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3-Fluoro-5-(Trifluoromethyl)Benzoic Acid

    • Product Name 3-Fluoro-5-(Trifluoromethyl)Benzoic Acid
    • Alias 3-Fluoro-5-(trifluoromethyl)benzoic acid
    • Einecs 619-234-3
    • 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

    400117

    Product Name 3-Fluoro-5-(Trifluoromethyl)Benzoic Acid
    Cas Number 1000340-78-4
    Molecular Formula C8H4F4O2
    Molecular Weight 208.11
    Appearance White to off-white solid
    Melting Point 120-124°C
    Purity ≥98%
    Smiles C1=CC(=CC(=C1C(=O)O)F)C(F)(F)F
    Inchi InChI=1S/C8H4F4O2/c9-6-2-1-5(8(11,12)13)3-4(6)7(10)14/h1-3H,(H,10,14)
    Solubility Slightly soluble in water; soluble in organic solvents
    Storage Temperature Store at 2-8°C

    As an accredited 3-Fluoro-5-(Trifluoromethyl)Benzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, white screw cap, tamper-evident seal; labeled "3-Fluoro-5-(Trifluoromethyl)Benzoic Acid, 10g" with hazard symbols.
    Shipping 3-Fluoro-5-(Trifluoromethyl)benzoic acid is shipped securely in sealed, chemically resistant containers to prevent contamination and degradation. Packaging complies with relevant safety regulations for hazardous chemicals. Each container is clearly labeled, accompanied by a Safety Data Sheet (SDS), and shipped under appropriate temperature and handling guidelines to ensure product integrity during transit.
    Storage Store 3-Fluoro-5-(trifluoromethyl)benzoic acid in a tightly sealed container, protected from moisture and light. Keep at room temperature in a well-ventilated, dry area away from incompatible substances such as strong bases and oxidizers. Ensure the storage area is equipped with proper spill containment and labeled clearly. Avoid excessive heat and direct sunlight to maintain stability and prevent decomposition.
    Application of 3-Fluoro-5-(Trifluoromethyl)Benzoic Acid

    Applications of 3-Fluoro-5-(Trifluoromethyl)Benzoic Acid in Industrial Manufacturing

    3-Fluoro-5-(Trifluoromethyl)Benzoic Acid supports several advanced industrial sectors, serving as a key starting material or functional intermediate. Our expertise in synthesis and quality control enables downstream manufacturers to achieve reliable and consistent production with compliance to international standards.

    1. Pharmaceutical Intermediates for Active Ingredient Synthesis

    This compound acts as a critical building block in the synthesis of several fluorinated pharmaceutical APIs, including selective COX-2 inhibitors and antiviral agents. Process engineers utilize its unique fluorine-substituted phenyl ring to introduce metabolic stability and increase target selectivity. Material enters production during early-stage organic transformations, where precision in nucleophilic aromatic substitution or amidation delivers high purity intermediates for downstream coupling and deprotection steps. Regulatory documentation and batch traceability remain crucial during qualification for commercial drug substance manufacturing.

    Industry compliance standards

    • ICH Q7 Guidelines for Active Pharmaceutical Ingredient Production
    • Current Good Manufacturing Practice (cGMP) per 21 CFR Parts 210/211
    • USP and Ph. Eur. monographs, where applicable for intermediates
    • REACH registration for import/use in Europe

    Typical usage ratio

    • 5-25 mol% relative to total substrate, adjusted based on target molecule and route of synthesis
    • Scale-up protocols optimize charge to minimize waste streams

    Downstream process integration

    • Added at the initial coupling or ring-modification step of multi-step synthesis
    • Subjected to controlled reaction with amines or alcohols in polar aprotic solvents
    • Intermediate purification via crystallization or flash chromatography
    • Final conversion to API by hydrogenation or functional group transformation

    Final product types

    • Active pharmaceutical ingredients (APIs) such as anti-inflammatory drugs
    • Analytical reference standards for drug development
    • Regulatory documentation samples for batch release
    • Impurity markers for stability testing

    2. Agrochemical Synthesis for Herbicide and Fungicide Actives

    Manufacturers utilize 3-Fluoro-5-(Trifluoromethyl)Benzoic Acid as a core intermediate in the development of modern herbicides and fungicides, where the presence of the trifluoromethyl group imparts increased environmental persistence and enhanced bioactivity. Synthesis routes often involve direct esterification or amidation, with careful control of reaction parameters to maximize yield and minimize regulated byproducts. Downstream processes frequently require phase transfer catalysis, followed by purification and formulation for crop protection products.

    Industry compliance standards

    • FAO Specifications for pesticide active ingredients
    • ISO 9001:2015 Quality Management for production traceability
    • Regulation (EC) No 1107/2009 for Plant Protection Products (Europe)
    • US EPA 40 CFR Part 180 for residue analysis compliance

    Typical usage ratio

    • 3-12% by weight in core intermediate formation (based on overall batch mass)
    • Ratio adjusted according to type of ester or amide to be synthesized

    Downstream process integration

    • Fed to reaction vessels after solvent charging and catalyst addition
    • Reacted under inert atmosphere using automated pH or temperature control
    • Post-synthesis extraction followed by salting-out and solvent stripping
    • Formulated into technical concentrates or dispersible granules for end-use

    Final product types

    • Herbicide actives targeting broadleaf weeds
    • Fungicide active compounds with systemic properties
    • Technical concentrates for agricultural formulation
    • Standardized analytical samples for regulatory clearance

    3. Advanced Material Precursors for Specialty Polymers

    Producers of specialty fluorinated polymers and resins rely on this benzoic acid derivative to introduce functional aromatic motifs into high-performance plastics, coatings, and films. The presence of both fluorine and trifluoromethyl groups delivers high hydrophobicity and chemical inertness in the finished polymer matrices. During polymer synthesis, manufacturers implement staged esterification or activation as an acid chloride to facilitate copolymer incorporation. Strict polymerization controls prevent side reactions and achieve tight molecular weight distribution.

    Industry compliance standards

    • ISO 14001:2015 for environmental management of fluorinated processes
    • RoHS Directive 2011/65/EU for electronics sector polymers
    • China GB/T 19001 Quality Management System
    • SDS compliance with UN GHS classification

    Typical usage ratio

    • 0.5%-4% as comonomer or functional group source, depending on polymer type
    • Proportions guided by desired thermal and chemical properties of final resin

    Downstream process integration

    • Functionalization step prior to main polymerization (solution or bulk methods)
    • Acid converted to acid chloride for co-condensation with fluorinated diols or diamines
    • Quality control ensures consistent incorporation via NMR/FTIR verification
    • Final pelletization or film extrusion under controlled drying conditions

    Final product types

    • Fluorinated polyesters and polyamides for electronics
    • Specialty coatings for chemical resistance in industrial plants
    • Barrier films for high-purity packaging
    • Resin dispersions for high-end composite materials

    4. Fine Chemical Intermediate for Liquid Crystal Materials

    The compound serves as a core intermediate in the synthesis of high-performance liquid crystal monomers used in advanced display technologies. Its rigid aromatic structure and electron-withdrawing substituents play a decisive role in achieving desired dielectric anisotropy and thermal behavior. Production processes often require multi-step synthesis sequences, including selective cross-coupling and protection/deprotection tactics under controlled moisture exclusion. Downstream integration targets narrow impurity profiles to meet the stringent requirements of electronic display manufacturers.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for reproducibility
    • RoHS Directive on substances in electrical and electronic equipment
    • REACH registration for import and use within the EU
    • Customer-specific quality agreements for trace metals and halide content

    Typical usage ratio

    • 1-8 mol% of total monomer feed, based on the formulation of specific liquid crystal mixtures
    • Ratio optimized according to application (e.g., nematic, smectic, or cholesteric phases)

    Downstream process integration

    • Synthesized as an intermediate, then further functionalized via Suzuki or Heck coupling
    • Protection of acid group as methyl or ethyl esters during cross-coupling
    • Packed into inert containers to control moisture and oxygen exposure
    • Shipped with full batch traceability to display technology customers

    Final product types

    • Liquid crystal monomers for display alignment layers
    • Intermediate additives in LED and OLED substrate production
    • Dielectric materials for advanced optics
    • Performance enhancers for energy-saving display panels
    Free Quote

    Competitive 3-Fluoro-5-(Trifluoromethyl)Benzoic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Understanding 3-Fluoro-5-(Trifluoromethyl)Benzoic Acid: Insights From Inside Our Plant

    What We See on the Production Floor

    Manufacturing 3-Fluoro-5-(Trifluoromethyl)Benzoic Acid brings a set of challenges only hands-on experience reveals. We watch the reaction as chloro- or bromo-benzoic acids transform through a careful balance of fluorination and trifluoromethylation. The result—white to off-white crystalline powder—comes from patience and vigilance at every stage, helping us meet the quality bar researchers expect in advanced chemical synthesis.

    At each batch, our team observes crucial details: particle size, bulk density, and the unmistakable pungency that signals the proper structure. The process echoes practices adopted in the synthesis of many aromatic building blocks, but the presence of a trifluoromethyl group and a ring-positioned fluorine shifts reactivity, solubility, and behavior in downstream applications. Each run, we adjust based on real-time feedback, blending decades of bench experience into every kilogram we ship.

    Model and Purity: More Than Just Numbers

    Customers often ask about the purity and form of this compound. We report the chemical as C8H4F4O2 (CAS 327-74-2). Most clients request a minimum purity of 98% by HPLC, and having spent years handling fluorinated benzoic acids, we know that small shifts in purity can change a compound’s performance in coupling reactions or environmental studies. Impure batches can mean wasted time or expensive reruns in multi-step syntheses, so our plant puts extra attention on recrystallization and filtration.

    We maintain batch records that trace each lot back to its original feedstock. Trace solvents, small impurities, and even stable isotope ratios get checked by our in-house QC, providing data you can depend on when qualifying a raw material. Over time, we've learned that slight differences in water content, particle morphology, or residual solvents do not just affect compliance filings—they influence shelf life in storage and behavior in reaction flasks. This real-world knowledge only comes from being on the manufacturing line rather than reading third-party spec sheets.

    The Chemistry That Matters to End-Users

    Every chemist who reaches out asks, “Will this work for my Suzuki or Ullmann coupling?” Our production crew knows that the presence of both the trifluoromethyl group and ortho fluorine means this benzoic acid offers enhanced electron-withdrawing ability. That affects reactivity in cross-coupling, amide formation, and the introduction into complex small molecules. You see fewer side reactions with our carefully monitored batch conditions, which keeps downstream purification much simpler—no one wants to tease apart side-products with nearly identical retention times.

    We have heard from agrochemical and pharmaceutical partners who value fluorinated benzoic acids’ stability under harsh conditions. The reactivity profile changes compared to unsubstituted benzoic acids or even mono-fluorinated versions. Trial runs in our pilot plant revealed a higher melting point and lower solubility in many polar solvents, which suggests different crystallization and separation techniques in gram-to-kilo scale. We respond to these hurdles by offering advice from failed and successful runs, because practical outcomes always outshine theory.

    How It Differs From Close Relatives

    The trifluoromethyl group at the 5-position and the ortho-fluorine create a distinct set of physical and chemical properties. The electron cloud shifts, influencing acidity—something few recognize on paper but that stands out when the compound gets loaded into a reactor for esterification or amidation. Compared to straight 3-fluorobenzoic acid or 5-trifluoromethylbenzoic acid, our product often requires different mixing protocols and solvents. We fine-tuned our isolation process because off-the-shelf approaches led to build-up on reactor walls or excessive foaming. Engineers and technicians rely on real-world troubleshooting, not simple recipe-following.

    Chemically, the double bond strength and aromatic system in this molecule impact its interaction with catalysts. Some downstream manufacturers found that trace residual acids can deactivate palladium catalysts needed for coupling. From the factory floor, we doubled the number of post-processing washes, using data from failed reactions in partner labs as our test case. We learned that while other manufacturers might cut corners, close QC on residuals and trace metals makes the difference in large-scale synthesis programs.

    End Use In Research and Industry

    Most 3-Fluoro-5-(Trifluoromethyl)Benzoic Acid we produce ends up in two main arenas: pharmaceutical intermediates and crop protection agents. Researchers use it to introduce electron-withdrawing motifs into active molecular fragments, aiming to improve metabolic stability or binding affinity. From experience, we can say that modification with this acid leads to real, bench-tested improvements in drug candidates. We hear from labs that turned to our material when cheaper alternatives failed to meet their selectivity or solubility demands.

    Crop science moves fast, and the need for novel herbicide or pesticide scaffolds continues to grow. Many new molecules incorporate heavily fluorinated aromatic segments, which our product supplies. We've seen this acid used to develop new ring systems, as well as a robust coupling partner for generating emerging bioactive libraries. Scientists tell us that small changes—like going from a single fluorine to both trifluoromethyl and fluorine—produce big shifts in biological activity. Real trial and error, not just computer modeling, proves this out.

    Responsible Handling and Sustainable Manufacturing

    Making modern fluorinated aromatics involves complex chemistry. Fluorinated reagents and intermediates demand careful ventilation and specialist protective gear. Inside our plant, daily safety briefings go hand in hand with years of experience handling corrosive and potentially hazardous byproducts. We prioritize closed-system operations and continuous improvement on emissions control. Waste solvents and spent acids go through on-site neutralization and licensed disposal, well before new environmental standards demand it.

    Raw material sourcing plays its own part. We've shifted toward greener reagents and solvent recovery wherever possible. Our engineering team tracks the energy used per batch, and feedback from workers on the production floor prompted changes in heat exchange and reactive quenching. These are not cosmetic upgrades. They matter when you produce tons per year and want to meet the scrutiny of regulatory agencies without introducing variability batch to batch. Decades of hands-on learning sharpened our approach.

    Supporting Researchers Beyond the Drum and Bag

    We often guide customers troubleshooting unexpected clogs, precipitates, or color changes during formulation. Our technical team brings years of experience working with fluorinated benzoic acids, meaning we don’t simply quote data points from a database. We advise on best practices for dissolving the material, handling static electricity risks, and differences in weighing or blending compared to simpler acids. Feedback from teams around the world led us to supply a product with consistently tight particle size and moisture control, because we’ve seen failed reactions triggered by stray drops of water or over-milled powders.

    Sometimes research teams attempt to substitute similar benzoic acids, chasing lower cost. We’ve helped teams realize after costly pilot runs that those choices affect downstream yield, especially in scale-up. The minute influence of a single fluorine or CF3 can matter more than a theoretical fungibility chart suggests. Heading off repeated pilot failures, we keep a log of end-user stories to help future customers avoid the same mistakes. Direct experience delivers value far beyond a COA.

    Quality Assurance by People, Not Automation Alone

    A lot rides on QA and QC. Over years, we stopped relying on automated analytics alone. We assign experienced chemists to visually inspect each finished batch and run hands-on spot checks. Our GC and LC methods go well beyond regulatory minimums not because specs demand it, but because an early visual or olfactory cue often catches what a machine might miss. We trust our crew’s expertise, refined by actual production problems—not just textbook knowledge.

    Our commitment to quality shows in repeated customer testimonials. Over the years, our plant supplied multinationals and single-bench startups alike. Both groups need predictability. We saw early on that fluorinated aromatics amplify trace impurity effects, especially in downstream reactions catalyzed by precious metals or involving light-sensitive steps. Regular audits and sample holds, managed by long-tenured staff, lay the foundation for trust in every shipment.

    Regulatory and Documentation Support

    In today’s regulated market, supporting documentation matters as much as the product. Our experience tells us that gaps in TDS, impurity profiles, and residual solvent statements cause delays in project milestones and even regulatory filings. Our staff compiles full documentation packages with batch traceability, impurity mapping, and even historical quality trends for bulk programs. Over time, we found that this thoroughness heads off delays, reduces redundant questions, and lets technical teams focus on new chemistry instead of paperwork loops.

    Batch to batch consistency is king for those needing data for registration or formal compliance. We use validated analytical methods and participate in round-robin testing with client labs to make sure our reporting lines up, batch after batch, across different instruments or operators. It took years at the lab bench and in shipping rooms to learn how these reports make or break a project’s downstream chance of approval.

    Continuous Improvement Born From Field Feedback

    Customers in pharma and crop protection bring new challenges every season. Being the manufacturer, we hear each one directly. Silent changes—a new drum type, altered packaging, or a shift in air flow—created ripple effects in formulation rooms we could not predict. Lessons like those prompted us to increase adjustability in our plant setup, ready for tweaks on customer request. We have implemented changes in granulation, drying technique, and packaging options based on partner input, not just industry trends.

    We maintain direct lines of communication with both R&D and production teams across the chemical sector. Regular site visits, technical visits, and hands-on collaboration drive upgrades in our methods. Real user experience gives us a feedback loop to refine purity, consistency, and shelf life batch after batch. As new downstream reactions and regulatory constraints emerge, our crew evolves too—knowledge grows on the plant floor, not just in certificates or trade shows.

    Looking Ahead, Keeping Perspective

    Fluorinated benzoic acids continue to gain attention not just for their chemical novelty, but for their role in the toolbox of modern synthetic chemistry. Every step of producing 3-Fluoro-5-(Trifluoromethyl)Benzoic Acid reflects hard-won lessons in safety, troubleshooting, and continuous improvement. Innovation drives this field—customers’ projects grow more ambitious every year. Inside our plant, we carry forward time-tested practices, practical troubleshooting, and an open door to users’ feedback because technical progress never stays still.

    Choice of supplier carries real consequences on development programs, timelines, and budgets. Our role as manufacturer means we see problems and solutions before others, and share them freely to keep projects on track. Teamwork between production experts and researchers breaks new ground in chemical manufacturing even as challenges — like regulatory hurdles and competitive pressures — rise. No shortcut beats direct experience, and decades on the manufacturing floor inform everything we ship out.

    Each drum of 3-Fluoro-5-(Trifluoromethyl)Benzoic Acid represents both that experience and our ongoing promise to chemists everywhere. Trust in raw materials grows from long cooperation, steady improvement, and a willingness to solve problems together as science evolves.