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3-Ethoxy-2-Nitropyridine

    • Product Name 3-Ethoxy-2-Nitropyridine
    • Alias 3-ethoxy-2-nitro-pyridine
    • Einecs 629-052-9
    • 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

    166483

    Chemicalname 3-Ethoxy-2-nitropyridine
    Casnumber 50890-22-1
    Molecularformula C7H8N2O3
    Molecularweight 168.15
    Appearance Light yellow to yellow liquid
    Boilingpoint 159-161°C at 15 mmHg
    Density 1.26 g/cm3 (approximate)
    Solubility Soluble in organic solvents such as ethanol and DMSO
    Purity Typically > 97%
    Smiles CCOC1=C(N=CC=C1)[N+](=O)[O-]
    Inchi InChI=1S/C7H8N2O3/c1-2-12-7-5-3-4-8-6(7)9(10)11/h3-5H,2H2,1H3
    Storagetemperature Store at 2-8°C
    Synonyms 2-Nitro-3-ethoxypyridine

    As an accredited 3-Ethoxy-2-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, 25 grams, with tightly sealed screw cap; labeled with chemical name, structure, purity, hazard symbols, and manufacturer details.
    Shipping 3-Ethoxy-2-Nitropyridine is shipped in tightly sealed containers, protected from light, heat, and moisture. It is classified as a hazardous material due to its nitro group and should be handled according to relevant regulations. Shipping typically requires appropriate labeling, documentation, and compliance with local, national, and international chemical transport guidelines.
    Storage **3-Ethoxy-2-Nitropyridine** should be stored in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong acids, bases, and oxidizers. Keep the container tightly closed and properly labeled. Store in a chemical-resistant, tightly sealed container, and avoid exposure to moisture. Follow all relevant safety regulations and guidelines for toxic and combustible materials.
    Application of 3-Ethoxy-2-Nitropyridine

    Applications of 3-Ethoxy-2-Nitropyridine in Industrial Manufacturing

    We supply 3-Ethoxy-2-Nitropyridine to established manufacturers serving pharmaceutical, agrochemical, and advanced organic synthesis sectors. This compound acts as a functional building block for several regulated downstream products, where purity, regulatory compliance, and precise process integration drive formulation decisions. Below, we outline real-world applications, compliance benchmarks, usage ratios, process points, and resulting product types based on production experience and customer feedback from leading industry sectors.

    1. Pharmaceutical Intermediate Synthesis—Pyridine-based APIs

    Our material finds significant demand in the synthesis of pyridine-derivative active pharmaceutical ingredients, especially for anti-infective and anti-inflammatory drugs. During the multi-step synthesis of complex APIs, its ethoxy and nitro substituents facilitate selective transformations and heterocycle construction. Pharmaceutical manufacturers rely on traceable batch supply for documented GMP compliance and validated synthesis pathways.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • EU GMP Part II—Basic requirements for APIs
    • USP, Ph. Eur., and JP monograph specifications for final APIs
    • FDA DMF (Drug Master File) submission support

    Typical usage ratio

    • 0.5%–5% w/w relative to total starting materials, adjusted depending on desired final yield and target compound synthesis route

    Downstream process integration

    • Enters the synthesis at the initial or intermediate step during heterocyclic ring assembly, with subsequent nitro reduction, alkylation, or acylation stages

    Final product types

    • Anti-infective finished tablets and capsules
    • Anti-inflammatory oral and injectables
    • Pyridine-derivative APIs for licensing and direct formulation

    2. Agrochemical Synthesis—Herbicide Intermediate Production

    Contract agrochemical companies use this compound as a core intermediate when producing systemic pyridine-based herbicides. The nitropyridine scaffold enables precise chemical modifications, essential for synthesizing active ingredients in post-emergence weed controls that pass tight environmental registration requirements.

    Industry compliance standards

    • FAO/WHO Specification for Agricultural Pesticides
    • OECD Guidelines for the Testing of Chemicals
    • REACH Regulation (EC) No 1907/2006 for intermediates and final products
    • EPA Residue Chemistry Guidelines (OPPTS 860 Series)

    Typical usage ratio

    • 1%–4% by weight of total raw material input, depending on the target active’s yield optimization and specific synthesis pathway

    Downstream process integration

    • Added in the selective nitration or alkylation phase for construction of herbicidal moieties, followed by chlorination or esterification steps before formulation

    Final product types

    • Post-emergence herbicide technical concentrates
    • Herbicide formulation intermediates for export and domestic blends
    • Custom pyridine derivatives for proprietary agrochemical portfolios

    3. Fine Chemical Manufacturing—Specialty Dye Precursors

    Producers in the fine chemical sector formulate specialty dyes using this compound as a targeted pyridine precursor. It enables precise introduction of functional groups via nucleophilic aromatic substitution, allowing for tailored chromophores and enhanced dye-fastness properties. Strict raw material characterization supports international textile and leather dye standards.

    Industry compliance standards

    • ISO 9001:2015 Certified Quality Management for Fine Chemicals
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals—Manufacturing Restricted Substances List)
    • REACH for non-toxic dye components
    • Textile Eco-label criteria (e.g., OEKO-TEX® Standard 100)

    Typical usage ratio

    • Variable at 0.2%–1.5% within precursor mixes; modified according to desired tint strength and chromophore

    Downstream process integration

    • Introduced during the nucleophilic aromatic substitution phase or as a pre-condensation intermediate for custom dye molecule synthesis

    Final product types

    • Synthetic textile dyes (disperse and acid dye types)
    • Leather dye intermediates
    • Specialized colorants for medical equipment plastics

    4. Pharmaceutical R&D—Reference Standard and Analytical Uses

    R&D laboratories engaged in medicinal chemistry programs and custom synthesis leverage this compound as a research grade standard as well as a reactant for developing reference impurities. These activities demand analytically characterized lots, supporting qualification to regulatory and internal QC guidelines for novel pyridine analogs.

    Industry compliance standards

    • ISO/IEC 17025 for chemical analysis and laboratory competence
    • Good Laboratory Practice (GLP) Principles, OECD
    • FDA Guidance for Industry: Analytical Procedures and Methods Validation
    • ICH Q2(R2)—Analytical Method Validation

    Typical usage ratio

    • 0.1%–1% of total synthesis batch; depends on intended yield for reference material or impurity product

    Downstream process integration

    • Used as a standard in comparative NMR, HPLC, GC, and MS analytical runs or spiked in pilot reactions for method development

    Final product types

    • Pharmaceutical reference standards for QC and regulatory filings
    • Identified analytical impurities/markers for release testing
    • Custom-purified research samples for structure elucidation studies
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    Certification & Compliance
    More Introduction

    Introducing 3-Ethoxy-2-Nitropyridine: A Chemical Manufacturer's Perspective

    Understanding 3-Ethoxy-2-Nitropyridine in the Lab and Industry

    In the constant push to meet demands for specialty intermediates in both pharmaceuticals and advanced materials, we have come to know certain compounds quite closely. Among these, 3-Ethoxy-2-Nitropyridine stands out not only for its unique niche in synthesis but for the impact it brings to efficiency and reliability in downstream applications. Years in the lab and on the production floor give a unique window into the fine balance between batch precision, safety, and reproducibility, all especially relevant to this molecule.

    Our Experience Producing 3-Ethoxy-2-Nitropyridine

    Producing aromatic nitro compounds always requires tight control over several variables: nitration selectivity, solvent choice, byproduct suppression, and workup reliability. For 3-Ethoxy-2-Nitropyridine, experience emphasizes the importance of starting material purity and carefully managed reaction conditions. The ethoxy group presents certain stability perks, but it brings sensitivity to certain bases and acids, which calls for discipline in quality checks both upstream and downstream.

    Through the years, we learned that customers count on consistency batch to batch. Trace residues from raw materials or incomplete reactions can carry over and interfere with planned syntheses further along, so we monitor contaminants especially closely. By holding to tight specifications on purity — and offering detailed batch records — we keep our partners’ processes on track. The internal specification we follow generally looks for purity well above 98 percent, low water content, and absence of volcanic organics, which comes from fine-tuned filtration and drying processes.

    Key Properties and Common Uses

    This compound, with its nitro substitution adjacent to the pyridine ring and ethoxy at the third position, opens up interesting routes not only for added reactivity but for precise selectivity. From our own manufacturing projects and what we've learned in collaboration with pharma innovators, the majority is used as a building block in studies targeting anti-infective or central nervous system drug families. It also provides a starting point for producing certain specialty ligands and agrochemical intermediates.

    Its solubility in standard laboratory solvents — including acetone, dichloromethane, and ethanol — streamlines downstream processing. We keep a close eye on color, as product darkening flags unwanted side-products; clean, pale yellow crystalline powder signals good control at each step. The melting point we see in most batches lands in a narrow range, which reflects correct substitution and minimal residual solvents.

    With each kilo, we include a COA listing analytic details: purity, major and minor impurity profile, water content by Karl Fischer method, spectral confirmations by NMR (usually proton and carbon-13), and LC-MS data. This approach comes from years of feedback: end users want confirmation, not just a number on a label.

    Differences from Other Pyridine Building Blocks

    Drawing clear lines between 3-Ethoxy-2-Nitropyridine and structurally related nitropyridines changes planning in synthesis work. The ethoxy substitution provides a more electron-donating effect than methyl, changing both activation at adjacent positions and shifting reduction conditions for the nitro group. Colleagues testing routes to differently substituted benzo-fused targets find that the ethoxy group lends better reactivity in certain Pd-catalyzed couplings, compared to methyl or plain hydrogen.

    Another key difference rests in handling: we have seen over the years that the ethoxy group provides better stability than methoxy analogs under acidic conditions, as demethylation has always challenged both process safety and reproducibility. In our own facilities, losses to hydrolysis decrease sharply when switching to ethoxy, cutting rework rates and waste.

    Those switching from other nitropyridines with similar ring structures, but without the ethoxy group, often report shifts in TLC profiles and differences in column behavior. This means chemists in downstream production processes must tweak purification methods, but can still rely on robust, scalable reactions. From our repeated feedback sessions with both process development and production-scale customers, adjustment periods run short when using our materials and documented critical parameter sheets.

    Production Insights: Batch Control and Safety

    A transparent look at production management unlocks confidence not only for customers, but for our own teams. In our facilities, the most demanding step remains the initial nitration, as it demands precise control of time and temperature to minimize poly-nitration or low-yield side products. We standardized a procedure based on past process runs — no two runs are identical, but repeated analysis shows tight bands of parameter ranges keep quality high.

    Our plant engineers stress that solvent recovery, careful temperature ramping, and gradual addition help keep reactions under control. Continuous operator training matters. Routine inline analysis, including periodic HPLC checks during the run, cuts the risk of out-of-spec product. To keep our workplace safe and the product reliable, the team runs frequent reviews of any runaway reaction cases, seeking root causes and sharing lessons both internally and with key supply partners.

    For storage, experience teaches that moisture control counts for more than shelf life claims. Peroxide formation might threaten some pyridine derivatives, but the ethoxy group on this compound confers additional stability. Still, we store our drums and kegs with desiccant packs, in sealed containers away from sunlight and temperature swings, keeping actual risk to a minimum. This translates directly to more consistent product for repeat buyers, less headache over claims, and minimal environmental impact from discards or returns.

    Why Technical Support and Collaboration Matter

    Direct interaction between manufacturer and end user provides much more than just a technical spec sheet. Feedback loops — where the user describes issues, and the producer responds with analysis or process advice — dramatically cut troubleshooting time. We don’t see ourselves in a clean break with the customer after delivery. Instead, teams on both sides share experiences, from product solubility in scale-up gloved boxes to optimizing reaction temperatures and catalyst amounts for specific transformations.

    A few years ago, we worked closely with a leading pharma customer scaling up a Suzuki coupling involving this compound. Initial yields struggled under “book” conditions from literature, but our tech team, familiar with impurity profiles from our production runs, helped adjust temperature gradients and purification sequences. Combined process know-how improved both yield and product purity, with cost savings documented in later batches.

    This experience, repeated in different contexts, convinced us to keep extending our technical library with case reports — always anonymized, always securing permission — so that new customers don't repeat avoidable errors. No compound’s “one size fits all,” and open dialogue is worth more than any efficiency claim on paper.

    Quality by Design: From Sourcing to Shipping

    Maintaining consistent results batch by batch doesn’t come from chance. Supplier control of starting pyridine ring and alkyl halides, proactive impurity screening, in-process monitoring, and careful end-point selection all factor into final product integrity. Over time, we set up incoming inspection protocols, including supply chain audits when needed, to catch contaminants early and tighten batch variability. Our staff develops their own expertise in rapid detection methods, such as TLC plate analysis for raw input streams, making in-line adjustments possible before bottlenecks develop.

    Once crystalline product forms, drying and isolation techniques affect not just the next process yield but how well product ships and stores. The move to more energy-efficient drying equipment improved our solvents recovery while keeping product characteristics consistent. Each batch, after final testing, heads into double-lined containers, always inerted with nitrogen before transport. Documentation on every batch isn’t just compliance — it’s answering the unasked questions each user may have weeks or months later in their own investigations.

    Environmental and Regulatory Considerations

    With all aromatic nitro compounds, waste management and regulatory reporting draw constant attention. We invest steadily in closed-system nitration setups, continuous solvent recycling, and regular emissions tracking. Waste solvent and filtrate treatment avoids sending heavy loads of nitro organics out of plant boundaries. Without responsive process adjustments, the risks climb fast — for both worker safety and outside communities.

    The regulatory patchwork for substances in this space means constant updates to both SDS documentation and customs paperwork. Export to regulated pharmaceutical markets brings batch-level serialization and transparency for each drum or bottle. We keep priorities straight: accurate self-monitoring matters far more than a certificate issued post-facto.

    Years of audits by outside inspectors, and our own learning by digging into near-misses or other industry incidents, reinforced the importance of traceability. Easy recall paths, fully documented, matter more than after-the-fact risk assessments. Our own policies lean toward transparency with all partners, as shortcuts create bigger costs in the long run.

    The Real-World Difference: End-User Needs in Focus

    Across our customer base, the biggest feedback revolves around reaction predictability. Chemists in fast-paced labs and full-scale plants alike prefer working with intermediates they trust not just on paper, but from experience. Our approach balances the latest detection and monitoring tools with basic communication and process notes — so users know exactly how each lot will behave, or if a variation might affect yields.

    Some colleagues using related compounds, such as 3-Methoxy-2-Nitropyridine or unsubstituted nitropyridines, switch to 3-Ethoxy-2-Nitropyridine for better downstream yield in amine reductions or nucleophilic aromatic substitutions. They comment that reproducibility improves, especially when scaling into multi-kilo runs. Those switching back for certain reaction steps note small differences in reactivity they must plan for, but confirm stability and ease of handling rank high as benefits.

    With printed QC results and complete MSDS on every batch, process improvements don't stall on missing or ambiguous information. Downtime from off-spec intermediates drains project budgets — keeping a reliable starting material like this one on hand gives project managers and chemists alike one less variable to guard against.

    Key Lessons: Long-Term Manufacturing Perspective

    As a manufacturer focusing on functional pyridine derivatives, our practical insight grows from walking the line between development and reliable supply. The path from lab notebook to repeat industrial order brings new understanding with each round. Factors like reproducibility, stability, and safe handling set apart 3-Ethoxy-2-Nitropyridine from other available options.

    True long-term reliability rises from both technical capability and transparent process management. By trading notes with customers and internal teams about what goes right, what needs adjusting, and where blind spots hide, we built a track record. External audits may impose extra work, but the toughest checks often develop in open internal debriefs, post-batch analysis walks, and informal lessons shared over equipment breakdowns or root-cause sessions.

    In summary, our experience with this compound reinforces several themes: customer feedback and open technical notes feed back into production. Batch control, impurity review, and close data-logging ease user workload later on. Switching to 3-Ethoxy-2-Nitropyridine usually brings reliability, better performance in classic transformations, and smoother workflow for teams steadily marching toward tighter regulatory standards and project timelines.

    Developments Ahead: Demand, Innovation, and Process Change

    The chemical industry landscape evolves as new synthesis approaches and product needs shift across regions and sectors. Research groups and formulators look for intermediates delivering the right functional groups with maximum flexibility and minimum downstream clean-up. As demand patterns for nitro-pyridine intermediates climb — especially with parallel growth in custom pharma synthesis — we see growing orders, not only in Asia but also from Europe and North America.

    Current trends in API and fine chemical synthesis focus on cleaner, scalable reactions and greener routes. Producing 3-Ethoxy-2-Nitropyridine that meets both technical and environmental criteria requires ongoing adaptation, including solvent recycling and minimization of waste. Demands from regulatory agencies become steadily more detailed, so we invest accordingly — not just for compliance, but because audits and feedback help us tighten internal controls and find process improvements.

    Customer needs drive our upstream projects as much as regulatory frameworks do. Whether it’s supporting a new research program in CNS drugs or enabling a specialty material for electronics, each use case feeds back into how we tweak reaction pathways, purification routines, packaging design, and delivery logistics.

    Conclusion: Inside Knowledge Translates to End-User Value

    Real-world outcomes start long before a drum leaves our loading docks. They start in raw material selection, the patient review of data, careful temperature and reaction management, and the candid sharing of process “edge-cases” and minor failures. Manufacturing 3-Ethoxy-2-Nitropyridine at commercial scale taught us the value of direct feedback, invested staff, fine-tuned batch checks, and a willingness to share information up and down the chain. In daily practice, these disciplines turn a sometimes-overlooked intermediate into an asset for both innovation and predictable project planning.

    Few products show so clearly how ongoing collaboration, open communication, and constant process check-ins improve both our performance as a manufacturer and the results for every chemist, project owner, and production foreperson relying on high-performing, high-purity building blocks. Through each delivery, our lens stays fixed not only on technical benchmarks, but on the daily needs of users who move from idea to product — and who depend on us to keep their next reaction running, batch after batch.