|
HS Code |
574032 |
| Productname | 2,6-Difluoro-3-pyridinecarboxylic acid |
| Casnumber | 20742-27-6 |
| Molecularformula | C6H3F2NO2 |
| Molecularweight | 159.09 |
| Appearance | White to off-white solid |
| Meltingpoint | 150-154°C |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥98% |
| Synonyms | 2,6-Difluoronicotinic acid |
| Smiles | C1=CC(=NC(=C1F)C(=O)O)F |
| Inchi | InChI=1S/C6H3F2NO2/c7-3-1-2-4(6(10)11)9-5(3)8/h1-2H,(H,10,11) |
As an accredited 2,6-Difluoro-3-pyridinecarboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2,6-Difluoro-3-pyridinecarboxylic acid, 5g, supplied in a sealed amber glass bottle with tamper-evident cap and labeled for laboratory use. |
| Container Loading (20′ FCL) | 20′ FCL container loaded with securely packaged 2,6-Difluoro-3-pyridinecarboxylic acid, using sealed fiber drums/pallets, compliant with chemical transport regulations. |
| Shipping | 2,6-Difluoro-3-pyridinecarboxylic acid is shipped in tightly sealed containers, protected from moisture and light. It is handled as a chemical substance and transported according to standard hazardous material regulations, including proper labeling and documentation. Suitable temperature control and secondary containment are used to prevent spills or contamination during transit. |
| Storage | 2,6-Difluoro-3-pyridinecarboxylic acid should be stored in a cool, dry, and well-ventilated area, away from sources of ignition, moisture, and incompatible substances such as strong bases or oxidizers. Keep the container tightly closed when not in use. Store in a chemically resistant, labeled container and avoid prolonged exposure to air and direct sunlight to maintain stability. |
| Shelf Life | 2,6-Difluoro-3-pyridinecarboxylic acid typically has a shelf life of at least 2 years when stored in a cool, dry place. |
|
Purity 98%: 2,6-Difluoro-3-pyridinecarboxylic acid with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced by-products formation. Melting Point 178°C: 2,6-Difluoro-3-pyridinecarboxylic acid with a melting point of 178°C is used in agrochemical compound manufacturing, where stable processing conditions are achieved. Particle Size <50 µm: 2,6-Difluoro-3-pyridinecarboxylic acid with particle size under 50 µm is used in fine chemical formulations, where enhanced solubility and homogeneous mixtures are obtained. Moisture Content <0.5%: 2,6-Difluoro-3-pyridinecarboxylic acid with moisture content below 0.5% is used in solid-state reaction processes, where it minimizes hydrolytic degradation and improves storage stability. Stability Temperature 120°C: 2,6-Difluoro-3-pyridinecarboxylic acid with a stability temperature of 120°C is used in high-temperature synthesis reactions, where it maintains structural integrity and consistent reactivity. Assay ≥99%: 2,6-Difluoro-3-pyridinecarboxylic acid with assay of at least 99% is used in analytical reference standards preparation, where precise calibration and reproducible results are required. |
Competitive 2,6-Difluoro-3-pyridinecarboxylic acid prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@boxa-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Years of chemical manufacturing have brought us to understand not only the technical nature of our products, but also their actual role on research benches and in pilot plants. 2,6-Difluoro-3-pyridinecarboxylic acid is a prime example. While some might recognize it by a chemical formula or its systematic name, hands-on experience shows that it holds a specific utility in both research laboratories and process-scale environments. We’ve produced this material for diverse sectors and have learned why certain specifications become non-negotiable for our partners, especially those working toward pharmaceutical or agrochemical targets.
Chemists often notice the nuanced interplay between structural elements and function. 2,6-Difluoro-3-pyridinecarboxylic acid possesses two fluorine atoms at positions 2 and 6 of its pyridine ring, which isn’t just an aesthetic aspect on paper. Those substituents drive the electronic influence on the core, altering reactivity compared to mono-fluorinated or non-fluorinated pyridinecarboxylic acids. The carboxylic acid in position 3 introduces another layer of synthetic logic—it opens pathways for selective coupling, amidation, or esterification distinct from isomeric or structurally related compounds.
Our team has supported custom syntheses where users reported surprising outcomes when switching from difluorinated to monofluorinated species. In such cases, the di-fluoro pattern led to markedly different reaction rates and product profiles, often improving selectivity or enabling reactions which otherwise stalled. This difference isn’t trivial for medicinal chemists tracking structure-activity relationships or process chemists optimizing a scale-up route.
For most batches, we deliver 2,6-difluoro-3-pyridinecarboxylic acid as a free-flowing, off-white crystalline solid. Purity typically meets or exceeds 98%, by HPLC, with water and other residuals consistently monitored and held below determined thresholds. During scale-up, water content and minor impurities surfaced as challenges; batches intended for API intermediates must clear stricter scrutiny on these metrics.
Small variations in form—fine powder versus crystalline—can affect dissolution in organic solvents. Our drying and packaging controls aim to give customers material that easily transfers into flasks and reactors, minimizing clumping or static issues that slow down workflow. Customers in hot, humid regions once struggled with clumping during monsoon months, so airtight, double-sealed packaging was developed in response, based on those actual reports rather than theoretical risk assessments.
As a supplier working directly with laboratories and industrial synthesis teams, we see demand for 2,6-difluoro-3-pyridinecarboxylic acid concentrated in custom synthesis, drug discovery, crop protection, and material science. For pharmaceutical companies, the compound often acts as a precursor for development-stage APIs where difluorinated aromatics are integral to structure-activity optimization.
Medicinal chemists working on kinase inhibitors, for example, reported that the 2,6-difluoropyridine moiety enhanced metabolic stability compared to non-fluorinated analogues or variants fluorinated at alternative positions. The placement of the carboxylic acid at the 3-position further expands their synthetic toolbox, making coupling with amines or alcohols more efficient for downstream modifications.
Crop protection researchers choose this difluorinated scaffold when looking for more robust, photostable molecules. The pyridinecarboxylic acid core, when difluorinated at 2 and 6, presents improved environmental persistence and unique biological profiles, which set the groundwork for next-generation agrochemicals.
Advanced materials teams have tapped into this compound for functionalizing surfaces or as building blocks in specialty polymers. We’ve worked with customers integrating it into novel battery electrolyte formulations and light-absorbing coatings, noting that electron-withdrawing difluoro groups influence performance in organic devices by altering electron density and conjugation.
As an actual manufacturer, we oversee every step of the synthesis, purification, and QC. We run our reactors, manage solvent recovery, and optimize crystallization procedures after every scale-up batch. Troubles like unexpected byproduct formation and reactor fouling aren’t theoretical to us—we troubleshoot and adjust day by day. During a production run a few years ago, we observed new minor impurities emerging at higher temperatures; by adjusting the temperature ramp and refining the crystallization step, we eliminated these without sacrificing yield. Our staff’s familiarity with each stage keeps product reproducibility high and batch-to-batch variance low.
Quality isn’t just an internal checkpoint. Several customers, after receiving initial trial quantities, asked for full trace records and impurity profiles before moving to scale-up. By supplying analytical chromatograms and spectral data, including HPLC, NMR, and GC-MS results, we supported their regulatory filings and process validation directly. Years of working with strict pharma and agro buyers mean we expect these demands and have designed our verification systems accordingly.
We’ve fielded inquiries about elemental impurities, particle size distribution, halogen content, and even specific residual solvents. Our quality team tracks and controls these parameters, either by adapting in-house analytics or collaborating with accredited third-party labs. The documentation trail doesn’t just check a compliance box—it helps partners trust the foundation of their products.
Those new to difluoropyridinecarboxylic acids sometimes assume low differentiation between isomers or fluorination patterns, but even slight molecular changes shift reactivity or downstream performance. Compared to 2,5-difluoro- or 3,5-difluoropyridinecarboxylic acid, the 2,6-substitution pattern moves the electronic density close to the nitrogen, making nucleophilic aromatic substitution or cross-coupling reactions more predictable and consistent. Chemists working with the 2,6 difluoro isomer often report fewer side products or cleaner separation during purification.
For processes that hinge on regioselective reactivity, a single misplaced fluorine can alter the fate of a multi-step route. In our own kilo-lab, we compared 2,6- and 3,5- substitution patterns and witnessed real differences in conversion and isolation yields. Where customers’ synthetic pathways lagged due to low activity or side reactions, the 2,6-difluorinated version offered a more tractable, robust alternative.
Bulk users from the agrochemical industry have described sharp cost savings and steps eliminated when swapping to our 2,6-difluoro-3-pyridinecarboxylic acid from older, less reactive isomers or non-fluorinated analogues. Formulation scientists in both crop protection and pharma R&D stress that the cost per gram doesn’t tell the whole story—the right isomer saves hours in synthesis, streamlines purification, and ensures a more stable final active ingredient.
Other difluorinated pyridinecarboxylic acids occasionally offer similar physical forms or analytical purity, but actual downstream performance sets them apart. Lab-scale experiments end up wasted if a crucial substitution doesn’t match expectations; we’ve supplied emergency material to projects derailed by misunderstood isomer differences. That direct customer feedback has shaped both our own R&D and the advice we offer to new clients.
Even a well-made product loses value if storage or shipping permits decomposition or contamination. Our packaging line uses airtight HDPE containers, double-sealed to block out moisture and air. A few seasons ago, a multinational client in southeast Asia documented material clumping and small-scale hydrolysis during monsoon shipments. We investigated their storage conditions, adjusted our post-packing drying procedures, and now run routine stability checks on every batch destined abroad.
In standard climate-controlled conditions, the product maintains integrity and flow for extended periods. Exposure to open air or direct sunlight can compromise both physical characteristics and chemical purity, particularly in larger, bulk containers where minor condensation remains a risk. That led us to develop vacuum-sealed, inert gas-flushed alternatives for partners with especially long shipping or storage times.
Our experience says that small differences in quality, lot-to-lot uniformity, and supply reliability become more critical as projects mature. We’ve engineered our workflow not only for nominal purity, but for confidence across multiple batches and production cycles. Chemists planning multi-step syntheses, scale-up processes, or regulatory submissions rely on uninterrupted supply and complete transparency about each batch, not just a technical sheet.
Clients in pharmaceuticals ran into surprise phase changes or reactivity issues using off-brand or resold material that originated outside a manufacturing environment. This was common among startup teams or contract researchers evaluating suppliers only by price and quick lead times. Out of several remediation stories, one stands out: a customer’s trial batch from a web-based reseller caused batch failure due to higher-than-spec residual fluoride. Our direct engagement with their technical team traced the specific contaminate to a storage problem at another site—an avoidable setback if buying from a direct producer. That episode laid the groundwork for our current customer support system, which includes technical troubleshooting and direct feedback loops.
Every chemical process meets unanticipated hurdles, even with well-established intermediates. Years ago, we hit snags with dehalogenation byproducts forming during high-temperature stages. Initial attempts to modify reaction time and temperature didn’t fully resolve the problem. Involving our R&D and scale-up staff together, we tested a set of purity-boosting crystallization solvents and adjusted pH and seed charge ratios, eventually suppressing unwanted side reactions. Transparent dialogue between production and client chemists often uncovers these issues fast—one partner caught a sharp spike in an off-target byproduct using a new analytical method. Together, we sampled the process stream, tracked the origin, and revised pre-treatment steps to prevent recurrence.
Input cost volatility in specialty chemicals remains a pain point, both in procurement and supply planning. To buffer customers against disruptive pricing shifts, we contracted forward on key fluorinating reagents and established a secondary supply route for the core pyridine starting material. That lets clients lock in volume purchases or forecast costs over larger projects, building trust in long-term partnerships rather than one-time sales.
The world of custom synthetics moves fast: regulatory changes, new synthesis routes, and performance requirements evolve rapidly with new discoveries. We’ve received requests to adjust specification ranges, particle size, moisture limits, or even packaging methods based on specific downstream processes or target market needs. Sometimes, these changes reflect regulatory filings that demand trace documentation, or they may respond to efficiency needs during formulation or process validation.
Instead of formulaic batch production, we build flexibility into our upstream raw material checks and batch records, so quality adapts to new guidelines without major delays. During a recent switch in EU API regulations, pharmaceutical clients altered their impurity profiles’ reporting requirements; we brought online LC-MS and expanded GC testing capabilities to provide the trace analytical data and documentation needed. The shift required resources, but the result was stronger customer retention and greater participation in collaborative R&D.
Supply chain disruptions exposed a fragility in chemical workflows during recent years. Looking at delayed shipments or lost product under global logistics pressure, many downstream processors and R&D directors reached out, asking for verified chain of custody, real-time status updates, and batch-level tracking. We responded by refining our shipping documentation, scanning batch numbers into digital logs and automating notifications at each transfer point.
Frequent communication with customers ensures that if there are shipment delays or customs hold-ups, both sides can adapt before any real project risks develop. That open channel—absent from tradable or brokered material supply—has become central to ongoing commercial relationships and confidence in the entire supply chain.
Bringing a product like 2,6-difluoro-3-pyridinecarboxylic acid from small-scale synthesis to kilograms or metric tons involves more than repeating a reaction and bottling the outcome. Each scale jump involves unique equipment, safety protocols, environmental controls, and process adjustments. With this compound, intricate steps—such as precise fluorination and carboxylation under controlled conditions—require both robust SOPs and continual learning from batch history.
We keep an eye on developments in fluorination technology, greener reaction conditions, and improved separation techniques. The regulatory climate continues changing, too. Overlapping recommendations from European, North American, and Asian authorities require that we maintain detailed records, supply chain mapping, and comprehensive documentation for every lot. Customers appreciate the ability to reference these records during audit visits, periodic reviews, or as part of regulatory filings and submissions.
Increasing collaboration with both academic and commercial labs keeps us attuned to shifts in demand and technical requirements. For example, we’ve provided small lots for university researchers characterizing novel catalytic cycles or developing advanced biomedical coatings. Feedback from syntheses, including failed attempts or scale-up hiccups, directly influences our process improvements—an ongoing loop where lessons from the field accelerate technical progress for every customer.
Our job doesn’t end at synthesis or shipping; we field questions about every step and are ready to troubleshoot when project directions shift or complications emerge. Every lot ships with full analytical summaries and a documented chain of production. Should a downstream synthesis reveal unexpected anomalies, we dive into the root cause, sometimes running side-by-side analyses or parallel pilot batches to isolate contributing variables.
We’ve encountered times where a project’s critical path rested on real-time troubleshooting support or immediate access to replacement material. Our direct oversight on inventory and logistics makes those pivots possible. The manufacturing environment means every inquiry finds a human with actual process experience, not just a paper trail.
From initial R&D orders to mature product supply, we adapt sourcing, documentation, and technical support to each requester’s workflow. The real-world challenges we solve and the feedback loop with our partners fuel the next phase of both process innovation and customer trust.
Looking over the journey with 2,6-difluoro-3-pyridinecarboxylic acid, value grows not only from molecular structure or measured purity. The trust our customers place in the material’s performance, batch-to-batch continuity, technical transparency, and responsive service matter most over the lifespan of a project. Every kilogram delivered reflects lessons learned at the bench, in the plant, and through close collaboration with real-world chemists across the globe.
This compound continues to draw new discovery and application, not only because of inherent properties but equally because of an evolving system built around reliability, openness, and practical support. Every innovation, troubleshooting session, and rigorous quality check leaves a tangible mark—one that reinforces why a direct relationship with the manufacturer pays dividends for those seeking more than just a commodity.