4-trifluoromethyl-3-pyridinecarboxamide

    • Product Name: 4-trifluoromethyl-3-pyridinecarboxamide
    • Chemical Name (IUPAC): 4-(Trifluoromethyl)pyridine-3-carboxamide
    • CAS No.: 54786-77-1
    • Chemical Formula: C7H5F3N2O
    • 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

    687033

    Iupac Name 4-(trifluoromethyl)pyridine-3-carboxamide
    Molecular Formula C7H5F3N2O
    Molecular Weight 190.12
    Cas Number 87460-18-4
    Appearance White to off-white solid
    Melting Point 110-112°C
    Solubility In Water Slightly soluble
    Smiles C1=CN=CC(=C1C(=O)N)C(F)(F)F
    Pubchem Cid 11796001
    Synonyms 4-(Trifluoromethyl)nicotinamide

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

    Packing & Storage
    Packing White, tightly-sealed 25g plastic bottle with hazard labels; product name, CAS number, and handling instructions clearly printed on the label.
    Container Loading (20′ FCL) Container Loading (20′ FCL): Securely packed 4-trifluoromethyl-3-pyridinecarboxamide in sealed drums/cartons, maximizing space and ensuring safe chemical transport.
    Shipping The chemical 4-trifluoromethyl-3-pyridinecarboxamide is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is typically packed according to relevant hazardous materials regulations, labeled with appropriate safety information, and transported at ambient temperature. Ensure documentation and compliance with local, national, and international shipping requirements for laboratory chemicals.
    Storage 4-Trifluoromethyl-3-pyridinecarboxamide should be stored in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, and well-ventilated area. Keep the chemical away from incompatible substances such as strong acids, bases, and oxidizers. Label the container clearly, and follow local regulations and safety guidelines for handling and storage of organic compounds.
    Shelf Life 4-Trifluoromethyl-3-pyridinecarboxamide is stable for at least 2 years if stored tightly sealed, protected from light and moisture.
    Application of 4-trifluoromethyl-3-pyridinecarboxamide

    Purity 99%: 4-trifluoromethyl-3-pyridinecarboxamide with Purity 99% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures minimal by-product formation.

    Melting Point 110°C: 4-trifluoromethyl-3-pyridinecarboxamide with Melting Point 110°C is used in solid dosage formulation development, where consistent melting behavior enhances process control.

    Molecular Weight 190.13 g/mol: 4-trifluoromethyl-3-pyridinecarboxamide featuring Molecular Weight 190.13 g/mol is used in high-throughput screening assays, where precise molecular properties optimize compound selection.

    Particle Size <20 μm: 4-trifluoromethyl-3-pyridinecarboxamide with Particle Size less than 20 μm is used in nanoparticle drug delivery systems, where fine particle distribution improves bioavailability.

    Stability Temperature 45°C: 4-trifluoromethyl-3-pyridinecarboxamide with Stability Temperature 45°C is used in ambient storage formulations, where elevated stability temperature extends shelf life.

    Water Content <0.2%: 4-trifluoromethyl-3-pyridinecarboxamide with Water Content less than 0.2% is used in moisture-sensitive catalytic reactions, where low hygroscopicity reduces reactivity loss.

    HPLC Purity ≥98%: 4-trifluoromethyl-3-pyridinecarboxamide with HPLC Purity ≥98% is used in analytical standard preparations, where high purity guarantees reliable quantification.

    pKa 4.1: 4-trifluoromethyl-3-pyridinecarboxamide with pKa 4.1 is used in buffer system optimization studies, where predictable acid-base properties ensure reproducible results.

    Solubility in DMSO >50 mg/mL: 4-trifluoromethyl-3-pyridinecarboxamide with Solubility in DMSO greater than 50 mg/mL is used in compound library stock solutions, where high solubility facilitates accurate dosing.

    Residual Solvents <0.05%: 4-trifluoromethyl-3-pyridinecarboxamide with Residual Solvents below 0.05% is used in active pharmaceutical ingredient production, where minimal solvent residues comply with regulatory standards.

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    Certification & Compliance
    More Introduction

    4-Trifluoromethyl-3-pyridinecarboxamide: A Closer Look from the Manufacturer’s Bench

    Rethinking Pyridinecarboxamides through Experience

    Every day in our production facility, the challenge centers on refining and improving chemical processes. Over years of manufacturing 4-trifluoromethyl-3-pyridinecarboxamide—known by its model CAS 33534-30-6—our team has woven practical experience straight into each batch. From early-stage research to large-scale synthesis, this compound’s unique structure—featuring a trifluoromethyl group at the 4-position on a pyridine ring and an amide function at the 3-position—offers clear value for researchers and industrial chemists who demand more than the basics.

    Structural Strengths: Why the Trifluoromethyl Group Matters

    In synthetic chemistry, even a small shift in molecular architecture can influence downstream reactivity, solubility, and metabolic stability. The trifluoromethyl substituent, for example, can entirely change how a molecule behaves in both organic transformations and biological assays. Over time, we’ve observed that analogues lacking this group rarely deliver the same degree of chemical durability or desired lipophilicity. That matters for medicinal chemists who want to improve absorption or resistance to metabolic degradation.

    A carboxamide at the 3-position also distinguishes this pyridine from other substituted pyridines. The amide functionality encourages hydrogen bonding, and the combined electron-withdrawing effects have given customers possibilities in fields ranging from agrochemical development to pharmaceutical intermediates.

    Process Development—Beyond the Textbook

    It’s easy to discuss purity and batch consistency, but on the floor, each run means revisiting temperature profiles, solvent systems, and crystallization conditions. We routinely take feedback from customer formulations and re-adjust isolation procedures accordingly. This doesn’t just produce a high-purity product—each lot reflects hands-on knowledge dealing with everything from air-sensitive intermediates to trace-level byproduct removal. Equipment fouling, for example, can threaten yield and introduce particulates. Overcoming these routine and often unpredictable hurdles is where years of scale-up experience make the crucial difference.

    4-Trifluoromethyl-3-pyridinecarboxamide can be provided in a range of grades to support medicinal and agrochemical investigations. Analytical support accompanies our product, ensuring chemists know exactly what’s in each delivered container—impurity profiling, certificate of analysis data, and batch history are always available for audit. Over the course of thousands of kilograms shipped worldwide, our results have reflected the obsession with consistency: the melting point sits reliably in the expected range, color and crystallinity stay true, and residual solvent levels comply with strictest international guidelines.

    From the Synthesis Bench to Production Tank

    Direct experience has shaped every aspect of our workflow—from sourcing raw trifluoromethylpyridines to selecting amide-coupling strategies that avoid excess side-product. Early on, we tested amidation protocols that worked on the gram scale but failed spectacularly in the reactor. Solvent swaps, poorly controlled pH, and scale-up of exothermic steps have challenged even our most senior engineers. Over years, we learned that in-process sampling and incremental reagent addition bring control, and the final filtration step—though tedious—consistently defines the finished product’s clarity. In practice, thorough wash protocols and low-hold-up transfer lines contribute more to the final outcome than any single parameter in a laboratory SOP.

    Practical Use Cases—Learning from Customer Outcomes

    Feedback from customers consistently steers our technical development. 4-Trifluoromethyl-3-pyridinecarboxamide often finds its way into the early-stage synthesis of active pharmaceutical ingredients and complex agrochemical building blocks. Its trifluoromethyl group helps modulate bioactivity and offers synthetic versatility, especially for chemists building heterocyclic scaffolds or working on structure-activity relationship studies.

    Some clients have reported increased yield stability when using our material instead of off-brand variants. In practice, predictable solubility and a manageable melting point greatly simplify process scale-up—and the difference is rarely subtle. One customer needed to scale a pilot synthesis of a pesticide intermediate: an unexpected side reaction with a low-grade amide forced costly reprocessing, but shifting to our product eliminated the impurity profile mismatch. Examples like this, from crops to clinical candidates, illustrate why purity and process know-how matter.

    Comparing 4-Trifluoromethyl-3-pyridinecarboxamide with Other Pyridinecarboxamides

    Chemical manufacturers often lump pyridinecarboxamides together, but the distinctive CF3 substituent at the 4-position interacts differently in chemical synthesis. Substituent effects on the pyridine ring—such as resonance and induction—change everything from reactivity in nucleophilic aromatic substitution to the stability of intermediates under hydrogenation. For instance, the trifluoromethyl group increases hydrophobic character, which is highly prized in pharmaceutical late-stage functionalization. It also impacts reactivity, providing a lever for selective reactions without resorting to elaborate protecting group strategies.

    We see the downstream differences when talking with customers adapting published procedures. Pyridinecarboxamides lacking this substituent rarely show equivalent behavior under the same set of reaction conditions. Analytical surveys confirm differences in NMR chemical shifts, UV absorbance profiles, and biophysical properties, which are critical when designing new compounds with intended biological activity.

    Analytical Verification—Delivering Data that Matters

    As a producer, we invest heavily in regular batch release testing. Instead of relying on third-party quality control post-synthesis, our in-house team reviews the spectral fingerprints of each lot. Proton and carbon NMR spectra, HPLC chromatograms, elemental analysis—all of these fill our product history archives. Any deviation—whether increased signal for an unknown impurity or a slight spectral shift—triggers a thorough investigation. In our experience, an uptick in HPLC baseline noise has warned of trace byproducts, sometimes eluding even skilled eyes. We’ve learned to trust subtle discrepancies and dig deeper, not just to meet regulatory standards but because product failures cost time and money for everyone along the chain.

    Monitoring for batch-to-batch variability, even at the parts-per-million level, reflects direct conversations with R&D chemists who have pushed formulations to the edge of stability. Years ago, a shift in trace metal content during one campaign highlighted the risk of cross-contamination from poorly cleaned reactors—this prompted stricter cleaning validation, which continues to pay dividends across our product lines.

    Scaling Responsibly—From Grams to Metric Tons

    Supplying kilo-scale materials brings environmental, safety, and efficiency issues into sharp focus. Waste minimization efforts led us into flow chemistry for some process steps, and raw material selection now accounts for both supply chain reliability and environmental footprint. Large-scale synthesis of 4-trifluoromethyl-3-pyridinecarboxamide relies not just on technical know-how but also on teamwork across the production floor. We continually review process changes—such as solvent swaps and workup improvements—by gathering plant feedback and examining near-miss incident reports.

    Maintaining robust supply chains for specialty intermediates like this one depends on stable planning and longstanding supplier relationships. Raw material shortages, unplanned maintenance, and regulatory changes have all forced rapid response at different times. Stock management, buffer inventory, and careful logistics planning all weigh in just as heavily as chemistry in keeping product available. A missed delivery matters more than a slight deviation in crystal form for customers facing tight R&D timelines.

    Supporting Pharmaceutical and Agrochemical Pipelines

    Our journey with this compound began via requests from early-phase pharmaceutical companies and crop science researchers. Each required stringent documentation and tailored analytical reports. We listened. The regulatory landscape never grows simpler—compliance demands traceability, documented origin of raw materials, cleaning records, stability data, and up-to-date safety records. We make sure that each drum and bottle leaving our plant carries a complete analytical history, ready for customer review during audits or filings.

    Many of the world’s largest pharmaceutical and chemical innovators look for a reliable supplier of 4-trifluoromethyl-3-pyridinecarboxamide not just for a batch, but for the entire run of a project. Whether destined for preclinical studies or field testing in agricultural trials, our experience tells us that proactive documentation support saves time during regulatory review. One client working on an active ingredient for a crop protection product used our full impurity profile—supported by targeted LC-MS data—to support environmental fate assessments required by international agencies.

    Troubleshooting and Continuous Improvement

    On the shop floor and in technical support calls, troubleshooting never takes a break. Residual moisture, trace solvent, and even specific crystal habits can complicate both downstream processing and analytical method development. Decades ago, unforeseen issues with certain grades turned into major learning opportunities. The importance of controlling residual methanol became obvious only after a customer detected a ghost peak during scale-up. Quick root-cause analysis, adjustment of dry-down conditions, and better use of drying agents made a permanent shift to our internal standards.

    Constant review of synthetic details—catalyst selection, reagent purity, order of addition—allows us to stay ahead of potential problems. High-throughput lab experiments go hand-in-hand with large batch production to validate process tweaks. We track every deviation, from temperature excursions to solvent substitutions, until no unexplained variation remains in finished lots. The confidence to supply analytical data to exacting regulatory agencies comes directly from this cycle of vigilance and refinement. We stand behind each delivery because we know exactly what it took to make it.

    Product Availability and Handling—From Factory to Lab Bench

    Long-handled bulk batches and small-scale lab samples both demand care in packing, handling, and shipping. Some customers need bespoke packaging for stability or safety, such as lined drums or moisture barriers. We adapt packaging solutions based on years of transportation experience, minimizing potential for contamination or degradation. Users often remark that our product’s stability, especially during long international shipments, outperforms previously sourced material. Consistent quality on arrival saves days—or even weeks—in laboratory qualification.

    Training our warehouse and logistics staff follows the same thoroughness as our chemists and engineers. Focusing on traceability, temperature controls, and documentation makes sure every shipment reaches its destination in original condition. Any deviation—be it from exposure at the dock or a delay during customs—gets tracked, reported, and analyzed at the management level. This hands-on approach, built on years of outbound shipments worldwide, underpins our reputation for reliability.

    Integrating Customer Feedback for a Stronger Product Line

    The circle of experience between producer and end-user constantly pushes our product higher. We watch how customers apply our 4-trifluoromethyl-3-pyridinecarboxamide in ways we never expected, whether as a key intermediate in an oncology therapeutic or as a building block for a selective herbicide. Each new application or feedback loop prompts lab trials and, often, a review of both upstream and downstream processing. Some innovations, including fine-tuned solvent systems or improved drying procedures, have stemmed directly from user-driven insight. Over the years, joint troubleshooting and open communication have set us apart, forging partnerships where solutions come faster and more reliably.

    The Human Element—Why Experience Trumps Textbook Knowledge

    Manufacturers face real-world complexity beyond any datasheet or initial literature review. Shortcuts and incomplete processing can show up unexpectedly months after a batch has shipped, but habits of thorough cleaning, rigorous documentation, and open communication catch most issues before they grow. Our commitment to direct, honest conversations with both suppliers and customers keeps our process transparent, makes root-cause analysis quick, and turns setbacks into clear steps for future improvement. The insights shared between our team and our clients' labs drive both innovation and reliability.

    For us, 4-trifluoromethyl-3-pyridinecarboxamide stands as an example of how attention to incremental detail—coupled with hands-on experience—produces a better product. From raw materials to packed drums, and from individual operator pride to full transparency, every step shapes what customers experience on their own bench. We view each batch as a new opportunity to deliver value, prove reliability, and continue the quiet process of technical advancement.