5-bromo-2-hydroxy-3-pyridinecarboxylic acid

    • Product Name: 5-bromo-2-hydroxy-3-pyridinecarboxylic acid
    • Chemical Name (IUPAC): 5-bromo-2-hydroxy-3-pyridinecarboxylic acid
    • CAS No.: 5470-05-1
    • Chemical Formula: C6H4BrNO3
    • 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

    275252

    Chemical Name 5-bromo-2-hydroxy-3-pyridinecarboxylic acid
    Cas Number 55220-78-9
    Molecular Formula C6H4BrNO3
    Molecular Weight 218.01
    Iupac Name 5-bromo-2-oxo-1H-pyridine-3-carboxylic acid
    Appearance White to off-white solid
    Melting Point 240-245°C
    Solubility Slightly soluble in water
    Smiles C1=CC(=C(C(=O)N1)O)C(=O)OBr
    Inchi InChI=1S/C6H4BrNO3/c7-3-1-4(6(10)11)5(9)8-2-3/h1-2,9H,(H,10,11)
    Synonyms 5-Bromo-2-hydroxynicotinic acid
    Storage Condition Store at room temperature, dry and away from light

    As an accredited 5-bromo-2-hydroxy-3-pyridinecarboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a 25-gram amber glass bottle, tightly sealed, with a white screw cap and a detailed label including chemical details.
    Container Loading (20′ FCL) 20′ FCL container loads 5-bromo-2-hydroxy-3-pyridinecarboxylic acid in securely sealed drums or bags, ensuring moisture and contamination protection.
    Shipping 5-Bromo-2-hydroxy-3-pyridinecarboxylic acid is shipped in tightly sealed containers, protected from light and moisture. It is packaged according to safety regulations for chemicals, typically using cushioned, leak-proof materials. Depending on quantity and local regulations, it may be shipped as a non-hazardous or limited quantity chemical, with proper labeling and documentation.
    Storage 5-bromo-2-hydroxy-3-pyridinecarboxylic acid should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from light and incompatible substances such as strong oxidizing agents. Protect from moisture and excessive heat. Ensure the storage area is clearly labeled and access is restricted to trained personnel. Follow all relevant safety and regulatory guidelines.
    Shelf Life 5-Bromo-2-hydroxy-3-pyridinecarboxylic acid typically has a shelf life of 2-3 years when stored in a cool, dry place.
    Application of 5-bromo-2-hydroxy-3-pyridinecarboxylic acid

    Purity 98%: 5-bromo-2-hydroxy-3-pyridinecarboxylic acid with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield reactions and minimal impurities.

    Melting point 220°C: 5-bromo-2-hydroxy-3-pyridinecarboxylic acid with melting point 220°C is used in high-temperature catalysis studies, where it provides reliable structural stability and thermal resilience.

    Particle size <10 μm: 5-bromo-2-hydroxy-3-pyridinecarboxylic acid with particle size less than 10 μm is used in fine chemical formulation, where it allows for improved dispersion and homogeneous mixing.

    Stability temperature up to 120°C: 5-bromo-2-hydroxy-3-pyridinecarboxylic acid with stability temperature up to 120°C is used in heterocyclic compound research, where it maintains chemical integrity during extended processing.

    HPLC assay 99%: 5-bromo-2-hydroxy-3-pyridinecarboxylic acid with HPLC assay 99% is used in analytical reference standards, where it enables accurate and reproducible quantification.

    Moisture content <0.5%: 5-bromo-2-hydroxy-3-pyridinecarboxylic acid with moisture content less than 0.5% is used in precision organic synthesis, where it prevents hydrolysis and guarantees product consistency.

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    Certification & Compliance
    More Introduction

    Introducing 5-Bromo-2-Hydroxy-3-Pyridinecarboxylic Acid: From Factory Floor to Your Lab

    A Chemist’s Perspective on Specialty Pyridinecarboxylic Acids

    Standing here in a chemical manufacturing plant, the settings feel less like a distant supply chain and more like an extension of our own effort and inquisitiveness. Facing the reactor vessel, a chemist can mark every stage—reaction, work-up, purification, quality checks—each step woven with experience. Among the wide variety of compounds we produce, 5-bromo-2-hydroxy-3-pyridinecarboxylic acid brings together challenges that only show up when raw chemistry meets modern synthesis.

    Shorthand in our process logs as 5-Br-2-OH-3-PCA, this molecule has carved out a place in laboratories and innovation pipelines, prized for its rare backbone and functional handles. Seeing it come together in a controlled production run, you recognize its value isn't just about a rare catalog number—it's shaped by the method, by what each molecule can mean to a researcher picking apart a tough synthesis or investigating new biological targets.

    From Raw Materials to Final Purity: A Process-Driven Approach

    Every successful batch begins with a clean plan for sourcing and handling intermediates, because subtle differences in starting material drive final result. We have seen that inadequate precursor purity or a hurried bromination stage can leave unwanted by-products—a headache down the line for both us and the researcher using the compound. This is why our protocol emphasizes staged addition, rigorous temperature control, and constant in-process monitoring using HPLC and NMR, not just at the end, but through multiple key hold points.

    The finished acid, after crystallization and vacuum drying, presents as a fine, almost white powder, denser than unhalogenated cousins, and notably less hygroscopic—an advantage for benchtop operations in humid environments. Most labs spot it by its well-defined melting point and its sharp NMR signals, confirming both purity and structure. We regularly analyze each batch for trace halogen and heavy metal residues, keeping within international requirements for research materials and downstream pharmaceutical use. Residual solvents are checked by GC—ensuring nothing extraneous rides along unnoticed.

    Where 5-Bromo-2-Hydroxy-3-Pyridinecarboxylic Acid Finds Its Purpose

    In pharmaceutical research, 5-bromo-2-hydroxy-3-pyridinecarboxylic acid often serves as a building block for complex heterocycles or specialty ligands. The combination of bromine and hydroxy groups at adjacent positions turns this into an ideal scaffold for cross-coupling reactions or late-stage derivatizations. Medicinal chemists in our client base routinely use it to construct new libraries of kinase inhibitors, with the bromine ready for Suzuki or Buchwald-Hartwig transformations, and the hydroxycarboxylic motif giving possibilities for hydrogen bonding or further functionalization.

    Agrochemical and material sciences have found it just as valuable, though for quite different reasons. The molecule’s electron-deficient core, with its unique activation patterns, appeals to those developing specialty dyes, corrosion inhibitors, and functional coatings. We routinely see requests for this compound from labs tuning ligand frameworks for custom catalysts, all seeking improved stability or activity. Our collaborators in polymer chemistry noted the difference the bromo group makes for introducing new cross-linking points, enhancing both mechanical strength and chemical resistance in finished materials.

    Understanding the Practical Differences: Not Just Another Pyridinecarboxylic Acid

    Having produced several related pyridinecarboxylic acids— some halogenated, some not— we witness first-hand the clear distinctions. The bromo substitution at position 5, together with the hydroxy at position 2, sets this one apart. Bromine brings a different kind of reactivity; electrophilic substitution patterns shift, and coupling possibilities multiply. By contrast, the 5-chloro or 5-iodo analogs don't always offer the same blend of stability and reactivity; the chloro forms, though cheaper, react less smoothly, especially for palladium-catalyzed cross-couplings and tend to lag in yield. Iodo variants, while more reactive, present additional handling issues, including shelf stability and higher cost.

    Non-halogenated versions miss out on the same breadth of transformations. Researchers report lower versatility when scaling up parallel syntheses, with fewer routes to extension or tailoring the electronic environment of the core. As for the hydroxy group, placing it away from the carboxy makes blocking or derivatization more difficult; some isomers force extra steps to achieve what the 2-hydroxy arrangement grants in a single reaction.

    In terms of handling, our product's solubility favors standard organic solvents—DMF, DMSO, acetonitrile—with clean filtration and straightforward crystallization. This makes purification less of a chore and lets us keep a narrow profile in batch-to-batch impurity content. Other carboxylic acids, particularly those with multiple substituents or longer carbon chains, often complicate matters by increasing oiliness or forming hard-to-remove emulsions during work-up.

    An Emphasis on Experience: Why Consistency Matters

    Working in manufacturing, you get a daily reminder that consistency underpins every research milestone depending on these materials. Subtle variations—trace water, microscopic dust, or a fraction of a degree off during crystallization—make big differences they don’t teach you about in the abstract. Each shipment that leaves the facility carries not just a certificate of analysis, but a story about choices, diligence, and fixes along the way.

    A product like 5-bromo-2-hydroxy-3-pyridinecarboxylic acid stands up to scrutiny because the workflow doesn't end at the reaction vessel. It continues through every analytical run— routine NMR crosschecks, HPLC every few hours, and spot GC/Mass Spectrometry to catch rare decomposition products. Clients have followed up years later, noting identical results from our batches— allowing clear, reproducible research, whether they’re working in academic labs or regulated pharmaceutical development.

    Supporting Researchers: From Custom Requests to Bulk Orders

    Sometimes, customers approach us with unusual needs. Maybe they want a specific polymorph, or a non-standard particle size for rapid dissolution. Our experience producing small batches as well as multi-kilo lots allows us to tweak parameters— adjusting crystallization solvents, switching up drying conditions, repeating wash cycles as needed.

    One project demanded a variant with sub-ppm halide content to support a delicate catalytic process. Another asked for isotope labeling, and our technical staff responded by redesigning synthetic steps to introduce the isotopic tags cleanly, minimizing both cost and waste. We found that open dialogue— sharing analytical data, commenting on unexpected blips in spectra— builds trust with clients who want to trace every facet of their supply chain.

    We keep lines open for custom analytical reports or split-lot shipments, prepared so researchers don’t have to gamble on uncertain quality. Rather than depending on warehouses or holding inventory for anonymous orders, each batch we produce reflects a specific need, a real experiment, a tight deadline, and someone’s next breakthrough.

    Troubleshooting and Continuous Improvement: Learning From Every Batch

    Not every production goes smoothly. Rainy spells spark changes in solvent uptake; a rumor of a shipping container snag at a port reminds us the supply of certain halogenated precursors can dry up. Sometimes, finishing yields unexpectedly drop, signaling issues upstream in bromination efficiency or downstream loss during filtration. On those days, the team reviews logs, rechecks materials, sometimes resorts back to smaller batch pilot reactions to root out the exact cause.

    Continuous improvement is more than jargon—it comes from tracking what works, tuning stepwise yields, tightening material flows, and updating control charts. Once, a small change in the pH during final acidification was traced as the culprit behind minor impurity spikes, so we fine-tuned the endpoint monitoring for better transition from reaction to isolation. Each fix finds its way into the next protocol revision.

    What’s true in a bustling chemical factory is true in downstream research lab: regular attention to minor details delivers outsized gains. Over time, we automate routine steps— inline quench monitoring, real time data capture, feedback loops for agitation rates— but never substitute machines for sense. Years watching hot reactors and cool crystals taught us that some judgments can’t be replaced by automation alone.

    Handling, Packaging, and Storage: Minimizing Risk, Maximizing Value

    The value of careful packaging often only becomes clear after a cross-country shipment arrives following days of rough travel. We select containers that fit the expected transit conditions, sometimes doubling seals or pre-packing with desiccant, but never losing sight of sustainability or safe handling. Researchers want to open a jar or drum knowing the material inside is fully protected, with no risk of cross-contamination or accidental degradation.

    Some products push packagers to new limits— hygroscopic salts, hydrophobic melts, low-melting acids that can slump at room temperature. Our 5-bromo-2-hydroxy-3-pyridinecarboxylic acid falls in the safer middle. Robust, crystalline, resistant to ambient moisture, it stores well in standard jars under dry nitrogen. Even after months in warehouse storage, provided containers remain sealed and cool, analytical spot checks have found no appreciable drop in purity.

    For institutions handling large volumes, we can offer supply chain insight—including shipping temperature logs, traceability from raw input to boxed product, and if requested, full batch production histories. It’s not uncommon for regulatory auditors to follow up on processes, and we provide all necessary documentation about sourcing, processing, and chain-of-custody with clarity.

    The Future: Meeting New Demands With Adaptability and Reliability

    As downstream research grows, calls for this specialty acid continue to shift. Years ago, the main demand ran almost exclusively through medicinal chemistry, but now, more interdisciplinary projects come in from advanced materials, environmental, and diagnostic fields. Requests aren’t just for sample vials, either— development teams now order kilograms at a time, seeking not just reliable product but also predictability in project budgeting and planning.

    Manufacturing in this sector means staring past simple demand curves and watching where the front lines of science head next. As new coupling techniques or functionalization strategies show promise, we keep up to date— not only to retain customers but because we share in their excitement for robust, cutting-edge chemistry.

    Any changes in regulatory standards or safety guidelines, or new studies about toxicological profiles, are woven into our practice as soon as available. Worker safety and environmental controls factor into any updated process, with regular reviews of solvent use, byproduct management, and emission controls. We cycle through greener alternatives where feasible, committed to maintaining quality even as regulatory and social expectations tighten.

    Collaborative Relationships: More Than Just a Product Number

    Our many years making 5-bromo-2-hydroxy-3-pyridinecarboxylic acid amount to more than mastering a technical recipe. The real strength lies in how closely we partner with the people using it—tracking new applications, troubleshooting odd side products, sharing insights about next-generation derivatives. Some of our closest partners send feedback after each synth run, flagging surprising outcomes or sharing ideas for improved yield or purity.

    We take pride not only in technical expertise but also in openness— whether fixing packaging hiccups or responding to unique custom syntheses. When a researcher suggests a tweak that later gets incorporated into our methodology, our staff knows their knowledge and care have echoed past the plant floor. The loop between production and research grows tighter each cycle, each improvement a reflection of mutual respect.

    All these practices stem from a simple realization— in chemicals, reliability and trust count as much as molecular structure. The compound matters, but so does the handoff from producer to end user, from raw ingredient to crucial step in something bigger. We stand behind each lot of 5-bromo-2-hydroxy-3-pyridinecarboxylic acid as a product of genuine experience— for us, that means accountability, pride, and a stake in each discovery it helps make possible.