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40918-51-2

40918-51-2 structure
40918-51-2 structure

Name L-Norvaline ethyl ester hydrochloride
Synonyms ZY3&VO2 &&L or S Form HCl
(2S)-2-Aminopentanoic acid ethyl ester hydrochloride
ethyl (2S)-2-aminopentanoate,hydrochloride
Ethyl L-norvalinate hydrochloride (1:1)
Ethyl (S)-2-Aminopentanoate Hydrochloride
(S)-2-Aminovaleric Acid Ethyl Ester Hydrochloride
L-Norvaline ethyl ester hydrochloride
L-Norvaline, ethyl ester, hydrochloride (1:1)
MFCD08458628
Ethyl (S)-2-Aminovalerate Hydrochloride
H-Nva-OEt·HCl
(S)-2-Aminopentanoic acid ethyl ester hydrochloride
H-NVA-OEt . HCl
H-Nva-OEt.HCl
Description L-Norvaline ethyl ester HCl is a valine 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.

Boiling Point 175.4ºC at 760 mmHg
Melting Point 104-106ºC
Molecular Formula C7H16ClNO2
Molecular Weight 181.660
Flash Point 48.4ºC
Exact Mass 181.086960
PSA 52.32000
LogP 2.17920
Storage condition Store at 0-5°C

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40918-51-2 structure

40918-51-2

Literature: Karanfil, Abdullah; Balta, Berrin; Eskici, Mustafa Tetrahedron, 2012 , vol. 68, # 49 p. 10218 - 10229,12 Title/Abstract Full Text Show Details Karanfil, Abdullah; Balta, Berrin; Eskici, Mustafa Tetrahedron, 2012 , vol. 68, # 49 p. 10218 - 10229

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40918-51-2 structure

40918-51-2

Literature: Meppen, Malte; Pacini, Barbara; Bazzo, Renzo; Koch, Uwe; Leone, Joseph F.; Koeplinger, Kenneth A.; Rowley, Michael; Altamura, Sergio; Di Marco, Annalise; Fiore, Fabrizio; Giuliano, Claudio; Gonzalez-Paz, Odalys; Laufer, Ralph; Pucci, Vincenzo; Narjes, Frank; Gardelli, Cristina European Journal of Medicinal Chemistry, 2009 , vol. 44, # 9 p. 3765 - 3770
Precursor  2

DownStream  1