| Identification | Back Directory | [Name]
DISUCCINIMIDYL SUCCINATE | [CAS]
30364-60-4 | [Synonyms]
DISUCCINIMIDYL SUCCINATE
Bis(2,5-dioxopyrrolidin-1-yl)
N,N'-(Succinyldioxy)disuccinimide
Succinic Acid Disuccinimidyl Ester
Bis(2,5-dioxopyrrolidin-1-yl) succinate
SUCCINIC ACID-BIS-N-HYDROXYSUCCINIMIDE ESTER
Butanedioic acid,1,4-bis(2,5-dioxo-1-pyrrolidinyl) ester
2,5-Pyrrolidinedione, 1,1'-[(1,4-dioxo-1,4-butanediyl)bis(oxy)]bis- | [Molecular Formula]
C12H12N2O8 | [MDL Number]
MFCD00228233 | [MOL File]
30364-60-4.mol | [Molecular Weight]
312.23 |
| Chemical Properties | Back Directory | [Melting point ]
305-306℃ | [Boiling point ]
471.6±55.0 °C(Predicted) | [density ]
1.58±0.1 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,Store in freezer, under -20°C | [solubility ]
Chloroform (Slightly, Heated, Sonicated), DMSO (Slightly) | [form ]
Solid | [color ]
White to Off-White | [Stability:]
Hygroscopic |
| Hazard Information | Back Directory | [Uses]
DISUCCINIMIDYL SUCCINATE can be used as a crosslinking agent. | [Synthesis]
General procedure for the synthesis of bis(2,5-dioxopyrrolidin-1-yl) succinic acid esters from N-hydroxybutanediimide and butanedioic acid: to a solution of THF (50 mL) of butanedioic acid (30 g, 254 mmol, 1.0 eq.) was added a solution of THF (50 mL) of N-hydroxybutanediimide (64 g, 556 mmol, 2.2 eq.). A THF (50 mL) solution of N,N'-dicyclohexylcarbodiimide (DCC, 11.5 g, 55.8 mmol, 0.22 eq.) was slowly added dropwise with stirring at 0 °C. After dropwise addition, the reaction mixture was stirred at room temperature overnight. The reaction progress was monitored by liquid chromatography-mass spectrometry (LC-MS). After completion of the reaction, the solid was collected by filtration and the filtrate was concentrated to obtain the crude product. The resulting solid was washed sequentially with THF and ethanol to give the final bis(2,5-dioxopyrrolidin-1-yl) succinate (24 g, 27% yield) as a white solid. | [References]
[1] Patent: WO2010/78449, 2010, A2. Location in patent: Page/Page column 291
[2] Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1980, vol. 29, # 5, p. 785 - 789
[3] Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1980, # 5, p. 1078 - 1081
[4] Chemical Papers, 2016, vol. 70, # 4, p. 505 - 514
[5] Patent: WO2016/205488, 2016, A1. Location in patent: Paragraph 0264 |
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