Chemistry:Ammonium succinate
From HandWiki
| Names | |
|---|---|
| IUPAC name
diazanium;butanedioate
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| Other names
Diammonium succinate
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| Identifiers | |
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PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C4H12N2O4 | |
| Molar mass | 152.150 g·mol−1 |
| Appearance | colorless crystals |
| Density | 1.601 g/cm3 |
| Boiling point | 236.1 °C |
| soluble | |
| Hazards | |
| GHS pictograms | |
| GHS Signal word | Warning |
| H315, H319 | |
| P261, P280, P302, P352, P305, P351, P338 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Ammonium succinate is a chemical compound with the chemical formula C
4H
4O
4(NH
4)
2.[2] This is an organic ammonium salt of succinic acid.
Synthesis
Succinic acid reacts with ammonium carbonate to form ammonium succinate.
Also, a reaction of ammonia water with succinic acid:[3][4]
- 2NH
4OH + H
2C
4H
4O
4 → C
4H
4O
4(NH
4)
2 + 2H
2O
- 2NH
Physical properties
Ammonium succinate forms colorless crystals, easily soluble in water.
Thermal decomposition of ammonium succinate produces succinimide.[5]
Uses
The compound is used a mediator in medicine, lacquer manufacture, and in the production of perfume esters. It is also used in food as a sequestrant, buffer, and neutralizing agent.[6]
References
- ↑ "Ammonium succinate". Sigma Aldrich. https://www.sigmaaldrich.com/RU/en/product/ambeedinc/ambh93e4c9e2?context=bbe.
- ↑ "Ammonium succinate | CAS 15574-09-1 | SCBT - Santa Cruz Biotechnology" (in en). scbt.com. https://www.scbt.com/p/ammonium-succinate-15574-09-1.
- ↑ Lloyd, John Uri (1883) (in en). The Chemistry of Medicines, Practical: A Text and Reference Book for the Use of Students, Physicians, and Pharmacists, Embodying the Principles of Chemical Philosophy and Their Application to Those Chemicals that are Used in Medicine .... R. Clarke. p. 216. https://books.google.com/books?id=6Vs3AAAAMAAJ&dq=Ammonium+succinate&pg=PA216. Retrieved 5 March 2025.
- ↑ Muter, John (1880) (in en). An Introduction to pharmaceutical and medical chemistry. W. Bater. p. 269. https://books.google.com/books?id=T_VbQ-IrQDQC&dq=Ammonium+succinate&pg=PA269. Retrieved 5 March 2025.
- ↑ "SUCCINIMIDE" (in en). Organic Syntheses 16: 75. 1936. doi:10.15227/orgsyn.016.0075. https://orgsyn.org/demo.aspx?prep=CV2P0562. Retrieved 6 March 2025.
- ↑ "MeSH Browser". meshb.nlm.nih.gov. https://meshb.nlm.nih.gov/record/ui?ui=D019802.
