JP5599793B2 - ジメトキシトリアジニル置換ジフルオロメタンスルホニルアニリド類を含む除草剤の組み合わせ - Google Patents
ジメトキシトリアジニル置換ジフルオロメタンスルホニルアニリド類を含む除草剤の組み合わせ Download PDFInfo
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- JP5599793B2 JP5599793B2 JP2011522419A JP2011522419A JP5599793B2 JP 5599793 B2 JP5599793 B2 JP 5599793B2 JP 2011522419 A JP2011522419 A JP 2011522419A JP 2011522419 A JP2011522419 A JP 2011522419A JP 5599793 B2 JP5599793 B2 JP 5599793B2
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- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
- 235000015424 sodium Nutrition 0.000 description 1
- MPYRGYZJJYMFTP-UHFFFAOYSA-M sodium 1,2,4-triazole-1-carbonylazanide Chemical compound [Na+].[NH-]C(=O)n1cncn1 MPYRGYZJJYMFTP-UHFFFAOYSA-M 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
- DHJHUXNTNSRSEX-UHFFFAOYSA-M sodium;2-(4-chloro-2-methylphenoxy)propanoate Chemical compound [Na+].[O-]C(=O)C(C)OC1=CC=C(Cl)C=C1C DHJHUXNTNSRSEX-UHFFFAOYSA-M 0.000 description 1
- AXKBOWBNOCUNJL-UHFFFAOYSA-M sodium;2-nitrophenolate Chemical compound [Na+].[O-]C1=CC=CC=C1[N+]([O-])=O AXKBOWBNOCUNJL-UHFFFAOYSA-M 0.000 description 1
- GABUSZPTCJGKGB-UHFFFAOYSA-M sodium;4-(4-chloro-2-methylphenoxy)butanoate Chemical compound [Na+].CC1=CC(Cl)=CC=C1OCCCC([O-])=O GABUSZPTCJGKGB-UHFFFAOYSA-M 0.000 description 1
- YPMAQKXGDCKXPE-WCCKRBBISA-M sodium;[(3s)-3-amino-3-carboxypropyl]-methylphosphinate Chemical compound [Na+].CP([O-])(=O)CC[C@H](N)C(O)=O YPMAQKXGDCKXPE-WCCKRBBISA-M 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- PQTBTIFWAXVEPB-UHFFFAOYSA-N sulcotrione Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O PQTBTIFWAXVEPB-UHFFFAOYSA-N 0.000 description 1
- OORLZFUTLGXMEF-UHFFFAOYSA-N sulfentrazone Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(NS(C)(=O)=O)=C(Cl)C=C1Cl OORLZFUTLGXMEF-UHFFFAOYSA-N 0.000 description 1
- ZDXMLEQEMNLCQG-UHFFFAOYSA-N sulfometuron methyl Chemical group COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(C)=CC(C)=N1 ZDXMLEQEMNLCQG-UHFFFAOYSA-N 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 125000001273 sulfonato group Chemical class [O-]S(*)(=O)=O 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 125000005537 sulfoxonium group Chemical group 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- RJKCKKDSSSRYCB-UHFFFAOYSA-N tebutam Chemical compound CC(C)(C)C(=O)N(C(C)C)CC1=CC=CC=C1 RJKCKKDSSSRYCB-UHFFFAOYSA-N 0.000 description 1
- IUQAXCIUEPFPSF-UHFFFAOYSA-N tembotrione Chemical compound ClC1=C(COCC(F)(F)F)C(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O IUQAXCIUEPFPSF-UHFFFAOYSA-N 0.000 description 1
- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000010496 thistle oil Substances 0.000 description 1
- 244000082735 tidal marsh flat sedge Species 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- IYMLUHWAJFXAQP-UHFFFAOYSA-N topramezone Chemical compound CC1=C(C(=O)C2=C(N(C)N=C2)O)C=CC(S(C)(=O)=O)=C1C1=NOCC1 IYMLUHWAJFXAQP-UHFFFAOYSA-N 0.000 description 1
- 230000014616 translation Effects 0.000 description 1
- 238000002054 transplantation Methods 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 description 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- IMEVJVISCHQJRM-UHFFFAOYSA-N triflusulfuron-methyl Chemical group COC(=O)C1=CC=CC(C)=C1S(=O)(=O)NC(=O)NC1=NC(OCC(F)(F)F)=NC(N(C)C)=N1 IMEVJVISCHQJRM-UHFFFAOYSA-N 0.000 description 1
- DFFWZNDCNBOKDI-UHFFFAOYSA-N trinexapac Chemical compound O=C1CC(C(=O)O)CC(=O)C1=C(O)C1CC1 DFFWZNDCNBOKDI-UHFFFAOYSA-N 0.000 description 1
- RVKCCVTVZORVGD-UHFFFAOYSA-N trinexapac-ethyl Chemical group O=C1CC(C(=O)OCC)CC(=O)C1=C(O)C1CC1 RVKCCVTVZORVGD-UHFFFAOYSA-N 0.000 description 1
- YNWVFADWVLCOPU-MAUPQMMJSA-N uniconazole P Chemical compound C1=NC=NN1/C([C@@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1 YNWVFADWVLCOPU-MAUPQMMJSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/26—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the group; Thio analogues thereof
Description
ここで、
(A)は、一般式(I):
R1はハロゲン、好ましくはフッ素又は塩素であり、
R2は水素であり、そしてR3はヒドロキシルであり、又は
R2及びR3は、それらが結合する炭素原子と一緒になってカルボニル基C=Oであり、そして
R4は、水素又はメチルである)
により表わされたグループからの1つ若しくはそれ以上の化合物又はその塩を意味し、そして
下記の除草剤から成るアルキルアミドのサブグループ(サブグループ1):
(B1−1)べフルブタミド(PM#55)、例えば、2−[4−フルオロ−3−(トリフルオロメチル)フェノキシ]−N−(フェニルメチル)ブタンアミド(施用量:5〜1000gAS/ha、好ましくは10〜500gAS/ha;質量比A:B=1:1000〜100:1、好ましくは1:100〜 20:1);
(B1−2)ブロモブチド(PM#95)、例えば、2−ブロモ−3,3−ジメチルN−(1−メチル−1−フェニルエチル)ブタンアミド(施用量:2〜3000gAS/ha、好ましくは4〜1500gAS/ha;質量比A:B=1:3000〜250:1、好ましくは1:300〜50:1);
(B1−3)ジメテナミド(PM#268)、例えば、(RS)−2−クロロ−N−(2,4−ジメチル−3−チエニル)−N−(2−メトキシ−1−メチルエチル)アセトアミド(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜50:1、好ましくは1:800〜7:1);
(B1−4)ジメテナミド(PM#268)、例えば、(S)−2−クロロ−N−(2,4−ジメチル3−チエニル)−N−(2−メトキシ−1−メチルエチル)アセトアミド(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜50:1、好ましくは 1:800〜7:1);
(B1−5)ジフェナミド(PM#284)、例えば、N,N−ジメチル−α−フェニルベンゼンアセトアミド(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜50:1、好ましくは1:800〜7:1);
(B1−6)ナプロパミド(PM#589)、例えば、N,N−ジエチル−2−(1−ナフタレニルオキシ)プロパンアミド、そのラセミ体又は異性体、例えば、(R)−(−)−又は(S)−(+)−異性体も含む(施用量:20〜3000gAS/ha、好ましくは30〜2500gAS/ha;質量比A:B=1:3000〜25:1、好ましくは1:500〜7:1);
(B1−7)ペトキサミド(PM#647)、例えば、2−クロロ−N−(2−エトキシエチル)−N−(2−メチル−1−フェニル−1−プロペニル)アセトアミド(施用量:10〜5000gAS/ha、好ましくは30〜4000 gAS/ha;質量比A:B=1:5000〜50:1、好ましくは1:800〜7:1);
(B1−8)MT−5950(コード番号)、例えば、N−[3−クロロ−4−(1−メチルエチル)−フェニル]−2−メチルペンタンアミド(施用量: 10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜50:1、好ましくは1:800〜7:1);
(B2−1)ナプタルム(PM#590)、例えば、2−[(1−ナフタレニルアミノ)カルボニル]安息香酸、その塩及びエステル、−塩形態(誘導体)、好ましくはNa塩も含む(施用量:20〜7000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:7000〜25:1、好ましくは1:800〜7:1);
(B2−2)プロピザミド(PM#701)、例えば、3,5−ジクロロ−N−(1,1−ジメチル−2−プロピニル)ベンズアミド(施用量:10〜4000gAS/ha、好ましくは30〜3000gAS/ha;質量比A:B= 1:4000〜50:1、好ましくは 1:600〜7:1);
(B3−1)ジフルフェニカン(PM#258)、例えば、N−(2,4−ジフルオロフェニル)−2−[3−(トリフルオロメチル)フェノキシ]−3−ピリジンカルボキサミド(施用量:1〜800gAS/ha、好ましくは1.5〜500gAS/ha;質量比A:B=1:800〜500:1、好ましくは 1:100〜170:1);
(B3−2)エトベンザニド(PM #330)、例えば、N−(2,3−ジクロロフェニル)−4−(エトキシメトキシ)ベンズアミド(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜50:1、好ましくは1:800〜7:1);
(B3−3)フルフェナセット(PM#381)、同義語、チアフルアミド、例えば、N−(4−フルオロフェニル)−N−(1−メチルエチル)−2−[[5−(トリフルオロメチル)−1,3,4−チアジアゾール−2−イル]オキシ]アセトアミド、(施用量:10〜3000gAS/ha、好ましくは 20〜2000gAS/ha;質量比A:B=1:3000〜50:1、好ましく、1:400〜10:1);
(B3−4)メフェナセット(PM#523)、例えば、2−(2−ベンゾチアゾリルオキシ)−N−メチル−N−フェニルアセトアミド(施用量:2.5〜2500gAS/ha、好ましくは5〜2000gAS/ha;質量比A:B=1:2500〜200:1、好ましくは1:400〜40:1);
(B3−5)メフルイジド(PM#525)、例えば、N−[2,4−ジメチル−5−[[(トリフルオロメチル)スルホニル]アミノ]フェニル]アセトアミド、その誘導体、例えば、メフルイジド−ジオールアミン(メフルイジド−ジエタノールアンモニウム)も含む(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B= 1:5000〜50:1、好ましくは1:800〜7:1);
(B3−6)ペンタノクロル(PM#643)、例えば、N−(3−クロロ−4−メチルフェニル)−2−メチルペンタンアミド(施用量:10〜5000 gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜50:1、好ましくは1:800〜7:1);
(B3−7)ピコリナフェン(PM#666)、例えば、N−(4−フルオロフェニル)−6−[3−(トリフルオロメチル)フェノキシ]−2−ピリジンカルボキサミド(施用量:1〜900gAS/ha、好ましくは2〜800gAS/ha;質量比A:B=1:900〜500:1、好ましくは1:160〜100:1);
(B3−8)プロパニル(PM#690)、例えば、N−(3,4−ジクロロフェニル)プロパンアミド(施用量:50〜5000gAS/ha、好ましくは 100〜4000gAS/ha;質量比A:B=1:5000〜10:1、好ましくは1:800〜2:1);
(B3−9)N−フェニルフタラミン酸(PM#654)、例えば、2−([フェニルアミノ]カルボニル)安息香酸、その誘導体も含む(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜50:1、好ましくは1:800〜7: 1);
(B4−1)アセトクロール(PM#5)、例えば、2−クロロ−N−(エトキシメチル)−N−(2−エチル−6−メチルフェニル)アセトアミド(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜50:1、好ましくは1:800〜7:1);
(B4−2)アラクロール(PM#14)、例えば、2−クロロ−N−(2,6−ジエチルフェニル)−N−(メトキシメチル)アセトアミド(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜50:1、好ましくは1:800〜7:1);
(B4−3)ブタクロール(PM#102)、例えば、N−(ブトキシメチル)−2−クロロ−N−(2,6−ジエチルフェニル)アセトアミド(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜50:1、好ましくは1:800〜7:1);
(B4−4)ジメタクロル(PM#266)、例えば、2−クロロ−N−(2,6−ジメチルフェニル)−N−(2−メトキシエチル)アセトアミド(施用量:30〜4000gAS/ha、好ましくは50〜3000gAS/ha;質量比A:B=1:4000〜170:1、好ましくは1:600〜4: 1);
(B4−5)メタザクロル(PM#543)、例えば、2−クロロ−N−(2,6−ジメチルフェニル)−N−(1H−ピラゾール−1−イルメチル)アセトアミド(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜500:1、好ましくは1:800〜7:1);
(B4−6)メトラクロル(PM#567)、例えば、2−クロロ−N−(2−エチル−6−メチルフェニル)−N−(2−メトキシ−1−メチルエチル)アセトアミド(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜500:1、好ましくは1:800〜7:1);
(B4−7)S−メトラクロル(PM#568)、例えば、(S)−2−クロロ−N−(2−エチル−6−メチルフェニル)−N−(2−メトキシ−1−メチルエチル)アセトアミド、及び(R)−2−クロロ−N−(2−エチル−6−メチルフェニル)−N−(2−メトキシ−1−メチルエチル)アセトアミドの80〜100%から20〜0%の割合の混合物(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜500:1、好ましくは1:800〜7:1);
(B4−8)プレチラクロル(PM#677)、例えば、2−クロロ−N−(2,6−ジエチルフェニル)−N−(2−プロポキシエチル)アセトアミド (施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜500:1、好ましくは1:800〜7:1);
(B4−9)プロパクロル(PM#688)、例えば、2−クロロ−N−(1−メチルエチル)−N−フェニルアセトアミド(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜500:1、好ましくは1:800〜7:1);
(B4−10)2−クロロ−6’−エチル−N−イソプロポキシメチルアセト−o−トルイジン(PM#142)、同義語、プロピソクロル、例えば、2−クロロ−N−(2−エチル−6−メチルフェニル)−N−[(1−メチルエトキシ)メチル]アセトアミド(施用量:10〜5000gAS/ha、好ましくは 30〜4000gAS/ha;質量比A:B=1:5000〜500:1、好ましくは1:800〜7:1);
(B4−11)テニルクロール(PM#809)、例えば、2−クロロ−N−(2,6−ジメチルフェニル)−N−[(3−メトキシ−2−チエニル)メチル]アセトアミド(施用量:15〜500gAS/ha、好ましくは20〜400gAS/ha;質量比A:B=1:500〜40:1、好ましくは1:80〜10:1);
(B5−1)アシュラム(PM#37)、例えば、[(4−アミノフェニル)スルホニル]カルバミド酸メチル(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜500:1、好ましくは1:800〜7:1);
(B5−2)カルバリル(PM#117)、例えば、メチルカルバミド酸1−ナフタレニル;1−ナフタレンオールメチルカルバマート(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜500:1、好ましくは1:800〜7:1);
(B5−3)カルベタミド(PM#119)、例えば、(R)−N−エチル−2−[[(フェニルアミノ)カルボニル]オキシ]プロパンアミド(施用量:50〜5000gAS/ha、好ましくは80〜4000gAS/ha;質量比A:B=1:5000〜500:1、好ましくは1:800〜7:1);
(B5−4)クロルプロファム(PM#149)、例えば、(3−クロロフェニル)カルバミド酸1−メチルエチル(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜500:1、好ましくは1:800〜7:1);
(B5−5)デスメディファム(PM#288)、例えば、[3−[[(フェニルアミノ)カルボニル]オキシ]フェニル]カルバミド酸エチル(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜500:1、好ましくは1:800〜7:1);
(B5−6)フェンメディファム(PM#649)、例えば、(3−メチルフェニル)カルバミド酸3−[(メトキシカルボニル)アミノ]フェニル、例えば、エチルエステル(フェンメジファム−エチル)などのそのエステルも含む(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜500:1、好ましくは1:800〜7:1);
(B5−7)プロファム(PM#695)、例えば、フェニルカルバミド酸1−メチルエチル(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量、A:B=1:5000〜500:1、好ましくは1:800〜7:1);
(B6−1)ブチレート(PM#110)、例えば、ビス(2−メチルプロピル)カルバミチオ酸S−エチル(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜500:1、好ましくは1:800〜7:1);
(B6−2)シクロエート(PM#190)、例えば、シクロヘキシルエチルカルバモチオ酸S−エチル(施用量:10〜5000gAS/ha、好ましくは 30〜4000gAS/ha;質量比A:B=1:5000〜500:1、好ましくは1:800〜7:1);
(B6−3)ジメピペレート(PM#265)、例えば、1−ピペリジンカルボチオ酸S−(1−メチル−1−フェニルエチル)(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜500:1、好ましくは1:800〜7:1);
(B6−4)EPTC(PM#311)、例えば、ジピロピルカルバミチオ酸S−エチル(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜500:1、好ましくは1:800〜7:1);
(B6−5)エスプロカルブ(PM#315)、例えば、(1,2−ジメチルプロピル)エチルカルバモチオ酸S−(フェニルメチル)(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜50:1、好ましくは1:800〜7:1);
(B6−6)メタスルホカルブ(PM#547)、例えば、メチルカルバモチオ酸S−[4−[(メチルスルホニル)オキシ]フェニル](施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜50:1、好ましくは1:800〜7:1);
(B6−7)モリネート(PM #578)、例えば、ヘキサヒドロ−1H−アゼピン−1−カルボチオ酸S−エチル(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜50:1、好ましくは1:800〜7:1);
(B6−8)オルベンカルブ(PM#612)、例えば、ジエチルカルバモチオ酸S−[(2−クロロフェニル)メチル](施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜50:1、好ましくは1:800〜7:1);
(B6−9)ペブレート(PM#636)、例えば、ブチルエチルカルバモチオ酸S−プロピル(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜50:1、好ましくは 1:800〜7:1);
(B6−10)プロスルホカルブ(PM#703)、例えば、ジプロピルカルバモチオ酸S−(フェニルメチル)(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜50:1、好ましくは1:800〜7:1);
(B6−11)ピリブチカルブ(PM#718)、例えば、(6−メトキシ−2−ピリジニル)メチルカルバモチオ酸O−[3−(1,1−ジメチルエチル)フェニル](施用量:5〜2500gAS/ha、好ましくは8〜2000gAS/ha;質量比A:B=1:2500〜100:1、好ましくは1:400〜25:1);
(B6−12)チオベンカルブ(PM#817)、同義語、ベンチオカルブ、例えば、ジエチルカルバモチオ酸S−[(4−クロロフェニル)メチル](施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜50:1、好ましくは1:800〜7:1);
(B6−13)トリ−アレート(PM#838)、例えば、ビス(1−メチルエチル)カルバモチオ酸S−(2,3,3−トリクロロ−2−プロペニル)(施用量:10〜5000gAS/ha、好ましくは30〜4000gAS/ha;質量比A:B=1:5000〜50:1、好ましくは1:800〜7:1);
(B6−14)ベノレート(PM #1517)、例えば、ジプロピルカルバモチオ酸S−プロピル(施用量:10〜5000gAS/ha、好ましくは 30〜4000gAS/ha;質量比A:B=1:5000〜50:1、好ましくは1:800〜7:1);
(B7−1)アミドスルフロン(PM#22)、例えば、N−[[[[(4,6−ジメトキシ−2−ピリミジニル)アミノ]カルボニル]アミノ]スルホニル]−N−メチルメタンスルホンアミド、その塩及びエステル、−塩形態−(誘導体)も含む(施用量:0.1〜100gAS/ha、好ましくは1〜80gAS/ha;質量比A:B=1:100〜5000:1、好ましくは1:16〜200:1);
(B7−2)アジムスルフロン(PM#43)、例えば、N−[[(4,6−ジメトキシ−2−ピリミジニル)アミノ]カルボニル]−1−メチル−4−(2−メチル−2H−テトラゾール−5−イル)−1H−ピラゾール−5−スルホンアミド(施用量:1〜1000gAS/ha、好ましくは1.5〜800gAS/ha;質量比A:B=1:1000〜500:1、好ましくは1:160〜160:1);
(B7−3)ベンスルフロン−メチル(PM#65)、例えば、2−[[[[[(4,6−ジメトキシ−2−ピリミジニル)アミノ]カルボニル]アミノ]スルホニル]メチル]安息香酸メチル、その他の誘導体も含む(施用量:1〜1200gAS/ha、好ましくは5〜500gAS/ha;質量比A:B=1:1200〜500:1、好ましくは1:100〜40:1);
(B7−4)クロリムロン(PM#138)、例えば、2−[[[[(4−クロロ−6−メトキシ−2−ピリミジニル)アミノ]カルボニル]アミノ]スルホニル]安息香酸、例えば、クロリムロン−エチル(例えば、2−[[[[(4−クロロ−6−メトキシ−2−ピリミジニル)アミノ]カルボニル]アミノ]スルホニル]安息香酸エチル)などのエチルエステルなどの塩及びエステル、−塩形態−(誘導体)も含む(施用量:1〜1200gAS/ha、好ましくは5〜500gAS/ha;質量比A:B=1:1200〜500:1、好ましくは1:100〜40:1);
(B7−5)クロルスルフロン(PM#152)、例えば、2−クロロ−N−[[(4−メトキシ−6−メチル−1,3,5−トリアジン−2−イル)アミノ]カルボニル]ベンゼンスルホンアミド(施用量:0.1〜100gAS/ha、好ましくは1〜90gAS/ha;質量比A:B=1:100〜5000:1、好ましくは1:16〜200:1);
(B7−6)シノスルフロン(PM#158)、同義語、モノスルフロン、例えば、N−[[(4,6−ジメトキシ−1,3,5−トリアジン−2−イル)アミノ]カルボニル]−2−(2−メトキシエトキシ)ベンゼンスルホンアミド(施用量:1.5〜1500gAS/ha、好ましくは2.5〜500gAS/ha;質量比A:B=1:1500〜350:1、好ましくは1:100〜80:1);
(B7−7)シクロスルファムロン(PM#192)、例えば、N−[[[2−(シクロプロピルカルボニル)フェニル]アミノ]スルホニル]−N’−(4,6−ジメトキシ−2−ピリミジニル)尿素(施用量:1.5〜1000gAS/ha、好ましくは2.5〜900gAS/ha;質量比A:B=1:1000〜350:1、好ましくは1:160〜80:1);
(B7−8)エタメツルフロン−メチル(PM#318)、例えば、2−[[[[[4−エトキシ−6−(メチルアミノ)−1,3,5−トリアジン−2−イル]アミノ]カルボニル]アミノ]スルホニル]安息香酸メチル(施用量:1〜500gAS/ha、好ましくは2〜300gAS/ha;質量比A:B=1:500〜500:1、好ましくは1:60〜200:1);
(B7−9)エトキシスルフロン(PM#326)、例えば、[[(4,6−ジメトキシ−2−ピリミジニル)アミノ]カルボニル]スルファミン酸2−エトキシフェニル、その塩及びエステル、−塩形態−(誘導体)も含む(施用量:1〜150gAS/ha、好ましくは2〜100gAS/ha;質量比A:B=1:150〜500:1、好ましくは1:20 〜100:1);
(B7−10)フラザスルフロン(PM#367)、例えば、N−[[(4,6−ジメトキシ−2−ピリミジニル)アミノ]カルボニル]−3−(トリフルオロメチル)−2−ピリジンスルホンアミド(施用量:1〜500gAS/ha、好ましくは3〜400gAS/ha;質量比A:B=1:500〜500:1、好ましくは1:80〜70:1);
(B7−12)フルピルスルフロン−メチル−ナトリウム(PM#397)、例えば、2−[[[[(4,6−ジメトキシ−2−ピリミジニル)アミノ]カルボニル]アミノ]スルホニル]−6−(トリフルオロメチル)−3−ピリジンカルボン酸メチル・モノナトリウム塩、その酸(フルピルスルフロン)、その他の塩及びその他のエステル、−塩形態−(誘導体)も含む(施用量:0.1〜100gAS/ha、好ましくは0.2〜90gAS/ha;質量比A:B=1:100〜5000:1、好ましくは1:16〜1000:1);
(B7−13)ホラムスルフロン(PM#414)、例えば、2−[[[[(4,6−ジメトキシ−2−ピリミジニル)アミノ]カルボニル]アミノ]スルホニル]−4−(ホルミルアミノ)−N,N−ジメチルベンズアミド、その塩及びエステル、−塩形態−(誘導体)も含む(施用量:1〜500gAS/ha、好ましくは3〜400gAS/ha;質量比A:B=1:500〜500:1、好ましくは1:80〜70:1);
(B7−14)ハロスルフロン−メチル(PM#438)、例えば、3−クロロ−5−[[[[(4,6−ジメトキシ−2−ピリミジニル)アミノ]カルボニル]アミノ]スルホニル]−1−メチル−1H−ピラゾール−4−カルボン酸メチル、その酸、ハロスルフロン(例えば、3−クロロ−5−[[[[(4,6−ジメトキシ−2−ピリミジニル)アミノ]カルボニル]アミノ]スルホニル]−1−メチル−1H−ピラゾール−4−カルボン酸)、塩、及びその他のエステル、−塩形態−(誘導体)も含む(施用量:1〜300gAS/ha、好ましくは2〜200gAS/ha;質量比A:B=1:300〜500:1、好ましくは1:40〜100:1);
(B7−15)イマゾスルフロン(PM#469)、例えば、2−クロロ−N−[[(4,6−ジメトキシ−2−ピリミジニル)アミノ]カルボニル]イミダゾ[1,2−a]ピリジン−3−スルホンアミド(施用量:1〜500gAS/ha、好ましくは2〜300gAS/ha;質量比A:B=1:500〜500:1、好ましくは1:60〜100:1);
(B7−16)イオドスルフロン−メチル−ナトリウム(PM#480)、例えば、4−ヨード−2−[[[[(4−メトキシ−6−メチル−1,3,5−トリアジン−2−イル)アミノ]カルボニル]アミノ]スルホニル]安息香酸メチルナトリウム塩、その酸(例えば、4−ヨード−2−(4−メトキシ−6−メチル−1,3,5−トリアジン−2−イルカルバモイルスルファモイル)安息香酸)及びその他の塩及びエステル、−塩形態−(誘導体)も含む(施用量:0.1〜50gAS/ha、好ましくは0.2〜30gAS/ha;質量比A:B=1:50〜5000:1、好ましくは1:6〜1000:1);
(B7−17)メソスルフロン−メチル(PM#532)、例えば、2−[[[[(4,6−ジメトキシ−2−ピリミジニル)アミノ]カルボニル]アミノ]スルホニル]−4−[[(メチルスルホニル)アミノ]メチル]安息香酸メチル、その酸(例えば、4−メチルスルホニルアミノ−2−(4,6−ジメトキシピリミジン−2−イルカルバモイルスルファモイル)安息香酸)、及びその他の塩、エステル、−塩形態−(誘導体)も含む(施用量:0.1〜150gAS/ha、好ましくは0.2〜100gAS/ha;質量比A:B=1:150〜5000:1、好ましくは1:20〜1000:1);
(B7−18)メトスルフロン−メチル(PM#574)、例えば、2−[[[[(4−メトキシ−6−メチル−1,3,5−トリアジン−2−イル)アミノ]カルボニル]アミノ]スルホニル]安息香酸メチル、その酸(例えば、2−[[[[(4−メトキシ−6−メチル−1,3,5−トリアジン−2−イル)アミノ]カルボニル]アミノ]スルホニル]安息香酸)、塩、及びその他のエステル、−塩形態−(誘導体)も含む(施用量:0.1〜20gAS/ha、好ましくは0.2〜10gAS/ha;質量比A:B=1:20〜5000:1、好ましくは1:2〜1000:1);
(B7−19)ニコスルフロン(PM#594)、例えば、2−[[[[(4,6−ジメトキシ−2−ピリミジニル)アミノ]カルボニル]アミノ]スルホニル]−N,N−ジメチル3−ピリジンカルボキサミド、その塩及びエステル、−塩形態−(誘導体)も含む(施用量:1〜120gAS/ha、好ましくは2〜90gAS/ha;質量比A:B=1:120〜500:1、好ましくは1:16〜100:1);
(B7−20)オルトスルファムロン(PM#614)、例えば、2−[[[[[(4,6−ジメトキシ−2−ピリミジニル)アミノ]カルボニル]アミノ]スルホニル]アミノ]−N,N−ジメチルベンズアミド(施用量:1〜500gAS/ha、好ましくは3〜400gAS/ha;質量比A:B=1:500〜500:1、好ましくは1:80〜70:1);
(B7−22)プリミスルフロン−メチル(PM#678)、例えば、2−[[[[[4,6−ビス(ジフルオロメトキシ)−2−ピリミジニル]アミノ]カルボニル]アミノ]スルホニル]安息香酸メチル、その酸(例えば、2−[4,6−ビス(ジフルオロメトキシ)ピリミジン−2−イルカルバモイルスルファモイル]安息香酸)、塩及びその他のエステル、−塩形態−(誘導体)も含む(施用量:0.1〜120gAS/ha、好ましくは0.2〜90gAS/ha;質量比A:B=1:120〜5000:1、好ましくは1:16〜1000:1);
(B7−23)プロスルフロン(PM#704)、例えば、N−[[(4−メトキシ−6−メチル−1,3,5−トリアジン−2−イル)アミノ]カルボニル]−2−(3,3,3−トリフルオロプロピル)ベンゼンスルホンアミド、その塩及びエステル、−塩形態−(誘導体)も含む(施用量:0.1〜300gAS/ha、好ましくは0.2〜200gAS/ha;質量比A:B=1:300〜5000:1、好ましくは1:40〜1000:1);
(B7−24)ピラゾロスルフロン−エチル(PM#714)、例えば、5−[[[[(4,6−ジメトキシ−2−ピリミジニル)アミノ]カルボニル]アミノ]スルホニル]−1−メチル−1H−ピラゾール−4−カルボン酸エチル、その酸、ピラゾロスルフロン(例えば、5−[[[[(4,6−ジメトキシ−2−ピリミジニル)アミノ]カルボニル]アミノ]スルホニル]−1−メチル−1H−ピラゾール−4−カルボン酸)、塩及びその他のエステル、−塩形態−(誘導体)も含む(施用量:0.5〜1200、好ましくは1〜1000gAS/ha;質量比A:B=1:1200〜1000:1、好ましくは1:200〜200:1);
(B7−25)リムスルフロン(PM#741)、例えば、N−[[(4,6−ジメトキシ−2−ピリミジニル)アミノ]カルボニル]−3−(エチルスルホニル)−2−ピリジンスルホンアミド、塩及びエステル、−塩形態−(誘導体)も含む(施用量:0.1〜120gAS/ha、好ましくは0.2〜90gAS/ha;質量比A:B=1:120〜5000:1、好ましくは1:16〜1000:1);
(B7−27)スルフォスルフロン(PM#772)、例えば、N−[[(4,6−ジメトキシ−2−ピリミジニル)アミノ]カルボニル]−2−(エチルスルホニル)イミダゾ[1,2−a]ピリジン−3−スルホンアミド、塩及びその他のエステル、−塩形態−(誘導体)も含む(施用量:0.1〜200gAS/ha、好ましくは0.5〜100gAS/ha;質量比A:B=1:200〜5000:1、好ましくは1:20〜1000:1);
(B7−28)チフェンスルフロン−メチル(PM#815)、例えば、3−[[[[(4−メトキシ−6−メチル−1,3,5−トリアジン−2−イル)アミノ]カルボニル]アミノ]スルホニル]−2−チオフェンカルボン酸メチル、その酸、チフェンスルフロン(例えば、3−[[[[(4−メトキシ−6−メチル−1,3,5−トリアジン−2−イル)アミノ]カルボニル]アミノ]スルホニル]−2−チオフェンカルボン酸)、塩、及びその他のエステル、−塩形態−(誘導体)も含む(施用量:0.1〜300gAS/ha、好ましくは0.2〜200gAS/ha;質量比A:B=1:300〜5000:1、好ましくは1:40〜1000:1);
(B7−29)トリアスルフロン(PM#839)、例えば、2−(2−クロロエトキシ)−N−[[(4−メトキシ−6−メチル−1,3,5−トリアジン−2−イル)アミノ]カルボニル]ベンゼンスルホンアミド、塩及びその他のエステル、−塩形態−(誘導体)も含む(施用量:0.2〜90gAS/ha、好ましくは0.5〜80gAS/ha;質量比A:B=1:90〜2500:1、好ましくは1:16〜1000:1);
(B7−30)トリベヌロン−メチル(PM#844)、例えば、2−[[[[(4−メトキシ−6−メチル−1,3,5−トリアジン−2−イル)メチルアミノ]カルボニル]アミノ]スルホニル]安息香酸メチル、その酸、トリベヌロン(例えば、2−[[[[(4−メトキシ−6−メチル−1,3,5−トリアジン−2−イル)メチルアミノ]カルボニル]アミノ]スルホニル]安息香酸)、塩及びその他のエステル、−塩形態−(誘導体)も含む(施用量:0.1〜100gAS/ha、好ましくは0.2〜80gAS/ha;質量比A:B=1:100〜5000:1、好ましくは1:16〜2000:1);
(B7−32)トリフルスルフロン−メチル(PM#859)、例えば、2−[[[[[4−(ジメチルアミノ)−6−(2,2,2−トリフルオロエトキシ)−1,3,5−トリアジン−2−イル]アミノ]カルボニル]アミノ]スルホニル]−3−メチル安息香酸メチル、その酸、トリフルスルフロン(例えば、2−[[[[[4−(ジメチルアミノ)−6−(2,2,2−トリフルオロエトキシ)−1,3,5−トリアジン−2−イル]アミノ]カルボニル]アミノ]スルホニル]−3−メチル安息香酸)、塩及びその他のエステル、−塩形態−(誘導体)も含む(施用量:0.1〜500gAS/ha、好ましくは0.2〜400gAS/ha;質量比A:B=1:500〜5000:1、好ましくは1:80〜2000:1);
(B7−33)トリトスルフロン(PM#865)、例えば、N−[[[4−メトキシ−6−(トリフルオロメチル)−1,3,5−トリアジン−2−イル]アミノ]カルボニル]−2−(トリフルオロメチル)ベンゼンスルホンアミド、その塩及びエステル、−塩形態−(誘導体)も含む(施用量:0.1〜200gAS/ha、好ましくは、0.5〜100gAS/ha;質量比A:B=1:200〜5000:1、好ましくは1:20〜1000:1);
(B7−34)HNPC−C9908(コード番号:Hunan Research Institute of Chemical Industry(HRICI)、中国;Agrow Magazine, Issue 17, October 2007, pp. 15-16を参照)、例えば、安息香酸2−[[[[[4−メトキシ−6−(メチルチオ)−2−ピリミジニル]アミノ]カルボニル]アミノ]スルホニル]メチルエステル、その他の塩及びエステル、−塩形態−(誘導体)も含む(施用量:1〜5000gAS/ha、好ましくは3〜4000gAS/ha;質量比A:B=1:5000〜500:1、好ましくは1:80〜70:1);
(B7−35)NC−330(PM#1352)、例えば、5−(4,6−ジメチルピリミジン−2−イルカルバモイルスルファモイル)−1−(2−ピリジル)ピラゾール−4−カルボン酸メチル(施用量:1〜500gAS/ha、好ましくは3〜400gAS/ha;質量比A:B=1:500〜500:1、好ましくは1:80〜70:1);
(B7−36)NC−620(コード番号)、例えば、Chemical Abstract Service登録番号[CAS RN:868680−84−6](施用量:1〜500gAS/ha、好ましくは3〜400gAS/ha;質量比A:B=1:500〜500:1, 好ましくは1:80〜70:1);
(B8−1)フルカルバゾン−ナトリウム(PM#376)、例えば、4,5−ジヒドロ−3−メトキシ−4−メチル−5−オキソ−N−[[2−(トリフルオロメトキシ)フェニル]スルホニル]−1H−1,2,4−トリアゾール−1−カルボキサミド・ナトリウム塩、その酸(フルカルバゾン)、その他の塩及びエステル、−塩形態−(誘導体)も含む(施用量:0.1〜500gAS/ha、好ましくは0.3〜400gAS/ha;質量比A:B=1:500〜5000:1、好ましくは1:80〜700:1);
(B8−2)プロポキシカルバゾン−ナトリウム(PM#699)、例えば、2−[[[(4,5−ジヒドロ−4−メチル−5−オキソ−3−プロポキシ−1H−1,2,4−トリアゾール−1−イル)カルボニル]アミノ]スルホニル]安息香酸メチル;ナトリウム塩、その酸(例えば、2−(4,5−ジヒドロ−4−メチル−5−オキソ−3−プロポキシ−1H−1,2,4−トリアゾール−1−イル)カルボキサミドスルホニル安息香酸メチル(N−酸に対して))、その他の塩及びエステル、−塩形態−(誘導体)も含む(施用量:0.1〜500gAS/ha、好ましくは0.3〜400gAS/ha;質量比A:B=1:500〜5000:1、好ましくは1:80〜700:1);
(B8−3)チエンカルバゾン−メチル(CPCN)、例えば、4−[[[(4,5−ジヒドロ−3−メトキシ−4−メチル−5−オキソ−1H−1,2,4−トリアゾール−1−イル)カルボニル]アミノ]スルホニル]−5−メチル−3−チオフェンカルボン酸メチル、その酸(例えば、4−[[[(4,5−ジヒドロ−3−メトキシ−4−メチル−5−オキソ−1H−1,2,4−トリアゾール−1−イル)カルボニル]アミノ]スルホニル]−5−メチル−3−チオフェンカルボン酸)、塩及びその他のエステル、−塩形態−(誘導体)も含む(施用量:0.1〜100gAS/ha、好ましくは0.3〜80gAS/ha;質量比A:B=1:100〜5000:1、好ましくは1:16〜700:1);
(B9−1)コロランスラム−メチル(PM#167)、例えば、メチル 3−クロロ−2−[[(5−エトキシ−7−フルオロ[1,2,4]トリアゾロ[1,5−c]ピリミジン−2−イル)スルホニル]アミノ]安息香酸メチル、その酸(例えば、3−クロロ−2−(5−エトキシ−7−フルオロ−[1,2,4]トリアゾロ−[1,5−c]ピリミジン−2−イルスルホンアミド)安息香酸)、塩及びその他のエステル、−塩形態−(誘導体)も含む(施用量:0.1〜500gAS/ha、好ましくは0.3〜400gAS/ha;質量比A:B=1:500〜5000:1、好ましくは1:80〜700:1);
(B9−2)ジクロスラム(PM#247)、例えば、N−(2,6−ジクロロフェニル)−5−エトキシ−7−フルオロ[1,2,4]トリアゾロ[1,5−c]ピリミジン−2−スルホンアミド(施用量:0.5〜150gAS/ha、好ましくは1〜120gAS/ha;質量比A:B=1:150〜1000:1、好ましくは1:30〜200:1);
(B9−3)フロラスラム(PM#370)、例えば、N−(2,6−ジフルオロフェニル)−8−フルオロ−5−メトキシ[1,2,4]トリアゾロ[1,5−c]ピリミジン−2−スルホンアミド(施用量:0.1〜500gAS/ha、好ましくは0.2〜300gAS/ha;質量比A:B=1:500〜5000:1、好ましくは1:60〜1000:1);
(B9−4)フルメツラム(PM#386)、例えば、N−(2,6−ジフルオロフェニル)−5−メチル[1,2,4]トリアゾロ[1,5−a]ピリミジン−2−スルホンアミド(施用量:0.5〜1500gAS/ha、好ましくは1〜1000gAS/ha;質量比A:B=1:1500〜400:1、好ましくは1:200〜200:1);
(B9−5)メトスラム(PM#570)、例えば、N−(2,6−ジクロロ−3−メチルフェニル)−5,7−ジメトキシ[1,2,4]トリアゾロ[1,5−a]ピリミジン−2−スルホンアミド(施用量:0.5〜1500gAS/ha、好ましくは1〜1000gAS/ha;質量比A:B=1:1500〜400:1、好ましくは1:200〜200:1);
(B9−6)ペノキススラム(PM#641)、例えば、2−(2,2−ジフルオロエトキシ)−N−(5,8−ジメトキシ[1,2,4]トリアゾロ[1,5−c]ピリミジン−2−イル)−6−(トリフルオロメチル)ベンゼンスルホンアミド(施用量:0.1〜500gAS/ha、好ましくは0.3〜400gAS/ha;質量比A:B=1:500〜5000:1、好ましくは1:80〜700:1);
(B9−7)ピロキシスラム(CPCN)、例えば、N−(5,7−ジメトキシ[1,2,4]トリアゾロ[1,5−a]ピリミジン−2−イル)−2−メトキシ−4−(トリフルオロメチル)−3−ピリジンスルホンアミド(施用量:0.1〜500gAS/ha、好ましくは0.3〜400gAS/ha;質量比A:B=1:500〜5000:1、好ましくは1:80〜700:1);
から成る(スルホン)アミドのグループからの1つ又はそれ以上の除草剤を意味し;
1.R1がフッ素であり、R2及びR3がカルボニル基C=Oであり、R4がメチルである一般式(I)の化合物、及びB1−2(ブロモブチド)、B7−3(ベンスルフロン−メチル)、B7−9(エトキシスルフロン)の化合物;
2.R1がフッ素であり、R2が水素であり、R3がヒドロキシルであり、R4がメチルである一般式(I)の化合物、及びB7−9(エトキシスルフロン)の化合物;
3.R1が塩素であり、R2及びR3がカルボニル基C=Oであり、R4がメチルである一般式(I)の化合物、及びB7−9(エトキシスルフロン)の化合物;
4.R1が塩素であり、R2が水素であり、R3がヒドロキシルであり、R4がメチルである一般式(I)の化合物、及びB7−9(エトキシスルフロン)の化合物;
は除外される。
(A−1)+(B1−1)、(A−1)+(B1−2)、(A−1)+(B1−3)、(A−1)+(B1−4)、(A−1)+(B1−5)、(A−1)+(B1−6)、(A−1)+(B1−7)、(A−1)+(B1−8)、(A−1)+(B2−1)、(A−1)+(B2−2)、(A−1)+(B3−1)、(A−1)+(B3−2)、(A−1)+(B3−3)、(A−1)+(B3−4)、(A−1)+(B3−5)、(A−1)+(B3−6)、(A−1)+(B3−7)、(A−1)+(B3−8)、(A−1)+(B3−9)、(A−1)+(B4−1)、(A−1)+(B4−2)、(A−1)+(B4−3)、(A−1)+(B4−4)、(A−1)+(B4−5)、(A−1)+(B4−6)、(A−1)+(B4−7)、(A−1)+(B4−8)、(A−1)+(B4−9)、(A−1)+(B4−10)、(A−1)+(B4−11)、(A−1)+(B5−1)、(A−1)+(B5−2)、(A−1)+(B5−3)、(A−1)+(B5−4)、(A−1)+(B5−5)、(A−1)+(B5−6)、(A−1)+(B5−7)、(A−1)+(B6−1)、(A−1)+(B6−2)、(A−1)+(B6−3)、(A−1)+(B6−4)、(A−1)+(B6−5)、(A−1)+(B6−6)、(A−1)+(B6−7)、(A−1)+(B6−8)、(A−1)+(B6−9)、(A−1)+(B6−10)、(A−1)+(B6−11)、(A−1)+(B6−12)、(A−1)+(B6−13)、(A−1)+(B6−14)、(A−1)+(B7−1)、(A−1)+(B7−2)、(A−1)+(B7−3)、(A−1)+(B7−4)、(A−1)+(B7−5)、(A−1) +(B7−6)、(A−1)+(B7−7)、(A−1)+(B7−8)、(A−1) +(B7−9)、(A−1)+(B7−10)、(A−1)+(B7−11)、(A−1)+(B7−12)、(A−1)+(B7−13)、(A−1)+(B7−14)、(A−1)+(B7−15)、(A−1)+(B7−16)、(A−1)+(B7−17)、(A−1)+(B7−18)、(A−1)+(B7−19)、(A−1)+(B7−20)、(A−1)+(B7−21)、(A−1)+(B7−22)、(A−1)+(B7−23)、(A−1)+(B7−24)、(A−1)+(B7−25)、(A−1)+(B7−26)、(A−1)+(B7−27)、(A−1)+(B7−28)、(A−1)+(B7−29)、(A−1)+(B7−30)、(A−1)+(B7−31)、(A−1)+(B7−32)、(A−1)+(B7−33)、(A−1)+(B7−34)、(A−1)+(B7−35)、(A−1)+(B7−36)、(A−1)+(B8−1)、(A−1)+(B8−2)、(A−1)+(B8−3)、(A−1)+(B9−1)、(A−1)+(B9−2)、(A−1)+(B9−3)、(A−1)+(B9−4)、(A−1)+(B9−5)、(A−1)+(B9−6)、(A−1)+(B9−7);
(A−3)+(B9−1)、(A−3)+(B9−2)、(A−3)+(B9−3)、(A−3)+(B9−4)、(A−3)+(B9−5)、(A−3)+(B9−6)、(A−3)+(B9−7);
(A−5)+(B3−6)、(A−5)+(B3−7)、(A−5)+(B3−8)、(A−5)+(B3−9)、(A−5)+(B4−1)、(A−5)+(B4−2)、(A−5)+(B4−3)、(A−5)+(B4−4)、(A−5)+(B4−5)、(A−5)+(B4−6)、(A−5)+(B4−7)、(A−5)+(B4−8)、(A−5)+(B4−9)、(A−5)+(B4−10)、(A−5)+(B4−11)、(A−1)+(B5−1)、(A−5)+(B5−2)、(A−5)+(B5−3)、(A−5)+(B5−4)、(A−5)+(B5−5)、(A−5)+(B5−6)、(A−5)+(B5−7)、(A−5)+(B6−1)、(A−5)+(B6−2)、(A−5)+(B6−3)、(A−5)+(B6−4)、(A−5)+(B6−5)、(A−5)+(B6−6)、(A−5)+(B6−7)、(A−5)+(B6−8)、(A−5)+(B6−9)、(A−5)+(B6−10)、(A−5)+(B6−11)、(A−5)+(B6−12)、(A−5)+(B6−13)、(A−5)+(B6−14)、(A−5)+(B7−1)、(A−5)+(B7−2)、(A−5)+(B7−3)、(A−5)+(B7−4)、(A−5)+(B7−5)、(A−5)+(B7−6)、(A−5)+(B7−7)、(A−5)+(B7−8)、(A−5)+(B7−9)、(A−5)+(B7−10)、(A−5)+(B7−11)、(A−5)+(B7−12)、(A−5)+(B7−13)、(A−5)+(B7−14)、(A−5)+(B7−15)、(A−5)+(B7−16)、(A−5)+(B7−17)、(A−5)+(B7−18)、(A−5)+(B7−19)、(A−5)+(B7−20)、(A−5)+(B7−21)、(A−5)+(B7−22)、(A−5)+(B7−23)、(A−5)+(B7−24)、(A−5)+(B7−25)、(A−5)+(B7−26)、(A−5)+(B7−27)、(A−5)+(B7−28)、(A−5)+(B7−29)、(A−5)+(B7−30)、(A−5)+(B7−31)、(A−5)+(B7−32)、(A−5)+(B7−33)、(A−5)+(B7−34)、(A−5)+(B7−35)、(A−5)+(B7−36)、(A−5)+(B8−1)、(A−5)+(B8−2)、(A−5)+(B8−3)、(A−5)+(B9−1)、(A−5)+(B9−2)、(A−5)+(B9−3)、(A−5)+(B9−4)、(A−5)+(B9−5)、(A−5)+(B9−6)、(A−5)+(B9−7);
(A−6)+(B3−6)、(A−6)+(B3−7)、(A−6)+(B3−8)、(A−6)+(B3−9)、(A−6)+(B4−1)、(A−6)+(B4−2)、(A−6)+(B4−3)、(A−6)+(B4−4)、(A−6)+(B4−5)、(A−6)+(B4−6)、(A−6)+(B4−7)、(A−6)+(B4−8)、(A−6)+(B4−9)、(A−6)+(B4−10)、(A−6)+(B4−11)、(A−6)+(B5−1)、(A−6)+(B5−2)、(A−6)+(B5−3)、(A−6)+(B5−4)、(A−6)+(B5−5)、(A−6)+(B5−6)、(A−6)+(B5−7)、(A−6)+(B6−1)、(A−6)+(B6−2)、(A−6)+(B6−3)、(A−6)+(B6−4)、(A−6)+(B6−5)、(A−6)+(B6−6)、(A−6)+(B6−7)、(A−6)+(B6−8)、(A−6)+(B6−9)、(A−6)+(B6−10)、(A−6)+(B6−11)、(A−6)+(B6−12)、(A−6)+(B6−13)、(A−6)+(B6−14)、(A−6)+(B7−1)、(A−6)+(B7−2)、(A−6)+(B7−3)、(A−6)+(B7−4)、(A−6)+(B7−5)、(A−6)+(B7−6)、(A−6)+(B7−7)、(A−6)+(B7−8)、(A−6)+(B7−9)、(A−6)+(B7−10)、(A−6)+(B7−11)、(A−6)+(B7−12)、(A−6)+(B7−13)、(A−6)+(B7−14)、(A−6)+(B7−15)、(A−6)+(B7−16)、(A−6)+(B7−17)、(A−6)+(B7−18)、(A−6)+(B7−19)、(A−6)+(B7−20)、(A−6)+(B7−21)、(A−6)+(B7−22)、(A−6)+(B7−23)、(A−6)+(B7−24)、(A−6)+(B7−25)、(A−6)+(B7−26)、(A−6)+(B7−27)、(A−6)+(B7−28)、(A−6)+(B7−29)、(A−6)+(B7−30)、(A−6)+(B7−31)、(A−6)+(B7−32)、(A−6)+(B7−33)、(A−6)+(B7−34)、(A−6)+(B7−35)、(A−6)+(B7−36)、(A−6)+(B8−1)、(A−6)+(B8−2)、(A−6)+(B8−3)、(A−6)+(B9−1)、(A−6)+(B9−2)、(A−6)+(B9−3)、(A−6)+(B9−4)、(A−6)+(B9−5)、(A−6)+(B9−6)、(A−6)+(B9−7);
ベノキサコル;
クロキントセット(−メキシル);
シオメトリニル;
シプロスルファミド;
ジクロルミド;
ジシクロノン;
ジエトラート;
ジスルホトン(=ホスホルジチオ酸O,O−ジエチルS−2−エチルチオエチル);
フェンクロラゾール(−エチル);
フェンクロリム;
フルラゾール;
フルキソフェニム;
フリラゾール;
イソオキサジフェン(−エチル);
メフェンピル(−ジエチル);
メフェナート;
ナフタル酸無水物;
オキサベトリニル;
「R−29148」(=3−ジクロロアセチル−2,2,5−トリメチル−1,3−オキサゾリジン);
「R−28725」(=3−ジクロロアセチル−2,2−ジメチル−1,3−オキサゾリジン);
「PPG−1292」(=N−アリル−N−[(1,3−ジオキソラン−2−イル)メチル]ジクロロアセトアミド);
「DKA−24」(=N−アリル−N−[(アリルアミノカルボニル)メチル]ジクロロアセトアミド);
「AD−67」又は「MON4660」(=3−ジクロロアセチル−1−オキサ−3−アザスピロ[4.5]デカン);
「TI−35」(=1−ジクロロアセチルアゼパン);
「ジメピペラート」又は「MY−93」(=ピペリジン−1−チオカルボン酸S−1−メチル−1−フェニルエチル);
「ダイムロン」又は「SK23」(=1−(1−メチル−1−フェニルエチル)−3−p−トリル尿素);
「クミルロン」=「JC−940」(=3−(2−クロロフェニルメチル)−1−(1−メチル−1−フェニルエチル)尿素);
「メトキシフェノン」又は「NK049」(=3,3’−ジメチル−4−メトキシベンゾフェノン);
「CSB」(=1−ブロモ−4−(クロロメチルスルホニル)ベンゼン);
「CL−304415」(=4−カルボキシ−3,4−ジヒドロ−2H−1−ベンゾピラン−4−酢酸;CAS登録番号:31541−57−8);
「MG−191」(=2−ジクロロメチル−2−メチル−1,3−ジオキソラン);
「MG−838」(=1−オキサ−4−アザスピロ[4.5]デカン−4−カルボジチオ酸2−プロペニル;CAS登録番号:133993−74−5);
(ジフェニルメトキシ)酢酸メチル(CAS登録番号:41858−19−9、WO−A−1998/38856より);
[(3−オキソ−1H−2−ベンゾチオピラン−4(3H)−イリデン)メトキシ]酢酸メチル(CAS登録番号:205121−04−6、WO−A−1998/13361より);
1,2−ジヒドロ−4−ヒドロキシ−1−メチル−3−(5−テトラゾリルカルボニル)−2−キノロン(CAS登録番号:95855−00−8、WO−A−1999/000020より)。
・植物中で合成される澱粉の改良を目的とした作物の、遺伝子組換え技術による改変(例えば、WO92/11376、WO92/14827、WO91/19806);
・除草剤、例えば、スルホニル尿素に抵抗性を示すトランスジェニック作物(EP−A−0257993、US−A−5013659);
・植物を特定の害虫に対して抵抗性にするバチルス・チューリンゲンシス毒素(Bt毒素)の産生能を有する、トランスジェニック作物(EP−A−0142924、EP−A−0193259);
・改変された脂肪酸組成を有するトランスジェニック作物(WO91/13972)。
Sambrook et al., 1989, Molecular Cloning, A Laboratory Manual, 2nd Edition, Cold
Spring Harbor Laboratory Press, Cold Spring Harbor, NY;又はWinnacker “Gene und Klone”, VCH Weinheim 2nd Edition 1996 or Christou, “Trends in Plant Science” 1 (1996) 423-431を参照。当該遺伝子組換え操作を行なうために、DNA配列の組み換えによる変異誘発又は配列変化を可能にする核酸分子をプラスミドに導入することができる。例えば、上記の標準法は塩基交換を行なうことを可能にし、部分配列を除去し、又は天然若しくは合成配列を付加することを可能にする。DNAフラグメントを互いに結合するために、アダプター又はリンカーをフラグメントに付加してもよい。
雑草に対する発芽後作用
方法
単子葉及び双子葉の有害及び有用植物の種子又は根茎片を砂壌土で満たした泥炭製ポット(4cm径)に置き、次いで土壌で覆った。ポットを最適条件下で温室内に維持した。加えて、水稲栽培において見られる有害植物は、土壌表面上2cmの水位でポット栽培した。
E=A+B−(A×B/100)
式中、
A、B= それぞれa及びb g(ai/ha=ヘクタール当りの活性物質グラム)の薬量における成分A及びBの百分率での活性;
E = a+b g(ai/ha)の薬量における%予測値。
グループ(A)からの除草剤及びグループ(B)からの除草剤の本発明の組み合わせを、広範囲スペクトルの重要な有害植物(イネ科雑草類、広葉雑草/カヤツリグサ科)及び有用植物:コムギ(TRZAS)、コハコベ(STEME)、イタリアンライグラス(LOLMU)、オオイヌノフグリ(VERPE)、ノスズメノテッポウ(Alopecurus myosuroides)(ALOMY)、イヌカミツレ(Matricaria inodora)(MATIN)、セイヨウアブラナ(BRSNW)、サンシキスミレ(VIOTR)、カラスムギ(AVEFA)、アオゲイトウ(AMARE)、トウモロコシ(ZEAMX)、マルバアサガオ(PHBPU)、エノコログサ(SETVI)、ソバカズラ(POLCO)、イヌビエ(ECHCG)、イチビ(Abuthilon theophrasti)(ABUTH)、ショクヨウガヤツリ(Cyperus esculentus)(CYPES)、イネ(ORYSA)で試験した。
(1)処理植物(上記参照)に対するEPPOコード(以前のバイエルコード);
(2)スコアリングの時間:DAT(処理後の日数);
(3)試験した成分A(識別番号);
(4)試験した成分B(識別番号);
(5)成分Aの薬量[ai(g)/ha];
(6)成分Bの薬量[ai(g)/ha];
(7)実測された%活性;
(8)E値(Colby法により計算;上記を参照);
(9)コメント:「SYNERGY」=協力的相互作用(E値<実測%活性);
「SAFENING」=有用植物に対する薬害軽減剤作用(E値>実測%活性)。
Claims (19)
- 成分(A)及び(B)を含む除草剤の組み合わせ物であって、
(A)は一般式(A−1):
(B)は、
(B3−1)ジフルフェニカン;
(B3−3)フルフェナセット;
(B3−4)メフェナセット;
(B3−8)プロパニル;
(B4−3)ブタクロル;
(B4−8)プレチラクロル;
(B6−7)モリネート;
(B7−6)シノスルフロン;
(B7−7)シクロスルファムロン;
(B7−8)エタメツルフロン−メチル;
(B7−16)イオドスルフロン−メチル−ナトリウム;
(B7−17)メソスルフロン−メチル;
(B7−20)オルトスルファムロン;
(B8−3)チエンカルバゾン−メチル;
(B9−6)ペノクススラム;
(B9−7)ピロクススラム;
から成る(スルホン)アミドグループからの1つ又はそれ以上の除草剤を意味する;
上記除草剤の組み合わせ物。 - 成分(B)として:
(B3−1)ジフルフェニカン;
(B3−3)フルフェナセット;
(B3−4)メフェナセット;
(B3−8)プロパニル;
から成るアニリド類のサブグループからの1つ又はそれ以上の化合物を含む、請求項1に記載の除草剤の組み合わせ物。 - 成分(B)として:
(B3−1)ジフルフェニカン;
(B3−4)メフェナセット;
(B3−8)プロパニル;
から成るアニリド類のサブグループからの1つ又はそれ以上の化合物を含む、請求項1に記載の除草剤の組み合わせ物。 - 成分(B)として:
(B4−3)ブタクロール;
(B4−8)プレチラクロル;
から成るクロロアセトアニリド類のサブグループからの1つ又はそれ以上の化合物を含む、請求項1に記載の除草剤の組み合わせ物。 - チオカルバマートのサブグループからの成分(B)として化合物(B6−7)モリネートを含む、請求項1に記載の除草剤の組み合わせ物。
- 成分(B)として:
(B7−6)シノスルフロン;
(B7−7)シクロスルファムロン;
(B7−8)エタメツルフロン−メチル;
(B7−16)イオドスルフロン−メチル−ナトリウム;
(B7−17)メソスルフロン−メチル;
(B7−20)オルトスルファムロン;
から成るスルホニル尿素のサブグループからの1つ又はそれ以上の化合物を含む、請求項1に記載の除草剤の組み合わせ物。 - 成分(B)として:
(B7−6)シノスルフロン;
(B7−7)シクロスルファムロン;
(B7−16)イオドスルフロン−メチル−ナトリウム;
(B7−17)メソスルフロン−メチル;
から成るスルホニル尿素のサブグループからの1つ又はそれ以上の化合物を含む、請求項1に記載の除草剤の組み合わせ物。 - スルホニルアミノカルボニル−トリアゾリノンのサブグループからの成分(B)として化合物(B8−3)チエンカルバゾン−メチルを含む、請求項1に記載の除草剤の組み合わせ物。
- 成分(B)として:
(B9−6)ペノキススラム;
(B9−7)ピロキシスラム;
から成るトリアゾロピリミジン類のサブグループからの1つ又はそれ以上の化合物を含む、請求項1に記載の除草剤の組み合わせ物。 - トリアゾロピリミジン類のサブグループからの成分(B)として化合物(B9−6)ペノキススラムを含む、請求項1に記載の除草剤の組み合わせ。
- 成分(A)及び(B)の質量比(A):(B)が、1:7000〜5000:1の範囲内
である、請求項1〜10のいずれか1項に記載の除草剤の組み合わせ物。 - 成分(A)及び(B)の質量比(A):(B)が、1:5000〜2500:1の範囲内
である、請求項1〜11のいずれか1項に記載の除草剤の組み合わせ物。 - 成分(A)及び(B)の質量比(A):(B)が、1:3000〜1000:1の範囲内
である、請求項1〜12のいずれか1項に記載の除草剤の組み合わせ物。 - 有効量の成分(A)及び(B)、及び/又は更に異なるタイプの農薬活性化合物、製剤補助剤及び作物保護における常用の添加剤のグループからの1つ又はそれ以上の更なる成分を含む、請求項1〜13のいずれか1項に記載の除草剤の組み合わせ物。
- 請求項1〜14のいずれか1項に記載の除草剤の組み合わせ物の成分(A)及び(B)を併用して又は別々に施用する、不要植生を防除する方法。
- 作物中の、又は牧草中の、葉物/芝生中の、果樹園中の又は非農耕地区における不要植生を防除するための、請求項15に記載の方法。
- 作物が、コムギ(デュラムコムギ及び普通コムギ)、トウモロコシ、ダイズ、サトウダイコン、サトウキビ、ワタ、イネ、マメ、アマ、オオムギ、エンバク、ライムギ、ライコムギ、アブラナ、ジャガイモ、キビ(モロコシである、請求項15に記載の方法。
- 作物がイネ作物である、請求項16に記載の方法。
- 不要植生を防除するための、請求項1〜14のいずれか1項に記載の除草剤組み合わせ物の使用。
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DE102008037620.5 | 2008-08-14 | ||
PCT/EP2009/005768 WO2010017930A2 (de) | 2008-08-14 | 2009-08-08 | Herbizid-kombination mit dimethoxy-triazinyl-substituierten difluormethan-sulfonylaniliden |
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Families Citing this family (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006056871A (ja) | 2004-07-23 | 2006-03-02 | Bayer Cropscience Ag | スルホンアニリド類の農園芸用殺菌剤としての利用 |
DE102008037631A1 (de) | 2008-08-14 | 2010-02-18 | Bayer Cropscience Ag | Herbizid-Kombination mit Dimethoxytriazinyl-substituierten Difluormethansulfonylaniliden |
WO2011082964A1 (de) * | 2009-12-17 | 2011-07-14 | Bayer Cropscience Ag | Herbizide mittel enthaltend flufenacet |
WO2012052408A2 (de) | 2010-10-22 | 2012-04-26 | Bayer Cropscience Ag | Herbizid-kombination mit einem dimethoxytriazinyl-substituierten difluormethansulfonylanilid |
DE102010042786A1 (de) | 2010-10-22 | 2012-04-26 | Bayer Cropscience Ag | Herbizid- Kombination mit einem Dimethoxytriazinyl-substituierten Difluormethansulfonylanilid |
CN103719126B (zh) * | 2011-07-01 | 2016-02-17 | 陕西美邦农药有限公司 | 一种含氟丁酰草胺与磺酰脲类的除草组合物 |
US8680010B2 (en) * | 2011-08-16 | 2014-03-25 | Dow Agrosciences, Llc. | Synergistic herbicidal composition containing penoxsulam and florasulam |
JP5898543B2 (ja) * | 2012-03-23 | 2016-04-06 | 三井化学アグロ株式会社 | 除草性組成物 |
CN109006847A (zh) | 2012-12-12 | 2018-12-18 | 美国陶氏益农公司 | 施用五氟磺草胺和苯噻酰草胺所引起的协同杂草防治 |
MY173055A (en) | 2013-02-25 | 2019-12-23 | Dow Agrosciences Llc | Synergistic weed control from applications of penoxsulam and acetochlor |
MX2015011043A (es) | 2013-02-25 | 2015-10-22 | Dow Agrosciences Llc | Métodos para el control de malezas en plantíos de piña. |
KR102230973B1 (ko) | 2013-03-15 | 2021-03-23 | 다우 아그로사이언시즈 엘엘씨 | 페녹술람 및 벤조비시클론 또는 클로마존 및 벤조비시클론의 적용으로부터의 상승작용적 잡초 방제 |
CN105188372B (zh) * | 2013-03-15 | 2017-10-31 | 美国陶氏益农公司 | 施用五氟磺草胺和烯草胺带来的协同杂草防治 |
CN104488884A (zh) * | 2014-11-26 | 2015-04-08 | 广东中迅农科股份有限公司 | 一种含有双草醚和氟酮磺草胺的农药组合物 |
CN104430451A (zh) * | 2014-11-27 | 2015-03-25 | 广东中迅农科股份有限公司 | 一种氟酮磺草胺和氯吡嘧磺隆的除草组合物 |
CN104430450A (zh) * | 2014-11-27 | 2015-03-25 | 广东中迅农科股份有限公司 | 一种氟酮磺草胺和吡嘧磺隆的除草组合物 |
CN105494373A (zh) * | 2015-12-18 | 2016-04-20 | 北京燕化永乐生物科技股份有限公司 | 一种除草组合物 |
BR112019011501B1 (pt) | 2016-12-07 | 2023-03-14 | Bayer Cropscience Aktiengesellschaft | Composição herbicida contendo triafamona e indaziflam, seu uso, e método para controle de vegetação indesejada |
CN107242243B (zh) * | 2017-06-27 | 2020-03-17 | 东南大学成贤学院 | 一种含氟酮磺草胺与哒草特的除草组合物及其应用 |
CN108946907A (zh) * | 2018-06-06 | 2018-12-07 | 中山大学 | 一种Fe(III)协同植物多酚活化过硫酸盐体系修复有机废水的方法 |
CN108739839A (zh) * | 2018-06-13 | 2018-11-06 | 安徽众邦生物工程有限公司 | 一种含氟酮磺草胺的水稻田除草组合物 |
CN109221170A (zh) * | 2018-11-13 | 2019-01-18 | 合肥喜田生物科技有限公司 | 一种含有氟酮磺草胺和丙草胺的除草组合物 |
CA3130265A1 (en) | 2019-02-19 | 2020-08-27 | Gowan Company, L.L.C. | Stable liquid compositions and methods of using the same |
EP3679794A1 (en) | 2019-11-27 | 2020-07-15 | Bayer AG | Herbicidal compositions |
CN111165501A (zh) * | 2019-12-27 | 2020-05-19 | 安徽众邦生物工程有限公司 | 一种含氟酮磺草胺和苯噻酰草胺的除草组合物 |
CN111226968A (zh) * | 2020-03-16 | 2020-06-05 | 南京吉星生物技术开发有限公司 | 一种氟酮磺草胺与苄嘧磺隆防除移栽水稻田杂草组合物及其应用 |
CN114766496A (zh) * | 2022-05-20 | 2022-07-22 | 河南省农业科学院植物保护研究所 | 一种用于紫花苜蓿田的含有氟酮磺草胺的除草组合物 |
Family Cites Families (103)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US555081A (en) * | 1896-02-25 | emond | ||
GB574995A (en) | 1941-05-12 | 1946-01-30 | Wilfred Archibald Sexton | Destruction of weeds |
US2556664A (en) | 1950-03-18 | 1951-06-12 | Us Rubber Co | Plant growth regulants and phytocides |
BE532981A (ja) | 1953-10-30 | |||
US2695225A (en) | 1954-05-21 | 1954-11-23 | Columbia Southern Chem Corp | Herbicidal compositions |
BE559977A (ja) | 1956-01-17 | |||
NL109343C (ja) | 1957-04-20 | |||
NL238088A (ja) * | 1958-04-14 | |||
BE587481A (ja) | 1958-08-07 | |||
BE597035A (ja) | 1959-11-17 | |||
NL269079A (ja) | 1960-09-09 | 1964-06-25 | ||
NL277794A (ja) | 1961-05-01 | |||
NL123687C (ja) | 1961-09-08 | |||
US3175887A (en) | 1962-05-10 | 1965-03-30 | Wright Anderson South Africa L | Apparatus for the aerobic digestion of night soil |
US3175897A (en) | 1962-08-21 | 1965-03-30 | Stauffer Chemical Co | Asymmetric thiolcarbamates as herbicides |
DE1567151C3 (de) | 1965-04-09 | 1974-02-21 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | Diurethane, Verfahren zur Herstellung dieser Verbindungen sowie diese enthaltende herbizide Mittel |
US3534098A (en) | 1967-01-10 | 1970-10-13 | Rohm & Haas | 3,5-disubstituted benzamides |
US3582314A (en) | 1967-02-10 | 1971-06-01 | Ihara Chemical Co | Method for killing grassy and broadleaf weeds |
US3442945A (en) | 1967-05-22 | 1969-05-06 | Monsanto Co | Phytotoxic alpha-halo-acetanilides |
US3480671A (en) | 1969-01-16 | 1969-11-25 | Stauffer Chemical Co | Alpha-naphthoxy acetamide compositions |
US3636524A (en) * | 1969-12-08 | 1972-01-18 | Tel Tech Corp | Multiplex communication system |
JPS4824728B1 (ja) * | 1970-07-16 | 1973-07-24 | ||
BE795021A (fr) * | 1972-02-07 | 1973-08-06 | Ciba Geigy | Halogeno-acetanilides pour influencer la croissance des plantes |
DD112988A5 (ja) * | 1972-06-06 | 1975-05-12 | ||
US3894078A (en) | 1973-02-12 | 1975-07-08 | Minnesota Mining & Mfg | 5-Acetamido-2,4-dimethyltrifluoromethanesulfonanilide |
US3836524A (en) | 1973-04-26 | 1974-09-17 | Stauffer Chemical Co | Preparation of esters of thiocarbamic acids |
OA05625A (fr) | 1976-04-07 | 1981-04-30 | Du Pont | N-(hétérocyclique aminocarbonyl) aryl sulfonamides herbicides, compositions les contenant et procédés les utilisant . |
DE2648008C3 (de) * | 1976-10-23 | 1980-09-04 | Basf Ag, 6700 Ludwigshafen | Acetanilide |
HU176582B (en) | 1977-07-02 | 1981-03-28 | Nehezvegyipari Kutato Intezet | Process for producing n-aryl-phtalaminic acides |
DE2822155A1 (de) | 1978-05-20 | 1979-11-22 | Bayer Ag | Substituierte carbonsaeureamide, verfahren zu ihrer herstellung und ihre verwendung als herbizide |
US4394506A (en) | 1978-05-30 | 1983-07-19 | E. I. Du Pont De Nemours And Company | Agricultural sulfonamides |
EP0007677B1 (de) | 1978-07-24 | 1982-03-24 | Ascom Autophon Ag | Schaltungsanordnung zur Ueberwachung des Verlaufs der Potentiale auf mehreren Leitungen |
AU522026B2 (en) | 1978-09-19 | 1982-05-13 | Sumitomo Chemical Company, Limited | N-benzylhaloacetamide derivatives used as herbicides |
JPS55127302A (en) | 1979-03-27 | 1980-10-02 | Nippon Kayaku Co Ltd | Disinfectant for rice plant seedling culture box |
JPS5673055A (en) | 1979-11-20 | 1981-06-17 | Hodogaya Chem Co Ltd | Benzamide derivative and herbicide containing the same |
DK172396B1 (da) | 1979-11-30 | 1998-05-18 | Du Pont | Thiophencarboxylsyrederivater, middel til bekæmpelse af væksten af uønsket vegetation, fremgangsmåde til bekæmpelse af uønsket vegetation samt mellemprodukter til fremstilling af de nævnte derivater |
CA1330438C (en) | 1980-07-17 | 1994-06-28 | Willy Meyer | N-phenylsulfonyl-n'-pyrimidinyl-and-triazinylureas |
IL64220A (en) | 1980-11-21 | 1985-06-30 | May & Baker Ltd | Nicotinamide derivatives,their preparation and their use as herbicides |
NZ201284A (en) | 1981-07-27 | 1985-08-16 | Stauffer Chemical Co | S-benzylthiolcarbamates as herbicides |
US4420325A (en) | 1981-09-29 | 1983-12-13 | E. I. Du Pont De Nemours & Company | Herbicidal sulfonamides |
MA19680A1 (fr) * | 1982-01-11 | 1983-10-01 | Novartis Ag | N- arylsulfonyl - n' - pyrimidinylurees. |
CH655312A5 (de) | 1982-02-09 | 1986-04-15 | Sandoz Ag | Chloracetamide. |
US4954164A (en) | 1982-02-27 | 1990-09-04 | Nissan Chemical Industries, Ltd. | Pyrazolesulfonylurea derivatives, preparation thereof, herbicide containing said derivative as active ingredient and herbicidal method by use thereof |
ATE35888T1 (de) * | 1983-03-28 | 1988-08-15 | Ciba Geigy Ag | N-phenylsulfonyl-n'-pyrimidinyl- und triazinylharnstoffe. |
JPS604181A (ja) | 1983-06-22 | 1985-01-10 | Tokuyama Soda Co Ltd | N−置換−クロロアセトアニリド |
DE3324802A1 (de) | 1983-07-09 | 1985-01-17 | Hoechst Ag, 6230 Frankfurt | Neue n-alkoxy- und n- alkylsulfonylaminosulfonylharnstoffe, und neue (pyrimido) triazino-thiadiazinoxide als vorprodukte |
US4548638A (en) | 1983-08-22 | 1985-10-22 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonylureas |
JPS6067463A (ja) | 1983-09-26 | 1985-04-17 | Toyo Soda Mfg Co Ltd | チオカ−バメ−ト誘導体の製造法 |
EP0142152B1 (en) | 1983-11-14 | 1991-03-20 | The Dow Chemical Company | Novel substituted 1,2,4-triazolo- [1,5-a] pyrimidine-2-sulfonamides and compositions and methods of controlling undesired vegetation and suppressing the nitrification of ammonium nitrogen in soil |
JPH0660176B2 (ja) | 1984-03-22 | 1994-08-10 | 日産化学工業株式会社 | ピラゾールスルホニルウレア誘導体、製法および選択性除草剤 |
US4744814A (en) | 1984-12-06 | 1988-05-17 | Ishihara Sangyo Kaisha | N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-3-trifluoromethylpyridine-2-sulfonamide or salts thereof, herbicidal composition containing the same |
FI855180A (fi) | 1985-01-18 | 1986-07-19 | Nissan Chemical Ind Ltd | Pyrazolsulfonamidderivat, foerfarande foer dess framstaellande och det innehaollande ograesgift. |
CA1230120A (en) | 1985-05-10 | 1987-12-08 | Gerald E. Lepone | Herbicidal o-carbomethoxysulfonylureas |
US5010195A (en) | 1988-05-25 | 1991-04-23 | The Dow Chemical Company | Herbicidal alkoxy-1,2,4-triazolo(1,5-c)primidine-2-sulfonamides |
NZ216253A (en) | 1985-05-27 | 1989-07-27 | Mitsui Toatsu Chemicals | N-(3-chloro-4-isopropylphenyl)-carboxamide derivatives and herbicidal compositions |
JPS61293956A (ja) | 1985-06-21 | 1986-12-24 | Tokuyama Soda Co Ltd | クロロアセトアミド化合物及びその製造方法 |
US4789393A (en) | 1986-03-07 | 1988-12-06 | E. I. Du Pont De Nemours And Company | Herbicidal pyridine sulfonamides |
JPH0657684B2 (ja) | 1986-03-28 | 1994-08-03 | 宇部興産株式会社 | N―ベンジル2―(4―フルオル―3―トリフルオルメチルフェノキシ)ブタン酸アミド及びそれを含有する除草剤 |
JPS62242679A (ja) | 1986-04-11 | 1987-10-23 | イ−・アイ・デユポン・デ・ニモアス・アンド・カンパニ− | スルホニル尿素化合物 |
CA1308101C (en) | 1986-12-08 | 1992-09-29 | Paul Hsiao-Tseng Liang | Herbicidal pyridinesulfonylureas |
IN167606B (ja) | 1987-08-31 | 1990-11-24 | Takeda Chemical Industries Ltd | |
JPH0748894B2 (ja) | 1987-10-09 | 1995-05-24 | 日本電信電話株式会社 | 無線選択呼出方式 |
US5009899A (en) * | 1987-11-05 | 1991-04-23 | Land O'lakes, Inc. | Whey permeate-derived sweetener |
CA1321851C (en) * | 1988-01-11 | 1993-08-31 | Kathleen Anne Hughes | Process for preparing functionalized polymeric compositions |
JP2615228B2 (ja) | 1988-03-24 | 1997-05-28 | イー・アイ・デユポン・デ・ニモアス・アンド・カンパニー | フルオロエトキシアミノトリアジン |
DE4110795A1 (de) | 1991-04-04 | 1992-10-08 | Bayer Ag | Sulfonylaminocarbonyltriazolinone mit ueber sauerstoff gebundenen substituenten |
DE3821600A1 (de) * | 1988-06-27 | 1989-12-28 | Bayer Ag | Heteroaryloxyessigsaeure-n-isopropylanilide |
US4895857A (en) * | 1988-07-14 | 1990-01-23 | Thames Pharmacal Co., Inc. | Anti-infective methods and compositions |
HU208224B (en) | 1989-04-27 | 1993-09-28 | Nitrokemia Ipartelepek | Composition and process for preemergent control of monocotyledonous and partly dicotyledonous weeds |
GB9005965D0 (en) | 1990-03-16 | 1990-05-09 | Shell Int Research | Herbicidal carboxamide derivatives |
US5009699A (en) | 1990-06-22 | 1991-04-23 | American Cyanamid Company | 1-{[O-(cyclopropylcarbonyl)phenyl]sulfamoyl}-3-(4,6-dimethoxy-2-pyrimidinyl)urea herbicidal composition and use |
ZA917435B (en) | 1990-09-26 | 1992-05-27 | Takeda Chemical Industries Ltd | Herbicides |
DE4038430A1 (de) | 1990-12-01 | 1992-06-04 | Basf Ag | Herbizide n-((1,3,5-triazin-2-yl)-aminocarbonyl) benzolsulfonamide |
EP0496701B1 (de) | 1991-01-25 | 1996-03-06 | Ciba-Geigy Ag | Sulfonylharnstoffe als Herbizide |
HU217652B (hu) | 1991-03-07 | 2000-03-28 | E. I. Du Pont De Nemours And Co. | Egy piridin-szulfonamid-vegyület, sói, hidrátjai, komplexei, intermedierjei, előállításuk, valamint a vegyület alkalmazása herbicidként |
UA44220C2 (uk) | 1991-11-07 | 2002-02-15 | Агрево Юк Лімітед | Сульфонаміди,що мають гербіцидну активність,спосіб їх одержання, гербіцидна композиція та спосіб боротьби з бур'янами |
US5457085A (en) | 1992-11-16 | 1995-10-10 | Sandoz Ltd. | Optical isomer of dimethenamid |
CN1028314C (zh) | 1993-02-27 | 1995-05-03 | 南开大学 | 防治玉米田杂草组合物 |
US5330821A (en) | 1993-05-05 | 1994-07-19 | New Paradise Enterprise Co., Ltd. | Decorative device for concealing the top of curtains and certain fixtures |
DE4335297A1 (de) | 1993-10-15 | 1995-04-20 | Hoechst Schering Agrevo Gmbh | Phenylsulfonylharnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
DE4415049A1 (de) | 1994-04-29 | 1995-11-02 | Hoechst Schering Agrevo Gmbh | Acylierte Aminophenylsulfonylharnstoffe, Verfahren zu deren Herstellung und Verwendung als Herbizide und Wachstumsregulatoren |
DE19520839A1 (de) | 1995-06-08 | 1996-12-12 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel mit 4-Iodo-2-[3- (4-methoxy-6-methyl-1,3,5-triazin-2-yl) ureidosulfonyl] -benzoesäureestern |
DE19521355A1 (de) | 1995-06-12 | 1996-12-19 | Hoechst Schering Agrevo Gmbh | Sulfonamide, Verfahren zu deren Herstellung und ihre Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
JPH09106236A (ja) | 1995-10-12 | 1997-04-22 | Fuji Xerox Co Ltd | 画像形成装置用の光学的検出装置及びそれを用いた画像形成装置 |
WO1997041112A1 (en) | 1996-04-25 | 1997-11-06 | Novartis Ag | Sulfonylurea salts as herbicides |
WO1998013361A1 (en) | 1996-09-26 | 1998-04-02 | Novartis Ag | Herbicidal composition |
US6071856A (en) | 1997-03-04 | 2000-06-06 | Zeneca Limited | Herbicidal compositions for acetochlor in rice |
IT1290062B1 (it) * | 1997-03-13 | 1998-10-19 | Isagro Ricerca Srl | Amminosolfoniluree ad attivita' erbicida |
EP1101760B1 (en) | 1998-07-29 | 2003-10-15 | IHARA CHEMICAL INDUSTRY Co., Ltd. | Difluoromethanesulfonyl anilide derivatives, process for the preparation of them and herbicides containing them as the active ingredient |
DE19933260A1 (de) | 1999-07-15 | 2001-01-18 | Bayer Ag | Substituierte Thien-3-yl-sulfonylamino(thio)carbonyl-triazolin(thi)one |
CN1128140C (zh) | 2000-05-11 | 2003-11-19 | 湖南化工研究院 | 具除草活性的含烷硫基或丙烯(炔)氧基磺酰脲类化合物及其制备方法 |
ATE261440T1 (de) | 2000-10-12 | 2004-03-15 | Lg Chem Investment Ltd | Pyridinsulfonylharnstoffderivate mit herbizider wirkung |
AU780115B2 (en) | 2000-11-03 | 2005-03-03 | Corteva Agriscience Llc | N-(5,7-dimethoxy(1,2,4)triazolo(1,5-a)pyrimidin-2-yl) arylsulfonamide compounds and their use as herbicides |
TWI327462B (en) | 2002-01-18 | 2010-07-21 | Sumitomo Chemical Co | Condensed heterocyclic sulfonyl urea compound, a herbicide containing the same, and a method for weed control using the same |
JP2006056870A (ja) * | 2004-04-01 | 2006-03-02 | Bayer Cropscience Ag | ジフルオロメタンスルホンアミド誘導体及び除草剤 |
KR101014328B1 (ko) | 2004-04-27 | 2011-02-14 | 닛산 가가쿠 고교 가부시키 가이샤 | 피라졸술포닐우레아화합물 및 제초제 |
JP2006056871A (ja) | 2004-07-23 | 2006-03-02 | Bayer Cropscience Ag | スルホンアニリド類の農園芸用殺菌剤としての利用 |
CN102578085B (zh) * | 2004-08-11 | 2014-06-11 | 组合化学工业株式会社 | 农药组合物 |
WO2007028505A2 (de) * | 2005-09-08 | 2007-03-15 | Bayer Cropscience Ag | Neue sulfonamid-haltige feste formulierungen |
JP2007106745A (ja) * | 2005-09-16 | 2007-04-26 | Bayer Cropscience Ag | スルホンアニリド類の除草剤としての利用 |
JP2007186460A (ja) * | 2006-01-13 | 2007-07-26 | Bayer Cropscience Kk | 水田用除草剤組成物 |
JP4850529B2 (ja) | 2006-02-09 | 2012-01-11 | 三菱電機株式会社 | 入退室管理システム |
JP2008201693A (ja) | 2007-02-19 | 2008-09-04 | Bayer Cropscience Ag | 水田用混合除草剤組成物 |
-
2008
- 2008-08-14 DE DE102008037620A patent/DE102008037620A1/de not_active Withdrawn
-
2009
- 2009-08-08 WO PCT/EP2009/005768 patent/WO2010017930A2/de active Application Filing
- 2009-08-08 BR BRPI0917659-4A patent/BRPI0917659A2/pt not_active IP Right Cessation
- 2009-08-08 KR KR1020117005828A patent/KR101663021B1/ko active IP Right Grant
- 2009-08-08 JP JP2011522419A patent/JP5599793B2/ja active Active
- 2009-08-08 EP EP09777760A patent/EP2317855B1/de not_active Not-in-force
- 2009-08-08 AT AT09777760T patent/ATE539612T1/de active
- 2009-08-08 CN CN200980140930.4A patent/CN102186346B/zh active Active
- 2009-08-12 AR ARP090103116A patent/AR075449A1/es unknown
- 2009-08-12 TW TW098127137A patent/TW201019856A/zh unknown
- 2009-08-13 US US12/541,072 patent/US20100099564A1/en not_active Abandoned
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Also Published As
Publication number | Publication date |
---|---|
BRPI0917659A2 (pt) | 2015-08-18 |
DE102008037620A1 (de) | 2010-02-18 |
ATE539612T1 (de) | 2012-01-15 |
CN102186346B (zh) | 2016-09-21 |
KR20110053241A (ko) | 2011-05-19 |
CN102186346A (zh) | 2011-09-14 |
EP2317855B1 (de) | 2012-01-04 |
WO2010017930A3 (de) | 2010-10-14 |
EP2317855A2 (de) | 2011-05-11 |
AR075449A1 (es) | 2011-04-06 |
WO2010017930A8 (de) | 2011-03-17 |
CO6351691A2 (es) | 2011-12-20 |
JP2011530557A (ja) | 2011-12-22 |
WO2010017930A2 (de) | 2010-02-18 |
TW201019856A (en) | 2010-06-01 |
KR101663021B1 (ko) | 2016-10-14 |
US20100099564A1 (en) | 2010-04-22 |
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