4-Chloro-2-hydroxy-5-nitropyridine

    • Product Name: 4-Chloro-2-hydroxy-5-nitropyridine
    • Chemical Name (IUPAC): Please provide the name or structure of the product for which you want the IUPAC chemical name.
    • CAS No.: ''
    • Chemical Formula: I am sorry, but you did not specify the product name. Please provide the name of the product so I can give you its chemical formula.
    • 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

    547229

    Cas Number 4318-95-2
    Molecular Formula C5H3ClN2O3
    Molecular Weight 174.54 g/mol
    Appearance Yellow crystalline powder
    Melting Point 173-177°C
    Solubility In Water Slightly soluble
    Purity Typically ≥ 98%
    Smiles c1c(cnc(c1O)[N+](=O)[O-])Cl
    Inchikey UZHHQARGTITDSP-UHFFFAOYSA-N

    As an accredited 4-Chloro-2-hydroxy-5-nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25 g of 4-Chloro-2-hydroxy-5-nitropyridine is supplied in a sealed amber glass bottle with a tamper-evident cap.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 4-Chloro-2-hydroxy-5-nitropyridine: Typically packed in 25kg fiber drums, totaling about 9–10 metric tons per container.
    Shipping 4-Chloro-2-hydroxy-5-nitropyridine is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is classified as a hazardous material and is transported according to relevant regulations, with appropriate labeling and documentation. Ensure temperature control if required, and handle with suitable personal protective equipment during receipt and unpacking.
    Storage 4-Chloro-2-hydroxy-5-nitropyridine should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing or reducing agents. Keep the container tightly closed and clearly labeled. Protect from moisture and direct sunlight. Use chemical-resistant containers, and ensure proper secondary containment to prevent spills or contamination.
    Shelf Life 4-Chloro-2-hydroxy-5-nitropyridine typically has a shelf life of 2–3 years when stored in a cool, dry, airtight container.
    Application of 4-Chloro-2-hydroxy-5-nitropyridine

    Purity 98%: 4-Chloro-2-hydroxy-5-nitropyridine with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal side product formation.

    Melting Point 185°C: 4-Chloro-2-hydroxy-5-nitropyridine with a melting point of 185°C is used in solid-formulation processes, where it offers precise thermal stability during compound preparation.

    Molecular Weight 176.55 g/mol: 4-Chloro-2-hydroxy-5-nitropyridine with a molecular weight of 176.55 g/mol is used in analytical research calibration, where it allows accurate standardization in HPLC methods.

    Particle Size < 50 μm: 4-Chloro-2-hydroxy-5-nitropyridine with a particle size less than 50 μm is used in fine chemical mixing, where it enables homogeneous blending and uniform reactivity.

    Stability Temperature up to 120°C: 4-Chloro-2-hydroxy-5-nitropyridine with stability temperature up to 120°C is used in elevated-temperature synthesis, where it maintains chemical integrity throughout the process.

    Water Content ≤ 0.5%: 4-Chloro-2-hydroxy-5-nitropyridine with water content not exceeding 0.5% is used in moisture-sensitive reactions, where it reduces unwanted hydrolysis and improves reproducibility.

    Assay ≥ 99%: 4-Chloro-2-hydroxy-5-nitropyridine with assay not less than 99% is used in active pharmaceutical ingredient development, where it assures consistency and high pharmacological performance.

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    Certification & Compliance
    More Introduction

    Introducing 4-Chloro-2-hydroxy-5-nitropyridine: A Versatile Solution in Fine Chemistry

    Meeting the Demands of Modern Chemical Synthesis

    Chemistry never slows down. Each year, researchers and professionals search for new tools to boost reaction yield, craft better products, and trim waste. 4-Chloro-2-hydroxy-5-nitropyridine has captured attention for its reliability in both lab-scale innovations and industrial manufacturing lines. This compound doesn’t just exist to fill a spot in a catalog. It stands out because of its adaptability. With a unique structure, it offers direct pathways to effect targeted modifications on the pyridine ring, allowing greater flexibility than traditional halogenated pyridine derivatives.

    Breaking Down the Structure

    Plenty of people talk about “derivatives,” but the details matter. With a chlorine atom at the fourth position, a hydroxyl group at the second, and a nitro group at the fifth, this compound brings reactive centers that don’t just sit idle. Chemists leverage these features to build more complex frameworks or introduce specific functional groups where they need them most. The arrangement offers possibilities that 2-hydroxy-5-nitropyridine or un-substituted pyridine can’t match. Its chemical fingerprint gives room for targeted adjustments by electrophilic and nucleophilic substitution reactions.

    Why Structure Matters in Real Applications

    From my years working alongside organic chemists, one truth rings clear: small changes to a molecule can open huge opportunities. Let’s say you’re exploring new pharmaceutical leads, or seeking a dye intermediate that gives deeper shades. The nature and position of substituents on a ring can affect everything from reactivity to final color. 4-Chloro-2-hydroxy-5-nitropyridine’s structure creates reactivity points not found in its closest cousins. That sets it up as a reliable building block when more common pyridine derivatives fail to deliver the selectivity, reactivity, or ease of downstream processing you need.

    Purity and Standards in Today’s Market

    Quality in the chemical industry carries consequences far beyond paperwork. Even minor impurities can derail a reaction or spoil a batch. Producers of 4-Chloro-2-hydroxy-5-nitropyridine know labs expect tight controls. Most batches reach a minimum purity of 98 percent, sometimes nudging higher, and that level has become necessary for both R&D and scale-up work. High-performance liquid chromatography and nuclear magnetic resonance tests confirm identity and purity, and it’s not just about pride—it’s about reliability when labs run reactions on tight timelines or with limited resources.

    Applications in Pharmaceuticals and Material Science

    From my experience supporting scale-up for pharmaceutical intermediates, the real world rarely mirrors textbook simplicity. Regulator scrutiny means every input needs a clear specification and traceability. 4-Chloro-2-hydroxy-5-nitropyridine steps up as an intermediate for synthesizing biologically active compounds, especially those integrating nitroaromatic and heterocyclic scaffolds. Its reactivity profile fits projects involving kinase inhibitors, anti-infective agents, and CNS-active molecules. Some development teams also look to this material for sensor dye synthesis and electronic material research, where small shifts in molecular features can shift an entire class of properties.

    This compound doesn’t just show up in patented reaction schemes. Its presence appears in scientific literature around nitroaromatic functionalization, Suzuki and Buchwald-Hartwig couplings, and ring modification projects. Anyone looking to move from milligram experiments to kilogram preparation soon finds that high yield reactions and manageable workup hinge on the right starting materials. 4-Chloro-2-hydroxy-5-nitropyridine smooths the path by behaving predictably and efficiently during such transformations.

    Environmental and Safety Considerations

    It pays off to think about more than just handling and reactivity. Safer alternatives frequently come up in meeting rooms these days, since environmental impact and occupational safety concerns point the entire industry in a new direction. 4-Chloro-2-hydroxy-5-nitropyridine presents fewer hazards than some older nitroaromatic starting materials, especially those that carry volatile or unstable functional groups. Still, solid handling routines, fume hood work, and robust storage standards matter. Nothing replaces responsible stewardship and adherence to up-to-date guidance for chemical safety and waste disposal. In my experience, preparation and good documentation do more to keep teams safe than any single piece of personal protective equipment.

    Stability, Storage, and Shipping Factors

    Pyridine derivatives can bring unpredictable issues if stability isn’t taken seriously. 4-Chloro-2-hydroxy-5-nitropyridine, compared to less stable nitro compounds, has proven its resilience under standard shipping conditions. Companies typically package it in sealed containers to block moisture uptake and ensure the crystalline product arrives intact. The nitro group demands respect under storage, as improper conditions might cause unwanted decomposition over longer periods or at higher temperatures. Making sure climate control, inventory rotation, and periodic testing all line up keeps the material ready for use and reduces waste along the supply chain.

    Comparison With Other Pyridine Derivatives

    Chemists have easy access to a range of pyridine compounds. Some lack a nitro group, others miss a halogen, and many don’t include hydroxyl functionality. Experience shows each functional group changes both the chemical and practical profile of a material. Take 2-hydroxy-5-nitropyridine, which offers nucleophilicity but doesn’t bring the same versatility for selective halogenation or downstream coupling reactions. In contrast, 4-chloro-5-nitropyridine skips the hydroxyl, missing some of the hydrogen bonding and coordination properties that make its sibling so useful in pharmaceutical research and catalysis.

    Because of these unique features, teams can swap out multi-step transformations that require heavy workups for simpler, more manageable reaction paths. This means fewer resources spent on purification or troubleshooting side products. In critical applications where reproducibility and product profile matter, this difference becomes much more than theoretical.

    Handling Supply Chain Complexity

    The global chemical supply chain has grown more complex in recent years. Sourcing niche intermediates like 4-Chloro-2-hydroxy-5-nitropyridine often means working with specialty producers and navigating customs hurdles. Delays or shortages can stall research and production. Based on my time working with procurement teams, early forecasting and regular engagement with trusted suppliers reduces surprises. Some projects benefit from dual sourcing, but real peace of mind comes from partnering with outfits that understand documentation, offer Certificates of Analysis, and keep product quality consistent between batches.

    Freight costs, customs procedures, and warehousing feed into total project expenses. Knowing a material holds its quality across time and environmental changes prevents expensive setbacks. I’ve found that choosing suppliers with good track records ends up saving time, avoiding headaches, and protecting tight project timelines.

    Adaptability in Research and Development

    Not every lab has the same needs. In my own experience, small academic groups push boundaries, while development arms in large companies demand repeatability and documented performance. 4-Chloro-2-hydroxy-5-nitropyridine supports both. For custom synthesis, it brings reactivity for targeting rare functionalizations or doing rapid analog development. In industrial trials, the substance carries enough data behind it so scale-up teams feel confident predicting performance based on past runs.

    With R&D spending rising each year, shortening the gap between discovery and scaled manufacture brings a clear cost advantage. A dependable building block like this reduces downtime and makes it simpler to pivot or adapt synthesis schemes without prolonged vetting of new raw materials. Reports from medicinal chemists, material scientists, and process developers make it clear: investing in reliable, well-characterized starting materials pays off over the lifespan of a project.

    Supporting Regulatory and Quality Demands

    Regulation in chemical manufacturing means navigating ever-changing expectations. Projects touching anything pharmaceutical, electronic, or agrochemical face audits and paperwork trails that grow thicker every year. In my work, sound documentation on raw materials—not just purity and lot number but full traceability—has become the ticket to faster approvals and smoother operations. 4-Chloro-2-hydroxy-5-nitropyridine sourced from experienced producers supports compliance efforts by arriving with analytical data, batch records, and, in many cases, detailed risk assessments.

    My colleagues in quality assurance have shared that fewer unknowns in a supplier’s documentation chain significantly cut the risk of delays at regulatory checkpoints. This attention to detail also builds confidence among project managers and technical directors, since every team member knows what goes into the end product, whether that’s a tablet, a pigment formulation, or an optical sensor.

    Market Trends and Price Sensitivity

    Price remains at the front of decisions, especially as inflation and global events squeeze margins. Producers of specialty pyridine derivatives watch feedstock costs, energy, and labor markets as closely as researchers look for new reactivity patterns. Customers want competitive prices but won’t cut corners on things like purity or documentation. My experience working with both buyers and chemists shows negotiation works best when suppliers can share transparency about raw materials, quality protocols, and delivery expectations.

    Bulk orders often bring better cost per gram, but even for modest lab quantities, guarantees around authenticity and consistency matter more than ever. Sourcing off-brand or from unverified online shops occasionally looks tempting, especially for initial trials, but often leads to wasted time or worse—unstable product that derails progress. Investment in proven sources repeatedly shows its value in higher project throughput, better overall results, and less troubleshooting down the line.

    Improving Green Chemistry Outcomes

    Anyone involved in chemical synthesis today faces growing expectations to cut waste, lower emissions, and replace hazardous intermediates. The move toward greener chemistry isn’t just a slogan; it’s becoming the foundation of R&D and commercial production. With its specific substitution pattern, 4-Chloro-2-hydroxy-5-nitropyridine supports strategies aiming to reduce the number of synthetic steps, eliminate hazardous reagents, and improve atom economy. These improvements directly address concerns raised by environmental review boards and internal sustainability teams.

    Instead of relying on legacy methods that generate excess by-products, teams have reported success using this compound to streamline routes and switch to milder reaction conditions. Projects that succeed here get more than just good press—they see cost savings, stronger investor backing, and longer-term customer loyalty. In my experience, practitioners who share positive case studies around green metrics can drive adoption industry-wide, reshaping both regulatory compliance and public trust.

    Training and Knowledge-Sharing

    A technical compound like 4-Chloro-2-hydroxy-5-nitropyridine may seem intimidating for newcomers just entering synthetic labs. People gave me the best advice early in my career: put as much effort into learning best handling practices as you do in learning theory. Solid mentorship and access to technical data can raise the baseline of safety and precision in a lab. Senior chemists often pass down procedural insights—how to dissolve, filter, and quench reaction mixtures, or how to safely recover and store excess stock. Building a knowledge-sharing culture helps everyone operate at a higher level and avoid mistakes that cost time or compromise safety.

    Institutional knowledge around new compounds, including thoughtful disposal routines and tips for optimizing synthetic routes, makes it easier for each generation of scientists and engineers to pick up where others left off. The industry’s best outcomes often come from collaborative care—sharing what works, capturing mistakes, and documenting new victories and challenges with each new product or process.

    Future Directions in Pyridine Chemistry

    Scientific progress rarely follows a straight line, and the niche filled by 4-Chloro-2-hydroxy-5-nitropyridine continues to shift each year as new demands arise. Research trends point toward expanded use of pyridine derivatives across life sciences, material sciences, and analytical technology. Flexible, multifunctional intermediates like this one allow for creative experimentation, giving chemists room to re-imagine what’s possible in both targeted and exploratory synthesis.

    Investment in automation, data analytics, and process modeling promises to multiply what can be done with adaptable building blocks. Projects can now access rapid screening tools to optimize reaction conditions or predict reaction outcomes, directly benefiting from materials that perform predictably across batches. Companies and academic labs report greater confidence taking on complex syntheses when they have solid, tested intermediates at hand, shortening the route from hypothesis to real-world solution.

    Closing the Loop: Toward Better Outcomes

    When chemists share their real-world experiences, patterns emerge. Reliable starting materials, handled with care, underlie every successful research and production story. 4-Chloro-2-hydroxy-5-nitropyridine has earned its spot because users value its predictability, clarity of reactivity, and role in achieving sustainable, cost-effective, and high-performance outcomes. Laboratories and production teams that focus on building strong relationships with reputable suppliers, investing in ongoing training, and adopting new sustainable technology consistently outperform those that treat these materials as mere commodities.

    My own work across several sectors confirms that ongoing investment in process improvement, safety, and responsibility pays dividends. Collaborative efforts—between suppliers, chemists, engineers, and regulators—form the backbone of every major leap forward. 4-Chloro-2-hydroxy-5-nitropyridine stands as more than another item on an inventory sheet. For those who care about quality, innovation, and results, it’s a trusted ingredient helping to push boundaries in chemistry and industry alike.