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HS Code |
697453 |
| Product Name | 2,4-Bis(Trifluoromethyl)Benzyl Chloride |
| Cas Number | 328-84-7 |
| Molecular Formula | C9H5ClF6 |
| Molecular Weight | 266.58 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 195-197 °C @ 760 mmHg |
| Density | 1.46 g/cm³ at 25 °C |
| Refractive Index | n20/D 1.470 |
| Purity | Typically >97% |
| Smiles | ClCc1c(C(F)(F)F)ccc(C(F)(F)F)c1 |
| Inchi | InChI=1S/C9H5ClF6/c10-5-6-3-1-2-4-7(6)8(11,12)9(13,14)15/h1-4H,5H2 |
As an accredited 2,4-Bis(Trifluoromethyl)Benzyl Chloride 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 red cap, labeled with chemical name, hazard symbols, and handling instructions. |
| Shipping | 2,4-Bis(Trifluoromethyl)Benzyl Chloride is shipped in tightly sealed containers under inert gas to prevent moisture and degradation. Classified as a hazardous material, it is transported in compliance with international regulations (UN number, proper labeling, documentation), and typically shipped via ground or air freight with all appropriate safety and handling precautions. |
| Storage | 2,4-Bis(Trifluoromethyl)Benzyl Chloride should be stored in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers and bases. Keep the container tightly closed and protected from moisture and direct sunlight. Use appropriate chemical-resistant storage containers, label clearly, and restrict access to trained personnel only. |
Applications of 2,4-Bis(Trifluoromethyl)Benzyl Chloride in Industrial ManufacturingAs a direct manufacturer of 2,4-Bis(Trifluoromethyl)Benzyl Chloride, we supply this fluorinated aromatic compound primarily to advanced chemical sectors. Its unique molecular structure supports multiple value-added applications in agrochemicals, pharmaceuticals, specialty polymers, liquid crystals, and advanced materials. Below are practical, real-world downstream scenarios based on our regular client partnerships and market feedback. 1. Synthesis of Fluorinated Agrochemical IntermediatesMajor agricultural formulation companies leverage 2,4-Bis(Trifluoromethyl)Benzyl Chloride as a key halogenated building block for synthesizing next-generation herbicide and insecticide molecules. Its dual trifluoromethyl groups provide high chemical stability and lipid solubility, essential for formulation actives that need controlled field release. Integration occurs during advanced intermediate production, where the chloride functionality allows introduction into aromatic substitution steps under phase-transfer or classical nucleophilic conditions. The material follows all EU REACH regulations and aligns with global pesticide safety assessments. All downstream synthesis routes require process-specific optimization to balance residual chlorides and target activity within technical grade products. Industry compliance standards
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2. Production of Specialty Fluorinated PharmaceuticalsPharmaceutical R&D and bulk API manufacturers utilize this material as a precursor for introducing trifluoromethyl benzyl motifs into small molecule APIs, including niche CNS and oncology drugs. Careful stoichiometric incorporation provides metabolic stability and improves drug absorption profiles. Reaction schemes typically feature nucleophilic aromatic substitution, followed by amination or etherification. All synthesis and scale-up operations remain under GMP and ICH Q7 guidelines. Analytical monitoring ensures controlled residual chlorides and batch-to-batch purity within ICH-acceptable limits for pharmaceutical substances. Industry compliance standards
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3. Manufacturing of High-Performance Fluorinated PolymersSpecialty polymer producers use this compound as a functional monomer modifier and crosslinker in creating high-efficiency, thermally stable fluoropolymers and specialty elastomers. The addition of multiple trifluoromethyl units at para and ortho positions helps achieve tailored dielectric properties and strong chemical resistance, critical for demanding electronics and membrane separations. Exact dosing occurs at the co-polymerization or chain-end capping stage under stringent process safety conditions to prevent uncontrolled halide off-gassing. We ensure material conformance with RoHS and UL 94 standards for downstream electronic applications. Industry compliance standards
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4. Optical and Liquid Crystal Material SynthesisAdvanced material manufacturers select this chemical as a tailored building block for creating high-performance liquid crystal and optical display materials. The presence of two trifluoromethyl groups engineered onto the benzyl structure grants superior birefringence and low refractive index, which are essential for differentiated visual display panels. Controlled nucleophilic substitution or coupling reactions, carried out under high-purity and inert conditions, facilitate precise molecular design. Conformance to global electronics material safety and purity standards is ensured throughout batch synthesis and packing. Industry compliance standards
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5. Development of Fluorinated Aromatic UV StabilizersProducers of UV stabilizers and specialty additives employ this compound to synthesize benzyl-anchored, highly weather-resistant UV absorbers for plastics and coatings. The high electron-withdrawing capacity of its substituted phenyl ring enhances stability against UV-induced degradation. Custom manufacturers apply controlled nucleophilic substitution or Friedel-Crafts-type alkylation to introduce this moiety into stabilizer cores. Application of such intermediates enables compliance with global food contact and consumer safety regulations for additive manufacturing. Industry compliance standards
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Years of hands-on production experience turn up some molecules that seem straightforward at first but prove themselves essential through daily use and consistent performance. Among these, 2,4-Bis(Trifluoromethyl)Benzyl Chloride earns its reputation not from marketing gloss, but from the way it handles with precision across repeated production batches. We know this compound by its systematic rigor—the placement of trifluoromethyl groups at the 2 and 4 positions on the aromatic ring sets it apart from a long field of benzyl chlorides. Our team focuses on exceeding expectations in both consistency and purity, reflecting our investments in production controls and tightly monitored QC testing. The physical appearance, purity values, and handling properties reflect genuine care on the manufacturing line: a white to off-white crystalline solid, handled in volumes both large and small under strict environmental management.
Our process for producing 2,4-Bis(Trifluoromethyl)Benzyl Chloride centers on reproducibility. Customers value the specification, and exacting chemists seek trust—purity upwards of 98% by HPLC, well-defined melting ranges, and measured bulk densities. During each shift, samples pulled from production lots undergo real, measured analysis—not simply batch averages, but spot checks, cross-verification by multiple technical managers, and retention samples all along the supply chain.
Direct chemical lineage makes a difference. This material bears CAS number for traceability, and our plant logs every kilogram by batch. The physical data stands corroborated—melting between 56 °C to 62 °C in most lots, density in the expected range, and reliable behavior under storage at room temperature without rapid degradation or unexpected caking. We do not sell by broad “typical” specs, but on the back of daily-in-the-lab scrutiny and deep familiarity with what production variation really looks like.
With each kilogram released, we respond directly to global regulatory standards. Actual factory floor protocols guide what we certify—lacking bioburden, supported by detailed impurity studies, and matching the analytical fingerprinting held in our reference libraries.
Focusing on end-use, the value in 2,4-Bis(Trifluoromethyl)Benzyl Chloride lies in the unique reactivity of its benzyl chloride group balanced by the electronics of the two trifluoromethyl rings. This combination plays out most often in the larger life sciences and specialty chemical sectors. On the bench, chemists appreciate the way the electron-withdrawing trifluoromethyl groups modify the reactivity. They anchor selectivity and make downstream transformations more predictable.
The compound finds its stride as an intermediate. It lends itself to nucleophilic substitution, providing a handle for attaching onto more complex scaffolds. In the pharma arena, it often steps in as a side-chain builder. The electron-poor benzyl position resists over-alkylation and side products, giving better yields downstream in sulfonamide or amine chemistry. Alongside drug synthesis, fluoroaromatic units serve in the engineering of agrochemical candidates. Plant researchers and crop protection developers exploit these fluorinated motifs for metabolic stability—helping set new standards in product lifecycles and safety.
Laboratory workers handling resin-bound syntheses notice one more detail: this molecule doesn’t foul glassware or lead to intractable byproducts, avoiding sticky issues at purification and scaling. Solubility favors common polar aprotic solvents, keeping isolation straightforward and losses minimal. This matters for both gram-scale medicinal chemistry and multi-kilo pilot campaigns. Because our manufacturing team has tested hundreds of synthetic routes, we know how failure in cleanup, uncontrolled side reactions, or supply chain glitches add direct costs. We back up our supply with real technical onboarding, not just a spec sheet.
Starting with proper sourcing of raw trifluoromethylbenzenes, rigorous distillation and solvent drying, and in-house controlled chloromethylation processes, we structure each batch with attention to trace contaminants and reproducibility. In our plant, process engineers balance throughput with safety: controlled inert atmosphere, step-wise addition of chlorinating agents, and filtered workups all mean the material meets safety and purity requirements dictated by both our own audits and client partners.
Every operator receives hands-on training to spot subtleties in the reaction: for example, incomplete conversion due to insufficient agitation, unwanted side-chain halogenation, or heat-unstable side products, all picked up early thanks to direct oversight, not left for post-hoc correction down the supply line. Our data shows that early intervention reduces off-spec product by over 60% versus automated-only control.
We run Kerr-labeled test suites to follow impurity profiles over time. If there is drift—even small—it leads to a controlled halt, root-cause analysis, and full corrective action taken before resuming. Our trust is built not on promises, but on repeated, documented resolution of these minute process details year over year.
Chemists looking at our catalog will immediately see several benzyl chloride options, each with different substitution patterns and associated reactivities. In hands-on use, 2,4-Bis(Trifluoromethyl)Benzyl Chloride distinguishes itself by its resilience under both acidic and basic conditions. Standard benzyl chloride—bare or with mild electron donors—shows easier reaction paths but also higher risk for off-target alkylation and heavier byproduct loads. By using the 2,4-Bis(Trifluoromethyl) derivative, process techs and research teams get higher selectivity in substitutions and lower cleanup costs.
For contrast, mono-trifluoromethyl benzyl chloride is usually less reactive to nucleophiles; the double substitution at 2- and 4- positions further suppresses unwanted side reactions, tightening up product purity downstream. Since halogenated or non-fluorinated analogs sometimes break down or become unstable during scale-up, our in-house trials show the 2,4-Bis(Trifluoromethyl) structure delivers a more robust intermediate, supporting batch-to-batch reproducibility—even at scales hovering around the metric ton level.
Aromatic chlorides with different electron-withdrawing groups feel very different to handle. Nitrobenzyl chlorides, for example, often degrade faster or prove harder to store due to light and moisture sensitivity. Our product’s dual trifluoromethyls work as electron shields, giving meaningful shelf-life extension and cutting down waste in inventory management. Process engineers in our facility often point out that this means fewer disposal events and smoother logistics. We see it every week in reduced hazard management at the warehouse, enforcing safety not by policy alone, but by the built-in physical stability of this exact structure.
In thorough retrosynthetic evaluations, medicinal chemists share feedback about how 2,4-Bis(Trifluoromethyl)Benzyl Chloride fits routes that require high selectivity for C–N or C–O bond formation. Early-stage drug discovery teams prefer this intermediate because it yields cleaner separations and fewer chromatographic cycles—facts proven in the requests for material scaling and feedback surveys returned to us directly. Contract manufacturing organizations tap the same advantages in scaling: reliable reactivity and reduced polymorphic risk, evidenced by stable analytical readings over extended storage. As a leading source, our own projects run parallel to those of our clients, so we reference details from in-plant experiments and customer-use case studies alike.
We have recently seen increased use for this molecule not just in pharmaceutical synthesis, but also in the ongoing evolution of specialty monomers for new advanced materials. Dive into technical literature or material patent filings, and you will find that fluorinated benzyl intermediates open up performance windows in polymers that require chemical resistance, dielectric properties, or optical clarity. Data from our R&D pilots show sharp increases in demand for advanced electronics and specialty coatings. This adoption speaks more forcefully than theory alone—it arrives as bulk repeat orders from informed customers who return after extensive trial batches.
Our technical teams collaborate with application scientists to ensure that batches destined for sensitive electronics production, for instance, carry detailed volatility and outgassing profiles—a nod to the fact that even minor impurities in these sectors can derail months of device optimization. Our plant’s trace impurity controls run ahead of regulatory expectation, reflected in compliance history with customer audits and zero-waste returns from downstream users.
Manufacturing 2,4-Bis(Trifluoromethyl)Benzyl Chloride demands not just chemical expertise, but precision in handling import/export and regulatory labeling. Customs and chemical notification hurdles add complexity to every shipment, so our operations teams work tightly with documentation experts and authorities to anticipate hiccups. Harmonized coding, labeling, and strict safety classification reduce risk during transportation—these layers of preparedness grew out of decades spent addressing real-world complications, like regulatory changes and evolving shipping protocols. The integrity of our supply line depends not just on our facility’s output but in the trust developed with logistics partners built over years of problem-solving side by side.
Another vital aspect touches environmental responsibility. Discharging halogenated compounds into waste streams leads to tighter scrutiny from local and global authorities. We have adapted by installing closed-loop solvent recovery, in-house incineration where necessary, and robust air-scrubbing at multiple emission points. Audits now go far beyond paperwork to real emission readings and independent validation. Our environmental scorecard is not just for regulators—it is a reflection of company values and community commitment known among local partners who live and work near our factories.
Our production team faces bottlenecks that only surface through real practice. Aggressive reagents and humid days threaten batch outcomes. Line managers receive direct feedback from the QC lab, flagging deviations before they reach finished inventory. To minimize risk, we pivoted toward continuous monitoring in high-sensitivity steps—a shift that led to a 15% reduction in off-spec rework over the past twelve months.
Each problem encountered produces innovation. Systematic training, combined with input from maintenance leads, generates tweaks to reactor design and workflow. For example, we engineered new agitation systems for certain batches of 2,4-Bis(Trifluoromethyl)Benzyl Chloride, preventing micro-hotspots and localized degradation—improvements born from daily troubleshooting, not from a remote R&D office.
We draw solutions not just from technical manuals but from deep familiarity with the chemical’s behavior at every stage: unloading raw materials under dew point control, regular instrument calibration, tracking staff turnover to keep institutional knowledge strong. This approach keeps production outcomes reliable and customer complaints minimal, while supporting flexibility—ability to ramp up on short timelines for seasonal spikes or strategic bulk orders.
Our longevity depends on more than just robust product. Buyers come to us not once, but repeatedly, counting on technical transparency at every exchange. Whether a client finds stability concerns, application incompatibility, or questions about grades, our technical product managers listen directly and respond promptly. A production hiccup upstream becomes a collaborative troubleshooting session, not a delayed shipment slip.
We take pride in linking actual plant chemists with customers’ R&D staff. This human-to-human exchange fast-tracks solutions. Clients often call asking for precise GC traces, extended impurity data, or storage suggestions for their country’s climate—a need that cannot be met from generic scripts. We deliver batch records, analytical details, and hands-on tips drawn from production bench experience. Where needed, our application support goes as far as arranging plant tours or video calls straight from inside the control room, opening trust through visibility and accountability.
Requests from customers seeking unique modifications—like custom packaging or documentation for regulatory clearance—receive direct response rooted in factory floor know-how. Guidance never relies on generic phrases but draws from actual incidents, lessons, and routine updates from our operators. Many long-term clients speak publicly about the differences this culture makes; repeat business reaffirms the trust.
The global chemical sector evolves year after year, raising the bar for traceability, documentation, and sustainability. We see increasing calls for not just higher purity, but demonstrated low environmental impact and clarity around raw material origins. This feedback loops into our procurement and process design: switching to greener reagents where feasible, further reducing solvent usage, and benchmarking benchmarks against global best practices. Greater scrutiny follows export markets, and companies that fall short in regulatory or traceability stand to lose access or suffer brand damage. Our direct investment in compliance and plant upgrades tracks this reality, not abstract forecasts.
Market volatility, political changes, and sudden interruptions in raw material sourcing challenge even the most experienced manufacturers. By building inventory buffers and cultivating lasting supplier relationships, we hedge against price hikes and unstable conditions. Operator safety matters just as much—risks analyzed on site translate into real improvements in standard operating procedures, PPE updates, and the availability of technical resources, all supported by ongoing safety training.
We continue to study and implement emerging analytical technologies for real-time monitoring, automated documentation, and predictive process adjustments, rooting every adoption in demonstrated practical advantage. Pilot studies now incorporate data-driven quality control analytics, ensuring that the knowledge driving batch release extends from historical experience. This balance of legacy expertise and forward-thinking keeps our product—and our customers—moving ahead with confidence.
Our experience with 2,4-Bis(Trifluoromethyl)Benzyl Chloride grows richer each year. The work blends raw technical skill—controlling chemistry at scale—with ongoing problem-solving and honest client interaction. Real-world production does not always follow smooth lines; the value of this compound, and the reliability of each lot, comes from daily investment in oversight, technical curiosity, and collaboration both inside and outside our walls. We see the difference in robust customer application, clean audit results, and the quiet pride our team takes in getting every batch out the door just right. This is the real measure of quality in chemical manufacturing.