| Name | N~6~-[(Benzyloxy)carbonyl]-L-lysine |
|---|---|
| Synonyms |
(2S)-2-amino-6-{[(benzyloxy)carbonyl]amino}hexanoic acid
N(ε)-Benzyloxycarbonyl-L-lysine 6-N-Cbz-L-lysine N6-(Benzyloxycarbonyl)-L-lysine MFCD00002638 (2R)-2-ammonio-6-[[oxo-(phenylmethoxy)methyl]amino]hexanoate NSILON)-BENZYLOXYCBONYL-L-LYSINE N6-Carbobenzyloxy-L-lysine SILON-CBOBENZOXY-L-LYSINE N-SILON-Z-L-LYSINE Nε-Z-L-lysine (Assay) H-LYS(Z)-OH L-Lys(Z)-OH H-L-Lys(Z)-OH N6-Cbz-L-lysine, [N N-6-CBOBENZYLOXY-L-LYSINE Nsilon-Cbobenzyloxy-L-lysine N(E)-BENZYLOXYCBONYL-L-LYSINE N-SILON-CBZ-LYSINE (S)-2-Amino-6-benzyloxycbonylaminohexanoic acid ε-(Benzyloxycbonyl)-L-lysine H-Lys(Z)-OH /K(Z) LYS(Z) N(5)-BENZYLOXYCBONYL-L-LYSINE N-BENZYLOXYCBONYL-L-LYSINE Nsilon-Cbz-L-lysine H-Lys(Z)-OH N6-CBOBENZYLOXY-L-LYSINE N-SILON-CBOBENZYLOXY-L-LYSINE N&si:-Cbobenzyloxy-L-lysine (S)-N6-Benzyloxycarbonyllysine L-LYS(Z) Nsilon-Cbobenzox (2R)-2-ammonio-6-(benzyloxycbonylamino)hexanoate N-[(Benzyloxy)carbonyl]-L-lysine Nepsilon-Carbobenzyloxy-L-lysine N-SILON-CBZ-L -LYSINE N(sup 6)-cbobenzyloxy-L-lysine (2R)-2-azaniumyl-6-(phenylmethoxycbonylamino)hexanoate LYSINE(Z)-OH (2R)-2-amino-6-[[oxo-(phenylmethoxy)methyl]amino]hexanoic acid N6-Cbz-L-Lysine //BP Nε-Carbobenzoxy-L-lysine Nε-Cbz-L-lysine N6-benzyloxycbonyl-L-lysine L-LYSINE(CBZ) (2R)-2-amino-6-(phenylmethoxycbonylamino)hexanoic acid N6-Cbz-L-Lysine SynonyMs H-Lys(Z)-OH Nsilon-Cbobenzyloxy-L-lysine, R (2S)-2-amino-6-(phenylmethoxycbonylamino)hexanoic acid H-LYS(CBZ)-OH N6-[(Phenylmethoxy)carbonyl]-L-lysine NSILON-CBOBENZOXY-L-LYSINE N6-[(Phenylmethoxy)carbonyl]-D-lysine H-Lys(Z)-OH N6-[(phenylmethoxy)carbonyl]-L-lysine N6-Cbz-L-Lys-OH N-ε-Benzoyloxycbonyllysine EINECS 214-585-7 N-silon-CBZ-L-Lysin L-Lysine, N6-[(phenylmethoxy)carbonyl] H-Lys(Z)-OH >= (NT) Nε-Z-L-lysine, N6-Cbobenzyloxy-L-lysine Nsilon)-Cbz-L-Lysine L-Lys(Cbz)-OH N6-[(phenylMethoxy)carbonyl]-L-lysine hydrochloride Nsilon)-cbobenzoxylysine N-SILON-CBZ-L-LYSINE |
| Description | H-Lys(Z)-OH is a lysine derivative[1]. |
|---|---|
| Related Catalog | |
| In Vitro | Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. |
| References |
| Density | 1.2±0.1 g/cm3 |
|---|---|
| Boiling Point | 499.6±45.0 °C at 760 mmHg |
| Melting Point | 259ºC (dec.) |
| Molecular Formula | C14H20N2O4 |
| Molecular Weight | 280.320 |
| Flash Point | 255.9±28.7 °C |
| Exact Mass | 280.142303 |
| PSA | 101.65000 |
| LogP | 1.36 |
| Vapour Pressure | 0.0±1.3 mmHg at 25°C |
| Index of Refraction | 1.550 |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | Xi |
| Safety Phrases | S24/25 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| Precursor 10 | |
|---|---|
| DownStream 10 | |