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H-DL-Ala-DL-Leu-OH

Names

[ CAS No. ]:
1999-42-4

[ Name ]:
H-DL-Ala-DL-Leu-OH

[Synonym ]:
(+-)-N-Alanyl-leucin
D,L-alanyl-D,L-leucine
(+-)-N-alanyl-leucine
alanylleucine
opt.-inakt. N-Alanyl-leucin
(S,S)2-(2-amino-propionylamino)-4-methyl-pentanoic acid
DL-ALA-DL-LEU
DL-Alanyl-DL-Lencine
D-Ala-D-Leu-OH/D-Ala-L-Leu-OH/L-Ala-D-Leu-OH/L-Ala-L-Leu-OH,(1:1:1:1)
DL-ALANINE-DL-LEUCINE
DL-Alanyl-DL-leucine
H-DL-ALA-DL-LEU-OH
DL-Alanyl-DL-leucin
MFCD00025555

Biological Activity

[Description]:

2-(2-Aminopropanamido)-4-methylpentanoic acid is a leucine 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]:
1.108 g/cm3

[ Boiling Point ]:
409.7ºC at 760 mmHg

[ Molecular Formula ]:
C9H18N2O3

[ Molecular Weight ]:
202.25100

[ Flash Point ]:
201.6ºC

[ Exact Mass ]:
202.13200

[ PSA ]:
92.42000

[ LogP ]:
1.04030

[ Storage condition ]:
−20°C

MSDS

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Safety Information

[ WGK Germany ]:
3

Synthetic Route

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Precursor & DownStream

Precursor

DownStream

Related Compounds