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2-(4-Methylpiperazin-1-Yl)Aniline

    • Product Name 2-(4-Methylpiperazin-1-Yl)Aniline
    • Alias 4-Methyl-2-(piperazin-1-yl)aniline
    • Einecs 629-725-6
    • 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

    328527

    Chemicalname 2-(4-Methylpiperazin-1-yl)aniline
    Casnumber 60484-69-5
    Molecularformula C11H17N3
    Molecularweight 191.28
    Appearance Off-white to yellow powder
    Meltingpoint 70-74°C
    Solubility Soluble in DMSO, methanol
    Purity Typically ≥98%
    Smiles CN1CCN(CC1)C2=CC=CC=C2N
    Synonyms 2-Aniline-4-methylpiperazine, 2-(1-Methylpiperazin-4-yl)aniline
    Storagetemperature 2-8°C

    As an accredited 2-(4-Methylpiperazin-1-Yl)Aniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle with a secure screw cap, labeled “2-(4-Methylpiperazin-1-Yl)Aniline,” hazard symbols, and handling instructions.
    Shipping 2-(4-Methylpiperazin-1-yl)aniline is shipped in tightly sealed containers, protected from light and moisture. The packaging complies with chemical safety regulations, including labeling for hazardous materials if applicable. Transport is conducted via certified carriers, ensuring temperature control and safe handling to prevent leakage, degradation, or accidental exposure during transit.
    Storage 2-(4-Methylpiperazin-1-yl)aniline should be stored in a tightly closed container, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizing agents. Protect from light and moisture. Store at room temperature (15-25°C). Ensure proper labeling and avoid exposure to air. Use secondary containment to prevent spills and accidental release.
    Application of 2-(4-Methylpiperazin-1-Yl)Aniline

    Applications of 2-(4-Methylpiperazin-1-Yl)Aniline in Industrial Manufacturing

    As a direct manufacturer, we supply 2-(4-Methylpiperazin-1-Yl)Aniline for advanced industrial applications requiring consistent quality and precise formulation controls. Below we detail key downstream segments utilizing this intermediate, with industry standards, recommended ratios, process information, and representative end product types.

    1. Pharmaceutical Active Ingredient Synthesis

    Global pharmaceutical companies utilize this intermediate in multi-step organic syntheses to construct specific heterocyclic structures in regulated drug APIs, particularly in oncology and central nervous system projects. The material enters amidation or reductive amination stages for synthesis of final bioactive molecules subject to extensive validation and quality checks prior to regulatory submission.

    Industry compliance standards

    • ICH Q7 GMP (active pharmaceutical ingredient manufacture)
    • EU GMP Part II (European Commission)
    • USP/NF and EP monograph conformance for downstream API
    • FDA 21 CFR Part 210/211 (US drug process controls)

    Typical usage ratio

    • 10–25 mol% relative to final API yield, optimized by step yield and intermediate conversion rates

    Downstream process integration

    • Engaged post-core scaffold assembly, serving as a key nucleophilic partner in specific functional group introduction and ring closure reactions

    Final product types

    • Kinase inhibitor small molecules
    • Psychotropic drug active substances
    • Specialty anti-infective APIs
    • CNS disorder candidate molecules

    2. Agrochemical Intermediate for Herbicide Synthesis

    Leading agrochemical formulators source this compound for synthesis routes targeting modern herbicidal actives that require piperazine-linked aromatic amines. It supports downstream integration into multi-stage coupling and cyclization reactions for next-generation selective herbicides, following environmental and application safety reviews for the finished agricultural products.

    Industry compliance standards

    • FAO/WHO specification for technical active ingredients
    • REACH (EC No 1907/2006) chemical safety registration (EU)
    • US EPA FIFRA registration for finished herbicides
    • ISO 9001 certified process control

    Typical usage ratio

    • 5–18 mol% depending on target herbicide selectivity, adjusted for crop/no-crop application efficacy

    Downstream process integration

    • Introduced following key halogenation and activation steps, acting as a coupling partner for arylation and nitrogenous bridge formation in active ingredient cores

    Final product types

    • Selectivity-patterned weed control actives
    • Pre-emergent and post-emergent field herbicides
    • Rice and cereal crop protection agents
    • Herbicide intermediate isolates

    3. Specialty Dye and Pigment Manufacturing

    Major pigment and dye manufacturers employ this raw material in the synthesis of advanced chromophores, particularly for specialty azo and anthraquinone dye segments requiring piperazine ring substitution for fastness properties across technical textiles and plastics. The material enables specific color keying and improved substrate compatibility within controlled batchwise reactions and continuous processes.

    Industry compliance standards

    • OEKO-TEX Standard 100 (textile chemical safety)
    • EN 71-3 (migration of certain elements in toys for dye use)
    • GOTS v6.0 (for organic textile pigment approvals)
    • ISO 105-X12 (rubbing fastness testing for end product)

    Typical usage ratio

    • 2–12 wt% of crude dye batch, value adjusted per final shade, tinctorial strength, and application method

    Downstream process integration

    • Utilized at core azo-coupling stage or amidation for ring-modified colorant buildout, before downstream salting, milling, and blending

    Final product types

    • High-washfast textile dyes
    • Specialty plastic colorants
    • Automotive coating pigments
    • Non-woven fabric dyes

    4. Organic Electronic Material Synthesis

    Specialty electronics fabricators use this chemical for synthesis of aromatic amine intermediates designed for high-performance organic semiconductors and OLED display applications. Its role centers on the formation of conductive and emissive layers requiring precise molecular design to achieve specific electrical and photonic properties under high-purity regimes.

    Industry compliance standards

    • JEITA ET-7306 (organic electronic material guidelines, Japan)
    • ISO 14644 (cleanroom manufacturing standards, electronic materials)
    • RoHS 2011/65/EU (hazardous substance restrictions)
    • IPC-6012DA (rigid printed boards with organic semiconductive layers)

    Typical usage ratio

    • 1–7 wt% in emissive layer formulations, with batch variation for film uniformity and target mobility

    Downstream process integration

    • Introduced as a nucleophilic agent during precursor construction and polymerization for organic semiconductor backbone preparation, followed by purification and device-layer deposition

    Final product types

    • OLED panel base compounds
    • Organic transistor materials
    • Flexible display coatings
    • Photodetector specialty resins

    5. Advanced Polymer Additive Manufacturing

    High-end polymer compounders incorporate this molecule as a functional additive and chain modifier in custom engineering thermoplastic resins to impart specific anti-static, impact, or electrical properties. The compound integrates during extrusion or in situ polymerization for control of microstructure and performance, especially for high-value technical films and component housings.

    Industry compliance standards

    • UL 94 (flammability standard for plastic materials)
    • FDA 21 CFR 177.1810 (regulation for indirect food contact in polymers, where applicable)
    • ISO 11357 (thermal property testing for plastics)
    • REACH registration for all specialty additive components

    Typical usage ratio

    • 0.1–3 phr (parts per hundred resin), selected to balance property improvement with processing stability

    Downstream process integration

    • Directly fed to extruder or in melt-blend for matrix modification, followed by pelletizing, film blowing, or injection molding as per final application

    Final product types

    • Antistatic polyamide films
    • Polycarbonate electrical housings
    • Specialty conductive thermoplastic compounds
    • Protective casing polymers for electronics
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