Molecular structure of Glyoxal, 40 % Solution, CAS Number: 107-22-2
Glyoxal, 40 % Solution (CAS 107-22-2)
See product citations (1)
Alternate Names:
Ethanedial; oxalaldehyde
Application:
Glyoxal, 40 % Solution is used to denature nucleic acids by forming stable complexes with guanine residues
CAS Number:
107-22-2
Molecular Weight:
58.04
Molecular Formula:
C2H2O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
QUICK LINKS
Ordering Information
Product Citations
Description
Technical Information
Safety Information
SDS & Certificate of Analysis
Glyoxal, 40 % Solution is used to denature nucleic acids by forming stable complexes with guanine residues. Glyoxal attacks the amino groups of proteins, nucleotides, and lipids with its highly reactive carbonyl groups. A sequence of non-enzymatic reactions, called glycation, yields stable advanced glycation end-products (AGEs). Glyoxal is a linear aliphatic dialdehyde that participates in the synthesis of glyoxylic acid. It is widely employed in the textile and paper industries. It also has a role as a pesticide, an agrochemical, and an allergen.
Glyoxal, 40 % Solution (CAS 107-22-2) References
- Temperature dependent near-UV molar absorptivities of glyoxal and gluteraldehyde in aqueous solution. | Malik, M. and Joens, JA. 2000. Spectrochim Acta A Mol Biomol Spectrosc. 56: 2653-8. PMID: 11145331
- Thermodynamics and kinetics of glyoxal dimer formation: a computational study. | Kua, J., et al. 2008. J Phys Chem A. 112: 66-72. PMID: 18067276
- [Determination of glyoxal and glyoxalic acid in aldehyde solution by high performance liquid chromatography]. | Zhu, Y., et al. 2010. Se Pu. 28: 59-63. PMID: 20458922
- Thermodynamics and kinetics of imidazole formation from glyoxal, methylamine, and formaldehyde: a computational study. | Kua, J., et al. 2011. J Phys Chem A. 115: 1667-75. PMID: 21322623
- Glyoxal in aqueous ammonium sulfate solutions: products, kinetics and hydration effects. | Yu, G., et al. 2011. Environ Sci Technol. 45: 6336-42. PMID: 21721547
- Raman spectroscopy of glyoxal oligomers in aqueous solutions. | Avzianova, E. and Brooks, SD. 2013. Spectrochim Acta A Mol Biomol Spectrosc. 101: 40-8. PMID: 23099158
- Novel Magnetic Silica-Ionic Liquid Nanocomposites for Wastewater Treatment. | Atta, AM., et al. 2019. Nanomaterials (Basel). 10: PMID: 31905704
- Preparation of chromium (III) ion-imprinted polymer based on azo dye functionalized chitosan. | Elsayed, NH., et al. 2022. Carbohydr Polym. 284: 119139. PMID: 35287888
- The reaction of acetaldehyde, glyoxal, and ammonia to yield 2-methylimidazole: thermodynamic and kinetic analyses of the mechanism. | Tuguldurova, VP., et al. 2022. Phys Chem Chem Phys. 24: 9394-9402. PMID: 35384955
- Brown Carbon from Photo-Oxidation of Glyoxal and SO2 in Aqueous Aerosol. | De Haan, DO., et al. 2023. ACS Earth Space Chem. 7: 1131-1140. PMID: 37223425
Inhibitor of:
βB2-crystallin, and KRTAP9-4.Activator of:
AKR1B10, H2-Db, RAGE, and TAP2.Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Glyoxal, 40 % Solution, 25 ml | sc-285868 | 25 ml | $87.00 | |||
Glyoxal, 40 % Solution, 50 ml | sc-285868A | 50 ml | $117.00 |