|
HS Code |
856017 |
| Chemical Name | 4-Amino-2-fluoropyridine |
| Molecular Formula | C5H5FN2 |
| Molecular Weight | 112.10 |
| Cas Number | 367-21-5 |
| Appearance | Off-white to light yellow solid |
| Melting Point | 70-74°C |
| Boiling Point | 242°C at 760 mmHg |
| Density | 1.28 g/cm3 |
| Solubility In Water | Slightly soluble |
| Flash Point | 99°C |
| Purity | Typically ≥98% |
| Pka | 5.0 (amino group) |
| Refractive Index | 1.570 |
| Smiles | c1cc(N)cc(F)n1 |
| Inchi | InChI=1S/C5H5FN2/c6-4-2-5(7)1-3-8-4/h1-3H,7H2 |
As an accredited 4-Amino-2-fluoropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g 4-Amino-2-fluoropyridine is supplied in a sealed amber glass bottle with tamper-evident cap and safety labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 4-Amino-2-fluoropyridine: Securely packed, moisture-protected, labeled drums or bags, ensuring safe transport and regulatory compliance. |
| Shipping | 4-Amino-2-fluoropyridine is shipped in tightly sealed containers, protected from moisture and direct sunlight. It should be handled as a hazardous chemical, following all relevant regulations. Packaging must prevent leaks or spills, and appropriate hazard labels should be used. Shipping documentation includes safety information and complies with chemical transportation standards. |
| Storage | 4-Amino-2-fluoropyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents and acids. Protect it from moisture and direct sunlight. Label the container clearly, and avoid exposure to heat or open flames. Use appropriate safety equipment when handling and storing this chemical. |
| Shelf Life | 4-Amino-2-fluoropyridine should be stored tightly sealed, protected from light and moisture; shelf life is typically 2–3 years under proper conditions. |
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Purity 98%: 4-Amino-2-fluoropyridine with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures efficient product yield and minimized impurities. Melting point 52-56°C: 4-Amino-2-fluoropyridine with a melting point of 52-56°C is used in fine chemical manufacturing, where precise melting ensures reliable process scalability. Stability temperature up to 120°C: 4-Amino-2-fluoropyridine stable up to 120°C is used in heterocyclic compound preparation, where thermal stability enables sustained reaction conditions. Particle size <50 µm: 4-Amino-2-fluoropyridine with particle size less than 50 µm is used in catalyst formulation, where fine particle distribution enhances catalytic surface area. Water content <0.2%: 4-Amino-2-fluoropyridine with water content below 0.2% is used in active pharmaceutical ingredient (API) formulation, where low moisture content improves product stability and shelf-life. Molecular weight 112.10 g/mol: 4-Amino-2-fluoropyridine with a molecular weight of 112.10 g/mol is used in organic synthesis, where defined molecular mass facilitates accurate stoichiometric calculations. Trace metal content <10 ppm: 4-Amino-2-fluoropyridine with trace metal content below 10 ppm is used in electronics material synthesis, where low metal contamination reduces risk of electronic failure. Residue on ignition <0.1%: 4-Amino-2-fluoropyridine with residue on ignition below 0.1% is used in specialty coatings, where minimal inorganic residue ensures high film purity. |
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Walking through a chemical laboratory and spotting a small bottle labeled “4-Amino-2-fluoropyridine” reminds me that some of the world’s biggest innovations start from unassuming origins. This compound, with its unique structure—a fluorine atom at the second position and an amino group at the fourth on the pyridine ring—holds its own in research and manufacturing alike. Some might look at the name and think it’s just another case of letters and numbers, but chemists know this is a workhorse molecule offering possibilities that set it apart from standard pyridines and related building blocks.
Products like this aren’t just about making something new for the sake of it. Researchers and developers turn to 4-Amino-2-fluoropyridine because of how the substitution pattern changes its behavior during synthesis. Having both an amine and a fluorine on the ring, spaced apart, lets scientists tweak reactivity in ways that can open doors to new strategies. Many consider fluorine a ‘game-changer’ — it brings stability, tunes electronics, and even helps bioactive molecules stick around in the body. An amine in the mix brings its own set of opportunities, from classic coupling reactions and catalytic transformations to new pathways for drug discovery.
Chemical suppliers see demand growing whenever pharmaceutical development heats up, because this compound fits so many custom synthesis pipelines. Medicinal chemists rely on these functional handles to assemble molecules one step at a time. In my own lab days, I watched folks reach for fluorinated pyridines every time they wanted to fine-tune binding properties or create a new analog. You quickly learn that not all substitution patterns are equal. Small changes to the scaffold turn into big changes in biological activity.
When purchasing a material like 4-Amino-2-fluoropyridine, chemists don’t stop at the catalog page. They want to see what form the product arrives in, the purity, batch reproducibility, and sometimes fine details like particle size or specific trace contaminants. Most commercial batches of this compound ship as an off-white to tan solid, in crystalline or powder form, depending on how it’s isolated and purified. Chemists often check for purity above 98% by HPLC and NMR, with water and residual solvent levels well below pharmaceutically acceptable limits. Handling is straightforward compared to more sensitive fluorinated materials—no need for special storage, just keep it sealed away from excess moisture.
Choosing this product depends on getting it in the form most useful for the intended reaction, and those tiny details matter. An ultra-pure batch supports sensitive catalysts and tricky coupling steps. On the other hand, for large-scale early synthesis, a technical-grade sample delivers enough quality without breaking the bank. In-house experience shows that a single well-made batch can move a medicinal chemistry project forward for months, especially if the key steps go as planned.
Some substances sit unused on the shelf, arriving with promise but not fitting real needs. 4-Amino-2-fluoropyridine avoids that fate. I’ve watched scientists grab it for Suzuki couplings, nucleophilic aromatic substitution, or straightforward amidations—all reactions that connect the small pyridine ring to larger, often bioactive frameworks. The amino group brings reactivity; it couples with acids, forms imines, or supports diazotization. The fluorine at position 2 doesn’t just act as a spectator either. It adjusts electron density across the ring and sometimes even directs the next substitution step by making the ortho and para positions more or less reactive.
In medicinal chemistry, incorporating fluorine can make a world of difference. A small fluorine atom often blocks metabolic degradation in the body, which means a promising drug candidate stays active longer. With the pyridine structure serving as a common fragment in drug design—think about many commercial antivirals, antifungals, and antihistamines—it only makes sense to look for new versions that improve performance or open the door to patents. That’s the way innovation moves forward: incremental improvements based on tools chemists trust.
Outside pharmaceuticals, demand comes from agrochemical research and specialty material science. Fluorinated pyridines sometimes show up in herbicide or pesticide projects, where the aim is more precise molecular recognition and environmental stability. Even if you’re not working on blockbusters, the nuanced balance between the amino and fluoro groups provides an entry point to explore reactivity and tailor-make molecules for specific targets.
Practical use means being able to scale up reactions, avoid tough purification steps, and manage hazards. Some specialty intermediates create headaches—unstable, moisture sensitive, or just plain hard to handle. Most commercial batches of 4-Amino-2-fluoropyridine bypass these issues, shipping as a stable solid that stores for extended periods and withstands the rigors of scale-up. That’s an underrated quality in research; fewer headaches, more progress.
Years in the lab taught me to recognize subtle differences among similar-sounding reagents. One might assume replacing a hydrogen for an amino or a fluorine makes little difference, but real-world chemistry tells a different story. Pyridine itself serves as a backbone for solvents, ligands, and even food additives, but doesn’t offer the same versatility for molecular elaboration. Switch in a fluorine atom, and you gain more control over acidity, basicity, and oxidative stability. Add an amino group, and coupling partners multiply.
What sets 4-Amino-2-fluoropyridine apart is the placement of both the amino and fluoro on a single aromatic ring, and how they work together. Chemically, these groups influence each other more than one might expect. Many research groups favor this molecule in SAR (structure-activity relationship) studies, where small adjustments drive big results on the biological end. It holds unique reactivity compared with 2-fluoropyridine or 4-aminopyridine alone. If you swap the positions, the chemistry shifts. Move the amino group to another location, and the compound handles differently during coupling. Choose a derivative without the fluorine, and you lose the chance to push stability further or control metabolic liability in biological screens.
Standard 2-fluoropyridine still matters for direct substitutions, but as soon as a synthetic plan calls for more diversity or complexity, 4-Amino-2-fluoropyridine takes the spotlight. Sometimes, the subtle interplay between substituents even nudges the molecule to favor one tautomer over another, which affects how it reacts and what products are possible. These details sound obscure unless you’ve run enough experiments to watch the changes unfold up close.
Researchers who aim to replace older aromatic building blocks with new ones for IP protection, enhanced safety, or improved pharmacokinetics usually start screening variants like this before moving on to more complex and costly intermediates. It’s a practical call: gain the power of a tried-and-true pyridine core, but with targeted electronics and reactivity.
Sometimes people outside of chemistry ask whether tweaking small molecular features really matters beyond research programs. From experience, watching project after project rise or fall based on the properties of a single intermediate reveals just how central a compound like 4-Amino-2-fluoropyridine can be. Time and again, teams in drug discovery, agriculture, and even dye chemistry turn to this molecule because it streamlines synthesis and creates a path for new discoveries. The ability to introduce both electron-withdrawing and electron-donating groups in controlled sequence unlocks new routes to targets previously considered off-limits.
Many projects focus on more sustainable syntheses, minimizing waste and hazardous reagents. Using 4-Amino-2-fluoropyridine, chemists often replace older, less selective routes with direct couplings or one-pot reactions, saving time and cutting down on extra purification. As regulatory systems evolve and demand greener chemistry, access to these specialty intermediates—especially those that enable cleaner transformations—becomes more than just a nice-to-have.
On the commercial side, companies keep an eye on supply chain stability. Reliable sources of specialty building blocks act as the glue that holds development timelines together. Global experience has shown how disruptions—even for relatively minor compounds—can slow or halt multi-million dollar projects. Suppliers that keep quality up, batches consistent, and prices competitive end up helping a lot more than just a chemist working at a fume hood; they keep pharmaceutical pipelines robust and innovation moving.
For all its potential, accessing high-quality 4-Amino-2-fluoropyridine hasn’t always kept pace with demand. The synthesis itself can be tricky. Making it from scratch in a small lab can tie up valuable time and expose workers to hazardous reagents and waste. That’s why most teams prefer to let specialized suppliers handle the manufacturing and purification. Regulatory compliance and full documentation add peace of mind, but the best suppliers go further, providing certificates of analysis that detail impurities, batch traceability, and even storage recommendations.
Where safety and environmental exposure are concerned, most routine practice keeps hands covered, the work in a ventilated hood, and solid waste collected for proper disposal. Yet the low volatility and modest toxicity profile compared to some other fluorinated intermediates reduce headaches. Training helps, but choosing intermediates that pose fewer risks matters at every stage, especially in pilot plants or scale-up scenarios.
Looking forward, scalable processes using milder reagents, greener solvents, and cleaner workups can boost both safety and cost-effectiveness. New catalytic methods, including cross-coupling using transition metals under milder conditions, offer hope for broader accessibility and fewer side-products. If chemists can buy exactly what they need, in the right grade, and in volumes that match current demand, projects move from idea to outcome much faster.
The most exciting part for many is how fast applications keep evolving. Novelty in drug research often leans on new building blocks, and compounds like 4-Amino-2-fluoropyridine play a key role in getting ahead of resistance, improving selectivity, or addressing neglected indications. As researchers react to new global challenges, ranging from superbugs to climate-driven pest outbreaks, specialty intermediates become building blocks for breakthrough solutions rather than just routine steps.
Even in material science, where function often comes from smart molecular design, the careful arrangement of substituents on a pyridine ring lets engineers create new scaffolds for sensors, light-harvesting, and energy storage. As techniques in organic electronics advance, there’s every reason to think that building blocks offering complementary reactivity find new life in unexpected fields. The mix of robust manufacturing, straightforward handling, and familiar chemistry means fewer barriers as science pivots toward real-world outcomes.
Educators also benefit. Teaching advanced organic synthesis or the subtleties of structure-property relationships means giving students a hands-on look at what refinements can mean. Lab classes working with fluorinated and amino-substituted aromatics demystify complex reaction sequences, making the next generation ready for industry challenges.
As labs and companies push to move faster and more efficiently, bottlenecks from unreliable sourcing or inconsistent quality quickly rank among the most frustrating setbacks. Teams that count on a steady supply of specialty building blocks value clear communication and quality records almost as much as the chemistry itself. More partnerships between manufacturers, suppliers, and end-users help build feedback that keeps improvements on track.
Long-term, supporting research into scalable, cleaner synthetic routes—especially those that generate less hazardous waste—creates both industry and environmental benefits. Investment in this kind of process innovation means more labs, from startup to established players, have fair access to the same tools. In practice, tweaking an old synthetic route or switching from a hazardous precursor to a safer one means less downtime, lower costs, and more sustainable science. The experience of working behind the bench—and seeing these problems firsthand—drives home how much difference thoughtful product development and robust support make.
Online platforms that allow rapid ordering, transparent stock updates, and quick access to documentation close the remaining gaps. Building digital bridges, along with flexible packaging that meets both milligram-scale and multi-kilo needs, makes modern chemistry nimble. The best suppliers listen to the changing needs, update their offerings, and deliver customer support that’s based on more than just shipping boxes.
From dozens of projects, the same advice holds true: don’t just choose a building block based on a catalog description. Look for real-world feedback, both from your own bench and from published literature, to see how products respond under different conditions. In many cases, subtle batch differences—moisture, color, texture—can flag issues that impact sensitive reactions. Over-the-counter isn’t always over-the-hurdle in terms of performance.
A small amount of upfront diligence pays off through the project’s lifetime. Checking certificates, reviewing stability data, and running early small-scale tests catch problems before they cross into more expensive territory. In company labs, we always set aside a portion of each batch for verification and contingency planning. Resourcefulness saves time, and for a molecule with as much potential as this, the return on investment is clear.
If you’re designing a drug discovery campaign, lining up a robust supply of 4-Amino-2-fluoropyridine means one less unknown when new analogs show promise. For new researchers, experimenting with this intermediate provides hands-on insight into the significance of electronic effects and regiochemistry. What seems routine from the outside rarely is in practice.
The world of specialty chemicals thrives on knowledge sharing. Seasoned chemists know which suppliers stand by their products, which materials over-perform, and which process tweaks make the most difference. Trust grows with every successful reaction, every shipment that matches its label, and every consultation that solves a problem rather than just logging a sale.
Sitting at the crossroads of classic chemistry and cutting-edge applications, 4-Amino-2-fluoropyridine represents an example of what’s possible when industry and scientific communities collaborate. Its story is about more than one molecule—it reflects how incremental changes can have outsize impact in practice. Small as it is, the pairing of fluorine and amine groups on a pyridine ring keeps research moving, manufacturing reliable, and innovation steady.
I have watched those who dare to run the extra experiment, who swap in a new scaffold on a risky bet, often finding breakthroughs hiding in plain sight. What gets missed in technical specifications and routine protocols is the long chain of work, trouble, and teamwork that turns a specialty chemical into a launchpad for discovery.
Every project brings a chance to do a bit better—at the bench, in the supply chain, or at the policy table. With the right tools, reliability, and new process knowledge, compounds like 4-Amino-2-fluoropyridine provide real value far beyond the bottle. They help make tomorrow’s big ideas a practical reality, not just a line in a proposal.