N-Hydroxysulfosuccinimide (sodium salt)
N-Hydroxysulfosuccinimide (sodium salt) (CAS No.: 106627-54-7) is a hydrophilic, non-cleavable linker reagent widely employed in bioconjugation chemistry, particularly in the development of antibody–drug conjugates (ADCs) for targeted therapeutic research. As a sulfonated derivative of N-hydroxysuccinimide, it facilitates efficient coupling reactions with primary amines, promoting the formation of stable covalent bonds that enhance conjugate stability and improve pharmacological targeting properties. Its high aqueous solubility and reactivity make it especially suitable for modifying biomolecules under mild conditions, thereby preserving biological activity during conjugation processes. In biomedical research, it is commonly utilized to activate carboxyl groups in peptides, proteins, and other macromolecules, supporting the generation of stable amide linkages essential for drug delivery systems and molecular labeling strategies. While it does not directly interact with classical biological targets or signaling pathways, its role in enabling precise molecular assembly underpins its importance in drug discovery workflows, including in vitro conjugation studies and optimization of antibody binding characteristics. Experimental usage typically varies depending on the system and desired conjugation efficiency, with concentrations adjusted according to specific assay conditions and molecular substrates.
| Physical Appearance | A solid |
| Storage | -20°C |
| M.Wt | 217.13 |
| Cas No. | 106627-54-7 |
| Formula | C4H4NNaO6S |
| Synonyms | Sulfo-NHS |
| Solubility | insoluble in EtOH; ≥21.7 mg/mL in DMSO with gentle warming and ultrasonic; ≥30.3 mg/mL in H2O |
| Chemical Name | sodium 1-hydroxy-2,5-dioxopyrrolidine-3-sulfonate |
| Canonical SMILES | ON1C(CC(S([O-])(=O)=O)C1=O)=O.[Na+] |
| 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. |







