|
HS Code |
570199 |
| Chemical Name | 2-Amino-3-nitro-5-trifluoromethylpyridine |
| Cas Number | 94467-16-6 |
| Molecular Formula | C6H4F3N3O2 |
| Molecular Weight | 207.11 |
| Appearance | Yellow to brown crystalline powder |
| Melting Point | 77-81°C |
| Solubility | Slightly soluble in water |
| Smiles | C1=CN=C(C(=C1N)[N+](=O)[O-])C(F)(F)F |
| Inchi | InChI=1S/C6H4F3N3O2/c7-6(8,9)3-1-2-4(10)5(12(13)14)11-3/h1-2H,(H2,10,11) |
| Storage Temperature | Store at room temperature |
| Purity | Typically ≥98% |
As an accredited 2-Amino-3-nitro-5-trifluoromethylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 25g amber glass bottle with a secure screw cap, labeled with safety and chemical identification details. |
| Container Loading (20′ FCL) | 20′ FCL loads 2-Amino-3-nitro-5-trifluoromethylpyridine securely in sealed drums or bags, ensuring safe, moisture-proof, bulk chemical transport. |
| Shipping | **Shipping Description for 2-Amino-3-nitro-5-trifluoromethylpyridine:** This chemical is shipped in tightly sealed containers, protected from moisture and light. It is classified as hazardous—handle with care according to local and international regulations. Ensure proper labelling, use of secondary containment, and provision of SDS documentation during shipping and handling. Avoid extreme temperatures and physical damage. |
| Storage | **2-Amino-3-nitro-5-trifluoromethylpyridine** should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Store in a cool, dry, and well-ventilated area, preferably in a chemical storage cabinet. Keep separate from incompatible substances such as strong oxidizers, acids, and bases. Follow all relevant safety protocols and ensure appropriate labeling of the storage container. |
| Shelf Life | 2-Amino-3-nitro-5-trifluoromethylpyridine has a shelf life of at least two years when stored in a cool, dry, and dark place. |
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Purity 98%: 2-Amino-3-nitro-5-trifluoromethylpyridine with a purity of 98% is used in pharmaceutical intermediate synthesis, where high purity ensures minimal side product formation. Melting point 92°C: 2-Amino-3-nitro-5-trifluoromethylpyridine with a melting point of 92°C is used in organic synthesis reactions, where predictable thermal properties support efficient processing. Molecular weight 209.1 g/mol: 2-Amino-3-nitro-5-trifluoromethylpyridine at 209.1 g/mol is used in agrochemical research, where precise molecular weight enables accurate formulation and dosage. Solubility in DMSO 50 mg/mL: 2-Amino-3-nitro-5-trifluoromethylpyridine with a DMSO solubility of 50 mg/mL is used in medicinal chemistry screening, where high solubility facilitates rapid compound evaluation. Moisture content <0.5%: 2-Amino-3-nitro-5-trifluoromethylpyridine with a moisture content below 0.5% is used in heterocyclic compound development, where low moisture prevents decomposition and preserves integrity. Chemical stability up to 120°C: 2-Amino-3-nitro-5-trifluoromethylpyridine with stability up to 120°C is used in high-temperature coupling reactions, where thermal stability ensures consistent product yields. Particle size <100 µm: 2-Amino-3-nitro-5-trifluoromethylpyridine with particle size under 100 µm is used in formulation science, where fine particle size enables uniform dispersion and increased reactivity. Appearance yellow solid: 2-Amino-3-nitro-5-trifluoromethylpyridine as a yellow solid is used in reference standard preparation, where distinct color allows for straightforward material identification. |
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Every day in our chemical production plant, we work with a range of specialized pyridine derivatives meant for intricate organic synthesis. One compound that often draws attention on our production floor is 2-Amino-3-nitro-5-trifluoromethylpyridine. Over the years, our factory teams and lab staff have become intimately familiar with its qualities, uses, and the reasons clients in pharmaceuticals, agrochemicals, and material sciences come knocking specifically for this molecule.
We call this compound by its familiar shorthand in the plant—sometimes just "AN-TFM Pyridine." Our batches run to a high standard of purity, typically not less than 98.5% by HPLC. The yellowish to light brown crystalline appearance serves as a visual indicator for our line operators, who check stability and contamination day in and out. These aren’t abstract measures; we have seen how even a minor color shift under ultraviolet examination can point to air or moisture creeping into a batch, which can throw off complex syntheses downstream.
Hydration control is a daily concern. Because trace water content can prompt degradation, our management of humidity and inert atmosphere is something every technician at our site takes seriously. Not all pyridine compounds are equally sensitive; we’ve handled many, but 2-Amino-3-nitro-5-trifluoromethylpyridine rewards diligence with greater batch uniformity and yields. The trifluoromethyl group on the pyridine ring brings both increased metabolic stability and profound electronic effects compared to many simpler analogs. As manufacturers, we’ve observed this functional group can sometimes enhance the biological activity of final products, which has given chemists in drug discovery more room to maneuver.
Since rolling out this product a decade ago, we have shipped it to laboratories pursuing a variety of objectives. Pharmaceutical researchers reach for it most often, especially during the synthesis of complex heterocyclic scaffolds. The amino group in the two-position acts as a versatile synthetic handle, opening up routes to amides, sulfonamides, and even custom ligands for metal coordination. The nitro group in the three-position also offers controlled reactivity, particularly in reduction or displacement reactions. These facts aren’t pulled from brochures—they show up every week in the reaction logs we read when clients troubleshoot a route or report an unexpected yield.
Another group of customers works in agrochemical ingredient development. Feedback from their R&D chemists consistently highlights the value of this compound’s electron-donating amino and electron-withdrawing nitro groups on the same ring. These customers tend to pursue molecules that require fine balancing of lipophilicity and metabolic robustness—the kind of tuning that the trifluoromethyl substituent is built for. Our production teams, having seen the reaction progress at every scale from pilot to commercial, recognize that AN-TFM Pyridine streamlines steps that, with other pyridines, would demand extra protection-deprotection cycles or result in unwanted byproducts.
Some of our longest-standing relationships have involved supplying research facilities where new materials for electronics are developed. 2-Amino-3-nitro-5-trifluoromethylpyridine’s rigid aromatic framework and high fluorine content serve as a starting point for building blocks in specialty polymers and OLED intermediates. These clients often request the highest purity grades, and our experience tells us any deviation in the nitro content or presence of unidentified traces can severely impact luminescence and conductivity in their final products.
People often ask what makes this molecule more valuable than a basic 2-aminopyridine or a straightforward 3-nitropyridine, both of which we also manufacture. From the perspective of our team, the answer lies in the interplay of aromatic substitution: this trifluoromethyl group changes the electronic landscape in a way that doesn’t just alter reactivity—it enables new reaction pathways. In practice, we see that derivatives tend to form more cleanly and often offer improved selectivity, especially during difficult cyclization or coupling steps.
Our chemists also point out that the combination of groups on the pyridine ring results in intermediates that don’t always require harsh conditions for further chemical modifications, which reduces side products and improves overall yield. The same trifluoromethyl group that offers synthetic advantages also imposes demands on production: specialized ventilation and scrubbing systems are essential for handling fluorine-containing residues. These aren’t textbook concerns—they show up daily in our environmental monitoring, process engineering huddles, and equipment maintenance logs.
Comparing AN-TFM Pyridine to its non-fluorinated counterparts, process reliability comes up again and again. During scale-up trials, our data shows that thermolability is less of a concern here than with certain halogenated pyridines. Customers regularly report back that this translates to fewer surprises during kilo-lab and pilot-plant campaigns.
We don’t approach quality assurance as just a checkbox. For a molecule like this, batch records are audited regularly, not only for regulatory reasons but as the only way to guarantee every drum, flask, or container leaving the plant matches the performance clients expect. High-performance liquid chromatography remains our analytical backbone, with nuclear magnetic resonance and mass spectrometry employed for lot-release as well as for customer-requested certifications. There’s no shortcut here. Over the years, we’ve adjusted our crystallization steps, solvent selection, and drying parameters to reduce the formation of colored byproducts—always a risk, especially when handling reactive nitroaromatics.
We see the importance of batch stability extending beyond shipping and storage. Outside temperature shifts during transit or a delay in customs inspection can degrade a less robust material. To address this, our packaging incorporates barrier layers and desiccants that our logistics crew checks personally as part of our release protocol. Maintaining a batch’s purity over months, not days, is where AN-TFM Pyridine demonstrates advantages—the trifluoromethyl group helps moderate hydrolysis and slow environmental breakdown.
Our inspectors track customer complaints and returns systematically. When a batch falls outside the target specification, we identify the cause at the reactor or during workup and update procedures. This discipline helps us maintain long-term supply contracts with companies that can’t risk a lab shutdown due to a minor change in a reagent as crucial as this.
A strong dialogue with customers teaches us the practical requirements for a product like AN-TFM Pyridine. More than once, chemists at top pharmaceutical firms have requested a specific crystal habit or particle size distribution to minimize static and dust during weighing. Some applications are sensitive enough that trace metal content from reaction vessels pushes a whole project off spec, so we regularly switch out glassware and employ PTFE-lined vessels for select lots.
Our familiarity with regulatory filings means we keep records of impurity profiles over years, so repeat clients can comply with their own internal documentation or international filing requirements with confidence. Those details, cross-checked across production runs, have allowed clients to pass audits smoothly.
On several occasions, our technical team has worked closely with customer R&D groups to troubleshoot solubility or scale-up obstacles. Sometimes this has led us to recommend different forms—powder versus crystalline, for instance—depending on downstream process needs. Our laboratory staff tests each lot’s melting point range as a critical control: too narrow, and there could be sublimation issues; too broad, and purity has drifted.
Our hands-on experience with the health and safety profile of this compound far surpasses what a regular data sheet can predict. The nitro and trifluoromethyl groups together mean we’ve invested in dedicated local exhaust and spill management. Staff who load product drums into shipping containers never skip over training in safe handling—not all pyridine derivatives pose similar respiratory or dermal hazards. Regular atmospheric monitoring in work areas ensures that vapor concentrations stay well below exposure limits documented in the literature.
Our environmental program focuses on capturing and neutralizing any pyridine- or nitroaromatic-laden effluents. Unlike less substituted pyridines, trifluoromethylated pyridines demand a more sophisticated waste treatment approach, often involving activated carbon and custom incineration cycles. Years of hands-on oversight prove that those steps cut hazardous emissions and protect both the workforce and the neighboring community.
We also run regular mock drills with fire brigades and emergency medical services. Experience tells us that storing and moving this compound safely requires more than labels—staff awareness and agility make changes in an emergency scenario, and we budget for those drills annually as a core part of operations.
Our procurement team keeps a pulse on global sources for the building blocks needed to produce AN-TFM Pyridine. Some precursors, including the right trifluoromethylated intermediates, go through periods of tight supply based on global fluorspar mining or shifts in specialty chemical production. Over the years, we've developed backup suppliers in several countries. These relationships didn’t come overnight; they developed through shared troubleshooting of purity and logistics snags, ensuring continuous production even during the rare supply crunch.
Shipping regulations for nitroaromatic chemicals require strict compliance, and every consignment draws on our years of documentation for smooth movement across borders. Drying agents, packaging seals, and custom labeling help minimize the risk of product contamination or regulatory detention. We’ve learned from callbacks and export delays; our in-house staff keep emergency response plans and customs documentation updated for every major destination.
Customer inventories tie directly into our delivery reliability. There are sometimes last-minute requests to expedite a consignment to avoid a lab shutdown or missed product launch, and our crew sees these situations as a normal part of the job—working overtime shifts or arranging after-hours dispatches based on real client needs, not a schedule dictated by a distant distributor.
Every month, we see new papers and patents citing 2-Amino-3-nitro-5-trifluoromethylpyridine as a reagent or intermediate in fields as diverse as kinase inhibitor synthesis, crop protection molecule development, and optoelectronic materials research. Its recurring presence isn’t an accident. The distinctive pattern of activation and deactivation on the pyridine ring means chemical transformations happen more predictably and with less effort adjusting reaction conditions.
Our technical support staff field questions daily from client project teams aiming to push downstream products past regulatory and scientific hurdles. The reliability of our manufacturing and analytics helps smooth out uncertainties for those working at the frontiers of new drugs or pesticides. We hear regularly from scientists moving quickly into animal models or pre-clinical assessment thanks to the shortcuts this compound allows in multi-step syntheses.
We have seen the learning curve for handling AN-TFM Pyridine flatten with repeat use and feedback. Our clients often identify unexpected selectivities or byproduct profiles arising from the trifluoromethyl group, adjusting routes to their benefit. The collective experience across hundreds of project cycles accumulates in our process improvements, which in turn show up the next time somebody orders ten kilos rather than ten grams.
No production campaign is without its obstacles. Controlling trace byproducts during large-scale synthesis requires constant reevaluation of mixing speeds, reagent grades, and purification sequences. We maintain an open line to our clients’ troubleshooting chemists and tracking analytical reports signals to our site managers when a procedural tweak could eliminate days of rework. Asking our veteran plant operators for insights often reveals subtle causes—overzealous drying temperatures or lagging valve seals—that can spell the difference between a pass and a reject batch.
Clients aiming for increasingly stringent purity cutoffs or compliance standards have led us to invest in updated purification systems every few years. Investments in in-line analytics and automation have paid off, letting us spot out-of-trend data before a batch gets too far along. These systems, combined with the human eye of an experienced operator, keep us ahead of the evolving demands, especially from clients seeking low ppm metal contaminants or trace fluorinated side-products documentation.
Sustainability pressures grow every year. Our engineering teams have worked to lower solvent consumption and shift to greener alternatives where possible, without sacrificing product quality. We monitor waste streams for persistent organics and partner with waste handlers specializing in halogen-rich materials. This ongoing commitment has allowed us to maintain supply relationships with firms who have to pass their own sustainability audits.
Producing 2-Amino-3-nitro-5-trifluoromethylpyridine well isn’t a one-off achievement. What matters in the manufacturer’s seat is predictability, adapting processes in light of new technological capabilities and outside feedback. Over the years, every improvement in handling, purification, or packaging has come from recognizing a recurring gap, devising a practical response, and working with clients as real partners. Our staff know the process history for each lot and can trace it back through archived process changes and analyst notes; transparency like that builds trust across the supply chain.
We don’t view this molecule through the lens of a sales pitch. It’s a product whose success rides on the skill of everyone who touches it—from operator loading raw material in the early shift, to the lab chemist drawing release samples, to the drivers assuring on-time delivery. These shared experiences and lessons learned permeate every aspect of how we make, test, and deliver this compound to researchers and manufacturers worldwide.
This hands-on reality and iterative improvement have cemented 2-Amino-3-nitro-5-trifluoromethylpyridine's reputation among high-performing pyridine derivatives. Our years behind the reactor, in the QC lab, and at loading docks shape how we see this product—not just as a chemical, but as the sum total of shared knowledge and collaborative progress.