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HS Code |
100937 |
| Chemical Name | 2-Chloro-5-Fluorobenzoic Acid |
| Cas Number | 2905-62-6 |
| Molecular Formula | C7H4ClFO2 |
| Molecular Weight | 174.56 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 150-154°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water |
| Density | 1.55 g/cm³ (approximate) |
| Synonyms | 2-Chloro-5-fluorobenzoic acid; Benzoic acid, 2-chloro-5-fluoro- |
| Smiles | C1=CC(=C(C=C1Cl)C(=O)O)F |
| Inchi | InChI=1S/C7H4ClFO2/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3H,(H,10,11) |
| Storage Temperature | Store at room temperature |
As an accredited 2-Chloro-5-Fluorobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2-Chloro-5-Fluorobenzoic Acid is supplied in a 100g amber glass bottle, featuring a tight screw cap and safety labeling. |
| Shipping | 2-Chloro-5-Fluorobenzoic Acid is shipped in tightly sealed, chemical-resistant containers to prevent leaks or contamination. It should be labeled according to hazardous material regulations, stored in a cool, dry area, and protected from incompatible substances. Appropriate documentation accompanies each shipment to ensure safe handling and regulatory compliance during transit. |
| Storage | 2-Chloro-5-fluorobenzoic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Use appropriate personal protective equipment (PPE) when handling. Store in a clearly labeled container and follow all safety and regulatory requirements. |
Applications of 2-Chloro-5-Fluorobenzoic Acid in Industrial ManufacturingAs the direct factory producer of 2-Chloro-5-Fluorobenzoic Acid, we support key industrial sectors in need of high-purity aromatic intermediates for complex synthesis chains. This compound reliably serves as a core building block in the production of advanced pharmaceuticals, agrochemicals, liquid crystal monomers, specialty dyestuffs, and polymer processing aids. Below, you will find tailored application scenarios recognized in actual downstream practice. 1. Pharmaceutical Intermediate SynthesisOriginating from validated multi-step synthesis routes, this acid acts as a controlled aromatic precursor in non-steroidal anti-inflammatory drugs (NSAIDs) and advanced anti-infective agents. Our material consistently meets strict validation for traceability and structural integrity, serving pharmaceutical manufacturers running multi-ton batch operations. Usage ratio depends on target molecule structure and scales according to molar demand in cyclization, amino substitution, or esterification reactions. Industry compliance standards
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2. Herbicide and Pesticide SynthesisChlorofluorinated benzoic acids provide essential ring structure for selective herbicides and crop protection agents. Agrochemical formulators requiring precise halogen positioning rely on this material during target-specific chemical synthesis. Our output supports continuous processing and batch production, ensuring rapid supply chain compatibility with major patent-expiring crop protection products. Industry compliance standards
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3. Liquid Crystal Monomer ManufacturingProducers of high-performance display materials utilize halogen-substituted aromatic acids in early-stage syntheses of liquid crystal monomers. The material supports precision alignment and high-purity cyclization reactions, directly affecting electro-optical properties in finished display components. Detailed QC and metal trace analysis ensure batch-to-batch consistency for panel manufacturers. Industry compliance standards
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4. Specialty Dye Precursor ProductionTextile and pigment companies source this compound for advanced structure dyes, where precise electron-withdrawing halogen substitution enhances color fastness, UV resistance, and molecular stability. Dyestuff formulation teams employ rigorous checking on melting point range and impurity profile to assure desirable chromophore formation in downstream azo or anthraquinone dye synthesis. Industry compliance standards
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5. Polymer Processing Additive SynthesisManufacturers in high-performance plastics use aromatic acids with dual halogenation for functional group insertion, creating additives that enhance flame retardancy, UV stability, and melt-process control. 2-Chloro-5-Fluorobenzoic Acid enters specific steps in copolymer modification or additive formulation lines, with process controls set on residual solvent and halogen content. Industry compliance standards
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After years of working with aromatic acids and their derivatives, we’ve learned that subtle substitutions on the benzene ring create significant changes in how a product performs in synthesis. 2-Chloro-5-fluorobenzoic acid, C7H4ClFO2, offers a blend of chlorine and fluorine atoms on the same moiety, providing functionality for a diverse range of transformations that are central to pharmaceutical, agrochemical, and material science research. In our facilities, each batch goes through vigilant monitoring for isomeric purity, color, melting point—which usually ranges between 162 and 164 °C—and water content, ensuring it serves both demanding industrial processes and exacting laboratory applications. Our chemists choose this molecule for synthetic versatility, reliability, and consistent handling, informed by firsthand troubleshooting and iterative batch improvements.
2-Chloro-5-fluorobenzoic acid distinguishes itself not just by its CAS number or chemical identifiers, but by the way it behaves where it counts—in the reaction flask. Both positions 2 and 5 on the aromatic ring are occupied by functional atoms. This dual halogenation pattern creates a unique balance: the electron-withdrawing effects of chlorine and fluorine tug at different strengths and angles. Using this specific substitution pattern, chemists can direct subsequent reactivity with greater predictability, especially when introducing further complexity on the ring through cross-coupling or nucleophilic substitution. In comparison, switching the fluoro or chloro groups to other positions—say, 3-chloro-5-fluorobenzoic acid—shifts the electron distribution, impacting reaction rates and selectivity. That distinction becomes clear not just on a reaction scheme, but in day-to-day plant yields and customer outcomes. Years of in-house tests have shown that these differences translate to tangible results in scale-up settings.
Most texts gloss over the time, labor, and scrutiny behind a kilo of 2-chloro-5-fluorobenzoic acid. Our setup uses a tried-and-tested approach to chlorination and fluorination, drawing upon both catalytic and direct substitution routes, depending on available precursors and downstream sensitivity. We’ve encountered every problem imaginable: solubility issues, exothermic surges when reagents are too eager, and stubborn byproduct formation clogging columns during purification. Our crews have tinkered with reaction temperatures, solvent proportions, and even stirring rates to squeeze every percentage point of yield. All raw inputs go through preliminary analysis—GC-MS, moisture checks, trace metal determination—to avoid downstream surprises. Our quality assurance team maintains chain-of-custody for analytical documentation. This level of oversight comes from years of risk management and regulatory compliance—not just for signature, but for peace of mind for both our chemists and the end users.
For larger scale runs, crystallization conditions demand special attention. We learned, after several trial-and-error attempts, that crystal habit and particle size can swing widely depending on cooling profiles. We opt for gradual temperature reductions and staged seedings to achieve manageable batch filtration. Once, we ran into sticky, greasy masses by omitting this discipline, which not only slowed production, but created dust and airborne particle hazards—an often-overlooked safety factor. By keeping a close watch, we now routinely produce a clean, white, odorless crystalline solid, with impurity levels consistently under two tenths of a percent for related aromatic acids. We store all finished product in sealed, low-humidity environments to stave off hydrolysis and darkening.
End users demand this acid for one main reason: functional group flexibility. In pharmaceutical development, 2-chloro-5-fluorobenzoic acid serves as a precursor for fluoro- and chloro-substituted benzamides, benzoxazoles, and even direct coupling to heterocyclic frameworks. The presence of both halogens opens the door for stepwise functionalization. Agrochemical firms use it for intermediates in herbicide and pesticide active ingredients, often as a building block for more complex heterocycles that require predictable reactivity in each successive step.
Another frequent user base includes companies working in specialty polymers and advanced materials, where the interplay of electron-rich and electron-poor segments affects binding and material stability. Fine-tuning electronic properties by adjusting site-selective halogenation allows these firms to move quickly from benchtop screening to pilot-scale production without retooling fundamental synthetic routes. That agility depends on reliable product performance as much as it does on supply chain consistency—both of which we work to guarantee in our operation.
Switching from 2-chloro-5-fluorobenzoic acid to another positional isomer, like 3-chloro-5-fluorobenzoic acid or mono-halogenated acids, changes practically everything about a downstream route. For instance, the ortho-chloro group in our product means reactions favor adjacent substitutions and often proceed under milder conditions than their para- or meta-substituted cousins. Our staff has plenty of stories of pilot chemists frustrated by the limited scope of less tailored benzoic acids. Results in cross-coupling reactions differ by catalytic choice, solvent, and purification approach, not to mention product purity and isolation techniques. Sometimes a switch in supplier triggers invisible shifts in impurity profiles, impacting catalyst poisoning or chromatography efficiency. Over time, we’ve become adept at documenting and comparing these subtle but critical differences, sharing our data with partners who also keep close tabs on risk, yield, and reproducibility.
Our product stands out due to tight melting range, low residual solvent, and robust batch-to-batch purity control. Monochloro- or monofluorobenzoic acids offer a lighter electron deficit, and so support a more limited scope of downstream reactions. Many users start with these simpler acids, only to switch once they see the selectivity boost in their synthetic procedures with a dual-substituted intermediate. In today’s climate of cost control, the efficiency these changes bring—fewer purification steps, higher isolated yields, less wasted solvent—is impossible to ignore for commercial process teams working with thin margins.
Many outside the manufacturing space underestimate how physical behavior during operations shapes daily workflow. We have adjusted our procedures after some batches caked, refusing to flow through standard hoppers. Particle morphology matters, especially for customers feeding the product straight into reactors. Over several campaigns we optimized grinding, sifting, and even antistatic precautions. Water pick-up once plagued our warehouse until we invested in better dehumidification and tighter secondary containment. That paid off not just in stability but safety, as handling wet benzoic acids can invite both hydrolysis and workplace slips.
Sensitivity to light and air usually remains low, but keeping material sealed preserves brightness and prevents trace degradation. By holding storage below ambient humidity, we’ve reduced caking and improved both process efficiency and final purity scores in our in-house QC. Regular checks on color, particle size, and appearance keep product standards tight—and let customers run, not troubleshoot, their own chemistry.
The para and ortho positions in aromatic acids matter to anyone doing direct substitutions or palladium-catalyzed cross-couplings. The double halogenation in 2-chloro-5-fluorobenzoic acid means extra departure points for reagents and more options for further modification. In some cases, this increases reaction speed during nucleophilic aromatic substitution, reducing both energy input and reaction times. Our product goes into Suzuki, Buchwald-Hartwig, and direct amidation reactions, regularly tested by R&D partners pushing innovation in lead compound development. Reproducibility remains the touchstone: poorly differentiated isomers undermine screening programs, while tightly specified starting materials form the backbone of scalable chemistry. It’s not unusual for pharma and agrochem development teams to request extra certificates of analysis or onsite inspections. We’ve handled those requests, furnishing samples for cross-lab verification and working side-by-side with outside process teams making the move from grams to kilograms.
Comparing this compound to less halogenated versions, users benefit from accelerations in acylation and amide-forming reactions. The presence of both bulk and electron-withdrawing effects supports cleaner transformations, particularly when companies need high yield and selectivity to minimize downstream separation challenges. Our product helps shave days off project timelines due to straightforward purification and low isomeric impurities—details that go unnoticed until a batch halts due to an unidentified contaminant. Those experiences turned us into fierce defenders of traceability and analytical transparency.
Large and small customers require careful packing to avoid losses to moisture and trace contamination. For mid-sized volumes, polyethylene-lined fiber drums provide the right mix of rigidity and barrier protection against ambient air and humidity. Our packing teams wear nitrile gloves and handle each load as if it’s destined for clinical validation. Shipment on pallets and protected with weather-resistant wraps keeps the product within spec during long transits, whether by road or air. Traceability never takes a day off: we keep photographic records at loading, logging of temperature and humidity conditions, and issue each shipment with batch-level documentation for chain of custody. This lets our end users trace back any analytical discrepancy, speeding followup and minimizing the cost of error investigation.
Over time, we developed relationships with international logistics partners who share our obsession with reliability. Import and export rules change often, and new requirements for labeling, documentation, and tracking emerge every year—especially for specialty chemicals with sensitivity to both quality and security. We maintain a robust internal compliance program led by specialists who monitor trends in ADR, REACH, and US DOT standards, and who engage directly with regulatory officers to keep our exports moving smoothly across borders. This reduces downtime for both us and our partners, ensuring continuity of supply without bureaucratic bottlenecks interrupting production campaigns.
The global landscape for halogenated benzoic acids has grown more complicated. Regulatory pressures on solvent choice and emissions, instability in raw material prices, and supply chain slowdowns from global unrest all impact operations. We have responded by investing in process intensification—optimizing smaller volume, higher throughput reactors—and by maintaining inventory on-site that covers several months of demand. In years with major supply shocks, this approach allowed us to avoid passing price spikes down the chain to critical users, including those in lifesaving drug research.
Purification technology plays another crucial role; by implementing continuous processes for solvent recovery and solid-liquid separation, we cut down on both waste and operating cost. Waste minimization forms part of every campaign. Our solvent recovery units bring down emissions and generate reusable fractions. In some cases, we revisit synthetic routes to skirt around less green reagents, switching to catalytic routes with improved atom economy. While not every process fits every product, our ongoing review ensures we keep both environmental impact and cost front of mind. We routinely audit our waste streams, tracking hazardous and nonhazardous outputs down to kilogram levels, driven by both regulation and personal belief in responsible manufacturing.
Nothing stands still in fine chemicals. Years ago, stray particles or inconsistent melting points prompted costly recalls and long nights in the lab. Each challenge shaped our current approach, where production, analysis, storage, and transport are scrutinized by hands-on staff. We keep datasets on each batch—IR spectra, NMR, HPLC purity, TLC patterns—and benchmark our results to external analytical labs as a double-check. Customers value that transparency: a few percent in improved yield or purity can mean the difference between a promising new drug and a lost patent opportunity.
Our in-house training covers both GMP and analytical best practices, run by staff with decades in chlorination chemistry. Spot audits and ongoing proficiency testing keep our team sharp, and open feedback from customers leads to tweaks both large and small—changing grind size, adjusting lot labeling, adding new analytical checks as emerging science demands. Long-term partnerships depend on more than just a competitive price or a flashy data sheet. We built our business—batch by batch—based on reliability, consistency, and an unflagging willingness to do the work others avoid.
Innovation in chemistry depends on a robust supply of pure, reliable intermediates. We see the demand shifting as customers seek more sustainable solutions and tighter timelines to market. Advances in catalysis, solvent selection, and green chemistry highlight the need for high-quality starting materials prepared with close attention to trace impurities and physical form. We continue exploring improvements in both production and logistics, meeting the requirements of research and industry partners who rely on hassle-free, direct communication and full technical support—not just a delivered drum or a specification sheet. As the landscape changes, we remain committed to evolving with it, leveraging our experience and hard-won expertise to support discovery, scale, and global impact through every batch of 2-chloro-5-fluorobenzoic acid we put into the world.