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Clearsynth is a leading innovator in pharmaceutical reference standards, offering high-quality Reference Standards for Idoxuridine, including both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope products, and nitrosamines (N-NO products). Our Idoxuridine 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 Idoxuridine-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.

Idoxuridine Related Compounds

API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Idoxuridine API CS-T-29109 54-42-2 Enquire


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
ent-Idoxuridine Impurity CS-T-56590 162239-35-2 Enquire


Secondary Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Idoxuridine Secondary Standards CS-SS-25632-500MG 54-42-2 Enquire