Description

Hydromadinone Acetate is a synthetic steroidal progestin of significant importance in pharmaceutical research and development. This compound serves as a key intermediate in the synthesis of advanced hormonal active pharmaceutical ingredients (APIs). It is primarily required by pharmaceutical manufacturers and research institutions engaged in the development of hormone-based therapies and contraceptive formulations.

Application

• Pharmaceutical Intermediate: A critical building block in the synthesis of steroidal progestins and other hormonal APIs.
• Contraceptive Research: Used in the development and study of novel hormonal contraceptive agents.
• Hormone Therapy Development: Serves as a precursor in creating treatments for hormone-related conditions.
• Biochemical Research: Employed in laboratory studies to investigate progestin receptor activity and metabolic pathways.
• Reference Standard: Utilized as a high-purity analytical standard for quality control and method validation in pharmaceutical analysis.

Basic Information

Product Name	Hydromadinone Acetate
CAS No.	33125-90-5
Molecular Formula	C23H30O4
Molecular Weight	370.49 g/mol
Synonyms	6-Chloro-17α-hydroxy-6-dehydroprogesterone acetate; 6-Chloro-17α-hydroxypregna-4,6-diene-3,20-dione acetate; 17α-Acetoxy-6-chloro-4,6-pregnadiene-3,20-dione; SH-714; 6-Chloro-δ6-17α-acetoxyprogesterone; 6-Chloro-17α-acetoxypregna-4,6-diene-3,20-dione
EINECS	Contact for details

Quality Control

Our Hydromadinone Acetate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical research and development. Certificates of Analysis (COA) detailing identity, purity, and impurity profiles are provided with 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 to prevent moisture absorption.

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%
Related Substances (HPLC)	Total impurities ≤2.0%
Loss on Drying	≤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.