Ala | |
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Esters [] | |
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Alanine acetate | |
Alanine benzoate | |
Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C3H7NO2[1] |
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Molecular mass | 89.09 g/mol[1] |
Predicted LogP | -3[1] |
Solubility | Solublein water[1] |
Chirality | racemic[2] |
Identifiers [] | |
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IUPAC name | 2-aminopropanoic acid[1] |
SMILES | CC(C(=O)O)N[1] |
InChI | InChI=1S/C3H7NO2/c1-2(4)3(5)6/h2H,4H2,1H3,(H,5,6)[1] |
InChIKey | QNAYBMKLOCPYGJ-UHFFFAOYSA-N[1] |
Dosing |
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Alanine
Alanine (also known as DL-ALANINE, DL-2-Aminopropionic acid, D,L-Alanine, DL-2-Aminopropanoic acid, AI3-08908, CCRIS 8596, Dl-alanine, Fema no. 3818, DLαAlanine or D,LAlanine) is a substance of the amino acid class.
Chemistry
Alanine is typically found in the form of its acetate and benzoate esters.
Stereochemistry
DL-Alanine is a racemic mixture of the logical stereoisomers:
Stereoisomers [] |
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See also
External links
- Alanine / L-Alanine (Wikipedia)
- Alanine / D-Alanine / L-Alanine (Wikidata)
- Alanine / D-Alanine / L-Alanine (PubChem)
- Alanine / D-Alanine / L-Alanine (ChEMBL)
- Alanine / D-Alanine / L-Alanine (ChEBI)
- Alanine / D-Alanine / L-Alanine (Common Chemistry)
- Alanine / D-Alanine / L-Alanine (HMDB)
- Alanine / D-Alanine / L-Alanine (KEGG)
- Alanine / D-Alanine / L-Alanine (UNII)
- Alanine / D-Alanine / L-Alanine (EPA DSSTox)