| API | Active Pharmaceutical Ingredient |
| BGE | Background Electrolyte |
| β-CD | β-Cyclodextrin |
| CD | Cyclodextrin |
| CE | Capillary Electrophoresis |
| COSY | Correlation Spectroscopy |
| DIPE | Diisopropyl Ether |
| DIPEA | N,N-diisopropylethylamine |
| DMF | Dimethylformamide |
| DMSO | Dimethyl Sulfoxide |
| DoE | Design of Experiments |
| DS | Degree of Substitution |
| ee | Enantiomeric Excess |
| EMO | Enantiomer Migration Order |
| HMBC | Heteronuclear Multiple Bond Correlation |
| HOESY | Heteronuclear Overhauser Effect Spectroscopy |
| HPLC | High-Performance Liquid Chromatography |
| HP-β-CD | Hydroxypropyl-β-Cyclodextrin |
| HSQC | Heteronuclear Single Quantum Coherence |
| ICH | International Council for Harmonisation |
| IDE | Idelalisib |
| LOQ | Limit of Quantification |
| LOD | Limit of Detection |
| MeOH | Methanol |
| NMR | Nuclear Magnetic Resonance |
| NOESY | Nuclear Overhauser Effect Spectroscopy |
| pD | pH Measured in Deuterated Solvent |
| PI3Kδ | Phosphoinositide 3-Kinase Delta |
| R-IDE | R-Enantiomer of Idelalisib |
| ROESY | Rotating-frame Overhauser Effect Spectroscopy |
| Rs | Resolution |
| RSD | Relative Standard Deviation |
| S-IDE | S-Enantiomer of Idelalisib |
| TGA | Therapeutic Goods Administration |
| UV | Ultraviolet |