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3-Hydroxy-6-Methyl-2-Nitropyridine

    • Product Name 3-Hydroxy-6-Methyl-2-Nitropyridine
    • Alias 3-Hydroxy-6-methyl-2-nitro-pyridine
    • Einecs 252-166-5
    • 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
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    Specifications

    HS Code

    139076

    Name 3-Hydroxy-6-Methyl-2-Nitropyridine
    Molecularformula C6H6N2O3
    Molecularweight 154.12 g/mol
    Casnumber 60270-58-0
    Appearance Yellow solid
    Meltingpoint 170-174°C
    Solubility Soluble in DMSO and methanol
    Purity Typically ≥98%
    Chemicalclass Nitropyridine derivative
    Iupacname 6-methyl-2-nitropyridin-3-ol
    Smiles CC1=NC=C(C=C1N(=O)=O)O
    Storagetemperature 2-8°C
    Hazardstatements May cause skin and eye irritation

    As an accredited 3-Hydroxy-6-Methyl-2-Nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of 3-Hydroxy-6-Methyl-2-Nitropyridine supplied in a sealed amber glass bottle with tamper-evident cap and hazard label.
    Shipping 3-Hydroxy-6-Methyl-2-Nitropyridine is shipped in tightly sealed, chemical-resistant containers to ensure stability and prevent contamination. The package includes appropriate hazard labeling and documentation according to international shipping regulations. It is transported as a limited quantity chemical, away from incompatible substances, and stored in a cool, dry environment during transit.
    Storage **3-Hydroxy-6-Methyl-2-Nitropyridine** should be stored in a tightly sealed container in a cool, dry, well-ventilated area, away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers or acids. Store at room temperature or as recommended by the manufacturer. Ensure proper labeling, and restrict access to trained personnel. Avoid moisture and ignition sources to maintain chemical stability.
    Application of 3-Hydroxy-6-Methyl-2-Nitropyridine

    Applications of 3-Hydroxy-6-Methyl-2-Nitropyridine in Industrial Manufacturing

    As a manufacturer dedicated to the production and global supply of 3-Hydroxy-6-Methyl-2-Nitropyridine, we provide this pyridine derivative to downstream sectors that require stringent quality consistency for regulated and high-value end products. The applications below represent the real, traceable industries where this material supports process efficiency and end-use performance. We detail each sector’s requirements on compliance, incorporation rates, integration into downstream processes, and end-product profiles, according to current industrial standards and audited manufacturing routes.

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

    This compound serves as a valuable intermediate in synthesizing specific heterocyclic APIs, particularly within anti-inflammatory and anti-infective drug classes. Its selective reactivity supports critical scaffold construction steps under validated process parameters. Customers rely on this raw material for routes involving pyridine core expansion or substitution necessary for proprietary drug compounds, integrating it at a defined stage to ensure batch-to-batch consistency during quality audits and regulatory filings.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP <1092> Pharmaceutical Dosage Forms
    • European Pharmacopoeia Monographs (where applicable)
    • cGMP as enforced by US FDA and EMA

    Typical usage ratio

    • 1–8% of the total reaction mass, depending on final API structure and stepwise conversion, with precise scale determined by target batch size and impurity profile controls

    Downstream process integration

    • Introduced during heteroaromatic ring assembly or selective nitro group functionalization stages in multi-step batch synthesis
    • Participates in solution phase synthesis under controlled temperature and inert atmosphere protocols
    • Utilized in both small molecule and extended structure formation prior to downstream workup and final purification

    Final product types

    • Anti-inflammatory API intermediates
    • Anti-infective heterocyclic drugs
    • Key intermediates for specialty APIs targeting CNS and respiratory indications

    2. Agrochemical Pyridine Derivative Synthesis

    Leading crop protection manufacturers use this compound to construct advanced pyridine frameworks for new-generation herbicides and selective insecticidal products. The compound enables precise placement of hydroxy and nitro substituents, facilitating unique activity profiles and regulatory-compliant residue properties in final actives. Integration occurs under tightly controlled reaction monitoring protocols to meet field application requirements and residue safety regulations globally.

    Industry compliance standards

    • FAO/WHO Maximum Residue Limit (MRL) guidelines
    • REACH registration for environmental safety in Europe
    • OECD Good Laboratory Practice (GLP) for registration studies
    • ISO 9001:2015 Quality Management System in synthesis

    Typical usage ratio

    • 0.5–5% of total synthetic formulation mass, adjusted based on target pyridine derivative potency and subsequent derivatization efficiency

    Downstream process integration

    • Charged at the stage of pyridine ring assembly within closed-system manufacturing lines
    • Enters into nitro group conversion sequences either pre- or post-reactive halogenation
    • Operates under monitored byproduct filtration to improve downstream yield consistency

    Final product types

    • Selective herbicide actives
    • Precursor compounds for insecticide synthesis
    • Intermediate for fungicide building blocks

    3. Specialty Dye and Pigment Intermediate Manufacturing

    Dye formulation facilities employ this nitropyridine derivative to generate high-performance colorant precursors for applications requiring photostability and precise chromophore control. The compound’s functional groups facilitate nucleophilic aromatic substitution and coupling reactions, essential for creating dyes with specified emission profiles and fastness properties in textile, plastic, and ink industries. Controlled addition ensures reproducibility over large-scale runs for international colorant compliance.

    Industry compliance standards

    • OEKO-TEX Standard 100 for restricted substances
    • REACH Annex XVII for textile colorants in the EU
    • ISO 105-A02 Color Fastness Certification
    • ZDHC MRSL for zero discharge of hazardous chemicals

    Typical usage ratio

    • 1–7% by weight in the synthesis of dye intermediates, depending on targeted hue and chromophore substitution pattern

    Downstream process integration

    • Introduced into ring coupling steps during organic pigment precursor synthesis
    • Used in substitution reactions following nitro group activation or reduction modules
    • Integrated under high-shear mixing and monitored temperature ramp to ensure product uniformity

    Final product types

    • High-stability textile dyes
    • Organic pigments for plastics and coatings
    • Specialty colorants for inkjet and packaging applications

    4. Electronic Material Intermediate for OLED and Display Chemistry

    Producers of optoelectronic materials integrate this molecule as a core-building block for customized aromatic heterocycles within organic light-emitting diode (OLED) fabrication. Selected for its electron-withdrawing and donating substituents, the compound supports consistent charge transport and light emission layer performance. Manufacturing protocols require close monitoring to comply with sector-specific purity and trace metals criteria, optimizing both efficiency and panel qualification rates in end-use applications.

    Industry compliance standards

    • RoHS Directive (EU) 2011/65/EU on hazardous substance restriction
    • IEC 61249-2-21 for halogen-free electronic materials
    • ISO 14001 Environmental Management for electronics production
    • Corporate critical impurity limits for OLED grade chemicals (<50 ppm metal ion content)

    Typical usage ratio

    • 0.1–3% by mass in the precursor blend for electronic functional material synthesis, tailored based on desired optoelectronic properties and purity specifications

    Downstream process integration

    • Incorporated during solution-phase preparation of heteroaromatic monomers
    • Used in condensation reactions or Suzuki coupling for advanced host-guest material formation
    • Participates directly in charge transport matrix assembly prior to device deposition steps

    Final product types

    • OLED emitter and transport materials
    • High-performance components for display and lighting modules
    • Intermediate layers for organic semiconductors

    5. Advanced Fine Chemical Building Block for Research-Grade Synthesis

    Specialty fine chemical companies and research institutes employ this compound as a defined building block in the development of novel heterocyclic scaffolds, particularly for exploratory medicinal and agrochemical applications. Stringent quality traceability is essential as the material enters synthesis routes where minor impurities could hinder downstream SAR elucidation or analytical reproducibility for publication and patent filing. Formulation chemists often adjust input loads based on targeted functionalization schemes and expected downstream transformations.

    Industry compliance standards

    • ISO 9001 quality management for laboratory reagents
    • Internal analytical methods for research-grade purity (HPLC/GC >98%)
    • GLP practices for documentation in preclinical research
    • Customer-specific compound traceability requirements

    Typical usage ratio

    • 2–10% in planned reaction mass, calibrated against projected yield and functional group compatibility for downstream modifications

    Downstream process integration

    • Dosed in pilot-scale or bench-top runs during initial ring construction or selective substitution
    • Integrated at the step of scaffold diversification for early stage SAR studies
    • Processed under inert conditions to safeguard against unwanted oxidations affecting downstream reactivity

    Final product types

    • Heterocyclic research intermediates
    • Library compounds for biological screening
    • Reference standards for structure-activity relationship validation
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    Certification & Compliance
    More Introduction

    3-Hydroxy-6-Methyl-2-Nitropyridine: In-Depth Insights from the Manufacturer

    Our Approach to 3-Hydroxy-6-Methyl-2-Nitropyridine

    For over twenty years, we have worked at the intersection of research, process chemistry, and industrial production. Among hundreds of pyridine derivatives we produce, 3-Hydroxy-6-Methyl-2-Nitropyridine stands out due to its unique reactivity and the specific demands it draws from both pharmaceutical and specialty chemical sectors. Its chemical structure—the substitution pattern of hydroxy, methyl, and nitro groups on the pyridine ring—brings valuable benefits in synthesis. Every pilot batch and kilogram-scale run pushes us to refine our methods, striving for purity, process safety, and reproducibility.

    Model and Specifications as Practiced by Industrial Chemists

    The chemical formula for 3-Hydroxy-6-Methyl-2-Nitropyridine, with a molecular weight of 154.13 g/mol, stays consistent across our output, as does its strict adherence to targeted impurity limits. We focus on crystalline material, with color ranging from pale yellow to orange-yellow. Over years of feedback from medicinal chemists and agrochemical formulators, we found a typical assay expectation surpassing 98%, and our process control enables us to deliver consistently above this benchmark. Water content, as measured by Karl Fischer, remains below 0.5%, preventing hydrolysis events that have spoiled so many development efforts in less meticulous hands.

    Trace residual solvents come under strict monitoring. Methylene chloride, which sometimes sneaks in from extraction, is kept beneath instrument detection—GC testing is routine, not an afterthought. Consistent melting range and particle form, though they may sound secondary, turn out to be decisive in downstream process yields. We have reconfigured drying and milling steps more than once to adapt to customer feedback, highlighting the importance of collaboration between producer and end-user.

    Why Process Matters: From Bench Scale to Tonnes

    Making kilogram and tonne quantities means managing variable batch reactions, heat transfer, and scale-up impurities. Unlike small laboratory samples, larger output can introduce by-products if reaction parameters drift. We have learned to maintain nitrate concentration and temperature profiles rigorously. Oxygen-sensitive intermediates demand careful exclusion of air, otherwise the hydroxy group can oxidize and trigger a range of side products, many producing colored impurities that complicate purification.

    Solvent recycling affects more than cost—it changes impurity profiles and environmental risk. Early process runs revealed that solvent re-use affected product consistency more than theory textbooks would have us believe. By implementing a closed-loop system with real-time GC monitoring, we established tighter control, not only reducing waste but ensuring lot-to-lot reproducibility demanded by both pharmaceutical candidates and advanced materials applications.

    The Role of 3-Hydroxy-6-Methyl-2-Nitropyridine in Advanced Synthesis

    Many leading-edge pharmaceutical projects rely on effective pyridine intermediates. The 3-hydroxy and 2-nitro positions give synthetic chemists versatile entry points—whether for nucleophilic aromatic substitution, reduction to amines, or functionalization for heterocyclic scaffolds. We have witnessed its use in several early-stage drug discovery programs, enabling sulfonamide derivatives that are difficult to synthesize by other means.

    Agrochemical researchers value this molecule for its adaptability in ring transformations and oxidative couplings. Modifying the nitro group—through reduction or rearrangement—opens up heterocyclic frameworks vital for crop protection agents. Over time we have seen new patents referencing this compound as a core building block, particularly in pyrazole and pyrimidine libraries.

    Outside of life sciences, electronics companies approach us for specialized applications. Certain functional materials, particularly conductive polymers, employ pyridine building blocks to adjust electronic properties. Quality requirements extend beyond purity—particle size, polymorphism, and residual ions can influence device reliability. Having seen how subtle impurities impact finished goods, we keep a close eye on these variables, offering custom pre-milling or sieving when engineers request it.

    Setting It Apart: Comparison with Other Pyridine Derivatives

    Among pyridines, the location and combination of substituents completely transform utility and handling. The presence of both hydroxy and nitro groups at specific positions separates 3-Hydroxy-6-Methyl-2-Nitropyridine from more common analogues, such as 2,6-dimethylpyridine or 3-nitropyridine. Unlike simple methylated pyridines, the hydroxy group introduces potential for hydrogen bonding and adds water solubility—features particularly appreciated in synthetic routes seeking green chemistry benefits.

    Compared to 2-nitro-5-methylpyridine, which is less reactive in substitution and more prone to forming intractable tars during high-temperature reactions, this product offers more predictable conversion yields and simpler work-up steps post-reaction. We have received feedback from research partners who tried cheaper alternatives and found their downstream yields suffered as a direct result of unexpected reactivity from non-optimal substitution patterns.

    Stability also sets our product apart. By tightly controlling process impurities and inerting during sensitive stages, we extend storage suitability far beyond competitors' products. Moisture present during extended storage can trigger decomposition or browning, especially where the nitro group is present. Our process deliberately minimizes exposure, locks in shelf life, and offers customers confidence even during international shipping or hot-season storage. Feedback from quality-control chemists underscores how less stable materials complicate batch records and delay pilot-to-plant scale-up.

    Direct Experience with End Uses and Downstream Impact

    Chemical intermediates often disappear into the black box of our customers’ labs; our experience is different. We receive technical inquiries from chemists fighting throughput bottlenecks, material failures, or unexplained reactivity. Tracing these issues, we’ve seen how trace impurities, moisture, or variable physical forms in 3-Hydroxy-6-Methyl-2-Nitropyridine affect not only reaction margins but the sheer reliability of entire synthetic routes.

    One case from a multinational pharmaceutical client involved an unexpected color formation during a key reduction. Investigation traced this directly to a by-product formed during a poorly controlled nitration on our end. Re-working our crystallization protocol eliminated the impurity, improved their API yield, and led to a long-term supply partnership. This example, among many, shows how quality beyond mere assay figures determines process success.

    Further down the innovation pipeline, agricultural R&D labs return feedback about material processability in pilot reactors. Certain physical parameters—clumping, poor dispersibility, or static issues—delayed scale-up and led them back to us for direct solutions. We altered granulation and packing, optimizing flow and reducing operator risk in their pilot plant. These real-world adjustments, based on continuous dialogue with process engineers and operators, matter more than the abstract language found in so many catalogs.

    Some electronics applications require even tighter control on residual metal ions or solvent traces. These end-use scenarios have driven us to adapt our purification methods, switching to all-glass equipment and expedited drying protocols. The result: batches that pass stringent electronics QC analysis. These changes stem directly from customer applications, reinforcing the difference a manufacturer makes when grounded in daily production rather than distant trading.

    Addressing Industry Challenges: Contaminants and Safety

    Pyridine derivatives pose specific risks during manufacture: hazardous gases, exothermic steps, and the potential for runaway nitration reactions. We have invested in real-time monitoring and pressure release protocols following early incidents in our facilities. Emergency handling instructions for staff, automatic shut-downs, and strict PPE rules show how evolved safety stems from real lessons, not just regulatory box-ticking.

    Customers often ask about the handling safety profile of 3-Hydroxy-6-Methyl-2-Nitropyridine, especially as the nitro group draws regulatory scrutiny. The nitro substituent increases the energetic potential of the molecule. We ship in moisture-resistant, double-sealed containers. MSDS documentation comes informed not only by generic chemical hazards, but by specific operational lessons: preserving material as installed, preventing static, and mitigating airborne dust. In our experience, downstream users benefit most from clear handling procedures shaped by active manufacturer involvement, not by off-the-shelf safety labels.

    Dealing with toxicological and environmental impact, especially where APIs or agrochemicals will result, motivates us to minimize extractables, avoid persistent organic pollutants, and document every lot’s residual chemistry with traceability. This commitment matches the rising global focus on sustainability—from green synthetic routes to responsible packaging and waste management in our own plants.

    Quality Control Measures Rooted in Experience

    Every batch starts with an in-depth QC plan derived from years of field experience and evolving international standards. Our lab teams use HPLC, NMR, and mass spectrometry to triple-check both main product and trace impurity profiles. Over time, we added GC-MS as a routine, not just for residual solvents, but to track subtle by-products invisible to standard UV methods.

    Each parameter on our certificates—assay, melting range, moisture, loss-on-drying, heavy metals, and residual organics—relates directly to lessons learned from returns, failures, or feedback. Investing in cross-departmental review before shipping shortens delivery times and reduces batch variability. For customers in regulated markets, this approach helps them streamline validation, avoiding costly re-testing and delays in their own development programs.

    We have seen first-hand how late batch failures or mismatches between analytical methods can halt projects. To address this, we offer cross-lab comparisons: if a client uses a different reference standard or method, our technical chemists can run parallel tests and help reconcile results. The main lesson: standardization matters, but real industry support means flexibility and quick response to shifting requirements.

    Refining Manufacturing and Supply: Lessons for the Future

    Consistent availability and short lead times for 3-Hydroxy-6-Methyl-2-Nitropyridine demand robust raw material sourcing and careful inventory management. Several years back, raw material shortages and logistical disruptions threatened to delay shipments. In response, we established a local network of audited suppliers and keep safety stocks based on actual customer usage patterns instead of theoretical forecasts. This approach has kept us responsive and shielded partners from industry-wide shortages.

    Supply chain transparency continues to surface in industry discussions. We provide clear lot traceability, shipment logs, and technical data sheets, informed by feedback from quality assurance teams. A direct relationship between producer and end customer removes many uncertainties. Project managers regularly tell us how much they value knowing not only what they’re buying, but how faithfully it’s been traced from tank to drum.

    Sustainability is reshaping customer expectations. Whether for active pharmaceutical research or industrial materials, demand grows for greener, safer, and better-documented source materials. We have re-engineered waste handling, increased solvent recovery, and lowered on-site emissions. Our teams have re-examined each synthesis step for compatibility with alternative green substitutes. This trajectory continues, spurred both by regulatory targets and direct customer input.

    Continuous Improvement: Partnering with Real-World Chemists

    Feedback cycles make the difference between a generic supplier and a reliable manufacturing partner. Our R&D teams work in tandem with customers to adapt batch sizes, packaging forms, and analytical paperwork. Some clients need pre-weighed sample packets; others require bulk fiber drums or hazardous materials protocols for air freight. Every request reflects a specific bottleneck or need in their workflow.

    The dialogue between bench chemist and manufacturer runs both ways: customers inform us of unexpected behavior in a reaction; process engineers report on downstream handling concerns. In response, we share insights about optimal storage, quenching procedures, and alternate purification tips learned from our own production troubleshooting. Collaboration extends the value of every shipment, reducing time-to-market and minimizing wasted effort.

    Looking Forward: Meeting Industry Evolution with Better Manufacturing

    3-Hydroxy-6-Methyl-2-Nitropyridine may serve as a fine chemical for specialized needs, yet the lessons from making and supplying it reflect the larger picture of chemical manufacturing. Each lot, each customer question, and each quality investigation marks a learning point. We believe bringing manufacturer insights directly to downstream users—sharing real-world troubleshooting, adapting formulation, and adjusting support—helps sectors innovate more quickly and with less risk.

    From process safety improvements to tighter impurity control and custom packaging, we continue to shape our offering around lived manufacturer experience and technical partnership. This approach, grounded not in marketing but in laboratory and plant-floor practice, keeps our customers ahead as research and industry applications evolve. The ongoing story of 3-Hydroxy-6-Methyl-2-Nitropyridine demonstrates, more than any spec sheet could, how diligent production makes tomorrow’s innovations possible today.