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HS Code |
589127 |
| chemical_name | 2,6-Dichloroaniline |
| cas_number | 608-31-1 |
| molecular_formula | C6H5Cl2N |
| molecular_weight | 162.02 g/mol |
| appearance | Pale yellow to brown solid |
| melting_point | 71-74 °C |
| boiling_point | 258-259 °C |
| density | 1.388 g/cm³ |
| solubility_in_water | Slightly soluble |
| flash_point | 131 °C |
| pubchem_cid | 12254 |
| synonyms | 2,6-Dichlorobenzenamine |
As an accredited 2,6-Dichloroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2,6-Dichloroaniline is supplied in a 100g amber glass bottle with a secure screw cap and hazard labeling. |
| Shipping | 2,6-Dichloroaniline should be shipped in tightly sealed, clearly labeled containers, protected from heat and moisture. It must comply with hazardous material transport regulations (Class 6.1, toxic substances). Use appropriate packaging, such as UN-approved drums or bottles, and provide safety documentation. Follow all local and international shipping and handling guidelines. |
| Storage | **2,6-Dichloroaniline** should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents and acids. Protect from moisture and direct sunlight. Store at room temperature, ensuring the storage area is free from sources of ignition and that containers are clearly labeled to prevent accidental misuse. |
Applications of 2,6-Dichloroaniline in Industrial ManufacturingAs a direct manufacturer of 2,6-Dichloroaniline, we enable its use across several key industrial sectors. Our material serves as a vital intermediate in complex synthesis routes, advancing precise downstream formulations in regulated industries. The following application scenarios demonstrate specific, validated use cases of this intermediate in global manufacturing chains. 1. Synthesis of Agrochemical Active IngredientsDownstream pesticide producers use this compound as a strategic intermediate for constructing chlorinated aniline-based herbicides and fungicides. Its chemical structure facilitates nucleophilic substitution, enabling reliable coupling steps in multi-stage synthesis paths for selective agrochemicals registered worldwide. Consistent quality and specification adherence are crucial for compliant registrations, with real-time analytical QC from our factory underpinning process reproducibility and output traceability. Industry compliance standards
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2. Intermediate for Pharmaceutical SynthesisPharmaceutical manufacturers rely on this material as a precursor in the synthesis of specialty APIs, particularly in the preparation of chlorinated heterocycles for investigational and generic drug molecules. Its high assay and controlled impurity profile are essential for GMP batch release. Each lot undergoes additional analytical verification to confirm suitability for regulated pharmaceutical synthesis where residual impurities may impact later purification processes and regulatory submissions. Industry compliance standards
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3. Precursor in Dye and Pigment ManufacturingProducers of specialty dyes and pigments apply this compound in the synthesis of chlorinated aniline-based azo and anthraquinone colorants. Tight control over input purity and isomer composition minimizes byproduct formation and ensures consistent shade, lightfastness, and application stability in textile, printing, and plastics sectors. Our supply enables downstream scale from pilot to continuous bulk runs, supporting reproducible color matching cycles. Industry compliance standards
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4. Raw Material for Polymer Modifier SynthesisIn the field of engineering polymers and specialty resin modifiers, this aniline derivative is introduced as a building block for halogenated chain extenders and crosslinking agents. Polymer compounders incorporate it during early-stage reactor charging, promoting thermal and chemical stability in high-performance plastics used across automotive, electronics, and coatings applications. Strict batch homogeneity and analyte consistency from our production control systems underpin reliable downstream polymer blend characteristics. Industry compliance standards
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2,6-Dichloroaniline stands out from other substituted anilines through the unique placement of its chlorine atoms on the aromatic ring. This structure shapes everything from reactivity to the role it plays in the synthetic process. As a chemical manufacturer with years of hands-on production experience, our understanding of this molecule goes beyond textbook chemistry. Making 2,6-Dichloroaniline starts with careful chlorination under controlled conditions, where choice of reagents and temperature impacts purity and consistency. Our procedures favor direct chlorination routes to keep unwanted isomers and byproducts at a minimum, which allows the resulting 2,6-Dichloroaniline to meet the high standards required by downstream processes.
2,6-Dichloroaniline arrives as an off-white crystalline solid, sometimes looking slightly pale yellow depending on the batch and storage. The melting point typically falls above 70°C, and the chemical keeps its integrity through careful packaging and transport. Our operational philosophy doesn’t overlook the fine details in color or odor, because even these ‘small’ things give clues about batch consistency and process optimization, especially for those using it as a starting material in pharmaceutical or agricultural synthesis.
We keep our technical standards transparent, because those buying 2,6-Dichloroaniline as an intermediate rely on unwavering specifications. Each batch undergoes analysis by HPLC and GC to monitor purity, with results regularly exceeding 99%. Trace moisture, identifiable by Karl Fischer titration, never creeps past 0.2%. Undesired isomers—such as the 3,5-dichloro or ortho/para substitutions—are efficiently purged. We take pride in handling the spirit of precision, not just hitting purity numbers. Every step, from production to storage, falls under continuous chemical process control.
We regularly encounter comparisons to similar compounds, such as 4-chloroaniline or 2,4-dichloroaniline. What most buyers notice is that the reactivity profile of 2,6-Dichloroaniline stands apart for coupling reactions, especially when dealing with steric effects in synthesis routes. The double chlorine substitution at the 2 and 6 positions on the ring nudges the molecule into unique positions—sometimes stalling other reactions or sometimes guiding them selectively. This behavior finds value in high-demand synthesis of dyes, agrochemicals, and specialty polymers.
We’ve learned that safety and environmental impact leave no room for shortcuts. Chlorinated aromatic compounds like 2,6-Dichloroaniline demand operational rigor. Modern containment, dedicated exhaust systems, and responsible effluent treatment keep both the shop floor and the outside environment safer. Wastewater streams get stringent scrutiny before release, removing chlorinated residues using neutralization and advanced oxidation. We build our workflows so that neither plant workers nor neighboring communities face avoidable chemical exposure. These steps require investment and ongoing vigilance, but they prove essential for sustainable manufacturing and reputation.
We source raw materials from known suppliers who meet our expectations, both in terms of technical quality and compliance with local and global chemical management laws. These relationships help avoid low-grade impurities entering the supply chain, which might otherwise complicate downstream use. For those purchasing 2,6-Dichloroaniline for fine chemical or pharmaceutical manufacture, these upstream choices matter, because they can directly impact regulatory submissions and end-product safety.
We see most 2,6-Dichloroaniline leave the plant in secure containers destined for dye and pigment synthesis. Its structure allows for fine control over color properties in azo and anthraquinone dyes, supporting color-fastness in textiles and specialty coatings. Because the chloro groups sit symmetrically, manufacturers gain advantage through better hue control and stability.
In crop protection, 2,6-Dichloroaniline forms a cornerstone of the chemical pathways leading to fungicides, herbicides, and insecticides. Some market segments blend it into intermediates for more targeted agrochemicals. Portfolio managers at agrochemical firms turn to us time and again, not out of habit, but because they understand that a minor irregularity in aniline substitution can magnify into downstream product failures.
Research labs and specialty polymer manufacturers also show interest, though their order volumes tend to run lower. Specialty plastics, especially those tuned for electronic or optical use, sometimes depend on 2,6-Dichloroaniline-based building blocks. Here, electronic properties and compatibility often govern selection, and a stable, uncontaminated supply makes the difference between a workable product and wasted R&D efforts.
Experience teaches respect for chlorinated aromatics in bulk quantities. At scale, 2,6-Dichloroaniline’s handling means all-metal piping, inert gas blanketing, and moisture control. Careful staff training and modern gear keep dust and vapor exposure within published guidelines. As manufacturers, we don’t rush packaging—every unit receives proper sealing and clear safety labeling with shipment tracking. Shipping and warehousing teams maintain records so that batch histories remain traceable long after delivery.
Clients in remote areas sometimes face challenges in storage due to fluctuating humidity or temperature. We recommend sealed storage in cool, controlled environments with periodic inspection for leaks or discoloration. Our technical support stands ready to answer handling or re-testing questions. Client feedback—whether from a major dye maker or a regional crop science firm—shapes our logistics solutions. Over time, we’ve seen routine communication turn into lasting partnerships, even in competitive markets.
As a manufacturer, we frequently field requests for tighter specifications—lower impurity thresholds or certificates tailored to a specific regulatory body. This adds cost, often in ways that are invisible to the end user, but the price usually equals higher process reliability later. Inconsistent batches, especially from suppliers using different synthesis routes, create bottlenecks and compliance headaches for customers. Reliable records, transparent impurity profiles, and batch-to-batch consistency form the fabric of a dependable supplier relationship.
Variability sometimes finds its way into melt-point or color depending on minor differences in production start materials and plant operating conditions. We document these variations rigorously, providing our partners with a complete batch record and impurity fingerprint. If a user seeks a material meeting an unusually tight spec, we work with them to tailor our production, often running smaller custom batches to ensure tighter control.
Comparing 2,6-Dichloroaniline to the more ubiquitous 4-chloroaniline or the trio 2,4,6-trichloroaniline uncovers clear distinctions. The 2,6-substitution pattern restricts reactivity in certain aromatic substituent positions, which reduces risk of overreaction in multi-step synthesis. This lets chemical engineers direct the course of oxidative or substitution reactions with greater intent. As an example, in azo dye manufacture, the desired shade or stability often turns on these small molecular geometry differences. In pharmaceuticals, the unique substitution pattern brings reactivity that supports selective coupling with heterocycles or peptides.
Other compounds, often close analogs, sometimes offer different performance properties but usually trade off something essential—yield, toxicity, or stability. The selection stems less from price, more from fit within a detailed synthetic pathway. Our customer service team regularly consults on which grade and substitution pattern best matches the job at hand, balancing process economics, environmental risk, and end-use function.
In the wider world, pressure builds for chemical producers to lessen the carbon load and increase process sustainability. We’ve invested in process improvements—lowering waste, recycling solvents, and updating older reactors for energy efficiency. Running a chemical plant carries responsibility not only for the product itself, but also for surrounding air, water, and soil integrity. Process audits, emissions checks, and repair of any leak, no matter how minor, make their way into our daily routine.
Some markets push for eco-label requirements even at the intermediate chemical level. We see this most strongly in dyes and pigments heading toward the textile or food packaging industries. In response, our technical team works with regulatory analysts and innovation partners to reduce residual solvent content and screen every input for persistent organic pollutants or heavy metals. Solutions come in incremental steps: switching to greener solvents, adjusting batch throughput, or collaborating with customers on new process introductions.
Quality control faces ongoing pressure from both buyers and regulators. As new residue limits and workplace standards roll out, we adjust production documentation and offer deeper disclosure of process aids, potential byproduct formation, and supply chain risks. Governments in Asia, Europe, and North America regularly inspect both paperwork and physical inventories; any lapses lead to prompt remedial action. Our teams stay updated through regular staff training and participation in chemical safety forums.
We also see customer audits with increasing frequency. Buyers visit, review our SOPs, inspect storage tanks, and check equipment maintenance records. These sessions run alongside traditional lab-based tests and leave us with useful feedback. Some concerns center around batch contamination with polychlorinated byproducts, or trace amounts of other aniline derivatives. Each concern gets systematic attention, and our project teams follow up in full, sometimes revising entire purification sequences based on a single audit finding.
Strong relationships with both raw material suppliers and end users keep our whole value chain running smoothly. We invest in these relationships through constant communication, shared technical development, and flexible responses to changing business needs. Our lab teams work closely with customer R&D groups, sharing data early to preempt any surprises. When product demand spikes unexpectedly, long-standing trust allows allocation of finished material without last-minute negotiation.
The ability to deliver on time, with clear documentation and support for end-user questions, doesn’t come from a rigid rulebook but from an ethos built over years on the shop floor. Some of our closest partners started with small orders, looking for custom grades of 2,6-Dichloroaniline. Through purchase cycles, batch troubleshooting, and new product launches, both sides expanded technical know-how. This cross-pollination benefits everyone—from us, the manufacturer, to the ultimate consumer.
Global demand for chlorinated aniline derivatives grows most rapidly in Asia, but nearly every region registers upward pressure for intermediates that enable new dyes, crop protection agents, and performance polymers. At the same time, each market brings its own regulatory hurdles and customer preferences, driving us to maintain supply flexibility and continual process refinement.
Digitization and real-time data tracking become more important in maintaining traceability and responding to client and regulatory requests. Our investment in plant automation includes live process monitoring, bar-coded batch control, and quick response to production anomalies. Inquiries from customers now regularly seek not only TDS and safety data, but details about sustainability, product provenance, and chain of custody.
Every call from a customer brings a fresh question: can 2,6-Dichloroaniline grades be tailored for a specific end-use, can residual solvent levels be reduced further, will it be possible to shorten lead times for urgent requirements? Our technical group sees these as opportunities for improvement, not burdens. Feedback generates new rounds of process optimization trials and guides our exploration of alternative technologies, whether in purification, yield improvement, or packaging solutions.
Our future investments emphasize cleaner technologies and greater agility in batch changeovers. The ongoing transition toward greener chemistry remains a major theme, and we use both experience and data to guide progress—a blend of careful stewardship and practical innovation. Advances in reaction engineering, better catalysts, and digital process analytics will shape how tomorrow’s 2,6-Dichloroaniline reaches chemical users worldwide.
From a manufacturer’s standpoint, producing and supplying 2,6-Dichloroaniline involves more than technical know-how or marketing claims. Every kilogram carries the history of materials, process adjustments, quality checks, and end-user feedback. As industry trends shift, supply chains stretch, and environmental scrutiny intensifies, we see the continued need for manufacturers who know their product at a granular level.
The distinctive substitution pattern of 2,6-Dichloroaniline defines its application and utility, influencing everything from color fastness in a finished dye to selectivity in a pharmaceutical intermediate. Supplying it means thinking ahead about purity, local and international rules, responsible sourcing, and partnership—values that don’t show up on a simple spec sheet. Every innovation, quality improvement, or sustainability upgrade stems from the on-the-ground realities faced daily in chemical manufacturing, linking our expertise directly to the success of our partners across the globe.