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HS Code |
805761 |
| Productname | 2,3,6-Trifluorobenzoic Acid |
| Molecularformula | C7H3F3O2 |
| Molecularweight | 176.09 g/mol |
| Casnumber | 403-27-6 |
| Appearance | White to off-white solid |
| Meltingpoint | 153-156°C |
| Boilingpoint | 303.6°C at 760 mmHg |
| Density | 1.595 g/cm3 |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | C1=CC(=C(C(=C1F)F)C(=O)O)F |
| Inchi | InChI=1S/C7H3F3O2/c8-3-1-2-4(9)6(5(3)10)7(11)12/h1-2H,(H,11,12) |
| Synonyms | 2,3,6-Trifluorobenzoic acid; Benzoic acid, 2,3,6-trifluoro- |
| Refractiveindex | 1.499 (estimate) |
| Pka | 2.89 |
| Storagetemperature | Store at room temperature |
As an accredited 2,3,6-Trifluorobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle with a secure screw cap, labeled "2,3,6-Trifluorobenzoic Acid, CAS 2458-29-1, 99% purity." |
| Shipping | 2,3,6-Trifluorobenzoic Acid is shipped in tightly sealed containers to prevent moisture entry and contamination. It should be labeled according to chemical hazard regulations, protected from excessive heat and direct sunlight, and stored upright. Transportation should comply with local and international regulations for handling and shipping hazardous chemicals. |
| Storage | 2,3,6-Trifluorobenzoic acid should be stored in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and bases. Keep the container tightly closed and protect it from moisture and direct sunlight. Store in a corrosive-resistant container, clearly labeled, and handle with appropriate personal protective equipment to avoid inhalation or contact with skin and eyes. |
Applications of 2,3,6-Trifluorobenzoic Acid in Industrial ManufacturingOur expertise in manufacturing 2,3,6-Trifluorobenzoic Acid ensures consistent quality for advanced industrial sectors. The following section details specific downstream industries where this compound serves as a critical formulation component, including technical data on regulatory frameworks, recommended dosages, integration methods, and typical end-use products. 1. Pharmaceutical Intermediate Synthesis2,3,6-Trifluorobenzoic Acid is a preferred intermediate in the synthesis of select active pharmaceutical ingredients (APIs), notably in fluorinated drug development pipelines. Our long-standing partnerships with pharma producers focus on manufacturing efficiency, scalability, and meeting global registration requirements. This compound's fluorinated aromatic ring structure underpins its role in scaffold construction for anti-infectives and oncology molecules. Chemists introduce it during multistep synthesis as a building block prior to key coupling, ensuring high-purity substrates for downstream derivatization. Industry compliance standards
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2. Agrochemical Active Ingredient ManufacturingIn agrochemical synthesis, 2,3,6-Trifluorobenzoic Acid acts as a feedstock for herbicides and fungicides targeting pest-resistant crop variants. Its unique substitution pattern confers desirable bioavailability and hydrophobic interactions within plant metabolic pathways. Downstream formulators value the predictable behavior of trifluorinated ring systems when constructing selective pesticides. Our facility supplies technical-grade material, subjected to additional user-side refinement for actives registration. Technical teams optimize batch addition at key esterification or amide bond formation stages. Industry compliance standards
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3. Specialty Polymer Monomer PreparationThis compound is incorporated as a specialty monomer precursor in the design of high-performance fluorinated polymers. Its trifluorinated structure imparts enhanced chemical resistance and reduced surface energy to the downstream resin matrix, essential for electronics, protective coatings, and advanced membranes. Industrial chemists leverage its carboxylic acid group for downstream esterification or ring-opening reactions prior to crosslinking. Our technical sales teams often consult on dosage and handling to align with end-use viscosity and reactivity needs in resin casting lines. Industry compliance standards
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4. Liquid Crystal and OLED Intermediate ProductionManufacturers serving the display technology industry source 2,3,6-Trifluorobenzoic Acid as a key intermediate for synthesizing specific liquid crystal compounds and OLED charge transport agents. Its precise substitution facilitates stable dipole moments, supporting robust mesomorphic behavior in display matrices. OLED formulators utilize the acid moiety for later functionalization stages. Entry into the production process occurs post-initial aromatic nitration and prior to specific aryl ether couplings, enabling batch-to-batch consistency in ultra-high purity environments. Industry compliance standards
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In the world of specialty chemicals, some compounds stand out for the steady results they deliver in real application. Over years of working with fluorinated aromatics, the production and application of 2,3,6-trifluorobenzoic acid have repeatedly illustrated the difference a well-crafted molecule makes. It carries a CAS number 2458-29-7, and its molecular formula C7H3F3O2 points to that balance between stability and reactivity which so many chemists demand when synthesizing advanced materials.
In-house production gives us a clear look at the challenges and potential found in this acid. The trifluorinated structure sits at a crossroads: three fluorines on the aromatic ring alter both the electron distribution and chemical behavior, setting this benzoic acid apart from simple mono- or difluoro variants. This difference becomes obvious in daily lab practice.
Our facility produces 2,3,6-trifluorobenzoic acid to strict standards because downstream users rely on predictable performance. Clients working in both pharmaceutical intermediates and specialty polymer sectors consistently highlight two required qualities: sharp purity and batch reliability. We push for a purity >99% by HPLC, with stringent controls on water content and trace impurities. Crystalline appearance, melting point repeatability, and spectral confirmation with NMR and IR back up those purity measures.
We avoid shortcuts such as outsourcing or blending low-cost intermediates, since inconsistency shows up fast when scaling a process. Chemists across different sectors have told us minor shifts in impurity profiles can upend a full week’s work, so maintaining ultra-low halide and non-fluorinated aromatic impurities is non-negotiable on our floor. We’ve put in place automated drying and advanced purification columns precisely to deliver high batch-to-batch repeatability.
With each batch, we prioritize traceability over sheer volume. QC data accompanies every shipment, and each lot is archived for cross-reference. Having lived through the frustration of chasing down an impurity in a final active ingredient or advanced material, our team does not cut corners on documentation or sample retention.
Many producers, especially those in custom synthesis, press us about why we pursue this specific isomer. In practice, having three fluorines in the 2,3,6 positions enables a unique mix of hydrophobicity and reactivity. Chemists designing agrochemical intermediates or advanced pharmaceutical building blocks look for these effects. The electronic properties of this structure make it much more than a substitute for benzoic acid or even for 2,4,6- or 2,3,4-trifluoro- derivatives.
Synthesis teams find that this configuration influences substitution chemistry at the aromatic ring—either facilitating or blocking certain reactions. With a genuine understanding of these mechanisms, our on-site team fine-tunes both the crystallization and drying phases, tailoring particle size and density. That hands-on feedback loop, unavailable to traders or outsourced producers, makes the difference when customers report back on scale-up issues or solvent compatibility.
There’s a tendency in the market to treat all trifluorobenzoic acids as interchangeable, failed syntheses often result from that shortcut. Our regular partners in the electronics chemicals and medicinal chemistry fields have experienced failed couplings or erratic yields when they switched to the 2,4,5- or 3,4,5-isomers out of convenience. Only after painstaking troubleshooting did those teams realize the subtle but critical difference in reactivity and solubility profiles.
The pharmaceutical sector, with its strict regulatory framework, calls for chemicals that deliver more than mere compliance. Working with small molecule intermediates, chemists recognize that any variability at the starting material stage can snowball into downstream risks—either via API impurity, altered bioavailability, or rejection of full batches. We use 2,3,6-trifluorobenzoic acid regularly as a starting fragment for active ingredient synthesis, especially in stepwise fluorination methods.
In-house synthesis of this acid gave us a front-row seat to the delicate balance demanded by innovators targeting halogenated drug candidates. The triple fluorination changes pKa and influences metabolite formation; such details can make or break patent portfolios. We actively support clients by tracking minor byproducts and feedback from pilot runs, with dedicated routes for impurity isolation and analysis. Several research partners have relied on our reference samples to debug adverse reactions at the preclinical stage.
The requirement for GMP-aligned documentation has prompted our investment in automated tracking and storage. We believe every bench chemist should be able to trace their bottle to the very reactor it was made in. Our lot traceability system has grown up over years of user feedback. Suggestions from lab and manufacturing teams now shape batch labeling and packaging, with barcodes integrating seamlessly into digital LIMS systems to support audits and regulatory filings.
Electronics and specialty polymer industries look to 2,3,6-trifluorobenzoic acid for properties that push beyond what non-fluorinated beans provide. The robust C–F bonds change both solubility and resistance to thermal and oxidative stress. This approach opens up options for custom monomer synthesis, high-stability ligands, and surface modification. We have worked directly with formulators and pilot plant managers on new fluoropolymer projects, supplying not only the acid itself but supporting data from accelerated aging studies.
Practical lessons emerge when the same product runs across multiple end-use scenarios. Some clients leverage the acid to tune polarity in functional copolymers; others tap into its chemical resistance profile for coatings that withstand the grueling environments of semiconductor fabrication. Users have described how the acid’s particular pattern of fluorine substitution helps them bypass solubility problems, and avoid unwanted side-reactions common with less substituted benzoic acids.
We routinely test powder flow and compaction properties for customers setting up automated dosing or continuous processing lines. Experienced engineers in toll manufacturing often offer feedback on packaging that stands up to both moisture exposure and rough handling during transit. Our packaging process draws on those lessons—triple-layer moisture barriers and heat seals come standard—because neither dusting nor caking has a place in high-value production environments.
Over time, direct experience has shown that not all “trifluorobenzoic acids” behave identically. As hands-on producers, we analyze side-by-side runs of 2,3,6- versus 2,4,5- and 3,4,5-trifluorobenzoic acids using the same reaction conditions. The impact on subsequent coupling or substitution steps can be pronounced: more nucleophilic ortho-fluorines accelerate or hinder reactions compared to their para or meta analogs. For those further downstream, this translates into altered chromatographic behavior and even color formation in cured materials.
Choosing the correct isomer avoids wasteful troubleshooting and testing. In practice, our process chemists have often run pilot reactions, logging every variable, taking nothing for granted. The familiarity with the quirks of 2,3,6-trifluorobenzoic acid—from its sublimation tendencies to solubility shifts with trace moisture—stems from years of practical work, not just reading spec sheets. That hard-won knowledge supports research platforms and helps our partners steer clear of production pitfalls.
Feedback from customer trials led us to refine our drying steps after a handful of users reported occasional specks in clear product runs. It took multiple cycles of root-cause analysis, including on-site visits and return material investigations, to arrive at tighter sieving and anti-static packaging. Batch uniformity became a topic of hands-on tinkering, not marketing slogans, and those improvements now benefit all users.
Innovation in fluorinated chemical building blocks often throws up surprises. The research cycle for new drug molecules or performance polymers includes many rounds of synthesis, scale-up, and reformulation. As producers, we get to see directly how even subtle changes in starting material quality ripple out into pilot plant or commercial scale processes. We design our workflow to support not only large-volume orders but also smaller, custom-sized batches for method development, validation or early-phase studies.
Our experience with tech transfer between lab and manufacturing scale taught us not to underestimate the hurdles that can arise. The same batch of 2,3,6-trifluorobenzoic acid that works well in hundred-gram quantities may cause headaches when turning out tens of kilograms unless its physical form—particle size, residual solvent, static behavior—lines up closely between lots. Our team regularly compares pilot-made and production samples, feeding back any divergence to process engineers for adjustment.
One key area in supporting scaling is close engagement with both safety and regulatory compliance teams. Regulatory trends in the US and EU have increased scrutiny on trace pollutants, risk of environmental persistence, and supply chain transparency. We routinely support clients with full impurity dossiers, toxicological summaries, and documentation to speed up filings. Our own internal audits reflect the same mindset we see in the most advanced research organizations—treating chemical quality as a non-negotiable asset.
Beyond documentation, we invest in operator training and equipment maintenance. Over the past five years, tighter quality specs have been matched by continuous upgrades to reactors, filtration gear, and analytical labs. This isn’t about chasing a certificate for its own sake, but staying ahead of the increasingly demanding requirements in advanced synthesis and manufacturing. Our people know how to spot anomalies, and aren’t afraid to call for a retest, because experience has proved it saves both time and money in the end.
Supporting new development sometimes means adjusting shipping schedules or batch splitting for clients running screening campaigns. Our logistics team, most of whom come from chemical process backgrounds, is intimately familiar with the quirks of this product’s stability across temperatures and humidity. Advance consultation when booking and packaging means the acid arrives ready to use, not in need of extra drying or filtration—a direct result of years spent handling specialty shipments.
Industrial chemistry is under a microscope today, and rightfully so. The responsibility for environmental stewardship lands directly on the producer’s shoulders. Our team has reviewed lifecycle analysis for every major input in the manufacture of 2,3,6-trifluorobenzoic acid. Given the nature of fluorinated organics, careful attention is paid to waste stream handling, solvent recycling, and emissions capture.
Over the course of multiple process redesigns, we reduced solvent loss by updating to closed-loop distillation, implemented real-time monitoring for halide discharge, and switched to greener alternatives for extraction where available. The same vigilance applies to energy use per kilogram produced. Our plant teams run regular kaizen (continuous improvement) sessions aimed at finding incremental environmental gains that don’t erode quality or reliability.
Supply security is a growing concern for everyone in the sector. Many coating and pharma clients now audit supply chains all the way back to primary producers. We open up our production flow to these inspections and invite feedback to reduce bottlenecks. By controlling each step of synthesis internally, our team has been able to weather raw material shortages that swept through the industry during volatile years. We maintain buffer stocks of high-risk inputs, track expiry tightly, and run parallel qualification for alternate suppliers, so clients can plan ahead with clearer lead times.
We engage with downstream users to map future demand and flag potential disruptions. Close connections between our planning and technical teams resulted in more transparent inventory updates and early warnings about tight situations, rather than leaving end users facing out-of-stock messages at the last minute.
It’s easy to see a fine chemical as just a code on a bottle—but the years spent in hands-on manufacture, testing, and direct communication with users reveal the human effort behind the numbers. Our role as a manufacturer is driven by feedback loops with applied chemists, product developers, supply planners, and regulators. Changes on the shop floor often unlock bigger wins for customers on the other side of the globe.
We welcome feedback on unusual outcomes—unexpected color shifts, handling problems, or downstream process snags. For example, an inquiry from a tablet manufacturer in Northern Europe, who noticed increased residual water content in warmer weather, led us to tweak our desiccant loading by season. Another client running advanced NMR analysis flagged a previously untracked impurity, prompting us to add a targeted cleanup step. These improvements have a habit of rippling backward into our SOPs, changing how new batches are made and how old habits are questioned.
While some outsiders assume chemical manufacturing stands still, our team knows that small but steady process improvements form the backbone of any long-term partnership. New regulatory landscapes, shifting application demands, and evolving analytical tools all shape how we produce and deliver specialty acids like this one. Collaborations with academic groups improve reference data and analytical methods, helping both our own process engineers and customers attempting new synthetic routes.
Over time, direct conversations between our technical and production teams enable us to chase optimal results, not just compliance. Routine inspections, tight process windows, and customer audits feed into updated best practices. We keep every operator and analyst in the loop, from the reactor floor to the sample dispatch room.
Trust in specialty chemistry comes down to visible commitment—commitment to consistent production, transparent documentation, and honest dialogue about limitations as well as strengths of each product. Our experience manufacturing 2,3,6-trifluorobenzoic acid demonstrates how much value grows out of intensive attention to feedback and a refusal to treat any batch as “just another job.”
In our world, every drum, every bottle, and every gram echoes the decisions made at every step: raw material selection, reaction controls, crystallization parameters, storage, logistics, and customer service. We stand behind our product—knowing its origins, its chemistry, and its impact on your process. That’s not a claim from the billboard; it’s the story written by hands-on experience, tested and refined by the demands of advanced chemical synthesis.