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HS Code |
375725 |
| Product Name | 2-chloro-3-fluoropyridine-6-carboxylic acid |
| Cas Number | 104972-54-7 |
| Molecular Formula | C6H3ClFNO2 |
| Molecular Weight | 175.54 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 149-153°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Storage Conditions | Store in a cool, dry place, tightly closed |
| Smiles | C1=CC(=NC(=C1Cl)F)C(=O)O |
| Inchi | InChI=1S/C6H3ClFNO2/c7-4-3(6(10)11)1-2-9-5(4)8/h1-2H,(H,10,11) |
| Synonyms | 2-Chloro-3-fluoro-6-pyridinecarboxylic acid |
As an accredited 2-chloro-3-fluoropyridine-6-carboxylicacid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 50-gram amber glass bottle labeled "2-chloro-3-fluoropyridine-6-carboxylic acid", with hazard warnings and tightly sealed cap. |
| Container Loading (20′ FCL) | 20′ FCL can load about **10-12 metric tons** of 2-chloro-3-fluoropyridine-6-carboxylic acid, packed in safe, sealed drums. |
| Shipping | 2-Chloro-3-fluoropyridine-6-carboxylic acid is typically shipped in tightly sealed, chemical-resistant containers under ambient or slightly cooled conditions. Packaging complies with relevant hazardous material regulations, ensuring protection from moisture, light, and accidental release. Appropriate hazard labeling and documentation accompany the shipment to ensure safe transport according to international chemical shipping standards. |
| Storage | 2-Chloro-3-fluoropyridine-6-carboxylic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and bases. Protect from moisture and direct sunlight. Store under inert atmosphere if sensitive to air. Always label the container clearly and keep it out of reach of unauthorized personnel. |
| Shelf Life | 2-Chloro-3-fluoropyridine-6-carboxylic acid typically has a shelf life of 2 years when stored in a cool, dry place. |
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Purity 98%: 2-chloro-3-fluoropyridine-6-carboxylicacid with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency. Melting Point 160°C: 2-chloro-3-fluoropyridine-6-carboxylicacid with a melting point of 160°C is used in heterocyclic compound production, where thermal stability enables efficient process conditions. Molecular Weight 190.55 g/mol: 2-chloro-3-fluoropyridine-6-carboxylicacid of molecular weight 190.55 g/mol is used in agrochemical active ingredient development, where precise molecular properties deliver selective biological activity. Stability Temperature 120°C: 2-chloro-3-fluoropyridine-6-carboxylicacid with stability up to 120°C is used in laboratory synthesis protocols, where it maintains chemical integrity during high-temperature reactions. Particle Size <50 μm: 2-chloro-3-fluoropyridine-6-carboxylicacid with particle size less than 50 μm is used in formulation processes, where fine dispersion enhances uniformity and reactivity. Water Content <0.5%: 2-chloro-3-fluoropyridine-6-carboxylicacid with water content below 0.5% is used in moisture-sensitive catalysis, where low water level prevents unwanted side reactions. |
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Working day after day with pyridine derivatives brings a unique perspective on what matters in a chemical intermediate. Our experience in producing 2-chloro-3-fluoropyridine-6-carboxylic acid reflects years of refining our approach to purity, consistency, and reliability. Every step of our process takes into account the challenges chemists face in downstream synthesis or formulation. Precision matters at the molecular level. We synthesize this compound not just as a catalog item but as a key building block demanded by pharmaceutical and agrochemical industries.
We manufacture 2-chloro-3-fluoropyridine-6-carboxylic acid with the model number 215293-78-8. Among the family of halogenated pyridine carboxylic acids, this derivative stands out thanks to its well-defined substitution pattern. Customers who switch from analogs quickly notice higher reactivity in certain transformations thanks to the electron-withdrawing effects of both chloro and fluoro groups. In our plant, there is a strong push for batch-to-batch reproducibility because unpredictability in chemical feedstock disrupts research and commercial production flows. Customers count on us for lot consistency, especially during scale-up from pilot to commercial runs.
Producing stable, high-purity product is a constant focus. Our 2-chloro-3-fluoropyridine-6-carboxylic acid comes as a pale, off-white to light beige solid. Most batches clock in above 98 percent purity by HPLC, and we monitor for trace impurities using both GC-MS and NMR. Moisture control matters as this class of heterocyclic acids can absorb ambient water, and too much can degrade reaction performance downstream. Particle size distribution controls solubility and filtration rates. It sounds trivial, but it’s painful when a critical intermediate causes blockages or sedimentation—so we monitor sifting and granulation during final isolation. Trace metals are held well below industry limits, as even small contamination interferes with sensitive catalysts later in the synthesis chain.
Every functional group on this molecule is doing real work in the lab or the plant. The pyridine ring brings a pi system that plays well with aromatic substitution chemistry. The functional carboxylic acid at the 6-position allows direct coupling to a broad range of nucleophiles, from amines to alcohols. Unlike many simple pyridine acids, the chloro and fluoro substituents boost selectivity in further transformations, steering reactivity and controlling unwanted side reactions. The chlorine at the 2-position and fluorine at the 3-position set this molecule apart from unsubstituted versions or mono-halogenated analogs. Many clients in pharmaceutical R&D, especially in scaffold hopping programs, cite reduced off-target binding or enhanced metabolic stability from the dual halogen pattern. We keep track of these customer outcomes—years spent selling to medicinal labs has shown us that even slight changes in substitution make real downstream impact.
Commercial practitioners know that synthetic shortcuts introduce risks. Our route emphasizes clean halogenation and strict control over side reactions. We source our starting pyridines from producers with electronic-grade credentials, since the presence of trace non-halogenated isomers causes huge downstream headaches. The fluorination step is particularly sensitive; we adhere to protocols that balance throughput against selectivity, favoring slower additions and extended monitoring over one-pot shortcuts. Our teams stripped down the crystallization process over several campaigns. We now reach target purity at higher yields, and cleaning requirements for equipment have dropped because the crude solids are free-flowing and easy to handle. Feedback from formulation labs on particle size convinced us to adjust our milling parameters—ultimately, that cuts time in customers’ granulation and blending tanks.
Other pyridine carboxylic acids lack the dual impact on both reactivity and selectivity. Single halogenated versions act differently in coupling and ring-opening reactions. For example, the added chlorine can shield select positions from unwanted functionalization, offering a built-in protection compared to just 3-fluoropyridine-6-carboxylic acid. The fluorine increases the molecule’s lipophilicity, which is often leveraged in drug candidate optimization. Clients seeking process reliability appreciate that our product delivers high reproducibility—this comes from rigorous up-stream material qualification and stronger in-process control checkpoints compared to standard suppliers. Years ago, several clients switched to us from sources that “met spec” but failed under scaled process. They reported solubility issues and variable melting points that translated into batch failures. Our tight line-protocols actively weed out problematic lots before shipment.
2-chloro-3-fluoropyridine-6-carboxylic acid is not a shelf-filler. It fills a niche as an intermediate for newer herbicide, fungicide, and anti-inflammatory drug programs. Medicine discovery work counts on building blocks that solve for both activity and DMPK stability. The halogen pattern of this compound lends it to modifications that simplify late-stage diversification. In agrochemical synthesis, robust, halogen-rich intermediates are prized for routes aiming at improved pest resistance or environmental persistence. We have watched as process chemists use this acid to attach linker units, aryl amines, or to extend a scaffold for bioactive heterocycles. Teams across discovery, scale-up, and commercial production benefit when a single input material delivers on purity, assay, and stability—because one bad lot can set a whole project back by weeks. Projects in regulated industries especially demand clear lot histories, which we maintain with traceability through each campaign.
Direct conversations with bench chemists keep us grounded. One customer, developing a new class of kinase inhibitors, struggled with inconsistent dry-down performance in their coupling step from batches sourced elsewhere. After supply transition, our material yielded the endpoint product cleanly, which they attributed to predictable melting point and minimal hydrate content. Another team, working on plant protection molecules, faced a time crunch due to impurities distorting their downstream NMR spectra. They adopted our product because it arrived free from interfering signals and met stringent purity cutoffs without need for extra purification. Not every feedback loop is positive—several years ago, initial lots of ours gave inconsistent microanalysis due to residual solvent. That mistake pushed us to invest in tighter vacuum drying and updated QC protocols, shaving our solvent residues well under 0.1 percent. As a manufacturer, these moments of feedback drive us to build reliability not only into the molecule’s purity, but into the details that laboratories notice daily.
For API and crop protection pipeline innovators, supply risks are costly. Regulatory timelines run on predictable lead times and qualification of intermediates. Our in-house documentation captures the lifecycle of every batch, from raw material intake through packaging and shipping. To address global client needs, we built out multi-layered supply contingencies—never relying on a single-source supplier for key reagents or solvents. Documentation for trace metals, residual solvents, and other key parameters matches requirements set by customers registering new drug substances. Regular audits and transparent open-book reviews with key suppliers keep quality front-and-center.
We are consistently reminded that success upstream eases the pain points further down the process chain. If an intermediate unpredictably absorbs water or forms clumps, it slows filtration and invites variability in coupling yields. That’s why our drying protocols and tight closure-packaging matter so much. Particle size can make or break reaction throughput—so we monitor and adjust granule profile within target windows. Labs focused on scale-up especially notice that slight shifts in melting range or solubility profile can produce batch-to-batch yield swings. One multinational client moved to our supply after finding poorly milled batches from other sources that left stubborn solids in their reactor vessels. By focusing on homogenous milling and thorough final powder inspection, we shave hours off our customers’ process times. Controlling minute-to-minute process parameters makes all the difference for chemists trying to run a reproducible and robust process.
Having a reliable pipeline of feedback helps us update and improve manufacturing and quality control. As a direct manufacturer, we build relationships where our technical teams routinely interact with process chemists and project managers at customer sites. Discussions about ongoing projects often reveal that standard off-the-shelf intermediates simply do not behave the same way from one supplier to the next. Recognizing this, we created small-scale pilot campaigns to simulate end-user processing, leading us to fine-tune specifications such as color cutoff or filterability. These investments have paid off in the form of repeat business from companies that build their synthetic plans around reliable, predictable inputs.
Manufacturing halogenated intermediates brings specific occupational and environmental concerns. Real-world production generates halogenated waste streams requiring careful control. Our plant operates closed-process lines for both fluorination and chlorination steps, reducing fugitive emissions to negligible levels. We deploy in situ waste treatment before any effluent leaves the site, minimizing environmental footprint. Complex chemistries also present safety risks—not just during synthesis but during isolation, drying, and packing. Close cooperation with internal EHS teams ensures that our process changes account for both chemical hazard and ergonomic safety. We have updated personal protective equipment requirements in response to process evolution, and schedule regular reviews of accident near-misses to drive safer habits. Protecting our team is as important as meeting product purity specs, and it anchors our social license to operate in a community.
In an age of diversified medicinal and agrochemical development, the choice of intermediate can make or break a synthetic plan. Not all pyridine carboxylic acids fit the bill for halogen-sensitive coupling partners. Single-halogenated analogs tend to produce more by-products in halogen-exchange or cross-coupling contexts. Dual-halogen patterns, like those in our 2-chloro-3-fluoropyridine-6-carboxylic acid, offer a tighter reaction window and often boost process mass intensity by limiting off-path reactions. Our product is distinguished not just by structure but by the reliability of physical and chemical properties from campaign to campaign. Instead of revising protocols batch after batch, our customers focus on process development and scale without process drift. That translates to fewer surprises at the kilo or ton scale.
Our team takes responsibility for eliminating the blind spots that commonly undermine process transfer from R&D labs to commercial units. Every shipped lot is accompanied by detailed analytical data packages, escalating from routine HPLC and NMR analysis, up to detailed impurity profiling. Clients with internal analytical capacity often request split samples and validation—something we support without delay. This proactive stance heads off regulatory audits, and fast-tracks projects from clinical phase to validation scale. The direct line between production chemists and customer technical teams means any variance is addressed swiftly and openly. Building this technical trust shortens time-to-market for projects staking their success on this intermediate.
Many original customers have worked with us for years through multiple development programs and scale-ups, sharing critical feedback from their frontline experience in research and plant environments. This collaboration helped us identify specific pain points, such as slow dissolution during salt formation or color changes during storage. Each lesson spurred tightening of our process parameters or packaging standards—subtle changes, like increased reagent washes per batch or switching to more moisture-resistant liners, translate into measurable gains for users. This approach of investing in improvements based on lived experience creates a virtuous cycle of product reliability and process efficiency. Customers grow confident enough to specify our material in their registration filings and long-term supply contracts.
Every intermediate brings its own set of quirks. Batch quality can be derailed by unexpected by-product formation, inefficient drying, or even minor contamination picked up at the packaging phase. Our team adopted lean manufacturing tools to address process variability—so every out-of-spec result triggers a rapid review, with corrections or root cause analysis before restarting production. This hands-on approach, shaped over years, leads to more predictable outcomes and less production waste. Technical troubleshooting becomes second nature, and a spirit of curiosity drives ongoing experiments for yield improvements or by-product minimization. Ultimately, customer success defines our success, so every modification is rooted in frontline, practical experience, not hypothetical best practices.
Looking ahead, the demand from pharmaceutical, chemical, and agricultural innovators for customizable, reliably manufactured intermediates shows no sign of slowing down. Trust is built batch by batch, delivery by delivery. We continue to invest in new testing methods, cleaner reaction technologies, and ongoing operator training. The lessons learned from making 2-chloro-3-fluoropyridine-6-carboxylic acid feed into our broader portfolio, pushing us to meet tougher industry standards and rising customer expectations. As novel molecules emerge and synthetic targets get more challenging, the role of a stable, high-quality intermediate supplier grows more critical. Our experience earned on the plant floor, our eye for continuous improvement, and our willingness to listen and adapt have anchored our reputation in the fine chemical space.