Norleucine
| Names | |
|---|---|
| Preferred IUPAC name
(2S)-2-Aminohexanoic acid | |
| Other names
Caprine Glycoleucine | |
| Identifiers | |
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3D model (JSmol) |
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| 1721748 | |
| ChEBI | |
| ChemSpider | |
| DrugBank | |
| ECHA InfoCard | 100.009.512 |
| EC Number |
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| 464584 | |
| KEGG | |
| MeSH | Norleucine |
PubChem CID |
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| RTECS number |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C6H13NO2 | |
| Molar mass | 131.175 g·mol−1 |
| Melting point | 301 °C (574 °F; 574 K) (decomposes) |
| 16 g/L at 23 °C | |
| Acidity (pKa) | 2.39 (carboxyl), 9.76 (amino) |
| Related compounds | |
Related Aminoacids |
Norvaline (2-amino-pentanoic) Aminocaproic acid (6-amino-hexanoic) Leucine (2-amino-4-methyl-pentanoic) Isoleucine (2-amino-3-methyl-pentanoic) Lysine (2,6-diamino-hexanoic) |
Related compounds |
Caproic acid (hexanoic) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Norleucine (abbreviated as Nle) is an amino acid with the formula CH3(CH2)3CH(NH2)CO2H. A systematic name for this compound is 2-aminohexanoic acid. The compound is an isomer of the more common amino acid leucine. Like most other α-amino acids, norleucine is chiral. It is a white, water-soluble solid.