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HS Code |
244077 |
| Iupac Name | 2,4-dimethylpyridine-3-carboxylic acid |
| Molecular Formula | C8H9NO2 |
| Molecular Weight | 151.17 g/mol |
| Cas Number | 63500-19-2 |
| Appearance | White to off-white solid |
| Melting Point | 128-132 °C |
| Solubility In Water | Moderately soluble |
| Pka | Approx. 4.3 (carboxylic acid group) |
| Density | 1.18 g/cm³ |
| Smiles | CC1=CC(=C(C=N1)C(=O)O)C |
| Inchi | InChI=1S/C8H9NO2/c1-5-3-6(2)9-4-7(5)8(10)11/h3-4H,1-2H3,(H,10,11) |
| Pubchem Cid | 23691499 |
As an accredited 2,4-Dimethyl-3-Pyridinecarboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2,4-Dimethyl-3-Pyridinecarboxylic Acid, with tamper-evident cap and chemical hazard labeling. |
| Shipping | 2,4-Dimethyl-3-Pyridinecarboxylic Acid is shipped in tightly sealed containers to prevent moisture and contamination. The package is clearly labeled with hazard information, handled under standard chemical transport regulations. It is stored and transported at room temperature, away from incompatible substances, and shipped with accompanying safety documentation. |
| Storage | 2,4-Dimethyl-3-pyridinecarboxylic acid should be stored in a tightly sealed container, away from moisture and direct sunlight, at room temperature in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizers. Clearly label the storage container, and ensure access is limited to trained personnel. Avoid excessive heat and physical damage. |
Applications of 2,4-Dimethyl-3-Pyridinecarboxylic Acid in Industrial Manufacturing2,4-Dimethyl-3-Pyridinecarboxylic Acid serves as a key intermediate in multiple advanced chemical sectors, consistently fulfilling critical functions across pharmaceutical synthesis, crop protection, fine chemicals, and materials science. As the direct manufacturer, we deliver this compound to specialized customers whose final products rely on its precise chemical properties for synthesis and performance. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)This compound acts as a strategic intermediate in the multi-step synthesis of several APIs, where it enables targeted functional group introduction on pyridine frameworks. In particular, its methylated pyridine ring structure makes it suitable for constructing molecules with specific bioactivity profiles, and downstream clients use it during early to mid-stage route development, especially for central nervous system and anti-inflammatory drug candidates. Strict process controls and batch traceability are required to ensure cGMP compliance in this application. Industry compliance standards
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2. Agrochemical Synthesis PlatformIn the crop protection segment, downstream formulators utilize this pyridinecarboxylic acid to build selective herbicide and pesticide scaffolds. Its unique substitution pattern supports the synthesis of molecules targeting weed or pest resistance mechanisms. Customers apply tight quality specifications to active ingredient syntheses, especially when using this material for new-generation low-toxicity pesticides. Industry compliance standards
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3. Fine Chemical Precursor for Dye ManufacturingPyridinecarboxylic acids with methyl substitutions provide reactivity platforms for advanced dye precursors, which are central in producing synthetic colorants with targeted absorption properties for textile, ink, and plastic sectors. The structure enables precise introduction of chromophore linkers, and downstream processors use analytical QC to guarantee batch color characteristics, ensuring consistent dye lot production for industrial and specialty applications. Industry compliance standards
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4. Raw Material for Advanced Polymer AdditivesManufacturers of specialty polymers integrate this carboxylic acid derivative to introduce functional sites in the macromolecular backbone, enhancing compatibility, thermal stability, and UV resistance. The compound enters copolymerization feeds for producing additives used in high-performance engineering plastics and coatings. Precise feed ratios are critical to avoid undesired molecular weight distribution or cross-link density variation. Industry compliance standards
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Back in our earliest batches, the challenge with specialty pyridinecarboxylic acids always came down to control and predictability through every stage of synthesis. Our experience with 2,4-dimethyl-3-pyridinecarboxylic acid, often called DM-3-PCA in technical discussions, grew from that kind of groundwork: long hours in production halls, regular tweaks to reactor settings, and steady communication from synthesis to finished lot. Each drum we put out owes something to those years of trial, hands-on adjustments, and customer conversations about where chemistry meets real-world demand.
This molecule brings a pair of methyl groups onto the pyridine ring, altering both its reactivity and its usefulness compared to simpler compounds like nicotinic acid. A crucial point that set the direction of our production process involved recognizing the difference a modest functional change could make—one methyl group here, another there, and suddenly new pathways open up in downstream synthesis. It’s why several pharmaceutical and chemical partners seek out this variant: those methyl groups influence the acid’s placement in synthesis routes or as a building block for more complex targets.
Every synthetic chemist knows variation shows up not in one-off reactions, but in what one batch will or won’t yield compared to the last. With 2,4-dimethyl-3-pyridinecarboxylic acid, years of iterative production led us to a model (99% min assay, water content under 0.3%, single-digit ppm levels for key impurities) that meets the demands of advanced applications. Sometimes customers ask if a lower-purity product could suffice for broader industrial use, but we’ve seen failed reactions or off-target product formation spike when neglecting trace differences between lots, especially with scale-up production.
Each tank of solvent and every cleaning process—chlorinated solvents or not, filtered air or ambient—translates into analytical readings post-synthesis. With this product, neglect leads to higher isomeric contamination or N-oxide formation during storage, which later trips up downstream reactions. Our solution: regular real-time monitoring, not only at final QC but after key crystallization and wash steps, most especially on pilot plant runs. This habit keeps outcomes repeatable. We’ve documented three consecutive years without a single out-of-spec shipment, and the underlying discipline stems from decades invested into procedural refinement.
Laboratories and industrial users often ask about differences between this acid and more widely recognized pyridinecarboxylic acid derivatives, such as nicotinic acid (a vitamin precursor) or its methylated cousins. Those methyl substituents on carbon 2 and 4 result in altered hydrogen bonding, affecting solubility in both polar and nonpolar media.
During gram-scale development work for a pharmaceutical intermediate, we found that using DM-3-PCA gave a pronounced shift in reactivity compared to unsubstituted forms—a fact not always visible on paper until pilot runs prove otherwise. The methyl groups block certain positions on the ring, steering selectivity in alkylation or acylation reactions. This capability wins praise from developers scaling up from university benches to continuous reactors. We’ve received reports from partners who swapped standard substrates for 2,4-dimethyl derivatives and saw not only higher yields but easier isolation of targets thanks to differences in solubility and product crystallization. Such distinctions only emerge in actual batch histories, and keeping a tight feedback loop with end users lets us fine-tune every run.
Another point worth noting comes from paint and resin researchers. They pursue higher-performance additives or cross-linking agents and frequently remark on how the methyl pattern yields more robust products during thermal cycling. This stems from the altered electron density on the ring, which changes both nucleophilicity and steric bulk. These qualities matter in processes exposed to real manufacturing conditions—wide swings in temperature, long storage times, or exposure to varied solvents. We’ve sent test lots to compounding labs and later traced product data through to end-of-life testing, building a database on how each adjustment echoes down the value chain.
Paper has room for catalog specs, but boots-on-the-ground experience tells the full story. From each lot, our physical analysis checks melting point (usually 144-148°C for this molecule), color (a pale beige to off-white), and bulk density for blending. Granulometry seldom enters the formal paperwork, yet feedback from formulation shops proves it worthwhile: powder flowability keeps automated dosing on track, avoiding process interruptions or machine jams.
A key sticking point for some clients comes from the form—should it be crystalline for precise weighing, or powder for quick dissolution? We build flexible production lines to fulfill both, knowing that process optimization means listening first, then adjusting, not the other way around. Early on, a contract synthesis partner needed a specific sieve cut to minimize dust and speed their batch processing. After on-site visits and lengthy exchanges, we introduced a secondary crystallization and grinding step, bringing both cleanliness and dosing speed within their range.
Moisture matters, especially for reactions sensitive to water or for warehouse storage. 2,4-Dimethyl-3-pyridinecarboxylic acid, with its relatively low hygroscopicity, performs well in closed bins, but we’ve received plenty of requests for extra-low-water grades. This is not just about meeting a published threshold—our practice brings Karl Fischer titration into every pre-shipment check, so even minor upticks in water content trigger a hold and rework instead of passage to dispatch.
Modern regulatory expectations demand traceability from raw material to end-use certification. Our plant management system keeps a living record for every raw chemical, each reaction run, and all solvents—traced from incoming tanker to packed, labeled drum. In the event of a recall or question from a client’s auditor, records go back a decade or more. That discipline came after watching peers struggle through compliance gaps, and from our own rough lesson after a single short-shipped lot caused unnecessary downtime for a longtime pharma partner.
Changes in global supply chain stability—delays at ports, shifting regulations—underscore the value of in-house synthesis rather than reliance on intermediates whose origins may shift unseen. We’ve invested consistently in our own source inputs, so if a run needs to pivot to a different precursor, our chemists review and revalidate procedures in-house. Clients get transparency, not guesswork, whenever a source adjustment happens. Complete transparency in raw material handling and process documentation—down to storage temperatures, pH drift during crystallization, or trace metals by ICP-AES—relieves the risk of surprises in critical batch campaign.
Experience in the lab and production line shapes how we support each customer. For example, 2,4-dimethyl-3-pyridinecarboxylic acid sees regular use as an intermediate for synthesizing specialty APIs (active pharmaceutical ingredients). Because trace byproducts—even isomeric impurities—can hurt reaction outcomes, our production rigor keeps deviation to a minimum. Chemists trust analytical readings from our labs: every COA reflects reality, not aspiration.
Agrochemical partners appreciate the acidity profile and methylation—attributes that lend themselves nicely in downstream reactions, whether for herbicide precursors or stabilizers. We worked directly with a formulator adjusting reaction conditions to cut down downstream waste. By tuning the batch grind and cleanliness, we achieved consistent flow and dissolution rates even on legacy equipment, reducing run times and improving batch-to-batch reproducibility. For this sector, fine-tuning physical and purity specs makes a real difference in process uptime.
Some advanced materials makers have tested DM-3-PCA in new applications: corrosion inhibitors for demanding environments, resin modifiers where controlled aromatic placement enables tighter physical performance windows. Our feedback circles don’t stop at the loading dock; continued conversation with process engineers guides tweaks for new needs. It’s direct experience with a real product—label, drum, and all—that enables such improvements.
Behind every ton of 2,4-dimethyl-3-pyridinecarboxylic acid shipped stands a cross-functional team. The reliability goes beyond instruments and specs: it comes from hands-on training, routine equipment audits, and regular communication from operators to managers. Over the years, we’ve mapped out each potential failure point—tank integrity, air handling, drying curves—so when new orders push production limits, staff can respond, troubleshoot, and deliver with minimal risk of off-spec output.
We meet spikes in demand through scheduled maintenance and maintaining excess buffer batches. It sounds mundane, but decades of schedule review helped us spot patterns before they disrupt customer timelines. Our team prioritizes proactive communication: if a blip threatens delivery, clients know within the day, not after a missed deadline. Batch histories, deviation reports, and incident logs all come together as part of a living process, stitched into our product as tightly as every molecule.
Compared to isomeric versions or non-methylated pyridinecarboxylic acids, 2,4-dimethyl-3-pyridinecarboxylic acid occupies a unique chemical space. End users have shared feedback on how the methyl groups add both steric hindrance and electron-donating power, shifting outcomes in regioselective reactions or conjugate additions. This matters most in pharmaceutical and specialty chemical synthesis, where controlling side products often means matching not just the base structure but specific ring substitution.
In practice, this product’s purity and batch performance make it a stronger candidate for consistency at scale. Unlike some 2,6-dimethyl or unmethylated counterparts, 2,4-dimethyl-3-pyridinecarboxylic acid shows more predictable melting and dissolution behavior, which supports smoother throughput. R&D groups at multiple partner sites confirmed that product lots originating from our facility showed narrower process windows—a direct byproduct of upstream cleanliness, updated reactor seals, and a habit of running batch checks instead of relying solely on automated alarms.
Some formulators mention cost as a deciding factor when pitting this molecule against other aromatic acids. The relative complexity of synthesis and purification usually pushes DM-3-PCA into the higher-cost category compared to single-methyl or parent acid forms. We invest in both energy-saving modifications and process intensification, aiming to limit that premium without compromising output quality. Our position as both manufacturer and ongoing technical partner means that every adjustment in process efficiency gets reflected back into stability, reliability, and fair pricing.
The main technical challenge with 2,4-dimethyl-3-pyridinecarboxylic acid lies in scaling from lab to full plant without sacrificing either purity or practical handling. Contaminant profiles shift when moving from small glassware to jacketed reactors, especially concerning N-oxides or ring-condensation byproducts. We take every scale-up as a learning opportunity: calibrating dosing pumps, reviewing agitation rates, and adjusting crystallization conditions to stabilize each lot. Several improvements originated from talking directly to plant engineers and responding to real-world pain points like caking, shelf life, or dissolution anomalies.
As some clients pivot toward greener processing, low-waste purification, and regulatory-compliant byproduct handling, our facility keeps pace through targeted upgrades. We switched to lighter solvent mixtures that keep process waste down and minimize environmental impact. Our solvent recovery now exceeds 92% per campaign, and remaining residues go to vetted downstream handlers. Staff training covers both process optimization and environmental compliance. In-house R&D spends hours each week on analytical verification, experimenting with new crystallization routines and filter media—all supported by both standard operating procedures and frontline team feedback.
Market requests for new forms—including pre-dosed blends or custom particle sizes—come up frequently, especially in fast-moving sectors like pharmaceutical development and electronics manufacturing. By keeping technical dialogue lively, we adjust processes for new specs even as market standards shift. This direct manufacturer’s approach means staff learn from one another, then fold that learning into each future improvement—there’s no standing still or relying solely on what worked last year.
Having produced and delivered 2,4-dimethyl-3-pyridinecarboxylic acid through fluctuating market cycles, shifting regulatory landscapes, and evolving customer needs, our viewpoint has changed. Lessons learned in batch consistency, customer communication, and technical agility continue shaping each new lot. Chemists, operators, and supply chain planners all contribute to maintaining a quality focus throughout the entire process. Information from production, warehousing, and laboratory analysis informs every detail, right down to the drum labels and the way products leave the dock.
Chemistry grows through iteration, feedback, and a willingness to fix problems as they emerge. The product stands not just as a result of chemical bonds made in the plant, but of years spent documenting, testing, and responding to real requests from the field. That history shows up in every shipment and every customer conversation about improving outcomes, batch after batch.
Over nearly two decades in this field, we’ve learned that no chemical product exists in a vacuum—especially not one as multi-use as 2,4-dimethyl-3-pyridinecarboxylic acid. Feedback from partners in pharma, agriculture, and specialty manufacturing informs our future plans. Our door stays open to direct queries, technical trials, and feedback from every corner of the supply chain. Running a transparent, responsive, and reliable facility ensures our output matches the demanding specifications and ambitious projects that move industry forward. Chemistry doesn’t stand still, and neither do we.