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4-Hydroxy-4'-Fluorobiphenyl

    • Product Name 4-Hydroxy-4'-Fluorobiphenyl
    • Alias 4-Fluoro-4'-hydroxy-1,1'-biphenyl
    • Einecs 624-357-6
    • 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

    430177

    Chemical Name 4-Hydroxy-4'-Fluorobiphenyl
    Molecular Formula C12H9FO
    Molar Mass 188.20 g/mol
    Appearance White to off-white solid
    Melting Point 103-107 °C
    Boiling Point Unknown
    Solubility In Water Slightly soluble
    Cas Number 348-51-0
    Pubchem Cid 202358
    Smiles C1=CC(=CC=C1C2=CC=C(C=C2)F)O
    Inchi InChI=1S/C12H9FO/c13-10-5-3-9(4-6-10)8-1-2-11(14)7-12(8)14/h1-7,14H
    Density 1.26 g/cm³ (estimated)

    As an accredited 4-Hydroxy-4'-Fluorobiphenyl factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g of 4-Hydroxy-4'-Fluorobiphenyl is supplied in an amber glass bottle, tightly sealed, with a chemical-resistant label.
    Shipping 4-Hydroxy-4'-Fluorobiphenyl is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is typically packed in accordance with relevant chemical safety regulations for transport. Ensure upright positioning, use secondary containment to prevent leaks, and include suitable hazard labels and documentation during transit. Transport by authorized carriers only.
    Storage 4-Hydroxy-4'-Fluorobiphenyl should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Protect from light and moisture. Store at room temperature and avoid sources of ignition. Properly label containers and ensure access is restricted to trained personnel, following relevant safety and chemical handling guidelines.
    Application of 4-Hydroxy-4'-Fluorobiphenyl

    Applications of 4-Hydroxy-4'-Fluorobiphenyl in Industrial Manufacturing

    4-Hydroxy-4'-Fluorobiphenyl serves as a specialized intermediate in advanced material science and chemical synthesis. This compound supports several critical downstream sectors by enabling tailored modifications in polymer, liquid crystal, and pharmaceutical industries, among others. Below are the core industrial scenarios where this material directly contributes to key value chains.

    1. High-Performance Liquid Crystal Materials

    Manufacturers use 4-Hydroxy-4'-Fluorobiphenyl as a structural core unit within the synthesis of liquid crystal monomers, specifically targeting the production of high-stability nematic and smectic phases for LCD panels. Its chemical structure introduces a high degree of thermal and electrical anisotropy, which is crucial for precision display applications. Integrators leverage its reactivity during etherification and esterification with various chain-extensions or terminal groups in multi-step synthesis, directly impacting the electro-optical properties of the resulting mixture based on detailed composition calculations and stringent purity requirements.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Electronic Chemical Materials
    • IEC 61249 for Printed Wiring Boards and Associated Materials – Flammability Testing
    • RoHS (Restriction of Hazardous Substances Directive, 2011/65/EU)
    • JIS C 62326 – Japanese Industrial Standard for Liquid Crystal Display Materials

    Typical usage ratio

    • 3–12 wt% of total liquid crystal mixture, customized according to viscosity and dielectric constant targets defined during formulation trials and in response to panel design requirements.

    Downstream process integration

    • Introduced at monomer synthesis stage, subsequently coupled via the Williamson ether synthesis and esterification before being subjected to stringent double-distillation purification and blending into LC mixtures by end-users.

    Final product types

    • TFT-LCD modules for consumer electronics
    • Automotive instrument cluster displays
    • Industrial control panel screens
    • Medical diagnostic flat panel displays

    2. Advanced Polymer Modifier for High-Temperature Engineering Plastics

    4-Hydroxy-4'-Fluorobiphenyl provides key structural reinforcement and enhances fire resistance in the manufacture of specialty polyaryletherketones (PAEK) and polyesters used for aerospace, automotive, and electrical insulation applications. Its rigid backbone and the electron-withdrawing fluorine group contribute to improved Tg, dimensional stability, and reduced moisture uptake. Its inclusion requires careful molecular weight distribution management during polymerization, with the incorporation process closely monitored via GPC and FTIR analytics according to industrial-grade QC protocols.

    Industry compliance standards

    • UL 94 V-0 – Standard for Safety of Flammability of Plastic Materials
    • EN ISO 1874-1 Plastics — Polyarylmethyl ketone (PAEK) Specifications
    • ASTM D6100: Standard Specification for Poly(arylether ketone) Materials
    • REACH Regulation (EC) No 1907/2006 for Chemical Registration and Risk Assessment

    Typical usage ratio

    • 0.5–4.0 mol% in co-monomer feed during melt or solution polymerization; exact ratios depend on final product application, hydrophobicity requirements, and mechanical property enhancement targets.

    Downstream process integration

    • Dosed directly into the polymer reactor with the primary diacid and dihalide monomers, followed by chain extension, vacuum dehydration, and solid-state post-curing steps.

    Final product types

    • High-performance PEEK and PEKK engineering plastic pellets
    • Electrical connector housings for aerospace and transportation
    • Heat-resistant insulation films and laminates
    • Micro-molding components used in medical and electronic devices

    3. Pharmaceutical API Intermediate for Antineoplastic Compounds

    As an aromatic biphenyl scaffold with both fluorine and hydroxy substituents, this material functions as a vital intermediate in the synthesis of select kinase inhibitors and hormone modulators. Medicinal chemists exploit its unique electronic distribution for targeted structure-activity relationship exploration, particularly in the assembly of molecules intended for breast cancer therapies. Synthesis routes rely on controlled Suzuki coupling or Ullmann-type reactions, with the intermediate’s purity closely monitored under GMP environments to ensure clinical suitability of downstream APIs.

    Industry compliance standards

    • ICH Q7 – Good Manufacturing Practice Guideline for Active Pharmaceutical Ingredients
    • Ph. Eur. European Pharmacopoeia Monographs for Intermediates
    • Current Good Manufacturing Practice (cGMP) per 21 CFR Parts 210/211 (FDA)
    • USP <797> Pharmaceutical Compounding – Sterile Preparations

    Typical usage ratio

    • Stoichiometric proportions depend on specific active pharmaceutical ingredient route; generally 1:1 or slightly in excess to maximize coupling efficiency and minimize byproduct formation during scale-up.

    Downstream process integration

    • Charged at early or mid-stage synthesis steps, coupled under palladium catalysis with arylboronic acids or halides, then directly isolated and purified prior to downstream closure or modification reactions.

    Final product types

    • Targeted kinase inhibitor active ingredients
    • Hormone therapy agents for oncology
    • Advanced intermediate blocks for clinical candidate evaluation
    • Research-grade reference standards

    4. Performance Coating Precursor in Electronic Protective Films

    Designers of ultra-thin and high-durability protective electronic coatings incorporate this compound in formulations aiming for increased chemical resistance and transparency. Its biphenyl core and fluorine substituent provide robust matrix stabilization when cross-linked with epoxide or polyol counterparts. Boiling-point control and reaction sequence timing play a critical role in batch formation, as do in-process checks for impurities and side product elimination to ensure functional group fidelity within the final cured coating layer.

    Industry compliance standards

    • IEC 61086-1:2014 – Coating Materials for Printed Board Assemblies
    • UL 746E – Polymeric Materials, Electrical Insulation Systems
    • RoHS (Directive 2011/65/EU) for heavy metal and halogen restrictions
    • ISO 2178:2016 – Non-magnetic Coatings Measurement Standards

    Typical usage ratio

    • 0.8–3.0 wt% in the total solids content, tunable according to barrier and dielectric property targets established during pilot lab evaluation

    Downstream process integration

    • Incorporated during pre-polymerization and cross-linking phases with functional prepolymers, after which the resin blend is filtered, precision-cast, and UV- or thermally-cured to form the finished protective layer

    Final product types

    • Printed circuit board conformal coatings
    • Display glass anti-scratch films
    • Mobile device internal protective films
    • Optoelectronic device encapsulation coatings

    5. Organic Electronics and OLED Host Material Synthesis

    Electronic material producers exploit the electronic and steric properties of the biphenyl structure for synthesizing host and charge-transport components in OLED emitters. The hydroxy and fluoro substituents facilitate further derivatization and enable control of molecular packing in the solid state. Integration occurs via Buchwald–Hartwig amination and cyclization with carbazole or triarylamine derivatives, supporting custom emission color profiles and efficiency improvements in advanced display electronics.

    Industry compliance standards

    • IEC 62341:2011 – Standard for Organic Light Emitting Diode Displays
    • ISO 14001 – Environmental Management for Electronic Raw Material Manufacturing
    • IPC-4101 – Specification for Base Materials for Rigid and Multilayer Printed Boards
    • RoHS-compliant materials for electronic components

    Typical usage ratio

    • Varies 0.5–5.0 mol% in the target precursor mixture, modulated by desired device emission wavelength and host system composition; precise level established by emission spectrum and quantum efficiency optimization studies

    Downstream process integration

    • Added during the organic synthesis of charge-transport and host layers, followed by purification (column chromatography, HPLC) before thin-film deposition using spin-coating or vacuum thermal evaporation techniques

    Final product types

    • OLED display panels for smartphones and TVs
    • Organic photovoltaic test modules
    • Flexible wearable electronic components
    • Small-molecule emitter blends for specialty lighting solutions
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    Certification & Compliance
    More Introduction

    4-Hydroxy-4'-Fluorobiphenyl: A Practical Insight from the Producer's Bench

    Understanding the Essence of 4-Hydroxy-4'-Fluorobiphenyl

    Producing 4-Hydroxy-4'-Fluorobiphenyl (CAS number 2088-70-0) in our own facility has sharpened our appreciation for both the scientific rigor and the real-world challenges that underpin every batch. This compound is more than a line item on a catalog. Those of us working directly with its synthesis and purification see first-hand how precise control over process conditions translates into consistent quality, batch after batch.

    4-Hydroxy-4'-Fluorobiphenyl serves chemists looking for a phenolic biphenyl core modified with a fluorine at the para position. In practice, this translates into a molecule that straddles the boundary between reactivity and stability – an unusual property that opens doors in pharmaceutical research, liquid crystal intermediate development, specialty polymer production, and more. Over the years, requests have ranged from gram-scale orders for academic research to much larger, multi-kilogram volumes supporting process development.

    From the Reactor to Your Lab: How Our Team Makes a Difference

    Producing this molecule goes beyond following a generic route from the literature. Every stage, from raw material selection through the workup, crystallization, and final handling, shapes the product qualities our customers rely on. We maintain a modern reactor setup with real-time temperature and reaction control, essential for managing the halogenation and phenolic substitution steps. The journey does not end at the end of the reaction. Strict solvent purification, multi-step washes, and drying under controlled conditions help avoid contamination that can compromise customer work downstream.

    Instrumental validation in our lab ties everything together. Each lot undergoes HPLC, NMR, and elemental analysis, not as routine chores but as crucial checkpoints. When specifications call for a purity over 99%, we see this as a bottom line, not just a statistic. End-users share feedback that off-colour product or persistent trace by-products create problems at their next synthetic stage. We treat these reports with urgency, treating each outcome as a direction for continuous improvement.

    Specifications Rooted in Application Demands

    Over years of fielding questions from customers, we’ve learned that the technical demands for 4-Hydroxy-4'-Fluorobiphenyl aren’t uniform. Academic labs might focus on purity and cost. Large manufacturers focus on scale, packing, and robust supply. The product we deliver meets a melting point range of 128-131°C, aligning with published literature. This transparency helps customers design reactions and avoid equipment blockages or uneven reactions. We maintain water content below 0.2% by Karl Fischer titration — a threshold tailored for moisture-sensitive reactions, especially Suzuki couplings or oxide formations.

    Our standard grade provides high purity (>99%), tightly controlled for trace halides and metal ions. These details matter most where the product goes directly into synthesis steps with sensitive reagents, as in ligands or catalytic intermediates. Over time, we’ve developed custom packaging solutions: amber glass bottles for laboratory use, lined HDPE drums for bulk shipments, and specialty sealed bags when users request inert-atmosphere packaging. These measures have cut down on the headaches customers previously faced with degradation or contamination during transit and storage.

    Differentiating Features in a Crowded Space

    On paper, the differences between one supplier’s 4-Hydroxy-4'-Fluorobiphenyl and another’s can seem minimal. But the devil really does live in the details. We work directly with raw material producers to ensure consistent quality, then perform multi-stage quality assurance checks through the process. The result shows up in the color, crystalline appearance, and reactivity of the product — subtle differences not always measurable by standard assays, but noticed by experienced chemists working at the bench.

    There have been instances where academic groups reported unexpected spots on their TLC readouts or a persistent residue after solvent evaporation. By working closely with technical teams and re-examining our traces for side-products, we traced these issues to supplier variability in raw halogenated phenyl sources. Today, our raw material qualification standards screen for obscure impurities that standard COA sheets sometimes miss.

    Handling logistics under tight deadlines happens routinely. We’ve managed urgent air shipments of temperature-sensitive lots and provided same- or next-day deliveries to customers running time-bound experiments. Years of collaboration with logistics partners have smoothed out many of the rough patches that once plagued specialty chemical shipments.

    Application-Driven Evolution

    Feedback from application labs often guides where we invest in process upgrades. Early on, researchers using 4-Hydroxy-4'-Fluorobiphenyl in pharmaceutical intermediate synthesis flagged batch-to-batch variations in reactivity, impacting project timelines. We responded by improving our impurity profiling with better chromatography and by extending our drying protocols to kill off hydrolysis-prone impurities. Diligence here went beyond ticking regulatory boxes — it came from responding to real disruptions experienced in the field.

    Another trend that has shaped product evolution is the growing number of high-throughput screening platforms. In custom screening applications for drug discovery and materials science, integration of automated liquid handling equipment places special demands on compound solubility and consistency. We have conducted solubility screenings in DMSO, DMF, and common organic solvents to ensure that pre-measured aliquots dissolve rapidly and completely. These tests revealed that even micro-traces of oxidized impurities can create bottlenecks downstream. Our dedicated QC team now screens for these before each batch is cleared for shipment.

    Supporting Scale-Up with Technical Know-How

    For many partners developing new pharmaceuticals or materials, starting with milligram quantities is only a first step. The challenge comes in scaling up to multi-kilogram or even pilot plant quantities without loss of quality or changes in impurity profile. As producers, we have handled numerous projects that began with test quantities and scaled to full-batch manufacture, often tightening specifications in the process.

    We’ve worked tightly with customers’ technical teams to anticipate changes that can arise during scale-up — shifts in crystal morphology, handling hazards, or differences in filterability. For 4-Hydroxy-4'-Fluorobiphenyl, scale-up required modifying the crystallization step to ensure batch uniformity and mitigate static charges, a problem that rarely surfaces at bench scale but becomes a safety concern in large vessels.

    Our investment in closed-system reactor setups further reduces the risk of environmental or cross-batch contamination, critical for upholding high-purity requirements as lot sizes grow. Equipment maintenance and frequent validation minimize run-to-run variability, an often overlooked detail that informs real-world reproducibility.

    Responding to Environmental and Regulatory Isssues

    As stewards of chemical manufacturing, we take our environmental and safety responsibilities seriously. We have implemented solvent recovery and waste neutralization steps, reducing both the environmental impact and the costs passed to customers. Regulatory expectations around halogenated organic handling continue to evolve. Where necessary, we collaborate with regulatory consultants to interpret updates affecting transportation, labeling, and export certification.

    We’ve encountered cases where end-users needed documentation to support registration of 4-Hydroxy-4'-Fluorobiphenyl as a research chemical or a notified intermediate. Our compliance staff have experience preparing detailed batch records, impurity profiles, and supplier qualification statements so that downstream users can navigate their own regulatory hurdles more easily.

    In responding to regulatory changes, we rely on lessons learned from previous inspections and audits. Teams collaborate across functions to prepare for new guidelines, and recent process revalidations demonstrate transparency in manufacturing practices. We treat each customer inquiry as an opportunity to explain, adjust, and, where practical, improve our own practices.

    Building Knowledge through Collaboration

    Long-term collaboration with customers and technical partners has fueled our knowledge base. Working side by side with university researchers, we have provided technical data that supports publications in peer-reviewed journals. For industrial partners, anonymized process data has enabled benchmarking and process improvements.

    The flow of questions and project feedback has deepened our own understanding of how 4-Hydroxy-4'-Fluorobiphenyl behaves in diverse applications: as a building block for novel ligands, a backbone for semi-conductor materials, or a component in advanced coatings. Each feedback loop closes the gap between lab-scale synthesis and real-world innovation, helping us refine both our process and our ability to support application-specific needs.

    With changing research and commercial landscapes, the properties end-users value can shift as well. Recently, interest has surged around using biphenyl derivatives in molecular electronics and artificial photosynthesis research. This trend pushes us to rethink traditional packaging and stability protocols, as such applications often demand ultra-high purity and special handling to preserve subtle electronic structure.

    Reliable Supply Chain and Crisis Management

    Pandemics, logistics bottlenecks, and market volatility have challenged the entire chemical supply chain. Our in-house production gives us agility when global shipping routes or customs regulations get snarled. We keep an on-site stock of raw materials so that unplanned supply stoppages have a minimal impact on customer projects. There have been times when alternative shipping solutions, such as “white glove” courier services for sensitive lots, made the difference between a successful project and a stalled timeline.

    We have strengthened connections with trusted carriers and cold-chain storage providers. In tight global markets, this preparation means consistent on-time delivery regardless of external disruptions. direct customer communication, from real-time shipment tracking to expedited order processing, has minimized confusion and frustration.

    Takeaways for the Practicing Chemist

    From our perspective as producers, 4-Hydroxy-4'-Fluorobiphenyl offers much more than a catalogue entry for synthetic chemists or R&D teams. Its specific properties make it valuable when only a phenolic biphenyl carrying a fluorine at the para position will do. Results depend on purity, trace contamination control, and the practical considerations of packing and shipping — all areas shaped directly by those who manufacture rather than those who merely resell.

    Customer trust develops through proven results across traditional and emerging applications. Decades of iterative improvement have shown that attention to detail — from raw material vetting to packaging design — carries more weight than generic claims of quality. By treating the product not as a transactional commodity but as the solution to a real experimental or production problem, we’ve stayed relevant in a rapidly changing field.

    Our commitment rests on clear communication, active feedback loops, and technical transparency. We see every inquiry as the start of a new collaboration and every order as an opportunity to prove, in practical terms, what difference careful manufacturing can make in demanding scientific work.