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75932-02-4

75932-02-4 structure
75932-02-4 structure

Name (2R)-2,6-bis(9H-fluoren-9-ylmethoxycarbonylamino)hexanoic acid
Synonyms Fmoc-Lys(Fmoc)-OH
N,N-Bis[(9H-fluoren-9-ylmethoxy)carbonyl]lysine
Lysine, N,N-bis[(9H-fluoren-9-ylmethoxy)carbonyl]-
N-(tert-Butoxycarbonyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-lysine
N,N'-Di-Fmoc-D-lysine
FmocHN-Lys(Fmoc)OH
D-Lysine, N-[(1,1-dimethylethoxy)carbonyl]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-{[(2-methyl-2-propanyl)oxy]carbonyl}-D-lysine
Fmoc-L-Lys(Fmoc)-OH
FMOC-D-LYS(FMOC)-OH
N2,N6-Bis-Fmoc-D-lysine
AmbotzFAA1331
N,N'-Di-Fmoc-D-lysine
Description N2,N6-Bis(((9H-fluoren-9-yl)methoxy)carbonyl)-D-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.

Density 1.2±0.1 g/cm3
Boiling Point 685.7±55.0 °C at 760 mmHg
Melting Point 130ºC
Molecular Formula C26H32N2O6
Molecular Weight 468.542
Flash Point 368.5±31.5 °C
Exact Mass 468.226044
PSA 113.96000
LogP 4.97
Vapour Pressure 0.0±2.2 mmHg at 25°C
Index of Refraction 1.566
Storage condition Store at 0-5°C
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