Description

16-o-Deacetylfusidic Acid is a key intermediate and derivative of the potent antibiotic fusidic acid. This compound is of significant interest in pharmaceutical research and development, particularly for the synthesis of novel antimicrobial agents. It is primarily utilized by research institutions and pharmaceutical manufacturers engaged in the development of new antibiotics and the study of bacterial resistance mechanisms.

Application

• Pharmaceutical Intermediate: Serves as a critical building block in the chemical synthesis of novel fusidic acid derivatives and semi-synthetic antibiotics.
• Antimicrobial Research: Used as a reference standard and active material in microbiological studies to investigate structure-activity relationships and mechanisms of action against Gram-positive bacteria.
• Biochemical Research: Employed in enzymatic studies, particularly those involving the modification of fusidic acid by bacterial enzymes, to understand resistance pathways.
• Analytical Standard: Functions as a high-purity certified reference material (CRM) for quality control and analytical method development in pharmaceutical testing laboratories.

Basic Information

Product Name	16-o-Deacetylfusidic Acid
CAS No.	13090-91-0
Molecular Formula	C31H48O6
Molecular Weight	516.72 g/mol
Synonyms	16-Deacetylfusidic Acid; 3α,11α,16β-Trihydroxy-29-nordammara-17(20),24-dien-21-oic Acid; Fusidic Acid Impurity C; 16-Desacetylfusidic Acid; 16-O-Deacetyl Fusidic Acid; 16-Deacetyl-fusidic Acid; 16-Deacetyl Fusidate
EINECS	Contact for details

Quality Control

Our 16-o-Deacetylfusidic Acid is produced and tested under a strict quality management system. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. Certificates of Analysis (COA) detailing specific results for all critical parameters are provided and available upon request, supporting compliance in research and development applications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). The product is light-sensitive and should be handled under appropriate conditions to maintain stability.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥ 95.0%
Related Substances (HPLC)	Total impurities ≤ 5.0%
Loss on Drying	≤ 2.0%
Residue on Ignition	≤ 0.5%

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