Description

Milveterol Hydrochloride is a high-purity pharmaceutical intermediate and active ingredient. This compound is critical for research and development in advanced therapeutic areas, offering a reliable building block for complex synthesis. It is primarily utilized by pharmaceutical manufacturers, biotechnology research organizations, and academic institutions engaged in the development of novel drug candidates.

Application

• Pharmaceutical intermediate in the synthesis of novel therapeutic agents.
• Key starting material (KSM) for active pharmaceutical ingredient (API) manufacturing.
• Reference standard for analytical method development and quality control in pharmaceutical labs.
• Biochemical research for studying specific biological pathways and receptor interactions.
• Pre-clinical and clinical research material for drug discovery programs.
• Production of high-value fine chemicals and specialty compounds.

Basic Information

Product Name	Milveterol Hydrochloride
CAS No.	804518-03-4
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Milveterol HCl; 804518-03-4; UNII-Contact for details; Milveterol Hydrochloride (USAN); Milveterol monohydrochloride; (Chemical IUPAC name - Contact for details)
EINECS	Contact for details

Quality Control

Our Milveterol Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency, meeting the stringent requirements for pharmaceutical development. Certificates of Analysis (COA) with detailed chromatographic and spectroscopic data are provided for every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0%
Water Content (KF)	≤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.