Description

Piperazine, 1-(1-Ethyl-1H-Benzimidazol-2-Yl)-4-(4-Fluorobenzoyl)- (9Ci) is a specialized heterocyclic organic compound featuring a piperazine core substituted with benzimidazole and fluorobenzoyl groups. This molecular architecture makes it a valuable high-purity intermediate for advanced chemical synthesis, particularly in the development of active pharmaceutical ingredients (APIs). It is primarily sought after by pharmaceutical R&D and fine chemical manufacturers engaged in creating novel therapeutic agents.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of novel drug candidates, particularly those targeting neurological or oncological pathways.
• Active Pharmaceutical Ingredient (API) Development: Serves as a core structural moiety in the research and production of new APIs.
• Biochemical Research: Used as a reference standard or reagent in pharmacological and biochemical studies to investigate receptor interactions.
• Fine Chemical Synthesis: Employed in multi-step organic synthesis for creating complex, high-value specialty chemicals.
• Agrochemical Research: Potential application as an intermediate in the development of advanced crop protection agents.

Basic Information

Product Name	Piperazine, 1-(1-Ethyl-1H-Benzimidazol-2-Yl)-4-(4-Fluorobenzoyl)- (9Ci)
CAS No.	604741-81-3
Molecular Formula	C20H21FN4O
Molecular Weight	352.41 g/mol
Synonyms	1-(1-Ethyl-1H-benzimidazol-2-yl)-4-(4-fluorobenzoyl)piperazine; 4-(4-Fluorobenzoyl)-1-(1-ethyl-1H-benzimidazol-2-yl)piperazine; 1-(1-Ethylbenzimidazol-2-yl)-4-(4-fluorobenzoyl)piperazine; 604741-81-3; 1-(1-Ethyl-1H-benzo[d]imidazol-2-yl)-4-(4-fluorobenzoyl)piperazine
EINECS	Contact for details

Quality Control

Our production of Piperazine, 1-(1-Ethyl-1H-Benzimidazol-2-Yl)-4-(4-Fluorobenzoyl)- (9Ci) adheres to stringent quality management protocols. Each batch undergoes comprehensive analytical testing, including HPLC, NMR, and MS, to ensure high chemical purity and structural identity. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming compliance with agreed specifications. Our quality system is designed to meet the rigorous demands of GMP-grade intermediate manufacturing for pharmaceutical applications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (typically 15-25°C). Keep away from incompatible materials. For long-term storage, consider an inert atmosphere to preserve stability.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Conforms to reference
Purity (HPLC)	≥ 97.0%
Related Substances (HPLC)	Total impurities ≤ 3.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%

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