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2-Hydroxy-6-Methyl-5-Nitropyridine

    • Product Name 2-Hydroxy-6-Methyl-5-Nitropyridine
    • Alias 6-Methyl-5-nitro-2-pyridinol
    • Einecs '-'
    • 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

    316724

    Chemicalname 2-Hydroxy-6-Methyl-5-Nitropyridine
    Molecularformula C6H6N2O3
    Molecularweight 154.12 g/mol
    Casnumber 50813-75-9
    Appearance Yellow crystalline powder
    Meltingpoint 176-178°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Density Approx. 1.43 g/cm3
    Smiles CC1=NC(=CC(=N1)O)[N+](=O)[O-]
    Iupacname 6-methyl-5-nitro-1H-pyridin-2-one
    Storagetemperature Store at room temperature, protected from light and moisture

    As an accredited 2-Hydroxy-6-Methyl-5-Nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 2-Hydroxy-6-Methyl-5-Nitropyridine, with a tamper-evident cap and hazard labeling.
    Shipping 2-Hydroxy-6-Methyl-5-Nitropyridine is shipped in tightly sealed containers, compliant with chemical safety regulations. The package is clearly labeled, protected from moisture, sunlight, and physical damage. It is transported as a non-flammable, toxic solid, accompanied by a safety data sheet (SDS), and handled by trained personnel with appropriate hazard precautions.
    Storage 2-Hydroxy-6-methyl-5-nitropyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers and reducing agents. The storage area should be clearly labeled, with access limited to trained personnel, and appropriate spill containment measures in place. Avoid moisture and keep container tightly closed.
    Application of 2-Hydroxy-6-Methyl-5-Nitropyridine

    Applications of 2-Hydroxy-6-Methyl-5-Nitropyridine in Industrial Manufacturing

    As a direct manufacturer of 2-Hydroxy-6-Methyl-5-Nitropyridine, we support a range of specialized downstream sectors with consistent product quality and technical formulation data for production line engineers and procurement managers.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    Several API producers utilize this compound as a key intermediate in the preparation of heterocyclic drug molecules, including anti-inflammatory and cardiovascular agents. The nitro and hydroxyl functionalities serve as reactive sites in multi-step synthesis routes, allowing for functional group transformations with high selectivity. Full traceability and process-specific batch control remain critical for GMP-regulated pharmaceutical manufacturing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) and USP monographs for bulk substances
    • 21 CFR Part 211 (US FDA cGMP requirements)
    • Certificate of Analysis with residual solvent and impurity profiling

    Typical usage ratio

    • Employed at 5–20 mol% of the total reactant mass in API intermediate stages, adjusted based on route efficiency and desired yield

    Downstream process integration

    • Introduced during the early stage of API synthesis in reactors equipped for nitration, hydrogenation, or amination steps
    • Subjected to further derivatization forming pyridine-based cores for finished APIs

    Final product types

    • Third- and fourth-generation antihypertensive drugs
    • Pyridine-based anti-inflammatory compounds
    • Intermediates for generic and custom APIs
    • Contract manufactured pharmaceutical intermediates

    2. Agrochemical Synthesis for Pyridine-Derived Pesticides

    Leading crop protection companies select this material as a strategic intermediate for synthesizing nitro-substituted pyridine herbicides and insecticides. Its reactive sites accommodate tailored substitution or reduction for new molecule development. Strict adherence to agricultural chemical regulations and environmental controls is enforced throughout the product integration process.

    Industry compliance standards

    • FAO and WHO standards for technical material purity
    • ISO 9001:2015 for agrochemical manufacturing
    • Regulation (EC) No 1107/2009 for EU plant protection products
    • EPA FIFRA guidelines (US) on raw material handling and registration

    Typical usage ratio

    • Used at 10–30% of the synthetic batch for targeted heterocycle formation in active ingredient production, variable with pesticide structure

    Downstream process integration

    • Charged into plant-scale reactors for stepwise building of pyridine-based agroactive scaffolds prior to final functionalization
    • Isolated or further processed to achieve regulated toxicity and efficacy parameters

    Final product types

    • Nitropyridine derivative herbicides
    • Pyridine-based fungicidal intermediates
    • Insecticide technical concentrates
    • End-use crop protection formulations (emulsifiable concentrates or wettable powders)

    3. Dye and Pigment Intermediate for Specialty Colorants

    Manufacturers of synthetic dyes and organic pigments incorporate this chemical into their molecules to introduce electron-withdrawing nitro and methyl groups for enhanced chromophore intensity and stability. Its use under controlled reaction parameters ensures consistent shade development and fastness properties valued in textile and plastics industries.

    Industry compliance standards

    • Oeko-Tex Standard 100 for restricted substances in dyes
    • REACH Substances of Very High Concern (SVHC) regulations
    • ISO 9001:2015 for pigment and dye manufacturing quality management
    • ZDHC chemical management protocols (Zero Discharge of Hazardous Chemicals)

    Typical usage ratio

    • Typically 15–25% by mass in target chromophore scaffold syntheses, modulated to balance color strength and reaction yield

    Downstream process integration

    • Added during diazotization or coupling stages for pigment and dye formation
    • Undergoes further sulfonation, reduction, or condensation for specific shade targets

    Final product types

    • Yellow and brown nitropyridine dyes for synthetic and natural fibers
    • High-stability pigments for plastics and inkjet formulations
    • Specialty organic colorants for automotive coatings
    • Reactive dye intermediates for cellulosic materials

    4. Electronic and Fine Chemical Precursor for Functional Materials

    Advanced material and electronic chemical suppliers apply this pyridine derivative as a precursor in the production of electron-acceptor ligands and specialty functional monomers. Applications include liquid crystal alignment agents, photoactive materials, and charge transfer complexes, where process purity and batch repeatability are essential to device performance and reproducibility.

    Industry compliance standards

    • IEC 61249 for materials in electronics
    • RoHS (Restriction of Hazardous Substances) compliance
    • ISO 14001:2015 for environmental management in specialty chemical plants
    • Customer-specific electronic grade purity specifications

    Typical usage ratio

    • Employed at 1–8% by mass in functional molecule synthesis protocols, controlled tightly per electronic material formulation requirements

    Downstream process integration

    • Introduced in the formation of functionalized pyridine ligands prior to metallation or polymerization
    • Used in micro-scale batch reactors for high-purity electronic chemical output

    Final product types

    • Photoresist additives for semiconductor lithography
    • Liquid crystal display (LCD) alignment and doping agents
    • Advanced charge-transport materials for OLED and OPV devices
    • Functionalized monomers for specialty polymer engineering

    5. Research Chemical Feedstock for Heterocyclic Library Synthesis

    Chemical research organizations and custom molecule developers employ 2-Hydroxy-6-Methyl-5-Nitropyridine as a building block for generating diverse pyridine libraries. The electron-withdrawing and donating group arrangement on the aromatic ring structure offers unique opportunities for exploring reactivity trends, preparing enzyme inhibitors, or facilitating SAR studies in medicinal chemistry programs. Direct factory supply ensures reliable documentation and traceability for regulated research environments.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for analytical and preparative research
    • ISO 17025 laboratory accreditation recognition
    • Material Transfer and Safety Data Sheet (MSDS) documentation
    • International Air Transport Association (IATA) restricted chemical shipping standards

    Typical usage ratio

    • Applied at 0.1–5 mmol scale for small-batch screening, or 50–100 g per batch in process development pilots, as determined by synthetic pathway complexity

    Downstream process integration

    • Used in parallel synthesis projects for heterocyclic diversification
    • Derivatized under controlled reaction conditions for structure-activity relationship exploration

    Final product types

    • Heterocycle-rich compound libraries for pharmaceutical discovery
    • Lead candidates for biological assay testing
    • Analytical standards for reference laboratories
    • Intermediate scaffolds in medicinal and process chemistry research
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    Certification & Compliance
    More Introduction

    Introducing 2-Hydroxy-6-Methyl-5-Nitropyridine: A Manufacturer’s Perspective

    What Sets 2-Hydroxy-6-Methyl-5-Nitropyridine Apart

    Working in chemical manufacturing for decades, I’ve watched the landscape change as demands for precision and traceability get sharper every year. 2-Hydroxy-6-Methyl-5-Nitropyridine, sometimes abbreviated as HMNP, has earned a steady place in our portfolio. It’s a yellow crystalline solid that draws attention from R&D departments in large pharma companies, as well as smaller labs pushing the frontier of heterocyclic chemistry. As we oversee each stage of its synthesis and purification, the reliability of active groups on the pyridine ring becomes a key advantage.

    This molecule’s structure—hydroxyl at position two, methyl at position six, nitro at position five—may not look striking on a chalkboard, but these details guide reactivity, solubility, and the types of transformations partners can expect. With the methyl group and hydroxyl locked into place, downstream chemistry opens up options that aren’t available with parent pyridines or related nitro derivatives.

    The Role It Plays in Today’s Synthesis Pathways

    We see most interest in HMNP from those engaged in medicinal chemistry, agrochemical discovery, and, not least, in the dyes and pigment sector. Medicinal chemistry teams value the balance between electron-rich and electron-poor centers because this enables stepwise derivatization—crucial for constructing advanced intermediates.

    Our connections with synthetic chemists working on kinase inhibitors and antibacterial scaffolds have underlined that subtle shifts in substitution—methyl or nitro positioning, for instance—lead to different selectivities or metabolic profiles. The responsive nature of the 2-hydroxy group, in particular, lets people anchor further functional groups for SAR studies or testing efficacy in biological systems. This difference becomes apparent in real projects, not just on paper.

    Specifications Backed by Direct Manufacturing Oversight

    Running several batches a month, our product consistently lands above 98% purity, confirmed by HPLC and NMR—data generated right here on-site. Some years ago, control over particle size became a theme during client audits, as it can affect reaction kinetics and safety when scaling up. For that reason, our standard process targets a controlled fraction, supporting both bench and plant-scale experiments.

    Handling HMNP safely means staying alert to its moderate sensitivity and providing adequate storage. Our team stores it under nitrogen, in tightly sealed containers, away from direct sunlight. This practice doesn’t come from manual-writing, but from observing the real effects of trace moisture or oxygen on batch stability over the years. Material handled with less care can yellow or clump, so we keep plenty of experience-based Standard Operating Procedures in place, ensuring each lot meets expectations after shipping as well as before.

    Choosing HMNP for Specialized Routes

    Chemists who compare HMNP to compounds like 2-hydroxypyridine or 5-nitropyridine spot the impact of the methyl group. It directs reactivity, particularly in nucleophilic aromatic substitutions, which simplifies certain protection or deprotection steps. Some customers once struggled with byproduct formation until switching to this exact isomer—proof that a small structural modification changes everything in a synthetic route’s success.

    Then, for those aiming to convert the hydroxy moiety to other groups—say, ether formation or esterification—the combination of methyl and nitro at those positions reduces undesired side reactions. Modifications proceed with superior selectivity, allowing for clearer separation and higher yield. I’ve watched partners save entire weeks of troubleshooting thanks to this predictable chemistry.

    Comparisons with Other Pyridine Derivatives

    Working upstream in chemical manufacturing puts us in touch with a broad catalog of pyridine derivatives. Some regularly compare HMNP with 2,6-dimethyl-5-nitropyridine or with simple 5-nitropyridine. In practical experience, HMNP handles differently—crystalline pinpoints at lower temperature, melts slightly above room temperature, and dissolves in organic solvents with a manageable exotherm.

    This matters for two big reasons: first, a shift in melting behavior allows tighter process control; second, changes in solubility profile ease work-up after reactions. If you’re performing reactions involving strong bases or reductants, HMNP’s robust molecular backbone resists over-reduction and provides a buffer against common impurities that plague similar compounds in large-scale settings.

    As an example, one partner transitioned from 2-hydroxy-5-nitropyridine and found that our product’s methyl group removed persistent instability during nitration at scale. Less decomposition led to a safer reactor environment, and less waste generated, both facts highlighted in their own safety debriefs. This reduction in error tracking and lost time isn’t measured in specification sheets—it’s seen in uninterrupted plant runs.

    How We Ensure Consistent Output Year After Year

    Real-world manufacturing regularly uncovers details that don’t show in technical brochures. For instance, in the post-synthesis wash cycle, solvent selection can affect not just cleanliness, but the chemical’s shelf life. Over hundreds of campaigns, our team has tested and tuned this step, seeking the balance between removing trace metallic impurities and retaining crystal integrity.

    We tailor temperature and humidity at each stage. Excess moisture or airborne contamination during final packaging encourages caking, so we control environmental conditions in the packing zone. While industry guidelines mention these things, it’s the daily experience of scrapped lots and costly reprocessing that has drilled in the practice. Our learning curve—sometimes steep, always ongoing—translates into cleaner, more reliable HMNP for every shipment.

    User-Focused Adjustments: Feedback Drives Us

    We’re not content to produce HMNP by formula alone. Feedback from academic groups and industrial labs comes directly to the plant floor. For example, some downstream users wanted a finer grade for microreaction platforms. After technical consultation, we modified our mill settings for those users, achieving a narrower particle distribution. Others sought validation for residual solvents beyond standard certificates, so our QC lab expanded verification protocols to fit their environmental policies.

    What sets our product apart isn’t just what leaves our factory. It’s the willingness to set up custom runs for clients needing particular impurity profiles, different packaging, or adjusted pH in the mother liquor stage. Each tweak adds challenge, but years of hands-on process improvement have shown us the return in client trust, project wins, and even the rare holiday card from a satisfied scientist.

    Regulatory Compliance Earned, Not Assumed

    If you’ve worked in manufacturing long enough, you’ve dealt with regulatory visits. Certificates of analysis only go so far; regulators need traceability from raw materials right down to the outer drum labels. For our HMNP, compliance doesn’t just mean meeting minimum standards. We’ve woven record keeping, batch tracking, and up-to-date documentation into the daily production rhythm. Auditors see not just papers, but staff ready to talk through their process knowledge or demonstrate cleaning logs in person.

    We frequently field requests about compliance with REACH, TSCA, and other frameworks. Our registry involvement started not out of obligation, but to remove delays for partners working to deploy new molecules in the EU, US, or Asia-Pacific zones. By investing early in compliance, we’ve avoided shipping problems and gained the confidence of purchasers facing tight development timelines.

    Environmental Responsibility in Manufacturing

    In chemical production, talk of sustainability can sound hollow—unless rooted in practical action. For HMNP, our facility reclaims and recycles wash solvents. Spent acids and bases get neutralized onsite rather than shipped for costly disposal. We test scrubbers for off-gassing from nitro-group processing, and log results not because a form demands it, but because the alternative is local air complaints.

    Supply chain transparency matters, too. Our raw material tracking uses supplier histories with visible quality trends, so we know which upstream changes might impact downstream quality. If a particular phenol source shifts in impurity profile, we can intervene before full-scale production. Environmental management, for us, is about prevention, not just remediation—and the results show in lower volumes of hazardous waste generated across campaigns.

    Industry Trends: Future Prospects for HMNP

    The way the market for heterocyclic intermediates is shaping up, demands for HMNP are likely to increase. Growth in personalized medicine, targeted agrochemicals, and high-durability pigments remains robust. Researchers keep probing new derivatives and conjugated molecules, placing reliance on building blocks that deliver exactly as advertised.

    From our vantage point as manufacturers, we see a desire for intermediates with more complexity, but still straightforward in terms of scale-up potential. HMNP fits into this niche perfectly: it’s stable enough for safe shipment in bulk, yet reactive enough for innovation downstream. Academic publications and patent filings referencing this compound have picked up, with plenty featuring successful late-stage derivatizations or bioconjugations that trace back to the quality of the starting material.

    Partnership: More Than a Transaction

    Direct manufacturing connections matter in today’s environment. With so many distributors and resellers in the mix, end users can end up uncertain about provenance, process variability, or even legal standing in patent-heavy fields. Clients working with us get direct answers on lot origin, contaminant testing, and supply continuity—because those are answers we have, not guesses or sales promises.

    When shortages swept the specialty chemical market during recent global events, our ability to source core reagents and pivot batch schedules kept partners supplied. That reliability has roots in long-term supplier relationships and an organizational habit of strategic stockpiling for at-risk inputs. We’ve ridden out monsoon disruptions, port slowdowns, and even local power cuts thanks to investments in redundancy. The result is measured not just in contracts, but in project milestones hit on time.

    Continuous Improvement: Listening to Labs, Not Just Metrics

    Every lot of HMNP carries the imprint of the feedback loop between our chemists and the people running the reactions. When clients point out solubility issues in rare solvents or need alternate crystallization solvents to enhance isolation, our process chemists work directly with theirs. This open channel identifies bottlenecks that never appear in spreadsheet analyses.

    For example, a US researcher struggled with color impurities after scaling a reaction. Our onsite staff visited, observed the filtration set-up, and suggested a double-wash using a different solvent mixture. Color dropped, purity rose, and the solution benefited future batches. These hands-on interventions are a world away from simple compliance or outsourced manufacturing, and they motivate our team daily.

    Summary: Why the Details Matter with 2-Hydroxy-6-Methyl-5-Nitropyridine

    Manufacturing 2-Hydroxy-6-Methyl-5-Nitropyridine is not a mechanical job. It’s a test of everything we know about fine chemical production. From molecule design to execution, to packing and support, each detail creates the foundation for inventing tomorrow’s products—whether they target diseases, enhance crops, or brighten new textiles. For many years, real progress has depended on reliability, flexibility, and the discipline to learn from every batch. That’s where the value of HMNP lies, shaped by attention, improvement, and the quiet knowledge that the right building block can set an entire project on the right path.