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HS Code |
760369 |
| Chemicalname | 2,4-Dichlorobenzyl Chloride |
| Casnumber | 1771-18-2 |
| Molecularformula | C7H5Cl3 |
| Molecularweight | 195.48 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Density | 1.37 g/cm³ |
| Meltingpoint | −12 °C |
| Boilingpoint | 242-244 °C |
| Refractiveindex | 1.583 |
| Solubilityinwater | Insoluble |
| Flashpoint | 116 °C |
| Purity | Typically ≥ 98% |
As an accredited 2,4-Dichlorobenzyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2,4-Dichlorobenzyl Chloride is supplied in a 500g amber glass bottle with a secure screw cap, labeled with hazard warnings. |
| Shipping | 2,4-Dichlorobenzyl Chloride should be shipped in tightly sealed, corrosion-resistant containers, clearly labeled according to hazardous material regulations. It must be transported in compliance with local, national, and international regulations for toxic and environmentally hazardous substances, avoiding exposure to heat, ignition sources, and moisture. Proper documentation and emergency procedures are required during shipping. |
| Storage | 2,4-Dichlorobenzyl Chloride should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from heat, direct sunlight, and sources of ignition. It should be kept separate from strong oxidizing agents, bases, and moisture. Properly label the storage area, and use secondary containment to prevent leaks or spills. Use personal protective equipment when handling. |
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Purity 98%: 2,4-Dichlorobenzyl Chloride with 98% purity is used in pharmaceutical synthesis, where it ensures the production of high-yield active intermediates. Molecular Weight 195.0 g/mol: 2,4-Dichlorobenzyl Chloride with a molecular weight of 195.0 g/mol is used in agrochemical formulations, where it provides consistent compound reactivity. Melting Point 37°C: 2,4-Dichlorobenzyl Chloride with a melting point of 37°C is used in fine chemical manufacturing, where controlled phase transition facilitates precise process control. Stability Temperature 60°C: 2,4-Dichlorobenzyl Chloride with stability up to 60°C is used in industrial resin production, where thermal stability prevents decomposition during processing. Particle Size ≤50 μm: 2,4-Dichlorobenzyl Chloride with particle size ≤50 μm is used in specialty coatings, where fine dispersion improves coating uniformity. Viscosity Grade Low: 2,4-Dichlorobenzyl Chloride of low viscosity grade is used in liquid formulations, where enhanced flow properties optimize blending and mixing. |
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2,4-Dichlorobenzyl Chloride isn’t a chemical most folks outside the industry have heard of, but for people making breakthroughs in pharmaceuticals and crop protection, this compound proves itself again and again. Going by the model 2,4-DCBC with a chemical formula of C7H5Cl3, it shapes the backbone of many active ingredients. Anyone who’s spent time in a synthesis lab knows the difference a reliable starting material makes: reactions go as planned, yields look consistent, and purity stands up to peer review.
A white to off-white crystalline powder, 2,4-Dichlorobenzyl Chloride brings a distinctive aroma—something you won’t forget after opening a drum. With a melting point generally reported between 40 and 42°C, it’s manageable for storage and for weighing in standard research environments. Boiling at roughly 245°C means it holds up to heating steps during manufacturing, while its solubility profile makes it easy to separate during workup. In my own experience, compounds with similar properties tend to attract fewer complaints from technicians, since routine handling stays simple.
Over the past decade, the demand for building blocks like 2,4-Dichlorobenzyl Chloride has stayed steady, particularly with the ongoing need for reliable intermediates in pharmaceuticals, veterinary medicines, and crop science. What sets this molecule apart from more generic benzyl chlorides comes down to its two chlorine atoms positioned on the aromatic ring. By introducing these electron-withdrawing groups, chemists get more selective reactions and, crucially, more powerful downstream chemistry.
2,4-DCBC often enters the conversation when laboratories gear up for the synthesis of fungicides, herbicides, and sometimes antiviral agents. I’ve watched teams spend months troubleshooting bottlenecks with less specialized benzyl chlorides, only to find that the right substitution pattern—provided by 2,4-DCBC—smooths out those steps. The presence of chlorine atoms at the 2 and 4 positions increases the reactivity at the benzylic site, opening up a broader range of alkylation possibilities. This flexibility lets formulators design complex molecules that would be tricky to access from monochlorinated or unsubstituted variants.
From a process chemistry standpoint, the value really shows when scaling up. Anyone who’s pushed through a few batches at pilot scale can appreciate a product that keeps its structural integrity through heating, mixing, and transfers. 2,4-DCBC stands up to real-world industrial conditions, cutting down on costly rework and waste disposal headaches.
It’s tempting to lump together all benzyl chlorides, but in practice, 2,4-Dichlorobenzyl Chloride holds its own space. Look at the pure benzyl chloride: less bulky, less electron-deficient, and less selective. Compare this with monochlorinated versions like 4-chlorobenzyl chloride—these work well for some applications, but run into selectivity and stability problems as reactions become more complex. Laboratories trying to produce advanced intermediates quickly come up against limits using the simpler forms.
2,4-DCBC’s specific pattern of chlorination lets manufacturers dial in the exact kind of reactivity or steric hindrance needed for synthesizing more sophisticated products. I’ve talked to process engineers who found yields climbing by 10 or 20% just by swapping in 2,4-DCBC for an unchlorinated benzyl chloride in key alkylation steps. This matters not only for cost control, but also for environmental responsibility—better yields mean less byproduct and smaller environmental footprints.
Reliability isn’t just about what’s on the label. It’s the performance batch after batch, year in and year out. Having seen the headaches caused by variability in raw materials—think color changes, odd-smelling batches, or unexpected reaction byproducts—I pay close attention to traceability and certification now. Reputable producers can usually provide certificates of analysis showing purity levels above 99%, often verified by independent labs using gas chromatography. Less reputable suppliers sometimes cut corners with chlorine content, leaving trace contaminants that can throw off reactions or even produce hazardous side-products.
For finished goods producers, regulatory compliance has become an everyday priority. Import restrictions and product recalls because of batch contamination can sink a project or ruin a company’s reputation. Choosing 2,4-DCBC from recognized sources cuts risk and reassures auditors. Supply chain disruptions left a lot of people scrambling over the last few years, making reliability in sourcing and compliance even more critical. Many manufacturers have responded by tightening contracts and performing their own routine QC checks, not just relying on vendor promises.
A lot of attention goes to major pharmaceuticals, but the impact of 2,4-Dichlorobenzyl Chloride runs wider. This compound finds its place in the coatings you see on certain seeds, where it helps deliver active substances in controlled-release forms. In disinfectants and preservatives, it works behind the scenes to suppress bacterial and fungal growth, especially in niche formulations where resistance can form to more generic antimicrobials.
I’ve watched startups in agricultural technology switch over to formulations based on 2,4-DCBC derivatives, not just for efficacy but for the easier regulatory paths in some jurisdictions. Its track record in legacy products means that research and regulatory reviews often go faster, since much of the toxicology portfolio has been established. For companies looking to bring innovation but avoid years in the queue, this compound provides a springboard.
Every chemical brings its own set of handling and environmental concerns. 2,4-Dichlorobenzyl Chloride is no exception—it’s a skin and respiratory irritant, so good laboratory hygiene and proper PPE can’t be skipped. In busy workshops, I’ve seen the difference a good fume hood and clear lab signage can make, turning what might have become a safety incident into a non-issue. Waste management adds another layer: being a chlorinated molecule, waste streams demand incineration at high temperatures or specialized chemical treatments to prevent environmental release.
Disposal isn’t the end of the story. Many labs and industrial sites now track chemical usage from “cradle to grave,” making sure that nothing slips through the cracks from manufacturing to final destruction. A few years back, regulations in the EU and parts of Asia got tighter on chlorinated organic waste, sometimes requiring explicit documentation for every kilo. This has pushed companies suppliers to offer more detailed batch records and to invest in environmentally preferable manufacturing routes.
If you ask around among experienced chemists, most agree that improvements in containment, automation, and analytical controls have made a real dent in workplace exposure and environmental releases. At the same time, groups focused on green chemistry are researching new synthetic pathways that could make production less dependent on harsh reagents and heavy chlorination.
Safe storage of 2,4-Dichlorobenzyl Chloride calls for attention to detail: sealed, moisture-free containers tucked away from direct sunlight and separated from incompatible chemicals. I’ve seen containers go sticky and off-color sitting too long in warm, humid corners—once that starts, purity takes a hit, and downstream chemistry can show variations. In transit, certified packaging and tight documentation keep the supply chain strong and help prevent mix-ups or accidental exposure.
Accidents during shipping once seemed rare, but with the rise in global logistics, they’ve made headlines from time to time. Most mishaps trace back to improper labeling or miscommunication between shippers and receivers. Thinking through chain-of-custody steps from warehouse to lab bench may sound bureaucratic, but in my own work, that attention to process often saved time, money, and a lot of stress.
Costs for specialty organochlorides like 2,4-Dichlorobenzyl Chloride have seen ups and downs in the last few years, with raw material shortages and global shipping delays throwing off predictions. During these squeezes, having a trusted distributor makes as much difference as the product itself. Labs that lean too heavily on price sometimes wind up with off-spec material and wasted resources, learning that lesson the hard way.
In my own purchasing experience, higher up-front costs for documented, high-purity batches often paid for themselves in savings on clean-up and rework. As regulatory agencies increase scrutiny on even routine intermediates, the value of traceability only climbs. More companies are now forging longer contracts to lock in supply security, and some build redundant supply chains split across vendors in separate regions.
Bulk availability usually depends on relationships with established suppliers, especially for kilogram or ton-scale projects. Smaller labs find that buying at smaller quantities comes with a premium, but group buying programs or collaborative purchasing among networks of researchers can level the playing field and keep costs grounded.
As conversations about green chemistry gain traction, attention has turned to the sustainability of specialty intermediates. 2,4-Dichlorobenzyl Chloride’s current synthesis relies on routes that generate hydrochloric acid as a byproduct, usually managed with scrubbers or neutralized in batch. Newer methods in development aim to reduce waste, cut energy consumption, and deliver a cleaner product. For instance, some groups are exploring more selective chlorination approaches or integrating continuous flow reactors to tighten up reaction controls.
Interest in bio-based alternatives continues to grow, though for aromatic chlorides, functional replacements might take time to arrive. Until then, improving energy footprints, maximizing yields, and responsible waste management offer the best paths forward. Large-scale users are finding ways to reuse or recycle auxiliary materials, and several manufacturers now publish environmental impact data for each batch, giving buyers a clearer sense of what they’re getting into.
These changes trace back to demand from buyers—farmers, pharmaceutical companies, even paint manufacturers—working under new sustainability mandates. That push flows up through their suppliers and, ultimately, the chemical producers. In one project I was involved in, customer questions about lifecycle impacts led directly to implementation of updated handling systems and switched packaging suppliers to better align with global recycling targets.
Advances in analytical chemistry and process control rarely make splashy headlines, but they make a practical difference in the world of specialty building blocks like 2,4-Dichlorobenzyl Chloride. Inline monitoring tools, for example, let process chemists spot impurities as they form, cutting down on lost time and improving both worker safety and the quality of the end product. Automation—the sort that’s been creeping into every corner of chemical manufacturing—promises tighter controls and, potentially, less reliance on human error.
Looking to the future, the role of AI-assisted design in synthesis routes could shorten the path to new 2,4-DCBC derivatives or more efficient forms of the base compound itself. These tools chew through data on reaction yields, impurity profiles, and solvent choices, offering optimized conditions that might have taken months or years to find otherwise.
For some, new applications may open up in unexpected directions. Work in material science points to uses in developing novel polymers or advanced coatings, tapping into 2,4-DCBC’s unique reactivity. Regulatory environments change fast; flexibility in chemical synthesis, supplied by established intermediates, will keep suppliers and users nimble. Education also plays a role—making sure practitioners at every level know the new standards, risks, and opportunities helps the industry adapt and thrive.
No matter where you sit in the supply chain, respect for detail wins every time with specialty chemicals. Check batch records, keep an eye on storage and handling, and stay plugged into both technical advances and shifting regulations. Companies that invest in training, transparent documentation, and sustainable practices turn out stronger, more resilient, and better prepared to ride out market bumps.
2,4-Dichlorobenzyl Chloride may not grab broad headlines, but its footprint is real. From safer medicines and higher-yield crops to streamlined industrial processes, this specialty ingredient reflects how the right starting point shapes the whole downstream story. My years on the laboratory floor and in project meetings taught me that choosing well at the outset—whether that means focusing on quality, sustainability, or technical support—makes all the difference. With this compound, as with most things in chemistry, the best results follow from proven choices and the willingness to question, adapt, and improve along the way.