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3-Methyl-4-Isoxazolecarboxylic Acid

    • Product Name 3-Methyl-4-Isoxazolecarboxylic Acid
    • Alias Methylisoxazole-4-carboxylic acid
    • Einecs 212-832-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
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    VTB
    Specifications

    HS Code

    221914

    Product Name 3-Methyl-4-Isoxazolecarboxylic Acid
    Chemical Formula C5H5NO3
    Molecular Weight 127.10 g/mol
    Cas Number 4922-47-6
    Appearance White to off-white crystalline powder
    Melting Point 187-191°C
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Storage Temperature 2-8°C
    Pka 2.7 (carboxylic acid group)
    Smiles CC1=CON=C1C(=O)O
    Inchi InChI=1S/C5H5NO3/c1-3-4(5(7)8)2-6-9-3/h2H,1H3,(H,7,8)
    Synonyms 3-Methylisoxazole-4-carboxylic acid
    Ec Number 207-704-2

    As an accredited 3-Methyl-4-Isoxazolecarboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 3-Methyl-4-Isoxazolecarboxylic Acid, 5g, supplied in a sealed amber glass bottle with tamper-evident cap and clear labeling.
    Shipping 3-Methyl-4-Isoxazolecarboxylic Acid is shipped in tightly sealed containers to protect from moisture and contamination. The package is labeled according to chemical safety regulations, handled as a laboratory chemical, and kept away from incompatible substances. Ensure proper documentation and transport under ambient conditions unless specified otherwise by the supplier.
    Storage 3-Methyl-4-Isoxazolecarboxylic Acid should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizing agents. Keep it in a cool, dry, and well-ventilated area, preferably in a chemical storage cabinet. Ensure proper labeling and avoid exposure to heat or direct sunlight. Always follow safety protocols and local regulatory requirements when handling and storing.
    Application of 3-Methyl-4-Isoxazolecarboxylic Acid

    Applications of 3-Methyl-4-Isoxazolecarboxylic Acid in Industrial Manufacturing

    As a specialized manufacturer of 3-Methyl-4-Isoxazolecarboxylic Acid, we engage directly with key industries that integrate this intermediate into advanced synthetic routes. Our continuous investment in QC, documentation, and technical support ensures reliable performance in all verified downstream applications. Below, we detail principal industrial uses across diverse chemical manufacturing sectors, addressing compliance, formulation, process integration, and the category of resultant finished products.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    3-Methyl-4-Isoxazolecarboxylic Acid serves as a critical heterocyclic building block in select API syntheses, particularly for central nervous system (CNS) agents and anti-inflammatory pharmaceuticals. Medicinal chemists incorporate this structure in multi-step synthetic processes, exploiting its reactivity for isoxazole ring functionalization. Adoption in these processes requires strict adherence to industry regulations, process validation, and thorough traceability from raw material intake to batch release.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA)
    • European Pharmacopoeia (Ph. Eur.) Monographs (where applicable)
    • China GMP (2010 Revision)

    Typical usage ratio

    • 0.5~3.0% w/w of synthesis batch mass, adjusted to stoichiometry and mole conversion targets during API intermediate formation.

    Downstream process integration

    • Charged at the ring construction or condensation step in the multi-stage API synthesis, followed by purification and crystallization prior to downstream functional group modifications.

    Final product types

    • CNS-active pharmaceutical intermediates
    • Anti-inflammatory drug intermediates
    • Final bulk APIs for branded and generic drug manufacturers after further processing

    2. Agrochemical Intermediate Production

    Major agrochemical producers employ 3-Methyl-4-Isoxazolecarboxylic Acid for synthesizing specialty herbicide and fungicide intermediates, where its scaffold supports the development of bioactive molecules with desirable selectivity and degradation profiles. Factory-scale operations require robust batch documentation, alignment with pesticide-specific regulatory dossiers, and responsive adjustment of input ratios to support tailored activity spectra in the final crop protection product.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH (EC No 1907/2006) as relevant to agchem substances
    • ISO 9001:2015 for supporting QC operations
    • GLP (OECD 21/2007) compliance for data traceability

    Typical usage ratio

    • 1.5~4.5% by batch mass, optimized based on intended downstream derivatization yields and required technical specification for active ingredient production.

    Downstream process integration

    • Dosed during the core heterocyclization step in the synthesis of active moieties, then incorporated into further functionalization and pre-formulation with inert carriers or solvents.

    Final product types

    • Herbicidal active ingredient intermediates
    • Fungicide molecule precursors
    • Granular and liquid technical concentrate formulations, after subsequent stages

    3. Fine Chemical Synthesis for Research and Development

    In research laboratories and commercial fine chemical companies, our material underpins the scalable synthesis and study of novel isoxazole derivatives, high-purity standards, and custom intermediates. End users require explicit COA traceability, batch-specific impurity profiles, and tailored batch sizes, with compliance focusing on laboratory safety and chemical management frameworks. The flexibility of the isoxazole ring enables structure-activity studies and the generation of analytical reference standards for regulated industries.

    Industry compliance standards

    • ISO 9001:2015 certified quality management systems for fine chemical manufacture
    • GHS (Globally Harmonized System) labeling and MSDS documentation
    • Local Chemical Registration (e.g., TSCA in USA, IECSC in China)
    • Lab safety standards (OSHA 29 CFR 1910.1450; EU Directive 2009/104/EC)

    Typical usage ratio

    • 0.01~1.0 molar equivalents per synthetic preparation, scaled to project requirements and purity demands of the target compound.

    Downstream process integration

    • Introduced at N-heterocycle assembly or functionalization steps, followed by chromatographic separation or crystallization for analytical and research uses.

    Final product types

    • Analytical reference standards
    • Screening compound libraries
    • Custom fine chemical intermediates for academia and discovery chemistry

    4. Veterinary Drug Intermediate Manufacturing

    Veterinary drug producers integrate this chemical to construct building blocks for specific veterinary medicinal products, specifically those aiming to introduce isoxazole motifs for target receptor affinity or metabolic stability. Producers observe compliance with national veterinary drug manufacturing regulations, ensure auditable production flows, and trace all key raw material lots throughout intermediate and final compound preparation.

    Industry compliance standards

    • US FDA Center for Veterinary Medicine (CVM) Guidance for Industry
    • EU Regulation (EC) No 2019/6 on veterinary medicinal products
    • VICH (Veterinary International Conference on Harmonization) Guidelines
    • China Veterinary Drug Standards (Ministry of Agriculture)

    Typical usage ratio

    • 1.0~2.2% per synthesis mass, determined according to the required activity and pharmacokinetic properties in the final molecule.

    Downstream process integration

    • Included in the early synthetic stages during assembly of the isoxazole ring structure, followed by multi-step derivatization and purification into compliant veterinary intermediates and APIs.

    Final product types

    • Veterinary anti-parasitic intermediate compounds
    • Veterinary CNS drug intermediates
    • Final veterinary bulk APIs after subsequent processing and regulatory review

    5. Specialty Polymer Modification

    Some specialty polymer formulators utilize the isoxazolecarboxylic acid motif to introduce selectively functional isoxazole groups into advanced polymer resins, impacting thermal properties, adhesive behavior, or electrical characteristics. This application requires conformity to quality management and polymer-specific safety guidelines, with exact ratios established by desired end-use properties and downstream polymer performance testing.

    Industry compliance standards

    • ISO 9001:2015 for Quality Management in manufacturing environments
    • REACH (EC No 1907/2006) for chemical inventory in the EU
    • RoHS Directive 2011/65/EU (if electronics cross-contamination risk exists)
    • Technical specifications of downstream OEMs

    Typical usage ratio

    • 0.2~1.5% w/w in the polymer matrix, balanced for target mechanical, thermal, or electrical requirements.

    Downstream process integration

    • Added as a co-monomer or chain-end modifier during resin or pre-polymer synthesis, preceding downstream compounding, molding, or extrusion steps.

    Final product types

    • High-performance engineering plastics
    • Polymer-based adhesives with specialized functionalization
    • Custom resin systems for electronics and automotive coatings
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    Certification & Compliance
    More Introduction

    3-Methyl-4-Isoxazolecarboxylic Acid: Purposeful Chemistry Backed by Manufacturing Experience

    Direct from the Source: Where Our Experience Shapes Quality

    Manufacturing 3-Methyl-4-Isoxazolecarboxylic Acid in our facilities opens a unique window into what real-world users expect from this isoxazole compound. We have seen requests grow, not only because of the molecule’s structure, but because of how it fits into the workflow of chemists chasing innovative drug candidates, crop protection materials, or specialized research projects. The difference starts with the raw inputs. Controlling the purity of every batch allows us to deliver material tailored for scale-up process development or consistent pilot runs. There is no mystery or middleman behind these drums and packs—everything begins with our own synthesis lines, managed by teams with decades behind the glass.

    Building for Use: Why Every Small Detail Matters

    Sourcing chemical building blocks used to mean accepting trade-offs. Here, we focus tightly on each stage from reaction to purification. The isoxazole core is sensitive; side reactions can introduce impurities that throw off downstream chemistry. Our team regularly inspects crystalline form, water content, and organoleptic characteristics to make sure every order meets expectations by the time it ships. Direct conversations with our end users—whether in pharma R&D, biochemistry, or agrochemical development—expose us to hard requirements, like tight control of residual solvents and accurate melting points. Quality assessments are done with in-house machines. Batch-to-batch reproducibility stands on our reactor control systems and the vigilant eyes of seasoned operators. We have learned that real-world use cases surface issues rarely covered in textbooks, and we’ve shaped our protocols to tackle those before they reach your bench.

    Understanding the Specifications: From Real-World Inquiry to Reliable Output

    Requests for 3-Methyl-4-Isoxazolecarboxylic Acid often focus on several technical details. Most labs ask for a powder with very high purity—sometimes over 98%—expecting it to dissolve well in standard organic solvents. In response, we calibrate our purification steps accordingly. Analytical HPLC ensures that even minor byproducts stand out, and we dial in the process so only the right molecular fingerprint passes final release. Chemists once flagged subtle variances in solubility from other sources, so we took on extra solvent compatibility tests. Our batches are regularly checked for particle size and uniform mixing, especially for users working with automated liquid handling systems or slow-feed synthesis modules. Each year, we revisit our processes based on user feedback, never fearing a return to the reactor if lab tests suggest a tweak will keep customers’ reactions trouble-free.

    Comparing Isoxazolecarboxylic Acids: What Sets the 3-Methyl Variant Apart

    Not every isoxazolecarboxylic acid offers the same utility. Chemists often debate the merits of 3-methyl versus other substitutions on the ring. 3-Methyl substitution on the isoxazole core introduces changes in electronic properties and steric bulk that influence reaction outcomes, particularly in heterocyclic synthesis and fragment-based drug discovery. From firsthand feedback, compound libraries built on the 3-methyl-4-carboxylic acid often display different biological profiles in screening programs compared to the unsubstituted or differently substituted analogs. For example, the extra methyl can influence metabolic liability in drug metabolism studies, or impact how intermediates behave in complex multi-step routes. Projects requiring site-selective transformations, like amide coupling or decarboxylative strategies, often gravitate toward this compound because it’s consistently reactive yet predictable. Our facility also produces several closely related analogs, so we’ve tracked the shift in research needs between these options, staying ready to pivot if customers’ requirements evolve.

    Beyond Purity: What the Lab Really Wants

    We hear often from research groups frustrated by inconsistencies—small differences in crystal morphology, unexplained trace residues, or packaging that exposes material to ambient air. These complaints shape our daily process. Our product does more than meet a number on a specification sheet: it arrives as anticipated, unaffected by transit or time in storage. We rely on moisture-resistant packaging for sensitive lots, sometimes using argon flush for projects that demand a low-oxygen environment. It is routine for our technical team to talk directly with downstream development chemists to understand lingering bottlenecks. We have fielded requests for custom batch sizes; sometimes a kilo for a pilot, sometimes just grams for screening. We know that each researcher has a slightly different end use, so flexibility and feedback are built into our customer management system. This hands-on, manufacturer-led approach accounts for our reputation among scientists seeking to avoid surprises.

    The Shift in Research Demands: How We Adapt

    We keep an eye on the scientific literature and patent filings, recognizing the direction of medicinal, biochemical, and agricultural research. Over the past five years, more projects demand higher-purity 3-Methyl-4-Isoxazolecarboxylic Acid with well-documented impurity profiles. Some teams want information on chiral purity, even when the molecule itself is not chiral, simply due to stringent project documentation. Our analytics department responds with reports tailored to these requests, drawn from actual batch data. We understand which regulatory standards matter to different regions, having exported to dozens of countries. If a customer in Europe requires additional certification for their regulatory filing, our staff is prepared to supply full certificates of analysis and traceability records back to input materials. We have learned to check stock solubility in the mixtures most often cited by researchers—acetonitrile, dimethylformamide, or buffered methanol—to make formulation work smoother downstream.

    A Closer Look at Synthesis and Cost Control

    Manufacturing a compound like 3-Methyl-4-Isoxazolecarboxylic Acid has layers of complexity. Tight control at every step helps keep costs in check for large-scale customers, while guaranteeing that the analytical results back up the price. We invest time in optimizing starting materials, process routes, and waste management strategies, always with eyes on sustainability and regulatory compliance. Our engineers have adjusted reaction scales in response to surges in demand, sometimes running three small batches instead of one big one to ensure tighter control. This hands-on approach delivers real savings, which gets passed on to the user. Occasional market disruptions—raw materials shortages or regulatory shifts—force us to adjust sourcing strategies, but close supplier relationships and our in-house reserve stocks help manage these hurdles without compromise. Every synthesis run builds operational knowledge, which sharpens our competitive edge and directly benefits our customers’ timelines and budgets.

    Analytical Methods: More Than Just Paperwork

    Years of production inform our familiarity with which analytical methods are most reliable for this compound. We use high-resolution NMR and mass spectrometry to confirm core structure, and our HPLC methods dig deeper into minor impurities that could confuse downstream results. Our lab staff takes part in industry proficiency testing to ensure our numbers mean something outside our own four walls. Real samples from research users sometimes come back for additional analysis—occasions where the compound’s performance didn’t match their protocols—giving us vital insights into edge-case performance and pushing us to refine our tests. Analytical method transfer is something we openly discuss with customers planning their own scale-up or regulatory filings, because turning over validated protocols improves trust and speeds success for both parties.

    Handling and Storage: From Production Line to Lab Bench

    The realities of handling 3-Methyl-4-Isoxazolecarboxylic Acid go well beyond the synthesis. Our staff packs orders in a controlled area, keeping the product away from moisture, light, and heat. Each lot ships with labels that show production date and lot number, so traceability is always at hand. In our experience, customers who keep the containers sealed and stored in cool, dry spaces rarely report any degradation, even after several months. We’ve developed special bulk packaging options for industrial users aiming to minimize waste on production lines. Because academic labs often require only small amounts, we offer aliquoting services to streamline sample management. Feedback from research partners helped us switch to more secure closures after a few cases of spillage, and our packaging solutions have developed based on real failures, not theory.

    Learning from Customer Setbacks

    Direct manufacturer involvement in customer troubleshooting leads to actionable improvements. Occasionally, a lab will struggle to integrate our compound into their multistep sequence, citing lower-than-expected conversions or unexpected color changes in their reactions. Our technical support team, which includes senior chemists with hands-on manufacturing experience, helps customers analyze each variable—solvent quality, order of addition, temperature ramps. Hearing about these problems directly has led us to refine not only product purity but also aspects like trace metal content and micro-particulate levels that would pass unnoticed with standard QC. As a manufacturer, sharing our own troubleshooting experience with customers speeds their own learning curve, prevents repeat issues, and sometimes sparks ideas for new synthesis pathways.

    Product Evolution: Responding to Research Realities

    A static product quickly fades from relevance. Research demands have prompted us to modify our 3-Methyl-4-Isoxazolecarboxylic Acid in several ways—sometimes to adapt solubility profiles, sometimes to address project-specific functionalization goals. The manufacturing process reflects knowledge gained from actual use cases, not just theoretical considerations. Recently, biotech firms requested larger volumes with reduced levels of unidentified impurities, prompting us to invest in a newer chromatographic system. Agricultural labs working with formulation development asked for consistently-sized crystalline powder for dust-free handling, which influenced how we dry and process the final product. Continuous dialogue with users keeps our manufacturing choices grounded in the needs of the people on the front lines of research, not the whims of marketers or catalogue trends.

    Safety and Responsibility in Practice

    Our approach to safety comes from a blend of regulatory compliance and real experience. Every worker handling the synthesis understands the risks and the required controls because their own health is at stake. Emergency protocols receive regular drills, and spill containment was engineered into our spaces after reviewing actual near-misses. For customers, we provide detailed storage and hazard guidance along with clear labels. Direct manufacturer oversight reduces communication gaps and makes it easier to pass along critical safety knowledge, answering user questions about proper handling, disposal, and decontamination without delay.

    Insight into the Academic and Industrial Divide

    We work with both research universities running cutting-edge experiments and commercial teams with deadlines. Each group values something different. Academic researchers often probe for spectroscopic data, side-product origins, or wish to test multiple analogs for SAR studies. They appreciate the flexibility and detailed documentation our manufacturing records provide. Industrial clients tend to value batch reproducibility, cost per kilo, and guaranteed delivery windows. Years in production have taught us to structure inventory, scheduling, and technical support with these user profiles in mind. We’ve shared protocols, raw data sets, and even application notes drawn from real synthesis runs, because rich, experience-based knowledge counts more to these clients than any certificate could.

    Future Directions: Preparing for Evolving Science

    Chemistry never stands still. The feedback loop between manufacturing and cutting-edge application provides the best chance to anticipate what research will need next from 3-Methyl-4-Isoxazolecarboxylic Acid. Emerging technologies like automated high-throughput screening or target-directed synthesis routines shape how production needs to evolve. We invest in analytics and reaction engineering that bring greater flexibility—batch sizes, packaging, delivery options—to match whatever innovations come to market. Partnering directly with end users lets us see around corners, picking up shifts in regulatory expectations, new therapeutic targets, or changes in agricultural chemical usage patterns long before specifications appear in formal requests.

    Responsible Sourcing and Environmental Impact

    As manufacturers, we recognize the importance of responsible sourcing and environmental stewardship in chemical production. Over the years, we’ve revisited our solvent recovery systems, optimized our waste minimization protocols, and sought out raw material sources that align with rigorous environmental and ethical standards. Refining process efficiency not only benefits our operational costs, but also reduces the environmental burden of large-scale synthesis. We actively monitor new developments in green chemistry, and our team experiments with route modifications whenever we spot an opportunity to cut hazardous waste or lower the process carbon footprint. We know our customers value transparency, so we document our raw material chain and share improvements annually to support those clients working with strict sustainability or regulatory mandates.

    Summary: Manufacturing as a Catalyst for Real-World Progress

    Every order of 3-Methyl-4-Isoxazolecarboxylic Acid carries traces of the hands that made it and the minds that refined it over years of continuous production. Our experience takes chemical manufacturing out of the abstract and into the everyday work of the laboratories and production lines that trust us. We have seen how the difference between a reliable product and a variable one can make or break an experiment, delay a project, or even affect a critical business decision. Our manufacturing process stays responsive, not only to market or regulatory pressures, but to every feedback loop that comes from those actually using our compound. Each step we take, from the synthesis kettle to the outgoing shipment, reflects lessons learned and insights gained from hands-on problem-solving. By reconnecting product quality to manufacturing expertise, we set a standard that speaks directly to the researchers and engineers moving science forward, one reaction at a time.