Ne-Boc-L-lysine

Modify Date: 2025-08-20 18:19:50

Ne-Boc-L-lysine Structure
Ne-Boc-L-lysine structure
Common Name Ne-Boc-L-lysine
CAS Number 2418-95-3 Molecular Weight 246.303
Density 1.1±0.1 g/cm3 Boiling Point 412.9±40.0 °C at 760 mmHg
Molecular Formula C11H22N2O4 Melting Point 250 °C (dec.)(lit.)
MSDS Chinese USA Flash Point 203.5±27.3 °C

 Use of Ne-Boc-L-lysine


(S)-2-Amino-6-((tert-butoxycarbonyl)amino)hexanoic acid is a lysine derivative[1].

 Names

Name Ne-Boc-L-lysine
Synonym More Synonyms

 Ne-Boc-L-lysine Biological Activity

Description (S)-2-Amino-6-((tert-butoxycarbonyl)amino)hexanoic acid 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

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

 Chemical & Physical Properties

Density 1.1±0.1 g/cm3
Boiling Point 412.9±40.0 °C at 760 mmHg
Melting Point 250 °C (dec.)(lit.)
Molecular Formula C11H22N2O4
Molecular Weight 246.303
Flash Point 203.5±27.3 °C
Exact Mass 246.157959
PSA 101.65000
LogP 0.74
Vapour Pressure 0.0±2.1 mmHg at 25°C
Index of Refraction 1.485
Storage condition 2~8°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2924199090

 Synthetic Route

 Customs

HS Code 2924199090
Summary 2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles11

More Articles
Adding l-lysine derivatives to the genetic code of mammalian cells with engineered pyrrolysyl-tRNA synthetases.

Biochem. Biophys. Res. Commun. 371(4) , 818-22, (2008)

We report a method for site-specifically incorporating l-lysine derivatives into proteins in mammalian cells, based on the expression of the pyrrolysyl-tRNA synthetase (PylRS)-tRNA(Pyl) pair from Meth...

Evidence that malondialdehyde-derived aminoenimine is not a fluorescent age pigment.

Chem. Res. Toxicol. 14(5) , 473-5, (2001)

It has been suggested that protein modifications by malondialdehyde (MDA), a major product of lipid peroxidation, contribute to the fluorescence formation of lipofuscin. Although early studies propose...

Nanoassembly of surfactants with interfacial drug-interactive motifs as tailor-designed drug carriers.

Mol. Pharm. 10(1) , 187-98, (2013)

PEGylated lipopeptide surfactants carrying drug-interactive motifs specific for a peptide-nitroxide antioxidant, JP4-039, were designed and constructed to facilitate the solubilization of this drug ca...

 Synonyms

Z-Lys(Boc)-OH
Ne-Boc-L-Lysine
NEPSILON-BOC-L-LYSINE
N-[(Benzyloxy)carbonyl]-N-{[(2-methyl-2-propanyl)oxy]carbonyl}lysine
N2-BENZYLOXYCARBONYL-N6-BOC-L-LYSINE
e-BOC-L-lysine.
MFCD00037221
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-lysine
H-L-LYS(BOC)-OH
L-Lysine, N-[(1,1-dimethylethoxy)carbonyl]-
L-LYSINE(BOC)
LYS(BOC)
Fmoc-Lys(Boc)-OH
Lysine derivative 1
N-(Tert-Butoxycarbonyl)-L-Lysine
Nε-Boc-L-lysine
N2-Benzyloxycarbonyl-N6-tert-butyloxycarbonyl-L-lysine
L-LYS(BOC)
Nε-Boc-Nα-Cbz-L-lysine
N6-Boc-L-lysine
Nepsilon-Boc-Nalpha-Cbz-L-Lysine
Nε-(tert-Butoxycarbonyl)-L-lysine
(S)-2-Amino-6-((tert-butoxycarbonyl)amino)hexanoic acid
LYSINE(BOC)-OH
(S)-2-(((Benzyloxy)carbonyl)amino)-6-((tert-butoxycarbonyl)amino)hexanoic acid
N2-benzyloxycarbonyl-N6-tert-butoxycarbonyl-L-lysine
H-Lys(Boc)-OH
L-Lysine, N6-((1,1-dimethylethoxy)carbonyl)-
AmbotzZAA1184
Lysine, N-[(1,1-dimethylethoxy)carbonyl]-N-[(phenylmethoxy)carbonyl]-
N-Cbz-N'-Boc-L-lysine
Nε-(tert-Butoxycarbonyl)-Nα-carbobenzoxy-L-lysine
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