2-Amino-4,6-dichloropyridine

    • Product Name: 2-Amino-4,6-dichloropyridine
    • Chemical Name (IUPAC): 2-amino-4,6-dichloropyridine
    • CAS No.: 19798-49-3
    • Chemical Formula: C5H4Cl2N2
    • Form/Physical State: Crystalline powder
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    212860

    Product Name 2-Amino-4,6-dichloropyridine
    Cas Number 22236-27-9
    Molecular Formula C5H4Cl2N2
    Molecular Weight 163.01
    Appearance Light yellow to brown crystalline powder
    Melting Point 111-115°C
    Density 1.56 g/cm³ (estimated)
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Smiles C1=CC(=NC(=C1Cl)N)Cl
    Synonyms 2-Amino-4,6-dichloro-pyridine
    Storage Temperature Store at room temperature

    As an accredited 2-Amino-4,6-dichloropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100-gram amber glass bottle with a tightly sealed screw cap, labeled "2-Amino-4,6-dichloropyridine," including hazard and handling information.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 2-Amino-4,6-dichloropyridine: Securely packed, 16–18 MT per 20’ FCL, in 25kg fiber drums or bags.
    Shipping 2-Amino-4,6-dichloropyridine is shipped in tightly sealed containers to prevent moisture and contamination. The chemical should be handled and transported according to local regulations for hazardous materials, typically under ambient temperature and with adequate labeling. Ensure the package is protected from physical damage, and consult the Safety Data Sheet for detailed handling and emergency instructions.
    Storage 2-Amino-4,6-dichloropyridine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of moisture, heat, and incompatible substances such as strong oxidizers. It should be kept out of direct sunlight, in a dedicated chemical storage cabinet, and handled with appropriate personal protective equipment to avoid exposure.
    Shelf Life 2-Amino-4,6-dichloropyridine shelf life is typically 2-3 years when stored in a cool, dry, tightly sealed container.
    Application of 2-Amino-4,6-dichloropyridine

    Purity 98%: 2-Amino-4,6-dichloropyridine with purity 98% is used in pharmaceutical intermediate synthesis, where high-purity levels ensure minimal side reactions.

    Melting Point 175°C: 2-Amino-4,6-dichloropyridine with a melting point of 175°C is used in heterocyclic compound preparation, where thermal stability enables precise reaction control.

    Particle Size <50 µm: 2-Amino-4,6-dichloropyridine with particle size less than 50 µm is used in fine chemical formulations, where small particle size promotes rapid dissolution and uniform mixing.

    Moisture Content <0.5%: 2-Amino-4,6-dichloropyridine with moisture content below 0.5% is used in agrochemical synthesis, where low moisture enhances shelf-life and prevents undesirable hydrolysis.

    Stability Temperature up to 100°C: 2-Amino-4,6-dichloropyridine with stability up to 100°C is used in dye manufacturing processes, where temperature resistance maintains pigment integrity.

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    Certification & Compliance
    More Introduction

    2-Amino-4,6-dichloropyridine: An Insider’s Perspective on a Trusted Pyridine Derivative

    Taking a Closer Look at 2-Amino-4,6-dichloropyridine

    Anyone who’s spent time in a chemical lab knows the range of compounds available for research and development can feel overwhelming. 2-Amino-4,6-dichloropyridine (often shortened to 2A46DCP among experienced chemists) stands out for its unique position among pyridine derivatives. Years spent handling specialty chemicals taught me the value of pinpointing compounds that deliver both consistency and adaptability. This molecule shows particular promise when reliable pyridine modifications matter.

    Examining Structure and Formulation

    2-Amino-4,6-dichloropyridine falls within the family of halogenated pyridines, bearing both an amino group at position 2 and chlorine atoms at positions 4 and 6 on the pyridine ring. The molecular formula, C5H4Cl2N2, places it near the compact end of this group. In practical terms, these small changes in structure can have a large impact on how chemists use it. The addition of chlorines increases stability and directs subsequent reactions, while the amino group expands the range of modifications and downstream applications.

    Products like 2A46DCP come as pale, sometimes off-white crystalline powders. In my lab, I’ve found the consistency of its granule size handy for weighing and solution preparation, leaving behind fewer surprises in yield or solubility. High purity versions hit upwards of 98%, which means far fewer side reactions and a cleaner baseline for developing synthetic procedures. Impurity levels—those trace bits that can spell trouble in research—tend to be tightly controlled by reputable suppliers, and that’s something anyone handling reactions with tight tolerances can appreciate.

    Why Chemists Reach for 2-Amino-4,6-dichloropyridine

    Over the years, I’ve seen first-hand how this compound earned its place in research labs and production lines. It acts as a potent building block for synthesizing active pharmaceutical ingredients and agrochemical products. The electron-withdrawing chlorines sharpen the ring’s reactivity, funneling reactions toward specific positions and giving synthetic chemists clear advantages in multi-step sequences. I’ve been involved in optimizing routes for specialty antifungals; 2A46DCP made challenging couplings manageable. Researchers found its behavior predictable, reducing the time spent troubleshooting failed reactions.

    Beyond pharmaceuticals, it’s found roles in dye synthesis and as a key intermediate for developing performance polymers. The flexibility of the amino group opens doors to modifications—replacing or transforming it depending on downstream goals. Few other pyridine derivatives deliver the same balance between chemical reactivity and control. Projects involving new heterocyclic scaffolds for electronic devices or sensor materials frequently tap into the unique reactivity profile this compound offers, as it streamlines the attachment of side chains or functional groups.

    How 2-Amino-4,6-dichloropyridine Stands Apart

    Experience handling other halogenated pyridines shows some are notorious for side reactions or instability under heat or light. 2A46DCP by contrast delivers a solid profile—its crystalline nature resists clumping, which I’ve found supports long-term storage and easier weighing. Pyrophoric hazards, a familiar concern in related chemicals, are much lower. This reduces the need for elaborate containment or frequent waste disposal, shaving hours off regular maintenance schedules in a high-throughput research setup.

    Stacking it side by side with simpler molecules like 2-chloropyridine or 4,6-dichloropyridine uncovers its value. Adding the amino group not only increases its range for follow-up reactions, but also lowers activation barriers for certain key reactions, notably those used in Suzuki and Buchwald-Hartwig couplings. Making the leap from more basic pyridines often means getting superior selectivity and an improved safety profile. That comes through not just from technical literature, but also in the day-to-day running of an R&D site, where wasted resources and failed runs have real financial impacts.

    Balancing Safety, Handling, and Environmental Impact

    Safe handling always stays on my mind, especially with halogenated compounds. 2-Amino-4,6-dichloropyridine’s toxicity sits well-below the more infamous dichlorinated aromatics. Following good chemical hygiene—wearing gloves, working in a ventilated hood, double-checking waste labels—has proven more than sufficient. Over the years, we’ve swapped it into workflows in place of more toxic or volatile reagents, cutting back on health risks without sacrificing output.

    Maintaining integrity in long-term storage relies on keeping this product dry and sealed away from direct sunlight. Both are straightforward, especially since its powder form resists humidity better than hygroscopic salts I’ve had to fight in other projects. For me, the reduction in unexpected decomposition cuts back on waste, unnecessary disposal costs, and reordering delays—problems that plagued older research workflows dependent on more fragile analogs.

    Disposal remains a consideration, as chlorinated compounds can run afoul of stricter environmental regulations. The predictability of 2A46DCP’s byproducts translates into a more routine waste handling process. Our in-house review found that switching to it trimmed down the variety of special waste streams, making compliance with lab safety and environmental rules less burdensome. This tight control stands in sharp contrast to my early-career experience, where multiple pyridine derivatives routinely triggered hazardous waste alarms with each new procedure.

    Real-World Application: From Lab Bench to Commercial Pipeline

    Colleagues in medicinal chemistry often highlight this compound’s utility in early-stage drug discovery. Its dual chlorine groups mark it as a versatile platform, letting teams staple on different side groups to chase new leads without reworking entire synthetic routes. Compound screening sets can be expanded rapidly, a tactic now standard in lead optimization campaigns.

    Process chemists in commercial plants often face the challenge of scaling up reactions that worked in the lab. I’ve witnessed 2A46DCP hold steady from gram to multi-kilogram batches, an attribute that can’t be overstated. Robustness on scale-up cuts not just technical headaches but also staggers costs in validation and regulatory paperwork, especially for pharmaceutical or agrochemical approvals.

    Polymer researchers also found it fit for building blocks in specialty plastics, with its reactivity fine-tuned through N-alkylation or acylation reactions. This flexibility enables the introduction of desired properties—rigidity, flame resistance, electrical conductivity—without returning to the drawing board for each new requirement. Over time, such reliability becomes invaluable, especially when timelines run tight during product development cycles.

    A Look at Sourcing and Supply Chain

    Reliable sourcing matters. Over the years, inconsistent supply quality and batch-to-batch variability annoyed plenty of my colleagues. With 2A46DCP, established suppliers offer transparent certification and clear impurity data—saving time that might otherwise go into redundant quality testing. Most of my positive experiences have come from suppliers who maintain close ties with academic consortia or industry groups, building trust through consistent documentation and stable batch purity.

    Regional manufacturing can sometimes shift the quality bar. Facilities with track records for environmental compliance, known safety training, and strong internal audits set themselves apart in the eyes of buyers. For our group, evaluating documentation for each delivery helps maintain standards set by larger regulatory bodies. Inconsistent flavor, odor, or color usually flags deviation quickly—reducing the risk of costly downstream mistakes. Any drop in initial sample quality often points to shortcuts on the supplier’s end, not inherent problems with the compound itself.

    Lasting Lessons from Years of Use

    Mid-way through my career, I watched early attempts to swap in cheaper pyridine alternatives backfire. The route looked cost-effective on paper, but produced unpredictable yields and headaches with purification. Returning to 2A46DCP restored reliability, as it matched published reactivity and handled downstream processing without extra steps. Experience taught me that paying upfront for high-purity intermediates often means bigger savings later from reduced troubleshooting and waste.

    Troubleshooting runs with inconsistent end-product often reveals the root cause: subpar intermediates. Purity checks on incoming 2A46DCP quickly confirm or rule out quality concerns, so resources aren’t wasted chasing phantom contaminants. Over time, our internal tracking showed distinctly fewer batch failures and clean scale-up transitions on projects centered around this compound. These are the sorts of real-world gains that get lost in standard technical sheets—and the ones that actually make the difference for day-to-day operations.

    Science in Practice: Building Knowledge, Supporting Innovation

    Researchers value this compound not just for its spec sheet, but for the reliability it brings when exploring new chemical territory. Building out new molecular scaffolds takes time, resources, and trust in core reagents. The real magic of 2A46DCP doesn’t lie in abstract descriptors, but in how it enables teams to dream up, build, and refine emergent molecules without taking on unnecessary technical risk. That freedom to innovate, grounded in consistent reagent quality, keeps countless projects alive that might otherwise falter under more temperamental compounds.

    Innovation in industries ranging from pharmaceuticals to electronic materials depends on shortcuts that don’t compromise downstream goals. My time in technology scouting highlighted that quick pivots in research direction require chemical tools that respond in predictable, repeatable ways. Relying on this compound in combinatorial chemistry, scaffold hopping, and route optimization let teams iterate quickly—bringing promising results to the decision point without bogging down in rework.

    The Bigger Picture: Responsible Chemistry in the Modern World

    Mainstream chemical production faces growing scrutiny for health, safety, and environmental risks. Stakeholders—from lab staff to regulators—now weigh not just synthetic performance but also the full profile of reagents. 2-Amino-4,6-dichloropyridine slots into this landscape as a compound where routine use brings fewer surprises and less regulatory friction. Lab teams can focus energy on inventive work rather than troubleshooting unpredictable hazards.

    Skeptics sometimes question whether “tried and true” intermediates like this one should keep their prominent spot in research pipelines. Flashy new reagents often show up, promising superior selectivity or greener credentials. Yet, long-term evidence from the bench keeps showing that performance stability, clear quality documentation, and well-understood handling protocols make the real difference. Replacing stable workhorses with unproven alternatives can undermine both research progress and operational safety.

    Moving Forward: Matching User Needs to Chemical Tools

    Looking back on projects that ran smoothly, the common thread has been robust intermediates like 2A46DCP. As calls for greener, safer, and more efficient chemistry grow louder, the next phase will likely focus on further minimizing synthetic waste, energy use, and human exposure. Ongoing work in solvent minimization, effluent recycling, and “design for degradation” all benefit from stable core building blocks.

    Communities of practice—professional networks, trade associations, university consortia—fuel continuous improvement by sharing hard-won lessons about reagents and workflows. Many push for transparent supplier audits, cross-lab verification of published data, and expanding digital databases of chemical performance records. Those support structures help end-users, new and experienced, avoid pitfalls and build confidence in their choices. 2A46DCP has remained a reliable reference point as that knowledge ecosystem expands.

    Focusing on Problem-Solving, Not Hype

    It’s tempting in a field driven by novelty to chase the next big thing. Still, my labs—and the broader community—have repeatedly come back to building blocks like 2-Amino-4,6-dichloropyridine for problem-solving. Not every challenge calls for a radical new compound. More often, established intermediates with deep technical documentation and a predictable performance profile keep both research and commercial synthesis on track.

    Supporting sustainable and pragmatic chemistry means backing molecules that support current needs and future ambitions. Whether developing a new drug lead, formulating high-performance dyes, or building advanced polymers, the unique balance of reactivity and reliability in this compound paves the way for innovation with fewer surprises.

    Shaping Tomorrow’s Research Landscape

    As regulatory frameworks tighten and expectations grow for responsible chemical sourcing, future choices in specialty reagents will lean ever more toward compounds with track records like 2A46DCP. That confidence stems not just from technical performance, but from supplier transparency, sustainable sourcing, and robust safety protocols. Teams looking to thrive in tomorrow’s market can learn from years of accumulated experience. Selecting intermediates with proven value clears space for risk-taking where it matters—in inventiveness, not in reliability.