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2-Fluoro-3-(Trifluoromethyl)Benzoic Acid

    • Product Name 2-Fluoro-3-(Trifluoromethyl)Benzoic Acid
    • Alias 2-Fluoro-3-(trifluoromethyl)benzoic acid
    • Einecs 246-230-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    165875

    Product Name 2-Fluoro-3-(Trifluoromethyl)Benzoic Acid
    Cas Number 104013-87-8
    Molecular Formula C8H4F4O2
    Molecular Weight 208.11 g/mol
    Appearance White to off-white solid
    Melting Point 104-108°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Smiles C1=CC(=C(C(=C1C(=O)O)F)C(F)(F)F)
    Inchi InChI=1S/C8H4F4O2/c9-6-3-2-4(8(13)14)5(1-6)7(10,11)12/h1-3H,(H,13,14)
    Storage Conditions Store at room temperature, in a tightly closed container
    Synonyms 2-Fluoro-3-(trifluoromethyl)benzenecarboxylic acid

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

    Packing & Storage
    Packing The 25g bottle is amber glass with a white screw cap, labeled "2-Fluoro-3-(Trifluoromethyl)Benzoic Acid" and safety warnings.
    Shipping 2-Fluoro-3-(Trifluoromethyl)benzoic acid is shipped in tightly sealed containers, compliant with chemical transport regulations. The package is protected from moisture, light, and extreme temperatures. Proper labeling ensures safe handling. Shipping is typically via ground or air, depending on destination, with accompanying safety documentation and material safety data sheet (MSDS).
    Storage Store 2-Fluoro-3-(trifluoromethyl)benzoic acid in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible materials such as strong bases and oxidizers. Protect from moisture, heat, and direct sunlight. Use appropriate personal protective equipment (PPE) when handling, and follow local regulations for chemical storage and disposal. Keep container clearly labeled at all times.
    Application of 2-Fluoro-3-(Trifluoromethyl)Benzoic Acid

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

    2-Fluoro-3-(Trifluoromethyl)Benzoic Acid functions as a specialized intermediate across defined sectors in chemical manufacturing. Our direct production and supply to industry leaders support high-volume projects demanding consistent purity and precise formulation. The following segments highlight specific and regulated implementation routes verified by actual downstream demand.

    1. Agrochemical Synthesis—Herbicide and Fungicide Active Ingredient Manufacturing

    This material is widely processed as a key building block for the synthesis of fluorinated active ingredients in advanced crop protection formulas. Leading manufacturers integrate it into multi-step syntheses for highly selective herbicides and fungicides. Its fluorine-rich structure supports the creation of molecules with improved metabolic stability in field application. Multi-ton batch runs implement stringent control at fluorination and coupling stages to meet product registration requirements for global agrochemical markets.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Certified QMS in manufacturing chain
    • REACH Registration for agrochemical intermediates (EU)

    Typical usage ratio

    • Input ratio typically 0.7–1.2 mole per mole active core, adjusted for targeted molecular configuration
    • Adjusted based on substitution pattern of downstream fluorinated products

    Downstream process integration

    • Charged into reactor during initial coupling stage
    • Followed by halogenation/condensation with primary amines or alcohols
    • Final purification via crystallization or distillation

    Final product types

    • Triazole-based fungicides
    • Pyrimidine herbicides
    • Aryloxyphenoxypropionate herbicides
    • Other proprietary crop protection compounds

    2. Pharmaceutical Intermediate—Antiviral and Oncology Drug Synthesis

    This compound functions as a core intermediate within the pharmaceutical sector for the production of selective fluorinated molecules. Process chemists utilize controlled halogenation and aromatic substitution to introduce performance-improving motifs in target drugs, especially in antiviral agents and oncology therapies. Manufacturing batches follow cGMP protocols during multistep synthesis and purification to secure APIs that meet ICH Q7 standards for regulated markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF and EP monograph references (where applicable)
    • ISO 15378:2017 Primary Packaging Materials for Medicinal Products
    • 21 CFR Part 211 (US FDA)

    Typical usage ratio

    • Typically 0.5–1.1 mole per mole of target API framework
    • Varies with required fluorine incorporation in lead structure

    Downstream process integration

    • Added in primary fluorination or acylation stage
    • Undergoes selective esterification or amidation
    • Further refined by chromatographic separation

    Final product types

    • Small molecule targeted oncology drugs
    • Antiviral therapeutic ingredients
    • Clinical trial quantity NCEs
    • Specialty fluorinated APIs for R&D

    3. Electronic Chemicals—Photoresist Monomer Manufacturing

    Producers of semiconductor materials use this acid derivative for synthesizing advanced fluorinated aromatic monomers applied in photoresist formulations. The presence of both fluoro and trifluoromethyl groups enhances chemical resistance and lithographic precision, which is essential for fine feature patterning in microchip production. Rigorous purification ensures compatibility with high-standard Class 10 cleanroom operations in the transfer to polymerization stages.

    Industry compliance standards

    • SEMI S2 and S8 Equipment and Chemical Safety Guidelines
    • ISO 14644-1:2015 Cleanroom Standard
    • RoHS Directive for electronics
    • REACH compliance for specialty monomers

    Typical usage ratio

    • 0.12–0.28 mole per mole of proprietary photoresist backbone
    • Precisely metered for end-use molecular weight and pattern fidelity

    Downstream process integration

    • Dosed into polymerization vessel with other monomer components
    • Followed by solution blending and solvent purification
    • Sent to microfiltration and packaging for fab-grade use

    Final product types

    • KrF and ArF photoresist polymers
    • High-resolution positive and negative photoresist solutions
    • Advanced lithography materials for integrated circuits
    • Display panel photoetching agents

    4. Specialty Polymers—High-Performance Fluoropolymer Additives

    Within the engineered polymers sector, formulators use the acid as a reactive co-monomer or modifying group introductor for specialty fluorinated resins. It allows precise control of dielectric and hydrophobic properties in wire insulation or membrane applications. Controlled dosages and process parameters help bridge compatibility between base polymers and advanced performance additives, frequently tracked via in-line FTIR and batch QC analytics.

    Industry compliance standards

    • UL 94 Flammability Standards for Plastics Materials
    • ASTM D543 (Chemical Resistance Testing)
    • ISO 10993-5 for medical polymer biocompatibility (if medical grade)
    • RoHS and REACH substance restriction compliance

    Typical usage ratio

    • 0.05–0.18 weight percent relative to total polymer blend
    • Tuned for target surface energy or electrical performance

    Downstream process integration

    • Pre-mixed into monomer stage or compounded during reactive extrusion
    • Integrated with fillers and stabilizers in melt blending
    • QC via melt index and dielectric strength tests

    Final product types

    • Low-loss dielectric cable insulations
    • Fuel cell membrane films
    • High-purity process tubing for aggressive media
    • Specialty medical device polymers (where biocompatible grades apply)
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    Certification & Compliance
    More Introduction

    2-Fluoro-3-(Trifluoromethyl)Benzoic Acid: Real-World Manufacture and Practical Insight

    Understanding the Compound from the Factory Floor

    Every batch of 2-Fluoro-3-(Trifluoromethyl)Benzoic Acid rolling off our reactors tells a story of close attention to detail. In the world of fine chemicals, this molecule brings unique value. Our technicians, engineers, and R&D lab crews move beyond recipes and formulas. With the CAS number 175277-96-6, this acid stands apart due to its combined fluorinated structure and carboxylic acid functionality. We’ve watched firsthand how these features impact not just its reactivity, but its performance across diverse synthesis applications.

    What Makes This Compound Stand Out

    From a manufacturer's point of view, the structure of 2-Fluoro-3-(Trifluoromethyl)Benzoic Acid presents opportunities and challenges. It combines a fluorine atom at the second position with a trifluoromethyl group at the third position on the benzene ring, leaving the carboxylic acid at the standard para location. This combination delivers a potent electronic impact, altering reactivity compared to plain benzoic acid or even simple monofluorobenzoic acids.

    We see chemists return to this compound for two main reasons: selective reactivity in complex molecule construction, and consistent physical properties during scale-up. Take the trifluoromethyl group—unlike standard methyl or ethyl, it brings significant electronegativity and lipophilicity. Whether you’re engineering a pharma intermediate or tuning polymers for specialty coatings, this molecular tweak yields properties not easily found elsewhere.

    How We Prepare and Confirm Quality

    Our process begins with purified raw benzene derivatives in high-grade reactors lined to resist fluorinated intermediates. The addition of fluoride sources and methyl trifluoromethylating agents calls for careful temperature moderation, as runaway reactions disrupt not just yield but also downstream purity. We’ve handled a wide range of reaction scales, from pilot runs at 5 kg in glassware to commercial volumes above 100 kg, and our protocols adjust accordingly.

    Each batch gets a full GC-MS and NMR profile. Residual solvents—be they acetonitrile, dichloromethane, or even DMF—require detection down to the ppm level. Our customers depend on the compound’s stability after long-distance shipping, so we check moisture uptake and potential hydrolysis. Nothing shifts out of our QC until it passes every threshold, from melting point determination to HPLC area normalization. Through the years, we’ve tweaked purification steps, using activated charcoal and precise pH adjustment, which reduces colored byproducts and ensures optical clarity for specialty applications.

    Differences Between Our Product and Others on the Market

    As a direct manufacturer, we know that everyone wants consistency batch to batch. Some sources invest only in bulk volumes, letting minor impurities slip through if specs are broad. We run every production sequence with the same analytical rigor, whether the order is a bottle for a research lab or a drum destined for a pharmaceutical plant. We avoid filler acids and keep particle size uniform, critical for anyone loading this acid into automated production lines or formulating reagents downstream.

    Trace metals come tightly controlled. Some syntheses, especially in electronics or medical intermediates, react poorly to iron and copper contamination. We monitor every feedstock for these elements and treat filtrates with chelating agents as needed. Cost-cutting at the level of raw materials or energy inputs always comes with trade-offs that hit people further down the supply chain. We’ve seen how that plays out—stalled production, dirty reactions, or failed registrations with regulatory agencies. Our commitment stands firm: no surprise contaminants, no poorly defined melting range, and always a clear Certificate of Analysis with data you can audit.

    How Customers Actually Use 2-Fluoro-3-(Trifluoromethyl)Benzoic Acid

    Through conversations with research chemists, scale-up supervisors, and process engineers, it’s clear this acid finds utility where site-specific functionalization is essential. Pharmaceutical companies often use it early in the synthesis of advanced drug candidates, particularly for molecules where metabolic stability requires extra fluorination. Its electron-withdrawing groups flatten aromatic reactivity, suppressing unwanted side reactions—especially in electrophilic aromatic substitution. Within the agrochemical industry, the compound gives rise to active ingredients with raised persistence and soil mobility, especially compared to plain benzoic acid derivatives.

    Coatings formulators and electronics material researchers seek out this acid for its impact on hydrophobicity and thermal resilience. Adding trifluoromethyl and fluoro groups simultaneously changes the surface energy profile of resins and polymers, resisting both wetting and chemical breakdown at high temperatures. In our own work, we’ve seen customers shave days off development cycles by dropping this building block into late-stage synthesis, passing purity specs on the first try.

    Typical Specifications We Achieve

    Our in-house quality comes down to numbers and data rather than vague promises. Melting points regularly fall between 98°C and 101°C with no sign of discoloration—an easy check for anyone equipped with a basic oil bath. Purity, measured via HPLC, runs above 99.0% area, usually higher. Water content, checked by Karl Fischer titration, often sits below 0.2%. Residual halides, metals, and organic solvents show up in trace amounts—rarely more than a few ppm for metals, and almost always undetectable by GC for chlorinated solvents.

    We maintain this quality in both analytical and preparative scale. Years ago, several customers pushed us for micronized particle options. On a variety of mechanical mills and air-jet pulverizers, we dialed in particle size distribution to sub-100 micron D-v50 for those using the acid in spray drying or granulation. Still, most production batches ship as crystalline powder, packed under nitrogen, in high-barrier PE-lined drums to cut moisture intrusion.

    Problems That Occur and How We Solve Them

    Fluorinated benzoic acids present handling and storage challenges. The main headache comes from their slight volatility under strong vacuum and their sensitivity to high temperatures during drying. We used to struggle with Teflon-lined drying ovens leaching trace perfluoro contaminants into the final product. After a batch was flagged for off-spec by a customer, we switched to glass and stainless steel containment for all post-reaction processing. Losses dropped and cross-contamination became negligible.

    Logistics also trip up many suppliers. Shipping acids with high fluorine content in hot, humid climates leads to package swelling and caking. We found the solution in thicker, multi-layer liners and deep-vacuum packaging that holds up even in ocean transit. Preventing humidity ingress preserves both flowability and chemical consistency—a detail too often overlooked in the race to trim logistics expenses.

    Comparisons to Related Benzoic Acids

    Some customers ask why not use simple 2-Fluorobenzoic Acid, or just 3-(Trifluoromethyl)Benzoic Acid. Working at the reactor, side-by-side tests show the difference. Monofluorobenzoic acids lack the electronic moderation and metabolic blocking power needed in complex molecules. The dual substitution—fluoro and trifluoromethyl—produces a subtle but strong field effect, which enables site-selective transformations hard to execute otherwise.

    We routinely ship custom analogues, yet few show the same stability during storage and transit. The specific substitution pattern of 2-Fluoro-3-(Trifluoromethyl)Benzoic Acid resists both oxidation and hydrolysis, two major causes of shelf-life reduction in related compounds. Chemists see better crystallinity, fewer byproducts during coupling steps, and strong recoveries during both chromatography and crystallization. For projects demanding tight reproducibility, few benzoic acid derivatives check as many boxes.

    Why Technical Support Matters

    Making a high-purity compound is just one piece. Explaining the subtleties of how our acid performs—why it dissolves a certain way, what crystallization speed to expect, or how minor pH adjustments change purity—is often what saves the day for downstream users. Our technical team includes people who have spent years on the actual shop floor and in kilo labs. Every year, we consult with end users both locally and abroad about everything from small-lab scale-ups to large reactor charge issues.

    Supporting a customer through a stuck filtration, or advising on compatible extraction solvents, comes from lessons learned the hard way. We once fielded a call from an API manufacturer whose batch began precipitating dark byproducts at the second step. By walking through their sequence and reviewing each solvent and pH inflection point, we helped them adjust workup. Their next run passed all in-process controls. We keep these experiences in mind as we guide every delivery out of our loading docks.

    Regulatory and Sustainability Considerations

    Few topics draw more discussion in our sector than safe manufacturing and compliance. 2-Fluoro-3-(Trifluoromethyl)Benzoic Acid, like many fluorinated chemicals, now faces tighter environmental scrutiny due to the persistence and bioaccumulative nature of the trifluoromethyl group. We monitor evolving regulatory frameworks in the EU, North America, and Asia. Internal audits double-check wastewater and vent streams for fluoride and organofluorine residues well under allowable thresholds.

    Waste processing gets close tracking—our on-site facilities neutralize fluorinated organics through controlled incineration, with exhaust scrubbing systems to capture and treat any off-gassing. We engage regularly in industry roundtables on green chemistry, aiming to substitute hazardous raw materials as better options become available. We invest in closed-loop solvent recovery, both for reducing environmental impact and lowering costs for customers.

    Ongoing Innovation

    Stagnation doesn’t serve anyone, least of all the innovators who rely on niche chemicals to crack tough research puzzles. Our R&D teams listen closely when formulators mention pain points—whether that means synthesizing close analogues of this acid, improving scale-up yields, or devising purer isolation methods. We’ve experimented with fluorination catalysts and greener methyl sources, shortening cycle times and tightening impurity profiles.

    Several years back, we worked with a contract manufacturer who needed rapid access to this product, but regulations in their market blocked one standard solvent. Through several iterations, our team switched to a solvent system cleared for medical drug synthesis in their territory. Their approval process sped up, their costs dropped, and our collaboration led to process improvements that we now use across multiple product lines. Customer feedback and regulatory signals feed directly into our process design, never getting lost in layers of distribution.

    Real-World Lessons from Years Manufacturing Fluorinated Benzoic Acids

    No one really understands the impact of a chemical until it arrives at scale—hundreds of kilos shipped, stored, blended, and reacted. 2-Fluoro-3-(Trifluoromethyl)Benzoic Acid has shown us that small details in production yield giant differences in application. Particle size modulation helps process yields and cuts downtime on high-throughput lines. Excluding colored impurities makes the difference in thin film applications, where color or haze impacts end-use. We collaborate with partners to revisit purification trains, adjusting for everything from temperature to washing solvents based on real-world data.

    Years spent inside the plant have proven that commodity mentality rarely holds up for compounds with specialty utility. Saving pennies on raw feedstock reagents only wrecks downstream reactivity or storage stability. Our focus rests on tight process control, rigorous analytics, and long-term trust with buyers. Suppliers who skip these steps can’t sustain repeat business or positive feedback from technical evaluators.

    Critical Value for Research and Scale-up

    The crossover value between lab-scale innovation and production-scale delivery often gets lost in translation. 2-Fluoro-3-(Trifluoromethyl)Benzoic Acid bridges this gap by replicating lab performance at scale. Process chemists bring us new coupling partners and ask for kilogram lots with the same purity they saw in gram-scale academic labs. We’ve learned to flex our batch sizes and purification runs, delivering just-in-time orders without losing analytical detail or documentation.

    We participate in multinational collaboration projects—each new market and industry sector spurring us to adjust offerings. Some research partners require pre-registered documentation for pharma filings, while new materials start-ups care most about batch-to-batch analytics and storage stability data. By engaging directly, we can supply detailed impurity profiles, stability curves, and support documentation that smooths the tech transfer process. The lessons from these collaborations feed straight back into every batch we start.

    The Human Element in Chemical Manufacturing

    At the heart of every 2-Fluoro-3-(Trifluoromethyl)Benzoic Acid delivery stands the combined experience of chemists, plant operators, and technical staff focused on reliability. Every day, new challenges crop up—contaminant surprises, packaging failures, scale-up headaches, and process glitches. Our answer comes in the form of hands-on troubleshooting, transparent communication, and a steady flow of technical evidence. We know which questions to ask, and which details will matter later during application—because we deal with those practicalities firsthand.

    This approach, grounded in plant-level and QA experience, builds real confidence for our partners. Whether the compound heads off to early discovery chemistry, down a commercial pharmaceutical route, or into new materials development, our commitment shows in the final product—crystal by crystal, batch by batch.

    Looking Ahead

    As research frontiers shift and regulatory expectations climb, we continue refining every step of our 2-Fluoro-3-(Trifluoromethyl)Benzoic Acid process chain. New requests come fast: lower impurity levels, custom particle morphologies, greener starting materials. Staying close to the realities of manufacturing and end-use means adapting quickly—not just on paper, but through shifts in how we handle, test, and deliver every kilogram. Years of direct production teach that quality never comes from shortcuts or generic approaches, but from steady, honest technical effort and constant dialogue with people who use the compounds every day.