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HS Code |
804361 |
| Cas Number | 603-82-9 |
| Molecular Formula | C8H9NO2 |
| Molecular Weight | 151.17 g/mol |
| Iupac Name | 1,2-dimethyl-3-nitrobenzene |
| Appearance | Yellow crystalline solid |
| Melting Point | 51-55 °C |
| Boiling Point | 264 °C |
| Density | 1.16 g/cm³ |
| Solubility In Water | Insoluble |
| Flash Point | 126 °C |
| Synonyms | 3-Nitro-o-xylene; m-Nitro-1,2-dimethylbenzene |
| Pubchem Cid | 13221 |
As an accredited 3-Nitro-1,2-Xylene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g amber glass bottle with airtight cap, safety labels displaying hazard symbols, chemical name, concentration, and manufacturer details clearly printed. |
| Shipping | **3-Nitro-1,2-xylene** must be shipped according to hazardous materials regulations. It should be packed in tightly sealed, chemical-resistant containers, clearly labeled, and cushioned to avoid breakage. Transport must comply with local, national, and international regulations (such as DOT, IATA, or IMDG), with appropriate documentation and safety precautions in place. |
| Storage | 3-Nitro-1,2-xylene should be stored in a cool, dry, well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers. Keep the container tightly closed and clearly labeled. Use only approved chemical storage containers. Protect from direct sunlight and moisture. Follow all local regulations and safety guidelines for hazardous chemical storage. |
Applications of 3-Nitro-1,2-Xylene in Industrial Manufacturing3-Nitro-1,2-xylene is a key intermediate utilized by specialty chemical manufacturers across several focused industrial segments. As a producer, we supply this material for downstream use where strict process requirements, precise formulation control, and adherence to regulatory frameworks are critical. The following sections highlight real-world integrations of 3-nitro-1,2-xylene in industrial synthesis, providing detailed information on compliance, formulation ratios, process integration, and finished product types. 1. Synthesis of Agrochemical Active IngredientsSpecialty crop protection compound producers depend on 3-nitro-1,2-xylene as an essential starting material during the nitration and subsequent derivatization steps in the creation of select herbicide and insecticide actives. Accurate addition of this intermediate during the coupling, reduction, and cyclization phases ensures reproducible activity and regulatory traceability. Strict quality and analytical controls support confident registration in regulated agricultural markets. Industry compliance standards
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2. Intermediate for Dye & Pigment ManufacturingSynthetic organic dye and pigment plants incorporate 3-nitro-1,2-xylene during azo and anthraquinone dye precursor synthesis. Maintaining accurate reaction conditions and dosage influences pigment shade intensity and fastness, critical for meeting established color indices and safety registrations. The raw material’s technical grade purity supports high-performance pigments for demanding textile and coatings applications. Industry compliance standards
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3. Building Block in Pharmaceutical API SynthesisRegulated pharmaceutical ingredient plants use 3-nitro-1,2-xylene as a core building block for several active pharmaceutical ingredient (API) precursors via nitration, reduction and halogenation transformations. Careful tracking of all raw material additions and analytical verification of conversion rates ensure cGMP and pharmacopeial compliance throughout the synthetic workflow. Its supply chain documentation supports DMF and regulatory filings globally. Industry compliance standards
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4. Specialty Chemical Synthesis for Polymer AdditivesProducers of polymer stabilizers, plasticizers, and flame-retardant intermediates utilize 3-nitro-1,2-xylene in complex multi-step syntheses. Stringent process monitoring is enforced due to the need for high purity intermediates suitable for polymer compounding. Its inclusion enables functionality enhancements in downstream plastics and rubbers by providing controlled aromatic substitution without excessive byproduct generation. Industry compliance standards
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5. Application in Photoresist and Imaging ChemistryElectronic chemical manufacturers deploy 3-nitro-1,2-xylene as an intermediate in the formulation of functionalized aromatic compounds essential for photoresist monomer and imaging agent development. This role requires exceptional control of residual catalyst levels, solvent quality, and trace impurity management to meet strict microelectronics and imaging performance objectives. Industry compliance standards
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6. Production of Antioxidant Intermediates for Specialty LubricantsChemical formulators rely on 3-nitro-1,2-xylene as a controlled aromatic feedstock in synthesizing intermediates subsequently functionalized for antioxidant applications. The effective stabilization of engine oils and synthetic lubricants requires highly consistent batch quality and traceability from raw material through the sulfonation and alkylation routes to active antioxidant agents. Industry compliance standards
Typical usage ratio
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As a chemical manufacturer with years of hands-on experience in aromatic nitro compounds, we see 3-Nitro-1,2-xylene filling a very specific niche. This nitroaromatic appears as a yellowish crystalline powder in its final purified form. Through repeated crystallization and careful control of parameters like reaction temperature, we maintain a product with high chemical purity, typically achieving less than 0.1% impurities on dry weight. Our QC team remains uncompromising; each batch’s melting point and chromatographic fingerprint are compared to previous standards to catch even the smallest deviation.
The molecular formula C8H9NO2 and CAS number 603-72-1 may sound abstract until you meet customers who depend on small molecular changes for their process yields. The difference between 3-Nitro-1,2-xylene and its structural isomers often confuses newcomers. What sets 3-Nitro-1,2-xylene apart is the nitro group fixed at the third position of the xylene ring, paired with methyl groups at the first and second. Minute changes in substitution, as we've witnessed in the lab, can shift entire reaction pathways for downstream chemical transformations. For instance, 3-nitro derivatives respond with different reactivity and solubility compared to 4-nitro or 2-nitro counterparts, which sometimes frustrates formulation chemists testing blend stability. Our customers trust us to keep such distinctions clear so their results don’t suffer from source material ambiguity.
Process engineers and technical managers in our plant keep close tabs on each stage, because small lapses translate to big headaches for our clients. Most buyers use 3-Nitro-1,2-xylene as an intermediate in dye and pigment synthesis. Its particular chemical structure steers diazotization and coupling reactions to high selectivity, reducing the formation of colored byproducts that would lower pigment tinting strength. In our feedback loop with downstream manufacturers, we see time and again that a pure cut of 3-Nitro-1,2-xylene helps to ensure their product shades run repeatable—no surprises in the final drum of pigment pastes.
Researchers and production chemists who work in agricultural and pharmaceutical sectors find use cases as well. At one major customer, 3-Nitro-1,2-xylene’s clean reactivity profile helps them move quickly through nitration and reduction sequences during early research phases for API intermediates. They have come to rely on our product to avoid side reactions that stalled their pilots with other batches in the past. This reliability builds confidence that scale-up won’t trigger unwanted surprises that show up as ghost peaks on HPLC traces.
We use reagent-grade starting materials for the nitration step, sourced directly from trusted upstream chemical plants. The sequence itself is sensitive: attacking the xylene ring under controlled acid conditions prevents uncontrolled oxidations or over-nitration that would ruin the product. Our team opts for precise additions and in situ monitoring; there’s no substitute for regular spot-sampling at each phase, especially during final purification. Waste treatment never becomes an afterthought, with secondary containment and dedicated acid recycling—decisions that reduce occupational hazards and environmental impact.
The reason we stress such vigilance: even trace contamination in nitro compounds can trigger isolated detonations or self-heating inside customer reactors. We’ve encountered and solved these real issues by fine-tuning our own parameters. Over decades in the field, we learned storage must consider both temperature and light exposure to avoid product discoloration or degradation. Many clients switching from repackaged materials to our fresh lots notice increased shelf stability and lower frequency of unplanned downtime.
Every product batch runs through a battery of direct analytical controls. Melting point is a quick first check—ours consistently falls within 74–77°C, which customer process chemists usually require for consistency in downstream reactions. We cap water content through vacuum drying, since micro-moisture can change how nitration or reduction passes behave. Chromatographic purity remains above 99%, confirmed by both HPLC and TLC side-by-side checks. We back this up by running parallel test reactions—real-world validation in addition to the numbers on a certificate.
Granular quality control matters most for customers using 3-Nitro-1,2-xylene in continuous reactors. In that environment, even a slightly oily or agglomerated batch requires downtime for filter changes or cleaning. Our decision to standardize storage under inert gas limits degradation, which translates to practically zero sediment on filters. These measures stem directly from site visits to user plants, where we see challenges firsthand. By keeping lines of communication open, we respond to feedback with tangible improvements that ease trouble spots.
We have seen customers initially confuse 3-Nitro-1,2-xylene with its isomeric siblings, including 3-Nitro-1,4-xylene and 4-Nitro-1,2-xylene. These molecules may appear similar on paper, but in practice, the positioning of substituents controls electronic effects and steric hindrance in subsequent reactions. For example, 3-Nitro-1,2-xylene offers a distinct balance of reactivity for building block synthesis, favored in dye houses seeking intense color without excessive process complexity. Our in-house trials with various isomers show differences in melting points, solubility profile, and even dustiness—which those charging reactors at industrial scale will appreciate.
Cost also differentiates these isomers, not just due to availability but also their purification demands. Standard operating procedures for 3-Nitro-1,2-xylene use less corrosive acid mixtures than certain meta- or para-nitro analogs, leading to higher equipment life and lower plant maintenance costs. This cost advantage carries through to customers looking to maximize value from their raw material spend. Downstream, we see fewer impurities stemming from the meta position, which leads pigment and API makers to select this isomer after running a side-by-side test on starter yields.
Bulk chemical purchasers rarely praise packaging, but repeated requests and issues over the years have taught us its importance. We pack 3-Nitro-1,2-xylene in airtight steel drums lined with inert coatings, which prevent contamination or water ingress during shipment and storage. Small orders head out in HDPE or glass containers to balance shipping safety and ease of handling. Packaging lines sit in a controlled room to minimize cross-contamination with dust, a decision based directly on feedback from clients plagued by erratic clumps or sticky residue from other suppliers. On receipt, our customers have reported fewer particulate issues clogging their dosing equipment.
Drums get batch-labeled for full traceability; end users never struggle to trace a problem to source. We implement first-in, first-out storage throughout our warehouse, minimizing shelf time and keeping the chemical as fresh as possible. By reducing transit obstacles, we know customers can start their interventions with less risk of delay or deviation in results.
Not all nitroaromatics behave or perform alike. Through both bench and pilot-scale testing, we’ve observed several practical differences. 2-Nitro-and 4-nitroxylenes each exhibit different reactivity, sometimes demanding excess reagent to push reactions to completion. Our process shows lower batch-to-batch reactivity spread with 3-Nitro-1,2-xylene, leading to higher overall process efficiency and less waste. This attribute matters for both small synthesis teams and major dye or pigment plants working on tight margins.
Downstream purification runs smoother with 3-Nitro-1,2-xylene because of its solubility and crystallization profile. Clients running pilot plants reflect that post-reaction filtration time drops slightly, which reduces labor cost and raises capacity. Other related compounds seem prone to froth formation or emulsion issues in wash steps—problems less common with our standard 3-Nitro-1,2-xylene. This is a detail few commercial specification sheets discuss, yet process engineers and operators value every small gain that makes the plant run easier.
We recommend cool, dry, and well-ventilated storage for long shelf life and have adopted these protocols ourselves at the plant. The compound does not tolerate high temperatures well—exposing drums to ambient heat, even temporarily, accelerates yellowing and fine particulate build-up. Many of our customers had experienced these issues with older or poorly stored lots from middlemen, prompting emergency cleanups and, in some cases, downtime. After switching to carefully staged inventory from our plant, incidents of discolored or off-spec product dropped sharply. We always keep unbroken, original packaging onsite; experience tells us even short-term repackaging during transfer can introduce static charges or moisture that impact handling safety.
Operators in our facility follow standard chemical safety protocols under well-lit and ventilated conditions. Nitrated xylenes require dedicated spill response materials and routine staff training, because accidents often follow complacency. We share these best practices with end users, not to alarm but to equip every handler with straightforward, proven controls. For long-term users of this compound, these granular safety routines have paid off with lower incident rates and fewer batch recalls.
Over the decade, our ongoing dialogue with users led directly to valuable improvements in both quality and logistics. We learned from a pigment manufacturer that their dispersion process failed repeatedly with low-concentration offcuts appearing in bulk drums sourced elsewhere. By adopting intensified in-process checks and improving our shipping documentation, their process interruptions dropped. These user-driven changes didn’t just benefit our own process or bottom line. They let end users improve their own capacity planning and batch yield projection.
We have run visits and pigment formulation studies alongside user technical teams, characterizing small improvements such as lowering dust formation or improving pour characteristics. Open communication means feedback doesn’t disappear in a suggestion box; our office and plant staff walk customer shops to see how real people interact with the product. The lessons we’ve captured—from how forklifts damage drum linings, to how powder fines can trigger filter changes—are fed back into production and packaging. These real-world tweaks hold more value than any theoretical optimization, because they cut direct costs and improve safety.
Data from the field continually shape our decisions. Unplanned downtime or search for alternate raw materials proves costly for chemical users, and reliable upstream partners becomes not just an advantage but a requirement. We track and follow up on outlier reports—an unexpectedly high ash content batch, or an odd odor complaint—by reviewing logs, pulling retain samples, and often shipping a replacement out before a formal request appears. This approach of rapid, transparent incident management prevents supply chain disruptions, sustains trust, and helps our partners grow with confidence.
Trends in specialty chemical production move toward tighter sources of control and verifiable traceability. As demand grows for pigments, coatings, and intermediates derived from nitroaromatic chemistry, project managers seek suppliers who match their need for stable quality and ethical handling. Our plant controls its own sourcing, verifies input lots for both purity and compliance, and adopts a policy of clear transparency because we stand behind each outgoing batch. Certificates come matched with real test data, not just template statements or bulk analysis.
Sustainability also shapes our approach; each nitroaromatic batch leaves residuals that require engineered handling. Our decision to build on-site wastewater and emissions controls isn’t just regulatory compliance—it ensures our team works in a safe and responsible environment, and our local community recognizes our commitment to shared resources. We regularly review emerging global chemical safety and plant emission guidelines, adjusting process designs and plant procedures accordingly. This responsible approach carries through to the quality and consistency of 3-Nitro-1,2-xylene and builds confidence among those who look beyond cost alone.
Markets continue to demand higher-quality intermediates for sophisticated syntheses. Variability in raw material or handling quality disrupts both costs and creativity for formulating teams down the line. In our own storied experience, staying ahead means treating every lot as part of an ongoing conversation with users. We see 3-Nitro-1,2-xylene’s unique reactivity, purity, and stability traits as a direct result of this commitment. As new applications emerge in pharmaceuticals, specialty materials, and fine chemicals, the push for higher traceability and lower risk stands only to accelerate.
Our own team—plant operators, technical managers, and customer support—all remain accessible. We listen to insights from large and small users and adapt quickly to changing technical demands. Our years of observation and course correction translate into a product that end-users depend on and return to project after project. True chemical manufacturing goes beyond the reaction vessel; it means understanding how products help other innovators build tomorrow’s solutions.