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HS Code |
765572 |
| Chemical Name | 2,6-Dichlorophenethylamine |
| Molecular Formula | C8H9Cl2N |
| Molar Mass | 190.07 g/mol |
| Cas Number | 1235-22-1 |
| Appearance | White to off-white solid |
| Melting Point | 38-41 °C |
| Boiling Point | Unknown |
| Density | Unknown |
| Solubility In Water | Unknown |
| Structure | Phenethylamine core with chlorine atoms at positions 2 and 6 of the phenyl ring |
As an accredited 2,6-Dichlorophenethylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A sealed amber glass bottle containing 50 grams of 2,6-Dichlorophenethylamine, labeled with safety data, batch number, and hazard symbols. |
| Shipping | 2,6-Dichlorophenethylamine is shipped in tightly sealed containers compliant with international chemical transport regulations. It is typically packaged in amber glass bottles to protect from light and securely cushioned against breakage. Shipments are labeled as hazardous, require appropriate documentation, and are handled by certified carriers to ensure safe and compliant delivery. |
| Storage | 2,6-Dichlorophenethylamine should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Properly label the container and avoid exposing the chemical to heat or open flames. Use secondary containment to prevent accidental spills or leaks. |
Applications of 2,6-Dichlorophenethylamine in Industrial Manufacturing2,6-Dichlorophenethylamine serves as a key intermediate for various industrial synthesis routes within high-value chemical sectors. Our manufacturing process aligns with strict regulatory frameworks and supports specialized downstream segments with controlled purity and consistent supply, ensuring traceability and process reliability. 1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis2,6-Dichlorophenethylamine functions as a primary building block in the multi-step synthesis of several pharmaceutical active ingredients, particularly those within selective serotonin, dopamine, and adrenergic modulators. Pharmaceutical manufacturers introduce it during early-stage alkylation or acylation reactions, forming critical cores for antihypertensive and psychoactive compounds. Detailed process documentation and batch traceability remain mandatory due to regulatory scrutiny. End users conduct stringent purification and chiral resolution after condensation or cyclization steps to ensure final API purity specifications. Industry compliance standards
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2. Agrochemical Active Compound ManufactureAgrochemical producers use 2,6-Dichlorophenethylamine to synthesize phenethyl-based pre-emergent herbicides and fungicides, employing it in selective alkylation or halogenation sequences. Its molecular structure enhances binding within target biochemical pathways in crops and broadleaf plant management products. Manufacturers blend it in tightly controlled reactions to minimize byproduct and residue formation, ensuring compliance with strict environmental and food safety limits. Industry compliance standards
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3. Specialty Polymer and Resin ModificationManufacturers in polymer and high-performance resin industries integrate 2,6-Dichlorophenethylamine as a hardener and functional group donor during epoxy and polyurethane formulation. The amine structure reacts with epoxy or isocyanate components, modifying mechanical performance, crosslinking density, and adhesion profiles. Its use improves thermal stability and resistance to chemical agents in specialty coatings, adhesives, and elastomers. Key process stages require closed-loop handling and real-time reaction monitoring to prevent off-stoichiometry or undesired branching. Industry compliance standards
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4. Fine Chemical Intermediate for Dye and Pigment SynthesisProducers of specialty dyes and organic pigments use 2,6-Dichlorophenethylamine as a primary amine source for constructing azo, methine, or phenylated chromophores, especially in high-performance textile and plastics coloration. The dichloro-substitution pattern supports increased color fastness and improved solubility. Process control includes pH-regulated coupling and diazotization steps, followed by multistage crystallization or solvent extraction. Close adjustment of concentration and temperature contributes to batch reproducibility and chromatic purity. Industry compliance standards
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Our journey with 2,6-Dichlorophenethylamine began with a simple demand—consistent, reliable building blocks for making advanced materials and pharmaceuticals. Anyone who has scaled up a specialty amine in the plant knows that quality and reproducibility can’t take a back seat. We work directly from raw materials at our own site, overseeing every part of the process, because we know an off-batch doesn’t just ruin a day’s work—it jeopardizes downstream chemistry. By investing in robust process controls and batch-by-batch analytics, we maintain the same crystalline, pale-to-off-white product lot after lot. This attention to detail matters, as trace variability can throw off sensitive syntheses or high-throughput screening in the lab.
Model and specification discussions often get abstract, but what matters day to day is what a chemist gets in hand. Our standard material targets a minimum purity of 99%, measured using both gas chromatography and HPLC. Residual solvents, like toluene or dichloromethane, are kept below 500 ppm and water content stands below 0.2%. Particle size influences ease of weighing and dissolution, so we tune bulk batches for coarse flowable crystals that dispense smoothly—important when you’re working with precise milligram quantities. Each drum or bottle goes through physical inspection, and we run spectral analysis to confirm structure. Analytical certificates ship attached with each consignment. Over time, our partners have come to expect this level of transparency, and if something drifts out of spec, we're the ones to answer for it.
Chemists in pharmaceutical labs, agrochemical companies, and material science research approach us with a range of needs. Some run pilot projects, others need regular shipments for commercial scale. In both cases, the risk matches the reward—cutting-edge research requires specialty amines that don’t just look right on paper but perform reliably, batch after batch. Because we manage production under controlled temperature and humidity, not only do we minimize byproduct formation, we also ensure the shelf stability of the product. It’s rare that a customer needs to ask us about requalification, but if curiosity strikes, we’re happy to pull retained samples and run side-by-side NMR and GC data to prove consistency over time.
Handling can trip up the best-laid plans. It’s not enough for 2,6-Dichlorophenethylamine to meet synthetic requirements; it must behave well in storage and transfer. We test for hygroscopic behavior—our product resists picking up ambient moisture, making it easier to weigh and less likely to clump. This is crucial during scale-up, since unpredictable clumping leads to dosing mistakes. Investment in material handling infrastructure pays off: cleanroom packaging lines, inert storage drums, and rapid environmental monitoring give us confidence that trace impurities stay low. It’s these details that keep reactivity and downstream coupling reactions predictable for end users.
Clients often ask how our 2,6-Dichlorophenethylamine fits into their own product pipelines. We see demand flowing from both established routes and new exploratory research. In medicinal chemistry, the phenethylamine backbone acts as a scaffold in a variety of drug discovery programs. Its dichloro substitutions bring electronic stabilization and modulate the molecule’s biological activity, influencing both potency and selectivity. Some downstream users convert our amine into sulfonamides, amides, or ureas; others use it for further aromatic substitution, benefiting from the ortho-chloro protection.
The agrochemical sector values the same features—chlorinated phenethylamines help build new herbicidal or fungicidal entities, exploiting their resistance to metabolic breakdown in harsh environmental conditions. As demand grows for greener, more selective crop agents, our chemists have worked with partners to refine process purity and remove haloaromatic side products, since these can cloud activity assays or trigger regulatory concern.
Beyond pharmaceuticals and pesticides, we also see materials scientists requesting this building block for advanced monomer synthesis. Properties like thermostability, rigidity imparted by the aromatic core, and the potential for crosslinking through the ethylamine handle, make it more than a simple reagent. Our flexible production lines allow us to meet requirements for whatever downstream application customers dream up—be it conductive polymers or high-durability coatings.
Questions about the difference between our 2,6-Dichlorophenethylamine and related amines come up in every meeting. Many organizations have experience with unsubstituted phenethylamine or other halogenated derivatives, such as 2,4-dichlorophenethylamine. The difference boils down to reactivity, position isomerism, and substitution pattern influencing electronic effects. The 2,6-configuration blocks both ortho positions, conferring a unique steric shield and driving selectivity in downstream coupling agents. Where 2,4-derivatives may show higher rates of nucleophilic aromatic substitution, 2,6-derivatives provide stability, especially under basic conditions, and a different profile in biological testing.
Sometimes the question turns practical: “Why not use standard benzylamines?” The 2,6-dichloro arrangement is about more than novelty. We’ve supported several projects where standard amines gave unwanted side reactions or decomposed rapidly under oxidative or metal-catalyzed conditions. By directing the chlorine atoms to the ortho positions, chemists gain control—minimized para substitution, limited radical formation, and a reduced chance of side-chain oxidation. This saves time in purification and increases yield further down the pipeline, translating directly into reduced costs and reduced development cycles.
Another fundamental point is the purity threshold. Many larger commodity producers might offer “technical grade” materials at a lower price, but their standard doesn’t approach ours. Trace metals, oxygenated residues, and colored byproducts slow down analytical labs and confuse product registration dossiers. Our team’s reputation has grown because we put purity and reliability first, not just on paper, but in the drum that chemists receive. This means fewer headaches at quality control windows, and a smoother path to the next project milestone.
Our direct relationships with laboratories and production facilities put us in a position to see the real impact of the material. One long-term partner uses 2,6-Dichlorophenethylamine to build libraries of neuroactive compounds. At first, they tried several vendor sources but landed back with us after inconsistencies affected test results—the difference came down to trace isomeric byproducts hiding in substandard lots. Our ability to guarantee no detectable levels of 3,5-dichloro impurities put their data integrity back on track and made regulatory filings straightforward.
Another customer in the pigment sector uses the compound as a modular nitro precursor. The substitution pattern ensures predictable reactivity, allowing for regioselective transformations without the risk of ring rearrangement or unexpected color impurities. Their end application needs a reliable supply, and our focus on logistical reliability—supporting both just-in-time orders and long-term warehousing—gives them a near-seamless production cycle.
Making 2,6-Dichlorophenethylamine at scale presents challenges not always visible to the end user. The synthesis often starts from 2,6-dichlorotoluene, which itself can vary in purity depending on global market conditions and supply chain disruptions. Our plant tackles this with a dual approach: in-house distillation to remove volatile chlorinated byproducts and close supplier relationships to assure regular, high-quality precursor deliveries. Equipment cleaning routines between batches guard against cross-contamination, particularly important when switching between chloroaromatic and non-chlorinated lines.
Our continuous improvement program relies on direct operator feedback—line technicians and quality control chemists spot trends in yield, recrystallization behavior, or waste stream content far faster than any top-down dashboard. For example, a switch in stirrer blade material improved purity and reduced unnecessary wear, cutting down on trace metal content in finished lots. These process tweaks don’t come from consultants; they arise from hands-on experience and a commitment to improvement at every step.
Waste management can't be ignored. Chloroaromatic synthesis generates regulated byproduct streams, particularly wash solvents and aqueous phases containing amine residues. Over the past decade, we have developed two solvent recycling lines and invested in catalytic neutralization technology to destroy residual organochlorines. This means not only do we reduce environmental impact, but our municipal compliance record remains spotless, and disposal costs go down, which customers appreciate in today’s margin-driven climate.
Many chemists are wary of new suppliers, and for good reason—shadowy sourcing and reselling can result in uncertain provenance and risk. As the actual manufacturer, we welcome technical audits and site visits. Visiting teams see exactly where raw materials enter, product lines run, and analytics labs operate. Our open-door policy builds trust and provides assurance that quality claims have substance.
Where documentation is requested, we supply batch records, origin details, and analytical certificates. Our flexibility extends beyond paperwork—custom filling, barcoded containers, and batch reservation provide real-world solutions to inventory management. Direct relationships mean questions get answered quickly. Customers aren’t bounced between sales reps; our chemists and plant supervisors provide firsthand answers, drawing on daily production experience. That kind of dialogue doesn’t just solve problems, it builds long-term partnerships.
Regulatory review has become stricter each year. Agencies monitoring chemical import, workplace safety, and downstream product registration demand unambiguous supply chains and detailed impurity profiles. Our team monitors evolving pesticide and pharmaceutical regulations, updating our product handling and testing protocols accordingly. This vigilance means our product helps customers dodge regulatory pitfalls—while some market alternatives trigger flags due to unclear impurity origins or ambiguous labelling, our clear documentation shortens review times and reduces requests for follow-up information.
Handling guidelines reflect real world needs. 2,6-Dichlorophenethylamine doesn’t present acute handling hazards at room temperature, but proper ventilation, gloves, and closed-system transfers are standard operating protocols in our plant. Regular safety audits and operator training maintain incident-free production. End users often rely on our direct advice for safe scale-up, especially in academic labs venturing into kilogram synthesis. Precautionary tales from our own experience—like preventing exposure to trace chloroamines or controlling dust—help downstream partners avoid their own mishaps.
End users increasingly value knowing who makes their products and how. With the complexity of today’s research pipelines and the cost of failed batches, transparent sourcing provides practical advantages far beyond price. Some of our most enduring customers prioritize not just product, but long-term consistency, technical support, and collaborative problem-solving. We treat every order as an opportunity to demonstrate our value, not through marketing promises, but through tangible support—helping with method development, troubleshooting unexpected reactivity, or suggesting alternative grades when a project pivots.
We pay attention to feedback with regular reviews, both internally and with major clients. That loop closes the gap between shop floor and laboratory workflow. New requests—such as reducing particle size for improved dissolution, or tightening up residual solvent limits for export compliance—go straight into our process development team’s project list. The relationship works both ways; innovative customers sometimes teach us new applications, spurring future investment and technical skill development.
As synthetic chemistry and materials science move into increasingly specialized territory, the demand for high-purity, consistent specialty amines will only grow. Our focus on 2,6-Dichlorophenethylamine fits into broader industry trends toward greener synthesis, traceable supply, and ever-tighter regulatory compliance. The pressures that define today’s market—reduction in waste, simplification of downstream purification, and lowering the environmental footprint—align well with our own philosophy as actual manufacturers.
We constantly evaluate improvements, whether it’s greener catalysts for amination steps, reusable packaging to reduce plastic volumes, or alternative solvents with lower emissions for purification. Customers see the benefit not just in reduced regulatory risk, but in simpler workflows and cleaner products. These incremental changes keep our product relevant, but more importantly ensure that our factory is built to last—a place where hands-on skill and modern process engineering create real-world value.
In summary, our experience with 2,6-Dichlorophenethylamine is shaped by years of production, technical troubleshooting, and partnerships with the world’s most demanding chemists. We back every drum and package with data, expertise, and direct accountability—the real markers of quality in specialty chemical manufacturing.