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132388-65-9

132388-65-9 structure
132388-65-9 structure

Name (2,3,4,5,6-pentafluorophenyl) 2-(9H-fluoren-9-ylmethoxycarbonylamino)-5-oxo-5-(tritylamino)pentanoate
Synonyms Fmoc-Gln(Trt)-OPfp
2-[[9H-fluoren-9-ylmethoxy(oxo)methyl]amino]-5-oxo-5-[(triphenylmethyl)amino]pentanoic acid (2,3,4,5,6-pentafluorophenyl) ester
N-alpha-Fmoc-N-gamma-trityl-L-glutamine pentafluorophenyl ester
N-Fmoc-N'-trityl-L-glutamine pentafluorophenyl ester
[2,3,4,5,6-pentakis(fluoranyl)phenyl] 2-(9H-fluoren-9-ylmethoxycarbonylamino)-5-oxidanylidene-5-[(triphenylmethyl)amino]pentanoate
(2,3,4,5,6-pentafluorophenyl) (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-5-oxo-5-(tritylamino)pentanoate
Description Fmoc-Gln(Trt)-Opfp 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 1.29g/cm3
Boiling Point 830.1ºC at 760mmHg
Melting Point 183-184℃
Molecular Formula C45H33F5N2O5
Molecular Weight 776.74600
Flash Point 455.8ºC
Exact Mass 776.23100
PSA 93.73000
LogP 9.86510
Vapour Pressure 4.48E-33mmHg at 25°C
Index of Refraction 1.604
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