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

Montelukast Sodium Related Compounds

API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Montelukast Sodium API Standards CS-O-01855 151767-02-1 In Stock


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Dihydro Montelukast Sodium Salt Impurities CS-T-53076 142147-98-6 In Stock
Dihydro Montelukast Sodium Salt Impurities CS-O-33060 142147-98-6 Enquire
ent-Montelukast Sodium Salt Impurities CS-T-82793 190078-45-6 Enquire
Montelukast EP Impurity F Impurities CS-O-11860 937275-23-5 In Stock
Montelukast EP impurity G Impurities CS-O-11861 774538-96-4 In Stock
Montelukast sodium racemate Impurities CS-EO-00151 Not Available Enquire