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(4-Nitro-Phenyl)-Piperazin-1-Yl-Methanone

    • Product Name (4-Nitro-Phenyl)-Piperazin-1-Yl-Methanone
    • Alias N-(4-Nitrophenyl)piperazine-1-carboxamide
    • Einecs 624-029-6
    • 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
    VTB
    Specifications

    HS Code

    557264

    Iupac Name (4-nitrophenyl)(piperazin-1-yl)methanone
    Molecular Formula C11H13N3O3
    Molecular Weight 235.24 g/mol
    Cas Number 32851-64-4
    Appearance Yellow to orange solid
    Melting Point 120-124°C
    Solubility Soluble in DMSO, slightly soluble in water
    Smiles C1CN(CCN1)C(=O)C2=CC=C(C=C2)[N+](=O)[O-]
    Boiling Point Decomposes before boiling
    Purity Typically ≥ 98%

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

    Packing & Storage
    Packing Sealed amber glass bottle containing 25 grams of (4-Nitro-Phenyl)-Piperazin-1-Yl-Methanone, labeled with hazard warnings and handling instructions.
    Shipping (4-Nitro-Phenyl)-Piperazin-1-Yl-Methanone is shipped in secure, airtight containers to prevent contamination and degradation. Packaging complies with chemical safety standards, including clear hazard labeling. Transport is by certified carriers with documentation to ensure compliance with local and international regulations regarding hazardous substances. Temperature and handling precautions are maintained throughout transit.
    Storage Store (4-Nitro-Phenyl)-Piperazin-1-Yl-Methanone in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect from moisture, heat, and direct sunlight. Handle in accordance with standard laboratory safety protocols, using appropriate personal protective equipment to prevent skin or eye contact. Dispose of according to local regulations.
    Application of (4-Nitro-Phenyl)-Piperazin-1-Yl-Methanone

    Applications of (4-Nitro-Phenyl)-Piperazin-1-Yl-Methanone in Industrial Manufacturing

    (4-Nitro-Phenyl)-Piperazin-1-Yl-Methanone is a critical intermediate for specialized industrial synthesis, supporting multiple chemical production segments. Below, we detail authentic downstream uses, integration points, control parameters, and resulting finished goods in each sector where this raw material provides tangible value to manufacturers.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Antipsychotic Drugs

    As a key raw material, this compound is systematically used in the multi-stage synthesis of several substituted piperazine pharmaceuticals, notably certain atypical antipsychotics. It participates in N-acylation or condensation reactions during the formation of pharmacologically active intermediates required for finished API production under regulated environments. Manufacturers carefully monitor impurity profiles at this stage, leveraging the material’s controlled reactivity and purity grade to ensure product qualification for further downstream processing in GMP-compliant API plants.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • USP Monograph procedures for intermediates
    • EDQM CEP guidelines
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • 0.9–1.2 molar equivalents relative to coupling reagent
    • Stoichiometry adjusted based on the desired yield, typically 10–30% by weight in precursor batch
    • Purity grades of ≥98% are standard

    Downstream process integration

    • Nucleophilic substitution or amide bond formation step
    • Integrated solvent phase purification—removal of excess reagent post-reaction
    • On-site or contract purification and crystallization for API-grade output

    Final product types

    • Antipsychotic finished APIs (e.g. quetiapine intermediates)
    • Therapeutic piperazine derivatives
    • Preclinical candidate molecules
    • GMP-certified pharmaceutical actives

    2. Veterinary Compound Manufacturing

    This compound finds reliable adoption within veterinary drug synthesis, especially for piperazine-based antiemetic and antiparasitic agents administered to livestock and companion animals. Manufacturers employ it during the route design of multi-step syntheses, ensuring robust impurity removal and batch reproducibility. Integration points often occur before core cyclization or heterocycle formation. Extensive analytical control throughout ensures compliance with veterinary pharmacopeia requirements and residue limits for animal health products.

    Industry compliance standards

    • VICH GL guidelines for veterinary chemical production
    • European Pharmacopoeia (Ph. Eur.) veterinary chapters
    • US FDA Guidance for Industry #205
    • ISO 9001:2015 systems in feed additive manufacturing

    Typical usage ratio

    • 10–25% by weight in the synthetic reaction mixture
    • 1:1 molar ratio versus starting amine core, adjusted by yield targets
    • Batch size scales from 50g R&D pilots to 200 kg GMP production

    Downstream process integration

    • First- or second-stage building block prior to heterocycle closure
    • In-line HPLC monitoring before neutralization and salt formation
    • Final product isolation by controlled precipitation or crystallization

    Final product types

    • Veterinary API intermediates
    • Antiparasitic actives (e.g., piperazine-based oral formula)
    • Feed additive precursors
    • Animal health injectable APIs

    3. Agrochemical Intermediate Synthesis

    In agrochemical plants, this molecule serves as a dedicated intermediate for the synthesis of nitrogen-containing protective agents and select fungicides. Producers use it to assemble specific piperazine-related scaffolds, critical to active molecule formation complying with international crop safety criteria. Material input is tracked precisely as part of multi-reactant syntheses, with in-process control for minimizing carryover of nitro-aromatic residues. The integration occurs ahead of active ingredient derivatization and microencapsulation steps, both of which require stringent adherence to agricultural chemical regulations.

    Industry compliance standards

    • FAO/WHO specifications for pesticide manufacture
    • REACH registration (EC 1907/2006) for intermediates
    • ISO 17025:2017 for analytical validation
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • 0.8–1.0 molar equivalents relative to secondary amine substrate
    • 5–12% by weight in formulated batch scale-up
    • Flux depends on final crop protection target compound

    Downstream process integration

    • Introduced during masked amine synthesis pre-oxidation
    • Mild base or acid catalysis at controlled temperature
    • Process validation by GC/MS—monitoring for residual parent compound

    Final product types

    • Nitrogen-rich agrochemical actives
    • Piperazine-derived fungicides
    • Herbicide precursor molecules
    • Seed coating synthesis intermediates

    4. Specialty Dye and Pigment Intermediate

    This material is employed by manufacturers requiring precise electron-withdrawing substitutions in the creation of performance dyes, pigments, or optical brighteners. Its introduction into the chromophore assembly processes enhances colorfastness and specific spectral properties of downstream pigment molecules. Used at set stoichiometries, it enters by direct coupling or as a bridge in building highly conjugated aromatic systems subject to rigorous environmental compliance for industrial dye production.

    Industry compliance standards

    • EN 71-3 safety for pigment product safety in toys and textiles
    • OEKO-TEX Standard 100 (input chemical restrictions)
    • REACH Substances of Very High Concern (SVHC) screening
    • DIN EN ISO 14001 for environmental management

    Typical usage ratio

    • 0.3–0.7 molar equivalents as chromophore modifier
    • 1–5% by mass in pigment batch blend
    • Ratio set by desired shade intensity and fastness

    Downstream process integration

    • Chemical insertion prior to aromatic system finalization
    • Color tuning via in-process HPLC/UV-Vis confirmation
    • Blending and dispersive milling ahead of packaging

    Final product types

    • Specialty textile dyes
    • Printing ink pigments
    • Optical brightener precursors
    • High-stability colorants for industrial use
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