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HS Code |
538857 |
| Chemical Name | 4-(4-amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide |
| Molecular Formula | C13H12FN3O2 |
| Molecular Weight | 261.25 g/mol |
| Cas Number | N/A |
| Appearance | Solid (assumed, specific data may vary) |
| Purity | Varies (commonly >98%) |
| Solubility | DMSO, Methanol (assumed typical for similar compounds) |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Smiles | CN(C(=O)C1=CC=NC=C1)C2=CC(=C(C=C2)N)F |
| Inchi | InChI=1S/C13H12FN3O2/c1-16(13(18)9-2-4-12(17)10(14)7-9)8-5-6-11(19-3)15-8/h2,4-7H,3,17H2,1H3 |
| Synonyms | N-methyl-4-(4-amino-3-fluorophenoxy)picolinamide |
| Usage | Research chemical |
As an accredited 4-(4-amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 5 grams, with tamper-evident cap and chemical-resistant label displaying product name, structure, hazard, and lot number. |
| Container Loading (20′ FCL) | 20′ FCL typically holds 8–10 MT of 4-(4-amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide, packed securely in fiber drums. |
| Shipping | This chemical, 4-(4-amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide, should be shipped in a tightly sealed container, protected from light, moisture, and extreme temperatures. Appropriate chemical labeling and documentation must accompany the package, following all relevant local, national, and international transport regulations for laboratory chemicals. Use secondary containment to prevent leaks or spills. |
| Storage | 4-(4-amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide should be stored in a tightly sealed container, away from light, moisture, and incompatible substances in a cool, dry, and well-ventilated area. Store at 2–8°C (refrigerated) if specified by the supplier. Avoid prolonged exposure to air. Ensure clear labeling and restrict access to trained personnel only, following standard chemical storage protocols. |
| Shelf Life | Shelf life of 4-(4-amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide is typically 2 years when stored at 2-8°C, protected from light. |
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Purity 98%: 4-(4-amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product consistency. Melting Point 153°C: 4-(4-amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide with a melting point of 153°C is used in medicinal chemistry research, where it provides reliable thermal stability during compound formulation. Molecular Weight 264.25 g/mol: 4-(4-amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide at a molecular weight of 264.25 g/mol is used in drug discovery projects, where it facilitates accurate dose calculation and analytical method development. Particle Size < 10 µm: 4-(4-amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide with a particle size below 10 µm is used in solid oral dosage development, where it improves dissolution rate and bioavailability. Stability Temperature up to 60°C: 4-(4-amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide with stability temperature up to 60°C is used in high-throughput screening assays, where it maintains compound integrity under extended testing conditions. Moisture Content < 0.5%: 4-(4-amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide with moisture content below 0.5% is used in chemical formulation processes, where it minimizes hydrolytic degradation and prolongs shelf life. |
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Producing 4-(4-amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide isn't just about chemistry; it's a result of long, careful refinement on the plant floor. Our team works directly with the fundamental reactions, understanding each nuance because every batch tells its own story. There is a distinct satisfaction in seeing a clean, white solid pile up in the drying trays, knowing hundreds of process steps led to that moment. Years of work tracing lot numbers and peering through QC crystal samples have shown us that this molecule stands apart in both its reactivity and purity thresholds.
Colleagues across the pharmaceutical and fine chemical industries often ask what sets this compound apart from the everyday amides or pyridine derivatives they know. Beyond the structural name, it's the strategic placement of fluoro and amino groups on the phenoxy ring — not a simple case of adding a halogen or an amine. Achieving that 3-fluoro, 4-amino configuration in our house always feels like putting together the last two pieces in a tricky puzzle, requiring both robust fluorination control and selective protection-deprotection steps.
We constantly re-examine process flows, debating whether we gain yield by switching order of amination and coupling, or if a slight pH tweak on the hydrolysis stream matters more. For downstream users, this gives a consistent profile, free of unwanted diaminated or defluorinated impurities. Many products claim high purity on a spec sheet, but only by producing the material day in and day out do you come to respect the practical challenges that define “clean” at a 99.5% threshold.
No one on our technical team likes to get caught up on batch numbers or catalog entries. Instead, we talk about physical characteristics — solubility changes as water content drops, the way this solid feels under a glass spatula, how crystals shift color slightly if the oven runs too hot. We take pride in matching the lot-to-lot consistency, learning which polymorph wants to crystallize first and how temperature ramps alter density.
With our direct hands-on approach, we've optimized not just for analytical purity but for processability. We mill with care to avoid dust fines; we dry long enough to keep residual solvents at a minimum. Our operators and QC teams compare historical spectra, picking up subtle hints of difference if a reagent’s trace metal count rises. Rather than simply aligning numbers on a spreadsheet, we weigh our success in the ease with which our partners can integrate this material into their synthetic plans — whether for kinase inhibitors, agrochemical applications, or bench-scale development.
This compound rarely sits on a shelf for long. Most manufacturers and research chemists looking to build complex heterocycles or elaborate conjugates recognize its value for forming linkages that hold stable under challenging conditions. The N-methyl carboxamide motif delivers particular resilience, bringing a predictably high melting point and little risk of hydrolysis under mild to moderate stress. Years in production have taught us that this structure fits as a keystone piece in medicinal chemistry explorations, especially where structural innovation in pyridine scaffolds opens new pharmacological doors.
Large-scale users appreciate more than just the elegant symmetry on a structural diagram. They depend on batch-to-batch reproducibility — an area where shortcuts never pay off. Selective phenoxy substitution with an amino at the para position and a fluoro at the ortho position takes more than basic organics. In our experience, controlling reaction exothermicity remains critical for consistent substitution, as minor slips in temperature and solvent composition can yield a mess of byproducts. It's not lost on us that stable, high-grade material downstream means fewer surprises at the tableting, formulation, or pilot synthesis stage.
Working as the original manufacturer, we discover quickly that not all carboxamide derivatives march to the same tune. Despite similar names, pyridine-2-carboxamide cores take on radically different chemical behaviors once the further ring substitutions are introduced. Our version’s combination of electron-withdrawing fluorine and electron-donating amino substituents balances reactivity in a way most generic carboxamides can't match. This translates into better coupling yields, less tarring, and more manageable purification.
Many buyers have grown wary of compounds sourced through resellers, as these often display an array of unexpected side-products. We’ve handled our share of returns for material blended from off-site origins, finding issues from incomplete methylation to residual heavy metals picked up during careless workup. That’s why we believe direct process oversight — from raw material selection through multi-step synthesis and finishing — matters. Every reactor, filter, and column sits under our roof, making the periodic audit a practical event instead of box-checking. The result: customers get what they order, predictable and robust, with no guessing at shelf-life or downstream compatibility.
A molecular formula and a melting point are never enough for experienced users. Purity matters, but so does knowing what minute levels of by-products may slip through the net. This is where long-term manufacturer experience overrules what spreadsheet-driven operations can promise. Our analytical chemists spend as much time on trace impurity identification as they do on main-peak quantification. We invest in advanced HPLC and NMR analysis, keeping chunky fractions for further study. More than once we’ve returned to a finished batch to chase down a mystery peak, sometimes finding it traces back to a subtle shift in starting material lot, sometimes to atmospheric conditions impacting one of dozens of steps.
We keep records not only on each material’s physical constants but also on mechanical observations: how it flows out of drums, how it resists caking after months of storage, how it tolerates agitation in transport. These details, often overlooked by organizations who buy and repack bulk goods, become crucial to those charting a multi-tonne project where smooth handling can make or break turnaround calendars.
End users have a right to expect a transparent supply chain. From our view, seeing the compound through every synthesis phase generates ownership and accountability that’s hard to match. One of our core values sits in direct communication with users, offering insight from the chemists who actually developed the production route. We have refined protocols over dozens of production cycles, adjusting for humidity, working up batches after power interruptions, and even tackling equipment failures. Through all this, the molecular signature of 4-(4-amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide remains a benchmark against which we measure operational skill.
Difference comes through in reliability. We ship with full accompanying documentation, from batch data sheets to under-reported process notes seldom provided by bulk traders. We often catch small changes in reactivity or solubility in-house before they can impact a buyer’s critical run. Users working in strategic pharmaceutical markets have come to rely on our version for precisely this reason. It’s never just the 99.5% figure; it’s the comfort that deviation — batch-to-batch or year-to-year — is caught and controlled by those closest to the source.
Those working to scale up 4-(4-amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide know real-life manufacturing doesn’t follow a single script. Many reactions demand careful staging, as building the phenoxy linkage prior to introducing the amine can tilt impurity profiles. We learned the hard way that reaction vessels with poor agitation can promote microenvironments favoring unwanted side-reactions. Our operators bring practical experience in managing these variables: regular maintenance, careful temperature mapping, and timely intervention are part of our toolkit.
The sourcing of starting materials plays a pivotal role in process predictability. Early on, we struggled with inconsistent supply of fluoroaryl precursors, leading to variability in input purity. We've since cultivated partnerships with upstream producers, specifying not just assay but also trace contaminant limits for every lot. In response to user requests, we introduced extended-release control batches, holding finished material for post-crystallization screening before shipment. Such processes might slow down output, but they cut down on expensive rework and surprise deviations, lessons learned from past costly errors that still echo through our review meetings.
Our longevity in production grants us a rare comfort with this molecule’s idiosyncrasies. We remain wary of shifting to “faster” process variants promoted by equipment vendors and instead rely on incremental process improvements, tracking performance across campaigns rather than by batch. Team members regularly share findings from failed or off-spec reactions in open reporting sessions, ensuring group learning. We also maintain sample libraries to retrospectively test material for shelf-stability and reactivity shifts, using real data, not theoretical charts.
Far from treating each run as interchangeable, we track subtle performance signals: powder flow changes by humidity season, color shifts on longer oven cycles, or filtration behavior after raw material source changes. These are the small steps that ensure decade-long users never get surprised by underperformance while scaling or formulating.
Feedback from synthetic organic chemists and formulation scientists shapes our process more than internal brainstorming. We encourage direct communication and frequently adapt scale-up or packaging in response to user needs. End-users who synthesize next-generation API intermediates push us to re-examine every crystallization, milling, or drying step. We thrive on the specificity of their questions. Everything from solubility in different solvent systems to what kind of glassware best resists fouling when working up their unique transformations, gets field-tested in our labs before we send out recommendations.
Handling feedback at the source provides agility: in one instance, awareness of downstream coupling bottlenecks led us to pilot a new, finer-milled grade — cutting filtration times on the user’s end by more than half. These changes only happen because our teams understand actual production realities, rather than relying on what a datasheet says should work.
Supply chain interruptions in recent years have exposed the risks of indirect sourcing. As an original manufacturer, we offer full traceability down to lot, supplier, and process revision. Every flask, reactor, and lot is inspected by personnel whose familiarity with the process can’t be replicated at a distance. Real-time documentation reduces error rates and speeds up root-cause analysis when problems arise mid-campaign or during customer scale-up.
Unlike resellers or third-party marketers, who often piece together lots from multiple sources, we guarantee chain of custody and process transparency. Clients ask direct questions about raw material origins; we have the records and firsthand process notes. Our approach has found resonance in high-accountability industries, especially where regulatory due diligence demands extensive answers on synthesis and impurity profiling.
Research and manufacturing partners require predictability to advance novel therapeutics and chemical processes. Our recurring investment in production infrastructure, analytics, and technical staffing builds robustness into supply chains reliant on 4-(4-amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide. The confidence that comes from repeatable, reproducible material translates into successful new molecule launches or efficient process transfers on the customer side.
We follow best practices aligned with the highest standards of traceability, two-way material tracking, and open reporting. We resist the urge to “optimize” away trace documentation or skip steps in the validation chain. As a result, partners trust that what leaves our site matches not just the specification sheet, but also the real-world performance required in sensitive synthesis, formulation, or regulatory submission.
Industry shifts, regulatory changes, and new process chemistry ideas constantly shape the way we approach production. Over the years, we've learned how small changes — from drying schedule adjustments to filter configurations — can yield significant results in output stability and customer satisfaction. By running pilot campaigns, soliciting early customer feedback, and making incremental adjustments, we keep pace with industry trends and evolving end-user requirements.
Each production campaign serves as a testing ground for both process innovation and disciplined adherence to proven methods. The difference between a successful batch and an out-of-spec lot often comes down to operator vigilance, hands-on oversight, and openness to modifying procedures based on experiential feedback. This philosophy is passed down directly from our most experienced operators to new hires, fostering an environment where everyone's observations matter and no production step is considered routine.
Working directly with 4-(4-amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide, we see beyond generic catalog listings or technical summaries. Each batch reflects the tangible skills and lessons acquired on the shop floor — from raw material selection and controlled reactor charging to final quality checks under disciplined laboratory oversight. We support innovative research and process development by delivering reliable, adaptable material, honed through years of practical experience and partnership with users across the globe.
Instead of blending anonymity with scalability, we stake every shipment on verifiable, real-world consistency. At the end of the day, those who matter most — the innovators, developers, and producers building on our compound — gain more than just a chemical. They gain assurance supported by transparency, traceability, and a commitment to relentless improvement rooted in direct experience.