|
HS Code |
812994 |
| Chemical Name | 4-Nitropyridine |
| Cas Number | 100-16-3 |
| Molecular Formula | C5H4N2O2 |
| Molecular Weight | 124.10 g/mol |
| Appearance | Yellow crystalline solid |
| Melting Point | 113-116 °C |
| Boiling Point | 310 °C |
| Density | 1.38 g/cm³ |
| Solubility In Water | Slightly soluble |
| Pka | 3.1 |
| Refractive Index | 1.624 |
| Smiles | c1cc(ncc1)[N+](=O)[O-] |
As an accredited 4-Nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 4-Nitropyridine is packaged in a 25g amber glass bottle with a secure screw cap and detailed hazard labeling. |
| Shipping | 4-Nitropyridine is shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. It should be packed according to hazardous material regulations, clearly labeled, and cushioned to avoid breakage. The packaging must comply with applicable transportation guidelines, and shipping should be via authorized carriers specializing in hazardous chemicals. |
| Storage | 4-Nitropyridine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers and reducing agents. Protect it from light, moisture, and physical damage. Properly label the container, and store it in accordance with local regulations for hazardous chemicals. |
Applications of 4-Nitropyridine in Industrial Manufacturing4-Nitropyridine is a specialty intermediate employed by industrial producers in several highly regulated downstream manufacturing routes. Below we detail practical field applications, specifying real compliance frameworks, typical formulation ranges, how the material is incorporated in processing, and the range of end products supported. 1. Pharmaceutical Intermediate for Antiviral and Anticancer AgentsPharmaceutical manufacturers rely on 4-nitropyridine for constructing pyridine scaffolds critical to small-molecule drug synthesis, especially in the targeted development of antivirals and oncology compounds. The compound’s distinctive electron-withdrawing nitro group facilitates regioselective nucleophilic substitutions in heterocyclic active pharmaceutical ingredient (API) synthesis, ensuring reliable batch-to-batch quality assurance aligned with regulatory guidelines. Controlled multi-step synthesis routes frequently start with 4-nitropyridine as a precursor for subsequent functional group manipulations yielding pyridine-modified APIs. Industry compliance standards
Typical usage ratio
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2. Agrochemical Synthesis: Pyridine-Based Herbicide ProductionAgrochemical producers use 4-nitropyridine as a key intermediate in manufacturing selective pyridine-herbicide actives. Its electron-deficient aromatic ring supports precise introduction of further functional groups necessary for developing herbicidal molecular structures. The process demands stringent traceability and documentation throughout each batch, reflecting requirements for residue standards and field registration. Industry compliance standards
Typical usage ratio
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3. Specialty Dye and Pigment ManufactureProducers of high-value dyes leverage 4-nitropyridine to create azo and heterocyclic colorants demanded by textile, printing ink, and specialty coating manufacturers. Its activated pyridine ring enables formation of stable, vibrant chromophores through direct coupling with aromatic amines, granting exceptional application performance in niche dye classes. This route is underpinned by geographical compliance for heavy metal and aromatic amine limits. Industry compliance standards
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4. Heteroaromatic Catalyst Ligand Precursor in Fine Chemical SynthesisChemical manufacturers specializing in organometallic catalysis adopt 4-nitropyridine in synthesizing chelating ligands for homogeneous catalysts. Its electron-poor aromatic system allows selective further functionalization, ultimately yielding bipyridine, terpyridine, and other multidentate nitrogen ligands required for high-activity catalytic processes. Ligand quality and traceability remain under strict scrutiny as part of customer and regulatory audits. Industry compliance standards
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5. Photoactive Material Intermediate for Electronic and Optical ComponentsElectronics and materials manufacturers use 4-nitropyridine in the synthesis of advanced molecular components employed in optoelectronics and photosensitive devices. Its nitro group provides strong electron-withdrawing characteristics necessary to modulate electronic properties within photoactive heterocycles. The integration process must demonstrate compliance with material purity, heavy metal, and halogen content regulations. Industry compliance standards
Typical usage ratio
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4-Nitropyridine plays a unique role in specialty chemical synthesis. As manufacturers, we recognize that few compounds offer its precise blend of reactivity and selectivity in scientific and industrial development. Unlike many aromatic nitro compounds, this structure brings a nitrogen atom directly into the ring, creating new pathways for interaction and functionalization. For years, we have shipped tonnage and smaller quantities globally, supporting both established manufacturers and research labs that rely on solid, repeatable quality.
Let’s look closer at what sets it apart in a crowded landscape of substituted pyridines and nitro aromatics. We always emphasize true consistency—reproducible purity, controlled particle size, and moisture content. Each parameter impacts downstream processes, yield, operator safety, and the final product profile whether you’re making API intermediates, ligands for catalysts, or exploring new materials.
We produce 4-Nitropyridine under strict controls. Typically, our batches come as a light-yellow crystalline powder. Analytical data, drawn from years of batch analyses, routinely confirms assay levels above 99 percent by HPLC, with trace impurities—like starting pyridine, 3-nitropyridine, or dinitro-pyridines—kept far below actionable thresholds.
Moisture plays a bigger role than some folks realize. Even tiny amounts change weight, flow, and reactivity, especially in air-sensitive or anhydrous processes. Our technical staff invests a lot of time screening for water and making sure packaging minimizes ingress from air. Most requests land on our dock for 25-kilogram fiber drums, but we can pull from stock in smaller sealed foil packs. All containers resist static and offer resealable closures for partial lots.
Odor is mild, with faint bitter notes typical of nitro aromatics—nothing overpowering or volatile under standard handling. Melting sits in the 67–70 °C range and the compound dissolves well in alcohols and polar aprotic solvents. We have noticed customer demand growing most in the pharma and electronics sectors, largely due to the predictable substitution pattern on the pyridine ring.
Scaling the nitration step of pyridine shows the need for safe and precise process control. Classic mixed acid nitration, despite its age, still requires careful heat management, real-time monitoring of water content, and rapid isolation to prevent by-product buildup. Over-oxidation or trace metallic catalysts in this step skew product purity. Our reactors use glass-lined steel, automatic temperature feedback, and closed nitrogen atmospheres, all helping us meet strict impurity profiles batch after batch.
Any slip in oxidant addition, or an unnoticed pH swing, throws off the nitration position, producing 3-nitropyridine or multi-nitro side products. We minimize these both through careful kinetic modeling and downstream fractional crystallization. While automation helps, our chemists constantly check colorimetric and chromatographic data, since seasonal changes and raw material lots do impact the final distribution.
One thing that surprises many users: even low-level contaminants show up during complex coupling or further transformations. Palladium- or copper-catalyzed processes, Suzuki reactions, and nucleophilic substitutions all demand clean feedstocks. Trace metals, unreacted pyridine, or byproduct nitro isomers lead to inconsistent yields, color issues, or harder purifications. We address these concerns straight at the source: multi-step recrystallization, micro-filtration, and periodic full-spectrum screening instead of just inline spot-checks.
Most downstream applications rely on the nitro function as a handle for further chemistry. Whether reduction to the amino group (for dye, pharma, or intermediate work) or cross-coupling to build more complex heterocycles, small differences in physical form can matter. Caking, static charge, or even invisible resinous films from equipment can confuse automated feeders or reduce blend homogeneity in large tanks. Feedback from bulk users in Japan and Europe led us to install additional sieving and metal detection right on the packaging line.
Some buyers ask about using cheaper or more available nitroaromatics, like 3-nitropyridine, 2-nitropyridine, or nitrobenzene, in the same synthetic steps. Over time, we have seen that 4-nitropyridine brings two key advantages. First, the 4-position on the pyridine ring is less hindered, making nucleophilic attack more straightforward. This reduces the risk of unwanted ortho rearrangement or ring-opening during tough conditions.
Second, nitrogen’s position in the ring affects electron density and the way catalysts or nucleophiles approach the molecule. Electrophilic substitutions and reductions proceed more smoothly at 4-Nitropyridine than with the benzene analog, avoiding polymerization. In some situations, we have tracked productivity improvements of 5 to 12 percent simply by switching to our material instead of a cheaper isomer. Less waste, cleaner workups, and better spectral matches in the final product end up saving both time and money.
In pilot campaigns, especially for active pharmaceutical ingredient (API) development or novel material chemistry, reliable scaling depends on physical and analytical repeatability. We use standardized protocols for every lot, constantly adjusting based on incoming chemical analysis data. In early years, one challenge was keeping batch-to-batch color and flow constant enough for fully automated dosing. We combat this with single-lot production and real-time PID control loops throughout critical thermal stages.
Not every synthesis needs beyond-99 percent purity, but tighter fractions pay off, especially in late-stage R&D or GMP manufacturing. End-users who previously accepted technical grade now return for advanced lots that meet custom particle size or sterility parameters. Large multinational customers report shorter cycle times and higher isolation yields when working with tailored batches—not because the chemistry changes, but because the material flows, dissolves, and reacts as expected every time.
Handling nitro aromatics comes with real safety responsibilities. We have spent time and resources reducing dust generation on site, with central vacuum extractors and electrostatic controls. Regular personal exposure monitoring and batch logbooks help keep operations in line with both national and international guidelines.
On transport, 4-Nitropyridine presents fewer HAZMAT headaches than some others, thanks to its lower volatility and flash point. But it still requires paperwork, training, and segregation from incompatible materials. Our logistics teams stay in close touch with shippers and overseas compliance offices, since even minor shipping delays can expose product to humidity or high temperature, working against shelf stability.
Many new customers ask about chemical or toxicological profiles. Acute oral, dermal, and inhalation studies point to moderate toxicity, typical of nitropyridine compounds. We always urge anyone handling drum-scale quantities to read the full SDS, connect with EHS professionals, and run in ventilated hoods or with dust collection in place. Our decades of safe operation stem from these simple, disciplined habits.
We’ve seen how a minor issue at the loading point or a miscommunication over purity levels can slow whole projects. Open lines of communication with chemists, engineers, and purchasing teams help resolve these challenges before they turn into headaches. If a customer notes diurnal weight shifts, for example, we trace back to environmental controls, investigate packaging seals, or review raw material data. For fine-tuning reactivity or blending, on-site support and pre-shipment samples let process engineers dial in their parameters before the main order leaves our gates.
Customers often challenge us with unique requirements: from micron-scale powders for ultrafine syntheses to coarser granulations needed for smooth bulk transfer in pneumatic systems. Over time, we have assembled a robust playbook based on real-world trouble tickets, not just textbook best practices. Speaking directly with operators and line managers, we recognize that getting a batch to flow properly into a feeder can matter more than hitting a percentage point of purity for certain applications.
Our job as chemical manufacturers is not just to ship a product, but to follow its entire lifecycle, picking up problems and process optimizations along the way. This approach results in both higher overall customer satisfaction and fewer emergency calls when something unexpected crops up in the reactor.
Supply stability often matters as much as the product’s technical merit. There have been challenging years: shortages of key raw materials, restrictions at border crossings, and logistics interruptions. Our team built out parallel trusted sourcing for feedstocks and invested in local warehousing closer to our biggest customers. Maintaining a living active relationship with shipping companies ensures fresh, on-time deliveries for those working with tight development timelines or regulatory deadlines.
Occasionally, off-shore material shows significant batch variability, both in physical appearance and impurity profile. As an original manufacturer, close control and fast feedback from in-house analytics gives us an edge. A surprising number of customers return after trying a more “available” product from a reseller, only to find it falls short on reactivity or leaves behind troublesome residues. Our long-term focus remains on stability—delivering the right lot, to spec, at the time it’s promised.
We often discuss with clients the consequences of choosing cheaper substitutes or over-relying on third-party material. Short-term cost savings rarely offset the cycle delays, extra purification steps, or regulatory headaches from unexpected side reactions. Drawing from the experience of multi-year, multi-ton supply partnerships, we emphasize building visibility and foresight into every part of the supply chain.
Most chemical manufacturing facilities face pressure to reduce waste and environmental footprint year over year. Our plant teams regularly audit water and energy use, tracking progress against concrete benchmarks. Small upgrades—from improved agitator seals to more sensitive batch-monitoring sensors—come straight from shop floor feedback. These practical steps help us maintain both product consistency and environmental stewardship.
Recent years have driven more R&D into process intensification—reducing reaction times, minimizing solvent needs, and recycling acids through in-house loops. Intellectual property protections aside, several improvements originated with young process chemists eager for more efficient, cleaner yields. By integrating these lessons back into everyday production, we both deliver higher-value products and prepare the ground for more rigorous regulatory futures.
Our involvement doesn’t stop at shipping. Collaboration with global research teams leads to new uses and better derivatives—not just as an end product, but as a stepping stone to custom building blocks for everything from OLED formulations to bioconjugates. Our legacy comes from listening to what the field needs, learning from both our successes and failures, and feeding that knowledge back into every batch that leaves our lines.
Producing 4-Nitropyridine at scale isn’t just about following procedures or ticking boxes. Each batch tells a story of learning, adaptation, and real-world constraints—unexpected temperature blips, minor logistics hang-ups, or evolving purity demands. As original manufacturers, we take pride in helping researchers, formulators, and engineers move faster, safer, and more reliably.
From behind the tanks and control panels, we know what it takes to keep quality high and surprises few. By building trust through real experience, rigorous data, and transparent communication, we give our partners what they need—a steady stream of a specialty material, always fit for its purpose. That’s what sets true manufacturing apart from trading—and it’s how we’ll continue to build value in a world that relies daily on fine chemicals such as 4-Nitropyridine.