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1999-42-4

1999-42-4 structure
1999-42-4 structure

Name 2-(2-aminopropanoylamino)-4-methylpentanoic acid
Synonyms (+-)-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
Description 2-(2-Aminopropanamido)-4-methylpentanoic acid is a leucine 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.

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
WGK Germany 3

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1999-42-4 structure

1999-42-4

Literature: Justus Liebigs Annalen der Chemie, , vol. 340, p. 171

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1999-42-4 structure

1999-42-4

Literature: Justus Liebigs Annalen der Chemie, , vol. 340, p. 171

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1999-42-4 structure

1999-42-4

Literature: Justus Liebigs Annalen der Chemie, , vol. 636, p. 140 - 143

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1999-42-4 structure

1999-42-4

Literature: Justus Liebigs Annalen der Chemie, , vol. 636, p. 140 - 143

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1999-42-4 structure

1999-42-4

Literature: Justus Liebigs Annalen der Chemie, , vol. 636, p. 140 - 143

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1999-42-4 structure

1999-42-4

Literature: Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, , vol. 154, p. 223