Description

Erythromyclamine CAS NO 13368-00-8 is a high-purity chemical intermediate of significant importance in advanced pharmaceutical synthesis. Its primary value lies in its role as a key building block for the production of specialized macrolide antibiotics and other active pharmaceutical ingredients (APIs). This compound is essential for manufacturers and R&D facilities in the pharmaceutical, biotechnology, and fine chemical sectors requiring reliable, high-quality raw materials for complex synthesis pathways.

Application

• Pharmaceutical Intermediate: A critical precursor in the synthesis of macrolide antibiotic APIs and related therapeutic compounds.
• Research & Development: Used in medicinal chemistry for the discovery and development of new antibacterial agents.
• Fine Chemical Synthesis: Serves as a specialized building block for constructing complex molecular architectures in custom synthesis projects.
• Bioconjugation Chemistry: Potential use in the development of targeted drug delivery systems and antibody-drug conjugates (ADCs).
• Process Chemistry: Employed in scale-up and optimization studies for commercial pharmaceutical manufacturing processes.

Basic Information

Product Name	Erythromyclamine
CAS No.	13368-00-8
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Erythromyclamine; Erythromycin amine; Desmethylaminoerythromycin; 6-Deoxy-6-demethylamino-6-oxoerythromycin; Erythromycin 6,9-hemiketal 9-(O-methyloxime); (8S,9R,10S,11R,12S,13R)-11-[(2S,3R,4S,6R)-4-(Dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-2-ethyl-3,4,10-trihydroxy-3,5,8,10,12,14-hexamethyl-7,15-dioxo-1-oxacyclopentadec-13-yl 2,6-dideoxy-3-C-methyl-3-O-methyl-α-L-ribo-hexopyranoside
EINECS	Contact for details

Quality Control

Our Erythromyclamine is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including chromatographic purity assays and identity confirmation, to ensure it meets the high standards required for pharmaceutical intermediate applications. A comprehensive Certificate of Analysis (COA) detailing purity, impurities, and physical characteristics is provided with every shipment to guarantee traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (typically 15-25°C). Keep away from incompatible materials. For long-term storage, consider conditions under an inert atmosphere to maintain optimal stability.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
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.