Description

Biperiden Lactate is a high-purity pharmaceutical active ingredient, a salt form of the anticholinergic agent Biperiden. This compound is critical for the formulation of injectable medications requiring precise neurological activity. It is primarily utilized by pharmaceutical manufacturers and research institutions in the development and production of treatments for Parkinson's disease and related movement disorders. Our supply ensures consistent quality and reliability for critical therapeutic applications.

Application

• Pharmaceutical Active Ingredient (API): Primary use in the formulation of injectable anticholinergic medications.
• Treatment of Parkinson's Disease: Used in drugs to manage symptoms such as tremors, rigidity, and bradykinesia.
• Management of Drug-Induced Extrapyramidal Symptoms (EPS): Key component in treatments for side effects caused by antipsychotic medications.
• Neurological Research: Serves as a reference standard and active compound in preclinical and clinical studies on cholinergic systems.
• Generic Drug Manufacturing: Essential for producing generic versions of established anticholinergic injectable therapies.
• Hospital Formulations: Used in pharmacy compounding for specific patient needs where commercial formulations are unsuitable.

Basic Information

Product Name	Biperiden Lactate
CAS No.	7085-45-2
Molecular Formula	C₂₁H₂₉NO₂ • C₃H₆O₃
Molecular Weight	401.52 g/mol
Synonyms	Biperiden L-lactate; 1-(Bicyclo[2.2.1]hept-5-en-2-yl)-1-phenyl-3-(piperidin-1-yl)propan-1-ol lactate; Akineton Lactate; α-Bicyclo[2.2.1]hept-5-ene-2-yl-α-phenyl-1-piperidinepropanol lactate; 1-Piperidinopropanol, α-bicyclo[2.2.1]hept-5-en-2-yl-α-phenyl-, lactate; Biperiden (as lactate); Biperidenum
EINECS	Contact for details

Quality Control

Our Biperiden Lactate is manufactured under strict quality systems to meet the rigorous standards of the pharmaceutical industry. Each batch is tested to ensure compliance with relevant pharmacopoeial monographs (e.g., USP, Ph. Eur.) for identity, purity, potency, and impurity profiles. A comprehensive Certificate of Analysis (COA) is provided with every shipment, detailing all analytical results. We support regulatory filings with full traceability and documentation.

Storage

Preserve in a tightly closed container, protected from light. Store at controlled room temperature (15-25°C) or as specified on the label. This material is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation. The container should be stored in a well-ventilated area.

Specification

Item	Specification
Appearance	White or almost 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)
Water (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 1.5%
Specific Rotation	Contact for details

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