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200616-40-6

200616-40-6 structure
200616-40-6 structure

Name Fmoc-N-methyl-L-glutamic acid 5-tert-butyl ester
Synonyms (2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl](methyl)amino}-5-[(2-methyl-2-propanyl)oxy]-5-oxopentanoic acid
MFCD00237028
(2S)-5-tert-Butoxy-2-{[(9H-fluoren-9-ylmethoxy)carbonyl](methyl)amino}-5-oxopentanoic acid (non-preferred name)
L-Glutamic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-, 5-(1,1-dimethylethyl) ester
N-Methyl glutamic acid
N-(9-Fluorenylmethyloxycarbonyl)-N-methyl-L-glutamic acid 5-tert-butyl ester
FMOC-L-MEGLU(TBU)-OH
Fmoc-N-Me-Glu(OtBu)-OH
FMOC-MEGLU(OTBU)-OH
FMOC-N-ME-GLUTAMIC ACID(OTBU)-OH
REF DUPL: Fmoc-N-Me-Glu(OtBu)-OH
Description Fmoc-N-Me-Glu(OtBu)-OH 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.

Density 1.2±0.1 g/cm3
Boiling Point 612.3±55.0 °C at 760 mmHg
Molecular Formula C25H29NO6
Molecular Weight 439.501
Flash Point 324.1±31.5 °C
Exact Mass 439.199493
PSA 93.14000
LogP 5.75
Vapour Pressure 0.0±1.9 mmHg at 25°C
Index of Refraction 1.570
Storage condition -15°C
Symbol GHS09
GHS09
Signal Word Warning
Hazard Statements H410
Precautionary Statements P273-P501
Hazard Codes N
Risk Phrases 50/53
Safety Phrases 60-61
RIDADR UN 3077 9 / PGIII