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HS Code |
663239 |
| Name | 2,4-Difluorobenzoic Acid |
| Cas Number | 455-86-7 |
| Molecular Formula | C7H4F2O2 |
| Molecular Weight | 158.10 |
| Appearance | White to off-white solid |
| Melting Point | 134-136 °C |
| Density | 1.44 g/cm3 |
| Solubility In Water | Slightly soluble |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=C(C=C1F)F)C(=O)O |
| Inchi | InChI=1S/C7H4F2O2/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3H,(H,10,11) |
| Storage Temperature | Store at room temperature |
| Synonyms | 2,4-DFBA |
As an accredited 2,4-Difluorobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2,4-Difluorobenzoic Acid is supplied in a 100g amber glass bottle with a secure screw cap, featuring hazard labeling. |
| Shipping | **Shipping Description for 2,4-Difluorobenzoic Acid:** Packaged in tightly sealed containers, 2,4-Difluorobenzoic Acid is shipped with appropriate labeling in accordance with chemical handling regulations. The material should be protected from moisture, extreme temperatures, and incompatible substances, and transported following relevant safety guidelines to ensure integrity and prevent hazard during transit. |
| Storage | 2,4-Difluorobenzoic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers and bases. Protect from moisture and direct sunlight. Properly label the container, and store at room temperature unless otherwise specified by the manufacturer’s guidelines or safety data sheet (SDS). |
Applications of 2,4-Difluorobenzoic Acid in Industrial ManufacturingAs a direct manufacturer with extensive expertise in specialty fluorinated intermediates, we supply 2,4-Difluorobenzoic Acid to a select range of global industries. Our material supports precise synthesis needs in advanced chemical processes, where compliance, formulation, and integration are tightly controlled for demanding downstream requirements. Below, we outline verified industrial application scenarios with key operational details. 1. Pharmaceutical Intermediate for Non-Steroidal Anti-Inflammatory Drugs (NSAIDs)This raw material serves as an essential building block in the synthesis of specific NSAID active pharmaceutical ingredients, including fluorinated analogues developed for improved metabolic stability. Pharmaceutical manufacturers incorporate it during multi-step reactions involving acylation, halogenation, and selective hydrolysis, benefitting from its reactivity and purity in regulated API synthesis. Industry compliance standards
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2. Agrochemical Intermediate for Selective Herbicide SynthesisProducers of modern crop protection agents use this raw acid to build active moieties in selective herbicide formulations, especially for fluorine-containing phenoxypropionate derivatives. Its incorporation provides enhanced chemical stability and environmental profile to finished actives, driving efficient crop protection product pipelines. Industry compliance standards
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3. Fine Chemical Intermediate in Liquid Crystal Monomer SynthesisDisplay technology manufacturers use it as a strategic raw material in the synthesis of specialty monomers for liquid crystal displays (LCDs). The difluoro motif enhances dielectric anisotropy and temperature range of liquid crystalline phases, enabling tailored optical and electrochemical performance in display panels and electronic components. Industry compliance standards
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4. Specialty Polymer Modifier in High-Performance FluoropolymersProducers of advanced engineering plastics and fluoropolymers adopt the acid in copolymer modifications, aiming to tune mechanical and chemical resistance in final polymer matrices. Its incorporation provides controlled fluorine content and alters crystallinity for demanding applications in coatings, membranes, and wire insulation sectors. Industry compliance standards
Typical usage ratio
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Our work with 2,4-Difluorobenzoic Acid has revealed just how versatile and robust this compound can be in the right applications. With the molecular formula C7H4F2O2 and CAS number 446-19-5, this industrial acid plays a role in both intermediate synthesis and direct application in pharmaceutical, agrochemical, and material science settings. Its unique structure, with two fluorine atoms at the 2 and 4 positions of the benzoic acid ring, brings chemical properties that distinguish it from single-fluorinated or non-fluorinated benzoic acids.
Chemists often look for ways to improve stability, reactivity, and selectivity during synthesis. In our production facility, we have experienced that introducing fluorine atoms to the aromatic ring opens new doors. Fluorine's high electronegativity influences the electron density across the molecule. With both fluorine atoms attached to specific positions, 2,4-Difluorobenzoic Acid shows a different reactivity profile compared to 2-fluorobenzoic acid, 4-fluorobenzoic acid, or the parent benzoic acid. These nuanced effects impact everything from solubility to how the acid reacts in esterification, halogen exchange, or amidation. In large-scale operations, a slight adjustment in molecular design, such as this one, often cascades through the process, affecting everything from yield to the cost of downstream purification.
At our plant, we consistently produce 2,4-Difluorobenzoic Acid to a minimum assay of 98 percent by HPLC, with trace moisture, chloride, and heavy metal levels below recognized thresholds. Our process capitalizes on stringent quality oversight, from raw material selection to final inspection. Color appears as white to off-white powder, and melt point often lands in the 136-140°C range. Particle sizing can be customized for those seeking uncoated or micronized formats; our team knows that a single process step can change everything from filtration time to final product bioavailability. Because labs and production lines require dependable outcomes, we back every batch with a complete certificate of analysis. Consistency across years of manufacture does not come by accident; it reflects tight control parameters, investment in modern analytical tools, and, most critically, a team trained to spot deviations before they grow into real issues.
2,4-Difluorobenzoic Acid rarely ends up in consumer products in its delivered form. Most of it flows downstream as an intermediate, especially in pharmaceutical and agricultural chemical synthesis. Among our major clients, crop science and specialty pharma projects stand out. Here, the compound is frequently converted to amide derivatives, coupled to nitrogen heterocycles, or utilized for further halogenation or reduction. Customers repeatedly tell us that when they switch from single-fluorine to our difluoro grade, parasitic side reactions tend to fall away, and cleaner yields become the norm. This is no accident; fluoro-aromatic chemistry changes the rules for reactivity and selectivity. For those seeking to introduce fluorine atoms into bioactive molecules, using 2,4-Difluorobenzoic Acid as a precursor offers a clear route. The electron-withdrawing effect stabilizes certain intermediates, reduces unwanted rearrangements, and can even help protect against enzymatic degradation in some biotech settings.
Handling difluorinated acids differs sharply from standard benzoic acids, especially during large-scale recrystallization, drying, or transfer. The dual fluorine modification impacts the hygroscopic nature and influences how we manage humidity during storage. In winter or in high-humidity environments, even small traces absorbed by the powder may alter both mass spectrometry results and final product potency. That is why every drum receives double sealing. Operators know from firsthand experience that even seemingly trivial changes in ambient temperature—or a small slip in pH adjustment during neutralization—may lead to clumping or off-spec product. Our teams have worked with lab groups to troubleshoot transfer losses and optimize solvent selection, since batch-to-batch reproducibility is not just a promise but a prerequisite. Years of direct feedback, both from chemists and plant engineers, have led to safer, faster, and more robust handling protocols.
Every manufacturing chemist faces the decision of which benzoic acid derivative fits a particular route. With 2-fluorobenzoic acid and 4-fluorobenzoic acid, you gain some of the benefits fluorine can bring—greater metabolic stability, altered lipophilicity, and changes to electronic structure. But the single substitution can leave some synthetic windows open, leading to different regioselectivity outcomes. By doubling the fluorination—and especially by placing these atoms at the 2 and 4 positions—our compound offers even more pronounced stability and a sharp reduction in certain oxygenation or nucleophilic attack side-reactions. This difference matters most during electrophilic aromatic substitution or esterification, where unwanted byproducts can waste solvents, lower yields, and clog downstream filters. Among all the benzoic acid variants we produce, 2,4-difluorinated stands out as a clean, efficient performer, especially on scale.
Bringing 2,4-Difluorobenzoic Acid to market at kilo or ton scale brings challenges not always seen in small-flask synthesis. During our earliest campaigns, tipping the stoichiometry even a fraction too high with fluorinating agents led to cumulatively higher unreacted substrate, so we refined the quench and washing steps with multiple trials. We learned to anticipate solids-handling issues, especially after workup. Equipment operators quickly noticed that filters and centrifuge socks required different materials to prevent breakthrough with this compound. Only by iterating process cycle after process cycle did we reach the throughput and purity customers now expect. Each plant run built more knowledge, honing solvent selection and optimizing drying times down to the hour.
By controlling particle size and moisture, we minimized caking and improved flow properties. External storage also received a rethinking, shifting away from standard fiber drums to lined drums with vacuum seals. This reduced contamination risk dramatically and ensured low, stable moisture content during storage. Customers who manufacture downstream actives have reported lower product loss and higher crystallization rates when processing our batches, thanks to these improvements. Having hand-in-glove conversations with those who actually run the reactors and pack the materials informs real-world change, not just paper policies.
Our batch size flexibility remains something we take pride in. Whether clients need a drum or a full ISO tank, the experience of shifting campaign priorities, adjusting upstream raw materials supply, and rapidly recalibrating reactor setups has fostered a nimble, technically adept production team. In a world where lead time trumps almost everything else, our long-term investments in scheduling software and multi-disciplinary training allow us to hit tight windows almost as a matter of routine. Each successful delivery adds to a culture of problem-solving and adaptation, which makes us better partners for those bringing new products to market.
Direct contact with any benzoic acid derivative requires a respect for reactivity and health-related issues beyond what’s found in textbooks. With 2,4-Difluorobenzoic Acid, the introduction of two fluorine atoms calls for an extra layer of attention. Even trace hydrolytic degradation requires tight exclusion of moisture during storage and shipment. From the production floor up, all team members participate in training on handling fluorinated organics, both for personal safety and environmental stewardship. Our long partnership with a regulated waste disposal provider reflects the need to manage spent solvent containing organofluorines under current environmental guidelines.
We discovered that discharges from cleaning reactors and transfer piping could carry more persistent residues compared to unsubstituted compounds. As a result, our process water treatment loop includes both activated carbon and advanced oxidation steps. Investments in abatement aren’t always visible to customers, but any manufacturer responsible for fluorinated building blocks knows that true sustainability comes from the inside out. We welcome plant tours for technical partners, because transparency in how materials move, react, and get managed after use remains essential to our credibility and commitment to responsible chemistry.
The trajectory of 2,4-Difluorobenzoic Acid in the market has expanded from a niche intermediate to a staple ingredient in innovative synthesis. In pharmaceutical R&D, lead optimization projects rely on our compound to boost stability and tweak pharmacokinetics by selective fluorination. Process chemists exploring new patent space often request small lots for custom reactions, only to return for commercial-scale drums a year or so later. Agrochemical developers seeking improved pest resistance and environmental persistence have found that difluorinated aromatics consistently outperform single-halogenated analogs.
Cooperation across product life cycles has taught us volumes about end-user challenges. In more than one instance, pharmaceutical clients uncovered formulation challenges when switching to difluorinated acids. We were able to provide granular technical data—solubility in mixed solvent systems, recrystallization behavior under different pH, details on absolute purity confirmed by NMR and GC-MS—that saved weeks or months in scale-up. Our experience built the muscle to troubleshoot alongside our clients, resulting in faster go-to-market timelines for their new therapies.
Outside health and crop science, materials developers have trialed 2,4-Difluorobenzoic Acid in modified polymer resins and specialty coatings. The stability offered by the dual fluorines impacts not only thermal properties but also long-term weather- and UV-resistance. Whether in ultra-thin films or bulk plastics, these unique characteristics can mean the difference between a passing grade and a failed product qualification in rigorous testing environments. Our technical team does more than ship chemistry; we consult directly with research teams to find out exactly what drives performance for their critical applications.
Time spent listening to customer challenges has spurred no small number of process refinements. With every new product launch or application trial, issues surface—sometimes a single micron of difference in particle size changes everything about a downstream mixing process. In one case, a customer found marginally higher ionic contamination affected their catalyst. We traced the concern back to trace raw material impurities and retuned sourcing and washing protocols, closing the loop in record time.
Our quality assurance lab interacts directly with pilot customers, not only at the validation stage but in post-delivery checks. That feedback comes straight back to the manufacturing team. Spikes in demand or sudden application surges have prompted us to double production runs at times. The result is a culture where unexpected questions from the field are welcomed rather than shunted aside. Those who source their 2,4-Difluorobenzoic Acid here know they can reach a process chemist or production lead, explain an issue, and expect both understanding and effective support.
Manufacturers rarely share the fine details of how minor building blocks shape blockbuster formulations, but we have been afforded a unique vantage point. Pharmaceutical companies have developed more stable ester prodrugs by starting with 2,4-Difluorobenzoic Acid, thanks to its selective reactivity and low impurity profile. In agrochemical textile coatings, the compound grants superior wash-fastness without leaching, a property directly traceable to bis-fluorination.
Innovators using next-generation sensor arrays or coatings for high-precision instruments have explored the compound’s potential for enhancing sensor performance in harsh environments. The chemistry of the difluoro system creates both polarity and electron density shifts that align with the requirements of these technically demanding endpoints. These projects are often so new to the market that few outside the manufacturing supply chain get to see the vital role that advanced building blocks play.
Teams developing application-specific protocols have leaned on our flexibility, whether needing rapid supply chain rerouting during global disruptions or highly unusual documentation packages for regulatory submissions. By anchoring operations firmly in our plant and keeping direct lines open both up- and downstream, we serve as more than just a supplier; we become an embedded part of our customers’ discovery engines.
Having boots on the ground in our own plant ensures that nothing gets lost in translation. Our staff monitor batch processes from start to finish, knowing just how such attention can tilt the outcome of later stages. Relying on direct manufacturing eliminates supply chain guesswork and allows for minute adjustments that ripple out to product quality. Rather than pushing paperwork through a bureaucracy, we share the same risks and rewards as our clients. They see this reflected in our willingness to run custom syntheses, troubleshoot process challenges, or source alternative raw materials when markets shift.
Every shipment carries the stamp of those who actually make the product. The pride in delivering lot after lot that meets tight targets shapes both our company culture and our place in the market. Customers rely on our people, not just our product, knowing that behind each drum or bottle stands a team able to adapt, explain, and improve. This is not a commodity process, but a living, evolving partnership between makers and users.
Changes in downstream industries keep shifting the requirements for intermediates like 2,4-Difluorobenzoic Acid. Pharmaceutical and agrochemical companies continue to demand higher purity, faster lead times, and documentation that stands up to the strictest regulatory scrutiny. As fluorinated synthetic chemistry evolves, new isotopic labeling and chirality challenges will likely emerge, requiring even tighter process control and real-time analysis. To keep pace, investment in plant-scale Green Chemistry initiatives remains at the center of our future strategy. We’re piloting solvent recycling units and exploring late-stage fluorination chemistries designed to lower environmental impact while maintaining product integrity.
New regulatory and market realities will require even greater transparency and innovation. Our teams are working closely with academic groups and industrial partners to design continuous process improvements, not only for the compound itself but for every input and output that touches its manufacture. We understand deeply that reputation—like purity—builds batch by batch, shipment by shipment. Those who use our 2,4-Difluorobenzoic Acid know they can trust in both our expertise and our commitment, built from generations of hands-on experience and direct, everyday engagement with the chemical realities of modern synthesis.
After years in the trenches of specialty chemical manufacturing, we have found that the success of 2,4-Difluorobenzoic Acid in the field owes as much to careful craftsmanship as it does to technical innovation. By working shoulder-to-shoulder with R&D chemists, process engineers, and end-users, we have built a flexible, knowledge-driven approach that adapts to the unpredictable realities of the chemical industry. Tomorrow’s breakthroughs depend on today’s attention to detail, and for us, that means never standing still. Each lot shipped is a real-world reflection of our ongoing commitment to reliability, problem-solving, and the real-world needs of those creating the next generation of products.