Aceturic acid
Names | |
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IUPAC name
2-acetamidoacetic acid | |
Other names
N-acetylglycine acetamidoacetic acid acetylglycocoll | |
Identifiers | |
3D model (JSmol) |
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Abbreviations | AcGly |
ChemSpider | |
ECHA InfoCard | 100.008.036 |
PubChem CID |
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Properties | |
C4H7NO3 | |
Molar mass | 117.10 g·mol−1 |
Appearance | White powder or needles |
Melting point | 206 to 208 °C (403 to 406 °F; 479 to 481 K) |
2.7% at 15 °C | |
Acidity (pKa) | 3.64 |
Hazards | |
S-phrases (outdated) | S24/25 |
Related compounds | |
Related compounds |
N-Acetylglycinamide |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Aceturic acid (N-acetylglycine) is a derivative of the amino acid glycine. Its salts are called aceturates.
Preparation
Aceturic acid can be prepared by warming glycine either with a slight excess of acetic anhydride in benzene,[1] or with an equal molar amount of acetic anhydride in glacial (concentrated) acetic acid.[2]
See also
References
- ↑ Curtius, Th.; Radenhausen, R. (1895). "Hydrazide und Azide organischer Säuren. X Abhandlung. 35. Ueber Hydrazide substituirter Amidosäuren und das Hydrazid der Fumarsäure". J. Prakt. Chem. 52 (1): 433–454. doi:10.1002/prac.18950520134.
- ↑ Dakin, H. D. (1929). "The Condensation of Aromatic Aldehydes with Glycine and Acetylglycine" (PDF). J. Biol. Chem. 82 (2): 439–446.
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