NO794206L - Herbicid preparat. - Google Patents
Herbicid preparat.Info
- Publication number
- NO794206L NO794206L NO794206A NO794206A NO794206L NO 794206 L NO794206 L NO 794206L NO 794206 A NO794206 A NO 794206A NO 794206 A NO794206 A NO 794206A NO 794206 L NO794206 L NO 794206L
- Authority
- NO
- Norway
- Prior art keywords
- bifenox
- herbicide
- salt
- ester
- weight ratio
- Prior art date
Links
- 238000002360 preparation method Methods 0.000 title claims description 27
- 230000002363 herbicidal effect Effects 0.000 claims description 55
- 239000004009 herbicide Substances 0.000 claims description 50
- SUSRORUBZHMPCO-UHFFFAOYSA-N MC-4379 Chemical compound C1=C([N+]([O-])=O)C(C(=O)OC)=CC(OC=2C(=CC(Cl)=CC=2)Cl)=C1 SUSRORUBZHMPCO-UHFFFAOYSA-N 0.000 claims description 37
- 239000005484 Bifenox Substances 0.000 claims description 36
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims description 27
- 150000002148 esters Chemical class 0.000 claims description 26
- 150000003839 salts Chemical class 0.000 claims description 26
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 20
- 241000196324 Embryophyta Species 0.000 claims description 19
- 239000002253 acid Substances 0.000 claims description 18
- 239000004480 active ingredient Substances 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 17
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 13
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 claims description 10
- 239000005711 Benzoic acid Substances 0.000 claims description 10
- 235000010233 benzoic acid Nutrition 0.000 claims description 10
- HUBANNPOLNYSAD-UHFFFAOYSA-N clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 claims description 10
- NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical group OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 claims description 10
- 229960002939 metizoline Drugs 0.000 claims description 10
- UFBJCMHMOXMLKC-UHFFFAOYSA-N 2,4-dinitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O UFBJCMHMOXMLKC-UHFFFAOYSA-N 0.000 claims description 9
- 239000005489 Bromoxynil Substances 0.000 claims description 9
- ZOMSMJKLGFBRBS-UHFFFAOYSA-N bentazone Chemical compound C1=CC=C2NS(=O)(=O)N(C(C)C)C(=O)C2=C1 ZOMSMJKLGFBRBS-UHFFFAOYSA-N 0.000 claims description 9
- 235000013339 cereals Nutrition 0.000 claims description 9
- OWZPCEFYPSAJFR-UHFFFAOYSA-N 2-(butan-2-yl)-4,6-dinitrophenol Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O OWZPCEFYPSAJFR-UHFFFAOYSA-N 0.000 claims description 7
- IIPZYDQGBIWLBU-UHFFFAOYSA-N Dinoterb Chemical compound CC(C)(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O IIPZYDQGBIWLBU-UHFFFAOYSA-N 0.000 claims description 7
- 239000007900 aqueous suspension Substances 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 7
- 239000012141 concentrate Substances 0.000 claims description 7
- MZHCENGPTKEIGP-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-UHFFFAOYSA-N 0.000 claims description 6
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical compound CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 claims description 6
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims description 6
- XZIDTOHMJBOSOX-UHFFFAOYSA-N 2,3,6-TBA Chemical compound OC(=O)C1=C(Cl)C=CC(Cl)=C1Cl XZIDTOHMJBOSOX-UHFFFAOYSA-N 0.000 claims description 5
- 239000005504 Dicamba Substances 0.000 claims description 5
- 239000004495 emulsifiable concentrate Substances 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- 231100001184 nonphytotoxic Toxicity 0.000 claims description 5
- 239000005476 Bentazone Substances 0.000 claims description 4
- CNBGNNVCVSKAQZ-UHFFFAOYSA-N benzidamine Natural products C12=CC=CC=C2C(OCCCN(C)C)=NN1CC1=CC=CC=C1 CNBGNNVCVSKAQZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000000969 carrier Substances 0.000 claims description 4
- 239000003085 diluting agent Substances 0.000 claims description 3
- 239000004563 wettable powder Substances 0.000 claims description 3
- NDNKHWUXXOFHTD-UHFFFAOYSA-N metizoline Chemical compound CC=1SC2=CC=CC=C2C=1CC1=NCCN1 NDNKHWUXXOFHTD-UHFFFAOYSA-N 0.000 claims 3
- -1 alkali metal salt Chemical class 0.000 description 10
- HYJSGOXICXYZGS-UHFFFAOYSA-N benazolin Chemical compound C1=CC=C2SC(=O)N(CC(=O)O)C2=C1Cl HYJSGOXICXYZGS-UHFFFAOYSA-N 0.000 description 8
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 8
- 239000004094 surface-active agent Substances 0.000 description 8
- 239000004615 ingredient Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- YIVXMZJTEQBPQO-UHFFFAOYSA-N 2,4-DB Chemical compound OC(=O)CCCOC1=CC=C(Cl)C=C1Cl YIVXMZJTEQBPQO-UHFFFAOYSA-N 0.000 description 5
- 239000002794 2,4-DB Substances 0.000 description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 5
- 229910052783 alkali metal Inorganic materials 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 240000005702 Galium aparine Species 0.000 description 4
- 235000014820 Galium aparine Nutrition 0.000 description 4
- 240000005979 Hordeum vulgare Species 0.000 description 4
- 235000007340 Hordeum vulgare Nutrition 0.000 description 4
- 240000005592 Veronica officinalis Species 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- 244000192528 Chrysanthemum parthenium Species 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 235000017945 Matricaria Nutrition 0.000 description 3
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 3
- 240000006694 Stellaria media Species 0.000 description 3
- 241000209140 Triticum Species 0.000 description 3
- 235000021307 Triticum Nutrition 0.000 description 3
- 241000405217 Viola <butterfly> Species 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 150000003863 ammonium salts Chemical class 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 125000004185 ester group Chemical group 0.000 description 3
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 3
- 239000002562 thickening agent Substances 0.000 description 3
- 235000007319 Avena orientalis Nutrition 0.000 description 2
- 244000075850 Avena orientalis Species 0.000 description 2
- 241000205407 Polygonum Species 0.000 description 2
- 235000007238 Secale cereale Nutrition 0.000 description 2
- 244000082988 Secale cereale Species 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 description 2
- 159000000001 potassium salts Chemical class 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 230000007928 solubilization Effects 0.000 description 2
- 238000005063 solubilization Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- WPRAXAOJIODQJR-UHFFFAOYSA-N 1-(3,4-dimethylphenyl)ethanone Chemical compound CC(=O)C1=CC=C(C)C(C)=C1 WPRAXAOJIODQJR-UHFFFAOYSA-N 0.000 description 1
- IBSQPLPBRSHTTG-UHFFFAOYSA-N 1-chloro-2-methylbenzene Chemical compound CC1=CC=CC=C1Cl IBSQPLPBRSHTTG-UHFFFAOYSA-N 0.000 description 1
- WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 description 1
- LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- UGDWWCJKEUBONY-UHFFFAOYSA-N 6-chloro-6-methylcyclohexa-1,3-dien-1-ol Chemical compound CC1(Cl)CC=CC=C1O UGDWWCJKEUBONY-UHFFFAOYSA-N 0.000 description 1
- RDJTWDKSYLLHRW-UHFFFAOYSA-N Dinoseb acetate Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(C)=O RDJTWDKSYLLHRW-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 241001289540 Fallopia convolvulus Species 0.000 description 1
- 244000044980 Fumaria officinalis Species 0.000 description 1
- 235000006961 Fumaria officinalis Nutrition 0.000 description 1
- 241001508646 Galeopsis tetrahit Species 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- 239000005574 MCPA Substances 0.000 description 1
- 239000005575 MCPB Substances 0.000 description 1
- 101150039283 MCPB gene Proteins 0.000 description 1
- 231100000674 Phytotoxicity Toxicity 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 240000003728 Spergula arvensis Species 0.000 description 1
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 1
- 240000000359 Triticum dicoccon Species 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000002528 anti-freeze Effects 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000007798 antifreeze agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 150000003997 cyclic ketones Chemical class 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- CRPOUZQWHJYTMS-UHFFFAOYSA-N dialuminum;magnesium;disilicate Chemical compound [Mg+2].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] CRPOUZQWHJYTMS-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 150000002169 ethanolamines Chemical class 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 239000011872 intimate mixture Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 235000019357 lignosulphonate Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- 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
- A01N37/44—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/48—Nitro-carboxylic acids; Derivatives 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; Derivatives 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; Derivatives thereof
- A01N39/04—Aryloxy-acetic acids; Derivatives 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
- 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
- A01N43/88—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 three ring hetero atoms
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Medicines Containing Plant Substances (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB7849440 | 1978-12-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO794206L true NO794206L (no) | 1980-06-24 |
Family
ID=10501858
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO794206A NO794206L (no) | 1978-12-21 | 1979-12-20 | Herbicid preparat. |
Country Status (24)
| Country | Link |
|---|---|
| JP (6) | JPS5589204A (ja) |
| BE (1) | BE880782A (ja) |
| BR (1) | BR7908349A (ja) |
| CA (2) | CA1129665A (ja) |
| CH (1) | CH641932A5 (ja) |
| DD (1) | DD147993A5 (ja) |
| DE (1) | DE2950682A1 (ja) |
| FR (1) | FR2444407A1 (ja) |
| GB (1) | GB2042339B (ja) |
| HK (1) | HK73985A (ja) |
| IE (1) | IE49337B1 (ja) |
| IL (1) | IL58962A0 (ja) |
| IT (1) | IT1162429B (ja) |
| JO (1) | JO985B1 (ja) |
| LU (1) | LU82017A1 (ja) |
| MA (1) | MA18678A1 (ja) |
| MX (1) | MX6293E (ja) |
| NL (1) | NL7909099A (ja) |
| NO (1) | NO794206L (ja) |
| NZ (1) | NZ192415A (ja) |
| PL (1) | PL220528A1 (ja) |
| RO (1) | RO78398A (ja) |
| SG (1) | SG44385G (ja) |
| TR (1) | TR20965A (ja) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8304102D0 (en) * | 1983-02-15 | 1983-03-16 | Rohm & Haas France | Herbicidal compositions |
| GB8403342D0 (en) * | 1984-02-08 | 1984-03-14 | Velsicol Chemical Ltd | Herbicidal compositions |
| AU5041085A (en) * | 1984-11-28 | 1986-06-05 | Ivon Watkins-Dow Ltd. | Herbicidal composition |
| GB8511998D0 (en) * | 1985-05-11 | 1985-06-19 | Fbc Ltd | Herbicides |
| NZ223585A (en) * | 1987-02-24 | 1990-09-26 | Rhone Poulenc Agrochimie | Herbicidal mixture of picolinic acid or 2-pyridyloxyacetic acid derivatives and a phenoxy benzoic acid derivative |
| DE4223465A1 (de) * | 1992-07-16 | 1994-01-20 | Bayer Ag | Herbizide Mittel auf Basis von Heteroaryloxyacetamiden |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR751855A (fr) * | 1932-06-04 | 1933-09-11 | Destruction sélective des plantes adventices et amélioration des récoltes | |
| US2192197A (en) * | 1936-09-03 | 1940-03-05 | Dow Chemical Co | Dinitro-alkyl-phenol |
| US3081162A (en) * | 1956-11-27 | 1963-03-12 | Heyden Newport Chemical Corp | Controlling bindweed with 2, 3, 6-trichlorobenzoic acid and salts thereof |
| BE562664A (ja) * | 1957-09-26 | |||
| US3013054A (en) * | 1958-08-04 | 1961-12-12 | Velsicol Chemical Corp | 2-methoxy-3, 6-dichlorobenzoates |
| NL108409C (ja) * | 1958-10-29 | |||
| GB977755A (en) * | 1962-09-04 | 1964-12-16 | Nippon Catalytic Chem Ind | Method of preparing aromatic nitriles |
| US3317549A (en) * | 1963-03-25 | 1967-05-02 | Dow Chemical Co | Picolinic acid compounds |
| FR1475686A (fr) * | 1965-11-30 | 1967-04-07 | Pechiney Progil Sa | Procédé de desherbage sélectif des céréales |
| US3708277A (en) * | 1966-08-30 | 1973-01-02 | Basf Ag | Herbicidal method |
| US3652645A (en) * | 1969-04-25 | 1972-03-28 | Mobil Oil Corp | Halophenoxy benzoic acid herbicides |
| NL175780C (nl) * | 1972-11-17 | 1985-01-02 | Rhone Poulenc Inc | Werkwijze voor het bereiden van een herbicide preparaat, dat ten minste een fenoxynitrobenzoaat bevat. |
| JPS562527B2 (ja) * | 1973-08-20 | 1981-01-20 | ||
| JPS5857402B2 (ja) * | 1973-08-20 | 1983-12-20 | ホクコウカガクコウギヨウ カブシキガイシヤ | ジヨソウザイソセイブツ |
| JPS5857403B2 (ja) * | 1973-08-20 | 1983-12-20 | ホクコウカガクコウギヨウ カブシキガイシヤ | ジヨソウザイソセイブツ |
| JPS5924122B2 (ja) * | 1973-08-20 | 1984-06-07 | 北興化学工業 （株） | 除草剤組成物 |
| JPS50125030A (ja) * | 1974-03-23 | 1975-10-01 | ||
| JPS5919081B2 (ja) * | 1975-04-28 | 1984-05-02 | 三井東圧化学株式会社 | 水田用除草剤組成物 |
| JPS52139719A (en) * | 1976-04-19 | 1977-11-21 | Mitsui Toatsu Chem Inc | Herbicidal composition |
| EP0001328A1 (en) * | 1977-09-23 | 1979-04-04 | FISONS plc | Method and composition for combating weeds |
-
1979
- 1979-07-13 CA CA331,754A patent/CA1129665A/en not_active Expired
- 1979-08-15 JO JO1979985A patent/JO985B1/en active
- 1979-12-14 IL IL58962A patent/IL58962A0/xx unknown
- 1979-12-14 MX MX798559U patent/MX6293E/es unknown
- 1979-12-15 DE DE19792950682 patent/DE2950682A1/de not_active Withdrawn
- 1979-12-15 MA MA18880A patent/MA18678A1/fr unknown
- 1979-12-17 GB GB7943358A patent/GB2042339B/en not_active Expired
- 1979-12-17 NZ NZ192415A patent/NZ192415A/xx unknown
- 1979-12-17 RO RO7999570A patent/RO78398A/ro unknown
- 1979-12-17 CH CH1114279A patent/CH641932A5/fr not_active IP Right Cessation
- 1979-12-18 NL NL7909099A patent/NL7909099A/nl active Search and Examination
- 1979-12-18 FR FR7930949A patent/FR2444407A1/fr active Granted
- 1979-12-19 BR BR7908349A patent/BR7908349A/pt unknown
- 1979-12-19 PL PL22052879A patent/PL220528A1/xx unknown
- 1979-12-20 LU LU82017A patent/LU82017A1/fr unknown
- 1979-12-20 CA CA342,403A patent/CA1131036A/en not_active Expired
- 1979-12-20 IE IE2488/79A patent/IE49337B1/en not_active IP Right Cessation
- 1979-12-20 JP JP16626679A patent/JPS5589204A/ja active Pending
- 1979-12-20 IT IT51151/79A patent/IT1162429B/it active
- 1979-12-20 DD DD79217958A patent/DD147993A5/de unknown
- 1979-12-20 BE BE6/47042A patent/BE880782A/fr not_active IP Right Cessation
- 1979-12-20 NO NO794206A patent/NO794206L/no unknown
- 1979-12-21 TR TR20965A patent/TR20965A/xx unknown
-
1985
- 1985-06-11 SG SG44385A patent/SG44385G/en unknown
- 1985-09-26 HK HK739/85A patent/HK73985A/xx not_active IP Right Cessation
-
1989
- 1989-02-07 JP JP1028524A patent/JPH01287004A/ja active Pending
- 1989-02-07 JP JP1028522A patent/JPH01308209A/ja active Pending
- 1989-02-07 JP JP1028520A patent/JPH01308207A/ja active Pending
- 1989-02-07 JP JP1028521A patent/JPH01308208A/ja active Pending
- 1989-02-07 JP JP1028523A patent/JPH01287003A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| NZ192415A (en) | 1982-03-30 |
| CA1131036A (en) | 1982-09-07 |
| MX6293E (es) | 1985-03-18 |
| IE792488L (en) | 1980-06-21 |
| LU82017A1 (fr) | 1981-07-23 |
| BR7908349A (pt) | 1980-09-23 |
| JPH01308207A (ja) | 1989-12-12 |
| MA18678A1 (fr) | 1980-07-01 |
| DD147993A5 (de) | 1981-05-06 |
| IT1162429B (it) | 1987-04-01 |
| JPH01287003A (ja) | 1989-11-17 |
| IE49337B1 (en) | 1985-09-18 |
| JPH01308209A (ja) | 1989-12-12 |
| DE2950682A1 (de) | 1980-07-17 |
| RO78398A (ro) | 1982-02-26 |
| JPS5589204A (en) | 1980-07-05 |
| GB2042339A (en) | 1980-09-24 |
| IT7951151A0 (it) | 1979-12-20 |
| CH641932A5 (en) | 1984-03-30 |
| HK73985A (en) | 1985-10-04 |
| SG44385G (en) | 1986-01-17 |
| JPH01287004A (ja) | 1989-11-17 |
| PL220528A1 (ja) | 1980-09-22 |
| GB2042339B (en) | 1982-10-20 |
| NL7909099A (nl) | 1980-06-24 |
| BE880782A (fr) | 1980-06-20 |
| JPH01308208A (ja) | 1989-12-12 |
| IL58962A0 (en) | 1980-03-31 |
| FR2444407B1 (ja) | 1984-09-28 |
| FR2444407A1 (fr) | 1980-07-18 |
| TR20965A (tr) | 1983-03-07 |
| CA1129665A (en) | 1982-08-17 |
| JO985B1 (en) | 1979-12-01 |
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