O-Phthalimide-C3-acid
O-Phthalimide-C3-acid (CAS No.: 3130-75-4) is a synthetic haptenic small molecule widely employed in biochemical and immunological research, particularly in antigen design and conjugation strategies. Structurally characterized by a terminal carboxyl functional group positioned on a flexible spacer arm, this compound readily reacts with primary amine groups on proteins, enabling efficient covalent coupling to carrier proteins such as albumin or keyhole limpet hemocyanin. This reactivity underlies its utility in generating well-defined hapten–protein conjugates for antibody production, epitope mapping, and immunoassay development. Although it does not directly target specific signaling pathways or biological receptors, its functional role lies in facilitating immune recognition of otherwise non-immunogenic small molecules through conjugation-based presentation. In vitro applications typically involve its use in protein labeling and conjugation workflows under mild coupling conditions, with effective concentrations generally falling within low micromolar to millimolar ranges depending on the system and coupling chemistry employed. O-Phthalimide-C3-acid is therefore primarily categorized as a chemical biology tool compound, supporting studies in immunochemistry, biomolecular engineering, and assay development, with experimental conditions tailored to specific research objectives and model systems.
| Physical Appearance | A solid |
| Storage | -20°C |
| M.Wt | 233.22 |
| Cas No. | 3130-75-4 |
| Formula | C12H11NO4 |
| Solubility | ≥35.7 mg/mL in DMSO; ≥12.17 mg/mL in EtOH; ≥6.74 mg/mL in H2O with ultrasonic |
| Chemical Name | 4-(1,3-dioxoisoindolin-2-yl)butanoic acid |
| Canonical SMILES | O=C(O)CCCN1C(=O)C=2C=CC=CC2C1=O |
| Shipping Condition | Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice. |
| General tips | We do not recommend long-term storage for the solution, please use it up soon. |







