Description

Lanreotide is a synthetic octapeptide analog of somatostatin, a naturally occurring hormone that regulates endocrine and exocrine secretion. This compound is of critical importance in the pharmaceutical industry for its potent and long-acting inhibitory effects on growth hormone, insulin, and glucagon. It is primarily required by pharmaceutical manufacturers and research institutions developing treatments for acromegaly and neuroendocrine tumors (NETs).

Application

• Pharmaceutical Active Ingredient (API): Primary use in the formulation of long-acting injectable depot therapies for chronic conditions.
• Acromegaly Treatment: Used in medications to reduce the production of growth hormone and insulin-like growth factor 1 (IGF-1) in patients.
• Neuroendocrine Tumor (NET) Management: Key component in therapies aimed at controlling symptoms like flushing and diarrhea associated with functional NETs.
• Research & Development: Serves as a critical reference standard and investigational compound in endocrinology and oncology research.
• Peptide Synthesis Studies: Used as a model compound in the development and optimization of solid-phase peptide synthesis (SPPS) techniques.

Basic Information

Product Name	Lanreotide
CAS No.	118992-92-0
Molecular Formula	C54H69N11O10S2
Molecular Weight	1096.3 g/mol
Synonyms	Lanreotide Acetate; BIM-23014; Somatuline; D-Phenylalanyl-L-cysteinyl-L-tyrosyl-D-tryptophyl-L-lysyl-L-valyl-L-cysteinyl-L-threoninamide, cyclic (2→7)-disulfide; (2R)-2-[[(2R)-2-[[(2S)-2-[[(2R)-2-[[(2S)-2,6-Diamino-1-hexanoyl]-N-methyl-L-valyl]-L-cysteinyl]-L-tyrosyl]-D-tryptophyl]-L-lysyl]-L-valyl]-L-cysteinyl-L-threoninamide cyclic (2→7)-disulfide acetate
EINECS	Contact for details

Quality Control

Our Lanreotide is manufactured under strict cGMP guidelines to ensure the highest standards of purity and consistency for pharmaceutical applications. Each batch undergoes comprehensive analytical testing, including HPLC for purity and assay, peptide mapping, and stringent controls for related substances and residual solvents. A Certificate of Analysis (COA) detailing all specifications is provided with every shipment to guarantee compliance with your project requirements.

Storage

Preserve in a tightly closed container, protected from light. Store at a controlled room temperature of 15-25°C or under refrigeration at 2-8°C as specified. The product is hygroscopic (moisture-sensitive) and must be kept in a dry environment. For long-term storage, consider desiccant use and inert atmosphere to maintain stability.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (HPLC)	Conforms to reference standard
Identification (MS)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Purity (HPLC)	≥ 97.0% (Total related substances ≤ 3.0%)
Single Impurity (HPLC)	≤ 1.0%
Water Content (KF)	≤ 5.0%
Acetate Content (HPLC)	5.0% - 12.0%
Residual Solvents (GC)	Meets ICH Q3C guidelines
Bacterial Endotoxins	< 10.0 EU/mg

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