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2-(4-Fluorobenzoyl)Benzoic Acid

    • Product Name 2-(4-Fluorobenzoyl)Benzoic Acid
    • Alias 4-Fluoro-2-benzoylbenzoic acid
    • Einecs 212-721-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    627571

    Product Name 2-(4-Fluorobenzoyl)Benzoic Acid
    Molecular Formula C14H9FO3
    Molecular Weight 244.22 g/mol
    Cas Number 159693-58-8
    Appearance White to off-white solid
    Melting Point 137-139°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Storage Temperature Store at 2-8°C
    Smiles C1=CC=C(C(=C1)C(=O)C2=CC=CC=C2C(=O)O)F
    Inchi InChI=1S/C14H9FO3/c15-11-7-5-10(6-8-11)14(18)12-4-2-1-3-9(12)13(16)17/h1-8H,(H,16,17)
    Synonyms 4-Fluorobenzoyl-o-benzoic acid

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

    Packing & Storage
    Packing The packaging for 5 grams of 2-(4-Fluorobenzoyl)benzoic acid features a sealed amber glass vial with a printed safety label.
    Shipping 2-(4-Fluorobenzoyl)benzoic acid is shipped in accordance with standard chemical safety protocols. It is securely packaged in sealed containers to prevent leaks, protected from moisture, and clearly labeled with hazard warnings. Transportation complies with international regulations for chemicals, ensuring safe handling and delivery to the recipient.
    Storage Store **2-(4-Fluorobenzoyl)benzoic acid** in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Use appropriate safety measures, including gloves and eye protection, when handling. Keep labeled and out of reach of unauthorized personnel.
    Application of 2-(4-Fluorobenzoyl)Benzoic Acid

    Applications of 2-(4-Fluorobenzoyl)Benzoic Acid in Industrial Manufacturing

    2-(4-Fluorobenzoyl)Benzoic Acid serves as a specialty intermediate in several advanced industrial synthesis processes, with established downstream uses limited to sectors where its molecular structure enables targeted performance characteristics. Below, we provide detailed, industry-verified application scenarios, each highlighting the relevant quality protocols, formulation practices, integration points, and common finished goods associated with this material.

    1. Pharmaceutical API Intermediate Synthesis

    In pharmaceutical manufacturing, 2-(4-Fluorobenzoyl)Benzoic Acid acts as a critical building block for synthesizing certain active pharmaceutical ingredients. Laboratories and plants incorporate it during specific coupling and acylation reactions for the creation of fluorinated aromatic compounds with enhanced bioactivity, following tightly regulated quality and traceability systems at every batch stage.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Annex 21: Importation of Active Substances
    • USP-NF monographs applicable to API fingerprinting
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • Provides a molar equivalent as determined by the target API’s route; concentrations typically range from 0.1 to 0.5 mol per API mol in stepwise synthesis, depending on conversion efficiency and impurity specifications.

    Downstream process integration

    • Introduced during aromatic ring-coupling or acylation steps, often following a purification stage; reacts directly in a stirred reactor under inert gas, after pre-mixing with solvents as specified by the validated process protocol.

    Final product types

    • Non-steroidal anti-inflammatory drug intermediates
    • Fluorinated quinoline and benzoxazole derivatives
    • Specialty anti-cancer pharmaceutical intermediates
    • Small-molecule R&D reference standards

    2. Agrochemical Active Ingredient Precursor

    Chemical crop protection manufacturers utilize 2-(4-Fluorobenzoyl)Benzoic Acid as a precursor for synthesizing select herbicides and fungicides. The fluorinated aromatic structure supports binding affinity in engineered agrochemicals where environmental persistence and bioavailability profiles must be precisely tuned, making specific feedstock selection critical for downstream compliance and field performance.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Annex XVII for hazardous and regulated precursors
    • ISO 9001:2015 for traceable input chemical qualification
    • EPA 40 CFR Parts 150 – 189 for pesticide registration

    Typical usage ratio

    • Integrated based on stoichiometric needs for target active; typically seen at 3–8% by weight relative to total synthetic mass in the core intermediate step, with adjustments for technical purity and desired reaction yield.

    Downstream process integration

    • Used in condensation or cyclization reactions, generally as a starting reagent in sealed vessel reactors equipped for temperature and pH control, forming the fluorobenzoyl core moiety in later synthesis stages.

    Final product types

    • Systemic triazole fungicides
    • Pre-emergent herbicide actives
    • Custom pesticide intermediate batches

    3. Specialty Dye and Pigment Intermediate

    Producers of advanced dyes and pigments employ 2-(4-Fluorobenzoyl)Benzoic Acid as a key aromatic raw material to impart halogenated chromophores in high-performance colorants. Application centers on industrial settings where precise hue stability and solvent resistance are critical, necessitating input raw materials of specified fluorination level and impurity profile to meet stringent end-user demands in textiles and specialty coatings.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for restricted substances in textiles
    • REACH Regulation (EC) No 1907/2006—Annex XVII
    • ASTM D4300 for synthetic organic pigments
    • ISO 9001:2015 for batch documentation and traceability

    Typical usage ratio

    • Used as a coupling component at 1–3% by mass in pigment formulations, with adjustments for target shade intensity and required lightfastness according to client specifications.

    Downstream process integration

    • Charged during a controlled diazo coupling or condensation step in pigment and dye synthesis lines, following solvent dissolution and pH adjustment to ensure high-coupling efficiency and color uniformity.

    Final product types

    • Fluorinated azo dyes for technical fibers
    • High-performance pigment dispersions for plastics
    • Solvent-resistant inkjet dye concentrates

    4. Liquid Crystal Intermediate for Electronic Displays

    Manufacturers of specialty liquid crystal compounds integrate 2-(4-Fluorobenzoyl)Benzoic Acid into the synthetic sequence for producing certain fluorinated liquid crystal molecules, enabling modulation of dielectric anisotropy and molecular alignment properties in advanced display technology. Strict quality and application standards apply to maintain the visual clarity and operational lifetime of end products.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for EEE chemicals
    • IEC 61249-2-21 for halogen-free electronic materials
    • JEITA EM-3510 for liquid crystal raw material quality
    • ISO 9001:2015 process QA

    Typical usage ratio

    • Employed at 0.5–2% by mass in precursor mixture, optimized based on the target dielectric constant and viscosity needed for specific LCD panel characteristics in commercial and industrial displays.

    Downstream process integration

    • Introduced during the condensation assembly of biphenyl or multi-ring liquid crystal structures, following precise pH, temperature, and reactant addition controls in multi-stage reactor setups.

    Final product types

    • Fluorinated biphenyl liquid crystals
    • High-resolution TFT-LCD panel materials
    • Specialized nematic and smectic phase display compounds

    5. Advanced Polymer Additive Preparation

    Several producers in the polymer modification sector incorporate 2-(4-Fluorobenzoyl)Benzoic Acid to synthesize tailored aromatic monomers and end-group cappers for engineering plastics. The fluorinated moiety allows for specific improvements in thermal stability, chemical resistance, and mechanical behavior in demanding industrial and electronics-grade polymers.

    Industry compliance standards

    • UL 94 for flammability of plastic materials
    • ISO 11357-1 for polymer thermal properties
    • RoHS and REACH substance thresholds (as applicable to plastics)
    • ASTM D1238 for polymer melt characterization

    Typical usage ratio

    • Added at 0.2–2% by weight in copolymer mixtures, determined according to polymer chain length and fluorination target for end-use temperature and chemical resistance needs.

    Downstream process integration

    • Incorporated during solution-phase polycondensation or as a reactive intermediate in melt-extruded batch production for functionalized monomer dispersion and end-group modification.

    Final product types

    • High-temperature fluorinated polyarylates
    • Functionalized engineering thermoplastics
    • Specialty plastic films for microelectronics
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    Certification & Compliance
    More Introduction

    2-(4-Fluorobenzoyl)Benzoic Acid: A Reliable Choice for Modern Synthesis

    Working in chemical manufacturing brings its share of daily challenges, from handling temperature-sensitive materials to maintaining consistency during large-batch reactions. Among the many products we have refined over the years, 2-(4-Fluorobenzoyl)benzoic acid continues to stand out, both in terms of reliability and the unique opportunities it offers for advanced synthesis applications. Our experience producing this compound, with model number 4FBA-1123, gives us plenty to reflect on—whether in the way it handles during production or the differences that make it an attractive intermediate for demanding chemists.

    Attributes Shaped by Real Conditions

    2-(4-Fluorobenzoyl)benzoic acid’s formula—C14H9FO3—tells only part of the story. The value comes alive on the production floor, where batch crystallization, purification stages, and final testing determine the product’s readiness for the most exacting users. In every run, we emphasize solid purity, low residual solvent content, and reliable crystalline appearance. Typical batches run with a purity above 98.5%, as determined by HPLC. Thanks to careful control over temperature during recrystallization and solvent exchange, we can avoid sticking points seen in lower quality materials. It moves with ease through reactors and downstream processes, reducing unexpected stoppages for maintenance or rework.

    Real-world users—those in contract research, pharmaceutical development, or specialty pigment design—watch for even modest differences batch-to-batch. Through careful calibration, we control fluorine content (one of several challenging analytical checks) and consistently minimize foreign ions and trace metals. A sample failed to meet specification? Back it goes to reprocessing or, if needed, full incineration, as there’s no shortcut for end users who expect certainty. This kind of quality assurance shapes the reputation of both the product and the business behind it.

    Unique Benefits on the Synthesis Bench

    Several attributes separate this fluorinated benzoic acid derivative from standard alternatives. The presence of the para-fluoro group on the benzoyl moiety makes the compound more reactive than benzoic acid itself. In multi-step synthesis, where regioselectivity and predictable electron distribution matter, this small change produces marked differences in outcomes. One quickly notices differences in reaction yields and side product profiles—users in medicinal chemistry often select 2-(4-Fluorobenzoyl)benzoic acid for exactly these reasons, especially while developing new kinase inhibitors or exploring fluorine’s impact on biological activity.

    Unlike some analogous compounds—such as 2-benzoylbenzoic acid or the chlorinated or methylated derivatives—our product demonstrates improved performance during Friedel-Crafts acylation and nucleophilic aromatic substitution. Persistent stability and resistance to moisture absorption allow for storage and use under standard lab conditions, without the need for desiccators or argon blanketing. Comparing processing loss rates between this material and non-fluorinated analogs reveals tangible savings in time and cost, translating directly into fewer interruptions between pilot-scale and commercial campaigns.

    Scaling Up Production Without Compromising Integrity

    Bench-top synthesis doesn’t always translate to reliable manufacturing, and we have met our share of setbacks. High concentrations of the starting acyl chlorides risk hydrolysis and decompose too quickly under some process conditions. Our engineers tweaked solvent ratios and implemented staged addition schedules to control exothermicity and prevent formation of unwanted by-products. Titrations and in-line pH controls, combined with a solid understanding of the chemical’s stability, have enabled tighter batch tolerances over the years.

    Replicating this consistency at larger scales meant investing in temperature and humidity controls, better agitation systems, and real-time analytics. The manufacturing equipment used is purpose-built for handling aromatic fluorinated intermediates: corrosion-resistant coatings, enhanced sealing, and redundant monitoring points ensure product purity through every stage. Regular investment in staff training goes hand-in-hand with new controls—chemical manufacturing remains, above all, an exercise in attention to detail.

    Direct Applications and End-User Expectations

    2-(4-Fluorobenzoyl)benzoic acid serves as a highly reliable intermediate in pharmaceutical research, agricultural chemistry design, and specialty polymers manufacturing. Many pharmaceutical developers appreciate how the fluorine atom alters drug metabolism and bioavailability, giving their candidate molecules a longer half-life or sharper selectivity. What often stands out in this particular acid is the predictability of its downstream transformations. In forming esters, amides, or even larger heterocycles, the compound’s structure favors well-defined reaction pathways—saving researchers from ambiguous results or hard-to-purify by-products.

    Beyond life sciences, formulators in the coatings and pigment sectors use this compound to introduce fluorinated properties—improving chemical resistance, gloss retention, or light stability in specialty materials. Experiences in those sectors have shown that minor shifts in purity or moisture can cause visible changes in final product appearance, leading to complaints or wasted runs. By focusing on precise, test-driven synthesis and confirming compositional benchmarks with every lot, we support partners who cannot tolerate ongoing process interruptions. Such collaboration builds trust over many years.

    Handling, Safety, and Environmental Responsibility

    No commentary on a fine chemical is complete without discussion on safe handling and responsible environmental stewardship. 2-(4-Fluorobenzoyl)benzoic acid, while not among the most hazardous organic intermediates, requires serious attention in storage and use. We ship each batch in high-density polyethylene drums sealed against moisture, labeled with non-fading inks for traceability. Operators in our own facility work with localized suction, gloves, and face protection. Even though the dust is low-irritant and non-volatile, repeated exposure—especially during powder transfer—requires full adherence to industrial hygiene standards.

    Disposal of unwanted or out-of-spec material aligns with government and industry regulations. Incineration at certified hazardous waste facilities ensures no residual fluorinated aromatic compounds reach groundwater or air. As a manufacturer, we shoulder responsibility for the environmental impact across the chemical’s full lifecycle and work with downstream users to improve packaging, transport, and waste minimization. The effort extends to careful monitoring of production effluent: real-world scrutiny goes beyond compliance paperwork, with trust built on actual performance, not promises.

    How 2-(4-Fluorobenzoyl)Benzoic Acid Differs from Similar Offerings

    On paper, there are many similar sounding compounds: 2-benzoylbenzoic acid, 2-(4-chlorobenzoyl)benzoic acid, or even trifluoromethyl-substituted versions. In practice, the subtle variation of the fluoro group at the para position delivers very specific behaviors. Fluorine’s small atomic size and high electronegativity influence reactivity in ways that chlorine or methyl simply cannot match. In our in-house tests during amidation and cyclization, the yields and impurity profiles change consistently in favor of the fluoro analogue. This lets downstream process chemists operate with more confidence, especially when outcomes depend on reproducibility.

    Another frequent conversation with users covers the appearance and handling properties of similar acids. Some alternatives are notorious for clumping after storage, making them hard to transfer or dose. With 2-(4-Fluorobenzoyl)benzoic acid, careful drying and anti-caking monitoring during bulk packaging—refined over years—result in a free-flowing powder through every season. This directly affects labor hours, spillage rates, and downstream automation. In return, users have one less material-related variable to control, allowing them to focus attention on more consequential process changes.

    Supporting Research and Continuous Improvement

    Early on, many teams in process development underestimate the importance of access to consistent, highly characterized intermediates. Plenty of research projects have stalled or failed because of slight shifts in trace impurity profiles, color, or crystallinity. Throughout hundreds of production lots, we have adjusted and improved spectral analysis, impurity tracking, and product release criteria based on user feedback. Not all users have the same sensitivity to minor color changes or hydrolytic stability. We work directly with technical staff—from method development groups to pilot plant managers—to ensure each lot supports the unique requirements at hand.

    This ongoing collaboration benefits both sides. It presses us to continually improve analytical practices and experiment with processing modifications, while end-users receive a material that reliably fits into workflows with minimal adjustment. We have invested in new HPLC columns, added mass spectral fingerprinting, and even run extended stability programs for long-term storage at various humidity levels. Feedback loops from users help us target critical-to-quality attributes—trapping trace fluorinated byproducts before release or retuning drying cycles to avoid agglomeration in larger drums.

    Investment in Quality: From Source to Final Product

    Producing specialty organofluorine compounds such as 2-(4-Fluorobenzoyl)benzoic acid consistently—at scale—calls for more than just reliable equipment or access to precursors. Our experience emphasizes the importance of qualified staff and tight controls on raw material sourcing. We select only pharmaceuticals-grade acyl chlorides and benzoic acid derivatives, backed by supplier audits and analytical confirmation. In sourcing, we refuse to cut corners on cost, as downstream problems quickly negate apparent savings. Each manufacturing run includes in-process controls: color checks, IR spectral confirmation, and real-time quantification of residual solvents.

    On the final stage, careful drying, controlled packaging, and double-checked labeling prevent cross-contamination or mix-ups. We also push ongoing investment in staff training—good manufacturing practice only delivers results when people pay attention to every lot. In the event of a rare deviation, such as color drift or the wrong melting point, corrective actions take priority over filling the next order. This builds a reputation in the market for dependability, a feature that brings more value than price alone.

    Navigating Future Demands: Innovation and Adaptability

    Markets continue to evolve, and so do user demands. Trends toward greener chemistry and biodegradable intermediates challenge all of us to think harder about the long-term implications of organofluorine production. Over the past five years, we have funneled more resources into waste minimization, solvent recycling, and finding non-halogenated alternatives for auxiliary reagents without sacrificing the end product quality. Users ask sharper questions now about sustainability, and chemical manufacturers have to answer with more than just paperwork—they need process transparency and evidence-based results.

    On the technical side, requests for custom particle sizing, solvent-free processing, or specialized impurity profiles have risen steadily. Users in life sciences increasingly expect product traceability—knowing exactly which raw material lot contributed to a specific batch. Digitalization and data transparency supplement traditional practices, allowing us to link every product drum or bag to unique batch records, spectral prints, and Certificates of Analysis that reflect real test results, not best guesses.

    Final Thoughts From the Production Line

    Some see 2-(4-Fluorobenzoyl)benzoic acid as just another “building block” along a crowded shelf of specialty chemicals. The daily work behind its manufacture paints a different picture: every promising pharma project, every breakthrough in agrochemical design, and every novel polymer starts with dependable supply and thoughtful manufacturing. Our long-term record with this compound proves there are no shortcuts in real-world chemical production. Trust develops from responsiveness—adjusting a process, troubleshooting a batch, or solving a supply chain hiccup with honesty and care. In consistently meeting tight specifications and tackling emerging environmental, safety, and sourcing challenges, we stand behind the product and the science it makes possible.

    The story of this compound, and those who rely on it, will keep evolving as technologies shift and industries adapt. Our job never stops at the endpoint of a drum or a batch certificate. It continues in listening, learning, and delivering proven quality—batch after batch, year after year.