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HS Code |
172155 |
| Cas Number | 89-87-2 |
| Molecular Formula | C8H9NO2 |
| Molecular Weight | 151.16 g/mol |
| Iupac Name | 2,5-Dimethyl-1-nitrobenzene |
| Appearance | Yellow crystalline solid |
| Melting Point | 58-60 °C |
| Boiling Point | 255-256 °C |
| Density | 1.13 g/cm³ |
| Solubility In Water | Insoluble |
| Flash Point | 120 °C |
| Smiles | CC1=CC(=C(C=C1)[N+](=O)[O-])C |
| Refractive Index | 1.556 |
| Pubchem Cid | 7298 |
As an accredited 2,5-Dimethylnitrobenzene 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 "2,5-Dimethylnitrobenzene," features hazard symbols, lot number, and tightly sealed with a screw cap. |
| Shipping | 2,5-Dimethylnitrobenzene should be shipped in tightly sealed containers, clearly labeled, and in compliance with local, national, and international chemical transport regulations. Store and transport away from heat, sparks, and open flames. It should be handled as a hazardous material, using appropriate protective measures to prevent leakage, accidental exposure, or environmental release. |
| Storage | 2,5-Dimethylnitrobenzene should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from heat, open flames, and direct sunlight. Keep it separate from strong oxidizers, acids, and reducing agents. Ensure proper labeling and access restriction, and follow standard chemical hygiene and safety protocols to prevent accidental exposure or contamination. |
Applications of 2,5-Dimethylnitrobenzene in Industrial Manufacturing2,5-Dimethylnitrobenzene serves as a vital intermediate in several specialized chemical value chains, enabling precise transformation steps in advanced manufacturing environments. As a direct manufacturer, we focus on supporting downstream producers in established industrial domains, delivering consistently controlled quality according to international process standards. 1. Synthesis of Pharmaceutical Intermediates (Key Intermediate for 2,5-Dimethylaniline Production)Pharmaceutical intermediate manufacturers utilize 2,5-Dimethylnitrobenzene in the reduction step to synthesize 2,5-Dimethylaniline, which feeds into the preparation of APIs for antihypertensive agents and select analgesics. This raw material ensures defined substitution patterns critical for the integrity of target molecules, supporting process reproducibility under regulated industry conditions. Manufacturers optimize the addition rate depending on batch target yield and process scale to maintain impurity profiles compliant with GMP requirements. Industry compliance standards
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2. Agrochemical Synthesis (Precursor in Fungicide and Herbicide Active Ingredient Manufacturing)Agrochemical formulators process 2,5-Dimethylnitrobenzene as a specific starting compound for the creation of specialized nitroaromatic substructures found in fungicide and herbicide actives. The compound’s substitution pattern resists side reactions in subsequent nitration or reduction steps, yielding intermediates required for active ingredient assembly. Ratio selection factors in subsequent alkylation/transformation efficiency and downstream purification strategies for regulatory compliance. Industry compliance standards
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3. Advanced Dye and Pigment Production (Nitroaromatic Feedstock in Colorant Chemistry)In specialty dye and pigment manufacturing, producers leverage 2,5-Dimethylnitrobenzene to synthesize core intermediates in azo and anthraquinone dye technologies, where controlled methylation supports desirable optical and fastness properties. Process chemistry calls for direct use of the material in coupling or condensation reactions, with ultrahigh purity grades critical to avoid off-shade formation and allergens in textile or paper contact products. Industry compliance standards
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4. Electronic Chemicals (Intermediate in High-Purity Aromatic Compound Synthesis)Electronics manufacturers incorporate this material into the multi-step synthesis of highly purified compounds utilized in organic semiconductors and specialty coatings. The aromatic structure with dual methylation supports charge transport properties essential for OLED and photoresist applications. Process engineers tightly monitor the entry point and purity to guarantee compatibility with wafer-grade electronic chemicals. Industry compliance standards
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Inside our manufacturing halls, we handle a wide range of aromatic chemicals, but 2,5-dimethylnitrobenzene holds a special role on our production lines. We synthesize this compound through meticulous nitration processes, keeping a close eye on each parameter to guide selectivity. While some may see it as just another isomer among many nitrobenzenes, we recognize the value its unique substitution brings. The presence of methyl groups at the 2 and 5 positions on the benzene ring, flanking the nitro group, shapes its reactivity, melting point, and downstream chemistry. Formed as an off-white to pale yellow crystalline solid, its molecular formula, C8H9NO2, may seem straightforward, yet the targeted arrangement of methyl and nitro groups grants it characteristics that chemists and engineers favor for certain syntheses over other isomers.
We produce 2,5-dimethylnitrobenzene using carefully chosen feedstocks, precise reaction temperature control, and vigilant purification steps, not just to chase purity but because our customers’ downstream reactions simply will not tolerate unpredictable impurity profiles. Even trace isomeric contamination, such as from the 2,4- or 3,5- variants, risks changing yields and side-products for those making dyes, pharmaceuticals, or advanced materials. Typical batches in our facility undergo purity checks using gas chromatography and spectroscopic analysis. Purity often exceeds 99%, but we refuse to cut corners because even a fraction of a percent in chemical manufacturing can mean the difference between a smooth process and an operational headache.
On a laboratory bench or inside a stirred reactor, 2,5-dimethylnitrobenzene shows off a melting point close to 52-55°C, which means it works well in applications that require either a solid state or manageable melting for further use. The compound does not give off much odor, and its low volatility at room temperature allows safer handling compared to some lighter nitroaromatics. Our team packages it to prevent moisture uptake and light-induced decomposition, because we have seen what happens if atmospheric oxygen or sunlight gets a chance at nitro compounds—a change in color, a reduction in shelf life, and an unwelcome splash of byproducts. We scale product from kilogram to tonnage quantities, but the quality does not shift with batch size, thanks to robust process engineering embedded into our operations.
Those on the development side know that 2,5-dimethylnitrobenzene isn’t just a building block; it often becomes the linchpin for certain molecular transformations. Chemical researchers and production chemists reach for this compound when making specific intermediates in pigment and dye synthesis, particularly where its substitution pattern brings selectivity in further nitration, reduction, or cross-coupling reactions. The nitro group, being electron-withdrawing, lets them tap into directed ortho metalation or hydrogenation conditions, and the methyls offer additional points for functionalization. We speak often with our partners about how this particular isomer offers more predictability in downstream steps than its 2,4- or 3,5- counterparts, saving time and solvent. In pharmaceutical research, we’ve seen teams leverage its manageable melting range when developing new solid forms or as part of scaffold modifications—not just for convenience, but because they cannot tolerate complexity in separating isomeric mixtures later.
Outsiders sometimes lump all dimethylnitrobenzenes together, but we learned long ago that this is a mistake. The arrangement of groups on the benzene ring makes a world of difference. The 2,4- isomer, for instance, exhibits altered reactivity patterns because the nitro group sits between the two methyls, raising the energy for some transformations and lowering yields for others. The 3,5- isomer lacks the same directing effects, which can matter enormously in catalytic cycles. We field questions every month from process chemists who tried a different isomer and encountered trouble in their hydrogenation step, or who found that downstream separation suddenly became more complex. Our experience on the manufacturing and technical support side allows us to anticipate these questions and guide customers toward the right choice for each application.
Handling nitro compounds, especially aromatic nitro products like 2,5-dimethylnitrobenzene, has no room for guesswork. We have honed processes over the years to manage safety, not just because regulations require it, but because we have seen what can go wrong. Maintaining constant nitrogen purging during synthesis, strict control of exotherm during nitration, and personal protective measures for staff make a measurable difference in outcomes. Our operation leans heavily on in-line sensors and early warning systems. The same applies through to packaging, storage, and shipping. Whenever possible, we share handling insights with our customers, explaining why storing the solid in cool, dry, shaded conditions helps maximize shelf life and minimize degradation. These practices spring from direct factory-floor experience, not from theoretical guidelines.
Talking about purity and quality sounds easy, but in practice, these demands drive many parts of our daily work. We routinely run NMR and HPLC analyses on outgoing batches, not just for our records but also to solve live issues for our partners. We know by sight and smell when a batch goes off-spec, but trust our instruments to catch anything our senses miss. If a downstream process calls for a higher melting point cut, we separate fractions using slow crystallization, rejecting any product that doesn’t meet agreed specs. Each batch receives unique identification, allowing full traceability in case of future questions or investigations.
Nothing concentrates the mind on environmental impact quite like handling nitroaromatics. Each ton we make brings potential liability if any byproducts enter the waste stream unchecked. We engineered our facilities with closed-loop solvent recovery, so every molecule used in synthesis enters waste treatment before being discharged—or more often, reused in the next batch. We can recount examples where failing to do so led to regulatory problems for others in our industry, so we would rather spend on upfront safeguards than pay down the road. Our customers, often bound by their own internal compliance standards, appreciate these efforts. Some have even toured our site to see solvent scrubbers and effluent treatment plants running in real time before ever signing on for regular supply.
Our technical service team spends as much time on the phone as they do on the plant floor. One recurring story involves a dye manufacturer who switched to our 2,5-dimethylnitrobenzene after months of fighting off-color batches. They had been using a blend containing multiple isomers sourced from another supplier, which led to unpredictable color development and reduced product acceptance in their export markets. After a few pilot runs with our material, their refusals dropped. Another research group reached out while scaling a novel API intermediate—selectivity for para-substitution led them to review all positional isomers, but only the 2,5 pattern delivered both reactivity and isolation simplicity. These stories repeat every quarter and show us which product attributes actually make the difference in the field.
We have seen strains in chemical supply chains caused by raw material shortages, shipping delays, and even political events. Our answer has been to build redundancy. Raw materials for 2,5-dimethylnitrobenzene come from multiple vetted suppliers, and we keep buffer inventories measured in months, not days. This way, customers relying on our timelines for their continuous processes do not have to shut down or scramble for alternatives. We also control logistics from the factory gate to customer delivery, using partners with proven safe handling of chemical cargo. These steps require extra investment and overhead, but lost trust costs much more.
Development teams in industries such as specialty chemicals, agrochemicals, electronics, and advanced materials constantly push for new ways to leverage 2,5-dimethylnitrobenzene. Our R&D group collaborates with clients who need specific crystal forms, particle size distributions, or tailored impurity profiles. We explore catalytic methods to lower process temperatures or enable greener chemistry routes, not because external forces dictate it but because operational efficiency impacts our own bottom line. Our investment in pilot facilities allows small-batch trials without disrupting ongoing commercial production, so new applications can be tested safely and rapidly.
Compliance isn’t just a paperwork exercise; it sets expectations for leadership and staff every day. We comply with REACH, TSCA, and local chemical regulations. Staff training is ongoing, not a one-off activity. Labels, packaging, documentation, and record-keeping are designed not merely to satisfy audits but to catch errors before they reach a customer. This approach stems from decades of facing audits—regulatory and customer-driven alike. We invite auditors on-site, not simply as a checklist, but because the best inquiries are those that expose blind spots. That openness saves both sides time and often leads to better processes going forward.
No product stays static in the chemical business, and 2,5-dimethylnitrobenzene has evolved through ongoing engagement with technical and procurement teams. Over the years, customers’ priorities changed—from specs centering around simple purity data to demands for full impurity profiles, extended shelf life, and documentation supporting every shipment. These requirements feed directly into how we run our reactors, dry our product, analytically release each lot, and package for transport. Each lesson learned flows through production meetings, so each batch improves on the last. If a customer’s process data highlights an unexpected interaction—say, with a trace metal catalyst or an unknown solvent—they reach out, and we investigate. This feedback loop improves reliability for everyone.
Greater scrutiny now lands on every chemical supply, both for regulatory and reputational reasons. Sustainability questions—lifecycle carbon footprints, origin certification, recyclability—now show up alongside routine technical specifications. In the early days, buyers focused purely on cost and speed. Now, their priorities address transparent reporting, renewable raw material sourcing where possible, and third-party certification. We have modified our supply and reporting systems to make answering these questions part of normal business, so our partners do not face surprises during audits, ESG reviews, or certification programs.
Through experience, we have learned the importance of managing both physical and chemical stability. 2,5-dimethylnitrobenzene holds up well under cool, dark, dry storage, but moisture, heat, or light quickly erode product quality. We remind end users that keeping containers tightly sealed, in stable temperature zones, helps prevent caking or decomposition. Cleanliness in preparation and transfer, avoidance of steel tools that might catalyze degradation, and proper PPE serve laboratory staff and plant operators alike. Over time, these habits protect not only product value but also the safety record of the site.
Within a given class of nitrobenzenes, selection of isomer matters just as much as overall purity. A team optimizing a route to a specific azo dye, for example, found their process only clicked into high yield and predictable color development with 2,5-dimethylnitrobenzene. The same holds for certain pharmaceutical R&D projects—one misplaced methyl group frustrates separation and raises costs by forcing extra chromatography or recrystallization steps. Lessons from these stories inform how we stock, analyze, and recommend product grades. It is no exaggeration to say that the smallest details on the ring distinguish success from a troubleshooting marathon.
Too many suppliers hide behind impenetrable technical sheets and slow service. We publish real test data, not just ranges, from every production lot. Testers on our line can tell you the NMR spectrum on a shipped product and describe exact storage or transit conditions across multiple warehouses. Working with closely held analytical records, our traceability standard covers not just origin but the full history of each drum or sack that leaves the factory.
Our journey with 2,5-dimethylnitrobenzene has been shaped by decades of listening, hands-on troubleshooting, and technical dialogue with customers. No two batches or seasons present the exact same challenge, but our methods and principles remain consistent. Purity matters not because it appears on a specification, but because it drives downstream consistency, yield, and quality for clients who manufacture products that end up everywhere—from textiles to pharmaceuticals and electronics. Lessons learned from each shipping, handling, and synthesis challenge feed continuous improvement within our plant, pressing us to innovate and deliver more reliably every year.