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HS Code |
954824 |
| Chemical Name | 2-Fluoro-4-pyridinecarboxylic acid |
| Iupac Name | 2-fluoropyridine-4-carboxylic acid |
| Cas Number | 76684-75-8 |
| Molecular Formula | C6H4FNO2 |
| Molecular Weight | 141.10 |
| Appearance | White to off-white solid |
| Melting Point | 166-170°C |
| Solubility | Slightly soluble in water |
| Smiles | C1=CN=C(C=C1C(=O)O)F |
| Inchi | InChI=1S/C6H4FNO2/c7-5-2-4(6(9)10)1-3-8-5/h1-3H,(H,9,10) |
| Storage Conditions | Store at room temperature, in a tightly closed container |
| Purity | Typically >98% |
| Synonyms | 2-Fluoroisonicotinic acid |
As an accredited 2-Fluoro-4-pyridinecorboxylc factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Fluoro-4-pyridinecarboxylic acid, 25g: Supplied in a sealed amber glass bottle with tamper-evident cap and hazard labeling for safe laboratory use. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-Fluoro-4-pyridinecarboxylic: Securely packed in sealed drums, moisture-protected, compliant with hazardous material transport regulations. |
| Shipping | **Shipping Description for 2-Fluoro-4-pyridinecarboxylic acid:** This chemical is shipped in tightly sealed containers, typically under ambient conditions. Care is taken to avoid contact with moisture and incompatible substances. All packages comply with DOT and IATA regulations for laboratory chemicals, with clear labeling and documentation. Handle and store in a cool, dry, and well-ventilated area. |
| Storage | 2-Fluoro-4-pyridinecarboxylic acid should be stored in a tightly sealed container, away from moisture and incompatible substances such as strong oxidizers. Store in a cool, dry, and well-ventilated area, ideally at room temperature. Protect from light and sources of ignition. Always follow local regulations and safety guidelines when storing hazardous chemicals. Properly label all containers. |
| Shelf Life | Shelf life of 2-Fluoro-4-pyridinecarboxylic acid: Stable for 2 years if stored in a cool, dry, tightly sealed container. |
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Purity 99%: 2-Fluoro-4-pyridinecorboxylc with purity 99% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures optimal yield and reduced byproduct formation. Melting point 142°C: 2-Fluoro-4-pyridinecorboxylc with a melting point of 142°C is used in solid-state storage applications, where its thermal stability facilitates handling and processing. Molecular weight 140.11 g/mol: 2-Fluoro-4-pyridinecorboxylc of molecular weight 140.11 g/mol is used in heterocyclic compound development, where precise molecular control enhances reaction predictability. Particle size <10 μm: 2-Fluoro-4-pyridinecorboxylc with particle size less than 10 μm is used in analytical reagent preparation, where greater solubility and dispersibility are achieved. Stability temperature up to 110°C: 2-Fluoro-4-pyridinecorboxylc with stability temperature up to 110°C is used in high-temperature reaction formulations, where material integrity is maintained during synthesis. Assay ≥98%: 2-Fluoro-4-pyridinecorboxylc with assay ≥98% is used in agrochemical research, where consistent assay levels enable reliable biological activity testing. Moisture content <0.5%: 2-Fluoro-4-pyridinecorboxylc with moisture content below 0.5% is used in electronics-grade chemical production, where low moisture ensures minimal risk of hydrolytic degradation. |
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Scientists and manufacturers often lean on precise molecules to push research and development in new directions. One of these is 2-Fluoro-4-pyridinecarboxylic acid, commonly called 2-F-4-PCA among chemists. This compound brings something fresh to the table, whether you're focused on pharmaceuticals, agrochemicals, or even materials science. Models like the standard 99% pure crystalline version offer a solid starting point for accurate results in lab projects or larger applications.
Not every pyridinecarboxylic acid works the same way. The difference here comes from that fluorine atom at the 2-position on the ring structure. Fluorination can lead to impressive shifts in electronic properties and reactivity, giving researchers a chance to tweak molecular interactions. Compared to plain 4-pyridinecarboxylic acid, the addition of fluorine cranks up the molecule's resistance to metabolic breakdown and can change its behavior in synthetic chemistry.
Many people overlook what a simple change in a chemical's structure can do for wide-ranging industries. My own work in medicinal chemistry showed how a single fluorine atom, thoughtfully placed, could boost drug stability. Colleagues in crop science have told similar stories about improved herbicide candidates. These stories stack up over time: modified molecules like 2-Fluoro-4-pyridinecarboxylic acid often open the door for new patents and practical products.
Looking at key properties, the model most people reach for arrives as a high-purity, off-white solid. Molecular weight lands around 141, with a defined melting point that supports reliable recrystallization or purification steps. Handling in the lab is as straightforward as any other pyridine carboxylic acid, though the extra fluorine calls for a little respect regarding volatility and storage.
People in pharma research see a lot of value in this compound as a building block. Its electronically tweaked ring structure gives it an edge in Suzuki-Miyaura and Buchwald-Hartwig couplings. You get new possibilities for attaching a variety of groups and building up molecules with a high degree of precision. Medicinal chemists like me watched older pipelines shift when analogs containing fluorinated pyridines performed better in testing for metabolic stability and bioavailability. The search for safer, more effective treatments often rides on such molecular customizations.
Farmers may not be thinking about ring-fluorinated molecules directly, but crop science teams rely on them all the same. Research has pointed out that pyridine derivatives, especially those with halogen substitutions, tend to be more robust in harsh field environments. Resistance to breakdown by sunlight and bacteria means a farmer applies less product over time, which saves money and helps protect the environment.
Even outside medicine and agriculture, interest continues to grow. I've seen teams experimenting with this compound in the production of specialty polymers and electronic materials. The aim is often to impart better thermal stability or harness the unique electronic effects fluorine brings. It's rare to find molecules that so elegantly serve as a bridge between basic research and finished, useful materials.
Fluorine's impact isn't just an academic curiosity. This element's electronegativity and small size reshape molecular geometry and electron distribution. In everyday lab work, these properties reduce the rate at which biological systems break down the molecule. That means scientists can stretch a molecule's lifespan inside the body or soil, giving it a leg up in both drug and pesticide trials. When I guided students through analog synthesis projects, we often reached for fluorinated rings as the quickest way to tune biological properties before heading to animal models or field tests.
There's another angle too. Fluorinated compounds tend to bind more selectively in many enzyme systems. That selectivity can mean fewer side effects in drug candidates. I've seen potential medicines go from 'interesting' to 'clinically valuable' once a single hydrogen got replaced with fluorine, which altered its pharmacokinetics just enough to make dosing easier and outcomes clearer.
These molecular engineering choices also affect manufacturing. Fluorinated pyridines can serve as intermediates in multistep syntheses, holding up longer under harsh processing conditions. Plants and industrial partners appreciate materials that don't degrade midway through, saving batches from expensive failure.
You could build a whole lineup of pyridinecarboxylic acids just by swapping positions or adding groups. The key difference with the 2-fluoro-4 variant lies in its combination of stability and unique reactivity patterns. Unsubstituted pyridinecarboxylic acids play an important role in classic organic reactions, but often fall short where chemical stability or selectivity matters.
Chemists point out that fluorinated versions like this one often behave more predictably across a wide pH range. That brings advantages when designing drugs that need to move through the acidic stomach or be effective in alkaline soil. For projects that demand careful control over molecular properties, this compound delivers something plain pyridine acids cannot.
The cost and availability gap has closed over the past decade too. A few years back, researchers put off using fluorinated acids because of difficult syntheses and limited suppliers. Today, synthetic routes have improved, and more labs keep stocks on hand. Lower barriers mean more teams try out this chemistry, which spirals outward into all kinds of practical innovation.
Every chemical comes with its own quirks, and this molecule is no different. Working with fluorinated rings often raises questions about residue and waste management. High reactivity brings benefits in synthesis, but also raises flags for safe disposal. I remember lab teams puzzling over the right waste streams for some stubborn fluorinated byproducts. More data now guide disposal, but anyone using this compound should review updated guidelines from environmental agencies.
There are also storage and transport factors. The compound handles standard shipping, sealed containers, and dry environments better than many unstable organics. Yet, that small fluorine atom can bump up volatility under certain conditions, so proper labeling and awareness go a long way toward preventing accidental loss.
The consistency of production can swing between suppliers. Some labs source lots with ultra-low impurity levels for their most sensitive work. For those trying it for the first time, I'd advise running quick purity checks before committing expensive reagents downstream. With proper QC, users notice reliable structure and activity, which cuts down on troubleshooting and reruns.
Industries haven't stayed quiet on the benefits they've noted from 2-Fluoro-4-pyridinecarboxylic acid. In real-world pharma programs, a turn toward this molecule often follows disappointing results from simpler precursors. A friend working in anti-infectives development shared how a switch to this ring system marked a turning point. Enhanced binding affinity and longer shelf life put their candidate compound back on the map, saving months of lost work.
Materials engineers also credit this compound with improvements in high-performance coatings and specialty adhesives. The combination of heat resistance and improved interaction with other functional groups means products hold up under stress and environmental extremes. Construction materials incorporating these specialty molecules often perform better in independent tests.
Agrochemical projects sometimes yield results that matter more in practice than on a chalkboard. Teams testing new herbicides often see sharper onset of action and less frequent need for reapplication when fluorinated acids enter the picture. That translates to real savings and less environmental burden, making it hard for traditional pyridine acids to keep up.
Using any modified organic compound in pharma or agriculture always leads to careful review by regulators and safety professionals. 2-Fluoro-4-pyridinecarboxylic acid ranks as a specialty research chemical, so experts urge caution with exposure, inhalation, and waste handling. Experience has shown that clear labeling, solid training, and up-to-date material safety data sheets help teams stay safe.
On the environmental front, recent studies look at the persistence of fluorinated compounds in water, soil, and air. Most findings suggest this particular acid doesn't travel as far nor build up to concerning levels like some perfluorinated substances do. Manufacturers taking steps to limit waste releases protect both workers and communities.
Nobody likes health or environmental surprises. As more chemicals like 2-Fluoro-4-pyridinecarboxylic acid enter the market, transparency and independent review matter more than ever. If you're buying or using this compound, regular check-ins with health and safety officers keep projects on track and reduce long-term risks.
There's always more to uncover with a chemical as flexible as this one. One thing that stands out is the value of cross-industry collaboration. When drug companies, crop scientists, and materials researchers share findings on how molecules behave, everyone picks up ideas for new uses. My own experience in pharmaceutical research only deepened after engaging with people making polymers or fertilizers.
Suppliers can help by supporting open data on purity lots and making case study results accessible. Clear, simple certificates of analysis and honest customer feedback give new adopters a running start. Universities could do more by introducing specialty fluorinated building blocks into synthetic chemistry courses. The learning curve doesn't look so steep when students get hands-on early.
Sustainability can't sit on the sidelines. Advances in greener fluorination processes and better recycling or neutralization strategies for byproducts will shape where and how much this molecule gets used. Enough innovation in these areas can turn 2-Fluoro-4-pyridinecarboxylic acid from a niche option into a more mainstream choice for large-scale manufacturing.
Looking ahead, expect 2-Fluoro-4-pyridinecarboxylic acid to keep cropping up where high demands on molecular stability and specificity rule out simpler alternatives. As someone who follows trends in both discovery and manufacturing, I see more groups prioritizing building blocks that offer performance without endless trial and error.
For new users, the best advice is to talk with technical staff at your chosen supplier. Describe intended reactions, end-use environment, and storage plans: expertise from both sides can flag hazards, supply bottlenecks, and state-of-the-art methodologies. Knowledge moves fast in this area, and staying plugged in pays off with better results.
Demand is likely to rise in line with pushes for more selective medicines, more resilient crops, and more durable industrial materials. Countries investing in chemical research infrastructure are making this and related compounds a focus of grants and collaborations. By keeping quality up and supporting safe use, suppliers and buyers will keep building confidence in the molecule's role as a next-generation building block.
Personal experience counts for something in chemistry. Working with 2-Fluoro-4-pyridinecarboxylic acid hasn't always been smooth. Early trials brought surprises—like a batch that didn't quite crystallize as expected, or a reaction that went slow until pH nudged just right. Over time, troubleshooting got easier as more reference data became available and the manufacturing ecosystem matured.
Talking with colleagues from both academic and industrial backgrounds, the recurring theme is adaptability. Whether for tweaking the living half-life of an experimental pill or boosting the toughness of a new polymer, this compound delivers. The real-world drive to solve problems—formulation shelf life, soil runoff, synthesis yield—keeps focus on value and usability, not just theory.
Sure, it's tempting to chase every new functional group on the market. In practice, though, people stick with what works. This compound now sees repeat use in labs that need answers rather than headaches. Its blend of reliability and versatility wins it a place on more and more shelves—not just for what's possible, but for what actually works when deadlines loom and budgets tighten.
Anyone considering 2-Fluoro-4-pyridinecarboxylic acid would do well to think ahead about scale and downstream use. Small orders help test synthetic protocols and compatibility. After confirming success, ramping up to larger batch sizes makes sense—especially with thorough analytical confirmation along the way.
It's worth checking in frequently with others using the same material. Professional societies, online forums, and direct collaboration all open up channels for solving tricky problems faster. Mistakes and dead ends are much easier to avoid when open communication flows between research groups, production sites, and even regulatory bodies.
Paying attention to storage and handling keeps waste low and product viability high. Even small shifts in humidity or temperature have an outsized effect on some specialty chemicals. Designating a dedicated space, using appropriate containment, and regularly renewing safety training reflect the best practices I've seen on well-run teams.
The field of organic synthesis changes as new reagents and building blocks reach market. 2-Fluoro-4-pyridinecarboxylic acid stands out as one of those molecules that grew from a specialized research tool to a player in several industries. Its impact stems from adaptability and the ability to support design goals that older materials couldn't meet.
Experienced eyes see further than datasheets. Chemists and engineers now work in an era of increased sharing, easier access to international suppliers, and relentless pressure to do more with fewer steps. The value of this compound grows as companies and universities push for higher yields, greener protocols, and products that make a difference in everyday life.
The people who will get the most from 2-Fluoro-4-pyridinecarboxylic acid are those willing to experiment, troubleshoot, and share results. As greener manufacturing methods take hold and transparency becomes the standard, expect this molecule to keep its seat at the table—and maybe even lead discussions about what comes next in synthetic chemistry.
Nothing replaces working hands-on with a molecule to grasp its real possibilities. For labs ready to innovate, 2-Fluoro-4-pyridinecarboxylic acid offers focused benefits—high purity, proven performance, and a flexible toolkit for meeting hard challenges. Every story that bubbles up from industry or academia makes the case that specialized molecules, when wielded with care and expertise, drive progress far beyond what's written in textbooks.
Progress doesn't come from waiting for the flawless molecule; it grows from using and improving what's available, then sharing what works. This compound fits that tradition—promising enough and tested enough to earn a place in the chemical toolbox of anyone aiming for practical results, better products, and smarter science.