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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375305Generated: November 1, 2026

Methylglyoxal → Quinoxaline

https://huagongshe.com/reaction/1375305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylglyoxalHCID 880—
ReactantO-PhenylenediamineHCID 7243—
ReactantGlyoxalHCID 7860—
ReactantPerchloric AcidHCID 24247—
Reactant3-DeoxyglucosoneHCID 114839—
SolventButanedioneHCID 650—
ProductQuinoxalineHCID 7045—
ProductO-PhenylenediamineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169407B1
Source datasetuspto-grants-2007_01
ORD IDord-eafb8e2f870947869aa998473a3afabb
Source noteuspto-grants-2007_01