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H-Gly-Ala-OH

Names

[ CAS No. ]:
3695-73-6

[ Name ]:
H-Gly-Ala-OH

[Synonym ]:
EINECS 223-019-8
Gly-l-ala
Glycyl-DL-alanine
Glycine-alanine
Glycyl-L-alanine
Gly-Ala-OH
MFCD00065112
Glcylalanine
H-Gly-L-Ala-OH
UNII:44L9158R9G
N-glycylalanine
Gly-L-Ala-OH
Alanine, N-glycyl-, L-
L-Alanine, glycyl-
(S)-2-(2-Aminoacetamido)propanoic acid
Alanine, glycyl-
Glycylalanine
DL-Alanine, N-glycyl-
Gly-Ala
L-Alanine, N-glycyl-
N-Glycyl-L-alanine
H-GLY-ALA-OH
H-Gly-β-Ala-OH

Biological Activity

[Description]:

Gly-Ala is a Glycine (HY-Y0966) 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]:
1.3±0.1 g/cm3

[ Boiling Point ]:
417.4±30.0 °C at 760 mmHg

[ Melting Point ]:
~ 230°C dec.

[ Molecular Formula ]:
C5H10N2O3

[ Molecular Weight ]:
146.145

[ Flash Point ]:
206.2±24.6 °C

[ Exact Mass ]:
146.069138

[ PSA ]:
92.42000

[ LogP ]:
-1.50

[ Vapour Pressure ]:
0.0±2.1 mmHg at 25°C

[ Index of Refraction ]:
1.498

[ Storage condition ]:
-15°C

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2924199090

Precursor & DownStream

Customs

[ HS Code ]: 2924199090

[ Summary ]:
2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Charge-based interactions between peptides observed as the dominant force for association in aqueous solution.

Angew. Chem. Int. Ed. Engl. 47(47) , 9059-62, (2008)

Epstein-Barr virus latent genes.

Exp. Mol. Med. 47 , e131, (2015)

Latent Epstein-Barr virus (EBV) infection has a substantial role in causing many human disorders. The persistence of these viral genomes in all malignant cells, yet with the expression of limited late...

Dissociative electron attachment to glycyl-glycine, glycyl-alanine and alanyl-alanine.

Phys. Chem. Chem. Phys. 13(10) , 4600-6, (2011)

The processes of negative ions formation of dipeptides glycyl-glycine, glycyl-alanine and alanyl-alanine in the conditions of resonant electron capture have been studied with a help of negative ions m...


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Related Compounds

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