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G4502

Sigma-Aldrich

Sodium glyoxylate monohydrate

≥93%

Synonym(s):

Glyoxylic acid sodium salt monohydrate, Oxoethanoic acid sodium salt

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About This Item

Linear Formula:
HC(O)COONa · H2O
CAS Number:
Molecular Weight:
114.03
Beilstein:
4003755
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

≥93%

storage temp.

−20°C

SMILES string

O.[Na+].[O-]C(=O)C=O

InChI

1S/C2H2O3.Na.H2O/c3-1-2(4)5;;/h1H,(H,4,5);;1H2/q;+1;/p-1

InChI key

VPWPWKBHCGJTTQ-UHFFFAOYSA-M

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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 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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Synthesis and breakdown of universal metabolic precursors promoted by iron
Kamila M B, et al.
Nature, 569, 104-107 (2019)
Rossana Canavesi et al.
Journal of pharmaceutical and biomedical analysis, 173, 154-161 (2019-05-28)
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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