|
HS Code |
805406 |
| Chemical Name | 2-hydroxy-6-(trifluoromethyl)pyridine-3-carboxylic acid |
| Molecular Formula | C7H4F3NO3 |
| Molecular Weight | 207.11 g/mol |
| Cas Number | 326-44-3 |
| Appearance | White to off-white solid |
| Melting Point | 124-128°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | OC(=O)C1=C(O)N=CC(C(F)(F)F)=C1 |
| Inchi | InChI=1S/C7H4F3NO3/c8-7(9,10)4-2-3(6(13)14)5(12)11-1-4/h1-2,12H,(H,13,14) |
| Density | 1.64 g/cm³ (estimated) |
| Pka | 3.7 (carboxylic acid group) |
| Storage Conditions | Store at 2-8°C, protect from light and moisture |
| Pubchem Cid | 17482 |
As an accredited 2-hydroxy-6-(trifluoromethyl)pyridine-3-carboxylic 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 with tamper-evident cap, labeled with product name, CAS number, hazard warnings, and manufacturer details. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-hydroxy-6-(trifluoromethyl)pyridine-3-carboxylic acid ensures secure, compliant bulk shipment in sealed drums or bags. |
| Shipping | 2-Hydroxy-6-(trifluoromethyl)pyridine-3-carboxylic acid is shipped in tightly sealed containers to prevent moisture absorption and contamination. The package is clearly labeled with hazard and chemical identification, and stored in a cool, dry place. Transport complies with all relevant chemical safety and regulatory requirements for non-flammable, non-corrosive laboratory reagents. |
| Storage | 2-Hydroxy-6-(trifluoromethyl)pyridine-3-carboxylic acid should be stored in a tightly sealed container, protected from moisture and light. Keep it at room temperature (15–25 °C) in a cool, dry, and well-ventilated area. Avoid exposure to strong oxidizers and incompatible substances. Ensure proper chemical labeling and follow standard laboratory safety protocols for handling and storage. |
| Shelf Life | Shelf life: Store 2-hydroxy-6-(trifluoromethyl)pyridine-3-carboxylic acid tightly sealed, protected from moisture and light, for at least two years. |
|
Purity 99%: 2-hydroxy-6-(trifluoromethyl)pyridine-3-carboxylic acid with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced byproduct formation. Melting Point 178°C: 2-hydroxy-6-(trifluoromethyl)pyridine-3-carboxylic acid with melting point 178°C is used in organic synthesis protocols, where it allows precise temperature-controlled reactions. Stability Temperature 120°C: 2-hydroxy-6-(trifluoromethyl)pyridine-3-carboxylic acid with stability temperature 120°C is used in agrochemical formulation processes, where it maintains compound integrity under processing conditions. Particle Size <10 µm: 2-hydroxy-6-(trifluoromethyl)pyridine-3-carboxylic acid with particle size less than 10 µm is used in fine chemical manufacturing, where it provides rapid dissolution and homogeneous mixing. Water Content <0.5%: 2-hydroxy-6-(trifluoromethyl)pyridine-3-carboxylic acid with water content below 0.5% is used in moisture-sensitive catalyst production, where it minimizes unwanted hydrolysis and ensures catalyst activity. |
Competitive 2-hydroxy-6-(trifluoromethyl)pyridine-3-carboxylic acid prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@boxa-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Experience in chemical manufacturing has taught us that some molecules demand more care than others during synthesis and handling. 2-Hydroxy-6-(trifluoromethyl)pyridine-3-carboxylic acid, with its highly functionalized pyridine ring and trifluoromethyl substituent, requires precise process control. Every batch brings lessons. Our team designed purification methods around the unique polarity and acidity imparted by the hydroxy and carboxyl groups. We use analytical methods, including HPLC and NMR, to verify that the product matches the precise profile set by both research and commercial needs. The trifluoromethyl group introduces a high degree of chemical stability, which, during manufacturing, means special attention must be given to controlling the reaction conditions to avoid unwanted side reactions that may degrade this valuable functional group.
Users in pharmaceutical and agrochemical research care about purity and consistency more than ever. The reason lies in the downstream chemistry: irregular batches wax havoc on reproducibility, waste costly reagents, and risk regulatory headaches. In our own experience, researchers rely on this pyridinecarboxylic acid as a building block for more complex molecules; the clean introduction of the trifluoromethyl group gives compounds unique metabolic stability and lipophilic properties, qualities sought after in both drug candidates and active ingredients for crop protection. Unlike many pyridine derivatives, this compound holds up during scale-up—yielding products that display fewer byproducts and better batch-to-batch consistency.
Several years back, side-by-side analysis of common substituted pyridines highlighted how this molecule stands apart. 2-Hydroxy-6-(trifluoromethyl)pyridine-3-carboxylic acid resists many oxidative and hydrolytic conditions that catch less robust analogs such as 2-hydroxy-3-pyridinecarboxylic acid or pyridinecarboxylic acids lacking the trifluoromethyl group. Incorporation of fluorine increases molecular weight and drastically alters electronic properties. As a result, pharmaceutical intermediates based on this scaffold display improved pharmacokinetic properties. Agrochemical innovators also remark on the environmental persistence and resistance to microbial breakdown that come from the trifluoromethyl group — a feature harder to harness with non-fluorinated analogs. In short, researchers can push the limits of their molecular designs farther with this unique compound.
Manufacturing fluorinated aromatics calls for specific reactor materials and environmental controls. Trifluoromethyl groups are introduced through reagents that do not play nicely with standard process equipment. We use corrosion-resistant reactors and continuously monitor for leakage or unwanted byproducts. Early in our scale-up efforts, a lesson learned: use of generic glass-lined tanks led to excessive cleaning cycles and increased downtime. Upgrading to reactors lined with specialized coatings solved residue issues and improved turnaround. Waste streams containing fluorinated materials require their own segregation, so plant design and training factor heavily in our procedures. Complying with evolving local and international regulations on per- and polyfluoroalkyl substances (PFAS) adds complexity; strict wastewater treatment and regular audits help us keep a clean track record.
Direct relationships with end-users allow prompt feedback on performance. Researchers in materials science have observed that our batches enable reliable crystallization and efficient downstream coupling reactions. A notable case involved a pharmaceutical customer who switched from a trader-sourced batch and immediately saw gains in both yield and product purity, credited to the absence of certain unreacted precursors that trace back to shortcut manufacturing. One agrochemical development team told us they achieved new actives with greater photo-stability, using our compound as a core scaffold. Results like these guide improvements in both process and packaging, as we look to minimize risk of degradation during storage or transport.
We manufacture 2-hydroxy-6-(trifluoromethyl)pyridine-3-carboxylic acid as an off-white to pale yellow powder. From batch to batch, key metrics remain within tight ranges: high purity (routinely greater than 98% by HPLC), minimal residual solvents, low trace metal content, and water limits suitable for most organic syntheses. Those working with automated synthesizers or sensitive catalytic reactions value consistent particle size distribution, which prevents clumping and allows for fast, reproducible dissolutions. Over the past decade, direct feedback from synthetic labs has shaped small-yet-important improvements, such as switching to more robust, low-static bottles after reports of powder adhesion under dry conditions. These practical shifts draw from daily realities on the customer side of the bench.
Speed to market often comes down to available building blocks. Many specialty molecules debut in journals, but bulk supply for expanded screening remains a bottleneck. Our direct synthesis approach for 2-hydroxy-6-(trifluoromethyl)pyridine-3-carboxylic acid answers this need. Developing custom derivatives in parallel for select clients, we have observed a meaningful reduction in hit-to-lead timelines. In an R&D campaign led by an external partner, our material reduced intermediate impurity levels, allowing the chemists to skip a chromatography step and accelerate the synthesis of their target compound. Another biochemist, working on kinase inhibitors, credited performance gains in cell assays to the high lot-to-lot consistency maintained during a multi-year research program—something that cheaper or repackaged alternatives simply could not offer.
Legal requirements for handling and documentation of speciality chemicals have grown steadily. Shipment records, material lineage, and full Certificates of Analysis require an airtight chain of custody. Our role as a direct manufacturer removes the uncertain “gray zone” around true product provenance—a reassurance for procurement teams and regulatory auditors. Updates to our compliance standards reflect input from both domestic and international partners, shaped by real inspection findings and feedback loops. We routinely update our internal protocols to reflect changes in regional chemical control laws, and all quality documentation is traceable to originating batch records. This transparency appeals to auditors preparing regulatory submissions and to researchers preparing critical data for publication. Experience reinforces one point: documentation diligence at the point of manufacture translates to confidence for downstream users.
A shelf-stable, predictable product saves time for researchers and operators alike. Our in-plant tests show this compound remains stable under typical laboratory storage conditions. Extreme humidity and long-term exposure to high temperatures have proven the only factors that degrade appearance or quality, so we advise sealed storage in a cool, dry location. During a heat wave last summer, a shipment delayed in customs maintained full specification upon arrival—thanks, in part, to our use of protective packaging chosen after years of trial and researcher complaints about caking or discoloration. Making continuous improvements in these small but critical packaging decisions all but eliminates waste and complaints.
Market conditions for fluorinated intermediates fluctuate with shifts in global demand and changes in upstream raw material pricing. Direct production lets us avoid the swings faced by traders and brokers, keeping costs steady. Our supply data shows buyers benefit most when volume commitments align with their R&D or manufacturing cycles, minimizing price volatility. Over time, clients who switched to direct purchasing reported fewer budget surprises and less time lost to sample qualification or returns. Building mutual trust through consistent delivery and technical clarity gives both parties peace of mind and predictability in planning. In an increasingly competitive market, this level of reliability becomes a real advantage for production teams aiming to hit tight deadlines.
New targets in pharmaceuticals and agricultural chemistry often stretch the limits of available raw materials. Our own research team regularly collaborates with industry and academia to tailor 2-hydroxy-6-(trifluoromethyl)pyridine-3-carboxylic acid derivatives for advanced applications. Rather than offering only standard catalog options, we draw on years of hands-on experience to develop new grades and specifications in response to customer requests for alternative purities, custom packaging, or unique particle characteristics. Close partnership between clients and our technical group makes rapid iteration possible—critical for fast-moving R&D pipelines. Several published case studies from academic laboratories acknowledge our role in providing tailored materials during early-stage discovery.
Manufacturing chemicals with high fluorine content invites scrutiny from environmental regulators. Early on, we analyzed our waste streams and adopted proven strategies to minimize environmental impact. Dedicated fluorine containment and separation protocols exceed minimum legal requirements and contribute to sustainable operation. We partner with licensed waste handlers for any byproducts, and ongoing investment in fluorine recovery cuts back on both costs and disposal volumes. Each year, our environmental audit compares our emissions to local and global benchmarks for best practices, and our team regularly reviews operational steps for additional improvement. Responsible stewardship in this area opens doors to supply agreements with companies that require evidence of sustainable sourcing.
Manufacturers hear one consistent request from laboratory scientists: reliable advice from someone who has physically handled the product. We provide direct consultation from staff chemists who developed the manufacturing process, rather than reading from a script. This means questions about solubility, scale-up, and downstream compatibility get prompt answers based on firsthand experience, saving users time during experimental setup. On one memorable project, a customer hit roadblocks dissolving the material in a mixed solvent system and turned to us. Drawing from our own purification process, we provided an approach that balanced pH and ionic strength, quickly clearing the issue. These day-to-day exchanges gradually improve both our product and the client experience.
Shifts in patent law and competitive dynamics influence demand for customized building blocks. Generic versions that overlook subtle differences—such as isomeric purity or trace impurity profiles—have occasionally run into legal or technical snags. Maintaining a consistent high quality for 2-hydroxy-6-(trifluoromethyl)pyridine-3-carboxylic acid gives our customers confidence that critical IP can withstand external scrutiny. Recent feedback from a university-based startup echoed the same point: patent applications for their new active pharmaceutical ingredients advanced smoothly due, in part, to the solid analytical data attached to every shipment. We track competitor offerings and routinely benchmark against new quality standards and analytical technologies, ensuring our product remains competitive both technically and legally.
Consumer expectations for transparency and traceability are driving rapid changes across chemical supply chains. The days of faceless intermediaries are fading. More clients want manufacturing details, origin information, and a real voice at the other end of the line. As a direct producer, our manufacturing data, traceability, and technical support are integrated from the start. This approach allows us to adapt to shifting demand across regions and end-user segments, whether the push comes from regulatory foresight or the pace of innovation in target markets. We stay flexible, investing in new equipment, compliance tools, and team training as needs arise.
The ever-rising complexity of pharmaceuticals, crop protection agents, and electronic materials keeps pushing the envelope on what manufacturers like us must deliver. 2-Hydroxy-6-(trifluoromethyl)pyridine-3-carboxylic acid represents a new class of enabling intermediates—combining stability, unique functionalization, and direct route synthesis. Teams counting on predictable, clean building blocks will see further gains as advances in reaction chemistry open up new possibilities. Strong, direct collaborations with customers, careful quality oversight, and nimble adaptation ensure we remain an active partner in pioneering research.