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Glyoxylic acid monohydrate

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Glyoxylic acid monohydrate Basic information

Product Name:
Glyoxylic acid monohydrate
Synonyms:
  • Formylformic acid, Oxoethanoic acid
  • Glyoxylic acid monohydrate, 98%, pure
  • Glyoxylic acid monoh
  • Oxoacetic Acid Monohydrate,50%
  • Glyoxylic acid Monohydrate, pure, 98% 25GR
  • Glyoxylic acid Monohydrate, pure, 98% 500GR
  • 2-Oxoacetic Acid Monohydrate
  • NSC 27785 Monohydrate
CAS:
563-96-2
MF:
C2H4O4
MW:
92.05
EINECS:
679-230-4
Product Categories:
  • Fine chemical
  • Aliphatics
  • 563-96-2
Mol File:
563-96-2.mol
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Glyoxylic acid monohydrate Chemical Properties

Melting point:
49-52 °C(lit.)
Boiling point:
100 °C(lit.)
Density 
1.33 g/mL at 20 °C
refractive index 
n20/D 1.414
Flash point:
>230 °F
storage temp. 
Store below +30°C.
solubility 
H2O: 0.1 g/mL, clear
form 
Liquid
pka
3.43±0.11(Predicted)
color 
White to light yellow
Water Solubility 
Freely soluble
Sensitive 
Hygroscopic
Merck 
14,4511
BRN 
969535
InChIKey
MOOYVEVEDVVKGD-UHFFFAOYSA-N
CAS DataBase Reference
563-96-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
C,Xi
Risk Statements 
34-43-41
Safety Statements 
26-36/37/39-45-37/39-24-27
RIDADR 
UN 3265 8/PG 2
WGK Germany 
1
RTECS 
MD4550000
3
TSCA 
Yes
HazardClass 
8
PackingGroup 
III
HS Code 
29183000

MSDS

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Glyoxylic acid monohydrate Usage And Synthesis

Description

Glyoxylic acid monohydrate is a versatile chemical used in various pharmaceuticals, agrochemicals, and cosmetics industries. It is commonly used as an intermediate in producing chemicals like vanillin, amino acids, and herbicides. It should be stored in a cool, dry place away from oxidizing agents and sources of ignition. Glyoxylic acid monohydrate may cause severe skin burns and eye damage, so it is essential to follow proper safety guidelines when handling it. The environmental impact of this product is minimal if it is disposed of according to local regulations.

Chemical Properties

white to light yellow crystalline powder or chunks

Uses

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.

Uses

Occurs in unripe fruit and in young green leaves; has also been found in very young sugar beets.

Glyoxylic acid monohydrate Preparation Products And Raw materials

Preparation Products

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