Description

Cycrimine Hydrochloride is a pharmaceutical active ingredient and a synthetic anticholinergic agent. It is a critical intermediate and reference standard in the research and development of treatments for neurological disorders, particularly Parkinson's disease. This compound is essential for pharmaceutical manufacturers, research institutions, and analytical laboratories engaged in neuropharmacology and drug discovery.

Application

• Pharmaceutical Active Ingredient: Used in the formulation of medications for managing symptoms associated with Parkinson's disease and other movement disorders.
• Reference Standard: Serves as a high-purity calibration standard in analytical chemistry for method development and quality control (QC) testing of pharmaceutical products.
• Biochemical Research: Employed in preclinical and in-vitro studies to investigate the mechanisms of anticholinergic agents and their effects on the central nervous system.
• Chemical Synthesis: Acts as a key chiral intermediate or building block in the synthesis of more complex therapeutic molecules targeting muscarinic receptors.

Basic Information

Product Name	Cycrimine Hydrochloride
CAS No.	126-02-3
Molecular Formula	C19H29NO•HCl
Molecular Weight	323.90 g/mol
Synonyms	Cycrimine HCl; 1-Phenyl-1-cyclopentyl-3-piperidinopropanol Hydrochloride; α-Cyclopentyl-α-phenyl-1-piperidinepropanol Hydrochloride; Pagitane Hydrochloride; Pargitan; 3-(1-Piperidyl)-1-cyclopentyl-1-phenyl-1-propanol Hydrochloride
EINECS	204-765-6

Quality Control

Our Cycrimine Hydrochloride 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 and reference materials. 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 area at controlled room temperature (15-25°C). The product is hygroscopic (moisture-sensitive) and should be handled in a dry environment to maintain stability.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.5%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 1.0%; Any single impurity ≤ 0.5%

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