Glycine
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| Glycine | |
|---|---|
| Names: | glycine aminоacetic acid 2-aminoethanoic acid Gly Е640 food additive |
| Formula: | NH2CH2COOH |
| Molar mass: | 75.067 g/mol |
| Density: | 1.1607 g/cm3 |
| Crystal system: | monoclinic (α-glycine) a=5.107 Å, b=12.04 Å, c=5.46 Åα=90°, β=111.82°, γ=90° monoclinic (β-glycine) a=5.0943 Å, b=6.286 Å, c=5.3831 Åα=90°, β=113.21°, γ=90° hexagonal (γ-glycine) a=7.035 Å, b=7.035 Å, c=5.481 Åα=90°, β=90°, γ=120° |
| Shapes: |
|
| Color: | colorless |
| Melting point: | 265 °C538.15 K <br />509 °F <br />968.67 °R <br /> (α-glycine) 266.7 °C539.85 K <br />512.06 °F <br />971.73 °R <br /> (γ-glycine) |
| Decomposition point: | 290 °C563.15 K <br />554 °F <br />1,013.67 °R <br /> |
| Refractive index: | 2.25 (γ-glycine) |
| Magnetic properties: | diamagnetic χ=-4.03 · 10-5cm³/mol |
| Stability: | stable |
Description
Organic compound, simple monobasic aminoacid. Doesn't form water hydrates.
Can be bought in pharmacy.
From water solution without impurities α-glycine crystals are formed. Some impurity like sodium chloride (>8g per 100g of water) or barium nitrate could form γ-glycine crystals.
In water solutions may form adducts with other compounds. Adduct crystals have different shapes and properties comparing to pure compounds.
Notes
Small crystals of α-glycine can spontaneously phase into γ-glycine, becoming opaque and craked. Larged crystals are stable
Keep in its original form or under several layers of varnish at average humidity and room temperature. Do not keep crystals near heaters.
| Temperature | g/100,00 g water | g/100,00 g ethanol 75% | g/100,00 g ethanol 90% | g/100,00 g ethanol | g/100,00 g methanol | g/100,00 g acetone | g/100,00 g pyridine | g/100,00 g formamide | g/100,00 g quinoline | g/100,00 g 1-butanol |
|---|---|---|---|---|---|---|---|---|---|---|
| 0°C273.15 K <br />32 °F <br />491.67 °R <br /> | 0.2 | |||||||||
| 25°C298.15 K <br />77 °F <br />536.67 °R <br /> | 25.3 | 0.448 | 0.053 | 0.0037 | 0.041 | 0.0029 | 0.61 | 0.555 | 0.07 | 0.00089 |
| 45°C318.15 K <br />113 °F <br />572.67 °R <br /> | 0.756 | |||||||||
| 60°C333.15 K <br />140 °F <br />599.67 °R <br /> | 1.23 | |||||||||
| 75°C348.15 K <br />167 °F <br />626.67 °R <br /> | 57.5 |
Gallery
Sources
- R.A.Kiper Properties of compounds. Handbook
- G. L. Perlovich, L. K. Hansen, A. Bauer-Brandl, The Polymorphism of Glycine. Thermochemical and structural aspects
- K. Srinivasan, Crystal growth of α and γ glycine polymorphs and their polymorphic phase transformations
- N. Sivakumar, V. Jayaramakrishnan, K. Baskar, G. Anbalagan, Synthesis, growth and characterization of γ-glycine – A promising material for optical applications
- M. Anis, M. S. Pandian, M. I. Baiq, P. Ramasamy, G. G. Muley, Monocrystal growth and characterization study of α- and γ-polymorph of glycine to explore superior performance of γ-glycine crystal
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