|
HS Code |
417819 |
| Chemicalname | 2-Amino-6-Methyl-5-Nitropyridine |
| Molecularformula | C6H7N3O2 |
| Molecularweight | 153.14 g/mol |
| Casnumber | 1835-53-4 |
| Appearance | Yellow to orange crystalline powder |
| Meltingpoint | 180-183°C |
| Solubility | Slightly soluble in water; soluble in organic solvents like ethanol and DMSO |
| Purity | Typically ≥98% |
| Storageconditions | Store at room temperature, in a tightly closed container, away from light and moisture |
| Synonyms | 2-Amino-6-methyl-5-nitropyridine; 6-Methyl-5-nitro-2-aminopyridine |
| Hazardstatements | May cause irritation to skin, eyes, and respiratory tract |
| Ecnumber | 217-408-8 |
As an accredited 2-Amino-6-Methyl-5-Nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2-Amino-6-Methyl-5-Nitropyridine, sealed with a screw cap and tamper-evident label. |
| Shipping | 2-Amino-6-Methyl-5-Nitropyridine is shipped in tightly sealed containers, protected from moisture and light. It should be packaged according to applicable regulations for hazardous chemicals, including appropriate labeling. Shipping is typically via ground or air, with documentation ensuring compliance with transport and safety guidelines for potentially harmful or irritant substances. |
| Storage | 2-Amino-6-Methyl-5-Nitropyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from direct sunlight and moisture. Properly label the container, and store it in a designated chemical storage area, preferably in a flammable materials cabinet. |
Applications of 2-Amino-6-Methyl-5-Nitropyridine in Industrial Manufacturing2-Amino-6-methyl-5-nitropyridine serves as a core intermediate across multiple chemical synthesis platforms, particularly in pharmaceutical, pigment, agrochemical, and specialty fine chemical industries. As a direct manufacturer, we supply this compound with consistent purity required for demanding downstream applications, supporting precisely controlled integration into critical production stages. 1. Pharmaceutical Intermediates for Antiviral Drug SynthesisThis compound acts as a foundational building block in the multi-step synthesis of select antiviral agents, functioning as a nucleophilic pyridine source for advanced heterocyclic frameworks. It enters the route during key condensation and cyclization steps, where controlled addition ensures the integrity of active pharmaceutical ingredient (API) backbones. Downstream, its reactivity with halogenating, acylating, or coupling reagents enables the introduction of target moieties, positioning the intermediate for GMP-validated purification and formulation into finished APIs. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Pigment Intermediate for High-Performance Yellow Organic PigmentsThis pyridine derivative plays a critical role in synthesizing yellow azo and quinophthalone pigments. Manufacturers routinely subject it to diazotization and coupling reactions, introducing functional groups essential for pigment chromophore formation. Strict reaction monitoring optimizes hue, brightness, and resistance properties, achieving pigment standards for plastics, coatings, and ink systems where lightfastness and chemical resistance are essential. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Advanced Agrochemical Synthesis for Pyridine-based HerbicidesOur material enables downstream synthesis of substituted pyridine herbicides, where, after activation, it participates in selective nitration and alkylation to produce active molecules for crop protection. Accurate formulation and controlled thermal processing are required, since excessive temperature can degrade precursor integrity. This ensures regulators can trace and verify the intermediates against safety and environmental criteria for large-scale field use. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Fine Chemical Synthesis for Electronic Materials PrecursorsElectronics industry partners use this compound as a synthesizing node for nitrogen-containing heterocycles, which serve in specialty electronic and optoelectronic applications. It functions during condensation and functionalization steps, promoting the development of charge-transport materials or photoactive layers. Its purity and reactivity under anhydrous conditions support molecular engineering processes that demand tight batch-to-batch consistency for device integration. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2-Amino-6-Methyl-5-Nitropyridine prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
From our work on the production line, 2-Amino-6-Methyl-5-Nitropyridine stands out among pyridine derivatives. On paper, the name looks long and somewhat intimidating, but in the reactor and in the hands of chemists, its real value comes through. Stepping into the plant each morning, the scent of organics hangs in the air, and the hum of vessels signals progress. Over the years, we have learned that not every substituted pyridine can withstand the demands of large-scale synthesis, variable temperature controls, or batch-to-batch reliability. This compound—known among the team by its shorthand, AMNP—has proven to be a workhorse, especially for those aiming for efficiency without compromise.
Consistency in quality doesn’t happen by chance. In our facility, tight control over batch parameters, starting material sourcing, and solvent selection ensures that every kilogram of 2-Amino-6-Methyl-5-Nitropyridine keeps to its specification target: a pure yellow-to-light amber crystalline powder, moisture kept low by careful drying, melting in a consistent and expected temperature range, and HPLC purity in the high nineties. Every production run brings the opportunity to fine-tune techniques—right down to how we dry the compound following crystallization, or how we monitor and control trace impurities.
Early in our production of substituted pyridines, purity would vary, and off-notes sometimes crept in. The analytical team at our plant could always spot a deviation, even before chromatograms confirmed it. Lessons learned on the line led to more rigorous handling of raw materials, thorough solvent distillation, and routine filter changes. Few outsiders appreciate just how much effort and careful planning it takes to achieve a bright, free-flowing batch, free of brownish flaws or sticky residues. Over time, we’ve dialed in our technique to reduce residual solvents and side-products far beyond the minimum standards many labs are willing to accept.
2-Amino-6-Methyl-5-Nitropyridine carries both an electron-donating amino group and an electron-withdrawing nitro group at strategic positions on the pyridine ring. That unique configuration makes it useful in synthesis, where subtle changes in substituents can make or break a downstream reaction. Unlike its cousin, 2-amino-5-nitropyridine, the methyl group on the sixth position tilts reactivity just enough to set it apart whenever a customer pushes the boundaries of heterocyclic chemistry.
In our experience, research labs and manufacturers choose AMNP as a starting point for creating novel pharmacophores, agrochemical actives, and specialty dyes. Customers have told us that they see defects in final products if small impurities in starting materials slip through. Time and time again, we’ve found that process consistency—no unexplained spikes in byproducts, no odd melting points—lays the foundation for success in subsequent steps like coupling reactions, cyclizations, and substitutions. AMNP’s well-defined reactivity stems from the deliberate way in which we design our process: we limit exposure to high temperatures, maintain vacuum conditions to avoid degradation, and use modern purification techniques instead of shortcuts.
In our company, we refer to AMNP with an internal model code that ties back to the precise production route we use. Over countless cycles, we have sifted through different approaches—one-pot methods, staged nitration with careful monitoring, and plant-wide efforts to minimize waste. The result: a lot-to-lot consistency on core parameters. The typical batch leaves the plant with purity verified above 98%, and less than 0.5% combined impurities, including trace pyridine isomers and any residual solvents. The compound melts between 140–146 °C, and the moisture content falls below 0.5%, measured via Karl Fischer titration on every final packout.
Those numbers come from hands-on experience, not just an idealized spec sheet created to look good for procurement. If a batch shows even a hint of deviation, our process experts trace the issue to its source before anything leaves the drum room. We’ve seen how a single off-spec batch can cause headaches down the entire value chain—yield loss, reprocessing, and even regulatory headaches. That discipline stems not from fear of rejection but from pride in the craft of manufacturing itself.
Most of the calls we get about 2-Amino-6-Methyl-5-Nitropyridine involve big questions—what solvent works best, how to handle scaling, how to ensure consistent yield in multi-step syntheses. Our technical team doesn’t take these lightly. Many users have ambitious targets for drug substance intermediates and specialty chemicals, and small process hiccups can bring years of work to a standstill.
In medicinal chemistry, 2-Amino-6-Methyl-5-Nitropyridine acts as a critical synthon for certain antitumor and antiviral leads. Pairing the amino group’s nucleophilicity with the nitro group’s activation potential, chemists can pull off transformations that might otherwise require multiple steps or riskier routes. The methyl group increases lipophilicity for applications where membrane permeability matters. For people developing new chemical entities, these small differences sometimes decide which candidate reaches the next development milestone.
Agrochemical research also turns to AMNP for constructing novel heterocyclic scaffolds with targeted activity on pests or weeds. Strong, stable intermediates let formulators work with confidence: fewer side-products during downstream coupling, and high stability during storage, which makes a big difference on the purchasing side. For pigment and dye synthesis, our partners in industry report that our AMNP delivers more reproducible results batch over batch, leading to tighter shade control and reduced waste.
After years of hands-on production, it’s clear that just selling molecules is not enough. Teams come to us for reliable supply, honest answers about product behavior, troubleshooting, and advice on getting reactions to work at scale without unwanted surprises. That trust comes from years spent understanding not just the chemistry but what really happens in application labs and large reactors.
One frequent customer, working on a new line of nitrogen heterocycles, reported that slight color changes in the AMNP from another supplier led to product variability, which set back timelines and prompted costly reruns. After switching to our production batches and cooperating on application support, they saw improved reaction yields and a significant reduction in downstream purification steps. Their story isn’t unique—it echoes what we hear from scale-up groups looking for less troubleshooting and more predictability.
The world of substituted pyridines can appear crowded, but years in manufacturing show real differences emerge through small adjustments in molecular structure. Take 2-amino-5-nitropyridine, a close relative. Missing the methyl group shifts its reactivity during electrophilic substitutions and can limit its usefulness in select ligand or pharmaceutical applications. Our synthesis of the 6-methyl variant consistently demonstrates a higher tolerance for downstream reductive or oxidative steps, and better yields during nitro reductions—this saves users time and cuts down on lost product.
Another distinction lies in physical handling. Some lower-grade analogs of 2-amino-6-methyl-5-nitropyridine offered by secondary suppliers arrive agglomerated, off-color, or hygroscopic, resulting in uneven dosing or variable reactivity. Through investments in precision drying equipment and real-time dust handling, we turn out batches that deliver the right blendability and stability for automated reactor dosing or manual weighing alike.
Our facility learned early that cheap shortcuts—taking a less rigorous purification route, skipping careful endpoint checking—cause downstream headaches for customers. Some products on the market meet only minimum assay requirements, but inconsistencies in minor impurity profiles can haunt a process days or weeks later.
We work alongside teams in the pharmaceutical, agricultural, and advanced materials sectors. In those jobs, time means everything, and a bad batch sets off a chain reaction—delays, increased costs, even the risk of missing critical regulatory filings. Knowing this, we center our approach around transparency and technical support at every stage.
For early-stage users developing a compound library, we offer guidance on solvent compatibility and suggest purification strategies based on what our own team has found works best. Industrial partners scaling up a lead candidate lean on us for advice on storage, optimal dissolution rates, and impurity monitoring. Every day brings fresh challenges—unexpected solubility problems or questions over how a trace byproduct will affect downstream crystallization. We take these discussions seriously, updating production documentation, tweaking batch production parameters, and feeding those improvements back into our process.
Compliance is not just about checking boxes, but about responsible stewardship. Ingredient traceability, solvent recycling, and consistent documentation ensure that users downstream can meet their own internal and external requirements. We work to keep our product traceable all the way from raw material intake to packaged delivery, providing transparency on every analytical certificate.
Environmental processes have evolved. Five years ago, our plant generated more high-strength waste streams, but continual investments in solvent recovery and catalytic treatment plants have paid dividends. Not only do we reduce our own footprint, but cleaner processes mean lower levels of problematic residuals carried into the final product. Every improvement made here reflects directly on the likelihood of smoother regulatory filings and avoids complications during audits.
No chemist wants to hear that the material they need for an urgent synthesis has run out, or will only arrive after weeks of delay. During recent supply chain disruptions, our team saw the value of maintaining safety stock, logistical agility, and honest communication about batch timelines. It isn’t enough to rely on paperwork and forecasts—real resilience grows out of hands-on management, redundant planning, and frequent communication with users.
A few years ago, a regional shortage of nitro reagents rippled through the sector. We worked closely with regular customers to prioritize allotments, avoid allocation crises, and schedule shipments to best fit genuine demand. These are moments that test the credibility of any manufacturer and reinforce the need for honest, realistic estimates—not just in production lead-time, but also in addressing potential bottlenecks or changes in transport regulation. Our policy has always been to inform partners clearly and adapt quickly, drawing on both modern tools and a commitment to direct engagement.
The chemistry doesn’t stand still, nor should our methods. With input from our own team, customers, and field research, we refine everything—handling methods, monitoring, and bulk packing solutions. We integrate new analytical techniques, from high-throughput chromatography to in-line particle size monitoring, reducing out-of-spec risk even further. Our specialists routinely take the extra step, whether that means spending the night monitoring a tricky crystallization or dissecting trace impurity peaks until they find the root cause.
Feedback matters. After one round of product improvements, a pharma customer told us they cut synthesis time by several hours, cutting costs and boosting throughput. Success in this business relies on tight feedback loops and a willingness to invest in better tools and processes—allowing us to anticipate rather than just react to common customer needs.
Running day-to-day operations reveals that customer needs rarely fit neatly into standard boxes or rigid lead-time charts. Development schedules change, new impurity limits appear from regulatory bodies, and cheaper production methods constantly emerge. Our team’s strength lies in staying open to feedback, constantly updating our know-how, and applying it practically to real-world issues.
From time to time, a user runs into solubility hiccups, minor discoloration, or questions on how AMNP will behave under new process conditions. These are everyday challenges, and our technical dialogue aims for practical fixes grounded in repeatable plant experience, not textbook theory or guesswork.
Real reliability grows not from marketing, but from evidence—consistent outputs, batch after batch, and hands-on engagement with real-world chemistry problems. Many customers expect suppliers to simply fill orders. In contrast, we view each shipment as a demonstration of the discipline, technical care, and customer partnership that define better chemistry manufacturing.
Years of working directly with synthetic chemists, plant engineers, and QC specialists have taught us to value straightforwardness. Our experience with 2-Amino-6-Methyl-5-Nitropyridine demonstrates that small details in sourcing, process design, and analytical rigor translate directly to downstream benefits—higher yields, fewer complaints, and smoother project timelines.
For anyone seeking to push the boundaries of heterocyclic chemistry, develop new pharmaceuticals, or build dependable specialty chemicals, we believe our way of manufacturing this key intermediate matters. Commitment to process control, transparency, and direct technical engagement lies at the core of every batch we deliver—and that makes a real difference where it counts most: in the lab, in the plant, and ultimately in the finished product.