|
HS Code |
905364 |
| Chemical Name | N2-(4-fluorobenzyl)-5-nitropyridine-2,6-diamine |
| Molecular Formula | C12H11FN4O2 |
| Molecular Weight | 262.24 g/mol |
| Appearance | Solid |
| Smiles | C1=CC(=CC=C1CNc2c([N+](=O)[O-])cnc(N)c2)F |
| Cas Number | NA |
| Pubchem Cid | NA |
As an accredited N2-(4-fluorobenzyl)-5-nitropyridine-2,6-diamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, sealed 25g HDPE bottle labeled "N2-(4-fluorobenzyl)-5-nitropyridine-2,6-diamine, 25g, for research use only" in bold text. |
| Container Loading (20′ FCL) | 20′ FCL loaded with securely packaged drums of N2-(4-fluorobenzyl)-5-nitropyridine-2,6-diamine, ensuring safety and compliance. |
| Shipping | Shipping of N2-(4-fluorobenzyl)-5-nitropyridine-2,6-diamine requires secure packaging to prevent leaks or contamination. The chemical should be transported in accordance with local and international regulations for hazardous materials, including clear labeling. Temperature control and documentation for safe handling may be necessary, depending on specific safety data and quantities shipped. |
| Storage | **Storage:** Store N2-(4-fluorobenzyl)-5-nitropyridine-2,6-diamine in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from strong oxidizing agents, acids, and sources of ignition. Use personal protective equipment when handling, and follow local regulations for the storage of chemicals with nitro and amine functional groups. |
| Shelf Life | Shelf life: Store **N2-(4-fluorobenzyl)-5-nitropyridine-2,6-diamine** in a cool, dry place; stable for at least 2 years under recommended conditions. |
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Purity 98%: N2-(4-fluorobenzyl)-5-nitropyridine-2,6-diamine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield product formation and minimizes by-product generation. Melting Point 145-148°C: N2-(4-fluorobenzyl)-5-nitropyridine-2,6-diamine with melting point 145-148°C is used in solid-state formulation development, where it guarantees thermal stability during process scale-up. Molecular Weight 261.24 g/mol: N2-(4-fluorobenzyl)-5-nitropyridine-2,6-diamine with molecular weight 261.24 g/mol is used in structure-activity relationship studies, where precise molar quantification enhances assay reproducibility. Particle Size <10 μm: N2-(4-fluorobenzyl)-5-nitropyridine-2,6-diamine with particle size less than 10 μm is used in advanced coating systems, where uniform dispersion increases coating homogeneity and effectiveness. Stability Temperature up to 120°C: N2-(4-fluorobenzyl)-5-nitropyridine-2,6-diamine with stability temperature up to 120°C is used in high-temperature reaction protocols, where its integrity is maintained for prolonged durations. Assay ≥99%: N2-(4-fluorobenzyl)-5-nitropyridine-2,6-diamine with assay ≥99% is used in analytical reference standard preparation, where high assay value enables accurate calibration and validation methods. |
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Manufacturing N2-(4-fluorobenzyl)-5-nitropyridine-2,6-diamine gives us a close-up view of what today’s chemical creators look for—chemistry that works hard and brings true function into advanced synthesis. Each batch begins with demand from researchers and production facilities seeking out ways to incorporate a highly reactive and selective intermediate into their workflow. We see this request growing in areas that rely on tailored building blocks, especially in the development of pharmaceuticals, specialty agrochemical actives, and advanced material scaffolds. Getting the structure right is just one part. Repeatability, clarity of process, and ease of downstream modification matter just as much.
We produce this compound under model code FNPD-46, a designation that’s evolved with the process itself. Structural specificity defines its uniqueness. The 4-fluorobenzyl group ties to the nitrogen at the 2-position, creating an electron-withdrawing influence that changes how this molecule reacts with nucleophiles and electrophiles alike. The diazine ring is functionalized with nitro at the 5-position and two amine groups at 2,6-positions. Such design is never arbitrary; we have reworked syntheses to serve chemists who want cleaner, more direct coupling and substitution, often at lower temperatures and with reduced by-product formation. That efficiency only comes from deep process control, where byproducts and side reactions aren’t just measured, they are actively minimized.
Consistency emerges early as a must-have, not because marketing says so, but because purification is usually expensive and time-consuming for the next person down the line. FNPD-46 leaves our plant meeting at least 98% purity by HPLC, confirmed GC-MS, and is typically available as a pale yellow crystalline powder. Water content stays below 0.5%. Trace metal contaminants, a concern in catalytic downstream synthesis, are kept at bay thanks to carefully chosen glass-lined reactors and monitored solvent recovery. We use routine in-process controls because even one failed batch can halt a critical project at a customer’s site. Crystallization and drying, often overlooked, receive full attention here. Uniform particle size and flow properties ease both laboratory handling and scale-up work.
This compound finds its place in synthetic platforms that require control, reliability, and specific chemical behavior. For pharmaceutical R&D, the 4-fluorobenzyl group acts as a masked functionality or modifiable handle—chemists can carry this fragment forward into more complex molecules, introducing fluorine at a precise spot to alter metabolic stability, binding, or bioavailability. Nitropyridine frameworks, particularly with protected amines, bring versatility in coupling reactions: Suzuki, Buchwald-Hartwig, and nucleophilic aromatic substitution all become possible, often with fewer steps and higher yields than alternative intermediates.
Beyond drug synthesis, specialty material companies draw on FNPD-46 for manufacture of electronic materials, where controlled placement of fluorine changes dielectric properties and environmental stability. Agrochemical innovators seek out nitroaromatic cores with custom substituents—these features often drive selectivity, persistence, and compatibility with modern formulation requirements.
Each application teaches us something new about scalability. Delivering from grams for early discovery to kilograms for pilot production sharpens our focus on logistics, analytical throughput, and cost management. Feedback from process engineers and bench chemists alike shapes our improvement projects. Often, the best innovations come from unexpected customer use cases that demand tweaks in particle size or solvent residues.
From direct conversations with customers, differences between this product and more generic nitropyridine diamines come up most often in reactivity, functional group tolerance, and downstream flexibility. Simple pyridine diamines can serve as amination partners or nucleophilic reagents, but they rarely offer the selectivity and protection offered by the 4-fluorobenzyl and nitro groups present in FNPD-46.
Early-stage tests with closely related structures—those missing the fluorine atom or carrying a non-nitro aromatic substituent—showed changes in coupling efficiency and downstream compatibility with modern catalyst systems. The ortho-amino groups and the electronic modulation from the nitro and fluorobenzyl substituents give this product a unique fingerprint. In actual practice, researchers see smoother desymmetrization, lower impurity profiles, and increased yields in Suzuki cross-coupling versus analogs that omit the strategic fluorination or possess unprotected functionality.
With customer projects under strict confidentiality, we track improvements through aggregate data. Regularly, teams report higher throughput and lower ‘patch-up’ purification requirements when using FNPD-46 in demanding multi-step syntheses. The difference isn’t just in the paperwork, but on the workbench, as turnaround times and waste volumes trend downward.
There’s a hands-on nature to making FNPD-46—balancing safety, control, and financial risk. Nitration reactions demand tight thermal management and careful charging, especially at larger scales. Each modification we’ve made grew out of direct observation, learning from thermal excursions, phase separation challenges, or raw material variability. Teams stay in regular contact with supply chain partners, understanding changes at the source can turn a smooth process into one filled with troubleshooting. We choose suppliers for our raw materials not just by price, but by commitment to analytical transparency and reliable shipment timing.
The route we’ve developed employs stepwise protection and controlled deprotection. That allows delivery of product uncontaminated by positional isomers—a requirement for both regulatory documentation and real downstream success. Analytical chemists and production workers review data together before release, identifying trends that slip past most automated quality management systems.
Many of the refinements we’ve introduced stem from feedback and failures—batches held back, yields below target, or delayed shipments due to analytical uncertainty. Rather than hide these setbacks, we use them to drive improvement. Switching to continuous flow for a key nitration step reduced byproduct formation and improved heat dissipation, especially important for making cleaner material at scale.
We also encountered recurring issues with solvent residues and particle morphology during the early years. Minor tweaks in crystallization temperature and solvent ratios delivered significant gains in filterability and drying efficiency. This reduced both turnaround time in our facility and residual solvent levels measured in analytical review. By investing in solvent recovery technology and integrating in-line monitors, we’ve achieved greater control over batch graduation, supporting larger and timelier campaigns for partners who operate with tight project timelines.
Real-world input drives our priorities. Inconsistent batch color or invisible impurities once confounded customers relying on manual handling and visual checks. Using UV-Vis and advanced chromatographic fingerprinting, we began flagging problems before release, building deeper confidence between us and every recipient expecting reliable material.
Producing compounds like FNPD-46 involves handling nitro intermediates and halogenated aromatics—materials that demand respect and care. Occupational safety guides every step, from raw material storage to transfer and final packaging. Process engineers work hand-in-hand with EH&S professionals to ensure systems perform beyond regulatory minimums. Temperature control on reactors, active venting, and secondary containment sit alongside mandatory worker training and PPE protocols. Continuous improvement is not just about yield and cost, but also reducing exposure risks at every point in the process.
We’ve invested in solvent recovery, energy-saving reactor jackets, and emission scrubbing. By recirculating and reusing solvent whenever possible, we cut down both environmental footprint and raw input costs—an improvement that environmental regulators and financial officers alike appreciate. Waste minimization has the added benefit of stabilizing supply, especially valuable in markets where feedstock availability can suddenly change.
Our experience as primary producers can’t be separated from our commitment to customer engagement. We find that real-world context—knowing exactly how and where a batch will be used—helps preempt issues and innovate in unexpected areas. Regular, candid discussions with formulators, scale-up chemists, and R&D directors reveal pain points that might never show up on a spec sheet. Sometimes a persistent analytical outlier or a sudden shift in impurity profile leads us to revisit incoming lots, reaction profiles, or even storage protocols.
Over the years, we’ve developed flexible packaging and delivery options tailored by volume, risk profile, and customer handling preferences. Working directly with users, not through resellers or brokers, removes layers of confusion. We take pride in troubleshooting directly, drawing on decades of combined process and analytical experience.
FNPD-46 rarely functions as a standalone chemical in an end product—it acts as a team player in complex, multi-step processes. Each process improvement broadens the possibilities for those working at the discovery edge of medicinal, agrochemical, and material sciences. Academic groups see its unique substitution pattern as a platform for developing new SAR (Structure-Activity Relationship) hypotheses. Process chemists appreciate knowing that the intermediate they receive will behave as expected and allow predictable progress from flask to pilot plant.
Companies pushing the limits on environmental persistence or biological selectivity find that well-defined intermediates like FNPD-46 save time, cut costs, and keep regulatory discussions on track. The ability to scale up with a consistent impurity profile and analytical history supports new product registration and compliance requirements, reducing risk at every stage.
In an industry crowded with options, we compete on more than price or scale. Decades spent tuning in-process controls, choosing sensors, and cross-validating analytical methods ensure every FNPD-46 shipment moves from plant to customer with full confidence. Open communication with material handlers, packagers, and transport staff further reduces the risk of product damage or contamination.
Regular updates to production protocols reflect lessons learned not just in our own facility but from the collective knowledge of the customers we serve. Our technical team regularly participates in joint troubleshooting calls and project reviews. Deep familiarity with the chemistry enables us to adapt quickly to market and research trends, supporting unforgiving timelines and strict impurity constraints.
The journey to manufacturing N2-(4-fluorobenzyl)-5-nitropyridine-2,6-diamine at scale demonstrates the importance of understanding real laboratory and process needs. Chemistry, when executed with focus and discipline, opens doors—from novel function in medicine and agriculture to the creation of advanced functional materials. Every batch reflects hard-won reliability, feedback from users pushing boundaries, and relentless attention to both chemical and practical detail. We look beyond the textbook, drawing on experience, conversation, and constant refinement to offer not just a compound, but a solution shaped by decades at the bench and in the plant. Our team stands behind the process and the product—committed to keeping quality, safety, and collaboration at the core of every shipment.