediate.

    Acidic, amine-laden building blocks often raise scale-up issues: solubility, crystallization, recoveries, and waste management. Over the years, we have customized filtration and drying systems specifically for bromopyridinecarboxylic acids, which reduces both losses and contamination risk. Good blending between automation and oversight improves reproducibility between lots, which means not having to debug the same impurity twice.

    Specifications That Matter

    In practical terms, the crude purity of 2-Amino-5-bromo-4-pyridinecarboxylic acid rarely tells the story on day one. Even before any secondary processing, we see that control over color and moisture for this compound sets it apart from structurally similar pyridines. Downstream users—whether running amide bond couplings or Suzuki-type cross couplings—almost always comment about solubility and filtration ease. Through repeated campaigns, our material emerges as a nearly white solid and stays free of the yellow tint that seems to haunt lower quality sources. Water content hovers below 0.5% because we use nitrogen-atmosphere drying, not only to protect the amine but also to prevent hydrolysis of the acid function.

    Small particle size matters for rate and consistency in further reactions, so we take that control to heart. Milling is performed only at the final stage, not before, which prevents bromine scrambling and ensures a more uniform particle profile. The lot-to-lot reproducibility isn’t luck; each QC phase, from melting point to HPLC analysis, is based on years’ worth of accumulated manufacturer-run calibrations against primary standards.

    Usages and End Market Applications

    On the synthesis floor, we constantly field questions about where this compound really earns its keep. Medicinal chemistry labs appreciate the unique substitution pattern: that bromine atom at the 5-position serves as a reliable functional handle for palladium-catalyzed coupling, creating opportunities for rapid exploration of SAR (structure-activity relationship) landscapes. Contract manufacturers in the pharmaceutical sector regularly remark on the ease of generating diverse analogs once they anchor this intermediate into their scaffolds. That 2-amino function stands ready for further derivatization—acylation or urea formation, for instance—offering medicinal and crop science teams direct access to next-step libraries.

    Researchers in the agrochemical sector tell us their synthesis time drops when they plug this molecule into their routes for potent pyridine-based actives. Instead of stitching together and protecting amino and carboxy intermediates repeatedly, having both in the right positions on a single molecule cuts down on steps and error rates. Our technical support team often addresses how reactivity and by-product profiles help avoid costly purifications: less column time, fewer decomposed materials, more efficient campaigns overall.

    Comparing With Other Pyridine Derivatives

    There’s always a temptation to reach for generic pyridine-2,5-diones or off-the-shelf aminopyridines, but most lack this specific combination of groups. For example, 2-aminopyridine offers versatility, but the absence of the bromo handle makes further elaboration through cross-coupling sluggish or messy. Meanwhile, 5-bromopyridinecarboxylic acid, without the amino group, restricts options for immediate downstream transformation. The trio—amine, bromine, and acid position—puts this molecule in a different league for both diversity-oriented synthesis and targeted analog campaigns.

    Chemical compatibility also differs substantially. We’ve measured less degradation under standard storage than with closely related compounds. Brominated analogs without extra polar handles often show gradual darkening or decomposition, particularly at elevated humidity. That comes up in long-term projects where consistent color and activity mean stable performance and reliable inventory for both pilot and commercial lots.

    Attention to Safety and Handling

    Handling pyridinecarboxylic acids with halogen and amine functionalities requires steady execution. These molecules draw water, so uncontrolled exposure to air often leads to clumping and inconsistent weighing. To avoid this, our operational protocols limit open handling, using sealed containers and dry rooms. This method proved its worth during export campaigns, as it kept the material within specifications from shipping dock to customer’s door. With generic sources, we see more fluctuation in sample-to-sample analysis, usually traced to less stringent control over humidity and oxygen.

    Our team encountered reactive episodes with non-optimized packaging in early years—pouching in low-barrier bags led to some off-tones and unwanted cycles of reprocessing. Rigid, moisture-tight containers now make the difference, especially for end-users with little margin for supply hiccups. Hazardous waste from pyridinecarboxylic acids used to be a source of worry, but modern containment and neutralization systems let us reduce emissions, even as batch sizes grow.

    Continuous Improvement and Direct Feedback

    There’s a difference between process documentation and learning from each batch. We actively solicit input from customers who test new reactions or new product lines. Several times, feedback on coupling performance—whether a reaction stalls early or finishes clean—has prompted us to adjust our purification steps or to switch up grade cutoffs. Over time, this helped build a more reliable supply chain for larger pharmaceutical requirements, with documented traceability from raw material lot to finished API intermediate.

    One area where direct manufacturing control truly matters: impurity tracking. Access to our own analytical equipment means shorter lead times for troubleshooting. For customers who require custom specification, having a dedicated process line allows us to adapt—whether that means adjusting specification thresholds, changing particle cut, or modifying drying protocols to fit a novel formulation approach.

    Environmental Responsibility

    Production of halogenated pyridine intermediates brings sharp environmental questions. We invest heavily in recovery and waste minimization steps. Off-gas scrubbing and solvent recovery are standard features of our facility. Our in-house catalysis team works to design cheaper and safer routes that avoid unnecessary by-products. More than one project has seen extensive work to switch from more hazardous brominating conditions to milder, safer procedures—cutting down hazardous effluent and improving worker safety.

    Where possible, we collaborate with downstream users to align on green chemistry opportunities. This sometimes means switching supply to aqueous neutralization, rather than sending material for incineration. These changes often go unremarked in official literature, but, from the manufacturer's side, they underpin reliable, long-term access and protect both the local community and the end market’s reputation for safety.

    Quality Assurance by the Manufacturer

    Ownership of the entire synthesis lets us make tight promises to pharmaceutical partners. We learned early on that batch recertification—sometimes required after lengthier transport or long storage—works best when the original manufacturer holds both the technical knowledge and the original analytical archives. More than once, our technical team resolved a customer supply question because our batch records covered the exact method and operator, going beyond standard COA information.

    Returns and tweaks don't erode trust when the same team that makes the product manages analytical review and customer support. Comparing this to trading firms, where information comes second- or third-hand, our approach reduces confusion. When an incident occurs—the rare detection of a process impurity, for example—the path from analysis to resolution is short, and lessons feed immediately back into manufacturing protocols.

    Supporting the Work of Innovators

    Our product does not become an end in itself; it exists for the innovation of researchers. Over years, we've seen this intermediate underpin the creation of new APIs and advanced agricultural chemicals. The potential for new heterocycles, bioconjugates, and fused aromatic systems sits directly on this building block, thanks to the flexible positions of the bromine and amino groups. Labs using our product design routes where direct substitution at the 5-position simplifies the make-up of future patent claims or reduces development cycles.

    The genuine difference, as we see repeatedly, comes from having a manufacturing partner who understands both upstream (raw materials, reaction control) and downstream (customer application, regulatory) perspectives. It is this perspective that lets us provide materials ready for stringent clinical trials, or for rapid iterative development in greenhouses and fields.

    Addressing Industry Challenges Directly

    Some challenges never really go away in the synthesis of compounds like 2-Amino-5-bromo-4-pyridinecarboxylic acid. Certain supply chain disruptions ripple through both chemical and pharmaceutical sectors. Market shifts in bromine or specialty amine sources test our ability to keep quality high without cost escalation. Our procurement specialists balance multi-sourcing and careful stockpile management, and this hands-on vigilance is what shields our customers from volatility.

    We also see evolving regulations around halogenated intermediates; those changes require regular adaptation, not just at the documentation level, but embedded into our everyday procedures. Compliance isn’t a box-ticking exercise: we routinely train staff to recognize the latest standards, audit our processes, and publish lot-specific information wherever required—all served by years of technical and regulatory experience.

    The point often missed is that manufacturing isn’t simply about making a product and shipping it. Each step, from raw material selection to shipment, directly shapes final application value. Our site supervisors and process chemists watch not only the obvious—yield and purity—but also those less quantifiable factors, such as ease of use in customer labs, adaptability to new downstream chemistry, and environmental performance.

    The Bottom Line for 2-Amino-5-bromo-4-pyridinecarboxylic Acid

    The reality of making and offering this product goes far beyond a simple supply transaction. We view ourselves as contributors to a larger ecosystem of innovation and reliability. Through iterative process optimization, a commitment to traceability, and genuine two-way relationships with innovators and manufacturers downstream, we deliver this compound not just as a reagent, but as a trusted foundation for scientific progress. The difference, as seen from our manufacturing floor, grows with every campaign, every troubleshooting challenge, and every shared success in new research and commercial achievements.