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1-(2-Aminophenyl)Pyrrole

    • Product Name 1-(2-Aminophenyl)Pyrrole
    • Alias 1-(2-Aminophenyl)-1H-pyrrole
    • Einecs 629-279-8
    • 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

    214816

    Productname 1-(2-Aminophenyl)Pyrrole
    Casnumber 28720-22-1
    Molecularformula C10H10N2
    Molecularweight 158.20
    Appearance Solid
    Color Off-white to pale yellow
    Meltingpoint 58-62°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Smiles c1ccc2c(c1)cccc2N
    Inchi InChI=1S/C10H10N2/c11-9-5-3-4-8-10(9)12-6-1-2-7-12/h1-8H,11H2
    Synonyms 2-(1H-pyrrol-1-yl)aniline
    Storageconditions Store at room temperature in a tightly closed container

    As an accredited 1-(2-Aminophenyl)Pyrrole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25 g quantity of 1-(2-Aminophenyl)pyrrole is supplied in a sealed amber glass bottle with a secure screw cap.
    Shipping 1-(2-Aminophenyl)Pyrrole is shipped in secure, airtight containers to prevent contamination and moisture absorption. Packaging complies with relevant chemical safety regulations, including labeling for hazardous substances. Shipments are handled through certified carriers, ensuring careful handling and tracking. Appropriate documentation and safety data sheets (SDS) are included with every order for safe transit and receipt.
    Storage 1-(2-Aminophenyl)pyrrole should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Protect it from light and moisture. Store at room temperature and avoid heat or ignition sources. Ensure labeling is clear and follow all standard laboratory chemical storage protocols.
    Application of 1-(2-Aminophenyl)Pyrrole

    Applications of 1-(2-Aminophenyl)Pyrrole in Industrial Manufacturing

    As a direct manufacturer of 1-(2-Aminophenyl)Pyrrole, we supply this advanced intermediate to key segments of chemical processing, supporting strict sector standards and downstream integration protocols. Below, we outline real industrial use cases across defined sectors, detailing compliance, recommended concentrations, production steps, and resulting finished goods.

    1. Pharmaceutical Active Ingredient Synthesis (API Intermediates for Antipsychotic Drugs)

    Major pharmaceutical manufacturers utilize 1-(2-Aminophenyl)Pyrrole as a core building block in multi-step syntheses of heterocyclic antipsychotic agents, notably including aripiprazole and its analogs. Its selective aminophenyl-pyrrole structure enables efficient construction of the aryl piperazine scaffold under closely regulated batch conditions. Adhering to regulatory standards, our material supports synthesis routines where yield, impurity profiles, and trace metal content directly impact API registration.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapters & Impurity Guidelines
    • EU Regulation 536/2014 on clinical trial APIs
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • Stoichiometric ratios commonly range from 0.8 to 1.2 mol equivalent relative to the subsequent cyclization agent. Final inclusion level varies with the arylpiperazine target structure and yield/reaction selectivity.

    Downstream process integration

    • Introduced during the condensation stage following precursor amide activation; often purified by crystallization prior to final piperazine ring-closure and acylation.

    Final product types

    • Aripiprazole APIs and their pharmaceutical salts (e.g., aripiprazole lauroxil)
    • Other quinolinone- or piperazine-based antipsychotic drug substances

    2. Specialty Dye Manufacture (High-Performance Pigments for Electronics & Printing)

    Key pigment producers rely on 1-(2-Aminophenyl)Pyrrole as an intermediate for synthesizing high-stability organic dyes, prized for their chromatic purity and lightfastness in OLED display coatings and advanced inkjet formulations. The unique electron-rich pyrrole ring confers exceptional chromophore rigidity for color-rich pigment backbones through targeted condensation and coupling chemistry. Precision in the handling and dosing of this material directly impacts hue specificity and thermal stability of the final pigment.

    Industry compliance standards

    • EN 71-3:2019 Safety of Toys—Migration of Certain Elements (for inks/dyes in toy applications)
    • RoHS Directive (2011/65/EU) for restricting hazardous substances in electronics
    • ISO 2846 Part 1: Color and transparency measurement for printing inks
    • Global Automotive Declarable Substance List (GADSL) for pigment chemistry in electronics

    Typical usage ratio

    • Integrates at 2–8% by weight relative to total pigment intermediate; adjusted for desired tinting strength and solubility in the final formulation matrix.

    Downstream process integration

    • Added during the high-temperature azo-coupling or oxidative cyclization step, preceding pigment grinding and dispersion for masterbatch compounding.

    Final product types

    • OLED display dyes and conductive pigment dispersions
    • High-purity printing inks for security and anti-counterfeiting applications

    3. High-Temperature Polymer Additives (Specialty Engineering Plastics and Composites)

    Advanced polymer compounders incorporate 1-(2-Aminophenyl)Pyrrole into specialty polymer matrices, exploiting its dual amine and pyrrole functions as a crosslinking promoter and electronic modifier within polyimide and polyarylamide backbones. This leads to improved thermal resistance and dielectric properties vital for aerospace, automotive, and high-performance electronics, where strict durability and reliability controls govern material adoption.

    Industry compliance standards

    • UL 94 Flame Retardancy Standard for Plastics
    • ASTM D5948: Thermoset Molding Compound Specifications
    • IEC 61249-2-21: Base materials for printed circuit boards (halogen-free requirements)
    • REACH Regulation (EC) No 1907/2006—Annex XVII restrictions

    Typical usage ratio

    • Formulation levels between 0.1–2.5% by weight of total resin, depending on the specific performance requirements for crosslink density and electrical properties.

    Downstream process integration

    • Incorporated during the pre-polymerization pre-mix; reacts under controlled temperature and vacuum in batch or continuous reactors prior to molding, extruding, or casting processes.

    Final product types

    • High-performance polyimide films and sheets
    • Specialty thermoset composite laminates for circuit boards and aerospace panels

    4. Specialty Chemical Synthesis (Precursors for Pest Control Agents)

    Producers of active pesticide compounds employ 1-(2-Aminophenyl)Pyrrole as a specific synthetic precursor in the route towards select heterocycle-based insecticides and fungicides. Its defined substitution pattern supports regioselective formation of bioactive rings and side chains during proprietary process scale-ups. Traceability and analytical purity are critical, as the material passes through multiple controlled transformations before final formulation.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Plant Protection Products
    • EPA 40 CFR Part 158: Data Requirements for Pesticides
    • OECD Guidelines for the Testing of Chemicals—Analytical Methods and Purity Criteria
    • Good Laboratory Practice (GLP) under OECD Principles

    Typical usage ratio

    • Ranges from 0.5–1.5 molar equivalents, calculated based on the core molecular scaffold of the desired active pesticide; variations determined by downstream reaction yield studies.

    Downstream process integration

    • Engaged as the primary aromatic amine in nucleophilic substitution or heterocycle ring-closing steps; intermediates isolated and purified prior to formulation into technical concentrates.

    Final product types

    • Crop protection active substances in technical grade form for further formulation
    • Commercial fungicide and insecticide finished products
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