Anodyne| Asp | |
|---|---|
 |
| Esters [] | |
|---|---|
| Aspartic acid acetate | |
|
| Molecular structure via molpic | |
| Conformer structure via 3Dmol.js | |
| Molecular formula | C4H7NO4[1] |
|---|---|
| Molecular mass | 133.10 g/mol[1] |
| Predicted LogP | -2.8[1] |
| Chirality | racemic[2] |
| Identifiers [] | |
|---|---|
| IUPAC name | 2-aminobutanedioic acid[1] |
| SMILES | C(C(C(=O)O)N)C(=O)O[1] |
| InChI | InChI=1S/C4H7NO4/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H,6,7)(H,8,9)[1] |
| InChIKey | CKLJMWTZIZZHCS-UHFFFAOYSA-N[1] |
| Dosing |
|---|
Aspartic acid
Aspartic acid (also known as Dl-aspartic acid, DL-Aminosuccinic acid, DL-Asparagic acid, DL-Asp-OH, Acid D,L-aspart, (+-)-Aspartic acid, (R,S)-Aspartic acid, (+/-)-2-Aminosuccinic acid, (+/-)-Aspartic Acid or L-aspartic-4-13c acid) is a substance of the amino acid class.
Chemistry
Aspartic acid is typically found in the form of its acetate ester.
Stereochemistry
DL-Aspartic acid is a racemic mixture of the logical stereoisomers:
| Stereoisomers [] |
|---|
|
D-Aspartic acid 
L-Aspartic acid 
DL-Aspartic acid 
|
See also
External links
- Aspartic acid (Wikipedia)
- Aspartic acid / D-Aspartic acid / L-Aspartic acid (Wikidata)
- Aspartic acid / D-Aspartic acid / L-Aspartic acid (PubChem)
- Aspartic acid / D-Aspartic acid / L-Aspartic acid (Common Chemistry)
- Aspartic acid / D-Aspartic acid / L-Aspartic acid (KEGG)
- Aspartic acid / D-Aspartic acid / L-Aspartic acid (UNII)
- Aspartic acid / D-Aspartic acid / L-Aspartic acid (EPA DSSTox)