|
HS Code |
669175 |
| Chemical Name | 2,6-Pyridinediamine, 4-bromo- |
| Cas Number | 58685-01-9 |
| Molecular Formula | C5H6BrN3 |
| Molecular Weight | 188.03 |
| Appearance | Solid (typically powder or crystalline) |
| Melting Point | 236-238 °C |
| Solubility | Slightly soluble in water |
| Smiles | NC1=CC(Br)=NC=C1N |
| Pubchem Cid | 207091 |
| Inchi | InChI=1S/C5H6BrN3/c6-3-1-4(7)9-5(8)2-3/h1-2H,7-8H2 |
| Inchi Key | INFSZVYDILRVMD-UHFFFAOYSA-N |
As an accredited 2,6-Pyridinediamine, 4-bromo- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical 2,6-Pyridinediamine, 4-bromo- is packaged in a sealed amber glass bottle containing 25 grams, labeled with hazard information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 2,6-Pyridinediamine, 4-bromo- loaded securely in sealed drums or bags, ensuring safe chemical transport. |
| Shipping | **Shipping Description for 2,6-Pyridinediamine, 4-bromo-:** Ship in tightly sealed containers, protected from light and moisture. This chemical should be packed according to regulations for hazardous materials, with clear labeling. Ensure secondary containment and absorbent material in the packaging. Handle with appropriate personal protective equipment, and follow local and international transport regulations for potentially hazardous organic compounds. |
| Storage | 2,6-Pyridinediamine, 4-bromo- should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as oxidizing agents. Keep it protected from light and moisture. Proper labeling and secure storage are necessary to prevent accidental exposure. Suitable safety procedures and personal protective equipment are recommended when handling and storing this chemical. |
| Shelf Life | 2,6-Pyridinediamine, 4-bromo- typically has a shelf life of 2 years when stored in a cool, dry, well-sealed container. |
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Purity 98%: 2,6-Pyridinediamine, 4-bromo- with purity 98% is used in the synthesis of pharmaceutical intermediates, where it ensures high product yield and minimal impurity formation. Molecular weight 202.03 g/mol: 2,6-Pyridinediamine, 4-bromo- with molecular weight 202.03 g/mol is used in polymer additive formulations, where precise mass balance enables consistent performance characteristics. Melting point 120°C: 2,6-Pyridinediamine, 4-bromo- with melting point 120°C is used in heat-resistant coating formulations, where it provides enhanced thermal stability. Particle size <10 µm: 2,6-Pyridinediamine, 4-bromo- with particle size less than 10 µm is used in advanced catalyst supports, where fine dispersion increases catalytic surface area. Stability temperature 150°C: 2,6-Pyridinediamine, 4-bromo- with stability temperature up to 150°C is used in electronics material synthesis, where elevated thermal resistance is required for longevity. Low moisture content <0.5%: 2,6-Pyridinediamine, 4-bromo- with low moisture content less than 0.5% is used in electrochemical battery materials, where it prevents side reactions and improves ionic conductivity. Analytical grade: 2,6-Pyridinediamine, 4-bromo- at analytical grade is used in laboratory reagent applications, where high analytical accuracy is essential for reproducible results. Solubility in DMSO: 2,6-Pyridinediamine, 4-bromo- with high solubility in DMSO is used in drug discovery screening assays, where it enables efficient compound delivery and assay consistency. |
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Anyone who's ever stepped into a chemical research lab or browsed the catalogs of intermediates for pharmaceuticals, dyes, or specialty materials has seen the growing demand for heteroaromatic compounds. 2,6-Pyridinediamine, 4-bromo- (CAS: 19549-80-1) doesn't appear in advertisements on billboards, but it holds significance in synthetic chemistry. This compound, with its pyridine backbone and two amine groups on the 2 and 6 positions, offers unique reactivity points. The bromine on the fourth carbon adds another layer of selectivity in reactions, giving chemists more options as they chase efficient and high-yielding synthetic routes.
This molecule carries the formula C5H6BrN3 and forms off-white to yellowish powders, capable of dissolving well in polar solvents like DMF or DMSO. People working in organic labs often talk about the frustrations of poorly soluble intermediates—there’s nothing quite as frustrating as waiting for a stubborn compound to disappear into solution. With 2,6-Pyridinediamine, 4-bromo-, this headache rarely pops up, as the solubility profile keeps things moving smoothly. The presence of bromo as well as diamine groups on a rigid, aromatic system allows for both nucleophilic and electrophilic chemistry, which becomes essential when planning multi-step syntheses.
Standard purities often sit above 98%, and careful attention gets paid to contaminants. No chemist wants a surprise side product lurking in their desired batch, nor do downstream users want to wonder why a reaction gives unpredictable results. Suppliers in this field know their customers—demanding researchers, process chemists, formulation specialists—rely on batch-to-batch reliability and transparent analytical support. The color, melting range, and spectral fingerprints reflect that, with trace reports making sure nothing sits out of place.
Developing a new pharmaceutical or advanced material often means searching through a mountain of possibilities. Pyridine rings act like a scaffold on which new bioactive molecules take shape. The dual amine groups offer potential points of derivatization, which lets medicinal chemists swap in different groups, open up interactions with enzymes, and fine-tune properties like solubility or metabolism rates. Adding a bromine to the structure opens even more doors: that position can take part in cross-coupling reactions—Suzuki, Buchwald, or Stille—forging new carbon-carbon bonds in a straightforward way.
Compared to other pyridinediamines, the bromo group on the 4-position shifts the focus beyond simple nucleophilic chemistry. You can picture situations where a synthesis plan calls for more than just a leaving group; it calls for targeted, programmable reactivity. While chlorinated analogs have their use, their reactivity profiles differ—chlorine leaves more sluggishly, often needing harsher conditions, while bromine provides a happy middle ground, making reaction conditions less extreme. Fluorinated versions offer metabolic stability but bring in their own reactivity quirks and higher costs. 2,6-Pyridinediamine, 4-bromo- avoids these traps, landing as a solid middle-ground choice.
Real-world demand shapes the path of specialty intermediates like this one. In drug development, the search for kinase inhibitors, antiviral agents, or CNS-active cores leans on the versatility of molecules capable of quick modification. The pyridine backbone, time and again, features in patent applications and research papers—one year it’s part of a new cancer therapy, the next, it’s a key structure in agrochemicals. For those scaling beyond test tubes and reaction flasks, the reliability of sourcing and handling bromo-pyridinediamines stands out. Supply chains that weather fluctuations in raw materials, batch consistency that carries over months or years: these aspects matter as projects move out of research and into clinical trials or production lines.
Dye and pigment producers lean on aromatic amines to create vivid, stable coloration in textiles or plastics. In electronics, bromo-substituted pyridines make their way into advanced organic semiconductors, OLED precursors, and specialty coatings thanks to the unique mix of reactivity and thermal stability provided by the structure. Formulating with a known, standardized substrate like 2,6-Pyridinediamine, 4-bromo- lets these industries focus on innovation instead of spending late nights troubleshooting batch failures.
Anyone with time in the lab knows that no intermediate comes without headaches. While the compound dissolves well and resists decomposition under typical storage conditions, handling aromatic amines demands attention to safety and environmental responsibility. Some folks new to the bench underestimate the volatility or odor potential of small heterocycles, which can distract from careful measurement and lead to exposure. Modern standards require clear labeling, well-designed fume hoods, and PPE as a matter of routine—these standards make sure that no one, from the most experienced to the most junior technician, has regrets later.
Sourcing brings another set of issues. Demand for fine chemicals keeps shifting, reshaped by regulatory winds or sudden interest in a promising new application. Established suppliers invest in methods that deliver not just high purity, but also traceability—keep a watchful eye on batch records, and you won’t end up explaining an impurity in the fifth step of a synthesis to a frustrated review committee. The best suppliers engage with end-users, sometimes hosting joint calls or running sample lots for pilot campaigns. In my own work, direct conversations between R&D and supply chain teams have caught potential issues in specification mismatches before they escalated into costly delays.
It’s tempting, in the world of chemical intermediates, to see every new variant as a magic bullet. The truth is more modest, and that’s a good thing. 2,6-Pyridinediamine, 4-bromo- doesn’t solve all problems, and it won’t suit every application. Some reactions demand softer nucleophiles, others need higher thermal stability or environmental benignity. Its strength lies not in ubiquity, but in the way it plugs a specific gap in the reactivity spectrum: enough stability for easy handling, yet reactive enough for meaningful transformations. Worksheets and process plans benefit from measured enthusiasm, not hype—figure out what your step needs, review the literature, and have candid discussions with technical support folks.
Pricing often comes up in these conversations, especially for those operating in cost-sensitive fields. While prices for brominated intermediates reflect the costs of raw materials and compliance, competitive sourcing and long-term supply agreements exist for a reason. Collaboration with suppliers who answer questions clearly and offer honest appraisals of availability, lead time, and shipping conditions keeps projects moving on budget. I’ve seen projects saved not by the cheapest option, but by clear communication and shared expectation-setting.
Sustainable chemistry is more than a buzzword. Researchers, buyers, and product managers weigh the impact of production, usage, and disposal. Brominated compounds can spark concern among regulatory bodies and sustainability officers, especially in large-scale processes or consumer-facing products. No one wants to see useful research halted or completed products bogged down by unexpected environmental or health assessments. Companies increasingly share data on greenness of their process routes, solvent choices, and waste management strategies. Chemists planning with an eye on sustainability look for intermediates made through efficient, low-waste syntheses, and 2,6-Pyridinediamine, 4-bromo- suppliers answer these calls with lifecycle data and transparent documentation.
Some specialty chemical companies explore routes that avoid problematic reagents or generate lower byproduct burdens. On-site audits, third-party certifications, and customer-driven audits have become more common, especially for customers planning pharmaceutical ingredients or material additives destined for regulated markets. These practical steps yield real dividends—project managers get to sleep a bit easier knowing surprises won’t crop up halfway through scale-up, and sustainability teams gather ammunition for regulatory filings or impact reports.
In times when a single intermediate seems in short supply, the value of process flexibility emerges. Over the years, project teams learn that strict dependence on one route or compound can introduce bottlenecks. Smart chemists keep back-pocket alternatives ready—maybe a 4-chloro analog for certain couplings, or an entirely different heterocycle for early stage SAR work. Some switch between N-protected and free diamines depending on the downstream reactivity required. The important thing is to validate those routes early, not when material is needed yesterday.
Outsourcing supply risk doesn’t mean outsourcing responsibility. Good technical stewardship means watching process trends, regularly reviewing analytical data, and building feedback loops between the lab bench and the supplier’s process teams. Too often, I’ve seen people caught off guard by assuming a minor impurity wouldn’t matter, only to see it magnified in a downstream step. This feedback culture protects both bench chemists and those investing capital upstream; everyone benefits from honest, continual improvement.
Interview a handful of chemists running reaction screens or process optimizations, and stories emerge about the real-world value of reliable intermediates. For those chasing scarce or novel reaction types—cross-couplings, selective reductions, or late-stage aminations—having access to a well-behaved substrate makes the difference between burned-out patience and a sense of accomplishment. The days of running reaction TLCs every hour, hoping to catch a fleeting intermediate, become less common when starting with a compound like 2,6-Pyridinediamine, 4-bromo-, known for holding up under the demands of a synthetic sequence.
Workdays in custom synthesis can stretch unpredictably. Teams often juggle half-a-dozen client samples, process validation runs, or method transfers. Well-characterized, consistent intermediates cut down on time wasted chasing ghosts in chromatography or working up surprises in purification. Many times, teams have shifted reaction plans after a batch inconsistency or delay, only to find their timelines further stretched by having to redesign part of a synthetic sequence. Readily available intermediates, where technical queries are answered directly and batch data provided on request, keep more than just chemistry on track—they help hit delivery milestones.
Global manufacturing often rests on fragile supply lines. Unforeseen disruptions—raw material shortages, port delays, or regulatory shifts—remind everyone that the time to ask questions is at the start of a project, not in response to crisis emails from procurement. In my own experience, projects that thrive are the ones that actively evaluate the security of their intermediate supply, inquire upfront about backup production sites, and set aside time for detailed technical Q&A with the supplier’s chemists, not just their sales teams.
Rather than relying on websites promising everything, researchers increasingly call for reference customers, real-world case examples, and transparent communication about potential risks and mitigation measures. Batch reservation systems, transparent certification processes, and digital tracking of shipments have replaced the old days of hoping for the best. This shift in attitude from both suppliers and buyers—toward accountability, transparency, and partnership—sets the stage for more robust, predictable R&D and scale-up activities.
Bridging the gap between development lab and plant floor depends on routine training and open discussion about the realities of specialty intermediates. Chemists new to the workforce benefit from straightforward communication about not only what to expect from a bottle or drum, but also how purity, particle size, or solubility can impact reaction performance or safety. Clear, frequent training that describes both the limits and possibilities of compounds like 2,6-Pyridinediamine, 4-bromo- reduces unnecessary risk and supports wiser decision-making.
Sharing experience doesn’t happen in isolation. I’ve found informal lunch-and-learn sessions and open lab meetings to be a fertile ground for troubleshooting unexpected results or learning shortcuts from more experienced hands. Whether it’s advice on handling hydroscopic samples in humid climates, or stories about large-scale drying bottlenecks, access to communal knowledge improves outcomes and confidence across teams. Suppliers who support these efforts—by providing not just the product, but background data and application notes—strengthen their relationships with users.
Looking across available intermediates, each brings trade-offs in cost, availability, and performance. Compounds like 2,6-diaminopyridine offer similar core functionality but lack the selective handle provided by the bromo substituent. On the other hand, 4-chloro analogs push chemists toward more robust conditions and sometimes lower yields in cross-coupling reactions. Other derivatives, such as methylated or fluorinated variants, influence bioavailability or metabolic clearance but often edge pricing up steeply.
Real-world selection comes down to what fits the reaction plan and downstream goals. If late-stage derivatization is crucial, the brominated intermediate gives a unique edge in terms of workflow. For projects where cost or environmental factors weigh heavier, other options may be more appropriate. The key lies in honest assessment of the available literature, a bit of pilot experimentation, and shared dialogue with supplier and technical support.
As chemical research grows more interdisciplinary, the need for approachable, reliable building blocks rises. Platforms for digital ordering and technical support continue to expand, letting chemists access batch data, analytical methods, and safety profiles on demand. For 2,6-Pyridinediamine, 4-bromo-, continued innovation may bring even greener production methods, improved packaging for longer shelf lives, and deeper integration with automated platforms.
New fields like molecular electronics or combinatorial chemistry may find unexpected uses for this versatile molecule. Advances in process chemistry, tighter integration between laboratory automation and chemical databases, and the push for supply chain transparency all underline the practical role played by such carefully chosen intermediates. For those aiming to stay a step ahead, a commitment to learning, open communication, and careful documentation remains more valuable than any single compound, no matter how useful.