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1-(4-Methoxyphenyl)Piperazine Hydrochloride

    • Product Name 1-(4-Methoxyphenyl)Piperazine Hydrochloride
    • Alias p-Methoxyphenylpiperazine HCl
    • Einecs 624-140-2
    • 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

    571796

    Chemical Name 1-(4-Methoxyphenyl)piperazine Hydrochloride
    Cas Number 5449-22-7
    Molecular Formula C11H16ClN2O
    Molecular Weight 226.71 g/mol
    Appearance White to off-white crystalline solid
    Solubility Soluble in water and methanol
    Melting Point 201-204 °C
    Purity Typically >98%
    Storage Conditions Store at room temperature, keep container tightly closed
    Synonyms 4-MeO-PP HCl; 1-(4-Methoxyphenyl)piperazine hydrochloride
    Smiles COC1=CC=C(C2CCNCC2)C=C1.Cl
    Inchi InChI=1S/C11H16N2O.ClH/c1-14-10-3-5-11(6-4-10)13-7-2-8-12-9-13;/h3-6,12H,2,7-9H2,1H3;1H
    Boiling Point No data available (decomposes)
    Density No data available
    Hazard Class No data available

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

    Packing & Storage
    Packing White, sealed HDPE bottle labeled "1-(4-Methoxyphenyl)piperazine Hydrochloride, 25g," with hazard pictograms and lot number on outer packaging.
    Shipping 1-(4-Methoxyphenyl)Piperazine Hydrochloride is securely packaged in sealed, chemical-resistant containers to prevent contamination and degradation. The shipment complies with all relevant safety and regulatory guidelines, including labeling and documentation. Appropriate cushioning ensures protection during transit, and temperature controls are maintained if required to preserve chemical stability.
    Storage 1-(4-Methoxyphenyl)piperazine hydrochloride should be stored in a tightly sealed container, away from moisture and direct sunlight. Keep the container in a cool, dry, and well-ventilated area, ideally at room temperature (15–25°C). Avoid exposure to incompatible substances such as strong oxidizing agents. Always ensure proper chemical labeling and follow standard laboratory safety protocols.
    Application of 1-(4-Methoxyphenyl)Piperazine Hydrochloride

    Applications of 1-(4-Methoxyphenyl)Piperazine Hydrochloride in Industrial Manufacturing

    As a direct producer of 1-(4-Methoxyphenyl)Piperazine Hydrochloride, we support multiple regulated industries with high-quality material for downstream synthesis. The following sections detail major application areas, including specific compliance requirements, typical formulation methods, integration steps, and final product types.

    1. Pharmaceutical Intermediates for Serotonin Receptor Modulator Synthesis

    Pharmaceutical manufacturers rely on our product for the synthesis of selective serotonin receptor modulators. The compound serves as a core fragment during multi-stage production of CNS-active molecules. Manufacturers incorporate it during the assembly of substituted piperazine frameworks, following precise molar ratios and GMP controls.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF Monograph standards for intermediates
    • EU EudraLex, Volume 4 GMP Guidelines
    • US FDA CFR Title 21 for API intermediates

    Typical usage ratio

    • Used at 0.8–1.2 molar equivalents relative to the core reactant in the coupling step.
    • Adjusted case-by-case for batch process yield or route optimization requirements.

    Downstream process integration

    • Added during the primary heterocycle coupling step.
    • Reacts via condensation or nucleophilic substitution in polar aprotic solvent systems.
    • QC sampling for purity and identity post-reaction before downstream transformation.

    Final product types

    • Serotonin 5-HT1A/5-HT2A antagonist drug substances
    • Mood disorder medication APIs
    • Anti-migraine drug precursors
    • Research reagents for CNS pharmacology

    2. Building Block for Agrochemical Active Ingredient Synthesis

    Agrochemical producers integrate our chemical as a piperazine core donor in the synthesis of phenylpiperazine-based insecticides and fungicides. It enters downstream formulations where strict regulatory and analytical procedures monitor purity, residual solvents, and target content in the multi-step reaction sequence.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 17025 Laboratory Accreditation for pesticide analysis
    • EU REACH registration for agrochemical intermediates
    • China GB 2763 standards for agrochemical residues

    Typical usage ratio

    • Used at 5–12% w/w of total intermediate batch mass, depending on end-use activity target.
    • Titration adjusts for crop-specific application profiles and degradation study results.

    Downstream process integration

    • Charged during the nucleophilic substitution phase of pyrimidine or triazine core construction.
    • Processes require moisture-free, controlled pH conditions for high-yield transformation.
    • Purity and traceability confirmed by HPLC/MS before packing into technical concentrate streams.

    Final product types

    • Systemic insecticide actives (e.g. phenylpiperazine chemotypes)
    • Cereal fungicide APIs
    • Seed coating primary actives
    • Intermediate concentrates ready for formulation into EC, SC, or WG agrochemical products

    3. Intermediate in Specialty Dye and Pigment Manufacturing

    Dye manufacturers introduce this substance into the synthesis pipeline for high-performance azo and anthraquinone pigment derivatives. The methoxy-substituted aryl ring modulates chromophore tone and enhances solubility characteristics, requiring close control of reaction stoichiometry and intermediate handling under regulated industrial guidelines.

    Industry compliance standards

    • OEKO-TEX® Standard 100 restricted substance compliance
    • EU REACH Annex XVII for dyestuff chemicals
    • ISO 9001:2015 Quality Management Systems (for pigment production)
    • GHS CLP Regulation (EC) No 1272/2008 for labeling and safety

    Typical usage ratio

    • Incorporated at 2–9% of total input mass during the dye substrate coupling step.
    • Levels precisely adjusted to achieve target color index value and lightfastness standard.

    Downstream process integration

    • Fed directly into diazotization and coupling reactors during pigment-linking stage.
    • Combined with sulfonated aromatic amines under controlled temperature and pH.
    • Crude intermediates are purified by recrystallization or solvent extraction prior to blending.

    Final product types

    • Textile dyestuffs with enhanced hue stability
    • Automotive and industrial pigment concentrates
    • Printing ink pigment dispersions
    • High-solids decorative paints

    4. Precursor in Fine Chemical Synthesis for High-Value Research Chemicals

    Producers focused on high-value fine chemicals employ this compound as a precursor in the custom synthesis of advanced piperazine derivatives. In R&D and pilot-scale contexts, it offers a controlled methoxy-para substitution profile for preparing ligands, standards, and test reagents used in molecular discovery and screening.

    Industry compliance standards

    • ISO 9001:2015 for fine chemical production & traceability
    • OECD Good Laboratory Practice (GLP) for analytical and reference materials
    • REACH Article 3 for research and development chemicals
    • IUPAC chemical nomenclature and reporting guidelines

    Typical usage ratio

    • Applied in 1:1 to 1:2 molar ratios with the functionalizing reagent.
    • Dosing flexes with downstream substitution pattern and desired throughput.

    Downstream process integration

    • Added at the stage of nucleophilic aromatic substitution or amidation.
    • Tool for library creation in medicinal chemistry, often in solid-phase or solution-phase combinatorial setups.
    • Final purification by flash chromatography and HPLC analytical confirmation before distribution to labs.

    Final product types

    • Molecular scaffolds for drug discovery
    • Reference standards for pharmaceutical and biotech research
    • Analytical marker compounds
    • Chemical ligands for receptor binding studies
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