|
HS Code |
346403 |
| Name | 3-Biphenylcarboxylic Acid |
| Synonyms | m-Biphenylcarboxylic acid, 3-Phenylbenzoic acid |
| Cas Number | 86-52-2 |
| Molecular Formula | C13H10O2 |
| Molecular Weight | 198.22 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 171-174°C |
| Solubility In Water | Slightly soluble |
| Smiles | C1=CC=C(C=C1)C2=CC(=CC=C2)C(=O)O |
| Inchi | InChI=1S/C13H10O2/c14-13(15)11-7-3-6-10(8-11)12-5-1-2-4-9-12/h1-9H,(H,14,15) |
| Density | 1.24 g/cm³ |
| Storage Conditions | Store at room temperature, tightly closed |
As an accredited 3-Biphenylcarboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 3-Biphenylcarboxylic Acid, with tamper-evident cap and chemical safety labeling. |
| Shipping | 3-Biphenylcarboxylic Acid is shipped in tightly sealed containers to prevent moisture and contamination. It should be handled with care, following all safety and regulatory guidelines. The package is labeled appropriately for chemical transport and protected from extreme temperatures during transit to ensure the integrity and stability of the product. |
| Storage | 3-Biphenylcarboxylic acid should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Avoid exposure to moisture and direct sunlight. Ensure proper labeling and keep away from sources of ignition. Use appropriate personal protective equipment when handling the chemical to prevent skin and eye contact. |
Applications of 3-Biphenylcarboxylic Acid in Industrial ManufacturingAs the direct manufacturer of 3-Biphenylcarboxylic Acid, we supply this intermediate to global partners across multiple key industrial segments. Our technical team collaborates closely with downstream users to address stringent regulatory, formulation, and process requirements unique to each sector. Below, we detail real-world application scenarios with specific industry practices. 1. Pharmaceutical Intermediates for Non-Steroidal Anti-Inflammatory Drug SynthesisIn pharmaceutical manufacturing, our material frequently serves as a key building block in the synthesis of certain non-steroidal anti-inflammatory drugs (NSAIDs), including biphenyl-structured actives. Drug substance producers introduce this intermediate during advanced amidation or acylation steps, after initial ring construction but before final functionalization and purification. Strict regulatory frameworks dictate impurity control and traceability from raw material to API batch. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. High-Performance Polymer Additive ManufacturingChemical formulators use this material during the production of polyarylate and polyether-based engineering resins to introduce rigidity and heat resistance in specialty plastics. The carboxylic acid group reacts with diols or diamines under high-temperature esterification or amidation protocols, allowing controlled copolymer architecture. Quality monitoring focuses on residual acid content and polymer intrinsic viscosity. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Liquid Crystal Display (LCD) Material IntermediatesWithin electronic chemicals, 3-Biphenylcarboxylic Acid acts as a precursor in the synthesis of tailor-made liquid crystal compounds. Its planar biphenyl core and functionalized carboxyl group provide essential anisotropic properties when condensed with substituted phenols or amines. Process engineers focus on purity grade, and minimization of trace metals or organic impurities to avoid display defects or conductivity losses in finished panels. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Agrochemical Synthesis (Herbicide and Plant Growth Regulator Intermediates)Our material functions as a core intermediate in the synthesis of certain biphenyl-derived herbicides and plant growth regulators. Crop protection manufacturers employ it during crucial coupling or ring-closing reactions to build specific aromatic backbones. Precision in raw material input and process parameters controls downstream crop safety and field persistence profiles, as specified by international agricultural regulations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Organic Synthesis for Dyes and Pigment PrecursorsSpecialty dye and pigment manufacturers use this raw material in multi-step organic synthesis to yield high-performance yellow, orange, and red colorants. The biphenyl structure offers chromophoric extension and stability, essential for textile and plastics coloration. Synthesis protocols typically involve diazotization or Friedel–Crafts acylation, allowing customized hue and lightfastness. Process chemists focus on solvent choice and purification at each stage to attain color intensity and batch-to-batch consistency. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 3-Biphenylcarboxylic Acid prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Like many producers in the specialty chemical sector, we tackle the challenge of meeting both performance and reliability demands from clients in pharmaceuticals, agrochemicals, and advanced materials. Among the aromatic carboxylic acids, 3-Biphenylcarboxylic Acid holds a particular value. It draws attention due to the stability imparted by its biphenyl backbone, as well as the carboxylic acid function set at the meta position. Our current main model has a molecular formula of C13H10O2 and offers a melting point range routinely checked at 108°C–111°C. We produce this compound in lots varying from kilo-lab scale up to several hundred kilograms, responding in real time to volume requirements without stockpiling unnecessary inventory.
This compound is no stranger to the synthetic chemistry lab. Its structure, a carboxylated biphenyl, offers dual advantages. The biphenyl core imparts both rigidity and electron delocalization. The meta-substituted carboxylic group (at the 3-position) distinguishes it clearly from 2-biphenylcarboxylic acid and 4-biphenylcarboxylic acid, both of which show different reactivity trends in coupling and acylation reactions. Engineers seeking to design advanced functional materials—either for liquid crystals, optical materials, or fine-tuning pharmaceutical intermediates—gravitate to this variant to harness distinct solubility, crystallinity, and reaction selectivity that meta configuration delivers.
From hands-on production batches and in-house R&D, we’ve learned that position matters far more than textbooks let on. Meta-carboxyl orientation subtly guides downstream reactivity, allowing for selective coupling, amide formation, and halogenation. Para- and ortho-substituted analogs favor alternative paths: ortho-derivatives often bring steric hindrance, leading to lower yields or sluggish kinetics; para-carboxylic acids may suffer from less favorable packing in solid-state applications, and sometimes underperform when targeting specific polymer architectures. Our experience has shown the meta arrangement in 3-Biphenylcarboxylic Acid to balance reactivity with process stability: the functional group remains readily accessible for activation, but doesn’t destabilize the biphenyl core during multi-step reactions.
With every warehouse survey and batch control audit, it’s clear why buyers choose this grade time and again for active pharmaceutical ingredient (API) synthesis. The meta position opens a practical window for site-specific derivatization. Chemists targeting amide linkage or wishing to build up to biaryl ethers benefit from this accessibility—minimizing side reactions that arise with ortho or para isomers. Processes using meta-carboxyl biphenyl yield cleaner products with less need for repeated purification, which matters deeply when scaling beyond benchtop.
Success in chemical manufacturing rarely springs from theoretical yield alone. Over the past decade, we've refined purification and crystallization routes that maximize recovery while holding the line on impurity profiles. Consistent purity—generally 99% or greater by HPLC, with single-digit ppm controls on halogenated residuals and trace metals—remains a non-negotiable standard for batches entering regulated pharmaceutical supply chains. Past pilot lots taught us that off-odors, coloration, or sub-visible particles can slip in with careless handling. That’s why our lines rely on closed transfers, nitrogen blankets, and carefully engineered drying conditions at each stage.
Bulk density, particle size, and moisture levels vary depending on downstream use. We monitor each parameter batchwise, knowing that a tablet formulator thinks very differently from a process chemist handling a Grignard coupling at high temperature. The tweaks we make—altering crystallization solvent, filtration sequence, or drying curve—directly impact handling ease. Other suppliers may default to a fixed granule size. Our teams stay responsive, open to adjusting particle cut or flowability in each contract, whether for direct cGMP synthesis or for advanced materials research.
Since direct empirical evidence matters most, our R&D team tracks how industry colleagues put this acid to work. In agrochemical discovery, biaryl motifs surface frequently owing to their metabolic stability and ability to disrupt targeted enzyme sites. The meta-carboxyl variant provides a valuable nucleus for building commercial herbicides and fungicides, especially those sensitive to positional isomerism. Our direct observation through customer-supplied feedback confirms greater synthetic efficiency for meta-based scaffolds, resulting in improved cost control for commercial launches versus analogous ortho or para acids.
Pharmaceutical customers serve as front-runners in repeated calls for secure supply and rapid response on custom modifications. They appreciate short communication lines with a manufacturer who’s seen the inside of a glass-lined reactor. For peptide coupling, for example, meta-carboxyl biphenyls offer key intermediates. We’ve also witnessed uptake in polymer industry pilots, where precise placement of carboxylic groups tunes optical properties and mechanical strength. Materials scientists from academia and industry check in with us yearly for special requests—sometimes seeking isotope-labeled analogs for mechanistic studies, sometimes asking for tailored impurity signatures that aid identification in quality control.
Every synthesis project faces a choice among positional isomers. Each brings its own baggage. We know ortho-biphenylcarboxylic acid can add real headaches in both solubility and byproduct formation. Complexes at the ortho position frequently show unpredictable crystallization patterns, requiring repeated solvent exchanges and sometimes leaving traces of mother liquor in the product. This means significant cleanup, greater material loss, and potential waste disposal issues—all factors we’ve measured and tracked during scale-up in our own facility.
The para-substituted form, on the other hand, streamlines some processes thanks to its symmetry, making it a staple for simpler biaryl extension or for cross-coupling protocols. Yet, the meta form stands apart: by providing a unique reactivity profile, it opens reactions such as selective nitration, halogenation, and C–N bond formation not always accessible with other isomers. Some of our long-tenured chemists remember specific pilot projects run for university consortia, where only 3-Biphenylcarboxylic Acid delivered the necessary intermediates, bypassing blocking steps that para derivatives could not sidestep. These lessons, learned firsthand, drive us to keep refining our processes for this product.
Through years of production, we’ve built analytical protocols that run hand in hand with each batch. Every lot receives not just basic melting point checks, but full panels for moisture by Karl Fischer titration, residual solvent screens by GC, and heavy metal sweeps down to single ppm. Such controls grow from lessons picked up on the shop floor. In the past, trace contamination by iron—originating from a poorly maintained pump head—forced remanufacture of an entire order destined for Europe. From that day, we established regular hardware audits and continuous in-process testing. Every anomaly gets logged, and every solution becomes a fixed part of our process documentation.
In addition to standard controls, our internal research capability allows for rapid problem solving. Last year, a customer running a key amidation step observed unexpected “shadow peaks” on HPLC. With quick turnaround, our QC team isolated the source: a small excess of biphenyl byproduct originating from incomplete oxidation in the upstream step. Modifying our catalyst blend and monitor points brought us back on specification within two production cycles. The direct connection between shop floor and QC lab matters. We pass these lessons to our clients, often troubleshooting their downstream bottlenecks as well as our own.
Industrial chemistry brings responsibility. We are accountable for the waste streams, water use, and emissions tied to each batch. For 3-Biphenylcarboxylic Acid, our plant has reworked solvent recovery lines and adopted batchwise distillation cycles to maximize solvent reuse. Ten years in, these changes have halved our per-kilo solvent demand, a concrete improvement stemming from mandates by regional environmental regulators. Where possible, we segregate high-biological-oxygen-demand (BOD) effluents for third-party treatment, keeping compliance records transparent and auditable. Experience shows that good environmental performance makes good business sense, as customers worldwide weigh supply security alongside sustainability credentials.
Regulatory documentation accompanies every shipment, including detailed batch records, signed certificates of analysis, and origin statements required for global audits. Our regulatory staff maintain close contact with authorities and industry consortia, updating technical files as pharmacopoeia or raw material watchlists evolve. Direct involvement in regulatory audits has taught us to anticipate and correct problems before they become issues for clients. Years spent answering questionnaires, hosting inspectors, and updating submission files have embedded a strong compliance culture in every department, from production techs up to senior leadership.
No process proves perfect from day one. Every synthesis route has kinks—unexpected exotherms, variable yields, unrecoverable mother liquors. From decades in batch production, we’ve learned that process hazards hide in the details. Scaling from gram to ton quantities stresses glassware, gaskets, and pumps; small leaks or undetected temperature swings can mean waste or, worse, out-of-spec product. Every year, our engineers refine reactor design, insulate transfer lines, and select high-compatibility sealants, all informed by direct experience with 3-Biphenylcarboxylic Acid’s unique solubility and thermal characteristics.
Continuous improvement cycles, set by in-house suggestions and customer feedback, push us to re-examine every filtration, isolation, and drying step. Five years back, a persistent challenge with product clumping during storage came to light. Through collaborative problem-solving between operations and QC, we introduced low-shear screening and anti-caking protocols that reduced batch failures by more than 60%. We’ve shared these improvements in technical seminars and published accounts, aiming to help partners avoid the same pitfalls.
Our technical teams regularly consult with research collaborators seeking to push the boundaries of aryl carboxylic acid chemistry. Whether the goal is a library for drug design, an intermediate for OLED material, or a tool for environmental remediation, the starting acid’s performance makes or breaks the campaign. We supply not just bulk product, but small pilot lots for fast-tracked projects, and field technical questions with specifics learned from real benches and reactors. Having encountered the full scope of scale-up issues, we bring practical solutions, whether a researcher needs an ultra-low water cut, a tighter particle size window, or advice for handling acid chlorides derived from this acid.
Thanks to stable production and ongoing technical development, our 3-Biphenylcarboxylic Acid functions as a reliable core molecule for a wide diversity of synthetic transformations. Applications stretch from ligands in complex metal catalysis, to custom building blocks for medical imaging tracers, to critical components in high-stability plasticizers. In each, physical and chemical purity matters as much as budget. By working alongside clients, listening to challenges, and refining material properties batch by batch, we've seen success stories multiply. The lessons from our own facilities—downtime events, contamination incidents, and breakthroughs—feed directly back into our product lines.
Hands-on familiarity with 3-Biphenylcarboxylic Acid doesn't just benefit our operations; it drives the communication lines we maintain with users worldwide. When requests for new derivatives roll in, the team pivots to run pilot syntheses, tweak purification, and troubleshoot as the project evolves. Our operators and chemists have supported partners in Europe tweaking UV-active additives, startups in the US making novel imaging agents, and academic labs in Asia working with isotope-labeled versions. Guidance doesn’t come from a catalogue; it grows from practical engagement with the molecule’s quirks and capabilities.
Supply chain disruptions in the past have reinforced the importance of robust, transparent manufacturing. Extended droughts disrupted water supplies for cooling in peak summer months, forcing us to replicate processing steps across two parallel lines—one drawing from groundwater, the other tied to municipal reserve tanks. Keeping product quality consistent took both flexibility and a track record of documentation. Sharing contingency protocols directly with our most sensitive customers made the difference in continued business.
Our approach has always involved a mix of technical rigor, iterative process improvement, and straightforward partnership with clients. Every innovation in our production line for 3-Biphenylcarboxylic Acid reflects the lessons absorbed from scaling new reactions, implementing environmental controls, and troubleshooting side reactions alongside end-users. The trust we earn comes from not just saying a batch will meet a certain standard but from demonstrating process transparency, consistency, and readiness to adapt formulations or batch records to unique end uses. Competitors may offer a product with a similar name, but we build confidence batch by batch, through auditable quality and a direct line to the people who make your critical materials.
From the lab to bulk, from bench to reactor, each day adds to our knowledge about what makes 3-Biphenylcarboxylic Acid valuable—differences that are not just measurable by spectrum or purity sheet, but validated by how seamlessly clients can move from concept to shelf. This material’s future looks as dynamic as the chemistries it enables, and we’re ready to help shape its next chapter wherever new challenges arise.