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Merck
CN

50170

Gly-Asp

≥99.0%

Synonym(s):

Glycyl-L-aspartic acid

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About This Item

Linear Formula:
NH2CH2CONHCH(COOH)CH2COOH
CAS Number:
Molecular Weight:
190.15
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
EC Number:
225-140-1
Beilstein/REAXYS Number:
1727387
MDL number:
Technical Service
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Quality Level

assay

≥99.0%

optical activity

[α]20/D +12.0±2°, c = 5% in H2O

reaction suitability

reaction type: solution phase peptide synthesis

mp

195-210 °C (dec.)

application(s)

peptide synthesis

SMILES string

NCC(=O)N[C@@H](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)/t3-/m0/s1

InChI key

SCCPDJAQCXWPTF-VKHMYHEASA-N



Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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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
Florian Rohm et al.
Molecular nutrition & food research, 63(5), e1801094-e1801094 (2018-12-07)
Peptide transporter 1 (PEPT1) function is well understood, yet little is known about its contribution toward the absorption of dietary amino acids in the form of di- and tripeptides. In the present human study, changes in plasma concentrations of a
Hyangmi Kim et al.
Archives of microbiology, 199(4), 597-603 (2016-12-29)
A Gram-negative, aerobic, non-motile, rod-shaped bacterial strain, designated MAB-07



Global Trade Item Number

SKUGTIN
50170-1G04061826222935