2-Pyridinecarboxylic acid, 6-(trifluoromethyl)-

    • Product Name: 2-Pyridinecarboxylic acid, 6-(trifluoromethyl)-
    • Chemical Name (IUPAC): 6-(Trifluoromethyl)pyridine-2-carboxylic acid
    • CAS No.: 34486-90-1
    • 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

    335575

    Chemical Name 2-Pyridinecarboxylic acid, 6-(trifluoromethyl)-
    Cas Number 53527-28-7
    Molecular Formula C7H4F3NO2
    Molecular Weight 191.11
    Appearance White to off-white solid
    Melting Point 133-137 °C
    Solubility Soluble in organic solvents (e.g., methanol, ethanol, DMSO)
    Smiles C1=CC(=NC(=C1C(F)(F)F)C(=O)O)
    Inchi InChI=1S/C7H4F3NO2/c8-7(9,10)5-2-1-3-11-6(5)4(12)13/h1-3H,(H,12,13)
    Pubchem Cid 3916567
    Storage Conditions Store at room temperature, keep container tightly closed

    As an accredited 2-Pyridinecarboxylic acid, 6-(trifluoromethyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, tightly sealed with a screw cap, containing 25 grams of 2-Pyridinecarboxylic acid, 6-(trifluoromethyl)-.
    Container Loading (20′ FCL) 20′ FCL container loading: Securely packed drums or bags of 2-Pyridinecarboxylic acid, 6-(trifluoromethyl)-, maximized to container capacity, compliant with chemical transport regulations.
    Shipping **Shipping Description:** 2-Pyridinecarboxylic acid, 6-(trifluoromethyl)- is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It should be labeled according to relevant hazardous material regulations and accompanied by a Safety Data Sheet. Transportation is conducted under controlled conditions, avoiding extreme temperatures and ensuring compliance with local and international shipping laws.
    Storage 2-Pyridinecarboxylic acid, 6-(trifluoromethyl)- should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and bases. Protect from moisture, direct sunlight, and sources of ignition. Ensure proper labeling and store according to chemical safety regulations. Use personal protective equipment when handling the substance.
    Shelf Life 2-Pyridinecarboxylic acid, 6-(trifluoromethyl)- typically has a shelf life of 2–3 years when stored in cool, dry, airtight conditions.
    Application of 2-Pyridinecarboxylic acid, 6-(trifluoromethyl)-

    Purity 98%: 2-Pyridinecarboxylic acid, 6-(trifluoromethyl)- with a purity of 98% is used in pharmaceutical intermediate synthesis, where high purity ensures optimal yield and reduced impurities in final products.

    Melting Point 153–156°C: 2-Pyridinecarboxylic acid, 6-(trifluoromethyl)- with a melting point of 153–156°C is used in solid-state formulation studies, where reliable thermal behavior facilitates stable formulation development.

    Molecular Weight 203.13 g/mol: 2-Pyridinecarboxylic acid, 6-(trifluoromethyl)- of molecular weight 203.13 g/mol is used in organic synthesis reaction planning, where precise molecular mass supports accurate stoichiometric calculations.

    Particle Size ≤10 µm: 2-Pyridinecarboxylic acid, 6-(trifluoromethyl)- with particle size ≤10 µm is used in catalyst preparation processes, where fine powder improves dispersibility and reactivity.

    Stability Temperature up to 120°C: 2-Pyridinecarboxylic acid, 6-(trifluoromethyl)- stable up to 120°C is used in high-temperature chemical syntheses, where thermal stability maintains structural integrity during reactions.

    Water Content ≤0.5%: 2-Pyridinecarboxylic acid, 6-(trifluoromethyl)- with water content ≤0.5% is used in moisture-sensitive synthesis applications, where low water levels prevent undesirable hydrolysis.

    Polarity Index 3.2: 2-Pyridinecarboxylic acid, 6-(trifluoromethyl)- with a polarity index of 3.2 is used in chromatographic separation protocols, where defined polarity enhances separation resolution.

    pKa 4.5: 2-Pyridinecarboxylic acid, 6-(trifluoromethyl)- with a pKa of 4.5 is used in buffer system development, where specific acid dissociation supports precise pH control.

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    Certification & Compliance
    More Introduction

    2-Pyridinecarboxylic Acid, 6-(Trifluoromethyl)-: Practical Insights from the Manufacturing Floor

    Understanding the Product: A Manufacturer’s Perspective

    For years, working on the synthesis of specialized pyridine derivatives, we’ve seen lesser-known compounds quietly play a massive role in driving pharmaceutical research. Among these, 2-pyridinecarboxylic acid, 6-(trifluoromethyl)- stands out—not just because of its structure, but also because of what it brings to the bench for both medicinal and chemical innovation. Its chemical backbone, the pyridine ring, already grants it a certain reactivity, and when we attach a trifluoromethyl group at the 6-position, the properties change.

    We don’t look at it as just another catalog item. Instead, years of process improvements have shown us that each added functional group can make a real difference, especially in pharmaceutical lead discovery and specialty chemical synthesis. The trifluoromethyl group alone can increase metabolic stability or alter acid/base behavior, which in turn opens up opportunities in bioactive compound development. 

    Among pyridinecarboxylic acids, there are a number of isomers and related acids, but the 6-trifluoromethyl derivative introduces a unique steric and electronic character. The resulting behavior isn’t just theoretical; researchers notice improved yield in Suzuki and Buchwald-type coupling reactions, reduced side-reactions, and selective transformations that don’t show up when working with non-fluorinated analogs.

    The Drive for Purity and Consistency

    A compound like this is only as good as the reliability of each batch. As an industrial manufacturer, we learned early that shortcuts in purification or crystallization mean wide swings in yield and purity downstream. We commit to producing material that consistently delivers above 99% purity for our clients, and our routine analytical checks go beyond spot testing.

    Each production line run offers us another chance to fine-tune parameters—reflux temperature, pH during separation, or solvent extraction steps. These details can mean the difference between a poor result and a smooth conversion in later synthetic work. For research labs, impurities that remain undetected may skew results, causing confusion about compound behavior or, worse, burying an otherwise promising research lead.

    Our plant-scale operations produce lots ranging from a few hundred grams up to multi-kilogram quantities. This isn’t a trivial matter—you can’t simply scale up lab procedures and expect unchanged performance. Temperature gradients, agitation rates, the residence time in crystallization tanks—all these matter. Over the years, stability studies and real-world feedback from end users have shaped our current protocols. We’re firm believers in sharing data from those experiences with our clients, giving a clearer picture of what to expect.

    Applications in Medicinal Chemistry and Beyond

    Many of our partners in pharmaceuticals use 2-pyridinecarboxylic acid, 6-(trifluoromethyl)- as a substrate for synthesis of heterocyclic intermediates. The molecule finds its way into potential anti-infectious agents, CNS-active compounds, and kinase inhibitors, especially since fluorine incorporation has become a cornerstone in modern drug design. It’s no coincidence that almost a quarter of new chemical entities approved over the last decade contain at least one fluorinated functional group. The ability of the trifluoromethyl group to increase bioavailability and lipophilicity, while maintaining acceptable toxicity profiles, draws continued investment among medicinal chemists.

    Outside the pharma world, custom catalysts and agrochemicals utilize this intermediate for constructing scaffolds that demand electron-withdrawing groups at specific sites to tune reactivity. We’ve had inquiries from clients in agricultural chemistry looking for reliable, high-purity sources because any contamination or substitution means a failed crop-protectant synthesis. Over the past five years, we’ve tracked projects where successful transitions from bench to pilot-plant hinges on the quality of starting materials, not just the final product.

    Material scientists have also joined the conversation. They’re seeking to exploit the electron-density distribution resulting from the 6-trifluoromethyl modification to prepare advanced ligands and coordination complexes for specialty chelates or NMR probes. From our viewpoint, clear communication about solvent compatibility, storage conditions, and solution-phase stability allows them to better design their own experiments. 

    Specifying the Model and Grade

    Much of the confusion seen among first-time users comes from overlapping naming standards and ambiguous grade definitions. We produce 2-pyridinecarboxylic acid, 6-(trifluoromethyl)- to a single-phased crystalline solid, white to off-white in appearance, available in both analytical and preparative grades. The typical melting point ranges from 170°C to 175°C, with confirmed structure using ^1H and ^19F NMR, mass spectrometry, and HPLC.

    Our specifications aren’t just paperwork. We designed our certificate of analysis to highlight even low-level residual solvents, halide content, and other trace impurities. We list batch traceability for every lot, with full access to archived analytical data for long-term partners. This kind of transparency fosters direct collaboration—when a client’s experimental result diverges from expectation, side-by-side scrutiny of batch records often reveals subtle but important contributing factors.

    Practical Differences from Similar Compounds

    Many clients arrive at this compound after working with more common nicotinic or isonicotinic acids. The trifluoromethyl group at the 6-position makes a material difference. In Suzuki couplings, it has improved solubility in polar aprotic solvents and higher resistance to hydrolysis. Where unsubstituted pyridinecarboxylic acids sometimes require harsher conditions, we’ve recorded increased yields under milder catalyst loads with the 6-trifluoromethyl variant.

    We also see this derivative behaving with greater thermal stability and delayed decomposition, attributes that matter most in step-reaction sequences with multiple heating cycles. Process chemists running continuous flow reactions report less fouling and improved handling—attributes rarely visible until you leave the glassware behind and start thinking about 10-liter jacketed reactors. This stands in contrast to isomeric trifluoromethyl pyridinecarboxylic acids, where group placement often governs everything from reaction rate to product isolation.

    The difference isn’t academic. Subtle structure-activity shifts can translate into millions of dollars at the commercialization stage. The 6-position substitution means distinct regioselectivity, which opens up new patent space and freedom-to-operate windows. This mirrors what medicinal chemists encounter with heterocyclic aromatic chemistry, where even a small change in substitution pattern can convert a marginal screening hit into a clinical candidate.

    Learning through Use: Real-World Feedback

    Every year, our technical support team fields questions about storage stability, solubility, and batch performance. Through site visits and pilot-plant troubleshooting, we’ve watched this particular compound help clients shorten optimization timelines. We receive requests to adapt particle size for solid-phase reactions or special solvent formulations for automated equipment.

    Unfiltered dialogue reveals what spec sheets don’t. A client shares a failed scale-up due to unexpected exothermic behavior, and our chemists go back through their process details, identifying both the expected and unexpected variables. In response, we’ve expanded our offering to include supplementary guidance on temperature ramping and solvent compatibility based directly on observed user challenges.

    Pharmaceutical teams using automated purification columns often comment on cleaner isolation and reduced carryover with our product compared to some lower-quality imports. These outcomes aren’t flukes. Years of batch-by-batch adjustment—filter aid choice, drying parameters, tweaking crystallization rate—have produced a consistent product our partners have come to rely upon. 

    Meeting Changing Regulatory and Sustainability Demands

    Increasing scrutiny of chemical manufacturing, particularly when handling fluorinated materials, forces us to keep pushing for safer and cleaner processes. Waste management for spent mother liquors, energy use minimization, and solvent recovery have all been a focus during our reviews. We harness closed-loop solvent recapture for all fluorinated intermediates, including 2-pyridinecarboxylic acid, 6-(trifluoromethyl)-, to both reduce cost and environmental impact.

    Regulatory authorities worldwide now demand tighter documentation. Our plant maintains a full batch manufacturing record, validated cleaning procedures, and explicit labelling in line with local and international shipping requirements. Each dispatch includes the relevant safety and storage guidelines, both as a compliance necessity and to ensure integrity through global logistics chains.

    Our team tracks shifting regulatory stances on fluorinated chemicals, especially regarding restrictions in Europe and North America on certain PFAS compounds. While 2-pyridinecarboxylic acid, 6-(trifluoromethyl)- doesn’t fit the profile of long-chain perfluoroalkyls drawing environmental concern, we share clear documentation about decomposition and disposal pathways with our users. This helps partners in the pharmaceutical, agrochemical, and material science sectors manage their own compliance strategies without surprises.

    Addressing Supply Security and Authenticity

    The value of a reliable supply chain for critical research intermediates remains as critical as ever. Market disruption—be it from raw material shortages or regulatory bottlenecks—has taught every producer the risk of relying on single-source suppliers. Our commitment involves integrating multiple raw material vendors with comprehensive pre-screening, both for consistency and for trace-level impurity control.

    Counterfeit and substandard material sometimes enters the supply chain, often at seemingly attractive prices. We receive samples of “lookalike” products with unexpected contaminant profiles and considerably lower yields in clients’ trials. Full spectral data accompanies every batch we ship; our clients know what they’re getting, and we invite them to compare with their historic results. Authentication, not just price, shields projects from costly setbacks and repeat failures.

    For our downstream partners scaling up for preclinical or pilot-plant programs, manageable lead times dictate experimental planning. We have learned to build buffer stock beyond just-in-time inventory, absorbing minor market fluctuations and affording a level of scheduling security to research teams. This minimizes last-minute sourcing or process interruptions, keeping programs on track.

    Safety, Handling, and Best Practices

    Physical safety cannot take a back seat, even for so-called benign solids like 2-pyridinecarboxylic acid, 6-(trifluoromethyl)-. Wearing the right gloves, eye protection, and using adequate ventilation stops minor irritations from turning into major headaches. In our experience, the compound remains stable under conventional storage, but exposure to high humidity or direct sunlight should be avoided to maintain optimal shelf life.

    We always remind users that working at scale introduces its own set of risks. Powder handling at several-kilogram quantities releases fine particulates, necessitating the use of dust-control equipment. Our own staff have benefited from consistent safety training, and we translate this into straight talk on risk as part of our product documentation and customer dialogue.

    Disposal, while straightforward, still requires deliberate action. Running used solutions through carbon filtration before disposal, or following approved incineration procedures, protects both people and the environment. We regularly update our recommended guidelines, integrating the most current regional information made available to industry partners.

    Moving Projects Forward: A Shared Commitment

    Producing 2-pyridinecarboxylic acid, 6-(trifluoromethyl)- isn’t just a technical achievement—every improvement, every customer success, links directly back to the dedication of the teams both inside our walls and in our partners’ labs. Our most successful relationships center around open technical exchange, not just transactional sales.

    We’ve walked through hundreds of process workflows with researchers, noting patterns in synthetic failures or process deviations that often trace to minute lot differences and misunderstood impurity profiles. Our team works side-by-side with some clients to explore alternative solvents, optimize catalyst recipes, or brainstorm safer reaction protocols that can withstand the realities of larger-scale manufacturing. 

    Years in the trenches have taught us that new regulations, shifting market dynamics, or innovations in fields like green chemistry all have ripple effects, not only for our manufacturing line but for our clients’ ability to innovate. Everyone benefits from honest feedback loops and sustained investment in process improvement. Each batch, each technical question, becomes a chance for everyone to move projects forward with better tools, clearer expectations, and more robust results.

    Looking Ahead

    As the demand for fluorinated building blocks grows, our production of 2-pyridinecarboxylic acid, 6-(trifluoromethyl)- reflects more than current best practices—it actively tracks with scientific progress, customer expectation, and our own internal benchmarks. The future for specialty chemicals rests on more than formula sheets or spec tables; it depends on real-world performance, adaptability, and integrity at every level of supply and technical support.

    We continue to work not just for consistent yield or purity, but for total dependability—batch after batch, year on year. Users can plan with confidence, knowing that each lot reflects cumulative experience and a commitment to supporting their goals. That’s how we’ve built trust in this evolving marketplace, one gram, one kilogram, one research breakthrough at a time.