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2-Amino-5-chloro-3-nitropyridine

    • Product Name 2-Amino-5-chloro-3-nitropyridine
    • Alias 5-Chloro-3-nitro-2-aminopyridine
    • Einecs 624-150-6
    • Mininmum Order 1 g
    • Factory Site West Ujimqin Banner, Xilingol League, Inner Mongolia, China
    • Price Inquiry sales7@bouling-chem.com
    • Manufacturer Bouling Chemical Co., Limited
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    227651

    Chemical Name 2-Amino-5-chloro-3-nitropyridine
    Molecular Formula C5H4ClN3O2
    Molecular Weight 173.56 g/mol
    Cas Number 24172-50-7
    Appearance Yellow to orange solid
    Melting Point 110-115°C
    Solubility Slightly soluble in water
    Pubchem Cid 256196
    Storage Conditions Store at room temperature, in a dry and well-ventilated place
    Smiles c1c(ncc(c1Cl)[N+](=O)[O-])N
    Inchi Key HIBPORVZVOSZRP-UHFFFAOYSA-N
    Hazard Statements May cause irritation to skin, eyes, and respiratory tract
    Synonyms 5-Chloro-3-nitro-2-pyridinamine

    As an accredited 2-Amino-5-chloro-3-nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Amino-5-chloro-3-nitropyridine (Sigma-Aldrich) is packaged in a 5-gram amber glass bottle with secure screw cap.
    Shipping 2-Amino-5-chloro-3-nitropyridine (Sigma Aldrich/Merck/TCI Chemical Grade) is shipped in tightly sealed containers, protected from light and moisture. It is transported in compliance with relevant hazardous material regulations, often with UN identification and appropriate safety labeling, ensuring safe handling and delivery to laboratory or industrial destinations.
    Storage 2-Amino-5-chloro-3-nitropyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Store at room temperature, protected from moisture, heat, and direct sunlight. Ensure appropriate chemical labeling and keep away from sources of ignition. Follow all relevant safety guidelines as specified by the manufacturer (Sigma-Aldrich/Merck/TCI).
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    Certification & Compliance
    More Introduction

    2-Amino-5-chloro-3-nitropyridine: A Core Intermediate for Modern Synthesis

    Our Experience with 2-Amino-5-chloro-3-nitropyridine

    In daily production, chemistry rarely stands still. Each molecule serves as a point of connection, not just a reagent. For over fifteen years, we have produced 2-Amino-5-chloro-3-nitropyridine (CAS 4214-76-0), watching demand gradually shift and expand. This compound forms an essential block for so many applications, thanks to its distinctive functional groups and stability.

    The factory line is where the sinew of chemical synthesis really shows itself. We synthesize this product by direct chlorination, optimizing for precise yields and minimal by-product formation. Our approach relies on automated monitoring, keeping purity above 99%. Over the years, we’ve seen just how sensitive downstream processes react to trace impurities, especially those introduced by imprecise handling or raw material variation. Our control starts at the raw material audit and does not loosen until the product sits sealed and ready for shipment.

    Chemical Features and Specifications

    2-Amino-5-chloro-3-nitropyridine carries a pyridine ring, amine, nitro, and chloro groups in defined positions—each influencing how it behaves later in synthesis chains. The presence of both electron-withdrawing and electron-donating substituents gives this molecule unique reactivity, which we regularly harness. It appears as a pale yellow to light brown crystalline solid under normal storage.

    Customers need clarity, so every batch is accompanied by spectral data, moisture analysis, and detailed chromatograms. We track melting point and HPLC purity not just for regulatory reasons but to serve process chemists who depend on reliable input. Our laboratory runs tests using modern UV-VIS and NMR equipment, correlating minor shifts to possible upstream changes. Troubleshooting at this stage has saved countless hours on multi-step synthesis projects for our partners.

    Role in Chemical Synthesis

    Practicality drives our focus here at the plant. Chemists choose 2-Amino-5-chloro-3-nitropyridine as a core intermediate in synthesizing active pharmaceutical ingredients and crop science materials. Its substitution pattern enables controlled transformations; for example, the nitro group offers handy reduction to amines or substitutions via nucleophilic attack, while the chlorine can be displaced in cross-coupling reactions. The amine segment often serves as the handle for further functionalization, facilitating the construction of benzimidazole or pyridine-fused compounds.

    Daily, we ship this material to R&D labs and pilot plants. Feedback plays a pivotal role in our ongoing process refinement. We recall a common challenge years ago: inconsistencies in particle size distribution led to sluggish filtration and variable yield for a major pharmaceutical transformation. Refining our crystallization step reduced these issues, resulting in reliable, free-flowing solid material. For us, it’s not about volume alone—it’s about how this intermediate performs in real-world, high-stakes applications.

    Why Purity and Handling Matter

    The chemical industry rarely forgets lessons from contamination or mishandling. Minor variations in trace metal content or residual solvents can derail a sensitive catalyst or fail a strict pharmaceutical audit. In our own work, we found that water content above 0.2% sometimes hindered subsequent reduction or substitution steps. In another situation, dust particles transferred during packaging caused filtration column clogging at a customer’s lab. By integrating HEPA filtration into our final packing stations and using multiple desiccators, we minimized such risks.

    Customers often ask about minimizing hazardous by-products and streamlining regulation-compliant paperwork. Most regulatory submissions hinge not only on a compound’s declared structure but its assured purity and well-documented handling. We keep archival samples of every lot, along with full analytical paperwork, to support long-term traceability.

    Comparisons with Other Pyridine Derivatives

    In our experience, process chemists may compare 2-Amino-5-chloro-3-nitropyridine with similar pyridine derivatives like 2-Amino-3-chloro-5-nitropyridine or 2-Amino-4-chloro-3-nitropyridine. Each variant presents different reactivity and synthetic utility due to the position of substituents on the ring. Our molecule, with a nitro at the 3-position, tends to offer better selectivity in nucleophilic aromatic substitution compared to its 4- or 6-position analogs.

    When scaling up reactions, some customers initially turned to less expensive, single-substituted pyridines. They soon realized that lack of functional group balance leads to poor conversions or unwanted regioisomers. We have observed this firsthand in scale-up projects where switching from a mono-chloro derivative to our 2-Amino-5-chloro-3-nitropyridine quadrupled the desired intermediate’s yield and trimmed purification steps.

    Certain crop protection syntheses require careful placement of electron-withdrawing groups to anchor later linking steps. In our own test series, alternatives sometimes elevated toxicological risk or brought unwelcome process bottlenecks. Sticking with our highly purified, doubly functionalized pyridine has demonstrated lower waste and fewer hazardous by-products in downstream production.

    End User Feedback and Adaptation

    The stories that stand out usually begin with a challenge: batch failures, sluggish chemical reactivity, unexplained impurities in a regulatory submission. One R&D partner in Europe once struggled to replicate their expected cyclization step when switching suppliers. After a joint analytical session, we pinpointed excess moisture and a subtle impurity—a residual amide—present only in non-dedicated production lines.

    We adapted by refining our drying and filtration, and sharing real-time batch data directly with their project chemists. The problem vanished instantly, restoring their downstream yields and helping avoid costly regulatory setbacks. These recurring collaborations drive us to push for continuous process improvements and transparent supply chain management.

    Not all adaptations are reactive; proactive changes stem from years of learning. For example, our method for storing the intermediate in inert atmosphere containers dates back to a customer who lost a month’s progress due to a humidity-driven decomposition issue. Now, all material leaves our site nitrogen-blanketed and vacuum-sealed, extending stable shelf life well beyond the standard recommendation.

    Impacts of Supply Chain Integrity

    A consistent supply of critical intermediates spares many headaches. Our direct control of the entire process, from sourcing basic reagents to custom finishing for sensitive blends, insulates our partners from market fluctuations, knock-off materials, or price gouging. Years ago, a sudden shortage in the region forced several local producers to substitute sub-optimal analogs, impacting yields and project timelines across several client facilities.

    By keeping our production onsite and internalizing quality control, we provided seamless continuity. The year that happened, we also invested in expanded warehousing and local logistics partnerships, ensuring buffer stocks that covered unpredictable surges in demand. Sharing logistics plans and raw data with clients cemented trust and allowed their own planning teams to optimize inventory and delivery schedules.

    More than once, process safety audits have flagged off-spec lots from non-manufacturer sources. Certificates of analysis alone do not always reflect true quality; minor color shifts, solubility changes, or unseen trace residues often reveal differences in control and commitment. Our process integrates batch-wise cross-verification, which filters out problem lots before leaving our storage, protecting downstream syntheses and project deadlines.

    Environmental Commitment and Regulatory Considerations

    Modern chemical manufacturing sits under a shifting landscape of regulation and environmental expectations. Effluent management, energy use, and personnel safety are not afterthoughts—they are daily concerns from the work floor to the laboratory. Our environmental practices stretch back to the earliest production runs, where excessive solvent waste and energy usage would eat into costs and raise compliance flags.

    Gradually swapping older, energy-hungry reaction vessels for continuous flow systems brought down both emissions and risk. Our multi-stage solvent recycling station now captures over 90% of organics, reducing landfill waste and discharge. These changes didn’t just happen in response to regulation; pressure from our largest customers led to major investments in green chemistry audits and third-party certifications.

    In the context of 2-Amino-5-chloro-3-nitropyridine, proper handling and disposal of waste streams and containment of dust matter immensely, as trace by-products from nitro or chloro substitutions can present regulatory reporting issues. Our commitment to fully documented chain-of-custody extends to internal environmental auditing, ensuring nothing escapes unnoticed, and no permit lapses go unaddressed.

    Practical Issues and Ongoing Solutions

    Scaling lab protocols to production volumes reveals challenges that can catch the unwary. Initially, we battled with batch-to-batch reproducibility, noting that subtle shifts in raw material sources—particularly with substituted chloro-pyridines—caused downstream process hiccups. Entering into long-term procurement agreements allowed us to better control variance, while implementing rapid spectroscopy at incoming inspection reduced surprises.

    The human factor also plays a role. Chemistry, even with all the automation and protocol checking, still relies on human oversight at critical stages. Our training programs keep every shift up to date—new hazards, revised procedures, trace contaminant identification. We hold regular technical exchanges, where both operators and R&D chemists review recent issues, flag new process variables, and suggest modifications. These gatherings often uncover ideas that have improved both efficiency and product reliability over time.

    Negotiating packaging, especially for international customers, revealed mismatches between required local labeling and our internal systems. Direct, repeated conversations helped us streamline regional compliance and documentation, lowering customs hold-ups and ensuring smooth transboundary movement.

    For industrial customers, the physical form of the product, whether as powder, granules, or crystals, can affect dissolution rates during feedstock preparation. We adapted our drying and milling methods for users needing a specific granularity. Ensuring consistently low dust content—often a cause of unexplained process fouling—has cut batch prep time in several downstream processes.

    Looking Forward: How 2-Amino-5-chloro-3-nitropyridine Fits into Evolving Chemical Synthesis

    As a manufacturer grounded in practical chemistry, we see 2-Amino-5-chloro-3-nitropyridine staying relevant for years. The growing demand for specialized pharmaceuticals, novel agrochemical agents, and advanced material science pushes the need for robust, high-quality intermediates. Our customers regularly return with requests for larger batch sizes or tighter specification limits—demands that challenge our engineers and drive process innovation.

    We continue investing in process improvements, broadening our analytical capabilities, and working with customers in joint development projects. Integrating machine learning tools into analytical data review helps us spot potential problems before they manifest, saving both cost and time for ourselves and our partners.

    For those developing new synthesis pathways, the specific substitution pattern of 2-Amino-5-chloro-3-nitropyridine opens routes that more common mono-substituted pyridines cannot match. This flexibility, coupled with the reliability that comes from direct control at every production step, keeps this molecule at the core of evolving chemistry.

    Our plant’s relationship with this compound mirrors the arc of modern synthetic chemistry: a blend of practical workmanship, ongoing scientific learning, and responsiveness to both environmental and market shifts. We draw from direct experience, standing behind our production line, as a partner to those building tomorrow’s molecules.