HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylglyoxal → Quinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylglyoxal | HCID 880 | — |
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | Glyoxal | HCID 7860 | — |
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | 3-Deoxyglucosone | HCID 114839 | — |
| Solvent | Butanedione | HCID 650 | — |
| Product | Quinoxaline | HCID 7045 | — |
| Product | O-Phenylenediamine | HCID 7243 | — |
Reaction Steps
The quantities of residual glyoxal, methylglyoxal, and 3-deoxyglucosone in the sample solution were determined by high-performance liquid chromatography (HPLC) following the incubation. More specifically, 40 μl of 2M perchloric acid, 40 μl of 1% o-phenylenediamine, and 100 μl of 25 μM 2,3-butanedione were added to 100 μl of the sample after the incubation; the mixture was stirred and incubated at 25° C. for 1 hour. Quinoxaline derivatives produced in the reaction of the dicarbonyl compounds and o-phenylenediamine were quantified by HPLC using a reverse-phase column according to the method of Ohmori et al. (Ohmori S. et al., J. Chromatogr. 414: 149–155,1987). Glyoxal, methylglyoxal, and 3-deoxyglucosone were used as standard samples.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07169407B1 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-eafb8e2f870947869aa998473a3afabb |
| Source note | uspto-grants-2007_01 |