Hydantoic acid is an acid with the chemical formula C3H6N2O3. Its molecule contains a total of 13 bonds including seven non-H bonds, two multiple bonds, two rotatable bonds, two double bonds, one carboxylic acid (aliphatic), one urea derivative, and one hydroxyl group.[1] It can be obtained from uric acid[2] as well as from glycine with urea in the presence of alkali. [3]
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| Names | |
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| IUPAC name
N-Carbamoylglycine
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| Systematic IUPAC name
(Carbamoylamino)acetic acid | |
Other names
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| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.006.663 |
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PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C3H6N2O3 | |
| Molar mass | 118.092 g·mol−1 |
| Hazards | |
| GHS labelling: | |
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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 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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References
edit- ^ "Chemical Structure of Hydantoic acid (C3H6N2O3)". MolInstincts Chemical Database.
- ^ Peter Wallwork Latham (1884). On the Formation of Uric Acid in Animals: Its Relation to Gout and Gravel, Together with an Explanation of the Therapeutic Effects of Some of the Remedies Used in the Treatment of Those Disorders. Deighton, Bell. p. 14.
- ^ V.K. Ahluwalia; R. Aggarwal, V.K. Ahluwalia. Comprehensive Practical Organic Chemistry: Preparations And Quantitative Analysis. Universities Press. p. 227. ISBN 978-81-7371-475-7.