Description

12,13-Didehydro-14-Hydroxy-12,12-o-Seco-13-Deoxymycinamicin I is a complex macrolide derivative, representing a key intermediate or reference standard in advanced pharmaceutical research and development. This compound is of significant interest for its structural relationship to bioactive macrolides, enabling critical studies in synthetic chemistry and antibiotic mechanism elucidation. It is primarily utilized by research institutions, pharmaceutical R&D departments, and fine chemical manufacturers focused on novel antibiotic discovery and process chemistry.

Application

• Pharmaceutical Reference Standard: Serves as a high-purity analytical standard for quality control and method development in antibiotic research.
• Chemical Intermediate: Used in the synthetic pathways for developing novel macrolide antibiotics and exploring structure-activity relationships (SAR).
• Biochemical Research: Employed in studies investigating the biosynthesis, mode of action, and resistance mechanisms of macrolide-class antimicrobial agents.
• Process Development & Scale-up: Acts as a critical benchmark or starting material in the optimization of fermentation or synthetic routes for complex molecules.
• Academic Research: Utilized in university and institutional labs for fundamental research in medicinal chemistry and microbiology.

Basic Information

Product Name	12,13-Didehydro-14-Hydroxy-12,12-o-Seco-13-Deoxymycinamicin I
CAS No.	73684-72-7
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	13-Deoxymycinamicin I, 12,13-didehydro-14-hydroxy-12,12-o-seco-; 12,13-Didehydro-14-hydroxy-12,12-o-seco-13-deoxymycinamicin I; A derivative of Mycinamicin; Macrolide antibiotic intermediate; 12,12-o-Seco-mycinamicin derivative; Antibiotic research compound; CAS 73684-72-7
EINECS	Contact for details

Quality Control

Our 12,13-Didehydro-14-Hydroxy-12,12-o-Seco-13-Deoxymycinamicin I is produced and handled under strict quality management protocols to ensure batch-to-batch consistency and reliability for research applications. Each lot is supported by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and other critical parameters. We adhere to cGMP principles where applicable, and our quality systems are designed to meet the stringent requirements of pharmaceutical R&D and fine chemical synthesis.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept under anhydrous conditions. For long-term storage, consider storing under an inert atmosphere.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 95.0%
Water Content (KF)	≤ 5.0%
Residue on Ignition	≤ 1.0%

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