Fmoc-Sar-Opfp

Names

[ Name ]:
Fmoc-Sar-Opfp

[Synonym ]:
Fmoc-Sar-OPfp
FMOC-SARCOSINE-OPFP
FMOC-N-METHYLGLYCINE PENTAFLUOROPHENYL ESTER
Glycine,N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-,pentafluorophenyl ester (9CI)
2,3,4,5,6-pentafluorophenyl 2-[(fluoren-9-ylmethoxy)-N-methylcarbonylamino]ace tate
FMOC-N-ME-GLY-OPFP
Fmoc-sarcosine pentafluorophenyl ester

Biological Activity

[Description]:

Fmoc-Sar-OPfp is a Glycine (HY-Y0966) derivative[1].

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

[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.

Chemical & Physical Properties

[ Density]:
1.434g/cm3

[ Boiling Point ]:
549.5ºC at 760 mmHg

[ Molecular Formula ]:
C₂₄H₁₆F₅NO₄

[ Molecular Weight ]:
477.38000

[ Flash Point ]:
286.1ºC

[ Exact Mass ]:
477.10000

[ PSA ]:
55.84000

[ LogP ]:
5.16840

[ Vapour Pressure ]:
3.99E-12mmHg at 25°C

[ Index of Refraction ]:
1.567

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3