Methyl 4-(trifluoromethyl)pyridine-3-carboxylate

    • Product Name: Methyl 4-(trifluoromethyl)pyridine-3-carboxylate
    • Chemical Name (IUPAC): methyl 4-(trifluoromethyl)pyridine-3-carboxylate
    • CAS No.: 874637-41-1
    • Chemical Formula: C8H6F3NO2
    • Form/Physical State: solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    289190

    Chemical Name Methyl 4-(trifluoromethyl)pyridine-3-carboxylate
    Cas Number 874835-93-7
    Molecular Formula C8H6F3NO2
    Molecular Weight 205.13
    Appearance White to off-white solid
    Melting Point 41-44°C
    Boiling Point 273.6°C at 760 mmHg
    Density 1.39 g/cm3
    Solubility Soluble in organic solvents (e.g., DMSO, methanol)
    Smiles COC(=O)C1=CN=CC(C(F)(F)F)=C1
    Inchi InChI=1S/C8H6F3NO2/c1-14-8(13)6-5(2-12-4-6)7(9,10,11)3/h2,4H,1H3
    Storage Conditions Store at room temperature, in a tightly sealed container
    Refractive Index 1.485 (estimated)
    Purity Typically >98%
    Synonyms 4-(Trifluoromethyl)nicotinic acid methyl ester

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams, with tamper-evident seal, labeled with product name, CAS number, hazard symbols, and safety instructions.
    Container Loading (20′ FCL) 20′ FCL: Typically loaded with 13-14 MT of Methyl 4-(trifluoromethyl)pyridine-3-carboxylate in 25 kg drums.
    Shipping Methyl 4-(trifluoromethyl)pyridine-3-carboxylate is shipped in tightly sealed, chemical-resistant containers, protected from light and moisture. Packaging complies with regulations for handling hazardous organic compounds. Proper labeling, including CAS number and hazard information, is ensured. During transit, temperature control and secure placement prevent spillage or degradation, guaranteeing safe delivery to laboratories or facilities.
    Storage Methyl 4-(trifluoromethyl)pyridine-3-carboxylate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances like strong oxidizers. Protect from moisture, heat, and direct sunlight. Ensure proper labeling, and store in a chemical storage cabinet designated for organic reagents. Follow standard laboratory safety protocols and local regulations for chemical storage.
    Shelf Life Shelf life of Methyl 4-(trifluoromethyl)pyridine-3-carboxylate is typically 2–3 years if stored in a cool, dry, sealed container.
    Application of Methyl 4-(trifluoromethyl)pyridine-3-carboxylate

    Purity 98%: Methyl 4-(trifluoromethyl)pyridine-3-carboxylate with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and reduced impurity formation.

    Melting Point 48°C: Methyl 4-(trifluoromethyl)pyridine-3-carboxylate with a melting point of 48°C is used in agrochemical compound formulation, where it provides predictable processing and easy solid handling.

    Moisture Content <0.5%: Methyl 4-(trifluoromethyl)pyridine-3-carboxylate with moisture content below 0.5% is used in drug discovery screening libraries, where it guarantees consistent assay performance.

    Stability Temperature 60°C: Methyl 4-(trifluoromethyl)pyridine-3-carboxylate with stability up to 60°C is used in high-throughput chemical synthesis, where it maintains structural integrity during heated reactions.

    Particle Size <50 μm: Methyl 4-(trifluoromethyl)pyridine-3-carboxylate with particle size less than 50 micrometers is used in fine chemical manufacturing, where it enables homogeneous blending and improved dissolution rates.

    HPLC Purity ≥99%: Methyl 4-(trifluoromethyl)pyridine-3-carboxylate with HPLC purity of 99% or higher is used in analytical reference standards, where it ensures accurate quantification and reliable calibration.

    Single Impurity <0.2%: Methyl 4-(trifluoromethyl)pyridine-3-carboxylate with single impurity below 0.2% is used in active pharmaceutical ingredient development, where it reduces risk of side reactions and regulatory issues.

    Molecular Weight 219.16 g/mol: Methyl 4-(trifluoromethyl)pyridine-3-carboxylate at a molecular weight of 219.16 g/mol is used in structure-activity relationship studies, where it aids in precise mechanistic investigation.

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    Certification & Compliance
    More Introduction

    Methyl 4-(trifluoromethyl)pyridine-3-carboxylate: A Manufacturer's Perspective

    What Experience Teaches Us About This Compound

    Manufacturing chemicals like methyl 4-(trifluoromethyl)pyridine-3-carboxylate takes commitment. Our daily work in the plant, running reactors, monitoring purity, and troubleshooting batches, becomes an exercise in attention to detail. This molecule, with the model identifier MF-430C, reflects the technical leap in pyridine derivatives over recent decades. We do not just produce numbers or catalog entries, but substances that play important roles in pharmaceuticals, agrochemicals, and advanced materials. Over years of synthesizing this ester, the real story unfolds in the subtle challenges the process throws at every stage. We have seen how even small changes in temperature profiles or solvent grades can impact both purity and yield. Such lessons cannot be found in off-the-shelf product descriptions.

    Diving Into the Physical and Chemical Profile

    Methyl 4-(trifluoromethyl)pyridine-3-carboxylate has become a preferred choice for many synthetic pathways. The ester stands apart for its combination of reactivity, stability, and the unique character introduced by the trifluoromethyl group. The compound offers a molecular formula of C8H6F3NO2, and the trifluoromethyl substituent at the 4-position adds significant value for medicinal chemists who pursue molecules with both lipophilicity and metabolic stability. The product appears as a colorless to pale yellow liquid, though slight hue variations can emerge from batch to batch, depending on trace impurities and the condition of distillation setups. Over the years, we noticed that proper control of residual solvents, especially during the final purification steps, plays a large part in the shelf-life and downstream reactivity of products sent to clients. Many years ago, escaping even a percentage point over in moisture content from an imperfect vacuum process caused unnecessary rework. Precision matters.

    Why Chemists Rely on This Structure

    Demand for methyl 4-(trifluoromethyl)pyridine-3-carboxylate has grown steadily. Chemists appreciate a building block that brings both a pyridine ring, offering aromatic nitrogen to anchor further substitutions, and a trifluoromethyl group that influences biological properties. As a source manufacturer, we see this product leave our warehouse destined for drug discovery groups, crop protection research, and at times, specialty materials teams. Formulators value the ester function, as it lends itself to quick transformation into the corresponding acid, amide, or more complex heterocycles by simple saponification or amidation steps. The robust C-F bonds in the trifluoromethyl group withstand many reaction conditions that would degrade less protected moieties. This stability often preserves molecular features until the later stages of synthesis, reducing the chance of costly rework or failed assays on our customers’ benches.

    Facing Challenges and Solving Technical Problems

    Smooth production of a compound like this comes only after wrestling through process bottlenecks. Pyridine chemistry rewards careful choice of reagents and attention to containment. During the early years, we learned to take ventilation and operator safety seriously due to the volatility of pyridine starting materials and evolving fumes. Failures likely taught us more than textbook successes; once, an overheated batch left us with runaway side-products, prompting us to reconfigure the heat-exchanger logic and tighten batchwise monitoring. Those repairs translated into consistently higher assay results and fewer lot rejections. The dry ice-acetone baths, constant vigilance on impurity profiles, and diligence in waste management have shaped not just the quality of our output but the working culture in our facilities. Our technicians gain respect for every molecule they help produce.

    The Role of Quality Control In Outperforming Traders and Repackagers

    Manufacturers stand uniquely equipped to monitor quality from start to finish. Each production run of methyl 4-(trifluoromethyl)pyridine-3-carboxylate goes through a tailored regime of HPLC, NMR, and GC-MS checks. As those who operate the reactors and oversee purifications, we control the lot-to-lot consistency and can make immediate adjustments when an analysis flags even subtle deviations. We see customers' frustrations with inconsistencies in third-party lots. Some traders may blend or re-bottle with little understanding of the chemistry's demands, leading to batches with variable purity or stability. By keeping process records and archiving spectra for every batch, we provide both accountability and reference data for our partners’ troubleshooting needs. As issues arise—whether it concerns UV impurities or unusual retention times on HPLC—we can respond directly, without translation across multiple steps in a supply chain.

    What Sets Methyl 4-(trifluoromethyl)pyridine-3-carboxylate Apart

    Not every trifluoromethylated pyridine carries the same synthetic value. This compound stands out because it combines reagent versatility with manageable processing hazards. Several analogues—such as the 2- or 5-substituted isomers—present greater challenges during synthesis or often display less reactive ester groups, resulting in lower yields during follow-up chemistry. Our direct experience shows that 4-(trifluoromethyl) substitution tends to offer both electronic compatibility and steric accessibility. The methyl ester group speeds up common hydrolysis steps while resisting premature decomposition. Through years of scale-ups, we have seen how this structure tolerates a broader variety of transformation conditions compared to related molecules. Selecting the right isomer is never just an academic exercise—it becomes a matter of time, yield, and safety.

    Real-World Applications and Performance on the Bench

    Practical use cases drive ongoing production of this compound. Many clients, especially in pharmaceutical discovery, use methyl 4-(trifluoromethyl)pyridine-3-carboxylate as a starting point for new bioactive architectures. The ability to append new groups onto the pyridine or selectively convert the ester has put this substance in many lead-optimization libraries. Agrochemical developers prefer the compound as a scaffold for exploring improved crop protection agents, since the trifluoromethyl group encourages environmental persistence and optimized uptake in plant biology studies. Our own process data and client feedback highlight the compound’s tolerance to varied transformation protocols including Suzuki couplings, amidations, and selective reductions.

    Managing Purity and Stability: From Plant to User

    Delivering reliable chemistry takes more than isolated product. We track moisture and trace residues especially closely, since even minor contaminants alter reactivity and shelf-life. Consistent production methods—solvent choices, vacuum distillation, dedicated glassware—let us hit purity marks that customers expect. Over the years, we have explored different ways to suppress unwanted hydrolysis during storage, settling on bulk packing systems with moisture scavengers and light-impermeable drums. Each lot receives a certificate based on actual instrument data on assay and residual solvents. If a user finds deviations, we have direct line-of-sight to batch-specific processing data, allowing quick resolution rather than back-and-forth guesswork.

    Process Improvements Grounded in Experience

    Every production campaign adds to a knowledge base. As we scaled from pilot runs to multi-kilo lots, early minor issues—such as unoptimized crystallization temperatures or inefficient mixing—created bottlenecks. Collaborating with our chemists and engineers, we upgraded filtration equipment, modified temperature controls on jacketed vessels, and adopted in-line monitoring for critical intermediates. These steps increased yield and further reduced process impurities, a benefit that resonates directly in the quality of delivered product. Employee skill development, including structured troubleshooting and hands-on maintenance, has minimized downtime. Investing in staff and technology rather than just output volume means we connect the dots between process design and satisfied end users.

    Safety Considerations Unique to Manufacturers

    Plant operators see dangers that don’t show up in laboratory notebooks. Pyridine derivatives have strong, distinctive odors and can irritate skin or mucous membranes. The manufacture of methyl 4-(trifluoromethyl)pyridine-3-carboxylate involves handling raw materials that react exothermically if mishandled. The engineering team monitors air quality and personal exposure to ensure our team works in safe conditions. Automation has decreased the need for manual intervention at hazardous stages, especially during solvent addition and distillation. Where possible, we substitute less noxious solvents, opting for lower-toxicity, easier-to-recover options during washing or extractions. Over the past decade, strengthening our safety standard has cut the number of reportable incidents in half, while keeping uptime and morale high.

    Respecting Environmental Demands and Waste Management

    The reality of large-scale chemical manufacture demands attention to waste and environmental legislation. Our commitment to responsible production is more than a compliance checkbox; solvent recovery systems and emission controls have become standard upgrades. On-site treatment facilities neutralize liquid waste streams, and regular audits by internal and external inspectors keep us accountable. Raw material sourcing seeks to minimize impact, with a shift towards greener feedstocks and recyclable packing. For methyl 4-(trifluoromethyl)pyridine-3-carboxylate, we recycle solvents from the final crystallization wherever possible and track fluorine-containing byproducts for safe disposal. These practices both lower costs and meet expectations for responsible stewardship of synthetic chemistry’s environmental impact.

    Why Source Direct From the Manufacturer?

    Buyers weighing choices between direct sourcing and intermediary routes often report a key difference—transparency. We offer full production traceability, batch-specific technical backing, and direct replacement or support if issues arise. Where resellers often lack context, we can decode challenges at the molecular or plant level. Our technical team consults with users to adapt batch parameters for unusual application needs, such as custom solvent systems or narrower impurity profiles. Through regular dialogue with chemists, formulators, and logistical partners, we have seen stronger project outcomes and higher rates of process transfer success.

    Looking To The Future of Pyridine Chemistry

    Our ongoing work with methyl 4-(trifluoromethyl)pyridine-3-carboxylate marks only one facet of a larger trend. Demand for fluorinated heterocycles continues to grow as R&D shifts toward drug molecules and crop chemicals with improved properties. As researchers increase their requirements for both variety and quality, the value of direct manufacturer expertise rises. We invest in process innovation and analytical support, partnering with the next generation of chemists to bring reliable, high-performance intermediates into novel discovery platforms. This approach has moved us beyond transactional supply to collaborations where outcomes matter both in the laboratory and in the market.

    Differences That Matter: Comparing With Other Pyridine Esters

    Within our catalog, methyl 4-(trifluoromethyl)pyridine-3-carboxylate distinguishes itself on the production line and in real synthetic work. We produce several related structures—methyl 2- and methyl 5-(trifluoromethyl)pyridine-3-carboxylates, for instance—but the 4-position substitution achieves better downstream reactivity in many coupling and cross-coupling protocols. Physical handling differs, too; certain isomers crystallize less reliably, or may accumulate colored byproducts under standard purification. End-users repeatedly cite the 4-(trifluoromethyl) version’s clean spectra and predictable conversion behavior, which supports challenging process development with fewer analytical surprises. The right product is not just a matter of catalog entry, it is proven through batch records, plant experience, and dialogue with real-world users addressing tight development timelines.

    Practical Solutions For Process and Supply Chain Challenges

    Every compound introduces its own set of supply challenges. With methyl 4-(trifluoromethyl)pyridine-3-carboxylate, process reliability and timely shipment remain top priorities for us. Plant teams work in close shifts, maintaining running logs and process checklists at each unit operation. Inventory tracking systems flag raw material needs, adjusting orders dynamically to keep pace with seasonal demand swings. Where shortage or transportation blocks threaten, we use buffer stock and flexible scheduling rather than risky overproduction. By maintaining direct oversight of inventory and lead times, we meet global shipping schedules without compromising batch freshness or supporting paperwork. Quality assurance liaises directly with shippers, ensuring documentation accuracy and reviewing batch-specific data with customs and regulatory teams where necessary. Reliable supply is a hands-on effort, not just a paperwork exercise.

    Supporting Customized Research Needs

    Many research partners discover that off-the-shelf specifications do not meet their needs. We build production flexibility into our workflow, from variation in residual solvent targets to deliberate design of impurity cutoffs for specialized use cases. Discovery chemists frequently approach us seeking technical opinions on unusual transformations or downstream purification needs. With a full picture of each synthetic run, our chemists can recommend optimized batch parameters or process adjustments, based on access to side-product and impurity profiles unavailable to repackagers. This two-way communication goes far to close knowledge gaps and speed up troubleshooting. Open channels with our plant engineers and analysts have made it possible for us to pilot and validate new approaches alongside customers, an outcome that has streamlined development and reduced total project risk.

    Meeting Compliance and Regulatory Demands

    Regulation shapes how fine chemical manufacturers operate. Every lot undergoes documented batch review, and we archive raw data in compliance with regional and international guidelines. Our team participates in regular training on evolving hazard communication and transportation rules for fluorinated materials. These efforts make global distribution possible, with shipment documentation prepared to satisfy customs, regulatory, and end-user quality teams. Our ongoing engagement with health, safety, and environmental requirements reduces the risk of logistical or compliance hurdles.

    Closing The Gap Between Maker and User

    Producing methyl 4-(trifluoromethyl)pyridine-3-carboxylate is not just supply fulfillment. Every flask run, analytical test, or packing job puts years of chemical manufacturing experience into a tangible product that supports research and discovery worldwide. Feedback from chemists, process engineers, and product developers cycles back into improvements on our line, making each lot both a product and a promise. From lab bench to pilot plant, the differences between a true manufacturer and a distributor are written in every technical report, every support call, and every batch we stand behind.