204251-24-1

204251-24-1 structure
204251-24-1 structure

Name fmoc-glu(otbu)-oh h2o
Synonyms Fmoc-L-GlutamicacidmonohydrateO-t-butylester
FMOC-L-GLUTAMIC ACID (OTBU) MONOHYDRATE
FMOC-L-GLU(OTBU)-OH H2O
FMOC-L-GLUTAMIC ACID-O-T-BUTYL ESTER MONOHYDRATE
FMOC-L-GLU(TBU)-OH H2O
FMOC-L-Glutamic acid-O-tert-butyl ester monohydrate
FMOC-GLUTAMIC ACID(OTBU)-OH H2O
L-Glutamic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 5-(1,1-dimethylethyl) ester, hydrate (1:1)
Fmoc-L-Glu(otbu)-OH hydrate
FMOC-GLU(OBUT) H2O
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxy)-5-oxopentanoic acid hydrate
Fmoc-L-Glutamic acid-O-tert-butyl ester hydrate
(2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-5-[(2-methyl-2-propanyl)oxy]-5-oxopentanoic acid hydrate (1:1)
MFCD00150485
Description (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxy)-5-oxopentanoic acid hydrate is a glutamic acid 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 633.5ºC at 760mmHg
Melting Point 89-93ºC
Molecular Formula C24H29NO7
Molecular Weight 443.490
Flash Point 336.9ºC
Exact Mass 443.194397
PSA 111.16000
LogP 4.42680
Vapour Pressure 6.39E-17mmHg at 25°C
Storage condition -20°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Safety Phrases S22-S24/25
RIDADR NONH for all modes of transport
WGK Germany 3