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[4-(1H-Imidazol-1-Yl)Phenyl]Methanol

    • Product Name [4-(1H-Imidazol-1-Yl)Phenyl]Methanol
    • Alias 4-(1H-imidazol-1-yl)benzyl alcohol
    • Einecs 629-744-8
    • 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

    100001

    Chemical Name [4-(1H-Imidazol-1-yl)phenyl]methanol
    Molecular Formula C10H10N2O
    Molecular Weight 174.20 g/mol
    Cas Number 124045-40-1
    Appearance White to off-white solid
    Melting Point 139-142°C
    Solubility Soluble in DMSO, methanol
    Smiles C1=CC(=CC=C1CN)N2C=CN=C2
    Inchi InChI=1S/C10H10N2O/c13-7-9-1-3-10(4-2-9)12-6-5-11-8-12/h1-6,8,13H,7H2
    Iupac Name (4-imidazol-1-ylphenyl)methanol
    Storage Conditions Store at 2-8°C, keep container tightly closed
    Pubchem Cid 24201031

    As an accredited [4-(1H-Imidazol-1-Yl)Phenyl]Methanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The product comes in a 5g amber glass bottle with a tamper-evident cap, labeled with chemical name, formula, and hazard warnings.
    Shipping [4-(1H-Imidazol-1-yl)phenyl]methanol is shipped in compliance with chemical handling regulations. The substance is packaged securely in sealed containers, cushioned to prevent breakage. Shipments include all necessary safety documentation and labeling. Temperature and humidity are controlled as needed to ensure product integrity during transit, aligning with hazard classification requirements.
    Storage [4-(1H-Imidazol-1-yl)phenyl]methanol should be stored in a tightly sealed container, protected from light and moisture, and kept at room temperature (15–25°C) in a well-ventilated, dry location. Avoid exposure to strong oxidizing agents. Store away from direct heat sources and incompatible substances. Proper labeling and access restriction to trained personnel are recommended to ensure safe handling and storage.
    Application of [4-(1H-Imidazol-1-Yl)Phenyl]Methanol

    Applications of [4-(1H-Imidazol-1-Yl)Phenyl]Methanol in Industrial Manufacturing

    As the manufacturer, we provide [4-(1H-Imidazol-1-Yl)Phenyl]Methanol to enable key transformations within specialized chemical processing industries. The following application scenarios reflect actual downstream deployments, compiling regulatory, formulation, processing, and end product insights for each sector in which this material is commercially integrated.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    In pharmaceutical manufacturing, [4-(1H-Imidazol-1-Yl)Phenyl]Methanol is primarily employed as a crucial intermediate during the synthesis of various imidazole-based APIs, where it introduces a selectable functional group for subsequent derivatization or coupling steps. Process chemists leverage its unique imidazolyl-phenyl methanol backbone to build scaffolds for antifungal and cardiovascular drug candidates. Rigorous cGMP controls and validated analytical methods monitor input, traceability, and reactivity at every batch scale, given its integration at a critical path of reaction cascades that determines the stereochemistry and purity profile required for downstream drug substances.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (Finished Pharmaceuticals)
    • Ph. Eur., USP-NF as applicable for final API
    • EDQM Certification of Suitability (CEP) for API supply chains

    Typical usage ratio

    • 0.5–3.0 molar equivalents relative to core aromatic amination or etherification steps; adjusted based on the synthetic route yield and target API batch size

    Downstream process integration

    • Enters during multi-step reaction stages, especially the nucleophilic substitution, alkylation, or imidazole coupling phase leading to active intermediate formation before protection and final deprotection steps

    Final product types

    • Imidazole-based antifungal APIs (e.g., econazole intermediates)
    • Imidazolyl-substituted antihypertensive drug precursors
    • Generic and proprietary pharmaceutical intermediates

    2. Specialty Organic Electronic Materials

    Leading manufacturers of functional organic electronics incorporate this raw material as a building block for hole-transport layers and advanced molecular dopants in OLED and OPV devices. Its electron-rich imidazole-phenyl configuration provides well-defined interface properties and anchoring potential in multilayer stacks. Raw material lots undergo purity and moisture control per the requirements of semiconductor-grade production, integrating inline with high-vacuum deposition or solution-shearing fabrication routes for consistency of film morphology and charge transfer characteristics in next-generation display technologies.

    Industry compliance standards

    • IPC-1752 Material Declaration Standard (electronics materials transparency)
    • IEC 62474 Material Composition in Electronic Products
    • RoHS (Restriction of Hazardous Substances) Directive 2011/65/EU
    • REACH Registration (as applicable to final electronic functional layers)

    Typical usage ratio

    • 0.2–2.0 wt% relative to total organic semiconductor blend; concentration set to optimize conductivity, thermal stability, and interface adhesion

    Downstream process integration

    • Feeds into organic solution preparation prior to spin-coating, slot-die coating, or vapor phase deposition of charge transport and interface modification layers

    Final product types

    • OLED panel charge transport layers
    • Organic photovoltaic films
    • Field-effect transistor semiconducting blends

    3. Fine Chemical Catalysts and Ligand Systems

    [4-(1H-Imidazol-1-Yl)Phenyl]Methanol serves a key role for fine chemical producers formulating tailored ligand complexes, where its imidazole group coordinates with transition metals in homogeneous catalysis. These custom ligands boost selectivity and turnover rates in cross-coupling, hydrogenation, and C-H activation platforms. Proprietary catalyst recipes require detailed stoichiometric evaluation and iterative upscaling to accommodate changes in substrate profiles at production scale. Material QC focuses on trace metal, water content, and functional group integrity throughout the ligand synthesis and catalyst pre-activation protocols consistent with industrial batch processing.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management System for chemical production)
    • Responsible Care® Program (chemical process safety)
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals, for EU applications)
    • Internal downstream customer standards for ligand performance validation

    Typical usage ratio

    • 1.0–5.0 mol% as ligand precursor or co-ligand per mole of catalyst complex; adjusted according to metal-to-ligand electronic demands and substrate scope

    Downstream process integration

    • Undergoes direct condensation or esterification into ligand frameworks, entering prior to complexation and catalyst system formulation for deployment in flow reactors or stirred-tank systems

    Final product types

    • Transition metal ligand complexes
    • Homogeneous fine chemical catalysts
    • Custom catalytic systems for pharmaceutical and agrochemical synthesis

    4. Advanced Polymer Modification Additives

    Manufacturers of specialty polymers employ [4-(1H-Imidazol-1-Yl)Phenyl]Methanol as a functional modifier to introduce specific polar sites and imidazole reactivity into engineering plastics and thermoset resins. This addition enhances compatibility with metal surfaces, cross-linking efficiency, or ionic conductivity according to application needs in coatings, adhesives, and sealants. Process engineers tailor the additive loading and mixing conditions based on molecular weight targets, desired glass transition temperature, and environment-specific durability, fully documenting additive traceability for compliance under end-use quality systems.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management for polymer manufacturing)
    • RoHS compliance (where used in electronics applications)
    • UL 94 Flammability Standards (as required for appliance or electronics housings)
    • Customer-driven PPAP (Production Part Approval Process) for automotive or electronics applications

    Typical usage ratio

    • 0.1–1.5 wt% relative to resin mass; modified based on polymer matrix chemistry, processing temperature, and mechanical performance targets

    Downstream process integration

    • Incorporated during resin compounding and masterbatch preparation ahead of extrusion, injection molding, or in situ curing processes; often metered through gravimetric feeders in continuous production lines

    Final product types

    • High-performance engineering resins
    • Imidazole-functionalized epoxy adhesives
    • Antistatic polymeric films
    • Surface-modified plastic and composite coatings
    Free Quote

    Competitive [4-(1H-Imidazol-1-Yl)Phenyl]Methanol prices that fit your budget—flexible terms and customized quotes for every order.

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