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4-Methylquinoline

    • Product Name 4-Methylquinoline
    • Alias Gassman’s base
    • Einecs 202-604-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales6@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    324739

    Cas Number 491-35-0
    Molecular Formula C10H9N
    Molar Mass 143.19 g/mol
    Iupac Name 4-Methylquinoline
    Appearance Colorless to pale yellow liquid
    Boiling Point 258-259 °C
    Melting Point 12 °C
    Density 1.053 g/cm³
    Flash Point 111 °C
    Solubility In Water Slightly soluble
    Structure Quinoline ring substituted at the 4-position with a methyl group
    Pubchem Cid 10145

    As an accredited 4-Methylquinoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 4-Methylquinoline is packaged in a 100 mL amber glass bottle with a secure screw cap and hazard labeling.
    Shipping 4-Methylquinoline should be shipped in tightly sealed containers, protected from light and moisture. Transport must comply with local and international regulations for hazardous chemicals. Use appropriate cushioning and labeling to prevent leaks or spills. Ensure ventilation during transit and store away from incompatible substances, such as strong oxidizing agents, during shipment.
    Storage 4-Methylquinoline should be stored in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep the container tightly closed and properly labeled. Separate from incompatible substances such as strong oxidizers and acids. Store in a chemical-resistant container, ideally in a flammable materials cabinet, to prevent accidental release or contact.
    Application of 4-Methylquinoline

    Applications of 4-Methylquinoline in Industrial Manufacturing

    As the direct manufacturer of 4-Methylquinoline, we serve a range of industrial sectors that require high-purity quinoline derivatives for advanced synthesis. Each application area reflects established market usage and demonstrates our focus on compliance, controlled formulation, and integration into specialized downstream processes.

    1. Synthesis of Agrochemical Intermediates

    Leading agrochemical companies use 4-Methylquinoline as a crucial building block for newer classes of pesticides and herbicide intermediates. The methyl-substituted quinoline structure increases molecular reactivity in heterocyclic coupling, especially in constructing fungicidal scaffolds and selective weed control agents. Our product meets consistent purity specifications to prevent side-reactions that impact crop protection compounds’ performance. Production lines monitor quinoline input at every batch load, with traceability for regulatory audits and export documentation.

    Industry compliance standards

    • FAO/WHO specifications for pesticide precursors
    • REACH (EC 1907/2006) registration for chemical intermediates
    • ISO 9001:2015 quality management
    • China National Standard GB 2763 guidance for raw input substances

    Typical usage ratio

    • 2–12% by weight, varying according to the downstream heterocyclic synthesis path and required actives’ purity. Higher loading improves yield for specific methylated quinoline-based actives.

    Downstream process integration

    • Loaded into closed high-shear reactors for initial cyclization and alkylation stages
    • Batch input tracked for cradle-to-grave documentation
    • Subjected to solvent recovery and mother liquor recycling steps
    • Maintained under inert nitrogen during handling to minimize side reaction

    Final product types

    • Pyridine-derived herbicides
    • Quinoline-based fungicide intermediates
    • Rice and cereal crop protection active agents
    • Methylquinoline markers for environmental detection of pesticide drift

    2. Pharmaceutical Intermediate Manufacturing

    Pharmaceutical synthesis teams select 4-Methylquinoline for constructing regulated APIs, including anti-tuberculosis and antimalarial drugs where methylated heterocycles enhance biological activity. Strict GMP practices apply from raw material reception to wet hydrogenation and cross-coupling stages. Quality system alignment assures absence of unwanted isomers or halogenated by-products entering the route to final API crystallization. Customers benefit from reference batch COAs and impurity profiling.

    Industry compliance standards

    • ICH Q7 (GMP for Active Pharmaceutical Ingredients)
    • USP/NF reference for raw material identity and purity
    • FDA 21 CFR Part 211 requirements for process input documentation
    • European Pharmacopoeia 10.0 (EP) monographs for quinoline derivatives

    Typical usage ratio

    • 4–9% by mole relative to the target pharmacophore, exact dosage tailored to multi-step API yield optimization and chiral integrity.

    Downstream process integration

    • Added to glass-lined reactors during intermediate salt formation
    • Used in Suzuki-Miyaura or Buchwald coupling reactions for further derivatization
    • Monitored by HPLC and GC for residual raw material and methylated byproducts
    • Subjected to in-process QC checkpoints according to customer’s DMF requirements

    Final product types

    • Rifamycin derivatives
    • Synthetic antimalarial agents such as chloroquine analogs
    • Methylquinoline-substituted anti-infective intermediates
    • Research compounds for clinical trial API scale-up

    3. Dye and Pigment Intermediate Production

    Dyestuff manufacturers utilize 4-Methylquinoline in the synthesis of specialized organic pigments, particularly those needed in high-performance printing inks and plastics coloration. Reactivity at the 4-methyl position allows for tailored azo coupling, generating stable chromophores and UV-resistant colorants. Stringent specifications for color consistency and purity are validated through batch retention samples and spectroscopic analysis.

    Industry compliance standards

    • EU REACH for dye intermediates safety
    • ISO 9001:2015 certification for process traceability
    • RoHS Directive 2011/65/EU for pigment use in electronics
    • OEKO-TEX® Standard 100 for textile dyeing inputs

    Typical usage ratio

    • 3–10% of pigment precursor input, with adjustments based on chromophore yield and targeted fastness parameters.

    Downstream process integration

    • Formulated into condensation step for quinoline-based pigment chains
    • Controlled heating and pH regulation during integration
    • Subjected to solvent extraction and washing to eliminate unreacted material
    • Final product standardized for color depth and stability

    Final product types

    • Quinoline-derived yellow and orange pigments
    • Lightfast printing ink colorants
    • High-purity dyes for plastics compounding
    • Organic pigments for specialty film coatings

    4. Corrosion Inhibitor Formulation for Petroleum Refineries

    Major refinery and pipeline operators add 4-Methylquinoline during corrosion inhibitor blending to enhance protective efficacy against acidic and sulfur-rich environments. Its amine structure interacts with metal surfaces, providing a stable barrier layer in high-temperature and high-pressure circuit systems. Formulators monitor dosage for compatibility with pipeline transport and minimize risk of fouling or operational downtime. Safety and environmental compliance feature prominently in MSDS and logistics documentation.

    Industry compliance standards

    • ASTM D665 for rust-preventing characteristics in hydrocarbon fluids
    • ISO 15597 for refinery additive quality
    • API RP 939-C (Materials Selection and Corrosion Control for Downstream Operations)
    • Global GHS (UN Purple Book) for inhibitor labeling and handling

    Typical usage ratio

    • 0.5–3% by final inhibitor solution, optimized per crude grade and flow rate conditions. Adjustment based on local corrosion survey data.

    Downstream process integration

    • Pre-mixed with base oil and specialty surfactants in blending tanks
    • Injected online prior to metal surface exposure in pipelines or vessels
    • Routine sampling and corrosion rate measurement to verify efficacy
    • COA and lot tracking required for audits and spill response

    Final product types

    • Pipeline and refinery corrosion inhibitor concentrates
    • Aqueous and oil-soluble protective additives
    • Anti-rust packages for drilling fluids
    • Blended chemical treatment products for downstream petrochemical units

    5. Organic Electronic Material Synthesis

    Research and industrial customers in the field of organic electronics integrate 4-Methylquinoline as an intermediate in the synthesis of charge transport materials and small-molecule semiconductors. The molecule’s conjugated core and methyl substituent provide fine-tuning for electronic band gaps and optimize charge mobility, especially in OLED and OFET layers. Precision in raw material quality is fundamental to reproducibility of electrical characteristics in display and photovoltaic devices.

    Industry compliance standards

    • IEC 62679 standards for electronic display manufacturing
    • ISO 14644 cleanroom practices for material processing
    • RoHS 3 (EU 2015/863) for electronic product composition
    • Internal QC protocols for semiconductor-grade organics

    Typical usage ratio

    • 5–15% of organic blend by mole in charge-transport layer synthesis, adjusted according to device layer thickness and fabrication method.

    Downstream process integration

    • Dispensed into glovebox for controlled anhydrous reactions
    • Integrated into polymerization or co-evaporation steps
    • Subjected to thin-film deposition on pre-treated substrates
    • Quality verified through spectroscopy and charge mobility testing

    Final product types

    • Electron/hole transport materials for OLED displays
    • Semiconducting layers for organic photovoltaics
    • Active-layer blends in OFET devices
    • Research materials for flexible electronics R&D
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