Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2,4,6-Trifluorochlorobenzene

    • Product Name 2,4,6-Trifluorochlorobenzene
    • Alias 1-Chloro-2,4,6-trifluorobenzene
    • Einecs 217-230-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    606138

    Cas Number 20270-54-4
    Molecular Formula C6H2ClF3
    Molecular Weight 168.53 g/mol
    Appearance Colorless liquid
    Boiling Point 153-155°C
    Melting Point -12°C
    Density 1.444 g/cm³
    Refractive Index 1.487
    Flash Point 50°C
    Solubility In Water Insoluble
    Vapor Pressure 2 mmHg (25°C)
    Smiles FC1=CC(Cl)=CC(F)=C1F

    As an accredited 2,4,6-Trifluorochlorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with secure screw cap, hazard labels, and product information; contains 100 mL of 2,4,6-Trifluorochlorobenzene.
    Shipping 2,4,6-Trifluorochlorobenzene is typically shipped in tightly sealed containers made of compatible materials to prevent leaks and contamination. It should be transported as a hazardous material, following regulations for flammable liquids, with proper labeling and documentation. Keep away from heat, open flames, and incompatible substances during transit. Handle with appropriate safety precautions.
    Storage 2,4,6-Trifluorochlorobenzene should be stored in a cool, dry, and well-ventilated area, away from heat, sparks, open flames, and incompatible substances such as strong oxidizers. Keep the container tightly closed and clearly labeled. Store in a corrosive-resistant container with a resistant inner liner. Avoid direct sunlight and sources of ignition. Ensure appropriate spill containment measures are in place.
    Application of 2,4,6-Trifluorochlorobenzene

    Applications of 2,4,6-Trifluorochlorobenzene in Industrial Manufacturing

    2,4,6-Trifluorochlorobenzene serves as a key fluorinated aromatic intermediate in advanced pharmaceutical synthesis, agrochemical production, high-performance materials, and specialty UV-cure technologies. Below we share our in-depth experience regarding its practical uses across major industrial downstream sectors, with focused insights on regulatory standards, addition levels, process roles, and resultant product types.

    1. Pharmaceutical Active Ingredient Synthesis

    Major pharmaceutical companies utilize 2,4,6-Trifluorochlorobenzene as a halogenated arene building block in the preparation of APIs targeting anti-infective, oncology, and CNS segments. Its controlled reactivity profile supports multi-step transformations, including Suzuki, Buchwald, and nucleophilic aromatic substitution, to introduce trifluoromethyl and cyclized cores essential for patent-protected actives. Precision in dosage and impurity control is mandatory at every scale-up stage to meet regulatory demands for traceability and batch quality.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP 43/NF 38)
    • European Pharmacopoeia (Ph. Eur. 10.0)
    • FDA 21 CFR Parts 210/211

    Typical usage ratio

    • Employed at 0.5–4.5 molar equivalents relative to target API core, adjusted by the route of synthesis and target impurity threshold

    Downstream process integration

    • Introduced during intermediate coupling or ring-construction steps, often as the limiting reagent in regulated reactor trains under GMP protocols

    Final product types

    • Small-molecule APIs such as kinase inhibitors, anti-tuberculosis agents, and antidepressant scaffolds
    • Pharmaceutical intermediates for further functionalization

    2. Crop Protection Active Synthesis

    Leading agrochemical manufacturers incorporate 2,4,6-Trifluorochlorobenzene in synthetic pathways to craft fluoro-substituted herbicides, fungicides, and insecticidal actives. Its electron-withdrawing profile enables efficient nucleophilic aromatic substitution for downstream halogenation, amination, or etherification steps critical for field-proven activity and regulatory registration. Monitoring of environmental emissions and raw material traceability remains a key operational focus during scale-up and continuous processing.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • FAO/WHO Specifications for Plant Protection Products
    • European REACH Chemical Regulation (Regulation (EC) No 1907/2006)
    • ISO 9001 Quality Management System

    Typical usage ratio

    • Used at 1.0–2.5 molar equivalents according to target molecule substitution pattern and reaction conversion efficiency

    Downstream process integration

    • Dosed in controlled-batch or flow synthesis for substitution, cyclization, or coupling with heterocyclic backbones under stringent containment and solvent recovery schemes

    Final product types

    • Selective herbicide actives (e.g., triazine and pyridine derivatives)
    • Fluorinated fungicidal agents
    • Intermediate compounds for flagship insecticidal formulations

    3. Liquid Crystal Material Fabrication

    Manufacturers in the advanced display sector leverage 2,4,6-Trifluorochlorobenzene as a precursor in synthesizing aromatic segments for liquid crystal mesogens and alignment agents. Its substitution pattern introduces polarity and specific steric effects, crucial for the design of nematic and smectic liquid crystals. Stringent impurity control during each reaction stage is required to avoid downstream color defects and ensure display performance meets OEM standards.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for hazardous substances
    • IEC 61249-2-21 for halogen-free requirements
    • ISO 9001 and ISO 14001 for process and environmental management

    Typical usage ratio

    • Typically 0.8–2.0 molar equivalents in comparison to terminal or bridging aromatic units, tuned for fluidity and birefringence properties

    Downstream process integration

    • Fed into Grignard and organolithium coupling steps forming rigid mesogenic cores, with further purification to meet device-grade specifications

    Final product types

    • Nematic and smectic liquid crystals for LCD panels
    • Alignment layers for thin-film transistor (TFT) displays

    4. UV-Curable Coating Monomer Synthesis

    Producers of advanced coatings use 2,4,6-Trifluorochlorobenzene to generate specialty acrylate and epoxy monomers, especially for high-durability films exposed to chemical or UV stress. The fluorinated core imparts superior weatherability and dielectric properties, essential for electronics and automotive topcoats. Precise monitoring of input ratios and thermal process conditions ensures batch reliability and minimizes by-product formation impacting downstream cure speeds.

    Industry compliance standards

    • ISO 10993 for medical device coating applications
    • ASTM D3023 for chemical-resistant coating films
    • EN 71-3 Safety of Toy Coatings (for child-safe products)
    • ISO 14001 certified environmental management for emissions control

    Typical usage ratio

    • Typically 0.5–1.5 equivalents per acrylate group; proportions optimized based on desired hardness, gloss, and resistance levels

    Downstream process integration

    • Used in early-stage synthesis via aromatic substitution and ring-opening reactions, prior to monomer end-capping and oligomerization

    Final product types

    • UV-cure coatings for electronics
    • High-durability automotive topcoats
    • Specialty scratch-resistant varnishes

    5. Specialty Polymer Syntheses (High-Performance Polymers)

    Polymers engineers select 2,4,6-Trifluorochlorobenzene for introducing fluorinated aromatic sites during custom polyarylene and polyetherketone production. These functional groups deliver targeted modifications to dielectric constants, chemical inertness, and mechanical profile essential in aerospace, semiconductor, and barrier film applications. Accurate flow control and reaction stoichiometry help ensure lot reproducibility and downstream converting yield.

    Industry compliance standards

    • UL 94 for flame retardance testing
    • ASTM D638 for tensile property measurement
    • REACH Annex XIV and SVHC listing compliance
    • EN 60243-1 for dielectric strength

    Typical usage ratio

    • Routinely 1.2–2.0 equivalents per repeat unit or comonomer, variable by final property target and degree of fluorination required

    Downstream process integration

    • Fed into condensation polymerization or nucleophilic aromatic substitution steps under controlled temperature and vacuum cycles

    Final product types

    • Fluorinated polyarylene and polyetherketone resins
    • High-performance dielectric films for electronic circuit substrates
    • Aerospace-grade specialty plastics
    Free Quote

    Competitive 2,4,6-Trifluorochlorobenzene prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    2,4,6-Trifluorochlorobenzene: Experience from the Source

    At our chemical plant, 2,4,6-Trifluorochlorobenzene keeps showing up as a linchpin in manufacturing modern molecules for crops, medicines, and advanced materials. Our own production line meets the high purity levels demanded by these industries, because we've watched for years how even the subtlest impurity throws off entire syntheses. We talk to our clients on the pharma and agrochemical R&D benches. They want trifluorochlorobenzene that holds its spec—precise assay, low moisture, and the consistency they count on across batches. This is not niche chemistry. It's the foundation for building blocks that make blockbuster drugs or resilient herbicides possible.

    Producing a Reliable Building Block

    Experience has taught us what it takes to keep this material stable and pure. We source feedstock fluorobenzenes under strict controls. Batch parameters have been dialed in through years of adjustment. Our reactors and purification lines don’t drift. Down the road, you notice the effect. A route might be two or three steps shorter because the starting chemical does not bring hitchhiking byproducts. Less time debugging chromatography, fewer headaches in regulatory paperwork.

    All 2,4,6-Trifluorochlorobenzene does not behave the same. Our quality control uses gas chromatography and NMR to check for any scratch of hydrodehalogenation, for traces of isomeric contamination, for halide exchange that hasn't been fully wrung from the product. In the early days we chased these issues one at a time, fine-tuning distillation setups and swapping glassware to eliminate cross-contamination. It cuts into yield upfront but spares customers from reaction knock-ons and wasted screens. People in fine chemical R&D know that one impure drum can set back an R&D project by months.

    Understanding the Chemistry

    2,4,6-Trifluorochlorobenzene stays in such high demand thanks to its versatility. A nucleus carrying three fluorines with a lone chlorine opens up a unique pattern of reactivity for cross-coupling. It’s a prime substrate for nucleophilic aromatic substitutions, including classic SNAr reactions that bring in amines or thiols straight onto the ring. The ortho and para fluorines set up strong electron withdrawal, which helps the ring move through more exotic organometallic transformations. Some customers take all these positions—meta, ortho, para—with their own substitution routes, so the molecule must behave exactly as expected on every batch.

    Where does 2,4,6-trifluorochlorobenzene stand out? Compared to the more widely available mono- or difluorochlorobenzenes, the three fluorines give a sharper electronic profile. For some reactions, other isomers stub out yields, because they bring in extra reactivity or steric hindrance. Our engineers have compared multiple fluoroarene isomers in batch trials for large contracts. The 2,4,6 arrangement stands firm—reactive enough for Suzuki couplings, easy to halogen-metal exchange, resistant to unwanted polymerization. That means fewer surprises on the plant floor and a more predictable timeline for process development in downstream industries.

    Specifications and Batch Consistency

    Every drum our team ships carries a batch log that stretches back to its raw materials and shift operator notes. Each lot is tagged with its precise assay—typically above 99%—but numbers alone do not reveal the real performance. We document water content by Karl Fischer titration because a few hundred ppm can block organometallics. Our team runs NMR and GC-MS profiles against reference materials. If a fraction starts showing up with an isomeric peak, we track it through the synthesis line and strip out washing steps until it’s gone.

    The plant’s layout itself evolved as we responded to regulatory tightening and customer demand. Several years ago, after a leading crop science company pointed out trace acid halides in one sample, we specced in-line monitoring to spot even low-level degradation. Other producers without the same instrumentation or production history sometimes find their product rejected or reworked after failing advanced analysis. We do not ship unless in-house and third-party labs confirm every panel.

    The Uses That Drive Real Demand

    Walk into most pharmaceutical intermediate plants, and you’ll find processes that either start from 2,4,6-trifluorochlorobenzene or need its derivatives. Medicinal chemists reach for this molecule when designing kinase inhibitors or fluorinated aromatic scaffolds. One project we supported for an oncology lead candidate required tons of material within a three-month window. Our team had to scale up without dropping below 99.5% purity, and we communicated directly with the client’s QA and process chemists to tune for their synthesis requirements. The reliability of supply and reproducibility of product made the difference between proof-of-concept and full clinical production for their team. We later heard from colleagues at other manufacturing sites about delays caused by unanticipated reactivity—losses that could have been avoided if they’d started from better-quality trifluorochlorobenzene.

    Agrochemical labs keep 2,4,6-trifluorochlorobenzene near the top of their raw material lists, because so many modern fungicides and insecticides depend on the three-fluorine motif for both stability and selectivity. The difference between a patented active ingredient and a generic typically comes down to such nuances in substitution. Materials science teams reach for this compound in specialty polymers and dielectric layers, where precise substitution prevents cross-linking and gives thermal stability. Choosing the right producer affects the whole value chain—if the input does not match the design spec, coatings end up with variable breakdown or sub-optimal conductivity.

    How Production Practices Shape the Industry

    Producers familiar with global requirements have to keep up with evolving regulations and customer demands. As a chemical manufacturer, we are required to demonstrate traceability, environmental responsibility, and a concrete risk-management plan for each batch. Auditors from pharmaceutical and electronic materials customers have walked our lines, inspected raw material logs, and reviewed every operation before approving us as a supplier. Less stringent producers might skip these steps, but eventually customers realize the difference: batch failures, inconsistent lot-to-lot results, or even regulatory bottlenecks downstream. These setbacks ripple out through process development, affecting project timelines and budgets.

    Comparing with Other Halogenated Fluorobenzenes

    Not all halogenated fluorobenzenes serve with the same strength in industrial settings. The key differentiator comes from the interplay of electronegativity and position. For example, 2,4,6-trifluorobromobenzene carries a heavier bromine, which shifts reactivity and can complicate downstream functionalization with palladium catalysis. Mono- or difluorochlorobenzenes, though cheaper and easier to synthesize, often lose out in selectivity when medicinal chemists need a sharper electronic landscape. We field calls from researchers who switch to our compound after encountering wasted time on alternative isomers that fail to deliver either the targeted substitution or the required batch stability.

    The consistency of trifluorochlorobenzene’s behavior under a variety of reaction conditions—high-temperature couplings, strong nucleophiles, or even pilot-scale continuous-flow processes—makes it a preferred input. Its volatility profile sits well within the safe handling margins for most plant operators. In our own shop, we make sure every tank and line is dedicated to prevent any kind of halogen carryover from other chlorinated or brominated lines, as this has proven to be a source of trouble not caught until the final step on the customer’s side.

    Listening to Customers for Continual Improvement

    Our relationships with pharmaceutical and agrochemical manufacturers shape every upgrade we make to process or specification. Over the years, we’ve worked with process chemists and plant engineers to troubleshoot specific reactivity issues—sometimes as fine as a subtle impurity masking a catalyst or impacting isolation steps. Customers relay back their QA’s blind panel spot tests, their QC controls from each campaign, and their own regulatory filings. These direct feedback loops have enabled us to refine controls on moisture, residual solvents, and isomeric purity well before formal specification gets updated. Each learning gets funneled back into production: changing out Teflon seals, tightening process analytics, or resourcing raw materials to eliminate trace metal content from catalysts upstream.

    We’ve encountered situations where a research group, aiming to scale up a new chemical entity, asks for unusual packing or delivery. For example, a formulating plant might request custom drum liners or different headspace gases to avoid static buildup. The goal is always to keep the trifluorochlorobenzene at its purest, through every step from production to arrival at the blending tank. Years ago, a high-throughput screening facility noticed a drop in reactivity that traced back to traces of an incompatible stabilizer used in a supplier’s product. Since then, we regularly check all stabilizer and additive profiles before confirming a drum for shipment to any lab with sensitive processes.

    Handling, Logistics, and Real-World Challenges

    Plant operators and logistic staff know that no two jobs are alike. Because of its moderate volatility and halogen content, 2,4,6-trifluorochlorobenzene requires careful attention in filling, storage, and transport. On a humid day, condensation along a bulk tank can spike water content, so we maintain nitrogen blanketing and run leak checks on every loading session. Gloves, vented hoods, pressure-relief devices—these aren’t optional steps, they’re hard-won lessons. We’ve supplied both metric tons and lab-scale containers, always balancing efficient transport against the safety and purity concerns. We work closely with certified hazmat shippers and run our own site audits before signing off on a logistics partner.

    Unexpected issues do arise. We’ve had years when global supply chains saw shocks—raw material pricing, packaging shortages, regulatory shifts—and each time, we keep reserves of validated critical raw materials and packaging. Any change to the raw process gets regressed through historic data to check that final product specs are not drifting from validated windows. We keep open lines with fire marshals and regional environmental agencies to prevent costly downtime. Each precaution grows out of experience gained in addressing unexpected leaks, stuck valves, or customer returns from past decades in the field.

    Environmental and Safety Considerations

    Making halogenated aromatics carries environmental responsibilities. As fluorine and chlorine reactants pass through our reactors and into waste streams, we’ve built recovery systems that capture and neutralize byproducts. For chlorinated effluent, we run multi-stage scrubbing and pay stringent disposal charges to certified handlers. On the fluorine side, any released compounds are neutralized in situ before storage or shipment for further reclamation. These steps add cost and effort, but they also prevent environmental regulatory headaches and chemical spill incidents down the line.

    Safety protocols stem not just from legal requirements but from seeing the results of lapses: a small leak builds up, an incompatible solvent tank triggers excessive venting, or waste drums impose hazards from long-term accumulation. Our staff receive regular training in detecting halogen leaks, interpreter readings from dedicated fluorine sensors, and participating in system-wide safety drills. Buyer audits from multinational pharmaceutical and agrochemical producers reinforce these standards. We often get asked about specific verification for zero-contaminant transport drum cleaning—a focus born from direct industry experience with batch recalls due to cross-contamination from recycled packaging.

    Market Shifts and Application Trends

    What keeps 2,4,6-trifluorochlorobenzene at the forefront of modern molecule design? The movement in drug discovery toward more halogenated scaffolds, with their unique metabolic stabilities and enhanced biological activity, drives wider adoption. Newer classes of crop protection chemicals keep pushing for increased weather resistance and lower environmental persistence, a pattern favoring precisely fluorinated aromatic moieties. In the performance chemistry sector, deeper fluorination gives better thermal management and reduced degradation under harsh conditions for circuit boards, sensors, and specialty films.

    Our technical staff stay alert for shifts in synthetic methods—continuous flow processes, new catalytic systems, greener solvent routes—that require shifts in input stability or impurity profile. Over the past five years, several formulators switched to more sustainable solvents for downstream use, and that change meant adapting packaging requirements or purification routines to prevent incompatibilities. Each update in customer production flows comes back to impact our batch-making, shipping, or storage practices. Open communication and routine joint study sessions keep us ahead of what the end-user really needs from trifluorochlorobenzene today.

    Challenges and Solutions on the Factory Floor

    Making a product like 2,4,6-trifluorochlorobenzene at scale is an exercise in practical chemistry, planning, and risk mitigation. Over decades, our site has solved persistent problems—halide carryover bleeding into neighboring lines, heat exchanger fouling, or unexpected impurity profiles surfacing after shutdowns. We tackle each challenge by combining historical batch data, customer feedback, and advances in process analytics. Switching out an agitator design in one reactor cut down on microcontamination from metal particulates that only showed up at trace levels. Upgrading in-line monitoring reduced the time from deviation detection to root-cause response. Experience with broad regulatory regimes—from REACH to local planning authorities—means we plan upgrades and maintenance to avoid weeks of downtime due to overlooked paperwork.

    Every improvement in the process feeds directly into better customer confidence. Whether the client is operating from a GMP-compliant pharmaceutical pilot plant or a continuous-feed agrochemical facility in a remote location, they depend on our material to perform the same every time. A missed impurity triggers a chain of hassles—quarantined batches, process hold-ups, expensive troubleshooting—that echoes up the supply chain. By choosing a manufacturing partner with deep in-house knowledge and direct process control, clients cut out months of development frustrations and keep timelines on track. We hear the difference in the follow-up calls after a trouble-free campaign: production teams meet targets, development chemists keep their focus on innovation, and new compounds reach the market without unexpected delays or surprises.

    Looking Forward: Keeping pace with innovation

    The role of 2,4,6-trifluorochlorobenzene will only grow as chemists find new applications in pharmaceuticals, agrochemicals, and advanced materials. From years of producing and improving this molecule, we know the direct relationship between manufacturing quality and customer success. As new process routes and downstream requirements keep evolving, our commitment stands: keep quality high, communication lines open, and improvement ongoing. The lesson is as clear as ever. Consistent, traceable, and pure trifluorochlorobenzene doesn't just build molecules—it helps build the innovation pipelines for entire industries. We know this because we’ve seen it, step by step, from raw material to finished product and through to the breakthroughs it helps make possible.