tags
MethylRamadolsodiumIbuprofencarboxyliccarbonEthanolacetoneibuprofensodium salt
video tutorial Ibuprofen extraction and optical isomerism
- Topic: extraction and purification of ibuprofen from OTC tablets; analysis of the ibuprofen molecule, including chirality (optical isomers).
- Starting material: 40 tablets of 400 mg ibuprofen each (16 g ibuprofen total; 9 g filler/binder per 25 g tablet batch).
- First method (alkaline extraction): crush tablets, try dissolving with sodium hydroxide to form water-soluble sodium ibuprofen salt; fails due to gel formation from cellulose binders; water extraction not viable.
- Second method (organic solvent extraction): use acetone to dissolve ibuprofen while leaving binders intact; filter, evaporate solvent to obtain crude ibuprofen.
- Discussion of optical isomers: ibuprofen contains a chiral center; two enantiomers exist; general properties similar, but interactions with mirror-image molecules can differ; in biology, proteins are chiral, causing activity differences.
- Purification sequence: re-dissolve crude ibuprofen in sodium hydroxide to form sodium salt; re-precipitate with hydrochloric acid; filter and dry to yield pure ibuprofen (7.5 g) with ~94% recovery from the starting batch.
- Additional notes: some colored non-generic tablets have outer coatings that must be removed before organic extraction (soak in absolute ethanol can help); otherwise, coating disrupts extraction.
- Safety and future work: plan to rig up equipment and establish safety procedures before further experiments.
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