JP2009524597A5 - - Google Patents
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- JP2009524597A5 JP2009524597A5 JP2008547895A JP2008547895A JP2009524597A5 JP 2009524597 A5 JP2009524597 A5 JP 2009524597A5 JP 2008547895 A JP2008547895 A JP 2008547895A JP 2008547895 A JP2008547895 A JP 2008547895A JP 2009524597 A5 JP2009524597 A5 JP 2009524597A5
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- alcohol
- methyl
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- ester
- composition
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- 239000000203 mixture Substances 0.000 claims 21
- -1 2,6-diethyl-4-methyl-phenyl Chemical group 0.000 claims 15
- WVDDGKGOMKODPV-UHFFFAOYSA-N benzyl alcohol Chemical group OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 8
- 230000002363 herbicidal Effects 0.000 claims 8
- 239000004009 herbicide Substances 0.000 claims 6
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-Ethylhexanol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 claims 4
- IUGYQRQAERSCNH-UHFFFAOYSA-N Pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 claims 4
- KBPLFHHGFOOTCA-UHFFFAOYSA-N octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 claims 4
- 239000003799 water insoluble solvent Substances 0.000 claims 4
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-Methyl-2,4-pentanediol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 claims 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 3
- 235000019445 benzyl alcohol Nutrition 0.000 claims 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-N (E)-but-2-enedioate;hydron Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N Adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N Diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 claims 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N Dodecanol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 claims 2
- XPFVYQJUAUNWIW-UHFFFAOYSA-N Furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 claims 2
- JFCQEDHGNNZCLN-UHFFFAOYSA-N Glutaric acid Chemical compound OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 claims 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims 2
- BSYVTEYKTMYBMK-UHFFFAOYSA-N Tetrahydro-2-furanmethanol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 claims 2
- 239000001089 [(2R)-oxolan-2-yl]methanol Substances 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 150000007513 acids Chemical class 0.000 claims 2
- 239000003995 emulsifying agent Substances 0.000 claims 2
- 235000019387 fatty acid methyl ester Nutrition 0.000 claims 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 claims 2
- MZHCENGPTKEIGP-RXMQYKEDSA-N (R)-dichlorprop Chemical compound OC(=O)[C@@H](C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-RXMQYKEDSA-N 0.000 claims 1
- WNTGYJSOUMFZEP-SSDOTTSWSA-N (R)-mecoprop Chemical compound OC(=O)[C@@H](C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-SSDOTTSWSA-N 0.000 claims 1
- VJYIFXVZLXQVHO-UHFFFAOYSA-N 1-(2-chlorophenyl)sulfonyl-3-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)urea Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)Cl)=N1 VJYIFXVZLXQVHO-UHFFFAOYSA-N 0.000 claims 1
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N 1-Hexanol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 claims 1
- XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 claims 1
- CGNBQYFXGQHUQP-UHFFFAOYSA-N 2,3-dinitroaniline Chemical class NC1=CC=CC([N+]([O-])=O)=C1[N+]([O-])=O CGNBQYFXGQHUQP-UHFFFAOYSA-N 0.000 claims 1
- 239000005631 2,4-D Substances 0.000 claims 1
- MAYMYMXYWIVVOK-UHFFFAOYSA-N 2-[(4,6-dimethoxypyrimidin-2-yl)carbamoylsulfamoyl]-4-(methanesulfonamidomethyl)benzoic acid Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(CNS(C)(=O)=O)C=2)C(O)=O)=N1 MAYMYMXYWIVVOK-UHFFFAOYSA-N 0.000 claims 1
- IEGRLEZDTRNPRH-UHFFFAOYSA-N 2-hydroxyiminocyclohexan-1-one Chemical class ON=C1CCCCC1=O IEGRLEZDTRNPRH-UHFFFAOYSA-N 0.000 claims 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims 1
- LOQQVLXUKHKNIA-UHFFFAOYSA-N 3-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]thiophene-2-carboxylic acid Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C2=C(SC=C2)C(O)=O)=N1 LOQQVLXUKHKNIA-UHFFFAOYSA-N 0.000 claims 1
- MQWCXKGKQLNYQG-UHFFFAOYSA-N 4-methylcyclohexan-1-ol Chemical compound CC1CCC(O)CC1 MQWCXKGKQLNYQG-UHFFFAOYSA-N 0.000 claims 1
- 239000003666 Amidosulfuron Substances 0.000 claims 1
- CTTHWASMBLQOFR-UHFFFAOYSA-N Amidosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)N(C)S(C)(=O)=O)=N1 CTTHWASMBLQOFR-UHFFFAOYSA-N 0.000 claims 1
- 239000005711 Benzoic acid Substances 0.000 claims 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Natural products OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 1
- MRABAEUHTLLEML-UHFFFAOYSA-N Butyl lactate Chemical compound CCCCOC(=O)C(C)O MRABAEUHTLLEML-UHFFFAOYSA-N 0.000 claims 1
- 239000005496 Chlorsulfuron Substances 0.000 claims 1
- HUBANNPOLNYSAD-UHFFFAOYSA-N Clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 claims 1
- RWGFKTVRMDUZSP-UHFFFAOYSA-N Cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 claims 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N Cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 claims 1
- XCIXKGXIYUWCLL-UHFFFAOYSA-N Cyclopentanol Chemical compound OC1CCCC1 XCIXKGXIYUWCLL-UHFFFAOYSA-N 0.000 claims 1
- 239000005504 Dicamba Substances 0.000 claims 1
- IWEDIXLBFLAXBO-UHFFFAOYSA-N Dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims 1
- MZHCENGPTKEIGP-UHFFFAOYSA-N Dichlorprop Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-UHFFFAOYSA-N 0.000 claims 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N Dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 claims 1
- LZCLXQDLBQLTDK-UHFFFAOYSA-N Ethyl lactate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 claims 1
- 239000005529 Florasulam Substances 0.000 claims 1
- QZXATCCPQKOEIH-UHFFFAOYSA-N Florasulam Chemical compound N=1N2C(OC)=NC=C(F)C2=NC=1S(=O)(=O)NC1=C(F)C=CC=C1F QZXATCCPQKOEIH-UHFFFAOYSA-N 0.000 claims 1
- 239000005574 MCPA Substances 0.000 claims 1
- 239000005575 MCPB Substances 0.000 claims 1
- LLWADFLAOKUBDR-UHFFFAOYSA-N MCPB Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 claims 1
- WNTGYJSOUMFZEP-UHFFFAOYSA-N Mecoprop Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 claims 1
- 239000005576 Mecoprop-P Substances 0.000 claims 1
- 239000005577 Mesosulfuron Substances 0.000 claims 1
- 239000005591 Pendimethalin Substances 0.000 claims 1
- CHIFOSRWCNZCFN-UHFFFAOYSA-N Pendimethalin Chemical compound CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 claims 1
- XMIIGOLPHOKFCH-UHFFFAOYSA-N Phenylpropanoic acid Chemical compound OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 claims 1
- 239000005603 Prosulfocarb Substances 0.000 claims 1
- 239000005604 Prosulfuron Substances 0.000 claims 1
- LTUNNEGNEKBSEH-UHFFFAOYSA-N Prosulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)CCC(F)(F)F)=N1 LTUNNEGNEKBSEH-UHFFFAOYSA-N 0.000 claims 1
- 229940090121 Sulfonylureas for blood glucose lowering Drugs 0.000 claims 1
- 239000005619 Sulfosulfuron Substances 0.000 claims 1
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 claims 1
- 239000005626 Tribenuron Substances 0.000 claims 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 claims 1
- 239000005629 Tritosulfuron Substances 0.000 claims 1
- KGEKLUUHTZCSIP-FOGDFJRCSA-N [(1R,3R,4R)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] acetate Chemical compound C1C[C@@]2(C)[C@H](OC(=O)C)C[C@@H]1C2(C)C KGEKLUUHTZCSIP-FOGDFJRCSA-N 0.000 claims 1
- 239000001940 [(1R,4S,6R)-1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl] acetate Substances 0.000 claims 1
- 239000001361 adipic acid Substances 0.000 claims 1
- 235000011037 adipic acid Nutrition 0.000 claims 1
- 230000000240 adjuvant Effects 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 125000005907 alkyl ester group Chemical group 0.000 claims 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims 1
- 235000010233 benzoic acid Nutrition 0.000 claims 1
- 229940007550 benzyl acetate Drugs 0.000 claims 1
- 238000009835 boiling Methods 0.000 claims 1
- 239000001191 butyl (2R)-2-hydroxypropanoate Substances 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- OPGCOAPTHCZZIW-UHFFFAOYSA-N diethyl 1-(2,4-dichlorophenyl)-5-methyl-4H-pyrazole-3,5-dicarboxylate Chemical group CCOC(=O)C1(C)CC(C(=O)OCC)=NN1C1=CC=C(Cl)C=C1Cl OPGCOAPTHCZZIW-UHFFFAOYSA-N 0.000 claims 1
- 239000000839 emulsion Substances 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- MWKVXOJATACCCH-UHFFFAOYSA-N ethyl 5,5-diphenyl-4H-1,2-oxazole-3-carboxylate Chemical group C1C(C(=O)OCC)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 MWKVXOJATACCCH-UHFFFAOYSA-N 0.000 claims 1
- 229940116333 ethyl lactate Drugs 0.000 claims 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N fumaric acid Chemical compound OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims 1
- 239000001530 fumaric acid Substances 0.000 claims 1
- NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 claims 1
- 239000011976 maleic acid Substances 0.000 claims 1
- 101700021309 mcpB Proteins 0.000 claims 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N o-xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims 1
- IBBMAWULFFBRKK-UHFFFAOYSA-N picolinamide Chemical class NC(=O)C1=CC=CC=N1 IBBMAWULFFBRKK-UHFFFAOYSA-N 0.000 claims 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propanol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims 1
- NQLVQOSNDJXLKG-UHFFFAOYSA-N prosulfocarb Chemical compound CCCN(CCC)C(=O)SCC1=CC=CC=C1 NQLVQOSNDJXLKG-UHFFFAOYSA-N 0.000 claims 1
- 239000011780 sodium chloride Substances 0.000 claims 1
- 239000001384 succinic acid Substances 0.000 claims 1
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 claims 1
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Substances CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 1
- 125000003944 tolyl group Chemical group 0.000 claims 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 claims 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 claims 1
- 239000008096 xylene Substances 0.000 claims 1
Claims (18)
- 乳化剤及び水不溶性溶媒に加え、
a)2,2−ジメチル−プロピオン酸8−(2,6−ジエチル−4−メチル−フェニル)−9−オキソ−1,2,4,5−テトラヒドロ−9H−ピラゾロ[1,2−d][1,4,5]オキサジアゼピン−7−イルエステル及び
b)アルコール、
を含んで成り、当該アルコールが、プロパノール、ヘキサノール、オクタノール、ドデカノール、2−エチルヘキサノール、イソトリデカノール、ジプロピレングリコール、2−メチル−2,4−ペンタンジオール、フルフリルアルコール、テトラヒドロフルフリルアルコール、ベンジルアルコール、4−ヒドロキシ−4−メチル−2−ペンタノン、乳酸エチル、乳酸ブチル、シクロペンタノール又はシクロヘキサノールである、乳剤の形態の除草用組成物。 - アルコールとして、2−エチルヘキサノール、n−オクタノール、ベンジルアルコール、テトラヒドロフルフリルアルコール、2−メチル−2,4−ペンタンジオール、4−ヒドロキシ−4−メチル−2−ペンタノン又はシクロヘキサノールを含んで成る、請求項1に記載の組成物。
- アルコールとして、ベンジルアルコール、テトラヒドロフルフリルアルコール又は2−メチル−2,4−ペンタンジオールを含んで成る、請求項2に記載の組成物。
- 除草剤が3〜30重量%存在しており、当該除草剤が2,2−ジメチル−プロピオン酸8−(2,6−ジエチル−4−メチル−フェニル)−9−オキソ−1,2,4,5−テトラヒドロ−9H−ピラゾロ[1,2−d][1,4,5]オキサジアゼピン−7−イルエステル単独あるいは1又は複数の追加の除草剤との混合物である、請求項1〜3のいずれか1項に記載の組成物。
- 1〜97重量%の前記アルコールを含んで成る、請求項1〜4のいずれか1項に記載の組成物。
- 5〜50重量%の前記アルコールを含んで成る、請求項1〜4のいずれか1項に記載の組成物。
- 10〜30重量%の前記アルコールを含んで成る、請求項1〜4のいずれか1項に記載の組成物。
- 2〜30重量%の乳化剤を含んで成る、請求項1〜7のいずれか1項に記載の組成物。
- 前記アルコールと水不溶性溶媒の混合物を含んで成り、
前記水不溶性溶媒が、トルエン;キシレン;クメン;160〜180℃又は180〜210℃又は230〜290℃の沸点を有する芳香族炭化水素の混合物;脂肪族又は脂環式炭化水素;脂肪アルコールの酢酸塩;酢酸イソボルニル;酢酸ベンジル;マレイン酸、フマル酸、コハク酸、グルタル酸又はアジピン酸の低級アルキルエステル;安息香酸エステル;C 8 -C 10 脂肪酸メチルエステル;又はC 16 -C 18 脂肪酸メチルエステル、である、請求項2、3、6又は7に記載の組成物。 - 10〜70重量%の前記水不溶性溶媒を含んで成る、請求項9に記載の組成物。
- 1〜50重量%の2,2−ジメチル−プロピオン酸8−(2,6−ジエチル−4−メチル−フェニル)−9−オキソ−1,2,4,5−テトラヒドロ−9H−ピラゾロ[1,2−d][1,4,5]オキサジアゼピン−7−イルエステルを含んで成る、請求項1に記載の組成物。
- 2,2−ジメチル−プロピオン酸8−(2,6−ジエチル−4−メチル−フェニル)−9−オキソ−1,2,4,5−テトラヒドロ−9H−ピラゾロ[1,2−d][1,4,5]オキサジアゼピン−7−イルエステルと適合性のある、1又は複数の追加の除草剤を含んで成る、請求項2、3、6又は7に記載の組成物。
- スルホニルウレア、アリールオキシフェノキシプロピオナート、トリアゾロピリミジン、アリールカルボン酸、アリールオキシカルボン酸、シクロヘキサンジオンオキシム、チオカルバマート、ヒドロキシベンゾニトリル、ジニトロアニリン及びピリジンカルボキサミドから成る群から選択される、追加の除草剤を含んで成る、請求項12に記載の組成物。
- トリアスフロン、トリベヌロン、メツルフロン、チフェンスルフロン、フルピルスルフロン、クロルスルフロン、プロスルフロン、アミドスルフロン、メソスルフロン、スルフォスルフロン、トリトスルフロン、クロジナホッププロパルギル、フェノキサプロップ−P−エチル、ジクロホップメチル、シハロホップブチル、フロラスラム、メトスラム、フルメツラム、ジカンバ、クロピラリド、2,4−D、2,4−DP、メコプロップ、メコプロップ−P、MCPA、MCPB、ジクロルプロップ−P、フルオキシピルのエステル、トラルコキシジム、トリアラート、プロスルホカルブ、ブロモキシニル、ブロモキシニルオクタノアート、アイオキシニル、アイオキシニルオクタノアート、ペンジメタリン、トリフルラリン、及びジフルフェニカンから成る群から選択される、追加の除草剤を含んで成る、請求項12に記載の組成物。
- セーフナーを含んで成る、請求項1、2、3、6又は7に記載の組成物。
- クロキントセット−メキシル、メフェンピル−ジエチル又はイソキサジフェン−エチルを含んで成る、請求項15に記載の組成物。
- アジュバントを含んで成る、請求項1、2、3、6又は7に記載の組成物。
- 不所望な植物の生長を制御する方法であって、除草剤として有効量の請求項1、2、3、6又は7に記載の組成物を前記植物又はその場所に施与することを含んで成る方法。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH20752005 | 2005-12-27 | ||
CH2075/05 | 2005-12-27 | ||
PCT/EP2006/012539 WO2007073933A2 (en) | 2005-12-27 | 2006-12-27 | Herbicidal composition |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2009524597A JP2009524597A (ja) | 2009-07-02 |
JP2009524597A5 true JP2009524597A5 (ja) | 2011-11-24 |
JP5086272B2 JP5086272B2 (ja) | 2012-11-28 |
Family
ID=38080896
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2008547895A Active JP5086272B2 (ja) | 2005-12-27 | 2006-12-27 | 除草用組成物 |
Country Status (22)
Country | Link |
---|---|
US (3) | US10952437B2 (ja) |
EP (1) | EP1965646B1 (ja) |
JP (1) | JP5086272B2 (ja) |
CN (1) | CN101453894B (ja) |
AR (1) | AR058747A1 (ja) |
AT (1) | ATE460839T1 (ja) |
AU (1) | AU2006331031B2 (ja) |
BR (1) | BRPI0621268B1 (ja) |
CA (1) | CA2632323C (ja) |
DE (1) | DE602006013038D1 (ja) |
DK (1) | DK1965646T3 (ja) |
EA (1) | EA018654B1 (ja) |
ES (1) | ES2341891T3 (ja) |
MA (1) | MA30087B1 (ja) |
PL (1) | PL1965646T3 (ja) |
PT (1) | PT1965646E (ja) |
SA (1) | SA06270491B1 (ja) |
SI (1) | SI1965646T1 (ja) |
TN (1) | TNSN08282A1 (ja) |
UA (1) | UA92512C2 (ja) |
WO (1) | WO2007073933A2 (ja) |
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EP1891855A1 (de) * | 2006-08-05 | 2008-02-27 | Bayer CropScience AG | Neue Mikroemulsionskonzentrate |
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JP5181592B2 (ja) * | 2007-09-14 | 2013-04-10 | 住友化学株式会社 | 除草用組成物 |
JP2009067740A (ja) * | 2007-09-14 | 2009-04-02 | Sumitomo Chemical Co Ltd | 除草用組成物 |
JP5353120B2 (ja) * | 2007-09-14 | 2013-11-27 | 住友化学株式会社 | 除草用組成物 |
US10307862B2 (en) | 2009-03-27 | 2019-06-04 | Electro Scientific Industries, Inc | Laser micromachining with tailored bursts of short laser pulses |
PL2672826T3 (pl) | 2011-02-11 | 2015-10-30 | Basf Se | Kompozycje chwastobójcze zawierające topramezon, pinoksaden i klokwintocet |
CA2835187A1 (en) | 2011-05-06 | 2012-11-15 | Syngenta Participations Ag | Herbicidal composition comprising pinoxaden and fluroxypyr, and methods of use thereof |
CN102326562A (zh) * | 2011-05-27 | 2012-01-25 | 陕西韦尔奇作物保护有限公司 | 一种含唑草酮与唑啉草酯的除草组合物 |
CN102283217B (zh) * | 2011-06-27 | 2014-08-13 | 陕西美邦农药有限公司 | 一种含双氟磺草胺与唑啉草酯的除草组合物 |
GB201115564D0 (en) | 2011-09-08 | 2011-10-26 | Syngenta Ltd | Herbicidal composition |
BR112014019372B1 (pt) * | 2012-02-27 | 2022-08-23 | Huntsman Corporation Australia Pty Limited | Formulação, e, método de obtenção de uma formulação |
JP6315702B2 (ja) * | 2012-02-27 | 2018-04-25 | ハンツマン・コーポレーシヨン・オーストラリア・ピーテイワイ・リミテツド | 農薬乳化性濃厚調剤 |
US10314305B2 (en) * | 2012-10-19 | 2019-06-11 | Syngenta Participations Ag | Liquid agrochemical compositions comprising a polymeric thickener and an alcohol-containing solvent system, and liquid herbicidal compositions having an alcohol-containing solvent system |
CN104585188B (zh) * | 2014-12-22 | 2018-06-19 | 广东中迅农科股份有限公司 | 含有氟氯吡啶酯和吡草醚以及唑啉草酯的除草组合物 |
HUE044475T2 (hu) * | 2014-12-22 | 2019-10-28 | Mitsui Agriscience Int S A /N V | Tribenuron-tartalmú folyékony herbicid kompozíciók |
CN104920396A (zh) * | 2015-06-01 | 2015-09-23 | 安徽华星化工有限公司 | 一种含唑啉草酯与吡草醚的除草组合物 |
CN104982450A (zh) * | 2015-07-10 | 2015-10-21 | 广东中迅农科股份有限公司 | 含有甲基二磺隆和唑啉草酯以及双氟磺草胺的农药组合物 |
CN105580820A (zh) * | 2016-02-24 | 2016-05-18 | 陕西上格之路生物科学有限公司 | 一种含三甲苯草酮和唑啉草酯的除草组合物 |
WO2018013721A1 (en) | 2016-07-12 | 2018-01-18 | Monsanto Technology Llc | Pesticidal compositions |
CN106538558B (zh) * | 2016-10-13 | 2018-10-16 | 北京明德立达农业科技有限公司 | 一种除草剂组合物及其应用 |
AU2018209803B2 (en) | 2017-01-23 | 2023-09-21 | Syngenta Participations Ag | Method of controlling weeds in warm season turfgrass |
CN109757478A (zh) * | 2017-11-09 | 2019-05-17 | 山东润博生物科技有限公司 | 一种麦草畏型乳油及其制备方法 |
KR102064661B1 (ko) * | 2018-03-14 | 2020-01-09 | 장인국 | 적화용 조성물 및 이를 이용한 적화 방법 |
CA3135509C (en) | 2019-04-01 | 2023-10-03 | Oriental (Luzhou) Agrochemicals. Co., Ltd. | Conjugated triene compound, and preparation and application thereof |
CN111372914B (zh) | 2019-04-01 | 2022-09-23 | 泸州东方农化有限公司 | 一种卤代共轭二烯类化合物及其制备和应用 |
ES2936283T3 (es) * | 2019-07-18 | 2023-03-15 | Adama Agan Ltd | Formulación estable que comprende herbicidas |
WO2021012173A1 (en) * | 2019-07-23 | 2021-01-28 | Jiangsu Rotam Chemistry Co., Ltd. | Emulsifiable concentrate formulations and their uses |
WO2021205448A1 (en) | 2020-04-06 | 2021-10-14 | Adama Agan Ltd. | Co-crystals of antioxidants and active ingredients and use of antioxidants as stabilizer |
WO2021226566A1 (en) * | 2020-05-08 | 2021-11-11 | Cjb Applied Technologies, Llc | Pesticidal compositions and related methods |
WO2023066695A1 (en) * | 2021-10-22 | 2023-04-27 | Syngenta Crop Protection Ag | Herbicide transport system |
CN113663543B (zh) * | 2021-10-22 | 2022-02-01 | 苏州丰倍生物科技有限公司 | 一种难溶有机化合物的溶解方法和乳化方法 |
GB2621169A (en) * | 2022-08-05 | 2024-02-07 | Rotam Agrochem Int Co Ltd | Herbicidal composition and use thereof |
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DE3573511D1 (en) * | 1984-03-15 | 1989-11-16 | Ciba Geigy Ag | Use of quinoline derivatives to protect cultivated plants |
PH22836A (en) * | 1985-06-07 | 1989-01-19 | Ciba Geigy Ag | Herbicidal compositions |
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WO2000047585A1 (en) * | 1999-02-11 | 2000-08-17 | Novartis Ag | 3-hydroxy-4-aryl-5-pyrazoline derivatives as herbicides |
ATE260035T1 (de) * | 1999-09-07 | 2004-03-15 | Syngenta Participations Ag | Herbizides mittel |
EP1209972B1 (en) * | 1999-09-07 | 2003-05-28 | Syngenta Participations AG | Herbicidal composition |
AR031027A1 (es) * | 2000-10-23 | 2003-09-03 | Syngenta Participations Ag | Composiciones agroquimicas |
ES2258570T3 (es) * | 2000-12-04 | 2006-09-01 | Syngenta Participations Ag | Composiciones agroquimicas. |
GB0121580D0 (en) * | 2001-09-06 | 2001-10-24 | Syngenta Ltd | Novel compounds |
MXPA05008647A (es) * | 2003-03-13 | 2005-10-18 | Basf Ag | Mezclas herbicidas basadas en 3-feniluracilos. |
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- 2006-12-27 AT AT06841168T patent/ATE460839T1/de active
- 2006-12-27 BR BRPI0621268A patent/BRPI0621268B1/pt active IP Right Grant
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- 2006-12-27 CA CA2632323A patent/CA2632323C/en active Active
- 2006-12-27 EP EP06841168A patent/EP1965646B1/en active Active
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- 2006-12-27 WO PCT/EP2006/012539 patent/WO2007073933A2/en active Application Filing
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