Val | |
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Esters [] | |
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Valine acetate | |
Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C5H11NO2[1] |
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Molecular mass | 117.15 g/mol[1] |
Predicted LogP | -2.3[1] |
Solubility | Soluble in water; Insoluble in ether[1] |
Chirality | racemic[2] |
Identifiers [] | |
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IUPAC name | 2-amino-3-methylbutanoic acid[1] |
SMILES | CC(C)C(C(=O)O)N[1] |
InChI | InChI=1S/C5H11NO2/c1-3(2)4(6)5(7)8/h3-4H,6H2,1-2H3,(H,7,8)[1] |
InChIKey | KZSNJWFQEVHDMF-UHFFFAOYSA-N[1] |
Dosing |
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Valine
(Redirected from L-Valine)
Valine (also known as DL-Valine, 2-Amino-3-methylbutanoic acid, FEMA No. 3444, CCRIS 8604, D,L-VALINE, D,l-valine, AI3-18308, Valine, DL, 2Aminoisovaleric acid, DL or αAminoisovaleric acid, DL) is a substance of the amino acid class.
Chemistry
Valine is typically found in the form of its acetate ester.
Stereochemistry
DL-Valine is a racemic mixture of the logical stereoisomers:
Stereoisomers [] |
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See also
External links
- Valine (Wikipedia)
- Valine / D-Valine / L-Valine (Wikidata)
- Valine / D-Valine / L-Valine (PubChem)
- Valine / D-Valine / L-Valine (ChEMBL)
- Valine / D-Valine / L-Valine (ChEBI)
- Valine / D-Valine / L-Valine (Common Chemistry)
- Valine / L-Valine (HMDB)
- Valine / D-Valine / L-Valine (KEGG)
- Valine / D-Valine / L-Valine (UNII)
- Valine / D-Valine / L-Valine (EPA DSSTox)