Description

9-Hydroxy Propantheline Bromide is a high-purity pharmaceutical intermediate and active metabolite of propantheline bromide. This compound matters for its critical role in the synthesis and analytical profiling of anticholinergic and antispasmodic drug substances. It is primarily needed by pharmaceutical R&D laboratories, quality control departments, and manufacturers engaged in the production of gastrointestinal therapeutics and reference standards.

Application

• Pharmaceutical Intermediate: A key synthetic precursor in the manufacture of anticholinergic medications.
• Reference Standard: Used in analytical chemistry for method development, validation, and quality control testing of drug products and metabolites.
• Metabolite Studies: Essential for pharmacokinetic and pharmacodynamic research to understand the metabolism of propantheline bromide.
• Impurity Profiling: Serves as a known impurity standard to ensure the purity and safety of final drug formulations.
• Research Chemical: Utilized in biochemical and pharmacological research to study muscarinic receptor antagonists.

Basic Information

Item	Detail
Product Name	9-Hydroxy Propantheline Bromide
CAS No.	93446-02-7
Molecular Formula	C23H30BrNO4
Molecular Weight	464.40 g/mol
Synonyms	9-Hydroxypropantheline Bromide; Propantheline Bromide Hydroxy Metabolite; 9-Hydroxy Propantheline; 2-Hydroxypropantheline Bromide; 9-Hydroxy-9-carboxymethyl-3-diisopropylmethylaminopropylxanthene-9-carboxylate Bromide; 9-Hydroxy-9-carboxymethyl-3-(2-diisopropylaminoethyl)-9H-xanthene-9-carboxylic Acid Bromide; Propantheline Impurity; Propantheline Related Compound
EINECS	Contact for details

Quality Control

Our 9-Hydroxy Propantheline Bromide is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC, NMR, and mass spectrometry, to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing all relevant specifications. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%

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