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HS Code |
801703 |
| Chemicalname | 2,3-Difluorophenylacetic Acid |
| Casnumber | 122775-46-0 |
| Molecularformula | C8H6F2O2 |
| Molecularweight | 172.13 |
| Appearance | White to off-white solid |
| Meltingpoint | 82-86°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically ≥97% |
| Smiles | FC1=CC=CC(=C1F)CC(=O)O |
| Inchi | InChI=1S/C8H6F2O2/c9-6-3-1-2-5(7(6)10)4-8(11)12/h1-3H,4H2,(H,11,12) |
As an accredited 2,3-Difluorophenylacetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 2,3-Difluorophenylacetic Acid is supplied in a sealed amber glass bottle with a tamper-evident cap and label. |
| Shipping | 2,3-Difluorophenylacetic Acid is shipped in tightly sealed containers, protected from moisture and light. Packaging complies with regulatory standards for chemical transport. During transit, the material is securely cushioned to prevent breakage or leakage, and shipped with proper labeling and documentation to ensure safe handling and compliance with safety regulations. |
| Storage | 2,3-Difluorophenylacetic acid should be stored in a tightly sealed container, away from moisture, direct sunlight, and incompatible substances such as strong oxidizers. Store at room temperature in a cool, dry, and well-ventilated area. Properly label the container and avoid contact with skin or eyes. Handle under fume hood if necessary, following standard laboratory safety protocols. |
Applications of 2,3-Difluorophenylacetic Acid in Industrial Manufacturing2,3-Difluorophenylacetic acid supports precision synthesis and process efficiency in select chemical industries. As an experienced manufacturer, we supply to regulated downstream sectors where this compound ensures consistent integration and quality output in complex production lines. The following application scenarios reflect actual industrial usage supported by established compliance frameworks, detailed usage ratios, downstream process roles, and final product types. 1. Pharmaceutical Active Ingredient SynthesisAPI manufacturers employ 2,3-difluorophenylacetic acid during multi-step syntheses for fluoroaromatic building blocks. Its structure allows for site-selective substitution and functionalization, crucial in developing drug intermediates such as CNS and oncology candidates. GMP-regulated plants introduce the acid after initial condensation reactions to deliver the difluorinated phenyl core, followed by subsequent amide coupling or further halogenation. This use supports traceability from intermediate to final compound, underpinning batch integrity throughout clinical and commercial scale production. Industry compliance standards
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2. Agrochemical Intermediate ProductionProducers of advanced herbicide and insecticide intermediates select this acid for incorporation into fluoroaromatic cores, enhancing the biological activity spectrum and persistence in field conditions. Used in synthesis of active components such as substituted phenoxyacetic acid herbicides, the compound enters the process as a functionalized aromatic acid directly after initial alkylation or halogen exchange. Regulatory-compliant plants monitor residuals and integrate the acid to meet specific active molecule design criteria, supporting field formulation standards for crop protection products sold in Asia, EU, and Americas. Industry compliance standards
Typical usage ratio
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3. Specialty Fluorinated Polymer SynthesisAdvanced materials companies use this acid as a functional monomer source in the synthesis of specialty polymers, resins, and adhesives requiring high fluoride incorporation. It provides targeted chemical resistance and lowers surface energy properties in high-performance coatings and engineered plastics. The acid is dosed accurately during monomer preparation and polymerization sequences, where batch reactors or continuous lines require real-time ratio control to achieve desired molecular weight and distribution properties. Downstream, polymer suppliers validate the raw's input against ISO and ASTM requirements for end-use mechanical and chemical resistance. Industry compliance standards
Typical usage ratio
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4. Fine Chemical and Fragrance Intermediate ManufacturingProducers of specialty fine chemicals employ 2,3-difluorophenylacetic acid as a precursor for controlled aromatic substitution in fragrance and flavor compound synthesis. Its unique fluorination pattern helps modulate volatility and olfactory profile for custom esters and derivatives in premium aroma formulations. The acid is introduced after formation of the aromatic core and before final esterification, with reaction control focusing on color and purity to industry standards set by IFRA and RIFM. This approach yields differentiated fine chemical stocks demanded by top-tier fragrance blenders and flavor houses with strict organoleptic requirements. Industry compliance standards
Typical usage ratio
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Each day in our plant, we see dozens of raw materials move through the warehouse, often just numbers and names on shipping manifests. Some names, though, mean a little more because of the time spent perfecting them on the line and testing them in labs. 2,3-Difluorophenylacetic Acid belongs to that small club. Chemically, it’s C8H6F2O2, which may not say much to those outside our trade, but we see the work behind each letter and number.
From the first batch run to the latest drum filled, we manufacture this compound not because it’s famous, but because research chemists, process managers, and even pharmaceutical innovators keep finding new ways to use it. That speaks louder than any marketing.
What truly distinguishes our product isn’t a generic list of numbers, but the actual process behind each kilogram. The 2,3-Difluorophenylacetic Acid we make typically arrives in a fine, off-white solid. Purity is not just a number here—it’s the outcome of repeated filtration, washing, and careful distillation. We keep an eye on HPLC results batch after batch, aiming for purity above 98.0% because the chemists who buy from us ask for that as a base requirement, not as a selling point.
Our typical melting point range sits around 65–70°C, verified by repeated lab checks. Impurities, especially trace halides or organic residuals, create much more trouble during scale-up processes than most datasheets suggest. We constantly test for them even in lots destined for internal use.
Moisture content is also checked rigorously. Controlled drying ensures each container ships below 0.5% moisture—because we know from troubleshooting that even small shifts can change reactivity and byproduct formation. Overly dry samples tend to be hard to dissolve, while excess water can ruin coupling reactions. Every process engineer here has had that experience at least once.
Pack sizes vary according to customer need, but in the plant we focus on minimizing cross-contamination and breakdown between batches. Every drum and bottle is mono-lot, meaning traceability from raw fluorobenzene all the way through final shipment. The line workers scanning every drum are the same ones who worry about glassware cleanliness and the right sealing method.
Demand for 2,3-Difluorophenylacetic Acid ties closely to its value as a versatile synthetic intermediate, especially in the pharmaceutical sector. Talking to researchers, the fluorine atoms at the 2 and 3 positions on the phenyl ring allow this compound to stand out among other phenylacetic acids. Fluorine’s presence changes how molecules behave in biological environments. Drug discovery teams rely on these kinds of building blocks to improve metabolic stability, alter receptor binding selectivity, or protect active sites in new drug candidates.
Our customers usually carry this into Suzuki couplings, amide formations, or other key steps in producing more complex molecules—from antihypertensive leads to novel agrochemical scaffolds. The acid group provides ready access to functionalization, and direct substitution patterns from the difluoro configuration result in derivatives less prone to metabolic degradation, a subtle but real advantage for scalability. Formulation scientists often consult with us about how minor impurities or even counter-ion loadings can influence later crystallizations. We don’t just ship out bulk chemical; we solve practical problems as they arise.
Beyond the world of pharma and life science, custom synthesis outfits order it for developing photoactive materials, specialty polymers, and even crop science test compounds. In the past year, we fielded unusual requests for this material from electronic device R&D teams, attempting to leverage its unique fluorinated aromatic properties for new semiconductor applications.
A lot of times, people ask about the difference between this compound and other, more common phenylacetic acids. On paper, it’s all rings and substituents, but hands-on work tells a different story. The placement of both fluorines ortho and meta to the acetic acid group makes specific hydrogen-bonding patterns, influencing solubility and reactivity in a way that single-fluorinated or non-fluorinated analogues simply can’t offer.
For those working on new active pharmaceutical ingredients, even tiny changes in fluorine position can tilt a molecule from inactive to potent, or from unstable to robust. Our QCs often compare this with 2-fluorophenylacetic acid and 3,4-difluorophenylacetic acid, and the differences are clear both on HPLC traces and in customer feedback. Selectivity, yield, and final product stability all shift with substitution pattern, and you only need to ruin one pilot batch to care about those differences.
Working with such a compound day in and day out, process engineers learn that the subtleties in reactivity save time and money. The difluoro pattern avoids over-halogenation in late-stage synthesis, and controls unwanted byproduct formation compared to chloro or bromo analogues. Product managers come to us not because 2,3-Difluorophenylacetic Acid is common, but because its unique profile means less troubleshooting at later stages.
A lot of people outside the factory assume making something like 2,3-Difluorophenylacetic Acid is just a matter of running a reaction and shipping the product. On the floor, though, we see it differently. The introduction of two fluorine atoms in the precise locations takes more than a single-step synthesis. Materials, times, and waste control need detailed monitoring because incomplete reactions can leave behind mono- or even tri-fluorinated byproducts, which throw off everything downstream.
Reaction scale-up often uncovers hidden problems that never appeared in the flask. Maintaining even temperature through a full reactor charge, avoiding localized overheating, and handling the unique volatility of fluorinated intermediates—these can turn an easy-looking transformation into a week-long troubleshooting affair. Our team sees the benefit of close process monitoring, not just in “optimized” lab work, but in keeping each batch within the specs real-world applications demand.
Waste management and environmental issues matter in our operation. Fluorinated waste is not handled like typical organic residues. Regulations on fluorine emissions, resources for proper neutralization, and attention to operator safety come with the territory. Over time, we built in both scrubbers and closed systems, not only to meet compliance but to keep our own team safe. This experience means our real cost of goods sometimes runs higher than what traders or middlemen might expect, but the difference appears in the consistency that researchers and manufacturers receive.
Shipping also tests our logistics. Strict moisture control, appropriate container materials (fluorinated compounds sometimes interact with plastic liners), and a focus on clear documentation all affect not just customs clearance but actual usability on receipt. Few things are more frustrating than getting a “high purity” product that arrives clumped, yellowed, or contaminated.
It’s one thing to claim high purity; it’s something else to prove it daily through practical steps. Every kilogram of 2,3-Difluorophenylacetic Acid we send out passes through checks at every part of the workflow. Instruments run regular calibration, lab techs track chain of custody, and plant staff regularly log batch numbers—all so that every client down the line knows what they’re working with and can trust each gram.
Impurity profiles matter especially at the kilo-to-multi-kilo scale. Our in-house testing covers not just HPLC but GC-MS and NMR scans, with full records going back five years. Pattern recognition plays as much a part in our work as formal specification, because over time, small deviations tend to grow if left unchecked. It’s this discipline that customers value most, especially those in regulated environments looking to scale from research bench to pilot plant.
We also maintain samples of each lot in controlled conditions for at least two years, sometimes longer if requested by partners. Whenever feedback comes in about a downstream issue—say, an unexpected impurity in a reaction intermediate—we quickly pull the original sample and actually run comparative testing rather than relying on paperwork. This rarely makes it into sales presentations, but those who work late in the lab or on the shift floor know it can save months of development time.
Because we run synthesis both for catalogue and on contract, we hear customer concerns straight from the source. Over the past decade, requests for 2,3-Difluorophenylacetic Acid often tie into exploratory work where reliability means everything. We offer more than a drum of chemicals; we serve as practical problem-solvers. When a client prepares to scale-up from grams to kilograms, we invite their chemists to review our actual batch records and tour the facility.
Some clients need unusually tight impurity controls or particular particle size profiles. Others worry about compatibility with automated handling systems and solvent systems unique to their process. Our in-house team provides guidance based on first-hand experience—sometimes even running pilot batches on our line with customer input. Miscommunication over something as manageable as particle size can cost weeks of work; hands-on collaboration fixes that before it starts.
Failures and breakthroughs both reach our ears. In one case, a pharmaceutical team tried to use a competitor’s material in late-stage amide coupling, only to run into trouble with residual catalyst and color change. Looking at their sample, we detected trace levels of monofluorinated byproduct, which threw off their purification scheme. Fixing the issue meant adjusting their workup protocol and providing cleaner material—a direct lesson for both our production line and our partners.
Fluorinated aromatics have come under scrutiny due to both their persistence in the environment and their involvement in regulated synthetic routes. Handling and shipping 2,3-Difluorophenylacetic Acid responsibly goes beyond checking regulatory boxes. Our workers receive regular training on best practice for handling, storing, and disposing of fluorinated chemicals. Every year, we update our plant protocols to reflect new safety findings and global guidance.
Legal compliance means tracking controlled precursor rules and export documentation, especially for clients in regulated industries or working with sensitive applications. As manufacturers, we continually invest in new monitoring and reporting technologies because we experience inspectors’ expectations first-hand. Sometimes, we field calls from customs agencies to provide detailed manufacturing records and chain-of-custody documentation. We know how much uninterrupted research and commercial operations depend on clear, rapid answers.
Manufacturing 2,3-Difluorophenylacetic Acid isn’t just a one-off project. Over the years, regular feedback from high-standard partners has pushed us to refine purity, yield, and physical handling properties. Projects that start as custom synthesis often turn long-term, and we work closely with technical teams to adjust everything from crystallization technique to final grind size, inventory management, and logistics.
Despite the new technologies and shifts in regulatory focus, the central value of this compound remains its tough-to-match combination of reactivity and selectivity. Each year, we see more demand not just for “good enough” but for reliable, scalable supply that fits real-world timelines and project goals. Lab managers, plant supervisors, and project engineers all value these partnerships, and resolve most technical problems through direct communication rather than layer after layer of standardization.
Research into new pharmaceuticals, agricultural solutions, and advanced materials continues to drive inquiry into building blocks like 2,3-Difluorophenylacetic Acid. More teams pursue complex, halogenated scaffolds for their unique biological and physical profiles. As a result, we see traditional manufacturing approaches challenged by new demands: tighter analytical standards, greener synthesis, improved traceability, and on-demand supply chain flexibility.
Internally, we invest in greener alternatives for fluorine incorporation and waste reduction, knowing that regulatory and client expectations are only set to rise. Partnering with universities and process chemistry groups, we test and scale methods to minimize hazardous inputs and outputs. Some new approaches rely on direct C–H activation rather than halide exchange or harsh reagents, which streamlines the path and cuts down individual processing steps. Although new technology often brings higher cost upfront, experience proves it saves time and compliance headaches long-term.
We recognize that collaboration with end-users improves not just product quality but also the design of new synthetic routes. Regular discussion with researchers or manufacturing partners challenges us to anticipate needs around physical forms, impurity profiles, and order scalability. That feedback cycle, which starts on the plant floor and carries through to the customer’s lab bench, truly shapes the way we produce and deliver 2,3-Difluorophenylacetic Acid.
Developing and supplying 2,3-Difluorophenylacetic Acid continues to be a real-world test of our capabilities as chemical manufacturers. The daily work—line checks, QC sampling, troubleshooting unexpected outcomes, and talking directly to customers—keeps us moving forward. Whether for a new research project or a commercial production campaign, we understand how much trust and reliability matter.
Every lot represents hundreds of hours of planning, testing, and real-time adjustment. We take pride in the calls returned directly from those using our products at the bench, scale-up suite, or production line. Their insight feeds back into our own knowledge, helping every new batch improve on the last.
Supply chain disruptions, evolving client needs, shifts in regulatory oversight, and the dynamic pace of scientific discovery mean that no two years look exactly the same. We keep pace because experience has taught us that excellence isn’t achieved in isolation. It means showing up every day prepared to learn, adapt, and deliver where it counts. For 2,3-Difluorophenylacetic Acid, that means more than just another name or number in the catalogue—it means a real investment in transparency, ongoing partnership, and hands-on care at every step.