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HS Code |
925410 |
| Chemical Name | 2,3-diamino-6-methoxypyridine |
| Cas Number | 5467-74-3 |
| Molecular Formula | C6H9N3O |
| Molecular Weight | 139.16 |
| Appearance | Light yellow to brownish solid |
| Melting Point | 98-101°C |
| Solubility | Soluble in organic solvents such as ethanol and methanol |
| Smiles | COc1ccc(N)nc1N |
| Inchi | InChI=1S/C6H9N3O/c1-10-5-3-4(7)2-6(8)9-5/h2-3H,1H3,(H4,7,8,9) |
| Purity | Typically >98% |
| Storage Conditions | Store in a cool, dry place, tightly closed |
As an accredited 2,3-diamino-6-methoxypyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is supplied in a 25-gram amber glass bottle, securely sealed, with a printed label detailing "2,3-diamino-6-methoxypyridine." |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Packed in 25kg fiber drums, 8 metric tons per 20’ FCL, secured on pallets, moisture-protected. |
| Shipping | 2,3-Diamino-6-methoxypyridine is shipped in sealed, chemical-resistant containers to prevent moisture or air exposure. It is carefully packaged in accordance with hazardous materials regulations. Proper labeling, documentation, and, where necessary, accompanying Safety Data Sheets (SDS) ensure compliance during transport. Storage and transit should be in cool, dry conditions away from incompatible substances. |
| Storage | Store **2,3-diamino-6-methoxypyridine** in a cool, dry, and well-ventilated area, tightly sealed in a chemical-resistant container. Keep away from sources of ignition, moisture, and incompatible materials such as strong oxidizers and acids. Label the container clearly, and ensure proper grounding to prevent static discharge. Access should be restricted to trained personnel using appropriate personal protective equipment. |
| Shelf Life | The shelf life of 2,3-diamino-6-methoxypyridine is typically 2-3 years when stored dry, tightly sealed, and protected from light. |
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Purity 99%: 2,3-diamino-6-methoxypyridine with purity 99% is used in API intermediate synthesis, where it ensures high yield and reduced process impurities. Molecular Weight 139.15 g/mol: 2,3-diamino-6-methoxypyridine with molecular weight 139.15 g/mol is used in heterocycle synthesis, where it provides precise stoichiometric control for reproducible product formation. Melting Point 160–163°C: 2,3-diamino-6-methoxypyridine with melting point of 160–163°C is used in pharmaceutical compound formation, where it enables efficient solid-state processing. Particle Size D90 < 50 μm: 2,3-diamino-6-methoxypyridine with particle size D90 < 50 μm is used in tablet formulation, where it allows for uniform dispersion and consistent tablet integrity. Stability Temperature up to 120°C: 2,3-diamino-6-methoxypyridine with stability up to 120°C is used in high-temperature reaction protocols, where it maintains chemical integrity and reaction consistency. Viscosity Grade Low: 2,3-diamino-6-methoxypyridine with low viscosity grade is used in ink formulation, where it facilitates smooth application and even pigment distribution. Moisture Content <0.5%: 2,3-diamino-6-methoxypyridine with moisture content less than 0.5% is used in peptide coupling reactions, where it prevents hydrolytic side reactions and improves product purity. Assay ≥98%: 2,3-diamino-6-methoxypyridine with assay not less than 98% is used in dye intermediate production, where it offers consistent chromophore intensity and batch-to-batch reliability. Solubility in DMSO: 2,3-diamino-6-methoxypyridine with high solubility in DMSO is used in biochemical assay development, where it enables accurate dosing and homogeneous test environments. Chromatographic Purity HPLC ≥99%: 2,3-diamino-6-methoxypyridine with HPLC purity ≥99% is used in analytical reference standard preparation, where it ensures precise calibration and data validity. |
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In the world of fine chemicals, certain compounds stand out because they open new doors for research and manufacturing. 2,3-diamino-6-methoxypyridine has earned a place among them. Drawing from years spent pushing beakers and balancing equations, many researchers will vouch for the unique ways this molecule transforms a project. As a derivative of pyridine, it marries two amino groups and a methoxy group in a structure that both synthetic chemists and pharmaceutical innovators find more valuable than the sum of its parts.
Few chemicals can claim the same balance between versatility and specificity. This compound tends to draw attention from teams hunting for ways to accelerate synthesis or introduce specific reactivity. Adding a methoxy group at position six and amino groups at both the two and three positions brings out reactivity patterns that straight pyridine or less substituted analogs do not offer. These differences are not just a matter of chemical curiosity; they determine outcomes in synthesis, catalysis, and drug design.
On a molecular level, 2,3-diamino-6-methoxypyridine carries the formula C6H9N3O. Its crystalline nature, moderate melting point, and good solubility in polar solvents makes it easier to work with on the bench than many other substituted pyridines. One clear point from lab experience: reproducibility is often tied not just to the presence of functional groups, but to predictable physical properties. Batch-to-batch uniformity can make the difference between a successful scale-up and hours of troubleshooting. When pure, the compound shows a yellow to brown hue and a characteristically sharp odor, helping trained eyes and noses spot impurities early in the process.
Purity in this context isn’t a buzzword. Trace contaminants in pyridine derivatives can alter reactivity, render bioassays unreliable, or gum up reaction monitoring. Having worked in both academic and industrial settings, it becomes clear that rigorous HPLC and NMR testing are essential checkpoints for those handling this molecule at scale. Reliable vendors provide certificates that detail heavy metals, water content, and organic impurities — evidence that matters when costs and results hang in the balance.
What truly sets 2,3-diamino-6-methoxypyridine apart is its reach across several high-impact fields. The most immediate and visible impact appears in pharmaceutical research. Drug designers reach for this compound when they need to build complex heterocycles or introduce amino groups into aromatic systems. Its backbone supports further functionalization, leading to molecules with greater bioactivity against cancer, infection, or neurological disorders. The combination of electron-donating methoxy and two reactive amine groups unlocks routes that stall out with simpler pyridines or non-methoxylated isomers.
Besides its impact in medicinal chemistry, it plays a foundational role in material science and coordination chemistry. During the years working on functional dyes and polymer films, the unique donor properties of this molecule have proved useful for creating stronger metal-ligand complexes. The result: materials with novel magnetic or electronic properties. Not every compound brings this mix of synthetic flexibility and manageable reactivity. Tinkering with electronic devices or optical sensors, scientists see the benefit of coupling this ligand to transition metals and engineering band gaps or fluorescence profiles that would otherwise be out of reach.
In practice, teams working in agrochemicals and specialty materials also turn to this compound to construct bioactive scaffolds, stable intermediates, and molecular probes. Having a single molecule that can do the job of multiple building blocks improves efficiency and reduces project timelines. Anyone who’s assembled combinatorial libraries can appreciate the value in a versatile, robust starting material like this. Carefully designed, the molecule throws its support behind molecular diversity in a measurable way.
There is a lot of noise in the specialty chemicals market about high purity, narrow specifications, and custom blends. That said, most buyers soon notice the difference not in labels but on the bench. Take, for instance, more basic pyridine derivatives: while they offer simplicity, they lack the differentiated reactivity and fine-tuned handling profile of 2,3-diamino-6-methoxypyridine. Classics like 2,6-diaminopyridine or 3,4-diaminopyridine might find use in specific parts of a reaction sequence, but often fall short in building out complex substitution patterns with one-pot processes.
Reflecting on years of compound screening, researchers often talk about the headaches from trial-and-error with less selective pyridine analogs. A compound that avoids side reactions, tars, or hard-to-purify byproducts simply translates to fewer failed runs and reduced waste. Real-world comparisons, supported by peer-reviewed data, show that the two amines and a single methoxy group in 2,3-diamino-6-methoxypyridine push reactivity into regions left untouched by more symmetrical or unsubstituted molecules. Sizable boosts in yield, shorter reaction times, and cleaner workups aren’t just theoretical claims; they end up on the monthly performance chart.
Imagine a project focused on kinase inhibitors, a hot area in today’s pharmaceutical pipeline. Out of a panel of heterocycles, compounds built from this diamino-methoxypyridine core showed both higher potency and improved selectivity. The lesson? Choice of starting material ripples through every step — cost, safety, intellectual property, and final efficacy.
Not every supply story goes smoothly. Finding true high-purity 2,3-diamino-6-methoxypyridine can still pose problems, especially for specialty labs in smaller markets. Bulk buyers sometimes complain of long lead times, variable pricing, or paperwork tangles tied to cross-border deliveries. Proper storage becomes an issue, too. Amine groups can absorb CO2 or moisture from ambient air, giving rise to unwanted changes and complicating both storage and analytical testing. It pays to check for sealed, light-resistant packaging and a careful chain of custody, not just vendor claims of purity.
Anyone in process R&D knows what happens when a batch arrives out of spec: overnight delays, spike in overtime, extra screening protocols and, ultimately, higher costs. Companies focused on sustainable synthesis point to the need for green solvents and waste minimization, since pyridine derivatives can pose ecological risks. Many teams have already transitioned to closed systems, regular air monitoring, and planned disposal — practical strategies that not only safeguard results but protect workers and the environment.
As chemical research continues to evolve, 2,3-diamino-6-methoxypyridine stands poised to play a greater role. The structure itself attracts attention from AI-driven drug discovery, where its substitution pattern feeds into predictive models seeking new therapeutic leads. Advances in catalysis have turned to this compound for stabilizing reactive intermediates, improving turnover rates, and engineering asymmetric syntheses. Years ago, computational chemistry was barely able to model these effects — today, molecular dynamics and machine learning push discovery based on data sets built around such advanced heterocycles.
A fundamental part of its growing appeal lies in the agility it brings to synthetic planning. Instead of laboriously building up each functional group, researchers get a head start with built-in handles for further modification. This opens up options in medicinal chemistry, materials development, and chemical biology. Whether crafting next-generation enzyme inhibitors or tailoring polymer side chains, this compound serves as both raw material and inspiration. After repeated rounds of lab work, one lesson keeps returning: flexible starting materials cut complexity and spark creative problem-solving.
Handling amine-bearing pyridines brings certain safety routines. While not as hazardous as some acylating agents or organometallics, exposure to vapors calls for basic PPE — gloves, eye protection, fume hoods. Repeated contact can cause skin irritation or respiratory reactions, so well-ventilated workspaces and prudent storage practices matter as much as reliable sourcing. Labs moving toward greener protocols now seek water-based processes and tighter recovery of solvents to cut down on VOC emissions.
Disposal remains a sticking point. Waste streams from pyridine chemistry may call for dedicated incineration or professional treatment, not simple drain disposal. At my first industrial posting, regulators made clear that even low-volume users needed tracking and documentation. Audits became regular, teams updated training and tracking logs, and on-site waste segregation protocols grew stricter. This extra attention isn’t just about compliance; it helps responsible labs build trust with partners and communities.
As developers look for ways to boost productivity and innovation, evidence increasingly underscores the value of versatile heterocycles. Peer-reviewed papers, patent records, and anecdotal reports all point to 2,3-diamino-6-methoxypyridine’s distinct contribution. Compared to generic starting materials or less-challenging intermediates, it often cuts the number of synthetic steps, trims costs, and improves reproducibility. Manufacturers who invest in robust supply chains and quality assurance end up outpacing competitors stuck with variable or hard-to-source ingredients.
Academic collaborations offer especially compelling proof. Consortiums tackling antimicrobial resistance or neglected tropical diseases reach for advanced building blocks like this one; their results echo the sentiment found in every well-run kitchen — good ingredients lead to better results. Careful attention to storage, purity, and handling wins out over cut corners and false economies. More and more research teams find themselves advocating for smarter sourcing decisions and collective bargaining with suppliers to secure stable, high-quality material flows.
The network effect cannot be ignored. As more research groups publish novel synthetic methods, access to technical know-how and smarter protocols grows fast. In my own circles, exchanging notes on purification or scale-up tricks frequently makes the difference between a failed run and a headline result. Online forums, open-access journals, and conference workshops spark improvements not just in science but in procurement, safety, and workflow management. Engineers tweak reactors, QC teams introduce new verification routines, and legal teams sort out IP boundaries — all to make sure advanced building blocks keep flowing into the pipeline.
Innovation at ground level sometimes starts with a single bottle — a new grade, a new supplier, a test batch that runs smoother than expected. Users quickly realize which suppliers stand behind their promises and which cut corners. Trust is currency, one that is hard-earned and quickly lost. Many buyers turn to user-generated reviews or jointly negotiated sourcing agreements to keep standards high. This self-policing dynamic has fed directly into improved standards, clearer documentation, and a shared push for reliability in the specialty chemical market.
Every path to innovation brings obstacles. For those facing supply bottlenecks or quality issues, several proven tactics offer real relief. Stronger supplier vetting — including random batch testing and secondary sourcing — reduces the risk of sudden interruptions. Smart buyers ask for detailed batch records, QA documentation, and access to staff with real-world lab experience. In distributed teams, rotating stock and pre-ordering during slow quarters gives a buffer when delays hit.
Labs hoping to cut their ecological footprint invest in solvent recycling and closed-loop systems. These may seem niche, but the payoff shows up quickly in reduced raw material waste and lower regulatory scrutiny. Moving away from single-use plastics or non-recyclable packaging helps as well; some suppliers now ship in compostable packing or offer bulk refills to trusted customers. Experience shows that a little up-front investment in sustainable practices pays for itself, in both regulatory peace of mind and corporate reputation.
Training and documentation stand out as low-cost risk reducers. Too many incidents trace back to complacency or misunderstanding. Regularly refreshed SOPs, scenario-based drills, and clear logbooks make it less likely for small errors to escalate into major setbacks. In settings where turnover runs high, staff testimonials suggest that mentorship programs speed up onboarding and lift performance across the board. Here, the old wisdom applies: an ounce of prevention beats a pound of regret.
As research climbs new heights, expectations for quality, transparency, and collaboration only increase. Specialty chemicals like 2,3-diamino-6-methoxypyridine become more than just parts of a reaction; they serve as barometers for the maturity and interconnectedness of the chemical supply chain. Teams prepared to invest in careful sourcing, thoughtful handling, and open exchange of best practices set themselves apart. They not only achieve better technical outcomes but build resilience into projects and partnerships that stretch across countries and industries.
Looking forward, the true value of this compound will continue to grow, not just as a chemical entity, but as a signal of scientific intent and capability. As the toolbox expands, materials like 2,3-diamino-6-methoxypyridine remind researchers, engineers, and manufacturers that great science comes from a blend of curiosity, discipline, and reliable building blocks. The ongoing commitment to responsible use, quality assurance, and sustainable practices ensures that this molecule will drive progress for years to come.