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2-Methylpyrimidine-5-Carboxylic Acid

    • Product Name 2-Methylpyrimidine-5-Carboxylic Acid
    • Alias 2-Methyl-5-pyrimidinecarboxylic acid
    • Einecs 629-566-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    728692

    Name 2-Methylpyrimidine-5-Carboxylic Acid
    Cas Number 50890-19-2
    Molecular Formula C6H6N2O2
    Molecular Weight 138.12 g/mol
    Appearance White to off-white solid
    Melting Point 190-195°C
    Solubility In Water Slightly soluble
    Pka Approx. 4.5 (carboxylic acid)
    Smiles CC1=NC=C(C(=O)O)N=C1
    Inchi InChI=1S/C6H6N2O2/c1-4-7-2-5(6(9)10)3-8-4/h2-3H,1H3,(H,9,10)
    Synonyms 2-Methyl-5-pyrimidinecarboxylic acid
    Storage Temperature Room temperature

    As an accredited 2-Methylpyrimidine-5-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle with a secure screw cap, labeled “2-Methylpyrimidine-5-Carboxylic Acid” and safety information.
    Shipping 2-Methylpyrimidine-5-Carboxylic Acid is shipped in tightly sealed containers to prevent moisture and contamination. It should be stored and transported at room temperature, avoiding direct sunlight and extreme conditions. Proper labeling and documentation are included in compliance with chemical shipping regulations to ensure safe handling and transit.
    Storage 2-Methylpyrimidine-5-carboxylic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect it from moisture, direct sunlight, and sources of heat or ignition. Keep the storage area clearly labeled and ensure spill containment measures are in place for safe handling.
    Application of 2-Methylpyrimidine-5-Carboxylic Acid

    Applications of 2-Methylpyrimidine-5-Carboxylic Acid in Industrial Manufacturing

    As a direct manufacturer, we supply 2-Methylpyrimidine-5-Carboxylic Acid for high-value synthesis and formulation processes across several industrial segments. Below, we outline specialized downstream fields and detailed application requirements based on customer processes and compliance needs.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical companies utilize this compound primarily as a pyrimidine moiety source in the synthetic sequence of certain antiviral and anti-cancer drug candidates. Its distinct carboxylic group supports amide coupling and heterocycle building, integrating into regulated GMP APIs. In typical API production, the acid intermediates undergo purification and salt conversion to meet stringent monograph criteria. Chemists control residual solvent and metal content per ICH Q3C/Q3D requirements throughout multi-step reactions, ensuring full traceability of input materials. Downstream manufacturers rely on its stable chemical profile for batch-to-batch synthesis consistency.

    Industry compliance standards

    • ICH Q7 GMP for API manufacturing
    • USP / EP monograph specifications (reference for related structures)
    • FDA CFR 21 Part 211
    • ISO 9001 Quality Management System

    Typical usage ratio

    • 0.5–7 molar equivalents per step, depending on target molecule structure; adjusted based on yield and impurity profile targets.

    Downstream process integration

    • Activated amidation or esterification step for API intermediate formation
    • Salt formation and crystallization as part of final API purification
    • Documented as starting material in DMF/CEP for regulatory submission
    • Integrated into multi-step continuous or batch synthesis lines

    Final product types

    • Antiviral pharmaceutical actives
    • Anticancer drug substances
    • Pyrimidine-containing intermediates for advanced pharmaceutical research
    • Drug candidate API reference standards

    2. Crop Protection Active Ingredient Synthesis

    Leading agrochemical formulators incorporate this pyrimidine derivative into novel heterocyclic ring systems for fungicidal and herbicidal actives. The robust reactivity of its carboxyl group allows selective acylation and condensation steps to construct functionalized pesticide scaffolds. Product quality must comply with FAO and EPA technical requirements to support registration and downstream field application. Our QC team performs trace impurity and residual solvent analysis to meet strict environmental and toxicology data demands. This ensures that downstream partners achieve reliable synthesis for their technical-grade actives and formulation bases.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides
    • EPA FIFRA Registration Technical Bulletin
    • ISO 17025 Laboratory Accreditation (for analytical testing)
    • REACH Registration (if imported to the EU market)

    Typical usage ratio

    • 0.2–5 molar equivalents per intermediate step, optimized according to the synthetic route and yield objectives; higher ratios can address scale-up requirements for fine-tuning downstream structural modifications.

    Downstream process integration

    • Condensation reactions with amine and hydrazine derivatives for active ingredient formation
    • Incorporation in heterocyclic core assembly during protected intermediate manufacturing
    • Analytical release and documentation for technical active production lots
    • Support for process validation and impurity profile establishment in plant-scale batches

    Final product types

    • Pyrimidine-based fungicide technical concentrates
    • Novel herbicidal actives targeting resistant weed species
    • Seed treatment additive actives
    • Research-scale reference standards for agricultural R&D

    3. Fine Chemical Building Block for Electronic Materials

    Electronic chemical manufacturers use this pyrimidine acid for constructing specialty intermediates used in high-purity conductive polymers and active layer materials. Its molecular configuration enables precise control over electronic properties in dielectric film precursors and photoresist additives. These downstream processes require significant impurity control, including ultra-low metal analysis and detailed documentation for traceability, as dictated by the electronics and display manufacturing sector. QC testing ensures sub-ppm metal contents and full analytical verification, responding to rising market quality demands and regulatory standards.

    Industry compliance standards

    • SEMI C-93-0914 purity protocols for electronic chemicals
    • IPC-4101 (for dielectric materials)
    • RoHS and REACH for restricted substance compliance
    • ISO 14001 for environmental management in chemical production

    Typical usage ratio

    • 0.1–2 weight percent of total monomeric input, precisely adjusted for desired electrical performance and film characteristics in downstream compounding operations.

    Downstream process integration

    • Direct raw material charge for precursor polymerization
    • Solution blending for spin-coating in electronics fabrication
    • Addition at oligomerization step for dielectric layer synthesis
    • Analytical verification in QC labs before downstream clean-room use

    Final product types

    • Polymer-based dielectric films for printed circuit boards
    • Photoresist additives for semiconductor lithography
    • Active materials for organic light-emitting diodes (OLEDs)
    • Functional coatings for touch panel sensors

    4. Biochemical Research Tools and Molecular Probes

    Biotech and diagnostics firms deploy this compound as a functionalized aromatic intermediate in research reagents and enzyme substrate design. Custom synthesis teams use its pyrimidine scaffold to build fluorescent tags, affinity labels, and small molecule probes for protein assay development. Downstream product batches require compliance with laboratory reagent purity standards such as ACS and ISO, with trace contamination studies and batch-specific CoA documentation. Biotech QC staff depend on consistent structure and reactivity to support reliable probe synthesis, labeling kits, and quality certification for diagnostic use.

    Industry compliance standards

    • ISO 13485 (Medical Devices Quality Management)
    • ACS Reagent Grade Specifications
    • OECD GLP guidelines (for labeled substances used in testing and validation)
    • REACH Annex IV (for laboratory use compounds in specific regions)

    Typical usage ratio

    • 0.05–1.2 mol per probe synthesis batch, determined by probe complexity and required labeling intensity for bioassay readouts.

    Downstream process integration

    • Covalent coupling in linker chemistry for fluorescent or affinity labeling
    • Reagent formulation in research kit assembly lines
    • Documentation for custom synthesis orders and end-user traceability
    • Analytical validation and identity confirmation before kit integration

    Final product types

    • Enzyme substrate probes for biochemical assays
    • Fluorescent labeling reagents for microscopy and cell analysis
    • Affinity probes for pull-down and protein interaction studies
    • Diagnostic kit intermediates for life science markets

    5. Specialty Polymer Modifier Synthesis

    Performance polymer producers select this carboxylic acid to introduce controlled pyrimidine substitution into specialty engineering plastics and thermoset resins. The functional group ratio offers tunable chemical resistance, adhesion, and UV stability in customized resin systems. Controlled addition prevents undesired crosslinking, and QC staff routinely monitor active group conversion and residual acid in line with industry quality standards. Product developers specify documented purity and trace metal analysis to prevent downstream processing issues such as gel formation or color instability in molded or extruded plastic goods.

    Industry compliance standards

    • ASTM D4000 (Standard Classification System for Polymers)
    • ISO 9001 Quality Management for specialty plastics
    • FDA 21 CFR 177.1520 (for polymers in regulated applications)
    • REACH for polymeric substances

    Typical usage ratio

    • 0.3–2.5 weight percent per resin batch, varies by desired modification level and matrix compatibility; process engineers define the final ratio based on detailed performance validation.

    Downstream process integration

    • Direct copolymerization for monomer functionalization
    • Additive blending in extrusion or compounding lines
    • Dispersal before thermoset curing to ensure uniformity
    • Monitoring of carboxyl conversion for QC sign-off prior to downstream processing

    Final product types

    • UV-resistant engineering thermoplastics
    • Custom-modified polyurethane or epoxy resin systems
    • Plastic adhesion promoters for composite applications
    • Functionalized injection-molded components
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    Certification & Compliance
    More Introduction

    2-Methylpyrimidine-5-Carboxylic Acid: A Manufacturer’s Perspective

    Stepping Into the Chemistry

    Every molecule we bring to the industry teaches us something new, and 2-Methylpyrimidine-5-Carboxylic Acid stands out as a fine example. We’ve produced this compound in our own facilities for years, watching its demand shift with evolving pharmaceutical and agrochemical trends. Each time we run a batch, we commit to controls tighter than any regulatory minimums. Years of fine-tuning have taught us that even subtle impurities affect the way chemists and formulators can use this molecule. We watch for color, odour, and trace ions, knowing their presence could shift reaction outcomes.

    Model and Customization Through Practice

    Our typical production centers around the 98% pure material, which we supply as a stable, faintly yellowish powder. The melting range holds steady batch after batch, a sign that no leftover solvents or side reactions linger. Lab teams in the next room monitor each process halfway and at the end, relying not just on machines but also on decades of trained eyes. We’ve learned over time which filtration steps yield the cleanest product and which reagents trigger trace contaminants. It’s a skillset built on countless production runs, not on borrowed know-how.

    As a manufacturer, we take pride in our ability to adjust production size according to our customers' project needs. Small samples for lab work roll off the same lines as large runs for manufacturing. Structuring shipments like this came from fielding real supply chain challenges, including last-minute orders from R&D teams and bulk requests from pharma partners moving to pilot scale. Handling unexpected requests has become routine, and we build slack into each schedule for that reason.

    What Sets This Material Apart

    Comparing 2-Methylpyrimidine-5-Carboxylic Acid with other building blocks highlights how functional groups on the pyrimidine affect the reactivity and use. The methyl at the 2 position and the carboxylic acid at the 5 position give this compound a unique profile. In contrast, other pyrimidine acids missing this substitution, or with changes elsewhere, behave differently in coupling reactions. In synthesis, we see 2-Methylpyrimidine-5-Carboxylic Acid react more selectively with certain amines or nucleophiles, which enables medicinal chemists to build specific scaffolds that resist side reactions.

    Over the years, researchers have relied on this molecule not just for its core structure, but for the confidence that each batch comes with clean, well-understood impurity profiles. We avoid cross-contamination by scheduling dedicated production runs, a practice we learned after early missteps with other heterocycles years ago. Trends in research also show that this acid supports work in nucleoside analogues and small-molecule drugs. Our clients confirm structure-activity data with our reference samples, and those data reinforce the value of quality at the source.

    Usage in Pharmaceutical and Chemical Work

    We see 2-Methylpyrimidine-5-Carboxylic Acid turn up most often in medicinal chemistry. Teams use it to assemble experimental drug candidates, especially those that need tight control over functional-group placement. In our experience, the compound’s dual reactivity—carboxylic for coupling, methyl for further substitution—opens up options in combinatorial libraries. Direct feedback from R&D teams echoes the need for high-purity material to avoid false negatives and ensure clean characterization.

    Process chemists working on scale-up have identified this compound as a gateway to analogues with promising biological effects. The controlled reactivity helps them introduce further modifications—halogenations, amidations, and others—without complex side reactions. By providing consistent product, we help these teams move from milligrams in test tubes to kilograms in reactors without changing the synthetic scheme.

    Outside pharma, some customers in agrochemicals use this acid as a starting point for new herbicide and pesticide leads. Once we started asking about end-use, we realized that even slight changes in metal content could cause problems later down the line, especially if the target molecules need regulatory approval. This feedback changed some of our purification methods and we introduced extra analytical checks—not because a certificate required it, but because real users hit walls that specs alone didn’t uncover.

    Technical Specifics That Matter in Practice

    In our facility, the product typically shows up as a crystalline solid, and it stores well in sealed drums under dry conditions. We don’t rely on theory alone; we’ve seen storage mishaps where exposure to moisture led to clumping or minor hydrolysis. To prevent issues, we use nitrogen blanketing and double-sealed packaging. It only took one customer returning caked material for us to change our handling entirely. Feedback like this is part of our routine improvement.

    Over several years, our quality team fine-tuned drying times and solvent choices, optimizing yield and minimizing process waste. Each parameter affects not just cost, but performance for the teams formulating new actives. It’s rare now to field a purity complaint, but each time we do, the full batch records are right at hand for cross-checking component by component.

    Differences from Other Heterocyclic Acids

    Many researchers move between various substituted pyrimidines, and their feedback has taught us crucial differences. When compared to 4-methyl versions or to unsubstituted pyrimidine-5-carboxylic acids, 2-Methylpyrimidine-5-Carboxylic Acid often reacts faster in forming bonds at the carboxyl. This saves steps for chemists, a claim we’ve confirmed with timed reactions in our own labs. The extra methyl also shifts the acid’s solubility, making it a better fit for some organic solvent systems—not something everyone reads from a catalog or paper.

    Others ask how this building block compares to pyridine or pyrazine acids. The electronic environment on the ring changes everything: as we’ve learned running similar syntheses head-to-head, 2-Methylpyrimidine-5-Carboxylic Acid gives different yields and selectivities, sometimes favoring products that alternate heterocycles wouldn’t allow. Groups developing new drug series have shown us how those differences, playing out over dozens of analogues, help narrow down the next candidate for animal trials. By supporting direct comparison batches, we provide real-world evidence of where our compound fits best.

    Real-World Production: Lessons Learned

    We spend a lot of time on reliability. In chemical manufacturing, the work doesn’t stop with a reaction’s end. Each kilogram we prepare is tracked with full lot numbers, traceable back to each raw material. We built this system after facing a few too many traceability requests from pharma teams working under strict audit. At first, it seemed like bureaucracy, but over time, we found root causes to quality issues that would have stumped us before—metal shavings from old blenders, or solvent residue from lines switched too hastily between runs.

    Sampling represents another critical point. Before anything ships, multiple staff pull out grams, test them, and compare against analytical standards made in-house. This multi-point sampling guards against “hot spots” of impurity—a lesson we learned years ago with a run that produced visual outliers undetectable by bulk testing. Even though high-end instruments can pick up down to ppm levels, there’s nothing like trained eyes and established processes to confirm results.

    Impact on the Supply Chain

    For us, on-time delivery never just means handing off a box to a courier. We keep buffer stock of key materials and pre-arrange logistics with transport specialists familiar with hazardous substances. Through hard experience, we’ve mapped out the pitfalls—customs holdups, temperature excursions, and documentation errors. We share tracking before the material even leaves the plant, so customers can prepare for arrival. The industry expects more than a tracking number; they want to know their shipment sits in the right conditions every step of the way.

    Building these routines took investment in people as much as in plant equipment. At one point, delays from customs almost caused a customer to miss a grant milestone. We stepped in, assembled an emergency document pack, and kept constant phone contact with everyone in the logistics chain. This kind of engagement keeps researchers coming back for more than the molecule’s specs alone.

    Sustainability in Manufacturing

    In recent years, we faced a growing demand for greener chemistry practices in manufacturing. Some customers requested detailed reports on solvent and energy use. Taking this seriously, we overhauled some routes to cut waste streams and recover solvents from distillation. Not only did this reduce our disposal bills, but it also made us rethink how each parameter affects total environmental impact. We moved away from certain reagents with questionable by-products, shifting to greener alternatives even when the switch meant longer process development hours.

    The drive for sustainability isn’t just a trend; it lines up with our own long-term savings and values. The product hasn’t changed functionally—the core 2-Methylpyrimidine-5-Carboxylic Acid stays the same—but our footprint shrinks year over year. Industry partners have commented favorably after receiving lifecycle analysis reports, showing lower overall burden thanks to changes we put in place on the production floor itself.

    Technical Support Backed by Direct Experience

    Technical support starts at the factory. Some inquiries might look simple on the surface but require real production experience to answer fully. Whether customers face solubility mismatches in scale-up or odd color changes in certain solvents, we bring observations from our own efforts. Over time, we built internal protocols and frequently asked questions, not by copying standards, but by collecting real situations from labs and packaging lines alike.

    We often connect with teams over troubleshooting, sometimes sending out parallel samples made under different conditions, helping researchers pinpoint what works best in their systems. Catching chatter about new uses, we’ve even run custom syntheses for off-spec material, providing modified 2-Methylpyrimidine-5-Carboxylic Acid for truly novel projects. These collaborative experiences drive home how direct access to the manufacturer allows research to advance with fewer supply roadblocks.

    Regulations and Documentation

    Navigating global shipment rules can trip up companies who don’t stay in close contact with regulators. Routine audits, changes in documentation, and local chemical controls each add new steps to the process. We’ve adapted our paperwork, training, and labeling based on hard-learned lessons—once, a minor mislabel nearly stranded our product at a port. Every learning point led to a new document or process, so each box matches regulations for destination countries.

    The discussions with compliance experts, coupled with our day-to-day production realities, taught us that clear traceability, up-to-date safety information, and proactive customer communication avert countless problems. Being ready with Certificates of Analysis, traceability records, and MSDS is a given, but explaining results and decisions in a way that helps users qualify and trust the product is just as essential. That’s a skill built on ongoing dialogue with regulatory agencies, industry audits, and unfiltered customer feedback.

    Driving Continuous Innovation

    Some manufacturers stick with the same route year in, year out. Our crew thrives on iteration. Direct feedback from customers in pharmaceuticals, biotech, and agriculture steers us toward tweaking conditions for better yield, purer product, or smoother crystallization. We run small test campaigns with tweaks, logging the results so every change builds toward the next improvement. At times, a simple filter swap or a pressure adjustment led to a far cleaner final compound, and those lessons flow back into each subsequent run.

    In my years watching customer successes, I’ve learned that predictable supply—backed by open forensic work behind each batch—beats the flashiest new process. Clients routinely plan whole drug-discovery cascades around batch availability. By delivering this acid on time and to agreed standards, we help accelerate new medicines and crop solutions from bench to field or clinic.

    Listening and Responding to Industry Needs

    Standing inside a chemical manufacturer, one truth becomes clear: the market for 2-Methylpyrimidine-5-Carboxylic Acid doesn’t stay still. New pharmacological leads and regulatory frameworks all push demand in new directions. Our role isn’t just making molecules, but adapting to what the next round of innovation needs. Requests for higher-purity lots, micronized grades, or documentation suited to new regulatory filings keep the production teams on their toes.

    Direct conversations with users drive many of our investments. If academic teams ask for analytical standards, or if review boards in major pharma want custom impurity profiles, we set up secondary purification or custom QC. Sometimes, our technical team sits with researchers over video calls, reviewing process diagrams or discussing the best way to dissolve the compound for their analytics.

    Long-Term Partnerships and Trust

    Decades in chemical manufacturing show a single trend: research programs reward reliability. Checking in with clients after shipment, offering technical details, and sharing lessons from our own synthesis runs build the kind of trust a spec sheet can’t. Experienced chemists know the value of a manufacturer who shows work behind every claim and doesn’t disappear after delivery.

    Using feedback for new product developments, managing scale-up challenges together, and supporting audits all contribute to partnerships that last. The confidence researchers show by returning each project cycle pushes us to maintain and improve our 2-Methylpyrimidine-5-Carboxylic Acid offering for long-term collaboration.

    Looking Forward

    The demand for 2-Methylpyrimidine-5-Carboxylic Acid continues to rise alongside research into new medicines and advanced agrochemicals. We dedicate ourselves to delivering material whose quality matches the ambition of the scientists who use it. Every production run, delivery, and support request reminds us that chemical manufacturing rests on a foundation of trust, attention to detail, and the willingness to adapt based on experience. A compound’s value grows through reliable supply, technical partnership, and lessons learned with every batch—a perspective only a manufacturer can fully appreciate.