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

Buserelin Related Compounds

API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Buserelin API Standards CS-O-01043 57982-77-1 In Stock


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Buserelin EP Impurity A Impurities CS-P-08920 1872434-99-5 Enquire
Buserelin EP Impurity B Impurities CS-P-08921 1926163-21-4 Enquire
Buserelin EP Impurity E Impurities CS-P-08924 1926163-20-3 Enquire
Buserelin EP Impurity F Impurities CS-P-08925 Not Available Enquire
D-His-Buserelin Impurities CS-O-47529 Not Available Enquire


Intermediates

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Buserelin Acetate Intermediates CS-T-49962 68630-75-1 Enquire