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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 | 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. |
Applications of 3'-Fluoro-Biphenyl-2-Carboxylic Acid in Industrial ManufacturingAs 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 SynthesisPharmaceutical 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
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2. Liquid Crystal Mixture ComponentProducers 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
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3. Agrochemical Active Ingredient Building BlockAgrochemical 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
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4. Specialty Polymer Monomer AdditiveAdvanced 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
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5. Electronic Chemicals for Photoresist SynthesisSemiconductor 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
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6. Analytical Reference MaterialAccredited 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
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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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.