Octreotide EP Impurity A Acetate CAS CATO-C4X-15208

Description

The occurrence of Octreotide EP Impurity A Acetate is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

Octreotide EP Impurity A Acetate (CAS CATO-C4X-15208) is a certified pharmaceutical impurity reference standard with the molecular formula C49H64N10O11S2C2H4O2 and a molecular weight of 1093.28 g/mol.

Based on its molecular formula C49H64N10O11S2C2H4O2, Octreotide EP Impurity A Acetate contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 1093.28 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

This reference standard supports related-substances testing and method development in line with ICH Q3A/Q3B guidance on impurity control, and is suitable for system suitability testing and forced-degradation studies.

CATO manufactures Octreotide EP Impurity A Acetate under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

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