Description

Propiverine Hydrochloride is a high-purity pharmaceutical active ingredient (API) and a key intermediate in advanced therapeutic formulations. This compound is a potent antimuscarinic agent, valued for its role in the development and manufacturing of medications targeting overactive bladder (OAB) syndrome. It is essential for pharmaceutical manufacturers, R&D laboratories, and fine chemical suppliers engaged in urological and neurological drug production. Our supply ensures the stringent quality and consistency required for critical pharmaceutical applications.

Application

• Primary Pharmaceutical API: Core active ingredient in the commercial manufacture of prescription medications for overactive bladder (OAB) and urinary incontinence.
• Drug Formulation R&D: Used in research and development for new dosage forms, including extended-release tablets and combination therapies.
• Reference Standard: Serves as a high-purity chemical reference standard for quality control and analytical method development in pharmaceutical labs.
• Clinical Trial Material: Supplied as a critical raw material for the production of drugs used in clinical studies and trials.
• Fine Chemical Synthesis: Acts as a key intermediate in the synthesis of more complex anticholinergic and antispasmodic drug molecules.
• Generic Drug Manufacturing: Essential for companies producing generic versions of antimuscarinic medications.

Basic Information

Product Name	Propiverine Hydrochloride
CAS No.	54556-98-8
Molecular Formula	C23H29NO3·HCl
Molecular Weight	403.94 g/mol
Synonyms	Propiverine HCl; 1-Methyl-4-piperidyl diphenylpropoxyacetate hydrochloride; 2,2-Diphenyl-4-(1-methyl-4-piperidyl)but-2-yloxyacetate hydrochloride; Mictonorm; Mictonetten; Toviaz Intermediate; Bropiverine Hydrochloride (common misnomer); 4-(2,2-Diphenyl-2-propoxyethoxy)-1-methylpiperidine hydrochloride
EINECS	Contact for details

Quality Control

Our Propiverine Hydrochloride is manufactured under strict quality management systems. Every batch undergoes comprehensive analytical testing to ensure it meets high-purity pharmaceutical-grade specifications, potentially aligning with ICH guidelines and pharmacopeial standards (e.g., USP, EP) for APIs. A detailed Certificate of Analysis (COA) documenting identity, purity, and impurity profiles is provided with each 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). This product is hygroscopic (moisture-sensitive) and must be kept under conditions that minimize exposure to atmospheric humidity to prevent degradation and clumping.

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% Any single unknown impurity ≤0.5%
Water Content (KF)	≤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.