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204777-78-6

204777-78-6 structure
204777-78-6 structure

Name (2S)-6-[[1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl]amino]-2-(9H-fluoren-9-ylmethoxycarbonylamino)hexanoic acid
Synonyms Fmoc-K(ivDde)-OH
Fmoc-Lys(ivDde)
L-Lysine, N-[1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
N-Fmoc-N'-[1-(4,4-Dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl]-L-lysine
9-fluorenylmethyloxycarbonyl-K(1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl)-OH
Nalpha-Fmoc-Nepsilon-[1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl]-L-lysine
N-[1-(4,4-Dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-lysine
Fmoc-Lys(IvDde)-OH
Fmoc-Lys(Ddiv)-OH
Description Fmoc-L-Lys(ivDde)-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.

Density 1.2±0.1 g/cm3
Boiling Point 765.6±60.0 °C at 760 mmHg
Molecular Formula C34H42N2O6
Molecular Weight 574.707
Flash Point 416.8±32.9 °C
Exact Mass 574.304260
PSA 121.80000
LogP 6.08
Appearance Powder | White
Vapour Pressure 0.0±2.7 mmHg at 25°C
Index of Refraction 1.570
Storage condition 2-8°C
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