Description

Hexoprenaline Sulphate is a selective β2-adrenergic receptor agonist, primarily recognized for its tocolytic properties. This compound is valued for its high purity and consistent quality, which are critical for reliable research and pharmaceutical development. It is essential for researchers and manufacturers in the pharmaceutical industry, particularly those focused on developing treatments for premature labor and respiratory conditions.

Application

• Pharmaceutical Intermediates: Serves as a key active pharmaceutical ingredient (API) or intermediate in the synthesis of tocolytic agents.
• Biochemical Research: Used as a reference standard and research tool in pharmacological studies of β2-adrenergic receptor activity and smooth muscle relaxation.
• Formulation Development: Employed in the development and stability testing of parenteral and inhalation drug formulations targeting bronchospasm.
• Quality Control Standards: Acts as a certified reference material (CRM) for analytical method development and validation in QC laboratories.

Basic Information

Product Name	Hexoprenaline Sulphate
CAS No.	3215-70-1
Molecular Formula	C22H32N2O10S
Molecular Weight	516.56 g/mol
Synonyms	Hexoprenaline Sulfate; Ipradol; 1-(3,5-Dihydroxyphenyl)-2-{[4-(1,2,3,4-tetrahydro-1-naphthyl)butyl]amino}ethanol sulfate; 4-[1-Hydroxy-2-(hexahydro-1H-azepin-1-yl)ethyl]-1,2-benzenediol sulfate; EINECS 221-739-7; Delaprem; GU 119
EINECS	221-739-7

Quality Control

Our Hexoprenaline Sulphate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling, to ensure it meets stringent specifications suitable for research and development. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept in a dry environment to maintain stability and potency.

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%
Water Content (KF)	≤ 5.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0%

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