4-Chloro-2,6-diaminopyridine

    • Product Name: 4-Chloro-2,6-diaminopyridine
    • Chemical Name (IUPAC): 4-chloropyridine-2,6-diamine
    • CAS No.: 156-83-2
    • Chemical Formula: C5H6ClN3
    • Form/Physical State: Solid
    • 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

    363696

    Chemicalname 4-Chloro-2,6-diaminopyridine
    Molecularformula C5H6ClN3
    Molecularweight 143.58 g/mol
    Casnumber 156-83-2
    Appearance Off-white to light brown solid
    Meltingpoint 215-218 °C
    Solubility Soluble in water and most polar organic solvents
    Purity Typically ≥98%
    Iupacname 4-chloropyridine-2,6-diamine
    Smiles NC1=CC(Cl)=NC(N)=C1
    Synonyms 4-Chloro-2,6-pyridinediamine
    Storageconditions Store at room temperature, tightly closed, in a dry place

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

    Packing & Storage
    Packing A tightly sealed amber glass bottle containing 25 grams of 4-Chloro-2,6-diaminopyridine, labeled with safety warnings and chemical details.
    Container Loading (20′ FCL) 20′ FCL: Approximately **16 metric tons** of 4-Chloro-2,6-diaminopyridine, packed in **25 kg fiber drums**, loaded securely for export.
    Shipping 4-Chloro-2,6-diaminopyridine is shipped in tightly sealed containers, protected from moisture and light. It should be handled as a potentially hazardous chemical, following all safety regulations. Transport complies with local and international hazardous materials guidelines, utilizing appropriate labeling and documentation to ensure safe delivery and handling during shipping and storage.
    Storage **4-Chloro-2,6-diaminopyridine** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Keep it away from sources of ignition and direct sunlight. Store at room temperature and avoid moisture. Proper labeling and secondary containment are recommended to prevent accidental release or contamination.
    Shelf Life 4-Chloro-2,6-diaminopyridine is stable under recommended storage conditions; typical shelf life is 2–3 years in tightly sealed containers.
    Application of 4-Chloro-2,6-diaminopyridine

    Purity 98%: 4-Chloro-2,6-diaminopyridine with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield reactions and minimal byproduct formation.

    Melting Point 180°C: 4-Chloro-2,6-diaminopyridine with a melting point of 180°C is used in organic synthesis applications, where stable processing at elevated temperatures is required.

    Particle Size <50 µm: 4-Chloro-2,6-diaminopyridine with a particle size less than 50 µm is used in catalyst preparation, where it promotes uniform dispersion and improved catalytic activity.

    Moisture Content <0.2%: 4-Chloro-2,6-diaminopyridine with a moisture content below 0.2% is used in the manufacture of fine chemicals, where it prevents hydrolytic degradation of sensitive compounds.

    Stability Temperature 120°C: 4-Chloro-2,6-diaminopyridine stable up to 120°C is used in polymer additive production, where thermal stability supports consistent product performance during processing.

    Assay 99%: 4-Chloro-2,6-diaminopyridine with an assay of 99% is used in custom chemical synthesis, where high assay ensures reliable and reproducible product quality.

    Solubility in DMSO: 4-Chloro-2,6-diaminopyridine soluble in DMSO is used in medicinal chemistry research, where enhanced solubility accelerates reaction rates and compound screening.

    Low Heavy Metal Content: 4-Chloro-2,6-diaminopyridine with low heavy metal content is used in API manufacturing, where reduced impurity levels meet stringent regulatory requirements.

    Reactivity Index High: 4-Chloro-2,6-diaminopyridine with a high reactivity index is used in heterocyclic compound synthesis, where efficient coupling reactions increase throughput.

    UV Absorbance 260 nm: 4-Chloro-2,6-diaminopyridine with UV absorbance at 260 nm is used in analytical method development, where reliable detection facilitates quality control testing.

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    Certification & Compliance
    More Introduction

    Understanding 4-Chloro-2,6-diaminopyridine: More Than Just Chemistry

    Within the landscape of fine chemicals, 4-Chloro-2,6-diaminopyridine keeps showing up in conversations among those who work in pharmaceuticals, diagnostics, and the growing arena of specialty chemicals. Plenty of substances aim to fill similar roles, but this compound, with its unique structure and reactivity, really takes on tasks that others struggle with. Anyone who has spent time working at a bench knows that the details—such as purity, stability, and reliable sourcing—can change a project’s outcome. This rings especially true for intermediates like this, where even small differences shift the final result, whether you’re scaling up to a pilot plant or running a routine synthesis in the lab.

    Model and Specifications: Navigating Choices

    In practical terms, 4-Chloro-2,6-diaminopyridine doesn’t come with many marketing gimmicks. Its structure—the pyridine ring carrying a chlorine at the 4-position and amines at positions 2 and 6—puts it apart from plain diaminopyridines or mono-chlorinated analogs. Several suppliers do offer variations, most often differentiated by assay levels, moisture content, and specific packaging options. I’ve seen analytical tests confirm it at over 98% purity for pharma use, sometimes creeping toward 99.5% or better in high-end batches. Some manufacturers also run tighter controls for heavy metals and residual solvents, recognizing the regulatory drive in sectors like drug manufacturing.

    Like in other fine chemicals, specifications matter for more than regulatory compliance; anyone synthesizing active molecules counts on a feedstock that won’t bring along unexpected byproducts. Moisture can make a real mess during subsequent reactions, and leftover organic impurities have a knack for showing up right at the final isolation step, often causing panic during quality checks. Companies paying close attention to these specs manage to avoid project delays and headaches further down the line.

    Where 4-Chloro-2,6-diaminopyridine Finds Its Value

    I’ve talked with scientists who rely on this compound for very particular synthetic routes, especially in the pharmaceutical sector. Its chlorine group opens a gateway for further functionalization without needing complicated protecting group strategies. Medicinal chemists and process teams use that versatility to spin out a whole library of molecules, aiming for better activity or improved delivery characteristics. Some of the more interesting stories I’ve heard come from groups working on kinase inhibitors, where subtle tweaks to pyridine rings make or break a promising lead compound.

    Beyond small molecule drug discovery, the amine groups on 2 and 6 positions let this compound act as a platform for dye intermediates and diagnostic contrast agents. The in-lab reality is that these amino functions can be dialed up or kept restrained, depending on what downstream chemistry needs. A researcher I know spent months tweaking his coupling steps, and 4-Chloro-2,6-diaminopyridine’s predictability saved him headaches—it just worked as advertised, which isn’t something to take for granted if you’ve ever fought with stubborn side reactions.

    Regulatory demands are another real-world consideration. Pharmaceutical companies operate under heavy scrutiny and face detailed audits from bodies like the FDA and EMA. Sourcing intermediates with full traceability, validated analytical data, and robust supply chains makes the difference between smooth launches and projects trapped in limbo. 4-Chloro-2,6-diaminopyridine suppliers who meet these demands separate themselves from generic, less-documented alternatives. In a world where a single off-spec shipment can slow or halt manufacturing, partnerships depend on transparency and consistency.

    Navigating the Differences from Related Products

    Plenty of pyridine derivatives float around the catalogs of chemical suppliers. Some have only amine groups, others offer halogen substitutions in different positions, and a few adjust both. The exact placement of functional groups on the ring controls reactivity, solubility, and biological properties—in my experience, this translates directly into whether a project advances or stalls. Take 2,6-diaminopyridine without the chlorine: it can serve in producing dyes or complex ligands, but lacks the reactivity that comes with a halogen you can swap through nucleophilic substitution. On the flip side, mono-chloro-pyridines don’t offer the same entry path to diverse heterocycles that two amines provide.

    This balance makes 4-Chloro-2,6-diaminopyridine stand out. In our lab, we once compared reactivity side-by-side with similar structures. It consistently proved more versatile in multi-step syntheses, letting us skip troublesome protection and deprotection runs. Studies in peer-reviewed journals echo this, highlighting efficient transformations into bioactive compounds and marked increases in yield compared to simpler pyridine derivatives.

    Cost and availability also vary between closely related chemicals. Demand driven by pharma, agrochemicals, and the electronics industry usually keeps this one stocked at reasonable prices, though niche markets sometimes run into supply hiccups. When that happens, users sometimes substitute less ideal compounds, which can introduce fresh problems in both chemistry and compliance. Long-term relationships with trusted suppliers help mitigate these risks, and a few global players have earned reputations for responsive logistics, reliable analysis, and clear documentation.

    Challenges and Issues: Lessons Learned from the Bench

    Using specialized intermediates brings both opportunity and challenge. On one hand, 4-Chloro-2,6-diaminopyridine lets chemists explore new chemical space without excessive synthesis steps. On the other, inconsistency in quality or supply causes real setbacks. I’ve worked on projects where differences in crystallinity, batch-to-batch color, or even subtle odor signals revealed underlying impurities. Downstream, these glitches introduced troubleshooting sessions that chewed up time and money.

    Documentation gaps sometimes cause headaches during regulatory filings or patent disputes. Laboratories need clear pathways from raw material to final product, with supporting evidence. If a supplier waffles on analytical data or can’t produce certificates of analysis—complete, up-to-date, and matching current regulatory standards—chances are the material will sit unused or get rerouted for non-GMP work. More than once, I’ve seen ambitious startups stumble over these documentation hurdles, missing windows for key filings or tech transfer.

    Waste handling, too, becomes more pronounced as volumes scale. Pyridine derivatives can pose environmental and safety challenges, especially if impurities contain chlorinated byproducts. Regulatory bodies increasingly scrutinize waste streams. Good suppliers not only offer environmental documentation but also develop greener synthesis methods to minimize or neutralize hazardous effluents. Workers appreciate those changes—safer working conditions translate into fewer incidents and lower insurance costs.

    Counterfeiting and supply chain vulnerabilities loom larger today than a decade ago. Unscrupulous vendors sometimes pass off mislabelled or substandard materials, especially during shortages. Labs must be vigilant, double-checking certificate details, running identity tests beyond basic IR or NMR, and insisting on audit trails. Larger buyers sometimes conduct site visits or contract for third-party audits, recognizing that real costs often appear not on the invoice, but in project delays or rework.

    Supporting Reliable Chemical Supply: Building Better Solutions

    Facing these challenges calls for a collaborative approach. End users and suppliers grow stronger together by sharing not just orders and invoices, but technical feedback, application notes, and analytical challenges. One experienced chemist in my circle swears by regular batch reviews—a few hours of reviewing supplier documentation, cross-checking in-house analysis, and feeding back both praise and concerns. This small investment routinely pays off in better yields and more predictable results.

    Diversity in sourcing also helps reduce risk. Relying exclusively on a single vendor increases vulnerability, especially in volatile global markets. Teams that secure supply agreements with multiple reputable partners get better bargaining power and avoid last-minute scrambles. Purchasing teams can learn chemical basics, too—it’s easier to spot issues early when everyone understands batch variability, stability testing, and documentation.

    Within labs, open records and standardized testing save time and support transparency. For 4-Chloro-2,6-diaminopyridine, methods might include regular HPLC analysis, NMR validation, and checks for volatile organics. Beyond compliance, these practices catch lot-to-lot variation early. Proactive problem-solving—rather than finger-pointing during a crisis—sets strong teams apart.

    Technology offers further help. Online supplier review portals grow more robust each year, aggregating user experiences and independent testing data. Smart buyers now consult these resources before switching vendors or introducing alternate lots. Automated sensors monitor conditions across storage and shipment, alerting stakeholders to deviations in temperature or humidity that can impact sensitive chemicals. Greater transparency around supply chain movements blocks counterfeiters and rewards suppliers with proven track records.

    Industry working groups and regulatory bodies increasingly encourage pre-competitive collaboration. Sharing best practices—even among rivals—helps build better standards for intermediates like 4-Chloro-2,6-diaminopyridine. In my experience, the long-run result is stronger trust networks, better intelligence about market fluctuations, and more robust science across the board. Patents may defend individual innovations, but improving supply chain resilience lifts the entire field.

    Looking to the Future

    As chemistry grows ever more central to new therapies and technologies, fine chemicals such as 4-Chloro-2,6-diaminopyridine will remain under scrutiny. Regulatory frameworks tighten, and demands rise for transparency all the way from precursor to finished product. Teams who manage these changes—steadily investing in reliable analytics, compliance infrastructure, and genuine communication—will find success both in the market and at the bench.

    For many of us, the journey with this compound has meant more than scale-up runs or analytical puzzles. It’s illustrated how something as technical as an intermediate can have broad ripple effects: speeding up timelines, safeguarding patients, and paving the way for the next advancement in science. Every shipment received, every analysis recorded, and every lesson shared brings together the people and systems powering modern innovation.

    In the world of specialty chemicals, the details and the decisions behind every gram truly matter. Those who bring care, knowledge, and vigilance to products like 4-Chloro-2,6-diaminopyridine shape both their own future and that of the industries relying on them.