Description

Oxeladin Citrate is a pharmaceutical active ingredient with the CAS registry number 52432-72-1. This compound is valued for its specific pharmacological activity, making it a critical intermediate in the synthesis of specialized therapeutic agents. It is primarily required by pharmaceutical manufacturers and advanced research institutions engaged in drug development and production.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of active pharmaceutical ingredients (APIs) for specific therapeutic applications.
• Research & Development: Used in preclinical and clinical research for pharmacological studies and new drug entity development.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method validation in pharmaceutical laboratories.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for the production of specialized drug formulations.

Basic Information

Product Name	Oxeladin Citrate
CAS No.	52432-72-1
Molecular Formula	C20H27NO7
Molecular Weight	393.43 g/mol
Synonyms	Oxeladin Citrate; Oxeladine Citrate; 2-(2-Diethylaminoethoxy)ethyl 1-phenylcyclopentanecarboxylate citrate; 1-Phenylcyclopentanecarboxylic Acid 2-(2-Diethylaminoethoxy)ethyl Ester Citrate; Pectamol; Silopentol; Tussimol; Oxeladinum
EINECS	Contact for details

Quality Control

Our Oxeladin Citrate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency, meeting the stringent requirements for pharmaceutical intermediates. A Certificate of Analysis (COA) detailing specifications and test results is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed to minimize exposure to atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥ 98.0%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 1.5%

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