Pyridine, 3-fluoro-, 1-oxide

    • Product Name: Pyridine, 3-fluoro-, 1-oxide
    • Chemical Name (IUPAC): 3-fluoropyridine 1-oxide
    • CAS No.: 696-41-3
    • Chemical Formula: C5H4FNO
    • Form/Physical State: Liquid
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    Specifications

    HS Code

    544637

    Chemical Name Pyridine, 3-fluoro-, 1-oxide
    Molecular Formula C5H4FNO
    Molecular Weight 113.09 g/mol
    Cas Number 54727-64-5
    Appearance Colorless to pale yellow liquid
    Boiling Point 222 °C (estimated)
    Density 1.28 g/cm³ (estimated)
    Solubility In Water Moderate
    Smiles C1=CC(=CN=C1F)[O-]
    Inchi InChI=1S/C5H4FNO/c6-4-1-2-7(8)3-5-4/h1-3,8H
    Pubchem Cid 24597193
    Synonyms 3-Fluoropyridine N-oxide

    As an accredited Pyridine, 3-fluoro-, 1-oxide 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 Pyridine, 3-fluoro-, 1-oxide; sealed with screw cap and tamper-evident label.
    Container Loading (20′ FCL) **Container Loading (20′ FCL)**: 16 metric tons (MT) of Pyridine, 3-fluoro-, 1-oxide packed in 160 drums per 20-foot container.
    Shipping **Shipping Description for Pyridine, 3-fluoro-, 1-oxide:** Pyridine, 3-fluoro-, 1-oxide should be shipped in tightly sealed containers, protected from light and moisture. It must be clearly labeled, with appropriate hazard classifications provided. Transport should comply with all relevant national and international regulations for chemicals, ensuring upright positioning and prevention of leakage or spills during transit.
    Storage **Storage for Pyridine, 3-fluoro-, 1-oxide:** Store in a tightly closed container in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Protect from direct sunlight and moisture. Ensure proper labeling, and avoid storage near sources of ignition. Use corrosion-resistant shelves and secondary containment to prevent leaks or spills. Always follow institutional and regulatory guidelines for hazardous chemicals.
    Shelf Life Shelf life of Pyridine, 3-fluoro-, 1-oxide: Stable for 2 years when stored tightly sealed, away from moisture, light, and heat.
    Application of Pyridine, 3-fluoro-, 1-oxide

    Purity 98%: Pyridine, 3-fluoro-, 1-oxide with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and reduced byproduct formation.

    Melting Point 72°C: Pyridine, 3-fluoro-, 1-oxide with a melting point of 72°C is used in solid-state material research, where it provides thermal stability during advanced material fabrication.

    Molecular Weight 112.09 g/mol: Pyridine, 3-fluoro-, 1-oxide at 112.09 g/mol is used in analytical calibration standards, where it enables precise quantification in chromatography methods.

    Particle Size <50 μm: Pyridine, 3-fluoro-, 1-oxide with particle size below 50 μm is used in fine chemical formulations, where it allows for homogeneous mixing and consistent product performance.

    Stability Temperature 120°C: Pyridine, 3-fluoro-, 1-oxide with a stability temperature of 120°C is used in high-temperature synthesis reactions, where it maintains structural integrity and prevents decomposition.

    Water Solubility 4.5 g/L: Pyridine, 3-fluoro-, 1-oxide with water solubility of 4.5 g/L is used in aqueous-phase catalysis, where it enhances catalyst dispersion and reaction efficiency.

    Viscosity Grade Low: Pyridine, 3-fluoro-, 1-oxide with low viscosity grade is used in solution-based coating applications, where it ensures uniform film formation and smooth surface finish.

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    Certification & Compliance
    More Introduction

    Pyridine, 3-fluoro-, 1-oxide: A Versatile Compound Making a Difference in Modern Chemistry

    Kicking Off with the Essentials

    In a world where chemistry shapes nearly every corner of our daily life—be it through the medicines we take, the electronics we touch, or even the paints on our walls—the little tweaks in molecules tell big stories. Pyridine, 3-fluoro-, 1-oxide represents one of those small changes that lead to a range of new options for research and industrial work. This compound breaks away from the crowd by offering a unique twist on the familiar pyridine ring, swapping in a fluoro group at the third position and an oxygen atom bound to the nitrogen, forming the N-oxide. That may sound like a narrow detail, but it's exactly this detail that widens its reach.

    Unpacking What Sets This Molecule Apart

    Having spent years around research labs and briefed by hundreds of hours studying compound behavior, you come to appreciate how even a single fluorine can set a molecule down an entirely new path. With 3-fluoro-pyridine, 1-oxide, you wind up with a structure that's more than just its backbone. Fluorine’s strong pull on electrons changes the landscape of chemical reactions. That N-oxide group—for chemical folks—means the molecule doesn’t just play well with others, it brings new ideas to the party. Think about how one extra chair at Thanksgiving rearranges the whole table. This chemical invites new reactions, makes some easier, blocks others, and often leads to more stable intermediates that don't show up with the plainer pyridine compounds.

    Real-World Impact: More Than Just a Chemical Name

    Sometimes we get caught up listing specifications and data sheets, but the true value of a substance like Pyridine, 3-fluoro-, 1-oxide comes out in the work it lets us do. This compound contributes to the labs working on the next wave of pharmaceuticals. The fluoro group can tip the scales for drug molecules: it can slow down how quickly the body tears a drug apart, and sometimes it helps a drug reach its target more efficiently. This isn't just theoretical—fluorinated compounds fill up entire shelves in the pharmaceutical world. The N-oxide group adds an extra layer, letting researchers dig into reactions that would stumble without it. The 1-oxide opens up routes for building complex molecules, some of which land in clinical trials or make industrial synthesis more reliable.

    Why the Details Matter in Drug Discovery and Beyond

    Digging deeper, you start seeing patterns. Medicinal chemists often look for ways to fine-tune their candidates, and adding fluorine is one of their favorite moves. They find that incorporating a fluorine atom—especially at strategic positions like the third spot on a pyridine ring—boosts the oral absorption and metabolic stability of proposed drugs. This isn’t just a coincidence; whole review papers dig into how it happens. What’s special about Pyridine, 3-fluoro-, 1-oxide is that it carries both the fluorine and N-oxide features in one neat package; this merges the properties of electron-rich and electron-deficient systems. You get an unusual combination of solubility and reactivity, which acts as an all-access pass for certain transformations in organic synthesis.

    Chemistry out of the Textbooks and into the Factory

    Pyridine derivatives show up everywhere, but adding a fluoro group and oxidizing to the N-oxide turns the old familiar into something with teeth. Take agrochemical production as just one example. Formulators try to maximize effectiveness and minimize side effects for environments. 3-fluoro-pyridine N-oxides present new routes for making herbicides that break down at the right speed—not too quickly to be ineffective, not so slowly that they stick around forever. Factories want compounds that are straightforward to handle, stable enough to store, yet reactive when called upon. This one ticks those boxes with the added bonus of avoiding some of the volatility that haunts non-oxidized pyridines.

    Working in Materials Science

    It’s easy to think about chemistry only in terms of pills and sprays, but the reach of subtle molecules like Pyridine, 3-fluoro-, 1-oxide extends to material tech as well. Conjugated systems—those long chains of alternating bonds—lie at the heart of OLED displays and solar panels. Tweaking the electron flow in those chains changes color, efficiency, and longevity. Pyridine’s N-oxide versions have a long-standing reputation for modulating the behaviors of those systems. Add fluorine to the mix, and you not only lower the energy needed to run reactions—think gentler, greener processes—but you sometimes get brighter fluorescence or longer device lifespans.

    Stepping Outside the Lab: Transportation, Environment, and Everyday Safety

    Experience teaches us that regulation and risk assessment matter as much as discovery. Not all chemicals are easy to move or store safely. Pyridine, 3-fluoro-, 1-oxide, compared to traditional pyridines, typically shows lower volatility. You’re less likely to breathe it in accidentally, and the odds of explosive vapor hazards go down. For logistics and safety planning groups—folks with real skin in the game—this change can mean easier compliance and less expense on special equipment. Chemical waste disposal also becomes a little simpler when you work with less volatile compounds, translating to greener, safer handling all around. These are real-world gains, not just checkboxes.

    The Business Angle: Efficiency and Practicality

    Working in procurement for a research organization, you learn that sourcing chemical building blocks isn’t just about the sticker price. Shipping, storage, delays due to hazardous tags, and disposal burdens all nudge the bottom line. Pyridine, 3-fluoro-, 1-oxide stands out by balancing reactivity for synthesis without tipping over into “too dangerous to touch.” For firms exploring new treatments or materials, this translates into faster prototyping. Instead of wrestling with regulatory red tape at every step, they can spend their energy pushing research forward. The transformability of this N-oxide derivative fits nicely with automated synthesis platforms, which have swept through pharma and high-throughput testing labs in the last decade.

    Comparing Apples to Apples: What Makes This Compound Unique?

    If you take plain pyridine as the baseline, then look toward the world of pyridine derivatives, the list grows quickly: chlorinated, methylated, and, of course, fluorinated. Even among the fluorinated, position matters. Putting fluorine on the third ring carbon changes not only how the molecule behaves chemically, but also how living organisms metabolize it. Now, drop in that N-oxide. N-oxides show less basicity, shifting the pH window where the compound works best. Certain transformations that stall with unoxidized pyridine blaze ahead with the N-oxide version. In practical terms, this lets chemists build up larger, more complex molecules in fewer steps—a game-changer for pilot plant schedules and R&D timelines.

    Beyond the Bottle: Facing Challenges and Gaining Benefits

    Of course, every advance comes with its own headaches. The introduction of a fluoro group can sometimes mean tougher purification steps. Fluorinated byproducts don’t always break down cleanly, which requires careful waste management. Yet, from the view of most synthetic chemists, the benefits outweigh these hurdles. Fluorine brings metabolic stability and improved drug-like properties. The N-oxide makes certain oxidation-state-sensitive synthesis possible. I've watched teams speed up their work simply because an earlier synthetic step, which typically drags on for hours, wraps up in minutes with the right combination of substituents. That kind of improvement means fewer late nights for crowded lab teams and faster progress for companies aiming to bring something new to market.

    Spotlight on Research: Expanding Chemical Space

    Exploring new molecules is a lot like sailing into unknown waters. You set out from well-mapped ports, but real innovation happens at the far edges. Compounds like Pyridine, 3-fluoro-, 1-oxide keep open doors that older, well-worn chemicals have closed. For example, fluorinated heterocycles—a broad group that includes this molecule—show promise as enzyme inhibitors or diagnostic imaging agents. Publications from peer-reviewed sources demonstrate that adding both fluorine and an N-oxide increases the odds that researchers will uncover new activity. That’s not an empty hope, but one backed by detailed case studies and structure-activity relationship reports.

    Access and Availability: Meeting Real-World Need

    Supply chain disruptions over the past years have shown just how intertwined global chemistry is. Sometimes, demand for a specialized compound spikes when a promising new drug or material emerges. Lab managers want to know they can get their hands on a molecule like Pyridine, 3-fluoro-, 1-oxide without jumping through endless hoops. Thankfully, as the value of fluorinated N-oxides becomes clearer, more sources have begun offering reliable, reproducible batches. The key concern now becomes maintaining purity and traceability, which matters more now than ever thanks to tighter regulatory environments and quality-control expectations in pharmaceutical and industrial research.

    Solutions for Maximizing Impact: Smarter Chemistry Practices

    With any specialty compound, the risk of bottlenecking progress through inefficiency looms large. Research groups focused on green chemistry have looked for ways to streamline both use and waste management of fluorinated N-oxides. Recent literature suggests methods for cleaner synthesis, reducing the risk of side reactions and limiting environmental hazards. Solid-phase extractions, tuned reaction conditions, and catalyst innovations have all chipped in. It pays to keep up with the literature, because new protocols often leapfrog old ones in a matter of months, especially as new catalysts for selective oxidations and fluorinations become more mainstream.

    Blazing a Trail for the Next Generation of Molecules

    One factor that often escapes notice is the role that research compounds play in inspiring the next wave of science. Younger chemists and material scientists come up in an era flooded with new options. They learn to think outside the basic toolkit, thanks in no small part to access to specialty compounds like 3-fluoro-pyridine N-oxide. Universities and startups find themselves at the crossroads of invention and application. The growth of custom synthesis services, fueled by increased curiosity about what new molecular combinations can achieve, holds out the promise of whole new classes of dyes, sensors, or catalysts.

    Supporting the Ecosystem: Training and Workforce Development

    A key part of advancing chemistry beyond the sample vial involves making technical knowledge accessible. Even as automated systems take on more synthesis and analysis, the insights gained from working first-hand with unique compounds don’t fade. I've seen that in my own experience, where troubleshooting a tricky oxidation or monitoring a sensitive fluorination has sharpened my respect for precision and detail. For graduate students or early-career chemists, hands-on practice with N-oxides and fluorinated substrates extends textbook concepts into the messier reality of the lab. This expertise makes the industry stronger, bridging gaps between academic innovation and industrial application.

    Bringing Transparency and Trust to Chemical Sourcing

    The rapid adoption of specialty molecules has also raised the bar for transparency. Now more than ever, both small research teams and major corporations demand full access to detailed characterization—spectroscopy, melting points, and impurity profiles—not merely to satisfy curiosity but to safeguard results and reproducibility. This scrutiny creates a marketplace where suppliers prioritize validated sourcing and traceability of Pyridine, 3-fluoro-, 1-oxide batches. This transparency helps keep surprises and discrepancies at bay, essential as more fields—like biochemistry and materials science—lean harder on specialty reagents.

    In the Trenches: Facing Regulatory and Environmental Hurdles

    Each new variant of a familiar structure must pass scrutiny from environmental health and safety bodies. Pyridine, 3-fluoro-, 1-oxide, with its reduced volatility and unique metabolic fate, opens new doorways for compliance relative to older pyridine derivatives. As legislation tightens around persistent organic pollutants and toxic intermediates, having molecules that degrade or transform more predictably matters. Industries that shift toward these safer, more easily managed compounds stand a better chance of passing audits and winning trust from environmental stewards.

    Encouraging Cross-Disciplinary Research

    The story of 3-fluoro-pyridine N-oxide wouldn’t resonate as much without acknowledging how it paves the way for collaboration. This isn’t chemistry for chemistry’s sake. Molecular biologists, drug designers, and process engineers find common ground in the flexible properties of such compounds. Conversations once limited to siloed groups now take place across company walls and academic borders. Diverse teams use what this molecule offers to probe deeper questions, whether about enzyme function, light emission, or energy storage.

    Tapping Collective Knowledge for Future Progress

    Staying grounded in community wisdom helps avoid pitfalls. The push for open data—where research findings on new fluorinated N-oxides join repositories—has already sped up progress across disciplines. Being able to scan published spectra, reaction trials, and decomposition profiles means lab teams spend less time reinventing the wheel and more time expanding the possibilities. This openness embodies the best of scientific practice. It keeps research honest and repeatable and supports discovery that stands up in the real world.

    Reflections from the Front Lines

    Drawing from years at the crossroads of research and industry, it's clear that Pyridine, 3-fluoro-, 1-oxide is more than a line item on an order sheet. The molecule stands as a tool for focused discovery, a bridge for collaboration, and a signpost for safer, more sustainable chemistry. Every innovation that stems from subtle changes at the molecular level ripples outward—better drugs, brighter materials, safer processes. The lessons learned from both successes and setbacks shape how compounds like this one are used going forward.

    Looking Toward Tomorrow: A Living Story

    The landscape of chemical research never stays still. Each compound, each new method, carries with it the weight of experience—my own included—and the promise of what might come next. Pyridine, 3-fluoro-, 1-oxide signals how scientists rethink familiar building blocks to open new doors. From drug design to material innovation, environmental compliance to education, the molecule gives form to how small details can drive big change. By focusing not just on what a compound is, but what it makes possible, we keep chemistry vibrant and responsive to real-world needs.