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4-Hydroxy-4'-Iodobiphenyl

    • Product Name 4-Hydroxy-4'-Iodobiphenyl
    • Alias 4-Iododiphenylol
    • Einecs 629-048-1
    • 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

    967595

    Chemicalname 4-Hydroxy-4'-Iodobiphenyl
    Casnumber 38623-35-7
    Molecularformula C12H9IO
    Molecularweight 296.10
    Appearance Off-white to pale yellow powder
    Meltingpoint 146-150°C
    Solubility Insoluble in water; soluble in organic solvents
    Purity Typically >98%
    Smiles C1=CC(=CC=C1C2=CC=C(C=C2)O)I
    Inchi InChI=1S/C12H9IO/c13-11-5-3-9(4-6-11)8-10-1-2-12(14)7-10/h1-8,14H

    As an accredited 4-Hydroxy-4'-Iodobiphenyl 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 10 grams of 4-Hydroxy-4'-Iodobiphenyl, labeled with product details, hazard warnings, and safety instructions.
    Shipping 4-Hydroxy-4'-Iodobiphenyl is packaged securely in sealed containers to prevent contamination and moisture exposure. It is shipped according to standard chemical safety guidelines, typically by ground or air, with appropriate labeling, documentation, and hazard information. Ensure compliance with local regulations for handling, transport, and storage of laboratory chemicals.
    Storage 4-Hydroxy-4'-Iodobiphenyl should be stored in a tightly sealed container, away from light, moisture, and incompatible materials such as strong oxidizing agents. Keep the chemical in a cool, dry, and well-ventilated area, ideally in a designated chemical storage cabinet. Ensure proper labeling and restrict access to trained personnel. Comply with local regulations for handling and disposal.
    Application of 4-Hydroxy-4'-Iodobiphenyl

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

    As the original manufacturer of 4-Hydroxy-4'-Iodobiphenyl, we support a range of specialized, high-value downstream industrial sectors by supplying this raw material in consistent specification batches. The following application scenarios reflect direct, established industrial utilization, adhering to relevant regulatory and quality standards in each field. Our technical team collaborates closely with customers to optimize integration, ensure regulatory compliance, and address real-world processing and formulation requirements.

    1. Advanced Liquid Crystal Intermediate for Display Materials

    Our material serves as a core functional intermediate in the synthesis of complex liquid crystal monomers for state-of-the-art LCD and OLED screens. Its para-iodo and hydroxy groups enable precise downstream derivatization, facilitating the fine-tuning of dielectric and alignment properties tailored for high-performance display panels in electronics manufacturing. Introduced during the intermediate step of monomer assembly, it supports exacting purity and process consistency, critical to subsequent polymerization and panel fabrication lines.

    Industry compliance standards

    • IEC 61747 for LCD display components
    • RoHS Directive (EU) 2015/863 for hazardous substance content
    • REACH Regulation (EC) No 1907/2006 Annex VII for chemical intermediates
    • ISO 9001:2015-certified QMS for specialty chemical production

    Typical usage ratio

    • 5–20 mol% of diphenyl intermediates in custom monomer synthesis; adjusted based on desired birefringence and volatility targets for target display grades

    Downstream process integration

    • Added at the core monomer assembly stage prior to final etherification, halide exchange, or coupling, allowing for targeted substitution and reactive blending under inert conditions

    Final product types

    • Liquid crystal monomers for TFT-LCDs
    • Reactive mesogen components for OLED alignment layers
    • High-relaxation-rate LC mixtures for advanced television and monitor displays

    2. Specialty Pharmaceutical Intermediate for Synthesizing Selective Estrogen Receptor Modulators (SERMs)

    This compound acts as a controlled aromatic precursor in the synthesis of key intermediates for non-steroidal pharmaceuticals, especially selective estrogen receptor modulators. The unique iodo-aryl structure provides a handle for regioselective coupling reactions, essential during the assembly of multi-ring pharmacophores. Integration takes place in medicinal chemistry routes prioritizing substitution fidelity, serving research-based and commercial pipeline development under cGMP oversight.

    Industry compliance standards

    • ICH Q7A for active pharmaceutical ingredient (API) manufacturing
    • Ph. Eur. (European Pharmacopoeia) monograph standards (for intermediates)
    • 21 CFR Part 211 (US FDA cGMP)
    • USP-NF General Notices (where applicable for process chemicals)

    Typical usage ratio

    • 0.8–1.3 mol equivalents per batch in SERM precursor coupling, adapted to stoichiometry for desired ring substitutions

    Downstream process integration

    • Reacted during Pd-catalyzed arylation steps or SNAr displacements, typically after protected amine or ether block creation to maintain target functional orientation

    Final product types

    • Active pharmaceutical intermediate for tamoxifen and raloxifene analog development
    • Advanced intermediates for estrogen modulator R&D pipelines

    3. Building Block in Organic Semiconductor Synthesis

    In the semiconductor materials industry, it enables the creation of functionalized polyarylene backbones, critical for manufacturing organic field-effect transistors (OFETs) and organic light-emitting diode (OLED) substrates. Its functional groups ensure reliable reactivity in metal-catalyzed cross-coupling, supporting precisely structured polymers with controlled charge transport properties needed in next-generation, printable electronics lines.

    Industry compliance standards

    • JEITA EM-3600 for organic semiconductor specifications
    • RoHS 3 (EU) on environmental compliance
    • ISO 14001 for environmental process controls in chemical synthesis
    • REACH Annex XIV for pre-registered substances and downstream user notifications

    Typical usage ratio

    • 2–10 mol% in Suzuki or Stille cross-coupling reactions, tailored according to backbone length and degree of polymerization needed for target device

    Downstream process integration

    • Introduced at the conjugated polymer chain-forming stage, enabling controlled substitution patterning prior to end-group capping for batch-to-batch consistency

    Final product types

    • Polyarylenevinylene and polyfluorene-based OFET layers
    • Electron/hole transport materials in OLED stack fabrication
    • Printable semiconducting inks for flexible electronics

    4. Intermediate in Agrochemical Active Ingredient Synthesis

    Leading agrochemical manufacturers use this compound for constructing halogenated biphenyl scaffolds with selective bioactivity, acting as a key building block in crop protection active ingredient development. Its targeted reactivity supports regioselective halogen incorporation in advanced fungicide and herbicide chemistry, entering the process at the controlled aromatic substitution and coupling stages prior to biological activity optimization.

    Industry compliance standards

    • FAO/WHO JMPR guidelines on pesticide active ingredient manufacturing
    • ISO 17025-accredited analytical verification during QC testing
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • China GB 2763-2021 (Maximum Residue Limits for Pesticides)

    Typical usage ratio

    • 3–15 mol% as an aryl halide donor in fungicide intermediate synthesis, adjusted for target substitution patterns and downstream performance screening

    Downstream process integration

    • Combined with specific amines or other aromatic precursors during early or intermediate coupling, followed by oxidation and final ring-activation reactions

    Final product types

    • Halogenated fungicide active substances for seed treatment
    • Herbicide intermediates used in broadleaf weed control formulations
    • Specific antiparasitic veterinary drug ingredients

    5. Dye Intermediate for High-Performance Polymer Colorants

    Leading polymer and industrial dye houses deploy this raw material in the custom synthesis of functional biphenyl chromophores, enhancing migration resistance and UV stability in fiber and engineering plastic coloration. Its iodo functionality supports site-specific coupling with diazo or anthraquinone groups, optimizing color intensity and fastness in polyester and polyamide coloration lines. It enters the workflow during the controlled chromogen assembly stage, where precise molecular engineering determines end-use stability and compatibility in melt-extruded plastics.

    Industry compliance standards

    • OEKO-TEX STANDARD 100 for human-ecological safety of textiles
    • EN 12852 for coloring agents in plastics
    • REACH-Regulation (EC) No 1907/2006 for dye intermediates
    • ISO 105-B02 for color fastness to light

    Typical usage ratio

    • 2–7 mol% as chromophore-forming core in dye intermediate synthesis, with dosage adjusted by target shade depth and resistance specifications based on plastic or textile substrate

    Downstream process integration

    • Employed during core chromogen coupling step, serving as a coupling base for azo, anthraquinone, or diaryl systems prior to melting and dispersion in plastic masterbatch or fiber spinning lines

    Final product types

    • High-migration-resistance colorants for PET fibers
    • Engineering plastic masterbatches for automotive components
    • Lightfast azo and anthraquinone dyes for synthetic textile coloration
    Free Quote

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