616281
L -Glutamic acid-2,3,3,4,4-d5
97 atom % D, 98% (CP)
Synonym(s):
(2S)-2-amino-2,3,3,4,4-pentadeuteriopentanedioic acid, Glutamicol-d5
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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:
Isotopic purity:
97 atom % D
Assay:
98% (CP)
Mass shift:
M+5
Form:
solid
isotopic purity
97 atom % D
Quality Segment
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
SMILES string
[2H]C([2H])(C(O)=O)C([2H])([2H])[C@]([2H])(N)C(O)=O
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
InChI key
WHUUTDBJXJRKMK-NKXUJHECSA-N
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.
Appl-
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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