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HS Code |
613752 |
| Iupac Name | 1-(3,4-dichlorophenyl)piperazine |
| Cas Number | 119532-26-2 |
| Molecular Formula | C10H12Cl2N2 |
| Molecular Weight | 231.13 |
| Appearance | White to off-white solid |
| Melting Point | 92-96°C |
| Solubility In Water | Slightly soluble |
| Density | 1.22 g/cm³ (approximate) |
| Smiles | C1CN(CCN1)C2=CC(=C(C=C2)Cl)Cl |
As an accredited 1-(3,4-Dichlorophenyl)Piperazine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100-gram bottle of 1-(3,4-Dichlorophenyl)piperazine is sealed in amber glass with a tamper-evident cap and hazard labeling. |
| Shipping | 1-(3,4-Dichlorophenyl)piperazine is shipped in tightly sealed containers, clearly labeled according to safety regulations. The chemical is handled as a hazardous material and packaged to prevent leaks or contamination. Shipping is conducted via approved carriers, with all documentation complying with regional and international chemical transportation guidelines. |
| Storage | Store **1-(3,4-Dichlorophenyl)piperazine** in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect from direct sunlight, moisture, and sources of ignition. Clearly label the storage area and ensure access is restricted to trained personnel. Follow appropriate chemical hygiene and regulatory guidelines for hazardous materials. |
Applications of 1-(3,4-Dichlorophenyl)Piperazine in Industrial Manufacturing1-(3,4-Dichlorophenyl)Piperazine serves as a critical intermediate in several specialized industrial sectors. Our manufacturing process ensures high purity and consistent quality for advanced downstream production. The following sections detail distinct real-world application segments, each with dedicated compliance benchmarks, formulation insights, process entry points, and reference end products. 1. Active Pharmaceutical Ingredient Synthesis (Antipsychotic Drugs)Major pharmaceutical producers use this compound as a key intermediate in the synthesis of arylpiperazine-based antipsychotic agents. Its dichlorophenyl-piperazine structure forms the core for multiple generations of psychiatric medications, including specific atypical antipsychotic molecules. Chemical engineers incorporate it during multi-step reactions for building complex active structures, adhering to strict GMP and pharmacopeial quality standards throughout all stages of API manufacture. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Pharmaceutical Research and Development (Central Nervous System Agents)R&D labs within large pharma companies and CROs rely on this intermediate during the synthesis of novel CNS-active compounds, such as investigational drugs for anxiety and depression. Medicinal chemists leverage the electronic and steric profile of the dichlorophenyl-piperazine segment to generate, via scaffold hopping, a broad array of trial molecules for structure-activity screening. Rigorous documentation and traceability support compliance within regulated research environments. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Agrochemical Intermediate for Fungicide SynthesisSpecialty agrochemical manufacturers utilize the dichlorophenyl-piperazine moiety as an intermediate to produce next-generation fungicides for crop protection. The compound’s structural motif underpins potential agents targeting fungal cell growth, often within multi-step synthesis for new triazole or imidazole class fungicides. Tightly controlled material traceability is mandatory, especially for production lines targeting export to regulated markets. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Chemical Intermediate for Veterinary Drug SynthesisContract manufacturers and animal health producers rely on this dichlorophenyl-piperazine derivative as a key starting material in veterinary pharmaceuticals, especially for the development of antiemetic and behavioral management agents in companion animals. The compound’s substitution pattern supports desired pharmacological profiles in formulations subjected to species-specific safety and efficacy requirements. Processing lines require precise material control to ensure compliance with veterinary GxP and pharmacopoeial standards. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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