Difenoxuron

Difenoxuron (commercially known as Lironion) is a phenylurea herbicide used to control annual broad-leaved weeds and grasses in allium crops (predominantly onions),[3][4] carrots, jojoba, and celery.

Phenylureas inhibit photosynthesis at photosystem II by binding to the serine 264 residue of the D1 protein, occupying the Qb (secondary plastoquinone) binding site and hence halting electron transfer from the primary acceptor Qa to the secondary acceptor Qb.

[11] Moreover, this blockade prevents chlorophyll from transferring energy to Qa, increasing production of triplet-state chlorophyll, which reacts with molecular oxygen to form singlet oxygen, a highly reactive species that oxidatively damages the pigments, lipids and proteins of the photosynthetic thylakoid membrane.

[11] Liming in Boddington soil has been shown by a 1976 study to increase the herbicidal toxicity of difenoxuron by two to three times compared to soil without the additional level of liming.

There are very few studies about the genotoxicity of difenoxuron and these studies are inconcordant but there appears to be a dose dependent relationship between the concentration of difenoxuron and rate of observed chromosomal aberrations.

NFPA 704 four-colored diamond Health 0: Exposure under fire conditions would offer no hazard beyond that of ordinary combustible material. E.g. sodium chloride Flammability 0: Will not burn. E.g. water Instability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogen Special hazards (white): no code