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6-Fluoroindole-2-Carboxylic Acid

    • Product Name 6-Fluoroindole-2-Carboxylic Acid
    • Alias 6-Fluoro-1H-indole-2-carboxylic acid
    • Einecs 607-158-2
    • 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

    269010

    Product Name 6-Fluoroindole-2-Carboxylic Acid
    Cas Number 398-30-1
    Molecular Formula C9H6FNO2
    Molecular Weight 179.15 g/mol
    Appearance Off-white to light tan powder
    Purity Typically ≥98%
    Melting Point 244-248°C
    Solubility Slightly soluble in water, soluble in organic solvents (e.g., DMSO, methanol)
    Smiles C1=CC2=C(C(=C1)F)NC(=C2)C(=O)O
    Inchi InChI=1S/C9H6FNO2/c10-6-2-1-3-7-8(4-6)11-5-9(7)12/h1-5H,(H,11,12)
    Storage Temperature 2-8°C (refrigerated, dry conditions)
    Synonyms 6-Fluoro-1H-indole-2-carboxylic acid

    As an accredited 6-Fluoroindole-2-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 6-Fluoroindole-2-Carboxylic Acid, labeled with chemical details, hazard warnings, and batch information.
    Shipping 6-Fluoroindole-2-Carboxylic Acid is shipped in tightly sealed, clearly labeled containers, protected from moisture and light. Packages comply with chemical safety regulations and are cushioned to prevent breakage. All shipments include safety data sheets and handling instructions, ensuring safe and compliant delivery to laboratories or authorized industrial facilities.
    Storage Store 6-Fluoroindole-2-carboxylic acid in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, ideally at 2–8°C (refrigerated). Ensure the container is clearly labeled and kept away from incompatible substances such as strong oxidizing agents. Follow relevant safety and chemical handling guidelines.
    Application of 6-Fluoroindole-2-Carboxylic Acid

    Applications of 6-Fluoroindole-2-Carboxylic Acid in Industrial Manufacturing

    6-Fluoroindole-2-Carboxylic Acid serves as a specialty organic intermediate in several tightly regulated industrial manufacturing streams, providing indispensable molecular features to downstream formulators. As a dedicated producer, we enable precise integration of this fine chemical into advanced synthesis workflows while addressing key regulatory, formulation, and process requirements defined by leading application segments.

    1. Small Molecule Drug Synthesis: Oncology Pharmaceuticals

    Pharmaceutical manufacturers utilize 6-Fluoroindole-2-Carboxylic Acid as a fluorinated building block in the synthesis of active pharmaceutical ingredients (APIs) targeting kinase inhibition and novel cytotoxic agents. Its indole core and fluorinated position permit the construction of bioactive heterocycles and influence metabolic stability, playing a vital role during structure-activity relationship optimization in medicinal chemistry campaigns. Production batches are typically executed within FDA- and EMA-inspected facilities with full traceability and process validation.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • 21 CFR Parts 210/211 (US cGMP for pharmaceutical production)
    • European Pharmacopoeia (Ph. Eur.) monograph references for relevant final APIs
    • FDA/EMA New Drug Application (NDA/MAA) impurity threshold requirements

    Typical usage ratio

    • 5–20 mol% relative to the API main core structure; actual ratio adjusted by medicinal chemists for each target molecule’s synthetic sequence

    Downstream process integration

    • Enter at the heterocyclic core assembly stage, commonly via palladium-catalyzed coupling, followed by functionalization steps and direct incorporation into the central pharmacophore scaffold

    Final product types

    • Antineoplastic small molecule APIs (approved and clinical phase compounds)
    • Key intermediates for fluorescent probe-labeled kinase inhibitors
    • Specialty research compounds for preclinical oncology development

    2. Agrochemical Intermediate Manufacturing

    Producers in the crop protection sector require 6-Fluoroindole-2-Carboxylic Acid as a precursor in advanced synthetic routes for fluoroindole-based herbicides and systemic fungicides. Its defined substitution pattern establishes unique molecular recognition profiles with target enzymes in weeds and pathogenic fungi, supporting the development of next-generation crop protection agents. Compliance with quality and environmental standards is mandatory for downstream access to global markets.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for agrochemical ingredient production
    • OECD Good Laboratory Practice (GLP) for toxicological testing intermediates
    • EU Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market
    • FAO/WHO specifications for pesticide active ingredient production

    Typical usage ratio

    • 3–10% by weight in multi-component synthesis streams, with adjustment based on the desired level of fluorination and biological assay requirements

    Downstream process integration

    • Employed as a coupling partner during the indole ring construction phase, followed by sequential esterification, halogenation, and protective group removal steps, enabling scalable batch consistency

    Final product types

    • Patent-protected herbicides for broadleaf weed control
    • Systemic fungicide actives for cereal and fruit protection
    • Key raw materials for registered agrochemical active substances

    3. Active Ingredient for Veterinary Pharmaceuticals

    Veterinary drug manufacturers incorporate 6-Fluoroindole-2-Carboxylic Acid in the synthesis of small molecule APIs used for antiparasitics, targeting advanced metabolic stability and tissue selectivity in companion and farm animals. Rigorous veterinary pharmacopoeia requirements and GMP certification present key quality benchmarks for bulk chemical supply to finished dose producers.

    Industry compliance standards

    • VICH GL3: Stability Testing for New Veterinary Drug Substances
    • Veterinary medicinal products Good Manufacturing Practice (Directive 91/412/EEC)
    • Japanese Veterinary Pharmacopoeia references for actives
    • US Pharmacopeia (USP) general chapters for veterinary APIs

    Typical usage ratio

    • 4–12 mol% depending on the specific veterinary drug chemical route, adjusted to enable efficient stage-wise synthesis and downstream purification ease

    Downstream process integration

    • Introduced in early-stage heterocycle formation, commonly via direct fluorination or amidation, then funneled through sterilizable synthetic routes to meet veterinary use requirements

    Final product types

    • Antiparasitic actives for livestock injectable solutions
    • Oral veterinary drug formulations for companion animal care
    • Intermediate compounds for extended-release veterinary pharmaceuticals

    4. Chemical Synthesis of Organic Electronics Materials

    Manufacturers of organic electronic devices utilize 6-Fluoroindole-2-Carboxylic Acid as a functional building block in the development of semiconducting polymers and charge transport materials. The fluorinated indole structure imparts increased molecular planarity and alters electronic characteristics, addressing key operational parameters in polymer light-emitting diodes and photovoltaic applications. Consistent quality, traceability, and integration with advanced material QC protocols are tightly maintained throughout the formulation and device assembly process.

    Industry compliance standards

    • RoHS 3 Directive (EU 2015/863) for hazardous substances in electronic components
    • ISO 14001:2015 Environmental Management Systems for electronics manufacturing
    • REACH Regulation (EC) No 1907/2006 for chemical substance registration and traceability
    • IEC 62899-201 series for printed electronics materials testing

    Typical usage ratio

    • 1–5 wt% as a monomer feedstock in initial polymerization batches, ratio optimized based on target electrical mobility and film formation profile

    Downstream process integration

    • Fed during the monomer synthesis phase, followed by in-line purification and controlled copolymerization to yield custom electronic grade polymers

    Final product types

    • Semiconducting polymers for organic TFT backplanes
    • Active layer materials in organic photovoltaic cells
    • Indole-based emissive components for OLED displays
    Free Quote

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