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HS Code |
929121 |
| Product Name | 5-Bromo-6-fluoro-3-pyridinecarboxylic acid |
| Cas Number | 1806243-88-4 |
| Molecular Formula | C6H3BrFNO2 |
| Molecular Weight | 236.00 g/mol |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | C1=CC(=C(C(=N1)C(=O)O)Br)F |
| Inchi | InChI=1S/C6H3BrFNO2/c7-4-2-3(6(11)12)1-9-5(4)8/h1-2H,(H,11,12) |
| Storage Condition | Store at room temperature, in a dry and cool place |
As an accredited 5-Bromo-6-fluoro-3-pyridinecarboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 10 grams, screw cap, white label stating "5-Bromo-6-fluoro-3-pyridinecarboxylic acid," CAS number, and hazard symbols. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 5-Bromo-6-fluoro-3-pyridinecarboxylic acid: Maximum load 12–14 metric tons, securely packed in sealed, chemical-safe containers. |
| Shipping | 5-Bromo-6-fluoro-3-pyridinecarboxylic acid is shipped in tightly sealed containers, protected from moisture and light. It is classified as a non-hazardous chemical for transport, but should be handled with care. Packaging complies with relevant regulations to prevent leakage or contamination. Temperature-controlled shipping is recommended to maintain stability. |
| Storage | Store 5-Bromo-6-fluoro-3-pyridinecarboxylic acid in a tightly sealed container, protected from moisture, light, and incompatible substances such as strong oxidizers. Keep in a cool, dry, and well-ventilated area. Avoid excessive heat and direct sunlight. Ensure proper labeling and secondary containment to prevent leaks or spills. Always follow local regulations and material safety data sheet (MSDS) recommendations for safe storage. |
| Shelf Life | 5-Bromo-6-fluoro-3-pyridinecarboxylic acid remains stable for at least 2 years when stored tightly sealed at room temperature, away from moisture. |
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Purity 98%: 5-Bromo-6-fluoro-3-pyridinecarboxylic acid with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and product quality. Molecular weight 218.01 g/mol: 5-Bromo-6-fluoro-3-pyridinecarboxylic acid with a molecular weight of 218.01 g/mol is used in agrochemical research, where it provides precise stoichiometric calculations for formulating target compounds. Melting point 190-193°C: 5-Bromo-6-fluoro-3-pyridinecarboxylic acid with a melting point of 190-193°C is used in organic synthesis screening, where it guarantees thermal stability during high-temperature reactions. Particle size <10 µm: 5-Bromo-6-fluoro-3-pyridinecarboxylic acid with particle size less than 10 µm is used in catalyst preparation, where it enhances the surface area for improved reactivity. HPLC assay ≥99%: 5-Bromo-6-fluoro-3-pyridinecarboxylic acid with HPLC assay ≥99% is used in medicinal chemistry applications, where it delivers accurate dosing and maximizes reproducibility. Stability temperature up to 60°C: 5-Bromo-6-fluoro-3-pyridinecarboxylic acid with stability up to 60°C is used in long-term storage conditions, where it prevents degradation and maintains compound integrity. Water content ≤0.5%: 5-Bromo-6-fluoro-3-pyridinecarboxylic acid with water content ≤0.5% is used in sensitive chemical reactions, where it minimizes side reactions caused by moisture. Low heavy metals content (<10 ppm): 5-Bromo-6-fluoro-3-pyridinecarboxylic acid with heavy metals content below 10 ppm is used in electronic material synthesis, where it ensures the purity required for advanced functional materials. |
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For years in the chemical industry, precision and reliability have set the bar for what defines a trustworthy supplier. As a manufacturer, we have watched new molecules find their way from bench chemistry to industrial synthesis and global supply chains. One such molecule, 5-Bromo-6-fluoro-3-pyridinecarboxylic acid, has earned its place among building blocks for advanced intermediates and active pharmaceutical ingredients.
5-Bromo-6-fluoro-3-pyridinecarboxylic acid brings together halogen and carboxylic acid chemistry in a single heterocycle. The bromine atom at the fifth position and fluorine at the sixth create distinct reactivity. Modifying the pyridine ring in this way offers important entry points for regioselective reactions. During scale-up production, consistency makes all the difference. We have set tight controls for purity, keeping residual solvents and related substances well within narrow thresholds. It has become clear, batch after batch, that even slight impurities or variation in form cause problems for partners further down the supply chain. We conduct HPLC and NMR analysis with each lot, publishing results that have earned the trust of process chemists who need to avoid plant stoppages and regulatory headaches.
Our journey with this particular acid started in the laboratory over a decade ago. Scaling up production called for tackling solubility issues and managing halogenated waste. Our technical team has worked closely with reactor operators, chemists, and quality engineers to refine every process step. Today, synthesis runs at multi-kilogram scale, with batch reproducibility as a priority—frequent in-process checks and a pragmatic eye for what helps or hinders downstream synthesis.
We take the trouble to source only stable and low-moisture starting materials. Pyridine derivatives can turn messy if exposed too long to air or trace water, which often shows up later as byproducts in complex syntheses. We store our intermediates under inert gas, account for trace fluoride and bromide content, and monitor each stage with spectroscopy before moving forward. This often adds time, but saves resources in terms of less rework, lower out-of-spec rates, and a smoother handoff to formulation teams.
The chemical landscape for substituted pyridine acids is broad. We manufacture a range of analogues, yet both our R&D customers and production partners keep returning to this compound for several reasons. The bromine-fluorine substitution pattern opens two halo handles for cross-coupling reactions. This allows for Suzuki-Miyaura, Buchwald-Hartwig, and other palladium-catalyzed couplings. Earlier analogues, especially the singly substituted acids, tend to lack such selective reactivity, often leading to mixed products or lower yields.
A major benefit shows up in the development of pharmaceuticals and fine chemicals. Medicinal chemists have shared that having both halides strategically located enables sequential functionalization without resorting to tedious protection and deprotection cycles. In agrochemical R&D, the compound’s flexibility lets formulators test several analogues quickly, saving weeks otherwise spent on parallel syntheses. Our technical support team often trades notes with these researchers, sharpening our own production methods based on real-world lab feedback that only surfaces with routine, hands-on handling.
Supply trends often tell us a lot about where this acid helps most. Pharmaceutical synthesis accounts for more than half our annual shipments. Here, it acts as a key intermediate in the route to kinase inhibitors, CNS-active compounds, and some antiviral scaffolds. We have observed that companies scaling from milligram to kilogram batches bring up certain recurring challenges—product stability under ambient storage, flowability, and the need for clean reaction profiles, especially during scale-up.
Our process engineers have spent time at client manufacturing sites, understanding usage in real reactors, not just on paper. Some partners run continuous processes, while others still rely on batch technology. We get regular feedback about solubility in aprotic polar solvents, filtration properties after work-up, and the consequences of minor moisture uptake. Earlier in our experience, customers shared that certain competitors’ material tended to clump, while others left residual halide content that stained glassware or complicated QC checks. We’ve set specifications accordingly and work with packaging engineers to ensure dry, manageable material, even for extended transit or storage.
Agrochemical research makes use of the compound as a starting point for crop protection libraries and some herbicide screens. Here, the need centers more on speed and cost than on ultra-purity. One of our agricultural clients highlighted how lot-to-lot stability reduces downstream requalification, which saves direct labor hours in field trial cycles.
Specialty chemical development, including advanced dyes and organic electronics, follows a similar pattern. Heterocyclic carboxylic acids with well-positioned halogens allow for greater control in “late-stage” modification. That can unlock faster prototyping in sectors where application-specific tweaks to physical properties mean market advantage. Our own R&D team continues to develop new transformations built on this acid’s backbone, broadening what we and our partners can offer next.
As a manufacturer, questions about handling, shelf life, or safety reach us almost daily. Our experience running several hundred batches of this acid has taught us to watch for three recurring pain points: sensitivity to moisture, the need for efficient purification, and safe storage. On the plant floor, we have learned not to skimp on desiccation steps, especially in monsoon-prone regions. Early on, we moved to nitrogen-blanketed storage tanks, helping to keep hydrolysis below detection thresholds. Transport containers come vacuum-sealed and lined to limit humidity exposure, and we furnish third-party stability data so quality managers see proof, not just claims.
Purification can challenge both manufacturers and customers. We tackled this by working closely with filter manufacturers to identify a medium that retains ultra-fine particulate without blinding or compressing. It took several cycles of trial and error, but now our downstream purities run higher, reducing the cost and time needed for customers to meet their internal release standards. These improvements stem directly from running continuous lots in our own lines, not from third-party reports or generic recommendations.
On the safety side, the combination of halogen atoms demands respect in handling. We run annual training with both lab and plant staff to reinforce correct glove, goggle, and ventilation protocols. Reviewing incidents across the industry, it becomes clear that most near-misses with this class of molecule involve either poor ventilation during scale-up or improper disposal of filtrates. We collaborate with waste management partners to ensure halogen-bearing effluents receive proper treatment, both to maintain regulatory compliance and safeguard our neighbors. Passing on this rigor to customers through transparent documentation, not just claims or basic labels, keeps our technical relationships open and practical.
Across regulated industries, scrutiny continues to rise. Regulatory bodies ask for full traceability, and in some markets every lot must tie back to validated starting materials and fully qualified equipment. Over the past several years, we have invested in a digital log system linking every step in the product lifecycle—from incoming raw goods to final dispatch. This records every analytical result, operator sign-off, and deviation, giving us and our customers evidence for any audit. We can pull up certificate of analysis and batch records within minutes on customer request, reducing the back-and-forth that often delays approval.
Raw material bottlenecks can threaten supply consistency. Pandemics, shipping route disruptions, and political volatility have all tested our contingency plans. By diversifying our supply base and working with more than one upstream provider for key reagents, we have managed to keep output consistent, even through bumps in the global supply chain. We have also formed reciprocal buying agreements with other trusted producers, so raw goods keep moving even during tight market conditions. It means absorbing some extra inventory cost, but our long-term partners have found this preferable to surprise shortages.
Every manufacturer tells stories about their best batches and hardest lessons. For us, the most useful changes arise directly from feedback by experienced chemists who use this acid daily in their synthesis work. We keep active records of on-site trials, tracking yield and purity results from our product versus previous lots or alternative suppliers. In the last year alone, one process improvement—switching our final recrystallization solvent to a less hygroscopic option—cut impurity profiles by roughly 40%. Another shift, optimizing our milling process, gave us finer, free-flowing powder, which clinicians report handles better in automatic dispensing.
Small changes in particle size or moisture level, easy to ignore at first glance, show big impact as batches grow from gram to hundreds of kilograms. We continue to test our assumptions by sending multiple samples from each lot to quality control teams in separate regions, catching issues before they snowball. Realistically, not every run goes perfectly; we maintain a dedicated rework bay and set aside finished goods that do not meet full specification. Any deviations get documented, traced to source, and rolled back into monthly production meetings for open discussion and process evolution. This culture of strict quality, combined with a willingness to admit and learn from mistakes, proves itself over years of repeat partnerships.
With halogenated intermediates, environmental stewardship takes extra diligence. Disposing of brominated and fluorinated byproducts safely costs more, but we put these costs into our calculations from the outset. Our plant handles solvent recovery and hydro-halide scrubbing as an integrated part of daily production, not as an add-on. Effluent is neutralized, tested, and released only under strict compliance.
Research into greener approaches continues to drive our process development team. We are piloting alternative halogen sources with lower waste profiles, and our analytical chemists work steadily to map minor byproducts that could raise future compliance hurdles. Partnership with downstream users also helps—several have joined projects aimed at reusing side-streams or reclaiming valuable residuals. Together, progress toward safer, cleaner chemistry is incremental, but experience shows it is possible with persistent effort and shared accountability.
Chemistry never stands still. Applications for 5-Bromo-6-fluoro-3-pyridinecarboxylic acid remain in flux. New routes to pharmaceutical scaffolds, agricultural actives, and specialty materials rely on fresh thinking and constant process tweaking. Our own researchers stay in active contact with leading university groups and industrial labs, sharing samples and lessons learned. One advantage of running a full-scale plant alongside a flexible pilot line is that we can test method tweaks in real production conditions, not just at the gram scale.
We open our facilities regularly for technical exchanges—inviting partners to suggest, prototype, and scale new transformations. The insight gained from hands-on collaboration becomes obvious in production performance. Last year, a university collaborator suggested a minor adjustment in reaction concentration for a key coupling step; after trying it at plant scale, we cut average reaction time by nearly 15%. Small shifts like this feed directly into customer benefit in the form of faster turnarounds and lower costs.
Our technical team makes a habit of responding directly to client questions, not routing them through sales or generic support. Incoming technical requests—ranging from solubility, compatibility, to scalable workup conditions—often reveal blind spots we address collectively. Many customers share their downstream data with us, providing a feedback loop that leads to better product for the entire user community. In one instance, a European pharmaceutical processor flagged phosphate buffer incompatibility, prompting our R&D group to publish new solvent compatibility data and adjust packaging recommendations.
Documentation comes from trial, not theory. Shelf life and batch stability claims reflect storage under both ideal and real-world conditions—from controlled environments to hot and humid warehouses. We make lab reserves of every manufactured lot and store these under varied conditions, using them to answer customer questions years down the line, well after product leaves our gates. This builds trust and repeat business, making the entire value chain more resilient.
Experience across hundreds of lots confirms the value of 5-Bromo-6-fluoro-3-pyridinecarboxylic acid as a robust, reliable, and versatile intermediate. Differences from similar pyridine carboxylic acids play out clearly in both laboratory and plant-scale applications: improved selectivity for cross-coupling, smoother batch reproducibility, and better storage performance all stem from years of direct production feedback and continuous optimization. Beyond technical benefits, thoughtful handling of environmental impact, supply chain risk, and practical documentation builds deeper trust along an increasingly demanding chemical supply network.
The pace of new discovery means requirements will keep evolving, calling for both consistency and the agility to adapt. Our own experience guides us—solving day-to-day hurdles in production and responding directly to user feedback, so each shipment stands up to scrutiny once it leaves our doors. Whether in drug discovery labs, process R&D groups, or the front lines of formulation, this acid continues to help drive progress, one carefully controlled batch at a time.