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HS Code |
839359 |
| Chemical Name | 5-(Trifluoromethyl)Pyridine-2-Carboxylic Acid |
| Cas Number | 874412-67-6 |
| Molecular Formula | C7H4F3NO2 |
| Molecular Weight | 191.11 |
| Appearance | White to off-white solid |
| Melting Point | 102-106°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=NC=C1C(=O)O)C(F)(F)F |
| Inchi | InChI=1S/C7H4F3NO2/c8-7(9,10)4-2-1-3-11-5(4)6(12)13/h1-3H,(H,12,13) |
| Storage Temperature | 2-8°C (Refrigerated) |
| Synonyms | 5-(Trifluoromethyl)picolinic acid |
| Ec Number | None assigned |
As an accredited 5-(Trifluoromethyl)Pyridine-2-Carboxylic Acid 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 5-(Trifluoromethyl)Pyridine-2-Carboxylic Acid, tightly sealed with screw cap, labeled for laboratory use. |
| Shipping | 5-(Trifluoromethyl)pyridine-2-carboxylic acid is shipped in tightly sealed containers, clearly labeled with hazard information. It is handled in compliance with chemical safety regulations, typically packaged to protect against moisture and contamination. Shipping is via certified carriers, following all local and international regulations for safe handling and transport of chemical substances. |
| Storage | Store 5-(Trifluoromethyl)Pyridine-2-Carboxylic Acid in a cool, dry, and well-ventilated area, away from heat sources, ignition sources, and incompatible substances such as strong bases and oxidizers. Keep container tightly closed and properly labeled. Protect from moisture and direct sunlight. Use appropriate chemical storage cabinets and avoid prolonged exposure to air. Handle under recommended laboratory safety protocols. |
Applications of 5-(Trifluoromethyl)Pyridine-2-Carboxylic Acid in Industrial Manufacturing5-(Trifluoromethyl)Pyridine-2-Carboxylic Acid serves as an advanced intermediate in several specialized industries. Its functional groups enable precise reactivity for downstream formulation and synthesis, supporting quality-driven manufacturing in demanding sectors. Below, we detail verified application sectors and key industrial practices for each use. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisThis compound functions as a targeted building block in the pharmaceutical sector, especially for fluorinated heterocyclic drug candidates. Pharma manufacturers utilize this acid in multi-step synthesis of enzyme inhibitors and specialty CNS or cardiovascular agents, allowing the introduction of the trifluoromethyl-pyridine motif at specific synthetic stages under controlled conditions. Processing involves integration into protected pyridine frameworks followed by functional group transformations for clinical candidate APIs. Industry compliance standards
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2. Agrochemical R&D and Commercial SynthesisAgrochemical producers apply this ingredient as a core scaffold for designing next-generation active substances, especially triazine and pyridine-based herbicides or insecticides with enhanced bioavailability. Its structural features allow high selectivity in source methylation reactions and facilitate downstream halogenation or amide linkage. The material is introduced during intermediate coupling stages to produce actives with fluorine-enriched pyridine rings. Industry compliance standards
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3. Electronic Materials and Advanced CoatingsLeading electronic chemical manufacturers use this carboxylic acid in the synthesis of specialty liquid crystal display (LCD) alignment layers and as a fluorinated doping agent for conductive polymers. Its distinctive trifluoromethyl substitution supports tight control of dielectric properties and enhances chemical stability in optoelectronic components. Downstream use includes site-specific introduction in precursor blends and polymer backbones where low polarizability and precise functionalization are required. Industry compliance standards
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4. Chemical Synthesis of Specialty Ligands and CatalystsFine chemical and catalyst producers choose this pyridine acid for the preparation of customized ligands to support metal-organic catalyst systems. The electron-withdrawing trifluoromethyl group enhances ligand stability and enables effective chelation in homogeneous catalytic applications. Synthesis processes include esterification, amide formation, and subsequent metal complexation tailored to catalytic cycle demands in fine organic synthesis and pharmaceutical transformations. Industry compliance standards
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Decades in fine chemical manufacturing have shaped our views about what drives progress in pharmaceutical and agrochemical synthesis. In any production environment, people often fixate on the obvious—purity, cost, and lead times. But there are subtler challenges that become apparent only after you’ve spent years scaling up processes, troubleshooting batches, and working alongside end users who demand more than just a spec sheet. 5-(Trifluoromethyl)Pyridine-2-Carboxylic Acid is a good example of these subtleties becoming the real difference-makers.
5-(Trifluoromethyl)Pyridine-2-Carboxylic Acid benefits from the inclusion of the trifluoromethyl group, a structural addition that often changes everything about how a pyridine ring behaves. Trifluoromethyl groups don’t just tweak reactivity—they can fundamentally alter the physicochemical properties of the compound, such as its electron density and metabolic stability. This alteration sometimes means pushing forward with a tough target molecule in discovery, finding that a parent compound simply can't offer the same performance in a reaction cascade or in final biological activity.
Colleagues working in early-stage drug design look for strong candidates that balance reactivity with robust stability under a broad range of conditions. Over the years, we have watched medicinal chemists gravitate towards this compound as a preferred core for bioisosteric replacements. The carboxylic acid at the 2-position lends itself to further derivatization, opening a pathway for many creative modifications.
Producing 5-(Trifluoromethyl)Pyridine-2-Carboxylic Acid was not simply a business decision but a response to repeated requests from development chemists dealing with stubborn intermediates. Our experience began with small-batch syntheses tailored for structure-activity relationship work. On the bench, it quickly became clear that managing the volatility and moisture sensitivity of certain intermediates required meticulous handling. A manufacturer’s advantage reveals itself through consistent solvent control, careful isolation at each step, and rigorous purity verification by HPLC and NMR—not just ticking minimum acceptance boxes, but diving one or two steps further when subtle impurities haunt process reproducibility.
Clients explained frustrations with inconsistent lot performance when they sourced this compound from brokers or non-specialist suppliers. These issues didn’t always show up on initial QC reports but became evident in downstream processes—yield drops, sticky residues, or extra chromatographic bands during analytical runs. It’s not a matter of just meeting a standard; a stable, well-defined supply chain cuts troubleshooting time for chemists, keeping projects on schedule when funding clocks run out fast.
Product specifications reflect the realities of process chemistry and continuous improvement. In the bulk chemical trade, listing purity at 98% or 99% often carries little meaning until examined from the lens of trace impurities and their impact on sensitive reactions. For 5-(Trifluoromethyl)Pyridine-2-Carboxylic Acid, our team gathers extensive NMR and LC-MS data for each lot. If a process repeatedly flags a minor contaminant during scale-up, the entire synthetic route receives reevaluation. This iterative effort enables reliable lot-to-lot consistency, reassuring experienced synthetic chemists who rely on predictable reactivity, especially when moving to kilo or ton scales.
The solid form of the compound is crucial as well. Particulate size, solubility, and the absence of clumping determine how quickly a lab can get from receipt to in-bottle reaction. We’ve fielded inquiries from clients dealing with “free-flowing” descriptions on datasheets only to receive bricks of material requiring grinding or excessive drying. Insights from front-line production teams sharpened our drying protocols. Finished product exits the reactor after precise temperature control—neither underdried nor overheated, both of which threaten stability and shelf life.
A growing list of pharmaceutical companies and academic groups turn to 5-(Trifluoromethyl)Pyridine-2-Carboxylic Acid for its key role in medicinal chemistry, especially scaffold hopping and targeted library design. The trifluoromethyl moiety brings lipophilicity and electronic effects, which significantly influence biological binding and ADME profiles. This property cannot be understated: the move from a methyl to a trifluoromethyl group often means the difference between a compound’s early failure and a candidate worthy of pursuit.
We have seen this acid routinely serve as a feedstock for amide bond formation, coupling with heterocyclic amines or other aromatic systems. Academics value this versatility, delivering novel analogs quickly for SAR studies. For commercial process chemists, this structure speeds up the search for actives by allowing late-stage diversifications using well-established coupling protocols (like EDC, HATU, or even less finicky thermal methods, depending on group compatibility).
Agricultural research teams also request this compound, aiming to introduce fluorinated motifs that delay metabolic breakdown in crops or pest targets. Not every pyridine-2-carboxylic acid core delivers the same balance of reactivity and resistance to biotransformation—a distinction that has practical, field-level outcomes.
A major burden falls on manufacturers to control costs without sacrificing reliability. Much of this hinges on process optimization: solvent selection, catalyst efficacy, and the avoidance of costly, tightly regulated reagents. Over five years of regular campaign runs, our engineers have driven down solvent waste, switched to greener oxidants where possible, and concentrated mother liquors to yield higher. Each refinement reflects a distillation of real-world lessons: batch failure root causes, operator feedback, and long-term data from clients reporting unexpected side products.
Batch-to-batch reproducibility shapes the reputation of any manufacturer. Years ago, a client in southern Europe ran into plateaus in their large-scale transformations, linking the issue to trace halides in starting acids. Feedback like this triggers internal troubleshooting—retesting archived samples, tweaking reagent grades, auditing incoming raw materials, and then validating changes across multiple production runs. The trust we build through this diligence is hard-earned and sometimes invisible to the procurement manager, but scientists in the labs appreciate every hour saved downstream.
Shipping and storage pose additional hurdles with moisture-sensitive products. Not all freight companies understand how a stray day in humid climates can impact a 25-kilogram drum. We invest in robust inner- and outer-packaging, working with partners familiar with handling fine chemicals that do not bounce back from careless warehousing. This hands-on outlook, built from hard experience, stands in contrast to the sometimes cavalier attitude found with generic commodity suppliers.
There are several commercially available pyridine-2-carboxylic acid derivatives, yet the trifluoromethyl variant leaves a distinctive mark in both synthesis and application. Where a methyl-substituted version may fall short, the enhanced polarity and metabolic stability of the trifluoromethyl group redefine the outcome in both pharmaceutical and agricultural applications.
We hear from development teams who tried to push through with lower-cost analogs, only to find the yields, profiles, or lifetimes disappointing. In our routine discussions with senior medicinal chemists, certain projects only reached completion once a reliable supply of 5-(Trifluoromethyl)Pyridine-2-Carboxylic Acid was established. This is not about a specification sheet or price negotiation—it’s the molecular output and downstream developmental success that count.
Besides property tuning, scalability sets high-grade material apart from research-only alternatives. Attention to trace contaminants, polymorph consistency, and thermal history become increasingly important above bench scale. A lot that performs well in milligram experiments may behave quite differently during a 10-kilogram scale-up; we’ve seen this scenario play out, both in our own pilot plant and at client sites. Those lessons inform every kilo we deliver.
Our technical teams work directly with R&D chemists to support complex synthesis needs, ranging from custom salt forms to particle engineering. Researchers often contact us not just for supply, but for insight into how subtle changes in process variables affect their own synthetic pathways. As manufacturers, our best contributions come from understanding the pressures of early-stage discovery, IP timelines, and the regulatory checkpoints that lean heavily on traceability and documentation.
Requests sometimes come in for alternate salt forms of 5-(Trifluoromethyl)Pyridine-2-Carboxylic Acid, such as the sodium or potassium salt, to match unique protocols in high-throughput settings. We keep close communication here, as each change affects downstream solubility, stability, and even waste handling procedures. It becomes a partnership aimed at troubleshooting together, drawing on years of collective manufacturing and research experience.
Feedback loops with clients have highlighted several best practices. For instance, protecting the acid during long-term storage eliminates loss of active compound, cutting rework and preserving batch integrity. Quick turnaround on paperwork—COAs, analytical spectra, chain-of-custody logs—matters almost as much as the product itself, especially in heavily regulated development sectors.
Our work doesn’t end at dispatch. Every batch shipped returns lessons. We track rare deviations, study end-user reports, and benchmark our own output against new industry findings. These practices reinforce a culture focused not just on what leaves the plant, but on the scale and impact of our clients’ results. We encourage clients to report any unusual findings or suggestions. The most robust improvements often arise from an unplanned, late-night phone call detailing a subtle side reaction in a new synthetic route.
Operator know-how shapes a plant’s safety record as much as the inherent hazard of the chemicals themselves. 5-(Trifluoromethyl)Pyridine-2-Carboxylic Acid, with its specialized handling and containment needs, pushed us to invest heavily in training. Seasoned operators guide new team members through hands-on sessions, teaching not just SOPs but the nuanced habits—listening for subtle changes in equipment tone, monitoring shifts in filtration rate, catching the earliest signs of unexpected precipitation.
Investments in ventilation, PPE, and automated monitoring equipment reduce incidents and keep expertise alive. Our safety protocols evolve every year, capturing both fresh regulatory guidance and lessons from our own near-misses. As a result, both the product’s integrity and worker safety remain at a premium, never sacrificed to the pressures of tight delivery schedules.
Years of focused manufacturing teach respect for every step affecting final compound quality—from the purity of fluorinating agents to the order and timing of reagent additions. Unlike broad-spectrum trading houses, a manufacturer learns to spot the telltale signs of a less-than-ideal batch early, not after hundreds of kilos leave the warehouse. Regular revalidation of critical steps, sample archiving, and investment in new analytical tools all add up to a higher-confidence supply.
Customers return to us not just for the compound itself, but for the assurances built into every kilogram: reproducibility, deep documentation trails, and consistently responsive technical support. By keeping all key operations in-house, from synthesis to packaging, we minimize supply chain disruptions and retain direct oversight of quality.
As chemical synthesis challenges grow tougher, researchers in both pharmaceuticals and agrochemicals focus ever more on fluorinated building blocks. The demand for materials like 5-(Trifluoromethyl)Pyridine-2-Carboxylic Acid will only rise as more projects move toward complex, highly selective chemistries. We watch regulatory standards climb, requiring analytical documentation, trace removal of residuals, and ever-broader impurity screens.
Meeting these standards means investing in new technology—on-line sensors, advanced NMR and mass-spectrometry capabilities, and robust batch history software that captures everything from operator shift records to post-packing environmental controls. Progress in the lab often depends on advances on the shop floor; this connection isn’t just a slogan. Our people see the difference best-in-class material makes when a top-tier pharma client reports a clean scale-up, saving weeks of cycle time.
Our long history with 5-(Trifluoromethyl)Pyridine-2-Carboxylic Acid comes down to lessons embedded in each production run and cemented by feedback from chemists who transform these grams and kilos into real-world answers. The compound represents more than a molecular structure or a catalog entry; it illustrates the value manufacturers can add by drilling into complexity, troubleshooting in partnership, and staying responsive as science moves forward.
For us, progress in fine chemistry is measured batch by batch, report by report, and above all by the usefulness of each delivery to those pushing science ahead. On the manufacturing floor, these challenges are not hypothetical. They shape the reality of discovery, scale-up, and quality—every day of the year. Our goal remains to deliver material that stands up to the front-line tests: clean reactions, reliable data, and steady progress on the toughest chemical problems.