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HS Code |
401298 |
| Chemical Name | 4-Hydroxy-3-Nitropyridine |
| Molecular Formula | C5H4N2O3 |
| Molecular Weight | 140.10 g/mol |
| Cas Number | 5470-18-8 |
| Appearance | Yellow crystalline solid |
| Melting Point | 179-183°C |
| Solubility In Water | Slightly soluble |
| Pka | Approx. 7.3 (hydroxyl group) |
| Smiles | C1=CN=C(C=C1O)[N+](=O)[O-] |
| Inchi | InChI=1S/C5H4N2O3/c8-4-1-2-6-3-5(4)7(9)10/h1-3,8H |
As an accredited 4-Hydroxy-3-Nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled "4-Hydroxy-3-Nitropyridine, 25g." Safety symbols, product code, and CAS number displayed on white label. |
| Shipping | 4-Hydroxy-3-nitropyridine is shipped in tightly sealed containers to prevent moisture and contamination. It should be packed according to standard chemical transport regulations, with clear hazard labeling. Shipments are typically handled by trained personnel and may require temperature control and documentation, depending on regulatory classifications and quantity being shipped. |
| Storage | 4-Hydroxy-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 oxidizing and reducing agents. Protect it from light, moisture, and heat. Ensure the storage area is equipped with proper spill containment. Label the container clearly and restrict access to trained personnel only. |
Applications of 4-Hydroxy-3-Nitropyridine in Industrial Manufacturing4-Hydroxy-3-Nitropyridine is a highly specialized intermediate, primarily used in select advanced manufacturing processes across pharmaceuticals, agrochemicals, dyestuffs, and fine chemical segments. Our facility supports scalable, quality-assured supply to industrial buyers demanding regulatory-compliant input materials for complex synthesis routes. 1. Pharmaceutical API Intermediate SynthesisPharmaceutical manufacturers incorporate 4-Hydroxy-3-Nitropyridine as a key building block during multi-step synthesis of certain heterocyclic active pharmaceutical ingredient (API) cores. This material enters custom routes for third- and fourth-generation quinolone antibiotics and related nitrogen-heterocyclic molecules. Its hydroxy and nitro functional groups enable selective substitution and ring construction, supporting process chemists in optimizing batch purity and minimizing side products. Each production campaign aligns to client-specific monograph and documentation requirements for regulatory filings. Industry compliance standards
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2. Agrochemical Heterocycle ManufacturingMajor crop protection formulators use 4-Hydroxy-3-Nitropyridine during synthesis of pyridine-based pre-emergent herbicides and insecticides. The controlled nitration and hydroxy orientation allow for precise coupling in later stages with functionalized chlorides and amines, forming active compound rings with defined substitution profiles. QC teams require batch homologation and full traceability from this upstream input as part of multi-country product registration dossiers. Industry compliance standards
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3. Dyestuff Intermediate for Electronic MaterialsChemical dye manufacturers utilize 4-Hydroxy-3-Nitropyridine during manufacture of pyridine-based high-performance dyes, frequently destined for OLED or LCD electronic applications. Its defined ring substitutions serve as nucleophiles in cross-coupling and azo dye synthesis, targeting intense chromatic purity and stable electronic characteristics for thin-film device deposition technologies. The controlled impurity profile suits circuit printing and optoelectronic grade requirements. Industry compliance standards
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4. Fine Chemical Synthesis for Analytical StandardsProducers of chemical standards and laboratory reagents deploy 4-Hydroxy-3-Nitropyridine as a matrix precursor for certified reference materials targeting trace analysis and LC-MS calibration needs. Stringent requirements on starting input traceability, purity (typically above 99.5%), and defined isotopic composition mean close batch-to-batch analytical monitoring at our QC labs, with full COA and mass spectral data issued for each delivery lot supporting metrology and industrial analytics sectors. Industry compliance standards
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Working with 4-Hydroxy-3-Nitropyridine has revealed its steady role as an important building block for pharmaceutical and agrochemical research. Our team crafts each batch in-house, following deliberate synthesis and purification steps shaped by years of hands-on handling. The powder’s distinctive pale yellow color signals its purity long before it meets any analytical device. Often, similar pyridine derivatives struggle with color consistency or residual odor—ours stands out through persistent efforts to refine both aspects. After spending years behind glassware and filter presses, we know these details matter for anyone depending on predictable benchwork.
Chemical structure guides both the application and constraints. Our 4-Hydroxy-3-Nitropyridine runs under CAS number 15152-81-5, with molecular formula C5H4N2O3 and a precise molecular weight. The hydroxy and nitro groups at specific sites on the pyridine ring create a distinct electron distribution, lending the compound reactive versatility uncommon in closely related agents. As operators, we keep moisture control a priority—hydroxy derivatives absorb water without strict environmental controls, so silica desiccators or sealed drums become part of our daily routine. Nothing replaces trained eyes when tracking batch color, feel, or flow; we measure melting point and chemical identity regularly.
Unlike products dominated by mass-produced traders, our approach holds to sample-by-sample tracking. Quality assessment includes not only HPLC but also IR spectroscopy and TLC, which helps catch minor byproduct signals. Particle size control stands right alongside purity; clumping or inconsistent grains cause trouble on the user’s side, especially during scale-up, and repeated sieving and observation keep lots reliable. Every person in our small production unit learns to spot off-notes in the freshly made material. Here, consistency is a hands-on affair, not a buzzword copied from brochures.
We supply this intermediate to direct users such as pharmaceutical R&D labs, crop protection developers, and some materials science groups. Nearly all requests relate to further derivatization—customers target nucleophilic aromatic substitution, Suzuki couplings, or cyclization steps. The hydroxy group acts as an anchor for selective substitutions, while the nitro group directs reactivity or, in some reactions, serves as a reducible functional handle. The balance between electron-donating and electron-withdrawing groups on a five-membered ring isn’t just theory—seeing these reactions succeed or fail in practice shows why this combination attracts synthetic chemists hungry for new scaffolds.
Process safety teams and technical buyers often want details on handling characteristics. Our weighing rooms have seen nearly every scale of operation, and our records confirm the powder stays free-flowing as long as humidity and temperature remain in check. The compound’s inherent stability leaves plenty of window for routine storage, though extreme conditions risk slow decomposition—something all pyridine derivatives share to a degree. Many new clients seek sample verification: our shelves always hold several vials under inert gas for quick turnaround, so no down time sits between inquiry and bench testing. This approach draws repeat business from researchers tired of guessing about quality or delivery times.
Comparing 4-Hydroxy-3-Nitropyridine to other substituted pyridines uncovers some stark contrasts. Mono-nitro or mono-hydroxy compounds lack the chemical finesse seen here; two distinct functional groups on a single ring enable regioselective syntheses otherwise impossible or impractical with simpler reagents. Experienced chemists appreciate the creative latitude opened by dual functionality, and our production logs routinely document customizations upon request. For example, the steric arrangement in 4-Hydroxy-3-Nitropyridine makes certain couplings smoother or more predictable due to ring activation and substituent positioning, which reduces byproduct formation in challenging reactions.
We rarely see this paired functionality from large-volume commodity suppliers. Most synthesize either hydroxy or nitro pyridines in isolation, chasing lower costs and maximum output, not subtlety or modularity. For those strategies that demand such versatility—a fine-tuned coupling with an aryl boronic acid, or the build-out of novel heterocyclic cores—the straightforward reagents just don’t perform as needed. Years working inside this niche have shown that end-users return to well-made, multi-functional intermediates even if alternatives seem cheaper upfront. Our records confirm repeat orders cluster around this product line, reflecting trust built project-by-project, not through marketing claims.
Production at scale demands attention beyond simple batch tracking. Standard routes for 4-Hydroxy-3-Nitropyridine involve careful nitration and hydrolysis under tightly controlled temperatures—without vigilant temperature and pH control, negative outcomes stack up fast. We install extra monitors across reactors, and assign line operators to spot suspicious exotherms before they escape correction. Scaling up from a kilo lab to larger runs can reveal hidden heat transfer bottlenecks. Once, a pilot batch drifted past control points, prompting our crew to redesign jacketed reactor protocols. Lessons from this near-miss now underpin every shift’s checklist.
Material losses can come from unexpected sources. The starting pyridine rings from upstream partners rarely arrive without impurities, so routine pre-purification counteracts knock-on effects down the chain. Our staff also manages waste streams actively—spent acid, residual salts, or organics all head straight for treatment benches, not general drains. Supervising every outlet keeps both safety and compliance in steady hand. As more jurisdictions tighten emissions and disposal standards, the team adapts by investing in containment and neutralization systems. Failures to enhance production hygiene have caused headaches—equipment fouling is expensive, and regulatory headaches can bring even experienced groups to a halt.
Development teams in drug and crop research ask for flexibility in both order sizing and documentation. Our laboratory supports requests from as little as a couple of grams up through multi-kilogram lots. Each delivery is matched with in-house COA sheets and certificates of origin. Researchers push us for thorough impurity profiles, not boilerplate documentation. The company hosts annual visits to allow long-term partners to audit our workflow, providing first-hand access to our line staff, raw material storage, and analytical records. This transparency supports technical dialogue, and we’ve responded more than once to requests to tweak drying methods or modify packaging on short notice.
Many organizations hesitate to share R&D information with outsiders. Our approach focuses on supplier-user collaboration from early exploratory phases onward. By tracking questions and feedback, and allocating technical staff to help troubleshoot synthetic obstacles, we see fewer surprises and accelerated time-to-solution. Access to key decision-makers helps us fine-tune the purity profile for specific synthesis routes, rather than serving up a fixed “industrial grade” unsuitable for high-sensitivity reactions. This level of adaptability shines against providers moving mass quantities without regard to downstream customization.
Daily experience with 4-Hydroxy-3-Nitropyridine shows that packaging format makes as much difference as batch purity. We rely on HDPE containers with gasketed closures, plus desiccant bags for anything stored long-term. On more than one occasion, a loose lid led to caked, unusable product—valuable loss anyone working in a production line feels. We’ve shifted our policy to double-check fastening and run shelf-life studies quarterly to catch early signs of degradation. Each year brings minor adjustments in drum liners or secondary containment, responding to the unending drip of real-world challenges.
Shipping concerns differ for large versus small users. For tightly scheduled pilot plants, a delayed order can stall downstream synthesis—all it takes is a hiccup in local customs or a misprint on the manifest. Our logistics arm monitors shipments until user confirmation, tracking everything from temperature swings in transit to scan failures at distribution points. The staff remains on-call to help decode tracking messages or arrange alternate routings if necessary. Regular communication with end users resolves interruptions far more smoothly than arms-length distribution desks.
Regulatory scrutiny for intermediates like 4-Hydroxy-3-Nitropyridine always finds its way to the production bench. Hazard labeling, GHS-compliance, and safety data management stay at the center of our compliance policy. Working in our environment, bulk storage means air handling and emergency cleanup familiarity—spills, even small ones, create slip hazards or potent odors. Every new hire receives explicit chemical hygiene training, with mock spills and hands-on interventions. This focus stems from hard-earned experience; minor lapses in housekeeping can snowball, affecting both worker welfare and bottom line.
We hear concern about downstream environmental impact and exposure risk, particularly from university groups and smaller pharma teams. These concerns have led us to revisit raw material sourcing, emphasizing vendor audits for responsible handling and restricted use chemicals. Record keeping tracks every bag or barrel through each room and each operator. By keeping this paper trail detailed, we answer technical queries and audit requests with specifics, not vague recounting. This level of rigor shields not only our staff but all downstream users who may face questions from their own safety committees or customers.
Chemists, materials scientists, and crop protection experts shape the evolving landscape for molecules like 4-Hydroxy-3-Nitropyridine. Our shop learns from each customer’s unique method of use. Pharmaceutical intermediates sometimes require extra purification steps; crop science batches call for documentation about trace heavy metal content, while academic queries probe mechanism or solubility for new reactions. Our support team works to gather, interpret, and present results in ways that speak to technical priorities rather than just regulatory minimums.
Sharing direct feedback from applied research back into production closes quality gaps that only theory would miss. For example, after months of testing solvent crystallization options, one customer improved their drug synthesis yield by nearly 8% after adjusting for minor byproducts found in our HPLC trace. Timely reporting and a willingness to adapt methods raised everyone’s game, minimizing delays from troubleshooting or wasted runs. This flexibility cannot come from faceless material brokers or generic distribution warehouses; it belongs to organizations willing to invest resources into every container, label, and report.
All chemical manufacturing impacts the environment, and 4-Hydroxy-3-Nitropyridine presents its own footprint. We collect, neutralize, and recycle as much process solvent as equipment allows. This ongoing effort cuts both overhead and environmental risk, as evidenced during regular site inspections. Implementing closed-loop water handling or evaporative recovery units required up-front investment, but our ongoing records show sustained reductions in hazardous discharge and waste output. Customers ask about green chemistry credentials; we source intermediates from suppliers with third-party environmental accreditation when available. Routine audits and lab tours for buyers provide firsthand assurance that stated policy matches actual practice.
The challenge of balancing production with environmental stewardship never disappears; rule changes across regions push us to stay current with both practice and paperwork. Our staff revise SOPs annually, and conference attendance keeps the team aware of safer alternatives or policy shifts. This cycle of review and improvement not only meets regulation but drives process efficiency. Over the years, this focus has delivered not just a better product, but a closer trust between our technical leads and the researchers depending on every shipment.
Direct involvement in the supply chain offers clear advantages for everyone involved. Our operators sit on audit panels, review complaints, and update documentation, keeping expertise in-house rather than outsourcing. This approach built up a core team who understand both technical and practical drivers—there’s little substitute for seeing a warehouse, a drum, or a spreadsheet firsthand. Many industry colleagues rely on outside consultants or arm's-length communication, and gaps often appear during problem resolution. Experience on the ground is hard to replicate, and the network built through repeated engagement fosters a level of problem-solving rarely present in more fragmented operations.
Cross-industry dialogue keeps us from becoming complacent. Attending technical workshops and benchmarking against global standards show us both our strengths and fields where we must adapt. Whether overcoming a production bottleneck, addressing new downstream requirements, or responding to customer audits, we’ve seen improvement comes fastest with open communication across processing, QA, and technical support. Trial and error across diverse customer applications sharpens both production and documentation—there is no shortcut to this kind of learning curve.
Markets for heterocyclic intermediates continue to shift. As new therapeutic targets, regulatory regimes, and environmental priorities emerge, our output must evolve at the same pace. Today’s users ask for granular impurity profiles, tailored packaging, and real-time analytical support. Our crew continues to invest in both analytical hardware and technical training, aiming to keep step with rising standards in each market served. Years of direct engagement on the manufacturing floor build both pride in the product and familiarity with its quirks and hazards.
New synthetic targets on our customers’ lines lead to fresh requests: higher purity fractions, lower metal content, more detailed contaminant tracking. By delivering on each new requirement, and learning from every success or misstep, we forge relationships with teams who value expertise over speed or price alone. The broader aim, from our perspective, is not only to ship reliable material but to act as problem solvers alongside each partner. We measure progress by project completions and customer reports, not simply tonnage of powder handled.
4-Hydroxy-3-Nitropyridine may stand as a small cog in larger systems, but close control and ongoing attention separate dependable supply from unreliable options. On the factory floor, where people and machines translate plans into product, every action counts. Each batch of powder is shaped by dozens of steps and people, combining tradition, innovation, and accountability. Developing every gram through careful stewardship, transparent reporting, and real partnership makes a difference that downstream users feel in the lab, the pilot plant, and beyond. No shortcut or generic alternative can replace a rigorous, user-centered manufacturing approach.