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HS Code |
472791 |
| Iupac Name | 4-(Trifluoromethyl)pyridine-3-carboxylic acid |
| Cas Number | 144060-86-6 |
| Molecular Formula | C7H4F3NO2 |
| Molecular Weight | 191.11 |
| Appearance | White to off-white solid |
| Melting Point | 114-118 °C |
| Solubility In Water | Slightly soluble |
| Smiles | C1=CN=CC(=C1C(=O)O)C(F)(F)F |
| Inchi | InChI=1S/C7H4F3NO2/c8-7(9,10)5-2-1-4(3-11-5)6(12)13/h1-3H,(H,12,13) |
| Storage Conditions | Store at room temperature, away from moisture and light |
As an accredited 4-(Trifluoromethyl)-3-pyridinecarboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle labeled “4-(Trifluoromethyl)-3-pyridinecarboxylic acid,” sealed with a screw cap and tamper-evident band. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 16 MT per 20′ full container load, packed in 25 kg fiber drums, for 4-(Trifluoromethyl)-3-pyridinecarboxylic acid. |
| Shipping | 4-(Trifluoromethyl)-3-pyridinecarboxylic acid is shipped in tightly sealed containers, protected from moisture and light. It is handled as a chemical substance, following standard safety protocols. Packages are labeled according to regulations and often shipped by ground or air, ensuring compliance with local, national, and international hazardous material transport guidelines. |
| Storage | Store **4-(Trifluoromethyl)-3-pyridinecarboxylic acid** in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong bases or oxidizers. Protect from moisture and sources of ignition. Clearly label the storage area, and ensure access is limited to trained personnel using appropriate personal protective equipment. |
| Shelf Life | 4-(Trifluoromethyl)-3-pyridinecarboxylic acid is stable under recommended storage conditions; shelf life typically exceeds two years when properly stored. |
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Purity 99%: 4-(Trifluoromethyl)-3-pyridinecarboxylic acid with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and low impurity levels. Molecular weight 189.1 g/mol: 4-(Trifluoromethyl)-3-pyridinecarboxylic acid with molecular weight 189.1 g/mol is used in drug discovery research, where it facilitates accurate compound formulation. Melting point 161°C: 4-(Trifluoromethyl)-3-pyridinecarboxylic acid with melting point 161°C is used in solid-phase organic synthesis, where it exhibits thermal stability during reaction sequences. Particle size <10 µm: 4-(Trifluoromethyl)-3-pyridinecarboxylic acid with particle size less than 10 µm is used in fine chemical production, where it promotes rapid and uniform dissolution. Stability temperature up to 120°C: 4-(Trifluoromethyl)-3-pyridinecarboxylic acid stable up to 120°C is used in process scale-up studies, where it maintains integrity under prolonged heating. Water content <0.5%: 4-(Trifluoromethyl)-3-pyridinecarboxylic acid with water content below 0.5% is used in moisture-sensitive formulations, where it prevents unwanted hydrolysis and degradation. HPLC assay >98%: 4-(Trifluoromethyl)-3-pyridinecarboxylic acid with HPLC assay greater than 98% is used in analytical reference standards, where it delivers reproducible quantification results. |
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As a chemical manufacturer with years in fine chemicals and fluorinated building blocks, we approach each product with practical experience and deep knowledge of its applications. 4-(Trifluoromethyl)-3-pyridinecarboxylic acid stands out in our catalog for the unique edge it brings to fields such as pharmaceuticals, crop protection, advanced materials research, and more. Based on direct feedback from formulation scientists and firsthand handling in our plant, this compound delivers consistent results in synthesis challenges that demand both structural complexity and robust stability.
Synthetic chemists seek out precisely substituted pyridine rings because of the distinct molecular recognition features they give to bigger compounds. The trifluoromethyl group is a strong electron-withdrawing function, often appearing in modern drugs and agricultural actives for the enhanced metabolic stability it provides. In our workshops, customers point to the need for crystal-clear quality, material traceability, and a minimized impurity profile to speed up development timelines. Our technical teams regularly observe that off-the-shelf options fall short, either in terms of batch-to-batch purity or in how easily the compound handles during scale-up. That motivated us to refine our own synthesis and offer a grade that meets reliable standards for R&D and kilogram-level pilot production.
Our analysts track regulatory filings and published synthesis routes closely. A key driver comes from the increased demand for fluorinated building blocks in small-molecule innovation. The global pharmaceutical landscape increasingly calls for options that meet international guidelines for purity and documentation. We answer this by offering our material only after thorough structure confirmation by NMR, GC/MS, and HPLC, directly from our own controlled process. Our in-house work confirms that the compound’s behavior under different reaction conditions matches or exceeds published protocols from peer-reviewed sources and industry leaders.
Handling properties in the lab and at the plant scale matter just as much as listed specifications. 4-(Trifluoromethyl)-3-pyridinecarboxylic acid typically forms a white to pale crystalline solid with high chemical stability under ambient conditions. Chemists appreciate its solubility profile, which includes good compatibility with polar organic solvents—like methanol, ethanol, and dimethyl sulfoxide—and practical, moderate solubility in water. This supports use in both standard organic synthesis and high-throughput screening.
Our technical staff frequently confirms the melting point range, and monitor for moisture content that can alter performance in moisture-sensitive reactions. Material produced here meets strict set points on water content, as measured by Karl Fischer titration, and all batches are subject to full traceability from raw material intake through to final packing. We track shelf life in our own stability chambers and provide real-world advice for storage, supporting shipment and stockpiling for longer development projects.
Our work with 4-(Trifluoromethyl)-3-pyridinecarboxylic acid finds its strongest interest among medicinal chemists and agrochemical researchers. The compound works as a versatile intermediate for coupling reactions, especially for the construction of novel heterocyclic structures that drive drug discovery programs. In conversations with customers, the pyridine ring, decorated with a trifluoromethyl group, is often described as a “privileged motif”—one that imparts key pharmacological properties, and can modulate solubility, metabolic rates, or target binding affinity.
Crop protection scientists come to us looking to enhance the activity or field longevity of experimental herbicides or fungicides. This compound often forms the backbone of synthesis for new candidate molecules, particularly where metabolic resistance is a concern. We have seen firsthand how a single substituent change using this acid can translate into half-life improvement or even unlock new biological pathways. Coordination with these teams lets us align our QC to their most pressing analytical needs, whether related to isomeric purity or trace metals content.
In-house production gives us direct oversight over every processing parameter. Batch records capture the actual observed melting point, which typically sits in the 160-170°C range, alongside specific purity by HPLC—commonly above 99% area by our standard test methods. The trifluoromethyl group’s signature signals appear clearly by both 1H and 19F NMR, and every lot comes with a full spectrum printout for customer technical files.
Careful characterization identifies not just the main compound, but also the route-dependent impurities that can creep in at ppm levels. We run regular impurity profiling to capture any process drift, and act swiftly on feedback from customer labs that may observe issues in late-stage synthesis or analytical development. Purity, in practical terms, is not just about overall assay but also about control over specific, structurally similar contaminants that can “ghost” the final API or formulated product.
Direct sourcing from a manufacturer sidesteps many pitfalls associated with unknown or poorly tracked supply chains. Traders and distributors sometimes repackage and relabel, breaking the link between the final batch and its real origin. Stories from customers include unreliable delivery, mismatched documentation, or the discovery of unexpected solvents or stabilizers added for unknown reasons. We built our own integrated supply not just to avoid these problems, but to give customers a relationship with a technical team that can answer detailed questions, provide extra COAs, and adjust schedules or packaging as demand requires.
Our R&D teams work side-by-side with operations, and that’s vital when a process needs tweaking for scale-up—such as switching from glassware in the kilo lab up to stainless reactors at the pilot plant. One key difference we often see: products supplied by third parties may meet basic chemical IDs but diverge in physical properties like particle size distribution, clumping tendency, or the presence of trace coloring, all of which influence throughput and downstream process performance.
Fluorinated pyridinecarboxylic acids span a range of positional isomers and substitution patterns. Our 4-(Trifluoromethyl)-3-pyridinecarboxylic acid offers unique regioselectivity compared to, for example, the 2- or 5-substituted isomers. Chemically, the position of the trifluoromethyl group relative to the carboxylic acid changes reactivity in coupling reactions. From our research collaborations and feedback, even small shifts in substitution can determine whether an intermediate channels smoothly into an amide, ester, or direct arylation.
The electron-withdrawing effect of the trifluoromethyl at the 4-position makes this molecule a stronger partner in cross-coupling than some analogous acids lacking the fluorine content. Many of our projects with external labs rely on this unique activation to open up reactivity with aryl halides or boronic acids. In drug design or in agricultural chemistry, even if the molecular formula looks similar on paper, the end performance in-field or in-vivo changes dramatically based on such substitution differences.
From the manufacturing angle, synthesizing this compound presents different challenges compared to ordinary pyridinecarboxylic acids—such as the need to carefully manage fluorination steps, handle specialized raw materials, and precisely control the environmental parameters during crystallization. This means not every supplier actually produces it in-house or at scale, and we often see downstream users report out-of-spec materials from less experienced outlets.
From raw material selection to packaging and logistics, each decision shapes the reliability of the finished product. We partner only with vetted primary vendors for trifluoroacetic derivatives and closely inspect each incoming shipment. Operations follows validated cleaning protocols to avoid cross-contact with other fluorinated or halogenated stocks. Our in-process controls use both manual inspection and automated analytical measurement at critical stages. As batches move forward, we sample before and after each key step to catch any drift early.
Once crystallized, we thoroughly dry and mill the product to homogenize particle size, then run repeated assays to ensure phase consistency across the lot. Packaging happens in humidity-controlled areas, with re-tested samples pulled immediately before bagging. We then seal in inert atmospheres using packaging grades specified for pharmaceutical intermediates, supporting long shelf life and safe transit across a broad range of climates from customer feedback.
Final release authority stays with a designated quality expert who reviews the process stack, analytical records, and stability data before certifying new lots for sale. Customers get full batch traceability and our tech teams answer any batch-specific queries—such as detailed impurity profiles, residual solvents, or advice on scale-up adaptation—because we make and test the product directly, not by relabeling another facility’s output.
Sometimes an inquiry comes from a university lab looking to trial a few grams in a catalyst study, other times from a multinational’s pilot plant ready to step up to 50 kilograms for preclinical intermediates. Our experience with both settings means we stay ready for process customization, whether that involves accommodating special documentation, specific packaging requests, or advice on solvent compatibility for critical reactions. Requests for custom grind, alternate packaging, or accelerated delivery get routed straight to our in-house teams, not lost in a third-party chain.
For end-users scaling from bench chemistry to commercial demonstration, rapid feedback on questions—down to the actual reaction sequence and reactor setup—is essential. Our chemical engineers draw from both batch and continuous production backgrounds. That perspective allows us to give real-world advice on how our product will behave in new or scaled-up conditions, e.g., solvency curve adjustments, possible issues due to exotherm management, or the right filtration step to minimize material loss at large scale.
While fluorinated organic compounds contribute essential properties to modern medicines and materials, their production and disposal require careful stewardship. We address these challenges by minimizing the use of hazardous reagents, reclaiming solvents wherever feasible, and strictly controlling waste disposal in compliance with international and local regulations. Staff receive ongoing training in safe fluorine chemistry, and we partner with responsible downstream processors for off-spec or returned material.
Our environmental health and safety (EHS) department runs regular audits on effluent streams—particularly hydrofluoric acid, a well-known byproduct of some fluorination reactions. We invested in closed-system reactors and real-time monitoring to ensure safe handling at every stage. In addition, green chemistry initiatives in our R&D group test out evolving synthetic methodologies that reduce the environmental footprint of trifluoromethyl introduction or make use of bio-based feedstocks. When a safer or more sustainable process reaches practical readiness, we integrate it directly rather than wait for regulatory mandates.
Geopolitical events and raw material price volatility challenge everyone in the specialty chemicals field. Tight regulation of fluorinated organics in some export regions has changed the way these raw materials move across borders. Our supply model accommodates these realities by maintaining multiple sourcing lines for key precursors, long-term contracts, and safety stock stored in multiple regions. Internal forecasting tools track both demand cycles and incoming global regulatory changes, so we can anticipate needs and deliver continuity—even as external conditions fluctuate.
Customers have seen sudden disruptions in the past, ranging from shipment delays to reclassification of chemical products. To avoid cascading supply shocks, we keep communication direct with end users. Advance notification of major supply changes, periodic market updates, and technical bulletins support labs and plants in planning their own inventory needs. We believe reliability means more than a declared stock level—it comes from understanding each customer’s application, process tolerances, and criticality of continuous supply.
Whether troubleshooting a stalled coupling step involving 4-(Trifluoromethyl)-3-pyridinecarboxylic acid or exploring alternative synthetic approaches, customers frequently request detailed technical support beyond basic COA data. Our in-house application chemists have worked through a range of typical and complex use cases. Their direct experience—ranging from reactivity assessment in Grignard additions to performance in Suzuki-Miyaura cross-coupling—brings pragmatic advice that’s shaped both by literature precedent and by direct lab observation.
We support method development by offering actual chromatograms, alternative dissolution methods, and impurity profiles based on specific customer reagents. Our analytics team even advises on atypical results, such as unexpected retention times or signal splits, that can stem from minor variations in lab setup. As a producer, we know how small changes—ambient humidity, tank calibration, or a grinder setting—can ripple through a process and show up as surprising results.
Scale-up support is part of our technical package. Practical tips, such as the handling of powder charging, ability to withstand freeze-thaw cycles, or solvent switch protocols, often make the difference between a successful large-batch run and avoidable downtime. End-users get direct phone or email access to the staff who have made, analyzed, or scaled up the product themselves, not a distant distributor chasing answers from someone upstream.
Open communication with industry partners shows the constant pressure on development teams to shorten project timelines, manage costs, and prove innovation. 4-(Trifluoromethyl)-3-pyridinecarboxylic acid fits into a toolkit that bridges known synthetic pathways with emerging needs for differentiated molecular scaffolds. Our team stays engaged in the field, learning from each project and feeding those lessons back into process improvements, safety initiatives, and portfolio planning.
We keep technical documents transparent, with up-to-date regulatory information, practical handling hints, and a realistic estimate of expected lead times based on seasonal factors or global trends. Where requests emerge for modifications to the process or product specification—more stringent impurity cutoffs, special grades for GMP development, or truly custom fine-tuning—we assess feasibility openly, share prospective timelines, and only commit where our direct in-house expertise guarantees the result.
As industry standards grow ever more demanding, product integrity and technical depth decide real outcomes. We continue to listen to our customers, adapt to changing market needs, and maintain the exacting standards that brought 4-(Trifluoromethyl)-3-pyridinecarboxylic acid into our lineup in the first place. Whether the requirement is gram-scale research or multi-ton campaigns for new pipeline candidates, direct-from-manufacturer sourcing gives both transparency and agility from project kickoff through long-term supply.
Continuous improvement in both product and process is the only way to keep up with the pace of discovery in fluorinated organics. By backing every shipment with proven analytical data, technical insight, and a commitment to ongoing collaboration, we see both our compound and our customers’ projects reach their strongest potential.