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1-(4-Chlorophenyl)-1H-Pyrrole

    • Product Name 1-(4-Chlorophenyl)-1H-Pyrrole
    • Alias CL-220
    • Einecs 629-135-9
    • 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

    187828

    Iupac Name 1-(4-chlorophenyl)-1H-pyrrole
    Molecular Formula C10H8ClN
    Molecular Weight 177.63 g/mol
    Cas Number 13682-46-3
    Appearance Off-white to pale yellow solid
    Melting Point 79-83°C
    Solubility Slightly soluble in organic solvents
    Smiles c1cc(ccc1n2cccc2)Cl
    Inchi InChI=1S/C10H8ClN/c11-9-4-6-10(7-5-9)12-2-1-3-8-12/h1-8H

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

    Packing & Storage
    Packing Amber glass bottle with tamper-evident cap, labeled "1-(4-Chlorophenyl)-1H-Pyrrole, 25g." Includes hazard warnings and handling instructions.
    Shipping 1-(4-Chlorophenyl)-1H-Pyrrole should be shipped in compliance with all applicable regulations for hazardous chemicals. The product must be securely packaged in appropriate, sealed containers, clearly labeled, and protected from moisture and light. Transport should occur under ambient conditions, with material safety data sheets (MSDS) included for handling and emergency reference.
    Storage Store **1-(4-Chlorophenyl)-1H-pyrrole** in a cool, dry, well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers. Keep the container tightly closed and protected from light. Handle under inert atmosphere if possible. Use appropriate personal protective equipment and comply with all safety guidelines and regulations for handling organic chemicals.
    Application of 1-(4-Chlorophenyl)-1H-Pyrrole

    Applications of 1-(4-Chlorophenyl)-1H-Pyrrole in Industrial Manufacturing

    1-(4-Chlorophenyl)-1H-Pyrrole serves as a targeted intermediate for the fine chemical sector. Our production process ensures batch consistency, traceability, and suitability for regulated industries. Presented below are key application fields supported by robust regulatory, formulation, and downstream process data.

    1. Pharmaceutical Intermediate for Antifungal API Synthesis

    Pharmaceutical companies use this compound in the synthesis pathway of certain triazole and imidazole antifungal actives. Its aromatic pyrrole structure enables regioselective coupling, particularly in late-stage heterocycle functionalization before final API crystallization. We supply this grade with a well-defined impurity profile, supporting validated process chemistries and regulatory clearance across major export markets.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) as per ICH Q7
    • 21 CFR Part 210/211 (USA)
    • EDQM CEP qualification for intermediate documentation (EU)
    • Ph. Eur., USP, and JP impurity limits for synthetic route acceptability

    Typical usage ratio

    • Applied at 0.3–0.6 molar equivalents relative to final API batch size
    • Adjustment based on pathway selectivity and impurity carryover risks

    Downstream process integration

    • Integrated in heterocycle-forming condensation step prior to triazole ring construction
    • Requires dry, inert handling with nitrogen blanketing for moisture-sensitive sequences
    • Enters process before purification and crystallization train

    Final product types

    • Active pharmaceutical ingredients (APIs) for topical and systemic antifungals
    • Key intermediates for veterinary drug actives

    2. Agrochemical Intermediate for Azole and Pyrrole-Based Fungicides

    Major agrochemical formulators select this molecule as a coupling partner in multi-step syntheses of advanced fungicidal actives, especially azole and pyrrole families. Its electron-rich core and selective halogen functionality ensure tailored reactivity during Suzuki or Buchwald-type coupling stages. Our material supports high-throughput, continuous-flow production setups typical in large-scale pesticide manufacturing.

    Industry compliance standards

    • ISO 9001:2015 certified quality management
    • REACH (EC 1907/2006) supply chain documentation and registration (EU)
    • EPA FIFRA technical-grade registration (USA)
    • FAO/WHO technical material purity specification for active ingredients

    Typical usage ratio

    • Blended at 0.45–0.75 molar equivalents in batch or continuous reactors
    • Titration aligns with yield optimization and downstream product selectivity

    Downstream process integration

    • Introduced during C–C or C–N bond-forming steps in azole skeleton assembly
    • Enters post-chlorination, pre-cyclization for pyrrole core construction
    • Handled under contained addition to prevent environmental release

    Final product types

    • Technical-grade fungicidal actives such as propiconazole derivatives
    • Emulsifiable concentrate and wettable powder pesticide formulations

    3. Chemical Intermediate for Electronic Materials and OLED Compounds

    Specialty electronic chemical manufacturers employ this compound in the controlled synthesis of functional pyrrole monomers. These monomers act as precursors for organic semiconductors and electroluminescent dyes. Its structural specificity supports high purity requirements for optical and electronic-grade downstream integration, particularly in the fabrication of OLED emitter layers and HTL (hole transport layer) materials.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) compliance for electronics manufacturing
    • IEC 62474 material declaration (EU/global)
    • ISO 14001:2015 for environmental management in electronic chemical production
    • Customer-validated impurity thresholds for optoelectronic applications

    Typical usage ratio

    • Used at 0.1–0.2 weight fraction relative to total monomer feed
    • Dosage tailored to target polymer characteristics and emission spectra

    Downstream process integration

    • Enters into controlled polymerization reactions for functionalized pyrrole backbones
    • Feeds directly to coupling reaction vessels ahead of purification and fractionation
    • Processed in solvent- and temperature-controlled environments to ensure batch uniformity

    Final product types

    • Precursor monomers for OLED device fabrication
    • Intermediate building blocks for organic field-effect transistor (OFET) materials

    4. Fine Chemical Intermediate for Specialty Dyes and Colorants

    The dye and pigment industry uses this compound for the targeted synthesis of pyrrole-based chromophores where a defined chloro-aryl substitution is needed to modulate light absorption. Its robust chemical profile allows precise control during azo-coupling or condensation dye routes, particularly in processes requiring tight shade control and reactivity for high-value performance pigments.

    Industry compliance standards

    • EN 71-3 (Toy Safety) for pigment use in consumer applications (EU)
    • Registration under TSCA for pigment intermediates (USA)
    • Comprehensive HSE and trace impurity documentation as per customer audit
    • Alignment to ETAD standards for dye intermediate production

    Typical usage ratio

    • Added at 0.15–0.38 molar equivalents, depending on chromophore target
    • Adjusted according to final pigment shade and lightfastness parameters

    Downstream process integration

    • Introduced during the coupling of pyrrole units in mixed aromatic dye frameworks
    • Handled in closed-system reactors prior to isolation and filtration of final pigment
    • Stable under high-temperature, water-based, or organic solvent synthesis steps

    Final product types

    • Performance organic dyes for specialized textile and coatings markets
    • Functional pigments for inks, plastics, and automotive coatings
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