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4-Amino-3-(Trifluoromethoxy)Benzoic Acid

    • Product Name 4-Amino-3-(Trifluoromethoxy)Benzoic Acid
    • Alias 4-Amino-3-(trifluoromethoxy)benzoate
    • Einecs 619-285-2
    • 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

    122739

    Productname 4-Amino-3-(Trifluoromethoxy)Benzoic Acid
    Casnumber 169057-16-7
    Molecularformula C8H6F3NO3
    Molecularweight 221.13
    Appearance White to off-white solid
    Meltingpoint 157-160°C
    Purity >98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Synonyms 4-Amino-3-(trifluoromethoxy)benzoic acid; ATBA
    Smiles C1=CC(=C(C=C1N)C(=O)O)OC(F)(F)F
    Inchikey BMORDPCXLKZCIK-UHFFFAOYSA-N
    Storageconditions Store at room temperature in a tightly sealed container

    As an accredited 4-Amino-3-(Trifluoromethoxy)Benzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is supplied in a 25g amber glass bottle with a white screw cap, labeled with product name, formula, and safety warnings.
    Shipping This product, 4-Amino-3-(Trifluoromethoxy)benzoic acid, ships in secure, leak-proof packaging designed for chemical transport. It is dispatched via regulated carriers with proper labeling and documentation. Temperature control and hazard compliance are ensured throughout the shipping process. Delivery typically occurs within 5-7 business days, depending on destination and import regulations.
    Storage Store 4-Amino-3-(Trifluoromethoxy)benzoic acid in a tightly sealed container, protected from light and moisture, in a cool, dry, well-ventilated area. Avoid exposure to incompatible substances such as strong oxidizing agents. Label the container clearly, and keep away from direct sunlight, heat sources, and ignition sources. Follow all relevant safety guidelines and local regulations for laboratory chemical storage.
    Application of 4-Amino-3-(Trifluoromethoxy)Benzoic Acid

    Applications of 4-Amino-3-(Trifluoromethoxy)Benzoic Acid in Industrial Manufacturing

    As the manufacturer, we support advanced industrial sectors with 4-Amino-3-(Trifluoromethoxy)Benzoic Acid produced under strict quality control. This material serves as a crucial building block in specialized molecule synthesis across high-value downstream segments. Each field requires well-defined compliance, precise formulation, robust process integration, and targeted end-use applications.

    1. Pharmaceutical API Intermediate Synthesis

    Innovators in the pharmaceutical sector utilize this compound as an advanced intermediate for the synthesis of selective kinase inhibitors and fluorinated benzamide APIs. Its electron-withdrawing trifluoromethoxy group enables the controlled installation of pharmacophores during multi-step organic transformations, often under cGMP batch processing. The raw material enters acylation, coupling, and cyclization stages, where stringent impurity controls apply to meet drug substance quality targets.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • 21 CFR 210/211 (US FDA GMP for finished pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) monograph requirements for related substances
    • DMF (Drug Master File) support documentation

    Typical usage ratio

    • 10–30% relative to total intermediates in batch reactions, adjusted by API yield strategy
    • Adjusted based on molar conversion, process mass intensity, and desired final purity

    Downstream process integration

    • Introduced during amidation or coupling step with heterocyclic partners
    • Processed under nitrogen or argon to limit moisture
    • Removal of side products followed by HPLC or UPLC in-process control
    • Usually isolated as a crystalline intermediate for further conversion

    Final product types

    • Targeted oncology small molecule APIs
    • Fluorinated benzamide pharmaceuticals
    • Preparation of preclinical research compounds for CNS therapeutics
    • Reference standards or impurities for analytical labs

    2. Agrochemical Active Ingredient Development

    Agrochemical formulators use this raw material to construct novel trifluoromethoxy-containing herbicide and fungicide actives. Its amino functionality supports formation of substituted benzoic acid frameworks, often used for selective mode-of-action pesticides. Control over substitution patterns is critical to pass regulatory reviews for environmental safety and efficacy, and scale-up occurs in closed reactors to prevent by-product contamination.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • EPA 40 CFR Part 158 (Data requirements for pesticides)
    • FAO/WHO JMPR (Joint Meeting on Pesticide Residues) purity requirements
    • ISO 9001:2015 for manufacturing process documentation

    Typical usage ratio

    • 12–20% by weight in synthetic route to benzoic-based actives
    • Ratio fine-tuned for yield optimization and impurity minimization

    Downstream process integration

    • First used in amide bond formation via coupling agents in closed batch reactors
    • Followed by protection/deprotection steps to control final molecule configuration
    • Downstream, intermediates subjected to flash chromatography for purification
    • Final actives isolated after hydrolysis or halogenation as required

    Final product types

    • Trifluoromethoxy-substituted herbicidal actives
    • New-generation benzoic acid fungicides
    • Experimental crop protection agents
    • Analytical standards for residue labs

    3. Specialty Fluorinated Polymer Monomer

    Producers of high-performance fluoropolymers select this compound as a monomer precursor for custom-engineered resins. The unique combination of amino and trifluoromethoxy moieties imparts controlled polarity, solubility modification, and increased thermal stability during emulsion or solution polymerization. Validation batches establish the impact of loading rates and reactivity ratios before larger-scale production.

    Industry compliance standards

    • ISO 14001 (Environmental management for chemical manufacturing)
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) for monomer registration
    • ASTM D4000 (Standard Classification System for Polymer Materials)
    • Customer-specific non-volatile residue and extractable limits

    Typical usage ratio

    • 3–8% by mol as a comonomer, depending on resin property targets
    • Lower ratios preferred for minor property adjustments, higher for specialty effects

    Downstream process integration

    • Prepolymerized with other fluoro-monomers via radical or ionic mechanisms
    • Used in pilot plant test runs to determine processability and finished resin properties
    • Functionalized further post-polymerization if higher performance is required
    • QC monitoring via GPC and FTIR spectrometry after cure

    Final product types

    • High-performance fluorinated engineering plastics
    • Resistant coatings for electronics and aerospace applications
    • Protective fluoropolymer films and sheets
    • Membranes for aggressive chemical environments

    4. Advanced Organic Pigment Synthesis

    Manufacturers in the specialty pigment sector use this compound to introduce both amino and trifluoromethoxy substitutions, enabling new chromophoric structures for use in high-stability colorants. The process involves diazotization and subsequent coupling or cyclization to access unique azo- or anthraquinone-based pigments. Close control of process parameters is essential, as the incorporation ratio directly impacts lightfastness and solvent resistance.

    Industry compliance standards

    • EN 71-3:2019 (Safety of toys — Migration of certain elements, for pigments in consumer goods)
    • REACH Annex XVII (Restrictions on pigments with hazardous content)
    • ISO 105-A02 (Color fastness testing method)
    • Chinese GB9685 (Standards for pigment migration in food contact materials)

    Typical usage ratio

    • 5–10% by mol in pigment backbone formation
    • Modification based on desired color strength and chemical resistance

    Downstream process integration

    • Diazotized and coupled under controlled pH and temperature
    • Purified post-coupling via recrystallization or chromatography
    • Final pigment subjected to milling and dispersant mixing before end use
    • QC analysis for particle size and tinting power

    Final product types

    • High-stability organic pigments for inks and coatings
    • Specialty colorants for plastics and synthetic fibers
    • Automotive and industrial paint colorants
    • Digital printing pigment concentrates

    5. Electronic Chemical Synthesis (Semiconductor Ancillaries)

    Fabricators in the semiconductor and electronics sector select this material for downstream synthesis of intermediates used in liquid crystal display components and antistatic treatments. Its trifluoromethoxy group confers dielectric and hydrophobic properties, critical for fine pattern etch resists and functionalized surface treatment agents. The compound enters high-purity synthesis stages, with all batches documented for traceability and material lot certification.

    Industry compliance standards

    • IEC 62474 (Material declaration for electronic industry supply chains)
    • RoHS Directive (2011/65/EU) for hazardous substance restrictions
    • IATF 16949 (Automotive quality system standard for electronics)
    • Customer-defined ultra-trace impurity specifications

    Typical usage ratio

    • 1–6% by mol in organic intermediate synthesis for microelectronic materials
    • Exact ratio determined by target resistivity or optical characteristics

    Downstream process integration

    • Activated with alkylation reagents for integration in photoresist precursors
    • Subjected to vacuum distillation or microfiltration to minimize contamination
    • Incorporated into pilot line verification processes
    • IC-grade quality assurance and documentation per shipment

    Final product types

    • Liquid crystal intermediate chemicals
    • Spin-on dielectric and etch resist materials
    • Semiconductor antistatic coating concentrates
    • Organic semiconducting agent precursors

    6. Analytical Reference Material Production

    Producers of analytical and quality control standards employ this compound to prepare traceable benzoic acid derivatives. Calibration standards require exceptional purity, and our manufacturing supports lot certification with documented impurity profiles. The compound is formulated into calibration blends and certified reference standards for laboratories conducting environmental, pharmaceutical, and industrial analysis.

    Industry compliance standards

    • ISO 17034:2016 (Competence of reference material producers)
    • ISO/IEC 17025 (General requirements for the competence of testing and calibration laboratories)
    • Sigma-Aldrich/USP primary reference standard traceability guidelines
    • Customer-defined documentation for traceability and impurity specification

    Typical usage ratio

    • 95–100% in neat reference material prep for analytical use
    • Dilution to ppm or ppb as calibration solutions in specified matrix solvents

    Downstream process integration

    • Recrystallized and validated by NMR, HPLC, and GC-MS
    • Dosed into calibration standard solutions under ISO cleanroom
    • Packaged under inert atmosphere with COA and batch documentation
    • Integrated into round robin or proficiency testing schemes for laboratories

    Final product types

    • NIST-traceable calibration standards for HPLC/GC/LC-MS analysis
    • Certified reference materials for environmental water/soil residue analysis
    • Analytical controls for pharmaceuticals and industrial quality labs
    • Proficiency test samples for laboratory accreditation bodies
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    Certification & Compliance
    More Introduction

    4-Amino-3-(Trifluoromethoxy)Benzoic Acid – Perspective from Our Manufacturing Floor

    Unpacking Demand and Chemistry

    Walk through our production lines any day, and there’s a good chance you’ll see a batch of 4-Amino-3-(Trifluoromethoxy)Benzoic Acid in some stage of synthesis. Requests for this compound have climbed steadily among pharmaceutical R&D teams, especially those focused on building out new active ingredients or exploring lead compounds with metabolic stability. In our experience, the trifluoromethoxy group has shifted from an oddity to an integral motif, and the amino-benzoic backbone offers a familiar platform for a broad range of synthetic transformations.

    Our model 4A3TFMB is based on direct coupling steps that minimize byproducts and reduce isolation headaches, so batch repeatability is higher than older routes. We monitor purity by HPLC and NMR; contaminants sit consistently below 0.3%, so researchers see the same results regardless of shipment size or destination. Most customers order as a white to off-white crystalline solid, which moves well in solution and carries over minimal odor. Granule size stays within our QC window to simplify handling in both pilot scale and high-throughput screening.

    Why This Trifluoromethoxy-Aromatic?

    Anyone who‘s worked with trifluoromethoxybenzoic acids understands their value in drug discovery. That CF3O– twist brings electronic and steric behaviors you won’t see in more basic aryl acids. Teams exploring kinase inhibitors or anti-inflammatory series appreciate how the electron-withdrawing group affects interactions with biological targets, especially compared to non-fluorinated analogs. Over the last few years, we’ve watched medicinal chemistry programs shift toward these motifs, not simply for activity, but also for metabolic resilience and unique ADME profiles.

    Equipment choices at our site reflect the stubbornness of the trifluoromethoxy group under typical conditions. Early experiments with aggressive temperature swings led to heavier degradation, lowering yield and introducing inconsistent side-products. Now, by holding reaction temperatures tighter and swapping out certain catalysts for higher selectivity, we see more predictable conversions and, ultimately, less waste to manage.

    The Experience Behind Each Kilo

    As a chemical manufacturer, we follow standard process analytics, but after years of running these synthesis blocks, the team has learned to “read” each batch based on subtle cues. Inconsistent color changes or shifts in exotherm hint at batch-to-batch quirks often missed in smaller labs. By integrating remote monitoring points—sometimes with custom probes—we’ve ironed out many of the surprises that show up in final purifications. It’s a rhythm that suits kilo-scale runs, especially where customers are strict about trace metal levels or residual solvents.

    On our end, one critical decision separated our 4-Amino-3-(Trifluoromethoxy)Benzoic Acid apart from generic material: we enforce a double recrystallization step. Yields run marginally lower, but every gram meets pharmaceutical screening grades, free of colored impurities or hard-to-purge oligomers that show up with rushed workups. That’s kept our material in libraries where batch consistency translates directly into reproducible biological readouts.

    Specifying for R&D Benchwork

    Most interest in this compound comes from pharmaceutical and agrochemical circles, but we see movement in specialty colorant and performance polymer segments too. We don’t cut corners on drying—free-flowing product matches the demands from automated lab systems and manual prep alike. Water content sits below 0.1% by Karl Fischer, which avoids annoying clumping in solution feeds, especially for larger screening campaigns.

    Customers exploring SAR (structure-activity relationship) series have shared feedback that our product’s trace impurity profile simplifies downstream purification after coupling or amidation. Less time spent teasing apart unknown contaminants saves them critical hours during deadline pushes. The trifluoromethoxy group distinguishes itself from methyl or ethyl ethers in the same positions, offering greater lipophilicity and lower basicity. Research teams often substitute our material in as a benchmark when testing alternative fluorination strategies.

    Differences from Competing Aromatic Acids

    Comparisons frequently arise between our 4-Amino-3-(Trifluoromethoxy)Benzoic Acid and the more common 4-aminobenzoic acid or 3-(trifluoromethoxy)benzoic acid. The combined presence of the amino and CF3O– groups alters reactivity; chemists aiming for further functionalization or coupling to heterocycles find options broaden. Function in peptide synthesis varies from the simpler precursors, due to steric protection and the influence on coupling rates. Bench feedback tells us the product copes better with harsh acylation steps and lessens side reaction rates involving free amino sites—useful for streamlined synthetic sequences.

    We’ve seen generic versions in the open market that cut corners on process control, leading to higher residual halides and unexpected side-isomers. Our QC rejects those. High purity translates directly into better yields downstream, whether customers push toward sulfonamide derivatives, amide linkages, or further ring expansion. Our internal experience shows that even trace impurities at 0.5% can cause headaches in demanding programs, so we hold tighter specs regardless of seasonal market volatility.

    Trusted Sourcing and Transparent Manufacturing

    We handle all stages from raw material preparation to packaging on site. This full ownership helps us track trends in raw material pricing and adjust stock strategies before supply disruptions ripple out. Our technical team keeps a log of every lot for five years, so tracking issues or answering audit queries has never caught us off guard. Customers in regulated sectors regularly audit our facility; each time, we welcome the extra scrutiny that drives improvements in our cleaning and material handling protocols.

    Feedback channels stay open, and close communication with experienced chemists among our customer base has led to continuous improvements—finer controls during temperature holds, additional analytical checks, and responsiveness to new process hazards. Our facility engineers have built in dedicated lines just for fluorinated organics, avoiding cross-contamination risks and preserving batch purity.

    Market Movement and Regulatory Considerations

    The regulatory landscape around aromatic amines and trifluoromethoxy groups won’t sit still. We keep our eyes on shifting limits from environmental and worker exposure authorities—this impacts everything from effluent handling to stack emissions, and ultimately shapes cost. Customers in pharma or crop-protection are painfully aware of how a single impurity or out-of-date protocol can throw a wrench in regulatory submissions. Years of working directly with these sectors gives us a strong edge in both pre-empting risks and supplying compliance documentation. We provide full impurity profiles, supply chain traceability, and documented storage procedures with each order.

    We don‘t just react to new guidance—we participate in industry workshops to stay ahead of updated hazard classifications and reporting requirements. New country markets occasionally require extra audits or adjustment in labeling, which we address through ongoing training and a lean supply chain designed for flexibility rather than speed at all costs.

    Lessons from the Floor: Process Evolution and Risk Control

    Our plant team has seen enough cycles to know that process risk creeps in at the pressure points—delivery schedules, increased batch sizes, or changes in upstream raw material sourcing. We monitor reaction endpoints with in-line spectroscopy; this gives us real-time control that’s allowed smoother scaling and fewer failed runs. Early trials took days, but with these upgrades, we shave hours while keeping yields up and waste down.

    Environmental controls play a role not only for compliance, but for operator safety. Handling aromatic amines, especially in open systems, required air control investments and more robust PPE at critical exposure points. Now, there’s no guesswork; teams rely on layered access controls, and we log monitoring data for all risk audits. This attention to safety doesn’t slow the process—it makes for steadier operations and fewer near-miss events.

    Application-Specific Perspectives

    Pharma leads usage, but not every customer follows the same pathway. Some agrochemical researchers source 4-Amino-3-(Trifluoromethoxy)Benzoic Acid as a building block for modified growth regulators. Early-stage performance polymer specialists favor the strong electron-withdrawing motif for boosting backbone rigidity and solvent resistance. Our technical team often fields queries on alternative solvent systems or reaction parameter tweaks; we share process learnings openly, aiming to help customers avoid classic pitfalls with scale-up.

    Since the material handles well with ultrasound-assisted couplings and Suzuki reactions, it attracts attention from researchers building high-complexity heterocyclic libraries. Our team benchmarks multiple purification methods, from flash to preparative HPLC, to recommend process-friendly options that minimize solvent footprints and operator time. Whether a customer orders grams or multi-kilo drums, feedback lets us spot preferred solvent mixes or additional processing steps, and we adjust future batches accordingly.

    Long-Term Partnership Approach

    Real-world manufacturing never stands still. Market swings, new competition, and the always-present squeeze for tighter quality mean today's process can feel outdated in less than a year. We discovered that direct customer collaborations produce more than just good delivery records; they shape better technical solutions to problems before they dog the industry. For projects running on tight IP windows or regulatory deadlines, we schedule pre-production meetings, share reliability metrics, and make process data available well beyond COAs.

    Production doesn’t pause at the last drum out the door. After-sale technical follow-up and detailed documentation are the standard in our plant—chemists know to expect transparent batch histories and root-cause analysis in the rare case of a setback. These practices help us keep pace with both evolving customer standards and shifting global regulations.

    Environmental Approach and Supply Security

    Waste and emissions always shadow fluorinated chemistry. Our facility embraces closed-loop recovery systems for solvents and uses selective oxidation to minimize aromatic amine residuals before waste stream discharge. This reduces ecological footprint and maintains good relations with regulators and local communities. Even with stricter fluorinated organic discharge guidelines, process tweaks and equipment upgrades allowed us to avoid production slowdowns or unplanned shutdowns.

    Supply security ranks as a close second to consistency in customer feedback. We carry buffer stocks of proprietary intermediates and prequalify two alternate sources for every key raw material. Years ago, we weathered a global shortage of a specific fluorinating agent by keeping communication open with strategic partners and not over-promising on delivery times. Instead of chasing single lowest-cost sources, we push for reliability, even when markets tighten and spot prices spike.

    Supporting Innovation and Driving Progress

    Feedback from biotech and pharmaceutical researchers has shaped much of our process development. Requests for custom salt forms, ultrapure grades free from alkali trace metals, or specific particle size distributions led us to introduce new production lines. Healthy dialogues with innovation-driven customers keep our approach practical, and knowledge transfer from our process engineers often leads to faster, more cost effective synthesis for emerging applications.

    We also make room for faster pilot run turnarounds. By investing in smaller reactor trains dedicated to niche fluorinated building blocks, we help teams validate new assay routes and lock in structure-activity relationships before investing in full-scale campaigns. Open data sharing on impurity formation and process reproducibility remains one of our core strengths, building ongoing trust from the research community.

    Retrospective: What Decades in Manufacturing Have Taught Us

    Few projects are ever as straightforward as a synthesis paper might suggest. The real value in 4-Amino-3-(Trifluoromethoxy)Benzoic Acid comes not just from clean HPLC traces or strong NMR signals, but from how predictably the product integrates into tough synthesis campaigns. Each improvement in process control, raw material resilience, and analytical feedback grants customers clarity at critical R&D milestones.

    Decades in aromatic chemistry manufacturing leave an unmistakable impression: customer priorities never stop evolving, and neither can production strategies. That means constantly scanning for tighter specs, building stronger feedback channels, and investing in both people and equipment. Supporting the wider market with dependable, tailored material—delivered transparently and refined by real-world feedback—forms the foundation of our long-term approach to specialty chemicals like 4-Amino-3-(Trifluoromethoxy)Benzoic Acid.