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G3640

Sigma-Aldrich

Glu-Glu

≥98% (TLC)

Synonym(s):

L-α-glutamyl-L-glutamic acid

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About This Item

Empirical Formula (Hill Notation):
C10H16N2O7
CAS Number:
Molecular Weight:
276.24
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.26

product name

Glu-Glu,

Assay

≥98% (TLC)

form

powder

color

white

storage temp.

−20°C

SMILES string

NC(CCC(O)=O)C(=O)NC(CCC(O)=O)C(O)=O

InChI

1S/C10H16N2O7/c11-5(1-3-7(13)14)9(17)12-6(10(18)19)2-4-8(15)16/h5-6H,1-4,11H2,(H,12,17)(H,13,14)(H,15,16)(H,18,19)

InChI key

KOSRFJWDECSPRO-UHFFFAOYSA-N

Biochem/physiol Actions

Glu-Glu is a small anionic dipeptides that may be used in physicochemical analysis of conformations states and protonation patterns.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

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C J Jeon et al.
Visual neuroscience, 14(2), 387-393 (1997-03-01)
Glutamate is the probable neurotransmitter of both retinal and cortical afferents to the cat superior colliculus (SC). The present study shows that glutamate is also contained in many postsynaptic neurons in SC. The distribution, morphology, and ultrastructure of neurons in
Marieke Schor et al.
Physical chemistry chemical physics : PCCP, 13(22), 10457-10467 (2011-04-20)
Triblock copolymers consisting of a silk-based ((Gly-Ala)(3)Gly-Glu) repeat flanked by hydrophilic outer blocks self-assemble into micrometer long fibrils in response to a trigger. Since the exact mechanism of the fibril formation remains unclear, we employ a multiscale modelling approach in
I A Kostanyan et al.
Bioorganicheskaia khimiia, 23(10), 805-808 (1998-03-07)
A specific interaction of [3H]Glu with T lymphocytes from the blood of healthy donors (Kd = 0.236 microM) was revealed and described. It was found that unlabeled quisqualate, a structural analogue of L-glutamic acid, and unlabeled dipeptides Ala-Glu, Glu-Ala, and
M Ohnishi et al.
Bioscience, biotechnology, and biochemistry, 59(6), 1002-1006 (1995-06-01)
The taste responses to the optical isomers of potassium warfarin, dipotassium glutamyl glutamate, and a mixture of both the substances in laboratory mice were studied using licking activity as an indicator of taste effectiveness. The offensive effectiveness of the optical
Muhammad A Hagras et al.
The journal of physical chemistry. B, 119(46), 14637-14651 (2015-10-28)
The most detailed and comprehensive to date study of electron transfer reactions in the respiratory complex III of aerobic cells, also known as bc1 complex, is reported. In the framework of the tunneling current theory, electron tunneling rates and atomistic

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