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2-Chloro-5-Fluorobenzoic Acid

    • Product Name 2-Chloro-5-Fluorobenzoic Acid
    • Alias 5-Fluoro-2-chlorobenzoic acid
    • Einecs 243-960-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of 2-Chloro-5-Fluorobenzoic Acid

    Applications of 2-Chloro-5-Fluorobenzoic Acid in Industrial Manufacturing

    As 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 Synthesis

    Originating 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

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF Monograph (applicable for registered pharmaceutical intermediates)
    • EU EudraLex Volume 4 Part II GMP
    • 21 CFR Part 211 (US FDA cGMP for drugs)

    Typical usage ratio

    • 0.8–1.2 mol per mol of target API precursor, adjusted based on downstream stoichiometric pathway in the synthesis process

    Downstream process integration

    • Charged at nucleophilic aromatic substitution, amidation, or condensation step after initial benzoic acid activation

    Final product types

    • Non-steroidal anti-inflammatory drugs
    • Intermediate blocks for quinolones and other anti-infectives
    • Contrast agent intermediates for medical imaging

    2. Herbicide and Pesticide Synthesis

    Chlorofluorinated 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

    • FAO/WHO Specifications for Pesticides
    • ISO 9001:2015 for agrochemical production
    • China GB 20810-2006 (Pesticide Registration Standards)
    • REACH (EU) Registration for agro intermediates

    Typical usage ratio

    • 15–25% of total formulation by weight in precursor stage, adjusted for specific molecule design and crop selectivity requirements

    Downstream process integration

    • Intake as a key aromatic building block during acylation, halogen exchange, or esterification in pesticide backbone assembly

    Final product types

    • Selective systemic herbicides
    • Pre-emergent weed control agents
    • Active ester intermediates for insecticides

    3. Liquid Crystal Monomer Manufacturing

    Producers 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

    • IEC 61249 (Requirements for Thin Film Materials in Displays)
    • SJ/T 11363 (China RoHS for electronic components)
    • ISO 14001:2015 (Environmental Management)
    • REACH SVHC Screening for electronic raw materials

    Typical usage ratio

    • 2–8% in step-growth polymerization feedstock, precisely controlled via HPLC purity analysis and batch-specific reaction design

    Downstream process integration

    • Input as feedstock during monomer cyclization or as a substituent in aromatic synthesis for LC host structure development

    Final product types

    • Twisted nematic and super-twisted nematic LCD monomers
    • Polymer-dispersed liquid crystals for displays
    • Reactive mesogen intermediates

    4. Specialty Dye Precursor Production

    Textile 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

    • OEKO-TEX Eco Passport for dye chemicals
    • ZDHC MRSL v3.1 (Zero Discharge of Hazardous Chemicals)
    • EU REACH for colorants
    • ISO 105-C06 (Textile colorfastness testing)

    Typical usage ratio

    • 5–15% in dyestuff reaction feed, calibrated based on desired chromophore properties and customer end-application testing

    Downstream process integration

    • Added during coupling or condensation with heterocyclic amines to form complex dye core structures

    Final product types

    • Azo and anthraquinone dyes
    • Reactive dyes for textile fiber processing
    • Specialty pigments for inks and digital textile printing

    5. Polymer Processing Additive Synthesis

    Manufacturers 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

    • UL 94 (Flammability rating for plastic materials)
    • ISO 9001:2015 (Quality assurance for polymer production)
    • EU RoHS Directive 2011/65/EU
    • ASTM D2565 (UV exposure of plastics)

    Typical usage ratio

    • 0.5–3% by weight in masterbatch compositions, tailored through lab melt index and migration studies

    Downstream process integration

    • Incorporated at polymer compounding or extrusion feed stage for new additive systems

    Final product types

    • Flame-retardant additives for engineering plastics
    • UV-stabilizing masterbatches for polyolefins
    • Functionalized copolymers for specialty plastics
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    Certification & Compliance
    More Introduction

    Introducing 2-Chloro-5-Fluorobenzoic Acid: The Specialist’s Choice in Fine Chemical Production

    From the Manufacturer’s Bench: Practical Knowledge of 2-Chloro-5-Fluorobenzoic Acid

    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.

    The Heart of the Matter: Why Subtle Structure Matters

    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.

    Production Insight: Decades of Process Refinement

    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.

    Applications: Why Our Customers Keep Coming Back

    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.

    Comparison to Other Benzoic Acid Derivatives

    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.

    Physical Handling and Storage: Lessons from the Factory Floor

    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.

    Structural Insight and Synthetic Uses in Real-World Situations

    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.

    Packing, Transport, and Scale: Practical Challenges and Commitments

    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.

    Challenges in a Changing Market: Our Response and Solutions

    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.

    Commitment to Quality: Lessons in Continuous Improvement

    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.

    Looking Ahead: 2-Chloro-5-Fluorobenzoic Acid in Tomorrow’s Chemicals

    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.