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| | 3-(2,4-ジクロロフェノキシ)-6-ニトロ安息香酸メチル 製品概要 |
| | 3-(2,4-ジクロロフェノキシ)-6-ニトロ安息香酸メチル 物理性質 |
| | 3-(2,4-ジクロロフェノキシ)-6-ニトロ安息香酸メチル Usage And Synthesis |
| 外観 | ごくうすい黄色～黄色, 結晶～結晶性粉末 | | 溶解性 | アセトンに溶け、水に極めて溶けにくい。 | | 農薬用途 | 除草剤 | | 使用 | Selective preemergence or postemergence herbicide used to effectively control a wide variety of broad-leaved weeds (such as bindweed, jimsonweed, kochia, mustards, pigweeds, sesbania, smartweed and velvet-leaf) in tolerant crops (corn, grain sorghum, maize, rice and soybeans). | | 使用 | Herbicide. | | 定義 | ChEBI: MC-4379 is a nitrobenzoic acid. | | 农业用途 | Herbicide: Used to control a variety of broadleaf weeds and
grasses in legumes such as soybeans and peanuts, and
post-emergent weed control in wheat, barley and sugar
beets. Not currently registered in the U.S. However, it is
used in 21 European countries and there are 27 global
suppliers. | | 製品名 | ALIBI®; FOX®; MODOWN®[C]; MC-
4379®; SABINE® | | 環境運命予測 | Soil. Bifenox degrades in soil forming 5-(2,4-dichlorophenoxy)-2-nitrobenzoic acid
and methyl 5-(2,4-dichlorophenoxy)anthranilate (Hartley and Kidd, 1987; Smith 1988).
The average half-life in soils is 7–14 days (Hartley and Kidd, 1987; Humburg et al., 1989)
Plant. Rapidly undergoes ring hydroxylation and subsequent conjugation in rice plants
(Ashton and Monaco, 1991).
Photolytic. The UV photolysis (λ = 300 nm) of bifenox in various solvents was studied
by Ruzo et al. (1980). In water, 2,4-dichloro-3′-(carboxymethyl)-4′-hydroxydiphenyl ether
and 2,4-dichloro-3′-(carboxymethyl)-4′-aminodiphenyl ether were identi |
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