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4-Chloro-3-Nitroquinoline

    • Product Name 4-Chloro-3-Nitroquinoline
    • Alias 4-chloro-3-nitroquinoline
    • Einecs 249-620-7
    • 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

    165531

    Chemicalname 4-Chloro-3-Nitroquinoline
    Molecularformula C9H5ClN2O2
    Molecularweight 208.60 g/mol
    Casnumber 181950-60-3
    Appearance Yellow crystalline powder
    Meltingpoint 120-124°C
    Solubility Slightly soluble in organic solvents
    Purity Typically ≥98%
    Storageconditions Store in a cool, dry place, protected from light
    Smiles Clc1ccc2nccc([N+](=O)[O-])c2c1
    Inchikey VIAHZUPIQNPACl-UHFFFAOYSA-N

    As an accredited 4-Chloro-3-Nitroquinoline 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 4-Chloro-3-Nitroquinoline, sealed with a screw cap, labeled with safety and hazard information.
    Shipping 4-Chloro-3-Nitroquinoline is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. Packages are labeled according to regulatory requirements, with appropriate hazard warnings. The substance is transported under controlled conditions—protected from light, moisture, and incompatible materials—to ensure safety and chemical integrity during transit.
    Storage 4-Chloro-3-nitroquinoline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Store separately from strong oxidizing or reducing agents, acids, and bases. Proper labeling and secondary containment are recommended to prevent accidental release or contamination. Use appropriate chemical storage cabinets for additional safety.
    Application of 4-Chloro-3-Nitroquinoline

    Applications of 4-Chloro-3-Nitroquinoline in Industrial Manufacturing

    We directly supply 4-Chloro-3-Nitroquinoline to global manufacturers seeking reliable upstream intermediates for advanced industrial applications. Below, we detail its integration across major verified downstream sectors, focusing on real-world compliance, practical formulation guidelines, downstream production methods, and delivering end-use product types.

    1. Pharmaceutical Intermediate Synthesis for Antineoplastic Agents

    Leading pharmaceutical production sites source our material as a key quinoline intermediate to construct molecular cores for anticancer drug APIs, specifically fused heterocyclic scaffolds in late-stage synthesis. Its electron-withdrawing substituents provide controlled reactivity for selective palladium-catalyzed reactions, supporting rigorous process controls mandated for regulated medicine ingredient supply.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • EU GMP Part II
    • US FDA 21 CFR Part 211
    • European Pharmacopoeia, section 2.6.13 (Residue on Ignition)

    Typical usage ratio

    • 0.7–2.0 molar equivalents; exact aliquot set by target yield and purification constraints

    Downstream process integration

    • Palladium-catalyzed C-N or C-C coupling as Stage III or IV in multi-step API synthesis route; introduced after core scaffold formation, prior to deprotection and purification

    Final product types

    • Quinoline-based antineoplastic APIs (e.g., kinase inhibitors)
    • Key intermediates for investigational oncology drugs

    2. Agrochemical Intermediate for Crop Protection Products

    Commercial crop protection actives manufacturers employ our material for synthesizing substituted quinoline derivatives, serving as chemical precursors in the construction of insecticidal or herbicidal agents. Companies depend on its predictable halogen-nitro substitution pattern to enable reliable downstream coupling and nucleophilic aromatic substitution for scalable batch processing.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management System
    • China GB 2763 (Pesticide Maximum Residue Limits in Foods)
    • REACH Registration (EC No. 1907/2006) for import to Europe

    Typical usage ratio

    • Between 0.4% and 1.8% w/w in intermediate step compounds, adjusted depending on downstream target molecular structure and impurity control requirements

    Downstream process integration

    • Charged to the main reactor vessel during nucleophilic aromatic substitution with amines or thiols, in a mid-stream stage after initial chlorination; followed by neutralization, extraction, and further functionalization

    Final product types

    • Herbicide active ingredient intermediates (e.g., quinoline-based herbicides)
    • Precursors to broad-spectrum insecticides

    3. Fluorescent Probe and Dye Intermediate for Analytical Chemistry

    Suppliers of specialty dyes and analytical reagents use this compound to synthesize highly substituted quinoline chromophores, necessary for developing fluorescent probes and chemical sensors. Its nitro and chloro substituents facilitate site-selective functionalization and yield high-purity dye building blocks essential for fluorescence intensity and low background interference in analytical tools.

    Industry compliance standards

    • ISO/IEC 17025:2017 Laboratory Accreditation (for QC measurements)
    • RoHS Directive 2011/65/EU (for electronic and optical applications)
    • EN 71-3:2019 (Safety of Toys – migration of certain elements, relevant for dyes)

    Typical usage ratio

    • 0.1–2.5% of reaction batch, tailored by desired chromophore intensity and probe stability needs

    Downstream process integration

    • Undergoes electrophilic substitution in the core dye synthesis reactor; used as a starting intermediate for coupling with electron-rich arenes or alkylamines under controlled temperature and oxygen exclusion

    Final product types

    • Fluorescent probe precursors for biological staining
    • Quinoline-based analytical dyes for laboratory and diagnostic applications

    4. Electronic Material Precursor for OLED and Semiconductor Sectors

    In high-purity electronics, chemical materials developers specify this compound for advanced organic synthesis routes that deliver functionalized quinoline derivatives. It acts as a core building block in manufacturing charge-transporting materials, emitters, and hole-transport layers for organic light-emitting diode (OLED) displays and thin-film devices. Highly specialized process and purity controls underpin the formulation for electronics compatibility.

    Industry compliance standards

    • JEITA ED-7303 (Standard test methods for organic semiconductors)
    • IPC-1752A (Material Declaration Management Standard)
    • ISO 14001:2015 Environmental Management (relevant for cleanroom use)

    Typical usage ratio

    • 0.15–1.1 molar equivalents per target compound, with final range optimised according to film-forming and photostability characterization during thin-film deposition trials

    Downstream process integration

    • Introduced in early-stage organic synthesis prior to cyclization or Suzuki coupling; material purity monitored through HPLC before integration into polymerization or co-evaporation steps for OLED stack assembly

    Final product types

    • Monomers for OLED hole transport and emission layers
    • Quinoline-based electron transport additives for display, photovoltaic, and sensor applications
    Free Quote

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