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N4-(2-Methylpropyl)-3,4-Quinolinediamine

    • Product Name N4-(2-Methylpropyl)-3,4-Quinolinediamine
    • Alias PQ15
    • Einecs 629-783-4
    • 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

    208431

    Chemical Name N4-(2-Methylpropyl)-3,4-Quinolinediamine
    Molecular Formula C13H19N3
    Molecular Weight 217.31 g/mol
    Cas Number 164776-48-1
    Appearance Solid
    Color Pale yellow to brown
    Solubility Slightly soluble in water
    Purity Typically >97%
    Storage Conditions Store in a cool, dry place
    Synonyms 4-(2-Methylpropylamino)quinoline-3-amine

    As an accredited N4-(2-Methylpropyl)-3,4-Quinolinediamine 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 100 grams of N4-(2-Methylpropyl)-3,4-Quinolinediamine, with tamper-evident cap and hazard labeling.
    Shipping **Shipping Description:** N4-(2-Methylpropyl)-3,4-Quinolinediamine should be shipped in tightly sealed containers, protected from moisture and direct sunlight. Handle with appropriate chemical safety procedures. Transport in accordance with local, national, and international regulations, ensuring compatibility with other substances. Include proper labeling, safety documentation, and emergency contact information with the shipment.
    Storage N4-(2-Methylpropyl)-3,4-Quinolinediamine should be stored in a tightly sealed container, protected from light and moisture. Store at room temperature in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Ensure proper chemical labeling, and keep away from sources of ignition or heat. Use secondary containment to prevent spills or leaks.
    Application of N4-(2-Methylpropyl)-3,4-Quinolinediamine

    Applications of N4-(2-Methylpropyl)-3,4-Quinolinediamine in Industrial Manufacturing

    As a direct global manufacturer of specialty quinoline derivatives, we supply N4-(2-Methylpropyl)-3,4-Quinolinediamine to precision markets with proven downstream integration. Below we outline real-world deployment across key industrial segments, detailing regulatory considerations, formulation guidance, incorporation procedures, and the variety of high-value finished goods our partners produce.

    1. Antioxidant Agent in Rubber Compounding

    Downstream tire and technical rubber formulators rely on this quinolinediamine derivative as a key antioxidant to inhibit thermal-oxidative degradation and prolong service life under demanding load and temperature cycles. Manufacturers of conveyor belts, automotive weather seals, and industrial hoses require slow-migrating, high-performance amine antioxidants that withstand repeated flexing and ozone exposure, ensuring dimensional integrity and resistance to brittle cracking in harsh real-world applications.

    Industry compliance standards

    • ASTM D3156: Standard Specification for Rubber Antioxidants
    • ISO 9001:2015 Quality Management Systems for rubber production
    • REACH (EC 1907/2006) chemical registration and safety compliance
    • US EPA TSCA Inventory for rubber chemical use

    Typical usage ratio

    • Range: 0.5%–2.0% by weight in the total elastomer matrix; modified upward in low-filler, high-thermal-stress applications, and downward in blends with synergistic antidegradants.

    Downstream process integration

    • Added during internal mixing, following elastomer polymer charge but before curatives; uniform dispersion ensured by pre-blending with reinforcing fillers.

    Final product types

    • Radial passenger car and truck tire treads
    • Industrial conveyor belts
    • Automotive sealing profiles and hoses
    • Heavy-duty agricultural equipment tires

    2. Intermediate in Synthesis of Antimalarial Pharmaceuticals

    Chemical manufacturers active in pharmaceutical synthesis utilize this quinolinediamine as a privileged intermediate in the multi-step preparation of active pharmaceutical ingredient (API) scaffolds for quinoline-based antimalarials. Its aminated structure enables site-selective coupling and functionalization crucial for downstream medicinal synthesis, supporting large-scale implementation in cGMP-compliant environments for global healthcare markets.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • USP-NF monographs (specific to downstream API synthesis)
    • European Pharmacopoeia 11.0 (contaminant and impurity profiling)
    • FDA 21 CFR Part 211: Current Good Manufacturing Practice for Finished Pharmaceuticals

    Typical usage ratio

    • Stoichiometric; typically equimolar feed in condensation or cyclization with on-site optimization based on yield trials and impurity minimization.

    Downstream process integration

    • Charged as a primary building block in batch or flow chemistry set-ups; initial combination with acylating agents or aldehydes, followed by purification and intermediate isolation prior to final API formation.

    Final product types

    • Chloroquine analog intermediates
    • Novel 4-aminoquinoline antimalarials
    • Precursor blocks for anti-parasitic drug development

    3. Polymer Stabilizer for Industrial Coatings

    Leading producers of polyurethane and epoxy systems employ N4-(2-Methylpropyl)-3,4-Quinolinediamine as a process stabilizer and antioxidant to inhibit yellowing, viscosity drift, and oxidative crosslinking during both storage and curing. Non-migrating amine stabilizers are critical in high-durability coatings that require extended shelf stability, UV resistance, and color retention in outdoor architectural and marine applications.

    Industry compliance standards

    • EN 1504-2: Products and systems for protection of concrete surfaces
    • ISO 12944-6: Paints and varnishes for corrosion protection
    • REACH (EC 1907/2006) chemical registration for coating additives
    • ASTM D16: Standard Terminology for Paint, Related Coatings, Materials, and Applications

    Typical usage ratio

    • 0.2%–1.0% by weight of total resin solids; raised in multi-layer systems exposed to high UV or industrial pollutants, and adjusted in concert with pigment load to minimize reactivity side effects.

    Downstream process integration

    • Dispersed pre-polymerization into resin batch; optionally co-dispersed with other stabilizer packages in pigment grinding phase to ensure homogeneous integration.

    Final product types

    • Outdoor polyurethane architectural coatings
    • High-gloss epoxy floor finishes
    • Protective ship deck and hull paints
    • Chemical-resistant storage tank linings

    4. Chemical Intermediate in Agrochemical Synthesis

    Producers of agrochemical actives incorporate the quinolinediamine backbone to construct nitrogen heterocycle structures in select herbicide and fungicide molecules. This aromatic diamine offers rapid integration in stepwise condensation and alkylation reactions, essential for producing advanced heterocyclic actives with controlled release and target selectivity required by modern integrated crop management programs.

    Industry compliance standards

    • FAO/WHO JMPR Guidelines for pesticide technical grade materials
    • ISO 17025:2017 for agrochemical analytical testing
    • REACH (EC 1907/2006) for crop protection chemical substances
    • Chinese GB 2763—National Food Safety Standard for Maximum Residue Limits for Pesticides

    Typical usage ratio

    • Batch-dependent; typically 1.0–1.5 equivalents relative to halogenated intermediates in the first condensation, with fine-tuning based on reaction stoichiometry and minimization of by-products.

    Downstream process integration

    • Fed as the key aminating agent post-halogenation and prior to final molecular derivatization; product purified for downstream microencapsulation or carrier formulation.

    Final product types

    • Quinoline-based systemic fungicides
    • N-heterocyclic selective herbicide actives
    • Precursor molecules for next-generation crop protection products
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