50660
Glyoxal solution
~40% in H2O (~8.8 M)
Synonym(s):
Ethanedial, Oxalaldehyde
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About This Item
Linear Formula:
OHCCHO
CAS Number:
Molecular Weight:
58.04
PubChem Substance ID:
UNSPSC Code:
12352200
Beilstein/REAXYS Number:
1732463
MDL number:
concentration
~40% in H2O (~8.8 M)
refractive index
n20/D 1.409
SMILES string
[H]C(=O)C([H])=O
InChI
1S/C2H2O2/c3-1-2-4/h1-2H
InChI key
LEQAOMBKQFMDFZ-UHFFFAOYSA-N
Other Notes
This form of glyoxal is composed of 3 moles of glyoxal and 2 moles of water in a relatively stable configuration.
Disclaimer
May precipitate on storage; redissolve at 50-60 °C.
may precipitate on storage; redissolve at 50-60°C
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Catherine Lambert et al.
Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 18(1), 59-69 (2012-10-30)
The molecular basis of Alzheimer's disease has not been clearly established, but disruption of brain metal ion homeostasis, particularly copper and zinc, might be closely involved in the pathogenesis of this disease and its characteristic β-amyloid neuropathological features. The use
Yu Wang et al.
Chemical Society reviews, 41(11), 4140-4149 (2012-04-18)
Methylglyoxal (MGO) and glyoxal (GO), known as reactive carbonyl species, can be generated endogenously and exogenously (human body and food system). They are attracting increased attention because of their relationship with diabetes and flavour generation. In this review, their characteristics
Niklas Bosaeus et al.
Nucleic acids research, 42(12), 8083-8091 (2014-05-20)
Overstretching of DNA occurs at about 60-70 pN when a torsionally unconstrained double-stranded DNA molecule is stretched by its ends. During the transition, the contour length increases by up to 70% without complete strand dissociation. Three mechanisms are thought to