|
HS Code |
424212 |
| Chemical Name | 2,4-Diamino-6-Chloro Pyridine |
| Cas Number | 5350-41-4 |
| Molecular Formula | C5H6ClN3 |
| Molecular Weight | 143.57 g/mol |
| Appearance | Off-white to light yellow crystalline powder |
| Melting Point | 185-189 °C |
| Solubility In Water | Slightly soluble |
| Purity | Typically ≥98% |
| Storage Conditions | Store in a cool, dry, and well-ventilated place |
| Odor | Odorless |
As an accredited 2,4-Diamino-6-Chloro Pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2,4-Diamino-6-Chloro Pyridine, sealed with a screw cap and labeled with hazard warnings. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 8.5–9.5 MT packed in 25 kg fiber drums with inner polythene liner, securely palletized for export. |
| Shipping | 2,4-Diamino-6-Chloro Pyridine is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is packaged according to regulations for chemical substances, ensuring safe transport and handling. The packaging is clearly labeled with hazard information, and all shipments comply with local and international shipping regulations for laboratory chemicals. |
| Storage | 2,4-Diamino-6-Chloro Pyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat and direct sunlight. It should be kept away from incompatible substances such as strong oxidizers and acids. Appropriate chemical storage cabinets and proper labeling are recommended. Personal protective equipment (PPE) should be used when handling this chemical. |
| Shelf Life | 2,4-Diamino-6-Chloro Pyridine typically has a shelf life of 2–3 years when stored in a cool, dry, and airtight container. |
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Purity 98%: 2,4-Diamino-6-Chloro Pyridine with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency. Molecular Weight 158.59 g/mol: 2,4-Diamino-6-Chloro Pyridine at 158.59 g/mol is used in drug discovery, where precise molecular targeting enhances lead candidate optimization. Melting Point 165–168°C: 2,4-Diamino-6-Chloro Pyridine with a melting point of 165–168°C is used in tablet formulation processes, where thermal stability maintains compound efficacy during granulation. Particle Size <50 μm: 2,4-Diamino-6-Chloro Pyridine with particle size under 50 μm is used in fine chemical synthesis, where improved solubility enables faster reaction kinetics. Stability Temperature up to 120°C: 2,4-Diamino-6-Chloro Pyridine with stability up to 120°C is used in high-temperature batch reactions, where thermal resistance preserves structural integrity during processing. Water Content <0.5%: 2,4-Diamino-6-Chloro Pyridine with water content below 0.5% is used in anhydrous formulations, where low water presence minimizes unwanted hydrolysis. Assay ≥99%: 2,4-Diamino-6-Chloro Pyridine with assay ≥99% is used in active pharmaceutical ingredient (API) manufacture, where high assay facilitates dosage accuracy and regulatory compliance. Solubility in DMF: 2,4-Diamino-6-Chloro Pyridine soluble in DMF is used in organic synthesis, where solubility increases reaction efficiency and product yield. |
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It’s not every day you come across a compound that manages to stay under the radar, yet quietly shape the backbone of high-value laboratory work and industrial innovation. 2,4-Diamino-6-Chloro Pyridine (let's call it DACP) brings something different to the table with its unique chemical composition and targeted applications, standing out in the field of pyridine derivatives. DACP combines a 6-chloro and two amino groups on a pyridine ring, an arrangement that has generated strong technical interest among chemists who are eager to push boundaries in the pharmaceutical, agricultural, and specialty chemical sectors.
There’s something immediately practical about DACP. It isn’t a household name; most people won’t ever see it outside a chemistry lab. But in those circles, DACP’s role proves to be more than incidental. The compound’s molecular structure (C5H6ClN3) gives it unusual reactivity and versatility. Those in pharmaceuticals or agrochemicals recognize how a unique setup like this can spark new reactions and lead to the construction of more complex and functionally active molecules.
Many times, the advances that make life-saving drugs or improved agrochemicals possible begin with subtle modifications around a pyridine core. DACP, with its 6-Chloro position and those diamino groups at 2 and 4, offers a different reactivity pattern compared to standard mono- or di-chloro pyridines, or even simple diamino analogs. I remember working with its close molecular relatives, hoping for properties just like what DACP brings—greater selectivity, potent activity in downstream reactions, and reliable yields.
DACP isn’t some esoteric research curiosity—it’s a tool, and it brings lab practitioners tangible benefits. For starters, the typical physical presentation is as a pale crystalline powder, stable under ambient conditions, dissolving well in polar organic solvents like DMF and DMSO, and showing reasonable solubility in water when gently heated. Chemists work best with solid compounds that don’t break down or require special handling at every turn, and DACP offers that kind of stability. Purity often exceeds 98% in reputable preparations, which matters—a cleaner starting material turns into a cleaner end product.
Batch consistency shapes long-term research outcomes. Quality control teams want to see minimal color variation, low moisture content, and restricted levels of trace contaminants. DACP answers those requirements in ways better than older, less refined derivatives used in similar spaces. Having spent years running syntheses where a trace impurity shut down a whole project, I see the value in being able to trust that every bottle will perform like the last.
The central value of DACP lies in how directly it acts as a building block for more advanced molecules. Chemists in drug discovery often turn to pyridine scaffolds to anchor their synthetic schemes. Substituting a chloro and two amino groups just so, as in DACP, allows for selective substitutions, condensation reactions, or cyclizations. If you’ve ever sat at a bench, chasing a promising lead compound, you know how even a single reactive handle on a pyridine ring can open up a series of related structures. Some research groups use DACP’s amino groups to attach peptide fragments, others aim for heterocycle assembly or amide formation. The 6-chloro moiety acts as a leaving group in nucleophilic aromatic substitution, further amplifying its synthetic flexibility.
In the pharma world, new drug candidates often begin with simple, robust pieces. DACP offers a dependable entry point to ring-expanded, condensed, or fused systems—what eventually become kinase inhibitors, antibacterial leads, and CNS-active scaffolds. Just as importantly, DACP’s scale of availability fits the transition from early-stage medicinal chemistry to pilot-scale manufacturing. That step—moving from gram to kilogram quantities—is one of the toughest any research project faces, so having a reliable upstream feedstock removes a major barrier to progress.
Amino-chloro pyridines like DACP aren’t just for drug discovery. In crop protection, these compounds anchor a number of selective herbicides or fungicides. The ability to introduce further substitutions at well-defined positions makes the molecule adaptable to designing actives with the right environmental fate or mode of action. Synthetic teams focusing on pigment intermediates or specialty resins turn to DACP too—it’s a chemistry hub, not just a one-trick reagent.
People tend to lump all pyridine derivatives together, but the details matter. Many alternative products feature monosubstitution—either just a chloro or a single amino group—which limits the diversity of follow-up chemistry. Others lean on di- or trisubstituted positions like 3,5 or 2,6, which can create steric problems or less desirable regioselectivity. DACP’s arrangement at 2,4-diamino and 6-chloro unlocks tailored functionalization that just isn’t possible with simpler scaffolds.
Encore attempts to build similar intermediates from 2,6-diamino or 2,4-dichloro pyridines show that each twist of the molecule’s framework results in different reactivity and application scope. For instance, 2,4-diamino-3-chloro pyridine can be trickier to selectively functionalize without side reactions, and basic 2,6-dichloro pyridine resists nucleophilic aromatic substitution precisely where DACP excels. There’s a reason experienced chemists reach for DACP first when a target molecule requires functional diversity, strong electron-donating effects, and reliable scale-up characteristics.
In my own research, switching from monoamine or monochloro analogs to a compound set up like DACP often made the difference between a frustrating dead end and a clear, repeatable route to success. Anyone who’s lost hours chasing difficult purifications or low-yielding side products appreciates the difference a tuned reagent makes. DACP doesn’t just promise efficiency; it delivers real, practical value where it counts.
I’ve seen what happens when sourcing goes awry. Technical-grade reagents with undefined byproducts often set back entire projects—nothing is more frustrating than tracing a reaction failure back to a poorly characterized starting material. DACP, in its better commercial forms, undergoes rigorous checks for purity, trace solvent, and residual heavy metals. Analytical reports from reliable suppliers confirm structural integrity by NMR and HPLC, so research teams waste less time second-guessing their resources.
DACP stores best in tightly sealed containers at room temperature, away from direct sunlight and sources of moisture. Its crystalline nature gives it solid shelf stability, which lab managers appreciate when stocking up for ongoing projects. The compound does not emit strong odors or volatiles, so day-to-day operations avoid the extra restrictions common with more reactive halogenated pyridines.
Handling safety always comes upfront in any discussion about specialty chemicals. For DACP, common-sense PPE—lab coat, gloves, goggles—keeps direct contact at bay. The compound shows low volatility, so dust inhalation risk stays low during routine weighing or transfer. Like other pyridine derivatives, its main hazards relate to toxicity if ingested or from prolonged skin exposure, but its manageable physical properties make common lab containment procedures effective.
A responsible approach to chemistry includes keeping an eye on waste streams, potential health effects, and wider ethical concerns. DACP does not belong to major hazard categories for persistence or bioaccumulation, which gives it an advantage over many older industrial pyridines now on their way out. Even so, proper waste disposal follows strict guidelines, and material safety data provides clear handling and first aid protocols.
Industrial users often look for regulatory compliance in raw material sourcing. DACP manufactured in certified facilities meets expectations for responsible supply chains, minimizing unexpected impurities or prohibited byproducts that could put health or environmental systems at risk. For chemists in regulated industries like pharmaceuticals or crop science, traceability in raw materials ensures products hold up under the toughest inspections.
Every researcher knows the value of documentation. Suppliers who provide detailed analysis sheets and transparent audit trails not only enable better science but help teams stay on the right side of environmental safety standards. Having worked in labs that audit every incoming product, I know how much easier it is to trust and focus on innovation when the basics—like DACP quality—never need questioning.
No compound sits above criticism, and DACP faces challenges of its own. The first issue comes with scale—while access to research volumes is reliable, high-purity, multi-kilogram supply still depends on the capabilities of advanced custom synthesis firms. Smaller labs sometimes face long lead times or cost premiums, especially when global supply chains run tight. Collaborative efforts between buyers and manufacturers, backed by transparent demand forecasts, help keep projects fully supplied and prices stable.
Another concern touches on downstream process waste. Multi-step syntheses starting from complex intermediates like DACP can generate organic solvents and byproducts that need effective treatment. Forward-looking facilities address this by investing in solvent recycling systems and green chemistry protocols—some even push for catalytic processes that cut down on the number of steps and reagents required. For academic and industrial groups alike, sharing learning and analytical data across the community makes continuous improvement possible.
Health monitoring also matters. Even with low volatility and moderate toxicity, chronic exposure poses risks. Regular review of in-lab practices, supported by up-to-date safety training and access to new analytical techniques, keeps teams safer and more productive. It’s not just about checking a compliance box—creating a culture of responsibility builds trust from the bench to executive management.
Over the past couple of decades, demand for precision synthesis has only grown. The world needs new molecules for drugs that beat resistant infections, crop protectants that avoid environmental persistence, and high-tech materials with tailored electronic or optical properties. Every one of those end goals can trace its origin to smart choices in early synthetic pathways. DACP finds itself firmly rooted as one of those decisions—a stepping stone that makes complex targets possible.
Compared to more established analogs, DACP’s profile cuts a rare combination of usability, versatility, and manageable risk. New advances in catalytic chemistry and automated synthesis may yet unlock even more ways to take advantage of its reactivity. In my experience, the best chemists keep an open mind about novel pyridine derivatives—sometimes a subtle change in substitution, like that in DACP, leads to chemical “shortcuts” that would have been impossible with classic materials.
Many academic papers, patent applications, and industrial case studies document new downstream products made possible starting with DACP. Its role in developing next-generation antifungals, kinase inhibitor probes, and imaging dyes continues to expand as synthetic strategies mature. Having followed this evolution from bench projects in grad school to leadership in industry consortia, I’ve seen how small technical victories—like a better pyridine supply—create outsized impacts on innovation timelines.
Researchers, suppliers, and end users all benefit from clear communication across the chemical value chain. Open discussions about purity standards, best handling practices, and new application case studies raise the overall competency level in the field. Conferences and peer-reviewed forums increasingly include DACP-based syntheses, reflecting its rising importance in both fine chemistry and broader industrial transformations.
I’ve seen great progress come from collaborative partnerships. For example, when a university lab needs access to larger amounts of DACP for scale-up trials, partnering with specialty chemical firms or contract manufacturers helps bridge the gap between research discovery and commercial viability. Direct dialogue enables fast troubleshooting of supply or purity challenges, helping everyone stay focused on the scientific advances that matter.
Online resources also open up vital access to technical benchmarks, impurities profiles, and best practices. Industry groups maintaining up-to-date monographs and protocols surrounding DACP ensure safer, more successful chemistry regardless of user experience. My own learning curve got much easier after engaging with these knowledge networks, saving both time and frustration during difficult projects.
As research pushes towards more sustainable and precise synthesis, DACP’s relevance only increases. Labs focusing on drug discovery, green crop protection, and electronics materials consistently find value in having access to such a versatile intermediate. Researchers continue to innovate in coupling methodologies, greener reaction conditions, and automated systems that make best use of DACP’s unique substitution pattern.
Addressing challenges, such as securing consistent large-scale supply and reducing downstream environmental impact, calls for ongoing commitment from both manufacturers and users. Knowledge-sharing and cross-sector cooperation can help make DACP-based science more accessible and sustainable. My own experience suggests that progress accelerates when information moves freely—vendors supporting with full transparency, end-users providing feedback from the front lines, auditors and regulators working not just to enforce rules but to facilitate advancement.
2,4-Diamino-6-Chloro Pyridine is not just another chemical—rather, it exemplifies the kind of agile, thoughtful design that modern chemistry depends on. By enabling new synthetic directions, supporting a strong safety and quality record, and encouraging community-driven learning, DACP earns its place in any well-equipped laboratory or process scale setup. The next big breakthrough may just begin with selecting the right intermediate, and for many ambitious projects, DACP is the obvious choice.