3-Ureidopropionic acid
In this article, we will delve into the world of 3-Ureidopropionic acid, exploring its many facets and manifestations. From its origins to its relevance today, 3-Ureidopropionic acid has captured the attention of people of all ages and backgrounds. Through this comprehensive analysis, we will seek to better understand what makes 3-Ureidopropionic acid so fascinating and what impact it has on our society. Regardless of whether you are an expert on the subject or simply curious to learn more, this article will provide you with the information necessary to fully understand the phenomenon of 3-Ureidopropionic acid. Get ready to immerse yourself in a journey of discovery and knowledge!
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| Names | |
|---|---|
| Preferred IUPAC name
3-(Carbamoylamino)propanoic acid | |
| Other names
3-Ureidopropanoic acid
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| Identifiers | |
3D model (JSmol)
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| 1705263 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.255.338 |
| EC Number |
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| 675230 | |
| KEGG | |
| MeSH | N-carbamoyl-beta-alanine |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C4H8N2O3 | |
| Molar mass | 132.119 g·mol−1 |
| Appearance | White crystals |
| log P | −1.23 |
| Acidity (pKa) | 4.408 |
| Basicity (pKb) | 9.589 |
| Hazards | |
| GHS labelling:[1] | |
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| Warning | |
| H302, H315, H319, H335 | |
| P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, P501 | |
| Related compounds | |
Related alkanoic acids
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Related compounds
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).
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3-Ureidopropionic acid, also called N-carbamoyl-beta-alanine, is an intermediate in the metabolism of uracil. It is a urea derivative of beta-alanine.
References
- ^ "3-Ureidopropionic acid". pubchem.ncbi.nlm.nih.gov. Retrieved 11 December 2021.
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