Description

Butocrolol is a selective β-adrenergic receptor antagonist (β-blocker) with significant pharmacological activity. This compound is a crucial intermediate in the research and development of cardiovascular therapeutics, offering a pathway to more targeted and effective treatments. It is primarily utilized by pharmaceutical R&D laboratories and fine chemical manufacturers engaged in the synthesis of advanced active pharmaceutical ingredients (APIs).

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of novel β-blocker APIs for cardiovascular drugs.
• Biochemical Research: Used as a reference standard or tool compound in pharmacological studies of adrenergic receptors.
• Preclinical Development: Serves as a starting material for creating analogs and derivatives in drug discovery programs.
• Fine Chemical Synthesis: Employed in multi-step organic synthesis for producing complex, high-value molecules.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for cGMP production.

Basic Information

Product Name	Butocrolol
CAS No.	55165-22-5
Molecular Formula	C16H25NO3
Molecular Weight	279.38 g/mol
Synonyms	Butocrolol; 1-(tert-Butylamino)-3-[(5,6,7,8-tetrahydro-cis-6,7-dihydroxy-1-naphthyl)oxy]-2-propanol; (±)-Butocrolol; Butocrololum; DL-Butocrolol; Bunitrolol Impurity; Adrenergic β-Antagonist
EINECS	Contact for details

Quality Control

Our Butocrolol is manufactured under strict quality management systems. Every batch undergoes comprehensive analytical testing, including HPLC for purity, identity confirmation by IR and NMR spectroscopy, and residual solvent analysis. A detailed Certificate of Analysis (COA) is provided with each shipment, ensuring traceability and compliance with your research or manufacturing specifications.

Storage

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

Specification

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

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