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HS Code |
417156 |
| Chemical Name | 6-Chloro-2,3-diaminopyridine |
| Molecular Formula | C5H6ClN3 |
| Molecular Weight | 143.57 g/mol |
| Cas Number | 33278-54-7 |
| Appearance | Light yellow to beige solid |
| Melting Point | 170-174°C |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥ 98% |
| Storage Conditions | Store at room temperature, tightly closed |
| Synonyms | 6-Chloro-2,3-pyridinediamine |
| Smiles | C1=CC(=NC(=C1Cl)N)N |
| Pubchem Cid | 2724362 |
As an accredited 6-Chloro-2,3-diaminopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 6-Chloro-2,3-diaminopyridine is supplied in a 25g amber glass bottle, sealed with a screw cap and labeled with hazard information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 10 MT (packed in 200 kg net UN-approved HM-HDPE drums, securely palletized, suitable for export shipment). |
| Shipping | 6-Chloro-2,3-diaminopyridine is shipped in tightly sealed containers, protected from moisture and light. Packaging complies with relevant regulations for hazardous chemicals, with proper labeling and documentation. Transport is typically via ground or air freight, ensuring temperature control if required, and includes Material Safety Data Sheets for safe handling and emergency measures. |
| Storage | **6-Chloro-2,3-diaminopyridine** should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers. Protect from light and moisture. Store at room temperature and avoid prolonged exposure to air. Ensure proper labeling and access is restricted to trained personnel. Use appropriate personal protective equipment when handling. |
| Shelf Life | 6-Chloro-2,3-diaminopyridine typically has a shelf life of 2-3 years when stored in a cool, dry, airtight container. |
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Purity 98%: 6-Chloro-2,3-diaminopyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal impurities in the final product. Melting Point 210°C: 6-Chloro-2,3-diaminopyridine with a melting point of 210°C is used in high-temperature reaction processes, where thermal stability prevents decomposition during manufacturing. Particle Size 10 μm: 6-Chloro-2,3-diaminopyridine with a particle size of 10 μm is used in fine chemical formulations, where it allows for improved dispersion and reaction kinetics. Moisture Content ≤0.3%: 6-Chloro-2,3-diaminopyridine with moisture content ≤0.3% is used in catalyst preparation, where low water content prevents unwanted side reactions. Stability Temperature 180°C: 6-Chloro-2,3-diaminopyridine with stability up to 180°C is used in polymer modification, where it provides consistent performance under elevated processing temperatures. HPLC Assay ≥99%: 6-Chloro-2,3-diaminopyridine with HPLC assay ≥99% is used in agrochemical synthesis, where high analytical purity ensures reproducible product quality. Residual Solvent <0.1%: 6-Chloro-2,3-diaminopyridine with residual solvent below 0.1% is used in dye intermediate production, where it guarantees safe handling and regulatory compliance. Bulk Density 0.75 g/cm³: 6-Chloro-2,3-diaminopyridine with a bulk density of 0.75 g/cm³ is used in tablet formulation, where flowability enhances uniform compaction. Storage Stability 24 months: 6-Chloro-2,3-diaminopyridine with storage stability of 24 months is used in long-term inventory management, where extended shelf life reduces material wastage. Solubility in Ethanol 50 mg/mL: 6-Chloro-2,3-diaminopyridine with solubility in ethanol at 50 mg/mL is used in solution-phase synthesis, where fast dissolution accelerates processing time. |
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Anyone who has spent time around chemical labs or in pharmaceutical development understands the significance of specialty compounds. 6-Chloro-2,3-diaminopyridine belongs to that list. This compound, known by its molecular formula C5H6ClN3, plays a distinct role in today’s dynamic research landscape. The structure itself draws attention; the chlorine at the sixth position of the pyridine ring plus two amine groups creates unique properties for downstream synthesis and functionalization.
Anyone handling advanced pharmaceutical intermediates already knows: small changes in molecular structure can shift an entire process. In the case of 6-Chloro-2,3-diaminopyridine, the addition of that chlorine atom turns it into a valuable scaffold. Synthetic chemists don’t just see it on paper; they recognize it for the actual differences it brings to nucleophilic substitution, cross-coupling reactions, and beyond. Having worked with several amine-substituted pyridines, I’ve run into roadblocks when it comes to purity, solubility, and reactivity. So seeing a compound that merges easy derivatization with stable handling stands out right away.
The model or grade isn’t mere jargon. High-quality 6-Chloro-2,3-diaminopyridine offers precise purity specifications, with top-grade batches often exceeding 98% purity. Looking at it from a bench chemist’s perspective—contaminants hurt yields, cause side reactions, and spin out projects into weeks-long troubleshooting. What’s more, when tracking impurities in analytical runs, an impure batch ends up costing far more than the initial price difference. Lab teams don’t always get second chances before deadlines.
Physical properties matter in daily use. Researchers usually work with a pale to off-white solid, melting somewhere above 140°C—a handy detail if you’re scaling up a reaction and want to avoid decomposition. Solubility in polar solvents like ethanol and dimethyl sulfoxide opens doors in formulation and in biological screening. It’s no secret: most teams prefer a solid that can be weighed easily and cleaned up without extra headaches from clumping or contamination. I still remember a run-in with an older lot from another supplier, full of yellowish tints and unhelpful debris. That sort of thing erodes confidence fast.
Talk to a medicinal chemist or a material scientist and you’ll see that every tool on their bench needs to justify its place. 6-Chloro-2,3-diaminopyridine brings a versatile combination that many other pyridines simply can’t match. In my own projects, I’ve seen it take center stage in work on kinase inhibitors. The positioning of amines makes it a great intermediate for molecules that hinge on specific hydrogen bonding. That added chlorine atom gives medicinal chemistry teams an extra handle—an easy site for further transformations, such as Suzuki or Buchwald-Hartwig reactions.
Medicinal chemistry is a world of endless small modifications in pursuit of better efficacy and safety. A compound like 6-Chloro-2,3-diaminopyridine, with both electrophilic and nucleophilic handles, empowers teams to create analogs rapidly. This kind of flexibility saves costs on synthesis and shaves months off timelines for screening new entities. Teams also use it for structure-activity relationship (SAR) studies, tweaking molecular geometry to find the sweet spot for biological interactions. Having stepped through this maze of SAR cycles, I can attest that having a reliable starting point makes all the difference.
On the industrial side, those who focus on agrochemicals look to compounds like this for lead optimization in insecticides and fungicides. That same combination—a modifiable ring, positioned amines, and a reactive chlorine—opens up vast synthetic routes for fine-tuning activity and resistance profiles. Not all building blocks offer this balance of reactivity and stability. Many competitors—especially standard diaminopyridines—fail to offer the same versatility or introduce unwanted by-products in chlorination or reduction steps. As someone who’s helped troubleshoot pilot-scale syntheses, I’ve seen entire batches scrapped due to inferior starting materials.
Most labs know the cost of switching out familiar compounds. Upgrading from regular 2,3-diaminopyridine to a chloro-derivative might seem incremental, but the differences become obvious during actual runs. In terms of reactivity: adding that chlorine creates a precise site for further reactions—think Suzuki couplings or nucleophilic aromatic substitutions—where regular diaminopyridines lack that handle. This means fewer steps in route design and lower waste, something I care about deeply for both budgets and the environment.
Stability and safety also enter the picture. Some pyridine derivatives have a reputation for being volatile or break down under mild conditions. 6-Chloro-2,3-diaminopyridine stands out for a robust profile, lending itself to storage and shipping in regular lab environments. From my experience, compounds unstable at room temperature create a chain reaction of costs: extra packaging, refrigeration, and wasted time resolving degradation issues. If one can opt for a stable compound, there’s little reason to invite extra headaches.
Purity is another pain point. Cheaper alternatives may promise low cost per gram but deliver on headaches instead, from insoluble residues to embarrassing TLC streaks. Quality product brings peace of mind; yields track more closely to theoretical values, QC issues drop, and teams spend more time on development, not damage control. I’ve had teams that hesitated to upgrade, only to realize that cleaner input meant less purification and faster project turnaround. In my years organizing synthesis efforts across a range of teams, I’ve found that purity, batch consistency, and straightforward handling save hundreds of collective hours over the course of a year.
Market data points to growing demand for high-quality pyridine intermediates, especially those serving the pharmaceutical and crop protection sectors. Reports from recent years show continued investment in heterocyclic research, with over seventeen thousand patents over the last decade referencing functionalized pyridines as critical intermediates. This isn’t surprising. Trends in drug discovery keep pulling in new families of molecules that need tailored, reliable intermediates. Teams that work with mass spectrometry, HPLC, and other analytical methods value nearly invisible impurities—so the call for top-grade material only gets louder.
Regulatory trends reinforce the same message. Traceability and batch documentation must meet global standards—especially in pharma. Teams face pressure to prove every compound has a known, consistent profile. Firms that can trace purity and lot consistency across multi-kilo runs win long-term trust. It’s easier to meet those demands with intermediates produced under strong quality systems—less time lost to internal investigations or external audits. No chemist wants to explain an unexpected impurity spike to a regulatory board.
Labs and manufacturing floors have no time for delays caused by inconsistent supplies. In my own work, I’ve sent critical samples across continents, only to learn that batches from lesser-known suppliers failed purity or turned brown after a few weeks. Handling 6-Chloro-2,3-diaminopyridine from trusted sources makes supply planning easier. Quality suppliers publish analysis certificates, chromatograms, and contamination limits. This transparency helps teams compare lots and avoid redundant QC testing, which can eat up budgets quickly.
Every research lead knows the hidden cost of downtime. If a batch triggers regulatory red flags or fails repeat steps, recovery is painful. Over time, working with intermediates like 6-Chloro-2,3-diaminopyridine that trace back to trusted vendors reduces friction. Large manufacturers take this seriously. Their lot tracking, impurity profiling, and post-shipping support all work to build resilience against the types of problems that slow down product development.
There's also environmental impact to consider. Green chemistry principles favor intermediates that avoid wasteful side reactions, cut out hazardous reagents, and allow for easy handling. The structure of 6-Chloro-2,3-diaminopyridine lends itself to clean conversions, whether forming amide, urea, or new aryl derivatives. Having followed the increasing regulatory push for sustainability metrics, I know project leaders value building blocks that create less solvent load and require milder workup conditions.
Standing at the frontier of synthetic chemistry, one quickly realizes that real productivity comes from reliable building blocks that behave as predicted. Cut corners on intermediates, and every subsequent reaction inherits those flaws. 6-Chloro-2,3-diaminopyridine consistently proves itself as a dependable, modifiable core. I’ve worked on process development teams—very few compounds rival the combination of reactivity and stability it brings. It’s no secret in the medicinal chemistry community: successful teams stack the deck in their favor with strong fundamentals, and that begins with solid starting materials.
Project managers and chemistry directors routinely ask, “Is the supply chain bulletproof?” Picking a standardized, high-purity intermediate answers a whole series of questions before they’re asked. Years ago, I watched a small biotech lose momentum due to repeated inconsistencies in their heterocycle intermediates. Switching to a trusted source of 6-Chloro-2,3-diaminopyridine cut their risk sharply—QC headaches all but vanished, logs became easier to reconcile, and collaboration across continents went smoothly.
The role of this compound stands out not just in how it reacts, but how it cultivates reliability throughout the project lifecycle. Anyone budgeting for late-stage trials, regulatory filings, or global rollouts pays sharp attention to the risk profile of each ingredient. 6-Chloro-2,3-diaminopyridine merits that attention not only for its contribution in the synthetic path but for the way it slashes hidden costs, builds quality at each step, and unlocks future flexibility in analog development.
Looking out at trends in medicinal and materials chemistry, there’s no sign of slowing demand for problem-solving intermediates like this one. Every year brings new screening targets and molecular classes. The adaptability of 6-Chloro-2,3-diaminopyridine serves researchers eager to pivot between target classes without swapping out core intermediates or retraining staff on new protocols. From scaled pilot batches for up-and-coming therapies to minute analytical samples for cutting-edge disease models, the same properties that built its reputation keep driving its relevance.
It’s important to credit the teams working behind the scenes—quality chemistry rarely happens in isolation. Each synthetic chemist, QC technician, and procurement specialist acts as a vital link, ensuring every gram poured meets its project’s demands. The story of 6-Chloro-2,3-diaminopyridine is really the story of how small structural innovations echo through the entire field, driving progress, reliability, and trust at every stage from benchtop experiment to marketed product.
Having steered dozens of development cycles—and watched how single weak points can stall progress—I look to proven intermediates like 6-Chloro-2,3-diaminopyridine as keys to reliability and confidence. It stands as a prime example of how advanced design, precise manufacturing, and steady supply form the backbone of top-tier research and industry. Far more than a catalog entry, this compound makes itself known by the reliability and innovation it supports—every successful project owes much to the quiet competence of quality intermediates under the hood.