Description

Hexoprenaline Sulfate is a selective β2-adrenergic receptor agonist, a high-purity pharmaceutical active ingredient. It is valued for its bronchodilatory properties, making it a critical intermediate in the synthesis of specialized respiratory medications. This compound is essential for pharmaceutical R&D and manufacturing sectors focused on developing treatments for asthma and other obstructive pulmonary conditions. Hexoprenaline Sulfate CAS NO 34459-26-2 is supplied under stringent quality control to ensure batch-to-batch consistency.

Application

• Pharmaceutical Active Ingredient (API): Primary use as the key active component in prescription bronchodilator formulations.
• Respiratory Drug Development: Critical intermediate in the R&D and synthesis of new therapeutics for asthma, chronic obstructive pulmonary disease (COPD), and bronchospasm.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method validation in pharmaceutical laboratories.
• Clinical Research Material: Used in preclinical and clinical studies investigating β2-adrenergic agonist efficacy and safety profiles.
• Formulation Studies: Employed in the development of various drug delivery systems, including inhalers and nebulizer solutions.
• Tocolytic Agent Research: Investigated for potential use in pharmaceutical preparations aimed at suppressing premature labor, leveraging its uterine relaxant effects.

Basic Information

Product Name	Hexoprenaline Sulfate
CAS No.	34459-26-2
Molecular Formula	C22H32N2O10S
Molecular Weight	516.56 g/mol
Synonyms	Hexoprenaline Sulphate; 4,4'-[1,6-Hexanediylbis(iminomethylene)]bis[1,2-benzenediol] Sulfate; Ipradol; GU-082; (±)-Hexoprenaline Sulfate; DL-Hexoprenaline Sulfate; 1,6-Bis(3,4-dihydroxyphenyl)hexamethylenediamine Disulfate
EINECS	Contact for details

Quality Control

Our Hexoprenaline Sulfate is manufactured under current Good Manufacturing Practice (cGMP) principles. Each batch undergoes comprehensive analytical testing to ensure it meets stringent specifications for identity, purity, and potency. We provide full traceability and detailed Certificates of Analysis (COA) for all shipments, confirming compliance with relevant pharmacopeial standards (e.g., USP, EP) as required.

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) and must be kept in a dry environment to prevent degradation. For long-term storage, consider desiccated conditions.

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% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 5.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%

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