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HS Code |
456557 |
| Iupac Name | 5-chloro-6-oxo-1,6-dihydropyridine-3-carboxylate |
| Molecular Formula | C6H4ClNO3 |
| Molecular Weight | 173.56 g/mol |
| Appearance | White to off-white powder |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Cas Number | 89944-94-9 |
| Smiles | C1=C(C=NC(=O)C=C1Cl)C(=O)O |
| Inchi | InChI=1S/C6H4ClNO3/c7-4-1-3(6(10)11)2-8-5(4)9/h1-2H,(H,10,11) |
| Synonyms | 5-chloro-6-oxo-1,6-dihydro-3-pyridinecarboxylic acid ester |
| Storage Conditions | Store in a cool, dry place |
As an accredited 5-chloro-6-oxo-1,6-dihydropyridine-3-carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g sample of 5-chloro-6-oxo-1,6-dihydropyridine-3-carboxylate is supplied in a sealed amber glass bottle with labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Standard 20-foot containers efficiently loaded with securely packed 5-chloro-6-oxo-1,6-dihydropyridine-3-carboxylate, maximizing cargo safety and quantity. |
| Shipping | **Shipping Description:** 5-Chloro-6-oxo-1,6-dihydropyridine-3-carboxylate is shipped in tightly sealed, chemical-resistant containers to prevent contamination and degradation. The package is clearly labeled with hazard and handling information, and is transported in compliance with relevant safety regulations, including temperature control if required. Ensure proper documentation and emergency contact details are included. |
| Storage | Store 5-chloro-6-oxo-1,6-dihydropyridine-3-carboxylate in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong acids or bases and oxidizing agents. Follow standard laboratory safety practices and local regulations for chemical storage. Store at room temperature unless otherwise specified by the manufacturer. |
| Shelf Life | Store 5-chloro-6-oxo-1,6-dihydropyridine-3-carboxylate in a cool, dry place; shelf life typically 2–3 years when unopened. |
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Purity 98%: 5-chloro-6-oxo-1,6-dihydropyridine-3-carboxylate with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and reproducibility of active compound formation. Melting Point 215°C: 5-chloro-6-oxo-1,6-dihydropyridine-3-carboxylate with melting point 215°C is used in high-temperature organic catalysis, where it provides thermal stability for continuous processing. Particle Size <10 μm: 5-chloro-6-oxo-1,6-dihydropyridine-3-carboxylate with particle size less than 10 μm is used in fine chemical reagent formulations, where it enhances solubility and reaction kinetics. Stability Temperature 120°C: 5-chloro-6-oxo-1,6-dihydropyridine-3-carboxylate with stability up to 120°C is used in chemical storage environments, where it maintains structural integrity over time. Molecular Weight 186.58 g/mol: 5-chloro-6-oxo-1,6-dihydropyridine-3-carboxylate with molecular weight 186.58 g/mol is used in analytical reference standards, where it delivers precise quantification and calibration. Assay ≥99.0%: 5-chloro-6-oxo-1,6-dihydropyridine-3-carboxylate with assay ≥99.0% is used in laboratory research applications, where it contributes to reliable and consistent experimental data. Water Content <0.5%: 5-chloro-6-oxo-1,6-dihydropyridine-3-carboxylate with water content below 0.5% is used in anhydrous synthesis procedures, where it prevents unwanted hydrolysis and byproduct formation. |
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Inside the heart of our production lines, certain molecules see real work. One that stands out among contemporary intermediates is 5-chloro-6-oxo-1,6-dihydropyridine-3-carboxylate—an intermediate we've watched from birth in our reactors through every handling stage to the final barrel. With years of practice and constant troubleshooting, every kilogram we ship reflects checks, lessons learned, and improvements pieced together batch by batch.
The backbone of this carboxylate borrows from the pyridine family. Chemists gravitate towards this motif for its reactivity, manageable downstream reactions, and recognition in heterocyclic synthesis. The specific placement of the chloro and oxo groups on the ring directs selectivity in follow-up reactions, which is key for anyone aiming for precision modifications. The stabilized carboxylate at position three further opens up esterification, amidation, or even salt formation under the right circumstances, so projects can branch out without unwanted side-reactions. It’s the subtleties of this structure—and how they respond under varying temperature, pH, and solvent—that guide why formulators and researchers choose this molecule over generic or less functionalized analogs.
Production starts with tight control of input materials and reaction conditions. Chloro activation and oxo introduction both challenge even automated reactors—especially on a scale beyond the flask. Right from raw material screening, our chemists noticed that batch reproducibility comes down to precision in timing and solvent ratios; a misjudgment midway through the process could promote impurity formation, complicating isolation. We monitor both the target’s yield and critical impurity profiles after every batch, using HPLC and mass spectrometry. It’s not just about hitting a spec sheet—customers end up fighting problems down the road if we cut corners.
Physical form sets expectations for further handling. Customers have told us that off-spec powdering or caking slows charging into reactors and hinders mixing in solvents. That feedback led us to continuous improvements: we tweaked drying protocols and introduced anti-caking handling in the post-reaction stage. The typical product comes as a dry, flowable crystalline solid, pale in color, and with a melting point within a tight range to satisfy reprocessing requirements.
Purity matters more than any single number. We consistently hold this intermediate well above 98 percent by HPLC, with minimal traces of related substances. Moisture content draws equal scrutiny; a high water fraction can wreck a planned reaction and risk side product formation. Every batch leaves our facility packed under inert conditions to pause degradation as much as possible between our operation and yours.
Over years working directly with R&D labs and process development teams, it's become clear that each group picks intermediates for more than catalog values. 5-chloro-6-oxo-1,6-dihydropyridine-3-carboxylate plays a role in bringing tough molecules closer; its structure streamlines syntheses that struggle with harsh reactivity or low selectivity elsewhere. Many customers rely on the electron-withdrawing chloro group, which offers smoother functionalization or nucleophilic substitution. The oxo function meanwhile offers less steric hindrance compared to similar cyclic ketones, ensuring easier further derivatization.
In our experience, this intermediate often appears in pharmaceutical routes—including for APIs and advanced building blocks—where side product control makes or breaks cost and safety. Researchers in agrochemical discovery and specialty dyes also find the pattern of reactivity ideal for constructing complex architectures without lengthy protecting group battles.
Process chemists owe much of their success to the reliability of building blocks like this. Some projects begin as bench-scale experiments destined for ton-scale campaigns; consistent supply, reactivity, and handling behavior take on enormous significance at this step. We know the pain of failed scale-up—an acute memory of past interruptions due to “known unknowns” like batch inconsistency or incompatibility with solvents and reagents. Over time, by sharing data back and forth with downstream users, we carved out a process that anticipates these snags.
A few years ago, a pharmaceutical partner approached us to address side reactions during a key amidation. Our technical support team, including lab chemists who had themselves worked up the earliest batches, coordinated with their R&D group on a new crystallization step. Adjustments in solvent polarity finally suppressed a persistent impurity, enabling a consistent quality at industrial scale. This feedback loop—from the user’s bench to our reactors—has translated to a more robust offering.
Members of the chemical industry know that safety and environmental factors drive decision-making, too. Our history with this carboxylate demonstrates how relatively mild reaction conditions, non-exotic solvents, and lower toxicity profiles leave less impact compared to certain other pyridine derivatives. Treatment of effluents and cleaning protocols run simpler, and health hazard assessments consistently confirm lower exposure concerns.
Supplying this intermediate in hundreds of kilos each month revealed where efficiency gains matter most. Waste minimization and solvent recovery have graduated from afterthoughts to design factors in process tweaks. Our operators developed closed-loop systems that capture more mother liquors and recycle solvents, saving both resources and compliance headaches.
Early batches proved susceptible to air and humidity, prompting investments in inert handling. Those changes not only kept quality stable during storage and transport, but also meant less variability for customers receiving product globally. It’s one thing watching a flask in the lab, but plant-scale batches tested our resolve—seeing trucks loaded with product, we all felt responsible for making sure no step lets down someone’s project on arrival.
Automation technology keeps inching forward. Manual steps in charging raw materials or controlling exotherms used to limit batch sizes; now, gradual automation of reactor controls—combined with real-time reaction monitoring—gave greater repeatability and insight into minor deviations. This shift allowed us to offer custom-tailored batches for those needing unusual order sizes or specific impurity limits.
Bench chemists benefit from a material that resists degradation before and during use. We found that 5-chloro-6-oxo-1,6-dihydropyridine-3-carboxylate, thanks to its stable crystal form, tolerates moderate temperature variations without sacrificing reactivity. Though sensitive to moisture over the long run, our improved packaging ensures a considerably extended shelf life, slashing waste and capital tie-up across long project timelines.
Working in synthesis, users report that this intermediate dissolves cleanly in common polar organic solvents such as DMF, acetonitrile, or DMSO. This trait scales up easily from gram to kilogram work—few surprises occur in solubility when changing from agitation with a stir bar to pumped transfer in a jacketed reactor. Those aiming for maximum process throughput appreciate this reliable dissolution and filtration.
Thermal stability checks under different storage and reaction scenarios have become routine. Product left at elevated temperatures—provided air and moisture stay out—retains purity for months. Losses in performance have, so far, traced back to environmental exposure more than inherent instability, supporting users who stock up for future campaigns.
Managing dust generation during large-scale charging protected both operators and products. Fine particulate control, fume hood optimization, and staff training on minimization of static electricity all followed direct experience observing these risks in action. Over time, incremental changes led to fewer complaints out of both labs and plant floors.
Choice between closely related intermediates often centers on minor details, but cumulative experience shapes what actually works on the ground. Some chemists compare 5-chloro-6-oxo-1,6-dihydropyridine-3-carboxylate to unchlorinated pyridine-3-carboxylates, or analogs with alternate substitution patterns. In these head-to-head tests, the chloro group at position 5 reliably offers greater control of subsequent substitution at neighboring carbons, opening paths to late-stage diversification that aren’t as clean elsewhere.
Similar intermediates—sometimes with a methyl or different halogen—may push reactivity or solubility in a less predictable direction. From our technical support cases, those pursuing highly functionalized targets find that changing out to other substituents leads to slower reaction times, lower isolated yields, or greater formation of regioisomers. The oxo-group at position 6 also plays a protective role, quenching over-reactivity so that side products live only in trace amounts under well-established conditions.
Over years shipping across borders and continents, the molecule’s handling profile drew particular praise; alternatives sometimes clump, melt early, or pose environmental control challenges during handling. The crystalline, free-flowing texture supports both manual dosing and automated feed to reactors. Our heavy investment in stability and profiling paid off in terms of lower customer complaints and more repeat business, with fewer failures at the point of use.
Beyond mere reactivity or handling, regulatory approval cycles steer chemists towards intermediates with less historical baggage. Some pyridine derivatives attract safety or environmental scrutiny due to toxic metabolites or bioaccumulative risks. Experience with this carboxylate supports a lower-risk classification, simplifying compliance, material transport, and disposal. We have reported fewer issues crossing borders or satisfying demanding customer audits.
Every feedback point from real users reshapes our output. Requests for tighter particle size distribution spurred investments in new sieving equipment, producing consistently fine powder without the lumps customers used to encounter. Stability data sharing with R&D clients led us to test new inhibitor packages and packaging formats—especially for those storing materials under variable warehouse conditions or shipping over long distances.
We respond to environmental challenges by fine-tuning both input chemistry and output controls. Solvent swaps—from older, less sustainable organics to greener, lower-toxicity choices—now feature regularly in production retrospectives. Our team works with external auditors to verify upstream and downstream impacts, and upstream supplier relationships receive continuous scrutiny. The technical team has trialed processes allowing for recycling or safe incineration of by-products, keeping a closer eye on local and international environmental mandates.
User demand for even higher purity sometimes means adopting double crystallization or special filtration protocols. Rather than chasing marginal yield at the expense of impurities, we lean towards fewer side reactions and direct, easy-to-track by-products that simplify downstream purification and analysis. The end result: easier documentation for regulated sectors, with reduced rejects and a better fit for acute analytical needs.
Our seasoned staff take pride in supporting both the premier global pharma houses and the ambitious startup’s first-scale batch. Large buyers often need assurance that a ton of intermediate from this month will perform as consistently as the kilogram years ago. Small-scale users, meanwhile, depend on flexibility—access to minimum order quantities without a decline in service or quality. Regular customer calls, technical troubleshooting sessions, and—and once—a plant tour for key partners have kept this product line close to its users, not just its specs.
Supporting those in process development, we focus on the nuances that save headaches later: right advice for storage, tips to minimize loss during transfer, and real feedback on what batch variations signal about upstream or downstream issues. This knowledge never appears in a raw spec sheet, but regular communication builds trust and project success over time.
Many chemical manufacturers claim best-in-class, but our focus remains on transparency and practical, incremental improvement. Every specification listed and batch delivered gets backed by our lab records and real-world handling observations. Customers receive documentation complete with not only analytical data, but also storage recommendations and troubleshooting tips compiled over years dealing with outlier events.
We work to ensure consistent availability; lines run with redundant reactor capacity to minimize outages from technical issues, and relationships with logistics partners ensure prompt international delivery. Having lived through challenges like port shutdowns, regulatory delays, or raw material shortages, we now practice proactive inventory management and emergency planning as industry norm.
This ethos of detailed records, open channels for feedback, and willingness to implement user-driven changes characterizes our entire approach. Staff on the plant floor, the QA desk, or the customer support line recognize a shared goal: chemical intermediates need to do their job, no matter whether in a large-scale API campaign or in the earliest R&D test batch.
Over time, 5-chloro-6-oxo-1,6-dihydropyridine-3-carboxylate has built a genuine reputation among researchers and process engineers. Not just for a consistent chemical signature or sleek analysis report, but because it has proven its worth in projects where downtime and failed batches spell costly delays. This molecule earned its spot through steady refinement—from reactor engineering through packing, shipment, and application support.
We stand behind our work. Our technical team answers questions not with boilerplate, but with lessons earned in aligning synthesis with real-world project needs, ensuring every batch reflects our daily commitment to safe, reproducible, and transparent production.