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HS Code |
476470 |
| Chemical Name | 2,6-Dichloropyridine-3-carboxamide |
| Molecular Formula | C6H4Cl2N2O |
| Cas Number | 7154-54-7 |
| Appearance | White to light yellow powder |
| Melting Point | 210-215 °C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Inchi | InChI=1S/C6H4Cl2N2O/c7-4-2-1-3(6(9)11)5(8)10-4/h1-2H,(H2,9,11) |
| Smiles | C1=CC(=NC(=C1C(=O)N)Cl)Cl |
| Storage Conditions | Store in a cool, dry place, tightly closed container |
| Synonyms | 2,6-Dichloro-nicotinamide |
| Ec Number | 230-472-1 |
As an accredited 2,6-Dichloropyridine-3-carboxamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed in a 100g amber glass bottle, labeled "2,6-Dichloropyridine-3-carboxamide," with hazard information and batch details. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 2,6-Dichloropyridine-3-carboxamide is packed in 440 kg fiber drums; total 16 tons per container. |
| Shipping | 2,6-Dichloropyridine-3-carboxamide is shipped in tightly sealed containers to prevent moisture and contamination. It is typically packaged in amber bottles or HDPE containers, cushioned for safe transit. The shipment complies with relevant chemical safety regulations, including appropriate labeling and documentation for classification, handling, and emergency procedures. Store and transport at ambient temperature. |
| Storage | 2,6-Dichloropyridine-3-carboxamide should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from direct sunlight and moisture. Store at room temperature and ensure proper labeling. Handle with appropriate personal protective equipment to prevent skin and eye contact, inhalation, or ingestion. |
| Shelf Life | 2,6-Dichloropyridine-3-carboxamide is stable under recommended storage conditions; shelf life is typically 2–3 years when stored properly. |
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Purity 99%: 2,6-Dichloropyridine-3-carboxamide with 99% purity is used in pharmaceutical synthesis, where it ensures high yield and low impurity formation. Molecular weight 192.01 g/mol: 2,6-Dichloropyridine-3-carboxamide with a molecular weight of 192.01 g/mol is used in agrochemical formulation, where precise dosing is facilitated for consistent biological activity. Melting point 200°C: 2,6-Dichloropyridine-3-carboxamide having a melting point of 200°C is used in high-temperature reaction processes, where it provides thermal stability and robustness. Particle size D90 < 50 µm: 2,6-Dichloropyridine-3-carboxamide with particle size D90 less than 50 µm is used in solid dispersion preparation, where it promotes uniform mixing and dissolution rates. Stability temperature up to 120°C: 2,6-Dichloropyridine-3-carboxamide stable up to 120°C is used in intermediate storage conditions, where it maintains chemical integrity and minimizes degradation risks. Water content < 0.5%: 2,6-Dichloropyridine-3-carboxamide with water content below 0.5% is used in moisture-sensitive syntheses, where it prevents side reactions and improves reproducibility. HPLC assay ≥ 98%: 2,6-Dichloropyridine-3-carboxamide tested by HPLC assay ≥ 98% is utilized in active pharmaceutical ingredient production, where it ensures compliance with regulatory standards. Residual solvent < 500 ppm: 2,6-Dichloropyridine-3-carboxamide with residual solvent below 500 ppm is used in fine chemical manufacturing, where it supports product safety and quality for downstream use. |
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For years, our facility has supported custom chemistry with the production of 2,6-Dichloropyridine-3-carboxamide, a compound that carves out a specific space in our catalog given its straightforward structure and the reliability it offers in more demanding synthesis applications. The core skeleton includes a pyridine ring with chlorine atoms at the 2 and 6 positions, plus an amide group at position 3. This arrangement matters—every detail of substitution, from ring halogenation to polar amide positioning, influences its role when inserted into larger synthesis schemes.
On our production floor, batch consistency and control over impurity profiles come up not as marketing lines, but as daily engineering targets. Each run demands precise temperature ramps and measured reagent addition. We have seen firsthand how minor deviations ripple down to yield, solubility, and — ultimately — suitability in downstream drug or crop-protectant manufacturing. We supply 2,6-Dichloropyridine-3-carboxamide as a pale powder with particle size tailored by final grinding, and we keep our moisture content low to avoid caking and flow issues in automated systems.
We make this compound for customers who value material they can trust to avoid side reactions. Our standard model features a minimum purity of 98%, achieved by column chromatography and analytical HPLC monitoring. Impurities, particularly persistent halogenated byproducts or over-chlorinated analogs, lead to headaches in scale-up if not watched closely. With strong internal controls and regular GC-MS checks, we can pick up on out-of-spec shifts before they trigger yield loss in downstream pilot trials.
Bulk densities, color, and melting point all tie into ease of use for plant chemists. A sudden deviation here — for example, a batch with a lower melting point or sticky feel — tends to point toward either incomplete drying or unrecorded process fluctuations. From years of feedback, we know that crystalline, free-flowing granules save labor on both measuring and tank charging.
Customers rely on 2,6-Dichloropyridine-3-carboxamide mainly as a building block in the agrochemical and pharmaceutical sectors. Most of the requests coming through involve either conversion to more elaborate ring systems or straightforward derivatization to amide- or ester-linked products. The compound’s dichloro substitution pushes reactivity in nucleophilic aromatic substitution while the carboxamide group enables amidation, coupling, or even directed ortho-metalation. Process teams report smoother routes to final targets in many synthetic trees where clogging, side chlorination, or solubility limits would otherwise bog down early steps.
Traditional pyridines lacking full halogenation don’t deliver the same range of reactivity. For example, if only one chlorine atom is present, nucleophilic substitution slows, and selectivity issues creep up in later transformations. Too many halogens crowd the ring, making it less cooperative in subsequent coupling stages. Tuning the core to two chlorines brings a sweet spot: robust enough to block unwanted metabolic transformation in agrochemical development, but still open to clean, predictable modification.
We have seen this compound used in new anti-infective research, plant health product prototypes, and concept pesticides—a handful of which progressed past early screening thanks in part to the reliable downstream behavior of our 2,6-Dichloropyridine-3-carboxamide. Repeat orders from these sectors keep us vigilant; feedback from purification teams, biologics groups, and analytical labs all cycle back to continual process improvement.
We often compare our mainstay to several close cousins—mono-chlorinated and tri-chlorinated pyridine carboxamides stand out as the most common benchmarks. Where others see basic similarities, we know through lab trials and scale-ups that even a lone ring substitution swap shifts the reactivity in catalytic couplings, hydrogenations, or halide redistributions.
Mono-chloro analogs tend toward ambiguity in selectivity. That means more by-product, extra column passes, and higher solvent usage per kilo of final intermediate. By dialing in two ring chlorines, we support cleaner single-step transformations. Tri-chloro versions, produced elsewhere by specialty shops, often hit solubility snags or require exotic bases in downstream N-arylation. That elevates both process risk and cost.
In our experience, the double-chloro, amide-functionalized ring sees substantially fewer analytical red flags when examined by NMR, LC-MS, or X-ray crystallography compared with adjacent systems. It helps shave unexpected variables out of multi-step compound campaigns.
From a manufacturing and logistical angle, safety rightly absorbs a major slice of our attention. 2,6-Dichloropyridine-3-carboxamide’s crystalline nature makes dust control a recurring operational point. We maintain enclosed transfer and dust extraction during grinding, not out of regulatory compliance ritual, but because repeat exposure to its fine particles irritates respiratory tissues for operators. PPE standards stem from incident investigations and close calls from the pre-modern plant era.
Handling this material also calls for attention to chemical compatibility. Most customers request it dry-packed, with nitrogen blanket if air sensitivity is a concern downstream. While this compound earned a reputation for chemical stability compared to other pyridine derivatives, thermal exposure above 160°C kickstarts slow decomposition and potential short-chain amide hydrolysis. Real-world storage in most plants (controlled room temperature with low humidity) matches the way we move it from mill to shipping dock.
Container selection emerges as crucial for bulk buyers. Polyethylene drums with anti-static lining fend off moisture ingress and minimize static spark risk. We routinely train carriers on correct drum handling for Class III chemicals—not because regulations insist, but because small lapses in the field cause leaks and headaches, both for us and for anyone using our product in a pilot or plant run.
Testing against the spec sheet marks the start, not the end, of our commitment. Each lot ships with batch impurities characterized by HPLC and GC, and atypical profiles trigger investigation. We capture stability data for each manufactured batch—smaller, recurring customers often ask for these to support regulatory filings or in-house qualification.
Long-term relationships with customers develop not from initial order performance, but from responding quickly if a batch deviates, a standard slips, or an audit flags something new. We provide full certificates of analysis based on real-time, batch-specific data. If a customer ever triggers a non-conformance ticket, we close the loop with both replacement product and process modification. It’s a continuous conversation between our plant, our QC team, and the chemists actually working up the material in scale.
Our manufacturing operation keeps a close eye on yield efficiency, solvent recovery, and energy use throughout the main synthetic process. Over the last decade, we have shifted from batchwise to semi-continuous flows on the key halogenation step, which has driven not only cost reductions but also lower impurity profiles. These investments grew from both internal goals and external audit feedback.
Polymer-lined reaction setups, real-time IR monitoring, and digital data logging sharpen our ability to head off process drift, and any change in our SOP triggers a new hazard analysis. Sustainability efforts have driven us to recycle chlorinated solvents wherever possible; the tighter control reduces both waste and overhead.
Over the years, we learned the hard way that recycled waste streams sometimes degrade purity beyond acceptable limits, so any resin used for solvent cleaning passes QC before touching product workups. By tracking key quality metrics, we can spot developing issues long before they would ever compromise a customer's process.
Our purchasing department maintains links with raw material producers and transporters, tracking seasonal and regulatory changes that affect amide precursor and halogen feedstock supply. Natural disasters, price shocks, or sudden customs shifts occasionally compress lead times or force last-minute search for alternate suppliers. Maintaining supplier transparency and running qualification batches with new sources repeatedly safeguards against these risks.
Close partnerships with customers — especially in pharma and agchem — mean we face our share of rush requests, pilot-scale upsizing, or just-in-time logistics. Last-minute troubleshooting, respecification, or blending to tighter particle windows keeps both our quality team and operations on alert.
Retrospective reviews, both annual and per-customer, feed into continuous improvement meetings. A spike in customer sample rejections gives an early sign that a new issue in synthesis might require a process tweak or extra purification.
A large part of the value in 2,6-Dichloropyridine-3-carboxamide, from our vantage point on the plant floor, involves its balance between properties needed by R&D chemists and the practical parameters that drive high-throughput production. Its physical stability eases day-to-day handling without need for heavy refrigeration, reducing overall shipping costs and making it a low-maintenance material in any formulation lab.
We maintain a focus on lot-to-lot uniformity, which frequently wins positive comments from customers reporting seamless transitions between development and commercial scale batches. Some alternative halogenated pyridines generate troublesome fumes, elevate storage risk, or lose activity through ring hydrolysis; experience has shown this compound avoids those pitfalls, especially when customs or transport time extends beyond the usual window.
For formulators needing more aggressive reactivity, some triple-chlorinated pyridines surpass this product, but reliability, scalability, and cost-effectiveness keep 2,6-Dichloropyridine-3-carboxamide as a practical default wherever its profile fits the broader synthetic plan.
Dustiness and static electricity present real operational risks during grinding, sifting, and pneumatic transfer; we control these with local exhaust ventilation, conductive hoses, and anti-static flooring in the packing area. Batching machinery undergoes inspection after every shift, and cleaning logs are reviewed daily by supervisors. We know from experience that lax control here can lead to product cross-contamination, both a safety and a compliance risk.
Solvent odor and minor off-gassing accompany large-scale synthesis, particularly in open-vessel reflux or during initial halogenation. We have invested in reactor covers, high-throughput scrubbing systems, and closed-loop air monitoring to minimize workplace exposure and environmental loss. Process engineers work directly with our EHS team whenever unusual readings crop up—a partnership that avoids surprises in either emissions reporting or regulatory review.
Occasionally, an aging batch picks up extra water or slight discoloration. To prevent this, desiccant packs and real-time humidity sensing form part of every shipment packet. Anomalies get flagged both by automated cameras and final manual inspection in the dispatch zone.
Our technical team keeps close contact with procurement, quality, and research groups at downstream facilities. Whether a lab hits a wall with process yield, or a plant flags a new impurity signal, we share not only analytical data but also help rework processes or suggest storage changes that fit local circumstances. In the last year, two major customers requested on-site visits for troubleshooting scale-up snags, and we dispatched both production and R&D leads to get a firsthand look at what’s happening outside our walls.
This hands-on, back-and-forth approach delivers better outcomes than impersonal paperwork or distant helplines. Growth in product interest overseas has led us to launch a multilingual document support effort, keeping data, COAs, and shipment details available for global regulatory and lab teams.
As regulatory frameworks for chemicals evolve, demand for cleaner downstream transformations and fully traceable intermediates continues rising. We are currently piloting greener nitrile conversion routes and exploring chlorine alternatives in response to customer requests for more sustainable processes. Every formulation change or process improvement cycles through joint review with both our QC lab and, increasingly, customers’ own technical teams.
The persistent goal remains the same: provide trustworthy, batch-consistent 2,6-Dichloropyridine-3-carboxamide that supports reliable R&D and full-scale manufacturing. We view compound innovation — whether through less hazardous feedstocks, tighter impurity controls, or improved downstream compatibility — not as marketing points, but as necessary steps to meet the real-world needs and challenges we’ve learned by standing side-by-side with plant and laboratory chemists.