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HS Code |
181193 |
| Chemical Name | 2-Amino-6-nitropyridine |
| Cas Number | 4348-60-7 |
| Molecular Formula | C5H5N3O2 |
| Molecular Weight | 139.11 |
| Appearance | Yellow to orange crystalline powder |
| Purity | 97% |
| Melting Point | 163-166°C |
| Solubility | Slightly soluble in water |
| Smiles | C1=CC(=NC(=C1N)[N+](=O)[O-]) |
| Synonyms | 6-Nitro-2-aminopyridine |
| Storage Temperature | Store at 2-8°C |
| Ec Number | 222-437-8 |
As an accredited 2-Amino-6-nitropyridine97% factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2-Amino-6-nitropyridine 97% is packaged in a 25-gram amber glass bottle, sealed for moisture and light protection. |
| Container Loading (20′ FCL) | 20′ FCL container loading: 2-Amino-6-nitropyridine 97% packed in drums or bags, palletized, and securely stowed for safe transport. |
| Shipping | 2-Amino-6-nitropyridine (97%) is shipped securely in tightly sealed containers, protected from moisture, light, and incompatible materials. The packaging complies with safety and regulatory standards to prevent leaks or contamination. The shipment is clearly labeled with hazard and handling instructions, and is transported under conditions specified by chemical safety regulations. |
| Storage | **2-Amino-6-nitropyridine (97%)** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from heat, light, and sources of ignition. Avoid moisture and incompatible materials such as strong oxidizing agents. Keep container tightly closed when not in use, and store under recommended temperature conditions indicated by the supplier, typically at room temperature. |
| Shelf Life | Shelf life of **2-Amino-6-nitropyridine 97%** is typically 2–3 years when stored tightly sealed in a cool, dry place. |
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Purity 97%: 2-Amino-6-nitropyridine97% with purity 97% is used in pharmaceutical intermediate synthesis, where high purity ensures reproducible reaction yields. Melting Point 159–162°C: 2-Amino-6-nitropyridine97% with a melting point of 159–162°C is used in organic chemistry reactions, where thermal stability prevents decomposition during processes. Molecular Weight 139.11 g/mol: 2-Amino-6-nitropyridine97% with molecular weight 139.11 g/mol is used in heterocyclic compound development, where precise dosing enhances product consistency. Particle Size < 100 µm: 2-Amino-6-nitropyridine97% with particle size less than 100 µm is used in fine chemical manufacturing, where uniform dispersion improves product homogeneity. Stability Temperature up to 80°C: 2-Amino-6-nitropyridine97% stable up to 80°C is used in dye precursor synthesis, where heat resistance ensures reliability during processing. Water Content < 0.5%: 2-Amino-6-nitropyridine97% with water content less than 0.5% is used in moisture-sensitive reactions, where low water level prevents unwanted side reactions. Solubility in Ethanol: 2-Amino-6-nitropyridine97% soluble in ethanol is used in solution-phase synthesis, where high solubility enables efficient mixing and reaction rates. Chemical Stability up to 12 Months: 2-Amino-6-nitropyridine97% with chemical stability up to 12 months is used in laboratory storage, where long shelf life allows prolonged usability. |
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The complexities of chemical research often come down to the right building blocks. 2-Amino-6-nitropyridine 97% is drawing the attention of chemists not only because of its purity but also due to its adaptability in a wide range of applications. As someone who's navigated the challenges of compound selection in organic synthesis and materials science, I’ve learned that the source and specification of a chemical has ripple effects on experimental outcomes. For colleagues working on advanced heterocyclic compound synthesis or drug discovery, this molecule offers serious advantages that can’t be overlooked.
Let's get technical for a moment. 2-Amino-6-nitropyridine is a pyridine derivative, featuring both amino and nitro groups positioned on the aromatic ring. This structure opens doors for modifications at multiple points, making the compound well-suited for creating new analogues in medicinal chemistry and functional materials. The 97% purity, confirmed by chromatographic analysis, signals reliable quality. Many research goals demand materials where impurities have been kept to a minimum, otherwise, results can show unwanted noise or mislead with inconsistent data.
Having worked in labs where results depended on small variations in chemical purity, I noticed consistent success when using compounds like this one. Trace impurities can interfere with coupling reactions or side-chain modifications. If you need confidence in your data or reproducibility in your synthesis, then purity cannot become an afterthought. 2-Amino-6-nitropyridine 97% manages to strike a solid balance between performance and cost, sitting above technical grades that might only reach the low 90 percentile but without the prohibitive price tag of ultra-high grades that go far beyond most project needs.
There’s no substitute for experience when it comes to finding molecules that work well as intermediates. In the lab, I watched teams use 2-Amino-6-nitropyridine during the syntheses of both pharmaceutical compounds and complex dyes. The amino group, sitting next to the nitrogen in the ring, is reactive enough to allow for diverse derivatizations, while the nitro group supports further chemical manipulation, such as reduction to an amino group or substitution reactions. This kind of flexibility is valuable because it reduces the time spent sourcing and testing dozens of similar compounds.
In pharmaceutical research, this compound often forms the backbone for more elaborate target molecules. The ability to introduce modifications at the 2- and 6-positions facilitates quick analog development. For academics and industrial chemists tackling structure-activity relationships, this means less bottleneck in the production process. In my experience, projects move faster when starting materials like 2-Amino-6-nitropyridine are readily available at a predictable purity.
Dye and pigment synthesis also benefits. The electron-rich nature of the amino group, combined with the electron-withdrawing nitro moiety, creates opportunities for advanced chromophore construction. These chemical features often affect optical properties, leading to materials with specific absorption and emission characteristics—something crucial for anyone designing photosensitive devices or fluorescent labels. Reliable batches with 97% purity help ensure the color outcomes remain consistent, batch after batch.
Chemical synthesis is unforgiving when it comes to quality. Over the course of several years in both industry and academic settings, I saw firsthand how minute contaminants—from dust in the lab to side-products in reagents—could derail entire experiments. With fine chemicals, purity sets the tone for what’s possible in downstream use. At 97%, 2-Amino-6-nitropyridine keeps impurity levels low enough that side-reactions remain rare. Higher grade materials may seem attractive, but in most scenarios, the small incremental gain in purity doesn't justify the additional strain on budgets.
This is more than just a matter of precision. Reproducibility forms the backbone of published results and patent applications alike. Too many times, researchers have tried to repeat the synthesis of a known molecule, only to discover that a slight impurity in the starting material sent yields plummeting or created an unanticipated byproduct. With an option like this, which provides high purity without going overboard, there is room to focus on core scientific work instead of chasing down sources of variability.
There are plenty of pyridine analogues on the market. Some lack functional groups in key positions, while others carry similar substitutions but at different ring locations. 2-Amino-6-nitropyridine offers a combination that feels tailored for the exploratory mindset of chemists and researchers who want both reactivity and selectivity. The 6-nitro and 2-amino pattern is less common than the 3- or 4-substituted variants, so it fills a gap many standard commercial compounds tend to leave open.
In the past, I’ve run into issues sourcing these less mainstream substitution patterns, often having to make them from scratch or pay exorbitant prices for very small batches. There’s now less need to sacrifice time or funding, since a reliable 97% grade is widely available in quantities that match experimental and scale-up work. For anyone who remembers the hassle of chasing after rare chemicals or dealing with cryptic supplier paperwork, this offers some relief and extra efficiency.
Safety remains a constant concern, even for those with decades behind the bench. 2-Amino-6-nitropyridine 97% should be handled with the same attention as other nitroaromatics and amines. My own lab routine involves wearing gloves and eye protection, and I make sure ventilation is more than an afterthought. The dry powder has a habit of becoming airborne, which underlines the need for careful transfer and labeling.
This attention to handling isn’t based on excessive caution. Cases of skin or respiratory irritation have been reported with many aromatic amines and nitro compounds, and the yellow hue of the powder serves as a visual reminder not to skip basic precautions. Having solid training in chemical hygiene isn’t just about avoiding problems; it supports a cleaner, safer, and more reliable research environment. In my experience, taking the extra few minutes up front saves days lost to accident investigations or wasted material.
Tracking down a steady supplier for advanced intermediates like 2-Amino-6-nitropyridine used to be a headache. Prices and purity grades fluctuated wildly from batch to batch. Inconsistent suppliers made it difficult to plan experiments or budget departmental funds. With more established, quality-focused suppliers, I see less concern about fluctuating specifications or paperwork snags. Certificates of analysis and third-party validation reports now come as standard, so you get clarity about what’s actually going into your reaction vessels.
Chemists are pragmatic. Cost, quality, and reliability all matter, especially in research environments where every delay translates to lost time and missed opportunities. Having a dependable source means less stress about failed reactions due to out-of-spec material. It also means cleaner documentation for regulatory reviews or patent drafting—a point that’s come up more than once in my career when questions about chemical provenance appeared at the least convenient moment.
2-Amino-6-nitropyridine 97% is not just for small-scale academic explorations. Larger pharmaceutical companies and industrial outfits have found value in using it during early lead development as well as scale-up of promising candidates. The molecular layout is optimal for creating new analogues of known drugs or for assembling stepwise syntheses where managing reactivity at each step becomes non-negotiable.
Processes that work at the gram scale in university settings can stumble during pilot plant expansion if raw materials shift in purity or granular quality. Using a consistently pure grade, without splurging on overkill, minimizes translation issues between small flask synthesis and batch reactors. As someone who’s worked alongside both process chemists and scale-up engineers, I witnessed firsthand how reliable intermediates smooth the transition from idea to reality, keeping costs down and timelines on track.
Today’s chemistry landscape cares about more than just what happens inside the reaction flask. Environmental impact and safety have become primary considerations, with many organizations reviewing every chemical used under the microscope of sustainability and hazard minimization. Choosing a compound like 2-Amino-6-nitropyridine 97% with a clear analytical pedigree helps teams comply with regulatory standards for trace metals, solvents, and known impurities.
Regulatory documentation matters. I’ve been through audits where auditors cared little for the color of a powder but scrutinized where it came from, how pure it was, and what potential contaminants existed. Documented sources and regular independent analysis reassure inspectors and clear the road for grant compliance or commercial product registration. For groups seeking FDA or EMA approval—or simply aiming to publish reproducible results—these factors matter as much as the synthetic route itself.
Troubleshooting experimental failures can consume entire weeks, especially when the culprit turns out to be something with the starting materials. Using a high-purity intermediate almost always reduces the uncertainty. There’s satisfaction in spending more time on design or mechanism and less on fruitless detective work, a lesson learned after chasing down the causes of unexpected spectral data.
My habit of holding back some starting material for future checks has paid off. With 2-Amino-6-nitropyridine 97%, chromatography or NMR runs rarely show surprises. Uncharacterized peaks cause less confusion, making it easier to pinpoint problems in the route or process. A clear, consistent starting material also opens the way for collaboration across labs or with external partners, as it lowers the chance of miscommunication about what’s in the vial.
Trends in drug development and material science fuel the search for new heterocyclic compounds. Many of the top-selling pharmaceuticals trace their roots back to modified pyridines. Analogs of 2-Amino-6-nitropyridine are providing fresh hope in areas like kinase inhibition, anti-infective design, and smart material synthesis. Having an accessible supply of this building block lets smaller labs compete with larger counterparts and fosters an environment where new ideas get a fighting chance.
In collaborative research projects, quick access to high-purity reagents can make or break proposals. Colleagues mention how delays in sourcing core intermediates set back entire grant cycles. 2-Amino-6-nitropyridine 97% is increasingly featuring in project wish lists, especially for teams investigating new platforms in catalysis, imaging probes, and environmental testing kits. This isn’t just a nod to utility—it’s an acknowledgment that time saved in procurement gets reinvested in discovery.
In a tight funding climate, every dollar counts. Overbuying on purity can drain resources, while cutting corners often comes back to haunt projects with unreliable or irreproducible results. I’ve been in budget meetings where the debate over $100 per bottle could determine the fate of a whole research initiative. 2-Amino-6-nitropyridine 97% tends to fit nicely into these discussions, offering evidence of quality without requiring special justification.
Researchers are no strangers to grant reporting or the need to demonstrate impact. Being able to show that every purchase supports clarity and replicability adds weight to spending decisions. With this compound, teams meet both financial targets and scientific expectations, rather than sacrificing one at the expense of another. The middle ground here makes sense, backed up by years of practical experience—especially for labs juggling multiple projects or sharing resources across groups.
There’s always room for better analytical data and advanced packaging. Some suppliers now include additional impurity breakdowns or offer custom lot analysis at request. It saves time during method development and supports regulatory submissions. I’ve appreciated tamper-evident bottles and extra lot validation, especially in teaching labs where chain of custody needs to be as clear as the synthetic scheme itself.
Waste reduction and greener chemistry are becoming major drivers for both corporate and academic buying choices. Better packaging options—like recyclable or reduced-plastic containers—would add further value to products like 2-Amino-6-nitropyridine 97%. Even small steps, such as packaging in the ideal batch sizes to cut down on leftover material, help keep labs efficient and environmentally responsible.
Direct communication between research teams and suppliers remains crucial for overcoming bottlenecks. I found it valuable to ask for updated analytical data or recommendations for storage and transport directly from technical representatives. This open line of contact prevents mishaps, such as using an older lot that degraded during shipping. Regular audits of stock rooms and clear labeling also stave off problems that crop up when bottles are misidentified or used past their shelf life.
Collaboration tools and better digital inventory systems can aid in tracking consumables. Integrations with chemical management software allow rapid checks of expiration dates, safety records, and prior use history. For compounds like 2-Amino-6-nitropyridine, being systematic about record-keeping means fewer surprises down the line. My advice to new labs is to document not only where and when the chemical was purchased, but also its precise grade and use case in experiments—a habit that’s borne out during audits or troubleshooting.
Education and training make the ultimate difference. Workshops or onboarding sessions focused on handling aromatic amines and nitro compounds keep colleagues safe and procedures up to code. Incorporating these compounds into safe chemical management plans ensures everyone, from students to senior researchers, gets the most out of their purchases without cutting corners. As the market shifts toward demanding more transparency in quality and handling, these habits only grow more important.
2-Amino-6-nitropyridine 97% has earned a solid spot in research settings that value flexibility, consistency, and reasonable cost. By supporting precise analog synthesis, streamlining troubleshooting, and mitigating common sources of experimental variance, it enables scientific teams to focus on discovery rather than detective work. As demands in research and regulation continue to grow, having a reliable, well-documented supply chain will remain central to both productivity and peace of mind in the lab. For those building tomorrow’s breakthroughs today, the right chemical building blocks make all the difference—a lesson reinforced with every experiment that goes right the first time.