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Clearsynth is a leading innovator in pharmaceutical reference standards, offering high-quality Reference Standards for Flavoxate Hydrochloride, including both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope products, and nitrosamines (N-NO products). Our Flavoxate Hydrochloride impurity reference standards are invaluable for pharmaceutical research, supporting product development, ANDA and DMF submissions, quality control (QC), method validation, and stability studies. They also aid in identifying unknown impurities and assessing genotoxic potential.
Our Flavoxate Hydrochloride-related products undergo thorough characterization and are supplied with detailed Certificates of Analysis (COA) and analytical data that meet regulatory requirements. All supplied products are re-tested at regular intervals to ensure ongoing quality and compliance.

Flavoxate Hydrochloride Related Compounds

API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Flavoxate Hydrochloride API CS-O-11651 3717-88-2 In Stock


Metabolite

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Flavoxate EP Impurity A Metabolite CS-O-06097 3468-01-7 In Stock


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Flavoxate EP Impurity C Impurity CS-EO-01811 1286165-14-7 Enquire


Secondary Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Flavoxate hydrochloride Secondary Standards CS-SS-25995-500MG 3717-88-2 Enquire