Description

Landiolol is a highly selective, ultra-short-acting β-1 adrenergic receptor antagonist. This compound is of significant interest in the pharmaceutical industry due to its rapid onset and offset of action, making it a valuable agent for precise cardiovascular control. It is primarily utilized in clinical and research settings for the management of acute tachyarrhythmias and perioperative hypertension. Our supply of Landiolol CAS NO 133242-62-3 ensures high purity and reliability for critical pharmaceutical development and manufacturing processes.

Application

• Pharmaceutical Active Ingredient (API): Core component in the formulation of injectable drugs for rapid heart rate control.
• Clinical Research: Used in studies investigating the management of supraventricular tachyarrhythmias (SVTs), including atrial fibrillation and flutter.
• Perioperative Medicine: Administration during and after surgery to manage tachycardia and hypertension without prolonged effects.
• Cardiac Stress Testing: Employed as a pharmacological agent to simulate controlled cardiac stress in diagnostic procedures.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method development in pharmaceutical laboratories.
• Drug Development: Key intermediate or final compound in the R&D of new ultra-short-acting cardiovascular therapeutics.

Basic Information

Product Name	Landiolol
CAS No.	133242-62-3
Molecular Formula	C25H35N3O4
Molecular Weight	441.57 g/mol
Synonyms	ONO-1101; Landiolol Hydrochloride; 2-Propanol, 1-[4-[2-hydroxy-3-[(1-methylethyl)amino]propoxy]phenyl]-3-[4-(1-methylethyl)phenyl]-; (RS)-1-[4-[2-Hydroxy-3-(isopropylamino)propoxy]phenyl]-3-(4-isopropylphenyl)propan-1-ol; ONO1101; Landiololum
EINECS	Contact for details

Quality Control

Our Landiolol is manufactured and tested under strict quality management systems to meet the rigorous standards required for pharmaceutical intermediates and active ingredients. We provide comprehensive analytical data to support your regulatory filings. A detailed Certificate of Analysis (COA), including purity by HPLC, identification (IR, NMR), and impurity profile, is available for every batch upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and should be handled 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%
Water Content (KF)	≤1.0%
Residue on Ignition	≤0.1%

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