Skip to Content
Merck
All Photos(1)

Documents

Safety Information

483834

Sigma-Aldrich

γ-L-Glutamyl-L-alanine

98%

Synonym(s):

gamma-Glu-Ala

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
CH3CH[NHCOCH2CH2CH(NH2)CO2H]CO2H
CAS Number:
5875-41-2
Molecular Weight:
218.21
MDL number:
MFCD00037215
UNSPSC Code:
12352200
PubChem Substance ID:
24871921

Assay

98%

optical activity

[α]20/D −26.5°, c = 5 in H2O

reaction suitability

reaction type: solution phase peptide synthesis

mp

188-192 °C (lit.)

application(s)

peptide synthesis

SMILES string

C[C@H](NC(=O)CC[C@H](N)C(O)=O)C(O)=O

InChI

1S/C8H14N2O5/c1-4(7(12)13)10-6(11)3-2-5(9)8(14)15/h4-5H,2-3,9H2,1H3,(H,10,11)(H,12,13)(H,14,15)/t4-,5-/m0/s1

InChI key

WQXXXVRAFAKQJM-WHFBIAKZSA-N

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

483834-VAR:
483834-BULK:
483834-500MG:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 2

1 of 2

Resorufin 95%

Sigma-Aldrich

73144

Resorufin

γ-Aminobutyric acid ≥99%

Sigma-Aldrich

A2129

γ-Aminobutyric acid

M E Anderson et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 3(13), 2527-2531 (1989-11-01)
Glutathione metabolism and transport in the choroid plexus were probed by determining the effects of administration to rats of several compounds (buthionine sulfoximine, L-2-oxothiazolidine-4-carboxylate, L-(alpha 5,5S)-alpha-amino-3-chloro-4,5-dihydro-5-isoxazole acetic acid, gamma-glutamyl alanine, and glutathione monoethyl ester) on the levels of glutathione and
T Takahashi et al.
Biochemical medicine and metabolic biology, 38(3), 311-316 (1987-12-01)
gamma-Glutamyl cyclotransferase activity is assayed in tissues by a colorimetric method using gamma-glutamyl alanine as a substrate coupled with alanine dehydrogenase from B. sphericus, to measure the formation of NADH. In order to avoid interference by the reaction catalyzed by
M J York et al.
European journal of biochemistry, 184(1), 97-101 (1989-09-01)
Spin-echo NMR spectroscopy was used to record the cleavage of a gamma-glutamyl--amino-acid by (5-L-glutamyl)-L-amino-acid 5-glutamyltransferase (cyclizing) (gamma-glutamylcyclotransferase) in human erythrocyte hemolysates. The Michaelis-Menten steady-state kinetic parameters were obtained by fitting the integrated Michaelis-Menten equation to the reaction time curves. The

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service