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HS Code |
773546 |
| Productname | 4-(Trifluoromethyl)pyridine-2-carboxylic acid |
| Casnumber | 874-23-7 |
| Molecularformula | C7H4F3NO2 |
| Molecularweight | 191.11 |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Meltingpoint | 142-145°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | C1=CN=C(C=C1C(=O)O)C(F)(F)F |
| Inchi | InChI=1S/C7H4F3NO2/c8-7(9,10)5-2-1-4(6(12)13)11-3-5/h1-3H,(H,12,13) |
| Synonyms | 2-Carboxy-4-(trifluoromethyl)pyridine |
| Storagetemperature | Store at room temperature |
As an accredited 4-(Trifluoromethyl)pyridine-2-carboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g bottle of 4-(Trifluoromethyl)pyridine-2-carboxylic acid is securely sealed in an amber glass container with safety labeling. |
| Container Loading (20′ FCL) | 20′ FCL container typically holds 12–14 metric tons of 4-(Trifluoromethyl)pyridine-2-carboxylic acid, packed in secure fiber drums or bags. |
| Shipping | **Shipping Description:** 4-(Trifluoromethyl)pyridine-2-carboxylic acid is typically shipped in sealed, chemically resistant containers to prevent contamination and moisture ingress. Packages comply with local regulations for handling organic acids and may require labeling if considered hazardous. Transport is conducted under controlled temperature conditions to maintain product stability during transit. |
| Storage | Store **4-(Trifluoromethyl)pyridine-2-carboxylic acid** in a tightly sealed container, away from moisture and incompatible substances such as strong bases or oxidizers. Keep in a cool, dry, well-ventilated area, protected from direct sunlight. Ensure the storage area is equipped with appropriate spill containment and clearly labeled. Follow all standard chemical safety and storage protocols. |
| Shelf Life | **Shelf Life:** 4-(Trifluoromethyl)pyridine-2-carboxylic acid is stable for at least two years when stored tightly sealed in a cool, dry place. |
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Purity 98%: 4-(Trifluoromethyl)pyridine-2-carboxylic acid with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced byproduct formation. Melting Point 155°C: 4-(Trifluoromethyl)pyridine-2-carboxylic acid with a melting point of 155°C is used in solid-phase organic synthesis, where it provides thermal stability for high-temperature reactions. Molecular Weight 191.11 g/mol: 4-(Trifluoromethyl)pyridine-2-carboxylic acid at a molecular weight of 191.11 g/mol is used in agrochemical research, where it enables accurate stoichiometric calculations for reproducible formulations. Particle Size <100 μm: 4-(Trifluoromethyl)pyridine-2-carboxylic acid with particle size less than 100 μm is used in fine chemical manufacturing, where it enhances dissolution rates and uniform mixing. Solubility in DMSO 10 mg/mL: 4-(Trifluoromethyl)pyridine-2-carboxylic acid with DMSO solubility of 10 mg/mL is used in screening assays, where it allows for high-concentration solution preparation and consistent dosing. Stability Temperature up to 80°C: 4-(Trifluoromethyl)pyridine-2-carboxylic acid with stability up to 80°C is used in catalytic process development, where it maintains chemical integrity during process optimization. HPLC Purity ≥99%: 4-(Trifluoromethyl)pyridine-2-carboxylic acid with HPLC purity of at least 99% is used in API manufacturing, where it minimizes impurities for regulatory compliance. |
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In our plant, we’ve worked with a range of pyridine derivatives over the years, but 4-(Trifluoromethyl)pyridine-2-carboxylic acid truly highlights the kind of advancement chemists seek in modern synthesis. We put practical focus on purity, stability, and scalability—not just to meet quotas, but to create something useable on both the lab and industrial scale with confidence. Our teams worked to refine every stage, from the sourcing of starting materials through to the final purification, aiming to hit benchmarks demanded by medchem and agrochem sectors.
We’re always watching for contamination from side-products, since minute differences in impurity levels can throw off pharmaceutical applications. Through constant monitoring of process parameters and real-world feedback from users, we’ve learned how to keep byproducts in check. That’s crucial because anything left behind can compromise downstream reactions or trigger costly reworks. By targeting a high assay and minimizing specific impurities that pose problems for downstream synthetic chemistry, we’ve been able to reach a market standard that supports consistent research and production.
What makes 4-(Trifluoromethyl)pyridine-2-carboxylic acid unique in its utility comes down to its electronic and structural characteristics. The trifluoromethyl group doesn’t just tweak lipophilicity; it can influence chemical reactivity in a way not seen with other pyridine carboxylic acids. It helps medicinal chemists searching for optimized pharmacokinetics and synthetic route flexibility. Researchers noticed the value right away—the electron-withdrawing trifluoromethyl isn’t just cosmetic, it’s often the difference between a promising hit and a lead that fails in vivo. As a manufacturer, seeing that kind of feedback from ongoing medicinal chemistry projects validates the effort that’s gone into our purification and handling procedures.
We offer this material in multiple packaging options with consistent particle size and flow—factors that often go underappreciated until you’re in the middle of a long synthesis run with jammed feeders or irregular weighing. By focusing on drying, granulation, and bulk transfer approaches that are well-understood but carefully monitored, we avoid the inconsistencies that trouble smaller batch processes. We manage every shipment so users don’t have to worry about batch-to-batch drift in moisture or residual solvents that could impact sensitive organometallic steps later in the process.
Scaling up any fluoroaromatic is never just a larger batch—process nuances show themselves in new ways. Specific to 4-(Trifluoromethyl)pyridine-2-carboxylic acid, exothermicity during some condensation steps required active monitoring and tight temperature control. In early runs, local hotspots risked decomposition or extra fluorination, which caused headaches that ripple down to customers. Our engineering team installed additional heat exchangers and set up automated real-time temperature feedback loops that flag abnormal behavior, which kept things straightforward and our yield up.
Solvent choices matter more at large scale, as recycling streams can introduce unexpected traces from previous campaigns. Choosing a reliable solvent system that doesn’t promote side-reactions or interfere with downstream isolation took time. We learned through firsthand trial and error that small changes in solvent composition alter solubility and purity profiles. We trap and monitor any low-level residuals against benchmarks, ensuring material passes stringent customer requirements for residual solvents, especially for those directing the chemical into pharmaceutical routes.
Managing fluorinated byproducts remains a real task since disposal requires regulatory compliance and genuine care for safety and environment. Instead of treating effluent like an afterthought, we invested early in specialized scrubbing and distillation areas specific to halogenated compounds. Our operators receive ongoing training for handling pressurization, run-off capture, and emergency protocols that consider fluorine-based hazards.
We’ve seen requests for ever-larger batch sizes as chemists scale their projects, and we respond with openness about what batch size changes mean for lead times, purity assurance, and overall logistics. We don’t hide challenges when they arise, and our customers trust us because we keep them informed about possible process transitions or raw material disruptions—a relationship built over years, not just transactions.
Supplying a useful specialty acid means providing comprehensive analytical support. Our in-house analytical chemists use methods matched to the real-world impurities you get from pyridine functionalization. Each lot gets confirmed by NMR and HPLC, but also by more specific tests—such as LC-MS and GC—because the low-level fluorinated impurities that escape standard detection can still matter. Reporting every trace; not just those mandated by compendia, builds trust with R&D-focused and regulated industry customers alike.
Having been on the receiving end of inconsistent COAs from third-party traders, we vowed to provide technical support that understands what questions come from those at the lab bench. Our team answers requests for extra spectral data, secondary verification, or in-process controls with urgency, because we’ve seen deadlines slip due to incomplete or unclear documentation. Every batch’s paperwork is double-checked and prepared with the researcher in mind, not just compliance.
For end-users demanding high-purity, analytical transparency reduces troubleshooting time and lets them move straight to synthesis. When unforeseen issues—like unknown impurity peaks—do pop up, having the production batch documentation and retention samples helps us trace back and work proactively with customers to pinpoint root causes, rather than just issuing replacements and moving on.
4-(Trifluoromethyl)pyridine-2-carboxylic acid stands out as a preferred intermediate for building complex pyridine-containing scaffolds, particularly those with bioactivity. Medicinal chemists rely on its electron-deficient nature to facilitate selective coupling, cyclization, or further functionalization. Customers tell us it serves as a crucial building block for kinase inhibitors and modulators with improved metabolic stability, often outperforming non-fluorinated alternatives on both synthetic yield and downstream screening.
The trifluoromethyl group promotes metabolic resistance, helping research teams create drug candidates with better in vivo persistence. In agrochemical research, this compound enables the synthesis of actives that benefit from the altered reactivity introduced by the electronegative fluorine atoms, allowing chemists to tune both potency and selectivity against pests or pathogens.
Years of supplying this compound to the global R&D and production sector means we get a constant stream of feedback about what works and where challenges appear. Some want extra dry material for water-sensitive reactions; some ask about alternative crystal forms or reactivity in cross-coupling protocols. We document user reports and use them to adapt our product and service—those user perspectives matter more than theoretical spec sheets could. For example, a feedback loop with a pharmaceutical partner revealed a subtle solvated impurity interfering with a downstream amide coupling. Adjustments in drying and filtration based on that knowledge now benefit all our customers.
In one program, a research group used our acid to couple with heteroaromatic amines, supporting a pipeline of antimalarial candidates. The reactivity profile gave them the selectivity and yields they wanted, avoiding the extra purification steps that dogged their previous work with less robust intermediates. This translates directly to faster project timelines and less wasted resource—a win for both sides.
This acid differs substantially from straight pyridine-2-carboxylic acid or methylated alternatives not just in electronic properties, but in its handling and regulatory requirements. The trifluoromethyl group means increased hydrophobic character and higher electron-withdrawing effect, shifting the reactivity and solubility in both organic and aqueous media. We worked directly with formulators who needed precise control over compound partitioning and clearance rates in bioassay development, and saw real performance benefits over simple methyl or non-substituted analogs.
Some users compare it to 4-fluoropyridine-2-carboxylic acid, but the three-fluorine substitution tends to outdo the mono-fluoro for both synthetic utility and end-stage activity. Rates of nucleophilic aromatic substitution shift, and final product stability improves. By maintaining tight control over our process chemistry, we have been able to keep impurities related to incomplete trifluoromethylation at low levels, which means the full substitution effect is present batch after batch.
Working alongside chemists in both academic and industrial settings, we learned early that not just any pyridine carboxylic acid will do. Structure drives biological results, but consistent material eases the process bottlenecks scientists dread. Our approach does not attempt to crowd the market with overlapping analogs—rather, we focus on providing the version chemists reach for when optimizing new reactions, expanding library collections, or finalizing lead compounds for regulatory submission.
Managing a specialty fluorinated acid at consistent quality means keeping a sharp eye on sourcing and transport. Our approach builds redundancy into raw material supply, favoring vendors with proven reliability and compliance history. Volatility in starting material markets has, on a few occasions, forced us to adjust timelines and batch planning. Instead of shifting the burden onto customers or resellers, we stay transparent and make adjustments in-house, finding alternate routes and scaling as possible to avoid extended shortages.
Environmental stewardship is not just an add-on. Handling and disposing of perfluorinated byproducts is strictly controlled, not only due to regulatory oversight, but because our reputation as a supplier comes from responsible conduct. The fluorine content raises stakes—we maintain specialized containment and recycle what we can. Waste streams see active management for fluorine removal and neutralization before disposal, following best practices adopted from ongoing process safety research. Our operators rotate through environmental training and safety simulation drills, so protocols do not exist just on paper.
Regulatory shifts in Europe, North America, and East Asia increase scrutiny for compounds featuring strong electron-withdrawing groups like trifluoromethyl. Regulatory files submitted by customers now require more documentation on origin, chain of custody, and contaminant history than ever before. We document every step—showing both the pedigree of each lot and supporting documentation for where our raw materials come from, how solvents are reclaimed, and what testing each batch undergoes.
Our customers include medicinal researchers, formulators, contract manufacturers, and startup companies. Their needs differ as widely as their project scopes, so we keep our lines open all the way from inquiry to post-delivery support. Direct feedback from users often guides the improvements in our process—shifts in drying dynamics, requests for lower metal content, or standards for tighter control on particle size distribution.
Our technical service teams are chemists, not call-center responders. More than once, we have received urgent messages about a failed catalytic cycle traced to trace metals and adjusted filtration and batch processing in response. Users who require custom documentation, specific labeling, or lot tracing beyond standard paperwork find our team ready to assist. These extra steps are not formalities—they demonstrate respect for the science being done on the other side of each shipment.
We regularly review experiences from returned lots and customer projects to identify where improvement makes sense. For example, a recurring issue with absorbance in UV assays pushed us to offer documentation on optical purity and process controls, preventing troubleshooting delays on analytical methods further down the line. Our learning never stops at specification compliance; we want to see customers achieve their project goals with fewer uncertainties about the building blocks they choose.
Specialty chemicals like 4-(Trifluoromethyl)pyridine-2-carboxylic acid don’t succeed based on formula alone. They need thoughtful handling, supported by practical knowledge from people who’ve run the reactors, managed the waste, worried about timelines, and fielded late-night troubleshooting calls from researchers in other time zones. Our legacy as a manufacturer comes from years in the trenches, not from relabeling or repackaging.
As the market for complex heterocycles grows, so does the scrutiny on every step—safety, environmental care, and supply continuity. We keep eyes on emerging synthetic methodologies, regulatory developments, and user feedback from the latest drug discovery and agrochemical programs. The feedback loop runs both ways; what matters in the field pushes us to better methods, tighter controls, and better-informed decisions about scaling production or pivoting to new product grades.
New developments in catalysis and fluorine chemistry suggest early adopters may want still greater control over particle size, dust levels, or extra-dry lots. Our R&D and production teams already work together to build prototypes for particularly sensitive transformations, collaborating directly with end users to tweak and refine.
By listening to those pushing the boundaries in the lab and understanding the real-world logistical, regulatory, and technical challenges, we stay committed to delivering material that advances projects, not just fills space on a product list. We have learned lasting lessons from every scale-up, every tough customer call, and every analytical blip—those collective experiences define the difference users experience with our 4-(Trifluoromethyl)pyridine-2-carboxylic acid.