Description

11-Deoxy Prednisone Acetate is a synthetic steroid derivative and a key pharmaceutical intermediate. This compound is valued for its role in the synthesis of more complex corticosteroid APIs, offering a critical building block for advanced pharmaceutical manufacturing. It is primarily utilized by research institutions and pharmaceutical companies engaged in the development and production of steroidal anti-inflammatory drugs and other therapeutic agents.

Application

• Pharmaceutical Intermediate: A crucial precursor in the multi-step synthesis of potent corticosteroid active pharmaceutical ingredients (APIs).
• Steroid Research & Development: Used in laboratory settings for the research and development of new steroidal compounds with potential therapeutic applications.
• Reference Standard: Serves as a high-purity analytical reference standard for quality control and method validation in pharmaceutical analysis.
• Biochemical Studies: Employed in biochemical research to study steroid metabolism, receptor binding, and structure-activity relationships (SAR).

Basic Information

Product Name	11-Deoxy Prednisone Acetate
CAS No.	1249-67-8
Molecular Formula	C23H28O5
Molecular Weight	384.47 g/mol
Synonyms	11-Deoxyprednisone Acetate; 17α,21-Dihydroxypregna-1,4-diene-3,11,20-trione 21-Acetate; 1,4-Pregnadiene-17α,21-diol-3,11,20-trione 21-Acetate; 21-Acetoxy-11-deoxyprednisone; NSC 10481; 11-Desoxyprednisone Acetate
EINECS	Contact for details

Quality Control

Our 11-Deoxy Prednisone 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 exacting standards for pharmaceutical intermediate use. Certificates of Analysis (COA) documenting all critical quality attributes are available upon request.

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 should be handled in a low-humidity environment to prevent degradation.

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%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Loss on Drying	≤ 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.