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HS Code |
773421 |
| Chemical Name | 2-Ethoxy-5-Nitropyridine |
| Molecular Formula | C7H8N2O3 |
| Molecular Weight | 168.15 g/mol |
| Cas Number | 4535-22-6 |
| Appearance | Yellow solid |
| Melting Point | 60-64°C |
| Solubility | Soluble in organic solvents |
| Smiles | CCOC1=NC=C(C=C1)[N+](=O)[O-] |
| Inchi | InChI=1S/C7H8N2O3/c1-2-12-7-6(9(10)11)4-3-5-8-7/h3-5H,2H2,1H3 |
| Pyridine Ring Presence | Yes |
| Storage Conditions | Store in a cool, dry place, protected from light |
As an accredited 2-Ethoxy-5-Nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Ethoxy-5-Nitropyridine, 25 grams, is supplied in a tightly sealed amber glass bottle, labeled clearly with hazard and handling instructions. |
| Shipping | 2-Ethoxy-5-Nitropyridine is shipped in tightly sealed containers to prevent moisture and light exposure. It is classified as a hazardous material and must be handled with care. Shipping complies with all regulations for chemical substances, typically using UN-approved packaging to ensure safe transportation and delivery. |
| Storage | 2-Ethoxy-5-nitropyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from heat sources, incompatible materials like strong oxidizers or acids, and direct sunlight. Proper labeling is essential. Use appropriate secondary containment and avoid exposure to moisture. Store at room temperature and keep away from ignition sources. Follow standard chemical storage protocols and local regulations. |
Applications of 2-Ethoxy-5-Nitropyridine in Industrial Manufacturing2-Ethoxy-5-Nitropyridine, manufactured to high-purity specifications at our facility, serves as a critical intermediate across several advanced chemical synthesis sectors. Its nitro and ethoxy functional groups provide essential reactivity for demanding applications in pharmaceutical, agrochemical, and specialty material production lines. Below are key validated industrial downstream fields with technical breakdowns based on customer feedback and manufacturing expertise. 1. Pharmaceutical API Intermediate SynthesisOur clients in the pharmaceutical industry utilize this material to introduce the nitro-pyridine motif during key stages of small-molecule drug development. It often participates in nucleophilic aromatic substitution, reduction, and functionalization steps, delivering structural fragments crucial for advanced active pharmaceutical ingredient (API) cores. The ethoxy group offers predictable reactivity, while downstream hydrogenation and coupling operations leverage the nitro substituent to build medical APIs meeting regional market authorizations. Industry compliance standards
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2. Agrochemical Synthesis of Pyridine-Based Herbicide IntermediatesLeading agrochemical manufacturers incorporate this raw material in multi-step syntheses of herbicide active ingredients, especially within the pyridine and nitroaromatic product families. Its structure allows precise functionalization using selective reduction, facilitating access to intermediates involved in weed control compound synthesis. Rigorous impurity profiling assures alignment with regulatory standards governing crop-protection chemistry. Industry compliance standards
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3. Electronic Chemicals – Synthesis of Organic Semiconducting MaterialsDevice manufacturers employ this intermediate during the preparation of soluble, electron-rich oligomers for use in organic light-emitting diode (OLED) and photovoltaic (PV) technologies. The nitro and ethoxy groups enable effective tuning of energy levels through post-synthetic modifications, ensuring uniformity in charge transport layers and supporting the manufacture of reliable, high-purity optoelectronic materials. This process requires precise material attributes to achieve performance specifications and reduce contamination risk. Industry compliance standards
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4. Specialty Chemical Manufacturing – Advanced Dye and Pigment IntermediateProducers of dyes and technical pigments use this pyrridine-based intermediate for the introduction of nitro functionality during colorant synthesis. It plays a crucial part in nucleophilic aromatic substitution and downstream reduction to amines, which support the development of high-performance pigments for inks, plastics, and coatings. The downstream processes demand rigorous control over purity and physical characteristics to guarantee product consistency and regulatory acceptance for consumer and industrial applications. Industry compliance standards
Typical usage ratio
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We focus on pyridine chemistry because it shapes many essential compounds in fields from pharmaceuticals to agrochemicals. Over the years, 2-Ethoxy-5-Nitropyridine has taken on a particularly valued role for its unique structure and reactivity. Its nitration and ethoxy substitution provide practical flexibility for advanced synthesis. When chemists need to build more complex nitrogen heterocycles or tailor molecular frameworks for specific targets, this molecule often stands out as a logical building block.
In practice, 2-Ethoxy-5-Nitropyridine delivers results where other nitropyridines do not. Its solubility profile, moderate melting point, and compatibility with strong nucleophiles make it much more than a lab curiosity. At manufacturing scale, small differences in impurity profiles or solvent requirements cause significant operational headaches. Through years of refinement, we’ve optimized not just yield, but also reliability in lot-to-lot purity. Each batch gets HPLC, NMR, and GC-MS checks to ensure practical utility, not just paper specifications. Customers running tightly controlled synthesis campaigns know that even a minor deviation in a starting intermediate can derail an entire schedule—so we set internal thresholds above typical industry baselines.
Our approach begins by listening to working chemists and process engineers. They appreciate that 2-Ethoxy-5-Nitropyridine opens routes that less accessible analogs cannot. Ethoxy substitution at the 2-position locks in favorable electron density, making downstream reductions, substitutions, or cross-couplings more selective and reproducible. The nitro group at the 5-position activates the adjacent ring carbons, which is a huge advantage for many palladium-catalyzed or metal-free transformations. This sets it apart from isomers such as 2-nitro-5-ethoxypyridine where the reactivity and selectivity profiles diverge.
The compound exhibits stable handling under ambient conditions, although we advise reasonable caution for large-scale transfers or extended exposure to sunlight. Its crystalline powder form also reduces inhalation risks compared to dustier nitroheterocycles that sometimes pose operator health issues. The ethoxy chain resists hydrolysis, unlike similar compounds with bulkier alkoxy groups, which tend to break down or absorb water during long-term storage.
In pharmaceuticals, 2-Ethoxy-5-Nitropyridine supports efficient heterocycle construction for API and intermediate synthesis. Examples include anti-infective agents, kinase inhibitors, and central nervous system therapies that require specific pyridine modifications only accessible from this scaffold. We have seen this compound move seamlessly from early discovery to pilot scale, where its straightforward structure allows for predictable regulatory submissions and patent boundaries. Biotech startups and major API integrators both value our technical documentation and transparency around spectral analyses, impurity limits, and material safety data.
In agrochemicals, many modern crop protection agents trace their lineage to such pyridine cores. Plant scientists want intermediates that can handle oxidizing and reducing conditions without excessive byproduct formation. Our experience with 2-Ethoxy-5-Nitropyridine synthesis shows excellent tolerance for a range of downstream chemistry, including selective hydrogenations and halogenations, and stands up to demands for scale-ups to the hundred-kilogram range without purity dropping below 99.5%. Integrated supply contracts keep rural chemical operations running smoothly, as their schedules depend on accurate lot release and logistics support—not just the base material.
In our facility, we work closely with customers who previously relied on related pyridine nitro derivatives. Some attempted to reformulate pharmaceutical processes around 2-methoxy-5-nitropyridine or unsubstituted nitropyridines and reported inconsistent yields or heavier purification burdens. The switch to the ethoxy derivative almost always drops the need for repeated column chromatography, freeing up both labor and solvent resources. Particularly in reactions involving nucleophilic aromatic substitution or metal-catalyzed couplings, 2-Ethoxy-5-Nitropyridine shows more robust reactivity, likely thanks to its balanced electron-withdrawing and electron-donating substituents. We regularly see improved selectivity when customers scale beyond the kilo-lab to pilot plant. Process teams avoid a host of scale-up headaches—unexpected exotherms, gas evolution, or product discoloration—simply by switching to this intermediate.
Some ask about alternatives such as 2-ethoxy-3-nitropyridine or nitrated pyridines with cyano or halogen substituents. In practice, those compounds tend to be trickier or harsher to handle. Unwanted side products, sensitivity to temperature swings, or the need for slower addition protocols often crop up. We’ve learned that modest adjustments in substituent pattern frequently pay major dividends in synthetic success. That pragmatism underpins our focus on 2-Ethoxy-5-Nitropyridine as a platform intermediate.
Our customers demand more than a label reading “99%” purity. The difference between 99.0% and 99.7% can mean the difference between a project delivered on time and one bogged down in troubleshooting. Over time, we have built analytical routines to provide not just assay numbers but also detailed spectral overlays so clients can spot lot-to-lot variation before a batch even reaches their reactors. Packing into double-lined polyethylene bags (within rigid drums) keeps material dry and protected from light, a protocol we put in place after real-world customer feedback about driveway loading and outdoor storage conditions.
Because 2-Ethoxy-5-Nitropyridine handles well as a free-flowing crystalline powder, chemists working in automated or semi-automated systems see reduced instrument clogging, even during swept-vessel transfers or loss-in-weight dosing. Our facilities have adopted closed-system loading where possible to further protect operators from exposure. If issues crop up during downstream handling—such as slow dissolution in certain solvents or color change after long-term storage—we work with lab teams to troubleshoot root causes, drawing on our own parallel trial data.
Manufacturing this compound requires controlled nitration and ethoxylation steps with careful attention to temperature ramp, reagent addition, and quench protocols. Early on, we experimented with a range of batch and continuous flow setups aiming for reproducible yields with minimal byproduct. The current method uses a nitration protocol with high selectivity at the 5-position, followed by installation of the ethoxy group using alkoxide chemistry optimized for limited over-alkylation. These choices address customer demand for reliable scale-up as well as straightforward environmental and safety controls. Waste stream minimization, solvent recycling, and energy-efficient operations remain central to our process design, rooted in both regulatory pressure and practical cost control. Our team regularly reviews process safety data and environmental impact to keep production both compliant and sustainable.
During lab and pilot trials, we learned that solvent quality, mixing speed, and reactant addition sequence each affect both impurity formation and downstream handling. For instance, switching to more highly refined ethanol led to a ten percent boost in crude product recovery due to reduced contamination, while adjusting cooling rates minimized crystalline byproduct formation that previously hampered filtration rates. This hands-on learning becomes part of our continuous improvement cycle—direct input from the shop floor to our R&D team.
Our clients often ask about compliance and regulatory transparency. We prepare regulatory support packages drawing on our internal data and third-party validation. The streamlined synthetic route helps customers provide clear impurity mapping and consistent reporting to global regulatory agencies. In addition, our multilayer approach to supply chain management—raw material qualification, dual sourcing, and forward stocking—keeps our commitments strong even in the face of storms, shipping disruptions, or raw material shortages. That’s crucial in markets like pharmaceuticals, where missing a single delivery can cause broad project delays and lost commercial opportunities.
Across the industry, supply security sometimes gets taken for granted. We keep detailed logs of raw material traceability, review storage facilities for compliance annually, and maintain rolling forecasts in consultation with end-users. Lessons from recent years underline the value of backup plans and strong communicative relationships with downstream partners. As one example, we worked with an agrochemical producer to adjust delivery intervals during a surge in demand, filling the gap with redirected inventory and just-in-time quality inspection. The lesson always comes back to flexibility married to transparency—qualities that distinguish us as a direct manufacturer attuned to ground realities.
Customers across the globe contact us about tailored packaging, expedited shipping, and special batch sizes. We’ve responded by adapting logistics, formalizing multi-container packouts, and developing temperature tracking protocols for shipments during extreme summer or winter conditions. We have even dispatched process engineers alongside technical samples when pilot trials run into difficulties, supporting customers as they adjust reaction parameters or troubleshoot unexpected impurity streaks on their HPLC traces.
A common challenge involves subtle differences in reactivity between batches from different suppliers. Switching supplier mid-project sometimes creates sourcing “surprises”: downstream reactions run slower, isolated yields drop, or trace byproducts pop up in finished product. Our clients tell us they want consistency, not just compliance. That honesty has pushed us to standardize process monitoring and digital record-keeping. Our site maintains control charts tracking physical and chemical specifications not just for regulatory needs, but because our operators and QC teams find proactive monitoring flags problems early, when changes still cost little to fix.
Direct manufacturing gives us a close look at the way intermediates like 2-Ethoxy-5-Nitropyridine behave outside academic settings. Published papers outline model transformations, but a ten-liter Buchi reactor at scale presents different risks than a Schlenk flask in a university setting. We learned the value of considering operator safety, batch-to-batch reproducibility, and downstream compatibility long before these topics became popular in industry publications. Over the years, optimizing crystal size distribution for smooth filtration saved thousands of labor hours, and fine-tuning our product drying cycle cut material loss rates, reducing both environmental load and client complaints about “sticky” product that clumped during feeding.
We invest time in supporting our materials through direct troubleshooting and bench-level experimentation, not just references to analytical literature. For example, we recently helped a pharmaceutical group adjust solvent selection for a SNAr reaction by sharing direct data from our internal trials rather than theoretical calculations. Not every process is the same, but decades of practical hands-on experience let us offer relevant data and walk through real-world solutions instead of passing the issue back to the client.
As the fine chemicals market evolves, new reaction classes often require alternate feedstocks and intermediates. 2-Ethoxy-5-Nitropyridine has seen increasing demand for applications in catalytic transformations, high-throughput screening, and new active pharmaceutical ingredient (API) programs. Feedback from both established and emerging markets guides our inventory planning and informs ongoing process development. By maintaining tight engagement with our clients and tracking regulatory and patent developments, we make sure our process route and quality controls remain ahead of marketplace shifts.
Recent conversations with formulation chemists and process engineers reveal that cleaner starting materials and predictable reactivity simplify not only the chemistry but the associated documentation and audit trails. Our technical service team runs training and troubleshooting workshops for clients bringing new compounds to scale. This practical partnership does more than move product: it helps entire teams avoid setbacks and accelerates route optimization. Over the years, we've built a reputation on results, backed by technical support built from the shop floor up, not dictated by marketing.
From work with high-throughput pharma labs to collaboratives with crop protection innovators, 2-Ethoxy-5-Nitropyridine delivers with consistency. Its tailored electronic properties, storability, and handling advantages often reduce bottlenecks and lower risk of extended downtime—both critical to staying lean and competitive in modern markets. Real operational feedback has guided how we handle everything from batch scaling to emergency response, logistics, and documentation. Rather than just shipping a commodity, we stay involved in our partners’ workflow, helping keep supply and process development on track.
For industry teams seeking a trusted source of 2-Ethoxy-5-Nitropyridine, working with a true manufacturer means gaining a partner committed not only to reliable supply, but to a broader view of operations, regulatory reporting, and everyday process headaches. Our ongoing efforts stem directly from practical experience, a focus on direct support, and an understanding that the difference between success and delay often lies in the small print—a drop in impurity level, a swap in packaging, or a quick troubleshooting call. The lessons learned from decades on the production floor continue to inform our work, and that depth of knowledge defines our reputation in the field.