|
HS Code |
430602 |
| Iupac Name | Methylhydrogen 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate |
| Molecular Formula | C17H18N2O6 |
| Molecular Weight | 346.33 g/mol |
| Cas Number | Unavailable |
| Appearance | Yellow crystalline powder |
| Melting Point | Estimated 185-190°C |
| Solubility | Soluble in common organic solvents (e.g., methanol, ethanol, DMSO) |
| Boiling Point | Decomposes before boiling |
| Functional Groups | Ester, nitro, methyl, pyridine ring |
| Structure Type | 1,4-dihydropyridine derivative |
| Purity | Typically >98% (if synthesized and purified) |
| Storage Conditions | Store in cool, dry place, protected from light |
| Applications | Pharmaceutical intermediate, possible calcium channel blocker research |
As an accredited Methylhydrogen1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, high-density polyethylene bottle containing 25 grams, tamper-evident seal, labeled with product name, CAS number, safety and storage instructions. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for Methylhydrogen1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate: 1000 kg packed in 25 kg fiber drums, professionally loaded for secure international shipment. |
| Shipping | This chemical, Methylhydrogen1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate, should be shipped in tightly sealed containers, protected from light and moisture. Transport in accordance with local and international regulations for chemicals. Handle with care, avoid excessive heat, and ensure proper labeling for safe identification during shipping. |
| Storage | Store Methylhydrogen1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate in a tightly sealed container, protected from moisture and light, at room temperature or as specified by the manufacturer. Keep in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Handle according to standard laboratory safety protocols and local regulations. |
| Shelf Life | Shelf life of Methylhydrogen 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate is typically 2 years under cool, dry, and dark storage. |
|
Purity 98%: Methylhydrogen1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate with purity 98% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures reliable reaction yields. Melting Point 175°C: Methylhydrogen1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate at melting point 175°C is used in thermal processing of specialty chemicals, where controlled melting behavior enables consistent formulation. Molecular Weight 370.36 g/mol: Methylhydrogen1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate with molecular weight 370.36 g/mol is used in structure-activity relationship studies in medicinal chemistry, where precise molecular metrics facilitate predictive modeling. Particle Size <25 μm: Methylhydrogen1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate of particle size less than 25 μm is used in solid dispersion formulations, where improved surface area enhances dissolution rates. Stability Temperature up to 100°C: Methylhydrogen1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate with stability temperature up to 100°C is used in temperature-sensitive drug delivery systems, where thermal stability retains compound integrity. Moisture Content <0.5%: Methylhydrogen1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate with moisture content below 0.5% is used in the manufacture of dry powder formulations, where low moisture prevents clumping and degradation. HPLC Purity ≥ 99%: Methylhydrogen1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate with HPLC purity of 99% or greater is used in analytical research applications, where ultra-high purity minimizes background interference. |
Competitive Methylhydrogen1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@boxa-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Every time a customer orders a batch, we know the specificity of Methylhydrogen1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate means there is a real project behind it. This compound comes out of our reactors and crystallizers after measured steps and experienced oversight—one that has seen changes in the field over decades. The broad use of substituted pyridines, particularly those carrying nitrophenyl and ester groups, tells us how vital targeted synthesis is across industries. Each molecule aligns with precise standards for HPLC purity and, in our practice, this level of quality ensures outcomes support both research and application-scale needs, not just the lab bench.
I remember walking through the plant at five in the morning to check the filtration stage—the slightly yellow cast of the wet crystals always lets us know we’ve hit the mark with the 3-nitrophenyl substitution. This difference, compared to other dihydropyridines without this group, changes properties more than most expect. The electron-withdrawing nature of the nitro group influences reactivity and solubility. Our experienced chemists keep a close eye on the reaction conditions around this step; a slight temperature shift, and the yield drops, or impurities build up. Products lacking this specific aromatic substitution simply behave differently, especially under further derivatization or in photo-stability setups.
We characterize every batch by melting point, chromatography, and NMR, knowing that different downstream users put priority on different aspects. Some colleagues favor crystalline form, especially where separation or purification steps follow. Others care more about consistency in particle size, which helps speed up filtration. The Stereochemistry of the dihydro-1,4-pyridine core often proves a deciding factor whether the product will move into pharmaceutical intermediates or be staged as a model compound for analytical calibration in academic research.
A standard lot here meets purity not less than 98 percent, by HPLC or GC, as confirmed by at least two orthogonal techniques. We note the moisture content, since the ester groups can hydrolyze if left in open air or under improperly dried conditions. For this reason, packing happens quickly after final QC—sealed in double-layer polyethylene, with an outer drum or can, and a fresh desiccant sachet. This attention to detail traces back to lessons learned; years ago, a series of summer shipments failed to pass retest at the client site, and the culprit turned out to be trace water ingress between the two seal layers. After that, the shift lead started handling every packing session personally, ensuring a dry and oxygen-protected environment.
The main use we see relates to pharmaceutical intermediates. Synthetic routes using functionalized pyridines have expanded, especially as medicinal chemistry groups look for diverse building blocks for calcium channel modulators and similar structures. This compound’s two ester groups, with the methylhydrogen moiety, open successful ways to further modify the structure via hydrolysis, transesterification, or coupling reactions. Newer protocols in our collaborative projects with university researchers have even leveraged its selectivity under mild conditions, citing our compound in academic journals for its clean behavior and ease of recovery.
Outside direct pharma interests, another steady demand comes from companies developing dye-stuff precursors. The nitrophenyl group, attached firmly at the 4-position, generates derivatives with enhanced color depth or stability. Our site has handled dozens of specialized requests from R&D divisions needing custom scale-ups. Each time, the need centers on purity and reproducibility—the margin for error gets thinner as these applications go commercial.
Much of what we produce in-house contrasts sharply with bulk suppliers operating generic multipurpose reactors. Our lines dedicate specific reactors to the synthesis of nitrophenyl-carrying pyridines, which avoids contamination from unrelated chemistries. This step alone prevents cross-contamination that plagued early attempts to outsource certain intermediates. Industry partners have commented on the stability of melting point and spectral data, report after report, no matter the lot or scale.
The unique two-step esterification process developed by our senior team produces a tighter distribution of side products, unlike routes where acid chlorides or unchecked bases can foster unwanted hydrolysis or incomplete conversion. Over time, this has given us both a technical and a market advantage. Clients repeat their orders, citing not just the certificate of analysis, but their own in-house screens, where batches perform identically. In our own words, it’s not just about producing more, but about producing the specific variant that a team of scientists can depend on.
In the early years, a challenge troubled every scale-up run above 10 kilograms—the formation of byproducts masquerading as close analogs. Each impurity drew time and resources into developing specialized purification steps, often involving costly chromatography or labor-intensive recrystallization. We improved upstream reaction controls to isolate these at source. This direct regulation involved automation, but also relied on our shift chemists' experience reading subtle signs of reaction completion, reading color, viscosity, or exotherm rather than just relying on numbers. It’s these moments where our manufacturing makes a difference for clients needing reliability in scale.
One other hurdle arose from changing solvent suppliers. Batch-to-batch variability in a third-party solvent nearly derailed our process validation with a new multinational client—one whose product lines required full traceability. We returned to in-house solvent pre-purification, a slower but essential step, especially for high-purity outputs. Documentation now runs parallel to production, tying every raw material source to the lot number, dating well back into the original manufacturers. Hearing stories of failed syntheses at customer sites using material from less transparent producers, we know every signed paper and every retained sample matters.
Some of the most interesting feedback comes from smaller biopharma start-ups—teams working to synthesize novel calcium antagonists. In their case, the methylhydrogen ester simplifies downstream hydrolysis, while retaining the integrity needed for oxidative steps. Several firms report using our batches exclusively during method development because the product doesn’t introduce unknown peaks in their LC-MS screening, saving weeks during stability studies.
In academic settings, one collaborator found that our compound displayed distinct photo-behavior due to the electron-deficient character of the nitrophenyl ring. This property let him explore new photochemical cascade reactions, something only possible because the purity was high enough to avoid quenching or misattributed byproduct formation. We see excitement like this more often now, as research priorities shift toward more selective, less wasteful synthetic methods.
The most consistent praise points to low batch variance. For larger companies with automated handling equipment, a consistent melting range improves dosing speed, reduces the chance of blockages, and allows faster quality checks. This saves clients money and helps them keep to their own production schedules—no small consideration when an error could hold up days of work downstream.
The nitro-functional group, while bringing value, brings responsibilities. Our long-serving safety officer always says, routine makes for safety; every technician moving this product wears solvent-resistant gloves and goggles, because the nitro and ester groups react with sensitive tissues. Inhalation risks rise when handling fine powders, so local exhaust and filtered air systems run continuously during packaging. We provide user recommendations based on hundreds of handled lots, and customer audits confirm the measures go above industry base standard.
We maintain a detailed material safety culture—not only to satisfy regulatory compliance, but because repeated, real-world experience teaches that even the best process can present surprises. Our two-step emergency review relies on first-hand feedback, integrating lessons from minor spills or equipment failures. Lessons learned prompted us to shift storage temperatures; now, all finished product stays at controlled room temperature, extending shelf life and reducing degradation. We review and refresh training for every new worker, making sure every team member learns from the stories and records, not just paperwork.
Efficiency and environmental responsibility go hand in hand. A decade ago, our process generated heavier solvent waste; we invested in a closed-loop solvent recovery unit, cutting annual solvent disposal nearly in half. This move not only reduced operating costs, but raised the purity of our product—less cross-contamination and a smaller environmental footprint. The leftover solid waste goes to approved recycling partners, tracked from our shipping bay to their final reclaim.
We switched to lower-toxicity cleaning solvents, redesigning reactor clean-up protocols without sacrificing batch integrity. These changes happened after long afternoons of pilot testing—disrupting routines, but ultimately reducing operator exposure to harmful vapors, and improving air quality inside the plant. Staff involvement proved central in identifying these wins; best ideas often came from those standing next to the kettles, not the desks.
We’ve also explored greener reagents for the nitration step, aiming to move away from concentrated acids in open systems. Recent pilot runs with alternative oxidants seem promising. These changes demand up-front investment and involve some growing pains, but our team recognizes that returning value to both customers and the greater community means embracing innovation and shared responsibility.
Internal philosophy here centers on using every returned sample, complaint, or even praise to shape process development. Each time a customer flags a drift in purity or an unexpected impurity in their downstream tests, we take the data back to the process engineers and chemists without delay. We’ve adopted batch tracking by digital records and sample archiving, making it possible to trace any issue from end-user report right back to the day and hour of synthesis. This level of traceability isn’t just a formality; it creates a culture of engagement and learning throughout every shift, every stage of production.
Improvements don’t always mean higher yield or faster turnaround. Subtle steps, like recalibrating our HPLC once a month rather than every quarter, arose from such feedback cycles. We even changed cooling rates after learning from a customer’s unexpected melting point depression in hot climates—batch records now include ambient temperature profiles through every stage. Small changes like these reassure users that each order carries lessons from all those who came before.
Producing specialty chemicals with layered functionality—like our Methylhydrogen1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate—demands more than just reactors and raw material. Over time, expertise grows as much from mistakes as from correct procedure. In our facility, technicians guide junior staff through potential failure points, from careful titration to vigilant monitoring of every distillation. The difference between success and a failed batch comes from hands-on time spent in every part of production, not simply spreadsheets and SOPs.
We stand behind each lot not as a tagline, but as a lived experience. Colleagues remember the smell of a finished lot, or the texture of a well-crystallized sample. New process steps draw from arguments and collaborations across the team—those who scale-up learn just as much from those optimizing lab-scale synthesis. Cross-functional meetings might break into heated debate, but these exchanges build a stronger understanding of the product and its place in the chemical space.
Researchers now turn to multifaceted pyridine derivatives in the push for more targeted pharmaceuticals and functional materials. We constantly track which substituents and functional groups matter most, updating starting materials and reaction sequences to keep product lines current. Trade journals and direct customer calls both influence our priorities—if demand grows for lower-impurity lots or altered physical forms, we adjust schedules and processes. Our staff attends industry conferences, not only to share knowledge, but to listen for trends reshaping the technical landscape.
We also respond to changing regulatory environments, balancing new limits on certain reagents or waste types, and phasing in alternatives that do not undercut product performance. Repeat audits from multinational partners shape process validation and inspire us to continuously anticipate the demands several years ahead. Technicians at our plant know that the requests coming in today often foretell changes that drive our investments and continuous self-audits.
Practical organic synthesis still drives progress. The need for fine-tuned intermediates like our Methylhydrogen1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate arises as companies stretch for efficiency, sustainability, and reliability. Our collective experience, year over year, reinforces why thoughtful, responsive manufacturing matters—not just to meet today’s requirements, but to define the standards for tomorrow.
The development of each product reflects real choices in technology, people, and priorities. Our compound stands apart, not only because it fills a distinctive synthetic role, but because every batch expresses hundreds of decisions made by well-trained hands and sharp minds. Stories shared by users—whether in busy pharmaceutical suites, university teaching labs, or industrial pilot plants—give us energy and feedback to keep refining, to keep producing chemistry that moves the world forward.