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3-(Trifluoromethoxy)Aniline

    • Product Name 3-(Trifluoromethoxy)Aniline
    • Alias m-(Trifluoromethoxy)aniline
    • Einecs 602-556-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    959431

    Chemical Name 3-(Trifluoromethoxy)aniline
    Cas Number 1535-73-5
    Molecular Formula C7H6F3NO
    Molecular Weight 177.13
    Appearance Colorless to pale yellow liquid
    Boiling Point 191-193°C
    Density 1.37 g/cm³
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Flash Point 73°C
    Refractive Index 1.484
    Smiles C1=CC(=CC(=C1)N)OC(F)(F)F

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

    Packing & Storage
    Packing 250g of 3-(Trifluoromethoxy)Aniline is supplied in a sealed amber glass bottle, labeled with hazard warnings and product details.
    Shipping 3-(Trifluoromethoxy)aniline is shipped in tightly sealed containers to prevent leakage and contamination. It should be labeled according to hazardous chemical handling guidelines, protected from moisture and direct sunlight, and transported at ambient temperature. Ensure compliance with local, national, and international regulations for the safe shipment of potentially hazardous laboratory chemicals.
    Storage Store 3-(Trifluoromethoxy)aniline in a tightly sealed container in a cool, dry, and well-ventilated area, away from heat, ignition sources, and direct sunlight. Keep it separate from incompatible materials such as strong oxidizers, acids, and bases. Use chemical-resistant secondary containment and ensure proper labeling. Standard laboratory precautions, including use in a fume hood, are recommended when handling.
    Application of 3-(Trifluoromethoxy)Aniline

    Applications of 3-(Trifluoromethoxy)Aniline in Industrial Manufacturing

    3-(Trifluoromethoxy)aniline serves as a critical intermediate in advanced chemical synthesis, supporting high-value sectors including pharmaceuticals, agrochemicals, specialty dyes, and polymer modification. As a direct manufacturer, we maintain strict sourcing and process controls to ensure stable supply for technical and commercial scale-up demands.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical companies use our 3-(Trifluoromethoxy)aniline as a core building block in preparing active pharmaceutical ingredients (APIs), particularly for next-generation anti-inflammatory and oncology therapies. The electron-withdrawing trifluoromethoxy group enables specific aromatic substitution reactions, yielding high-purity intermediates for regulated synthesis routes. Clients integrate this compound into their multistep process at the aromatic amination or Suzuki coupling stage, driving differentiation in structure-activity relationships for target drug candidates. Our facility ensures traceability and impurity profiling to meet pharma-grade expectations at every stage.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF and EP applicable monographs (project-specific)
    • 21 CFR Part 211 (cGMP for Finished Pharmaceuticals, US FDA)
    • REACH registration and SDS documentation (EU chemical safety)

    Typical usage ratio

    • 5–30% molar ratio in pharmaceutical synthesis steps, adjusted by target molecule structure and route yield optimization

    Downstream process integration

    • Entry during early-stage amination or reductive coupling in multipurpose reactors
    • Direct charge in high-pressure or catalytic batch reactors for API precursor assembly
    • Controlled dosing via automated powder feeders for reaction scale consistency

    Final product types

    • Pyridine-based kinase inhibitors
    • Novel arylamine class NSAIDs
    • Cancer therapy intermediates
    • Custom small-molecule synthons

    2. Crop Protection Ingredient Manufacturing

    Agrochemical formulators employ this raw material to construct key agroactive scaffolds, especially modern herbicides and fungicides requiring trifluoromethoxy functionality. The compound’s reactivity allows selective formation of substituted aniline or anilide linkages, enhancing target specificity for crop safety and pest control. Plant protection synthesis involves precise integration post-condensation to maintain functional group fidelity and regulatory compliance for technical-grade batches.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Technical Grade Material
    • ISO 9001:2015 Quality Management for Bulk Chemical Supply
    • US EPA 40 CFR Part 158 for active ingredient registration
    • OECD GLP for analytical verification in product development

    Typical usage ratio

    • 10–25% by weight in reaction mixture; ratio selected based on crop protection target and final AI structure

    Downstream process integration

    • Charged as a nucleophilic aromatic substitution partner in solvent-phase reactors
    • Reacted in closed-system vessels with chlorinated structures for anilide synthesis
    • Fed semi-continuously to control side products during heterocyclic group installation

    Final product types

    • Post-emergence herbicide technical concentrates
    • Novel fungicide actives for plantation crops
    • Aromatic urea and anilide-based insecticides
    • Registered generic pesticide intermediates

    3. High-Performance Dye and Pigment Manufacture

    Specialty dye suppliers integrate our material for precision tuning of color strength, fastness, and stability. The trifluoromethoxy substitution promotes unique resonance effects in azo and anthraquinone dye frameworks, providing saturated coloration for fiber, plastics, and ink markets. Customers dose the material during diazotization or coupling reactions under tightly monitored conditions to maximize chromophore uniformity and compliant hazardous control. Our product’s lot-to-lot consistency minimizes formulation drift in commercial batch runs.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile chemical safety
    • REACH Annex XVII for restricted dye substances
    • ISO 787/1 for pigment quality evaluation
    • EN 71-3 Toy Safety standard (for colorants in children’s products)

    Typical usage ratio

    • 2–12% w/w in pigment/dye synthesis; exact range defined by chromophore architecture and application end-use

    Downstream process integration

    • Charged at initial diazo salt formation or subsequent coupling reaction
    • Batch-fed during high-temperature organic synthesis for solid dye formulation
    • Metered liquid dosing for continuous pigment reactor systems

    Final product types

    • High-stability textile dyes (e.g., for polyester blends)
    • Special effect pigments for digital printing inks
    • Industrial plastics color masterbatches
    • Automotive coatings and plastic parts colorants

    4. Polymer and Material Surface Modification

    Compounders and resin manufacturers adopt this molecule to modify functional polymers, especially for imparting improved chemical resistance or targeting tailored dielectric properties. The trifluoromethoxy segment, integrated through copolymerization or end-group functionalization, alters polymer backbone polarity and stability without impacting main-chain structure. Integration typically occurs at the monomer activation or chain-transfer stage in controlled polymerization systems—resulting in finished resins that meet advanced electronics, membrane, or fluoropolymer industry requirements.

    Industry compliance standards

    • UL 94 and IEC 60695-11-10 flammability compliance (for electronics resins)
    • ISO 9001 Quality Systems for engineering plastics production
    • RoHS Directive 2011/65/EU for restricted substances in polymers
    • ASTM D638 tensile and performance standards for advanced polymers

    Typical usage ratio

    • 0.5–4 mol% in polymer modification reactions, tuned for desired resistance or electrical properties

    Downstream process integration

    • Added during monomer pre-reactor staging for free-radical or condensation polymerizations
    • Fed in end-capping stages for custom resin products
    • Blended post-polymerization for reactive extrusion or co-polyester applications

    Final product types

    • Dielectric films for electronics and capacitor industries
    • Acid-/solvent-resistant fluoropolymer coatings
    • Membrane polymers for specialty gas separation
    • Modified engineering thermoplastics for automotive components
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    Certification & Compliance
    More Introduction

    Get to Know 3-(Trifluoromethoxy)Aniline from the Manufacturer’s Bench

    A Story Written in the Synthesis Bay

    In our workshop, where the whiff of solvents hangs in the morning and glassware lines the shelves, 3-(Trifluoromethoxy)Aniline stands out in our daily synthesis routine. The chemists here handle dozens of anilines and fine intermediates every month, but this molecule, known on paperwork as model 98-TRI-MF-OXYAN or sometimes as 3-TFMA, brings both challenge and reward. Its chemical structure—an aniline core with a trifluoromethoxy group at the meta position—offers a fine balance of reactivity and stability. That makes it a building block we put forward with genuine confidence.

    Specifications We Focus on—And Why They Matter

    Purity holds the biggest piece of our attention. The grade of 3-(Trifluoromethoxy)Aniline coming off our lines usually reaches 98% and sometimes higher. That reflects hours of careful distillation and column purification. Water content needs tight restriction, generally holding well under 0.3%, since traces of moisture sabotage sensitive couplings down the line.

    Chemists often ask for lot-specific data. Our own project spreadsheets call up melting points—usually landing near 34 to 36°C—and spectral analysis: sharp NMR and clear GC-MS signatures. Each batch shows a faint but unmistakable hue, drifting from faint yellow to clear, matching the experience of those who handle it daily. These aren’t just marketing points. Every measure points back to function in the lab.

    Real Use Cases from the Plant Floor

    We can recall the first time an agrochemical client switched precursors, hoping to sharpen the efficacy of a new protective. 3-(Trifluoromethoxy)Aniline played its role as a substitution point—a scaffold for assembling new phenylureas or triazines. Some groups rely on its trifluoromethoxy for boosting lipophilicity and metabolic stability in crop protection agents. During API projects, med chem teams often use our product as a jump-off for more elaborate derivatizations. Switch positions, throw on a halogen, or add an amide, and suddenly the compound map branches out quickly. About a fifth of our demand comes from pilot drug candidates—never directly as a finished active, always as a handle to build further.

    We’ve walked teams through the scale-up snag where low-purity anilines ruined a hydrogenation run. Minute amounts of diphenylamine or ortho isomers—impurities that slip into lazier syntheses—do not slide past our in-process checks. Down at the kilo scale, little differences like that change waste profiles, affect downstream chromatography, and sometimes decide whether a project survives the quarter.

    Differences That Matter—Not Just for the Data Sheet

    Compared with 4-(Trifluoromethoxy)Aniline—the para isomer—3-(Trifluoromethoxy)Aniline behaves differently in cross-couplings and amidations. During reaction temperature ramps, the meta isomer keeps side-product formation lower. It often delivers more predictable conversions in Suzuki and Buchwald-Hartwig couplings, tracing back to both electronics and steric effects brought in by the meta position.

    Anilines from cheap sources sometimes carry hints of residual acid, leftover solvent, or mixed isomer content. Those slip-ups become headaches for formulation or further modifications. Our plant employs closed-loop nitrogen handling, in-line drying columns, and tightly controlled feeding—partly because we’ve endured enough botched yields and recall headaches in our earlier years. This is the kind of unglamorous process detail one rarely spots in a sales brochure, but it’s where the difference between “just making chemicals” and actually supporting an R&D team’s project lives.

    Safety and Handling Realities—Practical Observations

    Everyone here, from production chemists right down to logistics, respects the volatility of the product. While handled as a liquid under most conditions at room temp, it solidifies around 30°C, and that transition point creates logistical complexity. It can creep and freeze in pump lines or drum valves. So, we store, ship, and handle the compound under tightly managed temp conditions, using double-seal containers and vapor barriers. Routine housekeeping, frequent inspection, and clear hazmat training keep near-misses from becoming accidents. These routines do more for reliability and reputation than the most polished certifications.

    Direct skin or eye contact brings the same risk profile as most aromatic amines. The Health and Safety lead always reminds fresh hands: nitrile gloves, well-ventilated bays, and easy reach for safety showers. Years ago, a lapse with a cracked gasket taught us to never shortchange containment, even with a “routine” workup. Residues linger, odors stick, and the product’s volatility means something as minor as a warm afternoon can escalate warehouse risks quickly.

    Why Our Plant Invested in Advanced Purification

    A few years back, one of the bigger pharmaceutical companies flagged contaminants in an imported batch from a distributor. That caught our attention. On-site analysis revealed trace levels of ortho and para isomers, and a persistent solvent residue—remnants from older distillation setups with poor fractionation. Our response came quickly: updated fractionation columns, secondary ion-exchange cleanup, and stepped quality-release analytics.

    Investing in purification is not just about batch records; it changes how engineers think about waste, recycle streams, and solvent recovery. Pulling pure product from raw intermediates is where plant chemistry becomes an art. The drive is not about getting a certificate, but creating steady output that R&D teams count on over years, not just for a single delivery.

    Supporting Innovation from a Manufacturer’s Perspective

    See enough R&D projects, and it becomes clear that 3-(Trifluoromethoxy)Aniline does not just slot into finished products. The molecule serves as a backbone for ever-evolving chemical libraries. In pharma, it’s often incorporated into more esoteric heterocycles or as a hinge in SAR studies. Agrochemical projects use it to build out resistance-busting actives, and materials scientists occasionally select it to impart specific electronic properties in polymers.

    Our involvement often goes well beyond the drum. Customers circle back asking for modified volumes, custom packaging, or specific impurity profiles. On some runs, we dial the purification slightly differently to preserve minor byproducts that downstream teams want for method development. That flexibility only happens with a close link between the plant floor, tech-support chemists, and the customers. Being the origin of the product, not another handling node, puts us directly in the problem-solving loop.

    Environmental and Compliance Pressures—Behind the Bay Doors

    As regulations about aromatic amine handling grow tougher, the burden is not just compliance paperwork. Each production campaign has us tracking emissions, waste treatment, solvent recovery rates, and employee exposure. The fluorinated nature of 3-(Trifluoromethoxy)Aniline means paying special attention to scrubbers and chemical-resistant containment. Our solvent waste undergoes dedicated fluorine-destruction processes, a far cry from practices a decade ago. These steps cost more, but taking shortcuts eventually means costs that show up in fines, product rejections, or long-term reputational loss.

    On top of that, end users now ask for lifecycle documentation and traceability—questions driven by downstream ISO standards or industry codes. Our QA and compliance teams have built process-traceable records for each batch, linking raw material source to final drum. As the producer, we are responsible not just for selling a molecule, but for knowing and proving its origins and journey.

    Challenges and Lessons from Scale-Up

    Scaling from kilo-lab to plant lot is never just a matter of making things bigger. Each campaign gets its own quirks: some batches produce more colored impurities, some see clogging on the packing columns, others demand slower heating ramps. The fluorine moiety increases sensitivity to base and acid traces, so reactor linings and cleaning cycles get more attention than in runs with plain anilines.

    One of our earliest plant-scale runs saw a yield collapse due to reflux loss and unplanned exotherms. We traced it back to using a lower-grade starting aniline supplied at a steep discount. That single decision led to weeks of solvent refills and extra purification. From that point, every run starts with QC on all incoming materials, and records on each lot’s spectral purity stay tied to the batch all the way up to shipping.

    Collaboration with R&D—Feedback Loops That Improve Product

    Many improvements to our 3-(Trifluoromethoxy)Aniline process came from pushback on final batch reports and real feedback from project chemists. Early on, most feedback came shaded with frustration: unexpected GC peaks, trouble with redissolution, or odd behavior under specific catalytic conditions.

    Instead of brushing complaints aside, our technical support crew walks through the chemistry, retraces synthesis steps, and brings solutions—adjusting drying protocols, upgrading filtration, or even changing the order of quenching operations. This built rapport not just with regular buyers but with end-users at the bench.

    We recognize that much as technical bulletins and literature help, direct contact between the manufacturer and lab chemists gives an edge for problem-solving. Being able to walk through reasons for abnormal readings or explore alternate purification methods reflects a transparency and support level that builds long-term reliability.

    Facing Cost and Supply Chain Fluctuations

    Fluorinated intermediates like 3-(Trifluoromethoxy)Aniline often sit at the mercy of supply chain pricing swings. Global fluorspar shortages or HF price hikes push up both raw material and final product costs. Experience has taught us to secure raw stock through multiple vetted sources. Our purchasing group builds in inventory buffers so downstream projects rarely get delayed—not a luxury, but a necessity born from watching deliveries slip on imported batches in past years.

    Sometimes, the answer means weathering a price spike or negotiating with customers around timelines. In other cases, we adjust batch sizes or shipping priorities. Doing all this as the producer—not as a handler juggling global logistics—keeps more control over actual timelines and fewer surprises for project teams. We keep eyes out for regulatory and raw-material changes, tweaking workflow to suit without upending reliable supply.

    Looking Forward—Upgrades and the Next Generation

    The chemical business moves fast, but reliability comes from continuous tuning. Our process engineers test greener solvents and less energy-intensive cleanup steps as part of regular improvement cycles. Cleaner production of 3-(Trifluoromethoxy)Aniline is not just a compliance box; it’s become a market differentiator.

    Sustainability pressures mean increasing emphasis on closed-loop solvent recovery, opt-in renewable energy, and more robust monitoring for emissions. These shifts make day-to-day operations more data-heavy, but they also reduce future environmental and economic risk. Our technical team collaborates with universities and pilot plants to trial catalyst recovery, new purification techniques, and dynamic process control, thinking beyond just the next batch order.

    Trust Built Over Years, Not Just a Purchase Order

    A product like 3-(Trifluoromethoxy)Aniline does not create impact because it sits on a database. Its value comes from stability, consistency, and the confidence R&D teams can place in each drum. Most of our plant team has watched projects drag on for years, with teams relying on repeat purchases for their own pipeline continuity. That expectation of repeatability drives every upgrade and each lot’s sign-off.

    Distributors and third-party sellers can move tonnage quickly, but they rarely get pulled into reaction troubleshooting or batch cleanup issues that end-users face. Being the hands that synthesize and package each lot ties the final product’s success directly to the daily care and troubleshooting that goes into its manufacture.

    Conclusion—Why the Source Matters in Specialty Chemicals

    We have seen how a slight slip in manufacturing standards, dirty reagents, or careless logistics can unravel months of hard-won progress on a customer’s bench. For 3-(Trifluoromethoxy)Aniline, the trust in quality, predictability, and transparency forms the backbone of ongoing relationships with innovators in pharma, agrochem, and materials science.

    The experience and investment poured into every batch mean downstream confidence in scale-ups and product launches. Every order fulfilled, every challenge handled, and every process improvement brings us and our collaborators closer to the cutting edge of chemical innovation. Standing at the origin, with an unbroken window onto production, means seeing the results not just in yields but in every successful partnership that starts in our plant and ends in a new discovery somewhere further down the chemical value chain.