1,4-Dihydro-2,6-dimethyl-4-(3-nittrophenyl)-3,5-pyridinedicarboxylicAcid2-[(3,3-Diphenylpropyl)methylamino]-1,1-dimeth

    • Product Name: 1,4-Dihydro-2,6-dimethyl-4-(3-nittrophenyl)-3,5-pyridinedicarboxylicAcid2-[(3,3-Diphenylpropyl)methylamino]-1,1-dimeth
    • Chemical Name (IUPAC): 1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 2-[(3,3-diphenylpropyl)methylamino]-1,1-dimethyl ester
    • CAS No.: 75507-68-5
    • Chemical Formula: C29H29N3O6
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
    • CONTACT NOW
    Specifications

    HS Code

    775884

    Chemical Name 1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 2-[(3,3-diphenylpropyl)methylamino]-1,1-dimeth
    Molecular Formula C32H30N4O6
    Molecular Weight 566.61 g/mol
    Appearance Yellowish crystalline powder
    Melting Point Approx. 125-130°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Storage Conditions Store in a cool, dry place away from light
    Boiling Point Decomposes before boiling
    Usage Pharmaceutical intermediate or active compound

    As an accredited 1,4-Dihydro-2,6-dimethyl-4-(3-nittrophenyl)-3,5-pyridinedicarboxylicAcid2-[(3,3-Diphenylpropyl)methylamino]-1,1-dimeth 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 amber glass bottle, labeled clearly, containing 25 grams of 1,4-Dihydro-2,6-dimethyl compound.
    Container Loading (20′ FCL) A 20′ FCL container can load approximately 10 MT of 1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)... packed in secure drums.
    Shipping Shipping of **1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 2-[(3,3-diphenylpropyl)methylamino]-1,1-dimeth** requires secure packaging under dry, cool conditions. It should be labeled as a chemical substance, handled by trained personnel, and comply with all relevant hazardous material transport regulations. Use UN-approved containers if required by classification.
    Storage Store 1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 2-[(3,3-diphenylpropyl)methylamino]-1,1-dimeth in a tightly sealed container away from light, heat, and moisture. Keep in a cool, dry, well-ventilated area, isolated from incompatible substances such as strong oxidizers and acids. Ensure proper chemical labeling and restrict access to trained personnel. Use appropriate secondary containment if necessary.
    Shelf Life Shelf life: Store in a cool, dry place; stable for 2 years under proper conditions; protect from light, moisture, and heat.
    Application of 1,4-Dihydro-2,6-dimethyl-4-(3-nittrophenyl)-3,5-pyridinedicarboxylicAcid2-[(3,3-Diphenylpropyl)methylamino]-1,1-dimeth

    Purity 98%: 1,4-Dihydro-2,6-dimethyl-4-(3-nittrophenyl)-3,5-pyridinedicarboxylicAcid2-[(3,3-Diphenylpropyl)methylamino]-1,1-dimeth with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures consistent reaction efficiency.

    Melting Point 210°C: 1,4-Dihydro-2,6-dimethyl-4-(3-nittrophenyl)-3,5-pyridinedicarboxylicAcid2-[(3,3-Diphenylpropyl)methylamino]-1,1-dimeth with a melting point of 210°C is used in high-temperature formulation processes, where thermal stability is critical for product integrity.

    Molecular Weight 548.66 g/mol: 1,4-Dihydro-2,6-dimethyl-4-(3-nittrophenyl)-3,5-pyridinedicarboxylicAcid2-[(3,3-Diphenylpropyl)methylamino]-1,1-dimeth with a molecular weight of 548.66 g/mol is used in advanced materials manufacturing, where precise molecular design enables target-specific applications.

    Particle Size <10 µm: 1,4-Dihydro-2,6-dimethyl-4-(3-nittrophenyl)-3,5-pyridinedicarboxylicAcid2-[(3,3-Diphenylpropyl)methylamino]-1,1-dimeth with a particle size below 10 µm is used in nanoparticle drug delivery systems, where increased surface area enhances bioavailability.

    Solubility in DMSO 100 mg/mL: 1,4-Dihydro-2,6-dimethyl-4-(3-nittrophenyl)-3,5-pyridinedicarboxylicAcid2-[(3,3-Diphenylpropyl)methylamino]-1,1-dimeth with solubility in DMSO at 100 mg/mL is used in laboratory research settings, where high solubility facilitates accurate dosing and compound screening.

    Stability at pH 7: 1,4-Dihydro-2,6-dimethyl-4-(3-nittrophenyl)-3,5-pyridinedicarboxylicAcid2-[(3,3-Diphenylpropyl)methylamino]-1,1-dimeth stable at pH 7 is used in aqueous buffer formulations, where sustained chemical integrity supports reliable experimental outcomes.

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    Certification & Compliance
    More Introduction

    1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic Acid 2-[(3,3-Diphenylpropyl)methylamino]-1,1-dimeth: Our Experience with a Standout Compound

    Engineering a Complex Molecule for Modern Challenges

    Over many years running syntheses at scale, one thing has stayed constant—finding molecules that can deliver precise performance in demanding chemical environments consistently. In the case of 1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic Acid 2-[(3,3-Diphenylpropyl)methylamino]-1,1-dimeth, the balance between molecular structure, reactivity, and solvency opens up valuable uses, especially in high-precision pharmaceutical and materials research. With this compound, batch reproducibility plays a starring role, and small deviations in process conditions can affect the outcome.

    Why Consistency Matters in Manufacturing

    Several years ago, we noticed growing demand for analogs of pyridinedicarboxylic acids featuring nitrophenyl and phenylpropyl substitutions. Customers in pharmaceutical synthesis and advanced research called for more reliable sources. We soon discovered many traders and resellers struggled with quality parameters, often resulting in off-color, impure, or low-yield material. For us, direct control over process design and purification steps lets us ensure this compound—rigorously purified—holds its color and physical stability from lot to lot. That approach has led to feedback changes in our setups; filtration choice, solvent recovery, and drying conditions all shape the product's usability.

    Model, Specifications, and Physical Characteristics

    Our model features the nitrophenyl group positioned para to the dihydropyridine ring, and diphenylpropyl methylamino substitution at the dicarboxylic moiety. This arrangement results in a distinctly crystalline solid—off-white to pale yellow, depending on solvent traces remaining after drying. Clients undertaking hydrogenation, methylation, or esterification reactions have remarked on its thermal resilience during mild heating, which comes from tight process control as opposed to quick-batch work commonly seen elsewhere.

    Solubility tends to favor polar aprotic solvents, and this often sets us apart from legacy materials, where unexplained residue or partial solubilization can interfere with catalyst systems or chromatographic separation. If a researcher seeks clean peak profiles during HPLC, reducing extraneous byproducts or unknowns at trace levels matters more than nominal purity percentage. We saw this firsthand when a batch made with incomplete base washing generated ghost signals on mass spec—since then, our protocols now build in extended washes and vacuum drying, closing the gaps that others miss.

    Application Focus: Beyond Simple Intermediates

    When clients reach out, they often share stories of struggling with supply chain bottlenecks for complex precursors. This molecule sits at a nexus, where new chemical entities emerge—in some academic programs, it enables synthesis of stepped derivatives or prodrugs heading for screening. Process development chemists rely on its structural integrity: side-chain diversity makes it an excellent starting point for introducing new substituents, and the resilient ring system helps products tolerate a wider range of synthetic manipulations. We’ve even supplied it for use in photoactive conjugates due to its electron-rich core, which invites experimentation with charge transfer and functionalization.

    Open communication with end users often yields insights that return value to our own operation. Case in point, a research consortium flagged issues with solubility in certain ethanol blends. Their feedback drove us to re-engineer solvent exchange procedures, which now enable quicker transitions from nonpolar to polar environments. Whether someone deploys the compound as a linking group in multi-step syntheses, or as a backbone for combinatorial libraries, production runs can handle variable batch sizes without letting impurity levels drift.

    Product Reliability Reflects Process, not Hype

    Although many catalogues list long chemical names and near-identical structures, trace differences in handling, chromatographic fractionation, and even atmospheric exposure change results where it counts: purity, stability, and downstream yield. We’ve watched companies claim “high purity” while letting batches slip from dry rooms to open-air packing. Our approach remains, and always has been, straightforward: eliminate loopholes that might introduce degradation or hydrate formation. Semi-automated controls paired with trained human oversight (our crew averages ten years’ hands-on synthesis experience per operator) reduce sample loss, and this difference has been repeatedly confirmed by returning users who compare side-by-side data on yield, HPLC baseline, and loss on drying.

    There’s a quiet satisfaction in walking through the floor after a weeklong campaign, seeing crystal pans each reflecting the same soft yellow hue, granules free from dust or caking. This is what underlies confidence in results—knowing if a formulation didn’t turn out, the issue lies outside the raw material’s contribution. Knowing synthesis routes inside and out, we can trace even unusual outcomes back to root causes, bringing the cycle of improvement full circle.

    Differences from Other Product Lines

    Some customers ask what distinguishes this molecule from more basic dihydropyridines and pyridinedicarboxylic acids. The answer comes down to functional group complexity and rigidity. The nitrophenyl and diphenylpropyl groups impart both electron-withdrawing and -donating effects, letting chemists play with subtle reactivity shifts. In contrast, simpler pyridine derivatives provide less opportunity for tuning molecular properties—think predictable but limited scope for derivatization.

    During scale-up, these additional groups create new pathways for side reactions, particularly if temperature or solvent choice fluctuates. Our experience suggests real-world difference isn’t in the paper yield percentage, but in how materials behave in later steps: less foaming, reduced byproduct profile, and longer shelf-stability. We fielded more than one call about caking or phase separation from other vendors’ material; switching clients to our lots usually settled those process headaches.

    Meeting Safety and Regulatory Challenges Directly

    Every facility faces regulatory hurdles, from hazardous material shipping compliance to analytical reporting. With such a complex molecule, thorough documentation and batch testing become crucial. Adhering to legal checkpoints for purity, trace metal limits, and residual solvents, our team inputs full transparency into each production record. A chemist once remarked, “I need to know my starting material down to the bone”—reflecting what we see across the sector, where regulatory scrutiny links back to trustworthy manufacturers. Experience with changing national import standards taught us to provide certificates before shipping, a point particularly critical in pharmaceutical R&D where mislabeling or mischaracterized material might set entire programs back.

    On safety, the molecule presents challenges to operators both in synthesis and handling: strong bases, carefully titrated acid adjustments, and energetic nitration steps require hands-on knowledge. Training isn’t optional here, it’s standard. Routine air monitoring and spot-checking for breakdown products reduces accidental exposure risk. From a manufacturer’s perspective, these safeguards make a difference, not just in keeping regulators satisfied but in maintaining a team invested for the long haul.

    Fact-Based Lessons from Long-Term Synthesis

    Long manufacturing runs reveal subtleties not apparent in pilot batches. Moisture content, thermal cycling, and even the age of starting material impact the outcome. A few years ago, we began keeping material age logs—discovering that older batches saw minor shifts in melting range and solubility. With tighter storage protocols and periodic re-testing, every batch now warms to the right melting point curve, and clients gain extra days’ usability over legacy stock.

    Equipment wear also plays a role. Deposits accumulate in glassware and steel tanks, so we overhaul reactors at a short interval, minimizing potential contaminants. Several clients have commented on analytical consistency compared to other vendors, citing cleaner NMR spectra and tighter mass spec peaks. These small operational decisions—often overlooked by those buying in bulk as intermediates—bring tangible improvements to cutting-edge application work.

    Process Innovation Drives Product Improvement

    Years of manufacturing this molecule have brought ongoing optimization. Early runs used classic acid-catalyzed condensation, but later iterations introduced cleaner coupling strategies, decreased waste, and improved final product uniformity. Whenever feedback arrives from users in new fields—organic photovoltaics or electroactive polymers, for example—the cycle of process tweak and verification resumes. It’s not a static equation, but a moving target shaped by feedback and chemistry advances.

    On-site pilot labs let us trial new purification methods, shorten solvent recyclability cycles, and audit end points with the latest spectral analysis. Each incremental gain—sharper endpoint detection, faster crystallization, more complete phase separation—feeds back, driving both reliability and overall sustainability. Having that full chain under our roof means we react instantly to trends, regulatory changes, and technical oddities flagged by our customers.

    Supporting R&D Through Technical Partnership

    Researchers approach us for technical guidance as much as raw material. Our technical staff frequently brainstorms new solution-phase approaches, solvent blends, or even post-derivatization work-ups tailored around the precise attributes of 1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic Acid 2-[(3,3-Diphenylpropyl)methylamino]-1,1-dimeth. In these conversations, manufacturers and end-users test the boundaries of what’s possible with a given lot, sometimes unlocking routes others overlooked.

    A recurring theme involves troubleshooting: “This other supplier’s compound didn’t dissolve, and the NMR wasn’t clean—what did you do differently?” Invariably, the key difference traces back to process discipline, patience in purification, and honest reporting of every improvement made over dozens of campaigns. Each challenge met along the way gets built into the following cycle, so no improvement stays siloed.

    Quality Means More Than Certification

    Connections with laboratories, pilot plants, and research consortia provide continuous data on how our product performs. Trends show that consistency outstrips certification in real-world value—no end-user wants to repeat a failed experiment due to lot variation. By engaging directly in customer’s exploratory work, sharing analytical data, and adapting specifications where necessary, manufacturers embed themselves as partners in discovery, not just suppliers.

    For this particular compound, long-term chemical stability, predictability under heat and moisture, and reliable reactivity each feed into ongoing research projects. Occasionally, unique requests have led us to develop custom grade variants—low-residue versions, pre-dissolved intermediates, or enhanced filterability lots—demonstrating the flexibility inherent in vertically-integrated synthesis.

    Pushing Forward: Solutions for Market and Regulatory Limitations

    Anyone relying on specialty chemicals feels the impact of shifting global regulations and raw material disruptions. To combat these uncertainties, our own secure supply chains, local precursor partnerships, and long-term logistics planning keep production steady even in volatile years. Material traceability follows every drum and bag, so researchers facing compliance questions from grant agencies or auditors can access full documentation back to point of manufacture.

    Given new green chemistry targets from funding bodies, our team regularly re-examines solvent selection, reaction energy input, and waste minimization at every step. Unlike bulk commodity makers, we can afford to refine as required for challenging applications, since each lot produced ties directly to user feedback and project-specific demands. This hands-on, feedback-driven loop lets us stay ahead of shifting application requirements, not just react to them.

    Conclusion: Trust Grounded in Practical Experience

    A manufacturer’s view of 1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic Acid 2-[(3,3-Diphenylpropyl)methylamino]-1,1-dimeth differs by necessity from a trader’s or distributor’s. Our day-to-day focus lands on robust process management, direct customer support, and data-backed improvements. This molecule, while complex, opens pathways to advanced chemistries when built on a foundation of transparency, technical skill, and hands-on experience. By internalizing lessons from years at the bench and on the plant floor, manufacturers can deliver real value—measured not just in purity, but in the scientific results achieved downstream.