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

Levocloperastine Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Levocloperastine D10 Stable Isotopes CS-O-38344 Not Available Enquire
Levocloperastine D4 Stable Isotopes CS-O-38539 Not Available Enquire


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
(R)-1-[2-[(4-Chlorophenyl)-phenyl-methoxy]ethyl]piperidine h... Impurities CS-O-52902 Not Available Enquire
Rac-Cloperastine fendizoate Impurities CS-L-00015 85187-37-7 In Stock