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HS Code |
454404 |
| Chemical Name | N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide |
| Molecular Formula | C19H11F5N2O2 |
| Molecular Weight | 394.30 g/mol |
| Appearance | White to off-white solid |
| Cas Number | 127294-92-6 |
| Melting Point | 178-180 °C |
| Solubility | Slightly soluble in water, soluble in DMSO and methanol |
| Purity | Typically >98% |
| Storage Conditions | Store at 2-8°C, away from light and moisture |
As an accredited N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide 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 white screw cap, labeled with chemical name, hazard symbols, batch number, and storage instructions. |
| Container Loading (20′ FCL) | 20′ FCL container typically holds 14–16 MT of N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide, packed in drums or bags. |
| Shipping | This chemical, N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide, is shipped in tightly sealed containers under inert atmosphere, protected from moisture, heat, and direct sunlight. Appropriate hazard labeling and documentation accompany the shipment. Transportation complies with international regulations for handling specialty chemicals, ensuring safety and integrity during transit. |
| Storage | Store N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide in a tightly sealed container, protected from moisture and direct sunlight. Keep at room temperature, ideally between 2–8°C, in a well-ventilated, dry area away from sources of ignition and incompatible substances. Clearly label the container and ensure access is restricted to trained personnel. Employ appropriate personal protective equipment when handling. |
| Shelf Life | Shelf life: Stable for at least 2 years when stored in a cool, dry place, protected from light and moisture. |
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Purity 98%: N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide with 98% purity is used in agrochemical synthesis, where it ensures high crop protection efficacy and minimal impurity-related phytotoxicity. Melting Point 168°C: N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide at a melting point of 168°C is used in solid formulation processing, where improved stability during transport and storage is achieved. Molecular Weight 388.27 g/mol: N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide with a molecular weight of 388.27 g/mol is used in active ingredient development, where optimal dosage calculation and formulation accuracy are ensured. Particle Size D90 <10 µm: N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide with particle size D90 less than 10 µm is used in suspension concentrates, where enhanced dispersibility and uniform application are provided. Stability Temperature up to 60°C: N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide stable up to 60°C is used in tropical climate packaging, where long-term storage without significant degradation is achieved. |
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Decades in the lab and on the plant floor have taught us that progress in crop protection comes from more than just following market demand. N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide grew out of hands-on research into resistance management and active ingredient design. The molecular backbone fuses a pyridine-3-carboxamide scaffold with targeted fluorination, embedded in both phenyl rings, while integrating a trifluoromethyl-phenoxy side chain. This combination offers improved metabolic stability and selectivity, which most off-the-shelf generic actives struggle to deliver against evolving pest profiles.
Unlike conventional carboxamides—for example, older chlorinated analogs or non-fluorinated pyridine amides—our variant leverages structure-activity relationships developed over years of iterative synthesis and biological screening. Many chemicals on the market today come from long-standing generic routes. They often show lower specificity or break down quickly in the environment, leaving growers with inconsistent protection and the larger chemical companies scrambling to chase new regulatory limits. By contrast, our continuous-scale production methods ensure each batch maintains tight purity ranges, usually above 98%, with consistent crystalline structure, minimizing off-target metabolites and supporting robust field performance.
Agricultural production faces a shifting landscape—not just from climate pressure, but from the genetic arms race in pathogens and pests. Over-reliance on legacy crop protection agents has driven a steady rise in resistance, especially among problematic fungi in cereals, rice, and specialty crops. Our teams saw this trend firsthand on farms where old chemical classes lost ground season after season. That’s why N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide was conceived to intervene at biochemical sites where alternative actives stumble.
In field trials and controlled studies, this compound delivered persistent activity against key pathogens such as Pyricularia oryzae and Septoria tritici. That means extended windows between applications, lower overall chemical use, and more reliable crop protection under disease pressure. Many earlier products offered similar initial disease knockdown, but then fell short during periods of heavy rainfall or rapid pest influx due to weaker rainfastness or UV decomposition. The hexafluorinated core in our molecule resists environmental breakdown, while the carefully managed side groups maintain biological uptake by fungal membranes without leaching heavily into soil or waterways.
Our facility runs dedicated lines for fluorinated aromatics, drawing on years of experience with safe handling and real-time quality monitoring. Manufacturing N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide requires multi-stage synthesis—beginning with the selective halogenation of phenol derivatives and culminating in late-stage amide coupling. Each process parameter keeps the electrochemical reactivity of the difluoro and trifluoromethyl groups in mind; overheating or poor reagent choice leads to impurities, so we keep every batch under constant spectroscopic and chromatographic surveillance.
While high-throughput chemistry can cut corners, our approach proves that reproducibility means more than just volume. Even small shifts in crystalline phase or solvent residue crop up in downstream formulation and field stability. We’ve witnessed how rapid scaling introduces unpredictable contaminant profiles—some that evade routine detection and only show up as residue complaints from overseas importers. Years of feedback from real-world users have shown us the value of sampling every lot, analyzing for isomer purity and ensuring that storage under normal warehouse conditions will keep the active ingredient within spec across the full shelf life.
Large multinational agrochemical products often serve as global staples, but many compounds in circulation today stem from routes or design philosophies developed several decades ago. Chlorinated pyridines and sulfur-linked carboxamides, for example, can accumulate in soil and may lack selectivity between target and non-target species, contributing to resistance build-up or off-target toxicity—problems we’ve traced during review meetings with regulatory bodies and grower associations. Even when new analogs claim improved performance, variations in production standards often cause fluctuating impurity profiles, impacting everything from dispersion in water to off-odors noticed by users.
N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide was designed for metabolic stability and environmental safety from the start. Its physicochemical profile offers condensed partition coefficients and moderated solubility, translating to lower runoff risk compared to many older chemistries—a point we verified by comparing residual analyses and soil/leaf binding studies on trial plots. Generic manufacturers may produce visually similar white powders or crystalline solids, but lack the in-house fluorination expertise and residual impurity control possible only with full vertical integration.
We’ve seen firsthand how growers respond to more predictable disease management. Many existing products fail to provide lasting control under variable conditions. During our own field demonstrations, users commented on the extended protection window N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide delivers on wheat and barley—especially during prolonged wet periods that test the limits of less robust formulations. By measuring residual activity on foliage, we tracked how the dual fluorination mechanism promotes tight binding at disease target sites and delays enzymatic degradation.
Sprayer compatibility remains crucial, given farms now rely on multicomponent tank mixes. Our technical team builds application support data for the active ingredient in suspension concentrates and wettable granules, ensuring dispersibility and compatibility with modern surfactants and water conditioners. Many previous-generation actives delivered uneven coverage or posed foaming risks in hard water, which we’ve reduced through careful particle size management and minimized salt content following feedback from mixers and field applicators. We’ve worked alongside customers in both subtropical and temperate climates, reviewing which adjuvants boost adherence on crop surfaces and limit re-emission during high wind or rain.
The agrochemical industry faces complex, continuously evolving requirements surrounding environmental trace residues, toxicological profiles, and operator safety risk. These pressures shape every step of our product development and production scale-up. Formulators and growers alike want reassurance on persistence data, metabolite breakdown pathways, and field dissipation curves. We provide detailed analytical packages for each lot at release, focusing on trace impurity minimization and robust metabolite identification—critical for both domestic regulators and export-oriented producers facing multiple destination standards.
Sustainability has grown from a buzzword to field-level reality as policymakers, food processors, and local communities question every spray pass and residue profile. Our rigorous approach to atom efficiency, waste minimization, and solvent recovery in N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide synthesis reflects not just regulatory expectation but a commitment to long-term stewardship. Repeated soil and aquatic studies under both rotation and monoculture systems have demonstrated rapid breakdown to non-toxic species within the local environment—a claim supported by multi-year residue monitoring and validation.
No chemical plant or pilot R&D line runs in isolation from the needs and complaints of its end users. From crop trial supervisors in rice paddies of Asia to cereal growers in the Black Sea region, feedback has shaped our approach to both technical data generation and real-time field support. In multiple seasons, growers have highlighted the need for less dusting during application, which led us to re-engineer our crystalline milling and drying setups. Storage complaints in hot, high-humidity regions prompted us to invest in stabilized packaging and enhanced desiccant liners, which keep the active ingredient within moisture tolerance ranges across shipping lanes and storage conditions.
Users want traceability and transparency. We document every synthesis run, every lot analysis, and every shipment point with digital tracking, ensuring real-world verification—not just on paper but in random audits and regulatory spot checks. We stand by our analytics, opening up our instrumentation logs and GC-MS reports both to buyers and independent auditors. When potential for cross-contamination arises—a risk many in the trade overlook—we halt packing for full QC review, not to avoid paperwork but to keep long-term trust with partners that depend on the active ingredient’s predictability in their mandatory residue portfolios.
Many growers and agronomists ask about differences between our product and other pyridine- or phenoxy-based solutions on the shelf. The difference comes from both design and follow-through. Structural analogs may look broadly similar, but performance on the field tells the real story. We rely on mass balance studies, UV and field stability testing, and spectrum analyses to compare side chains, halogen substitution patterns, and environmental fate—not just general “activity” promises seen in data sheets.
Some off-patent or “similar” actives promise equivalent disease reduction on paper but exhibit inconsistent field performance due to varying impurity remnants, poor particle size control, or insufficient environmental breakdown data. With N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide, fluorine incorporation drives a higher level of metabolic resistance, meaning pronounced durability across consecutive application cycles. We’ve mapped these findings not just with chemistry but with season-by-season field logs—tracking response curves, wind drift, and even real-world operator feedback on handling and cleanup.
Each growing season brings new challenges, new pathogen mutations, and sharper regulatory oversight. Our ongoing work in synthetic route optimization and advanced analytics reflects an understanding that chemical innovation depends on both on-site experience and broader stewardship obligations. We keep full API trace logs, track environmental batch data, and adapt manufacturing protocols based on on-the-ground needs—whether that means rapid-release micro-batches for emergency disease outbreaks, or tailored granule size distributions for specific tank mixes dictated by changing weather or application equipment.
This isn’t the result of trend-watching or tertiary chemical translation. The dataset we rely on comes from investments in plant-level upgrades, repeated external lab partnerships, and an ear to every user complaint or technical question in the field. Our continual re-investment in production and analytical infrastructure ensures that, as disease patterns change and food system pressures mount, we have answers based on a real-world record—not theoretical or marketing claims.
We’ve long believed technical transparency underpins real trust in crop protection chemistry. Each batch manufactured undergoes comprehensive in-house and third-party laboratory assessments, with complete method logs, residue curves, and impurity breakdown reports available for scrutiny. The difference is felt not just by regulators but by growers who face increasing scrutiny from buyers and consumers asking about every input in modern crop production.
Our commitment to open documentation goes further than what’s required. With N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide, all major parameters—melting point, shelf-life, water-dispersibility, and resistance management—are monitored with each production cycle, with findings made available upon request as part of our ongoing support for supply chain partners and users under evolving transparency mandates.
Years in the chemical industry have shown us that making a difference means more than outcompeting on cost or chasing generic releases. To us, manufacturing N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide isn’t just about supply—it’s about setting a process-focused standard for what modern agrichemicals can achieve in durability, selectivity, and environmental impact. Each decision, from bench synthesis to final QC release, balances commercial viability with health and sustainability. As fresh disease threats and market pressures keep emerging, only real-world data, continuous feedback, and investment in both people and plant can keep the next generation of actives useful, accepted, and trusted.