Description

Tienoxolol Hydrochloride is a high-purity pharmaceutical intermediate and active pharmaceutical ingredient (API). This compound is critical for research and development in cardiovascular pharmacology, offering a key building block for advanced therapeutic agents. It is primarily utilized by pharmaceutical manufacturers, R&D laboratories, and academic institutions engaged in the synthesis of β-adrenergic blocking agents and related compounds.

Application

• Pharmaceutical API Synthesis: Serves as a key intermediate in the production of β-blocker medications.
• Cardiovascular Research: Used in preclinical and clinical studies targeting hypertension and arrhythmias.
• Metabolite Standard: Employed as a reference standard in analytical method development and bioanalytical studies.
• Process Chemistry: Acts as a starting material or intermediate for the scalable synthesis of novel drug candidates.
• Quality Control Laboratories: Utilized as a certified reference material for assay and impurity testing.

Basic Information

Product Name	Tienoxolol Hydrochloride
CAS No.	97067-66-8
Molecular Formula	C15H24N2O3 • HCl
Molecular Weight	332.82 g/mol
Synonyms	Tienoxolol HCl; 1-(tert-Butylamino)-3-[(2-methyl-1,3-thiazol-4-yl)methoxy]propan-2-ol Hydrochloride; Tienoxolol Hydrochloride; Tienoxolol Monohydrochloride; (±)-Tienoxolol Hydrochloride; rac-Tienoxolol Hydrochloride; 4-[[2-Hydroxy-3-[(1,1-dimethylethyl)amino]propoxy]methyl]-2-methylthiazole Hydrochloride
EINECS	Contact for details

Quality Control

Our Tienoxolol Hydrochloride is manufactured under a strict quality management system. Each batch is subjected to comprehensive analytical testing, including identification, assay, and impurity profiling, to ensure it meets high-purity standards suitable for pharmaceutical R&D. A Certificate of Analysis (COA) detailing all test results is provided with every shipment.

Storage

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

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.5%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 1.0% Any single impurity ≤ 0.5%

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