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4-Fluoro-2-Methoxybenzoic Acid

    • Product Name 4-Fluoro-2-Methoxybenzoic Acid
    • Alias 4-Fluoro-o-anisic acid
    • Einecs 229-008-6
    • 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

    753434

    Product Name 4-Fluoro-2-Methoxybenzoic Acid
    Cas Number 403-12-1
    Molecular Formula C8H7FO3
    Molecular Weight 170.14 g/mol
    Appearance White to off-white solid
    Melting Point 114-117 °C
    Solubility Soluble in organic solvents such as ethanol and DMSO
    Purity Typically ≥98%
    Smiles COC1=CC=C(C=C1C(=O)O)F
    Inchi InChI=1S/C8H7FO3/c1-12-6-4-5(9)2-3-7(6)8(10)11/h2-4H,1H3,(H,10,11)
    Storage Temperature Store at room temperature
    Synonyms 2-Methoxy-4-fluorobenzoic acid

    As an accredited 4-Fluoro-2-Methoxybenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White HDPE bottle with a secure screw cap, labeled "4-Fluoro-2-Methoxybenzoic Acid, 25g," including hazard symbols and storage instructions.
    Shipping 4-Fluoro-2-Methoxybenzoic Acid is shipped in secure, airtight containers to prevent contamination and moisture absorption. Packaging complies with relevant chemical transport regulations. Containers are clearly labeled with hazard information, handling instructions, and safety data. Shipping is conducted by licensed carriers with appropriate documentation to ensure safe and legal delivery.
    Storage 4-Fluoro-2-Methoxybenzoic Acid should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers. Keep the storage area free from moisture and sources of ignition. Properly label the container and store at room temperature, ideally between 2-8°C, to maintain chemical stability and safety.
    Application of 4-Fluoro-2-Methoxybenzoic Acid

    Applications of 4-Fluoro-2-Methoxybenzoic Acid in Industrial Manufacturing

    4-Fluoro-2-Methoxybenzoic Acid is a specialty building block widely used in multiple industrial manufacturing sectors. Below we present verified downstream applications, each with precise standards, processing details, and end-product insights based on direct manufacturer experience.

    1. Pharmaceutical Intermediate for Anti-Inflammatory Drug Synthesis

    This compound frequently serves as an intermediate in the production of non-steroidal anti-inflammatory drugs (NSAIDs), specifically in the synthesis of selective COX-2 inhibitors. Formulators introduce it during the construction of aromatic or heterocyclic cores under controlled temperature and pressure. Quality teams must monitor purity and trace impurity profiles throughout the batch process to meet registration requirements for final APIs exported globally to regulated markets.

    Industry compliance standards

    • ICH Q7 for API manufacturing
    • European Pharmacopoeia (Ph. Eur.) monographs for specific APIs
    • US FDA 21 CFR Part 211 (CGMP for finished pharmaceuticals)
    • REACH registration for exports to Europe

    Typical usage ratio

    • 5–15% of synthesis batch mass, depending on target molecule yield and route of synthesis; adjusted based on stoichiometric requirements and impurity tolerance.

    Downstream process integration

    • Introduced after initial alkylation steps in multi-stage batch reactors
    • Feeds into Suzuki or Buchwald cross-coupling reactions as an aryl source
    • Requires subsequent neutralization and phase separation
    • Purification by recrystallization or chromatography prior to next reaction stage

    Final product types

    • Active Pharmaceutical Ingredients (APIs): Celecoxib, etoricoxib
    • Pharmaceutical intermediates for contract synthesis
    • Reference standards for pharmacopoeial analysis
    • Custom developed NSAID molecules for clinical trials

    2. Agrochemical Synthesis for Herbicide Manufacturing

    Crop protection manufacturers use this material as an intermediate for synthesizing specific fluorinated aromatic herbicides. The methoxy and fluoro-substituted scaffold introduces key electronic and solubility properties essential for herbicidal action. Reaction controls must ensure minimal cross-contaminants and guarantee that the material meets agrochemical residual tolerances. Manufacturers perform scale-up under validated SOPs to maintain environmental compliance.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical materials
    • ISO 9001:2015 for agrochemical production
    • OECD Principles of GLP for analytical quality
    • China GB 2763 for pesticide maximum residue limits (MRLs) in food crops

    Typical usage ratio

    • 2–10% of total synthetic input, calculated according to the chlorination or amidation sequence in the formulation; adjusted for target molecule loading and minimum effective dose targets.

    Downstream process integration

    • Used in Friedel-Crafts acylation to introduce the aromatic acid moiety
    • Feeds esterification or amide bond-forming steps
    • Acts as a key precursor at the pre-crystallization stage prior to formulation
    • Waste mitigation and solvent recovery steps implemented routinely

    Final product types

    • Technical-grade herbicides (e.g., fluorinated benzoate herbicides)
    • Pre-emergent weed control agents
    • Custom active formulations for multinational agrochemical brands
    • Agrochemical intermediates in global contract manufacturing

    3. Specialty Chemical Intermediate for Liquid Crystal Materials

    Liquid crystal display (LCD) and specialty electronics manufacturers employ this raw material as a high-purity intermediate for synthesizing anisotropic aromatics. Its specific substitution pattern enables fine-tuning of mesogenic unit polarity and thermal performance. Producers must operate under stringent moisture and particle control systems, with detailed qualification programs for all inward and outward transfer to fabrication facilities.

    Industry compliance standards

    • ISO 14001 for environmental management at production sites
    • IECQ QC 080000 for hazardous substance process management in electronics
    • SEMI S2 for chemical safety in semiconductor and display manufacturing
    • Japanese Industrial Standards (JIS) for liquid crystal raw materials

    Typical usage ratio

    • 3–8% in the targeted reaction mass for core mesogen synthesis; varies based on molecular design and process scale-up yields.

    Downstream process integration

    • Integrated in the early stages of mesogenic core formation via etherification or acylation
    • Followed by halogen exchange and purification by vacuum distillation
    • Direct transfer to LC formulation or thin-film deposition units
    • Static and dynamic impurity monitoring throughout

    Final product types

    • Nematic and smectic liquid crystal mixtures for displays
    • Polymer-stabilized LC films for TVs and monitors
    • Anisotropic conductive films for touchscreen manufacturing
    • Advanced organic semiconductors for OLED or sensor arrays

    4. Fine Chemical Intermediate for Dye & Pigment Synthesis

    Leading dye manufacturers utilize this building block for the production of specialized aromatic pigment molecules, especially for applications requiring high stability and chromatic precision. As part of multi-step syntheses, color chemists select this compound to tailor electronic distribution in the final chromophore, controlling spectral absorption regions and lightfastness. The integration frequently involves catalytic coupling and controlled crystallization operations to prevent batch-to-batch shift.

    Industry compliance standards

    • REACH Substances of Very High Concern (SVHC) avoidance for dyes and pigments
    • ISO 9001 for quality in colorant manufacturing
    • ETAD (Ecological and Toxicological Association of Dyes and Pigments Manufacturers) Responsible Care requirements
    • ZDHC (Zero Discharge of Hazardous Chemicals) compliance for textile chemicals

    Typical usage ratio

    • 1-6% by weight in pigment core synthesis; optimized according to the structure-activity relationship and batch scale.

    Downstream process integration

    • Feeds into diazo coupling or Suzuki-Miyaura cross-coupling steps
    • Chromatographic purification prior to core pigment annulation
    • Filtration and milling for dispersible pigment batches
    • Ongoing colorimetric QC checks against reference standards

    Final product types

    • Aromatic monoazo dyes for plastics and fibers
    • High-performance pigments for inks and paints
    • Lightfast fluorinated pigments for automotive coatings
    • Dye intermediates for specialty organic colorants

    5. Intermediate for Active Ingredients in Veterinary Pharmaceuticals

    Animal health product manufacturers select this acid as a key intermediate in the synthesis of fluorinated benzoic acid derivatives used for anti-inflammatory and antimicrobial agents. Production facilities implement batch isolation and dedicated line cleaning between campaigns to prevent API carryover, complying with veterinary medicinal guidelines and local regulatory controls. Each batch supports supply to global and domestic veterinary pharmaceutical contract manufacturers.

    Industry compliance standards

    • VICH GL03 for GMP in veterinary active ingredient manufacturing
    • EU Regulation (EC) No 2019/6 on veterinary pharmaceutical products
    • US FDA Guidance for Industry #205 for veterinary APIs
    • Local Ministry of Agriculture product dossier submission

    Typical usage ratio

    • 4–10% per batch process, further optimized during pilot studies for target molecule conversion and minimal by-product formation.

    Downstream process integration

    • Enters amidation or esterification reactions to complete the veterinary API structure
    • Subject to direct crystallization and micronization for improved solubility
    • Secondary purification includes activated carbon treatment
    • Transferred to dosage form manufacturing following full QC release

    Final product types

    • Vet-grade anti-inflammatory APIs
    • Antimicrobial benzoate derivatives for animal use
    • Commercial veterinary dosage forms (powders, injectables)
    • API master batches for regional veterinary drug manufacturers
    Free Quote

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    Certification & Compliance
    More Introduction

    4-Fluoro-2-Methoxybenzoic Acid: Supporting Advanced Synthesis with Consistent Quality

    Introduction

    Our company produces 4-Fluoro-2-Methoxybenzoic Acid at scale, drawing on years of hands-on experience in refining halogenated aromatic acids for demanding researchers and industrial partners. This compound, sometimes referenced by its model number as 4F-2MBA, has earned a solid reputation with chemists focused on pharmaceuticals, agrochemicals, and performance materials. Unlike resellers, we carry the entire process, from sourcing fluorinated raw materials to packaging crystalline, high-purity batches ready for customer formulation or molecule building.

    Model and Purity: The Result of Tight Process Control

    Product consistency matters most for fine chemicals like 4-Fluoro-2-Methoxybenzoic Acid. Our main model, 4F-2MBA-99, delivers a certified 99.5% minimum purity level determined by HPLC and GC-MS, without trace solvent residues. Customers with specialized application needs sometimes require further customizations—we've supported projects requiring low-metal or low-moisture grades. From the production line, every batch passes through rigorous QA inspection, including NMR, melting point analysis, and checks for related substances below industry-relevant ppm limits.

    At this scale, reproducibility matters. Many clients have strict regulatory project requirements, so we avoid fluctuations between lots and keep analytical certificates traceable. Shipment always matches the lot tested—not simply a label.

    Material Handling and Appearance

    What we supply isn’t generic powder. The finished product forms a crystalline white to off-white solid, with bulk densities in a narrow, repeatable range. Years of adjusting milling and crystallization processes have produced a material that minimizes dusting and maximizes flow, critical for direct transfer to reactors or blending tanks. Minor batch differences, whether in moisture or particle profile, often matter more to a chemist than to a commercial trader, because these affect solubility rates and yields down the line.

    We don’t cut corners on packaging either. The acid typically ships in double-lined polyethylene drums with tamper-evident seals. Orders that require air shipment or extended storage can be packed under inert atmosphere protection. Redux shipments and custom pack sizes are available, subject to our QA cycle checks, to avoid risk of contamination or exposure.

    Comparing 4-Fluoro-2-Methoxybenzoic Acid to Related Compounds

    Several benzoic acid derivatives are available from manufacturers worldwide, but most are not designed for heavy-lifting research and pilot-scale synthesis. Our experience shows that the simultaneous presence of a fluorine at para and methoxy at ortho delivers unique reactivity compared to unsubstituted or single-substituted benzoic acids.

    For example, in contrast to 4-Fluorobenzoic acid, the 2-methoxy group increases solubility in certain organic media and modifies electronic effects. This often leads to higher selectivity during esterification or amide coupling—feedback from contract R&D firms supports this claim. In pharmaceutical discovery, fluorinated methoxybenzoates like this one act as key intermediates for synthesizing small-molecule APIs, specifically when looking to block or tune metabolic sites on aromatic rings.

    Researchers sometimes substitute 4-Fluoro-2-Methoxybenzoic Acid for analogues lacking either fluorine or methoxy, hoping for easier downstream processing or reduced reagent consumption, yet results are rarely identical. Our technical support team has seen clear yield improvements and process savings in custom coupling and cyclization protocols where the electron-donating and -withdrawing effects balance to give precise control.

    Where 4-Fluoro-2-Methoxybenzoic Acid Finds Its Strength: Usage and Real-World Projects

    Drug discovery teams lean heavily on this compound when assembling libraries of fluorinated analogues; it serves as a foundation for newer non-steroidal anti-inflammatory and central nervous system agent candidates. The unique substitution pattern helps researchers explore structural-activity relationships, aiming for higher receptor selectivity or metabolic stability.

    Beyond lab benches, scale-up teams pilot plant processes using our material to prepare specialty esters, amides, or biaryl linkages, crucial in agrochemical or polymer science exploration. Unlike most traders, we can support consistency throughout the transition from grams to multi-kilogram lots. For instance, agrochemical intermediates synthesized from this acid feature in modern herbicide projects where selective aryl substitution enables safer breakdown profiles in the environment.

    Polymer and materials science groups value the predictability of this compound in preparing chain-terminating agents, dyes, and specialty monomeric units. The dual electron-withdrawing (fluoro) and donating (methoxy) impacts allow for fine-tuned reaction rates in cross-coupling or protection-deprotection protocols.

    Another real difference comes out in fine-tuning process parameters. In complex Suzuki or Buchwald-Hartwig cross-couplings, for example, the unique substitution supports both activation and protection of specific ring positions. Experienced process chemists favor our product because they do not face unpredictable batch-to-batch absorption or side-reactions. Pilot studies for bioactive sunscreen ingredients and fragrance intermediates eastward of Europe have used our material in multiple stages, seeking the same attributes: clean conversion and straightforward purification.

    Practical Manufacturing Challenges and Solutions

    Experience tells us that halogenated aromatic acids need special care during their synthesis and isolation steps. Direct fluorination routes, favored for cost reasons, raise risks of halide scrambling and undesirable isomers. We’ve invested years into optimizing nucleophilic aromatic substitution and protecting group strategies, settling on a process that avoids the formation of polychlorinated byproducts. Careful monitoring and real-time sampling help us limit overreactions or formation of related impurities.

    Our system uses a closed reactor train with staged solvent recovery, cutting down waste output. Operators undergo annual refresher safety training, so even during large campaigns we maintain a record of zero reportable incidents with hazardous intermediates. Environmental compliance remains a top priority, with real solvent reclamation rates holding over 97%. Long experience has shown that investing in containment and extractor maintenance pays off—not just for compliance, but for avoiding yield loss and batch rework.

    Handling the crystallization and drying phases poses the greatest technical hurdles; 4-Fluoro-2-Methoxybenzoic Acid forms fine needles under some conditions that have poor filtration speed and can trap trace solvents. We’ve adopted a staged cooling cycle with in-line monitoring, developed through years of real production feedback. After initiating a move to vacuum tray drying, we sharply reduced time-to-dry while holding final moisture and solvent levels well below 0.2%. Test results from multiple production years confirm our approach outperforms older rotary evaporation systems, especially on scale.

    Analytical Insight—Traceability From Start to Finish

    We have seen how regulatory expectations have shifted, requiring attention to every detail—down to confirming the absence of persistent organic pollutants or ensuring compliance with REACH and other frameworks. Our on-site analytical laboratory maintains full batch traceability from the initial weighing to final release. Each drum picked for shipment accompanies a lot-matched COA with an NMR spectrum, HPLC chromatogram, heavy metals report, and—if needed—a full impurity profile.

    Feedback from European pharma customers illustrates the importance of transparent documentation and rapid Q&A response. Six sigma-style internal audits produced data showing that product non-conformities have dropped below 0.3% over the latest three-year stretch, reflecting how lessons from every scale-up feed back into our core manufacturing methods. This results in clear, reliable supply chains: one of the key reasons why researchers and process chemists keep returning instead of contacting broadline resellers.

    Occasionally, lab clients request single-batch trace impurity tracking to confirm negative responses in structure–activity studies—for example when correlating in-vitro test results with source material. We maintain product samples in refrigerated retention for at least three years. Trace data for every input reagent, handled through a digital protocol, can be accessed within 48 hours of written request, supporting scientific reproducibility.

    Case Studies in Real-World Applications

    A leading pharmaceutical partner in North America recently completed a multi-kilogram pilot using our 4-Fluoro-2-Methoxybenzoic Acid. The project goal—preparing a late-stage fluorinated API candidate with challenging solubilization requirements—relied on consistent reactivity. Lab notes credited the precise 2-methoxy and 4-fluoro pattern for offering extra kinetic control during intermediate step isolation, avoiding laborious chromatographic separations.

    In the field of specialty coatings, an EU-based R&D group purchased our acid to synthesize oligomeric additives with strong weather resistance. The downstream process needed acids stable under multiple heat-cool cycles and inert storage. Since our product holds to a controlled particle size and purity level, repeat analysis found no shift in optical properties between independent pilot runs.

    Local contract research organizations within our domestic network frequently use our 4-Fluoro-2-Methoxybenzoic Acid for testing new cyclization methodologies—a practical feedback loop which helps us further customize batch profiles. Coordination with their technical teams has led to development of a more filter-friendly crystallization regime, which we’ve since adopted for exporter lots with demanding downstream filtration steps. These case histories underscore a core truth: hands-on support and process responsiveness determine long-term supply relationships.

    Safety, Sustainability, and Support: Our Commitment in Practice

    Halogenated aromatic acids are not handled like basic bulk chemicals. They demand advanced technical controls during handling, both for operator safety and to prevent product degradation. Installing a comprehensive local exhaust and monitoring system came not from legal pressure but from our own close calls and near-miss investigations—personal lessons learned on the production floor. In addition to basic PPE training, we emphasize early intervention protocols for spills and skin contact, knowing from experience that delays raise risk dramatically.

    Moving toward broader sustainability goals, we've replaced a portion of virgin solvents with a closed-loop recycling system, tackling both resource use and emissions. Product yield and analytical data from the past five years show no degradation in purity or performance, reassuring partners that green chemistry shifts still maintain output. Real reductions in landfill output and improved energy use intensity per kilogram set a path many small-volume manufacturers have yet to follow.

    Beyond factory walls, clients know they can reach technical staff directly. Lab chemists and purchasing leads often reference our batch note archive, which links project numbers, scale-up notes, and customer feedback loops. For projects with tricky timelines or atypical processing needs, our rapid adjustment and open technical communication prevents costly delays—a lesson we embrace from both flagged complaints and positive reviews.

    We also maintain relationships with major regulators and international consortia, contributing anonymized impurity and handling data to promote safer industry practices. A standing technical liaison team tracks evolving legislative frameworks, ensuring that our synthetic and QA methods stay a step ahead of shifting compliance requirements. This practical approach protects customer projects from last-minute supply chain or documentation surprises.

    Choosing the Right Material for Modern Chemistry

    Chemists and process leads return to our 4-Fluoro-2-Methoxybenzoic Acid because it’s made by a partner who cares about scientific progress, not just sales volume. Experience matters—years spent optimizing flouride supply management, streamlining workups, learning from odd batch feedback. As fields like medicinal chemistry and advanced materials evolve, our clients find value in working with a producer who can link laboratory lessons to plant-scale production without compromise.

    4-Fluoro-2-Methoxybenzoic Acid remains more than another catalog compound. Reliable access, documented batch lineage, and an ongoing dialog between end-user and manufacturer distinguish our supply line from those passing through countless warehouses. It’s the difference between chasing purity on a spec sheet and achieving solid results in a file of project reports. For chemists and developers building future therapies or materials, every percent yield, every repeatable reaction step, and every traceable impurity count—at our factory scale, the details and expertise make all the difference.