Description

Oxyfedrine is a synthetic organic compound with significant pharmacological activity, primarily functioning as a β-adrenergic agonist and vasodilator. This compound is valued for its role in cardiovascular research and pharmaceutical development, offering a key intermediate for creating therapeutic agents. It is essential for research institutions, pharmaceutical manufacturers, and chemical suppliers engaged in the development of cardiac medications and related biochemical studies.

Application

• Pharmaceutical Intermediate: Serves as a critical building block in the synthesis of active pharmaceutical ingredients (APIs) for cardiovascular drugs.
• Biochemical Research: Used in laboratory studies to investigate β-adrenergic receptor mechanisms and coronary vasodilation.
• Reference Standard: Employed as a high-purity analytical standard in quality control laboratories for method development and validation.
• Preclinical Development: Utilized in the research and development phase for new therapeutic agents targeting angina and myocardial metabolism.

Basic Information

Product Name	Oxyfedrine
CAS No.	15687-41-9
Molecular Formula	C19H23NO3
Molecular Weight	313.39 g/mol
Synonyms	Oxyfedrine; 3-[(1-Methyl-2-phenoxyethyl)amino]-1-(3,4,5-trimethoxyphenyl)-1-propanone; 1-(3,4,5-Trimethoxyphenyl)-3-[(1-methyl-2-phenoxyethyl)amino]-1-propanone; Ildamen; Modacor; Oxyphylline; Oxyfedrin; Contact for additional synonyms.
EINECS	Contact for details

Quality Control

Our Oxyfedrine is produced and tested under a strict quality management system to ensure batch-to-batch consistency and high purity. We provide comprehensive analytical data, including identity confirmation, purity assay, and impurity profiling via techniques such as HPLC, NMR, and IR spectroscopy. A Certificate of Analysis (COA) detailing all specifications is available for every batch to support your quality assurance and regulatory compliance needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (typically 15-25°C). Keep away from incompatible materials and sources of ignition.

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)	≥ 98.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 1.0%

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