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HS Code |
485992 |
| Iupac Name | 3-(trifluoromethyl)pyridine-2-carboxylic acid |
| Molecular Formula | C7H4F3NO2 |
| Molecular Weight | 191.11 g/mol |
| Cas Number | 368-95-6 |
| Appearance | White to off-white solid |
| Melting Point | 114-116 °C |
| Boiling Point | 313.9 °C at 760 mmHg |
| Density | 1.532 g/cm³ |
| Solubility In Water | Slightly soluble |
| Smiles | C1=CC(=C(N=C1)C(=O)O)C(F)(F)F |
As an accredited 2-Pyridinecarboxylic acid, 3-(trifluoromethyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled "2-Pyridinecarboxylic acid, 3-(trifluoromethyl)-", 25g, with hazard symbols and product details. |
| Container Loading (20′ FCL) | 20′ FCL container loading: Securely packed 2-Pyridinecarboxylic acid, 3-(trifluoromethyl)- in drums/bags, maximizing space and ensuring safe transport. |
| Shipping | 2-Pyridinecarboxylic acid, 3-(trifluoromethyl)- is typically shipped in tightly sealed containers to protect against moisture and contamination. The package is clearly labeled and handled following regulations for chemicals, often shipped with Material Safety Data Sheet (MSDS). Transport may require temperature control and hazard labeling depending on quantity and destination. |
| Storage | Store 2-Pyridinecarboxylic acid, 3-(trifluoromethyl)- in a tightly sealed container in a cool, dry, well-ventilated area away from sources of moisture, heat, and incompatible substances such as strong bases or oxidizers. Protect from direct sunlight. Clearly label the storage area and follow all standard chemical safety protocols, including use of personal protective equipment when handling. |
| Shelf Life | 2-Pyridinecarboxylic acid, 3-(trifluoromethyl)- typically has a shelf life of 2-3 years when stored in a cool, dry, airtight container. |
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Purity 98%: 2-Pyridinecarboxylic acid, 3-(trifluoromethyl)- with 98% purity is used in medicinal chemistry synthesis, where enhanced yield and reproducibility are achieved. Melting point 142°C: 2-Pyridinecarboxylic acid, 3-(trifluoromethyl)- of melting point 142°C is used in organic electronic materials development, where consistent phase behavior is ensured. Molecular weight 189.10 g/mol: 2-Pyridinecarboxylic acid, 3-(trifluoromethyl)- with molecular weight 189.10 g/mol is used in pharmaceutical lead optimization, where precise stoichiometric control is possible. Particle size <50 µm: 2-Pyridinecarboxylic acid, 3-(trifluoromethyl)- with particle size below 50 µm is used in catalyst formulation, where improved dispersion and reactivity are gained. Stability temperature up to 120°C: 2-Pyridinecarboxylic acid, 3-(trifluoromethyl)- stable up to 120°C is used in high-temperature reaction processes, where product integrity is maintained. Water content <0.5%: 2-Pyridinecarboxylic acid, 3-(trifluoromethyl)- with water content below 0.5% is used in moisture-sensitive agrochemical synthesis, where hydrolysis risk is minimized. Flash point 180°C: 2-Pyridinecarboxylic acid, 3-(trifluoromethyl)- with flash point 180°C is used in safe handling during industrial scale-up, where fire hazard is reduced. |
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As a chemical manufacturer, each reaction run holds a promise. Among the many compounds we see in our synthesis halls, 2-Pyridinecarboxylic acid, 3-(trifluoromethyl)- stands out for its reliable performance as an intermediate and its well-documented properties. The journey behind putting this molecule in the hands of chemists and researchers reflects the wider changes in advanced material science and pharmaceutical development.
In our lab, the synthesis of this compound starts with selecting pure pyridine derivatives and carefully managing the trifluoromethylation step. Each step calls for controlled temperature, solvent selection, and post-reaction purification to remove by-products that can alter assay or downstream reactivity. Batch after batch, we analyze for moisture, identify trace impurities, and document melting points and spectral fingerprints. These tasks are not just box-checking—they matter because inconsistency in a fine chemical creates discord in every subsequent synthesis it enters.
This molecule is more than a modification of picolinic acid. Introducing the trifluoromethyl group delivers both significant electronic impact and metabolic stability. The CF3 group, well known for its ability to influence electron density and increase lipophilicity, upgrades picolinic acid chemistry in medicinal and agrochemical applications. We see this firsthand as project teams frequently approach us about customizing lot size or integrating 3-(trifluoromethyl)-functional groups into pharmaceutical candidates.
From a chemists’ viewpoint on our floor, the trifluoromethyl group’s bulk and strong electron-withdrawing nature set the molecule apart from other pyridinecarboxylic acids. It changes hydrogen bonding, alters solubility in organic solvents, and increases resistance to metabolic degradation. In practice, clients working with early-stage medicinal chemistry cite the consistent bioavailability improvements they see when using fluorinated carboxylic acids versus non-fluorinated analogs.
Every batch of 2-Pyridinecarboxylic acid, 3-(trifluoromethyl)- exits our reactors under strict quality control. Our team measures active ingredient content by HPLC or NMR, and investigates impurities down to the ppm level. Moisture content deserves special attention. Trace amounts can trigger unwanted side reactions, so our post-production drying and packaging aim for residual moisture well beneath 0.5%. These are not arbitrary points. When poorly controlled, excess water causes failed coupling reactions, costly project delays, and wasted research effort.
Beyond the routine numbers, our people handle the material’s physical form every day. Workers keep an eye out for clumping and caking, frequently linked to high humidity storage or too much exposure during transfer. Operators who spot such issues do not push the material forward but isolate and investigate, knowing even slight physical changes may hint at compromised quality.
The melting point on records typically sits between 145 and 147°C under controlled atmosphere, though small deviations occur based on crystallization rate and solvent of recrystallization. All product goes out in tightly sealed HDPE containers, inner bagged with liner to reduce breathing of air moisture.
Most requests we field for 2-Pyridinecarboxylic acid, 3-(trifluoromethyl)- revolve around three areas: pharmaceutical R&D, performance materials, and specialized catalysis. In drug discovery, the trifluoromethyl group has a reputation for increasing permeability and metabolic resistance in candidate molecules. We often supply research-grade quantities for SAR (structure-activity relationship) studies, where modifying the pyridine ring opens up new chemical space unexplored by non-fluorinated analogs.
Several biotechnology clients have shared positive feedback on the compound’s behavior in coupling reactions, particularly for forming amide bonds or preparing ligands for coordination complexes. The acid group offers a direct handle, while the trifluoromethyl substituent enhances binding selectivity in certain targets. As a manufacturer, we get to see the results in bioassay data, where analogs with and without the trifluoromethyl group reveal how one atom set changes biological response.
Outside pharmaceuticals, research teams exploring battery materials and new polymers leverage the CF3-containing pyridine acids for building blocks that bring oxidative stability and unique coordination geometries. In the hands of skilled synthetic chemists, such subtle changes often unlock properties unavailable through classic carboxylic acids.
In manufacturing, having several pyridinecarboxylic acids on hand offers a window into structure-function relationships. The standard 2-pyridinecarboxylic acid, for example, sees broad use in coordination chemistry and simple condensation reactions, but cannot match the metabolic stability delivered by the trifluoromethylated analog. The 3-trifluoromethyl group rewires reactivity, creating an electron-poor pyridine ring that steps outside typical aromatic substitution profiles.
Our group has synthesized dozens of substituted pyridines for decades. Adding a methyl or chloro substituent, for instance, yields improvements in crystal stability or reactivity, yet only the trifluoromethyl group reliably moves logP, boosts lipophilicity, and shields molecules from oxidative enzymes. Many customers who start with simple pyridinecarboxylic acids pivot to the trifluoromethylated version after hitting solubility or biostability roadblocks.
Fluorination steps are not trivial. The addition introduces cost, complexity, and safety precautions in handling reagents. Unlike methyl or ethylation, which use relatively benign agents, we must pay close attention to reagent exotherms and potential release of HF when scaling up. Our team monitors every run, logs waste, and trains operators in emergency procedures.
Producing this compound at kilogram scale brings its own set of lessons. Each batch run demonstrates the practical realities of fluorination work beyond gram-scale reactions published in academic journals. Reproducibility, often taken for granted in small-scale work, has proven elusive without investment in equipment upgrades and process controls.
By tuning solvent ratios, agitation rates, and crystallization steps, we offer consistent product year after year. Sudden demand spikes, typically driven by client project phases, create sourcing challenges for specialty reagents. This is where a manufacturer’s experience proves irreplaceable—preemptively securing key starting materials and building relationships with global suppliers shields customers from costly stockouts or winding down research due to lack of a niche intermediate.
Shipping and packaging call for careful documentation, especially for international shipments where customs and regulatory agencies request substantiation of material identity and purity. We have learned to anticipate such scrutiny, preparing certificates of analysis, detailed synthesis documentation, and stability data so clients do not face regulatory holdups.
Scaling up fluorine chemistry always requires vigilance. Low-yielding reactions, batch-to-batch variability, and potential exposure to harsh reagents keep us monitoring every detail. Rather than push for speed, we prioritize robust, stepwise scale-up to minimize loss and maximize safety. Investing in specialized glassware, robust corrosion-resistant reactors, and proper ventilation proved indispensable.
For example, at one point, we struggled with batch consistency due to a by-product forming during the trifluoromethylation stage. Through root cause analysis and collaboration with upstream suppliers, we traced the issue to a trace contaminant in the starting pyridine. Switching to a new supplier, implementing additional analytical testing, and adjusting the purification protocol restored the purity profile. Watching the data change after each intervention drives home that, in manufacturing, outcomes hinge as much on problem-solving as on following standard procedures.
Handling waste is another area that demands long-term commitment. Fluorinated waste must be properly neutralized and disposed of by licensed contractors. We’ve invested in in-house treatment capacity where possible and partner with reputable firms to ensure full traceability for each kilogram of waste material generated.
Working as a chemical manufacturer involves daily decisions with significant consequences for customers. Each lot is traceable to individual operators, processing conditions, and quality control results. Training documentation, SOP revisions, and open channels for employee feedback keep production on target and improve outcomes for our customers.
Customer audits and on-site visits are part and parcel of manufacturing life, and we treat them as opportunities to demonstrate process transparency and rigorous controls. Sharing raw data, walking clients through our QC protocols, and showing our analytical documentation backs up every purity figure reported on a certificate of analysis. Investing in KBr pellet FTIR, 400MHz NMR, and UHPLC systems may seem excessive, but for this molecule and its applications, data integrity and reproducibility mean everything.
We also listen. Pharmacologists sometimes request unusual impurity profiles for toxicity testing; materials scientists working on next-generation batteries have specific questions about trace metals. Each group pushes us to innovate, adapt, and sometimes rework our standard production pathways. In return, we gain early exposure to shifts in technology and evolving project needs across industries.
The demand for trifluoromethylated building blocks grows each year, driven by drug development that relies more and more on fluorine’s unique properties. It isn’t just about making drugs more lipophilic—today’s synthesists ask about environmental fate, long-term metabolic impact, and the durability of specialty chemicals under thermal or oxidative stress.
We are seeing a rise in projects blending computational modeling with synthetic work, allowing discovery teams to rationally select building blocks that offer the best chance at improved drug-likeness. This data-driven approach nudges manufacturers like us to maintain a broad product catalogue and invest in scale-up for new derivatives. 2-Pyridinecarboxylic acid, 3-(trifluoromethyl)- remains a steady performer, not a flash-in-the-pan molecule; year after year, research clients reorder and build new discoveries on its backbone.
Environmental and regulatory scrutiny has increased for all high-value intermediates, particularly those containing fluorine. As a result, we find ourselves documenting cradle-to-gate lifecycle impacts, registering substances for REACH, and pre-emptively building dossiers for North American and Asian regulators. The work takes sustained investment but reassures downstream customers that products from our sites align with the shifting regulatory landscape.
Being a manufacturer is more than running reactors and printing invoices. Every gram of 2-Pyridinecarboxylic acid, 3-(trifluoromethyl)- heading out the door carries the weight of our reputation. Reports from researchers that “your batch worked flawlessly” validate the long hours and quality controls, while occasional feedback on unexpected issues drives us to investigate, learn, and further tighten our processes.
Stories from the field underscore the product’s value. A pharmaceutical team recently shared that switching to our material reduced rework rates in a peptide coupling campaign. Another advanced materials group pointed to gains in oxidative stability for their battery electrolyte project, which they credited to the presence of the trifluoromethyl group. Direct engagement means our technical team can troubleshoot project challenges side by side with customers, rather than relying on intermediaries or distributors to relay late-breaking lab findings.
From a manufacturing standpoint, reliability rests on careful raw materials qualification. Starting the process with subpar feedstocks guarantees downstream problems, so we maintain dynamic supplier audits, in-plant quarantine zones, and routine documentation of every incoming drum.
Achieving true batch-to-batch consistency requires addressing the details others often gloss over. Strict calibration of analytical equipment, periodic revalidation of every cleaning procedure, and platforms to share improvement ideas among staff—all play a part. Our internal systems flag even minor deviations, prompting investigation rather than acceptance of “close enough” results.
The story of 2-Pyridinecarboxylic acid, 3-(trifluoromethyl)- underscores the complex nature of specialty chemical production today. This compound occupies a small but crucial space in countless research and manufacturing pipelines. Its subtle transformation of the pyridine ring through trifluoromethylation drives real-world impact, whether by enabling medicinal chemists to extend drug lifetime, materials scientists to build more robust polymers, or analysts to compare new analogs with known standards.
From raw material selection to final shipment, every step reflects decisions grounded in years of practical lab and plant experience. That perspective—a blend of chemical know-how, attention to end-user feedback, and hard-won lessons in scale-up—makes a difference that customers see in every bottle delivered.
We remain committed to innovation, safety, and supporting customer breakthroughs. The continued evolution of advanced fluorinated intermediates like this one promises to reshape the boundaries of what’s possible in the labs and production lines that rely on specialty chemicals each day. From our side of the process, the goal remains simple: dependable, high-quality material, produced sustainably and delivered with transparency.