Description

Afurolol is a specialized organic compound with significant utility in advanced chemical synthesis and pharmaceutical research. Its unique molecular structure makes it a valuable intermediate for developing novel active pharmaceutical ingredients (APIs) and fine chemicals. This product is essential for R&D laboratories and production facilities in the pharmaceutical, agrochemical, and life science sectors seeking high-purity building blocks.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of β-blocker and other cardiovascular drug candidates.
• Chemical Research & Development: Used as a precursor for exploring new chemical entities and reaction pathways in medicinal chemistry.
• Agrochemical Synthesis: Serves as an intermediate in the development of advanced crop protection agents and herbicides.
• Fine Chemical Production: Employed in the manufacture of complex, high-value specialty chemicals for various industrial applications.
• Academic Research: Utilized in university and institutional labs for pharmacological studies and biochemical research.
• Reference Standard: Can be supplied as a high-purity standard for analytical method development and quality control in API manufacturing.

Basic Information

Product Name	Afurolol
CAS No.	65776-67-2
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	65776-67-2; Afurolol; 1-(4-Fluorophenoxy)-3-[(1-methylethyl)amino]-2-propanol; 3-(Isopropylamino)-1-(4-fluorophenoxy)-2-propanol; 1-(p-Fluorophenoxy)-3-(isopropylamino)-2-propanol; (±)-1-(4-Fluorophenoxy)-3-(isopropylamino)-2-propanol; DL-Afuralol; DL-Afuralol hydrochloride
EINECS	Contact for details

Quality Control

Our Afurolol is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. Each lot undergoes comprehensive analytical testing, including identity confirmation, purity assay, and impurity profiling via techniques such as HPLC, GC, and NMR. Certificates of Analysis (COA) detailing all test results are provided with every shipment. We can support development and commercial projects requiring compliance with cGMP, ICH Q7, and other relevant pharmaceutical guidelines.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (typically 15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed to prevent moisture absorption, which may affect stability and handling properties. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white powder or crystalline solid
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Loss on Drying	≤ 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.