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1-[2-(2,5-Dimethyl-1H-Pyrrol-1-Yl)Ethyl]Piperazine

    • Product Name 1-[2-(2,5-Dimethyl-1H-Pyrrol-1-Yl)Ethyl]Piperazine
    • Alias DMPEP
    • Einecs 687-494-7
    • 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
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    Specifications

    HS Code

    110222

    Iupac Name 1-[2-(2,5-Dimethyl-1H-pyrrol-1-yl)ethyl]piperazine
    Molecular Formula C12H21N3
    Molecular Weight 207.32 g/mol
    Cas Number 881677-41-6
    Smiles CC1=CC(N1CCN2CCNCC2)=C
    Appearance Off-white to yellow solid
    Solubility Soluble in common organic solvents (e.g., DMSO, methanol)
    Purity Typically ≥ 98% (as provided by suppliers)

    As an accredited 1-[2-(2,5-Dimethyl-1H-Pyrrol-1-Yl)Ethyl]Piperazine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "1-[2-(2,5-Dimethyl-1H-Pyrrol-1-Yl)Ethyl]Piperazine, 5g". Tamper-evident seal; includes safety and handling instructions.
    Shipping The chemical 1-[2-(2,5-Dimethyl-1H-Pyrrol-1-Yl)Ethyl]Piperazine is securely packaged in sealed, chemical-resistant containers to prevent leakage or contamination. Shipped via certified carriers compliant with safety regulations, it includes appropriate hazard labeling and documentation. Care is taken to avoid temperature extremes, moisture, or direct sunlight during transit for product integrity.
    Storage Store 1-[2-(2,5-dimethyl-1H-pyrrol-1-yl)ethyl]piperazine in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep away from oxidizing agents, acids, and incompatible substances. Ensure storage area is equipped with spill containment and proper labeling. Follow standard laboratory chemical storage protocols for safe handling.
    Application of 1-[2-(2,5-Dimethyl-1H-Pyrrol-1-Yl)Ethyl]Piperazine

    Applications of 1-[2-(2,5-Dimethyl-1H-Pyrrol-1-Yl)Ethyl]Piperazine in Industrial Manufacturing

    As a direct manufacturer of 1-[2-(2,5-Dimethyl-1H-Pyrrol-1-Yl)Ethyl]Piperazine, we offer this specialty intermediate for select advanced chemical industries that demand strict process control and traceability. Industrial users rely on this compound for its defined chemical behavior and compatibility in complex synthetic routes. The following sections provide application-specific details, with a focus on real regulatory, processing, and product use in each downstream segment.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical manufacturers integrate this raw material in multi-step syntheses of piperazine-based APIs, particularly in the production of CNS-active agents and antihistamine derivatives. The compound serves as a key bridging segment, enabling specific side-chain chemistries while maintaining control of isomerism and impurity profiles. Strict adherence to validated synthetic protocols and batch records is required throughout the process.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US FDA cGMP for Finished Pharmaceuticals)
    • European Pharmacopoeia Monographs for related piperazine intermediates
    • Chinese Pharmacopoeia standards for intermediates (where applicable)

    Typical usage ratio

    • 5–15% by molar feed ratio in stepwise synthesis, adjusted according to API yield requirements and reaction kinetics

    Downstream process integration

    • Charged during the nucleophilic substitution step after initial heterocycle formation
    • Monitored by in-process HPLC to confirm completion prior to quenching, followed by thorough impurity analysis
    • Final stage: intermediate is isolated, dried under vacuum, and either transferred to in-house API facilities or packed for validated shipment to licensed contract manufacturers

    Final product types

    • CNS-active drug substances (e.g., certain antipsychotics, anxiolytics)
    • Second-generation antihistamines
    • Oncology therapy intermediates with tailored piperazine scaffolds

    2. Agrochemical Synthesis: Fungicide and Herbicide Precursor

    Selective agrochemical producers utilize this compound when engineering new classes of piperazine-derived fungicides and herbicides. The unique pyrrole-functionalized scaffold imparts desired bioactivity for narrow-spectrum plant protection, and precise control over formulation purity remains critical to meet both field efficacy and residue compliance.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • FAO/WHO Codex Alimentarius Maximum Residue Limits (MRLs)
    • ISO 9001-certified production controls for precursor chemicals
    • REACH (EC 1907/2006) pre-registration for European supply chains

    Typical usage ratio

    • 3–8% weight percent of total input for targeted fungicide/herbicide precursor pathways; adjusted per field trial results and toxicity profile

    Downstream process integration

    • Dosed into closed hydrogenation or condensation reactors after initial aromatic precursor preparation
    • Monitored using GC-MS and LC-MS to minimize by-product formation and improve active ingredient selectivity
    • Post-reaction purification by multi-stage crystallization and solvent exchange to meet residue standards prior to final formulation

    Final product types

    • Systemic fungicide actives with unique piperazine-pharmacophore linkages
    • Pre-emergent herbicides for cereal and maize protection
    • Raw actives for downstream formulation into SC, WG, or EC agricultural products

    3. Fine Chemical Intermediate for Specialty Polymers

    Advanced polymer manufacturers incorporate this molecular structure to achieve tailored flexibility and solvent resistance in high-performance resin systems. The compound acts as a bifunctional chain extender or cross-linker, offering unique electronic and steric effects due to its substituted pyrrole and piperazine domains. Formulators adjust feed ratio based on target mechanical properties and end-use compliance.

    Industry compliance standards

    • ISO 9001:2015 for quality management in specialty chemical operations
    • ASTM D638 and D790 for mechanical property testing of thermoset and thermoplastic resins
    • EPA TSCA Inventory Listing for manufactured intermediates
    • EU REACH compliance for downstream marketing in Europe

    Typical usage ratio

    • 0.8–4% by weight in the total polymer backbone, depending on the specific formula and crosslink density required

    Downstream process integration

    • Fed as a liquid or pre-diluted concentrate during in-reactor oligomerization or polycondensation steps
    • Chain-growth monitored via NMR and GPC to ensure consistent distribution of the functional groups
    • Polymer slurry subjected to devolatilization and pelletizing before compounding for industrial applications

    Final product types

    • High-temperature solvent-resistant coatings
    • Flexible printed circuit board substrates
    • Specialty elastomers with enhanced weatherability
    • Industrial adhesives for electronic assembly

    4. Electrochemical Material for Charge-Storage Devices

    Manufacturers of advanced battery and supercapacitor components exploit the redox-active properties of the dimethyl-pyrrole-piperazine moiety for novel electrolyte additives and conductive polymer matrices. Its chemical structure enables tuning of ion transport and interfacial stability in next-generation energy storage platforms. Consistent quality and trace impurity control are required throughout scale-up.

    Industry compliance standards

    • IEC 62660-2 for lithium-ion battery performance and safety
    • RoHS Directive (EU 2015/863) restriction of hazardous substances
    • UL 1973 certification process for stationary energy storage
    • SEMI S2 EHS evaluation for components used in semiconductor and cleanroom environments

    Typical usage ratio

    • 0.2–1.2% by weight as electrolyte additive, or 1–3% in the conductive polymer phase — optimized by electrochemical cycling performance

    Downstream process integration

    • Blended directly into liquid electrolyte formulations under inert gas conditions to avoid oxidative degradation
    • Copolymerized with other monomers during synthesis of electrode binder layers
    • Processed under controlled moisture and particle-size specifications to ensure reproducibility in slurries

    Final product types

    • Nickel-rich lithium-ion battery cells for electric vehicles
    • Industrial supercapacitor packs for grid balancing
    • Flexible thin-film batteries for wearable electronics
    • Polymer-electrolyte capacitors for consumer and automotive markets
    Free Quote

    Competitive 1-[2-(2,5-Dimethyl-1H-Pyrrol-1-Yl)Ethyl]Piperazine prices that fit your budget—flexible terms and customized quotes for every order.

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