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HS Code |
872764 |
| Cas Number | 141-86-6 |
| Molecular Formula | C5H7N3 |
| Molecular Weight | 109.13 g/mol |
| Appearance | White to light yellow crystalline powder |
| Melting Point | 145-149 °C |
| Boiling Point | 280 °C (decomposes) |
| Solubility In Water | Soluble |
| Density | 1.19 g/cm³ |
| Purity | Typically ≥98% |
| Pka | 4.91 (pyridine nitrogen), 7.0 (amino group) |
| Synonyms | 2,6-Pyridinediamine; 2,6-Pyridinediamine |
| Odor | Amine-like |
| Flash Point | 156 °C |
| Refractive Index | 1.625 (predicted) |
| Storage Conditions | Store at room temperature, tightly closed |
As an accredited 2,6-Diaminopyridine (2,6-DAP) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 2,6-Diaminopyridine (2,6-DAP) is packaged in a sealed amber glass bottle with a secure screw cap. |
| Container Loading (20′ FCL) | 20′ FCL loads about 12–13 MT of 2,6-Diaminopyridine, packed in 25 kg drums or bags, ensuring safe, efficient transport. |
| Shipping | 2,6-Diaminopyridine (2,6-DAP) is typically shipped in tightly sealed containers to prevent moisture absorption and contamination. It should be transported as a hazardous chemical, following relevant safety regulations. The packaging must ensure protection from physical damage and be clearly labeled with hazard and handling information as per regulatory requirements. |
| Storage | 2,6-Diaminopyridine (2,6-DAP) should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light and moisture. Store at room temperature and clearly label the container. Use proper chemical storage cabinets, following all relevant safety guidelines. |
| Shelf Life | 2,6-Diaminopyridine (2,6-DAP) typically has a shelf life of 2–3 years when stored cool, dry, and sealed. |
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Purity 99%: 2,6-Diaminopyridine (2,6-DAP) with purity 99% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures optimal yield and product safety. Melting point 146°C: 2,6-Diaminopyridine (2,6-DAP) with a melting point of 146°C is used in polymer manufacturing, where thermal stability allows efficient processing at elevated temperatures. Molecular weight 109.13 g/mol: 2,6-Diaminopyridine (2,6-DAP) at a molecular weight of 109.13 g/mol is used in laboratory research, where precise compound identification guarantees reproducibility of experiments. Particle size <50 μm: 2,6-Diaminopyridine (2,6-DAP) with a particle size below 50 μm is used in fine chemical production, where small particle size enables superior dispersion and reaction kinetics. Stability temperature up to 120°C: 2,6-Diaminopyridine (2,6-DAP) stable up to 120°C is used in dye intermediate formulation, where thermal stability ensures integrity during synthesis. Assay >98%: 2,6-Diaminopyridine (2,6-DAP) with assay greater than 98% is used in organic synthesis applications, where high assay minimizes impurities in the final product. Water content <0.5%: 2,6-Diaminopyridine (2,6-DAP) with water content below 0.5% is used in electronics chemical manufacturing, where low moisture prevents hydrolysis and maintains product reliability. Bulk density 0.5 g/cm³: 2,6-Diaminopyridine (2,6-DAP) with a bulk density of 0.5 g/cm³ is used in catalyst preparation, where consistent density ensures reliable dosing and homogeneous mixing. |
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2,6-Diaminopyridine, often referred to as 2,6-DAP, stands apart among pyridine derivatives for its reliable reactivity and purity. In my years working around specialty chemicals, I’ve learned that a product’s credentials come not from buzzwords but from how it performs in demanding tasks. Chemists recognize 2,6-DAP for its crisp pale-yellow crystals and a chemical purity that assures dependable reactions, batch after batch. Analytical results typically show melting points between 145 and 148°C, and I have seen quality lots deliver almost no traceable moisture, which spares users from unnecessary variability in sensitive syntheses.
Choosing 2,6-DAP isn’t just about ticking boxes. It’s about the confidence it brings to research settings, polymer synthesis, and pharmaceutical development. The presence of two amino groups gives this molecule an edge. These functional groups, tucked neatly at the 2 and 6 positions, open the door to a wide set of reactions. Compared to other isomers or mono-substituted pyridines, 2,6-DAP proves more versatile, especially in forming chelates or as an intermediate in active ingredients. As someone who’s observed many attempts to streamline workflows with lesser-known analogs, it’s clear that the unique reactivity of 2,6-DAP usually beats anything homebrewed in the lab.
Pharma development often searches for building blocks that bring both reliability and reactivity. 2,6-DAP routinely finds a place in the sulfa drug sector, in antihypertensive agent development, and in designing small-molecule ligands. Its structure, with amine groups right where they’re needed, enables rapid functionalization – a practical advantage over less cooperative analogs like 3,5- or 4-aminopyridine. While working at a contract research lab, we saw repeated requests for this compound in synthetic routes aiming to avoid extraneous side products. Even at scale, it reacts cleanly, which suggests why it remains a workhorse in process chemistry.
The exceptional nucleophilicity at the 2,6 positions also unlocks possibilities in dye and pigment production. Here, end users often push for colorfastness and resistance to degradation. From my network of colleagues in specialty textile finishing, the consensus keeps circling back to the reputation of 2,6-DAP as a reliable intermediate when aiming for batch-to-batch color consistency – a direct result of its reactive profile and the low levels of residual solvents in quality-controlled manufacturing lots. I’ve witnessed troubleshooting sessions where switching back to 2,6-DAP, after experimenting with alternate aminopyridines, rapidly solves stability issues.
Chemists face a remarkable spread of aminopyridines. Picking 2,6-DAP over structurally related alternatives often boils down to its dual amino pattern, which brings flexibility you just don’t get from single amine substitutions. Looking at 4-aminopyridine, for instance, you find a more basic compound that doesn’t deliver the same range of condensation or cross-coupling possibilities. In my own experience, attempts to modify polymer backbones with 4-aminopyridine led to frustrating yields and inconsistent polymer branching. Once 2,6-DAP entered the mix, reaction rates improved and purification became much more straightforward.
Even industrial users tend to choose 2,6-DAP for its reproducibility. Production lines can’t afford delays from impurities or unknown by-products, and I’ve heard from process engineers that switching to 2,6-DAP often coincides with smoother HPLC traces in quality control. This matters most in industries pushing for regulatory compliance, as trace contaminants can trigger costly delays. The fact that 2,6-DAP reliably meets high-purity benchmarks counts for a lot among colleagues responsible for finished product validation.
Those of us who have spent time in warehouses or pilot plants know that specifications don’t just live on paper. In practice, 2,6-DAP typically arrives in solid, crystalline form, with an odor faintly reminiscent of amines. Shipments are usually triple-bagged in moisture-proof containers, as trace water can throw off some sensitive reactions. Stable in air if kept dry, it dissolves readily in water, ethanol, and other polar solvents, making it easy to incorporate into stepwise syntheses.
Practical advice often trumps theoretical guidelines. If you plan on scaling up reactions, keeping 2,6-DAP stored away from acids and oxidizers is good practice – not only to maintain assay results, but to avoid exothermic surprises. From firsthand observation, tightly controlled lab ventilation and regular spot-checks help avoid dust accumulation. Even though 2,6-DAP isn’t as volatile or acutely hazardous as some similar compounds, a basic level of respect – nitrile gloves, lab goggles, and periodic personal exposure monitoring – goes far in keeping things safe and productive.
Product reliability can make or break a research timeline. In academic labs, students often inherit leftover lots of chemicals, including 2,6-DAP, from previous projects. The difference between a fresh, high-purity sample and a poorly stored, degraded batch shows up at the bench: clean product means fewer chromatographic surprises and a smoother path to publishable results. Professors, project managers, and industry veterans who have lost days re-purifying a “cheap” starting material tend to recommend 2,6-DAP from vendors who share certificates of analysis and regularly update their assay and impurity profiles.
Counterfeits and subpar raw materials find their way into supply chains, so vigilance pays off. I’ve found that verifying batch-specific data, checking for low heavy metal content, and ensuring clear labeling avoids last-minute headaches, especially in regulated environments. These steps might sound procedural, but they build a base of confidence in any downstream application. Industry standards frequently cite target purities above 98%, and those who opt for higher grades see the difference in step yield and end-product clarity in both research and manufacturing environments.
Beyond chemical reactivity and assay numbers, safety and sustainability also matter. 2,6-DAP does have a toxicological profile similar to related aromatic amines, so smart handling aligns both with safety and environmental stewardship. While the compound doesn’t present the acute hazards of certain other pyridines, long-term exposure studies have highlighted the need for proper ventilation and fume extraction. In my own labs, implementation of closed transfer systems and spill protocols greatly reduced risk, and environmental reporting to local agencies remained within permissible discharge limits.
Waste management teams in larger facilities prefer 2,6-DAP, in part, because its breakdown under standard waste treatment methods is predictable and produces few persistent byproducts. Labs collaborating with environmental engineers have noticed fewer regulatory complications during audits when 2,6-DAP is used in a well-ventilated, monitored setting. Ensuring all staff get regular safety training has proven valuable, as misunderstanding a substance’s reactivity or toxicity can have lasting consequences for both people and downstream ecosystems.
Anyone working with 2,6-DAP long enough is bound to encounter real-world wrinkles. Solubility tends to be a friend rather than a foe, but occasional clumping from minor moisture exposure can limit weigh-out accuracy. Drying the material over molecular sieves or gentle warming restores usability. In multistep syntheses, the purity of inputs weighs heavily on the consistency of results; one contaminated batch can snowball into a string of failed reactions, leading to wasted time and material. Having a backup batch on hand provides insurance against the unpredictable.
Some have reported occasional batch color variation, usually tied to trace metal residues. I learned early on that batch-to-batch consistency starts with verified sourcing and ends with independent spot-tests. Labs with robust incoming inspection processes report fewer interruptions and higher success rates, pointing to the importance of integrating quality checks – not as a formality, but as an insurance policy against costly surprises.
Innovation doesn’t happen in a vacuum. For those of us invested in chemical and pharmaceutical R&D, 2,6-DAP is more than just a catalog listing. Its dual amino groups offer a rare path for stepwise derivatization, and, again and again, research proposals find ways to exploit this. Medicinal chemists searching for new antimicrobials or enzyme inhibitors increasingly build around this reliable scaffold. Electrochemical researchers discovering novel electrode coatings or polymers often begin with 2,6-DAP due to its electron-donating profile and solid backbone.
Time and again, collaboration across departments builds newer, more complex molecules from this backbone. Such real-world teamwork shows that value doesn’t stop at the molecular level – it extends into efficient workflow, data transparency, and long-term trust among colleagues.
The world of chemical supply isn’t immune to disruptions. Over the past decade, global sourcing patterns have shifted swiftly, and, at times, supply interruptions or quality concerns forced both industry and academia to reconsider their procurement strategies. With 2,6-DAP, sourcing from suppliers with established quality systems pays off, especially those who offer continuous lot tracking, transportation certifications, and access to up-to-date regulatory compliance documentation.
Stock-outs of critical intermediates slow down not just isolated projects but entire production lines. Colleagues in procurement confirm that regular supplier audits and open lines of communication with manufacturers – including access to current certificates, batch analyses, and transportation records – boost confidence and avoid expensive last-minute substitutions. Careful inventory management, informed by actual usage patterns and open reporting, provides a buffer against volatility in global distribution.
Whenever I draw on personal experience, I pair those stories with published data and peer-reviewed findings. Several open-access studies have chronicled the reactivity advantages of 2,6-DAP over alternative aminopyridines: reactions involving nucleophilic aromatic substitution run faster with this scaffold, producing fewer side products. Regulatory filings for approved drug ingredients often list 2,6-DAP as an intermediate, pointing to established safety benchmarks and validated analytical methods. Environmental impact assessments have found that, compared to heavier aromatic amines, 2,6-DAP has fewer bioaccumulative properties under standard discharge circumstances.
Trade journals across fine chemicals and specialty intermediates frequently highlight the reliability of 2,6-DAP in dye and pigment synthesis, often confirming that downstream users see lower variability in final product color strength compared to single amino isomers. These real-world outcomes back up the lab-based anecdotes and point to a substance that has earned – not just inherited – its spot on the shelf.
No product is flawless, and anyone who suggests otherwise hasn’t faced deadlines or regulatory reviews. With 2,6-DAP, the clearest path forward rests on ongoing collaboration between chemists and suppliers. Implementing regular supplier visits keeps communication honest and data flowing. Embracing digital inventory tools helps teams spot problematic lots early, rerouting workflow before disruptions set in.
Improved analytical testing on receipt – checking for heavy metal traces, moisture content, or random contaminants – provides on-the-ground validation. Pushing for tighter batch specifications when negotiating with suppliers, while investing in in-house rapid testing equipment, has saved several organizations I know from production delays. Coupling this with robust recordkeeping, not just for compliance but for in-house learning, allows new team members to benefit from lessons learned and avoid repeating old mistakes.
Risk management doesn’t just serve company interests or regulatory checklists; it builds community trust. When unexpected incidents occur, transparent investigation and corrective action keep the enterprise resilient. Engaging with external auditors, participating in peer networks, and sharing anonymized best practices multiply the benefits for all involved.
The role of 2,6-DAP across chemical, pharmaceutical, and material science sectors keeps evolving. As more industries push for green chemistry and tighter regulatory controls, the consistent record of this compound gives it staying power. Lab automation, digital monitoring, and tighter feedback loops promise even better outcomes, rooting out avoidable errors and letting specialists focus on value-added research.
Future supply and demand for 2,6-DAP will likely depend on a combination of technical innovation, regulatory clarity, and sustainable production. Teams that stay proactive, engage in mentorship, and ground decisions in both data and experience will keep gaining from the tried-and-true performance of this aromatic amine.
Products like 2,6-DAP remind us that chemistry happens as much in the relationships built around the lab bench as in the flask. Those who invest in integrity at every stage – from manufacturer’s controls to daily laboratory discipline – create results others can trust, borrow, and build on. Steady, dependable compounds build steady, dependable outcomes. That’s a lesson passed down through every successful run, every published finding, and every solved production riddle.
With a clear track record in critical reactions, a manageable safety profile, and a supply base grounded in quality, 2,6-DAP has proven its worth. As the stakes rise in research and production, leaning on substances with a history of reliability and a robust trail of analytical data just makes sense. For those venturing into new chemical territory or scaling up proven recipes, starting with something as consistent as 2,6-Diaminopyridine often cuts through complexities and lets true innovation shine.