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

Escitalopram Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Escitalopram D4 Oxalate Stable Isotopes CS-EO-02395 219861-08-2 (Unlabelled) Enquire
N-Nitroso-Desmethyl Escitalopram-d3 Stable Isotopes CS-O-53621 Not Available In Stock


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Escitalopram EP Impurity I (oxalate salt) Impurities CS-EO-03540 920282-75-3 (Freebase) Enquire
Escitalopram Impurity 4 Impurities CS-EO-00978 Not Available Enquire
Escitalopram USP Related Compound A Impurities CS-O-32121 128173-53-5 In Stock
N-Nitroso-desmethyl Escitalopram Impurity C Impurities CS-EO-02124 Not Available Enquire