2-Methyl-3-nitropyridine-6-carboxylic acid

    • Product Name: 2-Methyl-3-nitropyridine-6-carboxylic acid
    • Chemical Name (IUPAC): 2-methyl-3-nitropyridine-6-carboxylic acid
    • CAS No.: 6968-60-1
    • Chemical Formula: C7H6N2O4
    • 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

    589896

    Product Name 2-Methyl-3-nitropyridine-6-carboxylic acid
    Cas Number 131747-57-8
    Molecular Formula C7H6N2O4
    Molecular Weight 182.13 g/mol
    Appearance Light yellow to yellow solid
    Melting Point 167-171 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Smiles Cc1nc(cc(n1)[N+](=O)[O-])C(=O)O

    As an accredited 2-Methyl-3-nitropyridine-6-carboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass bottle containing 25 grams of 2-Methyl-3-nitropyridine-6-carboxylic acid, labeled with safety, batch, and purity information.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 2-Methyl-3-nitropyridine-6-carboxylic acid ensures secure, moisture-free bulk packaging, maximizing space and maintaining product integrity.
    Shipping 2-Methyl-3-nitropyridine-6-carboxylic acid is shipped in tightly sealed containers to prevent moisture and contamination. It should be stored in a cool, dry place, away from incompatible substances. Packaging complies with chemical safety regulations to ensure secure transit. Always handle with appropriate personal protective equipment during shipping and handling.
    Storage 2-Methyl-3-nitropyridine-6-carboxylic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers and bases. Ensure appropriate labeling, and avoid moisture or humidity. Handle with suitable personal protective equipment and follow standard chemical safety protocols for storage and handling.
    Shelf Life **Shelf Life:** Store 2-Methyl-3-nitropyridine-6-carboxylic acid in a cool, dry place; shelf life is typically 2-3 years unopened.
    Application of 2-Methyl-3-nitropyridine-6-carboxylic acid

    Purity 98%: 2-Methyl-3-nitropyridine-6-carboxylic acid with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and consistency in active compound production.

    Melting point 174°C: 2-Methyl-3-nitropyridine-6-carboxylic acid with a melting point of 174°C is used in high-temperature organic reactions, where it provides thermal stability and controlled reactivity.

    Molecular weight 182.13 g/mol: 2-Methyl-3-nitropyridine-6-carboxylic acid with molecular weight 182.13 g/mol is used in agrochemical research, where precise dosing and formulation development are required.

    Particle size <50 μm: 2-Methyl-3-nitropyridine-6-carboxylic acid with particle size less than 50 μm is used in fine chemical manufacturing, where rapid dissolution and uniform mixing are essential.

    Stability temperature 120°C: 2-Methyl-3-nitropyridine-6-carboxylic acid with stability temperature of 120°C is used in catalyst development, where resistance to decomposition under process conditions is critical.

    Water content <0.5%: 2-Methyl-3-nitropyridine-6-carboxylic acid with water content below 0.5% is used in moisture-sensitive coupling reactions, where it minimizes hydrolysis and enhances product purity.

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    Certification & Compliance
    More Introduction

    2-Methyl-3-nitropyridine-6-carboxylic Acid: A Manufacturer’s Perspective

    Every product starts with a need. For years, research and manufacturing teams have looked for high-purity intermediates to unlock new possibilities in pharmaceuticals, crop protection, and specialty chemicals. Time and experience in chemical synthesis have shaped the way we produce 2-Methyl-3-nitropyridine-6-carboxylic acid. This unique compound doesn’t just represent another entry in our catalog. It is a response to demanding requirements, setting itself apart from the crowd in both performance and consistency.

    Understanding the Structure and Value

    2-Methyl-3-nitropyridine-6-carboxylic acid has earned its niche through a well-defined molecular arrangement. The presence of both the nitro and carboxylic acid motifs on the pyridine ring provides dual reactivity. Our team has observed, after years of process refinement, that this combination enhances the compound’s suitability as a substrate or building block where both electron-withdrawing properties and directed functionalization are needed. That distinction may sound technical, but it matters when aiming for reliable yield in scale-up reactions that impact a project timeline and bottom line.

    Typical Specifications from Our Bench

    We produce 2-Methyl-3-nitropyridine-6-carboxylic acid with high-purity thresholds, as measured by HPLC and NMR. Through tight process controls during nitration, methylation, and final oxidation, we consistently achieve purity specifications above 98%. The compound presents as a pale yellow solid, with a melting range confirmed by repeated batch testing, reflecting our commitment to reproducibility. We keep an eye on residual solvents and moisture—trace levels can throw off downstream reactions or crystallization steps in the hands of formulators. Regular GC and Karl Fischer titrations back up our labeling, a detail not always seen from trading intermediaries or brokered lots.

    Application Insights Rooted in Practice

    This compound owes its popularity to how it adapts to practical challenges in synthesis. In our own facility, and among partner labs, 2-Methyl-3-nitropyridine-6-carboxylic acid often acts as an intermediate in the assembly of heterocyclic scaffolds used in libraries for potential drug candidates. Teams value the controlled reactivity: the methyl group allows for further elaboration under mild conditions, while the nitro group can be selectively reduced or modified based on the pathway. The carboxylic acid moiety simplifies downstream conversion into amides, esters, or salts. Those who have struggled with less-functionalized pyridine analogs often hit bottlenecks in either reactivity or purification. This compound’s arrangement often opens up routes that would require protecting group strategies or laborious multi-step workarounds in other chemistries.

    In crop protection, formulation chemists make use of its electron-deficient ring as a core in new active ingredients, banking on its stability under varied reaction setups. The compound's solubility profile offers flexibility in selecting carriers or solvents for scale-up. Through live demonstration runs in our pilot plant, we have watched downstream partners reduce steps and purification overhead compared to using mixtures or less refined alternates.

    From Bench to Ton-Scale: Lessons Learned in Production

    Producing 2-Methyl-3-nitropyridine-6-carboxylic acid at scale brings challenges beyond what analytical chemistry can predict. Early attempts revealed how sensitive the process is to even slight changes in reaction temperatures or acid concentration during nitration. We learned to continuously monitor not only the main reaction but also side-product formation—like isomerized pyridine derivatives or over-nitrated impurities—which can compromise downstream utility. That attention to process hazards, supported by real-world accident data and in-house root-cause analysis, informs our current standard operating procedures.

    Adaptation comes in the form of incremental improvements. After scaling out the process from flask to reactor, we installed automated process monitoring to spot subtle heat releases. Our teams act fast, adjusting feeds and mixing speeds to keep impurity profiles narrow. Recrystallization parameters are not “one-size-fits-all”—each batch requires minor tweaks, depending on ambient humidity and starting material source. We instituted batch records for each lot, which provide transparency for users who insist on backward traceability.

    What Sets This Product Apart

    As direct manufacturers, we know substitutes exist in the market. Some traders offer materials described as “comparable,” but repeated customer feedback—and our own comparative tests—highlight tangible differences. We do not accept materials simply blended or repackaged from upstream sources lacking real process documentation. Outsourced or resold lots sometimes present a combination of higher aldehyde content, misaligned melting point, or contain trace byproducts that evade casual inspection. These factors become pain points for end-users who rely on clean, efficient conversions and reproducible yields.

    Our product emerges from validated, in-house processes, not as a one-off synthesis, but as the result of years spent refining each synthesis step. The consistency benefits both small-scale innovation and industrial runs where materials flow through packed columns or continuous flow reactors. High purity translates to less downtime—technicians spend less time unclogging reactors, and analysts spend fewer nights tracking down ghost peaks in spectra. Each kilogram delivered carries with it the assurance that both practical and technical insights from our team have shaped its journey.

    Common Applications: Real-World Scenarios

    Pharmaceutical researchers form the core user group for 2-Methyl-3-nitropyridine-6-carboxylic acid. Its reactivity profile supports the creation of fused bicyclic systems, core to kinase inhibitors and CNS-active compounds. We see medicinal chemistry groups use it as a strategic node in multi-step syntheses, especially when rapid library expansion is necessary. The reaction mechanism leverages both polarized positions and the acid group, which helps in controlling byproduct formation. In one customer project, moving from a methyl-only derivative to our nitro-carboxylic acid shortened total synthesis by two steps, unlocking not just time savings, but better overall yield.

    Crop protection companies report similar gains. In select herbicide and fungicide projects, the compound acts as a backbone. They modify either the methyl or nitro positions through classic nucleophilic substitution, then transform the acid into a salt or ester for field-use formulations. In our own pilot trials, these chemical modifications demonstrate stable shelf life—significant when shipping overseas or storing over multiple planting seasons. Other pyridine acids often degrade or discolor under these conditions, which can impact field efficacy and regulatory compliance.

    Specialty chemical development, particularly among OLED and advanced materials researchers, taps into its electron-withdrawing properties. Engineers pair this group with electron-rich partners to tune optical and electronic behavior, targeting display, solar cell, or sensor applications. Our technical support team works alongside development teams to troubleshoot unusual scale-up issues, offering insight from our analytic and operations staff. In contrast, off-the-shelf analogs rarely offer the same reliability in profile or responsiveness from source.

    Feedback, Problem Solving, and Continuous Improvement

    Collecting feedback matters. Years in contract manufacturing have shown us that the story doesn’t end at delivery. Users speak candidly about what works and what slows down their projects. Some flag concerns about solubility in polar aprotic solvents, prompting our R&D to test temperature stability and alternative crystallization methods. Others want to press the limits of purity—especially for regulated pharma applications—so we invest in routine upgrades to our detection and removal systems for trace contaminants.

    We also recognize unique, outlier requests: smaller particle sizes for micronization, enhanced lot-to-lot documentation, or support troubleshooting tough impurity profiles. Our hands-on process allows us to implement these changes without delay, passing the benefit directly to users. Feedback cycles feed into revised SOPs, investment in upgraded dryers, degassers, and environmental controls. In high-stakes environments, research groups value not just product, but the ability to reach live technical experts—the same individuals who monitor synthesis from raw material arrival through drum loading.

    Environmental Impact and Safety Practices from a Manufacturer’s Lens

    Responsible manufacturing extends beyond compliance. Our facility integrates solvent recovery and advanced air scrubbing to keep emissions in check. Wastewater, a focus for both environmental agencies and company conscience, is pre-treated and monitored for residual pyridine and nitro species before safe disposal. On the shop floor, technicians undergo routine safety training to grasp both acute and chronic hazards—including the risk of skin or respiratory contact. Supervisors enforce PPE standards, monitor air, and use incident tracking databases to predict and reduce accidents before they occur.

    Customers—especially in pharma and agtech sectors—look for assurances that suppliers adhere not only to local but also international process safety standards. Regulatory inspections and customer audits happen on schedule, and our open-door approach means data is always current and available. Material safety data sheets, technical files, and shipment records reflect direct, in-house experience—never outsourced compliance narratives. It’s not a marketing tick box; it’s a philosophy driven by the people who operate reactors, pack drums, and sign batch records.

    Looking Ahead: Research, Supply Assurance, and the Evolving Role of Manufacturers

    Scientific and supply landscapes change fast. Industry-wide headaches—ranging from disrupted shipping to raw material shortages—teach the importance of local manufacturing capacity and process adaptability. Our in-house development group continually scouts new process routes, alternative reagents, and energy-saving approaches that support both security of supply and greener practices. Partnerships with research universities help us keep pace with innovative reaction methods, whether that means biocatalysis, continuous flow, or novel purification strategies.

    A significant challenge in today’s chemical supply chains comes from market volatility for pyridine, nitric acid, or specialty oxidizers. By engaging suppliers early and often, we pre-qualify new sources and diversify critical material streams. Our logistics team plans not just for current contracts, but also for disasters—fires, storms, or sudden regulatory shifts. Inventory buffers, alternate shipping lanes, and facility upgrades stem from this risk-based thinking, not from hindsight after disaster strikes.

    We take pride in contributing not only to finished goods but to the advancement of chemical science itself. Our technical staff routinely participates in collaborative research, sharing anonymized performance data to help guide future process improvements. This extends to open discussions with customers about structure-activity relationships or synthetic bottlenecks. Such information exchange rarely occurs when working through trade brokers or silent, distant suppliers, reinforcing the value of real manufacturer partnerships.

    Conclusion: Experience Shapes Every Batch

    Every kilogram of 2-Methyl-3-nitropyridine-6-carboxylic acid represents thousands of hours spent in R&D, pilot runs, and feedback sessions. The substance does not reach the market as a mere commodity—it embodies a reliable, high-performance intermediate honed by real process insights and a continuous drive to meet challenges head-on. Our customers receive more than just a chemical; they gain a collaborative resource deeply invested in innovation, efficiency, and accountable production. Practical experience, real-world trials, and close feedback loops define every batch, setting a standard that others only reference. Serious research and manufacturing do not run on shortcuts, and neither do we.