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HS Code |
545584 |
| Iupac Name | 4-(trifluoromethyl)pyridine-2-carboxylic acid |
| Molecular Formula | C7H4F3NO2 |
| Molecular Weight | 191.11 |
| Cas Number | 875781-17-2 |
| Appearance | white to off-white solid |
| Melting Point | 110-113°C |
| Boiling Point | N/A (decomposes) |
| Solubility In Water | slightly soluble |
| Smiles | C1=CN=C(C=C1C(=O)O)C(F)(F)F |
| Inchi | InChI=1S/C7H4F3NO2/c8-7(9,10)4-1-2-5(6(12)13)11-3-4/h1-3H,(H,12,13) |
| Pka | approx. 3.5 (carboxylic acid group) |
| Logp | 1.7 (estimated) |
As an accredited 2-pyridinecarboxylic acid, 4-(trifluoromethyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2-pyridinecarboxylic acid, 4-(trifluoromethyl)-; tightly sealed with a screw cap, labeled with hazard information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-pyridinecarboxylic acid, 4-(trifluoromethyl)-: Standard 20-foot container; suitable for bulk packaging and efficient international shipping. |
| Shipping | 2-Pyridinecarboxylic acid, 4-(trifluoromethyl)- is typically shipped in airtight, chemically resistant containers, secured to prevent leaks or exposure. It is handled according to regulations for corrosive or hazardous chemicals, often with appropriate labeling and documentation, and transported via ground or air freight under controlled temperature and safety conditions to ensure stability. |
| Storage | 2-Pyridinecarboxylic acid, 4-(trifluoromethyl)- should be stored in a tightly sealed container, away from moisture and incompatible substances such as strong oxidizers and bases. Keep in a cool, dry, well-ventilated area, protected from direct sunlight. Ensure appropriate chemical labeling and secondary containment to prevent spills. Personal protective equipment should be used when handling the compound. |
| Shelf Life | 2-Pyridinecarboxylic acid, 4-(trifluoromethyl)- typically has a shelf life of 2–3 years when stored in a cool, dry place. |
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Purity 99%: 2-pyridinecarboxylic acid, 4-(trifluoromethyl)- with purity 99% is used in pharmaceutical intermediate synthesis, where high purity ensures minimized side product formation. Molecular weight 189.1 g/mol: 2-pyridinecarboxylic acid, 4-(trifluoromethyl)- with molecular weight 189.1 g/mol is used in agrochemical research, where precise molecular control enables reproducible formulation studies. Melting point 160°C: 2-pyridinecarboxylic acid, 4-(trifluoromethyl)- with melting point 160°C is used in high-temperature reactions, where thermal stability promotes process safety. Particle size <50 µm: 2-pyridinecarboxylic acid, 4-(trifluoromethyl)- with particle size <50 µm is used in catalyst preparation, where fine particles enhance reaction surface area and yield. Stability temperature up to 120°C: 2-pyridinecarboxylic acid, 4-(trifluoromethyl)- with stability temperature up to 120°C is used in continuous flow synthesis, where chemical integrity is maintained under process conditions. Water content ≤0.5%: 2-pyridinecarboxylic acid, 4-(trifluoromethyl)- with water content ≤0.5% is used in moisture-sensitive coupling reactions, where low water content prevents hydrolysis and degradation. LogP 1.2: 2-pyridinecarboxylic acid, 4-(trifluoromethyl)- with LogP 1.2 is used in medicinal chemistry screening, where optimal lipophilicity aids in drug-likeness evaluation. UV absorbance (λmax 273 nm): 2-pyridinecarboxylic acid, 4-(trifluoromethyl)- with UV absorbance at 273 nm is used in analytical reference standards, where strong UV response facilitates accurate quantification. Assay ≥98% (HPLC): 2-pyridinecarboxylic acid, 4-(trifluoromethyl)- with assay ≥98% (HPLC) is used in fine chemical manufacturing, where product consistency increases batch reliability. Residual solvent <0.1%: 2-pyridinecarboxylic acid, 4-(trifluoromethyl)- with residual solvent <0.1% is used in electronic materials development, where low solvent levels minimize contamination risk. |
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As the people who blend, monitor, and refine every batch of 2-pyridinecarboxylic acid, 4-(trifluoromethyl)-, we look at this molecule through a lens sharpened by daily work and practical concerns. Out on the chemical plant floor, every drum, every reaction, and every test bears out a truth: quality always starts at the molecular level. We see this organic acid as much more than a chemical structure or a line in a catalog. Each shipment to labs, pharmaceutical firms, and specialty synthesis plants stems from the small decisions we make in our reactors, where control of temperature, moisture, and purity sets the stage for the chemical’s performance downstream.
The 4-(trifluoromethyl) group built into the pyridine ring offers a fundamental shift in reactivity, one that regular pyridinecarboxylic acids cannot match. Scientists who reach for our batches in their explorations of pharmaceuticals and advanced agrochemicals do so because they rely on these nuanced differences—and we are here at the beginning, responsible for delivering consistency and trust. The layers of regulatory scrutiny and real-world research depend on raw materials that never waver in quality.
We never talk about purity as a mere number on a certificate. Each lot we produce of 2-pyridinecarboxylic acid, 4-(trifluoromethyl)- tells its own story, during chromatography and during physical handling. The material’s crystalline nature, solubility profile, and UV absorption character come under daily examination. Labs for pharmaceutical intermediates count on our attention to impurity profiles, matching real molecular fingerprints and ensuring each potential use—especially in regulated industries—remains uncompromised by by-products or trace contaminants.
For this specific compound, subtle shifts in the trifluoromethyl group’s position and electronic effects draw a line between our product and common pyridine derivatives. The fluorinated group shapes both the compound’s hydrophobicity and electron-withdrawing potential, ultimately guiding its selectivity in synthesis. In our experience, downstream reactions that struggled with the parent pyridinecarboxylic acid can often proceed more smoothly and with greater yield using this fluorinated version. Customers in pharmaceutical development and crop-protection see clear differences, and their feedback directly shapes the process improvements we implement. We keep in mind, always, how variance in lot-to-lot chemical characteristics could mean wasted time, failed runs, or worse—ruined opportunities for innovation. That is why checkpoints, from raw material selection to finished product analytics, line every step.
Each batch of 2-pyridinecarboxylic acid, 4-(trifluoromethyl)- leaves our facility meeting the most stringent purity standards we can uphold—typically upwards of 98% by HPLC. To reach this threshold, our team reviews not just the finished substance, but the environmental conditions through synthesis and isolation. We have found, after years of trial and feedback, that batch size meaningfully influences impurity profiles. For research and scale-up partners, we run adaptive batch cycles, favoring versatility in quantities while revalidating every scale increase.
Physically, the acid’s white to off-white crystalline appearance, its melting point curve, and its solubility in key solvents tell us almost as much as spectral data. Industrial users care about how it handles in real mixers and reactors—does it clump? Does it dissolve as predicted? Does it introduce unwanted foaming or byproduct precipitation? Our plant staff report these findings, and our technical teams shape advice for customers learning to optimize formulations on their own floors.
Questions from the field give us the sharpest insights into how 2-pyridinecarboxylic acid, 4-(trifluoromethyl)- functions in real-world chemistry. In pharmaceutical synthesis, the trifluoromethyl group not only enhances metabolic stability in candidate molecules, but it also shifts reactivity, enabling new coupling opportunities in heterocycle-rich targets that standard pyridinecarboxylic acids simply cannot achieve. Process chemists often reach out with requests for guidance about controlling reaction selectivity, predicting side reactions, or achieving consistent yields in scale-up stages.
Agrochemical firms tell us that the molecule, with its electronic tweaks from fluorination, often grants improved bioactivity in lead molecule development, especially in projects looking to enhance environmental persistence or modify mode of action. The voice of these researchers pushes us to maintain not just purity, but trace-level consistency from batch to batch. We know from experience that even minor background contamination in our acid can snowball into unreliable screening results in biological assays.
Researchers synthesizing advanced materials also report advantages with this fluorinated pyridine derivative. It participates effectively in cross-coupling and expands the palette of available building blocks for highly engineered molecular frameworks that regular, non-fluorinated pyridines cannot access.
The transition from non-fluorinated pyridinecarboxylic acids to a 4-(trifluoromethyl) derivative isn’t cosmetic. We’ve seen, time and again, how this adjustment changes reactivity. In the field, medicinal chemists rely on this difference to achieve increased binding affinity or improved pharmacokinetics in candidate molecules. From the perspective of our reactors and QA labs, the presence of three tightly bound fluorines introduces both challenges and benefits: greater demands in controlling fluorinated by-products, but far-reaching advantages once the compound heads out into clients’ synthesis streams.
Without the trifluoromethyl group, many substituted pyridinecarboxylic acids offer less potent electron-withdrawing behavior, and their solubility profiles differ. Our customers have flagged this in their process development—the fluorinated acid tends to show lower basicity and solubility in certain aqueous systems, a feature that downstream production chemists sometimes leverage to improve selectivity or purification. We reinforce our process design to keep these variations tightly controlled, giving buyers the trust that each delivered lot serves as a genuinely reliable and differentiated building block.
Logistics and shelf-life often get taken for granted. Direct feedback from both bench chemists and plant operators points out differences in handling between this fluorinated acid and less specialized pyridinecarboxylic acids. We see slightly elevated sensitivity to moisture uptake during storage, so our packaging team has moved over years of experience to triple-layered drum liners and tighter humidity controls. We store this product away from acids and basic fumes, knowing that trifluoromethyl substituents can sometimes amplify unwanted side reactions with atmospheric contaminants.
We also train our staff to prepare the compound for sampling and transfer with eye for dust and fine particulate control. 2-pyridinecarboxylic acid, 4-(trifluoromethyl)- forms a more disperse dust than most related acids, owing to its specific crystalline habit. This isn’t a mere annoyance—uncontrolled dust can throw off accurate weighing, alter reaction stoichiometry, or pose safety risks if inhaled. We found through repeated experience that installing finer mesh screens and automated transfer nozzles sharply reduced these problems for our customers down the supply chain.
Our approach to traceability grows out of practical collaboration with users. We register every lot against a unique molecular fingerprint, confirmed by a battery of in-house and third-party analytical methods—NMR, HPLC, GC-MS, and elemental analysis among them. When a client reports an unexpected analytical spike or an anomaly in reactivity, we track every blend and every step back to our own logs. There’s a reason our technical staff keeps a database of variance, process incidents, and operator notes all tied back to specific lots. Where issues emerge, we fold those lessons directly back into production standards.
This system lets us offer not just a product, but a history—a narrative of how the batch performed, who oversaw what, and what corrective actions put us on the right path. It also gives us insights into how storage duration or warehouse temperature fluctuations impact physical characteristics: discoloration, caking, shifts in crystalline habit. As a result, batches heading to tight-tolerance pharmaceutical processes are given priority both in terms of freshest stock and extra rounds of QC review.
In reality, the path from raw chemicals to high-grade 2-pyridinecarboxylic acid, 4-(trifluoromethyl)- involves more than just machines and protocols. Production teams learn to recognize quality through details not always visible in data: how the compound pours, how it smells, how it settles in a container. We build this hands-on experience into our customer support. When a scientist calls about a problematic filtration or an unusual solubility, our technical advisors draw on everything from batch records to old operator notebooks to solve the problem right at the source. The questions and troubleshooting never stop—we see this as essential to developing a better product over time.
Producing aromatic fluorinated acids brings environmental responsibilities that require more than simple compliance. Fluorine chemistry brings special waste and emissions concerns. Our plant invests heavily in closed system reactors, scrubbers for volatile organic compounds, and on-site fluorination by-product capture. All this work reduces not only our regulatory burden, but also downstream problems for customers in highly regulated spaces.
Our solvent recovery and by-product treatment units run in close integration with production. Batch effluents go through in-line monitoring, and we constantly search for new ways to recover or neutralize hazardous species before they leave our site. Our efforts here are not just about passing inspections—they tie directly into feedback from field users worried about residual solvents or unexpected trace contaminants in their own products. By keeping control at the source, we offer a tighter guarantee for every drum shipped.
As demand for specialized fluorinated building blocks grows in pharmaceuticals, crop protection, and high-performance materials, the technical demands placed on 2-pyridinecarboxylic acid, 4-(trifluoromethyl)- continue to escalate. Our relationships in the research and development community push us to go further: shortening delivery times for trial lots, tuning purification for ultra-sensitive projects, or running custom scale-ups on short notice. This is a daily dialogue, not a remote transaction. By sharing real-world technical notes and supporting open communication, we support innovators who are pushing synthesis boundaries.
We keep our focus sharp on not only what goes right, but also what needs improvement. Cross-company working groups, supplier audits, and direct field visits remain cornerstones for how we learn where our product succeeds and where it falls short. In one case, sustained feedback from a pharmaceutical partner led us to change our crystallization solvent, which cut down on a persistent filtration bottleneck in their process. These changes ripple out—new solvent systems, altered drying conditions, different packaging protocols—all the way from plant floor to customer.
Trust, in our view, means more than shipping a white powder with a label. It grows from a record of practical success and honest setbacks shared with the user. Whether the request comes in for a five-kilogram R&D lot or a full-scale production order, we treat each with the same combination of technical discipline and critical skepticism that defines long-term supplier relationships. This trust flows both ways—clients who share back issues, observations, and even hints of new chemistry help us lift the overall field another notch higher.
Continuous improvement underpins our operations, not as a slogan but as a response to the day-to-day challenges that emerge from both routine production and exceptional customer requests. If a plant operator flags a recurring issue with cake formation during the isolation of the acid, our team gathers for root cause analysis—bringing engineering, analytical, and synthesis know-how to bear in retooling the process. When a customer explores a radical new application, we dig through past batch records and internal studies to flag potential hazards or support a tailored approach.
Outside the plant, our technical outreach seeks to bridge the distance between basic manufacturing and complex real-world use. Customers can access not only typical specifications but also nuanced insights: advice on solvent selection, reminders about reactivity quirks, or shared data on downstream transformations where the 4-(trifluoromethyl) group is likely to impact coupling, isomer ratios, or metabolic fate. This exchange sharpens both our internal practice and the broader results clients see in their end-user applications.
2-pyridinecarboxylic acid, 4-(trifluoromethyl)- stands as a testament to the intersection of pure chemistry and daily, hands-on problem-solving. Its distinctiveness resides in the very features that define its handling, quality, and performance: the subtle signature of its trifluoromethyl group, the careful steps controlling reactivity and trace impurities, the collaborative exchange with the researchers and engineers building tomorrow’s solutions. From our long hours in the plant to the client labs shaping modern pharmaceutical and agrochemical breakthroughs, every step builds on careful observation, transparent communication, and lessons hard-won over years of production. Our experience tells us this: a molecule, carefully made and honestly delivered, can shift projects forward—one reaction, one partnership, one improvement at a time.