Chemistry:Glycinamide
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Preferred IUPAC name
2-Aminoacetamide | |
Identifiers | |
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PubChem CID
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Properties | |
C2H6N2O | |
Molar mass | 74.083 g·mol−1 |
Appearance | white solid |
Melting point | 65–67 °C (149–153 °F; 338–340 K) |
Boiling point | decomposes |
good | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Glycinamide is a organic compound with the molecular formula H2NCH2C(O)NH2. It is the amide derivative of the amino acid glycine. It is a water-soluble, white solid. Amino acid amides, such as glycinamide are prepared by treating the amino acid ester with ammonia.[1]
It is a ligand for transition metals.[2]
The hydrochloride salt of glycinamide, glycinamide hydrochloride, is one of Good's buffers with a pH in the physiological range. Glycinamide hydrochloride has a pKa near the physiological pH (8.20 at 20°C), making it useful in cell culture work. Its ΔpKa/°C is -0.029 and it has a solubility in water at 0 °C of 6.4 M.
Glycinamide is a reagent used in the synthesis of glycineamide ribonucleotide (an intermediate in de novo purine biosynthesis).[3]
References
- ↑ Yang, Peter S.; Rising, Mary M. (1931). "A Simplified Method of Preparation of Alpha Amino Acid Amides". Journal of the American Chemical Society 53 (8): 3183–3184. doi:10.1021/ja01359a505.
- ↑ Appleton, Trevor G. (1997). "Donor atom preferences in complexes of platinum and palladium with amino acids and related molecules". Coordination Chemistry Reviews 166: 313–359. doi:10.1016/S0010-8545(97)00047-7.
- ↑ "Glycinamide hydrochloride". https://www.goldbio.com/product/9582/glycinamide-hydrochloride.
![]() | Original source: https://en.wikipedia.org/wiki/Glycinamide.
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