Description

Bedoradrine Sulfate is a high-purity pharmaceutical intermediate and reference standard of significant importance in modern drug development and quality control. Its primary value lies in its role as a critical building block for the synthesis of novel therapeutic agents, particularly within the cardiovascular and respiratory domains. This compound is essential for pharmaceutical R&D laboratories, analytical testing facilities, and manufacturers engaged in producing advanced active pharmaceutical ingredients (APIs).

Application

• Pharmaceutical Intermediate: A key precursor in the multi-step synthesis of complex drug molecules targeting specific biological pathways.
• Reference Standard: Used in analytical laboratories for method development, validation, and quality control testing of APIs and finished drug products via HPLC, LC-MS, or NMR.
• Biochemical Research: Employed in in vitro studies to investigate pharmacological activity, receptor binding affinity, and metabolic pathways.
• Process Development & Scale-up: Serves as a benchmark material for optimizing synthetic routes and purification processes during technology transfer from lab to pilot and commercial scale.
• Impurity Profiling: Utilized to identify, characterize, and quantify related substances and degradation products in compliance with ICH guidelines.

Basic Information

Product Name	Bedoradrine Sulfate
CAS No.	1000308-25-7
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Bedoradrine Sulphate; (1R,2S)-2-[(3,4-Dihydroxyphenyl)methylamino]-1-(3,4-dihydroxyphenyl)ethanol sulfate; Norepinephrine analogue sulfate; Racemic mixture of Bedoradrine Sulfate (if applicable); AR-13324 (potential research code)
EINECS	Contact for details

Quality Control

Our Bedoradrine Sulfate is manufactured under strict quality management systems. Every batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide full traceability and detailed Certificates of Analysis (COA) that include results for assay, related substances, residual solvents, and other critical parameters. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates, ensuring reliability for your most demanding applications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (typically 15-25°C). The product is light-sensitive and should be handled under appropriate conditions to maintain stability. Keep the container tightly sealed when not in use to protect from moisture.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference standard
Identification (HPLC)	Retention time matches reference
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Water Content (KF)	≤ 1.0%
Residual Solvents (GC)	Complies with ICH Q3C
Heavy Metals	< 20 ppm

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