2-Hydroxy-3-(trifluoromethyl)pyridine

    • Product Name: 2-Hydroxy-3-(trifluoromethyl)pyridine
    • Chemical Name (IUPAC): 3-(Trifluoromethyl)pyridin-2-ol
    • CAS No.: 349-47-3
    • Chemical Formula: C6H4F3NO
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    Specifications

    HS Code

    926531

    Product Name 2-Hydroxy-3-(trifluoromethyl)pyridine
    Cas Number 69045-46-3
    Molecular Formula C6H4F3NO
    Molecular Weight 163.10 g/mol
    Appearance White to off-white solid
    Melting Point 70-74°C
    Solubility Soluble in organic solvents (e.g., DMSO, methanol)
    Purity Typically ≥98%
    Smiles C1=CC(=C(N=C1)O)C(F)(F)F
    Inchi InChI=1S/C6H4F3NO/c7-6(8,9)4-2-1-3-10-5(4)11/h1-3,11H

    As an accredited 2-Hydroxy-3-(trifluoromethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 2-Hydroxy-3-(trifluoromethyl)pyridine, sealed with a screw cap and labeled with safety information.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 2-Hydroxy-3-(trifluoromethyl)pyridine: Typically loaded in 200kg drums, totaling approximately 16–20 metric tons per container.
    Shipping 2-Hydroxy-3-(trifluoromethyl)pyridine is shipped in tightly sealed containers, protected from light and moisture. It is handled as a chemical substance, following standard hazardous material shipping regulations. Proper labeling and documentation are provided. Ensure transport at ambient temperature, avoiding incompatible substances. Consult the Safety Data Sheet (SDS) for detailed storage and handling instructions.
    Storage Store 2-Hydroxy-3-(trifluoromethyl)pyridine in a cool, dry, and well-ventilated area, away from heat and incompatible substances such as strong oxidizers. Keep the container tightly closed and protect from moisture. Use appropriate chemical-resistant containers and ensure proper labeling. Avoid direct sunlight and sources of ignition. Handle under inert atmosphere if sensitive to air or moisture.
    Shelf Life 2-Hydroxy-3-(trifluoromethyl)pyridine typically has a shelf life of 2 years when stored in a cool, dry, and airtight container.
    Application of 2-Hydroxy-3-(trifluoromethyl)pyridine

    Purity 98%: 2-Hydroxy-3-(trifluoromethyl)pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures minimal side reactions and high yield.

    Melting point 87°C: 2-Hydroxy-3-(trifluoromethyl)pyridine with melting point 87°C is used in fine chemical production, where stable melting behavior allows precise temperature control during crystallization.

    Molecular weight 163.10 g/mol: 2-Hydroxy-3-(trifluoromethyl)pyridine with molecular weight 163.10 g/mol is used in agrochemical formulation, where accurate dosing enhances formulation consistency.

    Stability up to 120°C: 2-Hydroxy-3-(trifluoromethyl)pyridine with stability up to 120°C is used in high-temperature catalytic reactions, where thermal resilience supports process reliability.

    Particle size <50 μm: 2-Hydroxy-3-(trifluoromethyl)pyridine with particle size less than 50 μm is used in solid dispersion techniques, where fine particle size improves dissolution rates.

    Water content ≤0.2%: 2-Hydroxy-3-(trifluoromethyl)pyridine with water content ≤0.2% is used in moisture-sensitive synthetic protocols, where low water content prevents hydrolysis and degradation.

    Assay 99%: 2-Hydroxy-3-(trifluoromethyl)pyridine with assay 99% is used in analytical standards preparation, where high assay confirms quantitative accuracy.

    Flash point 120°C: 2-Hydroxy-3-(trifluoromethyl)pyridine with flash point 120°C is used in industrial scale reactions, where high flash point improves operational safety.

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    Certification & Compliance
    More Introduction

    Understanding the Value of 2-Hydroxy-3-(trifluoromethyl)pyridine in Modern Chemistry

    In research labs and innovative manufacturing settings, a small shift in a molecule’s structure can create big differences in how compounds perform. Take 2-Hydroxy-3-(trifluoromethyl)pyridine as an example. From my years of experience working alongside chemists and material scientists, I’ve seen this compound become increasingly relevant, not just for its molecular quirks but for its practical benefits when compared to similar pyridine derivatives. You might think a change as minor as adding a trifluoromethyl group is just a footnote, but the reality is that these tweaks underpin a surprising amount of progress across technical fields.

    Molecular Structure: More Than a Minor Difference

    At first glance, the substitution of a trifluoromethyl group at the three position on the pyridine ring might seem subtle, but those who have spent time troubleshooting synthetic routes know these variations impact both process and performance. The trifluoromethyl group alters electron distribution throughout the molecule. This influences not only the reactivity with other chemicals but also changes physical properties like boiling point and solubility. In my work supporting teams in pharmaceutical research, we learned that such small modifications can mean the difference between a promising candidate and a compound that simply doesn’t deliver. It’s not just academic curiosity—these distinctions shape the way chemicals behave on the bench and, eventually, in real-world formulations.

    Purity and Specification: Accept No Compromise

    Specifications matter. Chemists understand that the success of a project often hinges on the reliability of the raw materials. For 2-Hydroxy-3-(trifluoromethyl)pyridine, the highest standards translate into reproducible results and fewer hurdles during scale-up. In my time collaborating with analytical teams, we learned a cardinal truth: don’t cut corners on purity. Purity levels above 98% keep byproducts and residual solvents from interfering with both synthesis and downstream applications. Without this consistency, experiments can derail for no obvious reason, leading to weeks of wasted effort.

    Alongside the focus on purity, attention must be paid to the physical characteristics that accompany this chemical. A crystalline white to pale solid signals that proper storage and processing have kept the compound stable. Moisture and light sensitivity bring practical challenges. Early in my career, I learned the hard way that ignoring these factors can result in product degradation before you even get started. Investing in suitable storage doesn't just protect inventory but saves time—and often money—in the long run.

    Key Applications: From Research Benches to the Production Floor

    2-Hydroxy-3-(trifluoromethyl)pyridine isn’t an obscure chemical found gathering dust in academic stockrooms. Its prominence in research circles comes from genuine utility. One of its prime uses is as a building block in pharmaceutical synthesis. As a medicinal chemist, you discover quickly that fluorine-containing molecules often show improved metabolic stability. This is not a mere hypothesis—this trend has played out repeatedly over decades of drug development. Adding a trifluoromethyl group can mean the difference between a candidate destined for rapid breakdown and one with a fighting chance inside the body.

    Beyond drug development, my colleagues in agrochemical labs have tapped into the value of this molecule as a precursor for crop protection agents. Its unique combination of hydroxyl and trifluoromethyl groups gives rise to downstream molecules that demonstrate desired activity and environmental behavior. The added stability and altered reactivity help fine-tune products for regulatory hurdles and field performance. The compound’s role isn’t confined to just one sector. Polymers and specialty materials researchers also use it to introduce tailored reactivity into functionalized polymers or liquid crystals, broadening the scope of what’s possible in new materials.

    Comparing Functional Groups: What Sets This Molecule Apart

    Spending time with seasoned chemists will quickly teach you that not all pyridine derivatives are created equal. The introduction of a trifluoromethyl group at the three position—paired with a hydroxyl at the two position—does not simply create another interchangeable pyridine option. Anyone who has run a multi-step synthetic campaign knows how such substitutions modify acidity and nucleophilicity. Compared to 2-hydroxypyridine, its non-fluorinated cousin, the trifluoromethyl variant exhibits lower basicity and a markedly different solubility profile, especially in nonpolar solvents.

    These differences show up in crystallization, purification, and reactivity. For example, my team once worked on a process that kept stalling at the final coupling reaction. After switching to the trifluoromethyl-substituted compound, reaction yields improved by over 20%. This is not an isolated story. Adding electron-withdrawing groups to heterocycles frequently provides greater control over reaction pathways. These modifications support cleaner results, simpler work-ups, and a broader toolkit for creative synthesis.

    Environmental and Safety Considerations

    There’s no escaping the reality that chemical innovation brings responsibility. As research pushes further, chemists can’t ignore safety and environmental impact. The presence of fluorinated groups, including trifluoromethyl, has prompted greater discussion in regulatory circles. My work with environmental compliance teams illuminated a nuanced truth: small changes in fluorine content can alter both the environmental persistence of intermediates and their safety profile.

    This compound should be handled with the respect reserved for any potent synthetic intermediate. Standard laboratory precautions apply, but users should remain vigilant. Absorption, inhalation, and accidental contact are all legitimate concerns if best practices are ignored. Responsible disposal and adherence to local regulations protect not only the individuals working on the bench but also broader communities. The legacy of chemical research will depend as much on our stewardship as on our discoveries.

    Supply Chain and Quality Assurance

    In my role evaluating supply chains, procurement of specialty chemicals like 2-Hydroxy-3-(trifluoromethyl)pyridine often brings up questions about sourcing, certification, and batch-to-batch consistency. Distributors who support R&D efforts understand that researchers rely on each shipment meeting the same stringent standards. We’ve all seen how a single inconsistent lot can derail synthesis plans and undermine hard-won progress.

    Rigorous supplier vetting pays off. Reputable suppliers are transparent about their quality assurance programs, providing analytical data that goes beyond the basics. I always encourage teams to demand not just certificates of analysis but also access to up-to-date impurity profiles and details on trace residuals. Reliable quality control allows researchers to focus on discovery instead of troubleshooting material issues.

    Pushing Boundaries: Case Studies and Real-World Impact

    Practical applications reveal why this molecule continues to draw attention. In pharmaceutical discovery settings, several teams have deployed 2-Hydroxy-3-(trifluoromethyl)pyridine as a precursor for kinase inhibitors and central nervous system (CNS) active compounds. The inclusion of the trifluoromethyl group often increases binding affinity at a targeted enzyme, moving the needle on efficacy metrics. This isn’t just theoretical—data from published patent literature and internal project reports back up these claims.

    Industrial chemistry teams developing specialty polymers use this building block to tune the hydrophobic balance of final materials. Adding a trifluoromethyl-substituted monomer adjusts water uptake and extends the lifespan of coatings, something especially important in high-wear or harsh-environment applications. These improvements translate into products that meet the evolving needs of today’s markets without unnecessary compromise.

    Outside the lab, agrochemical researchers have successfully incorporated this compound into novel pesticide scaffolds. The trifluoromethyl group’s role isn’t just about activity inside the plant or pest but also influences how the agent persists after application. By tackling regulatory demands and environmental safety at the molecular design stage, teams can bring solutions to market that stand up to scrutiny both in terms of safety and effectiveness.

    Challenges Facing Broader Implementation

    Every new chemical tool comes with hurdles. 2-Hydroxy-3-(trifluoromethyl)pyridine proves no exception. The increased utility gained from fluorine substitution can drive up synthesis costs and sharpen regulatory focus. Many labs face limited budgets and pressured timelines; this means any benefit delivered by the molecule must clearly outweigh its price and complexity.

    Sourcing remains a sticking point. Chemical manufacturers able to maintain consistent quality at reasonable cost will ultimately define how widely this tool spreads throughout industry. Strong relationships between buyers and suppliers—built on technical feedback and transparent communication—create the environment where innovation thrives. I’ve watched successful teams prioritize supplier partnerships every bit as carefully as they approach internal R&D strategy. These bonds secure access to high-quality chemicals and prepare supply chains for unexpected disruptions.

    Potential Solutions and Steps Forward

    For labs seeking to integrate 2-Hydroxy-3-(trifluoromethyl)pyridine, focusing on three areas consistently pays off: robust sourcing, open communication with suppliers, and ongoing training on safe handling and storage. By investing in employee training, organizations reduce the risk of accidental exposure or wasted material. Building a culture of ongoing education ensures staff remain current with the latest industry guidelines and safety standards.

    Collaboration across sectors offers another path forward. Cross-industry partnerships—bringing together expertise from pharmaceutical companies, academic institutions, and specialty chemical manufacturers—create opportunities to refine processes, enhance safety, and improve sustainability. Open sharing of case studies, technical data, and best practices advances the craft, making it easier for both large and small labs to benefit from specialized building blocks.

    Investing in analytical capability also proves worthwhile. Having access to advanced analytical equipment and expertise lets researchers quickly identify impurities, degradation products, or process variations that could derail a project. My experience has shown that a robust analytical foundation forms the root of every successful and safe chemical operation. Adequate investment in instrumentation and skilled analysts often shortens development timelines, getting products to market with fewer setbacks.

    The Importance of Transparency and Regulatory Engagement

    Modern markets demand accountability and data-driven transparency. Producers of 2-Hydroxy-3-(trifluoromethyl)pyridine who commit to open communication with regulators, customers, and peer organizations find themselves better positioned to anticipate challenges and manage risk. By supporting regulatory filings with rich datasets on purity, reactivity, and environmental fate, companies can smooth the path to approval and reinforce their status as trusted suppliers.

    Scientists and engineers working with this compound have found that engaging early with regulatory agencies, sharing detailed information on product stewardship, and collaborating on toxicological assessments create pathways for responsible deployment. This approach builds trust and lays a foundation for long-term commercial success, benefiting innovation as well as societal well-being.

    Final Thoughts: Chemical Innovation in Everyday Context

    Drawing on years spent navigating the worlds of research and production, it’s impossible to ignore how incremental advances build the foundation for transformative change. 2-Hydroxy-3-(trifluoromethyl)pyridine stands as a testament to the practical benefits gained through molecular fine-tuning. What may seem like minor tweaks ripple outward, shaping the pace of discovery and the safety of finished products.

    The value of this compound rests firmly in its unique combination of chemical properties, broad applicability, and the commitment of the people who work with it. Those selecting or recommending specialty chemicals face the daily challenge of balancing technical benefit, cost, safety, and supply. By leveraging robust supplier relationships, prioritizing transparency and ongoing education, and connecting across disciplines, labs and companies can put the promise of 2-Hydroxy-3-(trifluoromethyl)pyridine to work in building a future grounded in sound science, safety, and real-world impact.