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1-(4-Methoxyphenyl)-1H-Imidazole

    • Product Name 1-(4-Methoxyphenyl)-1H-Imidazole
    • Alias 4-Methoxy PHI
    • Einecs 629-947-8
    • 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

    290852

    Chemicalname 1-(4-Methoxyphenyl)-1H-Imidazole
    Casnumber 38468-20-1
    Molecularformula C10H10N2O
    Molecularweight 174.20 g/mol
    Appearance White to off-white solid
    Meltingpoint 110-113°C
    Solubility Soluble in organic solvents such as DMSO and methanol
    Structure Contains an imidazole ring substituted with a 4-methoxyphenyl group
    Smiles COC1=CC=C(C=C1)N2C=CN=C2
    Inchi InChI=1S/C10H10N2O/c1-13-9-4-2-8(3-5-9)12-7-6-11-10-12/h2-7H,1H3
    Purity Typically >98% (commercial grade)
    Storage Store in a cool, dry place, tightly closed
    Synonyms 4-Methoxyphenylimidazole

    As an accredited 1-(4-Methoxyphenyl)-1H-Imidazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "1-(4-Methoxyphenyl)-1H-Imidazole, 25g." Features hazard symbols, batch number, manufacturer details, and storage instructions.
    Shipping The chemical **1-(4-Methoxyphenyl)-1H-Imidazole** is shipped in tightly sealed containers to protect it from moisture and air exposure. Packaging complies with chemical safety regulations, ensuring secure transit. It is labeled according to hazard standards, with documentation provided for handling and emergency procedures. Only licensed carriers and authorized personnel handle shipments.
    Storage 1-(4-Methoxyphenyl)-1H-Imidazole should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of heat or ignition. Keep the container tightly closed and store it in a chemical-resistant, labeled container. Avoid exposure to strong oxidizing agents, acids, and bases. Follow all relevant safety guidelines for handling and storage of laboratory chemicals.
    Application of 1-(4-Methoxyphenyl)-1H-Imidazole

    Applications of 1-(4-Methoxyphenyl)-1H-Imidazole in Industrial Manufacturing

    As the original manufacturer of 1-(4-Methoxyphenyl)-1H-Imidazole, we support diverse customers across high-value sectors by supplying this advanced heterocyclic compound directly integrated within specialized downstream production processes. The following application scenarios reflect industrial practices validated by regulatory standards, strictly mapped to real-world use cases where our material drives core product performance and compliance.

    1. Active Pharmaceutical Ingredient (API) Intermediate in Antifungal Drug Synthesis

    Pharmaceutical manufacturers routinely use 1-(4-Methoxyphenyl)-1H-Imidazole as a critical building block in synthesizing imidazole-based antifungal agents such as ketoconazole and related APIs. Its specific structural characteristics support key steps in heterocyclization and functionalization, enabling precise molecular control during multi-stage organic synthesis under GMP environments.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211
    • European Pharmacopoeia (Ph. Eur. current edition)
    • USP–NF monographs when relevant intermediates are registered

    Typical usage ratio

    • 0.8–1.3 equivalents per mole of target API intermediate; dosage is adjusted to stoichiometric requirements based on the stepwise reaction protocol and purity of input material

    Downstream process integration

    • Charged during controlled N-alkylation or condensation steps; introduced into closed reactors under inert atmosphere, followed by purification and isolation of API-grade intermediates

    Final product types

    • Imidazole-based antifungal medicines (tablets, topical creams, injectables)
    • Generic and branded APIs supplied to formulation partners

    2. Curing Accelerator in Epoxy Resin Systems

    Epoxy formulators in electronics and advanced composites employ 1-(4-Methoxyphenyl)-1H-Imidazole as a highly efficient curing accelerator, favored for its ability to activate epoxy groups at controlled temperatures and reduce cure times while minimizing exothermic risk. Its electron-donating methoxy group enables finely tuned catalysis in production lines demanding precision in resin cross-linking.

    Industry compliance standards

    • IEC 61249-2-21 (halogen-free requirements for PCB laminates)
    • REACH Registration (Annex XVII ingredient limitations)
    • RoHS Directive 2011/65/EU—applicable to electronic encapsulants
    • ISO 9001:2015 Quality Management for specialty chemicals

    Typical usage ratio

    • 0.3–1.0 phr (parts per hundred resin); adjusted up to 1.5 phr for high-speed or low-temperature cure cycles in advanced composite molding

    Downstream process integration

    • Added to epoxy resin premixes or masterbatches prior to reactor charging; mixed under controlled agitation and temperature to prevent premature curing, followed by automated dispensing or casting in final component fabrication

    Final product types

    • Electronic potting compounds and PCB substrates
    • Structural adhesives in aerospace interior panels
    • Composite prepregs for high-performance automotive and sports equipment

    3. Chemical Intermediate in Agrochemical Synthesis

    Producers of specialty crop protection agents utilize 1-(4-Methoxyphenyl)-1H-Imidazole as an advanced intermediate for imidazole ring incorporation during the manufacture of systemic fungicides. It supports selective alkylation, facilitating high-purity active ingredient synthesis in multistep reaction cascades, often with demanding yield and environmental requirements under ISO-certified production.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 and ISO 14001:2015 Environmental Management
    • China GB 2763: National Food Safety Standard for pesticide residues (for downstream monitoring)
    • ECHA REACH compliance for intermediate registration

    Typical usage ratio

    • 0.7–1.2 molar equivalents relative to core halogenation or ring-fusion agent; dosage determined by target fungicide synthesis pathway and required batch scale

    Downstream process integration

    • Dosed directly during core condensation or cyclization stage in pilot or production reactors; reacts with alkylating agents under phase-transfer catalysis, followed by neutralization and washing prior to formulation

    Final product types

    • Broad-spectrum triazole and imidazole fungicides, including tebuconazole-type products
    • Emulsifiable concentrate (EC) agrochemical preparations
    • Wettable powder and water-dispersible granules

    4. Research Reagent in Organic Synthesis (Fine Chemicals, Custom Synthesis)

    Universities, process development laboratories, and custom synthesis companies source our material for its reliable purity and functionality in creating heterocyclic scaffolds and library compounds. It serves as an indispensable imidazole variant for synthesis of ligands, photoactive molecules, and specialty fine chemicals in process development, method validation, and high-throughput screening.

    Industry compliance standards

    • GLP (Good Laboratory Practice), OECD Series on Principles of GLP
    • ISO/IEC 17025: Testing and calibration for analytical labs
    • REACH Annex I and II for research and development substances
    • Local chemical registration within each region (e.g., TSCA in the US, K-REACH in South Korea)

    Typical usage ratio

    • 10–50 mmol per reaction or as required by specific synthesis protocols; actual scale driven by experimental design, with larger quantities for preparative research or pilot validation

    Downstream process integration

    • Weighing and direct introduction during initial coupling or cyclization step within solid- or solution-phase organic synthetic workflows; handled in dry, inert conditions to ensure reproducibility of research outcomes

    Final product types

    • Specialty ligands for catalysis and material science
    • Reference standards and analytical controls
    • Small-scale batches of drug discovery candidates and photoinitiators
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