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193954-28-8

193954-28-8 structure
193954-28-8 structure

Name (3S)-3-(9H-fluoren-9-ylmethoxycarbonylamino)-4-phenylbutanoic acid
Synonyms Fmoc-|A-HoPhe-OH
Fmoc-Beta-HoPhe-OH
(3S)-3-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-4-phenylbutanoic acid
MFCD01863055
Benzenebutanoic acid, β-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (βS)-
Fmoc-L-beta-homophenylalanine
AmbotzFAA1657
(S)-3-(Fmoc-amino)-4-phenylbutyric acid
(S)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-phenylbutanoic acid
Description Fmoc-B-HoPhe-OH is a phenylalanine 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):1793-914.

Density 1.3±0.1 g/cm3
Boiling Point 633.2±50.0 °C at 760 mmHg
Molecular Formula C25H23NO4
Molecular Weight 401.454
Flash Point 336.8±30.1 °C
Exact Mass 401.162720
PSA 75.63000
LogP 5.62
Vapour Pressure 0.0±2.0 mmHg at 25°C
Index of Refraction 1.624
Storage condition 2-8°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xn
RIDADR NONH for all modes of transport
WGK Germany 3