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Merck

616281

L-Glutamic acid-2,3,3,4,4-d5

97 atom % D, 98% (CP)

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About This Item

Linear Formula:
HO2C(CD2)2CD(NH2)CO2H
Molecular Weight:
152.16
NACRES:
NA.12
PubChem Substance ID:
UNSPSC Code:
12352209
MDL number:

Product Name

L-Glutamic acid-2,3,3,4,4-d5, 97 atom % D, 98% (CP)

InChI

1S/C5H9NO4/c6-3(5(9)10)1-2-4(7)8/h3H,1-2,6H2,(H,7,8)(H,9,10)/t3-/m0/s1/i1D2,2D2,3D

SMILES string

[2H]C([2H])(C(O)=O)C([2H])([2H])[C@]([2H])(N)C(O)=O

InChI key

WHUUTDBJXJRKMK-NKXUJHECSA-N

isotopic purity

97 atom % D

assay

98% (CP)

form

solid

optical activity

[α]25/D +31°, c = 2 in 5 M HCl

mp

205 °C (dec.) (lit.)

mass shift

M+5

Quality Level

Related Categories

Biochem/physiol Actions

Glutamic acid (or glutamate) functions as a neurotransmitter and also serves as a precursor to other neurotransmitters such as gamma-aminobutyric acid. Glutamic acid also plays a key role in many metabolic pathways that controls growth, reproduction, maintenance and immunity. It is converted to α-ketoglutarate, a key component of the TCA (tricarboxylic acid) cycle and a precursor for the biosynthesis of nucleic acids and certain amino acids. In cells, glutamine is converted to glutamate by the enzyme glutaminase.
Appl- L-Glutamic acid-2,3,3,4,4-d5 has been used as an internal standard in metabolomics and lipidomics profiling.

Packaging

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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The biology of cancer: metabolic reprogramming fuels cell growth and proliferation.
DeBerardinis RJ
Cell Metabolism, 7(1), 11-20 (2008)
Glutamic Acid, Twenty Years Later
S. Garattini
The Journal of Nutrition, 130(4), 901S-909S (2000)
Flavia Bianchi et al.
Insects, 11(11) (2020-11-22)
The production of phagostimulant and attractive volatile organic compounds (VOCs) by yeasts can be exploited to improve the efficacy of attract-and-kill formulations against the spotted wing drosophila (SWD). This study evaluated the persistence over one week of a yeast-based formulation
Metabolomics and lipidomics using traveling-wave ion mobility mass spectrometry.
Paglia G and Astarita G
Nature Protocols, 12(4), 797-797 (2017)
Amino acids: metabolism, functions, and nutrition.
Wu G
Amino Acids, 37(1), 1-17 (2009)

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