Names | |
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IUPAC name
3-Amino-2-hydroxypropanoic acid
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Other names
3-Aminolactic acid
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Identifiers | |
3D model (
JSmol)
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ChemSpider | |
PubChem
CID
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UNII | |
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Properties | |
C3H7NO3 | |
Molar mass | 105.093 g·mol−1 |
Hazards | |
GHS labelling: | |
Warning | |
H315, H319, H335 | |
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
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Isoserine is a non-proteinogenic α-hydroxy-β- amino acid, and an isomer of serine. Non-proteinogenic amino acids do not form proteins, and are not part of the genetic code of any known organism. Isoserine has only been produced synthetically.
The first documented synthesis of isoserine in a laboratory setting was by Miyazawa et al., who published their results in 1976. [1]