6-Bromo-5-fluoropyridine-2-carboxylic acid

    • Product Name: 6-Bromo-5-fluoropyridine-2-carboxylic acid
    • Chemical Name (IUPAC): 6-bromo-5-fluoropyridine-2-carboxylic acid
    • CAS No.: 573566-68-0
    • Chemical Formula: C6H3BrFNO2
    • 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

    306293

    Product Name 6-Bromo-5-fluoropyridine-2-carboxylic acid
    Cas Number 875781-65-2
    Molecular Formula C6H3BrFNO2
    Molecular Weight 232.00 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Soluble in DMSO and methanol
    Smiles C1=CC(=NC(=C1F)Br)C(=O)O
    Inchi InChI=1S/C6H3BrFNO2/c7-4-2-3(6(10)11)1-5(8)9-4/h1-2H,(H,10,11)
    Storage Conditions Store at 2-8°C, protected from light

    As an accredited 6-Bromo-5-fluoropyridine-2-carboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 5 grams of 6-Bromo-5-fluoropyridine-2-carboxylic acid, powder form, with tamper-evident cap.
    Container Loading (20′ FCL) Container Loading (20′ FCL): Securely packed 6-Bromo-5-fluoropyridine-2-carboxylic acid in drums or bags; moisture-proof, tightly sealed, weight optimized.
    Shipping 6-Bromo-5-fluoropyridine-2-carboxylic acid is shipped in tightly sealed, chemically resistant containers to prevent moisture or contamination. The material is handled under standard shipping regulations for laboratory chemicals, typically at ambient temperature, and accompanied by safety documentation. Ensure compliance with local and international transport guidelines for hazardous substances if applicable.
    Storage Store **6-Bromo-5-fluoropyridine-2-carboxylic acid** in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and sources of ignition. Keep the container tightly closed and labeled. Avoid storage near incompatible substances such as strong bases and oxidizers. Use proper chemical storage cabinets and follow all relevant safety guidelines for handling hazardous chemicals.
    Shelf Life 6-Bromo-5-fluoropyridine-2-carboxylic acid typically has a shelf life of 2 years when stored in a cool, dry place.
    Application of 6-Bromo-5-fluoropyridine-2-carboxylic acid

    Purity 98%: 6-Bromo-5-fluoropyridine-2-carboxylic acid with a purity of 98% is used in pharmaceutical intermediate synthesis, where high purity ensures optimal reaction yields and product quality.

    Melting point 144-147°C: 6-Bromo-5-fluoropyridine-2-carboxylic acid with a melting point of 144-147°C is used in solid-state organic compound development, where controlled phase transitions support reproducible crystallization.

    Stability temperature up to 80°C: 6-Bromo-5-fluoropyridine-2-carboxylic acid with stability up to 80°C is used in organic reaction processes, where resistance to thermal degradation enables reliable process scalability.

    Molecular weight 234.99 g/mol: 6-Bromo-5-fluoropyridine-2-carboxylic acid with a molecular weight of 234.99 g/mol is used in drug discovery research, where defined molecular characteristics support accurate structure-activity relationship studies.

    Particle size <10 microns: 6-Bromo-5-fluoropyridine-2-carboxylic acid with particle size below 10 microns is used in high-throughput screening assays, where fine particle dispersion increases assay sensitivity and reproducibility.

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    Certification & Compliance
    More Introduction

    6-Bromo-5-fluoropyridine-2-carboxylic Acid: A Manufacturer’s Perspective

    Introducing a Key Building Block

    In the world of synthetic chemistry, progress often hinges on small, well-characterized molecules. 6-Bromo-5-fluoropyridine-2-carboxylic acid stands out among these as a robust intermediate, widely sought by pharmaceutical and agrochemical research teams. Having spent years working directly with the development and production scale-up of halogenated pyridine carboxylic acids, I can say from experience that the pairing of both bromo and fluoro substituents gives this molecule special utility.

    What Our Laboratory Has Learned

    Every batch starts with carefully controlled halogenation and carboxylation reactions, monitored closely for byproducts. For 6-Bromo-5-fluoropyridine-2-carboxylic acid, mistakes in the reaction sequence or purification show up fast—impurities lead to less predictable behavior in downstream syntheses, especially in Suzuki or Buchwald-Hartwig coupling steps that many downstream users perform. Our facility runs strict quality chromatographic analyses and NMR confirmation to ensure consistent purity, as this directly impacts yields for medicinal chemists screening new kinase inhibitors or heterocyclic scaffolds.

    Usage and Industry Applications

    Most of the demand we see comes from teams exploring structure-activity relationship (SAR) studies in early drug discovery. A fluorine atom in the heterocycle gives chemists a useful handle for modulating electron density, which often leads to improved pharmacokinetics or shift in bioactivity. The bromo substituent makes this pyridine amenable to efficient C–C bond forming reactions. Medicinal chemistry groups often choose this carboxylic acid as a core because it gives them freedom to elaborate the structure efficiently, thanks to easy decarboxylation or amidation options.

    Beyond pharmaceuticals, agrochemical innovators have turned to halogenated pyridine acids to generate lead candidates with tunable environmental stability. Sometimes they require 6-Bromo-5-fluoropyridine-2-carboxylic acid specifically for selective herbicide or fungicide exploratory programs, where fine-tuned molecular properties make or break a project. Ironically, its popularity means researchers sometimes need quantities that outpace our annual predictions, pushing us to optimize scale-up and supply chain security.

    Our Model and Specifications—Why These Matter

    Some manufacturers sacrifice purity for throughput, particularly during campaign mode production, but our experience has taught us to avoid cutting corners. We target a purity benchmark matched to the sensitivities of rigorous medicinal chemistry workflows—typically >98% as determined by HPLC. This is not an arbitrary decision: low-level impurities or batch-to-batch variability introduces uncertainty for downstream teams, leading to unreliable SAR interpretations and wasted resources. Our own chemists have traced failed reactions back to unexpected contamination, a hard lesson that still shapes how we document and verify every lot.

    Physical form plays a practical role for end users—not all process flows tolerate clumping or unstable hydrates. We dry and mill our material to yield a free-flowing, crystalline powder, knowing full well how a sticky lump can clog feeders in larger reactors or dissolve poorly during automated dispensing. Our packing materials are selected after lengthy shelf-life and transport stress tests, since moisture and oxygen over weeks or months can degrade the halopyridine core. Chemists often appreciate that our bottles open cleanly, and we avoid static-charged packaging since fine powders tend to escape into laboratory air and can contaminate glove box environments.

    6-Bromo-5-fluoropyridine-2-carboxylic Acid Versus Similar Compounds

    Deciding between 6-Bromo-5-fluoropyridine-2-carboxylic acid and related compounds comes down to chemistry, not just availability. For synthetic chemists working on a new lead compound, the positional selectivity matters: shifting the bromo or fluoro substituent around the pyridine ring disrupts electronic effects and often changes reactivity. We have run model reactions that show how substitution at the 6-position, with fluorine adjacent, promotes clean coupling in cross-coupling chemistry—this is not always true for 2-bromo-3-fluoro analogs, for example, which often show lower yields in analogous reactions.

    Many commercial offerings of halogenated pyridine carboxylic acids contain a mix of regioisomers because separation is laborious. Our process, refined over hundreds of production lots, yields the target isomer with consistently low isomeric contamination, measurable both by HPLC and NMR. For SAR projects, such selectivity means fewer column purifications and less time spent identifying which impurity end up in active compounds.

    Compared to simple bromopyridines or fluoropyridine acids, this dual-substituted acid demonstrates improved robustness under a wider range of synthetic conditions. Our customers note fewer problems during scale-up steps—there is less decomposition, reduced formation of side products, and reactions with coupling partners proceed at lower catalyst loading, saving both time and cost. Having run hundreds of grams through Buchwald-Hartwig aminations ourselves, we know that operator experience with this acid translates directly to process predictability.

    Continuous Improvements and New Demands

    We see rising interest from specialized chemical biology teams who demand extremely low trace metals and residual solvent content. To meet this, our purification has shifted to solvent systems showing superior removal of polar impurities while minimizing product losses. Our analytical lab constantly checks for ethanol, methanol, and dichloromethane below ppm levels, reporting certificate of analysis numbers down to industry-recognized thresholds.

    Analytical rigor goes hand-in-hand with documentation. We have invested heavily in data logging and batch traceability, prompted by a few years ago when supply chain concerns forced our clients to request audit-ready transparency—something not all labs can provide. This now backs our product lines, giving customers peace of mind if regulatory questions arise downstream. We have learned that in regulated sectors, especially when our intermediates move into GLP toxicology studies, every certificate, every lot trace, and every impurity profile must stand up to third-party scrutiny.

    Supporting Early-Stage Innovation

    Some of the most innovative work we’ve witnessed comes from start-up biotech teams or academic labs ordering just a few grams, running trial syntheses that, years later, blossom into major drug candidates. Production on this scale demands flexibility—often custom lot sizes or tailored packaging. We have experimented with everything from heat-sealed vials for moisture-sensitive applications to small, repurposed glassware for courier shipments when speed matters over logistics protocol.

    Support for these smaller orders isn’t charity—it’s an investment in relationships. Several now-prominent researchers recall our willingness to provide a few extra grams or detailed NMR charts at no charge, building trust one project at a time. In either case, these direct partnerships feed back into our internal standards: invaluable feedback on crystallinity issues, solution compatibility, or subtle odor traces that signal residual solvents.

    Scaling Up—Production Insights

    Manufacturing at kilogram scale is rarely glamorous; every step presents its own headaches. Early pilot runs flagged issues such as clinging product on glassware, product loss during filtration, and solvent usage mismatches. Using jacketed reactors with direct temperature monitoring has reduced hot spots that lead to localized decomposition. We trialed several anti-solvent additions to optimize product precipitation, each tweak documented and assessed for cost and clean-up time.

    Local environmental regulations mean all mother liquors are tracked and processed with waste minimization in mind. We’ve installed closed-loop recycling for key solvents, based on experience that routine disposal is both costly and shortsighted. Pressure to deliver consignments reliably during supply chain hiccups taught us to keep critical raw materials in buffer stock—few outside a production environment appreciate how fast lead times collapse during annual shutdowns in raw material supply regions.

    Handling halogenated materials also brings safety aspects to the fore. We train staff regularly in spill protocols, and invest in improved ventilation after a single incident years ago revealed design shortcomings. Every process line update consults both front-line workers and technical experts to identify subtle failure points; this collaboration leads to safer working conditions and fewer health complaints.

    Environmental and Safety Considerations

    Halogenated intermediates, including 6-Bromo-5-fluoropyridine-2-carboxylic acid, need careful stewardship. We adopted real-time fume monitoring and upgraded PPE standards after observing recurring skin irritation linked to trace dust. Dust control solutions now include negative-pressure hoods, frequent cleaning, and powder transfer methods that minimize operator exposure—even as demands for throughput increase.

    Waste streams rich in brominated and fluorinated material are segregated and treated with customized protocols, not lumped together. We found that solvent distillation for reuse does not always prevent trace cross-contamination, so we reserve separate recycling lines for runs containing these pyridines. Our commitment to environmental responsibility is not just about compliance; fielding queries from research clients who want detailed data on our waste treatment led us to refine our reporting and emissions tracking far beyond legal thresholds.

    Our process audits capture both long-term trends and near-miss incidents to inform future upgrades. We participate in industry forums, sharing anonymized case studies with international peers, hoping our lessons help prevent similar accidents or inefficiencies elsewhere. Conversations with downstream partners regularly prompt us to try out less toxic reagents or pursue joint R&D on greener halogenation methods—giving us a stake in the sustainable future of specialty chemicals.

    Why Chemists Choose This Molecule

    Clients with deep experience often tell us that 6-Bromo-5-fluoropyridine-2-carboxylic acid brings a rare blend of performance and versatility. The carboxyl group grants access to a variety of functionalizations, while the bromo and fluoro atoms open distinct reaction pathways. Even challenging synthesis projects benefit from this flexibility—certain bioisosteric replacements or late-stage diversifications are only possible using dual-halogenated pyridine carboxylic acids.

    Repeat orders usually signal successful project milestones. We hear from medicinal chemists that switching to our manufacturing routes improved their successfully delivered analogs and cut troubleshooting time. During patent filings, they rely on the rigorous batch documentation and purity data we provide to demonstrate freedom-to-operate and robust analytical provenance—these are real, bottom-line advantages that elevate the importance of our approach.

    Our team has a saying—“every batch is a test, every client a partner”—reflecting the reality that small differences in purity, lot history, or packaging translate into tangible results in the lab. Over the years, we have supported not just routine synthesis but also urgent, time-sensitive campaign runs where the stakes include grant deadlines, regulatory applications, or pivotal milestones in clinical pipelines.

    Challenges and Solutions

    Production scale creates challenges in consistency, solvent usage, and impurity tracking. Our researchers chase down even faint signals of unusual peaks in the spectra, knowing that what looks like noise may become significant when transferred to sensitive downstream assays. Advanced process controls and customized documentation systems grew out of our own trial-and-error, with digital traceability now embedded at each production stage.

    Clients keen on continuous flow or automated chemistry platforms asked for higher solubility ranges and granular particle size distribution—demands that sent our team back to the lab, tuning crystallization conditions or post-processing steps. Integration of new milling equipment made a difference. We’ve run comparative dissolution and filtration trials tailored to specific customer platforms, fine-tuning protocols to reduce clump formation or powder loss.

    Transport conditions and cross-border shipping pose another set of issues. We validate temperature profiles and monitor humidity exposure, especially during warmer months or long customs holds. It matters for us that each bottle, whether traveling across continents or just a few hundred kilometers, arrives in the form and purity expected by research teams who can afford no delay.

    Looking Beyond the Label

    Behind every bottle of 6-Bromo-5-fluoropyridine-2-carboxylic acid stand years of cumulative experience—each production run, batch logbook, and customer feedback cycle informing the next. Our path as direct manufacturers connects us closely to the real needs of chemists on the front lines of discovery. We have learned to listen carefully to criticism, to tweak protocols, and to innovate not for the sake of change but for measurable results at the bench.

    Our ongoing investment in analytical technology, safety infrastructure, and process documentation reflects a long-term commitment. The pressures to cut costs and cut corners run high in this sector, but the complexities of advanced intermediates demand something different. Chemists in industry and academia have grown savvy in their questions, pushing each producer to differentiate not via mere compliance, but through provable, earned expertise.

    Each delivered batch represents compounded efforts from synthesis to shipping. Continuous improvement, attention to genuine feedback, and commitment to transparency—these form the backbone of our role as a manufacturer. We don’t just bridge supply and demand. We shape outcomes for researchers across the globe, one carefully crafted molecule at a time.