Description

26-Deoxymonensin A is a specialized derivative of the well-known polyether ionophore antibiotic, Monensin. This compound is valued for its role as a key intermediate in the research and development of novel veterinary pharmaceuticals and feed additives. It is primarily utilized by research institutions and manufacturers in the animal health sector focused on developing next-generation coccidiostats and growth promoters. The product is supplied to meet the stringent requirements of pharmaceutical R&D and fine chemical synthesis.

Application

• Pharmaceutical Intermediate: Serves as a critical building block in the synthesis of advanced Monensin analogs and derivatives for veterinary medicine.
• Veterinary Drug Research: Used in preclinical studies and development of new anti-coccidial agents for poultry and livestock.
• Biochemical Research: Employed as a tool compound in studies investigating ion transport mechanisms across biological membranes.
• Reference Standard: Functions as a high-purity analytical standard for quality control and method development in pharmaceutical analysis.
• Fine Chemical Synthesis: Utilized in custom synthesis and contract manufacturing of specialized bioactive molecules.

Basic Information

Product Name	26-Deoxymonensin A
CAS No.	122576-59-4
Molecular Formula	C35H62O10
Molecular Weight	642.87 g/mol
Synonyms	26-Deoxy Monensin A; Monensin A, 26-deoxy-; 26-Desoxymonensin A; 26-Deoxymonensin; Deoxymonensin A; Antibiotic X-206, 26-deoxy-; (2R,3S,4R,5R,6S)-5-[(2S,3R,4S,6R)-4,6-Dimethyl-3-(2R,3S,5R,6S)-3,5-dimethyl-6-[(1S,2S,6R,8S,9S)-1,2,8,9-tetramethyl-5-oxaspiro[2.13]hexadec-13-en-7-yl]heptan-2-yl]oxyoxan-2-yl]oxy-6-methyloxane-2,3,4-triol
EINECS	Contact for details

Quality Control

Our 26-Deoxymonensin A is produced under a strict quality management system. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via spectroscopic methods, to ensure it meets the high standards required for research and synthesis. A Certificate of Analysis (COA) detailing all test results is provided with every shipment. We support compliance with cGMP guidelines for advanced pharmaceutical intermediates.

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); ensure the container is sealed tightly after each use to minimize exposure to atmospheric humidity. 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%
Related Substances (HPLC)	Total impurities ≤ 5.0% Any single impurity ≤ 2.0%

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