Description

Anhydro Pridinol Hydrochloride is a high-purity pharmaceutical intermediate and active ingredient. This compound is critical for the development and production of specialized therapeutic agents targeting neurological and muscular conditions. It is primarily utilized by pharmaceutical manufacturers and advanced research institutions in the life sciences sector.

Application

• Pharmaceutical Active Ingredient (API): Key intermediate in the synthesis of anticholinergic and antispasmodic medications.
• Neurological Research: Used in preclinical studies for investigating treatments for Parkinson's disease, dystonia, and other movement disorders.
• Muscle Relaxant Formulations: A critical component in the development of central-acting muscle relaxants.
• Reference Standard: Serves as a high-purity analytical standard for quality control and regulatory testing in pharmaceutical labs.
• Process Development: Employed in process chemistry for route scouting and optimization of synthetic pathways.

Basic Information

Product Name	Anhydro Pridinol Hydrochloride
CAS No.	13150-57-7
Molecular Formula	C20H25NO•HCl
Molecular Weight	331.88 g/mol
Synonyms	Pridinol Anhydro Hydrochloride; 1,1-Diphenyl-3-piperidino-1-propanol Hydrochloride, Anhydro; α,α-Diphenyl-1-piperidinepropanol Hydrochloride; Pridinole Hydrochloride; AHPH; AKOS BBS-00004345; LS-176106; Pridinol HCl Anhydro Form
EINECS	Contact for details

Quality Control

Our Anhydro Pridinol Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets stringent purity and identity criteria, suitable for pharmaceutical development. A Certificate of Analysis (COA) detailing specifications such as assay, related substances, and residual solvents is provided with every shipment to guarantee traceability and compliance.

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). 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 reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.5%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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