Fmoc-N -Me-Lys(Boc)-OH

Modify Date: 2024-01-02 23:48:55

Fmoc-N -Me-Lys(Boc)-OH Structure
Fmoc-N -Me-Lys(Boc)-OH structure
Common Name Fmoc-N -Me-Lys(Boc)-OH
CAS Number 197632-76-1 Molecular Weight 482.569
Density 1.2±0.1 g/cm3 Boiling Point 665.4±55.0 °C at 760 mmHg
Molecular Formula C27H34N2O6 Melting Point N/A
MSDS Chinese USA Flash Point 356.2±31.5 °C

 Use of Fmoc-N -Me-Lys(Boc)-OH


N2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N6-(tert-butoxycarbonyl)-N2-methyl-L-lysine is a lysine derivative[1].

 Names

Name Fmoc-Nalpha-methyl-Ne-t-Boc-L-lysine
Synonym More Synonyms

 Fmoc-N -Me-Lys(Boc)-OH Biological Activity

Description N2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N6-(tert-butoxycarbonyl)-N2-methyl-L-lysine 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 1.2±0.1 g/cm3
Boiling Point 665.4±55.0 °C at 760 mmHg
Molecular Formula C27H34N2O6
Molecular Weight 482.569
Flash Point 356.2±31.5 °C
Exact Mass 482.241699
PSA 105.17000
LogP 5.45
Vapour Pressure 0.0±2.1 mmHg at 25°C
Index of Refraction 1.566
Storage condition 2-8°C

 Safety Information

Hazard Codes Xi
RIDADR NONH for all modes of transport

 Synonyms

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-methyl-N-{[(2-methyl-2-propanyl)oxy]carbonyl}-L-lysine
(2S)-2-[9H-fluoren-9-ylmethoxycarbonyl(methyl)amino]-6-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid
N'-Boc-N-Fmoc-N-methyl-L-lysine
Fmoc-N-Me-Lys(Boc)-OH
L-Lysine, N-[(1,1-dimethylethoxy)carbonyl]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-
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