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

Hexamidine Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Hexamidine-d12 Impurity A Hydrochloride Stable Isotopes CS-T-100247 Not Available Enquire
Hexamidine-D12 Stable Isotopes CS-P-01039 Not Available Enquire
Hexamidine-d12 Dihydrochloride Stable Isotopes CS-T-78221 1286461-12-8 Enquire


API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Hexamidine diisethionate API CS-ED-42211 659-40-5 In Stock
Hexamidine API CS-P-01037 3811-75-4 Enquire


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Hexamidine EP Impurity B Impurity CS-O-37190 2469554-78-5 Enquire
Hexamidine EP Impurity D Impurity CS-O-37193 2514722-87-1 Enquire
Hexamidine EP Impurity C Impurity CS-O-37192 Not Available Enquire
Hexamidine Impurity 4 Impurity CS-P-01038 74065-84-2 Enquire