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HS Code |
432733 |
| Chemical Name | 2,3-Dichloro-4-(trifluoromethyl)pyridine |
| Molecular Formula | C6H2Cl2F3N |
| Molecular Weight | 217.99 g/mol |
| Cas Number | 261762-38-7 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 181-183 °C |
| Density | 1.54 g/cm³ |
| Purity | Typically ≥98% |
| Refractive Index | 1.505 |
| Solubility | Soluble in organic solvents (e.g., DMSO, ethanol) |
| Flash Point | 77 °C |
| Smiles | C1=CN=C(C(=C1Cl)Cl)C(F)(F)F |
| Storage Conditions | Store at room temperature, tightly sealed |
As an accredited 2,3-Dichloro-4-(trifluoromethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams, sealed with a screw cap, labeled with chemical name, hazard symbols, and safety information. |
| Container Loading (20′ FCL) | 20′ FCL holds 12MT (240 drums × 50kg) of 2,3-Dichloro-4-(trifluoromethyl)pyridine, packed in HDPE drums. |
| Shipping | 2,3-Dichloro-4-(trifluoromethyl)pyridine is shipped in tightly sealed, chemically resistant containers to prevent leakage and contamination. Transport must comply with all local, national, and international hazardous materials regulations, including appropriate labeling and documentation. Store and handle away from incompatible substances, heat, and open flames. Use secondary containment to minimize risk during transit. |
| Storage | Store **2,3-Dichloro-4-(trifluoromethyl)pyridine** in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat sources and incompatible substances such as strong oxidizers and acids. Protect from moisture, direct sunlight, and ignition sources. Ensure proper labeling and access is restricted to trained personnel. Always use appropriate personal protective equipment when handling the chemical. |
| Shelf Life | 2,3-Dichloro-4-(trifluoromethyl)pyridine typically has a shelf life of 2-3 years when stored in a cool, dry, airtight container. |
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Purity 98%: 2,3-Dichloro-4-(trifluoromethyl)pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency. Melting Point 65°C: 2,3-Dichloro-4-(trifluoromethyl)pyridine with melting point 65°C is used in solid-state formulation development, where it enables controlled processing and reproducibility. Stability Temperature 120°C: 2,3-Dichloro-4-(trifluoromethyl)pyridine at stability temperature 120°C is used in agrochemical manufacture, where it maintains structural integrity during high-temperature reactions. Molecular Weight 216.98 g/mol: 2,3-Dichloro-4-(trifluoromethyl)pyridine with molecular weight 216.98 g/mol is used in fine chemical synthesis, where it supports precise stoichiometric calculations. Water Content ≤0.5%: 2,3-Dichloro-4-(trifluoromethyl)pyridine with water content ≤0.5% is used in catalyst preparation, where it prevents unwanted hydrolysis and ensures catalyst activity. Particle Size <75 μm: 2,3-Dichloro-4-(trifluoromethyl)pyridine with particle size <75 μm is used in slurry phase reactions, where it promotes rapid dissolution and efficient mixing. Color Index ≤10: 2,3-Dichloro-4-(trifluoromethyl)pyridine with color index ≤10 is used in material science research, where it provides high purity for optical clarity in final products. |
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The journey of manufacturing 2,3-Dichloro-4-(trifluoromethyl)pyridine offers a practical lesson in precision and patience. This compound, recognized by CAS number 3939-09-1, features a uniquely substituted pyridine ring. Every batch reflects more than formulaic synthesis; it mirrors years of tuning the process so quality remains consistent. Anyone who has stood on the production floor knows the difference between theory and reality: small details, like the rate of heating or the purity of starting reagents, make distinctly measurable shifts in outcome.
Compared to more basic pyridine derivatives, this molecule stands out for its trifluoromethyl group on the 4-position and the two chlorines on the 2 and 3 positions. These additions are not only structural quirks; they drive genuine performance gains in pharmaceutical and agrochemical development. Chemists sourcing intermediates for active pharmaceutical ingredients often turn to us for this molecule because it enables certain transformations that a common, unsubstituted pyridine simply cannot deliver.
Sourcing high-purity starting materials sets the stage for the rest of the process. Impurities don’t just disappear—they follow through to the final product, causing headaches in downstream applications. We’ve learned to screen suppliers and test incoming chemicals for trace contaminants and water content, since both can skew the halogenation steps required for 2,3-Dichloro-4-(trifluoromethyl)pyridine. The chemical’s utility in the synthesis of crop protection agents and specialty pharmaceuticals only matters if it meets stringent purity and performance profiles.
Each production run includes checkpoints: verification of reactant purity, NMR monitoring after chlorination stages, and analysis for residual solvents post-synthesis. By controlling these aspects, we have reduced batch-to-batch variation. In the chemical industry, “pretty close” never guarantees satisfaction, so we measure and re-measure. From a technical perspective, this compound’s melting point, specific gravity, and chemical stability can drift when handled incorrectly. Keeping storage temperature and moisture exposure in check isn’t just good practice—it’s necessary for maintaining shelf life and downstream reactivity.
We see most requests for 2,3-Dichloro-4-(trifluoromethyl)pyridine come from innovators pushing boundaries in crop protection and pharmaceuticals. This compound serves as a versatile intermediate for constructing key structural blocks found in active ingredients. The electron-withdrawing trifluoromethyl and dichloro substituents increase the molecule’s reactivity at the nitrogen, opening synthetic routes that would be closed to less substituted pyridines.
Pharmaceutical research teams have described the value of this intermediate in creating novel antifungal agents and anti-microbial compounds. The agricultural sector exploits its properties too, integrating it into molecules designed to deliver robust, long-lasting pest resistance. Unlike more common pyridine intermediates, this variation often shortens total synthesis steps—saving resources and reducing waste in final product preparation.
Strict regulations surrounding pharmaceutical and crop protection agents mean our facility operates with constant oversight, both from internal QA and external audits. By documenting procedures and regularly calibrating instruments, we ensure the 2,3-Dichloro-4-(trifluoromethyl)pyridine we supply has traceable provenance and meets customer expectations for reliability.
Comparing our 2,3-Dichloro-4-(trifluoromethyl)pyridine to more common pyridine derivatives quickly shows some defining technical characteristics. The presence of two chlorine atoms combined with the trifluoromethyl group produces a unique electronic environment on the ring. Synthetically, this impacts both the types of reactions you can perform and their yields. Customers trying to install particular function groups, such as amines or ethers, find this scaffold more accommodating than mono-substituted versions because the electron-withdrawing groups activate the ring towards nucleophilic substitution.
In past collaborative projects with pharmaceutical teams, we’ve measured higher selectivity and improved reaction rates using this compound over less-substituted benchmarks. It’s not a case of marketing boasting; it’s confirmed by technical data and, frankly, the number of repeat orders from process development teams. NMR and HPLC analyses from our QC labs back these claims, confirming tight control over isomeric purity and minimized impurities—details researchers and formulation chemists cannot afford to leave to chance.
Manufacturing small batches for R&D brings a different set of concerns compared to scaling for commercial demand. We’ve invested in both pilot-scale glass reactors and larger, automated stainless-steel setups so that neither speed nor consistency suffers under new project demands. Each scale presents its own challenges—heat transfer, mixing times, and gas venting for volatile intermediates all shift with batch size. Learning lessons the hard way—wasted batches, near-misses on moisture exclusion, or cross-contamination between production lines—has led us to implement closed-system transfers and inline monitoring systems.
Practical differences show when the request moves beyond kilograms. Large-volume orders test logistics and coordination among raw material suppliers, utility operators, and QC teams. Any chemical that picks up trace water or becomes exposed to light during shipment might lose potency or react unpredictably during customer use. Over years of dispatching this product domestically and worldwide, we have developed stable packaging solutions and niche methods for back-filling containers with inert gases. Customers don’t want surprises, and we’re at our best when shipments arrive exactly as intended, with supporting analytical data to prove it.
By now, most chemical manufacturers have experienced the tidal wave of new regulations regarding both pharmaceutical ingredients and agricultural intermediates. Even robust documentation and track records get reevaluated when agencies tighten standards. For a compound like 2,3-Dichloro-4-(trifluoromethyl)pyridine, regulatory transparency starts upstream and follows the molecule through every internal checkpoint. We maintain detailed lot histories and chain of custody documents, routinely updating our compliance documentation when new directives require it.
Researchers and product development teams working with our product know they may need batch-specific certificates or additional impurity profiles for regulatory submissions. We regularly receive custom requests for tighter impurity control, alternate packaging options, or specific drying protocols to meet final product applications. Sometimes, the answers depend on site-specific requirements or regulatory environments in customer countries. Experience has taught us to listen closely, adapt quickly, and document extensively.
Our technical partners in synthetic organic chemistry report notable improvements in both yield and process safety when using this pyridine variant. The electron-deficient ring resists unwanted side reactions under standard coupling conditions. That means downstream purifications become less demanding and reaction streams stay cleaner, saving solvent and time during scale-up. These are not theoretical benefits; they appear directly in reduced wastes, repeatable yields, and smoother technology transfers between R&D and production teams.
One pharmaceutical partner shared data showing that this intermediate shortened a new analog synthesis by a full day—and reduced organic solvent consumption by a measurable percentage. These are modest but important benefits in an environment where cost and resource efficiency drive competitive advantage. Our own process development chemists have also reported fewer problems during workups, due in large part to the chemical stability built into the structure of 2,3-Dichloro-4-(trifluoromethyl)pyridine.
The last few years have exposed vulnerabilities across the global chemical supply chain. Material shortages, transportation bottlenecks, and regulatory revisions slow down even the best-managed sourcing programs. We’ve learned to build redundancy into our sourcing for key precursors—especially halogenated benzenes and pyridines. Our QC team has been trained to detect not only obvious contaminants but subtle lot-to-lot variations in starting materials that might barely register at first but can cascade into real process headaches if ignored.
Early planning, including buffer inventory strategies and real-time supplier engagement, has sometimes made the difference between delivering on schedule or missing a seasonal production window for customers in agriculture. We document and track temperature exposures and shipping durations, logging data on every shipment. If a barrel spends too many hours in customs or a freight container gets delayed at port, we reevaluate stability and, if necessary, retest before release. These details are not just for internal peace of mind—they translate to fewer rejected lots and fewer production halts for our clients.
A chemical manufacturer’s credibility grows out of solving real-world problems. The greatest improvements in our 2,3-Dichloro-4-(trifluoromethyl)pyridine process have come not from internal brainstorming, but from the challenges our users faced. For example, a pharmaceutical customer working with particular hydrogenation conditions alerted us to trace-level reactivity with certain metal catalysts. That feedback led to additional screening steps for trace metals in our product QC, limiting problematic contaminants before packaging.
Listening to agricultural customers led us to re-examine the compound’s photo-stability under outdoor handling. Resulting changes to our packaging specifications—thicker drums with UV-resistant liners—delivered measurable stability gains without excessive cost. These are changes driven by experience, not conjecture.
Consistency in analytical data is fundamental—HPLC purity, residual solvent profiles, and water content tests show up on every batch record. But we know quality also means predictability during downstream operations for customers. Even small changes in microcontaminants or particle size can trigger unexpected behavior in fine-tuned pharmaceutical or agrochemical syntheses. Our plant chemists and analytical team meet regularly to compare process data with customer feedback, always seeking to close the loop between observed performance in the lab and the factory floor.
For many batches, we maintain retain samples for post-delivery testing, digging deeper when customers uncover anomalies in yield or reactivity. In one case, a new supplier of a minor reagent caused a shift in a trace impurity profile. Through root cause analysis and direct engagement with the client, we managed to restore normal function to their process and revise our internal supplier controls in the process.
Looking ahead, advances in green chemistry and process intensification are likely to change how intermediates like 2,3-Dichloro-4-(trifluoromethyl)pyridine will be produced and used. We’ve taken early steps towards solvent reduction, improved waste management, and process intensification through improved reactor design. Every improvement brings economic and environmental payoffs: less waste leaves our site, and more product gets into the hands of customers who need it to progress their own innovations.
Many of our industrial customers now ask not only for high purity but also for details about the energy and waste footprints behind each kilogram delivered. Requests for green certification or lifecycle analysis of our processes have prompted deeper dives into plant data and, in some cases, research collaborations to find better alternatives for reagents or process solvents. These shifts challenge us to rethink routines and explore new catalysts, solvent systems, or containment strategies. Our willingness to adapt becomes a competitive edge—and provides a foundation for customer trust that builds over years, not just shipments.
Training a reliable production crew for specialty chemicals demands time and patience. Every operator and technician rotating on our 2,3-Dichloro-4-(trifluoromethyl)pyridine line absorbs safety culture, process nuances, and troubleshooting best practices. In an environment filled with potent reagents and exacting schedules, shared knowledge of both routine and edge cases forms the real backbone of process reliability.
We maintain thorough operating manuals, facilitate frequent team huddles, and encourage transparent reporting of even minor process deviations. A close-knit team, rooted in mutual respect and shared purpose, has responded with flexibility during both routine production runs and unexpected contingencies. This human capital—seasoned chemists, line operators, and QC analysts—supports more than checklists; it underpins our ability to rapidly diagnose and fix issues, adapt to nonstandard customer needs, and stay ahead of evolving regulatory and technical requirements.
Open lines of communication widen the information pipeline. Technical support doesn’t end after product leaves our warehouse. We encourage customers to connect with our team during method development, scale-up trials, or troubleshooting efforts. Often, a short call or shared analytical report uncovers adjustments to production or packaging that pay dividends for all involved.
These collaborations help us optimize process steps, discover new synthetic applications, and anticipate upcoming regulatory or assay requirements. Jointly authored papers, in-house seminars, or technical visits create shared understanding. A collaborative approach, built on years of steady interaction, keeps the product relevant and helps shape future variations for new applications.
Producing and supplying 2,3-Dichloro-4-(trifluoromethyl)pyridine gives us a front row seat to changing expectations in global specialty chemicals. End users ask for more than a reagent; they seek solutions grounded in practical knowledge, technical rigor, and genuine partnership. From raw material inspection to finished product delivery and documentation, every step in our process reflects responsibility and pride.
This product’s differentiated profile—stability, purity, and reactivity—not only serves current market needs but provides a practical basis for future innovations in pharmaceuticals and crop protection. As both regulatory and market environments evolve, manufacturers who listen, learn, and stay ahead of both problems and opportunities will remain valuable partners in every breakthrough that follows.