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About This Item
Linear Formula:
HC(O)COONa · H2O
CAS Number:
Molecular Weight:
114.03
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4003755
Assay:
≥93%
InChI
1S/C2H2O3.Na.H2O/c3-1-2(4)5;;/h1H,(H,4,5);;1H2/q;+1;/p-1
SMILES string
O.[Na+].[O-]C(=O)C=O
InChI key
VPWPWKBHCGJTTQ-UHFFFAOYSA-M
assay
≥93%
storage temp.
−20°C
Quality Level
General description
Sodium glyoxylate monohydrate, also known as Glyoxylic acid sodium salt monohydrate, is often utilized in the reductive amination of glyoxylate/pyruvate intermediates and ketoacids with hydroxylamine.
Application
- Proteomic characterisation of polyethylene terephthalate and monomer degradation by Ideonella sakaiensis.: This paper details the degradation of polyethylene terephthalate and its monomers, highlighting the role of sodium glyoxylate monohydrate as a byproduct in biodegradable polymer production and its implications for environmental sustainability (Poulsen & Nielsen, 2023, Poulsen & Nielsen, 2023).
Sodium glyoxylate monohydrate is used as an intermediate in the transamination reaction in the formation of unstable keto esters during the synthesis of indolo [3,2-a] carbazoles.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Synthesis and breakdown of universal metabolic precursors promoted by iron
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In Anopheles gambiae, the most efficient vector of the malaria parasite Plasmodium falciparum, 3-hydroxykynurenine is endowed with a toxic potential. In adult mosquitoes, the excess of 3-hydroxykynurenine is removed by a specific transaminase (3-hydroxykynurenine transaminase, 3-HKT) which converts the compound
Chemistry and properties of indolocarbazoles
Tomasz J, et al.
Chemical Reviews, 118, 9058-9128 (2018)
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