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2,4,6-Trifluorobenzotrifluoride

    • Product Name 2,4,6-Trifluorobenzotrifluoride
    • Alias 1,3,5-Trifluoro-2-(trifluoromethyl)benzene
    • Einecs 216-676-5
    • 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
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    Specifications

    HS Code

    870256

    Chemicalname 2,4,6-Trifluorobenzotrifluoride
    Casnumber 98-08-8
    Molecularformula C7H2F6
    Molecularweight 200.08 g/mol
    Appearance Colorless liquid
    Boilingpoint 111-113 °C
    Meltingpoint -34 °C
    Density 1.506 g/cm³ at 25 °C
    Refractiveindex 1.364
    Flashpoint 34 °C (93 °F)
    Solubilityinwater Insoluble
    Vaporpressure 20.1 mmHg at 25 °C

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

    Packing & Storage
    Packing 500 mL amber glass bottle with secure screw cap, labeled "2,4,6-Trifluorobenzotrifluoride," hazard symbols, batch, and supplier details.
    Shipping 2,4,6-Trifluorobenzotrifluoride is shipped as a non-hazardous liquid in tightly sealed containers to prevent leaks and contamination. Containers are clearly labeled and protected from extreme temperatures and sunlight. Standard transport regulations apply, but check local guidelines for any specific requirements. Handle with care to avoid spills and inhalation.
    Storage **2,4,6-Trifluorobenzotrifluoride** should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Store in tightly sealed containers, protected from moisture and direct sunlight. Ensure proper labeling and keep away from heat and flames. Use appropriate chemical storage cabinets for flammable liquids, and follow all relevant safety regulations.
    Application of 2,4,6-Trifluorobenzotrifluoride

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

    Our facility produces high-purity 2,4,6-Trifluorobenzotrifluoride for customers in multiple specialized chemical manufacturing sectors. This material supports downstream producers with critical performance in established industrial processes, where precise formulation and regulatory compliance determine finished product quality and reliability.

    1. Agrochemical Intermediate Synthesis

    Producers in the agrochemical sector use this compound as a building block for advanced herbicide and fungicide active ingredients. Its high fluorine content improves the metabolic stability of target molecules in crop protection formulations. Downstream customers integrate this intermediate in multi-step synthesis, requiring strict in-process controls and compliance with regulations regarding residual fluorinated compounds in agricultural products.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius MRLs for agrochemicals
    • European Union Regulation (EC) No 1107/2009 for crop protection substances
    • US EPA guidelines for pesticide technical materials
    • ISO 9001 quality management in chemical synthesis

    Typical usage ratio

    • Raw material accounts for 15–35% of the starting material mass in the coupling step, adjusted by target yield and process route

    Downstream process integration

    • Fed at the nucleophilic aromatic substitution or cross-coupling reaction stage
    • Reacts with phenolic or amine substrates under controlled temperature and pressure
    • Residual content in the final API regulated by downstream purification and QC

    Final product types

    • Selective herbicides (e.g., trifluoromethylated anilines, phenoxy herbicides)
    • Triazole and strobilurin fungicides
    • Intermediates for synthesis of fluorinated crop protection agents

    2. Advanced Electronic Chemical Manufacturing

    In the electronics sector, this chemical functions as a fluorinated solvent and fluorinating reagent during the production of photoresists, liquid crystal display (LCD) materials, and semiconductor coatings. Its thermal and chemical stability meets strict requirements for high-purity processing. Close monitoring ensures trace-level introduction into formulas, with waste management aligning with sector environmental directives.

    Industry compliance standards

    • IEC 61249-2-21 for halogen content in printed circuit boards
    • RoHS 2011/65/EU restriction of hazardous substances
    • SEMATECH purity guidelines for semiconductor-grade chemicals
    • ISO 14001 environmental management

    Typical usage ratio

    • Concentration ranges from 1–8% by mass in solvent blends or precursor baths

    Downstream process integration

    • Introduced at microfabrication or cleaning steps in wafer production
    • Serves as a specialty solvent in lithography processes
    • Possible role as a precursor for fluorinated monomers in LCD and OLED manufacturing

    Final product types

    • Photoresist materials for integrated circuits
    • Liquid crystal and OLED display films
    • High-reliability semiconductor coatings

    3. Pharmaceutical Intermediate Synthesis

    This molecule supports APIs and pharmaceutical intermediates where fluorine functionality modulates biological activity, absorption, and stability. Medicinal chemistry groups employ this compound in key arylation and fluorination strategies as part of final-stage or penultimate intermediate syntheses. Stringent documentation and traceability apply, including full batch release analysis and risk assessment of extractables.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. monographs for residual solvents
    • REACH Regulation (EC) No. 1907/2006 substance registration
    • ISO 9001 process control in pharmaceutical synthesis

    Typical usage ratio

    • Usage rate at 8–20% relative to total synthetic input, basis adjusted based on target molecular scaffold

    Downstream process integration

    • Charged to arylation or trifluoromethylation steps in API intermediate synthesis
    • Monitored for potential hazardous by-products and residual solvent traces
    • Integration with column purification and in-process QC

    Final product types

    • Fluorinated pharmaceutical intermediates
    • Small-molecule APIs containing trifluoromethyl aryl groups
    • Research compounds for oncology and CNS therapeutics

    4. Specialty Coating Formulations

    This fluorinated aromatic contributes to high-performance industrial and aerospace coating systems, providing hydrophobicity and environmental resistance in thin films. Formulators use it as a co-monomer or additive in polyurethane resins or silicone-based coatings. Its use must comply with application-specific emissions and workplace safety standards during manufacturing and application.

    Industry compliance standards

    • OSHA 29 CFR 1910.1200 for hazardous chemical labeling
    • VOC content regulations under US EPA 40 CFR Part 59
    • REACH SVHC compliance for finished coatings
    • ASTM D5402 solvent resistance test for coatings

    Typical usage ratio

    • Dosage between 0.5–7% of total resin content, modified based on target hydrophobicity and film durability

    Downstream process integration

    • Blended into resin during pre-polymerization or post-additive stages
    • May require dissolution in approved solvents for homogeneous mixing
    • Controls on emission and exposure during application and curing

    Final product types

    • Aerospace-grade protective coatings
    • Anti-corrosion coatings for chemical equipment
    • Non-stick and stain-resistant architectural paints

    5. Advanced Polymer Synthesis

    Processors incorporate this raw material into specialty fluorinated polymers to enhance performance in highly demanding environments. It provides thermal stability, low surface energy, and chemical resistance in formulations for membranes and sealing components. Accurate dosing and controlled conditions ensure reproducibility in bulk polymerization or solution polymerization processes.

    Industry compliance standards

    • ISO 10993-5 cytotoxicity if intended for medical or food contact use
    • UL 94 flame rating for polymer materials
    • ASTM D543 chemical resistance testing
    • REACH SVHC screening for polymer additives

    Typical usage ratio

    • Loading at 2–14% by weight of monomer feed, with adjustment based on target polymer properties and processing method

    Downstream process integration

    • Introduced at polymerization reactor charging step
    • May require pre-dissolution or activation for co-polymerization
    • Polymer finalization includes devolatilization and granulation

    Final product types

    • Engineered fluoropolymers for electronics
    • Chemical-resistant gaskets and seals
    • Microporous membranes for filtration systems
    Free Quote

    Competitive 2,4,6-Trifluorobenzotrifluoride 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.

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    Certification & Compliance
    More Introduction

    2,4,6-Trifluorobenzotrifluoride: A Core Product from Our Manufacturing Line

    From Our Production Floor: Bringing 2,4,6-Trifluorobenzotrifluoride to Industry

    Decades on the plant floor have shown us how a selective approach in aromatic fluorination shapes the success of specialty chemicals. Among our fluorinated aromatics, 2,4,6-Trifluorobenzotrifluoride has stood out for clients working in advanced polymers, electronics, and crop science. Having run this compound through the loop from reactor start-up to final filtration, you learn the quirks and strengths that don’t make it onto a spreadsheet. Our routine production batches center on a purity grade over 99.5%, a mark we reach through controlled addition of reagents and continuous monitoring for common impurities such as isomeric trifluorotoluenes and residual starting materials.

    The Difference Begins with Real-World Manufacturing

    The journey for 2,4,6-Trifluorobenzotrifluoride starts with fluorobenzene derivatives and high selectivity during chlorination and subsequent fluorination. This multi-stage synthesis demands conditions few tolerate—a tight temperature window, robust venting, and constant vigilance for runaway exotherms. These are not details from a catalog; they come from years spent optimizing scale-up, fighting byproduct formation at every batch. During quality checks, routine use of GC and NMR ensures that we catch even the most elusive co-products, which can undermine downstream yields in fine chemical production. Stability under typical atmospheric moisture sets this product apart from more labile trifluoromethyl benzenes, reducing storage headaches for clients.

    Model and Specifications Rooted in Operational Excellence

    Current outputs run under the internal reference model TF-BTF-246, which our team applies in both solvent-grade drums and higher-specification lots for electronics use. Batch reports record moisture content below 200 ppm, trace metal residues consistently under 1 ppm for iron and copper, and color tracked by APHA below 10 for top-grade shipments. We take the view that lot retention matters, so our warehouse policy avoids batch mixing. Tanks are nitrogen-blanketed, not simply capped, to lock down hydrolysis and oxidation even during long-term storage.

    Physical properties only tell part of the story. 2,4,6-Trifluorobenzotrifluoride carries a molecular weight of 214.05 g/mol and boils in the ballpark of 139–142°C. Low aqueous solubility, combined with strong organic solvent compatibility, makes it a workhorse for specialty coatings and a robust intermediate in active ingredient manufacturing. Several research institutes have praised its chemical resilience, especially where long product lifetimes or exposure to harsh reagents are common.

    What 2,4,6-Trifluorobenzotrifluoride Brings to Downstream Chemistry

    Looking back at the process scale-ups, one lesson stands out: reliable intermediates drive innovation at the bench and pilot plant. Our 2,4,6-Trifluorobenzotrifluoride is used by customers turning out fluorinated aromatics for critical industries. Most see value in the way its three fluorine atoms tune electron density on the ring, providing routes into aryl aminations, metal-catalyzed couplings, and the kind of nucleophilic substitutions you encounter in advanced agrochemical synthesis. During process consultations, clients pointed out that our product enabled higher final yields in their coupling and substitution reactions, thanks to a low isomeric impurity profile.

    Custom polymer groups depend on this building block for both backbone rigidity and chemical inertness. Several partners in the semiconductor market choose this fluorinated aromatic over less substituted alternatives because its symmetrical substitution pattern lends a balance of polarity and processability. It’s common knowledge in the trade that the 2,4,6-trifluoro pattern prevents side reactions prevalent in less fluorinated rings, meaning fewer purification steps downstream and real cost savings on production campaigns.

    2,4,6-Trifluorobenzotrifluoride in Agrochemical and Pharmaceutical Applications

    Our customers don’t just buy another solvent—they invest in reliability for syntheses that set the tone for new molecule development. Several agrochemical producers look to this aromatic for its unique reactivity. Its fluorinated ring acts as a vector for introducing both electron-withdrawing and sterically demanding substituents, a feature beneficial in both active compound and protecting group chemistry. Over years working with pharmaceutical partners, we have supported projects that demand lower levels of halide and trace aldehydes, tracking these with high-sensitivity analytical methods.

    Technical teams in pharmaceuticals measure the subtle shifts in NMR spectra, searching for aberrations that may hint at process-side reactivity. A recurring theme in feedback: batches from our manufacturing line lead to smoother scale-up of functionalization steps, especially where precise selectivity is crucial. In bioconjugation work, process chemists appreciate that 2,4,6-Trifluorobenzotrifluoride opens doors for introducing fluorine in a controlled, predictable manner.

    Distinguishing Features Compared to Other Aromatic Trifluoromethyl Compounds

    Manufacturing lines across the world churn out a range of trifluoromethylated aromatics, but not all share the same stability, reactivity, or impurity profile. The 2,4,6-substitution pattern creates a uniquely shielded aromatic system, resulting in reduced para and ortho reactivity relative to 4-trifluoromethylbenzotrifluoride or 3,5-difluorobenzotrifluoride. Feedback from electronics sector partners has stressed that this symmetry supports consistency in dielectric properties, an edge in coatings for printed circuit boards and specialty films.

    Low vapor pressure, coupled with resistance to base-catalyzed decomposition, gives users more flexibility in storage and blending. Unlike more reactive fluorinated aromatics, 2,4,6-Trifluorobenzotrifluoride does not hydrolyze or degrade under typical warehouse conditions. Customers moving from 2,3,4-trifluorobenzotrifluoride to our product report fewer extractables during resin curing cycles, allowing for cleaner final articles with minimal post-cure treatment.

    Operational Insights: Safety and Handling

    From experience, the easy part is making a kilogram batch in the lab. The challenge sets in with tanker loads. Our operators have settled on best practices: transfer under closed systems, regular drum sampling, and continuous monitoring for trace HCl or other volatile byproducts. Workers on the line suit up with appropriate PPE, as skin contact with neat trifluoromethyl aromatics should be avoided. Over many years without injury reports, we credit clear procedures and early detection of line leaks or pressure imbalances.

    We willingly share with our customers lessons learned from decades of filling, blending, and dispatching this product. The drum residue management plan allows us to recapture and recycle off-spec or surplus material, turning waste streams into reprocessable feedstock and reducing overall environmental impact. Factory air handling systems get regular retrofitting based on how actual production volumes evolve over time.

    Meeting Regulatory and Sustainability Expectations

    Keeping pace with both regional and global expectations, each process batch runs through a compliance checklist, not just a technical spec sheet. Our output matches or exceeds REACH registration standards and is produced in a plant certified under ISO 9001:2015 and ISO 14001:2015. Traceability back to raw material sources forms the backbone of our quality assurance routine. During every audit, we present run records and analytical results—no surprises, no missing pages. This is a mindset sharpened by the realities of upstream disruptions and shifting regulatory landscapes.

    A growing number of clients ask about the lifecycle and environmental profile of our fluorinated aromatics. All spent streams undergo neutralization and removal of persistent organofluorines before effluent discharge. Our process engineers continuously seek catalysts and solvents that enable cleaner synthesis paths, shortening reaction times and minimizing halogenated byproducts. Energy and resource audits have sparked upgrades in refrigeration and waste gas scrubbing, movements that lower our operational footprint and answer the growing call for greener manufacturing.

    Supporting Client Innovation: Examples from the Field

    Engineers and technical teams from various industries regularly visit our site for collaborative troubleshooting. On a project with a specialty plastics firm, the downstream process had been plagued with off-odor and yellowing during extrusion. After a root-cause analysis, we found that tiny levels of halogenated side products from earlier suppliers triggered these faults. Switching to our 2,4,6-Trifluorobenzotrifluoride, the client logged production runs with consistently low impurity levels, opening the way for longer campaign durations and a drop in reject rates. That win came not from theoretical specs but from in-the-field experience and open communication.

    Another case involved custom crop protection products. A partner’s synthetic pathway stalled due to unpredictable side product formation in aromatic substitution. Joint work with our process chemists pinpointed how minor changes in raw material quality could trigger a domino effect, impacting their conversion and isolation yields. We implemented tighter raw material screening and fine-tuned process controls, which led to a measurable uptick in their active ingredient output.

    Shipping and Storage Informed by Factory Practice

    Drums and tankers leave our loading dock with more than just filled forms and checked boxes. Each shipment follows a tracked chain of custody, with regular temperature logging for longer routes. Warehouse workers follow a set schedule for air quality testing, using mobile sensors to alert us of even minor vapor build-ups. Double-sealed gaskets and corrosion-resistant liners for bulk shipments avoid mid-transport compromise. The lesson here is simple—invest in upfront packaging improvements, and both customers and producers enjoy fewer delays, fewer claims, and lower costs from spoiled inventory.

    We don’t shy away from customer queries about how our storage systems work. Instead, we invite teams to tour the facility, view the inert gas safeguard systems in place, and see firsthand how small improvements—like anti-static drum linings—cut down on workplace hazards and product degradation. Such transparency not only builds trust but also sets industry benchmarks to which newcomers aspire.

    Next Steps: Shaping the Future of Fluorinated Aromatics

    Markets will keep pushing for more selective, cleaner, and cheaper sources of critical intermediates. We hear from R&D teams across the spectrum—battery materials, polymer blends, fine chemicals—who look to us for input on how to adapt 2,4,6-Trifluorobenzotrifluoride for the next challenge. We return to pilot trials and tweak parameters, always noting how the smallest process variables cascade from glassware to reactor to customer’s line.

    Improvements don’t just appear overnight. Feedback from end users inspires in-house trials, tighter statistical controls, and trials with alternative feedstocks. Our long-standing view remains that durable partnerships, built on real transparency and honest sharing of technical detail, deliver more than any data sheet or glossy brochure. The success stories, lessons, even mishaps—these shape every new production batch as much as any recipe or piece of plant equipment.

    What to Expect in the Coming Years

    With regulatory landscapes tightening and application fields widening, manufacturers who can offer reliability, documented traceability, and constant technical feedback will set the pace. 2,4,6-Trifluorobenzotrifluoride—carried from plant floor to customer line—illustrates the value that experienced, detail-focused manufacturing brings to modern industry. After years of working at the junction of chemistry and applied engineering, we understand that putting out a higher-spec product isn’t a one-off achievement. It’s a routine, punctuated by feedback loops, careful analysis, and real-time improvements based on hands-on experience.

    We commit to supporting every user—researcher or plant manager—through products that don’t just pass tests but raise the bar in purity, stability, and process safety. In the story of high-value fluorinated intermediates, our 2,4,6-Trifluorobenzotrifluoride isn’t simply another name on a stock list. It’s the result of persistent inquiry, careful scale-up, and a daily focus on the needs of industries whose innovations depend on materials of unflagging consistency.