Description

10-Deoxymethymycin is a specialized macrolide derivative with significant research and development potential in the pharmaceutical sector. This compound is valued for its structural framework, which serves as a key intermediate or starting material for synthesizing novel bioactive molecules. It is primarily utilized by research institutions, pharmaceutical R&D laboratories, and fine chemical manufacturers focused on antibiotic development and medicinal chemistry. The product is supplied under stringent quality control to ensure consistency for critical applications.

Application

• Pharmaceutical Intermediate: Serves as a crucial building block in the synthesis of novel macrolide antibiotics and other therapeutic agents.
• Medicinal Chemistry Research: Used in structure-activity relationship (SAR) studies to develop new compounds with improved efficacy and reduced resistance.
• Biochemical Research: Employed as a reference standard or probe in studies investigating bacterial protein synthesis and ribosomal function.
• Fine Chemical Synthesis: Acts as a key precursor in multi-step organic synthesis for producing high-value, complex molecules.
• Antibiotic Development: Investigated for its potential in creating next-generation antibiotics to combat multidrug-resistant bacterial strains.

Basic Information

Product Name	10-Deoxymethymycin
CAS No.	36826-66-1
Molecular Formula	C22H39NO7
Molecular Weight	429.55 g/mol
Synonyms	10-Deoxymethymycin; 10-De-O-methylmycin; Demethylmycin; (3R,4S,5S,6R,7R,9R,11R,12R,13S,14R)-4-[(2,6-Dideoxy-3-C-methyl-3-O-methyl-α-L-ribo-hexopyranosyl)oxy]-14-ethyl-7,12,13-trihydroxy-3,5,7,9,11,13-hexamethyl-6-[[3,4,6-trideoxy-3-(dimethylamino)-β-D-xylo-hexopyranosyl]oxy]oxacyclotetradecane-2,10-dione; Antibiotic T-2636 C
EINECS	Contact for details

Quality Control

Our 10-Deoxymethymycin is produced and tested under a strict quality management system to ensure it meets the high-purity standards required for research and synthesis. Each batch is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. We adhere to cGMP principles where applicable, and specifications can be aligned with client requirements for advanced pharmaceutical development.

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 must be kept under an inert atmosphere or in a desiccator to prevent degradation. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 95.0%
Water Content (KF)	≤ 2.0%
Residue on Ignition	≤ 0.5%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 5.0%

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