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HS Code |
451470 |
| Productname | 3-Amino-2-(2,4-Difluorophenoxy)Pyridine |
| Casnumber | 120728-66-9 |
| Molecularformula | C11H8F2N2O |
| Molecularweight | 222.19 |
| Appearance | Off-white to light yellow solid |
| Meltingpoint | 95-98°C |
| Purity | ≥98% |
| Solubility | Soluble in DMSO, DMF |
| Storagecondition | Store at 2-8°C |
| Smiles | c1cc(F)ccc1Oc2nccc(c2)N |
| Inchikey | FCCZLLPGGZMVQC-UHFFFAOYSA-N |
As an accredited 3-Amino-2-(2,4-Difluorophenoxy)Pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle with a secure screw cap, labeled "3-Amino-2-(2,4-Difluorophenoxy)Pyridine, 98% purity, handle with care." |
| Shipping | **Shipping Description:** 3-Amino-2-(2,4-Difluorophenoxy)Pyridine is shipped in secure, chemically resistant containers, clearly labeled according to regulatory standards. The compound is protected from moisture, heat, and light. All safety data sheets accompany the shipment. Handling follows standard protocols for laboratory chemicals, with expedited and tracked delivery to ensure product integrity and compliance. |
| Storage | Store **3-Amino-2-(2,4-Difluorophenoxy)Pyridine** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Protect from direct sunlight and moisture. Ensure proper labeling and access for authorized personnel only. Use appropriate personal protective equipment (PPE) when handling the chemical to minimize exposure risk. |
Applications of 3-Amino-2-(2,4-Difluorophenoxy)Pyridine in Industrial ManufacturingAs a manufacturer specializing in high-purity pyridine derivatives, we serve global B2B partners with industrial-grade 3-Amino-2-(2,4-difluorophenoxy)pyridine for advanced chemical synthesis. The following sections detail downstream scenarios where producers rely on this intermediate as a critical building block, with specific focus on compliance, practical formulation use, integration routes, and target end products. 1. Agrochemical Active Ingredient SynthesisManufacturers of crop protection chemicals utilize this raw material as a pyridine scaffold for creating new herbicidal and fungicidal active ingredients. It is valued for introducing fluorinated moieties that improve the target compound’s resistance to metabolic degradation in agricultural fields. Actual process requirements define the point of addition, influencing both the yield and selectivity in key coupling and derivatization reactions during actives synthesis. Industry compliance standards
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2. Pharmaceutical Pyridine Derivative SynthesisIn pharmaceutical API (Active Pharmaceutical Ingredient) manufacturing, downstream companies employ this molecule as a key intermediate during heterocyclic core assembly. Its difluorophenoxy motif enables development of molecules with stronger bioactivity profiles for metabolic and CNS drug candidates. Controlled introduction into synthetic pathways preserves stereochemical and purity requirements for GMP production. Industry compliance standards
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3. Custom Fluorinated Fine Chemical SynthesisProducers specializing in custom-synthesized fine chemicals deploy this raw material when designing bespoke fluorinated building blocks for R&D and specialty chemical libraries. The dual fluorine pattern coupled with the pyridine base allows developers to tailor target properties ranging from electronic structure to hydrophobicity, critical in advanced material and specialty application research. Industry compliance standards
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4. High-Performance Pigment Intermediate ManufactureIndustrial pigment manufacturers integrate this pyridine derivative as a functional group donor for high-performance organic pigments with increased chemical and thermal stability. The difluorophenoxy group enhances the chromophore backbone, serving in the custom dye and pigment synthesis chain. Applications target coatings, plastics, and printed circuit board inks with high durability demands. Industry compliance standards
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5. Specialty Polymer Monomer SynthesisPolymer producers exploiting functionalized aromatics for specialty copolymer synthesis employ our compound for its electron-deficient pyridine ring and difluorinated phenoxy groups. It contributes to improving thermal and chemical resistance in fluorinated polyarylene and polyimide systems, supporting applications in microelectronics and advanced membranes. Industry compliance standards
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Working in the chemical manufacturing industry for years, I’ve watched subtle molecular tweaks shape game-changing advances downstream. 3-Amino-2-(2,4-Difluorophenoxy)Pyridine, known in our plant as one of our more refined heterocyclic intermediates, stands out among the growing roster of specialty chemicals. Shaped by industrial demand, this compound plugs directly into research where selectivity and performance edge out generic choices.
Our production model for 3-Amino-2-(2,4-Difluorophenoxy)Pyridine focuses on high reproducibility and purity, answering the strict requirements of pharmaceutical, agrochemical, and advanced materials clients. Each batch undergoes complete raw material traceability and end-to-end monitoring—habits learned not only from decades of continuous processing, but from the real-world consequences of impurity in tight synthesis chains.
Most of the product coming off the reactors records assay levels over 99% by HPLC, and the residue sullying crystallization or post-synthetic workup rarely shows up when following our dialed-in procedures. Tightly monitored conditions—an inert atmosphere, attention to stoichiometry, regular calibration, and purpose-driven work-up—keep the typical trace impurities, such as mono-fluorinated or non-aminated analogs, to levels below 0.3%. Moisture content checks finish each lot, generally landing at 0.2% or lower, since wet intermediates can disrupt high-sensitivity coupling steps at the customer’s end. Particle size sits on the finer side, averaging around 0.15 mm, as so many applications, especially those tied to solid-phase processing or solution-phase coupling, demand predictable handling and rapid dissolution without caking or retention troubles.
Packing the material, we use certified HDPE drums with foil linings for export, since cardboard fails under aggressive humidity swings during ocean shipment. We’ve learned from batches years ago that skipped measures mean return shipments. For local customers, vacuum-sealed polyethylene bags suffice, and secondary containers get labeled with full analytical records.
The typical end-user of 3-Amino-2-(2,4-Difluorophenoxy)Pyridine isn’t looking for a commodity aromatic amine; their synthetic route calls for deliberate electronic and steric control. Over the years, we’ve followed the journeys of our product through research and commercial syntheses. Medicinal chemists use this intermediate as a building block in kinase inhibitor programs, exploiting both the electron-deficient pyridine and the ortho- and para-fluoro substitutions on the phenoxy group. The two fluorines, in combination with the amino group para to nitrogen, create possibilities for selective bidentate ligation, hydrogen bonding, or improved metabolic profiles compared to non-fluorinated cousins.
Agrochemical innovators push our product through coupling reactions to invent new pesticide candidates. The fluorine atoms drive pest resistance and metabolic stability, while the amino functionality maps onto a variety of urea, amide, or sulfonamide structures that crop protection chemists favor for next-season field trials.
In custom and contract research, 3-Amino-2-(2,4-Difluorophenoxy)Pyridine crops up in hits from virtual screening programs, where its core quietly modulates activity at biological targets. Clients have described its influence in everything from anti-inflammatory research to diagnostic probe development. The trend seems clear: modest scaffold modifications lead to patents, and a thoughtful intermediate like ours often forms the skeleton of those innovations.
For startup labs working with lean budgets and tight schedules, access to liters of this intermediate means direct savings in man-hours. Instead of lengthy and multi-step preparations starting from fluorinated anilines, they plug in our product, cut down on their waste, and avoid hazardous by-products related to early-stage halogenations.
If chemistry was just about attaching the same groups in slightly different places, every catalog would look the same, but experience tells a different story. 3-Amino-2-(2,4-Difluorophenoxy)Pyridine stands out for more than just its CAS number and structure. The dual fluorine pattern isn’t just for show. Many competitive intermediates on the market rely on mono-fluorinated, tri-fluorinated, or fully hydrogen-substituted analogs. Each of these presents hurdles—whether it’s the unpredictable electronic pull on the pyridine ring, the risk of non-specific binding, or metabolic liabilities in in vivo tests.
Our version offers a balance between reactivity and selectivity. The 2,4-difluoro substitution creates both spatial and electronic terrain, nudging downstream reactions by tuning the nucleophilicity of the amino group and the electron density of the adjacent rings. Medicinal chemists banking on activity cliffs appreciate more than just a random placement of fluorines. Comparative studies with mono-fluoro or di-fluoro positioned differently have yielded shifts in IC50 values, solubility, and target affinity that can’t be ignored, especially once projects move out of early screening and into late-stage optimization.
Synthetically, our process reduces the risk of isomeric contamination. In contrast, resellers sometimes offer material derived from less selective routes; batch-to-batch inconsistencies plague those trying to reformulate or validate scale-up. With our continuous-improvement approach, analytical data seldom shows more than trace contamination with positional isomers or over-fluorinated derivatives, something our downstream clients routinely recognize as a selling point.
Markets for heterocyclic intermediates are crowded, but the unique fingerprint on our product, from IR to proton NMR, keeps it distinct. Repeat customers cite this reliability, and, as a manufacturer, there aren’t many compliments higher than seeing your material pulled into full-scale commercial launches, patent filings, or regulatory dossiers.
There’s also the critical matter of environmental handling. Our plant team worked out processes for in-process waste management from synthesis of this intermediate, building closed-loop solvent recovery and neutralization at every step. This isn’t something visible on a spec sheet. It matters for downstream users, especially those prepping regulatory filings for new actives, who need to audit supply chains. Such diligence on the production floor means fewer downstream headaches for everyone involved.
Competition with generics and rogue manufacturers is part of the business these days. Counterfeit and impure versions creep into supply chains, especially for compounds like this which sit one or two steps removed from high-value APIs or crop protection candidates. We vet raw material suppliers rigorously—with the dial on impurity detection turned all the way up, especially regarding residual halogenated by-products.
Maintaining purity through purification is neither trivial nor cheap. Our operations team learned through broken reactors, small fires, and missed deliveries that shortcutting’s not worth it. Separate purification lines handle potential side products, and stringent final filter checks and chromatography scans reduce rework and downstream contamination. Some competitors have lowered costs with open processes, but feedback from our customers, especially across Europe and the US, confirms their preference for the peace of mind our product brings.
Meeting rising demand from high-throughput screening labs and biotech startups has required flexible scaling. Every uptick in demand strains reactor scheduling and QC staffing. Our process engineers tinker with batch size, cycle time, and continuous versus stop-and-go production to balance speed with consistency. For instance, keeping batch records and traceability at scale proved more resource-intensive than anticipated, but regulatory trends show this level of transparency becoming the norm.
Transport infrastructure looms large in our decisions, too. Moisture control in shipment matters more than ever, given the sensitivity of the pyridine ring and difluoro-phenoxy group to hydrolysis under poorly managed conditions. Uncooperative summers, monsoon shipping routes, and cold snaps forced us to revise logistical protocols. Now, transport partners undergo inspection and product tracking continues through arrival at the customer’s dock.
End-use integration, especially with new automated synthesizers and microfluidic labs, challenged our historical protocols. Smaller batch customers using robotics value consistent handling properties—free-flowing, dust-minimized, predictable dissolution profile—so our downstream granulation and drying team adjusts to maintain these standards. Such responsiveness signals our willingness to listen and adapt, something manufacturers must embrace to stay relevant.
3-Amino-2-(2,4-Difluorophenoxy)Pyridine’s journey doesn’t end on the shelf. Its role as a seed for discovery means we share responsibility for how it gets used, both through honest QC reporting and by supporting supply chain audits. As regulatory authorities scrutinize both product and process, we stand ready with full-origin documentation, impurity profiles across multiple runs, and process safety records. Developers know corners cut in early supply bring headaches later during FIL (first-in-lab), FIH (first-in-human), or GLP toxicology.
We field plenty of questions from new customers—googling their way to the compound and wanting to confirm chain-of-custody, prior audit results, or environmental profile. Our long game is transparency, because one poorly documented supply break spells loss of product trust and client relationships built over years, not months.
In addition to simply producing the compound, we often collaborate on custom modifications. Requests come in for deuterated versions, non-standard particle sizes, or cross-linkable tethers for bioconjugation. Our chemists work alongside these partners, providing synthesis guidance and honest feedback. We are not just “selling a product,” we’re acting as active participants in ongoing scientific stories.
Chemists in industry and academia have no shortage of aromatic amines or fluoroaryl intermediates. So choosing the right scaffold shapes the project trajectory. Compared to 2,4-difluoroaniline or even 2,4-difluorophenoxy-substituted benzenes and pyridines, the 3-Amino-2-(2,4-Difluorophenoxy)Pyridine core creates unique binding interactions in drug and material design.
Structural biology work from our partners illustrates that even a single change—from the para to meta position for the amino group, or swapping out the relative positions of the fluorines—alters downstream affinity, selectivity, and ADME profiles. For some applications, overly electron-rich or electron-poor scaffolds encourage off-pathway reactions or create compounds unsuitable for IP protection.
Compared to monosubstituted analogs, our product gives researchers options for tuning lipophilicity and metabolic resistance. Multiple fluorine atoms in precise orientation discourage rapid degradation by cytochrome P450 enzymes; at the same time, our compound avoids the over-rigidity that arises in trifluorinated analogs which prevents target plasticity or bioavailability.
Real-world customer feedback underscores these competitive differences. Firms reporting improved hit rates in kinase screening series often link their results to the balanced electronics of the 3-amino–2-(2,4-difluorophenoxy) motif. Process chemists praise its crystalline, manageable solid-state form, favoring it over sticky, greasy or strongly hygroscopic mono- or tri-functional variants. No product is plug-and-play everywhere, but this intermediate fills a gap for tailored reactivity, effective binding, and manageable production costs.
The supply chain landscape keeps changing. Regulatory pressures mount, from REACH in Europe to EPA scrutiny in the US. We proactively report compliance to these frameworks, knowing that early openness saves last-minute headaches for our customers. Our raw material procurement relies more and more on closed-loop local suppliers, ensuring traceability and reducing transit-related contamination.
Questions of environmental stewardship shape our daily routine. Older processes for difluorinated intermediates often created non-trivial halogenated waste. We invested in waste minimization, both out of environmental principle and financial necessity. Modern solvent recovery, on-site incineration of byproducts, and re-use of off-gas heat for pre-reaction charging all form part of our workflow now.
One recurring issue, familiar in any intermediate-intensive industry, relates to IP and freedom-to-operate. Our documentation process clarifies and confirms non-infringement for our specific processes and routes; clients need hard proof that their work with our compound won’t set off legal skirmishes. We learned, sometimes the hard way, that preemptively providing patent landscapes and detailed origin disclosures supports our customers and builds confidence.
The feedback loop with end users drives our QC processes today. Whether it’s a researcher scaling from milligrams to kilos, or a multinational firm preparing a DMF (Drug Master File), their experience with our product directs our own internal process improvement. Rapid response to complaints—cloudiness, odor, or off-spec melting point—helps keep defects rare and satisfaction high. We routinely revise production SOPs after tough but fair customer feedback.
Collaborative innovation, whether for new fluorination strategies, greener manufacturing, or hybrid synthesis, reinforces our place in the field. Increasingly, we see requests for support in route scouting and sample prep beyond simple upscaling. Our team of in-house chemists offers synthesis support out of a responsibility for both the science and the safety of those who work with our material downstream.
Looking ahead, lab-scale supply constraints, shifting regulatory climates, and the need for traceable, consistent materials favor manufacturers willing to invest in transparency, process control, and customer dialogue. For 3-Amino-2-(2,4-Difluorophenoxy)Pyridine, reliability isn’t a marketing slogan—it’s the result of everyday experience at the reactor, the filter press, and the QA table.
We invest in R&D, listen to failures as much as successes, and aim to keep our product’s quality and utility at the level that partners trust. There’s no substitute for the incremental improvements, customer engagement, and direct accountability that only the manufacturer can provide.
The place of 3-Amino-2-(2,4-Difluorophenoxy)Pyridine in research and industry demonstrates the ongoing interplay between foundational chemistry and real-world application. Our commitment shapes its reliability, and the demands of synthetic chemists worldwide guide our continued progress, batch after batch.