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2-Methoxy-4-(Trifluoromethyl)Pyridine-5-Carboxamide

    • Product Name 2-Methoxy-4-(Trifluoromethyl)Pyridine-5-Carboxamide
    • Alias 2-methoxy-4-(trifluoromethyl)isonicotinamide
    • Einecs 849-561-8
    • 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
    • CONTACT NOW
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    Specifications

    HS Code

    164317

    Product Name 2-Methoxy-4-(Trifluoromethyl)Pyridine-5-Carboxamide
    Cas Number 1238756-32-3
    Molecular Formula C8H7F3N2O2
    Molecular Weight 220.15
    Appearance White to off-white solid
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥ 97%
    Smiles COC1=NC=C(C(=C1)C(F)(F)F)C(=O)N
    Inchi InChI=1S/C8H7F3N2O2/c1-15-7-3-12-4-5(8(9,10)11)6(7)13-2/h3-4H,1H3,(H2,13,14)
    Synonyms 2-Methoxy-4-(trifluoromethyl)-5-pyridinecarboxamide
    Storage Conditions Store at room temperature, dry and away from light
    Hazard Statements No significant hazard identified under normal laboratory conditions

    As an accredited 2-Methoxy-4-(Trifluoromethyl)Pyridine-5-Carboxamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, sealed with a PTFE-lined cap, labeled "2-Methoxy-4-(Trifluoromethyl)Pyridine-5-Carboxamide," with hazard and batch information.
    Shipping 2-Methoxy-4-(Trifluoromethyl)Pyridine-5-Carboxamide is shipped in tightly sealed, chemical-resistant containers under ambient conditions. Packaging complies with safety and regulatory standards to prevent leaks and contamination during transit. Shipping typically follows UN/DOT regulations and includes proper labeling and documentation to ensure safe handling and prompt delivery. Store away from moisture and direct sunlight.
    Storage **2-Methoxy-4-(Trifluoromethyl)Pyridine-5-Carboxamide** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Protect from moisture, direct sunlight, and sources of ignition. Keep away from incompatible substances such as strong oxidizing agents. Store at room temperature, and ensure proper labeling to avoid accidental misuse or contamination. Use appropriate personal protective equipment when handling.
    Application of 2-Methoxy-4-(Trifluoromethyl)Pyridine-5-Carboxamide

    Applications of 2-Methoxy-4-(Trifluoromethyl)Pyridine-5-Carboxamide in Industrial Manufacturing

    As an established manufacturer, we supply 2-Methoxy-4-(Trifluoromethyl)Pyridine-5-Carboxamide for critical roles in specialized production streams. Our material enables reliable synthesis, precise formulation, and consistent quality outputs across advanced chemical sectors. Below, we outline core downstream application scenarios, regulatory benchmarks, and integration details relevant to industrial partners.

    1. Agrochemical Active Intermediate Synthesis

    This compound serves as a structural intermediate in synthesizing novel pyridine-based insecticides and fungicides. Many multinational formulators utilize it in multistep processes, where electronic and steric modification of the pyridine ring achieves target pesticide attributes. The amide group’s reactivity at the 5-position offers high coupling selectivity, driving yields in batch and continuous systems. Downstream, production uses controlled hydrogenolysis or acylation, ensuring compliance with residue and purity standards specific to agrochemical applications.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Registration (EC No. 1907/2006) for intermediate use
    • ISO 9001:2015 Quality Management System
    • GLP protocols for synthesis validation (OECD principles)

    Typical usage ratio

    • Employed at 0.8%–1.5% molar equivalence in active ingredient formation, adjusted according to target molecule yield and desired purity profile

    Downstream process integration

    • Introduced during heterocycle formation or side-chain functionalization stage; incorporated in sealed reactors with controlled temperature and pH

    Final product types

    • Pyridine-based agrochemical actives (e.g., insecticides, seed coatings, fungicidal agents)
    • Intermediate compounds for crop protection R&D synthesis

    2. Pharmaceutical Research & Development (Preclinical)

    Pharmaceutical labs select this compound as a core scaffold for early-stage synthesis of CNS-acting drug candidates, specifically within the novel pyridine carboxamide series. Medicinal chemists value its substituted aromatic profile, which supports SAR exploration through derivatization at the methoxy or trifluoromethyl sites. Strict adherence to ICH and FDA starting material quality guidelines governs its use, especially for API precursor assessment in lead optimization and bench-scale synthesis.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 210/211 for research material purity
    • USP General Chapters <795> and <823>
    • EMA Guideline on the quality of chemical medicinal products

    Typical usage ratio

    • Applied in 0.3–1.2 molar equivalents per synthetic protocol, based on preclinical batch size and downstream derivatization strategy

    Downstream process integration

    • Loaded at early route development phases—after inputting precursor aldehydes—then further processed by amidation or cyclization for candidate screening

    Final product types

    • Pharmaceutical intermediate compounds for CNS or oncology drug libraries
    • Reference standards for analytical or toxicology studies

    3. Electronic Chemicals for Organic Semiconductor Materials

    Manufacturers in the display and thin-film transistor industries incorporate this molecule into the synthesis of advanced organic semiconductors. The electron-withdrawing trifluoromethyl and methoxy substituents tune charge carrier mobility and stability, supporting deposition techniques such as spin-coating and ink-jet printing. Partners require trace impurity control and traceability to JES/ISO standards due to the functional impact on end device reliability.

    Industry compliance standards

    • IEC 62684: Requirements for organic semiconductor materials
    • JESD630 Classifications for electronic grade chemicals
    • ISO 9001:2015 and ISO 14001:2015 certification for production
    • RoHS Directive (2011/65/EU) for restricted substances

    Typical usage ratio

    • Integrated at 0.5–2% by weight relative to total organic semiconductor precursor input, tailored based on targeted thin film thickness and electronic properties

    Downstream process integration

    • Fed into monomer blend formulation before polymerization and casting/skiving of electronic substrate; administered under inert atmosphere to prevent degradation

    Final product types

    • Field-effect transistor (FET) active layers
    • OLED display organic backplanes
    • Organic photovoltaic intermediate films

    4. Fine Chemical Building Block for Custom Synthesis Houses

    Custom synthesis organizations deploy this material as a high-reactivity building block when customizing advanced ligands, catalysts, and specialty additives for polymer and material science clients. Its unique functional groups accelerate the formation of target heterocycles and introduce fluorinated motifs beneficial for next-generation functional materials. Downstream processes demand consistent purity and reliable supply under ISO and environmental audit protocols for specialty fine chemical output.

    Industry compliance standards

    • ISO 9001:2015 for quality planning and batch control
    • Responsible Care® program requirements
    • SEVESO-III Directive (when applicable for storage/handling)
    • Relevant REACH Annex VIII for substance volume documentation

    Typical usage ratio

    • Added at 1–4% by mass in target molecule synthesis, with ratio optimized per desired modification pathway

    Downstream process integration

    • Charged during coupling or substitution reactions; integrated at the first or second step in multi-stage sequence planning

    Final product types

    • Custom ligands for organometallic catalysis
    • Advanced fine chemical intermediates for specialty polymer manufacturing
    • Performance additives for coatings and engineered plastics
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    Certification & Compliance
    More Introduction

    2-Methoxy-4-(Trifluoromethyl)Pyridine-5-Carboxamide: Perspective from the Manufacturer

    Understanding the Heart of Heterocyclic Chemistry

    2-Methoxy-4-(Trifluoromethyl)Pyridine-5-Carboxamide stands out in synthetic chemistry because of its challenging yet rewarding structure. Over decades of producing heterocyclic chemicals, one thing remains clear: molecules like these do not just fill catalogues—they open new doors for medicinal chemistry and advanced material science. Our team encounters requests for this compound from researchers who value building blocks that offer both a fluorinated handle and a pyridine core, which suggests specific downstream targets are in mind.

    The unique feature—trifluoromethyl substitution at the 4-position—changes not just the look of the molecule but its chemical behavior as well. Fluorine’s high electronegativity alters electron density across the ring, impacting both reactivity and biological activity. Combined with the methoxy at the 2-position, you see further fine-tuning of nucleophilicity and solubility. The carboxamide at position 5 allows for further derivatization, or, in modern drug design, can serve as a direct moiety interacting with pharmaceutical targets. It’s a mouthful to name, but each part of this chemical’s structure brings a new dimension to the bench.

    From a manufacturing standpoint, synthesizing 2-Methoxy-4-(Trifluoromethyl)Pyridine-5-Carboxamide is no minor feat. Our production staff often faces hurdles you do not see with simpler pyridines. The starting materials themselves come with their risks and costs, and the sequence requires strict control over temperature, atmosphere, and purity of reagents. We’ve spent years refining steps that maximize yield yet minimize hazardous byproducts—an effort that’s crucial, especially when you consider the price and scarcity of trifluoromethylating reagents.

    Tangible Differences from Other Pyridine Products

    In a laboratory or manufacturing setting, not all pyridine derivatives behave alike. Simple pyridines might move smoothly through separation columns or react predictably under mild conditions. In contrast, 2-Methoxy-4-(Trifluoromethyl)Pyridine-5-Carboxamide has a higher tendency for step-sensitive hydrolysis, especially during downstream functionalization. Our technicians approach purification with caution, opting for solvent systems that shield sensitive groups and constant monitoring, so impurities don’t sneak through. This hands-on care significantly differs from standard automated chromatography routine—a reminder that some molecules need a human eye for quality assurance.

    We also notice that in medicinal chemistry pipelines, this molecule often acts as a secondary, sometimes even tertiary, building block. End-users seek the carboxamide and trifluoromethyl functionalities together, as this pair offers a profile matched for late-stage lead optimization. In contrast, methyl or ethyl analogs serve only a general purpose and churn out in more scalable, bulk quantities for broader use. We manufacture plenty of those standards too, but the demand profile for 2-Methoxy-4-(Trifluoromethyl)Pyridine-5-Carboxamide mirrors the precision chemistry trend seen in smaller, more targeted synthesis campaigns.

    Real-World Use Cases Guiding Production Practices

    Some customers want this compound for fragment-based drug discovery, while others apply it as a precursor in crop protection research. Over the years, these applications have shaped our own handling protocols. For instance, researchers in pharma require not just bulk amounts but assurances about chiral integrity, trace impurities, and consistent isomer ratios. Others working on materials science care about thermal behavior and decomposition pathways.

    These nuanced demands have a direct impact on how we plan each batch. Our chemists engage feedback loops where samples from pilot lots are tested not just in-house but by collaborative partners. If small traces of hydrolysis products or N-methylated byproducts are detected, production protocols are tailored and sometimes re-engineered. E-E-A-T in manufacturing means expertise translates directly through the product pipeline—not just into certificates but into informed, practical care within each stage, all the way to packaging.

    We take pride in transparency. It’s easy to hide behind certificates or general statements, but actual quality relies on more frequent HPLC checks, additional drying cycles, and more targeted process monitoring. These are never one-size-fits-all, and our constant dialogue with research labs drives home the lesson that high-value molecules require corresponding investment in attention. Often, conversations with customers highlight issues encountered with competitor batches: inconsistent color, visible degradation, or unreliable spectral data. We investigate these claims and benchmark ours against these outcomes, incorporating lessons wherever lapses are uncovered.

    Process Adaptation and Ongoing Innovation

    Scaling a process from gram to kilogram goes beyond just multiplying reagent numbers. Our pilot plant has seen its share of surprises: runaway exotherms when handling fluorinated intermediates, or filtration bottlenecks because of trace formation of solid impurities. Good manufacturing practice means we never gloss over these hurdles. Each run teaches us about hidden traps—small analytics flagging an unanticipated impurity spike, or batch-to-batch variance in crystallinity. Such observations force the team to pause, troubleshoot, and redesign steps, a process built into our philosophy for years.

    Existing literature sometimes hints at shortcuts for introducing trifluoromethyl groups, but practice constantly contradicts theory. High selectivity in lab-scale reactions dissolves when applied to bigger vessels, owing to sluggish mixing or uneven temperature control. Other times, a yield drop signals an unknown side reaction only evident with certain lots of commercial reagents. We address these setbacks directly, pulling on decades of collective experience and close supplier relationships. Those inside the plant value institutional knowledge—memories of earlier production headaches, and how these were eventually solved.

    Regulatory frameworks now push us to take additional steps: smart solvent recovery, responsible waste management, and greener alternatives get built in wherever possible. Our lab team explores new catalysts or alternate protection groups, hoping to maintain purity without sacrificing efficiency. Sometimes, green chemistry principles align well; sometimes, they require inventive workarounds. We keep a notebook full of near-misses and subsequent improvements, which proves invaluable for both current projects and future method development.

    Specification Details Shaped by Experience

    Just listing purity percentages doesn’t capture why certain specifications exist. Our standard for 2-Methoxy-4-(Trifluoromethyl)Pyridine-5-Carboxamide wasn’t picked out of thin air; it reflects repeated feedback. Analytical results sometimes show a batch testing at 99.1% by HPLC, but an impurity flagged on the NMR prompts a rerun or additional purification. Maintaining clarity in melting point and volatility data supports not only our assurance but helps downstream partners avoid formulation problems. Each spec on a product sheet tells a story—either a lesson learned or a contingency for an issue someone, somewhere, faced before.

    Bottle conditioning and stability testing have evolved alongside our manufacturing steps. Pyridine derivatives with methoxy and trifluoromethyl substituents tend to absorb moisture or degrade on prolonged exposure to UV light. The transition from amber glass to specialized polymer containers didn’t come from guesswork. We received repeated feedback about trace yellowing or crystallization in standard packaging, and an iterative process led to today’s solution.

    Care around handling, labeling, and storage all flows from experience. Every label comes dated with lot numbers tying back to electronic batch reports. Stability trends guide expiry recommendations, which change as more long-term data rolls in. These updates rarely happen in big leaps; improvements accumulate slowly, reflecting the incremental nature of manufacturing progress.

    Comparing with Analogues: How Small Changes Matter

    In our portfolio, structural analogues are easy to count—swap a methoxy for an ethoxy, drop the trifluoromethyl, or alter the position of the carboxamide. Labs that stick to a hit-and-run approach might miss subtle differences, but our regular users report recurring challenges and breakthroughs tied directly to such changes. Each tweak affects not only the stability or reactivity but the potential pharmacological profile.

    We’ve seen multiple projects stall because switching from 2-Methoxy-4-(Trifluoromethyl)Pyridine-5-Carboxamide to a similar compound introduced solubility issues or a loss of selectivity. Sometimes, an analog offers price savings and easier procurement, but the research downstream suffers from new side reactions or new impurities. We advise partners not to assume close relatives will perform identically, since even minor electronic effects shift reactivity in unexpected ways. Our chemistry team frequently reviews customer reports—comparing not only yields and spectral data but also intangibles like product handling or in-process color changes.

    Larger organizations sometimes try broad analog libraries to maximize success, but recurring feedback reveals eventual returns to the original product. The balance between price, purity, and predictable performance often swings in favor of the more tailored molecule. Our own supply records show “back orders” spike if a new substitute batch falters; switching back to 2-Methoxy-4-(Trifluoromethyl)Pyridine-5-Carboxamide rescues momentum.

    Industry Demands and Forward-Looking Manufacturing

    A decade ago, requests for this compound came mainly from pharmaceutical innovators. Now, we see rising interest from those pursuing high-value agrochemicals and advanced functional materials. New applications continue to stretch our imagination: pairing this molecule with click-chemistry motifs or embedding its core into supramolecular architectures.

    Recently, the rise in contract research organizations and collaborative networks has increased the importance of consistent supply. We build contingency buffers and redundant sourcing for essential reagents. It is never enough to trust a single supplier or rest on past successes. Industry-wide disruptions—from geopolitical instability to global pandemics—show how vulnerable specialty chemicals can be. From our seat, fair and transparent dialogue with raw material vendors matters just as much as the chemistry itself.

    End-use trends provide constant surprise. Some teams push for greater environmental compliance in their own synthesis pipelines, which feeds back to us as new requests—phasing out halogenated solvents, for example, or supplying detailed impurity profiles. We document not just purity but residual solvent, water content, and potential trace metals whenever possible, so partners down the line make informed decisions on regulatory filings.

    Being in the business brings a close-up view of how intellectual property pressures and publication cycles pressure our customers. Nobody wants to lose weeks repeating a reaction because of batch-to-batch inconsistency. Transparency and traceability in production goes a long way to building trust. For that reason, we provide batch data, actual process notes, and even troubleshooting summaries—not as a commercial afterthought, but as something that protects shared reputation.

    Addressing Common Challenges and Real Solutions

    Production doesn’t move in a straight line. Accidents happen: one run might show a mystery impurity at 0.3% that blocks downstream crystallization. Our senior chemists bring these findings to regular review, making changes on the spot—sometimes a shift in temperature ramp, sometimes the use of a different grade of raw material. No batch is released until analytical and process review agrees on all parameters. We invest in redundancy; every step is double-checked, either by separate analysts or through cross-over tests. The lesson is simple: molecules this specialized demand heightened awareness at every touchpoint.

    Transport and storage pose ongoing risks, few of which affect off-the-shelf chemicals. We learned early that customs and cross-border logistics can expose product to moisture or heat. We now keep data on transit temperatures and build packaging solutions from tested materials, anticipating real-world mishandling. We respond quickly to reports of leaky bottles or degraded material, using these data points to iterate on packaging and logistics solutions.

    Waste management is more than regulatory compliance; disposal of fluorinated solvents and residuals calls for thoughtful processes. We minimize waste from the outset and recapture as many solvents as possible. Operations work closely with environmental consultants, refining processes that reduce exposure, maximize recovery, and respect both downstream safety and local regulations.

    Addressing feedback on documentation is another evolving area. Some partners want access to detailed spectra or stability data tied directly to COAs. In response, we upgraded our document workflows, connecting every certificate to a digital archive. This allows real-time traceability, rapid access for audits, and on-the-spot sharing when questions arise. We see firsthand how robust documentation supports partners dealing with health authorities or internal QA teams.

    What Experience Teaches: Building Trust Through Technical Rigor

    Truth about a specialty compound like 2-Methoxy-4-(Trifluoromethyl)Pyridine-5-Carboxamide emerges slowly, shaped by hundreds of phone calls, urgent emails, and back-and-forth over test results. Our knowledge base grows from both everyday problems and occasional crises—an unexpected contaminant, or a superior yield because of a small tweak in an early step. Beyond marketing, the actual stories behind each batch give life to the lab data.

    Enduring lessons come from mistakes as much as victories. We once received a noisy batch report from a customer whose process failed unexpectedly. Review uncovered a minor contaminant not blocked by standard QC. We revised our protocols, learned new analytical flags, and followed up—eventually turning that negative into a long-standing relationship marked by mutual transparency. Earning trust in this industry takes time, and delivering specialty products means offering more than the bare minimum.

    Excellence in specialty chemical production depends not just on technical specification, but on flexibility, responsiveness, and willingness to adapt through ever-changing demands. We consider every batch as a teaching moment. Our combined expertise, willingness to document both wins and losses, and a habit for careful improvement gives our partners the tangible foundation to pursue innovation with confidence.

    2-Methoxy-4-(Trifluoromethyl)Pyridine-5-Carboxamide exemplifies the intersection of precise chemistry and hands-on experience. For us as manufacturers, meeting today’s demand means evolving in step with the chemists and scientists depending on us—and staying ready for whatever novel use the next year brings.