2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine

    • Product Name: 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine
    • Chemical Name (IUPAC): dimethyl 4-(2,6-dimethyl-1,4-dihydropyridin-3-yl)butanedioate
    • CAS No.: 5398-36-7
    • Chemical Formula: C13H19NO4
    • 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

    741807

    Iupac Name 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine
    Cas Number 27245-47-6
    Molecular Formula C15H21NO4
    Molecular Weight 279.33 g/mol
    Appearance Yellow crystalline powder
    Melting Point 119-121 °C
    Solubility Soluble in organic solvents such as ethanol and acetone
    Boiling Point Decomposes before boiling
    Purity Typically ≥98% (may depend on supplier)
    Storage Conditions Store at room temperature, in a cool, dry place, protected from light
    Smiles CCOC(=O)C1=CN(C(=C(C1C)C)C(=O)OCC)C
    Density 1.18 g/cm³

    As an accredited 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a sealed 25-gram amber glass bottle with a secure screw cap and tamper-evident seal for protection.
    Container Loading (20′ FCL) 20′ FCL container loads approximately 12 metric tons of 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine, packed in 25kg fiber drums.
    Shipping The chemical **2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine** is typically shipped in tightly sealed containers, protected from light and moisture. It should be transported at room temperature, following standard regulations for non-hazardous organic compounds. Ensure proper labeling and documentation, and handle with care to avoid exposure or spillage during transit.
    Storage 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area. Protect it from direct sunlight, heat, and incompatible substances such as oxidizing agents. Store at room temperature or as specified by the manufacturer. Ensure it is labeled appropriately and kept away from moisture and sources of ignition.
    Shelf Life 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine should be stored cool, dry, protected from light; shelf life is typically 2–3 years.
    Application of 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine

    Purity 98%: 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine of purity 98% is used in pharmaceutical research synthesis, where high chemical purity ensures reproducible reaction outcomes.

    Melting Point 126–128°C: 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine with melting point 126–128°C is used in solid-state formulation studies, where narrow melting range enhances product stability.

    Molecular Weight 281.33 g/mol: 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine with molecular weight 281.33 g/mol is used in chemical intermediate production, where precise molecular identification supports accurate stoichiometric calculations.

    Particle Size <40 µm: 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine with particle size below 40 µm is used in fine chemical manufacturing, where smaller particles improve reaction kinetics.

    Storage Stability up to 25°C: 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine stable up to 25°C is used in analytical laboratories, where storage stability minimizes compound degradation over time.

    UV Absorbance λmax 364 nm: 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine with UV absorbance λmax at 364 nm is used in quantitative HPLC analysis, where distinct absorbance allows for precise detection and monitoring.

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    Certification & Compliance
    More Introduction

    2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine: Practical Insights from Our Manufacturing Floor

    Introduction to the Compound

    The work bench holds countless compounds and intermediates that make their way into a wide range of products, but among the ones that stand out through continual lab and plant experience is 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine. Over years of synthesis and scale-up, this compound, with its distinctive structure and reactivity, has become a reliable staple for many downstream use cases, especially for chemists working in drug discovery and materials science.

    A Closer Look at What Sets It Apart

    Anyone who has handled dihydropyridine derivatives knows that purity and batch-to-batch consistency can make or break a project. Our manufacturing team regularly audits process control data to make sure the product meets those high standards, especially since subtle differences in impurity profiles can influence downstream yields and reaction behavior. This compound’s diethoxycarbonyl substitution, combined with its dimethyl positioning, provides a structural backbone that’s both robust and versatile. Some may compare it to others in the family of 1,4-dihydropyridines, such as unsubstituted dihydropyridines or those with different ester groups, but with hands-on experience, you see tangible differences in solubility, crystallinity, and stability.

    Most of the material that rolls off our reactors finds its way into research labs and industrial R&D pipelines. Our in-house staff includes synthetic chemists who apply this compound in asymmetric catalysis, further hydride transfer reactions, and studies involving ion channels. In the real world, speed, data reliability, and reproducibility are the key drivers for scientists; we keep a close watch on these factors during each run so the next person down the stream faces fewer surprises.

    Process Knowledge and Safety at Scale

    Scaling up a complex intermediate like 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine means digging deep into the nuts and bolts of reaction controls, purification steps, and waste handling. From our experience, methyl and diethoxycarbonyl substitutions introduce additional sensitivity to water and oxidants; the team revises process parameters regularly in order to keep moisture and air exposure at strict minimums. Early on, the lab bench trials might only yield a few grams, but sitting in an industrial reactor, even a slight slip in atmospheric control can bring out unwanted by-products. Our process engineers have documented these troubleshooting cases—nothing substitutes for the real feedback of multiple full-scale campaigns.

    The esterification and hydrogenation steps in its synthesis generate specific effluents, and we route these streams for responsible treatment before disposal. Focusing on chemical safety is not a one-and-done checkmark but a daily practice. Face-to-face feedback from those who run the glass-lining and drying units drives continuous improvement, as does tracking odor levels and potential exotherms. You feel the advantage most during campaign launches: new employees learn from records left by those before them—a living knowledge base that helps avoid the errors of earlier runs.

    Why This Chromophore Catches Attention

    This compound’s distinct features give it an edge in research and development. The 1,4-dihydropyridine core structures often serve as charged intermediates in organic transformations. From our benchtop studies, the dual ester groups at the 3 and 5 positions expand its solubility profile, enabling easier handling in both organic and mixed solvent systems. The two methyl groups at the 2 and 6 positions increase electron density, providing stability against certain degradation pathways but making it more reactive in others; this balance allows chemists to adjust reaction conditions for their target transformations.

    It’s sometimes tempting to view these structural nuances as academic, but in practice, they determine real-world project timelines. During one pilot batch, a team using a simple methylated dihydropyridine reported longer purification cycles and higher levels of colored side products in comparison to batches using our diethoxycarbonyl-methylated variant. Direct in-process monitoring confirmed lower levels of by-product peaks, translating to fewer headaches at the isolation stage.

    Applications Backed by Experience

    The hands-on work in process optimization brings clear evidence that this compound fits applications where high chemical selectivity and manageable physical properties matter most. In calcium channel modulator screening projects, for example, purity and performance correlate directly with observational outcomes because impurities can interfere with activity measurements, even at trace levels. When our teams prepared the compound for use in ion transport models, consistent melting point and solubility characteristics became vital—reproducibility in those physical properties allows faster assay set-up and clearer interpretation of biological data.

    Pharmaceutical intermediates depend on reliability. The most common feedback received from clients revolves around ease of weighing, dissolution in standard solvents, and batch-to-batch color consistency. Each time questions surface about employing this compound as a precursor for custom API syntheses, our chemists find themselves drawing from batches kept on-hand as internal references. Comparing our material to similar compounds, like 3,5-diacetoxy substitutions or other branched dihydropyridines, brings up conversations about yield drifts: the diethoxycarbonyl groups, unlike bulkier or more rigid ester groups, give both better yields at scale and a manageable purification path.

    Differences From Other Dihydropyridines—Backed By Real-World Data

    Over repeated production campaigns, our records show that this compound handles better than many alternatives during crystallization. Where other dihydropyridines with bulkier substituents can form oily residues or stubborn amorphous solids, 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine reliably delivers a robust crystalline output after the final step. This practical feature shaves hours off the work in drying rooms and reduces the frequency of reprocessing—small changes with major impact in a busy plant.

    Some peers have tried switching to other esters, such as methyl or tert-butyl, looking for higher throughput, but our collective notes show how these alternatives complicate both purification and downstream functionalization. Low reactivity at some positions, coupled with unpredictable side reactions, tends to eat into both yield and margin. For clients looking to push reactions forward in a timely way, our team reports a preference for the smoother work-up provided by the diethoxycarbonyl variant. The reproducibility of these results in both internal and customer trials provides a level of confidence not always found in less thoroughly tested materials.

    Specifications That Matter in The Real World

    Lab teams and production managers often focus on what specifications make a difference at the bench and in the vessel. In our hands, purity typically exceeds 99 percent as measured by HPLC, and moisture control remains a key focus throughout all processing steps. Any trace of over-oxidation or incomplete reaction can affect both the chemical’s color and downstream transformations, so every batch undergoes visual and instrumental checks. By working closely with quality control chemists, production staff have learned to recognize early warning signs, like subtle shifts in melting behavior or color tone, which usually signal upstream issues that we work to catch before shipping.

    Granular sizing, ease of transfer, and non-hygroscopic nature often come up in daily conversations. This might sound mundane, but someone who has ever transferred a powder prone to clumping or static knows how an efficient transfer process saves time and mess in the lab. Reports from multiple campaigns bear out the observation that this compound requires fewer interventions in both weighing and transfer compared to products with different ester loads or less consistent particle sizing.

    Building in Quality from Start to Finish

    Our plant follows continuous improvement protocols rooted in real, practical lessons learned. Recording critical variables at each stage—from solvent charge to reflux time—enables us to spot trends and troubleshoot problems before they interrupt a campaign. Staff members regularly cross-train, and many have backgrounds working in both analytical labs and manufacturing roles, which fosters a broader sense of accountability and a team spirit focused on delivering a uniform product.

    Recent process optimization put a spotlight on solvent use and minimization of waste streams. By adjusting esterification step conditions, the team reduced solvent use and increased yield with no loss in purity, making a measurable difference in both throughput rate and environmental impact. Regular reviews and on-the-job training keep everyone informed, from operators on the floor to research scientists at the front end of new project development.

    Supporting Advances in Science and Industry

    Many key advances in medicinal chemistry trace back to the accessibility and reliability of core intermediates. Several pharmaceutical projects that rely on rapid prototyping of new dihydropyridine derivatives begin with stock of the 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine produced at our site. Our records highlight fewer impurities and simpler purification when compared to both commercial and in-house runs of alternatives. In published collaborations, the compound’s clean analytical profile has been cited as a factor in efficient structure-activity relationship mapping.

    Outside pharmaceuticals, the compound finds use as a model substrate in physical organic chemistry studies. Its predictable redox behavior—in contrast to unprotected or differently substituted dihydropyridines—allows researchers to map reaction mechanisms and explore new catalytic cycles. Routine supply of consistent material pays off in reduced downtime and fewer failed experiments, particularly in academic or high-throughput screening environments.

    Tackling Challenges in Production and Usage

    No plant run ever unfolds exactly according to plan, but much of our confidence in this intermediate comes from troubleshooting years. One challenge that recurred in early campaigns was sensitivity to trace water—demanding careful selection of drying agents and storage solutions. Teams iterated on drying cycles for both starting materials and final product, and logs show that small shifts in atmospheric controls correlated with higher stability and lower degradation patches.

    Another notable experience revolved around optimizing filtration rates. Like many cyclic compounds, the morphology of the crystals depends on both the mixing regime and the seeding strategy. Over time, adjustments in agitation speed and cooling rate helped us move away from batch-to-batch variability, leading to crystals that filter efficiently and dry evenly. These adjustments, documented and shared across shifts, not only speed up campaign cycles but also protect against reprocessing costs.

    Feedback That Drives Continuous Improvement

    Direct customer conversations often surface new insights into both strengths and potential pain points of the compound. Some users have stressed the importance of packaging that protects from accidental moisture ingress during long storage or transport. Taking that feedback seriously, our packaging team adopted new linings and desiccant combinations, further reducing the risk of product changes prior to use.

    A recurring topic is clarity around actual impurity profiles, not just summarized analytical numbers. We now share more detailed chromatograms and spectra with user shipments, giving research and manufacturing partners the transparency they need to make informed decisions about integration into their workflows. The improved documentation has come from direct experience: we’ve seen how misunderstandings about trace by-products can delay project milestones or introduce unnecessary troubleshooting at the user end.

    Environmental and Compliance Considerations

    The changing landscape of environmental regulations and responsible manufacturing directly affects how we conduct business every day. Our waste management protocols take special care with effluent streams produced during both synthesis and purification steps. Tracking and managing solvents, by-products, and spent reagents isn’t just an exercise in compliance—plant staff understand the need to balance operational costs with stewardship of the environment where we operate.

    Regular audits by safety officers, combined with feedback from local authorities, provide a reality check on both process and outcomes. In some cases, investing in better solvent recycling systems and more efficient scrubbers hasn’t just lowered total emissions but also created a safer work environment for the team. These investments spring directly from lessons learned during routine shutdowns and safety reviews—practical culture shifts powered by real people and real feedback.

    Concluding Thoughts Drawn from Practice

    Decades of direct experience with 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine have shaped the way we approach both production and customer collaboration. Each batch brings minor shifts and necessary adjustments, but the reliability of this compound over time has made it the preferred choice for many advanced syntheses, pilot projects, and research pipelines. Its consistent behavior, combined with safety- and environment-centered protocols, shows what can be achieved when deep process knowledge blends with a commitment to continuous improvement.