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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 | 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. |
Applications of 2-Methoxy-5-(Trifluoromethoxy)Benzoic Acid in Industrial Manufacturing2-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 SynthesisThis 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
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2. Pharmaceutical Intermediate for APIsThis 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
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3. High-Performance Polymer ModifierPolymer 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
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4. Specialty Dye and Pigment IntermediateProducers 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
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5. Advanced Electronic Material SynthesisManufacturers 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
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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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.