Description

Deoxycorticosterone Acetate CAS NO 56-47-3 is a synthetic steroid hormone and a key pharmaceutical intermediate. It is valued for its potent mineralocorticoid activity, making it a critical building block in the development of corticosteroid-based therapeutics. This compound is primarily required by pharmaceutical manufacturers and research institutions engaged in endocrinology, hormone replacement therapy, and advanced steroid synthesis.

Application

• Pharmaceutical Active Ingredient (API): A key intermediate in the synthesis of corticosteroid drugs.
• Reference Standard: Used in analytical laboratories for quality control and method validation in pharmaceutical testing.
• Biochemical Research: Employed in studies of adrenal cortex function, mineralocorticoid receptors, and electrolyte balance mechanisms.
• Veterinary Medicine: Utilized in formulations for treating adrenal insufficiency in animals.
• Hormone Replacement Therapy (HRT) Development: Serves as a precursor in the development of treatments for conditions like Addison's disease.

Basic Information

Product Name	Deoxycorticosterone Acetate
CAS No.	56-47-3
Molecular Formula	C23H32O4
Molecular Weight	372.50 g/mol
Synonyms	DOCA; Desoxycorticosterone Acetate; 21-Hydroxypregn-4-ene-3,20-dione 21-acetate; Cortexone 21-acetate; 4-Pregnene-21-ol-3,20-dione 21-acetate; Percorten Acetate; Deoxycortone Acetate; 11-Deoxycorticosterone Acetate
EINECS	200-278-5

Quality Control

Our Deoxycorticosterone Acetate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via IR and NMR spectroscopy, to ensure it meets high-grade pharmaceutical standards. A Certificate of Analysis (COA) detailing all specifications is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and light-sensitive; ensure containers are sealed tightly after each use to minimize exposure to air and humidity.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥ 98.0%
Loss on Drying	≤ 1.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Single Unknown Impurity	≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines

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