Glycinamide hydrochloride
Names | |
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IUPAC name
2-aminoacetamide:hydrochloride[1] | |
Other names
Glycinamide hydrochloride | |
Identifiers | |
EC Number | 216-789-1 |
PubChem CID |
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Properties | |
C2H7ClN2O | |
Molar mass | 110.541 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Glycinamide hydrochloride is one of Good's buffers with a pH in the physiological range and is a reagent used in the synthesis of glycineamide ribonucleotide (an intermediate in de novo purine biosynthesis)[2], [M(glycinamidato-N,N')(ptpy)2] where ptpy = 2-(p-tolyl)pyridinato) and M = Rh or Ir,[3] and the following glycinamide-based imidazolidinones:[4]
- (±)-2-(2-phenylpropyl)imidazolidin-4-one
- (±)-2-(2,4,4-trimethylpentyl)imidazolidin-4-one
- (±)-2-[(R)-2,6-dimethyl-5-heptenyl]imidazolidin-4-one
- (5R,6S,9R)-6-isopropyl-9-methyl-1,4-diazaspiro[4.5]decan-2-one
- (5S,6S,9R)-6-isopropyl-9-methyl-1,4-diazaspiro[4.5]decan-2-one
- (±)-2-methyl-2-pentylimidazolidin-4-one
- (±)-2-ethyl-2-(2-methylbutyl)imidazolidin-4-one
- (±)-2-(undecan-2-yl)imidazolidin-4-one
- (±)-2-pentylimidazolidin-4-one
- 2-(2,4-dimethylcyclohex-3-en-1-yl)imidazolidin-4-one
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 6.4M.
References
- ↑ "Glycinamide Hydrochloride". PubChem. 19 July 2005.
- ↑ "Glycinamide hydrochloride". Gold Biotechnology.
- ↑ Graf M, et al. (2013). "Synthesis and Characterization of New Bis-Cyclometalated Rhodium and Iridium Complexes Containing the Glycinamidato Ligand". Zeitschrift für Anorganische und Allgemeine Chemie. 639 (7): 1117–1121.
- ↑ Trachsel A, et al. (2012). "Preparation of Imidazolidin-4-ones and Their Evaluation as Hydrolytically Cleavable Precursors for the Slow Release of Bioactive Volatile Carbonyl Derivatives". European Journal of Organic Chemistry. 2012 (14): 2837–2854.
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