Description

Biperiden Hydrochloride is a high-purity pharmaceutical active ingredient (API) and fine chemical intermediate. This compound is a synthetic anticholinergic agent, valued for its precise pharmacological activity and chemical stability. It is primarily utilized by pharmaceutical manufacturers and research institutions in the development and production of neurological and therapeutic formulations.

Application

• Pharmaceutical API: Core active ingredient in the formulation of anticholinergic medications.
• Neurological Research: Used in preclinical and clinical studies targeting cholinergic pathways.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method validation in laboratories.
• Drug Development: Key intermediate in the synthesis of novel therapeutic agents and prodrugs.
• GMP Manufacturing: Supplied for use in Good Manufacturing Practice (GMP) compliant production processes.

Basic Information

Product Name	Biperiden Hydrochloride
CAS No.	1235-82-1
Molecular Formula	C21H29NO•HCl
Molecular Weight	347.92 g/mol
Synonyms	Biperiden HCl; 1-(Bicyclo[2.2.1]hept-5-en-2-yl)-1-phenyl-3-(piperidin-1-yl)propan-1-ol hydrochloride; Akineton Hydrochloride; α-Bicyclo[2.2.1]hept-5-ene-2-yl-α-phenyl-1-piperidinepropanol hydrochloride; 1-(5-Norbornen-2-yl)-1-phenyl-3-piperidino-1-propanol hydrochloride
EINECS	214-974-7

Quality Control

Our Biperiden Hydrochloride is manufactured under strict quality systems. Each batch undergoes comprehensive analytical testing to ensure it meets stringent specifications for identity, purity, and potency, suitable for pharmaceutical applications. A Certificate of Analysis (COA) detailing results for assay, related substances, residual solvents, and other critical parameters 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). Due to its hygroscopic nature, the container must be kept tightly sealed to protect from moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Related Substances (HPLC)	Individual impurity: NMT 0.5% Total impurities: NMT 1.5%
Water (KF)	NMT 1.0%
Residue on Ignition	NMT 0.1%
Heavy Metals	NMT 20 ppm

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