Description

Pasireotide (Aspartate) CAS NO 820232-50-6 is a high-purity synthetic peptide analog of somatostatin, specifically engineered for advanced pharmaceutical research and development. This compound is critical for its potent and selective binding to somatostatin receptor subtypes, offering a targeted mechanism of action. It is primarily utilized by pharmaceutical companies and research institutions engaged in the development of novel therapeutics for endocrine disorders, including Cushing's disease and acromegaly.

Application

• Pharmaceutical Active Ingredient (API): Core component in the formulation of injectable therapeutics for treating hormone-related conditions.
• Biomedical Research: Used as a critical reference standard and tool compound in preclinical studies investigating somatostatin receptor pathways.
• Drug Discovery & Development: Serves as a key intermediate in the synthesis and optimization of next-generation peptide-based drugs.
• Clinical Trial Material (CTM): Supplied as a high-grade material for use in Phase I-III clinical trials under Good Manufacturing Practice (GMP) guidelines.
• Endocrinology Studies: Applied in laboratory research to study the inhibition of growth hormone, IGF-1, and cortisol secretion.

Basic Information

Item	Detail
Product Name	Pasireotide (Aspartate)
CAS No.	820232-50-6
Molecular Formula	C58H66N10O9
Molecular Weight	1055.2 g/mol
Synonyms	Pasireotide Diaspartate; SOM230 (Aspartate); Cyclo(L-cysteinyl-L-phenylalanyl-D-tryptophyl-L-lysyl-L-threonyl-L-cysteinyl-L-tyrosyl-L-tryptophyl-L-lysyl-L-valyl-L-cysteinyl-L-threoninamide) (2→7)(7→12)(13→20)-tris(disulfide), L-Aspartate salt; Signifor (Aspartate); Pasireotide L-Aspartate; Pasireotide Aspartate Salt
EINECS	Contact for details

Quality Control

Our Pasireotide (Aspartate) is manufactured under strict quality systems to meet the exacting standards of the pharmaceutical industry. Each batch is subjected to comprehensive analytical testing, including HPLC for purity and assay, mass spectrometry for identity confirmation, and stringent tests for residual solvents and related substances. A comprehensive Certificate of Analysis (COA) is provided with every shipment, detailing compliance with specified parameters. We support development from research to commercial scale with appropriate documentation.

Storage

Preserve in a tightly closed container, protected from light. Store at a controlled room temperature of 15-25°C or as specified on the label. This product is hygroscopic (moisture-sensitive) and must be kept in a dry environment. For long-term storage, consider desiccated conditions at -20°C.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (HPLC/MS)	Conforms to reference standard
Assay (HPLC)	≥ 98.0%
Purity (HPLC)	≥ 97.0%
Water Content (KF)	≤ 5.0%
Acetate Content (HPLC)	3.0 - 8.0%
Single Impurity (HPLC)	≤ 1.0%
Total Impurities (HPLC)	≤ 3.0%
Residual Solvents (GC)	Meets ICH Q3C guidelines

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.