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1-Acetyl-4-(4-Hydroxyphenyl)Piperazine

    • Product Name 1-Acetyl-4-(4-Hydroxyphenyl)Piperazine
    • Einecs 609-658-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    487961

    Chemical Name 1-Acetyl-4-(4-Hydroxyphenyl)Piperazine
    Molecular Formula C12H16N2O2
    Molecular Weight 220.27 g/mol
    Cas Number 6602-61-9
    Appearance White to off-white crystalline powder
    Melting Point 157-159°C
    Solubility Soluble in DMSO, slightly soluble in water
    Synonyms N-Acetyl-4-(4-hydroxyphenyl)piperazine
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, protect from light and moisture
    Smiles CC(=O)N1CCN(CC1)C2=CC=C(C=C2)O

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

    Packing & Storage
    Packing The packaging is a sealed amber glass bottle containing 50 grams of 1-Acetyl-4-(4-Hydroxyphenyl)piperazine, labeled with hazard and handling information.
    Shipping Shipping of **1-Acetyl-4-(4-Hydroxyphenyl)Piperazine** is conducted in compliance with chemical safety regulations. The product is securely packaged in sealed containers, clearly labeled, and protected against moisture and light. It is transported as non-hazardous, but requires standard chemical handling protocols and documentation during domestic and international shipment.
    Storage Store **1-Acetyl-4-(4-hydroxyphenyl)piperazine** in a tightly sealed container, protected from light and moisture. Keep in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizing agents. Ensure the storage area is clearly labeled and only accessible to trained personnel. Follow all relevant safety guidelines and local regulations when handling and storing this chemical.
    Application of 1-Acetyl-4-(4-Hydroxyphenyl)Piperazine

    Applications of 1-Acetyl-4-(4-Hydroxyphenyl)Piperazine in Industrial Manufacturing

    As a dedicated manufacturer of 1-Acetyl-4-(4-Hydroxyphenyl)Piperazine, we supply this advanced piperazine derivative directly to selected industries where its chemical profile delivers unique functionality. The following application scenarios are grounded in actual large-scale utilization of the material, each reflecting precise compliance, blending, processing, and downstream product contexts observed in global manufacturing environments.

    1. Active Pharmaceutical Ingredient (API) Intermediates for Antipsychotic Compound Synthesis

    Major pharmaceutical companies integrate this substance into multi-step syntheses for producing high-value API intermediates, especially within the generation of certain atypical antipsychotic drugs. It enters amidation or acylation stages, serving as a key scaffold or side-chain precursor, which is essential for molecular designs requiring both piperazine and acetylphenol motifs. Manufacturers ensure batch traceability within each campaign due to regulatory scrutiny associated with CNS drug compounds.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Current Good Manufacturing Practice (cGMP) under US FDA 21 CFR Part 210/211
    • Ph. Eur. and USP monographs for relevant APIs
    • EU REACH Regulation (EC) No 1907/2006 for raw material registration

    Typical usage ratio

    • 0.6–1.4 molar equivalents relative to the primary amine or acid reactant, adjusted based on target API structural requirements and reaction scale; typical batch campaigns utilize 10–20 kg per reactor charge.

    Downstream process integration

    • Charged as a nucleophilic intermediate during amidation/acylation stage, often after purification/drying under controlled conditions; high-performance liquid chromatography (HPLC) monitors residual content post-reaction.

    Final product types

    • Antipsychotic drug substances (e.g., analogues used in risperidone, paliperidone synthesis)
    • Patent-protected CNS API intermediates
    • Development-stage compounds for psychiatric medication pipelines
    • Clinical trial lots of investigational drugs meeting cGMP traceability

    2. Chemical Building Block for Advanced Agrochemical Synthesis

    Chemical companies engaged in crop protection solutions use 1-Acetyl-4-(4-Hydroxyphenyl)Piperazine in the production of next-generation fungicide or herbicide actives, where the piperazine phenolic structure offers both reactivity and desired metabolic profiles. It is frequently incorporated at the substitution or derivatization steps, resulting in high selectivity during late-stage functionalization of heterocyclic rings essential for advanced agrochemical APIs.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • OECD Good Laboratory Practice (GLP)
    • European Union Plant Protection Products Regulation (EC No 1107/2009)
    • ISO 17025 for in-process and release analytical testing

    Typical usage ratio

    • 0.5–1.2 equivalents when used as a direct precursor or reactant; formulation scientists adjust ratio based on targeted yield and impurity control during key ring-closing or coupling steps.

    Downstream process integration

    • Fed during late-stage synthesis as coupling partner or functionalized building block; subsequent purification includes solvent extraction and crystallization, with QA/QC confirmation by GC-MS or LC-MS.

    Final product types

    • Novel triazole fungicides active ingredients
    • Selective piperazine-based herbicides
    • Pre-emergent weed control agents containing acetylphenylpiperazine subunits
    • Patent-pending crop protection molecules for regulatory submission

    3. Monomer/Chain Extender in Specialty Polymer Manufacturing

    Advanced materials manufacturers adopt this compound as a tailored monomer or chain extender in high-performance polymers, especially for specialty polyamides and polyurethanes where phenolic and piperazine units contribute to flame retardancy, chemical resistance, or controlled hydrophilicity. Integration occurs during prepolymer preparation under inert atmospheres, with batch-specific dosing validated by in-line spectroscopy to achieve targeted polymer architecture.

    Industry compliance standards

    • ISO 9001 Quality Management Systems—manufacturing and process control
    • UL 94 flammability standard for final polymer materials
    • REACH polymer-specific registration when used in Europe
    • FDA CFR 21.177.1580 (for engineered polymers in food-contact applications, if relevant)

    Typical usage ratio

    • 3–8% by weight relative to total monomer content; polymer scientists adjust based on targeted thermal, mechanical, or rheological performance.

    Downstream process integration

    • Incorporated during polycondensation or chain extension phase, typically added to reactor with other polyfunctional monomers or diisocyanates; monitored for uniform reactivity using FT-IR or NMR spectroscopy.

    Final product types

    • Flame-retardant polyamide fibers for technical textiles
    • Specialty polyurethane coatings for electronics
    • Functional thermoplastic blends for industrial applications
    • Precision-molded engineering plastics featuring enhanced chemical stability

    4. Modified Resin Hardener Additive in Epoxy-Based Systems

    Formulators of high-performance epoxy resins in electronics and industrial coatings rely on this piperazine derivative as a functional modifier for resin curing agents, leveraging its phenolic groups and secondary amide linkage to fine-tune crosslink density and balance toughness versus thermal resistance. Its introduction occurs during hardener pre-mix preparation, usually in application-dedicated blending suites with real-time viscosity control for downstream processability.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (for finished electronics components)
    • IEC 61249-2-21 for halogen-free laminate materials
    • ISO 9001/14001 for end-to-end traceability and environmental management
    • UL 746E safety certification for electrical insulation resins

    Typical usage ratio

    • 0.5–4% by weight relative to total hardener blend; adjustments based on test batches targeting gel time, exotherm profile, and cured modulus for specific end uses.

    Downstream process integration

    • Added to hardener pre-mix, which subsequently undergoes vacuum de-aeration and inline mixing with epoxy oligomers; batch QC includes monitoring of amine value and viscosity consistency.

    Final product types

    • Halogen-free electronic laminates for PCBs
    • Industrial-grade epoxy flooring compounds
    • 2K electrical potting compounds for transformer encapsulation
    • Specialty adhesive systems for automotive electronics

    5. Intermediate in Synthesis of Performance Dye Compounds

    Colorant manufacturers select this material as a reactive intermediate for the production of specialty dyes, particularly those designed for advanced textile and high-durability leather finishes. Its phenolic ring enhances chromophore attachment, while the piperazine core improves solubility and substantivity on synthetic fibers. Processing teams introduce it during diazotization or condensation coupling, with precision control of reagent feeding to ensure dye quality and purity.

    Industry compliance standards

    • OEKO-TEX Standard 100 for input chemical safety
    • ZDHC MRSL chemical compliance in dye manufacturing
    • DIN EN ISO 105 series for color fastness testing
    • National Inventory Listing for dyes (TSCA, REACH, IECSC, etc.)

    Typical usage ratio

    • 0.8–1.5 equivalents as a coupling partner in the chromophore synthesis stage; color chemists establish precise equivalents via lab scale-up and spectral analysis.

    Downstream process integration

    • Dosed as a coupling component in batch or semi-batch dye-forming reactions, followed by filtration, washing, and salt-forming steps to isolate the final dye structure; in-process HPLC used for checking conversion and byproduct levels.

    Final product types

    • Reactive dyes for polyester, nylon, and technical textile applications
    • Leather finishing colorants with enhanced fastness
    • Industrial printing inks for durable surface coloration
    • Dispersed dyes for microfiber and nonwoven fabrics
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