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3-(4-Fluorophenyl)-1-Isopropyl-1H-Indole

    • Product Name 3-(4-Fluorophenyl)-1-Isopropyl-1H-Indole
    • Alias Fluoroisopropylindole
    • Einecs 696-038-8
    • 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

    356031

    Iupac Name 3-(4-Fluorophenyl)-1-isopropyl-1H-indole
    Molecular Formula C17H16FN
    Molecular Weight 253.31 g/mol
    Cas Number 1479582-47-4
    Appearance White to off-white solid
    Solubility Soluble in organic solvents, insoluble in water
    Chemical Class Synthetic indole derivative
    Smiles CC(C)n1cccc2c1cc(c3ccc(F)cc3)cc2
    Inchi InChI=1S/C17H16FN/c1-12(2)19-9-8-13-10-15(11-16(13)19)14-4-6-17(18)7-5-14/h4-12H,1-3H3
    Pubchem Cid 139025882
    Storage Conditions Store in a cool, dry place, away from light
    Synonyms 4F-PI, 1-Isopropyl-3-(4-fluorophenyl)indole

    As an accredited 3-(4-Fluorophenyl)-1-Isopropyl-1H-Indole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass vial, 5 grams, tightly sealed with a screw cap, labeled with chemical name, quantity, batch number, and hazard warnings.
    Shipping The chemical 3-(4-Fluorophenyl)-1-isopropyl-1H-indole is shipped in sealed, clearly labeled containers, compliant with applicable safety regulations. Packaging ensures protection from moisture, light, and physical damage. Transport follows chemical safety guidelines, with accompanying documentation for identification and hazard information. Handlers must use appropriate personal protective equipment during shipping and receiving.
    Storage Store 3-(4-Fluorophenyl)-1-isopropyl-1H-indole in a tightly sealed container, protected from light and moisture. Keep at room temperature in a cool, dry, and well-ventilated area. Ensure storage is away from incompatible substances such as strong oxidizers, acids, and bases. Clearly label the container, and restrict access to trained personnel only. Follow all safety and regulatory guidelines regarding chemical storage.
    Application of 3-(4-Fluorophenyl)-1-Isopropyl-1H-Indole

    Applications of 3-(4-Fluorophenyl)-1-Isopropyl-1H-Indole in Industrial Manufacturing

    As the actual manufacturer of 3-(4-Fluorophenyl)-1-Isopropyl-1H-Indole, we support a diverse range of advanced industrial sectors. Our material enables high-value synthesis routes across multiple regulated downstream segments. Below are the main application scenarios based on direct industrial demand and regulatory requirements.

    1. Pharmaceutical Intermediate for CNS Drug Synthesis

    Pharmaceutical firms use this indole derivative as a key building block in synthesizing central nervous system (CNS) active agents, particularly those targeting serotonin receptors. Its substitution pattern enhances binding specificity in structure-activity explorations, supporting late-stage development under Good Manufacturing Practice (GMP). Production teams integrate it in multi-step syntheses, requiring careful control of impurity profiles and reaction yields. Quality assurance teams reference regional pharmacopoeia requirements during scale-up and batch release.

    Industry compliance standards

    • cGMP (ICH Q7, US FDA 21 CFR Part 211, EU GMP Vol 4)
    • USP/EP monograph compliance for APIs
    • REACH Regulation (EC No. 1907/2006) registration
    • ICH Q3A/B for residual and impurity limits

    Typical usage ratio

    • 0.3–2.5 molar equivalents relative to final API target structure; exact ratio determined by route efficiency and yield requirements in scale-up

    Downstream process integration

    • Charged during Stage 2–4 intermediate coupling or ring closure steps in multi-step synthesis
    • Undergoes direct N-alkylation, Suzuki-Miyaura, or Buchwald–Hartwig reactions
    • Material enters closed system reactors, with in-process control (IPC) validation

    Final product types

    • Active pharmaceutical ingredients (APIs) for psychotropic medications
    • Serotonin and dopamine receptor agonists/antagonists
    • Investigational CNS drug candidates
    • Clinical trial samples and bulk API for finished dosage forms

    2. Specialty Agrochemical Research and Development

    Agrochemical innovators select this compound for novel research into fungicides and insecticides. Laboratory and pilot teams use it as a core scaffold to develop active ingredients targeting specific pest pathways. Process chemists optimize synthetic conditions to maintain activity and minimize byproducts. Regulatory sciences require detailed records for all lab and pilot quantities, governed by laboratory safety standards and global chemical inventory rules before field trials.

    Industry compliance standards

    • OECD GLP for laboratory synthesis and evaluation
    • ISO 9001:2015 quality management system
    • EPA TSCA inventory compliance (United States)
    • REACH Annex VII–X data requirements for new actives

    Typical usage ratio

    • 5–15% by mass in lead compound library synthesis; ratio varies with analog generation and synthetic design for bioassay batches

    Downstream process integration

    • Used as core fragment in the parallel synthesis of candidate libraries
    • Integrated during early lead optimization cycles for potency and selectivity screening
    • Scalability testing in pilot facilities with semi-automated synthesis platforms

    Final product types

    • New chemical entities (NCEs) for crop protection R&D
    • Experimental fungicidal and insecticidal actives
    • Patentable backbone structures for agrochemical innovation
    • Small-lot intermediates for regulatory submission studies

    3. Advanced Material Science: Organic Electronic Components

    Materials science laboratories leverage this indole derivative in synthesizing next-generation organic semiconductors. Its electronic properties contribute favorably in hole-transport layer (HTL) and organic field-effect transistor (OFET) R&D. Materials engineers rely on consistent quality for batch-to-batch reproducibility during thin-film device fabrication and performance testing. Manufacturing and research controls reference international electronic grade quality systems and material purity benchmarks.

    Industry compliance standards

    • ISO 9001:2015 for quality management
    • IEC 60747-1 semiconductor device standards
    • RoHS (2011/65/EU) restricted substances compliance
    • REACH SVHC monitoring for R&D quantities

    Typical usage ratio

    • 1–10% w/w in donor-acceptor blend formulations; actual loading varies with device architecture and targeted charge transport, optimized in pilot lines

    Downstream process integration

    • Dissolved into casting solvents for spin-coating or inkjet deposition
    • Integrated into polymer blends in the preparation of thin films for device prototyping
    • Material introduced post-filtration prior to substrate application stages

    Final product types

    • Organic light-emitting diode (OLED) test structures
    • Experimental thin-film transistors (TFTs)
    • Evaluation-grade organic photovoltaics (OPVs)
    • Semiconductive research monolayers and sensor substrates

    4. Fine Chemical Synthesis: Custom Intermediates for Contract Manufacturing

    Fine chemical and contract manufacturing organizations (CMOs/CDMOs) choose this specialty indole to prepare highly specific intermediates as part of advanced synthesis projects. Its unique structure offers tailored reactivity for downstream derivatization steps, especially in high-value custom molecules. Technical and quality teams maintain traceability with batch-specific documentation and full analytical support. Projects follow client-directed synthesis under strict quality agreements and ISO/ICH frameworks.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 certification for manufacturing
    • ICH Q7, Q9, and Q10 for regulated synthesis
    • REACH and GHS (Globally Harmonized System) chemical safety compliance
    • Project-specific client quality agreements and DMF/CMC standards

    Typical usage ratio

    • 0.8–3.0 molar equivalents per custom project scheme; ratio determined by required conversion and selectivity during N-functionalization or aryl coupling

    Downstream process integration

    • Added as principal core substrate in stepwise or convergent custom synthesis
    • Material purified by chromatography and crystallization after intermediate formation
    • Lot traceability maintained throughout batch and minor scale-up manufacturing

    Final product types

    • Specialty intermediates for pharmaceuticals or fine chemicals
    • Custom R&D compounds for global biotech clients
    • Chiral building blocks for enantioselective chemical synthesis
    • Protected scaffolds for further functional group transformations
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