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4-(Trifluoromethoxy)Aniline

    • Product Name 4-(Trifluoromethoxy)Aniline
    • Alias p-(Trifluoromethoxy)aniline
    • Einecs 629-036-6
    • 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

    959749

    Name 4-(Trifluoromethoxy)aniline
    Cas Number 330-20-7
    Molecular Formula C7H6F3NO
    Molecular Weight 177.13
    Appearance White to off-white solid
    Melting Point 60-63°C
    Boiling Point 234-235°C
    Density 1.39 g/cm3
    Solubility In Water Slightly soluble
    Smiles Nc1ccc(OC(F)(F)F)cc1
    Inchi InChI=1S/C7H6F3NO/c8-7(9,10)12-6-3-1-5(11)2-4-6/h1-4H,11H2
    Synonyms p-Trifluoromethoxyaniline, 4-Aminophenyl trifluoromethyl ether
    Refractive Index 1.496

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

    Packing & Storage
    Packing A 25g amber glass bottle with a secure screw cap, labeled “4-(Trifluoromethoxy)Aniline,” includes hazard warnings and lot number.
    Shipping **Shipping Description for 4-(Trifluoromethoxy)aniline:** This chemical is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is typically packed according to international regulations for organic chemicals. Appropriate hazard labeling is included, and transport follows all relevant safety guidelines to ensure secure and compliant delivery.
    Storage 4-(Trifluoromethoxy)aniline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition, moisture, and incompatible substances such as strong oxidizing agents. Protect from direct sunlight and avoid prolonged exposure to air. Store at room temperature and ensure proper labeling to prevent accidental misuse or mixing with other chemicals.
    Application of 4-(Trifluoromethoxy)Aniline

    Applications of 4-(Trifluoromethoxy)Aniline in Industrial Manufacturing

    Our manufacturing expertise in 4-(Trifluoromethoxy)Aniline supports specialized downstream sectors with reliable quality and precise formulation control. Below we outline actual industrial application areas where this raw material is integrated to enable advanced product performance. Each scenario details compliance obligations, dosage ranges, process stage, and the types of finished goods manufactured by our global customers.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers source 4-(Trifluoromethoxy)Aniline primarily as a building block for active pharmaceutical ingredient (API) synthesis, such as in custom-designed arylamine-containing scaffolds and for the introduction of trifluoromethoxy moieties that improve drug metabolism profiles. Quality audits and regulatory inspections require full traceability, so production adheres strictly to traceable lot processes and validated synthetic routes. It is introduced at the stage of aromatic amine functionalization, which serves as a precursor for targeted amidation, acylation, or coupling reactions under cGMP oversight for both clinical and commercial API batches.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopeia (Ph. Eur.) requirements for API intermediates
    • US FDA guidelines for pharmaceutical ingredients
    • Chinese Pharmacopoeia ChP applicable for China market export

    Typical usage ratio

    • Added at 0.8–1.2 molar equivalents to core scaffold, ratio adjusted according to downstream yield optimization and impurity profile targets

    Downstream process integration

    • Charged during primary or secondary amine functionalization stages; involved in fine chemical coupling under inert atmosphere to minimize by-product formation

    Final product types

    • Small-molecule APIs featuring CF3O-aryl fragments
    • Pharmaceutical intermediates registered for DMF filing
    • Custom route drug candidates for oncology and CNS applications

    2. Agrochemical Synthesis (Herbicide & Fungicide Intermediates)

    Downstream agrochemical plants rely on our material for the introduction of fluorinated aromatic rings into advanced herbicide and fungicide molecules. Regulatory requirements around environmental residue and operator exposure make batch consistency and impurity control critical. Formulators typically dissolve it in chlorinated or polar aprotic solvents during the aromatic substitution stage before downstream transformation to target actives. The compound’s robust electron-withdrawing group delivers enhanced bioactivity by improving binding affinity and metabolic stability of the finished agrochemicals.

    Industry compliance standards

    • FAO/WHO Good Manufacturing Practice for Pesticide Production
    • EU Regulation No 1107/2009 for plant protection products
    • US EPA Pesticide Registration requirements (40 CFR Part 158)
    • SIN List (Substitute It Now) monitoring for new fluoroaromatic structures

    Typical usage ratio

    • Utilized at 1.0–1.5 molecular equivalents relative to coupling substrate, with optimization based on target molecule complexity and active loading

    Downstream process integration

    • Fed into aromatic nucleophilic substitution or Ullmann-type coupling reactors; follows with halogenation or sulfonylation as required by target structure

    Final product types

    • Fluorinated pre-emergent and post-emergent herbicides
    • Broad-spectrum triazole fungicides
    • Intermediate concentrates for formulation into field-ready crop protection agents

    3. Advanced Dye and Pigment Manufacturing

    Specialty dye and pigment makers integrate this aniline derivative for the synthesis of high-performance colorants where trifluoromethoxy substitution imparts enhanced lightfastness and resistance to chemical degradation. Our production batches meet the purity thresholds required for color consistency and low metal content as demanded by industrial coatings and textile dyeing sectors. Industrial users dose the material during the azo or anthraquinone dye synthesis step, balancing loading to achieve the targeted chromatic strength and fastness properties in the end-use matrix.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for pigments and dyes
    • OEKO-TEX Standard 100 for textile chemical safety and restricted substance list
    • ISO 9001 Quality Management System for colorant manufacturing
    • GB/T 22115-2008 (Chinese standard for reactive dyes)

    Typical usage ratio

    • Added at 5–20% of the total dye precursor mass, tuned according to target shade, brightness and intended textile or coating substrate

    Downstream process integration

    • Charged into the condensation or diazotization reactors; may participate in further coupling with sulfonic acid or other aryl groups to build complex chromophore structures

    Final product types

    • High-stability textile reactive dyes
    • Solvent-resistant organic pigments for paints and plastics
    • Photoresistant printing inks

    4. Electronic Chemicals for Liquid Crystal Display Materials

    Manufacturers of fine electronic chemicals employ this compound as a precursor in the synthesis of liquid crystal intermediates and alignment materials, where strict purity and trace ionic contamination controls are enforced. Integration occurs in high-precision, closed-system acylation or coupling reactions, allowing consistent fluorinated aromatic frameworks essential for modern LCD and OLED substrates. Detailed spectral analysis ensures batch reproducibility according to device specification tiers and accounts for the critical influence on electro-optic behavior in end products.

    Industry compliance standards

    • IEC 61249-2-21: Halogen-free requirements for electronic materials
    • RoHS Directive 2011/65/EU restriction of hazardous substances
    • ISO 14001 Environmental Management for electronics production
    • IPC-4101 standards for base materials in printed wiring boards relevant to flat panel display layers

    Typical usage ratio

    • Charged at 1.5–3.0 weight% of precursor blend, precisely quantified based on desired dielectric properties and molecular alignment uniformity in the liquid crystal host compounds

    Downstream process integration

    • Introduced during acylation or etherification steps in high-purity reactors with tight humidity and metal contamination control, forming functionalized aromatic cores used in liquid crystal mixtures or intermediate resins

    Final product types

    • Liquid crystal intermediates for LCD panels
    • Specialty polyimide alignment agents
    • Functionalized aromatic resins for display coatings
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    Certification & Compliance
    More Introduction

    4-(Trifluoromethoxy)Aniline: Building on Experience in Fine Chemical Manufacturing

    Direct from the Manufacturer: Understanding What Sets 4-(Trifluoromethoxy)Aniline Apart

    Anyone who works with advanced intermediates knows that subtle changes in a molecule’s structure can change everything—the outcome, the yield, the safety, and the reliability of what comes after. In our years of producing 4-(Trifluoromethoxy)Aniline, with model number TFMA-101, we have learned that the trifluoromethoxy functional group does not only provide chemical uniqueness: it creates a bridge between practicality in synthesis and downstream product performance.

    The model TFMA-101 signals a commitment to reproducibility. Each batch keeps its integrity in terms of moisture content, color, and purity, thanks to a production environment set up for moisture-sensitive, halogenated organics. We hold the purity at no less than 99.0% by GC, a threshold that fits the needs of most pharmaceutical, agrochemical, and material science projects where reliability is non-negotiable. Appearance varies from off-white to pale yellow crystalline solid; this comes from handling certain reaction intermediates and batch-to-batch micro-variations, which don’t touch downstream reactivity.

    What 4-(Trifluoromethoxy)Aniline Brings to Synthesis

    Out in the research labs and on the production floor, we have seen 4-(Trifluoromethoxy)Aniline offer a rare mix: electron-withdrawing power from the trifluoromethoxy group joined to the accessible amine scaffold. This feature flavors the way you build complex molecules—whether for medicinal chemistry or crop protection—where you want both stability in tough conditions and high synthetic flexibility.

    Colleagues in medicinal chemistry often tell us that the electron-withdrawing ability of –OCF3 improves metabolic resistance in final drug candidates and enhances bioavailability. We notice pharmaceutical groups choosing this aniline derivative for sulfonamide, urea, and carbamate formations, where the presence of the –OCF3 provides both steric bulk and lipophilicity. Every synthesis specialist faces bottlenecks with late-stage functionalization—the para-position aniline backbone often survives cross-coupling conditions, and doesn’t rearrange or decompose in the presence of challenging reagents. We source fluorinated intermediates when we need them ourselves, and we know it matters deeply that you do not find mystery peaks on your NMR or LC-MS.

    Usage in Everyday Chemical Production

    Our clients use 4-(Trifluoromethoxy)Aniline to introduce fluorinated aromatic rings in drug candidates, agrochemicals, dyes, and specialty polymers. Feedback shows that the compound’s stability, both in liquid and solid states, helps during the transport and storage phases. The boiling point of about 180°C at reduced pressure (a common figure, though always batch-verified) lets process teams recover the compound through simple vacuum distillation, avoiding decomposition seen with some nitro-analogs or more reactive para-substituted anilines.

    We've designed our facility air and dust handling with this molecule in mind; our approach is shaped by practical experience with fluorinated amines, which can generate low-level HF on decomposition and need line-by-line segregation from other halogenated waste. Many customers handle scaling up with confidence, as our product arrives free of expected byproducts, like dimeric anilines or oxidized traces, that sometimes sneak through with non-specialist suppliers.

    What Goes Into Quality: Hard Lessons from Batch-to-Batch Learning

    Years of manufacturing trifluoromethoxy series compounds have taught us some tough lessons about purification and stabilization. The presence of the strong electron-withdrawing trifluoromethoxy ring means every trace of residual acid, moisture, or high-boiling side product can cause off-color, slow decomposition, or tricky emulsification during workup. The high cost of raw materials drives constant scrutiny both in the initial amination and in the final recrystallization—every percent loss matters, not just for the balance sheet, but for what arrives at your door.

    During scale-up, we found a direct correlation between solvent dryness and final product shelf stability. Slight undetected moisture jump-starts hydrolysis if left unchecked. We triple-check our drying stages, including in-line Karl Fischer moisture analysis, before packaging, to reduce any chance you will face surprises later.

    Sensor drift on hydrogen fluoride monitoring, or slight air ingress during bulk final treatment, creates discoloration and co-crystallization of impurities, which jeopardizes your next synthetic step. We've put more eyes on in-process testing and real-time QC, so when we say 99% purity, it’s not just a sticker on the drum—it’s the cumulative lessons of dozens of scaled batches.

    Handling and Delivery: Working With Fluorinated Aromatic Amines

    Handling experience changes your attitude toward packaging and logistics. Every year, we field reports from teams who tried sample vials from traders, ran an initial reaction, and then found their main bulk shipment bore no resemblance to what worked in the lab. The truth is, fluorinated organics often degrade or discolor under marginal shipping, unclear labeling, or poorly flushed containers, especially in warm or humid climates. We ship only in fluoropolymer-lined or food-grade HDPE-lined containers, inerted with dry nitrogen, and coded for batch traceability.

    We send out every bulk shipment with a certificate of analysis tied directly to the batch, signed by our QC manager. The same tracking lives in our own systems, matching your feedback to the precise line in our production log. If your final HPLC result measures an anomaly, we want to hear about it. Only by owning the feedback loop with our buyers—the actual hands who weigh, dissolve, and react with TFMA-101—can we spot tiny drifts or rare contaminants, and build out better future lots.

    Once you have your drums or small packs, you store the product in a cool, dry place, away from acids and oxidizers. Based on our stability tests, product loses its punch if stored with fluctuating humidity, and the minimal level of volatile amines in headspace can initiate yellowing over many months. That’s why our drums are sealed, but easy to open and reseal as much as possible—because not every facility empties their order overnight.

    How 4-(Trifluoromethoxy)Aniline Differs From Other Anilines or Fluorinated Building Blocks

    We have worked with dozens of para-substituted anilines over the years—chloro, bromo, iodo, methoxy, methyl, and countless fluorinated analogs. Some bring more reactivity, some lower price, but not all offer the same combination of chemical resilience and downstream performability as TFMA-101.

    Chloro- or bromo-anilines tend to face issues with aromatic nucleophilic substitution, especially when handled under high-pH or elevated temperature. They often lag in solubility, making meta- and para-substitution more difficult for certain applications. The presence of the –OCF3 in TFMA-101 boosts solubility both in polar and moderately nonpolar solvents, streamlining reaction setup for sulfonylation or ring closure steps.

    Take para-methoxy aniline as another example. The electron-donating property often makes it poorly compatible with strongly oxidizing or basic environments. 4-(Trifluoromethoxy)Aniline, on the other hand, stands strong in a wider pH range, survives aggressive oxidation, and gives a much cleaner separation during chromatography. This gives an edge to synthesis chemists working with reactive, late-stage intermediates, or troubleshooting inconsistent yields in scale-up.

    Compare the reaction side by side in a Buchwald-Hartwig amination: with a para-fluoro, side reactions crop up in polar solvents, especially with less robust ligands. TFMA-101 resists these detours, giving high selectivity, minimal byproducts, and a more straightforward product workup. This is not a trivial point if you keep scaling up and need the downstream purification to remain manageable.

    Applications in the Real World: Feedback from the Field

    The majority of our high-volume TFMA-101 leaves the facility destined for pharmaceutical R&D, where medicinal chemists build libraries of fluorinated lead candidates. The para-trifluoromethoxy group gives better metabolic stability, a wider range of bioactivity, and—according to several customer feedback reports—noticeable boosts in CNS drug permeability. Formulators mention improvements compared to the corresponding para-fluoro or para-chloro anilines, where bioavailability stutters or clinical candidates show unplanned degradation.

    Another use, which we see growing year by year, lies in agrochemicals. The –OCF3 functionality not only bumps up activity against certain pests and weeds—it reduces the potential for off-target activity and environmental persistence, according to public patent filings and independent reviews. Our partners making new herbicides and fungicides report cleaner conversion and product stability through scale-up, especially compared to nitro- or methoxy- substituted anilines, which often need complicated downstream cleanup or reduction.

    Some of our volume finds its way to the electronics and dye sector, especially in photoinitiators and specialty pigments. Again, the unique fluorinated structure resists UV breakdown and offers a rare combination of solubility, color stability, and compatibility with demanding polymer systems. Technical support requests from this sector tend to focus on ways to keep the grade high during prolonged storage or after repeated handling, since many specialized applications stretch over years, not weeks.

    The Sustainability Question: Waste, Byproducts, and Process Improvements

    People sometimes overlook the environmental side of manufacturing specialty chemicals. We have direct experience with the waste streams these fluorinated compounds produce. Even a single-kilo batch generates distinct halogenated byproducts, which need high-temperature incineration, careful neutralization, or, for spent solvents, regulated third-party recovery or destruction.

    Everyone in the field faces regulatory pressure to reduce waste and avoid accidental emissions of fluorinated gases. In our own plant, years of process improvement have led us to recover much of the dichloromethane, acetonitrile, or methyl tert-butyl ether used in the synthesis. We condense and recycle off-gasses, with leak detection systems running around the clock, to prevent even trace venting of volatile fluorocarbons. These changes came from direct feedback—from regulators, customer audits, and colleagues working the line, not from greenwashing in the marketing department.

    Our current focus looks at safer catalytic amination and alternatives to toxic starting materials, both to improve yield and to reduce the handling risk and waste profile. Research collaborations with local universities help us test greener solvents and explore continuous flow setups, which substantially cut down solvent demand and waste. We know from years of troubleshooting that incremental steps, like better pH control or a slight tweak in reaction order, often cut failure modes and drive up final product safety.

    Problems Faced in Global Supply and Our Strategy to Answer Them

    Every year brings a new twist in raw material supply. Several years ago, a major supplier of trifluoromethoxy precursors tightened their export quotas, causing turmoil throughout the specialty chemical sector. Only careful inventory management, hedged contracts, and a willingness to pivot to parallel sourcing let us keep batches flowing out of the plant.

    We don’t hide the fact that the price for TFMA-101 fluctuates with global demand and fluorinated raw material costs. Fluctuating logistics—weather delays, port slowdowns, shifting import rules—can all pinch the supply chain at the worst possible moment. What we guarantee is transparency on lot origin, quality control, and as much predictive communication as we can give when timelines may slip.

    From our experience, the answer is not to promise the moon—it's to make clear what stock is ready, how quickly we can pivot between grades (technical, pharma, or custom), and to be upfront when uncertainty looms. Many buyers, especially those deep in pharma and biotech, prefer honest advance warning over soothing words and missed delivery dates.

    Health, Safety, and Our Day-to-Day Protocols

    Fluorinated anilines occupy a peculiar spot in handling safety. They don’t always show the volatility of simple anilines, and their acute toxicity sits lower than the nitro series derivatives, but there’s no place for complacency around fluorinated aromatics. Regular, direct handling of TFMA-101 means the right gloves, full eye protection, and local exhaust when weighing or charging reactors.

    On our floor, any process step that risks vaporizing a fluorinated compound relies on closed systems and remote monitoring. We treat spills with anhydrous sodium carbonate or calcium oxide, not just to mop up but to capture any possibility of free HF or acid fluoride forming during clean-up. Packed-activated carbon units scrub vented air before it meets the outside, and we cycle through regular maintenance of personal protective equipment stocks.

    Customers who reach out about incident procedures or safe handling rarely find an out-of-the-box answer. Our support team, made up of operators and engineers with real years on our plant floor, can answer questions about what’s worked—or failed—in our own experience. We keep detailed handling records, review near-miss events regularly, and update internal practices as new hazards are identified elsewhere in the industry.

    The Human Side: Long-Term Partnerships and Technical Support

    We’ve been in the business long enough to know that buyers want more than just tonnage and a COA. Most return business doesn’t come from flawless first runs, but from the follow-up after a problem: a batch that crystallizes poorly, a shipment question, or a reaction that behaves unpredictably.

    A fair percentage of our sales go to repeat partners—people building new pharmaceuticals, testing advanced materials, or pushing old processes to be quicker and cleaner. These long-term relationships let us spot shifts in the market, changes in regulatory requirements, and, most importantly, recurring technical issues before they turn into crises. We work hard to answer questions with direct, actionable details from our own facility, not boilerplate pulled from generic literature.

    For instance, one recurring issue among pharmaceutical process chemists is scale-up exothermicity during aromatic substitution, particularly if small-scale calorimetry is not performed early in project planning. Only direct communication and shared data helped prevent a serious runaway, and the partnership continues because those lessons got folded into better protocols by both sides.

    Looking Toward the Future: Better Practices and New Opportunities

    Being a direct manufacturer, we have a unique lens on where 4-(Trifluoromethoxy)Aniline is headed. The molecule sits, quietly but reliably, as an ingredient for the next generation of drugs, crop protectants, and functional materials. Continuous investment in process intensification—like flow chemistry or non-chlorinated solvent systems—not only points toward better safety but will gradually bring down costs and environmental impact.

    We track every trend, every regulatory change, and every shift in customer demand, refining our processes and product offering as the market shifts. Conversations with buyers, operators, and researchers shape every step we take, from how we train new plant staff to how we design new facility upgrades. We believe that by keeping our focus on reliable, reproducible production and open communication, we offer more than a chemical—we offer a foundation you can build great products on.

    Customers looking for a supplier with depth—technical knowledge, real process experience, and ongoing improvement—find value in what comes from years inside a real chemical manufacturing plant. We welcome new technical inquiries, trial batches, and the difficult conversations that come with honest feedback—because quality grows over time, and a thoughtful, experienced manufacturer never stops learning from those who know their chemistry best.