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3'-Fluoro-Biphenyl-2-Carboxylic Acid

    • Product Name 3'-Fluoro-Biphenyl-2-Carboxylic Acid
    • Alias 2-Carboxy-3-fluorobiphenyl
    • Einecs 696-009-8
    • 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

    146921

    Productname 3'-Fluoro-Biphenyl-2-Carboxylic Acid
    Molecularformula C13H9FO2
    Molecularweight 216.21 g/mol
    Casnumber 861939-64-8
    Appearance White to off-white solid
    Meltingpoint 128-132°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically >98%
    Smiles C1=CC=C(C(=C1)C2=CC=CC=C2F)C(=O)O
    Inchikey ZZICZWDEINPNHR-UHFFFAOYSA-N
    Storagetemperature 2-8°C
    Synonyms 3-Fluoro-2-carboxybiphenyl
    Chemicalclass Aromatic carboxylic acid

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

    Packing & Storage
    Packing A 5-gram amber glass bottle with a tamper-evident cap, labeled "3'-Fluoro-Biphenyl-2-Carboxylic Acid, 99%," includes hazard information.
    Shipping 3'-Fluoro-Biphenyl-2-Carboxylic Acid is shipped in secure, sealed containers to prevent contamination and ensure stability. Packaging complies with safety and regulatory guidelines for chemical transport. The product is labeled properly, shipped at ambient temperature unless otherwise specified, and accompanied by a Safety Data Sheet (SDS) for safe handling and storage.
    Storage **Storage for 3'-Fluoro-Biphenyl-2-Carboxylic Acid:** Store in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers or bases. Protect from direct sunlight and moisture. Handle under inert atmosphere if sensitive to air or humidity. Properly label containers and follow all relevant safety and regulatory guidelines.
    Application of 3'-Fluoro-Biphenyl-2-Carboxylic Acid

    Applications of 3'-Fluoro-Biphenyl-2-Carboxylic Acid in Industrial Manufacturing

    As an experienced manufacturer, we supply 3'-Fluoro-Biphenyl-2-Carboxylic Acid to critical downstream sectors requiring precise chemical functionality, high purity, and reliable batch consistency. The following application fields demonstrate key usage scenarios and their operational requirements within process industries.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers utilize this material as an advanced intermediate, particularly in the synthesis of fluorinated biphenyl core structures for non-steroidal anti-inflammatory drug (NSAID) candidates and kinase inhibitor scaffolds. Its role centers on introducing the fluorine atom at the 3'-position, which improves metabolic stability and binding affinity in several active pharmaceutical ingredient (API) pipelines. Only GMP-compliant plants can integrate this material, which typically enters the early-stage coupling or amidation steps. Chemical and process development teams determine the loading level according to desired reaction yield and downstream impurity control.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU EMA Guideline on Start Materials and Intermediates
    • USP <781> Spectrophotometric Identification
    • ISO 9001:2015 Certified Quality Management Systems

    Typical usage ratio

    • 10–25 mol% relative to the target pharmaceutical yield; adjusted for compound library needs or process scale-up

    Downstream process integration

    • Used in Suzuki-Miyaura or Buchwald-Hartwig coupling steps during complex API assembly
    • Can act as a carboxyl donor in selective amide bond formation pre-final stage purification

    Final product types

    • Small molecule APIs (e.g., kinase inhibitors, NSAIDs with fluoroaryl groups)
    • Advanced research intermediates for medicinal chemistry
    • Pharmaceutical reference standards

    2. Liquid Crystal Mixture Component

    Producers of liquid crystal display (LCD) materials use 3'-fluoro substituted biphenyl acids as fine-tuning building blocks within high-performance nematic liquid crystal mixtures. The carboxyl group acts as a functionalizable handle for ester exchange or derivative formation, which controls rotational viscosity, dielectric anisotropy, and clearing points in the formulated mixture. Material purity and consistent specification are crucial for panel image quality and production repeatability.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) restriction of hazardous substances
    • IEC 62321:2013 Analytical detection of hazardous substances
    • ISO 14001:2015 Environmental Management System

    Typical usage ratio

    • 1–5 wt% in the total liquid crystal formulation; varies by desired electro-optical response and mixture composition

    Downstream process integration

    • Feedstock for esterification or acylation during custom LC mixture synthesis, prior to mixing and cell filling
    • Derivative formation blending into pre-polymer or matrix phase under controlled dry-room conditions

    Final product types

    • Nematic and smectic liquid crystal mixtures for color TFT-LCD panels
    • Specialty LC modules for automotive and medical displays
    • OLED display alignment layers (by chemical modification)

    3. Agrochemical Active Ingredient Building Block

    Agrochemical research and scale-up facilities adopt this compound as a core intermediate for synthesizing novel herbicide and fungicide actives based on biphenyl carboxylic structures. Introduction of the fluoro-group at the 3'-position improves field stability and biological selectivity in target species. This intermediate is commonly deployed in the coupling or hydrolysis stages, with strict pesticide GMP and traceability measures in place during multi-step synthesis.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • ISO 17025:2017 Laboratory Testing Accreditation
    • OECD GLP in Chemical Testing
    • REACH Registration (EC 1907/2006) for chemical substances

    Typical usage ratio

    • 3–8 mol% of total agrochemical synthesis batch; fine-tuned according to desired bioactivity and cost control

    Downstream process integration

    • Direct input in palladium-catalyzed cross-coupling reactions to make active 3'-fluoro substituted biphenyls
    • Incorporation during ester hydrolysis or amidation before formulation into technical concentrates

    Final product types

    • Active ingredient concentrates (herbicides, fungicides with fluoroaryl motifs)
    • Water-dispersible granules and suspension concentrates for field use
    • Laboratory standards for residue analysis

    4. Specialty Polymer Monomer Additive

    Advanced material manufacturers employ this acid for copolymerization or graft modification in specialty engineering polymers, especially for applications requiring improved heat resistance, chemical durability, or dielectric properties. The fluorine substitution enhances polymer backbone rigidity and chemical inertia, while the carboxyl group enables direct incorporation into step-growth or radical polymerizations. Strict controls on residual acid and impurity content are vital to downstream extrusion or molding performance.

    Industry compliance standards

    • ASTM D4000 Classification System for Polymers
    • RoHS and REACH chemical use restrictions for electronic and automotive sectors
    • ISO 10993 for biocompatibility testing (for medical-grade use)

    Typical usage ratio

    • 0.5–2.0 wt% as a comonomer or chain-modifying monomer; dosage set by targeted molecular weight and application environment

    Downstream process integration

    • Charged into melt-polycondensation reactors for polyarylate or polyamide synthesis
    • Dosed in solution or emulsion polymerization reactors for hybrid copolymer production

    Final product types

    • High-performance polyarylates and polyamides (film, rod, fiber)
    • Polymeric dielectrics and coatings for electronic components
    • Specialty molded parts for automotive and medical devices

    5. Electronic Chemicals for Photoresist Synthesis

    Semiconductor chemical suppliers require aromatic carboxylic acids with specific halogen substitutions, using this intermediate in the production of custom photoacid generators and high-resolution negative-tone resists for advanced photolithography. Control over substitution pattern supports selectivity of light-activated reaction and stability during post-application bake. All production occurs under solvent-handling safety standards and semiconductor purity protocols.

    Industry compliance standards

    • SEMI C93: Purity Requirements for Electronic Chemicals
    • IATF 16949: Automotive Quality Management for Electronics
    • ISO 14644 Cleanroom Standards
    • RoHS and REACH for halogen content

    Typical usage ratio

    • 0.2–1.0 wt% in total resist or photoacid generator formulation; precise ratio set by UV sensitivity and etch resistance targets

    Downstream process integration

    • Serves as a precursor in diazonium or sulfonium salt synthesis before blending in photoresist matrices
    • Processed in cleanroom batch reactors with dedicated trace impurity analysis

    Final product types

    • Photoresist coatings for IC wafer lithography
    • Advanced packaging resists for MEMS and sensor devices
    • Photoacid generator blends for microfabrication

    6. Analytical Reference Material

    Accredited laboratories and standards producers use this highly pure acid as a calibration substance for analytical method development, particularly in HPLC, GC-MS, and NMR testing where precise fluorine positional isomers are needed. Material traceability, homogeneity, and batch documentation allow for robust method validation and system suitability checks.

    Industry compliance standards

    • ISO 17034:2016 Reference Material Producers
    • ISO/IEC 17025:2017 Analytical Laboratory Accreditation
    • USP Reference Standards Program

    Typical usage ratio

    • 0.1–10 mg per analytical sequence run; varies with detection limits and calibration curve requirements

    Downstream process integration

    • Prepared as neat or in validated solution for calibration, system suitability, and recovery checks
    • Distributed in certified ampoules or vials for cross-laboratory studies

    Final product types

    • Certified analytical reference materials
    • Calibration standards for instrument qualification
    • Round-robin proficiency testing samples
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    Certification & Compliance
    More Introduction

    3'-Fluoro-Biphenyl-2-Carboxylic Acid: A Closer Look from the Manufacturer’s Bench

    Practical Insights from Chemical Synthesis to Real-World Demand

    Years on the plant floor shape the way we view every compound we deliver. 3'-Fluoro-Biphenyl-2-Carboxylic Acid carries a reputation in the chemical industry that’s rooted in its structure and utility, not just its name. This molecule bridges traditional biphenyl carboxylic acids with modern fluorine chemistry, bringing unique reactivity and selectivity into hands-on lab and pilot plant work.

    As the manufacturer, we watch production from the earliest charge of raw materials to the finished, purified acid. There’s no shortcut with halogenated aromatics. Introducing fluorine at the meta position alters both the electronic nature and the steric character of the biphenyl core. Sure, other carboxylic acids have long been mainstays in pharmaceutical intermediates or advanced material science, but giving that molecule a fluorine atom turns open old doors and unexpected new ones. It’s not just another tweak for the sake of novelty. Specific reactivity shows up during Suzuki couplings, for instance, where meta-fluoro substitution resists undesired side reactions that plague non-fluorinated analogues.

    Model, Specifications, and Real-World Handling

    We produce 3'-Fluoro-Biphenyl-2-Carboxylic Acid under the reference model BPFA-3F-CA, targeting both routine and exploratory synthesis needs. From the specification standpoint, we keep a minimum purity of 98% by HPLC (water/acetonitrile gradient, diode-array detection at 254 nm), and each batch receives a full NMR assignment along with a controlled moisture content. Trace halide and residual solvent levels see close monitoring – not just for regulatory compliance, but because downstream applications depend on a high-quality input.

    Supply runs in both research and commercial batch sizes, and orders range from tens of grams to multi-kilogram lots. We’ve thrown out plenty of substandard material over the years – one watchful eye on color, particle size, and flow keeps the QA team alert. No one wants to risk stuck feed lines or filtration hangups halfway through a scale-up just because of inconsistent crystal habits. Our drying step holds solid between 55–60°C in forced-air ovens, usually yielding a brilliant off-white to light beige powder, free of visual contaminants.

    Understanding Why 3'-Fluoro Matters: Application Realities

    Compared to the parent biphenyl-2-carboxylic acid, the addition of a 3'-fluoro group is more than surgical chemistry; it’s tangibly helpful in building blocks for agrochemicals, advanced pharmaceuticals, and specialty catalysts. Medicinal chemists learned to respect fluorinated aromatics for their metabolic stability. A hydrogen and a fluorine atom seem similar at a glance, but only one fits the bill when a biologist requires resistance to enzymatic breakdown. Researchers in our own application labs use this compound to probe alterations in binding affinity for small-molecule ligands. We’ve even supplied custom isotopically labeled lots for tracking studies in metabolic profiling.

    Catalysis labs reach for this acid when tuning ligand electronics. Introducing fluorine shifts electron density without the extreme withdrawal seen in nitro substitution. The result is a fine-tuned process catalyst, suitable for both homogeneous and supported designs. This distinction matters: one step over, and the downstream yields take a hit. Beyond the technical, we always answer direct inquiries about solubility, reactivity, and recommended handling – not because it’s a sales pitch, but because hard-won bench experience trumps copy-paste advice.

    3'-Fluoro vs. Other Biphenyl Carboxylic Acids: Drawing Real Differences

    Not all biphenyl carboxylic acids are built equally. The ortho and para positions tend to dominate commercial supply lists, yet meta-fluoro substitution stands apart. The difference hits home in coupling chemistry. In classical Suzuki-Miyaura reactions, meta-fluorinated biphenyl isn’t simply another node on the reaction map. We find that it brings in a resistive effect to oxidative coupling, helping yield selectivity where other groups flop. This behavior isn’t theoretical – repeat batchwork in both our in-house pilot plants and at customer sites around the globe prove it out.

    Our own R&D chemists compared batch-to-batch impurity profiles between 2-carboxylic acid, 4’-fluoro, and 3’-fluoro forms. The meta-fluorinated lots consistently shone with lower levels of decomposition residues during elevated temperature runs. Our production team refines purification steps and solvent swaps specifically for this compound, since high-performance applications demand low baseline impurity counts.

    From a practical angle, 3'-Fluoro-Biphenyl-2-Carboxylic Acid exhibits enhanced crystallinity under our process conditions, which aids not only filtration but also product stability during extended storage. While unsubstituted biphenyl-2-carboxylic acid risks slow color drift in ambient light and varied humidity, the meta-fluoro analog holds up, resisting the gradual formation of colored oxidative byproducts. Those subtle differences, drawn from repeated storage tests and months-long shelf-life observations, don’t make it onto most datasheets. They matter to manufacturers who rely on predictable physical properties.

    Manufacturing Challenges: Lessons from the Field

    Putting a fluorine atom onto the biphenyl ring is no trivial task. Early routes relied on laborious electrophilic aromatic substitution, with waste streams and side products headache enough to turn any chemist gray. Once modern cross-coupling routes stepped onto the scene, efficiency and selectivity improved – but only for teams that did their homework on reagent purity, moisture control, and stepwise addition. We’ve logged more hours than we’d like troubleshooting batch failures where low-grade boronic acids, erratic solvents, or unfiltered bases sabotaged runs.

    Automated sensors help track reaction progress, but human intervention remains crucial. We check color, clarity, and exotherm signatures at each step, learning to spot trouble before it ends up in the final drum. Over time, our operators developed tricks like staged reagent addition and in-line filtration to cut back on waste and lift yields. What seems straightforward on paper turns far more complicated at the 50 kg scale, where a heat spike or emulsified side product can bring work to a halt. Each improved lot reflects lessons learned from good batches and bad.

    Why Consistency Wins, Not Just Compliance

    Plenty of regulatory checklists guide commercial manufacturing, but compliance doesn’t replace consistency. Some customers prize high-purity material; others focus on batch-to-batch behavioral reproducibility. Meeting both demands takes more than ticking boxes. We run back-to-back tests using our own retained archive samples to flag variation, whether in melting point, solubility, or spectral fingerprints.

    We’ve moved away from reliance on a single process. Instead, we maintain contingency routes for 3'-Fluoro-Biphenyl-2-Carboxylic Acid, letting us respond faster to raw material interruptions or price surges in fluorinated intermediates. Investment in reactor infrastructure and solvent recovery means we’re not hamstrung by outside pressures—a vital edge as global supply chains stretch and contract.

    From scaling up pilot runs to full-scale commercial batches, modifications never happen in the dark. We document procedural tweaks meticulously, using in-house analytical tools—GC, HPLC, multi-nucleus NMR, and LC-MS—checking that each production run matches or exceeds our initial target profile. This deep archive proves invaluable when customers question a subtle shift or need traceability down to the molecular fingerprint. For us, consistency isn’t a slogan—it’s a survival trait.

    Market Direction and Industry Trends: The Fluorine Uptick

    The last decade brought a surge in demand for fluorinated aromatic acids, fueled by both pharma’s push for metabolic stability and electronics’ search for new functional materials. We saw a clear uptick in requests for meta-fluorination, often tied to early-stage molecular discovery. Large pharmaceutical innovators frequently approach us not with off-the-shelf inquiries, but with precise requests for custom purities, salt forms, or isotopic enrichment of the 3'-fluorine position.

    Down the line, we see agrochemical developers, advanced polymer labs, and OLED manufacturers coming in for this compound. Meta-fluoro biphenyls slip into custom ligands, contrast agents, and as intermediates in synthesis of more complex polycyclic compounds. In our own trial collaborations, the addition of 3'-Fluoro-Biphenyl-2-Carboxylic Acid smoothed out scale-up pains that non-fluorinated analogues failed to overcome. Adjusting solubility, thermal stability, and reactivity isn’t a marketing flourish—it’s what keeps process teams returning to this building block.

    Sustainable Manufacturing: Practical Steps Forward

    Responsible chemistry doesn’t begin and end in safety briefings or compliance paperwork. For production work on 3'-Fluoro-Biphenyl-2-Carboxylic Acid, we constantly push for reduced solvent loads and more effective solvent recycling. Chlorinated solvents gave excellent selectivity in early synthesis routes, but environmental and disposal concerns push us toward greener, safer alternatives whenever possible.

    Batch process optimization delivered concrete improvements. Shifting to more benign base choices, tuning the order of addition, or switching out traditional phase-transfer catalysts with more biodegradable options shaved off hazardous waste burdens. Our production reports make clear: even small gains add up across hundreds of kilograms of final product per year.

    We also maintain a closed-loop cycle for waste acids and off-spec product streams, routing byproducts wherever feasible into auxiliary processes such as neutralization or energy recovery. Sometimes those choices mean increased capital expenditure, but they keep us ahead of evolving regulatory and community expectations. It’s not lip service—this approach opens new business with clients who share the same sustainability mindset.

    Quality Control: Learning from Trouble and Success Alike

    Years at the reactor controls taught us to expect surprises, both good and bad. Some batches reach final analysis with stellar spectral data yet underperform during shipping or long-term storage. Deeper investigation often reveals culprit microimpurities or subtle particle size anomalies. In one instance, a seemingly minor process tweak—changing a filtration cloth vendor—altered product morphology enough to impact ease of handling in customer blending tanks. We keep multiple failsafes: shipment retention samples, accelerated aging studies, and continuous process-probe monitoring.

    Customer feedback always hits our debrief meetings. If a particular lot clouds up faster or takes on a tint, QA digs until we isolate the source. Sometimes the answer lies in air exposure during drum filling; other times, minor process drift calls for recalibration. No customer appreciates surprises, especially with long lead times or validated downstream processes on the line. Through this cycle of vigilance, correction, and improvement, we hold our rate of returns to near zero.

    Supporting Formulators and Researchers on the Ground

    Technical support doesn’t stop with product shipment. Our in-house chemists field direct queries at all stages: advance order planning for pilot-scale work, best practices for dissolution into common solvents, and troubleshooting for downstream coupling reactions. Practical questions flood in: What are the best storage conditions against moisture and light? How does meta-fluoro substitution influence reactivity with standard activating agents? What’s the risk profile with common acetate or halide couplings?

    We keep a database of real-world troubleshooting logs, built not from literature assumptions but first-hand batchwork. More than one analytical chemist in our shop built protocols for resolving close co-eluting impurities in meta-fluorinated biphenyl batches on both classical and reversed-phase systems. Our priority remains clear: deliver not just a product, but the know-how that helps researchers and formulators push their own projects forward.

    Addressing the Unseen Challenges: Supply Chain and Regulatory Shifts

    In global chemistry, no player lives in a vacuum. Recent raw material shortages and evolving transport regulations for fluorinated intermediates stress-test every part of our operation. We maintain multi-vendor partnerships for critical raw materials, stock insurance, and backup routes for our staple starting materials. These weren’t put in place because of today’s headlines—they grew from past scramble-and-stretch cycles where supply shortfalls threatened on-time delivery and customer process schedules.

    Hazardous materials classifications, REACH directives, and country-specific shipping blips mean our team keeps pace with every update. Proactive communications with regulatory consultants ensures our product documentation stays both accurate and defensible. By investing in pre-clearance, export compliance, and trace certification for every outgoing lot, we protect both ourselves and our customers from last-minute border hangups.

    Our ability to pivot based on new regulatory demands or unforeseen logistic snags sets us apart. Whether the challenge is customs clearance of a single barrel or surge orders for clinical trial manufacturing, those with boots on the ground feel the impact first and hardest.

    In the End, Bench Knowledge Drives Value

    3'-Fluoro-Biphenyl-2-Carboxylic Acid stands as a product not built from theory, but from years of practical manufacturing, scale-up, and troubleshooting. The meta-fluoro group doesn’t just redefine a molecule’s reactivity; it forces a manufacturer to rethink purification, logistics, and customer support. Over time, product quality, predictability, and depth of technical knowledge build real trust—whether the order is a kilo or a hundred.

    As suppliers face rising expectations from pharmaceuticals, electronics, and advanced materials, those who can explain the real-world differences—backed by data and years on the reactor floor—cut through template talk and deliver genuine value. Every lot of this product we ship distills not just a chemical, but the hard-earned lessons, attention to detail, and partnership that keep our industry moving forward.