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Glyoxylic acid monohydrate, 97%, Thermo Scientific Chemicals
Catalog number: A16058.14
25 g, Each
Thermo Scientific Chemicals
Glyoxylic acid monohydrate, 97%, Thermo Scientific Chemicals
Catalog number: A16058.14
25 g, Each
Quantity
Catalog number: A16058.14
also known as A16058-14
Price (USD)
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42.65 45.65 Online priceSave 3.00 (6%)
Ends: 15-Oct-2024
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Chemical Identifiers
CAS
563-96-2
IUPAC Name
2,2-dihydroxyacetate
Molecular Formula
C2H3O4
InChI Key
GOCCREQJUBABAL-UHFFFAOYSA-M
SMILES
OC(O)C([O-])=O
Specifications
Specification SheetForm
Crystals or powder or crystalline powder or lumps or fused solid
Assay (Aqueous acid-base Titration)
≥96.0 to ≤104.0%
Appearance (Color)
White to pale cream to pale yellow
Water Content (Karl Fischer Titration)
10.85-26.74% (0.5-1.5 waters)
Identification (FTIR)
Conforms
Description
Glyoxylic acid is a reagent for sulfinylmaleate synthesis. It is one of the chemicals used in the Hopkins Cole reaction. It is involved to check the presence of tryptophan in proteins. It is condensed with urea and 1,2-diaminobenzene to form heterocycles. It also undergoes Friedel-Crafts and cyclocondensation reactions to form bis(pentamethylphenyl) acetic acid and a beta-carboline respectively. It is employed in the synthesis of a sulfinylmaleate, which serves as an efficient dienophile for enantioselective Diels-Alder cycloadditions.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Glyoxylic acid is a reagent for sulfinylmaleate synthesis. It is one of the chemicals used in the Hopkins Cole reaction. It is involved to check the presence of tryptophan in proteins. It is condensed with urea and 1,2-diaminobenzene to form heterocycles. It also undergoes Friedel-Crafts and cyclocondensation reactions to form bis(pentamethylphenyl) acetic acid and a beta-carboline respectively. It is employed in the synthesis of a sulfinylmaleate, which serves as an efficient dienophile for enantioselective Diels-Alder cycloadditions.
Solubility
Soluble in water, dimethyl sulfoxide and alcohol. Insoluble in diethyl ether and hydrocarbons.
Notes
Hygroscopic. Keep the container tightly closed in a dry and well-ventilated place. Incompatible withbases, oxidizing agents and reducing agents.
Glyoxylic acid is a reagent for sulfinylmaleate synthesis. It is one of the chemicals used in the Hopkins Cole reaction. It is involved to check the presence of tryptophan in proteins. It is condensed with urea and 1,2-diaminobenzene to form heterocycles. It also undergoes Friedel-Crafts and cyclocondensation reactions to form bis(pentamethylphenyl) acetic acid and a beta-carboline respectively. It is employed in the synthesis of a sulfinylmaleate, which serves as an efficient dienophile for enantioselective Diels-Alder cycloadditions.
Solubility
Soluble in water, dimethyl sulfoxide and alcohol. Insoluble in diethyl ether and hydrocarbons.
Notes
Hygroscopic. Keep the container tightly closed in a dry and well-ventilated place. Incompatible withbases, oxidizing agents and reducing agents.
RUO – Research Use Only
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