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HS Code |
362769 |
| Name | 3,5-Difluorobenzoic Acid |
| Cas Number | 446-35-5 |
| Molecular Formula | C7H4F2O2 |
| Molecular Weight | 158.10 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 162-165 °C |
| Density | 1.54 g/cm³ |
| Solubility In Water | Slightly soluble |
| Synonyms | 3,5-DFBA; Benzoic acid, 3,5-difluoro- |
| Smiles | C1=CC(=CC(=C1F)C(=O)O)F |
| Inchi | InChI=1S/C7H4F2O2/c8-4-1-5(9)3-6(2-4)7(10)11/h1-3H,(H,10,11) |
| Pka | 3.73 |
As an accredited 3,5-Difluorobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3,5-Difluorobenzoic Acid, 25g, packaged in a sealed amber glass bottle with a tamper-evident cap and clear labeling. |
| Shipping | 3,5-Difluorobenzoic Acid is shipped in secure, sealed containers to prevent contamination and moisture exposure. It is classified as a non-hazardous solid but should be handled with care. Packaging meets regulatory standards, and transport occurs via ground or air freight, with appropriate labeling and documentation for safe and compliant delivery. |
| Storage | 3,5-Difluorobenzoic acid should be stored in a cool, dry, and well-ventilated area, away from heat and sources of ignition. Keep the container tightly closed and protected from moisture. Store separately from strong oxidizing agents and incompatible substances. Ensure good laboratory practices and use appropriate personal protective equipment when handling. Store under inert atmosphere if required to minimize degradation. |
Applications of 3,5-Difluorobenzoic Acid in Industrial ManufacturingAs an established upstream producer, we supply 3,5-Difluorobenzoic Acid (3,5-DFBA) to a range of B2B partners operating in advanced chemical manufacturing sectors. Its molecular structure serves as a vital intermediate in several tightly regulated industries, supporting the development of pharmaceuticals, agrochemicals, specialty polymers, and advanced materials. Below we detail several industrial segments where 3,5-DFBA is integrally incorporated into downstream production, with explicit focus on authentic industry use and integration processes. 1. Pharmaceutical Intermediates for Non-Steroidal Anti-Inflammatory Drug (NSAID) SynthesisOriginating within the regulated supply chain for active pharmaceutical ingredients (APIs), 3,5-DFBA is a recognized intermediate in multi-step synthesis of select NSAIDs, notably for producing fluoro-substituted benzoic acid scaffolds. Pharmaceutical manufacturers employ this compound to introduce fluorinated aromatic motifs, which can modify biological activity and pharmacokinetic profiles within candidate drug molecules. The chemical enters the synthetic scheme as an early-stage reactant and undergoes conversion through controlled catalytic and coupling reactions. Industry compliance standards
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2. Crop Protection Agent Synthesis (Agrochemicals)Major agrochemical formulators rely on 3,5-DFBA as a precursor for developing modern herbicides and fungicides, specifically within triazole and phenoxy-substituted product lines. The presence of di-fluorinated aromatic rings in the raw material enhances both target selectivity and chemical stability of the end-use compounds in agricultural environments. It is introduced upstream during the assembly of phenyl-fluorinated structures, feeding into coupling and cyclization reactions that generate the final bioactive molecules. Industry compliance standards
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3. Advanced Polymer Material Additive ManufacturingSpecialty polymer producers use 3,5-DFBA to engineer high-performance polyesters and polyamides with enhanced chemical resistance, dielectric stability, and mechanical strength. By introducing this acid at the monomer formulation phase, manufacturers create polymer chains with distinct fluorinated aromatic content, yielding resins suitable for demanding electronics, insulation, and specialty coating applications. The inclusion level directly affects the thermal properties and end-use performance of the resulting polymer. Industry compliance standards
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4. Aromatic Building Block for Electronic Chemical SynthesisElectronic-grade chemical producers draw on 3,5-DFBA for the synthesis of functionalized intermediates used in manufacturing organic light-emitting diodes (OLEDs), liquid crystal displays (LCDs), and other advanced materials in electronics. The di-fluorinated aromatic core provides needed stability and performance in downstream application, and the compound enters the process as a primary aromatic building block for subsequent coupling or modification reactions. Strict control of purity and trace metal content is maintained throughout upstream handling to comply with electronics industry benchmarks. Industry compliance standards
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5. Fine Chemical Synthesis for Dye and Pigment IntermediatesManufacturers of high-performance dyes and pigments, particularly those formulated for specialized plastics, coatings, and fibers, integrate 3,5-DFBA as a core aromatic acid in azo and anthraquinone dye synthesis. Its incorporation facilitates the production of stable, lightfast coloration materials with distinct shades and high resistance to solvents and environmental degradation. The raw material enters targeted diazotization, coupling, or condensation steps unique to fluoroaromatic intermediates. Industry compliance standards
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Working day-in and day-out in the field of chemical synthesis, we come across a wide spectrum of intermediates and fine chemicals. Among these, 3,5-Difluorobenzoic Acid has carried a steady demand, serving as a reliable building block for a variety of operations. Its chemical structure, C7H4F2O2, places two fluorine atoms on the benzene ring at the 3 and 5 positions, creating particular physical and electronic effects valued in multiple downstream processes.
Our most actively requested grade of 3,5-Difluorobenzoic Acid comes as a white to off-white crystalline powder. Purity, traced using HPLC, generally surpasses 99%. Moisture content stays below 0.5%, and residual solvents rest securely under pharmacopeial thresholds. From an operator’s standpoint, these factors help standardize each batch and minimize surprises at the point of usage in the laboratory or at plant scale.
Particle size distribution typically falls beneath 250 microns, which delivers consistent reactivity and simple dispensing, whether for high-throughput screening or when preparing larger-scale reactors. Melting point centers between 156 and 159°C, offering a practical benefit for thermal cycling and processing in pilot facilities. Trace impurities—such as 2,4- and 2,6-difluorobenzoic acid—remain tightly restricted, due to rigorous in-process monitoring and batch QC. Each lot is assigned a unique tracking number for full traceability, a measure our technical teams rely on for process validation and troubleshooting.
Fluorinated aromatics like 3,5-Difluorobenzoic Acid stand apart from their monofluorinated and non-fluorinated cousins because of the way they alter the electron density and lipophilicity of the parent ring. Chemists leveraging this molecule in pharmaceuticals, agrochemicals, or advanced material synthesis gain tighter control over product reactivity, metabolic stability, and bioavailability.
In our experience, switching from unsubstituted benzoic acid to certain fluorinated analogs leads to real differences in target molecule properties. For example, in pharmaceutical R&D, adding two fluorine atoms at the 3 and 5 positions suppresses unwanted metabolic oxidation compared to the parent benzoic acid or simple para-fluorinated variants. This tweak increases half-life of target drugs in preclinical studies, a point closely tracked by project chemists and regulatory reviewers alike.
In crop protection, researchers look for analogs that balance activity, systemic mobility, and resistance to enzymatic breakdown in soil. The 3,5-difluoro arrangement often gives intermediates that last longer, resist photodegradation, and display lower volatility, allowing more efficient dosing in the field. This structural selectivity—down to the individual carbon-fluorine bond—carries through every step, from plant design to field testing.
Handling crystallized 3,5-Difluorobenzoic Acid, process chemists value the high chemical and thermal stability during reactions. It stands up well to basic and acidic media, and does not degrade under the mild oxidation or reduction conditions typically encountered in multi-step synthesis. The powder pours cleanly; clumping and static are minimized in our batches due to careful control of moisture and particle treatment.
For those scaling up, low impurity and consistent particle size reduce batch-to-batch variation and prevent filter clogging or unexpected delays during post-reaction workup. This technical predictability is hard-won, resulting from long-term investment in process analytics, equipment upgrades, and QA retraining.
In pharmaceuticals, 3,5-Difluorobenzoic Acid becomes a preferred core for designing drugs with higher metabolic resistance. Medicinal chemists incorporate it as a precursor to amides, esters, and other derivatives, harnessing its unique fluorine substitution pattern to nudge target affinity or slow down in vivo clearance. In our collaborations, we have seen it used in the development of several enzyme inhibitors, anti-inflammatory candidates, and central nervous system drugs where predictable pharmacokinetics are key.
The agrochemical sector continues pushing demand for multi-fluorinated benzoic acids, as regulatory limits on persistence and off-target toxicity get stricter every year. By supplying a tightly controlled intermediate like 3,5-difluorobenzoic acid, we contribute to the creation of novel fungicides and herbicides that both meet efficacy goals and fit evolving environmental profiles. Our technical team often works side-by-side with formulators during early process trials, helping fine-tune parameters for maximum yield and purity.
Outside the life sciences, specialty chemicals companies draw on this acid for electronic materials, photoresists, and fine-tuning of advanced polymers. Developers exploit the precise F-substitution for high thermal and chemical stability, as well as selective reactivity in downstream functionalization. The specific substitution pattern of 3,5-difluoro enables tuning of dielectric properties, allowing for innovation in lithium-ion batteries and specialty coatings.
Within the family of fluorinated benzoic acids, each isomer brings a distinct set of properties. The single-fluorine compounds, such as 4-fluorobenzoic acid, carry different electron distribution and typically show less resistance in biological systems. Isomers with both adjacent (ortho) or alternate (meta) substitutions affect reactivity and final product stability in different ways.
Lab experience shows 3,5-difluoro gives products a unique edge, especially when used as a starting point for compounds destined to serve in rigorous environments. It outperforms simpler analogs on resistance to metabolic breakdown, handling in high-purity applications, and reproducibility across scale. The specific positioning of the fluorines means regioselectivity during further reactions, especially halogenations or nitrations, can be dialed in more precisely than with other fluorinated benzoic acids.
Comparing price and availability, 3,5-difluorobenzoic acid sits between low-cost monofluorinated and much more difficult-to-access trisubstituted and perfluorinated benzoic acids. Our own manufacturing process capitalizes on this, making high-purity product widely available without the excessive costs associated with high-fluorine-content compounds.
Scaling up production means addressing technical and market realities head-on. Manufacturing 3,5-Difluorobenzoic Acid reliably takes considerable attention to raw material selection, reactor design, and purification techniques. Our experienced operators oversee every batch, making micro-adjustments to reaction parameters based on real-time process data rather than just following recipes. This hands-on approach pays off when customers receive a product that performs the same—every drum, every kilo—regardless of order frequency or size.
One operational lesson stands clear: switching synthetic routes mid-stream can introduce unexpected impurities and affect lot consistency. Our team frequently reviews reaction performance, optimizing reaction time, temperature profile, and crystallization conditions so the resulting acid meets customer expectations on color, odor, and purity every time. This dedication reduces downtime in our clients’ facilities, preventing bottlenecks that can delay critical R&D milestones or downstream production runs.
We developed feedback systems for capturing end-user experiences, which inform iterative improvements in our own operations. Whether a customer needs small R&D samples or metric ton lots for full-scale production, feedback about dissolution, reaction rate, and product handling flows directly back to process engineering. Changes in regulatory guidance or emerging needs—such as lower residual solvent content or alternative packaging—spur rapid response, not bureaucratic runarounds.
Purity requirements keep climbing, driven by tighter standards in pharma and green chemistry. Delivering on these standards takes significant reinvestment in refining isolation steps, automating process analytics, and tightening up environmental controls. Our QC lab routinely fields requests for expanded impurity profiling and is equipped to offer specialized analysis based on end-client needs.
One ongoing challenge we face is managing the balance between production cost and ever-higher purity targets. Fluorination steps tend to be less forgiving than chlorination or bromination, due to both safety considerations and the specialty nature of fluorine chemistry. Careful maintenance of F2, HF, or other fluorinating agents ensures not just product quality but worker safety and environmental responsibility.
Sustainable practices, like solvent recycling and heat integration, become more important each year. Regulatory scrutiny around emissions from halogenated compound manufacturing grows more stringent, so we have implemented closed-loop waste treatment and energy recovery. Monitoring a medium-sized reactor farm for organofluorine emissions or run-off isn’t showy work, but it makes a real difference on our operating permits and global environmental impact.
For most customers, the finished 3,5-difluorobenzoic acid ships in fiber drums with double PE liners, meeting both UN transport and local regulatory requirements. Our shipping group coordinates closely with freight forwarders and local partners so delivery matches the stability profile of the product—no defrosting, deliquescence, or packaging breaches, even during extended international transit.
Labs working with highly sensitive synthetic sequences have the option to request smaller, inert-atmosphere packed units, which eliminate risk of water ingress or static. Our technical sales team tracks requirements arising from both batch and continuous processing, adjusting fill weights or container materials as customer operations evolve.
Inventory management can cause headaches for production schedulers. A surge in demand for a promising drug candidate or a shift in customs clearance timelines can disrupt carefully planned supply chains. We manage safety stock based on both historical consumption and forecasted customer launches, ensuring partners receive uninterrupted product flow even as their project volumes shift.
The pace of innovation in specialty synthesis keeps climbing, and our R&D interface reflects that. Custom versions of 3,5-difluorobenzoic acid—ultra-high purity, extra-fine particle grade, or particular impurity profiles—are routinely developed in collaboration with customers seeking to cut process steps or improve yields. Process support doesn’t stop at the loading dock. Technical support specialists and senior chemists remain available to troubleshoot issues, suggest alternate synthetic routes, or assess ways to improve recovery or crystallization after scale up.
As the shape of demand changes, we stay flexible—stocking various packaging formats, adjusting batch sizes, and scaling purification runs as needed. This tight-loop feedback between field use and plant operations gives us a practical advantage, proven by repeat orders from customers developing treatments, crop solutions, and next-generation materials.
Dependable quality and supply of 3,5-difluorobenzoic acid turns into fewer delays across research and manufacturing. Our repeat customers, spanning small startup labs and global multinationals, cite fast turnaround, real-time lot tracking, and batch-to-batch consistency as key pillars. Raw material price swings or process bottlenecks can disrupt this reliability, so our procurement and process teams build agility into every phase, from supplier qualification to final QC.
Routine performance reviews of our raw material vendors and in-plant process analytics make it possible to isolate and resolve emerging issues before they affect finished product. Making that work takes deep collaboration across specialties: procurement, analytical, process, and logistics. Reliable supply wasn’t born overnight; it grew out of years addressing small failures and continually refining everything from fluorine handling to packaging closure verification.
Shifts in scientific discovery point to increasing use of multi-fluorinated benzoic acids for targeted therapies, greener agrochemicals, and advanced electronics. We’ve seen firsthand the uptick in specialized requests as researchers push into new areas, such as fluorinated peptides or ionic liquids. Continuous engagement with these emerging demands keeps us evolving—whether it means installing new purification lines, investing in safer fluorine chemistries, or adapting packaging to market shifts.
Investments in digital traceability, process intensification, and greener manufacturing illustrate where our priorities lie. Technologies like online NMR and process mass spectrometry allow tighter reflection of process control directly onto each drum shipped, delivering unmatched consistency. Adopting green chemistry approaches reduces our operational footprint and helps customers meet sustainability targets, a shift underscored by global environmental pressures and consumer expectation.
Knowledge gained from manufacturing 3,5-difluorobenzoic acid influences broader applications of fluorinated aromatics in our product line—better consistency, improved safety, and closer collaboration with customers working at the leading edge of innovation. Presence at the interface of chemistry, engineering, and logistics gives us a direct view of needs as they develop, informing where to invest and innovate next.
Supplying 3,5-difluorobenzoic acid isn’t just a matter of ticking boxes or meeting a spec sheet. It comes down to understanding how highly consistent, well-controlled batches support breakthroughs in medicine, agriculture, and technology. Experience teaches that no two orders are ever the same, and no two applications demand identical product attributes. Our boots-on-the-ground approach—listening to customers, refining every process variable, and pushing for safer, greener chemistry—defines the end result customers get.
3,5-difluorobenzoic acid stands as a proven intermediate in the hands of scientists and engineers across sectors, and producing it at scale, without compromise, channels decades of process knowledge and field experience. That reliability travels with every package shipped from our plant, building trust in each new project, and supporting targets that stretch far beyond the gates of any single manufacturer.