|
HS Code |
639959 |
| CAS_Number | 3209-22-1 |
| IUPAC_Name | 2,3-Dichloro-1-nitrobenzene |
| Molecular_Formula | C6H3Cl2NO2 |
| Molecular_Weight | 192.00 g/mol |
| Appearance | Yellow crystalline solid |
| Melting_Point | 54-57°C |
| Boiling_Point | 284°C |
| Density | 1.54 g/cm³ |
| Solubility_in_Water | Insoluble |
| Flash_Point | 170°C |
| PubChem_CID | 17514 |
| SMILES | C1=CC(=C(C(=C1Cl)Cl)[N+](=O)[O-]) |
As an accredited 2,3-Dichloronitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 500-gram amber glass bottle with a tightly sealed cap, labeled with hazard warnings and chemical information for 2,3-Dichloronitrobenzene. |
| Shipping | 2,3-Dichloronitrobenzene should be shipped in tightly sealed containers, clearly labeled, and compliant with hazardous material regulations. It must be kept away from heat, sources of ignition, and incompatible substances. Transport in accordance with local, national, and international regulations, typically classified as a toxic and environmentally hazardous substance. Use secondary containment if needed. |
| Storage | **2,3-Dichloronitrobenzene** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from heat, sparks, and open flames. Keep separate from incompatible materials such as strong oxidizers and reducing agents. Ensure the storage area is clearly labeled and equipped with proper spill containment and fire extinguishing systems. Store away from direct sunlight and moisture. |
Applications of 2,3-Dichloronitrobenzene in Industrial ManufacturingAs an established manufacturer, we supply 2,3-Dichloronitrobenzene to various industrial sectors where its chemical functionality supports specialized synthesis and performance. Below, we detail verified downstream application areas with clear information tailored to real manufacturing operations. 1. Agrochemical Intermediate for Herbicide SynthesisLeading agrochemical producers utilize 2,3-Dichloronitrobenzene as a core intermediate during the multi-stage synthesis of selective herbicides based on phenoxyphenoxyalkanoic acid chemistry. Its ortho-dichloro and nitro groups enable downstream halogenate coupling, crucial for controlling reaction specificity and yield, particularly in the production of niche, post-emergent products targeting resistant broadleaf weeds in cereal crops. Formulators adjust batch input strictly according to seasonal demand cycles and specific herbicidal actives under development for varied crop registrations. Industry compliance standards
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2. Intermediate in Pharmaceutical Sartan API PrecursorsContract API manufacturers and pharmaceutical raw material suppliers leverage 2,3-Dichloronitrobenzene during nitroaromatic condensation and reduction steps crucial for preparing key intermediates of angiotensin II receptor antagonists (sartans). Its dichloro functionalities direct regioselective transformations central to the active moieties used in cardiovascular drugs. Finished process designs incorporate full traceability of every batch according to GMP mandates for pharmaceutical synthesis, as the compound directly affects impurity profiles and yield accuracy of subsequent hydrogenation reactions. Industry compliance standards
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3. Precursor for Dyes and Pigment ManufacturingColorant and pigment producers rely on 2,3-Dichloronitrobenzene as a key starting molecule in synthesizing complex azo and anthraquinone dyes used in the textile, leather, and plastic industries. Its specific dichloro-nitro substitution profile enables highly controlled amination, coupling, and ring-extension reactions that dictate finished pigment hue intensity, migration resistance, and thermal stability, critical for compliance with strict coloration standards in major end-use sectors. Industry compliance standards
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4. Building Block in Specialty Polymer SynthesisAdvanced polymer manufacturers adopt 2,3-Dichloronitrobenzene as a functionalized aromatic monomer in the synthesis of heat-resistant, halogen-modified engineering polymers and specialty resins. The compound’s dichloro and nitro sites offer multiple points for nucleophilic aromatic substitution (SNAr) and reductive coupling, enabling the development of tailored polymer chains with enhanced thermal and flame-retardant properties. Technical teams monitor each integration step for consistent molecular weight distribution and end-use validation in demanding industrial applications. Industry compliance standards
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Each day, our team handles compounds that shape the future of countless industries. Working on 2,3-Dichloronitrobenzene, we’ve learned details and quirks you won’t see in typical catalogs or alphabetized lists. Our staff gets their hands on the actual batches, monitors every stage of crystallization, and responds to shifts in raw material purity during real production hours. That hands-on approach enables us to refine the consistency and purity of 2,3-Dichloronitrobenzene for the most demanding downstream processes.
2,3-Dichloronitrobenzene stands out as a core building block in fine chemical synthesis, especially where functionalized aromatic rings are required. The nitro and dichloro groups on the benzene ring set up a foundation for complex molecule creation. Small changes at the molecular level can tilt reactivity dramatically, and our years of production underscore just how sensitive this compound becomes to subtle impurities or process deviations. Imagine a reactor loaded with thousands of liters, every electron on the benzene ring dictating where reactions will go next.
It’s not enough to meet broad specifications. Our customers, especially pharmaceutical and agrochemical researchers, press for strict thresholds on residual solvents, isomer purity, and trace metals. From our perspective, chlorinated nitrobenzenes like this one must hit specific HPLC and GC readings—otherwise performance can drop, yields suffer, or reaction times bog down. Typical models of our product come as pale yellow crystalline solids, packed and sealed to preserve stability, with target assay values over 99% by weight. Yet what really counts is the reproducibility batch-to-batch, since inconsistent impurity profiles disrupt the entire downstream synthesis.
Our 2,3-Dichloronitrobenzene differs from its 2,4- and 3,4- isomers through both physical behavior and how it reacts in coupling reactions. The ortho-chlorine and meta-nitro placements drive different selectivities, and the position of the nitro group can steer reductions, halogen exchanges, or aromatic substitutions—real-world outcomes that hinge on the subtleties of molecular geometry. We’ve found certain pharmaceutical processes prefer this isomer because they achieve higher selectivity for target ligands, curbing unwanted side product formation at scale. Many agricultural active ingredients depend on this isomer for its predictable conversion to key intermediates under high-throughput, high-temperature conditions. It’s not a one-size-fits-all choice: research labs often test multiple isomers, but full-scale manufacturers like us see a definite industry trend toward batch-to-batch reliability for the 2,3- structure.
From sourcing raw chlorobenzenes to managing the nitration reaction's exothermic nature, every step brings practical decisions. Handling mixed acid systems and managing reaction heat transfer means investing in jacketed reactors, robust cooling systems, and constant in-line monitoring. As operators, we see first-hand how subtle temperature drifts can alter the isomer ratio. Optimizing these conditions has led to lower byproduct formation and more efficient purification workflows. It’s a balancing act—maximize conversions, minimize over-nitration, and ensure no halogen exchange throws off purity.
Working with downstream partners, we’ve learned that application needs drive every technical specification. Many pharmaceuticals demand high consistency because downstream reductions or coupling steps hinge on nitro group reactivity. In dyes and pigments manufacturing, even trace impurities can discolor final products or create filtering clogs. Some pesticide routes seek this isomer for better biological activity by virtue of its electron distribution. Research chemists contact us directly to discuss the limits of our detection for contaminants—not abstract numbers, but thresholds that dictate if a new process can go forward. It’s these collaborations that push us to refine solvent stripping, crystallization, and washing techniques, constantly working toward a product that performs seamlessly from lab to kilo lab to industrial plant.
After years of batch campaigns with different ring substitutions, we recognize 2,3-Dichloronitrobenzene’s balanced reactivity. Other isomers show up in literature and patents, but side-by-side trials reveal different thermal stability, volatility, and overall ease of handling. For example, 2,4- and 2,5-Dichloronitrobenzenes may demonstrate more volatility or reduced selectivity during hydrogenation. Supply chain reliability varies between these isomers, with some showing less robust historical data on scalability or regulatory compliance. Customers who experimented with imports found uneven melting points and difficult chromatographic separation, hinting at mixed isomer feeds or uncontrolled crystallization protocols. In our plant, 2,3- has become the preferred candidate for scale-up due to fewer purification cycles and more predictable solid handling during winter months.
Our plant operators log years of experience strictly on these types of aromatic nitrations. It’s more than managing equipment—we’ve trained generations of chemists and maintenance techs to anticipate the quirks of each campaign. Knowledge passes between shifts: how crystallization rates change with ambient humidity, how filter cloths need swapping based on residue stickiness, and which equipment seals degrade from trace acid carryover. Field experience taught us that subtle yellowing hints at process upsets that won’t show up on a raw assay figure. Customers depend on us for these insights, because reliable manufacturing isn’t born out of formulas—it’s shaped by habit, vigilance, and shared lessons from long hours on the floor.
Standard product descriptions will list melting point, appearance, or solubility, but those snapshots miss how 2,3-Dichloronitrobenzene behaves in the actual world. We’ve observed fallout during storage if residual water remains above 0.1%. Static buildup can cause issues unloading the crystalline product—our crews manage it with routine anti-static protocols, especially in the dry winter months. Fielding calls from partners who’ve changed their synthesis protocol, we’ve had to troubleshoot problems like unexpected emulsions upon mixing with toluene or cloudiness in dissolved mode. The details make all the difference to end users scaling pilot batches up to production runs.
Every manufacturer faces growing scrutiny over effluent, byproduct management, and waste minimization. Handling nitroaromatics like this one means investing in scrubbers and continuous monitoring to ensure chlorinated and nitrated byproducts don’t drift into water or air streams. Through years of process improvements, we’ve tightened reaction stoichiometry to avoid excess acid use and focused on solvent recovery to limit environmental exposure. Customer questions about sustainable chemistry aren’t theoretical for us—they shape production scheduling, wastewater treatment investment, and even raw material supplier reviews. These efforts have allowed us to minimize both visible and hidden environmental impacts, keeping our operation resilient in a landscape of tightening regulations.
From firsthand experience, packaging changes have real effects on product utility. Early in our production runs, we learned that not all containers maintain the necessary dryness. Paper-lined drums led to moisture uptake and surprising caking that customers flagged as bottlenecks on their lines. We switched to heavy-duty multilaminate bags within steel drums, then invested in dedicated dessicant canisters. Every shipment includes a moisture indicator, so receivers know the product hasn’t exceeded threshold limits during sea or overland transport. Surface stickiness, clumpiness, or changes in flow properties are all red flags—our shippers inspect every unit before loading, since any surprise at the customer’s door can halt an entire synthesis run.
More than once, our technical staff has traveled to client sites to examine an unexplained equipment blockage or to help resolve color changes in downstream products. These visits turn troubleshooting into shared improvement: we take lessons learned from both sides and reapply them to plant protocols. One memorable case involved a new pesticide intermediate where our crystallization endpoint needed tweaking by barely a single percentage point—but that shift eliminated a recurring haze that plagued the client’s product clarity. Through such cases, trust deepens, and small changes improve reliability for everyone.
Recent years have brought increased scrutiny from global regulators on both nitroaromatic handling and halogenated intermediates. Inspection teams look not only for paperwork and batch histories but also for on-the-ground practices—documentation of cleaning cycles, air exhaust readings, and traceability from raw input to outbound shipment. We keep detailed logs and internal audits to demonstrate compliance. Every new market entry comes with its own set of expectations: some require residual solvent levels far below ICH guidelines; others review color indices beyond standard visible light readings, especially in optically sensitive applications. Regulatory changes push us to upgrade sampling, invest in new analytical equipment, and keep technical staff trained on evolving protocols so there’s never a gap in documentation or process transparency.
A manufacturer’s perspective changes with every customer complaint or technical success story. Years ago, one batch failed to dissolve properly in a UK client’s reaction solvent, leading to off-spec conversion rates. After analyzing the lot, we identified unnoticed trace contaminants and shifted our filtration process. The next campaign produced no such problems, and the lesson stuck with us: problems echo through the supply chain until they’re solved at the origin. We appreciate hearing not only successes but also the rough edges—every phone call about unexpected crystal deposits or slow dissolution informs how we tweak parameters back at the plant.
Raw materials drive the tone for any specialty chemical campaign. For 2,3-Dichloronitrobenzene, we evaluate each supplier for predictability in both quality and logistics, especially as global transport faces new uncertainties. Unplanned shipping delays or force majeure events can compromise overall timelines, while inconsistent raw chlorobenzene purity affects end product outcome. To stay ahead, our procurement team maintains multiple qualified sources and monitors the physical stock holding at every partner location. Fluctuating supply costs prompt us to work with customers openly—transparency builds trust, especially in specialty segments where pricing can shift unexpectedly.
Handling nitration safely requires more than following written rules—it means learning from decades of production. Operators walk the floor during every sensitive stage, and we never leave temperature ramps to guesswork. Over-pressurization isn’t theoretical; we’ve dealt with false alarms, and our teams train regularly for unlikely but possible leaks or runaway events. Frequent in-house safety drills have produced a culture where every operator watches for early warning signs—the way solution viscosity thickens, subtle odors, or even the sound of agitation changing tone. Our plant upgrades reflect these experiences, as do our investments in redundant safety cutouts and remote monitoring technology. Staff well-being and asset safety sit at the center of every daily decision.
As a core intermediate in regulated industries, every campaign of 2,3-Dichloronitrobenzene requires airtight documentation. We track raw materials by lot, log every parameter from reaction start to final packaging, and archive analytical results for customer and regulatory review. Digitalization has helped, but we still combine it with hands-on review—our senior QC staff cross-checks key reports before product leaves the warehouse. Quick trace-back saves client time in the event of unexpected findings or regulatory audit reviews. Our goal is not only to ship on time, but also to provide support when downstream investigators need detailed histories.
Our approach to 2,3-Dichloronitrobenzene production reflects decades of accumulated know-how, where every detail—from reactor metallurgy to shipping label accuracy—affects customer results. We believe that transparency serves everyone better: what works, what could improve, which process steps might one day change as new technology emerges. This isn’t a product you choose from a drop-down menu. Clients want to see that someone stands behind the supply, understands both chemical and logistical realities, and is committed to ongoing improvement. Our history gives us the conviction to guarantee not only the assay on the package, but also a cooperative approach to its use and integration into advanced chemistries worldwide.