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Arbutamine CAS NO 130783-37-8


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CAS No.:130783-37-8

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Arbutamine is a synthetic catecholamine derivative and a potent β-adrenergic receptor agonist. This compound is of significant interest in pharmaceutical research and development, particularly for its cardiovascular effects. It is primarily utilized by pharmaceutical companies, research institutions, and contract development and manufacturing organizations (CDMOs) engaged in cardiac stress testing, cardiovascular drug discovery, and the synthesis of advanced pharmaceutical intermediates.

Application

  • Pharmaceutical Intermediate: Key starting material or intermediate in the synthesis of advanced cardiovascular drugs and diagnostic agents.
  • Cardiac Stress Testing Research: Used in preclinical and clinical research to simulate cardiac stress and study myocardial perfusion and function.
  • β-Adrenergic Receptor Studies: A valuable pharmacological tool for investigating β-1 and β-2 adrenergic receptor activity and signaling pathways.
  • Diagnostic Agent Development: Serves as a core component in the development of diagnostic pharmaceuticals for heart disease assessment.
  • Chemical Reference Standard: Employed as a high-purity standard in analytical laboratories for quality control and method validation (HPLC, LC-MS).
  • Academic & Institutional Research: Used in university and institutional labs for cardiovascular pharmacology and medicinal chemistry studies.

Basic Information

Product Name Arbutamine
CAS No. 130783-37-8
Molecular Formula C16H25NO3
Molecular Weight 279.38 g/mol
Synonyms (-)-Arbutamine; (R)-(-)-Arbutamine; (R)-4-[2-[[2-(3,4-Dihydroxyphenyl)-2-hydroxyethyl]amino]propyl]phenol; (R)-Arbutamine; Arbutamine [USAN:INN]; Gensar; (+-)-Arbutamine (racemic mixture); 1-(3,4-Dihydroxyphenyl)-2-[[(1R)-1-(4-hydroxyphenyl)-2-methylpropyl]amino]ethanol
EINECS Contact for details

Quality Control

Our Arbutamine is manufactured under a strict quality management system. Every batch undergoes comprehensive analytical testing, including HPLC for purity, identity confirmation by IR and MS, and residual solvent analysis to ensure it meets exacting standards for research and pharmaceutical use. A Certificate of Analysis (COA) detailing all test results is provided with each shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). The product is light-sensitive and should be handled under appropriate conditions to maintain stability.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time corresponds to reference standard
Purity (HPLC) ≥98.0%
Water Content (KF) ≤0.5%
Residue on Ignition ≤0.1%
Heavy Metals ≤20 ppm
Specific Rotation Contact for details

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

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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

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