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4-(Trifluoromethoxy)Ethylaminobenzene

    • Product Name 4-(Trifluoromethoxy)Ethylaminobenzene
    • Alias p-(Trifluoromethoxy)phenetidine
    • Einecs 629-334-7
    • 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

    226502

    Chemical Name 4-(Trifluoromethoxy)Ethylaminobenzene
    Molecular Formula C9H10F3NO
    Molecular Weight 205.18 g/mol
    Cas Number 24171-42-8
    Appearance White to off-white solid
    Boiling Point Unknown
    Melting Point Unknown
    Density Unknown
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles CCNCC1=CC=C(C=C1)OC(F)(F)F
    Inchi InChI=1S/C9H10F3NO/c1-2-13-7-3-5-8(6-4-7)14-9(10,11)12/h3-6,13H,2H2,1H3
    Storage Conditions Store in a cool, dry place, tightly closed
    Purity Typically ≥98%
    Synonyms 4-[(Trifluoromethoxy)phenyl]ethylamine
    Refractive Index Unknown

    As an accredited 4-(Trifluoromethoxy)Ethylaminobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 4-(Trifluoromethoxy)ethylaminobenzene, labeled with safety information, batch number, and hazard pictograms.
    Shipping **Shipping Description:** 4-(Trifluoromethoxy)ethylaminobenzene is shipped in tightly sealed, chemical-resistant containers. The package is clearly labeled according to regulatory guidelines and includes a Safety Data Sheet (SDS). Shipping occurs under ambient conditions unless otherwise specified and complies with all local, national, and international hazardous material transport regulations.
    Storage 4-(Trifluoromethoxy)ethylaminobenzene should be stored in a tightly sealed container, away from direct sunlight, heat sources, and moisture. Keep it in a cool, dry, and well-ventilated area, ideally in a designated chemical storage cabinet. Avoid storing near incompatible substances like strong oxidizers or acids. Proper labeling and handling using personal protective equipment are essential for safety.
    Application of 4-(Trifluoromethoxy)Ethylaminobenzene

    Applications of 4-(Trifluoromethoxy)Ethylaminobenzene in Industrial Manufacturing

    As an integrated chemical raw material producer, we supply 4-(Trifluoromethoxy)Ethylaminobenzene to several mainstream manufacturers who require its distinctive structural properties in modern organic synthesis. Proven performance drives its adoption in fine chemicals, pharmaceuticals, agrochemicals, specialty dyes, and advanced material sectors.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients

    End-users in the pharmaceutical sector deploy this compound as a building block in the synthesis of several advanced intermediates, particularly for the preparation of aromatic amines and substituted benzene derivatives that appear in antihypertensive and anticancer drug classes. Its electron-withdrawing trifluoromethoxy group enables targeted functionalization, improving yields during coupling steps and facilitating cleaner downstream transformations. Production focuses on batch reactor synthesis, monitored by in-process HPLC to maintain intermediate purity.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for API Production)
    • EU GMP Part II (Raw Materials for APIs)
    • USP <795>, <823> guidance for raw materials
    • EMA and US FDA registration standards

    Typical usage ratio

    • As an intermediate, 0.5–2.2 molar equivalents per active moiety depending on the complexity of the API scaffold; proportion adjusted to minimize impurities while maximizing yield

    Downstream process integration

    • Added during early or mid-stage condensation or amination steps in multi-step API synthesis; introduced under controlled temperature and inert atmosphere to preserve the functional group

    Final product types

    • Sartan class antihypertensive drugs
    • Fluorinated oncology intermediates
    • Research-stage kinase inhibitors
    • Bulk APIs for contract manufacturing organizations (CMOs)

    2. Agrochemical Synthesis: Herbicide and Insecticide Building Block

    Manufacturers in the crop protection sector use this molecule in the synthesis of select fluorinated herbicides and insecticides. The molecule’s trifluoromethoxy group enhances stability and bioactivity, which is critical for targeting specific enzyme systems in weed and pest control. Reactions generally occur under catalytic hydrogenation or cross-coupling conditions, following strict in-plant handling to comply with occupational exposure limits.

    Industry compliance standards

    • FAO/WHO specifications for technical active substances
    • EPA 40 CFR Part 180 (Tolerance for pesticide residues)
    • ISO 9001:2015-certified manufacturing environments
    • REACH registration for imported substances

    Typical usage ratio

    • 1.0–1.8 molar equivalent per active ingredient, adjusted according to crop target and regulatory restrictions on active substance concentration

    Downstream process integration

    • Functions as a key nucleophile or electrophile in late-stage cross-coupling, often under palladium catalysis; raw material dosing measured for conversion efficiency

    Final product types

    • Trifluoromethoxy-substituted herbicides (selective broadleaf weed control)
    • Systemic insecticides for seed treatment
    • Combination pest control agents
    • Intermediate stock for custom synthesis

    3. Material Science: Polymer and Coating Modification

    Producers in advanced materials use this specialty amine derivative to introduce fluorinated characteristics to high-performance polymers and coatings. Its integration enables the design of hydrophobic and chemically resistant surfaces, meeting demands for protective films or specialty adhesives. The raw material enters at the copolymerization or surface-grafting phase under controlled temperature to prevent decomposition, with process adjustments for viscosity and molecular weight control.

    Industry compliance standards

    • ISO 14001:2015 for environmental management
    • ASTM D2578 for surface energy testing
    • RoHS Directive 2011/65/EU for electronics applications
    • EN 71-3 (for coatings used on toys and children’s products)

    Typical usage ratio

    • 3–10 wt.% of monomer mix for copolymer systems; ratio adapted based on target film thickness and performance requirements

    Downstream process integration

    • Introduced during the monomer feed stage in batch or continuous reactors, often with radical initiators, or directly applied as a modifying agent in post-polymerization grafting

    Final product types

    • Fluorinated protective coatings for industrial equipment
    • Hydrophobic films for electronics and optics
    • High-durability adhesives
    • Insulating materials for automotive or aerospace applications

    4. Specialty Dyes and Pigments Synthesis

    Dye and pigment manufacturers utilize this compound to achieve desirable hues and fastness properties in functional colorants. The electron-withdrawing trifluoromethoxy group increases chroma stability under UV exposure, and supports synthetic transformations to produce fine-tuned azo, anthraquinone, and phthalocyanine derivatives. The raw material is introduced in key diazotization or reduction steps, and its amount is determined according to batch size and target shade.

    Industry compliance standards

    • OEKO-TEX Standard 100 (chemical safety in textiles)
    • REACH Annex XVII (specific restrictions on aromatic amines)
    • DIN EN ISO 105-X12 (color fastness specification)
    • Eco-Passport for chemicals used in dye manufacturing

    Typical usage ratio

    • 0.8–2.5 molar equivalents per colorant molecule, fine-tuned for desired chromophore and resistant properties; based on dye formulation and substrate

    Downstream process integration

    • Blended during controlled diazotization or condensation reactions, with pH and temperature regulated for yield and color purity

    Final product types

    • UV-stable specialty dyes for performance textiles
    • Solvent-resistant pigments for plastics and paints
    • High-performance colorants for automotive coatings
    • Inkjet and digital printing pigments

    5. Electronic Chemicals: Photoresist and Semiconductor Processing

    Major photoresist and electronic chemical manufacturers use this molecule to synthesize advanced intermediates for microelectronic fabrication. The addition of trifluoromethoxy functionality enhances resistance to plasma etching and improves line-edge definition in photolithography. It is commonly introduced during the late-stage synthesis of chemistries for positive and negative resists. Critical quality parameters include absolute material purity and consistent batch lot characteristics verified by GC/HPLC analysis.

    Industry compliance standards

    • SEMI C3 specification (chemicals for microelectronics processing)
    • IEC 62474 (material declaration in electronics)
    • Cleanroom ISO 14644-1 classification
    • RoHS compliance for device manufacturing

    Typical usage ratio

    • 0.5–2.0 wt.% of resist matrix for pattern transfer formulations; adapted per substrate and required lithographic resolution

    Downstream process integration

    • Incorporated during monomer synthesis or as a modifying agent in solvent blends for photoresist formulations, with filtration through 0.1 μm to remove particulates

    Final product types

    • Photoresist formulations for IC fabrication
    • Specialty etch-resistant chemicals
    • Microelectronic interlayer coatings
    • Wafer processing additives

    6. Fine Chemicals: Custom Synthesis of Fluorinated Aromatics

    Custom synthesis suppliers and contract manufacturers rely on this aromatic amine as a key starting material in the production of tailored fluorinated compounds for research, OLED materials, and analytical standards. Its predictable reactivity profile supports efficient routes to customized molecules targeting next-generation functional applications. End users prioritize traceability and consistency, verified through supplier batch documentation and spectral quality controls.

    Industry compliance standards

    • ISO 9001:2015 quality assurance for batch traceability
    • Good Laboratory Practice (GLP) for analytical intermediates
    • REACH registration and transport labeling
    • SDS documentation in line with GHS classifications

    Typical usage ratio

    • 0.2–1.5 equivalents per synthesized target molecule, depending on reaction type and final product requirement; adjusted for lab, pilot, or production scale

    Downstream process integration

    • Introduced as a defined reactant in nucleophilic aromatic substitution, Buchwald-Hartwig coupling, or oxidation protocols; processed in controlled environments for reproducibility

    Final product types

    • Research-grade fluorinated standards
    • Early-stage pharmaceuticals and lead compounds
    • OLED intermediates for display technologies
    • Analytical reference chemicals
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    Certification & Compliance
    More Introduction

    Introducing 4-(Trifluoromethoxy)Ethylaminobenzene: Moving Chemistry Forward

    Understanding the Role of 4-(Trifluoromethoxy)Ethylaminobenzene in Modern Synthesis

    From the start, the chemical industry demands more than routine performance. Every compound in the lab or plant has to add real value—a simple truth for those who have spent years behind reactors and fume hoods. 4-(Trifluoromethoxy)Ethylaminobenzene draws increasing attention because its trifluoromethoxy substitution unlocks characteristics prized by pharmaceutical chemists, agrochemical researchers, and specialty materials producers. Every batch reflects decades of process refinement, experience with scale-up hazards, and an insistence on clean, reproducible outcomes. The model chemists work with today stands on proven routes and reliable analytical control. Actual product handled in tanks and drums offers purity exceeding 99%, with careful attention to trace moisture and uncontrolled impurities.

    Chemists regularly wrestle with questions about selectivity and structure-activity relationships when planning new molecules. Inserting a trifluoromethoxy group can feel like flipping a switch: electron distribution in the aromatic ring shifts, metabolic stability climbs, and the balance of lipophilicity often falls in the medicinal “sweet spot.” That is not speculation—it is a pattern repeated across kinase inhibitor libraries, antipsychotic leads, crop protectants, and dye intermediates. The ethylamino substituent brings another angle. Its flexibility allows rapid access to further analogues through N-alkylation, acylation, or reductive amination, letting discovery teams rapidly iterate structural variants. Each of these pathways brings its own practical headaches, of course, but starting from a high-purity intermediate saves untold time and money downstream.

    Why Our Process Matters: Experience in Manufacturing and Product Quality

    Too many synthetic procedures forget what goes wrong during scale-up. Glancing at lab notes or a literature method is one thing, but running a 3,000-liter batch is another world. We learned that solvents chosen for pilot scale sometimes later wreak havoc—with product oils refusing to crystallize or side reactions quietly building unwanted by-products not seen at bench-scale. Years spent refining the 4-(Trifluoromethoxy)ethylaminobenzene process have eliminated stumbling blocks like incomplete conversion, unwanted isomer formation, and tough-to-remove tars. Control at each step isn’t an afterthought, it is the baseline. Crude isolates facing filtration headaches receive process modifications: solvent swaps, temperature profiles with real time analytics, and careful introduction of seeds for robust crystallization.

    Every shipment matches the same high standard, sampled for HPLC and NMR confirmation, so contract partners know what they are receiving. True reproducibility matters far beyond compliance—it determines the success of downstream reactions, influences regulatory filing quality, and gives project planners a real foundation for scale-up projection. Our technical team regularly moves from kilo-lab to plant-scale, keeping process notes honest about exotherms, gas releases, phase behavior, and filtration problems—no shortcuts, because surgeons and researchers later depend on the compound behaving as predicted.

    Applications Driven by Function, Not Trends

    It’s tempting to pitch a specialty intermediate as a cure-all for chemical development, but actual project work reveals a sharper picture. Most customers do not buy 4-(Trifluoromethoxy)ethylaminobenzene as a generic building block. They commit to it because fluorinated aryl ethers outperform alternatives in specific synthetic campaigns. For one team, that means searching for an extra point of metabolic stability in CNS drug programs. For another, the benefit comes from the way the ethylamino function enables switching to different heterocyclic scaffolds without rebuilding the synthetic route from scratch. That flexibility feeds medicinal chemistry, process research, and even efforts in advanced material science.

    We have supplied this compound for efforts as diverse as development of new agrochemicals—where the challenge lies in surviving photolytic breakdown in field conditions—to OLED material design, where trace impurities can quench efficiency in a finished electronic device. Each field weighs purity and structure-function relationships differently. For all, a clean fluorinated intermediate can pave the way for simpler downstream chemistry, fewer purification headaches, and more meaningful SAR (structure-activity relationship) data. Rather than treat the material as only a physical supply, researchers build it into the intellectual core of new discovery.

    What Sets This Material Apart from Similar Aromatic Amines?

    Comparisons usually begin with cost, but for technical teams, subtle differences in reactivity and ease of modification drive decision-making. Ordinary ethylaminobenzenes run into performance limits—positions unadorned by electron-withdrawing groups suffer from rapid oxidative breakdown, tricky side-reactions, or unpredictable behavior under cross-coupling conditions. Substituting with a methoxy group brings moderate improvements, but the leap to trifluoromethoxy substitution delivers more than just incremental benefit. The trifluoromethoxy increases oxidative and hydrolytic stability. That directly impacts storage and handling—no slow degradation in warehouse drums, fewer worries about product shelf life, and more predictable blending with other specialty reagents.

    Anecdotal reports from the field reinforce this. Client teams running palladium-catalyzed couplings see higher yields and fewer dehalogenation side-products. Medicinal chemists report improved cell-based assay consistency when working with derivatives built from this backbone. Over dozens of client projects and plant campaigns, feedback flows both ways—material purity makes new chemistry possible, yet we hear about bottlenecks and adjust crystallization steps to meet tougher downstream limits. Instead of one-size-fits-all, we tune physical properties to practical realities: solubility in targeted solvent systems, melting points just right for solid handling, and moisture controls that meet exacting analytical criteria.

    Meeting Industry Demands with Trusted Chemistry and Engineering

    Many new aromatic and heteroaromatic fluorine-rich compounds never make it out of the literature because they are tough to produce on real-world timelines or require compromise with downstream plant chemistry—crude mixtures, finicky liquid phases, or hard-to-isolate tars. Over years, our own process chemists have hit the same walls. Each time, determination and laboratory experience lead to practical solutions: new solvent choices, continuous extraction cycles, empirically-tuned addition rates, and thermal controls that prevent run-away exotherms. It isn’t textbook work, but the deep dive pays off with a material that delivers every time, batch after batch.

    Bulk handling practices have shaped the evolution of our plant and technology. Early methods relied on distillation and batch crystallization. As demand grew and projects called for higher material flow, we invested in continuous crystallization modules, inline moisture monitoring, and advanced filtration trains that grab every last milligram of delivered compound. That not only raises output, but sharply reduces the risk of contamination and product losses so common to one-pot runs. Our operators and engineers have kept careful logs through every major campaign, and those notes improve consistency at scale.

    Supporting Innovation Across Industries

    Whether supporting pharmaceutical process R&D or chemical biology screening, the demands for reliable supply and ultra-high purity shape every operational decision. Early on, we encountered investigative teams screening dozens, sometimes hundreds, of fluorinated aromatic scaffolds. They needed every batch to perform across a range of further transformations—Suzuki couplings, acylations, alkylations—without surprise reactivity or residual catalytic poisons. That requirement forced us to develop cleanup steps that remove residual palladium, copper, or other transition metals below single-digit ppm levels. Testing every drum is a non-negotiable part of release, both for legal compliance and to build trust with chemists down the supply chain.

    In agrochemical pilot projects, applications teams focus more on targeted field use, regulatory constraints, and the impact of even trace byproducts on environmental fate. Many suppliers overlook these factors or cut corners on analytical detail. From our end, transparency helps. We support customer pilot runs, rapid troubleshooting, and provide full analytical documentation. Pure supply lets formulation chemists focus on optimizing activity—not solving headaches caused by barrel-to-barrel variability. That collaboration has delivered breakthroughs in pre-emergent weed control projects and extended crop protection candidates’ field stabilization times, all built on the shoulders of smarter intermediates.

    Regulatory and Quality Concerns: Learning from the Factory Floor

    Modern chemical manufacturing faces unyielding pressure from regulatory authorities: documentation, traceability, REACH and EPA obligations, and client-specific auditing. Many promising projects have collapsed not from technical limitations, but from paperwork gaps, inconsistent quality, or unresolved impurity identification. Having grown up in this climate, we maintain real traceability for lots, not just batch numbers scribbled in a notebook. Whenever a client needs to trace back, we provide analytical runs, batch genealogy, and full process condition logs that speed up the investigation. Experience on both sides—the plant floor and the regulatory desk—has shaped every standard operating procedure.

    Training rounds out our approach. Every plant operator, lab analyst, and maintenance technician knows the weight of their signature on a batch record. This internal culture has reduced recalls and batch failures, strengthened relationships with multinational partners, and delivered real supply reliability where other ventures stall. That up-front investment in training and documentation isn’t just insurance—it keeps us real and responsive on technical calls. When researchers update target impurity limits or a new regulatory guideline surfaces, the plant adapts quickly. That sort of institutional memory, shaped by pressure and learning, is tough to download from a website and forms the backbone of our long-term technical partnerships.

    Environmental and Sustainability Considerations

    New demands for green chemistry and industrial sustainability have shifted how process plants approach aromatic fluorinated compounds. To many outsiders, fluorination chemistry screams high cost, energy intensity, and environmental headaches. Only true for outdated processes. Over the last decade, process upgrades have steadily trimmed unit operations, reduced reaction mass intensity, and eliminated most liquid waste streams that typically plague these syntheses. By reclaiming solvents, recycling reaction by-products where possible, and slashing reagent overuse, we’ve both trimmed operating expenses and taken a chunk out of the environmental load.

    Challenges remain. Perfluorinated impurities, unregulated vent emissions, and complicated solid waste streams can still trip up even the most disciplined operations. Instead of sweeping these under the rug, we work with external labs and client teams to characterize and minimize emissions, keep by-products under control, and adjust quench procedures without sacrificing yield. The shift is gradual but steady: more closed-loop recycling, pressure filtration systems to cut washing waste, and recycled input materials when purity allows. Rather than treat “green chemistry” as a slogan, we work toward reducing not just carbon footprint but the whole lifecycle impact, from raw materials to plant closure.

    Why This Compound Has Earned Trust Across Applications

    Real trust in specialty chemicals grows from repeated delivery and technical honesty. Across pharmaceutical, agrochemical, or materials science projects, our clients bet on us to deliver the same high standard every time. More than anything, 4-(Trifluoromethoxy)ethylaminobenzene demands this: precision in make, rigorous handling, and unflagging batch-to-batch repeatability. It isn’t magic. Years of feedback, continuous plant upgrades, deeper analytical capability, and above all, the daily attention of people who care about chemistry—the ones who troubleshoot filters, tweak wash cycles, and keep an eye on thermal monitors at shift change.

    Feedback from partner labs matters. We regularly review reports of reaction yields, impurity drift, and even storage conditions in far-away research sites. Each project teaches new lessons—minor protocol tweaks, cold-chain reminders, desiccation protocol updates—which then loop back into our manufacturing process. This reflection and recalibration doesn’t just refine the product, it helps set new benchmarks for what a specialty intermediate can deliver. Others may chase volume targets or commoditize the business. For us, building a reliable stream of 4-(Trifluoromethoxy)ethylaminobenzene means leaning on process intelligence, experienced hands at every stage, and a real partnership with those who run the project benches or keep the plant humming.

    Building Value Through Collaboration and Real Manufacturing Expertise

    Experience in chemical process development shapes every lot we make. That practical knowledge—dialing in reaction concentration, engineering for safe venting, and handling crystallization quirks—translates to product quality and user confidence at every link in the supply chain. Our R&D team works side by side with plant operators and quality analysts to build not just consistent chemistry but smooth workflows, quicker response to field requests, and tech transfer capabilities that keep projects on schedule. Each advance in manufacturing—a tweak in temperature control, a new purification bed, smarter mixing—builds on the last, cementing reliability not through paperwork alone but through hard-earned process gains.

    For all the talk about digitalization and AI in the plant, nothing replaces the experience learned by people with hundreds of batches under their belts. Practical lessons shape updates to standard operating procedures and training for newcomers. Advanced instrumentation helps, but raw experience—like knowing when a reaction smells off or a filtrate runs thin—makes the real difference in delivering a product trusted from preclinical bench chemists to commercial formulators. We keep improving, inch by inch, with eyes wide open to customer feedback and the daily reality of production floors.

    Looking Forward: Opportunities and Continuous Improvement

    No chemical product stands still. Industrial users and academic collaborators continuously push new boundaries: moving from discovery-phase synthesis to registered starting materials, working toward niche material applications, or responding to new market or legislative challenges. Each shift brings requests for bespoke modifications—specific impurity controls, alternate crystalline forms, or adapted reaction schemes tuned to local plant capabilities. We see this not as a burden but as a steady source of technical progress and a reminder why direct manufacturing experience counts.

    The future of 4-(Trifluoromethoxy)ethylaminobenzene rests on these collaborative advances. We keep close at hand a log of field requests: new polymorph screens, alternate salt forms, improved powder flow control, and custom packaging to match downstream plant constraints. These aren’t “added value features”—they grow from careful listening and translating bench chemistry reality into scalable, reliable, and safe process execution. Because real progress in chemical manufacturing rides on industry-wide participation—process chemists refining steps, analytical groups validating purity, and plant teams ensuring safe and predictable throughput.

    The Importance of Transparent, Experienced Chemical Production

    Transparent manufacturing, whether it’s batch notes, analytical methods, or tweakable SOPs, sets our plant apart and helps researchers and developers focus on what matters. Open dialogue lets us adapt quickly, fix problems before they mushroom, and deliver the steady supply chain projects run on. The goal remains unchanged: deliver reliable 4-(Trifluoromethoxy)ethylaminobenzene that fits customer ambition and project pace, supported by real stories from the shop floor—not theory or abstraction, but practiced technical insight.

    Looking back at years of process challenges and technical achievements, we know the material’s value grows with every challenge solved. The substance doesn’t just fill a specification—it helps companies, scientists, and engineers make real-world goods, develop safer pharmaceuticals, and move industries ahead. Each new project or application reflects the sum of that learning. By keeping things grounded in operational reality, we offer not just a better product, but peace of mind for every team putting it to work in tomorrow’s chemical solutions.