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HS Code |
921595 |
| Product Name | 2,4-Bis(Trifluoromethyl)Chlorobenzene |
| Cas Number | 328-84-7 |
| Molecular Formula | C8H3ClF6 |
| Molecular Weight | 252.55 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 153-155°C |
| Melting Point | -6°C |
| Density | 1.546 g/cm³ |
| Refractive Index | 1.418 |
| Purity | Typically ≥98% |
| Flash Point | 58°C |
| Solubility | Insoluble in water |
| Smiles | FC(F)(F)c1ccc(Cl)cc1C(F)(F)F |
As an accredited 2,4-Bis(Trifluoromethyl)Chlorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100 grams, with tamper-evident cap and hazard labeling for `2,4-Bis(Trifluoromethyl)Chlorobenzene`, manufacturer details displayed. |
| Shipping | 2,4-Bis(Trifluoromethyl)Chlorobenzene is shipped in tightly sealed containers to prevent leaks and contamination. It should be transported in compliance with all applicable regulations for hazardous chemicals, avoiding exposure to heat and moisture. Proper labeling and safety documentation, including Material Safety Data Sheets (MSDS), are mandatory during shipping and handling. |
| Storage | **2,4-Bis(Trifluoromethyl)Chlorobenzene** should be stored in a tightly sealed container in a cool, dry, and well-ventilated area away from heat, ignition sources, and incompatible materials such as strong oxidizers. Avoid exposure to moisture and direct sunlight. Use secondary containment to prevent spills and clearly label the container. Handle using appropriate protective equipment to minimize inhalation, ingestion, and contact risks. |
Applications of 2,4-Bis(Trifluoromethyl)Chlorobenzene in Industrial Manufacturing2,4-Bis(Trifluoromethyl)Chlorobenzene serves as a specialty intermediate in diverse chemical industries, where its unique trifluoromethylated aromatic structure imparts specific reactivity and stability required by advanced material and agrochemical synthesis. As the original manufacturer, we support downstream processors with traceable supply and formulation expertise for process-critical integration. Below, we detail major application sectors with specific compliance standards, recommended usage levels, relevant process stages, and typical finished products. 1. Advanced Agrochemical SynthesisThis intermediate contributes to the selective introduction of trifluoromethyl groups in the synthesis of herbicide and fungicide actives employed for crop protection. Its unique halogen-fluorine pattern improves target molecule stability against metabolic breakdown and photodegradation. Downstream producers carry out nucleophilic substitution and cross-coupling at the chlorinated position to construct complex molecules with regulated field activity and environmental persistence. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Pharmaceutical Intermediate for Active Ingredient SynthesisOur product finds targeted application as a building block in the synthesis of advanced pharmaceutical actives, especially for molecules containing aryl trifluoromethyl motifs that enhance metabolic stability and bioavailability. Medicinal chemists leverage its reactivity in Suzuki or Buchwald-Hartwig couplings, providing key step transformation toward late-stage pharmaceutical candidates in anticancer and CNS drug sectors under stringent GMP protocols. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. High-Performance Material Monomer SynthesisProducers of specialty polymers and electronic materials incorporate this molecule as a monomer precursor to generate high thermal stability aromatics for advanced applications. Its dual trifluoromethyl groups induce unique dielectric and chemical resistance properties. Facilities producing fluorinated resins, OLED intermediates, and specialty coatings require controlled monomer feedstock with consistent purity for critical polymerization reactions. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Custom Synthesis in Agrochemical Research and DevelopmentR&D labs engaged in the creation of next-generation crop protection actives regularly specify this intermediate for small-batch synthesis and structure-activity relationship (SAR) studies. Its reactivity profile supports iterative modification strategies, enabling exploration of molecular analogs to achieve improved selectivity, reduced toxicity, or IP-protected scaffolds. Such projects require analytical-grade supply and impurity control with defined traceability for regulatory submission purposes. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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In a chemical plant’s daily operations, few substances draw as much attention from synthesis teams as 2,4-Bis(Trifluoromethyl)Chlorobenzene. This compound, known within our walls as a dependable intermediate, carries the CAS number 328-84-7, and often finds itself referred to by its model name: 2,4-Bis(TFM)CB. With a structure that brings together a chlorinated benzene ring and two trifluoromethyl groups, it has staked its place as a core building block for high-performance applications.
Most of our manufacturing lines have worked with halogenated aromatics, but 2,4-Bis(Trifluoromethyl)Chlorobenzene stands out for its specific substitution pattern. Our teams have learned through years of handling, that the introduction of two -CF3 groups at the 2 and 4 positions on the benzene ring, alongside a chlorine at another site, doesn’t just change the basic chemistry—it completely shifts how the material behaves in reaction and downstream use.
Chemistry on paper is theory, but on our production floor, we focus on delivering a clear, colorless to pale yellow liquid with a typical purity above 99%, as confirmed by GC assay. Trace water and acid residues destroy sensitive reactions, so moisture content and acidic impurity control become part of every batch’s standard tests. The boiling point runs in the 170-172°C range under reduced pressure. Physical consistency and freedom from extraneous particulates mean less downtime during filtration or distillation, which is a priority for both us and our customers’ process teams.
Solubility is a recurring topic during production planning. 2,4-Bis(Trifluoromethyl)Chlorobenzene displays very low solubility in water and mixes well with common organic solvents like DCM, toluene, and ether. Our experience shows this helps in product isolation and downstream manipulation, especially when customers need to feed it directly into coupling or halogen-exchange reactions. The stability profile under standard storage conditions—dry, away from UV light, and in a nitrogen-blanketed drum—matches what we see for most halogenated aromatics with strong electron-withdrawing groups.
Our clients in agrochemicals and advanced materials maintain a steady demand for 2,4-Bis(Trifluoromethyl)Chlorobenzene. Their teams tell us that this molecule’s trifluoromethyl groups offer more than just chemical uniqueness: they drive up lipophilicity and metabolic stability in final products. In crop protection R&D, researchers have shifted toward molecules that feature multiple trifluoromethyl substituents to increase persistence and selectivity, because these effects are well-proven in field trials. Mouse bioassay and storage studies point to better environmental stability compared to non-fluorinated analogues.
In the polymer sector, engineers and researchers come to us for this product because traditional materials fall short where chemical resistance against aggressive chemicals or thermal stress matters. The -CF3 substituents on the aromatic ring exert a strong inductive effect, so the resulting polymers or resins resist hydrolysis, oxidation, and even solvent attack better than those made from simple chlorobenzenes. Performance coatings and specialty adhesives regularly incorporate derivatives of this molecule, improving bond integrity under harsh industrial conditions.
Producing 2,4-Bis(Trifluoromethyl)Chlorobenzene at scale brings lessons that never show up in textbooks. Fluorination chemistry is finicky, highly exothermic, and punishes careless process control. During initial runs years ago, we realized reactor metallurgy needs careful selection—otherwise, traces of free fluoride create pitting, even with specialized stainless steel. Our technical team invests much time in optimizing temperature ramps and dosing to suppress side reactions that yield mono-substituted or over-chlorinated byproducts.
Yield is only part of the equation in a full-scale plant. Consistency in product purity, absence of residual acid, and minimization of hydrolytically-labile side-products define a successful campaign. In-house GC-HPLC comparison studies allow us to catch even low ppm impurities which could scuttle a pharmaceutical or agrochemical scale-up on the customer’s end. Logistics also shape the process; moisture control during packaging and transit decides if the product will ship as a single-phase clear fluid or end up heterogeneous, wasting time and money.
We often field questions about the chemical’s advantages compared to other substituted chlorobenzenes or similar trifluoromethylated aromatics. The distinctive pattern—two CF3 groups at 2 and 4—translates into very different electronic properties from its mono-trifluoromethyl cousins. Electrophilic aromatic substitution, nucleophilic aromatic substitution, and cross-coupling reactivity each change dramatically, as demonstrated by reaction selectivity shifts in the lab.
Compared to simple chlorobenzene, which acts as a relatively benign starting material, the twin CF3 substitution pulls electron density away from the ring, toughening the molecule against unwanted nucleophilic attack. This extra stability is valuable in applications calling for residue resistance or longer shelf-life under extreme storage conditions. On the other hand, some customers new to working with such highly fluorinated aromatics encounter difficulties dissolving or activating the molecule without rethinking their conventional reaction conditions. We often consult on adjusting bases, solvents, or activating catalysts to match these new demands.
Looking at single-substituted trifluoromethyl chlorobenzenes, the difference in properties is no less dramatic. 4-Trifluoromethyl-chlorobenzene remains more reactive in some electrophilic reactions but fares poorly for applications that require more robust chemical inertia. Dual CF3 groups raise molecular weight and boiling point while dropping polarizability compared to non-fluorinated and mono-fluorinated peers. Our long track record gives us data to predict which applications align with these traits.
In large-scale synthesis, reliability and predictability often matter more than record-setting yields. We have seen customers repeatedly return for our 2,4-Bis(Trifluoromethyl)Chlorobenzene because its reproducibility simplifies troubleshooting in both pilot and plant settings. Analytical validation data spans liquid chromatography, mass spectrometry, and NMR—a necessity for regulatory submissions in regulated industries.
Many new materials, particularly pharmaceuticals or specialty polymers, begin as an idea in a research lab, but their real test starts in the plant reactor. Failures at gram or kilogram scale due to unknown impurity spikes or off-specification reactivity can cost weeks or months of development time. Over years of manufacturing, our background in continuous process controls and end-to-end batch documentation has helped both internal teams and external partners avoid these headaches by supplying product that performs predictably.
Partnerships grow out of trust and results, not just paperwork. We have collaborated with agricultural and pharma innovators to adapt product grades for high-pressure hydrogenation or ultra-dry crystallization routines. Feedback directly influences tightness of our recrystallization and solvent-drying steps, reflected in updated batch protocols and regular on-site training.
Day-to-day handling of 2,4-Bis(Trifluoromethyl)Chlorobenzene demands more than standard chemical routine. The same strong electron-withdrawing groups that help the product in applications also impact stability. Our crews store this compound in UV-opaque, nitrogen-flushed containers to arrest decomposition or moisture pick-up. Over time, we have worked out interventions for when storage environments deviate, for instance, hot summer loading bays or poorly-sealed drums. Batch stability studies are ongoing and data shows, under proper conditions, the product keeps its purity year over year.
On rare occasions, minor traces of decomposition byproducts have flagged new cleaning protocols for drums and valves. To get ahead of the problem, we've installed inline analytical checks during bulk loadouts, and those efforts have sharpened both safety and reliability.
Every batch of this product sent out the door marks an entry into innovation pipelines in synthetic chemistry, material science, and crop protection. Pharmaceutical chemists incorporate the 2,4-Bis(Trifluoromethyl)Chlorobenzene motif not just for molecular complexity but for confirmed metabolic stability against enzymatic degradation, streamlining development of actives tailored for long half-life or environmental resilience.
Polymer scientists and materials engineers turn to the molecule in formulating films, coatings, and resins that demand inertness and resistance to environmental wear. Coatings based on derivatives of this product withstand outdoor exposure and chemical cleaning cycles better than their predecessors. Direct feedback from end-users points towards easier maintenance and less downtime on high-value assets—upstream benefits made possible by the right chemical design, beginning with our 2,4-Bis(Trifluoromethyl)Chlorobenzene.
Agrochemical researchers look for specific attributes in intermediates, and this compound’s low bioaccumulation alongside high field persistence stands out in side-by-side soil mobility and breakdown studies. This feedstock has played a visible role in boosting efficacy and selectivity of crop protection solutions now registered around the globe.
Years of hands-on experience have taught us that process safety and sustainable practice must sit at the core of any chemical production. Working with fluorinated aromatics means detailed hazard controls for thermal excursions, strict ventilation management, and responsible waste treatment. Staff are trained on recognizing exothermic behavior and the correct step sequence during startup and shutdown operations, supporting a culture of safety.
Sourcing of upstream raw materials—chlorobenzene, trifluoromethyl donors, and all the rest—relies on partners who can document the integrity of their shipments. Tighter regulation and greater attention to planetary health mean recycling and minimizing effluent loads, especially with fluorinated residuals. Factory audits and environmental controls follow the product’s journey from reaction to packaging, ensuring real accountability.
Quality management for 2,4-Bis(Trifluoromethyl)Chlorobenzene starts long before the material lands in a storage tank. Each batch triggers a cycle of analytical checks, including NMR, FTIR, HPLC, and Karl Fischer titration. Our laboratories hold records reaching back through hundreds of campaigns, giving traceability and insight for troubleshooting or demonstrating compliance to regulatory bodies.
The chemical industry’s history is written in real-world feedback. Adjusting grades for different customer industries, working on purity profiles, improving logistics packaging, and responding to field data about decomposition or byproduct formation have each shaped the evolution of our 2,4-Bis(Trifluoromethyl)Chlorobenzene product line.
In collaborations with academic and industrial researchers, we have piloted different purification technologies—fractional crystallization, advanced membrane separations, and high-performance distillation. Each adjustment seeks to reduce impurities that could seed failure in pharmaceutical clinical trials or agricultural scale-up. Open dialogue with chemistry and engineering teams allows us to identify new bottlenecks and rapidly adapt.
Digital transformation across the plant has delivered more robust tracking and documentation for supply chain transparency, batch genealogy, and compliance checks. Real-world feedback from technical service visits, product returns, and scheduled audits cycles back into the plant floor to refine procedures even further.
The landscape of chemical manufacturing and innovation continues to shift. Our role grows with the needs of fields such as advanced electronics, battery materials, and medical imaging. Manufacturing 2,4-Bis(Trifluoromethyl)Chlorobenzene for these new areas poses challenges in purity, trace metals, and batch-to-batch consistency. Experience in fine-tuning existing production systems and investing in new analytic instrumentation puts our plant in a position to respond rapidly.
Field-driven change is constant. Input from partners testing new catalytic cycles or environmental breakdown pathways has prompted new directions in our process controls. As regulatory landscapes evolve, tighter limits on impurities and environmental releases push us further toward full lifecycle accountability.
Training and knowledge transfer, informed by years of steady production, secure new generations of staff for tasks that demand precision and judgment. Real incidents—planned and unplanned—teach lessons that can be weighted against the routine documentation and SOP rewrites. We keep learning which details actually make a difference on the floor and in a customer’s next big launch.
Manufacturing 2,4-Bis(Trifluoromethyl)Chlorobenzene has connected us with some of the world’s most determined problem solvers. Chemistry is never done by textbook alone. Each drum loaded, each batch certified, and each improvement made is the result of practical know-how, collaboration, and a deep commitment to the end user’s innovation. The story of this product, as seen from the plant, is evidence that trust grows through tackling detail after detail, one improvement at a time, empowering both our teams and every customer who puts our chemistry to the test.