Description

Oxyphencyclimine is a synthetic anticholinergic agent with specific pharmacological properties. This compound is valued for its role as a key intermediate in the research and development of pharmaceutical actives targeting the muscarinic acetylcholine receptor. It is primarily utilized by pharmaceutical R&D laboratories and fine chemical manufacturers engaged in the synthesis of specialized therapeutic agents.

Application

• Pharmaceutical Intermediate: Serves as a critical building block in the synthesis of anticholinergic and antispasmodic drug candidates.
• Biochemical Research: Used in in vitro studies to investigate receptor binding affinity and pharmacological mechanisms of action.
• Reference Standard: Employed as an analytical standard in quality control laboratories for method development and validation.
• Preclinical Development: Utilized in the early-stage development of new chemical entities (NCEs) for gastrointestinal and urinary tract disorders.

Basic Information

Product Name	Oxyphencyclimine
CAS No.	125-53-1
Molecular Formula	C20H28N2O3
Molecular Weight	344.45 g/mol
Synonyms	Oxyphencyclimine; Oxyphencyclimine Hydrochloride; 1-Methyl-4-piperidyl α-cyclohexyl-α-hydroxy-α-phenylacetate; Daricon; Antrenyl; Oxyphencyclimine HCl; α-Cyclohexyl-α-hydroxy-α-phenylacetic acid 1-methyl-4-piperidyl ester
EINECS	204-748-2

Quality Control

Our Oxyphencyclimine is produced under a strict quality management system. Each batch undergoes comprehensive analytical testing, including identification, assay, and impurity profiling, to ensure it meets the high-purity standards required for pharmaceutical research. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming compliance with specified parameters.

Storage

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

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%

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