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HS Code |
165741 |
| CAS_Number | 97-02-9 |
| Molecular_Formula | C6H5N3O4 |
| Molecular_Weight | 183.12 g/mol |
| Appearance | Yellow to orange crystalline powder |
| Melting_Point | 145-148 °C |
| Solubility_in_Water | Slightly soluble |
| Density | 1.53 g/cm³ |
| Purity | Typically ≥98% |
| Synonyms | 1-Amino-2,4-dinitrobenzene |
As an accredited 2,4-Dinitroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 500g amber glass bottle labeled "2,4-Dinitroaniline, C6H5N3O4," includes hazard symbols and tightly sealed screw cap for safety. |
| Shipping | 2,4-Dinitroaniline should be shipped as a hazardous material, in accordance with relevant regulations (such as DOT, IATA, or IMDG). Package in tightly sealed, chemical-resistant containers, clearly labeled, with suitable cushioning and secondary containment. Ensure appropriate documentation and safety data sheets (SDS) accompany the shipment, and handle away from heat, ignition sources, and incompatible substances. |
| Storage | 2,4-Dinitroaniline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from heat, sparks, and open flames. It should be kept away from incompatible materials such as strong oxidizers and reducing agents. Proper labeling and secure shelving are essential to prevent spills and accidental exposure. Store in compliance with local regulations. |
Applications of 2,4-Dinitroaniline in Industrial ManufacturingWe manufacture 2,4-Dinitroaniline for specialized industrial sectors requiring precise synthesis control, reliable downstream compatibility, and adherence to strict compliance frameworks. Explore primary application fields and technical integration details below. 1. Dyestuff Intermediate in Azo Dye ManufacturingMajor textile and pigment manufacturers apply 2,4-Dinitroaniline as a diazo component and coupling intermediate in azo dye synthesis. This chemical supports production of yellow and red shades with stable performance for fibers, leather, and plastics. It reacts with aromatic amines or phenols under controlled acidic conditions to generate required chromophores. Facilities use dedicated high-purity grades to meet color yield and environmental benchmarks defined by global textile markets. Industry compliance standards
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2. Pharmaceutical Synthesis Building BlockPharmaceutical process chemists employ 2,4-Dinitroaniline to construct nitroaromatic scaffolds incorporated into analgesic, antimalarial, and specialty drug molecules. Its two nitro substituents facilitate controlled reductions, amination, or heterocycle formation. This intermediate serves key roles in pilot-scale and GMP-compliant batch synthesis, ensuring batch-to-batch consistency for regulated drug substance manufacturing. Industry compliance standards
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3. Agrochemical (Herbicide) IntermediateSpecialist agrochemical manufacturers use 2,4-Dinitroaniline as a core nitroaromatic building block in pre-emergent herbicide production, particularly for dinitroaniline-based products such as pendimethalin and trifluralin. Its consistent purity enables reproducible reaction yields and potent selectivity against annual grasses and weeds. The integration into multi-stage synthesis requires strict residue and by-product management to meet agro-environmental guidelines. Industry compliance standards
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4. Rubber Antioxidant ProductionRubber chemical factories utilize 2,4-Dinitroaniline in the synthesis of certain antioxidant additives, notably nitroaniline-derived stabilizers for natural and synthetic rubbers. Its nitro groups permit stepwise transformation, introducing functional substituents that help resist oxidative polymer degradation in tires, belts, hoses, and molded products. This application demands traceability and batch uniformity across high-throughput continuous mixing and vulcanization lines. Industry compliance standards
Typical usage ratio
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Drawing on several decades of experience in the synthesis and refinement of nitroaniline derivatives, I have seen the market’s evolving needs pull industrial chemicals along in diverse directions. 2,4-Dinitroaniline, with the molecular formula C6H5N3O4 and a CAS number of 97-02-9, represents a versatile specialty chemical serving target markets that call for consistent purity and traceable manufacturing practices.
On the production floor, a faint yellow crystalline powder emerges from process streams, recognized easily by its distinctive hue and solid physical state at ambient temperatures. Standard operating procedures at our facility deliver this material with purity typically in excess of 99%, achieved through carefully controlled nitration and subsequent purification sequences. Batch documentation reflects true-to-scale process repeatability, since quality and trace impurity profiles hold significance for downstream reactions and for customer applications where small variances in raw material can rewrite an entire production day.
Sourcing reliable precursors and performing plant-level checks at each stage, our technical team flags any trace anomalies, from moisture content under 0.5% by Karl Fischer titration, to granular consistency assessments. 2,4-Dinitroaniline is hygroscopic; this means that improper handling during shipping or storage can lead to caking or decomposition. Real-world logistics demonstrate the value of vacuum-sealed and nitrogen-purged packaging, not just for shelf life but to preserve handling safety. For international clients, packaging shifts from 25 kg fiber drums to smaller units, matching the risk management profile each end user expects.
We have fielded calls from research groups struggling with inferior batches containing more than 0.3% ortho or para regioisomers. These impurities, trivial to some, can frustrate catalysis or yield inferior dye products. Our movement towards continuous improvement focuses on keeping these below detectable limits by HPLC and GC analysis. Receiving team feedback about off-color or persistent clumps usually points to inadequate drying at the finishing stage, something correctable with process discipline and measurable at every stage.
2,4-Dinitroaniline finds its value in multiple production lines—chief among them are the synthesis of dyes, pigments, and chemical intermediates. In azo dye chemistry, it stands as a preferred amine precursor, converting reliably to a range of vivid dyes that textile processors rely on for lasting colorfastness. The specific positions of the nitro groups in the aromatic ring drive reactivity in coupling reactions, making 2,4-dinitroaniline more predictable than mixed isomer blends. Feedback from dye technicians often mentions the reproducibility of shade development and batch-to-batch color matching—a direct consequence of strict upstream specifications.
Agrochemical innovation continues to depend on precise intermediates. Early-stage development compounds, ranging from herbicides to fungicides, demand raw materials free of trace interfering substances that could compromise biological activity. Our batches, consistently passing industry-accepted assays for elemental and heavy metal contaminants, enter this domain with a proven track record of zero batch failures for more than five years.
Outside of large-scale manufacturing, analysts and academic researchers use 2,4-dinitroaniline as a building block in synthesizing targeted conjugates, sensor molecules, and standards for spectrophotometric analysis. Lab-scale applications place even greater weight on homogeneous composition, since success or failure at small scales amplifies any background impurity.
Anyone experienced with aromatic nitro compounds understands the balance between precision and respect for inherent hazards. 2,4-Dinitroaniline exhibits moderate toxicity and poses risks typical of nitro aromatics, including potential explosive hazard if mishandled or exposed to extreme heat. Our operational experience leads us to emphasize closed-transfer systems, adequate ventilation, and robust PPE during transfer and weighing. Regulatory compliance starts at receipt and continues through production. Annual safety drills, monitored waste neutralization, and air emissions tracking—these are not optional. They form the backbone of modern, responsible chemical manufacturing.
As producers, we work alongside third-party auditors to perfect controlled disposal methods. Incinerators tailored to nitrogenous organics, rather than landfill or untreated aqueous discharge, provide a meaningful reduction in environmental impact. No shortcut replaces years of audit trails and honest documentation. Sustainable chemistry isn't achieved in a memo—it requires routing every kilogram of off-spec product through proper outlets, even at short-term expense.
Within our facility, periodic reviews of closed-vessel filtration, scrubbing of atmospheric releases, and employee exposure logs find their way into daily operations. Workers receive refresher training, and disaster drills don’t wait for something to go wrong. Feedback loops with local authorities and civil preparedness officers give our team a realistic reading—not just compliance but confidence in every shipment leaving the yard.
The “dinitroaniline” chemical class covers more than just the 2,4-isomer. Structural variations matter profoundly in practical chemistry. During my years at the plant, both 2,6- and 2,5-dinitroaniline have reached pilot or full-scale synthesis for select partners. Chemically, shifting a nitro group by just one ring position alters melting point, reactivity toward nucleophilic substitution, and azo-coupling tendencies. 2,4-dinitroaniline offers both a higher melting point and greater oxidative stability, which gives downstream processors more flexibility under variable storage or thermal conditions.
Handling characteristics differ between the isomers. Materials like 2,6-dinitroaniline tend toward a softer, oilier appearance with more tendency to compact or form sticky masses, challenging automated feeding mechanisms in bulk production. Over time, customers across dye intermediates, specialized agrochemicals, and pharmaceutical research have gravitated to 2,4-dinitroaniline because of its tried-and-tested performance record.
If a process can accept a broader impurity profile, commodity “mixed dinitroanilines” enter the conversation, priced with fewer specifications. Large-volume traders rarely satisfy the needs of pharmaceutical or fine chemical synthesis. There, even fractions of a percent impurity can dilute the value of a finished compound or generate regulatory headaches, as international quality systems place tight limits on impurities.
One persistent point of debate centers around scalability of purification. The more uniform the starting material, the less energy and solvent spend during downstream refinement. Engineering staff at both our site and at end-user plants corroborate this point: 2,4 isomer-packed batches feed into continuous reactors with minimal unplanned downtime, reducing costs over months and years.
Over the past ten years, the chemical sector has undergone a series of price swings, driven by fluctuations in precursor costs, regional market realignments, and waves of new environmental regulation. 2,4-Dinitroaniline, despite its modest volumes compared to base chemicals, consistently sits in the crossfire of these forces. Downturns in the nitrobenzene or aniline market inevitably ripple through to pricing in this specialty product. Our purchasing department has lived through both periods of scarcity and oversupply, adjusting strategies in response and investing in both local supplier relationships and direct import capabilities where risk warrants.
A new challenge for many manufacturers involves the ever-tightening restrictions on nitro compound discharge. Around our industry, compliance with standards from agencies such as EPA or ECHA means running more frequent analysis, reporting on every abnormal result, and holding ourselves directly accountable for any release, accidental or planned. The upside is a cleaner, safer workplace and river, though the investment in new sensors, treatment beds, or recovery processes proves anything but minor. In our factory, the money spent on effluent upgrades is easily justified—community trust and plant operating licenses rest on it.
Taxation and tariff policy create another level of uncertainty. International clients, especially those based in North America and Europe, sometimes delay or revise orders in response to new duties or changes to the Harmonized Tariff Schedule for specialty compounds. We have found agility an asset here, adapting quickly to label, document, and reroute shipments to keep pace with dynamic regulatory environments.
Not every day brings a textbook scenario in the production of 2,4-dinitroaniline. Our customer support and technical teams field requests running the gamut from minor color changes to more involved issues where unexpected side-reactions threaten high-value multi-step syntheses. Experience teaches that upstream diligence, such as rigorous drum labeling and well-trained material handlers, pre-empts most avoidable problems. A misstep in humidity-controlled storage can convert a top-spec batch into flowability complaints in an instant.
In downstream processes, users sometimes chase elusive yields or face filter-clogging due to unanticipated particulate formation. As manufacturers, our lab-replicated process simulations have uncovered that slow crystallization followed by staged drying gives crystalline material better stability in subsequent re-solubilization steps. The extra hours spent here save days in remediation—lessons learned through hard accountability and open communication with our customers’ technical teams.
Periodic reviews with production partners flag up the odd batch where off-specification attributes slip through—an unavoidable reality for any complex chemical operation. Rather than hiding these, our response involves quick recall, immediate investigation, and changes to process documentation that reach every shift. Mistakes open a path to collective learning, not blame.
Feedback from research chemists and downstream partners propels our investment in process intensification projects and real-time quality analytics. In the last several years, installation of in-line NIR spectroscopy and computer-controlled dosing systems has lowered the variance in pH, color, and isomer content. Greater precision, both in production and QC release, supports customers scaling up for new business or meeting their own regulatory audits.
Laboratory and pilot-scale teams trial green chemistry alternatives when feasible, testing safer solvents and exploring microwave-based synthesis techniques for process steps with high-energy or high-waste output. Cross-discipline working groups scrutinize the lifecycle impacts of every new change, balancing profitability with a responsibility to both employees and local communities.
Our schedule of biannual plant upgrades, combined with close relationships with component suppliers and local engineers, means the real-world production environment stays aligned with modern expectations. A successful manufacturer adapts faster than the market can throw problems in its path, and nowhere is this more evident than in the specialty intermediates sector. 2,4-Dinitroaniline represents not just a core product but a blueprint for quality management in action.
Regular knowledge exchange with chemical associations, global buyers, and regulatory agencies plays a defining role in our strategy as manufacturers. By hosting site visits and participating in standards-setting workshops, our team helps raise the bar not just internally, but across the industry. We aim for transparency in process documentation and encourage third-party assessments, opening our results and improvements to scrutiny.
Our technical manager sits on the review panels for several industry journals, helping to disseminate applied knowledge and advance best practices. This involvement translates directly to better products, more consistent performance, and a smoother dialogue with customers facing regulatory or technical barriers in their own businesses.
The market for high-purity 2,4-dinitroaniline faces steady, if not spectacular, demand. Growth sectors include digital textile printing, microelectronic component etching, and specialty pharmaceuticals. Each requires ever more consistent and cleaner intermediates. End users expect traceability, and as manufacturers, we deliver that confidence through investment in both people and technology, not shortcuts.
New environmental standards and advances in automation will keep pushing the sector to higher standards. Our own future plans include pilot runs using more sustainable process solvents, recovery of waste heat, and automated feedback loops that anticipate process drift before it affects a single kilogram of product. In this space, trust is an output of both legacy and daily action.
Day after day, producing 2,4-dinitroaniline isn’t about just filling orders—it’s about supplying a community of chemists, engineers, and researchers who expect solutions delivered with honesty and deep-rooted technical know-how. From the tangible feel of a freshly filled drum to the digital printout of a recent HPLC scan, our plant proves that quality starts on the shop floor.
Each improvement, each new hire trained in the details of safe manufacture and open reporting, strengthens the long-term viability of this niche but vital intermediate. 2,4-Dinitroaniline’s story in our hands is one of care, adaptation, and continuous attention to both the process and the people making it happen.