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Bixlozone

Herbicide Active Ingredient

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Bixlozone is a herbicidal active ingredient, announced by FMC in 2018, for commercial release in April 2021 in Australia. It is used to control broadleaf and grassy weeds

Bixlozone is a isoxazolidinone class herbicide, and is mildly lipophilic. It is the second herbicide with its mode of action, the other being clomazone (differing only by a single atom); they work by preventing carotenoid biosynthesis by inhibiting DXP synthase.

01Mechanism of action

Like clomazone, bixlozone blocks carotenoid synthesis in plants. The lack of protective carotenoid causes bleaching of leaves. Bixlozone is uptaken by the roots and shoots in germinating weed seedlings. It is mobile in xylem, but does not seem to move downward or between leaves.

Specifically, it blocks the terpenoid synthesis pathway, between isopentenyl pyrophosphate and geranylgeranyl pyrophosphate, which prevents the synthesis of plant pigments, chlorophyll, and carotenoids.

Bixlozone's HRAC Group is Group 13, Group F3 / F4, Group Q. (Numeric, Global, Australian)

Symptoms

Symptoms vary, but on grasses, typically bleaching in lines or streaks on the leaf, or whitening of the whole leaf. Chlorosis may occur at lower application rates between the veins and leaf margins. Some plants turn white. In particular, lolium (ryegrass) tends to turn pink.

Crop injury can happen under heavy rainfall after application, since bixlozone might wash into the seedbed.

02Safety

Bixlozone has low dermal, oral and inhalational actue toxicity, according to the APVMA. Nor is it an eye irritant or skin sensitiser, though it may be a mild skin irritant. If absorbed, it is excreted mainly in urine and the remainder in faeces. In the body, bixlozone and related metabolites have a half-life of 10-16 hours. Applied dermally, under 16% was absorbed from 0.25 g/L solution, and less at higher concentrations. It has a 21-day NOAEL of 1000 mg/kg/day, the highest dose tested on rats. On a chronic test, it has a NOAEL of 53 mg/kg/day, and showed no evidence of oncogenicity.

03Synthesis

3-Chloro-2,2-dimethylpropionyl chloride is transformed with hydroxylamine hydrochloride to a hydroxamic acid, which is then cyclised under strongly basic conditions to an isoxazolidinone. The isoxazolidinone can then be alkylated with 2,4-dichlorobenzyl chloride to produce bixlozone.

04Tradenames

Overwatch is a 400 g/L bixlozone suspension concentrate. Its viscosity is 103 mPa.s at 20°C, comparable to olive oil. Isoflex Active is technical grade bixlozone.

05Weeds controlled

Bixlozone can control annual grasses including ryegrass, barnyardgrass, crabgrass, foxtail, canarygrass, goosegrass, bluegrass, and (suppression only) blackgrass. It controls the broadleaf weeds common chickweed, speedwells, shepherd's purse and wild chamomile.

Herbicide resistance to this mode of action is rare, with only three global populations so reported by 2022.

Watch videos about BixlozoneExplainers and documentaries on YouTube (opens in a new tab)

Sources and credits

This article is adapted from the Wikipedia article Bixlozone, written by its contributors and licensed under CC BY-SA 4.0. Fathomly has changed the layout, removed citation markers, navigation and maintenance notices, and adjusted punctuation. This adapted version is shared under the same license. For references, see the original article.

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