Description

Ciclopramine CAS NO 33545-56-1 is a high-purity organic compound belonging to the class of piperazine derivatives. This versatile chemical intermediate is valued for its role in the synthesis of more complex molecules, particularly in the pharmaceutical sector. It is essential for manufacturers and R&D facilities engaged in developing active pharmaceutical ingredients (APIs) and other fine chemicals requiring precise structural control.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of various active pharmaceutical ingredients (APIs), particularly those with piperazine-based structures.
• Agrochemical Synthesis: Used in the research and production of advanced crop protection agents and pesticides.
• Organic Synthesis & Research: Serves as a versatile precursor in academic and industrial laboratories for creating novel organic compounds.
• Material Science: Potential application in the development of specialty polymers and functional materials.
• Chemical Reference Standard: Employed as an analytical standard for quality control and method development in analytical chemistry.

Basic Information

Product Name	Ciclopramine
CAS No.	33545-56-1
Molecular Formula	C15H22N2
Molecular Weight	230.35 g/mol
Synonyms	1-Cyclopentyl-4-(2-methoxyphenyl)piperazine; Ciclopramina; Ciclopraminum; 4-Cyclopentyl-1-(2-methoxyphenyl)piperazine; Lu 10-171; Citalopram Impurity A
EINECS	Contact for details

Quality Control

Our Ciclopramine is manufactured under a strict quality management system. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical intermediate applications. A detailed Certificate of Analysis (COA) confirming identity, purity, and impurity profiles is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Any single unknown impurity	≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 0.5%

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