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2'-Fluoro-Biphenyl-2-Carbaldehyde

    • Product Name 2'-Fluoro-Biphenyl-2-Carbaldehyde
    • Alias 2-Fluorodibenzaldehyde
    • Einecs 871-783-5
    • 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
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    Specifications

    HS Code

    747151

    Product Name 2'-Fluoro-Biphenyl-2-Carbaldehyde
    Cas Number 51558-21-7
    Molecular Formula C13H9FO
    Molecular Weight 200.21 g/mol
    Appearance Pale yellow solid
    Melting Point 48-50°C
    Purity Typically >98%
    Solubility Soluble in organic solvents such as dichloromethane and ethanol
    Smiles C1=CC=C(C(=C1)C2=CC=CC=C2F)C=O
    Inchi InChI=1S/C13H9FO/c14-12-7-3-5-10(8-12)11-6-2-1-4-9(11)13-15/h1-8H
    Storage Store at 2-8°C, protected from light and moisture
    Synonyms 2'-Fluoro-[1,1'-biphenyl]-2-carbaldehyde

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

    Packing & Storage
    Packing Amber glass bottle containing 5 grams of 2'-Fluoro-Biphenyl-2-Carbaldehyde, sealed with a tamper-evident cap and safety label.
    Shipping Shipping for 2'-Fluoro-Biphenyl-2-Carbaldehyde is conducted in compliance with all relevant chemical transportation regulations. The compound is securely packaged in sealed containers to prevent leakage or contamination. Shipments include appropriate hazard labeling and documentation, ensuring safe handling during transit. Expedited and temperature-controlled shipping options are available upon request.
    Storage 2'-Fluoro-Biphenyl-2-Carbaldehyde should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep the container tightly closed and protected from moisture. Store separate from oxidizing agents and strong acids. Use appropriate chemical-resistant containers and labeling to prevent contamination. Always follow institutional safety guidelines and local regulations for storage of organic chemicals.
    Application of 2'-Fluoro-Biphenyl-2-Carbaldehyde

    Applications of 2'-Fluoro-Biphenyl-2-Carbaldehyde in Industrial Manufacturing

    2'-Fluoro-Biphenyl-2-Carbaldehyde is a key fine chemical intermediate widely used in pharmaceutical synthesis, specialty agrochemical production, advanced material modifiers, and liquid crystal precursor development. As a direct manufacturer, we support clients engaged in high-value downstream manufacturing by ensuring controlled impurity profiles, strict regulatory compliance, and reliable supply consistency.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical companies employ 2'-Fluoro-Biphenyl-2-Carbaldehyde as a building block in the synthesis of selective kinase inhibitors, non-steroidal anti-inflammatory product precursors, and next-generation CNS drug candidates. It introduces a fluoro-substituted aromatic group that improves molecular binding and metabolic stability, critical for achieving specific pharmacological targets in regulated GMP environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP-NF, EP, JP for impurity and residual solvent limits (as applicable to the final API)
    • 21 CFR Part 211 US FDA cGMP for Finished Pharmaceuticals
    • China Pharmacopoeia (ChP) compliance for domestic products

    Typical usage ratio

    • 0.2–0.8 molar equivalents, depending on the coupling step and desired substitution pattern
    • Adjustment based on reaction efficiency and targeted API yield

    Downstream process integration

    • Introduced in Buchwald–Hartwig amination, Suzuki-Miyaura coupling, or reductive amination stages during API assembly
    • Purification via crystallization or column chromatography after key bond-forming reactions

    Final product types

    • Anticancer kinase inhibitor APIs
    • Non-opioid analgesic precursors
    • Fluoroaryl CNS active molecules
    • Synthetic pharmaceutical intermediates for veterinary compounds

    2. Agrochemical Intermediate for Novel Fungicides and Herbicides

    Major agrochemical producers use this compound to synthesize active ingredients targeting resistant weed species and fungal strains. Its biphenyl and fluoro group enhance biological activity and environmental stability, facilitating the development of next-generation crop protection agents under global food safety compliance frameworks.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • EU REACH Regulations (EC 1907/2006)
    • EPA 40 CFR Parts 150-189 for US crop protection chemical registration
    • ISO 9001:2015 quality management for manufacturing traceability

    Typical usage ratio

    • 5–15% by weight as starting material in key ring-forming and acylation steps
    • Exact ratio optimized according to desired active ingredient structure and synthesis scale

    Downstream process integration

    • Condensed with heterocycles or aliphatic amines during active molecule assembly
    • Incorporated before chlorination or methylation steps to impart definitive selectivity

    Final product types

    • Systemic fungicides for cereal and soy crops
    • Herbicides with post-emergent activity
    • Broad-spectrum pesticide intermediates
    • Chemical seed treatment actives

    3. Advanced Material Modifier for OLED and Electronic Chemicals

    Materials science companies select this compound as a precursor for the functionalization of high-performance organic semiconductors, liquid crystals, and OLED emitters. Its fluoro-biphenyl scaffold impacts electron density, alignment, and photophysical properties, essential in the fabrication of stable and efficient optoelectronic devices.

    Industry compliance standards

    • RoHS 2015/863/EU for electronic device materials (limitation of hazardous substances)
    • IEC 62474 material declaration
    • ISO 9001:2015 for advanced material production
    • IPC-4101 for base materials in electronic interconnect manufacturing

    Typical usage ratio

    • 0.05–0.3 molar equivalents, depending on the intended molecular weight and electronic properties
    • Adjusted during monomer synthesis and copolymer integration steps

    Downstream process integration

    • Engaged in Grignard or Stille cross-coupling for polymer backbone assembly
    • Used as a terminal aldehyde block for end-functionalization and alignment in small molecule emitters

    Final product types

    • Blue and green OLED emitters
    • Organic semiconductors for OFETs
    • Liquid crystal intermediates for display panels
    • Photonic polymer actuators

    4. Fine Chemical Intermediate for Specialty Aroma and Fragrance Compounds

    Specialty fragrance and aroma manufacturers incorporate this building block for creating high-value fluoroaromatic aldehyde derivatives, enabling unique scent profiles not achievable with conventional aldehydes. It supports synthesis of top-note fixatives and long-lasting aroma elements, processed under controlled batch and continuous flow setups meeting international safety requirements.

    Industry compliance standards

    • IFRA (International Fragrance Association) Safety Standards
    • EU Cosmetic Regulation (EC) No 1223/2009
    • ISO 9001:2015 for flavor and fragrance ingredient production
    • Hazardous Substances Classification (CLP Regulation EC No 1272/2008) for label compliance

    Typical usage ratio

    • 1–5% in synthetic routes for key aldehyde fragrance bases
    • Proportion adjusted for batch size and target olfactory profile

    Downstream process integration

    • Aldol condensation or reductive alkylation to produce unique aromatic bases
    • Subsequent functional group transformations leading to alcohols, acids, or esters

    Final product types

    • Fine fragrance top notes and fixatives
    • Long-lasting aroma aldehyde blends for perfumery
    • Flavor compounds in specialty food applications
    • Scented cosmetic ingredient bases
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    Certification & Compliance
    More Introduction

    2'-Fluoro-Biphenyl-2-Carbaldehyde: A Practical Perspective from Our Factory Floor

    Introduction to 2'-Fluoro-Biphenyl-2-Carbaldehyde

    Over the years, our work as a direct chemical manufacturer has shown us that every product batch tells its own story. 2'-Fluoro-Biphenyl-2-Carbaldehyde holds a particular place among our specialty aldehyde line, both for its distinctive molecular characteristics and for the way it fits into demanding project applications. The nickname “2'-fluoro BP-2-aldehyde” gets used around the plant, as our technicians try to keep things clear during synthesis or QC rounds. Production doesn’t rest on theory alone in this industry, and this material’s behavior and impact extend far beyond the lab sheets.

    The Product Profile: How We See It

    We produce 2'-Fluoro-Biphenyl-2-Carbaldehyde in a form that satisfies the high purity standards expected from intermediates in advanced organic synthesis. With a CAS number that distinguishes it from close relatives, its structural formula features a fluorine atom precisely at the 2'-position on the biphenyl spine, then an aromatic aldehyde group. This subtle substitution holds major implications for selectivity in reactions and for tuning the properties of target molecules.

    In practice, the fine white to pale yellow crystalline product is a sign of a smooth run, minimal side reactions, and tightly controlled process variables right through to the final workup. Consistency here does not arise by chance—it comes from investment in both equipment and technician skill, which lets us maintain tight purity windows batch after batch. Each time we send out a shipment, our QC data trails behind it, reassuring users in the pharma, agrochemical, and advanced material sectors of our attention to detail.

    Manufacturing Realities and Purification

    Production starts with sourcing dependable raw materials, including the needed fluorinated aromatics. Sourcing this grade of starting material, not always an easy feat, cuts out potential headaches later—impure feedstock only introduces costly bottlenecks. In our facility, dedicated glassware and reactors guard against contamination and cross-over with other aromatic lines.

    We run synthesis under scaled conditions that translate the principles of directed ortho-lithiation and Vilsmeier-Haack reactions into a process that maintains yield and safeguards personnel. The work doesn’t end at reaction completion. Our team performs iterative purification, mostly by column chromatography and recrystallization, and each step narrows the side product margin. The final compound gets dried under vacuum until it meets water content thresholds that prevent downstream reaction scatter or unwanted polymerization. Seeing those spectral fingerprints—sharp NMR peaks for fluoro substituents, clean aldehyde C=O stretches on IR—is a professional satisfaction unique to manufacturers.

    In-Use Performance in Synthesis

    Users want to know how a building block like 2'-Fluoro-Biphenyl-2-Carbaldehyde performs as a reagent. Several pharmaceutical R&D teams routinely incorporate this compound into their programs targeting bioactive scaffolds, especially when metabolic stability or fluorine’s unique pharmacokinetic tuning become necessary. The ortho-fluoro effect on the biphenyl framework often creates more desirable reactivity trends, changing both electronic effects and the way substituents interact with enzymes or active sites.

    Beyond pharma, the materials science crowd evaluates our batches for routes leading to novel polymers, ligands, or advanced OLED materials. Here, the precise placement of fluorine confers both chemical stability and a shift in physical properties, such as higher resistance to oxidative conditions or shifts in melting point. In agricultural chemistry labs, researchers use this building block to combine aromatic complexity with handleable reactivity, designing molecules where both persistence and breakdown rates must be dialed in.

    Direct customer feedback forms part of our improvement loop. A recurring theme: users value the reproducibility of their own key synthetic transformations—be it Suzuki couplings, imine formations, or downstream functionalization—when starting from our aldehyde. The confidence in our work comes through clean TLC plates and consistent HPLC traces, batch after batch.

    Comparing 2'-Fluoro-Biphenyl-2-Carbaldehyde to Related Aldehydes

    Aldehydes with biphenyl or substituted aromatic groups offer a range of reactivities, yet the introduction of a fluoro atom at the 2'-position defines this product’s identity. Compared to unsubstituted biphenylcarbaldehyde, the presence of fluorine can shift electrophilicity, stabilize certain intermediates, and impact downstream coupling efficiency. Our technical staff frequently points out how this affects route selection: a user working with 4'-fluoro variants, or methylated analogs, faces different outcomes in selectivity and yield when compared to this 2'-fluorinated backbone.

    Chemically, this means slower oxidation rates than some of the more activated aromatic aldehydes. That can prove useful when storage stability is a concern or when a controlled oxidation profile is part of the process design. We’ve seen our product outperform both 4'-chloro and 2-methoxy analogs in certain cross-couplings, based purely on workups run side by side in the technical team’s own comparative trials.

    Another layered benefit: the para-position on the adjoining ring remains open for further functionalization, thanks to the blocking nature of the ortho-fluoro. Synthetic chemists have called out this flexibility in SAR (structure-activity relationship) studies, attributing more robust data to higher yields and fewer byproducts.

    Key Specifications and Analytical Control (From the Production Line)

    Day-to-day, we keep our focus on metrics that actually matter for downstream use: purity, isomer content, moisture level, and particle size. We don’t just rely on COA certificates. On the line, our chemists run HPLC and NMR for every batch, verifying not only that the product is within spec, but that side impurities like biphenyl-dialdehyde or over-fluorinated analogs are tightly controlled. We measure trace metals spectroscopically to ensure no process artifacts slip through from catalysts used upstream. Often, internal benchmarks run stricter than the industry norms, as our sales team knows customers will test the same vials in their own incoming QC labs.

    Over the years, we’ve refined filtration procedures and drying techniques to maximize shelf-stability, keeping moisture content far below levels that risk unwanted hydrate formation. Packaging in inert atmosphere containers adds another barrier against air- or moisture-triggered degradation, especially for export shipments likely to encounter a range of storage conditions.

    Experienced-Based Tips from Our Manufacturing Floor

    Sharing what actually works matters more than just listing features. Our warehouse staff reports that controlling storage temperature around 2°C to 8°C keeps this aldehyde at peak performance through extended holding periods. Exposure to light can slowly impact color and is best avoided, based on old test samples tracked in our stability studies.

    Our technical support team often discusses usage with clients tackling tricky condensations or cross-coupling protocols. We advise filtering all solvents through activated alumina just before use—trace water or peroxide counts for more than theoretical calculations suggest. It took years of bench experience to realize that washing glassware with acetone, then drying in a vacuum oven, pays dividends in cleaner spectra and improved conversion rates.

    Handling our product in a glovebox environment, or under a steady nitrogen purge, further extends working time before any oxidation-related discoloration creeps in. Not all customers need extreme measures, but those developing high-value molecular targets often benefit from incremental improvements at each step.

    Solving Common Issues as a Producer

    Our years in chemical manufacturing have forced us to tackle persistent industry challenges head-on. One such challenge: residual odor. Sharp, lingering smells—common to many aromatic aldehydes—can persist unless distillation cuts hit a precise margin. Modifying our end-stage purification two years ago, we now achieve much lower odor levels than typical traders or generic suppliers. Lab techs and shipping staff both appreciate this improvement.

    Allergic reactions or skin sensitization deserve attention during packing; our SOPs go further than industry standard, requiring gloves and face protection even at the microgram scale. We train each new hire in incident handling, and maintain a direct route to on-site first aid, helping us keep accident rates well below sector averages.

    Another issue: minimizing exposure to trace metals originating from earlier synthetic steps. Customers running transition-metal catalyzed reactions are attuned to this. By upgrading purification columns and investing in metal scavenger resins, we’ve seen a marked reduction in customer complaints about reaction inhibition due to extraneous palladium, iron, or nickel traces.

    Regulatory and Safety Perspectives

    Strict regulatory awareness runs through production. Hazard classification of 2'-Fluoro-Biphenyl-2-Carbaldehyde informs both labeling and transport. Our safety protocols integrate lessons learned from past spills nationwide and on our own site. We implement targeted risk controls and keep strict logs for both domestic and export lots. Packaging, like our tamper-evident vials and sealed drums, stems from field feedback and regulatory site audits.

    Transport regulations can occasionally change, impacting transshipment windows. We preemptively work with forwarders skilled in handling aromatics, ensuring dynamic compliance with customs paperwork and local regulations, cutting down on delays or rejections at borders.

    Continuous Improvement and Richer Customer Feedback

    We keep our ears open to client feedback—researchers, plant operators, and method developers all spend time on the phone with our technical leads discussing process tweaks or new project needs. Requests for alternative packaging size, solvent-wetted material, or customer-set quality benchmarks shape the tweaks we make in subsequent production runs. Sometimes a gram-scale custom lot prefaces a full kilo-scale contract, giving us early warning signals about downstream synthetic bottlenecks.

    One surprising lesson came through requests for detailed impurity breakdowns. Our analytical lab expanded their reporting to include additional byproduct traces after a major pharma client found an unexpected impurity interfering with high-throughput screening. We adapted, we shared the new data, and as a result the client’s timelines stayed on track. This feedback loop lies at the heart of our manufacturing culture.

    Addressing Future Demand Shifts

    Shifts in research funding, new trends in fluorinated organic molecules, and advances in green chemistry all direct the flow of demand for this building block. As new polymer technologies emerge or as regulatory boundaries push agrochemical developers towards more engineered aromatic structures, we see upticks in production requests, sometimes compressing lead times. We allocate resources to keep pace, investing both in core reactor upgrades and in a skilled technical team able to troubleshoot at every turn.

    Domestic demand increasingly asks for full chain-of-custody documentation. Abroad, stringent purity specs and supporting data have become prerequisite for partnership. We grow our digital systems accordingly, giving clients real-time access to documentation and lot analysis. The customers driving technology—those demanding the cleanest, best-characterized chemical building blocks—keep us striving to raise our own game.

    Environmental Responsibility and Waste Management

    Our roots as a chemical manufacturer mean that every stream—solvent, solid, or gaseous—must be diligently tracked. We built waste minimization into our SOPs by reusing appropriate solvent fractions, capturing volatile organic compounds through engineered vapor scrubbers, and investing in spent media treatment. Over time, this approach cut handling costs and improved morale across shifts.

    Our approach isn’t about hitting sustainability targets just for certifications. We saw, firsthand, how recycling cleaned solvents not only trimmed operational spend, but improved workplace air quality—everyone in production benefits. What started with 2'-Fluoro-Biphenyl-2-Carbaldehyde production spread to other lines, and we share hard-earned tips with manufacturing partners who come through on site visits.

    Down the line, customers sometimes request documentation for green chemistry compliance. We maintain source traceability, processor logs, and emissions audits. Clients building precise environmental impact models for their own end products cite this transparency as a deciding factor in choosing our material over less-documented imports.

    The Human Element: Craftsmanship and Collaboration

    Throughout the plant, the people who steward 2'-Fluoro-Biphenyl-2-Carbaldehyde from bench to bulk shipment invest daily in craftsmanship. Our average technician brings a decade of batch production experience to bear, and new hires learn the ropes under close supervision. Morning meetings tackle issues from glassware wear and filter rebuilding, to tips on improving batch timing or modifying the packing team’s workflow for the busy season.

    Our shift leads keep an open door policy by design, so early detection of even subtle changes in product appearance or odor get reported, traced, and documented right away. This experience-driven approach anchors our quality culture. A client’s peace of mind starts here, not just with data but with the tacit knowledge built into every production run.

    Enabling Applied Research: Beyond the Catalog

    Every kilogram of 2'-Fluoro-Biphenyl-2-Carbaldehyde we produce gets shipped with an implicit promise—to support breakthroughs in research and product development. We have worked directly with academic collaborators who need batch-specific spectral libraries or want support troubleshooting reaction failures. Our technical team fields questions ranging from solubility profiles to hints for improved crystallization. Several successful projects started with a single phone call or email, followed by sample vials, then resulted in multi-year supply contracts as trust in our consistency grew.

    Innovation thrives in partnership. The wider chemistry community benefits from manufacturers willing to share lessons learned, and from those who remain invested in the science behind both the successes and failures. Our own methods, refined over years and based on measured outcomes, become a quiet foundation for ambitious clients to build on. Product innovation often starts with a foundation of reliable, high-purity materials—science progresses when these materials perform as expected.

    Looking Forward

    We see demand for 2'-Fluoro-Biphenyl-2-Carbaldehyde rising as the scientific community pushes boundaries in molecular design, materials engineering, and healthcare. Staying ahead means investing in both technology and people. Automated equipment joins hands with seasoned eyes on the production floor.

    Our close connection to both material and user stands as our most important asset. As a manufacturer, we translate every new order and every tough question into progress, not by sticking to template processes but by responding with practical know-how, proven process improvements, and a focus on the details that matter. The goal remains: to deliver reliable quality so our customers can innovate boldly, one batch at a time.