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

Dexchlorpheniramine Related Compounds

API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Dexchlorpheniramine Maleate API Standards CS-O-01285 2438-32-6 In Stock


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Dexchlorpheniramine Maleate EP Impurity B Impurities CS-P-06936 32188-09-3 Enquire
Dexchlorpheniramine n-Oxide Impurities CS-T-96042 142494-46-0 Enquire
N-Desmethyl N-Nitroso Dexchlorpheniramine Impurities CS-O-46572 Not Available Enquire