Description

Protokylol is a synthetic adrenergic agent with specific pharmacological activity. This compound is valued in research and development for its role as a β-adrenergic receptor agonist. It is primarily utilized by the pharmaceutical industry and research institutions for investigative and developmental purposes. Our supply ensures high purity and consistency for critical applications.

Application

• Pharmaceutical Research & Development: Used as a reference standard and active pharmaceutical ingredient (API) intermediate in the development of adrenergic drugs.
• Biochemical Studies: Employed in in vitro and in vivo studies to investigate β-adrenergic receptor mechanisms and signaling pathways.
• Analytical Standard: Serves as a high-purity certified reference material (CRM) for quality control and method validation in analytical laboratories.
• Preclinical Studies: Utilized in pharmacological profiling and safety assessment during early-stage drug discovery programs.

Basic Information

Product Name	Protokylol
CAS No.	136-70-9
Molecular Formula	C16H21NO3
Molecular Weight	275.35 g/mol
Synonyms	Protokylol Hydrochloride (common salt form); 1-(3,4-Dihydroxyphenyl)-2-(isopropylamino)butan-1-ol; (±)-Protokylol; N-Isopropylarterenol; Caytine (trade name); Ventaire (trade name); Protokylol HCl; 4-[1-Hydroxy-2-(isopropylamino)butyl]benzene-1,2-diol
EINECS	205-250-2

Quality Control

Our Protokylol is manufactured under a strict quality management system. Each batch undergoes comprehensive analytical testing, including identification, assay, and impurity profiling, to ensure it meets the highest standards for research and development use. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming identity, purity, and conformance to specifications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive); ensure the container is kept tightly sealed in a low-humidity environment to maintain stability and purity.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0%
Water Content (KF)	≤0.5%
Residue on Ignition	≤0.1%

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