Succinimide
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Names | |||
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IUPAC name
Pyrrolidine-2,5-dione | |||
Other names
Succinimide Succinic acid imide | |||
Identifiers | |||
ATC code | G04 | ||
123-56-8 | |||
ChEBI | CHEBI:9307 | ||
ChEMBL | ChEMBL275661 | ||
ChemSpider | 10955 | ||
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Jmol-3D images | Image | ||
PubChem | 11439 | ||
RTECS number | WN2200000 | ||
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UNII | 10X90O3503 | ||
Properties[1] | |||
Molecular formula |
C4H5NO2 | ||
Molar mass | 99.09 g·mol−1 | ||
Appearance | White crystalline powder | ||
Density | 1.41 g/cm3 | ||
Melting point | 125 °C (257 °F; 398 K) | ||
Boiling point | 287 °C (549 °F; 560 K) | ||
1 g/3 mL | |||
Acidity (pKa) | 9.5 | ||
Hazards | |||
MSDS | External MSDS | ||
Main hazards | Irritant Slightly Flammable | ||
R/S statement | S24/25 S28 S37 S45 | ||
LD50 (Median lethal dose) |
14 g/kg (rat, oral)[1] | ||
Related compounds | |||
Related Imides |
Maleimide, N-Chlorosuccinimide, N-Bromosuccinimide | ||
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |||
verify (what is: / ?) | |||
Infobox references | |||
Succinimide is a cyclic imide with the formula C4H5NO2. It is used in a variety of organic syntheses, as well as in some industrial silver plating processes. It may be prepared by thermal decomposition of ammonium succinate [2]
Succinimides
Succinimides refers to compounds that contain the succinimide group. These compounds have some notable uses. Several succinimides are used as anticonvulsant drugs, including ethosuximide, phensuximide, and methsuximide. Succinimides are also used to form covalent bonds between proteins or peptides and plastics, which is useful in a variety of assay techniques.
See also
References
- ↑ 1.0 1.1 Merck Index, 12th Edition, 9040
- ↑ {{http://www.orgsyn.org/demo.aspx?prep=cv2p0562}}