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HS Code |
860838 |
| Product Name | 2-Fluoro-3-(Trifluoromethyl)Phenylacetic Acid |
| Cas Number | 180276-26-7 |
| Molecular Formula | C9H6F4O2 |
| Molecular Weight | 222.14 |
| Appearance | White to off-white solid |
| Melting Point | 74-77°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents like DMSO and methanol |
| Smiles | C1=CC(=C(C(=C1)F)C(F)(F)F)CC(=O)O |
| Inchi | InChI=1S/C9H6F4O2/c10-6-2-1-5(4-7(15)16)8(3-6)9(11,12)13/h1-3H,4H2,(H,15,16) |
As an accredited 2-Fluoro-3-(Trifluoromethyl)Phenylacetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2-Fluoro-3-(Trifluoromethyl)Phenylacetic Acid, sealed with a screw cap and labeled for laboratory use. |
| Shipping | 2-Fluoro-3-(Trifluoromethyl)Phenylacetic Acid is shipped in tightly sealed containers to prevent moisture ingress and contamination. It is transported under ambient conditions unless otherwise specified. All packages are clearly labeled in accordance with regulatory standards and accompanied by appropriate safety documentation, ensuring compliance with chemical transport regulations for safe delivery. |
| Storage | Store 2-Fluoro-3-(trifluoromethyl)phenylacetic acid in a cool, dry, and well-ventilated area, sealed tightly in a clearly labeled container. Protect from moisture, heat, and direct sunlight. Keep away from incompatible substances such as strong oxidizers and bases. Avoid exposure to air to prevent degradation. Follow all relevant safety regulations and guidelines for handling and storage of chemical substances. |
Applications of 2-Fluoro-3-(Trifluoromethyl)Phenylacetic Acid in Industrial ManufacturingAs a manufacturer of 2-Fluoro-3-(Trifluoromethyl)Phenylacetic Acid, we supply this intermediate to downstream partners across several tightly regulated industries. Here are primary industrial sectors and practical usage details based on real-world application, industry standards, integration methods, and resulting end products. 1. Pharmaceutical Active Ingredient SynthesisThis intermediate plays a vital role as a building block in the synthesis of fluorinated active pharmaceutical ingredients, particularly for specialty APIs targeting oncology and central nervous system disorders. Pharmaceutical manufacturers rely on its high purity and precise chemical properties during multi-step synthesis, often following strict documentation and traceability workflows to ensure batch reproducibility and regulatory compliance throughout the API production chain. Industry compliance standards
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2. Agrochemical Herbicide Intermediate ProductionLeading agrochemical firms utilize this acid as a core intermediate for assembling selective herbicide molecules that demand precise fluorination patterns. Its unique structure enables downstream synthesis of modern herbicide actives targeting broadleaf and grass weed resistance. Our material complies with the trace metal and halogen specifications needed for large-scale herbicide intermediate production and registration dossiers. Industry compliance standards
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3. Advanced Materials for OLED and Liquid Crystal Precursor ManufacturingManufacturers in the electronic materials sector value the structural motif for assembling fluorinated precursors of organic light-emitting diodes (OLEDs) and next-generation liquid crystals. Controlled synthesis conditions and batch certification ensure finished material meets electronic grade purity and functional group performance needed in advanced display technologies. Complete batch traceability is documented per customer NDA or quality agreement. Industry compliance standards
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4. Specialty Chemical Synthesis for Analytical Reference StandardsContract research organizations and analytical laboratories utilize this compound as a reference standard precursor or labeled marker in analytical method development. Stringent batch documentation and impurity profiling ensure reliable traceability in certified reference material programs. Specification control supports stable isotope labeling and submission to accredited analytical bodies. Industry compliance standards
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Working daily with specialty compounds, we have seen how 2-Fluoro-3-(Trifluoromethyl)Phenylacetic Acid stands out in the landscape of advanced intermediates. This aromatic acid, known to some as a valuable building block, serves much more than a checkbox in a chemical catalog. The presence of both a fluoro and a trifluoromethyl group on the phenyl ring alters not only its physical attributes but also its impact on downstream synthetic pathways. These transformations continue to drive drug design, agrochemical innovation, and material sciences, giving researchers and formulation teams new levers to pull when standard chemistries start to fail. From first-hand experience, the complexity and precision required in manufacturing highlight both its potential and the challenges that come with handling such a molecule.
2-Fluoro-3-(Trifluoromethyl)Phenylacetic Acid does not belong to the family of bulk chemicals where marginal purity variations go unnoticed. The molecule is sensitive not only to impurities but also to storage and transit conditions. In our process, each batch undergoes meticulous monitoring through advanced chromatography and multiple rounds of quality assessment. Fine-tuning reaction temperature, solvent polarity, and isolation steps directly influences both yield and long-term stability. For instance, residual metal impurities or unreacted starting material persistently lead to side-product formation in scale-up trials, demanding an ongoing cycle of process optimization. Every step, from raw material verification to final isolation, loops back to earlier lessons learned—especially for those who have weathered the effects of scale-up inconsistencies or batch-to-batch drift.
Many of our pharmaceutical customers approach us looking for reliability, but also for flexibility as their projects scale from grams to kilograms and eventually tons. In these projects, 2-Fluoro-3-(Trifluoromethyl)Phenylacetic Acid offers something unique. The balance between a lipophilic trifluoromethyl group and an electron-withdrawing fluorine atom at the ortho position shifts its character compared to traditional phenylacetic acids. For medicinal chemists, these subtle changes translate into altered binding affinities, metabolic pathways, and physicochemical properties of final drug candidates. We have seen how fluorine substitution can increase the metabolic stability of lead molecules, a property invaluable in oral drug development.
Recent pipelines in kinase inhibitor and anti-inflammatory drug development rely on structures that struggle with metabolic degradation. The addition of a fluoro group, as seen in this compound, often makes a real difference. Our partners have reported increased half-life and decreased off-target reactivity, leading to more streamlined preclinical assessments. Even in early discovery, the proper choice of aromatic intermediates can add years to a compound’s patent life, reduce formulation headaches, and simplify toxicology profiles. From the synthetic chemist’s bench to the late-stage analytical reviewer, the advantages become apparent not just in final product profiles but during the entire research lifecycle.
Through the years, we have produced a broad spectrum of phenylacetic acids. Most classic variants lack the specific electronic effects that arise from perfluorinated substitutions. The dual impact of the ortho-fluorine (2-position) and the meta-trifluoromethyl (3-position) groups imparts a unique electron density and steric profile. These shifts can suppress unwanted byproduct formation during cross-coupling or activation reactions, an advantage valued by chemists working on scale-sensitive transformations. In contrast, working with standard phenylacetic acid substrates yields higher rates of decarboxylation or side-chain rearrangement under similar conditions.
On a practical level, fluorinated derivatives also display distinct solubility profiles and increased resistance to photodegradation. For teams tasked with long-term storage or complex purification, this reduces waste and supports easier batch tracking. The trifluoromethyl group especially influences partition coefficients, which improves extraction processes, making the intermediate easier to handle during multi-step synthesis. People often notice that even in simple crystallization trials, our 2-Fluoro-3-(Trifluoromethyl)Phenylacetic Acid behaves with greater predictability than non-fluorinated cousins. This translates into easier upscaling, reduced purification time, and lower solvent consumption, all of which feed directly into the sustainability metrics so many teams measure today.
From the operator’s side, not all specifications receive equal weight. We prioritize accurate assay determination, moisture content, and freedom from common side-products such as 2-fluorobenzyl alcohol and trifluoromethylated toluenes. During scale-up, trace residual organic solvents pose recurring problems if overlooked. Even with high-performance instrumentation, small changes in process water content can push a batch over specification limits. Deep experience working on the line has shown us that weather, plant environment, and subtle supply chain shifts produce tangible differences in analytical data.
A typical product specification focuses on assay (usually measured by HPLC or GC), water content (by Karl Fischer titration), melting point, and specific UV absorption peaks. But our team keeps an eye on broader factors. We track impurity profiles specific to the route—differences emerge depending on whether a nucleophilic aromatic substitution or a directed ortho metalation process is used. As manufacturers, we have learned to treat every run as a chance to learn, always watching for batch-specific signatures that may stand out months or years later during pharmacovigilance or regulatory review.
Though pharmaceutical development provides most of our case histories, 2-Fluoro-3-(Trifluoromethyl)Phenylacetic Acid has found a niche in agrochemical syntheses and functional materials. These industries appreciate the molecule’s robustness. Many next-generation crop protection agents demand trace-level impurity control and photo-stability. The same properties that benefit oral drug candidates—stability under environmental stress, lower rates of bioaccumulation, and tunable polarity—extend to these areas. Materials scientists have begun to specify fluorinated aromatics for their impact on polymer behavior and as surface modification units where weather resistance matters more than cost-per-gram.
From discussions with supply chain experts, margin for error shrinks as final products reach broader markets. A contaminant that may go unnoticed in a research context can prove disastrous in large-scale deployment, especially in regulated regions. Our work with agricultural clients has revealed that process consistency often matters more than theoretical maximum yield. Tighter control supports easier downstream blending, leading to less rework and lower energy use in subsequent manufacturing steps.
Scaling up production of such a compound brings daily reminders that theory must yield to hands-on troubleshooting. Our operators have faced routine issues with exotherm management, especially as batch sizes increase. The fluorinated groups slightly raise reaction enthalpy and can produce unpredictable foaming or sparging when paired with certain polar solvents. We have retooled reactor baffles, adjusted agitation regimes, and changed heat transfer strategies to overcome these hurdles. Years of direct feedback from operators and lab staff drive these incremental improvements, not top-down directives.
Another issue arises in crystallization trials. While the molecule displays helpful stability compared to others, subtle changes in cooling rates or antisolvent additions can rapidly shift the quality of finished product. Operators learn to trust their instincts, honed by repeated experience, to achieve target particle size and purity. Many of these solutions are not handed down by R&D labs, but emerge from repeated failures and successes during routine campaigns. Cross-training plant staff and sharing lessons across shifts helps smooth out bottlenecks. As much as process chemistry offers structured problem-solving, manufacturing reality rewards adaptability and honest assessment of root causes.
Over the years, the analytical toolkit used for 2-Fluoro-3-(Trifluoromethyl)Phenylacetic Acid has changed. Early batches relied on basic melting point and TLC assessments. Now we use high-resolution mass spectrometry, multidimensional HPLC, and even NMR-based quantitation for select projects. Regulatory requests often push for deeper impurity identification and batch traceability. Operators have learned that robust records mean faster responses to technical questions from clients or inspectors. What looks like overkill today becomes the starting standard next year.
Tighter analytical routines have a preventive function. Last year, a small change in raw material source resulted in a shift in impurity profile. Because our lab developed extra crosschecks, we caught the issue before delivery. Clients downstream noticed nothing, but internally we documented and shared the finding. These practices do not slow us down—they enable us to stop small problems before they become major ones. Many customers have come to depend on this approach as their own project teams grow leaner, knowing that they don’t need to flag every detail themselves. Mutual trust between manufacturers and end users builds project momentum.
On paper, 2-Fluoro-3-(Trifluoromethyl)Phenylacetic Acid keeps well in cool, dry storage. In the warehouse, things get more complicated. Even tightly sealed containers attract atmospheric moisture, especially on humid days or during seasonal changes. Residual solvent traces, if not controlled, can lead to gradual off-odors or color changes. Working alongside experienced warehouse staff, we learned to track not just batch location, but stacking height and airflow patterns, since these factors subtly influence product longevity.
Every shipment leaves with full documentation, but it’s the experience of shipment packers and forklift operators that closes the quality loop. Over-packing or using the wrong pallet finishes can trap heat and trigger condensation. Direct communication between warehouse and production ensures product consistency and supports timely resolution of logistical headaches. Each failed shipment or corrective action gets logged, reviewed, and used for future improvement. People may overlook these details, but ignoring them leads to returns and lost productivity.
Regulatory frameworks seldom stand still. Today’s compliance checklists evolve with changing environmental priorities and growing scrutiny on fluorinated molecules. Our technical and QA teams proactively monitor updates from watchdog agencies, anticipating how even minor specification changes ripple through customer supply chains. In recent years, calls for lower per- and polyfluoroalkyl substances (PFAS) levels have pushed us to update purification practices, revalidate processes, and extend documentation.
Our experience tells us that open, two-way communication solves more problems than formal statements or rapid responses. Project teams on both sides benefit when manufacturers share details about route changes, impurity controls, or alternate synthetic pathways. No customer wants to rewrite their regulatory filings because of an unexpected production tweak. Through regular technical exchanges, both parties lower the risk of surprise, clarify expectations, and keep projects moving even during market disruptions. This collaborative approach flows from decades of field experience, where accountability and transparency count more than short-term cost savings.
Years ago, sustainability discussions felt abstract. Operating a chemical plant brought home very real questions about solvent recovery, reactor energy use, and waste treatment. 2-Fluoro-3-(Trifluoromethyl)Phenylacetic Acid, with its reliance on specialty reagents and multi-stage syntheses, presents a regular test case for greener practices. We have moved toward solvent recycling where possible, use in-line water monitoring to cut down rinsing cycles, and test bio-sourced raw materials as commercial availability grows.
Changes imposed for one product line often benefit others. Installing energy-efficient heat exchangers for this compound, for example, reduced downtime across multiple products. By sharing actual impact data with downstream clients, we help inform environmentally-conscious procurement decisions. Customers increasingly require not just competitive quotes, but credible plans for supply continuity in face of regulatory or environmental shifts. The closer the collaboration, the greater the mutual benefit. Manufacturing reality rewards persistent, transparent, and incremental sustainability improvements over symbolic gestures.
Every project built around 2-Fluoro-3-(Trifluoromethyl)Phenylacetic Acid pushes the boundaries of what’s possible in modern synthesis. Working on the manufacturer’s side gives unique insight into why certain batches succeed and others do not. Our team’s accumulated expertise, from seasoned operators to technical support analysts, enables us to spot trends and share early warnings when up- or downstream conditions change. Through close feedback loops with research partners, custom manufacturing teams, and industrial clients, we contribute to a larger ecosystem of innovation.
As automation and digitization continue to shape production environments, we transfer lessons learned into digital logs and training packages, equipping new staff to troubleshoot and improve on legacy processes. Experience has taught us that trust, accumulated through quality outputs and open communication, far outweighs any one product’s technical documentation or price sheet. At the core, producing consistent, reliable 2-Fluoro-3-(Trifluoromethyl)Phenylacetic Acid supports progress across pharmaceuticals, agrochemicals, and materials—enabling customers to push new boundaries while knowing they have a solid foundation. Every batch reflects not only our technical expertise, but also our commitment to responsible, real-world chemical manufacturing.