|
HS Code |
813085 |
| Chemical Name | 2-Pyridinecarboxylic acid, 4-methyl-6-nitro- |
| Molecular Formula | C7H6N2O4 |
| Molecular Weight | 182.14 g/mol |
| Cas Number | 13874-82-1 |
| Appearance | Yellow solid |
| Melting Point | 209-211°C |
| Solubility In Water | Slightly soluble |
| Pubchem Cid | 36811 |
| Inchi Key | WZNHRKOHJAVTDC-UHFFFAOYSA-N |
As an accredited 2-Pyridinecarboxylic acid, 4-methyl-6-nitro- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 25 g of 2-Pyridinecarboxylic acid, 4-methyl-6-nitro-, is supplied in a sealed amber glass bottle with tamper-evident cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-Pyridinecarboxylic acid, 4-methyl-6-nitro-: Safely packed 20-foot containers, moisture-protected, labeled according to chemical transport regulations. |
| Shipping | 2-Pyridinecarboxylic acid, 4-methyl-6-nitro- is shipped in tightly sealed containers to protect from moisture, light, and incompatible substances. Packaging follows regulatory guidelines for hazardous chemicals. During transit, it is labeled appropriately and handled with care to prevent leaks or spills. Storage at controlled room temperature is recommended during shipping. |
| Storage | 2-Pyridinecarboxylic acid, 4-methyl-6-nitro- should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect it from light and moisture. Proper labeling and secondary containment are recommended to prevent leaks or spills. Store at room temperature and follow relevant safety guidelines for handling hazardous chemicals. |
| Shelf Life | 2-Pyridinecarboxylic acid, 4-methyl-6-nitro-, typically has a shelf life of 2-3 years if stored properly in cool, dry conditions. |
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Purity 98%: 2-Pyridinecarboxylic acid, 4-methyl-6-nitro- with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced side reactions. Melting point 180°C: 2-Pyridinecarboxylic acid, 4-methyl-6-nitro- with a melting point of 180°C is used in polymer research, where thermal stability during processing is achieved. Particle size <50 μm: 2-Pyridinecarboxylic acid, 4-methyl-6-nitro- with particle size under 50 μm is used in advanced material formulations, where enhanced dispersion and reactivity are obtained. Solubility in DMSO: 2-Pyridinecarboxylic acid, 4-methyl-6-nitro- with high solubility in DMSO is used in organic synthesis, where it facilitates homogeneous reaction mixtures. Stability at 120°C: 2-Pyridinecarboxylic acid, 4-methyl-6-nitro- with stability at 120°C is used in chemical process optimization, where consistent product quality is maintained under elevated temperatures. |
Competitive 2-Pyridinecarboxylic acid, 4-methyl-6-nitro- prices that fit your budget—flexible terms and customized quotes for every order.
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We’ve spent the better part of the past decade working directly with 2-Pyridinecarboxylic acid, 4-methyl-6-nitro-, a compound that doesn’t just pass through the lab as a number on a requisition slip. For those who haven’t spent a lot of time handling or synthesizing this compound, its importance might seem niche. The fact is, the interaction between the nitro and methyl groups on the pyridine ring opens a lot of doors in multi-step synthesis routes, particularly for pharmaceutical intermediates and advanced materials research. Seeing it move from raw ingredients to finished batches on our floor, we’ve come to respect its versatility and the reliable performance it offers in downstream applications.
Over the years, monitoring every step and tweaking everything from temperature ramps to solvent selection has taught us a lot about this molecule’s personality. The combination of the nitro group at the 6-position and the methyl at the 4-position of the pyridine ring isn’t just a structural variation—it’s the foundation of its particular behavior in condensation reactions, cross-couplings, and amidation. We learned early on that quality at the upstream synthesis stage reflects downstream in both performance and impurity profile. In our hands, it’s the difference between a product that delivers the desired yield in a single pass and one that creates headaches during purification.
Academic labs usually come to us with very specific purity and characterization requests. For more process-driven clients, it’s batch reproducibility and a manageable safety profile that matter most. By controlling reaction pathways and fine-tuning the nitration and methylation steps, our team’s experience helps us avoid by-products that can complicate analysis or scale-up. Our knowledge in scaling from grams to multi-kilogram lots stems from years of observing crystallization behavior and filtration challenges on the factory line.
This isn’t just a chemical listed in a catalog. Each batch reveals the subtleties of color, odor, and crystallinity—details that make a pronounced difference in downstream reactions such as Suzuki coupling or further functionalization. We’ve witnessed how minor impurities interact with organometallic reagents, especially under scale-up scenarios. Keeping unwanted side-products low isn’t just about compliance; it’s about trust in predictable chemistry.
Over repeated cycles, we have seen how a targeted melting point, a consistent crystal habit, and robust HPLC purity translate into fewer headaches in formulation or intermediate steps. Researchers ask us about fine points, such as limits for specific heavy metals or GC/LC data, because they know trace contaminants can derail an entire project or show up in regulatory filings. Using freshly analyzed raw materials, maintaining glycol and moisture controls, and performing small-scale piloting before every large run have formed the backbone of our quality protocol.
It’s easy to overlook, but the way our 2-Pyridinecarboxylic acid, 4-methyl-6-nitro- is filtered, washed, and dried directly affects downstream solubility and reactivity. More than once, in collaborative troubleshooting with our clients, a slightly uneven drying curve has revealed itself as the culprit behind a sluggish re-dissolving stage or an unexpected by-product. In these moments we lean on our process notes and decades of lab logs to mass-balance impurities and trace them back to specific steps.
Much of the chemical community turns to more common pyridinecarboxylic acids like picolinic acid or nicotinic acid isomers. The introduction of the 4-methyl and 6-nitro groups brings a shift in electronic character that changes how the molecule coordinates with metals, how it acts as a ligand, and how easily it enters into palladium-catalyzed processes. Through practice, we’ve learned one of the defining traits of our product is its balance between electron-withdrawing and electron-donating effects on the ring. Other structural isomers just don’t provide the same utility in processes like regioselective functionalization.
In crystallization and purification work, 2-Pyridinecarboxylic acid, 4-methyl-6-nitro- shows a certain resilience that allows a bit more flexibility in solvent use. We have watched as even minor tweaks—switching from ethanol to isopropanol in final washes—change the color and filterability. The stability under moderate heating and its clear, defined melting point have helped clients avoid the surprises that can pop up with less resilient derivatives.
Clients who return to us year after year nearly all put this material to work as a key intermediate for heterocycle construction or as a coupling agent precursor in medicinal chemistry. The combination of the acid, nitro, and methyl functionalities means the compound not only acts as a building block for more complex architectures but also simplifies downstream modifications for combinatorial libraries, small-molecule drugs, or pigment applications. In pilot plant projects, especially, researchers have told us how our product enables selective transformations without extensive post-reaction workup.
Our long-term partners in crop protection and specialty materials value its role in producing high-purity intermediates with minimal side-reactions. In practice, this reduces purification burden and supports high-throughput screening, two critical needs in fast-moving industrial settings. Over time, we’ve invested in refining each metric—particle size, moisture control, ease of filtration—because these nuances save time (and money) in manufacturing.
Working day in and day out with nitro-containing pyridine compounds, our personnel go through specialized handling and storage training. While some users may not see the difference between handling this acid and other pyridine derivatives, the nitro group changes the way we approach both reactivity and workplace safety. We take special care with dust control and containment, especially at charging, drying, and packing stages, as repeated exposure to nitroaromatic compounds can carry occupational health risks.
Over the past few years, we’ve adopted continuous monitoring for volatile organic compounds and installed specific extraction systems for areas where open handling occurs. Our waste-treatment protocols separate aqueous and organic waste streams, allowing us to minimize the risk of unwanted reduction or environmental discharge. Feedback from clients led us to design packaging that fits safely into their own hazard management systems, reducing the chances of stacking or rupture during storage.
It’s tempting to see batch certification and purity checks as box-ticking exercises. We’ve learned, often the hard way, how minor lapses—sloppy labeling, incomplete batch records, letting a batch sit with residual solvent—ripple through the production chain. Our QA approach rests on actual lab and shop-floor experience: spectra from FTIR and NMR don’t just go into a folder; experienced technicians check them against physical appearance, odor, and yield history. Every batch draws on years of accumulated knowledge, and unusual data prompts a double-check long before the material ever leaves our site.
Audits by outside partners, regulatory bodies, and ISO compliance checks keep us sharp, but the real assurance comes from the questions our long-term clients ask—whether this batch matches the critical impurity profiles from last year, whether the moisture content has shifted seasonally, and how the product behaves in their scale-up trials. We believe transparency and traceability make for lasting trust, and we encourage direct feedback from users who notice anomalies or have specialized needs.
The most valuable lessons emerge from moments of trouble. Several years ago, after a persistent batch color deviation, root-cause analysis and reprocessing not only improved the product but also exposed a sampling method that hadn’t kept pace with process changes. Addressing that, we upgraded not just lab equipment, but also staff training and in-process controls, leading to steadier results ever since.
Ongoing collaboration with universities and industrial partners drives our next round of process optimization. As demands shift—greener chemistry, lower residual solvents, improved trace analysis—we adapt upstream by experimenting with new solvents and safer catalysts in laboratory pilots before scaling up. The shift to continuous monitoring and digital record-keeping has cut errors and downtime. Bringing operators into troubleshooting meetings ensures practical ideas flow both ways; insights from the bench and production line guide improvements and ensure the product keeps meeting user needs with fewer deviations.
Over repeated runs, precision and predictability keep labs coming back. During production planning calls, clients ask about previous batch performance, request custom lot-specific certificates, and sometimes send back aliquots for side-by-side comparison with earlier years’ material. Input from medicinal and process chemists led us to tailor batch sizes and adjust impurity targets to reduce downstream work for their teams.
It’s common for new users to remark on the consistent orange-yellow color and quick response in coupling reactions, features that help with tracking progress in multi-step synthesis. Several partners reported improved step yields and faster purification when switching from competing sources. This speaks to the tight controls we maintain on particle morphology and solvent inclusion. We share these outcomes amongst staff as proof that listening and responding to practical challenges pays off in loyalty and reputation.
Historically, much of the demand for 2-Pyridinecarboxylic acid, 4-methyl-6-nitro- came from pharmaceutical and agrochemical intermediates. Lately, we have seen an uptick in materials science researchers using it for advanced polymers or as catalysts rests upon the electronic tuning possible thanks to the nitro and methyl positions. With this shift, the push toward greener chemistry methods has gained urgency. Our development team now focuses not only on improving product consistency but on reducing the energy footprint of thermal stages, switching to aqueous workups where possible, and reclaiming mother liquors for new runs.
Pressure from regulators and brand-conscious clients accelerated our move to low-waste production cycles. Minimizing solvent use, improving yield efficiency, and integrating process analytical technology have not only lowered costs, but also improved our site’s emissions data. Clients interested in lifecycle analysis or green claims find that these investments translate into measurable benefits, not just marketing gaps. Our internal green chemistry committee routinely reviews literature and collaborates with external researchers to adopt next-generation practices that increase both safety and sustainability.
After years of repeated syntheses, mid-night troubleshooting, and countless analytical runs, our perspective on 2-Pyridinecarboxylic acid, 4-methyl-6-nitro- has changed. The properties captured in any chemical handbook only tell one part of the story. The lessons we’ve drawn from scaling up, right-sizing packaging, and troubleshooting drying or reaction quirks allow us to offer a product that performs predictably under pressure. There’s no replacement for knowing how a product behaves after months in storage or through the rigors of overseas shipping.
By keeping a short feedback loop between production, lab, and client site, we’re able to catch potential issues early and tweak protocols as new application needs arise. Instead of seeing downstream challenges as “not our problem,” we tackle them alongside our users, drawing from years of hands-on practice and cross-lab dialogue.
Producing and supplying 2-Pyridinecarboxylic acid, 4-methyl-6-nitro- isn’t just about meeting a spec; it’s about making sure every shipment does its job in your process. The market for heterocyclic building blocks grows more competitive and demanding each year. Having a manufacturing partner who can talk specifics—moisture content, impurity fingerprinting, handling nuances—means fewer surprises in both research and production.
From synthesizing the first gram to shipping off multi-kilo lots, we’ve come to realize the greatest value we provide is the depth of lived experience behind each batch. Our approach folds together scientific rigor, practical feedback, and continuous process improvement. In the end, a reliable supply of 2-Pyridinecarboxylic acid, 4-methyl-6-nitro- stands as a testament to what experience, adaptability, and open communication can achieve. We look forward to supporting those pushing the limits of synthesis and innovation with the tools and know-how needed to succeed.