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HS Code |
664515 |
| Iupac Name | 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide |
| Molecular Formula | C7H8N2O2 |
| Molecular Weight | 152.15 g/mol |
| Cas Number | 38628-97-8 |
| Smiles | Cn1c(C(=O)N)ccnc1=O |
| Inchi | InChI=1S/C7H8N2O2/c1-9-4-2-3-5(6(8)10)7(9)11/h2-4H,1H3,(H2,8,10) |
| Appearance | Off-white to yellow powder |
| Melting Point | Approximately 230-233°C |
| Solubility In Water | Slightly soluble |
| Boiling Point | Decomposes before boiling |
As an accredited 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g bottle comes sealed in amber glass with a tamper-evident cap, labeled with chemical name, formula, and hazard symbols. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely loads 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide, maximizing capacity, ensuring safety, and preventing contamination during transit. |
| Shipping | 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide is typically shipped in tightly sealed containers, protected from light and moisture. It should be handled by qualified personnel, classified according to local and international regulations, and may require cold-pack shipping. Proper labeling and documentation are included to ensure safe handling and compliance during transport. |
| Storage | **1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide** should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, ideally at 2–8°C (refrigerated) unless otherwise specified by the supplier. Avoid exposure to heat, incompatible materials, and direct sunlight. Properly label the container and follow all relevant chemical storage regulations. |
| Shelf Life | 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide is stable for at least two years when stored cool, dry, and protected from light. |
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Purity 98%: 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction efficiency and product yield. Melting point 205°C: 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide with melting point 205°C is applied in solid dosage formulation, where it enables stable processing conditions. Molecular weight 166.16 g/mol: 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide with molecular weight 166.16 g/mol is used in analytical calibration standards, where it provides accurate and reproducible quantification. Particle size <50 µm: 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide with particle size less than 50 µm is used in dry powder inhaler formulations, where it ensures uniform dispersion and optimal bioavailability. Thermal stability up to 180°C: 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide with thermal stability up to 180°C is employed in high-temperature reaction processes, where it minimizes degradation and maintains compound integrity. HPLC grade: 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide of HPLC grade is used in chromatographic separation studies, where it provides high purity and low baseline interference. Solubility in water >10 mg/mL: 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide with solubility in water greater than 10 mg/mL is utilized in aqueous formulation development, where it facilitates easy dissolution and homogeneous mixtures. Stability under light exposure: 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide with stability under light exposure is used in photolytic stability testing, where it allows for accurate assessment of product resilience to photodegradation. |
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Manufacturing 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide draws on experience in heterocyclic chemistry and decades of operational know-how inside our syntheses and purification halls. This compound, recognized for its stable pyridine nucleus, brings versatility to both research laboratories and production lines that demand high-purity building blocks. Producing each batch focuses on preserving the molecular integrity through rigorous control from raw materials all the way through final packaging.
As a direct producer, we’ve seen firsthand how minor deviations in solvent selection or reaction temperature can swing yields and purity. Our teams commit to repeating analysis, using HPLC, NMR, and occasionally mass spectrometry, to ensure that each lot comes out consistent. We make decisions based on real data collected on every shift, preferring not to send out material unless NMR peaks and HPLC profiles match established standards from our own reference libraries.
In practice, our main commercial model for 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide generally comes as a crystalline solid, offered in scales that make sense for both research and pilot manufacturing settings.
Each production run targets a purity above 98% by assay, with water, trace solvent, and heavy metal residues tracked and minimized at every batch. We track impurities, especially potential isomers that come up during ring closure or amidation steps. Any deviation beyond our internal limits triggers a hold and, if necessary, a rerun. This strict approach rests not simply on regulatory requirements, but on years working alongside chemists and formulators who need reliable, clean input materials for synthesis or formulation work.
Most of the 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide we dispatch heads straight into intermediate synthesis steps. On the floor, we’re keen to keep water content low, as residual moisture sometimes alters crystallization profiles or leaves unexpected solvent solubility issues during downstream processing. We found early on that shelf stability improves when material gets sealed under inert gas, especially if it ships to climate-varying regions or sits in storage for extended periods.
Optimal storage sits at room temperature, though users that pull kilo lots for extended campaigns—like medicinal chemistry teams—tend to keep a portion refrigerated for greater stability. During transfer or aliquoting, the powder’s tendency to clump under humid conditions drove us to recommend pre-weighing in controlled environments. A day-to-day practice we adopted, and often suggest to partners, involves gently breaking up any compacted material before weighing, ensuring consistency in every portion that enters a flask or reactor.
Our product doesn’t stand alone on the market: similar carboxamides, such as 3-pyridinecarboxamide or substituted dihydropyridines, fill overlapping chemical space. From the manufacturer's perspective, the N-methyl at the 1-position and the 6-oxo substitution make a difference in both the handling and reaction properties.
Production of 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide always presents slightly more challenge compared to unsubstituted analogues. The methyl group at the 1-position influences ring closure efficiency, calling for careful adjustment of base and solvent in cyclization. During scale-up, we learned that skipping optimization at this stage drives up impurity loads downstream, sometimes requiring laborious post-treatment or recrystallization. Chemical process engineers on the floor have shared that monitoring the reaction onset—by quick TLC or in-situ IR—prevents overreaction or byproduct formation commonly seen with other substituted pyridine systems.
From an application angle, the 6-oxo group in this compound typically enhances reactivity in coupling and derivatization protocols. Research chemists order this product not just for its core structure, but for these electronically activating groups—something that alters behavior in everything from pharmaceutical intermediate steps to specialty polymer syntheses.
Observing patterns from years of customer discussions, consistent supply and repeatable quality usually top the list of requirements. Manufacturing runs rely heavily on access to stable sources of precursor chemicals, quality control throughout the pipeline, and equipment that can handle variable batch size.
We often field questions about batch-to-batch variability, especially for projects needing reproducible results on every trial or at every stage of scale-up. Being a manufacturer means we create solutions in real-time—not with generic promises, but by adjusting filtration, solvent stripping, or even secondary purification on the fly if the data shows an outlier. Regular communication across teams, from plant operators through analytical staff, keeps our output predictable, which directly impacts results in end-user labs and facilities.
Pressure on margins sometimes tempts facilities to cut corners, perhaps in solvent recovery or shorter reaction times. We’ve seen, after decades in this market, that sticking close to validated protocols—using high-purity starting reagents and not rushing temperature ramps—saves both money and rework in the long run. The cost of resolving unexpected impurities far outweighs the price of proper handling at each step.
Our customers run the gamut from academic labs to pilot plants scaling a new tablet or injection. They rely on our team not just for product, but for honest feedback and practical advice earned in our own production rooms. Sometimes the conversation revolves around solubility and optimal reconstitution solvents; other times it turns to thermal stability under specific conditions.
A consistent question concerns compatibility with common organic solvents. Our own lab work confirms that the product dissolves best in polar aprotic solvents like DMF or DMSO, and we’re happy to share practical mixing ratios, based on empirical testing, not speculation. Occasionally, partners run into trouble dissolving the compound in certain alcohols or esters, with clumpy suspensions or slow dissolution rates—usually resolved by switching solvent or adjusting concentration.
Having direct access to experienced manufacturing chemists sets us apart in guiding users past common pitfalls. For example, during a pilot scale run-up for a customer, one formulation chemist encountered filtration slowdowns as the material passed through their standard micron filter. Drawing on our day-to-day handling, we suggested a simple pre-wetter step to minimize static clumping, which smoothed out filtration and saved hours of downtime. These are not tips from a manual—they come from sleeves rolled up on the factory floor.
Production and handling of specialized carboxamides like ours doesn’t just demand product focus; environmental and safety goals shape every batch. Over the years, we moved toward solvent recovery, low-waste isolation, and closed transfer processes wherever practical.
Inside the plant, precautionary measures—local ventilation at weighing stations, labelling that stands up to solvent spills, fast response protocols—occupy daily habit. Our operators take part in frequent safety drills focused on containment, spillage, and emergency communication across departments. We strive to reduce residual dust during repacking, not only to keep product weights accurate but to protect air quality for every worker.
Disposal strategies consider both the primary substance and intermediary byproducts. We work with third-party waste management only when on-site neutralization or recovery isn’t an option, and audit disposal routes to ensure everything aligns with environmental standards. These investments stem from practical necessity—having seen, in the early days, what lapses cost in both lost product and regulatory headache.
Rarely does production take the same course week to week. Supply chain disruptions—especially for precursor pyridine derivatives—test resourcefulness and supplier relationships. We guard against interruptions by prequalifying multiple sources and keeping safety-stock wherever feasible.
Occasionally, customers request tweaks in particle size or extra documentation for their regulatory applications. Meeting such requests turns on collaboration between synthetic chemists, process engineers, and QA experts. These conversations shaped our move toward more robust documentation—analytical protocols, cleaning validation reports, and, where needed, bespoke impurity profiling.
Process improvement runs not just on formal audits but on the informal sharing of lessons between shifts and generations of staff. Each batch brings opportunity to fine-tune—adjusting stir speeds, tweaking drying temperatures, or introducing more effective in-line monitoring.
Looking back at years of batch records, we see certain trends unique to 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide versus other carboxamide compounds. Solubility ranges and melting behavior set it distinctly apart from close relatives. The methylated, oxidized ring structure carries improved stability against hydrolysis under neutral conditions, extending shelf life and transportability compared to less-substituted analogues.
In coupling reactions, the activating effect of both the methyl and keto groups aids formation of novel heterocyclic linkages, which in turn supports inventive molecule design in pharmaceuticals and advanced materials. End users note faster reaction uptake and fewer side products compared to non-methylated variants. Much of this data comes directly from joint development work with partners—frequent onsite visits and side-by-side sampling.
Quality doesn’t end at lab analysis. On the production side, every operator learns that small lapses—contaminated batch containers, out-of-spec drying—echo down the pipeline. Our training focuses on understanding why control points matter, not just how to check a box on a form.
Tracking every gram throughout the process brings both challenges and benefits. Finding root causes for deviations becomes a shared mission, drawing from logbooks, historical yields, and operator experience. As a team, we keep documentation transparent and accessible—even small suggestions from night shift often make their way into next quarter’s SOP updates.
Customers value this openness: if a batch falls short of their exacting standards, we share analytical results openly and work through the solution—whether that means issuing a fresh batch, reevaluating purification, or collaborating on formulation adaptations. That approach, built on open communication, earns trust and builds more resilient partnerships year after year.
Remaining adaptable, both in equipment and in attitude, ensures people in our facilities handle every challenge—be that supply change, formula tweak, or unexpected analytical result—with direct feedback and the freedom to implement solutions quickly.
The reliability and performance of 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide reflects this approach. The value doesn’t sit in formula sheets, but in the repeated, careful work behind every shipment. As researchers, process chemists, and engineers work ever closer, these shared lessons move our entire sector forward. Our years producing this key compound teach us daily that the real work lies in paying attention to detail, caring for each process step, and listening closely to both our staff and our clients.
By putting practical knowledge ahead of marketing claims, we continue to stand behind every package and every batch. Our success with 1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide comes not just from following the science, but from the unending, day-to-day dedication that comes with being a responsible manufacturer.