H-Gly-Ala-OH

Modify Date: 2025-08-26 13:42:09

H-Gly-Ala-OH Structure
H-Gly-Ala-OH structure
 Common Name H-Gly-Ala-OH
CAS Number 3695-73-6 Molecular Weight 146.145
Density 1.3±0.1 g/cm3 Boiling Point 417.4±30.0 °C at 760 mmHg
Molecular Formula C5H10N2O3 Melting Point ~ 230°C dec.
MSDS Chinese USA Flash Point 206.2±24.6 °C

 Use of H-Gly-Ala-OH


Gly-Ala is a Glycine (HY-Y0966) derivative[1].

 Names

Name Glycine-alanine dipeptide
Synonym More Synonyms

 H-Gly-Ala-OH Biological Activity

Description Gly-Ala is a Glycine (HY-Y0966) 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.

 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

 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

 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%

 Articles26

More 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...

 Synonyms

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
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