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3,5-Bis(Trifluoromethyl)-N-Ethylaniline

    • Product Name 3,5-Bis(Trifluoromethyl)-N-Ethylaniline
    • Alias 3,5-Bis(trifluoromethyl)-N-ethylaniline
    • Einecs 242-732-5
    • 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
    VTB
    Specifications

    HS Code

    446755

    Chemical Name 3,5-Bis(Trifluoromethyl)-N-Ethylaniline
    Molecular Formula C10H9F6N
    Molecular Weight 261.18
    Cas Number 328-69-8
    Appearance Colorless to pale yellow liquid
    Boiling Point 219-221 °C
    Density 1.406 g/cm3
    Purity Typically ≥98%
    Solubility Insoluble in water; soluble in many organic solvents
    Smiles CCNC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1
    Refractive Index n20/D 1.442
    Storage Conditions Store at room temperature, tightly closed, in a dry, well-ventilated place
    Flash Point 98 °C
    Ec Number 430-060-7

    As an accredited 3,5-Bis(Trifluoromethyl)-N-Ethylaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, tightly sealed with a screw cap, labeled with compound name, CAS number, and hazard warnings.
    Shipping 3,5-Bis(Trifluoromethyl)-N-Ethylaniline is shipped in tightly sealed containers under cool, dry conditions to prevent contamination and moisture absorption. Packages are labeled according to hazardous material regulations. Handle with care, avoiding heat and direct sunlight. Ensure compliance with local and international shipping guidelines for safe transport of chemicals.
    Storage Store 3,5-Bis(Trifluoromethyl)-N-Ethylaniline in a tightly sealed container, away from light, heat, and sources of ignition. Keep in a cool, dry, well-ventilated area, segregated from incompatible substances such as strong oxidizing agents. Use chemical-resistant containers and label clearly. Follow all applicable safety protocols and local regulations for storage of hazardous organic chemicals.
    Application of 3,5-Bis(Trifluoromethyl)-N-Ethylaniline

    Applications of 3,5-Bis(Trifluoromethyl)-N-Ethylaniline in Industrial Manufacturing

    As an advanced fluorinated aromatic amine, 3,5-Bis(Trifluoromethyl)-N-Ethylaniline supports key synthesis demands in high-value industrial applications. The following downstream segments represent actual areas where this material plays a critical technical role in manufacturing processes, with detailed compliance, dosage, integration, and product type references.

    1. Fluorinated Agrochemical Intermediate Synthesis

    Producers of next-generation agrochemicals incorporate this fluorinated aniline as an electrophilic coupling block in the synthesis of herbicide and pesticide actives. Its electron-withdrawing trifluoromethyl groups enable selective functionalization through Buchwald-Hartwig or Ullmann-type cross-coupling, particularly where high herbicidal activity and environmental stability are required. Process engineers adjust reaction stoichiometry to optimize yield against halogenated aryl partners, and in-situ QC tracks residual amine under process safety standards.

    Industry compliance standards

    • REACH registration (EC No 1907/2006) for intermediate use
    • OECD Guidelines for the Testing of Chemicals 108, 111 (physicochemical properties)
    • ISO 9001:2015 for chemical quality management
    • Relevant EPA Pesticide Registration (U.S. FIFRA)

    Typical usage ratio

    • 0.3–1.2 molar equivalents relative to target pesticide core; varies by active scaffold
    • Ratio adjusted based on desired fluorination density in target molecule

    Downstream process integration

    • Charged after deprotection or pre-activation step in batch reactors
    • Used as a controllable N-source during arylamine coupling stages
    • Removed overhead via solvent extraction post-reaction

    Final product types

    • Fluorinated phenoxy herbicides
    • Substituted pyrimidine insecticides
    • Trifluoromethylated azole fungicides

    2. Liquid Crystal Intermediate for Display Technology

    Manufacturers of specialty liquid crystals deploy this compound as an amine building-block during the synthesis of advanced, high-anisotropy nematic hosts. The strong inductive effects of the trifluoromethyl groups improve thermal and dielectric characteristics of the resulting liquid crystalline phases, meeting rigid display pixelation standards. Production batches require stringent QC to verify low metallic and halide trace levels, as dictated by electronic industry standards.

    Industry compliance standards

    • IPC-4101C (Specification for Base Materials for Printed Boards)
    • IEC 61249-2-7 (Materials for Printed Boards and Other Interconnecting Structures)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 14001 certification for environmental management

    Typical usage ratio

    • 0.5–2.5 molar parts per major core intermediate, adjusted by phase modulation targets
    • Ratio controlled via LC mixture formulation for viscosity and clearing point parameters

    Downstream process integration

    • Reacted with acid chlorides or anhydrides for nematic core construction
    • Purified via column chromatography or recrystallization for device-grade purity
    • Integrated into LC host formulation tanks prior to cell encapsulation for panel manufacture

    Final product types

    • High-transmittance liquid crystal display (LCD) panels
    • Active-matrix OLED precursors
    • Electro-optical switching films

    3. Advanced Pharmaceutical Intermediate Manufacturing

    Pharmaceutical synthesis routes targeting selective serotonin or dopamine receptor ligands may specify this material as an aryl amine precursor for trifluoromethylated N-alkylaniline scaffolds. Medicinal chemists value its electron-rich aromaticity for late-stage C-N bond formation, especially in structures requiring improved metabolic stabilities. Manufacturing follows cGMP requirements for APIs and strictly monitors identification and quantitation of any aniline impurities, using validated HPLC or GC-MS procedures.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP <823> Radiopharmaceuticals (where applicable in PET tracer synthesis)
    • EMA guideline: Impurities in new drug substances (EMA/CHMP/ICH/82260/2006)
    • 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • 0.6–1.4 fold per aromatic halide, depending on coupling protocol
    • Excess minimized by real-time HPLC analysis to control aniline carryover

    Downstream process integration

    • Introduced post-chlorination or via nucleophilic aromatic substitution step
    • Integrated within GMP synthesis line after validated intermediate release
    • Intermediate subjected to scale-up filtration and solid-state characterization prior to final API synthesis

    Final product types

    • Fluorinated CNS-active bulk drug substances
    • Specialty APIs for antipsychotic and antidepressant therapies
    • Intermediates for PET imaging agents

    4. High-Performance Polymer Additive Manufacture

    Chemical processors utilize this fluorinated aniline as a chain-modifying co-monomer for specialty polyimide and polyamide-imide resins. Its structure introduces high thermal stability and low dielectric constants into performance polymers, a requirement for the electronics and aerospace sectors. Formulation chemists control monomer feed ratios tightly, and processors execute purification processes that achieve ultra-low extractables, matching semiconductor-grade resin specifications.

    Industry compliance standards

    • UL 94 Standard for Safety of Flammability of Plastic Materials
    • IPC-4101E for polyimide base materials in electronics
    • ASTM D6456 for Polyimide Resin (Thermosetting)
    • ISO 10993-5 Biological evaluation (if medical device-related)

    Typical usage ratio

    • Up to 8% by weight of total monomer system, adjusted based on desired Tg and dielectric profile
    • Optimized experimentally for each polymer batch based on melt viscosity and end-use standards

    Downstream process integration

    • Fed during initial polymerization with dianhydrides under inert atmosphere
    • Excess monomer removed via sub-ppm solvent cleaning and devolatilization
    • Polymerized batches subject to FTIR and GPC for molecular weight confirmation

    Final product types

    • High-performance flexible printed circuits
    • Low-k dielectric films for microelectronics
    • Polyimide insulation used in aerospace cabling
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    Certification & Compliance
    More Introduction

    3,5-Bis(Trifluoromethyl)-N-Ethylaniline: A Closer Look from the Manufacturer’s Floor

    Understanding 3,5-Bis(Trifluoromethyl)-N-Ethylaniline

    Handling 3,5-Bis(Trifluoromethyl)-N-ethylaniline in production isn’t just about supplying another aromatic amine; it’s about serving customers who know exactly what they want for their synthetic goals. Its chemical structure, built around the aniline core with two trifluoromethyl groups on the aromatic ring and an ethyl group on the nitrogen, gives it a unique personality among fluorinated anilines. We manufacture this compound with an eye for purity and batch consistency because these features matter throughout a project’s lifecycle, from initial screening to process scale-up. Most researchers and formulators who choose this material seek an intermediate with a powerful electron-withdrawing influence from the trifluoromethyls while also looking to tune solubility and reactivity with the N-ethyl substituent.

    Behind the Scenes of Production

    In our facility, making 3,5-Bis(trifluoromethyl)-N-ethylaniline requires watching every variable. We pay attention to temperature ramps, reagent loading, solvent quality, and atmosphere control. Each batch draws on years of accumulated expertise. Cathodic protection, nitrogen blanketing, glass-lined vessels, and validated cleaning processes keep contamination risks low, so the finished product meets its specified profile. Our staff monitors color, melting range, GC-MS purity results, and other parameters before each shipment leaves the site. We keep comprehensive documentation for every lot. Sometimes that comes down to noticing a slight odor at the end of a workup or spotting a shift in a TLC spot. These are judgment calls informed by repeating the process over and over—not by reading manuals, but by standing over real reactors, day in and day out.

    Choosing the Right Model and Specifications

    For most of our pharmaceutical and agrochemical customers, traceability and rigorous analytical profiles matter even more than the headline assay number. Our typical product offers GC purity above 98%, with reference spectra and impurity data included. 3,5-Bis(trifluoromethyl)-N-ethylaniline comes as a crystalline solid, off-white to pale yellow, depending on storage and container conditions. Even small hints of colored byproducts signal upstream issues. Water or solvent residues get flagged, because minor contaminants can derail downstream reactions or lead to batch failures. We test for chloride, residual starting aniline, isomers, and process-derived marks. It’s the little details—QR-coded labels, tamper-resistant seals, single-source traceability for reagents and solvents—that separate a manufacturer’s offering from others.

    Where It Fits Best

    Most of the requests we see come from research pilots developing novel heterocycles, pharmaceutical intermediates, and specialty material blocks. The two trifluoromethyl groups on the 3 and 5 positions impact electron density dramatically, suppressing undesired side reactions during aromatic substitutions or metalation. Chemists also value the N-ethyl group for tuning lipophilicity and managing hydrogen bonding in target molecules, especially in medicinal or crop science applications. We routinely ship to labs scaling up sulfonamide syntheses, exploring new dye classes, and inventing ligands for catalysis. Sometimes the molecule finds its way into specialty polymers where thermal stability and hydrolytic resistance are essential.

    Differences from Other Anilines and Trifluoromethylated Compounds

    As a manufacturer, we see both the strengths and challenges of this compound, especially in comparison with other anilines or even methyl- or N-alkyl substituted variants. Some buyers ask for 3,5-bis(trifluoromethyl)aniline (without the N-ethyl), which brings higher crystalline melting points and lower solubility. The ethyl group not only shifts the melting range, making the compound easier to handle at room temperature, but also changes polarity just enough to improve compatibility in diverse organic solvents. As soon as the product shifts from small batch to hundreds of kilograms, these physical properties save time and resources. Stability improves with the N-ethyl; storage losses drop off, and end-users report lower degradation or color change over time—which means less waste and rework.

    Comparing 3,5-bis(trifluoromethyl)-N-ethylaniline to mono-trifluoromethyl anilines, the electron-withdrawing effect nearly doubles, impacting every downstream transformation. We often discuss these nuances with synthetic chemists—how the strong EWG behavior pushes selectivity in cross-coupling or halogenation runs, or how it tempers nucleophilicity so amide formations stay controlled. These aspects rarely come up in broad summaries, but they frame real-life decision-making in R&D routines. Even under identical reaction conditions, each substituent constellation gives the aniline backbone a different chemical voice. Our manufacturing documentation reflects these subtleties.

    Challenges in Handling and Solutions from Actual Experience

    Trifluoromethyl groups demand specific handling, both on the shop floor and in the laboratory. Vapors escape easily; trace impurities build up surprisingly in open handling. Shipping samples in glass ampoules rather than plastic avoids static buildup and unwanted leaching. We’ve worked through challenges like crystallization in transfer lines during winter or clumping under inadequate cooling. It’s tempting for newcomers to treat anilines as generic, but this molecule’s trifluoromethylation brings extra edge. We had to adjust our PPE and air extraction systems to offset minor offgassing, especially as loading rates increased. Training our staff on proper decanting techniques and HPLC prep kept batch integrity high and minimized skin contact risk.

    Downstream users often overlook solvent compatibility until they run into walling or phase-separation issues in their formulations. Conversations with customers lead to real process tweaks, like switching from relatively nonpolar diluents to more polar options or adding phase transfer agents. The storage environment—dry, moderate temperature, away from strong oxidants—plays a huge role in reducing hydrolysis or degradation over time. Even container headspace can matter, so we fill drums to reduce air volume, especially for long-haul shipments. Details like these reflect years of failures, fixes, and incremental gains in the chemical plant.

    User Feedback: The Real-World Proof

    We get specific feedback from customers working with novel heteroaromatic ring systems where standard nucleophilic aromatic substitutions stall out using plain N-ethyl aniline. Swapping in the bis(trifluoromethyl) version pushes yields higher and avoids tarry byproduct messes. Formulators in coatings and advanced polymer fields report that the combination of the two CF3 groups on the aromatic ring and the N-ethyl chain improves film hardness and chemical resistance. These aren’t just marketing lines—they’re claims substantiated by user trials and shared QC data from multiple consecutive runs. More than once, a project that flatlined with other intermediates hit its stride by changing this single raw material input.

    The analytical chemistry crowd appreciates our detailed certification approach. Even when a customer doesn’t specify by name, issues such as trace p-toluidine or ring-trifluoromethyl isomers can disrupt downstream HPLC, NMR, or LC-MS assays. We filter each batch by those standards, not just regulatory compliance. The result is less requalification work and fewer sudden surprises when scaling up from bench to pilot plant—which, as we’ve learned, saves weeks on a typical development calendar. Users ask for samples, try a small batch, and often return with feedback or a modified specification, which helps us fine-tune every future lot.

    Why Manufacturing Matters

    Anyone can sell a drum, but meeting commitments on this compound means building real relationships and technical dialog. Our experience in synthesizing, purifying, packing, and testing this aniline means issues get addressed before they ever arrive at a customer’s plant. When new impurities pop up, our response isn’t just to shrug and pass on the batch; production stops until the root cause points to an actionable process fix. It sometimes means rerunning a whole lot, tightening up temperature profiles, or revising cleanup stages. These aren’t visible to most buyers, but it’s where the difference gets made—especially for advanced intermediates destined for high-stakes applications.

    Shipping coordination is another layer many don’t see. Coordinating with forwarders about temperature swings during transit, or ensuring regulatory paperwork (especially for Asia-Pacific and European destinations), involves direct communication between our shipping desk and the carrier’s technical advisor. Customs delays, broken seals, wrong labeling—any one of these stumbles can cascade into missed production windows on the customer’s end. Reliable supply only happens when manufacturers own the complete chain from vessel to customer storage, so we push for answers instead of excuses.

    Regulatory and Sustainability Considerations

    The growing public and regulatory focus on fluorinated chemicals, especially PFAS and related compounds, drives us to examine the environmental footprint of every production run. We invest continuously in closed-loop recovery for spent solvents, waste stream monitoring, and emissions control. The industry faces stricter rules, especially in Europe and the Americas, aimed at trace fluorinated organic compounds in effluent waters and atmospheric discharges. Ongoing staff training, regular third-party environmental audits, and developing greener alternatives in the synthetic steps underpin our daily work. While 3,5-bis(trifluoromethyl)-N-ethylaniline remains in demand for its functional properties, we know customers want assurance it wasn’t produced in a way that leaves future liability.

    We’ve faced requests for documentation relating to sustainability metrics—carbon reporting, life cycle data, and even renewable feedstock percentages. That’s why we document not just our materials but also our energy and water use, with periodic reviews to spot improvement opportunities. Investing in new abatement and recovery tech brings costs, but long-term partnerships with multinational formulators depend on traceable, responsible manufacturing. Our ongoing job includes not just making and selling chemicals, but responding and adapting to a world that expects more from every part of that supply chain.

    Innovations and Future Directions

    Chemistry never stands still. We track literature for improved synthetic pathways—catalytic trifluoromethylation techniques, greener oxidants, or continuous flow options that reduce waste. Every process change on our line starts with a clear validation and customer dialogue. For a custom batch of 3,5-bis(trifluoromethyl)-N-ethylaniline headed to a novel oncology program, a customer wanted trace catalyst content lower than the norm. Our team reconfigured the reaction, adopted a new filtration medium, and hit the tighter spec comfortably—while making sure yield and purity didn’t drop. These real-world tweaks only come from direct dialog between the manufacturer and lab scientists at both ends.

    Requests for higher purity, tailored particle size, or bespoke packaging feed into our development queue. Automated monitoring and real-time analytics on the line speed up troubleshooting and batch release, closing the loop between QC, production, and user feedback. Our operational commitment extends from the shop floor up to the R&D lab, with teams cross-trained so that everyone understands what happens both in the flask and on the line. The results get shared not through memos, but in long-form production notes and direct team talks.

    Looking Ahead: Commitment to End-Users and Quality

    No matter how advanced the market becomes, the need for consistent, transparent, and high-quality intermediates remains unchanged. Each drum of 3,5-bis(trifluoromethyl)-N-ethylaniline represents hundreds of careful steps—intensive cleaning, validated analytical runs, rework for batches that don’t quite hit the mark. We invest in each of these not because a distributor requires it, but because end-users depend on inputs that won’t sabotage their research timelines or cost them in rework.

    When development teams specify our product, they rely on more than a spec sheet. They stake valuable projects on our attention to detail and willingness to respond fast, share process updates, and troubleshoot issues openly. We know, because our own teams expect suppliers who deliver the same level of detail, transparency, and accountability—standards we hold for every shipment out the door. The journey from raw materials to the labeled drum isn’t glamorous, but it builds the confidence that every successful synthesis run and new drug candidate program requires. That’s the real mark of a committed manufacturer.

    The Value of Direct Manufacturing

    Experience counts in shaping a better supply chain. Distributors and resellers serve many needs, but the true backbone of specialty chemicals lies with the people who scale up, manage risk, and keep customers in close communication. With 3,5-bis(trifluoromethyl)-N-ethylaniline, this means not just reacting to market requests, but anticipating challenges before they hit the plant floor at a customer site. It’s about sharing data openly, owning up to snags, and pushing for incremental excellence in every cycle.

    For development and technical teams who rely on our material, we stand ready to answer in-depth questions, provide supporting data, and adjust production approaches based on new chemistries. Whether it’s for pharmaceuticals, advanced coatings, or novel catalysts, our direct approach ensures that those who choose our 3,5-bis(trifluoromethyl)-N-ethylaniline receive not just a drum or bag, but a partner in their innovation process. Our team’s accumulated knowledge, commitment, and manufacturing discipline go into every lot—so our customers keep building, discovering, and improving, project after project.