|
HS Code |
375798 |
| Chemical Name | 1,4-Dihydro-2,6-Dimethyl-4-(3-Nitrophenyl)-3,5-pyridinedicarboxylic acid monomethylester |
| Molecular Formula | C17H16N2O6 |
| Molecular Weight | 344.32 g/mol |
| Cas Number | 6709-71-7 |
| Appearance | Yellow crystalline powder |
| Melting Point | 172-176°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Storage Conditions | Store at 2-8°C in a dry place |
| Purity | Typically ≥98% |
| Boiling Point | Decomposes before boiling |
| Iupac Name | methyl 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylate |
| Synonyms | Nifedipine intermediate |
| Ec Number | 229-409-6 |
As an accredited 1,4-Dihydro-2,6-Dimethyl-4-(3-Nitrophenyl)-3,5-pyridinedicarboxylic acid monomethylester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is supplied in a 25-gram amber glass bottle, sealed with a screw cap, and labeled with safety and identification details. |
| Container Loading (20′ FCL) | A 20′ FCL can load 8,000–10,000 kg of 1,4-Dihydro-2,6-Dimethyl-4-(3-Nitrophenyl)-3,5-pyridinedicarboxylic acid monomethylester securely packed. |
| Shipping | The chemical **1,4-Dihydro-2,6-Dimethyl-4-(3-Nitrophenyl)-3,5-pyridinedicarboxylic acid monomethylester** should be shipped in a tightly sealed container, protected from light and moisture. Use appropriate cushioning materials, label as a laboratory chemical, and comply with all regional hazardous material shipping regulations to ensure safety during transit and storage. |
| Storage | Store **1,4-Dihydro-2,6-Dimethyl-4-(3-Nitrophenyl)-3,5-pyridinedicarboxylic acid monomethylester** in a tightly sealed container, protected from light and moisture. Keep at 2–8°C in a well-ventilated, cool, and dry area, away from incompatible materials such as strong oxidizers. Ensure proper labeling, and avoid sources of ignition or extreme temperatures. Use gloves and eye protection when handling. |
| Shelf Life | Shelf life: Stable for at least 2 years when stored in a cool, dry place, protected from light and moisture, in sealed container. |
|
Purity 98%: 1,4-Dihydro-2,6-Dimethyl-4-(3-Nitrophenyl)-3,5-pyridinedicarboxylic acid monomethylester with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced impurity profile. Melting Point 180–183°C: 1,4-Dihydro-2,6-Dimethyl-4-(3-Nitrophenyl)-3,5-pyridinedicarboxylic acid monomethylester with a melting point of 180–183°C is used in solid dosage formulation development, where it provides consistent processing and stability. Particle Size <10 μm: 1,4-Dihydro-2,6-Dimethyl-4-(3-Nitrophenyl)-3,5-pyridinedicarboxylic acid monomethylester with particle size below 10 μm is used in microencapsulation applications, where it enhances dispersion uniformity and bioavailability. Stability Temperature up to 110°C: 1,4-Dihydro-2,6-Dimethyl-4-(3-Nitrophenyl)-3,5-pyridinedicarboxylic acid monomethylester with stability temperature up to 110°C is used in polymer modification processes, where it maintains molecular integrity and performance. Molecular Weight 346.31 g/mol: 1,4-Dihydro-2,6-Dimethyl-4-(3-Nitrophenyl)-3,5-pyridinedicarboxylic acid monomethylester with a molecular weight of 346.31 g/mol is used in medicinal chemistry research, where it allows precise dosage calculations and compound tracking. |
Competitive 1,4-Dihydro-2,6-Dimethyl-4-(3-Nitrophenyl)-3,5-pyridinedicarboxylic acid monomethylester 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@bouling-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@bouling-chem.com
Flexible payment, competitive price, premium service - Inquire now!
For those of us behind the reactors, the synthesis and precision behind each batch of 1,4-Dihydro-2,6-Dimethyl-4-(3-Nitrophenyl)-3,5-pyridinedicarboxylic acid monomethylester goes beyond the molecular formula. We know every variable in the process shapes the outcome. From strict raw material selection to steady temperature control during condensation and crystallization, our approach ensures a consistent product.
Our units run the full synthesis chain — solvent choice, catalyst addition, isolation, purification. After years maintaining this process, every stage has become a careful calculation of risk, yield, and effort. It has taught us the unpredictability of trace impurities, the need for in-process checks, and the value of extended drying cycles in controlling final moisture and residual solvents. There’s no shortcut to building that kind of reliability into a specialty chemical.
Half the benefit of working directly with the manufacturer comes from guaranteed transparency in what leaves the plant. Our main commercial offering of this compound keeps a controlled particle size, aiming for a fine crystalline powder, free-flowing and light yellow. We target an assay of no lower than 99.0% by HPLC or titration, which is a threshold we’ve modified after reviewing results from hundreds of scale-up batches.
Residual solvent and moisture content both tend to be grey zones in the market. We keep these low, well beneath pharmacopoeia allowances, even though most end uses don’t demand it. Reproducibility and process control show up not just in specification sheets, but when clients run their own analyses months after delivery and get matching results. We squeeze out unwanted nitro impurities using multiple washes, and our team documents every cleaning cycle.
We offer a standard packaging size, but the plant switches formats efficiently. This flexibility comes from designing our own blending and packing lines. There’s rarely confusion between batch lots, because the whole logistic line is run by operators who stamped their initials on original batch sheets. The relationship between a chemical and its lot of origin is never abstract — not here, with ownership rooted in every ton that leaves our yard.
Experience teaches which markets need this molecule on a regular schedule. The pharmaceutical intermediates sector looks for high-purity batches, typically as a building block for antihypertensive compounds or as a key fragment in dihydropyridine structures related to calcium channel blockers. Some laboratories in Europe and the United States use it for synthesizing custom active pharmaceutical ingredients. Small differences in purity or technical profile can translate to months lost in process validation.
Outside pharma, R&D teams in dye chemistry and specialty pigment manufacturers draw on this compound for the selective introduction of nitro-functionalized aromatic groups. Stability during elevated temperature steps matters to them, so our crystal habit and water content receive extra attention. Over the last five years, our records confirm that our material has matched technical grades requested by labs advancing experimental coatings and specialty polymers, even if these projects remain confidential.
Changing the scale of production for industrial users involves more than adding another reactor. A scale-up always means refining filtration and managing effluent, especially when nitroaromatic intermediates accumulate. Over time, our site has modified drying protocols, improved mother liquor recycling, and sharpened instrument calibration for better in-line monitoring. Fewer off-spec lots benefit everybody. For those handling sensitive syntheses, receiving a consistent product batch after batch means less troubleshooting and less downtime.
On the surface, buyers see a chemical name and an assay value, often supplied by several companies. It’s easy to miss differences unless you’ve run enough syntheses to recognize how tricky low-level impurities or inconsistent particle size can be. Competing lots in the market often pass basic tests but create headaches through sluggish dissolution or leave more weight behind in filtration. Those are not problems we ignore.
Running chromatography on raw material lots tells us how nitro content, moisture traces, and unidentified by-products shape up over time. As the actual producers, we notice how many commercial suppliers, especially aggregators and importers, cannot trace small deviations because they do not control the production floor. Distribution chains may introduce variable storage and repackaging. On our site, product never sits exposed or undergoes unnecessary transfers, so the risk of outside contamination drops away.
We observe that many traders lean heavily on a product made by facilities far removed from the customer. In direct contrast, our system keeps a tight feedback circle between the plant chemists and users — repeated feedback from process chemists using our batch records has sharpened how we tune solvent changes and timing on critical steps. That reality means buyers get a predictable product, not one that wanders lot-to-lot or introduces unwelcome process interruptions.
There’s a gulf between knowing a molecule’s formula and handling its quirks on the production floor. We’ve spent years resolving clumping, managing batch-to-batch variation, and improving yields by only a few percentage points each time. Root cause investigations have shown us how minor temperature deviations left unchecked can result in trace degradation products that laboratory tests don’t always flag immediately.
Our on-site QA team runs random long-term stability tests, sometimes storing retained samples months or years after shipment. These tests matter. We’ve opened up vials a year later, analyzed for impurities, and compared results to the original COA. Inconsistencies don’t stay hidden, and feedback cycles lead us to tighten the process. Clients in regulated sectors appreciate proof when their regulatory submissions call for long-term impurity profiles. We see our reputation reflected in audit reports and the absence of unexpected technical queries from critical users.
We have refined crystallization methods to improve filterability, which cuts down on labor and material loss during the downstream process. Filtration problems are something every chemist dreads, and they usually arise when the supplier loses track of process tweaks. This is never a distant concern for us. Our hands-on experience keeping the same equipment running batch after batch means a direct line from production detail to shipped drum.
Market data suggests the use of pyridine derivatives ranks among the steadiest demand drivers for fine chemical suppliers, especially across APIs and performance chemical sectors. Global supply chains are under strain from variable logistics and raw material spikes, so supply predictability makes the difference for users. Buyers who start with us tend to stay — not for reasons of price bargaining, but because switching suppliers introduces more variables and, in the worst case, failed validations.
We have tracked batch-level performance data over several years and rarely see significant negative feedback on performance metrics. When a deviation occurs, a full root cause analysis becomes mandatory, and client liaison keeps everyone informed. This reflects transparent information sharing, rather than burying or avoiding problems. We host audits for both local inspectors and global customers, exposing our plant practices to external review.
Quality certifications and documentation only go so far. The details live in how a plant operates on any given shift. We've invested in instrument upgrades, frequent calibration, and ongoing staff training, because repeated experience confirmed that process control drifts when maintenance lags. Audit scores and client retention rates back up that approach.
Quality manufacturing requires constant vigilance. Supply chain choke points challenge even the most careful producer. For raw materials, buying from reliable upstream partners maintains input integrity, which keeps the process steady. Last year, a supply-side interruption in a critical intermediate taught us the need for secondary qualification — having backup suppliers for raw nitrobenzene derivatives now keeps us ahead of future disruptions.
From process development to final packaging, the biggest lesson is the value of incremental improvement. Sometimes a filter cloth lasts fewer cycles than expected, or a temperature probe drifts out of calibration. Experience has shown that these minor factors cause most off-spec events. We set up a regime of preventive maintenance, regular staff training, and hands-on supervision from the plant manager. Responsibility never falls through the cracks — the team runs root cause checks immediately, minimizing the size of lost lots and preventing recurrence.
Client feedback ties into each improvement. Over years, clients have raised issues such as unexpected color changes or unaccustomed odor. Plant checks trace these back to subtle raw material shifts, not always readily apparent from COAs. Direct client dialogue accelerates our investigations and has led to more widely shared lessons internally. In a manufacturer’s business, reality always trumps theory — experience shared between the lab and the floor narrows the gap between promise and delivery.
Expertise in this area grows from years of running, monitoring, and improving every aspect of the production chain. Our staff floor has seen the entire process, from small glass reactors to commercial-scale production vessels. This exposure builds an ingrained respect for detail: minor pH drifts, small unknown peaks on an HPLC output, slight variations in color — all flagged and corrected based on that year-in, year-out routine of vigilance.
Authority comes not from claim, but from consistent delivery and the willingness to welcome audits. As direct producers, every order stands as a record of what our site can actually deliver, not a theoretical promise brokered by third parties. Our feedback loop stays close, with the manufacturing team reviewing every issue raised, not just sales or customer support.
Trust grows through openness about problems. For instance, our plant once noticed a deviation in moisture content that slipped past standard test procedures. Quick in-house retesting, open communication, and honest reporting back to clients recovered confidence. These events turn into training guides and root cause documentation, improving our processes and reducing odds of recurrence.
Experience reflects itself in every process improvement. Over time, our manufacturing books fill with handwritten notes: suggestions for faster filtration, reminders about particular hazards when heating specific intermediates, and flagging suppliers for specific raw materials. The weight of process memory means less risk of costly shortcuts or repeat mistakes. This always works to the customer’s advantage, though its value isn’t often visible in a price quote or product sheet.
Direct links to the production source let buyers track every batch, lot number, and process change. We share detailed traceability records, not just generic COAs. Our staff investigates client performance data to further tailor future runs, leading to a cycle of ongoing improvement. Communication lines are clear — from your technical team right back to our chemists, lab technicians, and plant managers — closing the feedback loop far more effectively than distant traders ever manage.
Physical and chemical testing can resolve many disputes, but only the producer logs every tweak to process conditions. We never leave data gaps. Our commitment extends to revalidating specifications whenever feedback or new regulations demand it. The real test of supplier value comes when a client’s synthesis shifts or tightens. Fast response, rooted in direct process knowledge, wins every time.
Clients buying direct avoid the pitfalls of supply chain opacity. Repacking, relabeling, and warehouse mixing common in distributed chemicals disappear from our product lines. Your material comes straight from the production plant, with detailed record chains attached. We watch shipment conditions, photograph outgoing drums or containers, and retain reference samples — ensuring that no batch slips through unmonitored.
Adaptation has shaped our process flow. As industry trends shift, our site has increased investment in lean manufacturing techniques — continuous process review, data-driven yield analysis, and steady debottlenecking. Input sourcing now follows a layered system, drawing from primary and secondary suppliers and documenting certificate checks at every intake. With rising global regulatory attention, batch analytics now extend beyond basic impurity checks, encompassing full traceable audits for long-term stability and safety.
Our site hosts periodic reviews with both equipment and process specialists, catching inefficiencies and refining batch turnaround times. Over the years, we have kept capital reinvestment focused — updating filtration, crystallization, vacuum drying, and solvent recovery. These changes may only trim costs or scrap rates modestly each year, but over a decade, the difference accumulates. What looks like minor advantage to the outside observer translates to smoother supply and a higher comfort level for buyers who need continuity and low risk.
Feedback from end-users drives much of our innovation. Large-scale buyers sometimes ask for supplemental technical data or customized certifications, and we’ve created cross-functional teams tasked exclusively with client audits and detailed documentation support. Several of our production steps have changed after client observations during site visits — from shifting a solvent supplier to adding extra drying time.
Some regulatory developments present challenges in labeling or data reporting. To answer these, our team stays in touch with global technical experts and industry groups, interpreting new standards to keep materials in compliance. Change never moves at a convenient speed, but our operational structure now supports rapid adaptation, reducing any lag from updated requirements to actual plant change.
Years of manufacturing this key intermediate have taught us the value of patience, process literacy, and collaborative transparency. Our 1,4-Dihydro-2,6-Dimethyl-4-(3-Nitrophenyl)-3,5-pyridinedicarboxylic acid monomethylester continues to meet high benchmarks for performance and technical reliability, underpinned by direct experience and deep process know-how.
We credit our clients for driving us to maintain not just consistency but accountability at every level. This compound, like many niche organics, is less forgiving of delay, impurity, or ambiguity. Manufacturing from the original plant, with tight process control and clear lines of communication, keeps us ahead of batch drift and industry uncertainty. Reliability, in our line of work, means producing more than a chemical — it’s a demonstration of continuous investment in craft and process.
If questions ever arise about the lot, process, or technical outcome, our operations team draws upon years of batch records, root cause files, and retained samples. We don’t manage this substance through paperwork alone, but by staying engaged with every customer, instrument, and reactor through the full lifecycle. Our confidence doesn’t rest on claims or marketing; it grows out of hands-on dialog, thorough tracking, and the daily demonstration of manufacturing skill.