Lys

Salts []
Lysine acetate
Lysine monohydrate
Lysine phosphate
Lysine malate
Lysine aspartate
Lysine carbonate
Lysine succinate
Lysine hydrochloride

Esters []
Lysine acetate
Lysine stearate

Molecular structure via molpic
Conformer structure via 3Dmol.js
Molecular formula	C6H14N2O2[1]
Molecular mass	146.19 g/mol[1]
Predicted LogP	-3[1]
Chirality	racemic[2]

Identifiers []
IUPAC name	2,6-diaminohexanoic acid[1]
SMILES	C(CCN)CC(C(=O)O)N[1]
InChI	InChI=1S/C6H14N2O2/c7-4-2-1-3-5(8)6(9)10/h5H,1-4,7-8H2,(H,9,10)[1]
InChIKey	KDXKERNSBIXSRK-UHFFFAOYSA-N[1]

Dosing

Lysine

(Redirected from L-Lysine)

Lysine (also known as DL-Lysine, (RS)-Lysine, CCRIS 8600, (+-)-2,6-Diaminohexanoic acid, DL-α,epsilon-Diaminocaproic acid, Ec 200-740-6, (+-)-Lysine, 200-740-6, (+/-)-2,6-Diaminocaproic acid or H-DL-Lys-OH) is a substance of the amino acid class.

Chemistry

Lysine is typically found in the form of its acetate, monohydrate, phosphate, malate, aspartate, carbonate, succinate and hydrochloride salts or its acetate and stearate esters.

Stereochemistry

DL-Lysine is a racemic mixture of the logical stereoisomers:

Stereoisomers []
D-Lysine L-Lysine DL-Lysine

See also

• Substituted amino acids
• Anodyne

External links

• Lysine (Wikipedia)
• Lysine / D-Lysine / L-Lysine (Wikidata)
• Lysine / D-Lysine / L-Lysine (PubChem)
• Lysine / D-Lysine / L-Lysine (ChEMBL)
• Lysine / D-Lysine / L-Lysine (ChEBI)
• Lysine / D-Lysine / L-Lysine (Common Chemistry)
• Lysine / D-Lysine / L-Lysine (KEGG)
• Lysine / D-Lysine / L-Lysine (UNII)
• Lysine / D-Lysine / L-Lysine (EPA DSSTox)