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4-Methoxy-2-(Trifluoromethyl)Benzoic Acid

    • Product Name 4-Methoxy-2-(Trifluoromethyl)Benzoic Acid
    • Alias 4-Methoxy-2-(trifluoromethyl)benzoic acid
    • Einecs 629-875-8
    • 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

    920444

    Productname 4-Methoxy-2-(Trifluoromethyl)Benzoic Acid
    Casnumber 19715-90-9
    Molecularformula C9H7F3O3
    Molecularweight 220.15
    Appearance White to off-white solid
    Meltingpoint 105-108°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Smiles COC1=CC(=C(C=C1)C(F)(F)F)C(=O)O
    Inchi InChI=1S/C9H7F3O3/c1-15-6-3-2-5(9(10,11)12)7(4-6)8(13)14/h2-4H,1H3,(H,13,14)
    Storagetemperature Room temperature

    As an accredited 4-Methoxy-2-(Trifluoromethyl)Benzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with screw cap, labeled “4-Methoxy-2-(Trifluoromethyl)Benzoic Acid, 25g,” includes hazard symbols and manufacturer information.
    Shipping 4-Methoxy-2-(Trifluoromethyl)benzoic acid is shipped in secure, chemically-resistant containers, labeled compliant with regulatory standards. The package is sealed to prevent leaks and protected against moisture and impact. Shipping follows all relevant safety guidelines, including provision of necessary documentation (SDS), and is handled by certified carriers specializing in chemical transport.
    Storage 4-Methoxy-2-(Trifluoromethyl)benzoic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and bases. Protect it from moisture and direct sunlight. Ensure proper labeling and keep it away from sources of ignition or heat. Follow relevant safety and regulatory guidelines when handling and storing this chemical.
    Application of 4-Methoxy-2-(Trifluoromethyl)Benzoic Acid

    Applications of 4-Methoxy-2-(Trifluoromethyl)Benzoic Acid in Industrial Manufacturing

    As the original manufacturer, we support global partners with consistent, high-purity 4-Methoxy-2-(Trifluoromethyl)Benzoic Acid for critical applications. This compound demonstrates proven value as a specialty intermediate in rigorously controlled downstream sectors, delivering traceable quality and reliable synthesis performance across specialized production networks.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical manufacturers use this compound as a building block in multi-step reactions to create advanced intermediates for active pharmaceutical ingredients, particularly in the development of anti-inflammatory and CNS drug scaffolds. It undergoes strategic coupling, activation, or derivatization—directly influencing the yield and purity of key heterocyclic and aromatic APIs destined for regulated markets.

    Industry compliance standards

    • GMP (Good Manufacturing Practice) – ICH Q7, FDA 21 CFR Part 210/211
    • EU EudraLex Volume 4 for API manufacturing
    • USP, Ph. Eur., and JP requirements for raw material traceability (as applicable)
    • REACH Registration (EU chemicals regulation)

    Typical usage ratio

    • 0.5–8 mol% relative to target API, depending on the synthesis step and process yield; optimized by stoichiometry and impurity profile requirements

    Downstream process integration

    • Input at the condensation, acylation, or selective ring formation stage; subject to phase transfer, metal-catalyzed coupling, or protection/deprotection sequences in continuous or batch reactor systems

    Final product types

    • Advanced API intermediates for small-molecule medicines
    • Regulated pharmaceutical ingredients used in finished tablets, capsules, and injectables

    2. Agrochemical Active Ingredient Synthesis

    Downstream agrochemical producers incorporate this acid into synthetic routes for complex herbicides or fungicides featuring trifluoromethyl- and methoxy-substituted aromatic rings. Its integration supports structure-activity optimization for selectivity and environmental fate, where precise impurity control and reaction reproducibility directly affect field-product registration.

    Industry compliance standards

    • ISO 9001-certified process control
    • FAO/WHO technical material requirements
    • EPA (US), REACH (EU) substance approval protocols
    • OECD Good Laboratory Practice (GLP) for synthetic study data

    Typical usage ratio

    • 1–12 mol% based on agrochemical target molecule complexity and required substitution density; adjusted according to active purity requirements

    Downstream process integration

    • Charged in initial aromatic ring formation, halogen exchange, or late-stage functionalization for target enrichment; implemented in both fixed-bed and stirred batch reactors operating under inert atmosphere

    Final product types

    • Registered herbicide technical concentrates
    • Fungicide raw actives for wettable powders and EC formulations

    3. Organic Electronics and Specialty Polymers

    Producers of specialized monomers and electronic-grade polymers use this compound during the synthesis of monomer units for advanced fluorinated resins and photoresist components. The methoxy and trifluoromethyl functionalities enable unique performance attributes in dielectric, UV-cured, and barrier materials deployed in semiconductor and display manufacturing.

    Industry compliance standards

    • RoHS (EU Directive 2011/65/EU) for restriction of hazardous substances
    • IEC 61249-2-21 (halogen-free requirements in electronics)
    • QC080000 (IECQ HSPM) hazardous substance process management
    • REACH SVHC listing for polymers

    Typical usage ratio

    • 0.3–6 mol% in the monomer mix, variable by desired polymer chain length, side-group loading, and dielectric properties

    Downstream process integration

    • Used in Suzuki, Heck, or Buchwald coupling reactions for monomer extension or functional end-group attachment; as an intermediate for final polymerization or photoresist formulation blending

    Final product types

    • Photoresist monomers for semiconductor lithography
    • Electronic-grade specialty polyarylethers and fluoropolymers for circuits, displays, and encapsulation films

    4. Fine Chemical and Dyestuff Intermediates

    Fine chemical producers integrate this aromatic acid within multipurpose dye precursor syntheses or as a structural motif in specialty colorants and UV-absorbing additives. The electron-withdrawing trifluoromethyl group in conjunction with methoxy substitution supports tunable spectral properties and chemical resistance critical to advanced pigment and dye innovations.

    Industry compliance standards

    • ISO 9001/14001-certified manufacturing for colorants and auxiliaries
    • Oeko-Tex Standard 100 for textile colorant safety (where applicable)
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) code of practice
    • REACH Annex VII–IX for advanced intermediates registration

    Typical usage ratio

    • 0.8–5 mol% as a key intermediate, ratio adjusted to target absorptivity and motif substitution patterns for end-use performance

    Downstream process integration

    • Introduced at key condensation, cyclization, or azo coupling steps as controlled-feed intermediate; incorporated before purification and final dye crystallization

    Final product types

    • High-stability dyes for electronic displays and industrial coatings
    • Specialty pigment precursors and photoactive additives for plastics and fibers

    5. Liquid Crystal Material Precursor

    Manufacturers supplying the liquid crystal (LC) sector use this compound in developmental fluorinated benzoic acid esters and related intermediates to enhance dielectric anisotropy and thermal stability in advanced LC mixtures tailored for display panels. Structural purity and substituent positioning are crucial to finished product performance.

    Industry compliance standards

    • ISO 14001-certified environmental management
    • IEC 61249-2-21 and RoHS for electronic materials
    • REACH compliance for intermediate registration
    • Customer-specific QC and purity requirements (≥99%) for LC applications

    Typical usage ratio

    • 0.2–2 mol% in precursor feed, controlled by LC formulation requirements and retention time in synthesis pathway

    Downstream process integration

    • Engaged during esterification and selective halogenation stages; followed by purification and blending into multi-component LC mixtures in closed-system reactors

    Final product types

    • High-performance LC mixtures for TFT-LCD and OLED display panels
    • Intermediate LC components for mobile device displays and optical shutters
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    Certification & Compliance
    More Introduction

    Introducing 4-Methoxy-2-(Trifluoromethyl)Benzoic Acid: Expertise from the Factory Floor

    Working on the production floor, we see compounds like 4-Methoxy-2-(Trifluoromethyl)benzoic acid pass through every stage of synthesis, purification, and packaging. For years, our chemists have watched the steady rise in demand for this particular aromatic acid, recognized not just for its niche structure but for how it unlocks new routes in chemistry that other benzoic acid derivatives simply cannot.

    Why 4-Methoxy-2-(Trifluoromethyl)Benzoic Acid Matters in the Chemical World

    Aromatic carboxylic acids have always formed a cornerstone in organic synthesis, and 4-Methoxy-2-(Trifluoromethyl)benzoic acid belongs to a class that truly stands apart. The combination of a trifluoromethyl group with a methoxy substitution on the phenyl ring changes reactivity in subtle ways. We see that effect every time a customer calls with a synthetic challenge: traditional benzoic acids can clog up a reaction or fail to deliver the electronic effects their synthesis demands. The presence of the methoxy group at the para position and the bulky, electron-withdrawing trifluoromethyl group at the ortho position guides transformations that would otherwise stall or misfire.

    From our own process chemistry teams, feedback keeps coming in. Adding fluorinated aromatic acids into synthetic routes has improved outcomes for pharmaceuticals, agrochemicals, and even specialty polymer industries. Over and over, 4-Methoxy-2-(Trifluoromethyl)benzoic acid shows itself as a versatile building block, introducing both electron-withdrawing and electron-donating influences into a molecule without losing the integrity of the phenyl backbone.

    Our Experience Manufacturing This Compound

    Manufacturing 4-Methoxy-2-(Trifluoromethyl)benzoic acid takes more finesse than turning out generic benzoic acids. The process starts with high-purity starting materials, sourced under close scrutiny. Impurities entering at this stage create headaches downstream, so our supply managers insist on analytical confirmation before batches move forward. Our team handles the delicate steps that introduce both trifluoromethyl and methoxy groups under strictly controlled temperature and solvent conditions. After many years refining this process, we can consistently achieve high yields and low residual solvents, because even trace leftovers will compromise performance in sensitive end-use sectors like drug development.

    Our reactors have seen their share of challenges scaling from pilot batches to multi-ton quantities. Fluorination chemistry is demanding — vents, seals, temperature controls, and even the cleaning routines after each batch need tight management. Worker safety comes first: PPE, scrubbers, and leak checks are part of daily routines. Early on, temperature spikes threatened to stall scale-up, but process optimization and in-line monitoring caught hot spots before fouling or thermal degradation could occur. There’s no replacement for hands-on experience here; it’s what earns customer trust batch after batch.

    Specifications That Reflect a Chemist’s Priorities

    Industry standards guide us, but it’s the feedback from bench chemists that shapes our specifications. Impurity profiles are tailored with the pharmaceutical and research chemist in mind, since downstream applications rely on minimal side-products. We keep moisture and residual solvent content low, as both the trifluoromethyl and methoxy groups can be sensitive to hydrolysis and other side reactions. Typical melting points and purity (assayed by HPLC and NMR) are confirmed for every batch, with full transparency in the certificate of analysis. Years of conversation with researchers taught us how even a fraction of a percent impurity can sink an entire synthesis. So we don’t “target” purity; we demonstrate it, with open results.

    Batch-to-batch consistency is a real measure of our facility’s discipline. Our QA lab tracks key specifications: color, clarity, melting range, and identity confirmation via NMR and mass spectrometry. Most of all, customers want reliability: the material from last shipment performs the same in their reaction flask as this shipment. We’ve put in the work (and sometimes long nights) to make that a point of pride.

    Applications and Unique Value to Synthetic Chemists

    4-Methoxy-2-(Trifluoromethyl)benzoic acid is not just another benzoic acid — the proof lies in its role as a strategic intermediate. Its utility shines in the synthesis of both proprietary APIs and research leads. The balancing act between electron-donating methoxy and electron-withdrawing trifluoromethyl fine-tunes the phenyl ring’s reactivity, granting new options in cross-couplings, esterifications, Suzuki reactions, and other transformations.

    On the plant floor, we’ve fielded stories from customers who swapped out more standard fluorinated benzoic acids only to find reaction profiles shift dramatically. The methoxy group opens doors for further functionalizations — especially in late-stage modifications — which can be tough to pull off on more simple analogs. The trifluoromethyl substitution doesn’t just tweak activity; it lends metabolic stability and influences physical attributes like solubility, all vital for pharmaceutical applications. Our customers in medicinal chemistry have pointed out better outcomes with molecules built off this scaffold, and we keep hearing how reactions run cleaner, with easier downstream purification.

    Unlike many multi-substituted benzoic acids, which bring stubborn impurities or require aggressive purification protocols, our product’s synthesis has been dialed in for minimal byproduct formation. This matters in scale-up reactions, where a few extra purification steps magnify costs and time. Laboratories aiming to generate libraries benefit by setting up reactions in parallel, knowing our material behaves as promised.

    Comparing With Other Benzoic Acid Derivatives

    Having produced a spectrum of benzoic acid derivatives, we see firsthand the differences subtle structural changes make. A simple 2-trifluoromethylbenzoic acid reacts very differently than the methoxy analogue. Adding the methoxy group boosts compatibility with certain palladium-catalyzed couplings and enables further oxygenation chemistry that pure trifluoromethyl benzoic acid misses. In competitive testing, this variant shows stronger shelf stability and improved recovery after storage, even at room temperature.

    Customers ask about whether to choose this compound or a para-methoxy version with no halogen, and our response comes straight from the lab: the reactivity difference is significant. One recent example from a medicinal chemistry workflow: the methoxy-trifluoromethyl combination provided an aryl core that allowed for selective amide coupling, with less over-reaction and cleaner API profiles by HPLC. Colleagues focusing on functional materials have found benefit too — the fluorinated analogue imparts useful properties into polymers, including hydrophobicity and enhanced durability, which the standard benzoic acids can’t deliver.

    We recognize the steady stream of inquiries about price and supply. For years, we’ve worked to keep costs manageable. The most common production bottleneck is reliable access to trifluoromethyl sources, which fluctuate with global demand. Knowing this, we keep strong links with suppliers and focus on buffer stocks, minimizing lead time risk — so researchers, purchasing teams, and production managers can move forward without worry over sudden shortages or spec changes.

    Real-World Challenges and Solutions

    On this side of the industry, problems crop up that rarely show up on glossy datasheets. During an uptick in global demand for specialty intermediates, our team encountered limited supply of high-purity trifluoromethyl precursors. Price hikes threatened to squeeze research budgets for both established and startup pharmaceutical firms. To counter this, we invested in alternate supply routes and formed direct, long-term partnerships with upstream producers. By managing the entire chain closely from material procurement to final QC, we protect our customers against both shortages and spec drift.

    Shipment and storage concerns are another frequent discussion point. Both the trifluoromethyl and methoxy groups bring sensitivity to prolonged heat and moisture. In the early days, we learned hard lessons about packaging — standard poly bags let moisture seep in and led to clumping, which complicated dissolutions on the customer end. Today, all outgoing shipments travel in moisture-proof, light-resistant containers, and we include handling tips based on our own warehouse trials. Our technical support team regularly fields questions on long-term storage, shelf life, and solubility — not just parroting textbook answers, but relaying what we see from our own retained samples year after year.

    Supporting Advanced Research and Development

    As drug discovery and advanced materials demand more sophisticated building blocks, compounds like 4-Methoxy-2-(Trifluoromethyl)benzoic acid become mission-critical. Our experience working with R&D teams gives perspective into some of the most challenging syntheses out there. Several industry partners used to struggle with unpredictability until switching to our product. It provided the consistent performance they needed to avoid costly re-runs.

    We’ve supported projects where a slight impurity, undetected by basic HPLC, derailed months of work. That drove us to establish secondary analytical controls and invest in higher-resolution NMR. Now, every shipment gives the recipient not just a product, but peace of mind. As a manufacturer, we see our job as reducing variables to clear the path for genuine scientific progress. By liaising with researchers, we continuously tweak production based on feedback, so material properties match end-use expectations as closely as practical chemistry allows.

    Looking to the Future: Sustainability and Reliability

    Chemical manufacturing faces pressure to address both environmental and supply chain stability. The processes that underpin 4-Methoxy-2-(Trifluoromethyl)benzoic acid synthesis once generated more waste than we were proud of. Through equipment investments, greener solvents, and catalyst recycling programs, we've steadily reduced output of hazardous byproducts. It wasn’t an overnight fix; each process step got scrutinized and optimized, sometimes by hand, sometimes by new automation. Environmental stewardship is now embedded in decision-making, from how we dispose of filtrate to how we plan expansions.

    We also track regulatory shifts. Some customers want documentation for REACH or TSCA, others seek details on impurity profiles to meet the next wave of regulatory demands. Our approach keeps compliance up to date, without holding up research or manufacturing. That makes things easier for those working in high-stakes fields like pharmaceuticals or electronics, where regulatory slip-ups carry big risks and big costs.

    Experience-Driven Innovation

    Chemical manufacturing isn’t about sitting still. Each batch, every late-night trouble-shoot, and all those emails with reaction updates — they drive our improvements. We solicit feedback — whether it points to a purity concern, a recurring shipment delay, or a successful application in a new synthesis. That feedback led to better monitoring for residual water, more robust packaging, and even optimization of particle size, after a customer’s filter press kept clogging. Our approach is grounded in direct dialogue with the chemists and operators across the industry who rely on our material.

    4-Methoxy-2-(Trifluoromethyl)benzoic acid represents more than just a molecule — it’s a testament to what patient process improvement, rigorous quality assurance, and transparent communication can deliver. Every drum, every bag that leaves our facility carries the fingerprints of our team, from R&D to the shipping dock. We know what it takes to make sure the product matches the customer’s needs, batch after batch.

    Commitment to Chemists, From Our Factory to Your Lab

    Ultimately, our mission is to deliver reliability along with every shipment of 4-Methoxy-2-(Trifluoromethyl)benzoic acid. Years of direct manufacturing give us a perspective that can’t come from stockrooms or catalogues. We've solved problems, large and small, often with only hours between identifying an issue and implementing a workaround. From dealing with supply shortages during peak demand, to developing analytical techniques that catch trace impurities, the biggest lessons come from the production line, not just from the lab bench.

    When new researchers call, they often ask about specific technical issues — solubility in mixed solvents, compatibility with high-throughput synthesis, or storage with advanced robotic workflows. We answer from real experience, not hypotheticals, because our teams run those same trials before we recommend solutions. We believe this hands-on approach helps researchers avoid pitfalls before they crop up, saving time, budget, and unnecessary frustration.

    Moving Forward Together

    The chemical industry depends on trust, innovation, and a willingness to tackle new problems. In supplying 4-Methoxy-2-(Trifluoromethyl)benzoic acid, our aim goes beyond making a sale — it’s about enabling new discoveries, powering advanced manufacturing, and creating materials for medicines and products that improve lives. Every experience on our production line, every conversation with a customer, shapes the way we make and deliver this compound. As applications broaden and the bar for purity and performance rises, we keep evolving, investing in both technology and people to serve the next wave of research and production needs.

    If you're a chemist or researcher pushing the boundaries of what’s possible with substituted benzoic acids, know that every bottle of our product reflects real expertise and a commitment to your success. We welcome technical discussions, feedback, and new challenges — it’s how our product, and our team, keep moving forward.