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2-Methoxy-5-(Trifluoromethoxy)Benzoic Acid

    • Product Name 2-Methoxy-5-(Trifluoromethoxy)Benzoic Acid
    • Alias 2-Methoxy-5-(trifluoromethoxy)benzoic acid
    • Einecs 630-930-5
    • 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
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    Specifications

    HS Code

    126855

    Product Name 2-Methoxy-5-(Trifluoromethoxy)Benzoic Acid
    Cas Number 132884-76-9
    Molecular Formula C9H7F3O4
    Molecular Weight 236.15
    Appearance White to off-white solid
    Melting Point 93-97°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Smiles COC1=C(C=C(C=C1)OC(F)(F)F)C(=O)O
    Inchi InChI=1S/C9H7F3O4/c1-15-8-4-6(9(13)14)2-3-7(8)16-5(10,11)12/h2-4H,1H3,(H,13,14)
    Storage Temperature 2-8°C

    As an accredited 2-Methoxy-5-(Trifluoromethoxy)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, 25 grams, tightly sealed with a screw cap, labeled with chemical name, CAS number, and hazard information.
    Shipping 2-Methoxy-5-(Trifluoromethoxy)benzoic acid is shipped in sealed, chemically resistant containers, protected from light and moisture. The package is clearly labeled with hazard information, handled per safety protocols for chemicals. Shipment complies with local and international regulations, with documentation included for safe transport. Store at room temperature unless otherwise specified.
    Storage Store 2-Methoxy-5-(trifluoromethoxy)benzoic acid in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong bases and oxidizing agents. Ensure clear labeling and use appropriate personal protective equipment when handling. Avoid sources of ignition and accidental contact with skin or eyes.
    Application of 2-Methoxy-5-(Trifluoromethoxy)Benzoic Acid

    Applications of 2-Methoxy-5-(Trifluoromethoxy)Benzoic Acid in Industrial Manufacturing

    2-Methoxy-5-(Trifluoromethoxy)Benzoic Acid is a specialty aromatic acid widely adopted in advanced industrial synthesis. As a direct manufacturer, we supply to key sectors requiring high purity and convincing traceability. Below, we detail core downstream application segments based on real industry demand, regulatory triggers, and in-use formulation practices.

    1. Agrochemical Active Ingredient Synthesis

    This compound serves as an essential structural intermediate in crop protection molecule pipelines, notably for herbicides and selective fungicides. Chemical development teams leverage its electron-withdrawing trifluoromethoxy group for structure-activity relationship (SAR) optimization during pre-formulation and scale-up. Integration occurs at critical condensation steps, supporting regulated product dossiers and batch consistency targets over multi-tonne scales.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for chemical synthesis
    • REACH (EC No. 1907/2006) registration, import and use authorization as a synthesis intermediate
    • US EPA requirements for active ingredient precursors
    • China GB 2763 MRL review for raw material approval in downstream actives

    Typical usage ratio

    • 5–20% in intermediate condensation reactions, adjusted by target actives’ molar input and process route

    Downstream process integration

    • Serves as a precursor in acylation or alkylation stages within fine chemical reactors
    • Introduced after initial aromatic core formation for late-stage functionalization
    • Requires controlled crystallization and isolation before downstream formulation

    Final product types

    • Modern herbicide and fungicide active ingredients
    • Crop-specific protective agents for wheat and rice segments

    2. Pharmaceutical Intermediate for APIs

    This compound is integrated at the intermediate stage of non-steroidal anti-inflammatory and central nervous system drug synthesis. Medicinal chemists employ this benzoic acid derivative during SAR-driven lead modification due to its electronic effects and solubilizing ether chain. Synthesis batches demand validated traceability and robust in-process controls to align with OECD and ICH guidelines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for active pharmaceutical ingredient intermediates
    • USP–NF, Ph. Eur. monograph alignment for aromatic pharmaceutical intermediates, where applicable
    • FDA 21 CFR Part 211 for drug manufacturing controls
    • China Pharmacopoeia ChP compliance for intermediate registration

    Typical usage ratio

    • 2–12% by weight, variable through hydrogenation or coupling stage; optimization guided by route efficiency and impurity profile

    Downstream process integration

    • Used after completion of initial benzene ring substitutions as a coupling or acylating intermediate
    • Reactive in amide and ester formation steps
    • Integrated into cGMP-compliant multi-purpose reactors under validated cleaning protocols

    Final product types

    • Non-steroidal anti-inflammatory agent APIs
    • Trifluoromethoxy-aniline pharmaceutical intermediates
    • Central nervous system drug scaffolds

    3. High-Performance Polymer Modifier

    Polymer manufacturers use this aromatic acid as a functional chain-terminating or branching modifier in specialty polyesters and high-performance copolymers. Its unique combination of trifluoromethoxy and methoxy groups modulates solubility, crystallinity, and chemical resistance in engineered plastics, especially for electronics encapsulation and fuel system components.

    Industry compliance standards

    • UL 94 V-0 and V-2 for finished polymer flame resistance
    • RoHS Directive (2011/65/EU) and REACH SVHC compliance for materials in E&E applications
    • ISO 9001:2015 for specialty polymer production
    • ASTM D256 (Izod Impact) and D638 (Tensile) as end-use properties benchmarks

    Typical usage ratio

    • 0.2–3% by total polymer mass, tuned to molecular weight and desired performance profile in the final resin

    Downstream process integration

    • Fed at oligomerization or polycondensation stage within continuous or batch reactors
    • Acts as end-group capping agent, processed under nitrogen protection due to volatility
    • Requires careful feeding to avoid prepolymer cross-linking

    Final product types

    • High-strength polyesters and liquid crystal polymers
    • Electronic encapsulants with improved dielectric properties
    • Fuel hose linings and chemical-resistant tubing

    4. Specialty Dye and Pigment Intermediate

    Producers select this benzoic acid for synthesizing high-stability organic pigments and specialty dyes, especially in applications requiring strong chemical resistance and color fastness, such as textile colorants and industrial coatings. Its electron-withdrawing groups provide improved chromophore performance and reduce off-shade risks in non-aqueous pigment dispersions.

    Industry compliance standards

    • DIN EN 71-3 (Toy Safety – Migration of Certain Elements) for pigment use in children’s products
    • OEKO-TEX® Standard 100 for textile dye safety
    • REACH Annex XVII compliance for restricted substances
    • ISO 18314 (Analytical measurement of color) in dye batch QC release

    Typical usage ratio

    • 1–10% as a coupling intermediate or precursor, depending on dye synthetic route and level of chromophore substitution

    Downstream process integration

    • Reacted via diazotization and subsequent coupling in pigment millhouses
    • Incorporated during phenol or aniline functionalization step for targeted absorption maxima
    • Kept under dry and inert atmosphere to avoid hydrolysis before use

    Final product types

    • Trifluoromethoxy-substituted azo dyes for textiles
    • High-stability pigments for automotive and coil coatings
    • UV-resistant decorative printing inks

    5. Advanced Electronic Material Synthesis

    Manufacturers of advanced electronic chemicals introduce this aromatic compound as a building block in the synthesis of functional monomers and specialty resins for printed circuit boards, photoresists, and sensor housings. The combination of the trifluoromethoxy and methoxy substituents enables fine-tuning of thermal and dielectric properties, critical for high-frequency device stability.

    Industry compliance standards

    • IPC-4101 for base materials in rigid and multilayer PCBs
    • ISO 14001 for environmental management during electronic chemical production
    • RoHS Directive (2011/65/EU) for hazardous substance control
    • UL 796 for polyimide resins in electronic interlayers

    Typical usage ratio

    • 0.5–4% in monomer and prepolymer synthesis for resins and laminates, based on resin backbone and desired end-use temperature resistance

    Downstream process integration

    • Fed as a co-monomer or modifier during etherification or imidization reactions
    • Introduced prior to final curing stage for resin cross-linking
    • Quality controlled for trace ionic content prior to downstream lamination

    Final product types

    • Photoimageable solder masks
    • Polyimide coverlays for flexible circuits
    • Dielectric layers in HDI and multilayer PCB substrates
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    Certification & Compliance
    More Introduction

    2-Methoxy-5-(Trifluoromethoxy)Benzoic Acid: Performance Rooted in Proven Chemistry

    Scientific research, process innovation, and new molecule discovery regularly steer the direction of fine chemical manufacturing. In our years of scaling, purifying, packaging, and shipping specialty chemicals, some molecules set themselves apart—not with marketing, but because demand comes from sincere results at the bench and in the plant. 2-Methoxy-5-(Trifluoromethoxy)benzoic acid is one of these compounds. Experience drives us to offer this specialty aromatic acid as a reliable, purified reagent for pharmaceutical synthesis, advanced material discovery, and unique custom projects where its structure enables progress.

    Model and Physical Consistency Backed by Experience

    The accepted molecular formula for 2-Methoxy-5-(trifluoromethoxy)benzoic acid, C9H7F3O4, only begins to tell its story. The trifluoromethoxy and methoxy groups bring electron-withdrawing and electron-donating properties together in a way that chemists know delivers distinct reactivity. Our batches undergo thorough assessment—not just testing for content, but hands-on confirmation of melting range, appearance, and solubility, judged by staff working daily with aromatic acids in various states and purities. With experience handling kilo projects right down to development-scale grams, our team recognizes subtle cues of purity that don't show up in automated printouts. The off-white to pale appearance, the crystalline nature, the ease of handling: these aren’t afterthoughts. These are hard-won insights built on actual lab work. Our material sees close scrutiny for residual solvents, trace metals, and organic impurities, since many customers require certainty when building toward regulated synthesis.

    We document reported melting points from the published literature and check them consistently, but real-world handling matters, too. If a powder clumps, retains odors, or shows unusual flow during dispensing, we look for the root cause. We test solubility by working with both typical polar and non-polar solvents, recognizing that longer contact times sometimes reveal edge-case behaviors. Our technicians see immediate use in solid-phase syntheses, bench reactions, and scale trials—feedback that loops constantly to our production supervisors.

    Application: Where Structure Meets Purpose

    Why introduce this particular benzoic acid to the market in the first place? Reactivity patterns open doors to new pharmaceutical intermediates, agrochemical candidates, and advanced electronics building blocks. Medicinal chemists routinely reach for the 2-methoxy-5-(trifluoromethoxy) substitution pattern as a platform for SAR studies. The benzoic acid core tolerates a wide range of transformations, but the combined influence of the methoxy group (at the ortho position) and the electron-starving trifluoromethoxy group (meta to the acid) gives it a unique profile absent in even closely related analogues. Electrophilic substitution rates, monoalkylation selectivity, and metabolic fate all shift; these are not theoretical effects but ones reported in peer-reviewed work and confirmed by our clients’ successful syntheses.

    Our chemists hear directly from colleagues in the pharmaceutical and agrochemical research space, noting that this acid enables clean amide formation under milder conditions than similar molecules lacking the fluorine boost. In multi-step synthesis, when a truncated yield or unexpected side-product ruins a project, it rarely traces to the benzoic acid if the intake is pure, well packed, and handled precisely. Plant operators need this confidence. The same functional groups that let medicinal chemists tailor molecules for better receptor affinity also serve polymer scientists and advanced materials teams seeking high-durability linkers. For these innovators, the difference between a single methoxy, trifluoromethoxy, or trifluoromethyl group cascades through the process—impacting curing times, thermal resistance, and even color stability. These are specifics acquired through hands-on collaboration, not abstract speculation.

    Distinction from Close Relatives: Why Precision Matters

    Suppliers often bracket 2-Methoxy-5-(trifluoromethoxy)benzoic acid with simpler benzoic acids or the more widely traded mono- or di-substituted analogues. Those of us who synthesize and purify such compounds know the distinction grows apparent inside the reactor, not just on a spec sheet. The presence of both methoxy and trifluoromethoxy groups sets it apart from 2-methoxybenzoic acid, 5-trifluoromethoxybenzoic acid, or parent benzoic acid. Electrophilic attack, hydrolysis, and coupling reactions push and pull on the aromatic ring in distinct ways. The energetic landscape in NMR, details of impurity profiles after a condensation, even the stability after a month on the shelf—all point to tangible differences.

    Sourcing by substitution pattern and traceable origin turns out to be critical, not a bureaucratic checkbox. We’ve traced back failed reactions to the smallest change in group position or the presence of minor rotamers. These aren’t “theoretical” risks or errors from desk research—they’re challenges solved by chemists and plant operators with years on the bench and the confidence to tweak parameters mid-run. Our plant commits to this exact structure at the micro-level because the differences reveal themselves down the line in customer workflows—from tighter LC-MS readouts to higher yields in deprotection or amidation steps. The thermostat in a reactor doesn’t care about product descriptors—it cares if a reaction is exothermic or sluggish due to the wrong structural isomer.

    Batch Reliability, Safety, and Traceability: Margin for Real-World Scale-Up

    Every batch of this benzoic acid gets tracked from precursor origin through final packaging. Our teams depend on documentation, barcoding, and hands-on inspection—not as a compliance burden, but as a hard-earned habit from years of troubleshooting narrowly missed specifications and learning from overlooked details. For researchers moving from bench to pilot, batch-to-batch predictability saves huge investment later. Every order ships with verifiable purity data tied directly to that lot—our team is reachable to talk through interpretation or answer follow-up questions based on observed results during synthesis or formulation.

    We supply this compound in bulk, working with containment and exposure limits in line with regulatory and worker safety guidelines. The purity and impurity profile don’t just matter for the customer’s chemistry—they also shape our procedures for filtration, drying, and storage. Our warehouse staff stays vigilant for any shifts in container seal, absorption pattern, or label legibility, drawing on years of direct feedback from companies relying on us to maintain compliant inventory and streamline safety reviews. Trace metals, color stability, and low-level impurities arrive at levels we’d accept for our own syntheses, because we still actively run internal bench tests and validations, never just reselling or repacking. These are the basics, but we treat them as cornerstones, not paperwork. Several clients have preserved their own pilot projects with late-stage material from our runs; their feedback forms the backbone of our lot-release practices.

    Usage: Not Just for Library Collections

    Labs might stock a series of substituted benzoic acids for reaction mapping or SAR work, but few molecules see repeat orders and scale-up requests like this compound. Direct feedback shows our 2-methoxy-5-(trifluoromethoxy)benzoic acid functions as a building block in active pharmaceutical ingredient (API) synthesis, lead optimization for crop protection agents, and as a linker for advanced polymers in optoelectronic devices. Synthetic routes that previously risked decomposition or low conversion rates see measurable improvement when switching to this precise substitution pattern. The methoxy group confers certain resonance stabilization, while the trifluoromethoxy substantially increases resistance to nucleophilic attack, enabling access to new coupling partners and higher selectivity.

    Process chemists running kilo-scale intermediates report smoother purification downstream, with fewer contaminants from unwanted ring activation or side-chain loss. Analytical teams confirm consistency run after run, giving project managers the confidence to move beyond bench trials. In some projects, the presence of this specific acid shortened total synthesis steps, saving months compared to processes relying on trial-and-error optimization of less suited analogues. Our history working side-by-side with formulation scientists means we know how crucial timely, reproducible delivery of specialty acids proves to be—especially when the current market faces ongoing supply chain delays and regulatory bottlenecks.

    Different from Commodity Chemicals: Handling and Service Mean More

    This is not a commodity product that sits in a bulk tank or flows through automated blend lines. 2-Methoxy-5-(trifluoromethoxy)benzoic acid requires handling with chemist-level care, where every lot gets packaged with attention to minimization of cross-contamination and excess exposure to heat or light. We recognize requests for specific particle sizes, customized packaging quantities, and specialized documentation, because real users often encounter roadblocks sourcing unusual chemicals via generic vendors. Direct feedback from allied industries informs how we pouch or drum the acid, right down to inert atmosphere considerations during sealing for moisture-sensitive processes.

    Our in-house QC spans more than HPLC and NMR—visual inspection from trained staff checks for clumping, discoloration, or trace label errors that can create confusion downstream. If a client reports even minor deviation at their site, our process team traces the chain of custody down to the sub-lot and raw material input. We’re a phone call or email away; our technical support desk consists of actual bench chemists, not just script readers, because that’s how we’d expect to be treated in their place. This is a culture built from years solving real process problems—not just pushing paper or sending out sales forms.

    Consistent Chemistry Enables Innovation Downstream

    The impact of this specialty benzoic acid on customer projects lands far outside our own gates. It travels into kilo-scale synthesis reactors, small vials for target validation, and modular material assembly lines. Regulatory trends, green chemistry protocols, and business innovation in pharmaceuticals all trace their timelines back to the reliability of intermediates like this—from compliance audits to peer-reviewed results. Recent years brought enormous pressure on sourcing, import documentation, and fire safety. Our response is an upgrade of containment protocols and user-friendly, comprehensive test reports (COAs) that speak the language of bench chemists and regulatory managers, not just procurement staff. We want users to see immediately how each lot stacks up—not in vague terms, but with purpose-driven transparency. This acid isn’t just a tick on a checklist—it’s a cascade point for patient trials, new crop treatments, and material science KPIs.

    Supply Relationships Driven by Long-Term Trust

    Long-term customers place repeat orders not just for convenience, but for peace of mind earned over years of reliable delivery, open communication, and technical troubleshooting. Where distributors tend to focus solely on price breaks or logistics, we invest upstream in process optimization: improving yields, tightening impurity specs, tweaking packaging, and scheduling runs to keep customer timelines intact. These changes happen only by talking with actual plant managers, synthetic chemists, and formulation heads—people with credibility gained from running their own syntheses and evaluating outcomes. We set aside time for troubleshooting odd reactivity or contamination issues and coach junior researchers on bench tips picked up across hundreds of batches. This iterative learning shapes every container and certificate leaving our site.

    The market continues to evolve, demanding not just purity but actionable traceability and robust support. Our plant invests in automation only where it frees up staff to focus on quality interpretation, not just to hit volume metrics. Every critical test instrument gets regular calibration by chemists who actually interpret spectra, not just push buttons. This hands-on approach means fewer surprises for downstream operators and better resilience in regulatory or audit events. The culture at our manufacturing facility revolves around open knowledge sharing—because the reality of specialty chemical supply is that a shortcut today becomes a recall tomorrow.

    Continuous Improvement: Feedback Turns Into Refinement

    Routine project work and recurring audits shape the way we handle this benzoic acid over time. Customer insight landed us on better drying schedules and more robust container labeling, for example. We build lessons from both power users and first-time clients into our training sessions and daily production briefings. Analytical standards shift as new regulatory updates flow down, so we stay proactive—implementing ELN-based lot tracking, updating our safety documentation, and running parallel validations so that no gap in data makes it out the door. Raw material spec changes, packaging innovation, and compliance with new environmental guidelines: these all reflect the market’s honest feedback loop, not just theoretical improvement.

    Right now, our scale extends from tens of grams for research to multi-kilo shipments for production, spanning custom requests such as extra QA analysis for niche regulatory filings or temperature loggers for sensitive shipments. Our account managers push for continuous improvement by spending time with actual users—shadowing process development, watching product get weighed and dispensed, joining troubleshooting calls, and feeding back field experiences into both process and product refinement. This is how we avoid the drift toward lowest-common-denominator supply; we stay focused on what chemists, formulators, and engineers actually experience.

    The Role of Rigorous Details in Specialty Benzoic Acid Supply

    Supplying pure, consistent, and well-characterized 2-Methoxy-5-(trifluoromethoxy)benzoic acid takes discipline, feedback loops, and a willingness to learn from setbacks as well as successes. We draw our technical confidence from years of running chemistry at varying scales—not just checking certificates, but tracing back every anomaly to its source. The subtleties of this molecule’s structure make it far more than an add-on to a product catalog: small changes in its synthesis, purification, handling, and storage will show up later in the customer’s data readouts. We address this through tight internal checks, a culture of curious chemists, and transparency about both the strengths and limitations of each lot.

    Over years, users have come to value not just the assay on the bottle but the story and certainty behind each unit delivered. We don’t gamble with analogues or tolerate hand-waving on impurity claims. For every container shipped, dozens of checks precede the moment it leaves our site, rooted in the same reality as those relying on it further down the value chain. We’re proud that our 2-Methoxy-5-(trifluoromethoxy)benzoic acid has played a role in making better medicines, safer crops, and more resilient advanced materials. The product’s unique blend of functional groups, stability, and reliable reactivity gives our partners a platform to innovate confidently—from bench test to market launch. That confidence comes not from promises, but from decades of shared outcomes, careful observation, and ongoing adaptation to real-world needs.