Description

Flavoxate Hydrochloride is a pharmaceutical-grade antispasmodic agent primarily used as a smooth muscle relaxant. It is a critical active pharmaceutical ingredient (API) valued for its efficacy in treating urinary tract disorders. This compound is essential for manufacturers in the pharmaceutical industry developing medications for conditions like overactive bladder and interstitial cystitis. Our supply ensures high purity and consistent quality for reliable formulation and production.

Application

• Primary Active Pharmaceutical Ingredient (API) in antispasmodic and urinary tract medication formulations.
• Key component in the production of tablets and capsules for the treatment of overactive bladder (OAB) symptoms.
• Used in pharmaceutical R&D for developing new therapeutic agents targeting smooth muscle spasms.
• Essential material for compounding pharmacies requiring high-purity bulk pharmaceuticals.
• Reference standard in analytical laboratories for quality control and method development.
• Intermediate in the synthesis of more complex pharmaceutical compounds.

Basic Information

Product Name	Flavoxate Hydrochloride
CAS No.	3717-88-2
Molecular Formula	C24H25NO4·HCl
Molecular Weight	427.92 g/mol
Synonyms	Flavoxate HCl; 3-Methylflavone-8-carboxylic Acid 2-Piperidinoethyl Ester Hydrochloride; 2-(Piperidin-1-yl)ethyl 3-methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylate hydrochloride; Urispas (brand name); Genurin; Bladderon; Urispadol; Rec-15/2051
EINECS	223-074-6

Quality Control

Our Flavoxate Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets stringent pharmaceutical standards, including identification, purity, and impurity profile assessments. A Certificate of Analysis (COA) detailing results for assay, related substances, residual solvents, and other critical parameters is provided with every 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 material is hygroscopic (moisture-sensitive) and light-sensitive; therefore, containers must be kept tightly sealed and away from moisture and direct light exposure to maintain stability and potency.

Specification

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

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