Metaxalone
General Information
Metaxalone Impurities and Metaxalone
Daicel Pharma offers the best-quality Metaxalone impurities and labeled standards. They are vital for evaluating Metaxalone quality, stability, and biological safety. Furthermore, Daicel Pharma specializes in the custom synthesis of Metaxalone impurities and ensures their worldwide delivery.
Metaxalone [CAS: 1665-48-1] is an oxazolidinedione derivative. It is a skeletal muscle relaxant and has sedative properties. As it has central nervous system depressant actions, it benefits people with musculoskeletal symptoms.
Metaxalone: Use and Commercial Availability
Metaxalone is a muscle relaxant but has no direct effect on muscle tissues. It treats chronic, acute, and inflammatory musculoskeletal disorders. It relieves pain from muscle spasms, sprains, and inflammation in patients. It is effective in treating spasticity associated with neurological disorders. It is available as an oral formulation under Skelaxin.
Metaxalone Structure and Mechanism of Action
The chemical name of Metaxalone is 5-[(3,5-Dimethylphenoxy)methyl]-2-oxazolidinone. The chemical formula for Metaxalone is C12H15NO3, and its molecular weight is approximately 221.25 g/mol.
The exact mechanism of action of Metaxalone is unknown.
Metaxalone Impurities and Synthesis
During Metaxalone synthesis1, impurities form that may affect the drug’s safety and efficacy. These impurities form during the manufacturing process, purification, or storage of Metaxalone. Therefore, Metaxalone impurities must be controlled and monitored throughout the drug’s development.
Daicel Pharma offers a comprehensive Certificate of Analysis (CoA) for Metaxalone impurities and labeled standards. We provide the CoA from a cGMP-compliant analytical facility. It gives complete characterization data2 such as 1H NMR, 13C NMR, IR, MASS, and HPLC purity. We provide additional analytical data on request. Daicel Pharma can prepare any unidentified Metaxalone impurity or degradation product. In addition, Daicel Pharma offers a highly purified, stable deuterium-labeled standard, Metaxalone Labelled Standard. We provide a complete characterization report to clients on delivery.
References
- 5-(polysubstituted phenoxymethyl)-2-oxazolidones, GB888594A, Jan 31, 1962, H. Robins Co., Inc. (https://www.lens.org/lens/search/patent/list?q=GB888594)
- Trivedi, Rakshit Kanubhai; Patel, Mukesh C., Development of a stability-indicating RP-UPLC method for rapid determination of metaxalone and its degradation products in solid oral dosage form, Scientia Pharmaceutica, Volume: 80, Issue: 2, Pages: 353-366, 2012 DOI: (10.3797/scipharm.1112-08)
Frequently Asked Questions
What is the analytical method to analyze Metaxalone from its degradation products?
RP-HPLC–UV method helps analyze Metaxalone from its degradation products.
What are the possible reasons for the formation of Metaxalone impurities?
Starting materials, reagents, unreacted catalysts during synthesis, and poor storage conditions may form Metaxalone impurities.
Why is it necessary to remove Metaxalone impurities from the drug?
Metaxalone impurities can affect drug safety and quality and pose health risks, so it is necessary to remove them from the drug.
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