|
HS Code |
418039 |
| Chemicalname | 2,3,6-Trifluoropyridine |
| Casnumber | 39546-32-2 |
| Molecularformula | C5H2F3N |
| Molecularweight | 149.07 |
| Appearance | Colorless liquid |
| Boilingpoint | 115-117°C |
| Meltingpoint | -32°C |
| Density | 1.376 g/cm3 |
| Refractiveindex | 1.446 |
| Flashpoint | 31°C |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥98% |
| Smiles | C1=CN=C(C(=C1F)F)F |
| Inchikey | ZKCPXKDWNWZBJE-UHFFFAOYSA-N |
As an accredited 2,3,6-Trifluoropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g amber glass bottle with tamper-evident cap, clear labeling: "2,3,6-Trifluoropyridine, 98%," hazard pictograms and manufacturer details. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2,3,6-Trifluoropyridine: 120 drums, 200 kg/drum, total net weight 24,000 kg. |
| Shipping | 2,3,6-Trifluoropyridine is typically shipped as a liquid in sealed, chemical-resistant containers. It should be stored and transported in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances. Proper labeling, adherence to relevant safety regulations, and use of protective packaging are required to ensure safe delivery. |
| Storage | 2,3,6-Trifluoropyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances like strong oxidizers. Store under inert gas if possible to prevent moisture and air exposure. Protect from direct sunlight and keep away from heat. Ensure that appropriate safety measures and labeling are in place. |
| Shelf Life | 2,3,6-Trifluoropyridine is stable under recommended storage conditions; shelf life is typically 2–3 years in tightly sealed containers. |
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Purity 99%: 2,3,6-Trifluoropyridine with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high-yield production of target compounds. Molecular Weight 119.06 g/mol: 2,3,6-Trifluoropyridine of molecular weight 119.06 g/mol is used in agrochemical research, where it enables precise molecular modifications in pesticide design. Melting Point -16°C: 2,3,6-Trifluoropyridine with a melting point of -16°C is used in low-temperature organic reactions, where it provides enhanced reaction control under sub-zero conditions. Boiling Point 119–120°C: 2,3,6-Trifluoropyridine with a boiling point of 119–120°C is used in chemical vapor deposition processes, where it allows efficient vapor-phase transport. High Chemical Stability: 2,3,6-Trifluoropyridine demonstrating high chemical stability is used in fluorinated material production, where it minimizes side-product formation and degradation. Low Water Content ≤0.5%: 2,3,6-Trifluoropyridine with low water content ≤0.5% is used in moisture-sensitive catalytic reactions, where it prevents hydrolysis and maintains catalyst activity. Analytical Grade: 2,3,6-Trifluoropyridine of analytical grade is used in laboratory scale synthesis validation, where it ensures reproducible and accurate experimental results. Refractive Index n20/D 1.431: 2,3,6-Trifluoropyridine with refractive index n20/D 1.431 is used in optical sensor material development, where it imparts tailored optical properties for sensing applications. Stability Up To 150°C: 2,3,6-Trifluoropyridine stable up to 150°C is used in thermally demanding coupling reactions, where it maintains compound integrity during high-temperature processing. |
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Every field has a few building blocks that quietly give shape to complex innovations. In synthetic chemistry, 2,3,6-Trifluoropyridine (CAS: 395-81-3) often pops up as one of those under-the-radar heroes. Whenever I walk through a research lab, I notice chemists reaching for specific reagents to tweak a molecule just right. 2,3,6-Trifluoropyridine stands out thanks to its blend of utility, purity, and reactivity. You don't see the name on everyday household products, but its impact runs through pharmaceuticals, agricultural research, and fine chemicals all the same.
What sets this pyridine derivative apart comes down to its structure: three fluorine atoms at the 2, 3, and 6 positions of the pyridine ring. Fluorine isn't just added for fun. In modern chemical design, adding fluorine tunes the electronic environment of a molecule in significant ways. The result tends to be improved metabolic stability, altered binding selectivity, or better bioavailability—essential benchmarks for drug and crop protection research. In my own bench experience, I’ve noticed how a single fluorination step, especially with a reagent like this, can mean the difference between a promising lead and a formula that fails halfway through animal testing.
Sometimes, the discussion around chemical intermediates boils down to practical details. Researchers and process chemists don’t want surprises. They want consistency, a controlled reactivity profile, and minimal unwanted byproducts. That’s what you typically get from high-purity 2,3,6-Trifluoropyridine batches. I’ve handled a fair share of off-target reactions due to poorly characterized starting materials, and it creates frustration while costing precious days. This product, produced through selective halogenation and refined for low residuals, typically offers purity above 98%. This can mean fewer headaches during downstream functionalization steps, less chromatography, and more time spent exploring promising molecules rather than troubleshooting.
2,3,6-Trifluoropyridine also holds a key advantage when scaling up reactions. In the pharmaceutical pipeline, repeatability is non-negotiable. The compound’s predictable reactivity with nucleophiles and organometallics unlocks a whole suite of cross-coupling reactions and nucleophilic substitutions. Medicinal chemists appreciate that trifluorinated aromatics can mimic natural metabolites or help a drug resist unwanted metabolic breakdown. I’ve seen colleagues use this intermediate as a springboard for designing everything from kinase inhibitors to pesticide scaffolds because it nudges structural activity into useful territory.
There are plenty of pyridine derivatives out there, but 2,3,6-Trifluoropyridine is a unique beast. Switch the fluorine positions or decrease the degree of fluorination, and you lose its specific reactivity. Compared to its cousin 2,6-difluoropyridine, for example, the additional fluorine at the 3-position tweaks the ring’s electron density and impacts how nucleophiles attack the molecule. Based on my own stints in medicinal chemistry, these minute differences translate into selective binding with proteins, changes in solubility, and, ultimately, in-vivo performance.
Industrial buyers and researchers should also note the difference in volatility and handling requirements compared to lower fluorinated analogs. The extra fluorines not only confer greater thermal stability but also limit competing side reactions under basic or acidic conditions. This stability provides a practical edge, especially for those running robust batch syntheses. Whenever I talk with scale-up chemists in agrochemical firms, they flag how this compound’s resilience saves headaches otherwise common in pilot-scale plants: less chance of decomposition means fewer re-runs and reduced downstream purification costs.
A conversation about any fine chemical in today’s research landscape demands a serious look at safety, traceability, and environmental impact. Trifluorinated compounds often raise questions since their persistence in the environment means they should be treated with respect. Chemical producers who are transparent about process impurities, trace metal content, and waste management protocols earn lasting trust. From first-hand experience, knowing your source provides a certificate of analysis with rigorous impurity data and a documented supply chain lowers anxiety, especially for research with regulatory requirements.
In my own projects, I’ve seen how poorly tracked reagents ripple through a workflow, causing regulatory headaches right before a patent filing or clinical submission. Responsible sourcing, ingredient traceability, and adhering to international standards for hazardous materials should never be treated as box-ticking exercises. That’s why researchers, myself included, prioritize suppliers who test and document every step, from raw material sourcing through final QA checks. Failing to do so jeopardizes not just research outcomes but public health, considering the persistence and sometimes toxicity of certain fluorinated molecules.
People outside of chemistry labs may never read a label with “2,3,6-Trifluoropyridine,” but they see the ripple effects everywhere. It’s an intermediate in the synthesis of specialty pharmaceuticals—especially kinase inhibitors—where precise targeting of disease proteins matters. More recently, it’s played a role in developing new insecticides that strike a delicate balance: potent against pests, less hazardous for the environment. These applications cross over with public health, food safety, and sustainability goals, raising the stakes for every step in the compound’s journey from raw material to finished product.
From years in the industry, I see how small tweaks in chemical structure—often made possible through compounds like this—can produce major shifts in drug dosing, half-life, and off-target interactions. The deceptively simple decision to incorporate a trifluorinated ring can lead to medications that require fewer pills per day, or crop solutions that degrade less in sunlight. These advances save money, reduce waste, and genuinely change outcomes for patients and growers alike.
Nothing in chemical manufacturing comes free of challenges. Synthesizing 2,3,6-Trifluoropyridine with consistent quality relies on access to specialized halogenation techniques—and not every lab is equipped for that. Fluorine chemistry sometimes means investing in corrosion-resistant reactors and strict ventilation, since hydrogen fluoride can form as a byproduct. From time to time, I’ve watched even well-funded pilot plants run into bottlenecks as they switch from lab-scale flasks to industrial reactors, especially when scaling up steps involving multiple fluorinations. This isn’t just about cost; a facility’s ability to handle aggressive reagents shapes the feasibility of entire R&D programs.
Even after production, storing and transporting a specialty pyridine derivative with high fluorine content asks for solid planning. Moisture or UV exposure can slowly degrade sensitive intermediates, and nobody wants spoilage before a critical round of development. Real-world logistics often force compromises, but keeping a close eye on container selection and inventory rotation cuts down on unexpected losses.
Green chemistry is no longer optional. Environmental standards around fluorinated chemicals have grown tighter, in part because their stability turns into persistence in soil and water. It’s not enough to chase high yields. Factories and research houses alike shift toward improved recovery of solvents, tighter waste management, and in-process recycling. I’ve seen the biggest leaps when companies invest in closed-loop systems, which reduce emissions and capture byproducts before they escape into the wider environment.
As a result, reliable producers of 2,3,6-Trifluoropyridine don’t just sell molecules—they become partners in compliance. Audit trails, batch records, and environmental impact assessments no longer float in the background. Young researchers coming into the field now expect clear communication of regulatory status and REACH registration for imported intermediates, especially when moving past academic settings into commercial drug discovery. These trends tilt the playing field in favor of companies that keep both product quality and stewardship front and center.
Rapid growth in pharmaceutical and agricultural research raised the demand for trifluorinated pyridines. The urge to push boundaries tempting, but history teaches the value of double-checking long-term effects. I've met scientists wrestling with the dual responsibility of bringing new medicines to market while avoiding tomorrow’s environmental problems. With potent chemical innovations come ethical questions: Will a new crop protection agent bioaccumulate? Can a breakthrough cancer drug avoid creating harmful byproducts in wastewater streams? These questions reflect my own frustrations and hopes as research expands its reach.
New analytical tools help a lot. Advances in mass spectrometry and environmental monitoring make it easier to trace even minuscule amounts of these compounds from rivers to food chains. Labs are not just troubleshooting synthetic routes—they’re taking part in the broader effort to keep industrial progress in sync with planetary boundaries. Building 2,3,6-Trifluoropyridine into a project now means weighing immediate gains against how future generations might be affected.
Coming up through the ranks as a chemist, I learned the importance of traceable, high-purity intermediates. There’s a world of difference between running screens with a batch contaminated by byproducts and using a reagent that pushes reactions toward predictability. Modern suppliers leverage advanced purification and analysis, routinely providing HPLC and NMR data along with shipments. These details may seem technical on the surface, but in drug discovery, they set in motion cascades of new patents and, ultimately, better clinical outcomes.
Quality doesn’t end with purity—homogeneity, stability, and reliable supply matter just as much. It’s one thing to succeed in a small pilot test; it’s another to deliver thousands of liters without a hiccup. During my time in process development, I saw the difference tested quality protocols make. They save millions in avoided recalls, lawsuits, and regulatory delays. A supply chain grounded in facts, transparency, and open dialogue with end-users turns a simple bottle of 2,3,6-Trifluoropyridine into a strategic asset.
Research and industry can’t afford to stand still. Better manufacturing practices—borrowing tools from green chemistry, investing in recycling systems, and sticking to the highest analytical standards—set the stage for broader acceptance and fewer roadblocks from regulators. Sourcing decisions grounded in full disclosure, traceability, and a clear ethical stance help safeguard both laboratory results and long-term public trust.
Collaboration makes the biggest difference. Sharing best practices, opening lines of communication between suppliers and research labs, and staying attuned to evolving guidelines on fluorinated chemical handling together create a healthier, safer ecosystem. From first-year graduate students to seasoned supply chain managers, everyone involved in the journey of 2,3,6-Trifluoropyridine shoulder some responsibility—and enjoy the opportunity to shape the future of applied chemistry. Balancing innovation with caution isn’t just a buzzword; it’s why the best companies and research groups continue to lead with integrity.
2,3,6-Trifluoropyridine sets chemists and product developers up for smarter, safer breakthroughs. Its selective reactivity, reliable production, and pivotal role in both pharmaceuticals and crop science make it a touchstone for anyone seeking to combine performance and responsibility. As research grows more complex, the choices made about sourcing, quality, and stewardship will ripple outwards, touching fields far beyond the laboratory bench. The journey from this molecule to tomorrow’s innovation shows just how much thoughtful groundwork shapes the value of every discovery.