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

Somatostatin Related Compounds

API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Cyclosomatostatin API Standards CS-T-73917 84211-54-1 Enquire


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Somatostatin Acetate Impurities CS-T-61385 38916-34-6 Enquire


Intermediates

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Somatostatin Intermediates CS-T-85833 51110-01-1 In Stock