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HS Code |
774994 |
| Product Name | 2,6-Dichloro-5-Fluoro-3-Pyridinecarboxlic Acid |
| Cas Number | 138379-77-4 |
| Molecular Formula | C6H2Cl2FNO2 |
| Molecular Weight | 224.99 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 157-161°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in organic solvents like DMSO and methanol |
| Boiling Point | Decomposes before boiling |
| Storage Conditions | Store at 2-8°C, keep container tightly closed |
| Synonyms | 2,6-Dichloro-5-fluoronicotinic acid |
| Smiles | C1=C(C(=NC(=C1F)Cl)C(=O)O)Cl |
| Inchi | InChI=1S/C6H2Cl2FNO2/c7-3-1-4(8)5(6(11)12)10-2(3)9 |
As an accredited 2,6-Dichloro-5-Fluoro-3-Pyridinecarboxlic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with tamper-evident cap, labeled “2,6-Dichloro-5-Fluoro-3-Pyridinecarboxylic Acid, 25g,” featuring hazard warnings and batch details. |
| Container Loading (20′ FCL) | 20′ FCL container loads 2,6-Dichloro-5-Fluoro-3-Pyridinecarboxylic Acid, securely packaged in drums or bags to ensure safe transit. |
| Shipping | 2,6-Dichloro-5-Fluoro-3-Pyridinecarboxylic Acid is shipped in tightly sealed containers, protected from moisture and light. It is labeled as a hazardous chemical and is transported in compliance with relevant regulations, including UN, IATA, and DOT standards. Appropriate documentation and safety data sheets (SDS) accompany each shipment for safe handling. |
| Storage | 2,6-Dichloro-5-Fluoro-3-Pyridinecarboxylic Acid should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area, away from incompatible substances such as strong bases and oxidizing agents. Protect the chemical from moisture and direct sunlight. Always ensure proper labeling and store at room temperature, following all relevant safety regulations for hazardous chemicals. |
| Shelf Life | 2,6-Dichloro-5-Fluoro-3-Pyridinecarboxylic Acid typically has a shelf life of 2 years when stored in a cool, dry place. |
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Purity 98%: 2,6-Dichloro-5-Fluoro-3-Pyridinecarboxlic Acid with 98% purity is used in active pharmaceutical ingredient synthesis, where high purity ensures minimal impurities in the final drug product. Melting Point 185°C: 2,6-Dichloro-5-Fluoro-3-Pyridinecarboxlic Acid with a melting point of 185°C is used in agrochemical intermediate manufacturing, where thermal stability allows for high-temperature processing. Particle Size < 50 μm: 2,6-Dichloro-5-Fluoro-3-Pyridinecarboxlic Acid with particle size below 50 micrometers is used in fine chemical formulation, where small particle size ensures uniform dispersion. Moisture Content < 0.5%: 2,6-Dichloro-5-Fluoro-3-Pyridinecarboxlic Acid with moisture content under 0.5% is used in catalyst production, where low moisture prevents unwanted side reactions. Stability Temperature up to 120°C: 2,6-Dichloro-5-Fluoro-3-Pyridinecarboxlic Acid with stability up to 120°C is used in electronic chemical processing, where elevated stability enables reliable device fabrication. Assay ≥ 99%: 2,6-Dichloro-5-Fluoro-3-Pyridinecarboxlic Acid with assay greater than or equal to 99% is used in material science research, where high assay leads to reproducible experimental outcomes. Solubility in Acetone: 2,6-Dichloro-5-Fluoro-3-Pyridinecarboxlic Acid soluble in acetone is used in solvent-based polymer synthesis, where good solubility allows efficient blending and mixing. |
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2,6-Dichloro-5-Fluoro-3-Pyridinecarboxylic Acid doesn’t just leave our reactors as another barcode in a catalog. Every batch reflects a series of precise chemical choices and thorough process control built on years watching pyridine derivatives pass from raw intermediate to active specialty chemical. With years of handling pyridinecarboxylic acids, we know that the right balance of substituents can change a routine intermediate into a linchpin for innovative synthesis work.
This compound’s structure—anchored by two chlorine atoms and a single fluorine attached to a pyridine ring—creates distinct properties. The carboxylic acid group at the 3-position offers reliable downstream functionalization. Each halogen atom influences reactivity and solubility, and these become evident when bench chemists are trying to push a yield above 98% or purify without sacrificing time on postreaction work-ups.
We’ve learned that purity makes or breaks efficiency in active pharmaceutical ingredient (API) synthesis and agrochemical formulations. Our typical output runs with purity above 98% (HPLC assay) because impurities cause unnecessary headaches: they complicate crystallization, clog columns, and force redundant filtering. Moisture content is always kept low, minimizing hydrolysis. Modern production lines let us ensure minimal residual solvents, in line with international regulatory limits.
Reliable specifications mean more than high numbers on a certificate. Grainy substances slow down filling equipment and can hold on to trace mother liquor. Finer, free-flowing powder supports rapid transfer, cleaner handling, and avoids cross-contamination when moving lots from bulk containers to reactors. Having observed batch-to-batch issues early in our careers, physical consistency is as non-negotiable as the chemical profile.
Many clients searching for pyridinecarboxylic acids run through a mental checklist: halogen pattern, ease of substitution, compatibility with catalytic systems, and downstream yields. This molecule, by design, combines electron-withdrawing effects from both chlorine and fluorine substituents. The impact? Heightened selectivity in electrophilic substitution, maintained integrity through multi-step synthesis, and improved environmental stability in final products.
You’ll find it in both high-throughput pharmaceutical discovery research and in scaling up fine chemicals. In crop protection, the unique halogen arrangement opens doors to bioactivity modulation, often serving as a scaffold to attach sidechains that tweak activity or solubility. Researchers at the bench, sourcing small quantities for method development, later call us for ton-scale production. They recognize that keeping consistent quality across scale reaps significant cost savings on regulatory compliance and downstream validation.
We see most usage scenarios split between pharmaceutical intermediate synthesis and agrochemical development, though custom manufacturing remains active for specialty catalysis and materials science. In medicinal chemistry, the 3-carboxy group often becomes an entry point for amide formation or esterification. Downstream, the molecule participates in Suzuki couplings, nucleophilic aromatic substitutions, or serves as a platform for creating diverse heterocyclic libraries.
Process chemists running pilot plants value predictable behavior—no surprise byproducts from unstable halogen positions, no unanticipated reactivity during chlorination, and consistent melting point for in-process QC checks. Agrochemical developers focus on field performance and toxicological profiles, so trace metal content and residual solvents aren’t just data points but critical factors controlling regulatory acceptance.
Direct production brings unique clarity to quality control and problem-solving. Distributors often serve as a useful stopgap but rarely relay feedback from plant operators who see, smell, and measure the shifts caused by different operating parameters. Our own investment in process optimization isn’t driven purely by cost; we have watched clients’ projects stumble on late-stage impurities or batch scale-out failures triggered by small specification drifts.
A transparent manufacturing process lets users ask for documentation beyond certificates of analysis—we provide impurity profiles, HPLC chromatograms, batch records, and customer audits for critical supply chains. Having these resources not only builds confidence but saves weeks during regulatory review or tech transfer to commercial teams.
The bulk of pyridinecarboxylic acids can be categorized by their position and choice of substituents. Many common derivatives swap out chlorine for methyl or nitro groups, or cluster all halogens on adjacent carbons. Few substitutions deliver both the reactivity and stability that the 2,6-dichloro-5-fluoro arrangement brings. The result is nuanced: chlorine at both ortho positions shields the nitrogen, reducing side reactions during nucleophilic substitution at neighboring carbons, while fluorine at the 5-position opens different synthetic vectors—especially when electron-deficient systems are a must.
This structure stands up to harsher reaction conditions without decomposing or losing yield in the core step. Not all analogues behave this way. Substituting with bulkier groups drives up cost and often complicates purification. Lighter halogens give more control and flexibility—chemists can swap fluorine or chlorine through well-studied substitution reactions, offering libraries of derivatives without needing to overhaul process chemistry.
Chemical synthesis at scale breaks down into a thousand small details that non-producers rarely notice. We clean our reactors to reduce cross-contamination and track incoming raw material purity to catch variances before they hit the main line. Using proprietary coupling reagents and finely tuned temperature profiles, we shave hours off reaction time. Optimizing pH in work-up reduces hydrolysis, so yields hold steady between batches.
Any experienced operator can tell you that batch yield isn’t a fixed number. It’s the outcome of choosing the right condensation temperature, fine-tuning catalyst loadings, and adjusting purification priorities based on past runs. In our production, every process is iteratively improved: solvent swapping, agitation speeds, in-process HPLC checks. Documentation from last year’s campaign guides this year’s adjustments, so process drift is minimized, and clients get the reliability they depend on.
From raw material sourcing through waste stream management, our involvement with 2,6-dichloro-5-fluoro-3-pyridinecarboxylic acid extends from chemical engineering to environmental stewardship. Multistep processes often generate mother liquors rich in halogenated byproducts, so we built containment and recovery systems that feed distillates back into upstream syntheses or neutralize them on site, lowering total emissions.
Packaging rarely attracts the limelight, but in practice, proper container lining and inert atmospheres prevent decomposition during longer shipments or storage. Dry nitrogen purges work to preserve chemical structure, while triple-bagged units reduce operator exposure and dust ingress. Every practice, from labeling protocols to tracking unique batch IDs with in-house systems, eliminates guesswork and lets clients trace every step from drum to lab bench.
Navigating international regulatory landscapes requires more than filling out a few forms. Government agencies and multinational customers expect detailed documentation, often running hundreds of pages. We maintain validated analytical methods, not just on paper but actively deployed for ongoing production, and tie these to digital archives for rapid, auditable data retrieval.
The evolution of REACH, EPA, and similar regulations reflects a push toward safer handling, better traceability, and well-documented impurity profiles. Adapting to these standards doesn’t happen overnight, so we stay ahead by running preemptive testing on heavy metals, trace solvents, and potential genotoxins. When asked for additional chromatographic proof or batch stability data, we root our answers in evidence, not guesswork.
Every year brings new requests—tighter purity cuts, custom particle sizing, or engineered blends. Balancing these orders with process consistency isn’t a theoretical concern, but a day-to-day operational necessity. Our teams work directly with chemists and process engineers on customer projects, bringing lessons learned on pilot-line failures or scale-up complications back to our methods group. This feedback loop lets us refine our production and anticipate new industry needs.
Take the example of method-driven modifications. If a partner wants a tailored impurity profile, we adjust purification or even the underlying synthetic route, rather than simply trying to re-run fractions off the failed batch. Wide-scale rollouts of a process change only happen after several cycles of lab, then kilo, then pilot plant validation—with side-by-side comparisons of yields, stability, and impurity drift.
We back every batch with qualified chemists who have actually run the reactions, troubleshooting alongside customers during tech transfers or scale-ups. Remote meetings with technical experts provide troubleshooting that goes beyond generic advice. Teams walk through real scenarios: column plugging, phase separations, batch hold-ups, or minor color changes that sometimes hint at deeper issues.
Experience also shows us where the documentation falls short of lived reality. Specifications, no matter how tight, can’t anticipate the quirks of every downstream system. So, customer feedback and firsthand knowledge blend to solve issues in real time. We draw on experiences from hundreds of campaigns, offering advice specific to the synthetic pathway, not just the chemical at hand.
No process is perfect every cycle, and setbacks teach us more than any success. Early rounds of scale-up often exposed new impurity profiles, triggering investigation into side reactions and off-spec batches. Adjusting crystallization temperatures, repeatedly washing and re-drying powders, or tuning catalyst concentrations helped build a process where deviations become rare events.
In some cases, customer needs forced us to explore new synthetic routes, switching out organometallics for safer, greener alternatives or moving from batch to flow chemistry to control exotherms and improve heat transfer. These pivots added upfront work, but the resulting routes offer better product quality, safer operations, and improved compliance.
With the rise in environmental scrutiny, chemists ask tougher questions. How is waste minimized? What about energy footprints? Our site recycles solvents where feasible—recovering, purifying, and reusing them through closed-loop systems. By mapping energy use during exothermic and endothermic steps, we cut heating and cooling costs, resulting in more sustainable production for every ton shipped out.
Wastewater treatment addresses halogenated effluents, using advanced oxidation, carbon treatment, and careful pH control to neutralize before discharge. Technical choices made at the reactor have direct consequences for environmental compliance, so ongoing upgrades remain a standing project.
The world of pyridine derivatives continues to evolve, with new methodologies—transition-metal catalysis, C-H activation, organofluorine chemistry—reshaping how researchers and manufacturers approach target compounds. We partner with academic consortia, joining collaborative programs in green chemistry, halogen functionalization, and continuous process development, sharing data and receiving valuable insight into the next generation of industrial synthesis.
Latest advances in analytical techniques, such as ultra-high-resolution mass spectrometry and two-dimensional NMR, let us maintain a cutting-edge grasp on trace impurity monitoring. We incorporate these tools directly into the QC pipeline, catching nuanced changes before they impact downstream users.
The last few years tested supply chain resilience worldwide, yet strong manufacturer relationships proved their worth. With our own warehousing, in-house logistics management, and well-coordinated shipping partners, we stabilized delivery even as upstream fluctuations occurred. On-the-ground communication with chemical shippers, customs agents, and regulatory departments made sure paperwork matched deliveries, containers remained intact, and timelines met project milestones.
Transparent updates on order and delivery status give partners realistic timelines. We maintain emergency stocks of key raw materials, which, when shortages strike, allow us to fulfill contracts without delay.
Science alone doesn’t keep products on spec or customers satisfied—teams of people do. Experienced engineers, plant operators, and laboratory analysts constantly inspect every step. Supervisors provide feedback on process improvements, plant workers notice aberrant smells or colors, and new hires challenge existing methods, prompting re-evaluation and improvement.
Plant tours, customer audits, and regular cross-training build a workforce adept in both chemical fundamentals and practical production. Our continuous investment in training and knowledge sharing pays off every time a new requirement arises or a novel intermediate hits the pipeline.
2,6-Dichloro-5-Fluoro-3-Pyridinecarboxylic Acid stands as a direct product of technical refinement, investment in people, and unending process improvement. Its combination of halogen substituents gives it a set of properties matched by few other pyridinecarboxylic acids—offering not just routine reactivity but reliability, flexibility in synthesis, and consistent performance at all scales. Thousands of kilograms leave our facility each year, destined for research, pharmaceutical production, crop protection, and special intermediates—each batch backed by the hands-on craftsmanship, knowledge, and experience accumulated on the floor.
The work doesn’t stop at the drum. Every reaction run, every process improvement, and every customer conversation guides tomorrow’s manufacturing choices, shaping a product and process that truly meet the needs of today’s innovators in fine and specialty chemical fields.