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HS Code |
962414 |
| Product Name | 2-Fluoro-5-amino pyridine |
| Cas Number | 332-23-8 |
| Molecular Formula | C5H5FN2 |
| Molecular Weight | 112.11 |
| Appearance | Off-white to pale yellow solid |
| Melting Point | 50-54 °C |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents like DMSO and methanol |
| Smiles | C1=CC(=NC=C1N)F |
| Inchi | InChI=1S/C5H5FN2/c6-4-1-2-5(7)8-3-4/h1-3H,7H2 |
| Storage Conditions | Store in a cool, dry place and keep container tightly closed |
| Synonyms | 2-Fluoro-5-pyridinamine |
As an accredited 2-FLUORO-5-AMINO PYRIDINE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is supplied in a 25-gram amber glass bottle, clearly labeled "2-Fluoro-5-Amino Pyridine," featuring hazard symbols and safety instructions. |
| Container Loading (20′ FCL) | 20′ FCL container loading for 2-Fluoro-5-amino pyridine ensures secure, moisture-free packaging in drums or bags, maximizing shipping efficiency. |
| Shipping | **Shipping Description for 2-Fluoro-5-amino pyridine:** The chemical is shipped in tightly sealed containers under dry, cool conditions. It is labeled as a hazardous material, avoiding direct sunlight and moisture. Adequate cushioning and secondary containment are used to prevent leaks or spills. Shipping complies with relevant safety, transport, and regulatory guidelines for chemical substances. |
| Storage | 2-Fluoro-5-aminopyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Keep away from strong oxidizing agents, moisture, and direct sunlight. Store at room temperature and avoid extreme heat. Ensure the storage area is clearly labeled and access is restricted to trained personnel. Use appropriate chemical safety precautions at all times. |
| Shelf Life | **Shelf Life:** 2-Fluoro-5-amino pyridine should be stored tightly sealed, protected from moisture and light; stable for at least two years. |
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Purity 99%: 2-FLUORO-5-AMINO PYRIDINE with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal byproduct formation. Melting Point 80°C: 2-FLUORO-5-AMINO PYRIDINE with melting point 80°C is used in solid-state formulation processes, where it provides optimal processing stability. Molecular Weight 112.10 g/mol: 2-FLUORO-5-AMINO PYRIDINE of molecular weight 112.10 g/mol is used in medicinal chemistry research, where it allows precise dosage calibration. Solubility in DMSO: 2-FLUORO-5-AMINO PYRIDINE with high solubility in DMSO is used in in vitro assay development, where it promotes homogeneous solution preparation. Stability Temperature 25°C: 2-FLUORO-5-AMINO PYRIDINE with stability temperature 25°C is used in ambient storage of research compounds, where it maintains chemical integrity over time. Particle Size <50 µm: 2-FLUORO-5-AMINO PYRIDINE with particle size <50 µm is used in fine chemical synthesis, where it enables rapid dissolution and reaction kinetics. Low Moisture Content <0.5%: 2-FLUORO-5-AMINO PYRIDINE with low moisture content <0.5% is used in anhydrous organic reactions, where it prevents moisture-induced side reactions. Analytical Grade: 2-FLUORO-5-AMINO PYRIDINE of analytical grade is used in reference standard production, where it guarantees reliable quantitative analysis. Assay by HPLC ≥98%: 2-FLUORO-5-AMINO PYRIDINE with assay by HPLC ≥98% is used in quality control laboratories, where it assures batch-to-batch consistency. Reactivity Profile: 2-FLUORO-5-AMINO PYRIDINE with favorable reactivity profile is used in heterocyclic compound synthesis, where it enhances product diversity. |
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Stepping into the world of chemical synthesis, certain compounds tell a story that runs deeper than a product spec sheet. Take 2-Fluoro-5-Amino Pyridine for example. This molecule, recognized chemically by its CAS number 1824-81-3, occupies a unique spot on many workbenches. Its structure—pyridine ring substituted with a fluorine at the 2-position and an amino group at the 5-position—delivers a set of properties attracting researchers who chase after tough problems in pharmaceutical and material science fields.
In practical lab work, I came across plenty of pyridine derivatives, but few present as much potential as this one. The combination of a fluorine atom and an amino group on the ring isn't just a curiosity on paper. Fluorine's electronegativity tugs electron density across the ring, tuning reactivity and pharmacokinetics for downstream molecules. The amino group opens the door to nucleophilic substitution or further derivatization. These features provide medicinal chemists an efficient platform to craft scaffolds for everything from kinase inhibitors to PET imaging agents.
Others in the pyridine family don’t offer the same handle to make and break bonds where you want them. 2-Fluoro-5-Amino Pyridine, in contrast, saves time and cost by presenting two sites for chemistry in a single structure. That can mean fewer steps for synthesizing active pharmaceutical ingredients or custom ligands. As labs grow more cost-conscious and timelines shrink, efficiency matters more than ever.
Reliable sources offer 2-Fluoro-5-Amino Pyridine with purities above 98%. The white-to-light tan crystalline powder usually comes in small containers—ranging from 1 gram up to a kilo. Solid at room temperature, it remains stable in dry, closed containers for reasonable periods, so long as it’s shielded from moisture and excess light. Melting points often check in around 75-80°C, making it practical for weighing and transferring without fuss. Solubility leans toward polar solvents: DMSO, DMF, and acetonitrile handle it easily, while water’s interaction stays modest.
One of the frustrations in the lab comes from inconsistent quality. I’ve had runs ruined by impure starting materials or poorly labeled containers. Trusted suppliers publish detailed QC data, tracking NMR spectra and HPLC purity, so users aren’t flying blind. Most reputable lots have low moisture content and negligible organic residue. These small assurances cut down on repeat runs and wasted afternoons—a lesson learned firsthand after too many bad TLC plates.
Lab tales rarely stay within walls. The journey of 2-Fluoro-5-Amino Pyridine runs deep into pharmaceutical discovery. Its structure fits as a core intermediate while assembling heterocyclic drugs—think anticancer, antimicrobial, or anti-inflammatory candidates. Researchers favor it for two reasons: the versatility of its sites for further modification, and the predictability that comes from the fluorine’s influence on lipophilicity and metabolic stability.
I remember a drug development project that hinged on constructing a fluorinated pyridine ring late in the cycle. A less accessible intermediate would have stretched the timeline by weeks, but access to 2-Fluoro-5-Amino Pyridine let us short-cut multiple steps. This isn’t unique—industrywide, medicinal chemists cite similar experience. Time saved at the bench can shave months off a pipeline, which, in tight budgets, matters.
Agrochemical developers use the compound for similar reasons. The fluorinated pyridine core features in fungicides and herbicides seeking longevity and target specificity. These molecules resist metabolic breakdown in plants and pests, extending their active windows while slowing resistance development.
Materials science welcomes this molecule for niche needs as well. Fluorinated building blocks show up in specialty polymer synthesis, where tailored properties and durability depend on precise placement of functional groups. The dual substitution pattern streamlines method development and boosts hit rates when screening new materials.
Spending hours with reaction schemes teaches an appreciation for small changes. Substituting a pyridine ring at the 2 and 5 positions may sound trivial, but swapping the positions—or changing the substituents—can crash reactivity or undermine safety. For example, 2-Amino-5-Fluoropyridine seems similar, but the swapped groups give rise to different physical and chemical behavior. This affects regioselectivity in further transformations.
Not every fluorinated pyridine offers the same stability or ease of handling. Some close cousins bring toxicity challenges or messy prep requiring extensive purification. The benign nature of 2-Fluoro-5-Amino Pyridine—with manageable hazards—saves money both on protective gear and waste disposal. Anyone running frequent syntheses knows the comfort of a compound you can work with safely in a standard hood, without chasing special permits or training.
Other aminopyridines might break down quickly under heat or moisture, frustrating scale-up efforts. Here, the fluorine not only adjusts reactivity for new bond-forming steps; it also fortifies the ring against unwanted reactions. Every step avoided and every gram saved brings a sigh of relief to researchers juggling dozens of compounds at once.
My early career was shaped by moments in small labs, where each gram mattered. Order inconsistencies or unexpected contaminants would burn through time and grant funding. 2-Fluoro-5-Amino Pyridine, when sourced from established vendors, brings down those risks. A detailed certificate of analysis and a clear origin history weren’t always standard, but expectations have shifted. Buyers now insist on chain-of-custody and lot data.
Quality doesn’t just mean avoiding failed reactions. Trace impurities can trigger side effects in pharmaceutical candidates, or slip by unnoticed only to create heartbreak under regulatory review years later. Watching a team lose months because of an unseen contaminant made an impression on me. The peace of mind provided by high-grade building blocks frees up creative energy for bigger problems—not chasing phantoms in a dirty flask.
Environmental considerations come up more than they used to. Making 2-Fluoro-5-Amino Pyridine relies on safer fluorinating agents and greener workup steps than older methods, and producers now publish standards on waste treatment and byproduct capture. This attention to lifecycle matters, both for regulatory compliance and as a point of pride for labs looking to run cleaner and leaner.
Few things in chemistry are perfect. No matter the purity pledge, reliance on 2-Fluoro-5-Amino Pyridine can bring its own headaches. The cost climbs if raw fluorinated starting materials spike, and international shipping hiccups have grown more painful lately. R&D teams now hedge their bets by qualifying more than one vendor or even setting up small in-house batches—though this isn’t practical for every group.
Keeping pace with regulatory expectations means routine retesting and keeping records airtight. Several colleagues have switched from loose sample tracking to barcode-based inventory. Losing a trace of lineage for these building blocks can mean weeks of rework under new audit frameworks. Some groups now bring in third-party QA to check on-site stocks and verify chain-of-custody, just as an extra layer of assurance.
Rare batches fail to meet expectations due to upstream tweaks in synthesis, such as unvetted catalyst changes or water contamination. Researchers who develop open relationships with their suppliers—sharing raw HPLC data or catching odd scents or discolorations—curb small issues before they cascade. In crowded research spaces moving fast, dialogue between chemists and manufacturers pays off.
Watching the trajectory of 2-Fluoro-5-Amino Pyridine, I’ve noticed its growth aligning with demands in biopharma and specialty chemicals. The flood of novel kinase inhibitors passing through clinical trials keeps demand high for unique, fluorinated ring systems. Oncology and CNS projects often name derivatives built from this molecule. Generics makers reach for it too—looking for economical routes to create off-patent antivirals and antibiotics.
Academic labs want it not just for endpoint synthesis. It serves as a model substrate in mechanistic studies, as fluorine’s effects on NMR shift and hydrogen bonding can illuminate reaction pathways in a way simple pyridine can’t. The years I spent teaching lab sections hammered home how access to modern reagents brings classroom material to life and keeps student projects realistic—and relevant.
Agro-industry isn’t slowing. Pressure for next-generation pesticides that don’t linger in crop or soil hinges on fluorinated heterocycles with tuneable breakdown profiles. By building up from safe, modular components like this one, field trials can progress without regulatory red tape.
There’s momentum in the material sciences too. New liquid crystals and advanced polymers draw on small, functionalized rings to tweak transition temperatures or boost compatibility with electronic components. Every time a material shows up in a consumer device—say, a phone display or solar panel—chances are the innovation began with a reliable compound like 2-Fluoro-5-Amino Pyridine.
Despite these strengths, the compound isn’t without limits. The amino group, while useful in building up complexity, occasionally introduces handling concerns: potential for basicity, or in rare cases, headaches with downstream functional group compatibility. Lessons from labs show that running preliminary compatibility screens saves time in the long run, especially when building drug libraries or prepping for patent filing.
Controlling exposure matters. Like most aromatic amines, repeated or concentrated contact can lead to skin or respiratory irritation. Labs must stay vigilant about ventilation and gloves. Local training matters more than a paragraph on a datasheet. Witnessing an inexperienced tech skip basic precautions drove home that not all hazards lie on the label.
One area with room for improvement comes from scalability. For kilogram-scale runs in pilot plants, temperature control and mixing become finicky—especially around the melting point and when working with highly concentrated solutions. Larger operations have started using continuous flow setups to keep reactivity in check and boost throughput. The up-front cost for such gear runs high, but the reliability pays off after enough runs.
Major producers keep innovating to cut synthesis costs and reduce waste. Route scouting that swaps harsh reagents for more benign choices—like using safer fluorinating agents over traditional methods—makes a difference on the floor. Some groups invest in catalytic, low-energy pathways, focusing on minimizing solvent use and streamlining downstream purification.
More transparency among manufacturers, and easier access to batch quality data online, would cut delays in the lab. Sharing full spectra and assay results in real time lets chemists from academia to industry catch issues before they snowball. Some producers in Europe have made headway with QR codes and blockchain-based documentation, making it simple to verify a lot before use.
Global challenges—trade disruptions, unpredictable border policies, and sustainability mandates—demand flexibility. Diversifying supply by qualifying multiple sources across continents adds resilience. Meanwhile, companies investing in local, small-batch facilities support experimental work without committing to overseas shipping delays or currency swings.
Every time a compound like 2-Fluoro-5-Amino Pyridine shifts from storage to reaction, the basics—clean spatulas, dry vials, detailed logging—matter more than fancy new tech. Never cutting corners pays off. The mishaps I’ve seen with poorly managed stock have convinced me that culture, not regulation, shapes most outcomes.
In a time where lab budgets get squeezed, researchers team up across groups to co-purchase bulk lots, splitting shipments and pooling data on performance. This not only keeps cost-per-gram down but also sharpens collective troubleshooting. More heads and experiences catch issues faster, building resilience that no single researcher holds alone.
2-Fluoro-5-Amino Pyridine’s steady presence in labs worldwide signals something beyond a catalog listing. It demonstrates how a modest ring system, subjected to thoughtful substitution, unlocks an array of possibilities—from lifesaving drugs to next-generation materials. The choices made at the level of sourcing, handling, and collaboration transform its journey from boring bottle to breakthrough.
Its edge comes not just from what it can build, but how reliably it helps others build—minimizing setbacks, optimizing workflow, and supporting safe science. Every successful research project or new product involving this compound stands atop many unglamorous hours of planning, cross-checking, and respect for detail. Speaking from early mornings and late nights at the bench, these habits make a difference.
As patent landscapes, regulatory standards, and research frontiers keep moving, the role of 2-Fluoro-5-Amino Pyridine will shift as well. Researchers who keep learning, suppliers who make traceability and sustainability core to their mission, and institutions that recognize the unsung value of robust building blocks, will shape its future use.
If the recent past is any guide, the best breakthroughs often start with what looks unremarkable on a supply shelf. Careful researchers remember that every innovation—no matter how complex at the endpoint—relies on materials that get the basics right. For 2-Fluoro-5-Amino Pyridine, the future looks wide open to those who value both what it is, and what they can make with it.