TW200803736A - Herbicidal composition - Google Patents
Herbicidal composition Download PDFInfo
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- TW200803736A TW200803736A TW095132768A TW95132768A TW200803736A TW 200803736 A TW200803736 A TW 200803736A TW 095132768 A TW095132768 A TW 095132768A TW 95132768 A TW95132768 A TW 95132768A TW 200803736 A TW200803736 A TW 200803736A
- Authority
- TW
- Taiwan
- Prior art keywords
- compound
- salt
- herbicidal composition
- herbicidal
- formula
- Prior art date
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- 159000000000 sodium salts Chemical class 0.000 description 1
- SZXAJDQTPWYNBN-NWBUNABESA-M sodium;4-methoxycarbonyl-5,5-dimethyl-3-oxo-2-[(e)-n-prop-2-enoxy-c-propylcarbonimidoyl]cyclohexen-1-olate Chemical compound [Na+].C=CCO\N=C(/CCC)C1=C([O-])CC(C)(C)C(C(=O)OC)C1=O SZXAJDQTPWYNBN-NWBUNABESA-M 0.000 description 1
- JRQGDDUXDKCWRF-UHFFFAOYSA-M sodium;n-(2-methoxycarbonylphenyl)sulfonyl-4-methyl-5-oxo-3-propoxy-1,2,4-triazole-1-carboximidate Chemical compound [Na+].O=C1N(C)C(OCCC)=NN1C(=O)[N-]S(=O)(=O)C1=CC=CC=C1C(=O)OC JRQGDDUXDKCWRF-UHFFFAOYSA-M 0.000 description 1
- HIEHAIZHJZLEPQ-UHFFFAOYSA-M sodium;naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 HIEHAIZHJZLEPQ-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000004550 soluble concentrate Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 210000003802 sputum Anatomy 0.000 description 1
- 208000024794 sputum Diseases 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 125000005504 styryl group Chemical group 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
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- FZXISNSWEXTPMF-UHFFFAOYSA-N terbutylazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C)=N1 FZXISNSWEXTPMF-UHFFFAOYSA-N 0.000 description 1
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
- 229960000278 theophylline Drugs 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- AHTPATJNIAFOLR-UHFFFAOYSA-N thifensulfuron-methyl Chemical group S1C=CC(S(=O)(=O)NC(=O)NC=2N=C(OC)N=C(C)N=2)=C1C(=O)OC AHTPATJNIAFOLR-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
- DQFPEYARZIQXRM-LTGZKZEYSA-N tralkoxydim Chemical compound C1C(=O)C(C(/CC)=N/OCC)=C(O)CC1C1=C(C)C=C(C)C=C1C DQFPEYARZIQXRM-LTGZKZEYSA-N 0.000 description 1
- 230000014616 translation Effects 0.000 description 1
- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
- YMXOXAPKZDWXLY-QWRGUYRKSA-N tribenuron methyl Chemical group COC(=O)[C@H]1CCCC[C@@H]1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 YMXOXAPKZDWXLY-QWRGUYRKSA-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
- 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
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
- 239000002383 tung oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 238000009333 weeding Methods 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000010457 zeolite Substances 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/08—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing solids as carriers or diluents
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/12—Powders or granules
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/12—Powders or granules
- A01N25/14—Powders or granules wettable
-
- 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
- A01N37/22—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 the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
-
- 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
- A01N43/713—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with four or more nitrogen atoms as the only ring hetero 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/86—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
200803736 ⑴ 九、發明說明 【發明所屬之技術領域】 本發明係有關一種除草組成物,其包含(A ) —種後 述式(I )之化合物或其鹽,和(B )至少一種選自由後述 化合物(B 1 · 1 )至(B 2 · 1 )或其鹽組成之群組的化合物, 作爲有效成分。 【先前技術】 WO 02/3092 1 或 WO 92/1 4728 揭示一種後述式(I) 之化合物,且後者例示已知除草成分,其可與後述式(I )之化合物(其中取代基R爲氫原子)混合。在該例示中 ,揭示一些後述(B )之化合物中的化合物。然而,它們 只被列爲已知除草成分和且沒有被明確地描述如後述本發 明之除草組成物中所指定者。 專利文件1 : WO 02/3 092 1 專利文件2 : WO 92/1 4728 【發明內容】 本發明之揭示 欲藉由本發明解決之問題 已發展和實際地使用許多除草組成物。然而,欲控制 之雜草類型也有許多,且其出現延伸一長時間。因此,需 要發展一種具有較廣除草範圍且其爲高活性和具有持久效 果之除草組成物。 -4- 200803736 解決問題之方法 本發明人已對解決上述問題進行硏究且結果,已發現 可能獲得一種具有高實用性之除草組成物,其係藉由混合 (A ) —種後述式(I )之化合物或其鹽,和(b )至少一 種選自由後述化合物(B 1 . 1 )至(B 2 · 1 )或其鹽組成之群 組的化合物,且本發明已根據此發現完成。 因此,本發明提供一種除草組成物,其包含(A ) — 種式(I )之化合物:
其中R爲氫原子或-COCH2〇CH3,或其鹽,和(B )至少 一種化合物選自由(B1.1)滅芬草(mefenacet) 、(B1.2 ) 四唑草胺 (fentrazamide ) 、 ( B1.3 ) 噁嗪草酮 ( oxaziclomefone )和(Β2·1)克普草(clomeprop)、或其 鹽組成之群組(後文簡稱爲化合物(B )),作爲有效成 分;一種控制不需要的植物或抑制其生長之方法,其包含 施用除草有效量之除草組成物;和一種控制不需要的植物 或抑制其生長之方法,其包含施用除草有效量之(A )之 化合物或其鹽,和(B )之化合物。 -5- (3) (3)200803736 發明的效果 本發明之除草組成物’也就是,包含式(I )之化合 物或其鹽和化合物(B )作爲有效成分之除草組成物能夠 控制廣泛範圍的在農作地或非農作地出現之雜草,且其令 人驚訝地呈現相乘之除草效果,也就是除草效果高於有效 成分之個別除草效果的單純相加。使用該本發明之除草組 成物,不只其可以低劑量施用,如與其中分別地施用個別 有效成分之情形比較,且除草範圍將也被擴大,和另外除 草效果將持續一段時間。 在組合二個有效成分之情形中,當除草活性大於二個 有效成分的個別除草活性之總和(預期活性)時,其稱爲 相乘效應。二個有效成分之組合所預期之活性可如下計算 (Colby S.R·,“Weed,,,第 15 冊,第 20-22 頁,1967)。 E = a + /3 -( α χ β -^-100) 其中 α :當用 χ ( g/a )之除草劑X處理時的生長抑制率 /3 :當用y ( g/a)之除草劑Y處理時的生長抑制率 E ··當用χ ( g/a)之除草劑X和y ( g/a)之除草劑Y 處理時所預期的生長抑制率。 即,當真實生長抑制率(觀察値)大於上述計算之生 -6- (4) (4)200803736 長抑制率(預期値)時’藉由組合之活性可被視爲顯示相 乘效應。本發明之除草組成物當以上述公式計算時顯示相 乘效應。 進行本發明之最佳模式 式(I)之化合物具有二個不對稱碳原子且因此具有 異構物例如赤式(erythro )或蘇式(thre〇 )。因此,在 本發明中式(I )之化合物包括每個該等異構物和該等異 構物之混合物。 式(I)化合物之鹽可爲任何鹽,只要其爲農業上可 接受的,且其可(例如)爲鹼金屬鹽例如鈉鹽或鉀鹽;鹼 土金屬鹽例如鎂鹽或鈣鹽;銨鹽例如二甲基錢鹽或三乙基 銨鹽;無機酸鹽例如鹽酸鹽、過氯酸鹽、硫酸鹽或硝酸鹽 ;或有機酸鹽例如乙酸鹽或甲烷磺酸鹽。 式(I )之化合物,也就是一種其中取代基R爲氫原 子之化合物(簡稱爲化合物A 1 )和一種其中R爲 -COCH2OCH3之化合物(簡稱爲化合物A2 ),二者在本 發明中皆顯示較佳效果。在他們之中,其中R爲 -COCH2OCH3之化合物A2 (俗名:福托沙隆( flucetosulfuron))在本發明中爲更佳。 化合物(B )包括具有各種異構物(例如幾何異構物 和互變異構物)之化合物,且在本發明中,其包括每個該 等異構物和該等異構物之混合物。 進一步地,化合物(B )包括於鹽形式之化合物,和 (5) 200803736 該類鹽可爲任何鹽,只要iMl包曲^ r —_ /、女其爲裊業上可接受的且可(例如 )與上述式(D化合物之鹽相同的鹽。 將進一步詳細地揭述化合物(B )。 化合物(Bl.l) f谷名爲滅芬帛且爲一 種具有下列化學結構之化合物:
/ο
T H2 C
IX (B 化口物(Β1·2)俗名爲四D坐草胺(fentrazamide)且 爲一種具有下列化學結構之化合物:
(B1.2) 化合物(B1.3)俗名爲11 惡嗪草酮(oxaziclomefone 且爲一種具有下列化學結構之化合物:
(B1.3) -8- 200803736
化合物(B2.1)俗名爲克普早(clomeprop)且爲一 種具有下列化學結構之化合物:
作爲有效成分的式(Ϊ )之化合物或其鹽和化合物(B )在本發明之除草組成物中的混合比視各種調配物、天氣 情況、欲控制之植物的類型和生長情況而改變而且通常不 能被定義。然而,通常,化合物(B)之量如下,每重量 份的式(I )之化合物或其鹽。 (B1.1)爲從1至500重量份,較佳從1〇至15〇重 量份。 (B1.2)爲從0.1至500重量份,較佳從1至50重 量份。 (B1.3)爲從1至100重量份,較佳從1至20重量 份。 (B2.1)爲從0.1至500重量份,較佳從1至50重 量份。 本發明包括具有上述混合比之除草組成物,和一種控 制不需要的植物或抑制其生長之方法,其包含施用除草有 效量之除草組成物。在其施用中,可任意地選擇施用至不 需要的植物或施用至植物生長之地(在不需要的植物出現 -9 - (7) (7)200803736 之前或之後)。 本發明之除草組成物的施用量通常不能被界定,因爲 其視各種條件例如作爲有效成分之式(I )化合物或其鹽 和化合物(B )的混合比、調配物、天氣情況、欲控制的 植物之類型和生長情況而改變。然而,式(I )之化合物 或其鹽通常爲從0.001至50 g/a,較佳從0.01至1 g/a, 和化合物(B )且其適當總施用量如下。 (B1.1)爲從 〇.〇5 至 2,000 g/a,較佳從 0.5 至 50 g/a,且其與式(I )之化合物或其鹽的適當總施用量爲從 0.051 至 2,050 g/a,較佳從 0.51 至 51 g/a。 (B1.2)爲從 0·1 至 1,〇〇〇 g/a,較佳從 1 至 1〇〇 g/a ,且其與式(I )之化合物或其鹽的適當總施用量爲從 0.101 至 1,050 g/a,較佳從 1.01 至 101 g/a。 (B1.3)爲從 0.001 至 50 g/a,較佳從 0.01 至 5 g/a ,且其與式(I )之化合物或其鹽的適當總施用量爲從 0.002 至 100 g/a,較佳從 0.02 至 6 g/a。 (B2.1)爲從 0·1 至 1,000 g/a,較佳從 1 至 100 g/a ,且其與式(I )之化合物或其鹽的適當總施用量爲從 0.101 至 1,050 g/a,較佳從 1.01 至 101 g/a。 本發明包括一種控制不需要的植物或抑制其生長之方 法,其包含施用分別在上述施用量的式(I)之化合物或 其鹽和化合物(B )或將其施用於上述適當總施用量。在 該施用中,可任意地選擇施用至不需要的植物或施用至植 物生長之地(在不需要的植物出現之前或之後)。 -10- 200803736 (8) 本發明之除草組成物在低劑量下能夠控制廣泛範圍之 不需要的植物例如一年生雜草和多年生雜草。不需要的植 物包括禾草類(或禾本亞目(gramineae))例如稱草( barnyardgrass)(稗草(Echinochloa crus-galli L.)、早 期水生禾草(Echinochloa oryzicola vasing)、海蓬子( crab grass )(馬唐(Digitaria sanguinalis L.))、狗尾 草(gr eenfoxtail )(狗尾草(S et ari a viri di s L ·))、谷 莠子(giant foxtail )、(大狗尾草(S et ari a fab eri Herrm.))、牛筋草(牛筋草(Eleusine indica L.))、 野生燕麥(野燕麥(Avena fatua L.))、強森草(強生 草(Sorghum halepense L.))、魁克麥草(偃麥草( Agropyron repens L.))、亞歷山大草(alexandergrass ) (Br achiaria pi ant aginea )、爬拉草(Panicum purpurascens ) 、蟣子草(千金子(Leptochloa chinensi s ))、紅蟣子草(蟣子草(Leptochloa panicea))、早 熟禾(annual bluegrass )(早熟禾(P 〇 a annua L.))、 黑色草 (大穗看麥娘(Alopecurus myosuroides Huds·) ) 和 cholorado 藍莖草(胎生鐵角蕨 (Agropyron tsukushiense (Honda) Ohwi ))、莎草(或莎草科( Cyperaceae ))例如稻莎草(荆三稜(Cyperus iria L.) )、香附子(purple nutsedge)(香附子(Cyperus rotundus L.))、黃香附子(yellow nutsedge )(油莎草 (CyperusesculentusL.))、日本大甲藺(螢藺(
Scirpus juncoides ))、莎草(7jc 莎草(Cyperus -11 - 200803736 (9) serotinus))、小花傘莎草(異花莎草(Cyperus difformis) )、slender spikerush (牛毛氍(Eleocharis acicularis))和荸薺(野荸薺(Eleocharis kuroguwai) )、澤潟科(alismataceae )例如日本緞帶 waparo ( Japanese ribbon waparo ) (矮慈姑(S agittaria pygmaea ))、慈蘇(野慈蘇(Sagittaria trifolia))和狹葉澤瀉 (窄葉澤瀉(Alismacanaliculatum))、雨久花科( pontederiaceae)例如雨久花 (鴨舌草(Monochoria vaginalis))和雨久花種(雨久花(Monochoria korsakowii))、玄參科(scrophulariaceae)例如泥花草 (false pimpernel) (母草(Lindernia p y x i d ar i a ))和 abunome (虫亡眼草(Dopatrium junceum))、千屈菜科( lythraceae )例如紅骨仔草(toothcup )(節節菜(Rotala India))和紅莖 (多花水莧菜(Ammannia multi flora) )、和闊葉例如絨葉草(商麻(Abutilon theophrasti MEDIC.))、紫花牽牛(Tall morningglory)(圓葉牽牛 (Ipomoea purpurea L.))、常見灰藿(lambsquarters ) (白藜(Chenopodium album L.))、多朿 fj 賽達草( prickly sida)(刺金午時花(Sida spinosa. L.))、豬母 乳(common purslane )(馬齒寛(P ortulaca oleracea L. ))、野竟菜(slender amaranth )(野竟(Am ar an t hu s viridis L.))、紅根寛(redroot pigweed)(反枝莧( Amaranthus retroflexus L.))、鐮刀豆(sicklepod )( 決明子(Cassia obtusifolia L.))、龍葵(Black. -12- (10) (10)200803736 nightshade )(龍葵(Solanum nigrum L.))、白蓼(旱 苗蓼(Polygonum lapathifolium L.))、繁縷(繁縷( Stellaria media L.))、長莖溝繁縷(三蕊溝繁縷( Elatine triandra SCHK.))、常見蒼耳(蒼耳(Xanthium strumarium L.))、彎曲碎米薺(彎曲碎米薺(
Cardamine flexuosa WITH·))、寶蓋草(henbit)(寶蓋 草(Lamium ampl exi c aul e L ·))、豬草(豬草(
Ambrosia elatior L.))、豬殃殃(catchweed)(豬狹狹 (Galium sp ur i um L·))、田旋花(田旋花(C a 1 y s t e g i a arvensis L.))、吉姆森草(曼陀羅(Datura stramonium )) 、萷(Breea setosa ( BIEB. ) KIT AM.)和 threeseeded 紅葉鐵寛(人莧(Acalypha australis L·)) 。進一步地,本發明之除草組成物當在雜草發芽之後或之 前的任一階段施用時能夠提供好的效果。 本發明之除草組成物可爲各種施用形式例如土壤施用 、葉施用和水施用且有效控制農田例如旱田、果園或水田 ,或非農田例如堤防、休耕地、遊戲場、空地、林地、廠 址、鐵路邊或路邊之不需要的植物。 進一步地,只要符合本發明之目的,本發明之組成物 除了上述有效成分之外可另外包含其他除草活性成分,因 此其有時可能改良例如除草活性,施用除草劑之時間安排 或欲控制之雜草範圍。該等其他除草活性成分包括(例如 )下列化合物(包括ISO核准之申請的俗名,或發展編號 )。甚至當在本文中沒有明確地提到時,在該等化合物具 -13- (11) (11)200803736 有鹽、烷基酯、等等之情形中,他們當然全部包括。 (1 )該等咸信藉由擾亂植物之激素活性而顯示除草 效果者,例如苯氧基類型例如2,4-D、2,4-DB、2,4-DP、 MCPA、MCPB、MCPP、殺奈丹(naproanilide )或克普草 (clomeprop)、芳族羧酸類型例如2,3,6-TBA、麥草畏( dicamba)、敵草腈(dichlobenil)、毒莠定(picloram) 、三氯比(triclopyr )、必克草(clopyralid )或氯氨基 口比D定酸(Aminopyralid )、和其他例如鈉得爛(n ap t al am )、草除靈(benazolin)、快克草(quinclorac)、氯甲 嗤啉酸(quinmerac)、二氟 Π比隆(diflufenzopyr)和噻草 口定(thi azopyr ) 。 (2 )該等咸信藉由抑制植物之光合作用而顯示除草 效果者,例如尿素類型例如綠麥隆(chlorotoluron)、達 有龍(diuron)、氟草隆(fluometuron)、理有龍( linuron)、異丙隆(isoproturon)、美托苯隆( metobenzuron)或得匍隆(tebuthiuron)、三嗪類型例如 草滅淨(simazine )、草脫淨(atrazine )、達諾殺( atratone )、西草淨(simetryn )、撲草淨(prometryn ) 、異戊乙淨(dimethametryn)、菲殺淨(hexazinone)、 滅必淨(metribuzin )、特 丁津(terbuthylazine )、氰乃 淨(cyanazine)、草殺淨(ametryn)、賽布殺淨( cybutryne)、三嗪氟草胺(triaziflam)或普拔根( propazine)、尿喷陡類型例如克草(bromacil)、環草定 (lenacil )或特草定(terbacil )、苯胺類型例如除草靈 -14- (12) (12)200803736 (propanil )或環草胺(cypromid )、胺甲酸酯類型例如 施威(swep)、甜菜安(desmedipham )或苯敵( phenmedipham )、羥基苯甲腈類型例如溴苯腈( bromoxynil )、溴苯腈-辛酸鹽或碑苯腈(ioxynil )、和 其他例如啦達特(pyridate)、本達隆(bentazon)、氨 D坐草酮(amicarbazone)和滅草 _ (methazole)。 (3)四級銨鹽類型例如巴拉刈(paraquat)或敵草快 (diquat ),咸信在植物體中其本身轉化成游離基而形成 活性氧。 (4 )該等咸信藉由抑制植物葉綠素之生物合成和在 植物體中異常地累積光敏性過氧化物物質而顯示除草效果 者,例如二苯基醚類型例如丁拉護谷(nitrofen )、甲氧 基護谷(chlomethoxyfen)、必芬諾(bifenox)、亞喜芬 (acifluorfen-sodium )、氟磺胺草醚(fomesafen)、復 祿芬(oxyfluorfen)、乳氟禾草靈(lactofen)或氯氟草 醚(ethoxyfen_ethyl )、環醯亞胺類型例如氯酞亞胺( chlorphthalim)、丙炔氟草胺(flumioxazin) 、米克拉 (flumi cl orac )—戊基或氟乙草酯(fluthi acet-methyl ) 、和其他例如丙炔惡草酮(oxadiargyl)、樂滅草( oxadiazon)、甲磺草胺(sulfentrazone)、乙基克繁草( carfentrazone-ethyl)、噻地立密(thidiazimin)、環戊 惡草酮(pentoxazone)、草芬定(azafenidin)、異丙口坐 (isopropazole)、霸草靈 (pyraflufen-ethyl )、雙苯喷 草(benzfendizone)、布他芬(butafenacil)、美托苯隆 15- (13) (13)200803736 (metob enzur on ) 、D引哄酮草酯(cinidon-ethyl)、胺草 口坐(flupoxam)、氟佐拉(fluazolate)、普氟佐( profluazol)、匹拉克尼(pyrachlonil)、氟芬比( flufenpyr)—乙基和苯卡巴隆(bencarbazone)。 (5 )該等咸信其特徵爲藉由抑制植物之色素形成的 白化活性而顯示除草效果者例如類胡蘿蔔素,例如嗒畊酮 類型例如諾氟隆(norflurazon)、氯草敏(Chloridazon) 或美氟隆(metflurazon )、啦11坐類型例如卩比哩特( pyrazolate )、匹 口坐芬(pyr azoxy fen )、苯芬那( b enzo fenap )、托拉美諾(topramezone ) ( BAS- 6 7 0 H ) 或匹拉沙托(pyrasulfotole )、和其他例如殺草強( amitrole)、氟 Π定酮(fluridone)、氟他酮(flurtamone) 、口比氟草胺(diflufenican)、甲氧苯酮( methoxyphenone )、可滅蹤(clomazone )、硫可三酮( sulcotrione)、甲基磺草酮(mesotrione) 、AVH-301、 異惡 D坐草酮(isoxaflutole)、地芬快(difenzoquat)、依 索氯托(isoxachlortole)、苯二環酮(benzobicyclone) 、氟 D比草胺(pieolinafen)和氟丁 醯草胺(beflubutamid )° (6 )該等特別對禾草植物顯示強除草效果者,例如 芳氧基苯氧基丙酸類型例如禾草畏(diclofop-methyl )、 麥草伏甲酯(flamprop-M-methyl )、匹立芬(pyriphenop )—鈉、伏寄普(fluazifop-butyl)、合氯氟(haloxyfop )-甲基、快伏草(quizalofop-ethyl ) 、丁基賽伏草( -16- (14) (14)200803736 cyhalofop-buty)、芬殺草(fenoxaprop-ethyl)或惡 D坐草 胺(metamifop ) —丙基、和環己二酮類型例如亞汰草( alloxydim-sodium )、勉草同(cl etho dim )、西殺草( sethoxydim)、苯草酮(tralkoxydim) 、丁 苯草酮( butroxydim)、得殺草(tepraloxydim)、卡羅斯地( caloxydim)、環苯草酮(clefoxydim)或普羅斯地( profoxydim ) 〇 (7 )該等咸信藉由抑制植物之胺基酸生物合成而顯 示除草效果者,例如磺醯基脲類型例如氯嘧磺隆( chlorimuron-ethyl )、磺土 龍甲酯(sulfometuron-methyl )、甲基氟赔礦隆(primisulfuron-methyl)、免速隆( bensulfuron-methyl)、氯硫昂(chlorsulfuron)、甲黃隆 (metsulfuron-methyl )、西速隆(cinosulfuron )、百速 隆(pyrazosulfuron-ethyl)、四哩嚼磺隆(azimsulfuron )、伏速隆(flazasulfuron)、颯嚼磺隆(rimsulfuron) 、煙嚼磺隆(nicosulfuron)、依速隆(imazosulfuron) 、環磺隆(cyclosulfamuron)、撲噻呋隆(prosulfuron) 、伏匹速隆(flupyrsulfuron)、醚苯磺隆(trisulfuron) —甲基、氯Π比嗤磺隆(halosulfuron-methyl)、甲基噻吩 磺隆(thifensulfuron-methyl)、亞速隆(ethoxysulfuron )、環氧嚼磺隆(oxasulfuron )、胺苯磺隆( ethametsulfuron )、啦竣喃擴隆(flupyrsulfuron)、碗擴 隆(iodosulfuron)、磺醯磺隆(sulfosulfuron)、三卩丫速 隆(triasulfuron)、三苯那隆(tribenuron)—甲基、三 -17- (15) (15)200803736 氟甲磺隆(tritosulfuron)、甲醢胺磺隆(foramsulfuron )、三氟D定磺隆(trifloxysulfuron)、異磺隆( isosulfuron)-甲基、甲磺胺磺隆(mesosulfuron-methyl) 或嚼草醚(orthosulfamuron)、三哇喷D定磺醯胺類型例如 氟滅索侖(flumetsulam)、磺草D坐胺(metosulam)、雙 氯磺草胺(diclosulam)、氯酯磺草胺(。1〇^113111&111-methyl)、雙氟磺草胺(florasulam)、美托草胺( metosulfam)或平速爛(penoxsulam)、咪〇坐啉酮類型例 如依滅草(imazapyr)、嗎兹紮比(imazethapyr)、嗎紮 嗤(imazaquin)、甲氧咪草煙(imazamox)、嗎兹美( imazameth )、咪草酸(imazamethabenz)或甲基咪草煙 (imazapic )、嘧啶基水楊酸類型例如嘧啶硫苯( pyrithiobac)—鈉、雙草醚(bispyribac-sodium)、嘧草 醚(pyriminobac-methyl)、嚼 B定膀草醚(pyribenzoxim )、環酯草醚(pyriftalid )或喃 D定沙方(pyrimisulfan ) (KUH-021)、磺醯胺羰基三唑啉酮類型例如氟酮磺隆( flucarbazone)或丙苯磺隆(procarbazone)—鈉、和其他 例如嘉磷塞(glyphosate )、嘉磷塞一銨、嘉磷塞—異丙 胺、硫復松(sulfosate)、固殺草(glufosinate)、固殺 草(glufosinate-ammonium )和必那松(bilanafos)。 (8 )該等咸信藉由抑制植物之細胞有絲分裂而顯示 除草效果者,例如二硝基苯胺類型例如三福林( trifluralin )、黃草消(oryzalin )、滅殺草(nitralin )、 施得圃(pendimethalin)、依沙氟林(ethalfluralin)、 -18- (16) (16)200803736 倍尼芬(benfluralin)或氨氟樂靈(prodiamine)、醯胺 類型例如地散磷(bensulide)、拿普醯胺(napronamide )或拿草特(pronamide )、有機磷類型例如安米羅松( amiprofos)—甲基、抑草磷(butamifos)、莎稗磷( anilofos)或哌草磷(piperophos)、苯基胺甲酸酯類型例 如苯胺靈(propham)、氯苯胺靈(chlorpropham)或燕 麥靈(barban)、異丙苯基胺類型例如殺草隆(daimuron )、草隆(cumyluron)或溴芬諾(bromobutide)、和其 他例如亞速爛(asulam)、汰硫草(dithiopyr)、噻草啶 (thiazopyr)、哩草胺(cafenstrole)和草酮(indanofan )° (9 )該等咸信藉由抑制植物之蛋白質生物合成或脂 質生物合成顯示除草效果者,例如氯乙醯胺類型例如拉草 (alachlor)、滅草胺(metazachlor) 、丁 基拉草( butachlor)、普拉草(pretilachlor)、莫多草( metolachlor) 、S-莫多草(metolachlor)、欣克草( thenylchlor)、佩索殺米(pethoxamid)、乙草胺( acetochlor)、毒草胺(propachlor)或異丙草胺( propisochlor)、胺甲酸酯類型例如稻得壯(molinate)、 峨草丹(dimepiperate)或稗草畏(pyributicarb)、和其 他例如乙氧苯草胺(etobenzanid)、滅芬草(mefenacet )、氟噻草胺(flufenacet)、曲地吩(tridiphane)、四 口坐草胺(fentrazamide) 、B惡嗪草酮(oxaziclomefone)、 汰草滅(dimethenamid)和呋草黃(benfuresate)。 -19- (17) (17)200803736 (10 )硫代胺甲酸酯類型例如EPTC、拔敵草( butylate)、萬隆(vernolate)、克草敵(pebulate)、草 滅特(cycloate)、卞草丹(prosulfocarb)、戊草丹( esprocarb )、殺丹(thiobencarb )、燕麥敵(dial late ) 或野麥畏(triallate)、和其他例如MSMA、DSMA、安豆 得歐(endothall)、卩坐草定(ethofumesate)、氯酸鈉、 壬酸、殺木鱗(fosamine)、匹諾沙得(pinoxaden)和 HOK-201。 (11)該等咸信藉由寄生在植物上而顯示除草效果者 ,例如野菜黃單胞桿菌(Xanthomonas campestris)、 Epicoccosurus nematosurus、尖角突臍胞菌(Exserohilum monoseras )和 Dr echsr el a monoceras ° 本發明之除草組成物可藉由根據農業化學品之習知調 配方法混合式(I )之化合物或其鹽,和化合物(B ),作 爲有效成分,與各種添加劑而製得,且以各種調配物之形 式施用例如粉劑、粒劑、水分散性粒劑、可溼性粉劑、銘 劑、九劑、膠囊(包括水溶性薄膜包裝之調配物)、水-基懸浮液、油-基懸浮液、微乳液、懸乳劑( suspoemulsions)、水溶性粉劑、乳劑、可溶性濃縮物或 糊劑。其可被形成通常使用於此領域的任何調配物,只要 因此符合本發明之目的。 於調配時,式(I )之化合物或其鹽和化合物(B )爲 了調配可被混合在一起,或它們可分開地調配且在施用時 混合在一起。 -20- (18) (18)200803736 欲使用於調配之添加劑包括(例如)固體載體例如矽 藻土、熟石灰、碳酸鈣、滑石、白碳、高嶺土、膨潤土、 高嶺土和絹雲母之混合物、黏土、碳酸鈉、碳酸氫鈉、芒 硝、沸石或澱粉;溶劑例如水、甲苯、二甲苯、溶劑油、 二噁烷、丙酮、異佛酮、甲基異丁基酮、氯苯、環己烷、 二甲亞》、N,N —二甲基甲醯胺、二甲基乙醯胺、N—甲 基- 2 -吡咯啶酮或醇;陰離子界面性劑例如脂肪酸之鹽 、苯甲酸鹽、聚羧酸鹽、烷基硫酸酯之鹽、硫酸烷酯、硫 酸烷芳鹽、烷基二乙二醇醚硫酸酯、醇硫酸酯之鹽、磺酸 烷酯、磺酸烷芳酯、磺酸芳酯、木質素磺酸鈉、烷基二苯 基醚二磺酸鹽、聚苯乙烯磺酸鹽、烷基磷酸酯之鹽、磷酸 烷芳酯、磷酸苯乙烯基芳酯、聚氧乙烯烷基醚硫酸酯之鹽 、聚氧乙烯烷芳基醚硫酸鹽、聚氧乙烯烷基芳基醚硫酸酯 之鹽、聚氧乙烯烷基醚磷酸鹽、聚氧乙烯烷芳基磷酸酯之 鹽、聚氧乙烯芳基醚憐酸酯之鹽、與甲醛縮合之萘磺酸或 與甲醛縮合之烷基萘磺酸鹽;非離子界面活性劑例如山梨 醇酐脂肪酸酯、甘油脂肪酸酯、脂肪酸聚甘油酯、脂肪酸 醇聚乙二醇醚、乙炔二醇、乙炔醇、氧化烯嵌段聚合物、 聚氧乙烯烷基醚、聚氧乙烯烷芳基醚、聚氧乙烯苯乙烯基 芳基醚、聚氧乙烯二醇烷基醚、聚乙二醇、聚氧乙烯脂肪 酸酯、聚氧乙烯山梨醇酐脂肪酸酯、聚氧乙烯甘油脂肪酸 酯、聚氧乙烯氫化蓖麻油或聚氧丙烯脂肪酸酯,·和蔬菜油 或礦物油例如橄欖油、木棉花油、蓖麻油、棕櫚油、山茶 油、椰子油、芝麻油、玉米油、米糠油、花生油、棉籽油 -21 - 200803736 (19) 、大_a油、油菜好油、亞麻仁油、桐油或液態石躐。這些 添加劑可適合地選擇單獨使用或以其之二個或更多之混合 物組合使用’只要符合本發明之目的。進一步地,可適當 地選擇使用除了上述之外的該等此領域已知的添加劑。例 如,可使用各種常用添加劑,例如塡充劑、增稠劑、抗沉 降劑、防凍劑、分散安定劑、保護劑(safener )、防霉劑 、發泡劑、崩解劑和粘合劑。在本發明之除草組成物中之 有效成分對該各種添加劑的重量混合比可爲從0.001 : 99.999 至 95: 5,較佳從 0.005: 99.995 至 90: 10° 作爲一種施用本發明之除草組成物的方法,視各種絛 件例如施用位置、調配物、欲控之植物的類型或生長情況 而可使用和適當地選擇使用各種方法。例如,可提及下列 方法。 1 ·混合式(I )之化合物或其鹽,和化合物(B )以 製備一種調配物,其係以其本身施用。 2.混合式(Ο之化合物或其鹽,和化合物(B )以 製備一種調配物,其用例如水稀釋至所預定之濃度且如果 需要,加入各種添加劑(界面活性劑、蔬菜油、礦物油、 等等),接著施用。 3 ·分開地調配式(I )之化合物或其鹽,和化合物( B )且如所調配的施用。 4 ·分開地調配式(I )之化合物或其鹽,和化合物( B )及分別地用例如水稀釋至所預定之濃度且如果需要, 加入各種添加劑(界面活性劑、蔬菜油、礦物油、等等) -22· (20) (20)200803736 ,接著施用。 5 ·分開地調配式(I )之化合物或其鹽,和化合物( B )及然後於用例如水稀釋至所預定之濃度時混合,且如 果需要,加入各種添加劑(界面活性劑、蔬菜油、礦物油 、等等),接著施用。 現在,將例示本發明之一些較佳體系。然而,本發明 絕不限制於其。 (1) 一種除草組成物,其包含(A) —種式(I)之 化合物,和(B)至少一種選自由(B1.1)滅芬草( mefenacet ) (Β1·2)四 Π坐草胺(fentrazamide)和( B1.3) B惡嗪草酮(oxaziclomefone)組成之群組的化合物 ,其顯示細胞分裂抑制作用,作爲有效成分;和一種控制 不需要的植物或抑制其生長之方法,其包含施用除草有效 量之該類除草組成物。 (2 ) —種控制不需要的植物或抑制其生長之方法, 其包含施用除草有效量之(A) —種式(I)之化合物或其 鹽,和除草有效量之(B )至少一種選自由(B 1 · 1 )滅芬 草(mefenacet) 、 (B1.2)四口坐草胺(fentrazamide)和 (Β1·3)噁嗪草酮(oxaziclonlefone)組成之群組的化合 物,其顯示細胞分裂抑制作用。 (3) —種除草組成物,其包含(A) —種式(I)之 化合物或其鹽’和(B) (B2.1)克普草(clomeprop), 其顯示生長素生物合成抑制作用,作爲有效成分;和一種 控制不需要的植物或抑制其生長之方法,其包含施用除草 -23- (21) (21)200803736 有效量之該類除草組成物。 (4 ) 一種控制不需要的植物或抑制其生長之方法, 其包含施用除草有效量之(A) —種式(I)之化合物或其 鹽,和除草有效量之(B) (B2.1)克普草(clomeprop) ,其顯示生長素生物合成抑制作用。 【實施方式】 實例 現在,將描述本發明之除草組成物的調配例,但本發 明絕不限制於其。 調配例1 (1) 化合物A2 0.45克 (2) 化合物(B 1.1 ) 20.62 克
(3) 與甲醛縮合之萘磺酸鈉(商標名:Lavelin FA-N,由第一工業製藥株式會社(DAI-ICHI KOGYO SEIYAKU CO·,LTD)製造) 3.00 克 (4) 二烷基萘磺酸鈉(商標名:NK.BX-C,由 TAKEMOTO OIL & FAT股份有限公司製造)3.00克 (5) 黏土 72.93 克 以上述混合比例混合上述成分和然後用離心磨機(具 有1.0 mm之直徑的篩子)磨碎以獲得可溼性粉劑。 -24- (22) (22)200803736 調配例2 > (1) 化合物A2 1.12克 (2) 化合物(B1.2) 15.79 克 (3) LavelinFA-N (與上述相同) 3.00 克 (4) NK.BX-C (與上述相同) 3.00克 (5) 白碳(商標名·· Carplex #8〇,由DSL·日本股份 有限公司製造) 10.00克 (6) 黏土 67.09 克 以上述混合比例混合上述成分和然後用離心磨機(具 有1 · 0 mm之直徑的篩子)磨碎以獲得可溼性粉劑。 調配例3 (1) 化合物A2 0.75克 (2) 化合物(B1.2) 10.52 克 (3) 聚氧乙烯苯乙烯基苯基醚和十二基苯磺酸鈣 (商標名:Sorpol 3661S,由TOHO化學工業股 份有限公司製造) 15.00克
(4) 芳族烴(商標名:Solvesso 150,由 EXXON 化學品公司製造) 23.73克 (5) N-甲基-2-吡咯啶酮 50.00克 於室溫下將化合物A2和化合物(B1.2)溶解在N-甲基- 2 -吡咯啶酮中,和然後以上述混合比例混合 -25- (23) (23)200803736
Solvesso 150 和 Sorpol 3661S 以獲得乳劑。 調配例4 (1)化合物A2 2.24 克 (2)化合物(B1.3) 8.42 克 (3)Lavelin FA-N(與上述相同) 3.00 克 (4)NK.BX-C(與上述相同) 3.00 克 (5)黏土 83.34 克 以上述混合比例混合上述成分和然後用離心磨機(具 有1.0 mm之直徑的篩子)磨碎以獲得可溼性粉劑。 調配例5 (1)化合物A1 0.45 克 (2)化合物(B1.1) 20.62 克 (3)Lavelin FA-N(與上述相同) 3.00 克 (4)NK.BX-C(與上述相同) 3.00 克 (5)黏土 72.93 克 以上述混合比例混合上述成分和然後用離心磨機(具 有1.0 mm之直徑的篩子)磨碎以獲得可溼性粉劑。 -26- (24) (24)200803736 調配例6 (1)化合物A1 1.12 克 (2)化合物(B1.2) 1 5.79 克 (3)Lavelin FA-N(與上述相同) 3 · 00 克 (4)NK.BX-C(與上述相同) 3 · 00 克 (5)Carplex #80(與上述相同) 10.00 克 (6)黏土 6 7 · 0 9 克 以上述混合比例混合上述成分和然後用離心磨機(具 有1.0 mm之直徑的篩子)磨碎以獲得可溼性粉劑。 調配例7 (1)化合物A1 0.75 克 (2)化合物(B1.2) 10.52 克 (3)Sorpol 3 66 1 S (與上述相同) 15.00 克 (4)Solvesso 150 (與上述相同) 23.73 克 (5)Ν·甲基-2-吡咯啶酮 50.00 克 於室溫下將化合物A 1和化合物(B 1 · 2 )溶解在N -甲基- 2 -吡咯啶酮中,和然後以上述混合比例混合 Solvesso 150 和 Sorpol 3661S 以獲得乳劑。 調配例8 (1)化合物A1 2.24克 -27- (25) (25)200803736 (2)化合物(B1.3) 8.42 克 (3)Lavelin FA-N(與上述相同) 3.00 克 (4)NK.BX-C(與上述相同) 3.00 克 (5)黏土 8 3.3 4 克 以上述混合比例混合上述成分和然後用離心磨機(具 有1.0 mm之直徑的篩子)磨碎以獲得可溼性粉劑。 調配例9 (1)化合物A2 〇·22 克 (2)化合物(B2.1) 3· 12 克 (3)NK.BX-C(與上述相同) 3.00 克 (4)烷基萘磺酸鈉(商標名:NK.WG-1,由 ΤΑΚΕΜΟΤΟ OIL & FAT股份有限公司製造) 3.00 克 (5)膨潤土 40.00 ^ (6)碳酸鈣 50.66 克 以上述混合比例混合上述成分和然後用離心磨機(具 有1 · 0 mm之直徑的筛子)磨碎。然後磨碎之混合物與水 捏合和用安裝具有1.2 mm之直徑的篩子之擠製機製粒。 藉由設定於60°C之流體化床乾燥器乾燥製粒之產物30分 鐘和然後過篩(以形成1 2至2 4網目)以獲得粒劑。 -28 - 200803736 (26) 調配例1 〇 (1)化合物A 1 〇·22 克 (2)化合物(B2.1) 3.12 克 (3)NK.BX-C(與上述相同) 3.00 克 (4)NK.WG-1(與上述相同) 3.00 克 (5)膨潤土 40.00 克 (6)碳酸鈣 50.66 克 以上述混合比例混合上述成分和然後用離心磨機(具 有1 · 0 mm之直徑的篩子)磨碎。然後磨碎之混合物與水 捏合和用安裝具有1.2 mm之直徑的篩子之擠製機製粒。 藉由設定於60°C之流體化床乾燥器乾燥製粒之產物30分 鐘和然後過篩(以形成1 2至24網目)以獲得粒劑。 測試例1 將水田土壤放進1 / 1 0,0 0 0公畝盆子中,和播種稗( 稗草(Echinochloa oryzicola vasing))的種子且留置在 3 · 5公分之水深度的灌溉條件下。當稗到達2.8至3.2葉 階段,分別地用水稀釋化合物A2和化合物(B1.1 )之可 溼性粉劑且在浸沉條件下施用以使有效成分分別地變成所 規定的量。在施用後第1 9天,目視觀察生長的狀態,和 根據下列評估標準評估之生長抑制率(% )(觀察値)和 以上述Colby方法計算之生長抑制率(% )(預期値)顯 不在表1。 -29- (27) 200803736 生長抑制率(%) = 0% (等於非處理區)至100%(完全殺死) 表1 化合物 有效成分之施用量(g/a) 生長抑制率(%) 觀察 預期 A2 0.165 73 0.11 68 0.083 55 (B1.1) 10 65 5 40 A2 + (B 1 .1) 0.165+10 100 90 0.165 + 5 100 84 0.11 + 10 100 89 0.11+5 100 8 1 0.083+10 95 84 0.08 3 + 5 94 73 測試例2 將水田土壤放進1/1〇,〇〇〇公畝盆子中,和播種稗( 稱草(Echinochloa oryzicola vasing))的種子且留置在 3.5公分之水深度的灌溉條件下。當稗到達2 · 8至3.2葉 階段,用水稀釋化合物A2之可溼性粉劑和化合物(B 1.2 )之乳劑且在浸沉條件下施用以使有效成分分別地變成所 規定的量。在施用後第1 9天,以與上述測試例1中相同 -30- (28) 200803736 之方法目視觀察和評估生長的狀態。結果顯示在表2中。 表2 化合物 有效成分之施用量(g/a) 生長抑制率(%) 觀察 預期 A2 0.165 73 塞 0.1 1 68 _ 0.083 55 _ (B 1.2) 3 65 1.5 30 A2 + (B 1.2) 0.165 + 3 99 90 0.165 + 1.5 100 8 1 0.11+3 99 89 0.11 + 1.5 100 77 0.08 3 + 3 95 84 0.08 3 + 1 .5 94 69 測試例3 將水田土壤放進1/1 0,000公畝盆子中,和播種稗( 稗草(Echinochloa oryzicola vasing))的種子且留置在 3.5公分之水深度的灌溉條件下。當稗到達2.8至3.2葉 階段,分別地用水稀釋化合物A2和化合物(B 1 . 3 )之可 溼性粉劑且在浸沉條件下施用以使有效成分分別地變成所 規定的量。在施用後第1 9天,以與上述測試例1中相同 -31 - (29) 200803736 之方法目視觀察和評估生長的狀態。結果顯示在表3 ψ 表3 化合物 有效成分之施用 1---- 生長抑制率(%) 量(g/a) 觀察 預期 A2 0.165 73 0.11 68 0.083 55 (B1.3) 0.8 30 0.4 5 A2 + (B1 .3) 0.165 + 0.8 95 81 0.165 + 0.4 92 74 0.11+0.8 100 77 0.11+0.4 90 69 0.083 + 0.8 90 69 0.083 + 0.4 83 57 測試例4 將水田土壤放進1 /1 0,000公畝盆子中,和播種稗( 稗草(Echinochloa oryzicola vasing))的種子且留置在 3 · 5公分之水深度的灌溉條件下。當稗到達2.7至3 . 1葉 階段,分別地用水稀釋化合物A 1和化合物(B 1 . 1 )之可 溼性粉劑且在浸沉條件下施用以使有效成分分別地變成所 規定的量。在施用後第2 1天,以與上述測試例1中相同 -32- (30) 200803736 之方法目視觀察和評估生長的狀態。結果顯示在表4中。 表4 化合物 有效成分之施用量(g/a) 生長抑f 率(%) 觀察 預期 A1 0.165 70 0.11 70 0.083 60 (B1.1) 10 40 5 35 Α1+(Β1.1) 0.165+10 85 82 0.165+5 88 8 1 0.11 + 10 85 82 0.11+5 85 8 1 0.083+10 99 76 0.083+5 85 74 測試例5 將水田土壤放進1/1〇,〇〇〇公畝盆子中,和播種稗( 稗草(Echinochloa oryzicola vasing))的種子且留置在 3 · 5公分之水深度的灌槪條件下。當稗到達2.7至3 . 1葉 階段,分別地用水稀釋化合物A 1之可溼性粉劑和化合物 (B 1.2 )之乳劑且在浸沉條件下施用以使有效成分分別地 變成所規定的量。在施用後第2 1天,以與上述測試例1 •33- (31) (31)200803736 中相同之方法目視觀察和評估生長的狀態。結果顯示在表 5中。 表5 化合物 有效成分之施用量(g/a) 生長抑f 則率(%) 觀察 預期 A1 0.165 70 0.11 70 0.083 60 (B1.2) 3 40 1.5 30 A1 +(B 1.2) 0.165 + 3 85 82 0.165 + 1.5 90 79 0.11+3 85 82 0.11 + 1.5 88 79 0.083 + 3 100 76 0.08 3 + 1.5 85 72 測試例6 將水田土壤放進1 /1 0,0 0 0公畝盆子中,和播種稗( 稗草(Echinochloa oryzicola vasing))的種子且留置在 3 · 5公分之水深度的灌溉條件下。當稗到達2.7至3 . 1葉 階段,分別地用水稀釋化合物A 1和化合物(B 1 . 3 )之可 溼性粉劑且在浸沉條件下施用以使有效成分分別地變成所 -34- (32) 200803736 規定的量。在施用後第2 1天,以與上述測試例!中相同 之方法目視觀察和評估生長的狀態。結果顯示在表6中。 表6 化合物 有效成分之施用量(g/a) 生長抑3 _ (%) 觀察 預期 A1 0.165 68 (B1.3) 0.8 60 0.4 55 Α1+(Β1·3) 0.165 + 0.8 88 87 0.165 + 0.4 95 86 測試例7 將水田土壤放進1/10,〇〇〇公畝盆子中,和播種稗( 稗草(Echinochloa oryzicola vasing))的種子且留置在 3.5公分之水深度的灌溉條件下。當稗到達2.7至3.1葉 階段,分別地用水稀釋化合物A 1之可溼性粉劑和化合物 (B2.1 )之粒劑且在浸沉條件下施用以使有效成分分別地 變成所規定的量。在施用後第2 1天,以與上述測試例1 中相同之方法目視觀察和評估生長的狀態。結果顯示在表 7中。 -35- (33) (33)200803736 表7 化合物 有效成分之施用量(g/a) 生長抑€ 則率(%) 觀察 預期 A1 0.165 70 0.11 70 0.083 60 (B2.1) 3 20 1.5 20 Α1+(Β2·1) 0.165 + 3 85 76 0.165+1.5 85 76 0.11+3 80 76 0.11 + 1.5 83 76 0.08 3 + 1 .5 80 68 測試例8 將水田土壤放進1/1〇,〇〇〇公畝盆子中,和播種稗( 稗草(Echinochloa oryzicola vasing))的種子且留置在 3.5公分之水深度的灌溉條件下。當稗到達2.7至3 · 1葉 階段,分別地用水稀釋化合物A2之可溼性粉劑和化合物 (B2.1 )之粒劑且在浸沉條件下施用以使有效成分分別地 變成所規定的量。在施用後第2 1天,以與上述測試例1 中相同之方法目視觀察和評估生長的狀態。結果顯示在表 8中。 -36- 200803736 (34) 表8 化合物 有效成分之施用量(g/a) 生長抑制率(%) 觀察 預期 A2 0.165 80 0.11 80 0.083 45 (B2.1) 3 20 1 .5 20 A2 + (B2.1 ) 0.165+3 85 84 0.165 + 1 .5 88 84 0.11+3 88 84 0.08 3 + 1.5 80 56 -37-
Claims (1)
- 200803736 (1) 十、申請專利範圍 I 一種除草組成物,其包含(A ) —種式(I )之化 含物:其中 R爲氫原子或- COCH2OCH3,或其鹽,和(B) 至少一^種選自由(B1.1)滅芬草(mefenacet) 、( B 1.2 ) 四哗草胺 (fentrazamide) 、 (Β1·3)卩惡嗪草酮 ( oxaziclomefone )和(B2.1)克普草(clomeprop)或其鹽 組成之群組的化合物,作爲有效成分。 2 ·根據申請專利範圍第1項之除草組成物,其進一 步包含另一除草活性成分。 3. 根據申請專利範圍第1項之除草組成物,其中(B )之化合物爲至少一種選自由(B1.1)滅芬草(mefenacet )、(Β1·2 )四唑草胺(fentrazamide )和(B1.3 )噁嗪 草酮(oxaziclomefone )組成之群組的化合物,其顯示細 胞分裂抑制作用。 4. 根據申請專利範圍第1項之除草組成物,其中(B )之化合物爲(Β2· 1 )克普草(clomeprop ),其顯示生 長素生物合成抑制作用。 •38- 200803736 (2) 5. 一種控制不需要的植物或抑制其生長之方法’其 包含施用除草有效量之如申請專利範圍第1項中所定義之 除草組成物。 6. 一種控制不需要的植物或抑制其生長之方法,其 ' 包含施用除草有效量之如申請專利範圍第2項中所定義之 ‘ 除草組成物。 ^ 7. —種控制不需要的植物或抑制其生長之方法,其 包含施用除草有效量之(A)之化合物或其鹽,和(B)之 化合物,該二者爲如申請專利範圍第1項中所定義。 8 · —種控制不需要的植物或抑制其生長之方法,其 包含施用除早有效量之(A)之化合物或其鹽,和(B)之 化合物’該二者爲如申請專利範圍第1項中所定義,和另 一除草活性成分。 -39- 200803736 七、指定代表圓: (一) 、本案指定代表圓為:無 (二) 、本代表圖之元件代表符號簡單說明:無 八、本案若有化學式時,請揭示最能顯示發明特徵的 化學式:無 -3-
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| 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 |
| CN102308829A (zh) * | 2011-10-11 | 2012-01-11 | 合肥星宇化学有限责任公司 | 一种稻田除草组合物及其制剂 |
| KR102015314B1 (ko) * | 2011-10-14 | 2019-08-28 | 구미아이 가가쿠 고교 가부시키가이샤 | 제초제 조성물 |
| 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 |
| CN103058782B (zh) * | 2013-01-31 | 2015-10-28 | 广西乐土生物科技有限公司 | 含苄嘧·苯噻酰的除草杀虫药肥及其生产方法 |
| CN103766367A (zh) * | 2013-12-09 | 2014-05-07 | 广东中迅农科股份有限公司 | 一种含有噁嗪草酮和氟吡磺隆的除草组合物 |
| CN104094955A (zh) * | 2014-06-25 | 2014-10-15 | 广东中迅农科股份有限公司 | 一种含有氟吡磺隆和异噁草松的除草组合物 |
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| Publication number | Publication date |
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| KR101261664B1 (ko) | 2013-05-06 |
| WO2007032532A2 (en) | 2007-03-22 |
| JP2012056959A (ja) | 2012-03-22 |
| CN101262771A (zh) | 2008-09-10 |
| CN101262771B (zh) | 2012-01-18 |
| WO2007032532A3 (en) | 2007-10-25 |
| JP5391255B2 (ja) | 2014-01-15 |
| KR20080047386A (ko) | 2008-05-28 |
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