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HS Code |
698743 |
| Iupac Name | methyl 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate |
| Molecular Formula | C8H9NO3 |
| Molecular Weight | 167.16 g/mol |
| Cas Number | 59513-99-8 |
| Appearance | White to off-white solid |
| Melting Point | 98-102°C |
| Solubility In Water | Slightly soluble |
| Smiles | CC(=O)C1=C(C=CN(C1)C)C(=O)OC |
| Pubchem Cid | 10674730 |
As an accredited methyl 1-methyl-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 | Amber glass vial containing 5 grams of methyl 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate, tightly sealed with tamper-evident cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 14 MT packed in 560 drums, each 25 kg net, loaded on pallets for secure chemical transport. |
| Shipping | **Shipping Description:** Methyl 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate should be shipped in tightly sealed containers, protected from moisture and direct sunlight. Transport at ambient temperature unless otherwise specified. Handle in accordance with standard chemical safety protocols. Include appropriate labeling and documentation according to local, national, and international regulations for non-hazardous chemicals. |
| Storage | Store methyl 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible materials such as strong oxidizers. Keep at room temperature (15–25°C). Ensure proper labelling and access is restricted to trained personnel. Use secondary containment to prevent leaks or spills and wear appropriate personal protective equipment when handling. |
| Shelf Life | Shelf life: Store methyl 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate in a cool, dry place; stable for 2 years unopened. |
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Purity 98%: methyl 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and consistent product quality. Molecular weight 179.17 g/mol: methyl 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate with molecular weight 179.17 g/mol is used in academic research applications, where precise dose measurements enhance reproducibility. Melting point 105°C: methyl 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate with melting point 105°C is used in organic solid-state chemistry studies, where it allows for controlled thermal analysis. Stability temperature up to 80°C: methyl 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate with stability temperature up to 80°C is used in storage protocols, where it maintains chemical integrity over extended periods. Particle size ≤ 50 µm: methyl 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate with particle size ≤ 50 µm is used in formulation development, where it enables uniform dispersion in composite blends. |
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In the world of fine chemicals, we spend a lot of time with compounds that might sound complex by name, but serve a clear purpose in the laboratory and on the manufacturing floor. Methyl 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate belongs to a group of pyridine derivatives that we—those of us who produce rather than simply source—know for their reliable chemistry. Every synthesis batch tells its own story. As a chemical manufacturer, the journey of this compound always weighs on our daily priorities. From the selection of starting materials and the precision required through every reaction step, to maintaining close controls during purification, we are reminded that what serves the end user best, starts well before packing the finished product.
Over the years, countless requests from pharmaceutical research labs, fine chemical formulators, and academic teams have shown us where methyl 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate fits into the real world. Its structure—centered on a dihydropyridine ring modified with a carboxylate ester and a ketone in the sixth position—brings together stability, reactivity, and solubility. This blend sets a foundation for predictable downstream reactions, especially when chemists want to build more elaborate molecules or screen new bioactive candidates. The methylation at the first position, which we achieve through a well-controlled alkylation process, improves the compound’s electronic characteristics. Lab researchers usually check these subtle differences using standard NMR and IR analysis, but those checks start with our in-house QC labs, using real-time spectroscopic feedback as a part of every run.
In our own facility, we control the product closely from the start. Most material leaves our plant at a purity above 98%, confirmed batch by batch. Color, as a quick sanity check, usually ranges from white to off-white powder—a telltale sign of purity and successful removal of trace side-products without needing extra chromatography. Moisture content is held tightly below 1% to avoid problems for those who need the compound for moisture-sensitive coupling reactions. Each kilogram or gram we ship traces back to a unique lot record, and we keep records of all analytical results, from HPLC to LC-MS, for years after each batch. As a team that interacts daily with real chemists using these materials, we respond to feedback about granularity and flow properties, adjusting milling or drying steps accordingly.
Sometimes users want the product packed in specific sizes—sometimes only a few grams for reference synthesis work, or several kilograms for scale-up. Having packed this compound in many forms, we have learned that glass is best for long-term stability, while sealed HDPE works well for shorter, high-turnover applications. Unlike more volatile or air-sensitive intermediates, this product handles moderate temperatures and standard warehouse conditions, which makes storage on the shelf less stressful for everyone down the supply line.
It often surprises those outside chemical production how much difference the chosen synthesis route actually makes. What may seem like just another intermediate is, to us, a timeline of careful choices with direct consequences for customers. For methyl 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate, we spent years refining a route that brings high yields and limits byproduct formation, so purification need not rely on column chromatography every time. That makes scale possible. The fewer the side products—especially regioisomers or over-methylated derivatives—the easier downstream work becomes for those who build new APIs or perform combinatorial screening with these molecules.
We’ve learned that not all batches—ours or from competitors—are made equally. Some sources focus only on yield or raw output, but those metrics mean little if additional impurities slip through. Researchers working to develop novel inhibitors, or those using this pyridine derivative to install functionality on more complex targets, expect more than just a prompt shipment. They count on transparency about residual solvents, metal content, and perhaps most of all, a willingness to trace quality issues to the root. We rarely see issues with our processes anymore, but in the past, we faced methyl group migration and minor oxidation during large-batch manufacturing. Solving these took not just green chemistry tweaks, but new reactor controls, better dry box infrastructure, and employee training. The impact on reproducibility and customer trust proved worth every hour invested.
A close look at methyl 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate tells a story through its crystalline structure. Our process avoids heavy metal catalysts and toxic alkylation agents, recognizing their downstream interference and regulatory risks in pharmaceutical or agrochemical work. We lean toward greener oxidants and environmentally safer solvents, without cutting the purity targets or yield as other industrial shortcuts might. The resulting powder flows easily, a byproduct of our controlled crystallization and drying, not accidental happenstance.
Comparing user experiences with versions from several sources, we see that not all products handle equally in the lab. Some present with persistent yellow tints, a sign of breakdown or incomplete purification, while others show variable solubility in common organic solvents. By investing in full solvent-exchange steps—making sure the final product is consistently deliquescent-free—our batches avoid the hassle and wasted material that comes when researchers must recrystallize on arrival. This leaves their focus on the discovery task at hand.
Where automation fails, human oversight prevails. On-site analytical teams check every backpack and container, making sure even a single gram or kilogram bag matches both structure and performance. Those who’ve gotten stuck with off-spec materials elsewhere know that shortcuts at this stage cost dearly downstream. New process control algorithms flag even slight deviations in melting point or spectral characteristics. We catch off-spec events before they leave our doors.
The practical significance of methyl 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate begins where glassware meets substance. A number of pharmaceutical R&D teams have used our material as a core building block in the synthesis of novel ion channel modulators. Due to the electron distribution imparted by the methyl group and the karboxylate moiety, their medicinal chemistry teams reported a more reliable outcome in both palladium-catalyzed coupling and acylation reactions. They’ve shared that our batch-to-batch reproducibility allowed faster development times, reducing the number of repeated trial-and-error runs. Having spent time on the line ourselves, these details matter as much as any printed certificate.
Specialty chemical developers, who routinely prepare next-generation light stabilizers or polymer additives, draw attention to the compound’s compatibility with a range of reagents. Our variant, with its low residual solvent threshold and consistently clean spectral fingerprint, often avoids the need for extensive pre-use cleaning. Those working on dye intermediates or heterocyclic ligands see similar benefit, reporting fewer unexpected byproducts during cyclization reactions. These landmark cases reinforce why persistent attention to detail at the manufacturing stage improves not only purity, but the efficiency of end-user chemistry.
Chemists often want to know the difference between closely related pyridine compounds, especially during project planning. Speaking from a production standpoint, we have handled a variety of substituted pyridines over decades. Compounds lacking the 1-methyl group typically show different reactivity profiles, especially regarding selectivity during further functionalization. The absence of the methyl at the first position pushes electron density elsewhere on the ring, making downstream addition reactions less predictable. Further, the 6-oxo function plays a dual role—serving as both an electron sink and a handle for derivatization—making this compound more versatile than simpler pyridine-3-carboxylates.
Users who switch between substituted pyridine analogs often mention differences in odor, color stability, and ease of work-up. Our product formulation ensures minimal odor, unlike lower-purity alternatives where unreacted methylating agents or side-products linger. During melt analysis, we routinely see this compound clear at narrow melting ranges, compared to the broader, multi-stage melting typical of mixed isomer lots from external traders or casual resellers. Our experience working directly with the reaction liquor, and not a sample from a multi-step upstream vendor, enables this distinction on a daily basis.
Transparency shapes our workflow at every stage. Early on, we hit several roadblocks—exothermic reaction spikes, batch inconsistency, and the perennial challenge of solvent recovery. Instead of cutting corners, each obstacle pushed us to tighten process controls, update analytical protocols, and invest in employee training. We adopted greener chemistry principles where possible, introducing less hazardous reagents and modern solvent recycling. Mistakes taught us that short-term savings never outweigh the overall cost of off-spec batches, especially given the risk of losing customer trust.
Over time, regular dialog with hands-on chemists shaped our approach. Where someone notes problems with their chromatographic run, or points out an unexpected impurity peak, we trace the issue—not to the reseller, but back to our own reactors. That accountability, a hallmark of genuine manufacturers, brings out the best in both process improvement and staff pride. Routine runs of methyl 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate now deliver a tighter range of analytical results than the industry average. Being nimble and detail-oriented means we can adjust specifications for demanding projects, provided the chemistry supports it. No automated line replaces a seasoned chemist who knows their batch inside and out. The proof, always, is in the final assay results and the repeat orders from seasoned clients.
As manufacturers, we don’t just fill orders; we build partnerships over years. Each lot of methyl 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate moving out our doors comes with a history of development, real-world testing, and open dialogue. Our site tours often welcome visiting researchers, who bring their own methods and share candid feedback about our last shipment. Those crash courses in user needs prompted real changes: from improving the temperature control in solvent removal, to investing in newer vacuum dryers that protect thermally sensitive batches better than the old heated trays ever did.
We maintain an internal database of issues and solution pathways, grounded in observations and action plans, not buzzwords. The most valuable knowledge usually comes from troubleshooting a single stubborn impurity or from watching a customer’s application protocol up close. After repeated collaboration, groups working on animal health products and crop science tools commented on the improved color stability and shelf life of our product batches. These are not just words on a website—they trace straight back to steps we took on our line, for real-world results.
Environmental responsibility no longer sits at the margins of chemical production. From solvent choice to waste handling, our team faces continual audits, internal and external. Each stage of manufacturing methyl 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate demands that we re-examine impact, not only for the sake of compliance but for the communities around our facility. Closed-loop solvent systems, responsible effluent management, and persistent upskilling of staff all play a role. We routinely work with regulatory consultants and local agencies, providing batch traceability and emission data, matching industry benchmarks and local ordinances in all areas where we operate.
Real change grows from day-to-day choices—favoring less hazardous chemicals, encouraging feedback from neighboring businesses, and maintaining transparency about our production schedules. Our team receives regular training in not only technical upgrades but in sustainability and workplace safety practices. In essence, we measure manufacturing advancement not only by product yield but by the growing connection with our regional partners. These roots keep our entire operation grounded.
Manufacturing never stands still. Each run of methyl 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate teaches new lessons. Sometimes a new filtration material increases throughput; at other times, a subtle tweak in temperature profile improves yield or purity. Most learnings stem from direct feedback from users: reports from academia, guidance from formulation teams, late-night calls from scale-up researchers tackling unforeseen filtration issues. These stories shape our direction more than any trade journal or industry report.
Bridging R&D, quality assurance, and final customer use, our site operates as an ongoing learning lab. The ideas from bench chemists and the experience of the manufacturing line combine every day. The value in listening—asking questions directly, inviting critique, keeping open records—continues to steer our decisions. Future directions focus on smarter process controls, next-generation analytical instruments, and a more circular model for chemical use and reuse, minimizing waste at every stage.
In sharing the real-world view of methyl 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate manufacturing, we hope to illustrate what takes place behind the final product. This compound, shaped by both knowledge and daily care, stands as more than a building block in a reaction scheme. It reflects the accumulated effort of every hand and mind in our plant, built on practical experience and transparent improvement. For those who choose to work directly with manufacturers, not traders or brokers, this difference is more than just a number or certificate—it’s the backbone of consistent, reliable chemical supply, batch after batch.