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Oxybutynin Hydrochloride CAS NO 1508-65-2


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CAS No.:1508-65-2

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Oxybutynin Hydrochloride CAS NO 1508-65-2 is a high-purity anticholinergic pharmaceutical active ingredient. It is a critical component in the formulation of medications used to treat overactive bladder and urinary incontinence. This compound is essential for pharmaceutical manufacturers and research institutions developing antispasmodic therapies. We supply this API with a focus on stringent quality control and reliable global supply chains.

Application

  • Pharmaceutical API: Primary active ingredient in prescription medications for overactive bladder (OAB) and neurogenic detrusor overactivity.
  • Extended-Release Formulations: Used in the development of controlled-release tablets and transdermal delivery systems for improved patient compliance.
  • Generic Drug Manufacturing: Serves as the key raw material for producing generic versions of antimuscarinic drugs.
  • Clinical Research: Utilized in preclinical and clinical studies for new urological and antispasmodic treatments.
  • Veterinary Pharmaceuticals: Potential application in formulations for urinary incontinence in animals.
  • Reference Standard: Sourced by analytical laboratories for use as a high-purity chemical reference standard in quality testing.

Basic Information

Product Name Oxybutynin Hydrochloride
CAS No. 1508-65-2
Molecular Formula C22H31NO3·HCl
Molecular Weight 393.95 g/mol
Synonyms Oxybutynin HCl; 4-(Diethylamino)but-2-ynyl 2-cyclohexyl-2-hydroxy-2-phenylacetate hydrochloride; Ditropan; Oxytrol; Oxybutynin Chloride; Trospium (related class); Antispasmodic agent
EINECS Contact for details

Quality Control

Our Oxybutynin Hydrochloride is manufactured under strict quality management systems. We provide material that meets or exceeds relevant pharmacopeial standards, including USP and EP monographs. Every batch is supported by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles, ensuring traceability and compliance for GMP-driven applications.

Storage

Preserve in a tightly closed container, protected from light. Store at controlled room temperature, typically between 15-25°C (59-77°F), in a dry environment. The product is hygroscopic (moisture-sensitive) and should be handled in conditions of low humidity to maintain stability.

Specification

Item Specification
Appearance White or almost white crystalline powder
Identification (IR) Conforms to standard
Identification (HPLC) Retention time corresponds to reference standard
Assay (HPLC) 98.0% - 102.0% (on anhydrous basis)
Water (KF) ≤ 0.5%
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.

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