Fmoc-L-Lys(Boc,iPr)-OH

Modify Date: 2024-01-03 13:57:33

Fmoc-L-Lys(Boc,iPr)-OH Structure
Fmoc-L-Lys(Boc,iPr)-OH structure
Common Name Fmoc-L-Lys(Boc,iPr)-OH
CAS Number 201003-48-7 Molecular Weight 510.622
Density 1.2±0.1 g/cm3 Boiling Point 677.1±55.0 °C at 760 mmHg
Molecular Formula C29H38N2O6 Melting Point N/A
MSDS N/A Flash Point 363.3±31.5 °C

 Use of Fmoc-L-Lys(Boc,iPr)-OH


Fmoc-Lys(ipr,Boc)-OH is a lysine derivative[1].

 Names

Name (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-6-[(2-methylpropan-2-yl)oxycarbonyl-propan-2-ylamino]hexanoic acid
Synonym More Synonyms

 Fmoc-L-Lys(Boc,iPr)-OH Biological Activity

Description Fmoc-Lys(ipr,Boc)-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

[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 677.1±55.0 °C at 760 mmHg
Molecular Formula C29H38N2O6
Molecular Weight 510.622
Flash Point 363.3±31.5 °C
Exact Mass 510.272980
PSA 105.17000
LogP 6.33
Appearance of Characters Solid
Vapour Pressure 0.0±2.2 mmHg at 25°C
Index of Refraction 1.558
Storage condition -15°C

 Synonyms

AmbotzFAA1447
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-isopropyl-N-{[(2-methyl-2-propanyl)oxy]carbonyl}-L-lysine
N-Fmoc-N'-Boc-N'-isopropyl-L-lysine
L-Lysine, N-[(1,1-dimethylethoxy)carbonyl]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-(1-methylethyl)-
Fmoc-Lys(Boc)(isopropyl)-OH
Fmoc-Lys(ipr,Boc)-OH
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