Description

Lusutrombopag CAS NO 1110766-97-6 is a potent, orally bioavailable, small-molecule thrombopoietin receptor agonist. This compound is of critical importance for its targeted therapeutic action in stimulating platelet production. It is primarily required by pharmaceutical manufacturers and research institutions engaged in the development and production of treatments for thrombocytopenia, particularly in patients with chronic liver disease who are scheduled to undergo invasive procedures.

Application

• Active Pharmaceutical Ingredient (API) in the manufacture of thrombopoietin receptor agonist medications.
• Clinical Research for investigating new therapeutic protocols for thrombocytopenia.
• Pharmaceutical Development for formulation studies, stability testing, and dosage form optimization.
• Reference Standard for quality control and analytical method validation in pharmaceutical laboratories.
• Biochemical Research for studying megakaryocyte proliferation and platelet biogenesis pathways.

Basic Information

Product Name	Lusutrombopag
CAS No.	1110766-97-6
Molecular Formula	C₂₉H₃₂Cl₂N₄O₅
Molecular Weight	563.49 g/mol
Synonyms	Lusutrombopag; S-888711; Mulpleta; 1-[3-Chloro-5-[[4-(4-chlorophenoxy)-2-fluorophenyl]carbamoyl]-2-pyridyl]piperidine-4-carboxylic acid; 3'-Chloro-5'-[4-(4-chlorophenoxy)-2-fluorophenyl]carbamoyl-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5-carboxylic acid
EINECS	Contact for details

Quality Control

Our Lusutrombopag is manufactured under strict quality management systems. It undergoes rigorous analytical testing to ensure compliance with high-purity standards suitable for pharmaceutical research and development. A comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles is provided with each batch to support your regulatory and quality assurance requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed in a dry environment to prevent degradation.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0% Any single impurity ≤0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Water Content (KF)	≤1.0%
Heavy Metals	≤20 ppm

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