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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 | 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. |
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 DrugsAs 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
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2. Veterinary Compound ManufacturingThis 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
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3. Agrochemical Intermediate SynthesisIn 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
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4. Specialty Dye and Pigment IntermediateThis 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
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