| Identification | Back Directory | [Name]
H-ALA-GLY-OH | [CAS]
687-69-4 | [Synonyms]
ALA-GLY
H-ALA-GLY-OH
L-Ala-Gly-OH
L-ALANYLGLYCINE
N-L-Alanylglycine
Glycine, L-alanyl-
Glycine, N-L-alanyl-
L-alpha-Alanylglycine
H-ALA-GLY-OH USP/EP/BP
L-Alanyl-glycine, ≥98%
Ala-Gly,L-Alanyl-glycine
L-ALANYL GLYCINE extrapure
(S)-2-(2-aMinopropanaMido)acetic acid
2-[[(2S)-2-aminopropanoyl]amino]acetic acid | [EINECS(EC#)]
211-699-9 | [Molecular Formula]
C5H10N2O3 | [MDL Number]
MFCD00065107 | [MOL File]
687-69-4.mol | [Molecular Weight]
146.14 |
| Chemical Properties | Back Directory | [Melting point ]
249-255 °C (dec.)
| [Boiling point ]
417.4±30.0 °C(Predicted) | [density ]
1.263±0.06 g/cm3(Predicted) | [storage temp. ]
−20°C
| [form ]
Solid | [pka]
3.14±0.10(Predicted) | [color ]
White to off-white | [BRN ]
1723438 | [CAS DataBase Reference]
687-69-4 |
| Hazard Information | Back Directory | [Uses]
H-ALA-GLY-OH is an amino acid reagent used in the synthesis of ternary copper(II)?-?L-?dipeptide-?neocuproine complexes used in cancer treatment. | [Definition]
ChEBI: A dipeptide formed from L-alanyl and glycine residues. | [Biological Activity]
Alanyl dipeptides such as ala-leuala-lysala-glyala-proala-tyr and ala-phe may be used in physicochemical studies or to evaluate dipeptide separation technologies. Alanyl dipeptides may also be used for studying cell uptake mechanismsdipeptide metabolism or cell growth supplementation benefits.''L-alanylglycine is a simple nutritional dipeptide also used for physical chemistry studies such as hydrogen bonding and heavy metal complexation. |
|
|