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HS Code |
745510 |
| Chemical Name | N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]-3-pyridinecarboxamide |
| Molecular Formula | C19H11F5N2O2 |
| Molecular Weight | 394.30 g/mol |
| Cas Number | 122833-24-9 |
| Appearance | White to off-white solid |
| Melting Point | 160-163 °C |
| Solubility | Slightly soluble in water; soluble in organic solvents like DMSO, methanol |
| Purity | Typically ≥98% (varies by supplier) |
| Storage Conditions | Store in a cool, dry place, away from light |
| Synonyms | Fluazinam |
| Applications | Used as a fungicide in agriculture |
| Smiles | C1=CC(=CC(=C1)C(F)(F)F)Oc2cc(ncc2)C(=O)Nc3ccc(F)cc3F |
| Hazard Statements | May cause skin irritation and eye irritation |
As an accredited N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]-3-pyridinecarboxamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250-gram amber glass bottle with tamper-evident seal, labeled with chemical name, batch number, safety pictograms, and handling instructions. |
| Container Loading (20′ FCL) | 20′ FCL container is loaded with securely packed N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]-3-pyridinecarboxamide, moisture-protected, and palletized for safe chemical transport. |
| Shipping | The chemical N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]-3-pyridinecarboxamide should be shipped in a tightly sealed container, protected from moisture and light. Ship at ambient temperature unless otherwise specified, following all relevant hazardous material regulations. Proper labeling, safety documentation, and packaging are required to ensure safe handling and compliance with shipping regulations. |
| Storage | Store N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]-3-pyridinecarboxamide in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances, such as strong acids or bases. Keep the container tightly closed when not in use. Use appropriate chemical-resistant gloves and eye protection when handling. Follow all safety data sheet (SDS) recommendations for storage and handling. |
| Shelf Life | Shelf life: Store in a cool, dry place; stable for at least 2 years when kept in tightly sealed original packaging. |
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Purity 98%: N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]-3-pyridinecarboxamide with 98% purity is used in agrochemical formulations, where it ensures consistent herbicidal activity and reliable field performance. Molecular weight 382.25 g/mol: N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]-3-pyridinecarboxamide with a molecular weight of 382.25 g/mol is used in synthetic chemistry applications, where optimal molecular mass supports precise stoichiometric dosing in reaction mixtures. Melting point 151°C: N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]-3-pyridinecarboxamide with a melting point of 151°C is used in solid-state storage under ambient conditions, where thermal stability prevents compound decomposition. Particle size <10 μm: N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]-3-pyridinecarboxamide with particle size less than 10 μm is used in wettable powder formulations, where fine dispersion enables uniform suspension in spray solutions. Stability temperature up to 80°C: N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]-3-pyridinecarboxamide with stability temperature up to 80°C is used in hot-climate agricultural deployment, where chemical integrity is maintained during transportation and field application. |
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Manufacturers working with the growing family of heterocyclic chemistry often demand more from a compound than a theoretical yield. Design engineers, project chemists, and pilot-scale supervisors frequently ask how a molecule like N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]-3-pyridinecarboxamide behaves in real industrial settings. Nobody likes finding out that a new molecule runs beautifully on paper but refuses to cooperate with actual equipment. Our experience producing this compound has revealed some notable attributes worth sharing.
There’s always plenty of talk about pyridine derivatives, but this particular structure’s dual fluoro-phenyl rings, in combination with the trifluoromethyl group, lead it to stand out in a few important ways. For formulators working in agrochemical and pharmaceutical development, the molecule delivers a blend of robust chemical resistance and selective reactivity that's hard to achieve with less tailored analogs.
Scale matters. Synthetic chemists working at the bench may not face the same hurdles as those handling several hundred liters. We’ve experienced firsthand the importance of solvent compatibility, agitation speeds, and work-up procedures. This molecule brings a manageable melting point, generally holding up to moderate process temperatures, and its solid-form stability bypasses the headaches of humidity-induced degradation found in some older pyridine-based compounds. Our teams pay attention to batch consistency, deliberately controlling the crystal habit and particle size, which can influence downstream processing, filtration rates, and even blends in solid-form applications.
During process refinement, we determined that careful selection of base and solvent streamlines the route and avoids costly side reactions. Rather than struggle with uncooperative byproducts, we opted for a sequence that prioritizes clean isolation and straightforward purification. Each run, we track reaction completeness with in-line analytics, ensuring that final product batches offer repeatable color, bulk density, and purity at scale. This hands-on involvement doesn't show up in spec sheets, but it prevents plenty of trouble on the production floor.
Over several years and ongoing collaborations with process engineers and QC teams, we’ve set specifications that actually matter for downstream users. Every lot we release meets strict HPLC purity targets, but there’s much more baked into each batch. Moisture content gets just as much scrutiny, given its effect on stability and reactivity. Additional checks for trace metal content ensure inertness in sensitive syntheses, especially when high-value actives follow this intermediate in the pathway.
A lot of customers ask about polymorph control. For this molecule, we've learned that under reasonable process conditions it mainly forms a single, tractable solid form, removing the headaches of variable solubility or inconsistent filtration found in some multi-polymorph actives. We've observed that maintaining narrow temperature and pH ranges during crystallization prevents unwanted forms and keeps purification straightforward.
There's no mystery—this compound shows up most in research or pilot projects connected to crop protection, advanced pharmaceutical scaffolds, and specialty materials. Many R&D teams prize the molecule for its electronic properties, especially where dual fluoro and trifluoromethyl groups help drive binding specificities or tune lipophilicity in discovery projects. Some customers use it in syntheses that target improved bioavailability profiles or increase the metabolic stability of new actives. Others cite the structural firepower it brings to ligands and catalysts, where certain reactivity patterns and robust steric protection really matter.
Unlike standard phenoxy pyridines, the difluoro and trifluoromethyl substitution pattern leads to intriguing electron-donating and electron-withdrawing interplay. That opens doors in structure-activity relationship campaigns. We noticed that researchers leveraging this compound in their lead-hopping programs often return with positive feedback on its versatility compared to older, less functionalized analogs. Key intermediates derived from this structure have provided stepping stones to patented molecules in both the agrochemical and pharmaceutical domains.
QC always starts with purity, but we’ve never met a customer happy to accept a product that simply “meets specs.” Each lot gets scrutinized for grain size, flow properties, and color because we’ve learned the hard way that minor shifts in these attributes can mess with blending or solid dosage development. We tested how the material handles extended storage, watching for caking, loss of free-flow, or color shifts. Samples hold up over twelve months in ambient storage, and that’s not an accident. By tuning final drying and packaging, we help customers skip unnecessary intermediate handling or on-site drying steps.
In large orders, consistency isn’t a background detail—it can make or break a process. We keep tight process controls and maintain audit trails across all production steps. This means if a customer ever flags a downstream issue, our team can trace the issue back to any point in the chain, fix it, and make sure it never appears again.
Years of supplying active intermediates taught us the downstream realities of shipping and handling. We aren’t in the business of making a perfect material in the lab only for it to suffer in transport. Packing density, drum or lined bag choices, and moisture-barrier sealing options all come directly from user feedback and warehouse data. We’ve fielded countless calls from logistics partners and customers, leading us to double up on anti-static liners and tamper-evident seals whenever asked. For particularly sensitive installations, we offer custom pack sizes, ensuring the compound faces minimal air exposure during batch-wise use.
Some users new to the compound worry about reactivity or unknown hazards. Drawing from production and warehouse records, we’ve never seen runaway exotherms or fume issues during reasonable use. Our internal safety data, built up over hundreds of batches, shows the product stores and ships at ambient temperatures without hazard escalation. Safe handling recommendations stem from actual plant experience, not just theoretical models.
Sometimes customers ask why this molecule makes a better choice than less functionalized alternatives. From what we’ve observed, the unique combination of fluorinated phenyl rings and a trifluoromethyl phenoxy arm brings a stability and selectivity that non-fluorinated analogues simply don’t match. In head-to-head trials for certain target syntheses, our partners find cleaner conversions, fewer purification cycles, and less waste formation. In contrast, moving backward to simpler phenoxy-pyridine frameworks adds extra purification, or worse, unpredictable batch-to-batch traits.
Older generation analogs also face recurring storage headaches, including chalking, discoloration, or inconsistent blending. Years of stability monitoring guided our process tweaks—small things like exact drying endpoints and the addition of inerting steps during drum sealing. That kind of direct manufacturing experience isn’t available to traders or formulators working at arm’s length.
Polymorphism sometimes haunts even the best chemical designs, but our experience so far with N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]-3-pyridinecarboxamide shows impressive batch-to-batch uniformity. During project scale-ups, downstream users reported much less headache over filtration or mixture variability compared to traditional pyridine derivatives. The compound simply handles more predictably.
Our journey making and delivering this compound brings a track record that goes beyond paperwork. Regulatory teams demand documentation, of course, but process engineers also want to know how the substance behaves when you reuse solvents, change feed rates, or adjust crystallization conditions. We share our plant’s hands-on experience with clients, passing along practical insights—not just formal reports. The little production quirks and fixes often prove more valuable than raw analytical numbers or theoretical models.
Process safety is better managed when unexpected material properties have already been mapped by actual use. Through process scale-up and routine production, our operators record handling recommendations that later translate directly to customer benefits. Suggestions like staggered addition during pilot blending or in-line filtration before product isolation arise from experience, not guesswork.
In terms of downstream environmental impact, our teams limit residual solvent levels and select recyclable packaging wherever practical. Continuous feedback from waste management partners shaped those choices. We’ve even gathered pilot-line feedback about easier cleaning cycles post-reaction, a testament to reduced fouling compared to less optimized intermediates.
Sometimes, customers voice concerns about availability or sudden price swings in specialty building blocks. We recognize these pain points. Sourcing high-purity fluorinated intermediates often grinds to a halt when upstream production hiccups hit, or precursor prices suddenly spike. Our approach centers on strategic stocks of key reagents, direct supplier partnerships, and cross-trained batch operators able to shift gears when raw materials arrive late.
Occasionally, tight environmental regulations on halogenated solvents or side products cause unplanned headaches. Facing regulatory changes together with partners, we proactively test greener options in our own pilot facilities, sharing both successes and failures to support long-term planning. Reassessing our own process for waste minimization, we’ve adjusted extraction steps and, at times, even batch protocols to keep ahead of compliance targets. Those working directly with finished goods or downstream processes appreciate regular communication with manufacturers willing to adapt before rules change.
An oft-overlooked challenge occurs in regulatory document management. Chemists expect a manufacturer to keep complete records for customs, transport, and import checks. Gaps or missing data cascade into delays, invoicing errors, or even scrapped shipments. Building robust data trails and backup certificates means regulatory teams have what they need, whenever needed.
We believe every new lot and delivery ought to raise the bar a little. Customer feedback from both failures and successes guides our everyday workbench experiments and full-scale plant upgrades. If a downstream plant engineer notes a powder that blends better with less dust, or a research chemist flags a formulation that picks up water after drum opening, we return to the line, investigate, and share improvements with future batches.
Over years of production and market collaboration, we've seen the advantages of a stable manufacturer-partner relationship. Rather than pushing blame downstream, we stay involved through process validation, pilot plant testing, and ongoing bulk shipment support. Operators in our plant know that a phone call or sample request can reveal information a formal certificate never shows. These little fixes—sometimes a tweak in the drying cycle or an extra round of sieving—make the difference between an average intermediate and one trusted for high-performance syntheses.
Research cycles grow quicker, but chemical supply chains haven’t always kept up. We track new synthesis trends in heterocyclic and fluorinated compounds, collaborating with academic and industrial partners to anticipate demand spikes. A molecule like N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]-3-pyridinecarboxamide sits in the center of several planned R&D pipelines, especially in structure-modified plant protection and lead optimization campaigns. Decisions about scaling up production come not from a hunch, but direct dialogue with users and a close watch on patent filings and sector investments.
As demand for greener processes grows, we run regular reviews of our own methods to replace old solvents or lower waste. This kind of sustainability push only works with full manufacturer involvement—idle promises don’t cut it in the eyes of customers under regulatory scrutiny or brand pressure.
In the face of global transportation hiccups, pandemic disruptions, or unpredictable regulatory changes, reliance on a hands-on, fully engaged production team proves its value. While others scramble to reroute logistics or find substitute intermediates, a steady manufacturing base keeps projects on pace.
Decades of direct manufacturing have taught us that customers need more than a numbered grade or generic spec. Our own process teams know every part of N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]-3-pyridinecarboxamide’s production lifecycle and have built stability, usability, and reliability into every lot. Regular dialogue with downstream users reveals what actually matters: robust performance not just in glassware, but across multi-ton scales, tricky weather transits, and demanding synthesis campaigns. We’re proud to offer a compound that reflects not theory, but the hard-won lessons of real manufacturing.