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Fmoc-L-beta-homovaline

Names

[ CAS No. ]:
172695-33-9

[ Name ]:
Fmoc-L-beta-homovaline

[Synonym ]:
Fmoc-β-Leu-OH
(3R)-3-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-4-methylpentanoic acid
Fmoc-L-beta-Homovaline
Pentanoic acid, 3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4-methyl-, (3R)-
(3R)-3-(9H-fluoren-9-ylmethoxycarbonylamino)-4-methylpentanoic acid
MFCD01862853

Biological Activity

[Description]:

Fmoc-β-HoVal-OH is a valine 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]:
1.2±0.1 g/cm3

[ Boiling Point ]:
563.9±33.0 °C at 760 mmHg

[ Molecular Formula ]:
C21H23NO4

[ Molecular Weight ]:
353.412

[ Flash Point ]:
294.9±25.4 °C

[ Exact Mass ]:
353.162720

[ PSA ]:
75.63000

[ LogP ]:
4.59

[ Vapour Pressure ]:
0.0±1.6 mmHg at 25°C

[ Index of Refraction ]:
1.583

[ Storage condition ]:
2-8°C

MSDS

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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

Synthetic Route

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Precursor & DownStream

Precursor

DownStream

Related Compounds