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HS Code |
489416 |
| Chemicalname | 2,6-dichloro-3-Pyridinecarboxylic acid |
| Casnumber | 65167-44-4 |
| Molecularformula | C6H3Cl2NO2 |
| Molecularweight | 192.00 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 220-224°C |
| Solubility | Slightly soluble in water |
| Density | 1.6 g/cm3 (approximate) |
| Smiles | C1=CC(=NC(=C1Cl)C(=O)O)Cl |
| Inchi | InChI=1S/C6H3Cl2NO2/c7-3-1-2-4(6(10)11)9-5(8)12-3/h1-2H,(H,10,11) |
| Ecnumber | 613-815-7 |
| Storagetemperature | Store at room temperature |
As an accredited 2,6-dichloro-3-Pyridinecarboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A white, labeled plastic bottle containing 100 grams of 2,6-dichloro-3-Pyridinecarboxylic acid, securely sealed with a tamper-evident cap. |
| Container Loading (20′ FCL) | 20’ FCL container loading: 2,6-dichloro-3-pyridinecarboxylic acid packed in 25kg bags, palletized, total 16 metric tons per container. |
| Shipping | 2,6-Dichloro-3-pyridinecarboxylic acid is shipped in tightly sealed containers, protected from moisture and light. Packages comply with relevant safety regulations and include accurate labeling and documentation. The chemical is handled and transported as per hazardous material guidelines to ensure safe delivery and to prevent contamination, degradation, or accidental release during transit. |
| Storage | 2,6-Dichloro-3-pyridinecarboxylic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Protect it from moisture, heat, and direct sunlight. Ensure proper chemical labeling and access by authorized personnel only. Always follow local and institutional chemical storage regulations for safety. |
| Shelf Life | Shelf life of 2,6-dichloro-3-pyridinecarboxylic acid is typically 24 months when stored in a cool, dry, and sealed container. |
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Purity 99%: 2,6-dichloro-3-Pyridinecarboxylic acid with purity 99% is used in active pharmaceutical ingredient synthesis, where it ensures reliable downstream reaction yields. Melting point 207°C: 2,6-dichloro-3-Pyridinecarboxylic acid with melting point 207°C is used in high-temperature organic reactions, where it provides stable performance during thermal processing. Particle size <10 µm: 2,6-dichloro-3-Pyridinecarboxylic acid with particle size less than 10 µm is used in precision agrochemical formulations, where it enables uniform dispersion and enhanced bioavailability. Moisture content <0.5%: 2,6-dichloro-3-Pyridinecarboxylic acid with moisture content below 0.5% is used in moisture-sensitive chemical syntheses, where it minimizes unwanted hydrolysis and improves product consistency. Stability temperature up to 120°C: 2,6-dichloro-3-Pyridinecarboxylic acid with stability temperature up to 120°C is used in controlled-release herbicide production, where it maintains compound integrity throughout processing. Assay ≥98%: 2,6-dichloro-3-Pyridinecarboxylic acid with assay of at least 98% is used in custom chemical manufacturing, where it assures batch-to-batch quality for regulatory compliance. Low heavy metals <10 ppm: 2,6-dichloro-3-Pyridinecarboxylic acid with low heavy metals content under 10 ppm is used in electronic material synthesis, where it prevents contamination and ensures high purity standards. |
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At our production site, 2,6-dichloro-3-pyridinecarboxylic acid goes through a journey involving strict control, specialty equipment, and years of experience handling pyridine chemistry. This compound, often known by its CAS number 35661-58-6, starts as a candidate for high-value synthesis thanks to the unique position of its chlorine substituents. We see rising demand from pharmaceutical, agrochemical, and materials science projects, where this arrangement on the pyridine ring alters reactivity in ways that unlock new pathways for downstream modification.
Manufacturing in-house means every batch meets the purity required by clients who leverage downstream chlorination or carboxylation chemistry. Each lot reaches at least 99% HPLC assay, run through repeat crystallization and vacuum-drying, ensuring consistent results for chemists developing new formulations or scaling up existing projects.
We package 2,6-dichloro-3-pyridinecarboxylic acid predominantly as an off-white to pale yellow powder, with melting points measured consistently within the 207-212°C range. Our analytical teams control moisture content below 0.5%. Purity stays high by preventing contamination during milling, sieving, and storage, never simply trusting theoretical process yields but measuring each output. Whether a client orders by kilograms or tons, we retain reference samples for every batch, which has proven invaluable for troubleshooting and backward compatibility for customers’ evolving specs.
Proper ventilation and dust control remain key in our plants—not every organic acid produces stubborn particles, but this one can settle in awkward corners. Our air-handling engineers tackled this issue by upgrading ductwork and introducing specialized extraction filters, which has reduced downtime for cleaning and improved operator safety. Over the years, these tweaks have prevented line stoppages that inevitably creep up when organic powders escape containment.
We ship in lined fiber drums or heavy-gauge polyethylene bags, double-sealed to slow hydrolysis and avoid accidental exposure to moisture in transit. Customers sometimes ask about glass containers, but experience shows these are impractical at scale due to risk of breakage during loading. Our current packaging approach comes from lessons learned through repeated handling—not everything works on the first try, but persistent refinement keeps the workflow moving.
Numerous clients utilize 2,6-dichloro-3-pyridinecarboxylic acid as a starting material for synthesizing pharmaceutical intermediates, especially where selective halogenation enables easy functionalization at available positions. Its structure allows further substitution on the pyridine ring without unwanted side reactions. We regularly get requests for technical details on coupling this acid with amines or alcohols, which led us to develop a technical support team able to trouble-shoot application-specific problems alongside clients’ own research staff.
In crop protection R&D, this acid often emerges in synthetic routes for new pyridine derivatives. Many syntheses demand a reliable chlorine layout to steer the reactivity of subsequent transformations, whether preparing esters, amides, or intricate bi-heterocyclic products. Early on, we saw a trend toward chlorinated pyridines in herbicide development, then wider adoption as researchers pushed for higher potency at lower application rates. Choosing a tightly controlled chlorination pattern can mean the difference between predictable scale-up and expensive downstream purification headaches.
Our product occasionally finds interest in electronic materials and ligands for advanced catalysis, where the acid moiety helps anchor molecules onto various support surfaces. We have helped users resolve solubility limitations by offering insights into solvent compatibility and stability under various reaction conditions. There’s no one-size-fits-all in this field—collaborating directly with researchers lets us tailor guidance based on direct process experience, not just abstract data.
Making and using 2,6-dichloro-3-pyridinecarboxylic acid feels different compared to handling non-chlorinated variants like nicotinic or isonicotinic acid. The two chlorine atoms at positions 2 and 6 both affect how the acid dissolves, its volatility, and reactivity with common reagents. We have seen this directly on the plant floor: technicians report faster filtration compared to mono-chlorinated analogs, but slower dissolution during charging in standard solvents, especially in cold conditions.
Some users, transitioning from 4-chloro or 2-chloro-3-pyridinecarboxylic acid, report lower rates of side-product formation with the 2,6-dichloro version—likely due to the electron-withdrawing effect on the remaining open positions of the pyridine, which tends to suppress undesirable coupling reactions. These subtle effects build up during process scale-up. Early pilot batches made clear that traditional purification schemes designed for less hindered pyridine acids required more aggressive solvent washes and filtration adjustments. Manually tweaking process windows, rather than relying on lab-sourced data alone, turned out to be essential for reliable bulk manufacturing.
Moving from laboratory to plant quantities, new pitfalls always show up. We struggled with exothermic behavior during chlorination, which couldn’t simply be controlled by adjusting batch size. Our engineering team responded with staged reagent addition and improved jacket cooling on reaction vessels. By monitoring temperature continuously and introducing more granular control steps, runaway reactions went from frequent occurrences to rare events.
Effluent management posed another learning curve. Chlorinated pyridine chemistry generated waste streams that traditional treatment units handled poorly—a fact apparent only after initial test runs. Retrofitting our effluent lines, we isolated these streams for targeted neutralization and carbon treatment, which allowed us to pass stringent discharge requirements and lowered our environmental footprint. These adaptations, both practical and regulatory, came about from direct feedback between the plant, environmental teams, and local regulators.
Quality control has required refinement. Each shipment’s HPLC and GC trace links back to storage silos and operation records, not just to satisfy clients but to resolve internal debates over potential contamination sources. This traceability also builds confidence with customers—when a rare complaint does arise, we rely on batch archives to provide answers backed by data rather than guesswork.
In our experience, even small impurities in 2,6-dichloro-3-pyridinecarboxylic acid can lead to unexpected final-stage failures, low yields, or complicated post-reaction cleanups. Intermediate grade material can introduce unknowns in pharmachem synthesis, especially if the goal is regulatory submission or production under GMP. Our plant teams accept only those inputs certified for trace metals, halide residues, and organic contaminants—a protocol refined after several rounds of costly troubleshooting in earlier years.
Clients focused on fine-tuning activity of chemical library candidates have a low tolerance for material drift. Our continuous monitoring—by titration, spectrophotometry, and chromatography—keeps purity on target, so results remain consistent from first kilo to full production scale. Supplying reference samples to longstanding research collaborators, we found that stability during storage can impact performance months after delivery. We recommend keeping the acid under nitrogen or dry atmosphere if long-term storage is planned, based on storage studies tracked since early production campaigns.
Direct feedback loops with our customers allow not just technical improvement, but also deeper understanding of where product specifications must evolve. For example, one client scaling up to pilot plant level discovered changes in flowability affected their tablet press uniformity. After site visits and hands-on trials, we installed a new milling line which improved not only their performance, but also opened up additional process windows for our broader user base. This partnership mindset, forged from years on the ground, brings more long-term value than faceless supply chains.
We answer questions about reactivity, compatibility with emerging synthetic routes, or potential product modifications by leveraging our own in-house expertise. Some requests arrive as fully developed protocols seeking custom blend, while others begin as simple queries about trace impurity profiles or alternative packaging. By responding with practical, experience-driven advice, both parties avoid unnecessary delays.
On the few occasions where product properties required gradual adjustment—say, tighter particle size distribution, or elimination of specific color impurities—open communication with users accelerated the process. A laboratory can validate a change in days, but confirming stable production over multiple batches under full plant conditions takes time and commitment. This two-way relationship forms the backbone of improvements in both process safety and output quality.
In recent years, the volatility in global logistics has underscored the importance of a secure upstream supply. We source raw materials from qualified, regionally diversified vendors—after past disruptions stemming from single-source supply, we changed purchasing systems to build resilience into our workflow. Our product flow undergoes constant review against projected demand, helping ensure steady availability for research and manufacturing projects operating on tight timelines.
Environmental sustainability matters ever more to both our operation and our customers. The chlorination reactions demand careful waste management, and our in-line scrubbers, solvent recyclers, and low-emission process designs signal a firm commitment to greener chemistry. Our metrics show a steady decrease in solvent losses and improved capture of fugitive emissions over multi-year horizons, a testament to both investment and operator vigilance.
We report progress on these efforts transparently through customer audits and third-party certifications—not merely to satisfy compliance, but to prove that improvements are not just aspirational. Each new generation of process modifications reflects collaboration among plant operators, engineers, and regulatory specialists, building a culture where accountability is shared.
Experience counts for a lot in the specialty chemicals industry. Over more than a decade of running this production line, we’ve seen new synthetic pathways emerge, regulatory shifts reshape client requirements, and expanded use cases driving continual process optimization. It’s not a fixed recipe, but a set of evolving best practices.
For example, bottlenecks we once faced in solid-liquid separation, due to stubborn crystal habits, got solved through rotary vacuum filtration and iterative tweaks in solvent blend ratios. Regular feedback from the analytical lab led to more robust sampling plans—which, in turn, detected trends before they became problems.
Never treating process steps as static pays dividends. Raw material quality can shift year to year, often going unnoticed until a subtle color or logbook discrepancy flags a deeper issue. We’ve built regular requalification cycles and supplier audits into our routine, tracking data over the long haul to back up procurement decisions.
Staff training matters as much as equipment upgrades. Handling chlorinated heterocycles brings risks both to product purity and worker health. Lessons learned from production upsets pushed us to invest in better operator training, PPE, and real-time air monitoring. These changes proved their worth during routine and unplanned maintenance shutdowns, ensuring safety doesn’t become a secondary concern.
Advances in pharmaceutical discovery, crop science, and advanced materials all increasingly need unique scaffolds as synthetic building blocks. Our role as a direct manufacturer lets us translate lab-scale advances into reliable, scalable output. Over time, stable access to 2,6-dichloro-3-pyridinecarboxylic acid has proved critical for customers taking a process from trial run to commercial launch, bypassing the frustration of inconsistent or impure reagent sources.
This acid’s particular chlorination pattern unlocks routes that would stall out or yield impurities with mono- or tri-chloro forms. We see this regularly with medicinal chemistry candidates, where the position of each substituent influences both biological activity and manufacturability. Formulation chemists investing in efficiency, reducing purifications or process steps, report fewer roadblocks when starting from this precisely constructed molecule.
A core benefit to direct partnerships emerges when regulatory or process hurdles call for documentation beyond the standard certificate of analysis. As the original manufacturer, our records stretch back through every lot produced, and technical staff can access full traceability, spectral archives, and historical correspondence. This supports regulatory filings, process audits, or simple troubleshooting in a way intermediaries struggle to maintain.
Staying ahead of changing application needs calls for a long-term perspective on product and process development. Our investment in both people and plant facilities reflects persistent demand for this acid in research and production environments that value reliability and responsiveness over cut-rate cost. Some process changes happened incrementally—like optimizing reaction isolation and reducing manual cleaning times. Others, such as moving to more sustainable chlorination technology, required coordinated effort across engineering and management.
As applications diversify, we remain committed to transparent, honest dialogue across the customer base. We don’t just read market trends—we participate in them, sharing insight and learning in both directions. Refining 2,6-dichloro-3-pyridinecarboxylic acid to higher consistency, safer packaging, and lower environmental impact continues to guide how we allocate resources and define success.
From the plant floor to the research lab, producing 2,6-dichloro-3-pyridinecarboxylic acid reveals chemical manufacturing as an iterative, hands-on enterprise. Careful tuning of specifications, embracing feedback from real-world application, and investment in worker safety make all the difference. Rather than simply offering another specialty reagent, we bring the collective learning of our production teams to ongoing collaborations, tackling each new challenge with practical knowledge and care. With each batch, our reputation rides on the ability to deliver consistent, high integrity material for innovators across the chemical landscape.