3-(Trifluoromethyl)pyridine-2-carboxylic acid

    • Product Name: 3-(Trifluoromethyl)pyridine-2-carboxylic acid
    • Chemical Name (IUPAC): 3-(Trifluoromethyl)pyridine-2-carboxylic acid
    • CAS No.: 872-50-4
    • Chemical Formula: C7H4F3NO2
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    232518

    Chemical Name 3-(Trifluoromethyl)pyridine-2-carboxylic acid
    Molecular Formula C7H4F3NO2
    Molecular Weight 191.11 g/mol
    Cas Number 875781-19-2
    Appearance White to off-white solid
    Melting Point 110-114°C
    Solubility Slightly soluble in water; soluble in organic solvents such as DMSO and methanol
    Smiles C1=CC(=NC=C1C(=O)O)C(F)(F)F
    Inchi InChI=1S/C7H4F3NO2/c8-7(9,10)4-2-1-3-11-5(4)6(12)13/h1-3H,(H,12,13)
    Purity Typically ≥98%
    Storage Conditions Store at room temperature; keep container tightly closed
    Synonyms 2-Carboxy-3-(trifluoromethyl)pyridine

    As an accredited 3-(Trifluoromethyl)pyridine-2-carboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 3-(Trifluoromethyl)pyridine-2-carboxylic acid is supplied in a sealed amber glass bottle with tamper-evident cap.
    Container Loading (20′ FCL) 3-(Trifluoromethyl)pyridine-2-carboxylic acid is loaded into a 20′ FCL using sealed, labeled fiber drums with pallets.
    Shipping 3-(Trifluoromethyl)pyridine-2-carboxylic acid is shipped in secure, chemical-resistant containers to prevent leaks or contamination. Packaging complies with international regulations for hazardous chemicals. During transit, it is protected from moisture, heat, and physical damage. Accompanying documentation includes safety data sheets and proper labeling to ensure safe handling and regulatory compliance.
    Storage Store **3-(Trifluoromethyl)pyridine-2-carboxylic acid** in a tightly sealed container, protected from moisture, light, and incompatible substances. Keep in a cool, dry, well-ventilated area away from sources of ignition and strong bases or oxidizers. Label containers properly and use appropriate personal protective equipment when handling. Follow all local, regional, and national regulations for storage of chemicals.
    Shelf Life 3-(Trifluoromethyl)pyridine-2-carboxylic acid is stable for at least two years when stored tightly sealed in a cool, dry place.
    Application of 3-(Trifluoromethyl)pyridine-2-carboxylic acid

    Purity 98%: 3-(Trifluoromethyl)pyridine-2-carboxylic acid with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction selectivity and reduced by-product formation.

    Melting Point 140°C: 3-(Trifluoromethyl)pyridine-2-carboxylic acid with a melting point of 140°C is used in solid formulation research, where it provides thermal stability during processing.

    Stability Temperature 120°C: 3-(Trifluoromethyl)pyridine-2-carboxylic acid with stability up to 120°C is used in agrochemical active ingredient manufacturing, where it maintains consistent efficacy under production conditions.

    Particle Size ≤10 µm: 3-(Trifluoromethyl)pyridine-2-carboxylic acid with particle size less than or equal to 10 µm is used in catalytic applications, where it offers increased surface area and enhanced reaction rates.

    Molecular Weight 191.11 g/mol: 3-(Trifluoromethyl)pyridine-2-carboxylic acid with a molecular weight of 191.11 g/mol is used in fine chemical synthesis, where accurate stoichiometric calculations enable precise formulation control.

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    Certification & Compliance
    More Introduction

    3-(Trifluoromethyl)pyridine-2-carboxylic acid: Practical Experience from the Manufacturer’s Floor

    Honest Work with Trifluoromethyl Pyridine Carboxylic Acid

    Every batch of 3-(Trifluoromethyl)pyridine-2-carboxylic acid we ship starts long before the drums get packed and labeled for outbound hauliers. This material speaks to anyone in agrochemical, pharmaceutical, and advanced material laboratories who understands the value of fluorinated heterocycles. We make it day after day, handle the raw materials ourselves, run the reactors, oversee purification, and respond fast to issues on our production line. Over the years, seeing its transformation from a set of base raw chemicals to a crisp, white-tinged powder on our warehouse shelves has given us direct insight into why the industry keeps coming back for more.

    Understanding the Model and Specifications

    For us, “model” means a single, well-defined compound using a fixed synthesis route. 3-(Trifluoromethyl)pyridine-2-carboxylic acid is not a generic quinoline with wishy-washy substitutions. Its structure carries the CF3 group at the 3-position of the pyridine ring, and a carboxyl group at the 2–position. We keep the batch quality reliable by starting with high-purity 2-chloronicotinic acid and integrating the trifluoromethyl group using pathways refined through explicit lab work—not borrowed literature procedures. The melting range stays consistently within expected limits when we nail the reaction, and HPLC area purity typically clocks above the 99% mark. Moisture content and residual solvents sit below the thresholds set by stringent pharma and crop science clients, not just the minimum “grade” categories stamped on commodity goods.

    Every shipment comes straight out of synthesis, filtration, and crystallization operations that run under the same roof. We oversee the drying and packaging right in-house. That gives us precise control over the final particle characteristics, which matter during dissolving, compounding, or tableting steps in later uses. This approach also minimizes batch-to-batch drift—a frustration often encountered by anyone trying to standardize their own reactions or scale up a process using unpredictable source material.

    Direct Comparison with Other Carboxylic Acid Compounds

    There’s no perfect substitute for the effect that the trifluoromethyl group delivers at the 3-position on the pyridine ring. We’ve worked with analogs and have fielded technical questions about placing the CF3 group on other parts of the ring, or swapping it for other electron-withdrawing groups. Each tweak changes reactivity, physical properties, and, most importantly, the outcome of the coupling or building-step in the customer’s synthesis plan. The 2-carboxylic acid function and the 3-CF3 arrangement in this molecule show real value in cross-coupling chemistry and amide formation.

    For chemists looking to prepare herbicides or pharmaceutical leads that depend on selective bioactivity and metabolite profiles, 3-(Trifluoromethyl)pyridine-2-carboxylic acid’s unique substitution proves especially useful. It resists breakdown under strongly basic or harsh oxidative conditions better than many non-fluorinated pyridines. That means fewer side-products and cleaner downstream reactions, which we see reflected in jobs clients run in scale-ups on their end. For example, switching to a methylpyridine acid or dropping the fluorines from the CF3 tail off entirely results in measurable losses—in both yield and selectivity—during Suzuki and Buchwald-Hartwig couplings, according to feedback and published data.

    Real-World Usage from the Manufacturer’s Experience

    From our factory to your project bench, applications of this acid span herbicide intermediate synthesis, pharmaceutical scaffold development, and the design of advanced organic materials. Large-volume buyers—particularly in agrochemical contract formulation—need the carboxyl group at the 2-position for efficient attachment to bulky aromatic rings, common in next-generation active substances. That precise configuration enables effective downstream construction steps: amidation, esterification, and ring closure.

    On the pharma side, we’ve watched clients grow pilot batches into multi-ton processes heavily reliant on the trifluoromethyl group’s influence. It shifts polarity and biological uptake characteristics, playing a pivotal role in tuning solubility, membrane permeability, and binding interactions in lead molecules. Some research groups have shown us stability data demonstrating how compounds derived from our 3-(Trifluoromethyl)pyridine-2-carboxylic acid survive simulated metabolic pathways better than their non-fluorinated analogs. That translates straight into value for those developing next-generation molecules for clinical evaluation.

    We often receive requests for subtle variations—pure ester or amide derivatives, for instance—which confirms the central role this acid plays as a versatile chemical building block. Since we manufacture the precursor ourselves, our ability to prepare custom derivatives often outpaces larger players relying on imported carboxylic acids or blended intermediates. From grams for proof-of-concept academic research, to hundreds of kilograms for commercial contract manufacturing—we know first-hand that material quality makes a difference in the lab and on the production line.

    Production Challenges and Solutions We’ve Learned

    Making this compound is no trivial task. Trifluoromethyl introductions bring regulatory scrutiny due to the fluorinated gas reagents and persistent waste issues. Our team has worked through setbacks caused by partial oxidations, catalyst deactivation, and even minor leaks during scale-up. Each problem led to real changes in plant procedure.

    Sourcing the right raw materials is a daily concern, as CF3 reagents trend with market changes in fluorine supply. We learned that keeping a robust supplier network—and qualifying secondary sources—keeps us flexible when inevitable shortages strike the global inventory chain. We also train team members to understand batch records in detail. That tight record-keeping helps track down the source of isolated off-specification batches and corrects issues in real time, not months later.

    On the purification side, we moved beyond standard crystallization to implement stepwise solvent systems and tailored pH control. Early on, we underestimated the effect trace iron contamination would have; it complicated downstream coupling steps for several large buyers. We invested in improved filtration equipment and tested glass-lined reactors, trading short-term cost for long-term reliability. Choosing not to cut corners on purification paid off, as clients reported fewer by-products and higher yields from their own synthesis runs.

    We face demands for ever-increasing product purity, driven by regulatory and patent litigation risks in agrochemicals and medicine. Responding to this, we run third-party analytics as standard, supplementing our in-house HPLC, GC-MS, and Karl Fischer titrations. No one likes to find out from a government lab that a by-product is lurking four decimal places deep in their active ingredient—the effort put in at our production site serves as an upstream risk shield for companies navigating tough legal environments.

    Environmental Responsibility as Actual Producers

    We see the risks that come with making fluorinated intermediates. Every kilogram of 3-(Trifluoromethyl)pyridine-2-carboxylic acid carries real emissions potential. Unlike outsourcing or distributing, being an actual manufacturer puts environmental compliance on our front step: our permits require regular audits, and neighbors count on us to keep stack emissions and waste within control. We’ve invested in scrubber systems sized for real peak flows, not just the theoretical capacity on paper. We recycle solvent streams and have moved to reclaim and reprocess liquid wastes where possible.

    Our experience with community oversight encourages transparency. We host tours for safety and local school groups, showing what it really takes to keep fluorine chemistry safe in a working plant. This kind of engagement not only builds trust but also sharpens our team’s day-to-day commitment to clean operation. For us, environmental action is not an abstract marketing claim; it’s down to routine maintenance, careful drum handling, and clear records from the plant floor.

    Supporting Customers With Product Knowledge and Real Answers

    Questions about 3-(Trifluoromethyl)pyridine-2-carboxylic acid don’t come from the procurement office—they come from scientists who know their chemistry. We regularly field calls and emails on spectral data, custom specifications, and odd-ball solubility issues. As the people who actually make the material, we can offer detailed answers grounded in what happens during our own syntheses, not just textbook generalities.

    One persistent question concerns long-term storage and shelf stability. From our production records, we see that batches kept dry and away from direct sunlight hold up for extended periods without significant decomposition. We recommend using airtight packaging based on our tests with open-vessel exposure to humid air, where degradation was noticeable after weeks, not months. Feedback from end-users in tropical climates leads us to suggest double-wrapping for sensitive bulk buyers.

    We’ve also witnessed firsthand how minor changes to particle size affect dispersion in organic solvents and water-miscible compounds. Watching clients struggle with sedimentation or slow dissolution prompted us to invest in more consistent micronization and sieving stages in the plant. The positive response from research groups—who need predictable handling—keeps the focus on process improvements.

    What Sets Our Compound Apart: A Manufacturer’s View

    Sourcing 3-(Trifluoromethyl)pyridine-2-carboxylic acid directly from a producer—especially one who manages the entire cycle from starting raw materials to finished, rigorously tested batches—gives buyers more than just a shipping slip. It delivers material traceability, verified batch purity, and honest answers to technical questions. Because we work up close with the product every day, we catch subtle quality control issues and address them before they impact a customer's project.

    Unlike bulk redistributors who may blend product from multiple plants or let inventory sit too long, we guarantee freshness and consistent analytical results. Direct synthesis enables us to accommodate custom particle sizes and offer short lead times on rush orders. We know what it’s like to watch the production schedule tick down and to “wait for the drum” that you can’t move your own process forward without—that urgency shapes how we prioritize workflows.

    Small and mid-sized buyers also benefit from clear feedback loops. Early-stage formulations often reveal requirements that don’t appear on a standard certificate of analysis. Since our technical team works in the same building as our synthesis crew, sharing data between customer and production lines is straightforward. This means tweaks are possible, not just promised. We’ve made subtle adjustments to impurity profiles, packaging types, and batch labeling—driven by feedback, not just regulatory demand.

    As a manufacturer with years of hands-on production, we approach each order of 3-(Trifluoromethyl)pyridine-2-carboxylic acid as a long-term partnership. Open communication and a willingness to solve specific application problems have built trust with the contract research and formulation labs who rely on high-purity starting materials.

    Shared Success Built on Real Quality

    For us, the story of this compound unfolds with every drum and every kilogram that leaves the production hall. Reaching high purity and reliable consistency doesn’t result from luck or formulaic procedure writing. It comes from careful selection of reagents, skillful operation, thorough documentation, and fast feedback between operators and laboratory analysts.

    The consistent physical and chemical performance of 3-(Trifluoromethyl)pyridine-2-carboxylic acid we deliver is why research teams keep coming back and why multi-ton buyers trust their large-scale processes to our material. Those who have tried cheaper, inconsistent sources often share stories of frustrated formulation, lower conversion rates, and lost project weeks. Consistency, rooted in production experience and commitment to continuous improvement, is what underpins the successful application of this product across so many sectors.

    Continuing Improvement Based on Experience

    We know that the demands on fluorinated heterocycles will only increase. Pioneering research in pharmaceutical, crop protection, and new materials regularly turns our attention to better ways of synthesizing, purifying, and delivering cutting-edge intermediates like 3-(Trifluoromethyl)pyridine-2-carboxylic acid. By listening to those at the bench and staying directly involved at the reactor level, we stay ahead of shifting requirements. Problems, both expected and new, show up as challenges to refine methods and elevate performance. The compound will remain a cornerstone in modern molecular design—and we aim to maintain its reputation for reliability, batch after batch, with every order shipped.