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HS Code |
219505 |
| Chemical Name | 2-Nitroaniline |
| Molecular Formula | C6H6N2O2 |
| Molar Mass | 138.13 g/mol |
| Cas Number | 88-74-4 |
| Appearance | Yellow solid |
| Melting Point | 71-74 °C |
| Boiling Point | 284 °C |
| Density | 1.37 g/cm³ |
| Solubility In Water | Slightly soluble |
| Flash Point | 180 °C |
| Pubchem Cid | 6942 |
| Iupac Name | 2-nitroaniline |
As an accredited 2-Nitroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle, labeled "2-Nitroaniline, 99%, 500g," with hazard symbols, barcode, batch number, and tightly sealed screw cap. |
| Shipping | 2-Nitroaniline should be shipped in tightly sealed, properly labeled containers to prevent leaks and contamination. It must be transported in accordance with local and international hazardous material regulations, typically as a toxic solid. Avoid contact with incompatible substances, moisture, and direct sunlight. Use secondary containment during transit to ensure safe delivery. |
| Storage | 2-Nitroaniline should be stored in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep the container tightly closed and properly labeled. Store separately from strong oxidizing agents, acids, and bases. Use appropriate chemical-resistant containers to avoid contamination. Comply with local safety regulations and ensure access to safety equipment in the storage area. |
Applications of 2-Nitroaniline in Industrial ManufacturingAs a direct manufacturer focused on quality consistency and supply transparency, we support the global industrial sector by providing high-purity 2-nitroaniline for targeted applications. Our product serves essential functions in colorant synthesis and specialty chemical intermediates manufacturing. The following downstream scenarios illustrate its differentiated industrial adoption, dosing practices, integration into processing, and end-market output, rooted in authentic sector usage and compliance expectations. 1. Azo Dye Manufacturing for Textile IndustryTextile dye producers use 2-nitroaniline as a diazo component in the synthesis of selected azo dyes, particularly for red, orange, and brown color shades. Its electron-withdrawing nitro group allows for stable coupling with aromatic amines, ensuring dye fastness on both natural and synthetic fibers. The processing window for ingredient dosage draws from both color intensity needs and washfastness standards, requiring adjustment between different dye formulations. Downstream integration prioritizes strict batch traceability and color reproducibility tested against established industry protocols. Industry compliance standards
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2. Intermediate for Agricultural Chemical SynthesisFormulators in agrochemical manufacturing employ 2-nitroaniline as a building block to construct active moieties found in certain herbicides and fungicides, relying on its reactivity for stepwise synthesis of heterocyclic scaffolds. Choice of concentration reflects downstream target molecule requirements and crop-specific regulatory thresholds. Integration focuses on continuous-flow synthesis lines, ensuring containment of intermediates and minimization of process impurities, with strict reference to regional and global agricultural standards. Industry compliance standards
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3. Pharmaceutical Intermediate SynthesisActive pharmaceutical ingredient (API) manufacturers utilize 2-nitroaniline to access specialty heterocyclic intermediates, especially in the construction of analgesic or antipyretic drug scaffolds. Precise dosing is imperative, as variation affects purity and yield of subsequent steps. Integration demands cleanroom processing and multi-stage reaction monitoring, adhering to international manufacturing practices for pharmaceutical actives and intermediates. Each lot undergoes rigorous quality certifying and documentation to ensure no cross-contamination or non-compliance with pharmacopeial limits. Industry compliance standards
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4. Base Material for Pigment Synthesis in Coatings SectorPigment producers in the coatings industry rely on 2-nitroaniline to manufacture monoazo and diazo pigments that deliver durable coloration for architectural paints, industrial coatings, and masterbatches. The compound’s chemical stability and controlled reactivity underpin its utility in achieving consistent batch shades within regulatory limitations. Usage ratios reflect pigment load and color target, while process integration combines in-situ coupling for high-chroma pigments and precision washing to remove unreacted precursor chemicals, supporting downstream dispersion performance in solvent and water-based formulations. Industry compliance standards
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5. Industrial Rubber Antioxidant PrecursorRubber compounding firms incorporate 2-nitroaniline as a precursor in the manufacture of select antioxidants that prevent polymer degradation under UV or thermal stress. The dosage used in antioxidant synthesis lines balances target antioxidant molecule concentration and minimization of nitro residue carryover. Process integration focuses on batch and continuous processing systems where the raw material is converted by hydrogenation and subsequent functionalization, closely monitored to align with rubber additive safety profiles and finished goods compliance directives. Industry compliance standards
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6. Specialty Chemical Intermediate for Photographic ChemicalsIn the photographic processing chemicals sector, 2-nitroaniline serves as a regulated intermediate in the synthesis of color couplers and stabilizers necessary for photographic paper and film development. The dosing aligns with color developer concentration and batch-scale adjustment, guided by analytical controls for both in-process and final product safety. Close-process integration ensures minimal nitro compound migration, meeting stringent imaging material standards and end-user durability criteria. Industry compliance standards
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Stepping inside a chemical manufacturing plant, one gets a real sense of what 2-nitroaniline means — to process technicians, researchers, and end users alike. This aromatic nitro compound, with the formula C6H6N2O2, stands out for its pale yellow crystalline appearance, distinct from many related materials that often come as white or off-white powders. As people who make and handle large volumes of 2-nitroaniline, we know it well: the way it reacts, the conditions it prefers, and what our customers look for to get best results in their own operations.
We specialize in the ortho-isomer of nitroaniline, known for its role in synthesizing dyes, pigments, pharmaceuticals, and certain agricultural chemicals. Every batch we produce comes with a focus on two things: controlling impurity levels and ensuring reliable lot-to-lot consistency. Because trace levels of contaminants can skew color outcomes in dye or pigment production, we monitor both nitro group position and amine group content. Our purification steps give a finished product with an assay over 99%, minimal moisture, and nearly undetectable heavy metals. These are not just numbers to us. They are proof that we understand which specifications matter most to chemists who depend on each shipment meeting critical standards.
2-Nitroaniline distinguishes itself from the related para- and meta-isomers. The ortho isomer’s unique electron placement means it participates in different coupling reactions, which leads to variation in the shades and stability of end products in color chemistry. We have learned, through experience, that customers seeking truest yellow-orange dyes will not achieve reproducible tones by substituting with the meta or para compounds. The ortho isomer’s melting point, roughly 70–75˚C, offers particular advantages in processing — it enables feeding directly into reactors, unlike para-nitroaniline, which has a higher melting point and forms crystals that are harder to dissolve quickly. Over the years, our operators have learned to tune temperature, stirring, and batch size for efficient throughput, focusing on the subtle melting and crystallization points characteristic of the ortho compound.
Not all nitroaniline sources deliver the purity that specialty applications demand. Lower-grade or recycled material, depending on upstream sources, may retain organic impurities leftover from original dinitration processes, leaching unreacted nitrobenzene or residual acids. While some competitors may not control for these byproducts, we have invested in both column and fractional crystallization systems that push quality above general industrial grade. Selecting our product means relying on traceability and transparency — our logging systems document every production run, and every outgoing order carries its own batch analysis. We’ve built this transparency not simply for compliance, but as a practical reflection of trust earned by long-term repeat buyers.
Our customers put 2-nitroaniline to use across a spectrum of industries, but nowhere is this more visible than in dye manufacturing. Many azo and anthraquinone dye syntheses begin with an aromatic amine; the ortho configuration can serve as a direct coupling agent for yellow, orange, and red pigments sought by textile houses and ink formulators. Over the decades, hundreds of thousands of metric tons of synthetic dyes have flowed through international markets, much of it built from just a handful of aromatic intermediates — 2-nitroaniline chief among them. Laboratory results only tell half the story. Plant engineers confirm what we observe: a single unreliable shipment can bring a color line to a stop, halting blankets of fabric on the production line, or spoiling an entire batch of ink.
Beyond dyes and pigments, pharmaceutical clients use our product in the synthesis of drugs like Benzocaine and certain sulfonamides. The aminonitrobenzene backbone provides a reactive site for additional functionalization, and selectivity at the ortho position enhances yields for these target molecules. Our relationships with formulation experts give us feedback on the significance of purity here — every fraction of a percent deviation in the main compound translates into a corresponding risk for end-product performance. Green chemistry researchers also investigate 2-nitroaniline as a potential building block for more biodegradable herbicides. These studies require input materials free of extraneous byproducts, as otherwise, any positive toxicity readings might be falsely attributed to the core compound instead of the impurity. For such research-driven uses, we provide data about trace components and, upon request, share the details of our analytical test methodologies.
The hands-on aspects of industrial 2-nitroaniline production can be demanding — especially where worker safety, regulatory compliance, and process reliability converge. We take the handling of nitro compounds seriously, knowing they require close attention to dust control, vapor extraction, and waste stream management. The bright yellow crystals and dust can discolor plant surfaces, and accidental exposure brings risk of skin or respiratory irritation. Our protocols include both personal protection and in-plant ventilation, with dedicated isolation and filtration of work zones. We conduct regular employee training. In conversations with operators, practical knowledge about spills, equipment cleanup, and first-aid procedures comes first, because lessons learned the hard way stay in memory longest.
Raw material quality plays a direct role in the final product we ship. Only selected batches of aniline and nitric acid, each sourced with certificates of origin and purity analysis, feed into the reactors. Careful dosing controls the exothermic nature of the nitration reaction. The process generates acidic byproducts — typically hydrochloric or sulfuric acid, depending on route — and these must be neutralized before crystallization. Inadequate neutralization leaves acidic residues and degrades long-term storage stability. By contrast, proper washing, staged under controlled pH, produces a product that maintains color, flowability, and chemical reactivity over extended warehousing.
Temperature monitoring matters on the production line. Excess heat can oxidize the product or exacerbate impurity formation. Modern sensors and digital logging now give us trends that, years ago, operators tracked on paper charts. We learn from every deviation captured in the system. If a temperature spike occurs in a certain cycle, investigations go beyond the immediate batch; retrospective process control lets us spot patterns and prevent reoccurrence in future runs. The result: each output lot more closely matches intended specifications, with shorter downtime and less waste.
Over the years, the specification requests we receive have grown stricter. Customers now expect certificates not only showing purity but also identity confirmation by NMR or HPLC, moisture analysis, ash content, and residual solvents. End users make decisions based on analytically measured data now, rather than simple visual checks. The move toward automated color matching, particularly in digital textile printing and high-speed pigment compounding, drives this evolution. Small variations invisible to the naked eye can trigger costly supply chain disruptions, forcing recalibration or halting runs. To address this, we work closely with in-house laboratory personnel, providing them with control samples, calibration curves, and check standards — a loop in which feedback never falls on deaf ears.
Traceability often separates industrial partners from quick-turnaround traders. As a manufacturer, we've found that maintaining a digital ledger of every lot produced, right down to the source of upstream raw materials, encourages reliability among our team members. It also proves valuable during audits or in case a customer reports an out-of-spec outcome. Our ability to match performance issues to a precise lot history has, on occasion, helped customers rescue a batch or identify procedural errors upstream. Consistency like this arises less from clever marketing than from decades spent cultivating a system that puts documentation and process control above cost-cutting shortcuts.
The impact of 2-nitroaniline doesn’t end at the shipping dock. Wastewater carrying traces of this material or its byproducts requires careful management. Our plant operates an on-site effluent treatment facility built on lessons from regulatory bodies and our own long-term water sampling data. The challenge: residual nitro compounds are hard to break down naturally, so we use advanced oxidation technologies and monitor outflows by both chemical test and bioassay. In our experience, plant neighbors appreciate candor about what leaves our site. Keeping open lines with local authorities, and even sharing monitoring results with interested stakeholders, builds the good will that paperwork cannot.
On safety, we've had our share of incidents, some minor, some near misses — never fatal, but always educational. Storing and transferring significant quantities forces us to think ahead. Fixed sensors for nitroaromatic vapors, automatic shutoff valves, regular maintenance of extraction fans: these are not extras, but core infrastructure that keeps our operation incident-free. Regular drills and emergency reviews keep the team alert. We have found that listening to our workforce about near misses and improvement ideas brings a level of awareness and accountability that written manuals alone cannot instill. The best ideas for risk reduction have come from technicians who know the hazards better than any consultant.
We do not produce 2-nitroaniline in a vacuum. Demand cycles shift, raw material costs fluctuate, and environmental rules tighten with each passing year. We adapt by keeping our technical leadership close to the production floor and reaching out to users who push our product into new applications. Sometimes the lessons are technical: a process tweak to minimize byproduct generation or to recycle a higher portion of spent acid. Sometimes they come from a customer who needs a tighter limit on a trace impurity — or faces a sudden regulatory need for a restriction on a specific metal. Our management champions ongoing dialog with all users, looking for ways to improve both material and service.
We have invested in pilot-scale reactors to test process innovations before plantwide deployment. By simulating slight changes in mixing rates, reagent ratio, or crystallization time, we can predict impacts before risking a larger batch. Recently, one such trial let us switch to a milder neutralization agent, reducing both effluent load and risk of batch “burning” — a phenomenon that leaves off-color residues and puts strain on downstream purification filters. Practical improvements like this take root only when teams on both lab and line communicate daily, exchanging notes and updating job tickets for the next shift. At the end of each month, we review production notes, tallying successes and losses, identifying potential for further cost or waste reduction. Every improvement is a win not just for us, but for the customers and communities relying on us to get it right every time.
Users evaluating 2-nitroaniline often compare it to similar compounds like 4-nitroaniline or related aromatic amines. The differences aren’t just in molecular placement but in performance and practicality. For instance, 4-nitroaniline creates different dye shades, leading to more muted hues than its ortho counterpart. We have seen labs attempt to substitute, only to find color fastness or light stability targets missed. Costs then balloon not from the price per kilo, but from lost batches or time spent remaking color masterbatches. 3-nitroaniline offers other reactivity, but rarely finds the same demand or processing ease as the ortho isomer. We have dealt with users who ran tests on all three before settling on 2-nitroaniline for its balance of solubility and reactivity under practical industrial temperatures.
From a safety standpoint, we know that the ortho compound’s relatively moderate toxicity and melting point allow for easier management versus some nitroaromatic alternatives. We’ve had conversations with both safety officers and plant engineers from partner companies who appreciated that our technical teams could answer specific questions about dust collection, fire hazard mitigation, and safe storage practices. Unlike more volatile nitrobenzenes, or those with uncontrolled exotherms on heating, 2-nitroaniline lends itself to established industry best practices — adaptable, predictable, and consistent from reactor fill to product shipment.
Manufacturing 2-nitroaniline connects us not just to big-name dye plants or international pharmaceutical companies, but to smaller innovators and academic research labs. We field requests every month for special studies: new analysis techniques, novel applications, regulatory data for new markets, and even customized blends for experimental use. Each inquiry shapes how we plan, invest, and allocate resources on the production line. We owe our success to the trust placed in our ability to deliver not only a chemical, but all the documentation, predictability, and technical backing that robust partnerships require.
We recognize that the world of chemical manufacturing faces growing pressure to minimize waste, improve energy efficiency, and increase transparency. For us, the challenge around 2-nitroaniline production is less about simply “making molecules” and more about how we manage every detail — from sourcing raw inputs to certifying analytical test results, from controlling what goes down the drains to teaching every new hire about the underlying risks and responsibilities. We expect that further shifts in end-user needs and regulations will keep us striving to do better. Internal process audits, continuous staff training, and investment in the latest analytical tools are part of our daily life.
As direct producers, we see ourselves as participants in a process that spans technology, people, and the wider community. Through years of hands-on engagement, we have learned to respect both the opportunities and responsibilities that come from making chemicals at scale. 2-nitroaniline’s significance, to us, is found not just in meeting grade specifications or filling orders — but in upholding safety, accountability, and trust at every step. That is how we judge our own progress as manufacturers, and how we intend to continue serving everyone who counts on us from lab bench to final application.