Glycinamide manufacturers
- Glycinamide
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- $0.01 / 1KG
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2020-01-08
- CAS:598-41-4
- Min. Order: 1KG
- Purity: 98%； 99%
- Supply Ability: 1kg; 5kg; 10kg；25kg
- Glycinamide
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- $1.00 / 1KG
-
2019-12-20
- CAS: 598-41-4
- Min. Order: 1KG
- Purity: 95%~99%
- Supply Ability: 1ton
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| | Glycinamide Basic information |
| Product Name: | Glycinamide | | Synonyms: | 2-Aminoacetamide;Acetamide, 2-amino-;Glycinamide;AMINOACETAMIDE;2-amino-acetamid;2-Amino-1-iminoethanol;Aminoacetimidic acid;2-azanylethanamide | | CAS: | 598-41-4 | | MF: | C2H6N2O | | MW: | 74.08 | | EINECS: | 209-932-4 | | Product Categories: | | | Mol File: | 598-41-4.mol |  |
| | Glycinamide Chemical Properties |
| Melting point | 65-67 °C | | Boiling point | 281.3±23.0 °C(Predicted) | | density | 1.122±0.06 g/cm3(Predicted) | | storage temp. | Keep in dark place,Inert atmosphere,Store in freezer, under -20°C | | pka | pK1: 7.95(+1) (25°C) | | Appearance | White to light yellow Solid | | InChI | InChI=1S/C2H6N2O/c3-1-2(4)5/h1,3H2,(H2,4,5) | | InChIKey | BEBCJVAWIBVWNZ-UHFFFAOYSA-N | | SMILES | C(N)(=O)CN | | NIST Chemistry Reference | H2NCH2CONH2 (glycinamide)(598-41-4) | | EPA Substance Registry System | Acetamide, 2-amino- (598-41-4) |
| | Glycinamide Usage And Synthesis |
| Chemical Properties | Needle-shaped crystals. Melting point 67-68℃. Soluble in water, ethanol and methanol, soluble in acetone, chloroform and ethyl acetate, slightly soluble in ether and benzene. Strong alkaline reaction, can absorb carbon dioxide. Glycine and ammonia are generated with hot water. | | Uses | 2-Aminoacetamide is a derivative of the amino acid glycine . It has been shown to inhibit the conversion of proparathyroid hormone to parathyroid hormone. It can be useful in the identification of yeasts. It can also be useful in the synthesis of Oxiracetam , which is a derivative of Piracetam and a nootropic drug useful for improving cognition and memory impairments. | | Definition | ChEBI:Glycinamide is an amino acid amide and a glycine derivative. | | Synthesis | The mild and effective aminodibromination reaction of nitroolefins with amphoteric ions as organocatalysts resulted in the efficient conversion of aminodibromo products to glycinamide.
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| | Glycinamide Preparation Products And Raw materials |
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