Description

1-(3-Fluorophenyl)-4-(2,4,4-Trimethylallophanoyl)Piperazine is a specialized piperazine derivative that serves as a high-value synthetic intermediate in advanced organic synthesis. This compound is critical for research and development in medicinal chemistry, particularly for constructing complex molecular architectures. It is primarily sought by pharmaceutical R&D laboratories and fine chemical manufacturers engaged in the development of novel active pharmaceutical ingredients (APIs) and other high-performance materials.

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of novel drug candidates, particularly in central nervous system (CNS) and psychiatric therapeutic areas.
• Medicinal Chemistry Research: Used as a core scaffold for structure-activity relationship (SAR) studies and lead optimization in drug discovery programs.
• Fine Chemical Synthesis: Serves as a precursor for the manufacture of complex, high-value specialty chemicals and advanced materials.
• Agrochemical Development: Potential intermediate in the research and synthesis of new generation crop protection agents and pesticides.
• Academic & Contract Research: Utilized in university and CRO settings for methodological development and exploratory synthetic chemistry.

Basic Information

Product Name	1-(3-Fluorophenyl)-4-(2,4,4-Trimethylallophanoyl)Piperazine
CAS No.	80712-24-9
Molecular Formula	C15H19FN4O2
Molecular Weight	306.34 g/mol
Synonyms	1-(3-Fluorophenyl)-4-[(2,4,4-trimethyl-1,3-diazetidin-1-yl)carbonyl]piperazine; 4-(2,4,4-Trimethylallophanoyl)-1-(3-fluorophenyl)piperazine; 1-(3-Fluorophenyl)-4-(2,4,4-trimethyl-1,3-diazetidine-1-carbonyl)piperazine; 80712-24-9; 1-(3-Fluorophenyl)-4-(2,4,4-trimethylallophanoyl)piperazine; 1-(3-Fluorophenyl)-4-(2,4,4-trimethyl-1,3-diazetidin-1-yl)formylpiperazine
EINECS	Contact for details

Quality Control

Our 1-(3-Fluorophenyl)-4-(2,4,4-Trimethylallophanoyl)Piperazine is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing including HPLC for purity, NMR and IR for structural confirmation, and residual solvent analysis to ensure it meets the stringent requirements of pharmaceutical R&D. A detailed Certificate of Analysis (COA) is provided with every shipment, documenting compliance with agreed specifications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at controlled room temperature (15-25°C). Keep the container tightly sealed in a dry environment to minimize exposure to moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Any individual impurity ≤ 0.5%
Total Impurities	≤ 2.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Water Content (KF)	≤ 0.5%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.