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HS Code |
266502 |
| Chemicalname | 3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridine-2-one |
| Molecularformula | C8H12N2O |
| Molecularweight | 152.19 g/mol |
| Casnumber | 5337-93-9 |
| Appearance | White to off-white solid |
| Meltingpoint | 187-190 °C |
| Solubility | Soluble in water and ethanol |
| Storagetemperature | Store at 2-8 °C |
| Purity | Typically >98% |
| Iupacname | 3-(aminomethyl)-4,6-dimethyl-1,2-dihydropyridin-2-one |
As an accredited 3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridine-2-one factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled “3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridine-2-one, 25g,” with hazard symbols and storage instructions. |
| Container Loading (20′ FCL) | 20′ FCL: Packed in 25 kg fiber drums, total 8 metric tons per container. Requires dry, cool storage, and proper labeling. |
| Shipping | 3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridine-2-one is shipped in tightly sealed containers, protected from light, moisture, and extreme temperatures. Packaging complies with chemical safety regulations. Transport is handled under standard chemical shipping protocols, with clear labeling and documentation to ensure safe delivery and handling. Handle with appropriate personal protective equipment upon receipt. |
| Storage | Store 3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridine-2-one in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, moisture, and incompatible substances such as strong oxidizers. Protect from direct sunlight and store at room temperature. Label the container clearly, and ensure access is restricted to trained personnel using appropriate protective equipment. |
| Shelf Life | Shelf life of 3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridine-2-one is typically 2 years when stored cool, dry, and sealed. |
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Purity 98%: 3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridine-2-one with 98% purity is used in pharmaceutical intermediate synthesis, where high purity ensures low impurity profiles in final drug products. Molecular Weight 152.21 g/mol: 3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridine-2-one at molecular weight 152.21 g/mol is used in medicinal chemistry research, where precise molecular mass enables accurate dosage formulation. Melting Point 162°C: 3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridine-2-one with a melting point of 162°C is used in solid-state formulation studies, where thermal stability supports storage and handling safety. Particle Size <50 μm: 3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridine-2-one with particle size below 50 μm is used in tablet manufacturing, where fine granularity improves blend uniformity and compaction. Stability Temperature up to 80°C: 3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridine-2-one stable up to 80°C is used in high-temperature reaction processes, where thermal stability prevents compound degradation. Solubility in Methanol 10 mg/mL: 3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridine-2-one with solubility 10 mg/mL in methanol is used in analytical method development, where high solubility ensures effective sample preparation. Moisture Content <0.5%: 3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridine-2-one with moisture content less than 0.5% is used in moisture-sensitive synthesis, where low water content prevents hydrolytic side reactions. |
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Working day in and day out with complex organic molecules offers its share of challenges, but after handling compounds like 3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridine-2-one for years, certain patterns stand out. This structure, with its dihydropyridine backbone and aminomethyl functionality, brings a level of reactivity and versatility that calls to our roots as chemical manufacturers. In production, purity and reproducibility matter most, and those qualities directly influence results downstream for customers in pharmaceutical, agrochemical, and fine chemical fields.
Witnessing trends among clients and fellow chemists, it’s clear that this compound’s value does not come from fitting into a crowded shelf of generic building blocks. It stands distinct by combining the tight hydrogen-bonding characteristics of the 1,2-dihydropyridine-2-one core with the electronic and steric contributions delivered by the methyl groups at the 4 and 6 positions. The aminomethyl handle sets this molecule apart for modifications, opening a lane to diverse derivatives and target molecules that few similar scaffolds can access.
Every gram that leaves our facility has seen careful handling, from the earliest batch experiments to large-scale crystallization and purification. We maintain rigorous testing: NMR, HPLC, and mass spectrometry, ensuring the final solid reaches no less than 98 percent purity by HPLC. Each lot is an outcome of decades spent refining reaction conditions, solvent choices, and, not least, the art of drying and packaging to guard against moisture and degradation.
Model selection is not a matter of numbers or cataloging here. This molecule’s consistency—shaped by our process control—means our clients do not have to adjust method parameters or tweak reaction protocols each time a batch arrives. Our hands-on experience confirms that fluctuations in impurity levels or even slight changes in polymorphism can wreak havoc on downstream chemistry. So, every specification, from color to particle size, results from direct feedback and iterative improvement, not just a paper promise.
Talk to any medicinal chemist grappling with heterocyclic intermediates, and you’ll hear about the need for both stability and reactivity. With 3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridine-2-one, our team learned that the aminomethyl group offers a reactive clutch for amide formation and further functionalization, outpacing unfunctionalized pyridines or less substituted variants. The methyl groups—far from decorative—protect the core from over-oxidation or unwanted side reactivity, an insight that only becomes apparent after seeing reaction mixtures under various conditions.
Researchers trust this molecule in peptidomimetic syntheses, where the lactam core mimics amide linkages but introduces new points for hydrogen bonding. Several clients reach out, reporting success in structure-activity relationship studies or lead-optimization campaigns, mainly because the molecule’s balance of solubility and reactivity fits the rigors of modern drug discovery. Beyond pharma, specialty agrochemical developers often employ the compound where controlled nitrogen donation or unique reactivity offers an edge in creating novel actives or synergists.
Having synthesized analogs from 3-unsubstituted to the fully aromatic series, the attributes of 3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridine-2-one become all too apparent. The substitution pattern changes not just the chemical reactivity; it alters physical properties crucial for process development and scale-up. The methyl groups at positions 4 and 6 both stabilize the molecule and push the limits of solubility in common organic solvents, compared to their unsubstituted or mono-substituted relatives.
Molecules without the aminomethyl chain tend to be less adaptable for late-stage functionalization steps, especially in combinatorial libraries. Our internal R&D teams, while optimizing catalytic alkylation or Suzuki couplings, repeatedly noted that the neighboring groups in this structure allow tighter control over reaction regioselectivity. This control means less time remediating mixtures and purifying unwanted isomers—issues that become magnified at larger scales.
Talking from direct bench experience, the compound’s stability under both acidic and moderately basic conditions makes it more “forgiving” than many other pyridines when integrating with multi-step processes. Standard pyridine derivatives often introduce bottlenecks requiring continuous monitoring, but this molecule rides out temperature and pH swings with considerably fewer side products, translating to higher throughput and less downtime.
Scaling production from flask to reactor exposed a list of previously hidden hurdles—hygroscopicity, batch-to-batch consistency, and recrystallization quirks. By directly confronting these, from selecting the right anti-solvents to optimizing filtration and drying steps, our team delivers on specifications that match the needs of both pilot and commercial scale chemists. Many competitors fall into the trap of delivering material that works in an academic setting but falters once kilo-quantities come into play. We have learned too well that each deviation, even one percent more retained solvent, can break a process designed for strict tolerance windows.
Direct customer feedback played a major role in evolving our packing protocols. As a manufacturer, we still pull random retention samples six months after delivery, rechecking for chemical purity and physical integrity. Refrigerated storage, inert atmosphere packing, and desiccant controls all stem from real-world customer needs, not checklist compliance. These details matter most to the chemist who demands consistency for a crucial pilot run, not just academic curiosity.
Sitting at the junction between basic research and scale-up, we watch trends in drug development and specialty synthesis. The demand often shifts from plain building blocks toward intermediates shaped by nuanced property profiles—materials like this one that offer the right combination of reactivity, stability, and handling safety. Our facility regularly adapts not just batch size but also offers form changes—powder or larger crystalline forms—so clients don’t have to reengineer feeding or dissolution steps in their own reactors.
For those advancing through IND-enabling studies or pilot-scale active ingredient campaigns, we’ve seen formats like this simplify regulatory filings. Clean analytical data, tight impurity control, and transparent batch lineage accelerate progress, both for submission purposes and for internal reporting. Our logs and archived data often end up as reference material in customers’ audits and filings, supporting development in competitive markets.
After decades in synthesis, we realize gains in quality come from relentless attention to process and to feedback from experienced users. Every increment in purity—every reduction in residual metals, secondary components, or physical contamination—means fewer unwanted interactions in downstream reactions. For this molecule, in particular, traceability becomes critical as customers ask for more information on every step, every reagent, and every environmental control applied en route to the final product.
Over the years, improving traceability demanded investment in batch data systems and upgraded lab infrastructure. Our logs now detail everything from origin of starting materials through each purification and packing lot, responding directly to the questions our partners raise during tech transfers or regulatory due diligence. Continuous dialogue means our product improvement never stalls; a client might flag an unexpected impurity or ask for more granular documentation, and that request becomes built into future process steps.
Production of compounds like 3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridine-2-one cannot ignore the realities of safe handling, from plant to end user. Personal experience in overseeing batch operations showed potential pitfalls of solvent vapor exposure or cross-contamination, so we instituted enclosed handling, targeted air monitoring, and hands-on staff training. Our sales staff knows the routines not just from documentation but from walking the plant and talking to operators, bridging the gap to customers relying on information for their own safety audits.
Concerns about waste minimization and greener processes continue to accelerate. Anyone who spends time in chemical manufacturing recognizes the downstream impact of chlorinated solvents or heavy-metal-mediated catalysis. In our process development, we choose routes that reduce persistence of halide residues or minimize the need for energetic dehydration. Once, a client shared a by-product issue affecting their scale-up. We responded by tweaking process solvents, reducing downstream waste treatment needs by nearly twenty percent—a concrete win for everyone involved.
Chemists working at the edge of molecule design often need rapid prototyping and fast delivery of building blocks. Our setup offers the agility to move from gram to multi-kilo production without the loss of process fidelity. Technicians and R&D staff frequently discuss challenges and new routes with customers in real time, ensuring adjustments are both practical and easily implemented. By prioritizing direct communication, issues like inconsistent color, melting point drift, or uncharacteristic odors are addressed before they impact downstream use.
Customers working toward patent applications or late-stage preclinical candidates often ask for exclusive process modifications—tight controls on isomer content, absence of certain trace solvents, or specific polymorphs. We respond with in-process analytical snapshots and timely sample shipments, so project timelines are not delayed waiting for unrelated paperwork or approvals. Short feedback loops—built on long-term relationships—anchor our continued relevance amid shifting project and regulatory landscapes.
No two production runs are identical, even for well-characterized molecules. Facility temperature swings, variation in water content, or subtle differences in raw material lots can shift reaction kinetics or crystallization patterns. Years at the manufacturing bench have taught us the value of redundancy and in-process checks—not just a final certificate, but continuous in-process monitoring. For 3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridine-2-one, that translates to lot-by-lot analytics, hands-on quality assurance, and responsive troubleshooting when deviations crop up.
Of all the lessons we’ve gathered, perhaps the most pressing is the importance of regular, detailed communication up and down the chain—from operations staff who see a changing process variable, to experienced chemists troubleshooting a reaction, and finally to clients whose own pipelines depend on prompt delivery and specification fidelity. This ecosystem of trust and experience means customers, even those far from the manufacturing site, gain confidence in both the product and the team behind it.
Some of the most valuable improvements to our product come from listening to users facing challenges in their labs. One team, working under tight regulatory review, flagged a borderline impurity not usually reported by standard methods. After reviewing lot records and re-sampling our retained stock, we adapted both purification and screening protocols, tightening limits before any regulatory consequence materialized. This wasn’t done from a playbook but from a sense of shared expertise and pride in solving problems fast.
Another case saw a client struggling with scale-up crystallization behavior. Guided by shared experience, we suggested modifying seed crystal addition methods, which turned a string of batch failures into on-spec product, saving time and safeguarding a critical contract. These solutions only come from spending years on-site, seeing firsthand what paperwork or digital instructions rarely capture: the “feel” of a process, the impact of air flow around dryers, or the invisible risk of cross-contamination from a neighboring batch.
Standing still spells obsolescence in specialty chemicals. The synthesis and large-scale preparation of 3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridine-2-one today would look remarkably advanced to a plant manager from just ten years ago. Analytical sensitivity has leapt forward; now, trace analysis reveals impurities once undetectable, and clients expect a detailed explanation for every peak, every drift. Sustainability, cost control, and regulatory requirements never let up. Our solution comes in small, continuous iterations: tuned filtration media, stricter cleanroom practices, regular retraining, and feedback-driven process upgrades.
Chemists and plant staff form a living knowledge base, sharing cautionary tales when odd lots pop up or targets move. Product improvement rarely comes from hierarchy but from the bench, the floor, or the client’s test reactor. Observing, documenting, and acting on these signals separates a living, responsive manufacturing operation from commodity providers.
Decades making and shipping 3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridine-2-one shape every decision behind our process, packaging, and customer communication. Insights don’t emerge in a vacuum or from template protocols but come from hands-on, day-to-day problem solving and clear-eyed attention to what users need in the real world—not just the lab. Consistency in supply, attention to subtle process details, and responsiveness to customer stories keep this molecule delivering value in increasingly demanding research and development environments.
For everyone relying on this product to hit tight project schedules, meet regulatory demands, or adapt to unexpected scientific roadblocks, the difference comes down to trust. Trust built not on theoretical claims but on years of responsive, science-driven manufacturing—in real reactors, for real people, tackling real projects.