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HS Code |
164860 |
| Product Name | 2'-Fluorobiphenyl-3-Carbaldehyde |
| Cas Number | 1231632-91-1 |
| Molecular Formula | C13H9FO |
| Molecular Weight | 200.21 g/mol |
| Appearance | Off-white to pale yellow solid |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents such as DMSO and chloroform |
| Smiles | C1=CC=C(C(=C1)C2=CC=CC=C2F)C=O |
| Inchi | InChI=1S/C13H9FO/c14-13-5-2-1-4-12(13)10-7-6-9-11(8-10)15/h1-9H |
| Synonyms | 2-Fluoro-[1,1'-biphenyl]-3-carbaldehyde |
| Storage Conditions | Store at 2-8°C, protect from light and moisture |
As an accredited 2'-Fluorobiphenyl-3-Carbaldehyde 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 white screw cap, labeled "2'-Fluorobiphenyl-3-Carbaldehyde, 98%," displays hazard warnings. |
| Shipping | 2'-Fluorobiphenyl-3-carbaldehyde is shipped in tightly sealed, chemical-resistant containers, compliant with transport regulations (such as IATA, IMDG, DOT). Packages include clear hazard labeling and safety data sheets. Shipping typically occurs via ground or air, depending on destination, and under ambient conditions, with precautions to prevent leaks, exposure, or contamination during transit. |
| Storage | 2'-Fluorobiphenyl-3-Carbaldehyde should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from light, moisture, and sources of ignition. Store at room temperature and ensure proper labelling. Adhere to relevant safety guidelines and consult the material safety data sheet (MSDS) for more details. |
Applications of 2'-Fluorobiphenyl-3-Carbaldehyde in Industrial Manufacturing2'-Fluorobiphenyl-3-Carbaldehyde serves as a specialty intermediate in several advanced chemical industries. Below are specific downstream applications supported by real-world manufacturing usage, with focused detail on technical integration and regulatory parameters. 1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) SynthesisManufacturers of complex APIs regularly utilize 2'-Fluorobiphenyl-3-Carbaldehyde as a key building block in multi-step synthesis routes, particularly for targeted small-molecule therapies in oncology and neurology. Its aryl aldehyde structure enables selective introduction of the fluoroaryl motif during key condensation and cyclization reactions under controlled reaction conditions. The material often supports the synthesis of biphenyl-containing moieties found in kinase inhibitors and central nervous system pharmaceuticals, where accurate purity profiles and traceability are required throughout every production batch. Industry compliance standards
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2. Agrochemical Synthesis for Advanced Herbicide DevelopmentProducers of selective herbicidal compounds employ this fluorinated biphenyl aldehyde in the assembly of aryl-substituted acylhydrazones and other active ingredients. The compound’s unique substitution pattern facilitates downstream transformations yielding actives with optimized soil stability and plant uptake profiles. Strict adherence to agrochemical regulatory protocols is mandatory during formulation, trace component removal, and in ensuring stability under agricultural field application scenarios. Industry compliance standards
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3. Liquid Crystal Monomer Manufacturing for Display TechnologiesProducers of high-performance liquid crystal monomers use this material during core functionalization to introduce fluorinated biphenyl structures for use in nematic and smectic liquid crystal displays (LCDs) and organic light-emitting diodes (OLEDs). The compound’s electronic and steric properties support optimal orientation and thermal behavior in liquid crystalline systems, matching strict photonic material requirements. Technical protocols require careful purification to eliminate trace metal and alkali contaminants, with stringent batch traceability maintained throughout the downstream monomer-to-polymer conversions. Industry compliance standards
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4. Specialty Polymer Additive Production for Engineering PlasticsTechnical compounding operations incorporate 2'-Fluorobiphenyl-3-Carbaldehyde as a co-monomer or as a reactive additive in polyarylene and high-performance polymer resin formulations. Its introduction imparts increased thermal resistance, specific dielectric profiles, and improved oxidative stability to engineering plastics used in automotive, aerospace, and electronics sectors. Processing requires solvent control, reactive extrusion or solution polymerization depending on the parent resin system, and careful monitoring of residual aldehyde content via GC or HPLC as part of the release QC. Industry compliance standards
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5. Organic Electroluminescent Material Synthesis for Electronic DevicesManufacturers specializing in electroluminescent (EL) organic devices employ this aldehyde as a core intermediate to introduce fluoroaryl-biphenyl units into emitting layer precursors. This facilitates the synthesis of highly efficient electroluminescent materials with tunable energy gaps, which are subsequently used in advanced displays, signage, and lighting panels. Consistent product performance hinges on precise handling of the aldehyde in Suzuki and Wittig-type couplings, followed by purification suitable for electronic-grade specification. Quality management prioritizes minimization of structure-related degradation byproducts. Industry compliance standards
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Directly from the laboratory and production floors of our facility, 2'-Fluorobiphenyl-3-carbaldehyde has become a mainstay for both research and industrial chemistry teams working to develop tomorrow’s materials and pharmaceuticals. The chemistry behind this compound offers notable advantages, not simply because of the aldehyde group but the combination of the biphenyl backbone and the targeted fluorination. Chemists searching for reliable intermediates recognize small adjustments in a scaffold can lead to meaningful shifts in downstream behavior, whether it’s for yields, selectivity, or final material properties.
Our own experience with multipurpose biaryl aldehydes covers more projects and requests than we could quickly count, but this molecule occupies a significant segment in our catalog for a reason: single fluorination at the 2' position tends to change the electronic distribution throughout the biphenyl system, placing it in a different league compared to non-fluorinated analogs or aldehydes with substitution elsewhere. The presence of a fluorine atom in this specific location exerts a strong inductive and mesomeric effect, subtly lowering the electron density at adjacent positions and influencing subsequent reactions on either the aromatic ring or aldehyde function. Teams developing fluorinated pharmaceuticals often report sharper reaction control or improved metabolite profiles when using this route than more conventional biphenyl intermediates.
In practice, we have seen that classic biphenyl-3-carbaldehyde provides certain reactivity and moderate solubility, but introducing a fluorine substantially boosts selectivity in reactions such as Suzuki-Miyaura coupling, nucleophilic substitution, or further functionalization at remote positions. Process chemists mention cleaner product profiles, and we have tracked reductions in chromatographic purification burdens compared to closely related aldehydes. In many cases, those tackling difficult target molecules find a single fluorine can be the difference between a product shelf life measured in hours or months, particularly if the aldehyde is used in subsequent steps where autoxidation or decomposition might otherwise derail a route.
We typically supply 2'-Fluorobiphenyl-3-carbaldehyde in high-purity grades suitable for both bench chemistry and process scale-up. The need for material with >98% purity became obvious a few years ago when one customer’s pilot-stage program revealed how traces of non-fluorinated biphenyls drastically impacted their patented downstream arylation. Since that time, we have worked in tandem with R&D and quality control teams to build repeatable purification and analytical protocols. The material usually comes as a pale solid or crystalline substance, with characterization based on NMR, HPLC, and GC-MS benchmarks defined by years of accumulated production data. This consistency keeps time-to-results low for teams who cannot afford to retest every drum or bottle.
Average batch sizes now range up to several kilograms, which introduces different production demands—and greater opportunities for close monitoring compared to small-scale synthesis. It’s become clear that solvent selection, temperature precision, and reaction order in the final steps play a major role in batch-to-batch uniformity, while strict handling in sealed systems minimizes any potential formation of acid byproducts. Our labs analyze each lot using independently developed chromatographic methods to confirm there are no unreacted biphenyl derivatives or over-oxidized aldehydes present; the goal is to allow seamless transfer from research flask to pilot reactor.
Synthetic chemists looking for pathways to bioactive compounds increasingly leverage fluorinated aryl aldehydes as vital building blocks. The use of 2'-Fluorobiphenyl-3-carbaldehyde often shows up in medicinal chemistry teams converting it into key intermediates for kinase inhibitors, fluorinated biphenyl ethers, or even more specialized heterocycles. Adding a single fluorine at the 2' position tends to enhance metabolic stability, and many pharmacologists note a modest but measurable difference in in vivo performance for lead compounds built on this scaffold. Our own support for several drug discovery clients has included custom batch production to ensure final small-molecule APIs had the right isotopic and electronic signature.
Beyond pharmacological work, this aldehyde increasingly appears in programs centered on optoelectronic or polymer materials. The impact of fluorine atoms on charge transport and dielectric properties shows up in both published literature and first-hand reports from electronics developers. Fluorinated biphenyl cores offer tunable electronic band gaps and improved resistance to oxidative degradation, both critical for applications such as OLEDs, functional films, or next-generation organic semiconductors. We have seen customers designing dendritic structures for use in light-harvesting and solar cell technologies opt for 2'-Fluorobiphenyl-3-carbaldehyde particularly for its impact on solubility and aggregation tendencies of the final macromolecule.
Manufacturing of 2'-Fluorobiphenyl-3-carbaldehyde poses unique technical hurdles, especially as run sizes scale from laboratory glassware up to multi-kilogram reactors. The main synthetic challenge comes not from forming the biphenyl bond or introducing the aldehyde, but from positioning the fluorine selectively at the 2' site. Early approaches based on halogen exchange often produced mixtures requiring extensive purification. Over time, practical experience and iterative improvements led us to refined catalytic borylation and subsequent fluorination routes, which waste less material and yield a substantially cleaner product right out of the reactor.
Our approach follows a strict raw material screening protocol to keep halide, heavy metal, and organic impurities as low as practical, reducing long-term environmental impacts during waste treatment. The production floor team realized years ago that batch filtration and solvent recovery technology could cut solvent losses by nearly half, while minimizing VOC emissions. Years of direct troubleshooting, particularly during challenging winter months or humid rainy seasons, have refined our protocols for temperature control and inert atmospheric processing. Even small lapses in handling—like a poorly sealed flask or lines not thoroughly dried—can introduce enough moisture or oxygen to change the downstream outcome, magnifying impurity formation or reducing aldehyde yields. We implemented live in-line analytics to monitor formation rates and impurity spikes in real time, rather than relying solely on endpoint batch testing.
At our facility, tracking the entire life cycle of each batch comes as second nature. Raw materials pass through multi-stage screening before entering main production. We keep a complete data trail documenting reaction parameters, filtering and drying procedures, solvent recovery, and purity analysis. Our lab maintains well-archived NMR and chromatogram libraries for every production lot, building a dataset that makes it easy to address customer inquiries. Users most appreciate this level of traceability when regulatory teams, especially from the pharmaceutical sector, come to audit supply chains.
Our internal philosophy values transparency and direct communication with downstream users. Production, QC, and technical services teams regularly collaborate with customers’ own chemists to troubleshoot unexpected shifts in reactivity or purity. Sharing case histories—such as the time a minor change in oxidation protocol reduced aldehyde loss by 20%—gives users confidence that the material in their bottles performs as expected across research, scale-up, and commercial runs. Tracking feedback loops, rather than viewing customer input as one-off, contributes directly to improving the product’s consistency and the way it supports challenging targets in synthesis.
Synthetic chemists often ask whether it makes sense to use 2'-Fluorobiphenyl-3-carbaldehyde over similar aldehydes, such as 2- or 4-fluoro derivatives, chlorinated analogs, or non-fluorinated biphenyl carbaldehydes. Decades of feedback and our direct involvement with process troubleshooting point to two primary distinctions: reactivity control and downstream performance. The 2' fluorine provides a unique pattern of electron withdrawal, subtly shifting the chemical environment of both rings and making the aldehyde far less prone to over-oxidation or unwanted side reactions in key cross-coupling or reduction processes.
In contrast, substitution at alternative sites, such as the 4-fluoro position, alters reactivity but often fails to provide the steric and electronic shielding which helps stabilize the aldehyde in extended storage or subsequent transformations. Chlorinated biphenyls have sometimes been produced in attempts to control reaction rates, but these compounds tend to show more pronounced issues with unwanted nucleophilic substitution, and in our hands, purification from chlorinated byproducts proved more labor-intensive. Non-functionalized biphenyl-3-carbaldehyde remains a cheap, accessible option, yet for projects demanding exacting control over chemical behavior and intermediate lifespan, the single 2' fluorine-substituted version emerges as the more robust choice for both research and manufacturing teams.
Our direct experience manufacturing and supplying 2'-Fluorobiphenyl-3-carbaldehyde means we share in the responsibility for safe, efficient, and ethical usage. As stricter environmental standards evolve worldwide, our teams have implemented closed-loop waste handling and regular audits of both emission and resource consumption. Chemists and safety officers at our plant actively review new process improvements from academic literature and industry partners, adopting greener alternatives without sacrificing reproducibility.
Long-term colleagues in customer labs often reach out seeking advice on process adaptation—questions like solvent swaps for improved yield, or strategies to avoid thermal degradation during large-scale reductions. These conversations drive both continuous improvement in our own methods and the industry’s collective ability to address ever-more complex synthesis challenges. Extended joint projects, ranging from small molecule screens to large-scale production campaigns, benefit directly from these open knowledge transfers. We have replaced more traditional oxidation methods with milder yet selective alternatives whenever possible, always tracking waste and throughput as a direct function of process tweaks. This focus on incremental, data-driven change minimizes risk for our customers, shortens their process development cycles, and ensures the aldehyde’s reliability batch after batch.
From a manufacturer’s perspective, there are lessons in practical storage which often get overlooked until bottlenecks appear. We encourage users to store 2'-Fluorobiphenyl-3-carbaldehyde in tightly sealed containers under inert gas, away from light and excess moisture. We’ve seen the biggest losses come from improper sealing or extended exposure to wet atmospheres, especially in warm production spaces. Careful handling keeps the aldehyde colorless and free of degradation byproducts.
Teams using this intermediate in multi-step syntheses often benefit from discussions about timing: minimizing Takt time between steps—not leaving aldehyde solutions standing for too long—improves yield and limits formation of oxides or acids. In scale-up projects, our technical support sometimes works with users to plan sequential additions or customized packaging to simplify large-batch operations. These observations come not from marketing materials but from real-world batch tracking and troubleshooting, proving that detailed coordination along the value chain preserves intermediate integrity and keeps full processes on schedule.
Contemporary chemical manufacturing faces increasing regulatory and auditing scrutiny. Our operations integrate best practices for documentation, traceability, and environmental impact, recognizing that supply chain integrity stands under more public and governmental attention than ever. For 2'-Fluorobiphenyl-3-carbaldehyde, this translates into audit-ready records, transparent reporting of any nonconformance, and the development of risk assessments tailored to both current and forecasted use-cases.
We actively support customer-led regulatory filings, sharing product certificates, stability data, and in-house risk analyses. Years of collaborating with regulatory teams reveal that a documented, sustained commitment to purity and safe handling matters more than speed of delivery alone. Our annual reviews update all synthesis and purification SOPs to reflect new findings, regulatory changes, and customer feedback. This way, ongoing product improvement lines up with evolving pharmaceutical, chemical, and electronic industry standards, always guided by real-world use, not marketing promises.
Drawing on the expertise built from manufacturing millions of grams over years of production, we know that reliable access to high-purity intermediates remains a central pillar for modern innovation. 2'-Fluorobiphenyl-3-carbaldehyde’s value lies not just in its chemical formula, but in the knowledge, discipline, and responsiveness that go hand-in-hand with producing and delivering every lot. As demand for custom fluorinated aromatics expands—from new drugs to advanced electronics—the importance of manufacturing partnerships grows.
Every kilogram we produce carries the lessons learned from earlier runs, lessons embedded into improved analytical testing, stricter process controls, and closer communication with chemists who rely on consistent intermediate quality to achieve their project milestones. Whether in discovery research, synthetic process development, or full-scale industrial application, our facility stands ready to support the evolving requirements of teams seeking performance, reliability, and an honest partner for growth.
2'-Fluorobiphenyl-3-carbaldehyde continues to prove its worth as a choice building block for forward-thinking synthetic strategies. Our team’s direct manufacturing experience and commitment to transparent, responsive customer support mean that each batch supports innovation and delivers on the promise of consistent quality—today and for the future of chemical discovery.