CARISOPRODOL

Carisoprodol is a muscle relaxant acting on CNS pathways to relieve acute musculoskeletal pain. Side effects include drowsiness, dizziness, and dependence risk.

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Product Description


Mechanism of action

Carisoprodol is a centrally acting skeletal‑muscle relaxant that modulates interneuronal activity in the spinal cord and reticular formation. Its primary mechanism involves enhancement of GABAergic inhibitory signalling, partly through its active metabolite meprobamate, which acts as a GABA_A receptor modulator. This reduces polysynaptic reflex activity and decreases muscle tone.

Benefits and advantages

Used in neuromuscular‑function modelling, spinal‑reflex research, GABA_A receptor pharmacology, sedative‑mechanism studies, musculoskeletal‑pain pathway research and comparative myorelaxant investigations.

Side effects and risks

Risks include sedation, dependence, headache, dizziness, impaired coordination, respiratory depression (high doses), and withdrawal symptoms. Handle as a CNS‑active substance with dependence liability.

Datasheet


Molecular Formula

C12H24N2O4

Molecular Weight

260.33 g/mol

CAS Number

78-44-4

Storage Condition

Carisoprodol tablets should be stored in well-closed containers at a temperature less than 40 °C, preferably at 15-30 °C.

Solubility

less than 1 mg/mL at 67.1 °F (NTP, 1992)

Purity

Purity information is available upon request (COA).

Synonym

carisoprodol; 78-44-4; Isomeprobamate; Carisoprodate; SOMA

IUPAC/Chemical Name

[2-(carbamoyloxymethyl)-2-methylpentyl] N-propan-2-ylcarbamate

InChl Key

OFZCIYFFPZCNJE-UHFFFAOYSA-N

InChl Code

InChI=1S/C12H24N2O4/c1-5-6-12(4,7-17-10(13)15)8-18-11(16)14-9(2)3/h9H,5-8H2,1-4H3,(H2,13,15)(H,14,16)

References

https://pubchem.ncbi.nlm.nih.gov/compound/2576;

3D Conformer.

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