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4-Phenylimidazole

    • Product Name 4-Phenylimidazole
    • Alias 4-Phenyl-1H-imidazole
    • Einecs 206-418-9
    • 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
    VTB
    Specifications

    HS Code

    824432

    Cas Number 7164-98-9
    Molecular Formula C9H8N2
    Molecular Weight 144.18 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 136-142°C
    Solubility In Water Slightly soluble
    Density 1.13 g/cm³
    Purity Typically ≥98%
    Synonyms 4-Phenyl-1H-imidazole

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

    Packing & Storage
    Packing White polyethylene bottle with a blue screw cap, labeled "4-Phenylimidazole, 25g", including hazard pictograms and manufacturer details.
    Shipping 4-Phenylimidazole is typically shipped in tightly sealed containers to protect from moisture and contamination. It should be packaged in accordance with regulatory guidelines, using chemical-resistant materials. Proper labeling, documentation, and hazard symbols are included to ensure safe handling and compliance during transportation. Store and transport in a cool, dry place.
    Storage 4-Phenylimidazole should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition. Protect from moisture, heat, and incompatible substances such as strong oxidizers or acids. Store at room temperature, avoiding exposure to light. Ensure the storage area is clearly labeled and follow all relevant safety and handling protocols.
    Application of 4-Phenylimidazole

    Applications of 4-Phenylimidazole in Industrial Manufacturing

    Our factory-grade 4-Phenylimidazole serves as a critical building block for industries where imidazole structures impart unique chemical functionality in targeted syntheses and downstream processes. Below we detail differentiated application scenarios, common integration ratios, compliance requirements, production stages, and representative finished goods as observed in our direct supply to industrial users.

    1. Epoxy Resin Curing Systems for Electronics Encapsulation

    In the electronics sector, manufacturers rely on this material as a latent curing accelerator in two-component and one-component epoxy adhesive systems. It activates polymerization at elevated temperature, allowing stable storage of uncured formulations while providing controlled reaction rates during final assembly. Specifically favored for encapsulating microelectronic modules, this imidazole derivative supports reliable crosslinking performance and stable electrical insulation in demanding environments.

    Industry compliance standards

    • IEC 60664-3 (Insulation Coordination for Electronic Equipment)
    • IPC-4101 (Specification for Base Materials for Rigid and Multilayer Printed Boards)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • REACH Regulation (EC) No 1907/2006 (Registration, Evaluation, Authorisation and Restriction of Chemicals)

    Typical usage ratio

    • 0.2–1.0% by weight of total epoxy system; formulators adjust ratio based on desired latency and cure schedule

    Downstream process integration

    • Incorporated during pre-mix stage of resin formulation, prior to vacuum de-gassing and final product packaging

    Final product types

    • Potting compounds for automotive sensors
    • Chip encapsulants in semiconductor packaging
    • Conformal coatings for PCB protection
    • High-reliability adhesive films for medical devices

    2. Corrosion Inhibitor Synthesis for Oilfield Applications

    Specialty chemical producers utilize this material as a synthetic intermediate in the preparation of custom imidazoline-type corrosion inhibitors designed for oil and gas processing equipment. Its aromatic character facilitates tailoring of molecular polarity and stabilization of surface-active agents employed in high-salinity and acidic production conditions. This approach directly impacts long-term pipeline and drilling tool protection under global field standards.

    Industry compliance standards

    • NACE MR0175/ISO 15156 (Materials for Use in H2S-containing Environments in Oil & Gas Production)
    • API RP 932-B (Corrosion Inhibitors in Oil Refineries)
    • OSHA 29 CFR 1910.1200 (Hazard Communication Standard)
    • REACH Regulation (EC) No 1907/2006

    Typical usage ratio

    • As a precursor: 10–20% in reaction batches for inhibitor active ingredients; batch ratios set by molecular design targets and desired chain length

    Downstream process integration

    • Reacted during imidazoline synthesis via cyclization and amidation stages, followed by neutralization and blending into inhibitor concentrates

    Final product types

    • Water-soluble pipeline corrosion inhibitors
    • Drilling fluid additives for offshore rigs
    • Process equipment protectants in acidizing operations
    • Downhole treatment chemicals

    3. Intermediate in Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers select this imidazole derivative as a heterocyclic precursor for several antimalarial and antifungal drugs, where its substitution pattern introduces desired pharmacophores for advanced synthesis. Multi-step routes involving this intermediate emphasize regulated traceability and consistent impurity profiles under cGMP standards, ensuring safe conversion to final actives in API plants with validated process controls.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for APIs)
    • Ph. Eur. (European Pharmacopoeia)
    • USP–NF (United States Pharmacopeia–National Formulary)
    • 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)

    Typical usage ratio

    • 0.5–1.5 molar equivalents as advanced intermediate; ratio defined by target synthetic pathway and molecule design

    Downstream process integration

    • Charged during heterocyclic coupling or N-substitution step of API synthetic route, followed by chromatographic purification and analytical QC

    Final product types

    • Active intermediates for antimalarial formulations
    • Building blocks for imidazole antifungals (e.g., miconazole derivatives)
    • Specialty veterinary drug actives
    • Research-grade impurity standards

    4. Polymer Additive for Fire-Resistant Engineering Plastics

    Plastic compounders employ this compound as a high-temperature chain modifier and catalyst for synthesis of flame-retardant polyphthalimides and specialty polyamides. Its aromatic imidazole structure participates in both end-capping and backbone integration, enabling finished plastics to meet stringent vertical burn standards in electrical insulators and transport parts.

    Industry compliance standards

    • UL 94 (Tests for Flammability of Plastic Materials for Parts in Devices and Appliances)
    • EN 45545-2 (Fire Protection on Railway Vehicles)
    • IEC 60695-2-11 (Glow-Wire Flammability Test)
    • ISO 1043 (Plastics – Symbols and Abbreviated Terms)

    Typical usage ratio

    • 0.1–0.5% by weight in masterbatch blending; loading depends on polymer system and melt viscosity adjustment needs

    Downstream process integration

    • Introduced during extrusion compounding before pelletization of base polymer; subsequent injection molding or extrusion shaping by end users

    Final product types

    • Flame-retardant polyamide sheets
    • Polyphthalimide electrical sockets
    • Railcar cable insulation jackets
    • Heat-resistant housing for electronic modules

    5. Analytical Reagent Manufacturing for Chromatographic Detection

    Specialty chemical labs manufacture derivatization reagents using this imidazole to modify analytes for improved retention and resolution in liquid chromatography (LC) and gas chromatography (GC) analysis. Its electron-rich aromatic nitrogen allows formation of stable adducts suitable for trace impurity detection or process monitoring in regulated QC laboratories.

    Industry compliance standards

    • ISO/IEC 17025 (General requirements for the competence of testing and calibration laboratories)
    • FDA 21 CFR Part 58 (Good Laboratory Practice for Nonclinical Laboratory Studies)
    • USP Chapter <621> (Chromatography)
    • REACH Regulation (EC) No 1907/2006

    Typical usage ratio

    • 0.05–0.2% by weight in reagent kits; reagent concentration optimized by analyte type and instrument configuration

    Downstream process integration

    • Blended into LC/GC derivatization solutions during kit assembly, then vialed and sealed under inert atmosphere for analytical use

    Final product types

    • Chromatographic derivatization kits for pharmaceutical analysis
    • Trace-level detection reagents for environmental monitoring
    • Quality control standard solutions
    • Research-grade analytical reference materials
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