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2389-48-2

2389-48-2 structure
2389-48-2 structure

Name methyl (2S)-2-amino-6-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoate,hydrochloride
Synonyms Methyl N-(tert-butoxycarbonyl)-L-lysinate hydrochloride (1:1)
2-Hexanaminium, 6-[[(1,1-dimethylethoxy)carbonyl]amino]-1-methoxy-1-oxo-, chloride, (2S)- (1:1)
MFCD00076959
H-lysine(Boc) methyl ester hydrochloride
Lys(Boc)-OMe HCl
N-Boc-L-lysine methyl ester hydrochloride
H-Lys(Boc)-OMe.HCl
H-Lys(Boc)-OMe hydrochloride
Nepsilon-Boc-L-lysine methyl ester hydrochloride
(2S)-1-Methoxy-6-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-1-oxo-2-hexanaminium chloride
(S)-Methyl 2-amino-6-((tert-butoxycarbonyl)amino)hexanoate hydrochloride
H-Lys(Boc)-OMe·HCl
N-Boc-L-lysine methylester hydrochloride
Description H-Lys(Boc)-OMe hydrochloride 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.

Boiling Point 364.6ºC at 760mmHg
Molecular Formula C12H25ClN2O4
Molecular Weight 296.791
Flash Point 174.3ºC
Exact Mass 296.150299
PSA 90.65000
LogP 3.07490
Vapour Pressure 6.2E-07mmHg at 25°C
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
Precursor  0

DownStream  1