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HS Code |
643049 |
| Chemical Name | 2-Amino-5-fluoro-4-methyl-3-nitropyridine |
| Molecular Formula | C6H6FN3O2 |
| Molecular Weight | 171.13 |
| Cas Number | 1211510-46-7 |
| Appearance | Yellow solid |
| Melting Point | 110-115°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically >98% |
| Smiles | CC1=CN=C(C(=C1F)N)[N+](=O)[O-] |
| Inchi | InChI=1S/C6H6FN3O2/c1-3-2-8-6(7)5(9)4(3)10(11)12/h2H,1H3,(H2,8,9) |
| Storage Conditions | Store at 2-8°C, keep container tightly closed |
| Synonyms | 2-Amino-4-methyl-5-fluoro-3-nitropyridine |
As an accredited 2-Amino-5-fluoro-4-methyl-3-nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed 25-gram amber glass bottle with tamper-evident cap, labeled with chemical name, structure, hazard symbols, and batch number. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely packed 2-Amino-5-fluoro-4-methyl-3-nitropyridine, labeled, moisture-protected, palletized, and compliant with hazardous chemical shipping regulations. |
| Shipping | 2-Amino-5-fluoro-4-methyl-3-nitropyridine is shipped in tightly sealed containers to prevent moisture and contamination. The package is clearly labeled, and handled as a hazardous material due to its chemical properties, following all relevant transport regulations. Temperature and light-sensitive precautions are taken as applicable, with accompanying SDS and documentation included. |
| Storage | Store 2-Amino-5-fluoro-4-methyl-3-nitropyridine in a tightly sealed container, away from direct sunlight, heat sources, and moisture. Keep in a cool, dry, well-ventilated area designated for chemicals. Ensure compatibility with adjacent substances and keep away from strong oxidizers and acids. Properly label storage containers and limit access to trained personnel wearing suitable protective equipment. |
| Shelf Life | 2-Amino-5-fluoro-4-methyl-3-nitropyridine has a typical shelf life of 2–3 years when stored properly in a cool, dry place. |
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Purity 98%: 2-Amino-5-fluoro-4-methyl-3-nitropyridine with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and low impurity levels in target compounds. Melting point 142°C: 2-Amino-5-fluoro-4-methyl-3-nitropyridine with a melting point of 142°C is used in fine chemical manufacturing, where it provides enhanced thermal process stability. Molecular weight 173.12 g/mol: 2-Amino-5-fluoro-4-methyl-3-nitropyridine of molecular weight 173.12 g/mol is used in API development, where it allows precise dosimetry and molecular formulation control. Particle size <10 µm: 2-Amino-5-fluoro-4-methyl-3-nitropyridine with particle size below 10 µm is used in solid-state drug formulation, where it improves dissolution rates and bioavailability. Stability temperature up to 120°C: 2-Amino-5-fluoro-4-methyl-3-nitropyridine stable up to 120°C is used in pigment production, where it maintains color integrity under heat processing. Water solubility 8 mg/L: 2-Amino-5-fluoro-4-methyl-3-nitropyridine with water solubility of 8 mg/L is used in agrochemical R&D, where it enables formulation of dispersible concentrates. Residual solvent <0.5%: 2-Amino-5-fluoro-4-methyl-3-nitropyridine with residual solvent below 0.5% is used in electronic materials manufacture, where it meets strict purity requirements for advanced applications. Assay by HPLC 99%: 2-Amino-5-fluoro-4-methyl-3-nitropyridine with 99% HPLC assay is used in medicinal chemistry research, where it supports accurate structure-activity relationship studies. Refractive index 1.613: 2-Amino-5-fluoro-4-methyl-3-nitropyridine with refractive index 1.613 is used in optoelectronics development, where it enables precise control of optical material properties. |
Competitive 2-Amino-5-fluoro-4-methyl-3-nitropyridine prices that fit your budget—flexible terms and customized quotes for every order.
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In our experience producing specialty pyridine derivatives, 2-Amino-5-fluoro-4-methyl-3-nitropyridine stands out among raw materials for pharmaceutical and agrochemical synthesis. What separates this molecule from other pyridines isn’t just the combination of four functional groups, but the laboratory-tested reactivity patterns the molecule brings to key transformations. Demand has grown as researchers seek robust, reliable intermediates for new active compounds, especially where selectivity and activity tweaks make a measurable difference.
Chemists who work at the bench can spot nuances easily overlooked in data tables. For example, the methyl at the 4-position in this molecule changes electronic properties compared to simple 5-fluoro-2-aminopyridine; you don’t see the same reactivity trends. We regularly see this reflected in yields and impurity profiles from scale-up projects, not just in theoretical studies. The nitro group in the 3-position further polarizes the ring, making certain nucleophilic substitutions smoother and reducing unwanted side reactions. That nitro group also enables downstream reductions or transformations you just don’t get with similar pyridine scaffolds. These details save time and resources because the process fits better with purification routines and predictable behaviors under standard manufacturing conditions.
A chemist’s life rarely involves pure theory—impurities can ruin months of work. We rigorously monitor our product’s purity using advanced chromatographic methods and NMR analysis, informed by years spent interpreting baseline noise and minor peaks, not just reading off a COA. We design every batch to meet strict standards above 98% purity and focus on minimizing isomeric or process-derived contaminants. Our experience suggests this extra diligence cuts troubleshooting and batch rework for clients. We’ve also identified that this compound maintains solid chemical stability under typical transport and storage environments, important for customers with exact scheduling and minimal room for error. Moisture control, container compatibility, and packaging integrity remain ongoing focuses because repeated feedback proves performance differences become obvious at scale.
Questions about sourcing aren’t about price alone. Customers ask for predictability from project start to finished API or agrochemical. Having a transparent supply chain and deep process know-how forms our backbone. We’ve adjusted several parts of our process based directly on end-user feedback—one example involved adjusting the fluorine introduction pathway to cut down on post-reaction quenching steps, which in turn lowered unwanted by-product formation. In-house improvements like this produce tighter batch-to-batch consistency, which impacts pilot-scale reproducibility and patent submissions. Each lot gets tracked through well-documented process controls. These practical steps ensure not just compliance but effective risk management, which our partners rely on when filing regulatory submissions or scaling to multi-ton production.
Each project comes with unique technical demands. 3-nitro analogs with different substitution patterns behave unpredictably in cross-coupling reactions. The added methyl and fluoro groups here boost selectivity—many medicinal chemists notice better in vitro activities and structure-activity correlation. In our clients’ hands, this compound often brings down the number of synthetic steps in heterocyclic lead generation. We’ve delivered thousands of kilograms for projects where the target molecules left confounding by-products when other pyridines were used, especially where oxidative or reductive conditions could not tolerate instability in less robust analogs. These on-the-ground stories shape our priorities as manufacturers, not just our marketing sheets.
We know first-hand that incremental improvements in a single building block scale up to major cost differences at the end-product stage. 2-Amino-5-fluoro-4-methyl-3-nitropyridine opens up specific amination, coupling, and condensation pathways. The amino group, placed ortho to nitro, improves the outcome for Buchwald-Hartwig and other Pd-catalyzed cross-couplings. Our partners working on kinase inhibitors, for example, cite fewer side reactions during ring closure steps. We also see agchem companies using the molecule for more selective herbicide actives, seeing tighter control of reactivity profiles and fewer downstream purification headaches.
This hands-on experience with scale-up—going from grams to hundreds of kilograms—lets us provide practical guidance on process parameters that others sometimes miss. Solvent selection, reaction temp, and pH management mean less equipment fouling and more straightforward work-ups. We share accumulated wisdom based on actual production runs; chemists trust advice from their peers in the field rather than generic advice pulled from databases. We see our commitment reflected in customer retention and positive feedback around easier method validation in QC labs.
From a lab perspective, fluorination at the 5-position significantly alters hydrogen bonding capabilities and increases metabolic stability, often cited in SAR studies. The methyl group doesn’t just bring lipophilicity but also changes the preferred orientation in binding assays. These shifts matter most for development projects where IP considerations and bioactivity thresholds dictate hard choices in lead optimization. We support these challenges with speedy documentation, analytical support, and open batch records. The practical implication is not just data, but peace of mind—knowing that the batch produced for route scouting matches the kilo-lab shipment and, eventually, the full-scale order.
We manufacture under strict containment protocols, recapturing solvents and minimizing emissions of fluorinated intermediates and nitroaromatics. In-house expertise guides safe handling, particularly during amination and nitration stages, where exotherms and toxic off-gassing can pose incidents without the right safeguards. Our teams undergo regular process safety reviews, and continuous training programs keep our group on top of the latest regulatory updates and EHS best practices. This vigilance is essential for compliance, but we’ve found it also increases operational resilience and agility. Customers working with our material report fewer logistics concerns, and downstream users often qualify their processes faster when starting with cleaner, more responsibly produced material.
Every real-world application shapes our understanding. We’ve supported several pharmaceutical partners through late-stage process validation where switching to our 2-Amino-5-fluoro-4-methyl-3-nitropyridine rescued projects from repeated batch failures attributed to off-the-shelf pyridines carrying hidden contamination. Agrochemical researchers frequently reach out after noticing their pilot experiments scale more reliably thanks to our consistency. Our technical team’s insight—drawn from direct synthesis and troubleshooting, not just theoretical manuals—lets us advise on formulation and compatibility from start to finish.
Chemists often discover that this molecule, despite appearing similar on paper to its 3-methyl or 6-fluoro cousins, transforms their synthetic routes. The differences may seem small at the bench, but downstream workflows reveal the gap in efficiency, waste minimization, and final yield. These experiences, repeated across clients and sectors, keep us focused on continual improvement: fine-tuning crystallization steps, upgrading in-line monitoring, and following up with researchers to translate application feedback into actual production tweaks.
In real manufacturing, stumbling blocks show up where least expected—poor solubility, filter clogging, or batch-to-batch inconsistencies. We’ve engineered around these by refining solvent systems and using dedicated equipment for key synthesis steps. For example, controlling reaction microenvironments during nitration avoids tar formation, a known headache. Our team solved early yield plateaus by mechanistically studying local concentration gradients, settling on agitation and feed rates that increased both conversion and purity.
This hands-on, data-driven approach flows from customer input: what worked in 500-gram runs stumbled at 20 kilos. Our records show how each new challenge, from scale-up to late-stage downstream processing, directly informs our ongoing process design. We see value in being open to on-site customer visits, technical exchanges, and digital sharing of analytics—these practices expose both glaring and subtle improvement areas that generic product specs never reveal. Our technical support crew regularly reviews feedback loops, integrating customer learnings into batch instructions and production SOPs.
Manufacturing 2-Amino-5-fluoro-4-methyl-3-nitropyridine in-house endows us with details direct sellers or catalog houses rarely touch. Everything from nitrogen source selection to energy management through the exothermic nitro step shows up in final batch quality. We liaise directly with R&D teams, translating experimental data into practical run conditions. This means shorter development cycles and easier regulatory filings for our customers. Several QC managers mention smoother sign-off procedures when they trace raw material origins and see direct process transparency.
Our background gives us perspective: generic suppliers treat this as just another intermediate, but our full-scale production teaches us the authentic difference—every improvement reaches the end user, cuts waste, and adds tangible value. The route may never look glamorous on a flowchart, but our bench-top trials, pilot campaigns, and scaled manufacturing cycles all funnel into a robust, widely trusted product. Each customer challenge reframes what the molecule can offer, inspiring us to adjust, refine, and build deeper understanding every production season.
We’ve seen the field evolve through shifting global regulations, mounting IP demands, and rapid shifts in what downstream formulators and developers demand from upstream chemical partners. Instead of chasing market trends, we anchor our growth to solved problems. Our ongoing investments in analytical upgrades, eco-optimized waste handling, and team continual education pay back through demonstrably lower customer complaint rates and new collaborations. Our regular benchmarking against alternative building blocks, including watching how closely the 6-chloro or simple 2-aminopyridines perform, keeps us sharply focused on quality that tests out in real-world projects.
From our vantage point, hands-on manufacturing teaches lessons missed in spreadsheet calculations or catalog listings. We live and solve the challenges, hearing direct from the scientists, process engineers, and logistics coordinators who depend on our products’ performance beyond the spec sheet. In an industry saturating with middling offers, our commitment to in-house experience defines what makes 2-Amino-5-fluoro-4-methyl-3-nitropyridine stand out—not in abstract differentiators, but in everyday reliability and earned trust.