Dimethyl-1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate

    • Product Name: Dimethyl-1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate
    • Chemical Name (IUPAC): dimethyl 1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate
    • CAS No.: 102342-63-2
    • Chemical Formula: C15H21NO7
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    485089

    Chemical Name Dimethyl-1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate
    Molecular Formula C15H21NO8
    Molecular Weight 343.33 g/mol
    Appearance White to off-white solid
    Solubility Soluble in organic solvents such as methanol, ethanol, DMSO, and DMF
    Purity Typically >98% (varies by supplier)
    Cas Number 74578-10-6
    Storage Conditions Store in a cool, dry place, protected from light
    Synonyms Dimethyl 1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydro-2,5-pyridinedicarboxylate
    Hazard Statements Handle with care; safety data sheet should be consulted
    Iupac Name Dimethyl 1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate

    As an accredited Dimethyl-1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a sealed amber glass bottle containing 5 grams of Dimethyl-1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate, labeled for laboratory use.
    Container Loading (20′ FCL) 20' FCL (Full Container Load) accommodates bulk shipment of Dimethyl-1-(2,2-dimethoxyethyl)...dicarboxylate, ensuring secure, efficient transport.
    Shipping Dimethyl-1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate is shipped in tightly sealed containers, protected from moisture and light. Transport follows standard chemical regulations, ensuring safe handling and storage. The package includes proper labeling and documentation, with temperature control as needed, and complies with all applicable local, national, and international transport guidelines.
    Storage Store **Dimethyl-1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate** in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong acids and oxidizers. Protect from moisture. Ensure the storage area is clearly labeled and access is limited to trained personnel. Handle under a fume hood if possible.
    Shelf Life Shelf life: Store tightly sealed at 2-8°C, protected from light and moisture; stable for at least 2 years under these conditions.
    Application of Dimethyl-1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate

    Purity 98%: Dimethyl-1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate with 98% purity is used in pharmaceutical intermediate synthesis, where high-purity ensures reproducible reaction yields.

    Molecular Weight 367.37 g/mol: Dimethyl-1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate of molecular weight 367.37 g/mol is applied in medicinal chemistry research, where accurate molecular mass supports precise compound formulation.

    Melting Point 142-146°C: Dimethyl-1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate with a melting point of 142-146°C is used in solid-state synthesis, where controlled melting allows for efficient processing.

    Stability Temperature up to 110°C: Dimethyl-1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate stable up to 110°C is utilized in high-temperature reaction protocols, where thermal stability prevents decomposition during handling.

    HPLC Assay ≥99%: Dimethyl-1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate with HPLC assay ≥99% is employed in analytical reference standards, where high assay values guarantee method accuracy.

    Particle Size ≤50 μm: Dimethyl-1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate with particle size ≤50 μm is incorporated in formulation development, where fine particle size enhances solubility and uniform dispersion.

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    Certification & Compliance
    More Introduction

    Introducing Dimethyl-1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate from the Manufacturer’s Perspective

    Real-World Chemical Manufacturing: The Road to a Reliable Active Intermediate

    Practical chemical manufacturing depends on one thing above all else—accuracy, both in synthesis and in every downstream step. Since early routine runs in our pilot plant, we have handled the synthesis of Dimethyl-1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate with close attention to process consistency and product purity. This compound has drawn attention as a versatile intermediate in pharmaceutical and specialty API labs, but its development as a robust, scalable product took years of iterative process improvements. Our laboratory teams learned early that theoretical yields or beautiful NMRs on a single batch mean little unless you can translate those results to each and every production run, with lot-to-lot repeatability.

    This particular molecule stands out for its tailored structure. The core dihydropyridine ring, featuring pendant methoxy and dimethoxyethyl groups, allows for a blend of electronic properties that reliably support various downstream modifications. During pilot trials, we challenged the influence of subtle temperature deviations, trace water levels, and reagent grades. When scaling to commercial reactors, real-world hurdles showed up—unexpected solubility behavior, need for precise pH conditions during ring closure, and the stubborn occurrence of byproduct esters under less stringent raw material controls. These practical setbacks drove us to reexamine every step, moving beyond mere compliance with literature procedures or standard operating protocols.

    Specifications That Matter to End-Users

    Direct user feedback informed vital production parameters in later batches. Researchers asked for consistent particle size for easier filtration, so we fine-tuned crystallization and post-synthesis drying. Early customers in contract synthesis pointed out the impact of residual solvents on downstream reactions; as a result, we introduced exhaustively monitored vacuum stripping and multi-stage washes. The feedback loop between our plant chemists and formulation technicians led us to refine the melting point to sit well within a reproducible range, reducing processing headaches for teams who count on smooth re-dissolution or coupling chemistry.

    More than a few buyers of specialty chemical intermediates have faced dead ends that stem from subtle spec slips—one or two percent higher impurity, moisture content exceeding a lab’s threshold, or off-color batches hinting at trace decomposition. To meet the expectations of advanced synthesis teams, every lot of Dimethyl-1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate leaving our facility passes rigorous inspection by HPLC, GC, and NMR in line with customer-supplied reference data, not generic catalog numbers.

    Our QA team instituted scheduled checks at every intermediate point in the production process. Instead of full reliance on batch-end QC, we monitor appearance and solution behavior at each critical stage. Those who have spent time in kilo labs know well the frustration of running a job with off-spec starting materials, only to discover the problem after several days of lost labor. We answer technical questions directly, connecting bench and plant chemists to speed up troubleshooting, whether for solubility, reactivity, or storage stability.

    Genuine Usage Scenarios: From Early Discovery to Commercial Manufacturing

    Our experience supplying Dimethyl-1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate spans from small-batch medicinal chemistry work to consistent production for scale-up campaigns. In new drug research, this molecule often serves as a core building block for modifications targeting enhanced pharmacological activity. Early-stage research teams appreciate its clean reactivity in functionalization at the 4 and 5-positions, whether for introducing side chains or protected amine groups.

    For pilot-scale manufacturing groups, the compound wins points for its manageable stability and ease of isolation. We make certain every shipment arrives with a certificate setting out moisture content, residual solvents, and assay, so formulation and process chemists know what to expect. Many of our customers run multi-step syntheses, and as their intermediates build value at each stage, they rely on a consistent starting point.

    Why This Molecule Performs Where Competitors Fall Short

    Comparing this compound to other similar intermediates, choices in the marketplace often boil down to three concerns: purity, real-world stability during storage and shipping, and genuine observed yields in downstream chemistry. Over the past few years, we have sourced and analyzed competitor batches, openly comparing our process output to those manufactured via slightly different synthetic routes.

    Some other producers lean on bulk-scale synthesis, sacrificing purity for high total yield. End-users later pay the price in side reactions or filtration headaches. In practice, those small differences in impurity profiles have a big impact, especially in multistep API synthesis. Process chemists from customer sites have shared details—traces of unreacted esters or wrong isomeric forms from less controlled batches leading to failed scale-ups or long troubleshooting cycles. We reserve material not just for in-house QC analysis, but for downstream simulation runs, using actual end-user protocols to ensure our material supports real-world success.

    Longevity and batch stability have always been cornerstones of our internal product reviews. Cold-chain shipment might look robust on paper, but frequent handling and variable environments test the limits of what a compound can reasonably withstand. Based on feedback from international customers managing long shipments, we validated our drum packaging and molecular sieving approach to ensure robust performance after weeks in transport. No more ruined runs from in-transit moisture pickup or color changes.

    Working with Industry Feedback to Improve Specifications

    Listening to customer needs has been part of our process since we supplied our first pilot batch as a custom run. Early on, a major European research institute described needing a particular polymorph for better compatibility with their automated synthesis robots. Our plant engineers and chemists adjusted the crystallization solvent system and temperature ramp to encourage the exact form needed, integrating additional drying and packaging checks to accommodate their automation requirements.

    We heard from biopharma teams setting up continuous flow runs, reporting difficulties in solubilizing certain grades of the compound. Reacting to those specifics, we detailed our drying curves, extended the vacuum step, and revised the filtration aid selection. The results—tighter control of bulk density and flow properties—helped several installations run for extended periods without plugging or downtime, saving our customers both time and significant cost.

    Addressing Down-the-Line Chemical Compatibility

    Practical manufacturing means anticipating not just the immediate transformation, but all the reactions and purification steps that follow. For companies making library compounds, our customers shared several workflow bottlenecks—slow reactivity under certain coupling protocols and inconsistent color development during methylation steps. Our team responded with test runs, slight process optimizations of precursor materials, and a line of open communication. This collaboration revealed that trace contaminants from earlier process reagents created subtle problems in late-stage chemistry. We worked backward, adjusting our own supplier qualifications and testing regimes to solve these compatibility issues.

    Our technical support doesn't hide behind layers of sales and distribution. Customers regularly reach our production chemists for troubleshooting, and that direct conversation leads to process tweaks on both sides—a rare value-add in chemical manufacturing. More than a few research partners have switched to our material out of frustration with inconsistent performance from multi-supplier blends, or after running into avoidable blockages caused by higher water or trace salt content. Offering transparency and speed in answering these questions is more effective than any brochure or marketing claim.

    Real Manufacturing Data, Not Just Paper Specs

    Lab-scale reactions may benefit from forgiving conditions, but kilogram-scale production brings up all the weak spots in process control and supply chain. Years ago, we struggled to meet a challenging moisture content target, with standard rotary evaporation and vacuum drying unable to reach the low levels needed for a particularly water-sensitive application. Learning from laboratory setbacks, we implemented nitrogen-purged gloveboxes for packaging sensitive lots and increased in-process control points. This extra work paid off with improved shelf-life and immediate customer trust. Many of the tightest specifications on water, solvent, and impurity content came directly from user runs, not from internal brainstorming or generic application notes.

    Shipping and storage conditions sometimes fall outside the direct control of a supplier. Still, we designed our container systems with long-haul international air and ocean shipments in mind, tested with repeated cycles of temperature and humidity swings. These “stress tests” exposed real-world risks—condensation inside drums, accidental seals breaking during customs inspection, or trace contamination from unsealed stoppers. Fixing these common issues drove us to move away from single-layer plastic packaging toward laminated foil and inert gas-flushed pouches. Not every manufacturer takes this approach; it takes frontline experience of ruined batches and wasted effort to make these adjustments.

    Supporting New Uses and Research Applications

    Research teams rely on new building blocks to push innovation, evaluate structure-activity relationships, and create novel candidates that address currently unmet medical needs. This dihydropyridine derivative has helped investigators design new ligands for calcium channel modulation, antioxidant molecules, and imaging agents by exploiting its unique methoxy and dimethoxyethyl substitutions. Rather than just fulfilling orders, we keep close contact with researchers trying the compound in unfamiliar chemistry, logging feedback on conditions where our material supports positive outcomes, but also where bottlenecks appear. Some users needed improved stability for late-stage glycosylation steps; others described difficulties with batch-to-batch color changes. Each scenario provided learning moments, building a robust, fact-driven process manual on which adjustments produce the most reliable downstream results.

    Our process teams focus on “getting it right at the source”—starting materials matter, and each time we see a new use proposed, a round of characterization follows. This due diligence builds confidence with partners who expect every delivery to perform like the last. Over the years, this attitude has encouraged several academic labs and pharmaceutical companies to ramp up projects, secure in the knowledge that raw material supply difficulty would not slow down their work.

    Practical Differences from Other Sourced Products

    The specialty building blocks market is filled with claims of high purity and easy handling, but by trialing dozens of competitor materials in a real-world setting, our material wins out under demanding conditions. While some suppliers emphasize large-batch efficiency, this often leads to higher impurity levels. Fine dust or off-color fractions may pass casual inspection, but downstream reactions reveal the accumulation of “silent” contaminants—resulting in lower yield, unexpected byproducts, or increased purification steps on the part of users.

    Our plant design centers on segregated production lines, each configured for a particular material stream, minimizing risk of cross-contamination from unrelated batches. This practice avoids the very real problem of minute carry-over between similar but functionally different intermediates, a problem reported by customer analytical teams performing deep-dive impurity profiling. Over time, this tight process segregration wins trust from clients performing regulated or high-value synthesis campaigns.

    Handling and storage processes also set our product apart. Not every competing producer will monitor and control for every conceivable risk—such as container outgassing, leaching from drum liners, or micro-interactions during storage in uncontrolled warehouses. Our production facility staff have seen the impact of small oversights, learning from every batch that gets flagged for physical change or minor deviation on retest. Direct conversations with process control and QA managers at user plants have generated practical ideas for shipping and handling—steering us toward overpacking and the use of twice-sealed containers for extreme climate transport.

    Learning from Shipping Setbacks and Solutions

    Moving high-value chemical intermediates across continents introduces risks that are invisible to most catalogs and spec sheets. Our teams have responded to issues like broken drums, regulator-mandated re-inspections, and customs clearance delays. Each time, we adapt—modifying labeling to withstand harsh environments, adding non-reactive desiccants, and building documentation that speeds up cross-border transit while minimizing the risk of unplanned exposure.

    Customers in demanding markets—where regulatory inspection is rigorous and paperwork intensely scrutinized—guide many of the shipping optimization protocols we use. After a batch lost clearance in a major port due to insufficient packaging, we introduced palletizing protocols and impact-resistant drum design, addressing real-world obstacles instead of waiting for the next expensive learning lesson. These details are often overlooked by other suppliers focused on a quick sale, but our frontline staff care about the long-term attachment of customer trust to each package delivered.

    Trustworthy Records, Continuous Access, and Direct Support

    Maintaining full transparency for every batch gives our end-users peace of mind. We keep batch records extending back beyond industry-average timescales, allowing users to audit and investigate historical quality any time a question arises. Chemists managing high-impact syntheses or regulatory dossiers value this direct access to batch records and spectral data, and we provide these rapidly and openly.

    Unlike distant resellers, our tech support and application chemists are available for consultation and troubleshooting, not just before a deal, but for years afterward. Many clients need support during unexpected troubleshooting episodes—a failed crystallization, inconsistent reactivity with coupling partners, or confusion over differences in spectral data. Our commitment remains: if something does not perform as expected in the user’s lab, we take rapid, direct action—sometimes producing new analytical reference spectra, sometimes reproducing user protocols in-house to locate an issue or validate a method.

    Conclusion: Hard-Won Knowledge and Continuous Improvement

    Dimethyl-1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylate earned its place in our lineup not through mere catalog listings, but through the knowledge gained from hands-on synthesis, repeated customer collaboration, and a shared commitment to getting every batch right. Supplier claims mean little until rigorous procedures and open, responsive support back them up. Each delivery carries the work of real people, real process learning, and end-user experience woven into the final product.

    By staying accountable to regulators, partnering with experienced users, and keeping communication lines open, we create more than a specification—we deliver a practical tool for real innovation. That is the standard by which we measure our manufacturing, not in abstract promises but in the visible success and satisfaction of the research and production teams we serve.