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2-Hydroxy-5-Methyl-3-Nitropyridine

    • Product Name 2-Hydroxy-5-Methyl-3-Nitropyridine
    • Alias 5-Methyl-3-nitro-2-pyridinol
    • Einecs 'EINECS 429-620-3'
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    275203

    Chemical Name 2-Hydroxy-5-Methyl-3-Nitropyridine
    Molecular Formula C6H6N2O3
    Molecular Weight 154.12 g/mol
    Appearance Yellow to orange crystalline powder
    Melting Point 176-180 °C
    Solubility In Water Slightly soluble
    Cas Number 6968-63-2
    Purity Typically ≥98%
    Smiles CC1=CC(=NC(=C1O)[N+](=O)[O-])
    Inchi InChI=1S/C6H6N2O3/c1-4-2-5(8(10)11)7-6(9)3-4/h2-3,9H,1H3
    Storage Conditions Store in a cool, dry place, tightly closed

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

    Packing & Storage
    Packing Sealed amber glass bottle containing 25 grams of 2-Hydroxy-5-Methyl-3-Nitropyridine, labeled with hazard symbols and product details.
    Shipping 2-Hydroxy-5-Methyl-3-Nitropyridine is shipped in tightly sealed containers, protected from moisture and light. It is transported according to chemical safety guidelines, typically as a non-hazardous substance. Standard labeling and documentation are included to ensure safe handling. Handle with appropriate personal protective equipment during transport and storage.
    Storage 2-Hydroxy-5-methyl-3-nitropyridine should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Separate from incompatible substances such as strong oxidizers or acids. Use secondary containment if necessary to prevent spills. Ensure proper labeling, and store at room temperature in a designated chemical storage cabinet.
    Application of 2-Hydroxy-5-Methyl-3-Nitropyridine

    Applications of 2-Hydroxy-5-Methyl-3-Nitropyridine in Industrial Manufacturing

    2-Hydroxy-5-Methyl-3-Nitropyridine serves as a critical intermediate in various specialized industrial processes, supporting high-value sectors with strict quality and regulatory demands. As the original manufacturer, we supply material tailored to enable specific transformations in pharmaceutical, agrochemical, dye, and specialty chemical manufacturing. Below, explore the key downstream applications based on real, established industry practice.

    1. Pharmaceutical API Intermediate Synthesis

    This material facilitates the construction of functionalized pyridine moieties in complex small molecule drugs, especially within anti-infective and oncology product pipelines. Manufacturers utilize it during the late stages of heterocycle assembly and functional group introgression to achieve precise molecular architecture as required by regulatory submissions for innovative therapies.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) General Chapter 1078
    • European Pharmacopeia (EP) Monograph-Relevant API Guidance
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • Employed at 0.3–1.2 molar equivalents relative to piperidine or other pyridine nuclei; weight percentage varies based on targeted drug substance yield, with adjustments during impurity profiling and process optimization.

    Downstream process integration

    • Introduced during pyridine ring-functionalization steps; used in batch or continuous flow reactors prior to coupling or reduction sequences that establish the parent API structure.

    Final product types

    • Active Pharmaceutical Ingredients (APIs) for anti-infectives
    • Heterocyclic oncology drug intermediates
    • Specialized anti-viral compounds containing modified pyridine backbones

    2. Agrochemical Active Ingredient Synthesis

    Recognized for its contribution to crop protection agents, this compound acts as a key nitro-pyridine building block for the synthesis of selective herbicides and fungicide actives. Agchem producers depend on its purity to achieve downstream catalytic hydrogenation and post-nitration transformations, ensuring batch consistency in accordance with regulatory requirements for large-scale pesticide manufacture.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications
    • ISO 9001:2015 Quality Management for Agrochemical Manufacturing
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • China GB 2763 Maximum Residue Limits for Pesticide Residues

    Typical usage ratio

    • Typically used at 0.5–2.0% w/w of total batch mass, depending on synthesis route; chemists adjust levels to balance targeted yield and conversion efficiency of nitro substitution reactions.

    Downstream process integration

    • Charged directly into the nitration or hydrogenation step of the active ingredient synthesis; may precede chlorination or alkylation as required for the specific crop protection molecule.

    Final product types

    • Selective herbicide technical concentrates
    • Systemic fungicide powder bases
    • Pre-mixed pesticide formulation intermediates for downstream formulation

    3. Azo Dye and Pigment Intermediate

    Downstream dye manufacturers select this compound as a coupling component and nitroaromatic precursor in the synthesis of high-performance yellow and orange azo dyes. The material’s consistent reactivity supports color tuning and shade reproducibility, meeting export standards for textile and plastics coloration lines in the EU and Asia-Pacific regions.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textiles and dye auxiliaries
    • REACH (EC 1907/2006) for Restricted Substances in Dyes
    • ISO 9001:2015 for Dye Manufacturing
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals) for Apparel Dyes

    Typical usage ratio

    • Added at 1.5–4.0% by batch weight, with formulation levels controlled according to the tone depth and completeness of diazotization reactions; ratios adjusted based on target pigment load for each dye series.

    Downstream process integration

    • Played into the diazo-coupling step, usually after preliminary sulfonation; further processed through azo-bond formation, filtration, and spray-drying for pigment stabilization.

    Final product types

    • Azo yellow and orange pigments for plastics and fibers
    • High-fastness textile dye powders and dispersions
    • Coatings-grade dye concentrates for automotive and industrial applications

    4. Specialty Chemical Synthesis Intermediates

    Producers of fine chemicals employ this material in the construction of custom pyridine derivatives and diversified heterocycles, particularly for specialty additives and chemical sensors. Its defined nitro and methyl substitution pattern allows efficient downstream functionalization favored by R&D and scale-up teams working within controlled pilot and kilo-lab environments.

    Industry compliance standards

    • ISO 9001:2015 for Fine Chemical Production
    • Responsible Care® Management Practices
    • Custom project QC standards based on client technical agreements
    • China JC/T or ASTM E260 for chemical purities

    Typical usage ratio

    • Utilized at 0.8–3.2% w/w depending on targeted structure complexity; amount is determined by specific stoichiometry of subsequent transformations relevant to the downstream molecule’s design.

    Downstream process integration

    • Inserted during the condensation step of heterocycle assembly or during nucleophilic substitution to install additional functionality; further transformed through reduction or coupling reactions before downstream formulation.

    Final product types

    • Specialty chemical intermediates for proprietary additive synthesis
    • Prototype functional materials for chemical sensing and analytical reagents
    • Precursor compounds for polymer modification additives
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    Competitive 2-Hydroxy-5-Methyl-3-Nitropyridine prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2-Hydroxy-5-Methyl-3-Nitropyridine: Expertise from a Chemical Manufacturer

    Built on the Factory Floor: How We Understand the Substance

    In a world full of chemical catalogs and intermediaries, it’s important to actually stand at the reactor, check the progress of the process, smell the faint, distinctive scent as the distillation kicks in, and physically watch purity levels edge up under the gaze of a seasoned QA manager. That’s where a manufacturer’s view on 2-Hydroxy-5-Methyl-3-Nitropyridine (also known by chemists as 3-Nitro-5-methyl-2-pyridinol) begins—in the plant, not behind a computer or at a reselling desk. This compound’s specialty synthesis firmly positions it in a category above generic pyridine derivatives, with decades of niche trial, adjustment, and feedback shaping its current specifications. The pathway to scale-up has never been merely academic. It’s been practical, grounded, and sometimes, a little stubborn—lessons in managing evolving regulatory reporting or in troubleshooting an unexpected spike in byproduct grade.

    What Goes Into Our 2-Hydroxy-5-Methyl-3-Nitropyridine

    Attention to raw material purity ranks high in our process. We source matched lots for the methylating and nitrating agents to avoid sudden variability that shows up even in advanced HPLC trace profiles. Temperature, pressure, and batch size don’t hide their personalities: we’ve learned to tune every step with real-world feedback to assure batch-to-batch consistency. This means an analytical certificate tied directly to a reactor, not a bulk trader’s shipment.

    Our typical output appears as a pale to yellowish crystalline powder. Particle form and color offer early hints about process control—darker material signals overreaction or contamination, calling for hands-on correction, not a written procedure. Water content holds well under 0.5%. With melting points solidly matching published values, this detail cements the product’s identity much more effectively than a fancy label could. The main impurity profile—mainly unreacted starting pyridine or a trace of 3-nitro-2-pyridinol—never escapes resin or charcoal treatment, and our in-house methods keep detection and removal up to date.

    Real-World Uses: Where This Molecule Matters

    Customers don’t pick 2-Hydroxy-5-Methyl-3-Nitropyridine for ornamentation. It goes into advanced intermediates for pharmaceutical R&D, agricultural product discovery, specialty colorants, and even some high-end materials research. Paint chemists look at the electron-donating and withdrawing effects of methyl and nitro groups for fine-tuning pigment properties. Specialists in medicinal chemistry use the structure’s reactivity to anchor unique scaffolds. The hydroxyl offers a handle for acylations; the nitro tweaks ring electronics. Versatile, reliable material supports ambitious design, but requires a controlled, reproducible foundation—our daily target.

    In pilot pharma environments, only a version with low-metal content (often less than a few ppm of any transition metals) supports downstream catalytic hydrogenation or coupling steps. You won’t see us selling “tech grade” on a whim; we have watched too many projects falter when trace impurities from upstream collapse a reaction or introduce unidentified byproducts. The discipline of repeated, small-scale validation informs how we manage our plant productions—the details get built in, not handed off to a late-stage QC technician.

    What Makes This Compound Different From Common Alternatives

    Several manufacturers list substitutions: 3-nitropyridine, 2-methyl-5-nitropyridine, hydroxy-3-nitropyridines without the methyl group, or even just pyridine rings with functional groups shuffled around the backbone. These might look similar in a table or a structural diagram, but downstream chemistry disagrees quickly. An ortho hydroxyl with a meta nitro and para methyl changes reactivity, solubility, and stability properties—especially under heat or in strongly basic environments. From personal observation, some researchers initially run screens with easier-to-source analogs, only to switch back to this exact structure after batches behave unpredictably or purification steps drag on forever.

    For researchers or production chemists, these small tweaks matter. The presence of a methyl substituent at position 5—rather than the more common 3- or 4- positions—affects polarity, melting point, and sometimes gives an edge during crystallization, reducing wash steps and solvent need. Nitropyridine analogs without a hydroxyl at the 2-position can’t form certain key bonds as easily, leaving gaps in the chemical toolkit. We’ve even seen some minor uses emerge in electrochemical devices, where an extra methyl fine-tunes electron mobility through a film. Such delicate uses never make it into the catalogs or commodity markets; they arise only through custom dialogues involving real samples and data exchanges, from people who handle kilogram runs and read their own waste logs, not just spreadsheets.

    Meeting Regulatory and Safety Demands

    Experienced plant managers expect more stringent reporting every year. Full traceability from raw material through isolation and packaging backs up every technical claim we make. Spec sheets don’t just pass from one warehouse to another; they build from original in-process controls, recorded in our actual production environment. We document solvent recycling rates, contaminant identification, and stability under warehouse conditions because we must pass ever-tougher audits, not just fill orders. For export, we chase ahead of evolving lists of restricted or controlled substances; even small changes to impurity limits affect how our drums land at a client’s site.

    Long-term, we adjust operations to anticipate new workplace exposure limits or preferred packaging formats. Customers with custom needs, whether ultra-low dusting or pre-packed portions, benefit directly from our close relationship with package lines and shipping staff. These lived realities—like confirming the right lining for a drum, not just assuming it’s chemically inert—are what keep downstream users protected. We know that a mistake in packaging, even a minor seal fault, can lead to exposure events or contamination. Fielding calls from experienced scientists in the middle of the night underscores the value placed on direct manufacturing accountability and practical, local fixes.

    Supporting Downstream Development

    True manufacturing isn’t about filling a spec sheet and walking away. R&D teams talk to our chemists about scale-up steps that textbooks gloss over. How does this batch behave as a solution in acetonitrile, compared to the last? Does a new filtration aid leave behind micro-particles, changing the clarity in final crystallization? These questions don’t stem from a sales pitch—they arise day to day, and the knowledge gained feeds right back into the reactor and the loading schedule. When a partner comes with a new application—say, as a starting point for a chiral ligand or a seed molecule for a next-generation herbicide—we work through the necessary modifications: boosting purity, drying protocols, or removing stubborn trace organics.

    We’ve seen requests for tighter particle size ranges, higher solubility, or specialized analytical fingerprints (like custom GC methods calibrated for process intermediates nowhere found in standard databases). Handling these changes demands a flexible production mindset. It’s not just about what the product is, but how it performs under conditions set by real-world users. Lab-scale trial runs give us fast feedback—sometimes painful if an adjustment blows out a filter or jams a pump. Those details stay with us and shape how each future ton gets handled.

    Why We Hold Academic and Industrial Collaboration Close

    Serving niche markets, especially in pharmaceutical and fine chemical R&D, puts us close to university labs and industrial research parks. Reproducibility issues or unforeseen side reactions can derail months of work, which puts the focus squarely on consistent manufacturing detail. We don’t ship just to meet quota—we track feedback, sample reproducibility, and performance in secondary syntheses. There’s no substitute for a call from an academic group reporting trouble or asking for a small tweak in specification. Sometimes, solution color changes, or yield drops point to minor differences invisible in standard QC. Listening and acting on these observations keep our production relevant.

    Sometimes, the input is as straightforward as switching packaging types to prevent static, or as complex as introducing orthogonal analytical methods to catch rare side products. We log these cases internally, ensuring future users benefit from previous troubleshooting—even if the batch meets basic published criteria. No abstract guarantee or faceless certificate serves users better than an ongoing, problem-solving collaboration between manufacturer and end-user.

    Potential Issues and Lessons from Experience

    Over the years, we’ve hit snags. Some early batches suffered from inconsistent drying curves, dragging moisture content above target—a nuisance in downstream reactions involving organometallics prone to hydrolysis. Others carried faint but stubborn halide traces from a process shortcut abandoned after just a few runs. Each post-mortem fed improvements down the line. Now, process adjustments get subjected to a reproducibility stress-test before scale-up. Analytical investments, including faster LC-MS mapping and thermal gravimetric profiling, save time on the tail end by catching non-obvious impurities upfront.

    Packaging, too, demanded close attention. Early shipments, especially for export or high-humidity destinations, sometimes triggered unexpected clumping or slow decomposition at the storage site. Switching to double-laminated foil and rigid drum linings worked better than previously imagined. User reports have directly shaped our labeling, safety, and shipping instructions—these lessons were not found in any manufacturer’s training manual but learned from keeping in touch with long-term customers who actually open the containers and run reactions, not just tick boxes.

    Solving for the Next Generation: Efficiency and Responsibility

    Process evolution doesn’t stop at synthetic yield. Energy inputs, solvent recycling, and waste minimization now play as big a role as actual output weight. We constantly review greener nitration routes and pilot less energy-intensive methylations. Lab and plant workers contribute directly to process optimization, catching ideas and failures that only hands-on practitioners notice. When a waste-stream separation lowered heavy metal content by twenty percent, it came from a suggestion by a day-shift engineer—and implementation got written back into future product safety sheets.

    Modern buyers—regardless of size—expect traceability, responsible sourcing, and transparent problem resolution. Meeting these expectations means more than keeping up with compliance requirements. It means running real trials, adjusting processes, and staying ready for a phone call after a customer’s experimental run reveals something unexpected. Every new regulatory update, every shift toward stricter workplace protections, influences how we adjust our systems—and how we guide clients who depend on our product to meet their own regulatory hurdles.

    Looking Ahead: Direct Manufacturing Involvement and Honest Communication

    Trust in a specialty chemical doesn’t settle at brand recognition or generic labeling. It grows with each batch—how impurities fluctuate, how packing materials interact with reagents, and even with direct support fielded to chemists handling the product late at night. We stay available and involved, providing input and learning from end-user challenges, strengthening production and technical support in a cycle that benefits all users.

    Every new order pushes us to reaffirm why direct manufacturing insight matters. Changes in supply chain, shifting research priorities, or regulatory adjustments bring uncertainty, but ongoing improvement and transparency stay at the center of what we do. 2-Hydroxy-5-Methyl-3-Nitropyridine isn’t just a line in a catalog—it is the product of real-world experience, day-to-day effort, and a commitment to detail that benefits chemists, formulators, and researchers who look beyond commodity alternatives.

    All told, our focus remains clear: reliable product, responsible practices, and an honest, experience-driven partnership with users. This foundation sets apart true manufacturing—and supports the innovation and safety required for tomorrow’s discoveries.