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G2754

Sigma-Aldrich

Gly-DL-Asp

≥98%, suitable for electrophoresis

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About This Item

Formule empirique (notation de Hill):
C6H10N2O5
Numéro CAS:
79731-35-4
Poids moléculaire :
190.15
Numéro MDL:
MFCD00066049
Code UNSPSC :
12352202
ID de substance PubChem :
24895102
Nomenclature NACRES :
NA.26

product name

Gly-DL-Asp,

Pureté

≥98%

Forme

powder

Technique(s)

electrophoresis: suitable

Couleur

white

Température de stockage

−20°C

Chaîne SMILES 

NCC(=O)NC(CC(O)=O)C(O)=O

InChI

1S/C6H10N2O5/c7-2-4(9)8-3(6(12)13)1-5(10)11/h3H,1-2,7H2,(H,8,9)(H,10,11)(H,12,13)

Clé InChI

SCCPDJAQCXWPTF-UHFFFAOYSA-N

Informations sur le gène

human ... SLC15A1(6564)

Application

Glycyl dipeptides such as glycyl-L-aspartate are useful as model compounds for the development of chiral separation technologies such as chiral ligand-exchange capillary electrophoresis and capillary electrochromatography (CEC).

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

D S Eggleston et al.
International journal of peptide and protein research, 19(2), 206-211 (1982-02-01)
The crystal structure of the acidic dipeptide glycyl-L-aspartic acid dihydrate, Gly-L-Asp X 2H2O, C6H10N2O5 X 2H2O, has been determined by means of three-dimensional counter X-ray data. The dipeptide crystallizes in space group P212121 of the orthorhombic system with four formula
R Chitra et al.
Acta crystallographica. Section C, Crystal structure communications, 63(Pt 1), o11-o13 (2007-01-09)
The title bis(glycyl-L-aspartic acid) oxalate complex {systematic name: bis[2-(2-ammonioacetamido)butanedioic acid] oxalate 0.4-hydrate}, 2C6H11N2O5+.C2O4(2-).4H2O, crystallizes in a triclinic space group with the planar peptide unit in a trans conformation. The asymmetric unit consists of two glycyl-L-aspartic acid molecules with positively charged
R Kaul et al.
Journal of neurochemistry, 56(1), 129-135 (1991-01-01)
Canavan disease, an autosomal recessive disorder, is characterized biochemically by N-acetylaspartic aciduria and aspartoacylase (N-acyl-L-aspartate amidohydrolase; EC 3.5.1.15) deficiency. However, the role of aspartoacylase and N-acetylaspartic acid in brain metabolism is unknown. Aspartoacylase has been purified to apparent homogeneity with
E C O'Brien et al.
Journal of inorganic biochemistry, 77(3-4), 135-139 (2000-03-04)
The first solution studies at physiological pH for the formation of metal complexes of taurine, +NH3CH2CH2S03-, one of the most abundant low molecular weight organic compounds in the animal kingdom, are reported. The complexes Cu(Gly-GlyH-1) (1) and [Cu(Gly-AspH-1)] (2) react
Martin G Schmid et al.
Journal of separation science, 29(10), 1470-1475 (2006-08-10)
The preparation and application of dynamically coated ligand-exchange chromatography phases for enantioseparation is described. The phases were prepared by pumping a solution of N-decyl-L-4-hydroxyproline, N-hexadecyl-L-4-hydroxyproline, or N-2-hydroxydodecyl-L-4-hydroxyproline through a commercially available monolithic RP-18 column. These coatings are stable against desorption
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