G1134
Glyoxylic acid solution
50 % (w/w) in H2O
Synonym(s):
Formylformic acid, Oxoethanoic acid
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About This Item
Linear Formula:
OHCCOOH
CAS Number:
Molecular Weight:
74.04
PubChem Substance ID:
UNSPSC Code:
12352100
Beilstein/REAXYS Number:
741891
MDL number:
concentration
50 % (w/w) in H2O
storage temp.
2-8°C
SMILES string
OC(=O)C=O
InChI
1S/C2H2O3/c3-1-2(4)5/h1H,(H,4,5)
InChI key
HHLFWLYXYJOTON-UHFFFAOYSA-N
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Met. Corr. 1 - Skin Sens. 1
Storage Class
8B - Non-combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
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Kelly C Fahnoe et al.
PloS one, 7(12), e51732-e51732 (2012-12-15)
Antibacterial compounds that affect bacterial viability have traditionally been identified, confirmed, and characterized in standard laboratory media. The historical success of identifying new antibiotics via this route has justifiably established a traditional means of screening for new antimicrobials. The emergence
Joseph P Dexter et al.
The Journal of biological chemistry, 288(8), 5770-5778 (2012-11-30)
An important goal of systems biology is to develop quantitative models that explain how specific molecular features give rise to systems-level properties. Metabolic and regulatory pathways that contain multifunctional proteins are especially interesting to study from this perspective because they
Kathrin Schneider et al.
Journal of bacteriology, 194(12), 3144-3155 (2012-04-12)
Oxalate catabolism is conducted by phylogenetically diverse organisms, including Methylobacterium extorquens AM1. Here, we investigate the central metabolism of this alphaproteobacterium during growth on oxalate by using proteomics, mutant characterization, and (13)C-labeling experiments. Our results confirm that energy conservation proceeds