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3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoic Acid

    • Product Name 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoic Acid
    • Alias 3-CFBA
    • Einecs 674-057-2
    • 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

    680093

    Productname 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoic Acid
    Casnumber 886372-38-5
    Molecularformula C8H3ClF4O2
    Molecularweight 242.56 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=CC(=C(C(=C1C(=O)O)F)Cl)C(F)(F)F
    Inchi InChI=1S/C8H3ClF4O2/c9-5-2-1-4(8(12,13)14)6(10)7(5)3(11)15/h1-2H,(H,11,15)
    Storageconditions Store in a cool, dry, well-ventilated place

    As an accredited 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100 grams of 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoic Acid, sealed in an amber glass bottle with a tamper-evident cap.
    Shipping **Shipping Description:** 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoic Acid is shipped in tightly sealed, chemical-resistant containers with appropriate hazard labeling. Transport follows regulations for corrosive and irritant organic chemicals. Protective packaging prevents leaks or contamination. Shipping complies with relevant national and international safety standards, including documentation for chemical identity, handling precautions, and emergency procedures.
    Storage **3-Chloro-2-fluoro-6-(trifluoromethyl)benzoic acid** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible materials such as strong bases and oxidizers. Avoid moisture to prevent decomposition. Use in a chemical fume hood and ensure appropriate labeling. Follow all standard laboratory safety and chemical hygiene practices.
    Application of 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoic Acid

    Applications of 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoic Acid in Industrial Manufacturing

    We supply 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoic Acid to global manufacturers specializing in complex chemical synthesis. This intermediate’s unique reactivity enables precision transformations across a focused set of advanced chemical sectors. Below, we detail actual industrial scenarios where this specialty acid is incorporated into downstream production at the formulation and synthesis stage, referencing compliance, process, and product output for each segment.

    1. Synthesis of Agrochemical Active Ingredients (Herbicides)

    Major agrochemical producers use this material during multi-step manufacturing of modern herbicide molecules, especially for fluorinated benzoyl fragments needed in selective weed control agents. The acid acts as a building block introduced at the benzoylation or coupling reaction stage, influencing both efficacy profile and environmental behavior of the final crop protection product.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • REACH (EC 1907/2006) European Plant Protection Product Regulation
    • US EPA 40 CFR Part 180 (Pesticide Chemicals in or on Food)
    • ISO 9001:2015 certified QMS in synthesis and release

    Typical usage ratio

    • 5–18% by weight in the active ingredient synthesis batch, adjusted based on target molecule

    Downstream process integration

    • Introduced during key condensation or Friedel–Crafts acylation steps before downstream halogenation or ring closure

    Final product types

    • Ready-to-formulate herbicide actives such as fluorinated benzoyl-based selective herbicides
    • Custom pre-registered technicals for multinational crop science companies

    2. Pharmaceutical Intermediate for Fluorinated Drugs

    Multistep drug synthesis strategies use this acid as a precursor for generating fluorinated and chlorinated intermediates vital to active pharmaceutical ingredient (API) construction. Its halogenation pattern fits both small-molecule oncology drugs and CNS agent scaffolds; precise introduction of this acid controls regioselectivity and purity at coupling or cyclization stages.

    Industry compliance standards

    • ICH Q7 (GMP for Active Pharmaceutical Ingredients)
    • USP/NF and Ph. Eur. monograph references (where downstream API applies)
    • 21 CFR Part 210/211 (cGMP for finished pharmaceuticals)
    • ISO 9001:2015 process traceability

    Typical usage ratio

    • 3–12%, variable depending on molecular scaffold and scale of API synthesis

    Downstream process integration

    • Fed into mid-stream amidation, Suzuki coupling, or esterification sequence before final API formation

    Final product types

    • Halogen-rich pharmaceutical intermediates
    • Bulk APIs (e.g., fluorinated oncology or CNS drugs); supplied to EU and US drug manufacturers

    3. Fluorinated Phenylether Synthesis for Specialty Polymers

    Producers of high-performance specialty polymers utilize this benzoic acid as a source for introducing fluorinated aromatic units. Industrial polymer chemists employ it in etherification or condensation steps, favoring the unique trifluoromethyl substitution for lowered dielectric constants, flame resistance, and increased chemical durability in electronics-grade materials and aerospace matrices.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 9001:2015 Quality Management for polymer/process manufacturers
    • UL 94 (Flammability Safety for Plastics)
    • IEC 61249 (Materials for Printed Circuits)

    Typical usage ratio

    • 2–7% by monomer content in custom polymer formulations, modified for targeted property balances

    Downstream process integration

    • Reacted during phenylether or polybenzoxazole condensation processing, before extrusion or casting

    Final product types

    • Dielectric films for flexible electronics
    • Flame-retardant composite panels used in aerospace interiors
    • Microelectronic substrates with tailored electrical properties

    4. Intermediate for Crop Protection Safener Molecules

    Manufacturers of herbicide safeners use this acid in the multi-step synthesis of benzoic acid derivative safeners that enhance crop tolerance to nearby herbicide use. The halogenated framework incorporates directly into the aromatic core of the safener, affecting both plant uptake and metabolic stability in the resultant field formulation.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Safeners
    • US EPA Tolerance Exemption for Inert Ingredients (40 CFR 180.920)
    • China GB 2763 Maximum Residue Limits for Pesticides
    • ISO 17025 laboratory release for batch QC

    Typical usage ratio

    • 6–14% of the total safener intermediate synthesis batch

    Downstream process integration

    • Charged during initial benzoic acid substitution, followed by esterification and further modifications before safener formulation

    Final product types

    • Finished safener active ingredients for mixing with pre-formulated herbicides
    • Co-granulated field-ready herbicide–safener blends

    5. Advanced Intermediate for Liquid Crystal Material Synthesis

    In the electronics sector, liquid crystal material manufacturers leverage this benzoic acid as a specialty intermediate to introduce unique halogen patterns required in the aromatic rings of high-performance liquid crystals. Its controlled reactivity contributes to customized phase transitions and improved electro-optical response in displays and optical devices.

    Industry compliance standards

    • IEC 61249-2-21 (Material Standards for LCD Applications)
    • RoHS and REACH Compliance for Electronic Grade Materials
    • ISO 14001:2015 Environmental Management in Manufacturing
    • Japanese JIS C 6471 (LCD Raw Material Quality)

    Typical usage ratio

    • 1.5–6% of the downstream organic synthesis batch depending on target liquid crystal parameter set

    Downstream process integration

    • Introduced at the aromatic coupling and acylation stage before final purification and crystal alignment processing

    Final product types

    • Liquid crystal compounds for LCD and advanced display panels
    • Optical alignment materials supplied to electronics producers
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    Certification & Compliance
    More Introduction

    3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoic Acid — Insights from the Manufacturer’s Bench

    A Closer Look at a Specialized Benzoic Acid Derivative

    In the chemical industry, the difference between standard intermediates and nuanced building blocks can mean success or endless troubleshooting in synthesis. 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoic Acid is one of those building blocks whose properties and performance draw interest from process developers and scale chemists alike. Over the years, we've produced this material in quantities ranging from pilot batches to multi-ton campaigns. Our experience in running this chemistry at scale, handling regulatory documentation, and supporting customers through technology transfer has granted us insight not just into this compound’s specifications, but its actual performance in today’s demanding synthetic routes.

    Putting the Molecular Profile in Context

    Every atom on this benzoic acid structure carries strategic weight. Chlorine at the 3-position, fluorine at the 2-position, and a trifluoromethyl group at the 6-position collectively adjust both the molecule’s electronic profile and its reactivity in downstream reactions. Manufacturers engaged in fluorinated or halogenated aromatic synthesis look to such motifs because of the way these electron-withdrawing groups allow precise control over selectivity, activate or deactivate the ring as required, and affect the behavior during challenging steps like cross-coupling or amidation.

    During manufacturing, the biggest hurdles typically involve selective halogenation and introduction of the trifluoromethyl group while keeping byproduct profiles in check. Not all suppliers manage to balance purity and throughput, since closely related impurities can result from over-fluorination, partial hydrolysis, or incomplete reaction. Our production line emphasizes in-process analysis with HPLC and NMR, not just to pass a spec sheet, but to reduce the time customers spend on purification after delivery. That saves time and money at the plant, which always matters more than theoretical purity claims.

    Production Experience and Its Impact on Utility

    Producing 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoic Acid at scale isn’t just about following a published route. Our researchers have invested in safer and more consistent methods for each step. For instance, engaging the trifluoromethylation using fluoroform or reagents like Togni’s and Umemoto’s, demands process robustness when you move from flask to reactor. As batch sizes climbed, we had to re-engineer mixing, address mass transfer, and ensure that localized hot spots didn’t degrade the sensitive intermediates. These sorts of details get overlooked in literature — they influence the overall quality and cost control.

    Customers in pharmaceuticals and agrochemicals frequently request material on tight impurity and moisture limits. From our perspective, the most persistent challenge is keeping the final acid free from residual inorganic salts without triggering decarboxylation or darkening of the product. In practice, that means multi-stage washing and careful control of pH, proven by lot-to-lot analytics. Product stability depends on controlling the form: too much residual solvent and the acid can ‘cake’ or change color; too little, and handling losses creep up due to static or dust. Experience has influenced not just how we purify, but also decisions on packaging and shipment.

    Model and Specifications — Not Just a List of Numbers

    The listed chemical identity — CAS number, molecular weight, assay — only tells part of the product’s story. Our experience shows real-world differences emerge in the impurity fingerprint and whether residual solvents meet downstream reaction needs. Some routes are more sensitive to specific byproducts like chlorinated or fluorinated benzoic acids, so consistent impurity profiling at ppm levels is more than a paperwork exercise; it enables chemists to skip unnecessary recrystallizations, boosting throughput.

    Our best batches have consistently delivered over 99% assay as measured by HPLC, with regulated levels of water and non-volatile residue. Typical lots ship with both the typical white to off-white appearance and correct polymorphic form; color changes or form changes can signal degradation or mishandling in transit, which we flag through stability testing and re-analysis if necessary. This kind of vigilance forms the backbone of reliability — something our customers have grown used to, especially across repeat orders spanning years.

    Usage and Key Applications — Lessons Learned in the Field

    In application, the compound serves most prominently as a building block in pharmaceutical, agrochemical, and specialty material synthesis. Over a decade of feedback from downstream users confirms the acid’s value for Suzuki and Buchwald-type couplings, trifluoromethyl-selective substitutions, and amidation processes. Customers leveraging it for amide or ester formation find that the balance of fluorine and chlorine on the ring boosts both yield and product purity, often streamlining workup protocols.

    Compared to traditional benzoic acids without extensive fluorination, this compound strikes a different solubility profile in solvents like DMSO, acetonitrile, or DMF. In our trials, process chemists working at kilo scale saw faster dissolution rates and better phase separation after acid-base extraction, sometimes cutting hours from the overall campaign. For anyone tasked with running multi-step synthesis, those hours add up, especially if you’re managing a tight deadline on a high-value intermediate.

    Further, the electron-withdrawing groups impact downstream reactivity: trifluoromethylated aromatics often enable access to metabolites or bioactives with improved metabolic stability and target engagement in pharmaceuticals. Fluorination at the ortho position also tunes acidity, which becomes a key factor during activation steps for peptide coupling or as a handle for further derivatization.

    Comparisons with Other Benzoic Acid Derivatives

    There is a crowded field of benzoic acid derivatives, but not all offer the same blend of selectivity or synthetic flexibility. For example, the parent 3-chlorobenzoic acid might be used widely, yet lacks the electronic profile needed for challenging couplings or activation-resistant conditions. Single-fluorinated alternatives, like 2-fluorobenzoic acid, don’t deliver the same hydrophobic character or metabolic stability for pharmaceuticals.

    Our chemists have compared this product’s performance against other multi-substituted analogs — such as 2,3,6-trifluorobenzoic acid — and noted that specific combination of chlorine and trifluoromethyl groups opens unique reaction windows. Clients running library synthesis have reported fewer side reactions, higher yields, and smoother purifications using our compound as the core scaffold. The substitution pattern also affects shelf life; material with para-electronic withdrawal tends to show greater thermal stability, which matters when large volumes spend months on the road or in warehouses.

    User Experience at Commercial Scale

    Scale brings surprises the literature doesn’t prepare you for. A customer once described how switching from a general supplier’s benzoic acid to our 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoic Acid cut their flash chromatography steps in half. These anecdotes highlight the value of true manufacturing consistency over time. Not all lots are created equal, and small upticks in specific byproducts — such as ortho-fluorinated impurity carryover or minor ring-chlorinated analogs — can force unexpected troubleshooting in kilo campaigns. We learned that strong, dedicated in-process controls benefit customers as much as us.

    Handling and safety considerations also shift with this class of compound. For instance, trifluoromethyl groups can increase volatility or affect perceived ‘cleanliness’ at the bench. We’ve worked out packing and shipping protocols that keep the acid free-flowing and protected from light, without relying on excess desiccants or over-engineering the packaging. Experienced handlers know that the right drum liner, the correct seal, and consistent particle size distribution make an outsized difference at scale.

    Process Support and Knowledge Sharing

    Many early-stage projects start with analytical grade quantities, but as programs move to pilot and commercial runs, documentation support and regulatory awareness grow in importance. We support our customers beyond just shipping the drums: offering full impurity spectra, stability assessments, and — where relevant — data for REACH or other regulatory filings. Projects in regulated markets can stall without robust evidence for impurity management and traceability.

    We also assist teams through technology transfer or troubleshooting scale-up. By sharing process notes on optimal solvent choices, isolation techniques, or recommended pH ranges during washing, we cut down the time needed to reach production qualified lots. Our plant operators understand the practicalities of filtered yield, filtration rates, and thermal ramping, building a base of shared knowledge that benefits all sides. Real-world manufacturing experience doesn’t just add a layer of trust, it shortens the project timeline.

    Quality, Repeatability, and Customer Feedback

    Continuous engagement with users shapes our approach to both product consistency and openness about limitations. For example, some think highly electron-deficient acids like this one can replace less substituted analogs directly in all transformations — our direct measurements and customer feedback show that base-catalyzed steps in certain solvents may slow or require tweaks. We keep customers informed about these nuances and offer side-by-side data from our application trials, supporting both the experienced pharmaceutical chemist and the new process development team.

    Quality isn’t a slogan here, it’s measured in turnaround reliability, package appearance, and the ability to track lots back to specific analytic records. Hundreds of batches have shown that critical limits on total halogen content, trace metals, and organic volatiles are practical only with good internal controls and swift lab support. Continuous improvement — be it an extra analytical checkpoint or helpline access for application chemistry — fosters a cycle where repeat clients keep offering us new challenges.

    Solutions for Ongoing Challenges

    One persistent concern across industries is the cost and environmental profile of manufacturing specialty intermediates like this one. Fluorination chemistry requires both specialty reagents and careful waste management. We’ve invested in solvent recovery, emission controls, and options for waste minimization at every stage. By tracking our own yields and byproduct streams, we have steadily pushed both the process mass intensity and waste generation curve down, even as demand scaled up. Large-scale users benefit from this too, as predictable cost bases enable better long-term planning.

    Further upstream, we’ve collaborated with raw material suppliers to ensure both child labor and conflict-mineral free sourcing, responding to concerns raised by our industrial partners about the wider context of specialty chemical manufacture. This level of transparency has solidified partnerships and allowed us to react faster to unexpected supply chain shocks, passing that stability on to end users.

    Looking Ahead — Where Manufacturing Meets Innovation

    The broad trend toward fluorinated scaffolds in pharmaceuticals and custom materials suggests demand for 3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoic Acid will only grow. As a manufacturer, we focus on refining the route, lowering cycle times, and supporting new application requests from discovery groups and process scale-up teams. Customization requests — whether for particle size, specific residual solvent limits, or co-crystallization studies — are increasingly common. In response, we keep updated on the landscape of greener fluorination techniques, safer halogen introduction, and improved analytical tools for lot certification.

    Researchers, formulation teams, and contract manufacturers rely on us not just for a drum or a kilogram, but for detailed, experience-driven feedback from people who've made, tested, and delivered this compound under real-world pressure. We thrive on pushing the process further, aiming to deliver not just the product, but the knowledge that streamlines production and innovation along every link of the value chain.

    Conclusion — The Value of Real Manufacturing Experience

    3-Chloro-2-Fluoro-6-(Trifluoromethyl)Benzoic Acid stands out in our line-up not because it’s rare, but because it demands focused process understanding from raw material selection through to drum shipping and post-sale troubleshooting. Customers don’t just want a benzoic acid — they want a product they can rely on, produced by a team who know every pitfall, every improvement, and every unexpected turn that comes with making something unique. The best outcomes always stem from deep, transparent collaboration between vendor and user, shaped by lessons only actual manufacturers have gathered. We take pride in delivering a product — and partnership — that reflect that depth of experience.