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Carisoprodol D6

Chemical Name Carisoprodol D6
CAT No. CS-O-02763
CAS Registry# 1218911-71-7
Status Prompt Dispatch
Category Stable Isotopes
Mol. Wt. 266.37 g/mol
Mol. For. C₁₂H₁₈D₆N₂O₄
Hazardous This is not a Hazardous Compound
COA View Sample COA

Additional Information


Controlled No
Parent API Carisoprodol
Purity 98
Smileys CC(COC(N)=O)(CCC)COC(NC(C([2H])([2H])[2H])C([2H])([2H])[2H])=O
Hazardous No


Usage and description


Carisoprodol D6 is a deuterated form of carisoprodol, a drug used as a muscle relaxant and pain reliever. It works by blocking pain sensations between the nerves and the brain. Carisoprodol D6 is used to treat acute muscle pain, spasms, and stiffness caused by injuries or other musculoskeletal conditions. The chemical formula of Carisoprodol D6 is C12H16D6N2O2, and its molecular weight is 230.34 g/mol. It is a deuterated form of carisoprodol, which means that some of the hydrogen atoms in the molecule have been replaced with deuterium atoms, a heavy isotope of hydrogen. Carisoprodol D6 is typically administered orally in the form of tablets or capsules. The recommended dosage for adults is 250 to 350 mg three times a day and at bedtime. The drug should not be taken for more than three weeks, as prolonged use can lead to dependence and withdrawal symptoms. Carisoprodol D6 is metabolized in the liver by the cytochrome P450 enzyme system to form meprobamate, a metabolite with sedative properties. The drug has a half-life of approximately 2 hours, and its effects can last up to 6 hours. In conclusion, Carisoprodol D6 is a deuterated form of carisoprodol used as a muscle relaxant and pain reliever. Its chemical formula is C12H16D6N2O2, and it is typically administered orally in tablets or capsules. The drug is metabolized in the liver to form meprobamate, and its effects can last up to 6 hours.

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