Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

148946

Sigma-Aldrich

DL-2-Methylglutamic acid hemihydrate

98%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
HO2CCH2CH2C(CH3)(NH2)CO21/2H2O
CAS Number:
Molecular Weight:
170.16
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

assay

98%

mp

160 °C (dec.) (lit.)

SMILES string

O.CC(N)(CCC(O)=O)C(O)=O

InChI

1S/C6H11NO4.H2O/c1-6(7,5(10)11)3-2-4(8)9;/h2-3,7H2,1H3,(H,8,9)(H,10,11);1H2

InChI key

UAHXIVOASZLFEG-UHFFFAOYSA-N

Application

DL-2-Methylglutamic acid hemihydrate may be used in chemical synthesis studies.

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

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

Visit the Document Library

P L Grant et al.
The Biochemical journal, 241(3), 699-704 (1987-02-01)
Several intermediates in the reaction of 2-methylglutamate with glutamate decarboxylase from Escherichia coli were detected by stopped-flow spectrophotometry and by rapid-scanning spectrophotometry after conventional mixing. Structures were assigned to intermediates on the basis of kinetic and spectral evidence. In the
G Hester et al.
Journal of molecular biology, 286(3), 829-850 (1999-02-20)
Phosphoserine aminotransferase (PSAT; EC 2.6.1.52), a member of subgroup IV of the aminotransferases, catalyses the conversion of 3-phosphohydroxypyruvate to l-phosphoserine. The crystal structure of PSAT from Escherichia coli has been solved in space group P212121 using MIRAS phases in combination
A tandem Michael addition ring-closure route to the metabotropic receptor ligand alpha-(hydroxymethyl)glutamic acid and its gamma-alkylated derivatives.
J Zhang et al.
The Journal of organic chemistry, 66(22), 7555-7559 (2001-10-30)
T W Stone
British journal of pharmacology, 81(1), 175-181 (1984-01-01)
Various synthetic analogues of quinolinic acid have been tested for agonist and antagonist properties when applied by microiontophoresis to neurones in the rat cerebral cortex. Quinolinic acid 2-methylester was a weak antagonist of N-methyl-D-aspartate (NMDA) and quinolinic acid, but also
M Kalman et al.
Molecular & general genetics : MGG, 225(3), 379-386 (1991-03-01)
The gltS gene is known to encode a sodium-dependent, glutamate-specific permease. We have localized the Escherichia coli K12 gltS gene with respect to the spoT gene, sequenced it, and recombined a null insertion-deletion allele into the chromosome without loss of

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