DE2435747C2 - Flüssige herbicide Zubereitung - Google Patents
Flüssige herbicide ZubereitungInfo
- Publication number
- DE2435747C2 DE2435747C2 DE2435747A DE2435747A DE2435747C2 DE 2435747 C2 DE2435747 C2 DE 2435747C2 DE 2435747 A DE2435747 A DE 2435747A DE 2435747 A DE2435747 A DE 2435747A DE 2435747 C2 DE2435747 C2 DE 2435747C2
- Authority
- DE
- Germany
- Prior art keywords
- alkyl
- oder
- udf54
- preparations
- udf53
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000004009 herbicide Substances 0.000 title claims description 20
- 238000002360 preparation method Methods 0.000 title claims description 20
- 230000002363 herbicidal effect Effects 0.000 title claims description 14
- 239000007788 liquid Substances 0.000 title description 3
- -1 cycloalkenyl ketone Chemical class 0.000 claims description 10
- LZGUHMNOBNWABZ-UHFFFAOYSA-N n-nitro-n-phenylnitramide Chemical compound [O-][N+](=O)N([N+]([O-])=O)C1=CC=CC=C1 LZGUHMNOBNWABZ-UHFFFAOYSA-N 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 239000012141 concentrate Substances 0.000 claims description 4
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 claims description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexyloxide Natural products O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 claims description 3
- 150000002576 ketones Chemical class 0.000 claims description 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- 235000008504 concentrate Nutrition 0.000 claims 1
- 125000002243 cyclohexanonyl group Chemical group *C1(*)C(=O)C(*)(*)C(*)(*)C(*)(*)C1(*)* 0.000 claims 1
- 235000014666 liquid concentrate Nutrition 0.000 claims 1
- 239000003995 emulsifying agent Substances 0.000 description 13
- 239000001257 hydrogen Substances 0.000 description 11
- 229910052739 hydrogen Inorganic materials 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- 241000196324 Embryophyta Species 0.000 description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 9
- 125000000217 alkyl group Chemical group 0.000 description 9
- 150000002431 hydrogen Chemical class 0.000 description 9
- 229910052736 halogen Inorganic materials 0.000 description 8
- 150000002367 halogens Chemical class 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- 239000004480 active ingredient Substances 0.000 description 7
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 6
- 235000013877 carbamide Nutrition 0.000 description 5
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 239000004202 carbamide Substances 0.000 description 4
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 description 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 description 3
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000003342 alkenyl group Chemical group 0.000 description 3
- 125000004414 alkyl thio group Chemical group 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 125000000081 (C5-C8) cycloalkenyl group Chemical group 0.000 description 2
- ZPVOLGVTNLDBFI-UHFFFAOYSA-N (±)-2,2,6-trimethylcyclohexanone Chemical compound CC1CCCC(C)(C)C1=O ZPVOLGVTNLDBFI-UHFFFAOYSA-N 0.000 description 2
- CGNBQYFXGQHUQP-UHFFFAOYSA-N 2,3-dinitroaniline Chemical class NC1=CC=CC([N+]([O-])=O)=C1[N+]([O-])=O CGNBQYFXGQHUQP-UHFFFAOYSA-N 0.000 description 2
- IITQJMYAYSNIMI-UHFFFAOYSA-N 3-Methyl-2-cyclohexen-1-one Chemical compound CC1=CC(=O)CCC1 IITQJMYAYSNIMI-UHFFFAOYSA-N 0.000 description 2
- UJBOOUHRTQVGRU-UHFFFAOYSA-N 3-methylcyclohexan-1-one Chemical compound CC1CCCC(=O)C1 UJBOOUHRTQVGRU-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 2
- 150000004996 alkyl benzenes Chemical class 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 239000003849 aromatic solvent Substances 0.000 description 2
- 125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 125000004093 cyano group Chemical group *C#N 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 231100001184 nonphytotoxic Toxicity 0.000 description 2
- 239000011877 solvent mixture Substances 0.000 description 2
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- OQQOAWVKVDAJOI-UHFFFAOYSA-N (2-dodecanoyloxy-3-hydroxypropyl) dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCC(CO)OC(=O)CCCCCCCCCCC OQQOAWVKVDAJOI-UHFFFAOYSA-N 0.000 description 1
- DRAWQKGUORNASA-UHFFFAOYSA-N (2-hydroxy-3-octadec-9-enoyloxypropyl) octadec-9-enoate Chemical compound CCCCCCCCC=CCCCCCCCC(=O)OCC(O)COC(=O)CCCCCCCC=CCCCCCCCC DRAWQKGUORNASA-UHFFFAOYSA-N 0.000 description 1
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 description 1
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 description 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 description 1
- IJBUWXMVBNUVME-UHFFFAOYSA-N 1,4-di(nonoxy)-1,4-dioxobutane-2-sulfonic acid Chemical class CCCCCCCCCOC(=O)CC(S(O)(=O)=O)C(=O)OCCCCCCCCC IJBUWXMVBNUVME-UHFFFAOYSA-N 0.000 description 1
- AILVYPLQKCQNJC-UHFFFAOYSA-N 2,6-dimethylcyclohexan-1-one Chemical compound CC1CCCC(C)C1=O AILVYPLQKCQNJC-UHFFFAOYSA-N 0.000 description 1
- CBQDTCDOVVBGMN-UHFFFAOYSA-N 2-methyl-3-octylphenol Chemical class CCCCCCCCC1=CC=CC(O)=C1C CBQDTCDOVVBGMN-UHFFFAOYSA-N 0.000 description 1
- LFSAPCRASZRSKS-UHFFFAOYSA-N 2-methylcyclohexan-1-one Chemical compound CC1CCCCC1=O LFSAPCRASZRSKS-UHFFFAOYSA-N 0.000 description 1
- OQJMHUOCLRCSED-UHFFFAOYSA-N 3,3,5,5-tetramethylcyclohexan-1-one Chemical compound CC1(C)CC(=O)CC(C)(C)C1 OQJMHUOCLRCSED-UHFFFAOYSA-N 0.000 description 1
- NOQKKFBBAODEHN-UHFFFAOYSA-N 3,5-dimethylcyclohex-2-en-1-one Chemical compound CC1CC(C)=CC(=O)C1 NOQKKFBBAODEHN-UHFFFAOYSA-N 0.000 description 1
- 244000003416 Asparagus officinalis Species 0.000 description 1
- 235000005340 Asparagus officinalis Nutrition 0.000 description 1
- 235000002566 Capsicum Nutrition 0.000 description 1
- 244000019459 Cynara cardunculus Species 0.000 description 1
- 235000019106 Cynara scolymus Nutrition 0.000 description 1
- 244000000626 Daucus carota Species 0.000 description 1
- 235000002767 Daucus carota Nutrition 0.000 description 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- 240000004658 Medicago sativa Species 0.000 description 1
- 235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 1
- 240000004370 Pastinaca sativa Species 0.000 description 1
- 235000017769 Pastinaca sativa subsp sativa Nutrition 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 241000758706 Piperaceae Species 0.000 description 1
- 240000004713 Pisum sativum Species 0.000 description 1
- 235000010582 Pisum sativum Nutrition 0.000 description 1
- 229920001213 Polysorbate 20 Polymers 0.000 description 1
- 235000008406 SarachaNachtschatten Nutrition 0.000 description 1
- 241000208292 Solanaceae Species 0.000 description 1
- 235000004790 Solanum aculeatissimum Nutrition 0.000 description 1
- 235000008424 Solanum demissum Nutrition 0.000 description 1
- 235000018253 Solanum ferox Nutrition 0.000 description 1
- 235000000208 Solanum incanum Nutrition 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- 235000013131 Solanum macrocarpon Nutrition 0.000 description 1
- 235000009869 Solanum phureja Nutrition 0.000 description 1
- 235000000341 Solanum ptychanthum Nutrition 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000017622 Solanum xanthocarpum Nutrition 0.000 description 1
- 241000219793 Trifolium Species 0.000 description 1
- BKZCZANSHGDPSH-KTKRTIGZSA-N [3-(2,3-dihydroxypropoxy)-2-hydroxypropyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)COCC(O)CO BKZCZANSHGDPSH-KTKRTIGZSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003302 alkenyloxy group Chemical group 0.000 description 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 125000005133 alkynyloxy group Chemical group 0.000 description 1
- 235000016520 artichoke thistle Nutrition 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000005228 aryl sulfonate group Chemical group 0.000 description 1
- 150000001896 cresols Chemical class 0.000 description 1
- 150000003997 cyclic ketones Chemical class 0.000 description 1
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 description 1
- FWFSEYBSWVRWGL-UHFFFAOYSA-N cyclohex-2-enone Chemical compound O=C1CCCC=C1 FWFSEYBSWVRWGL-UHFFFAOYSA-N 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical class CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical class CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 229940074049 glyceryl dilaurate Drugs 0.000 description 1
- 150000005108 haloalkylbenzenes Chemical class 0.000 description 1
- 125000004995 haloalkylthio group Chemical group 0.000 description 1
- 125000004970 halomethyl group Chemical group 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 230000002147 killing effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 235000010483 polyoxyethylene sorbitan monopalmitate Nutrition 0.000 description 1
- 235000010989 polyoxyethylene sorbitan monostearate Nutrition 0.000 description 1
- 235000010988 polyoxyethylene sorbitan tristearate Nutrition 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 125000002112 pyrrolidino group Chemical group [*]N1C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- HTSABYAWKQAHBT-UHFFFAOYSA-N trans 3-methylcyclohexanol Natural products CC1CCCC(O)C1 HTSABYAWKQAHBT-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 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<
- A01N47/30—Derivatives containing the group >N—CO—N aryl or >N—CS—N—aryl
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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3794573A GB1473105A (el) | 1973-08-10 | 1973-08-10 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2435747A1 DE2435747A1 (de) | 1975-02-13 |
| DE2435747C2 true DE2435747C2 (de) | 1987-02-26 |
Family
ID=10400132
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2435747A Expired DE2435747C2 (de) | 1973-08-10 | 1974-07-25 | Flüssige herbicide Zubereitung |
Country Status (19)
| Country | Link |
|---|---|
| JP (1) | JPS5944285B2 (el) |
| AT (1) | AT344439B (el) |
| BE (1) | BE818479A (el) |
| CA (1) | CA1032362A (el) |
| CH (1) | CH596755A5 (el) |
| CS (1) | CS185659B2 (el) |
| DD (1) | DD112336A5 (el) |
| DE (1) | DE2435747C2 (el) |
| DK (1) | DK140741B (el) |
| FR (1) | FR2239941B1 (el) |
| GB (1) | GB1473105A (el) |
| HU (1) | HU170845B (el) |
| IL (1) | IL45404A (el) |
| IT (1) | IT1021599B (el) |
| NL (1) | NL184935C (el) |
| PL (1) | PL94443B1 (el) |
| RO (1) | RO70571A (el) |
| SE (1) | SE430014B (el) |
| SU (1) | SU1243606A3 (el) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2534042A1 (de) * | 1975-07-30 | 1977-02-17 | Shell Int Research | Herbicide mittel |
| IT1131750B (it) * | 1980-06-06 | 1986-06-25 | Montedison Spa | Formulazioni stabili di n-(3,4-diclorofenil)-n'metossi-n'-metilurea (linorun) e 2,6-dinitor-n,n-dipropil-4-trifluoro metilanilina (trifluralin) in emulsione |
| CH652888A5 (de) * | 1982-08-25 | 1985-12-13 | Sintagro Sa | Stabile, fluessige zubereitung mit herbizider wirkung und verfahren zu ihrer herstellung. |
| IL116147A (en) | 1994-11-30 | 2002-05-23 | Aventis Cropscience Sa | Complexible composition for insect control |
| IL116148A (en) * | 1994-11-30 | 2001-03-19 | Rhone Poulenc Agrochimie | Complexible composition for insect control |
| MA40840A (fr) * | 2014-10-22 | 2017-08-29 | Ishihara Sangyo Kaisha | Composition herbicide |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2037265A1 (de) * | 1970-07-28 | 1972-02-03 | Badische Anilin & Soda Fabrik AG, 6700 Ludwigshafen | Herbizid |
| US3373010A (en) * | 1964-10-08 | 1968-03-12 | Du Pont | Herbicidal composition and method |
| DE1242936B (de) * | 1965-03-12 | 1967-06-22 | Schering Ag | Selektive Herbizide |
| US3322527A (en) * | 1965-04-30 | 1967-05-30 | Du Pont | Herbicidal compositions and methods employing 3-(3, 4-dichlorophenyl)-1-methyl-1-methoxyurea with 3-amino-1, 2, 4-triazole |
| BE705182A (el) * | 1967-10-16 | 1968-04-16 | ||
| DE1923545A1 (de) * | 1968-05-27 | 1969-12-04 | Du Pont | Fluessiges Konzentrat fuer Unkrautbekaempfungsmittel |
| BE754383A (fr) * | 1969-08-05 | 1971-02-04 | Ciba Geigy | 4-(n- ou iso-propoxy)-3-chlorophényl-urées, leur procédé de préparation et leur utilisation pour la destruction des parasites |
| CH533421A (de) * | 1970-02-02 | 1973-02-15 | Ciba Geigy Ag | Biozides Mittel |
| DE2106875A1 (de) * | 1970-02-23 | 1971-09-16 | Ciba-Geigy Ag, Basel (Schweiz) | Phenylharnstoffe, ihre Herstellung und ihre Verwendung als selektive Herbizide |
| IL36218A0 (en) * | 1970-02-27 | 1971-04-28 | Ciba Geigy Ag | 4-isopropylphenylureas,their manufacture and use in combating pests |
| IL36448A (en) * | 1970-03-26 | 1974-07-31 | Ciba Geigy Ag | N-(substituted phenyl)-ureas,their preparation and use as selective herbicides |
| IL36718A0 (en) * | 1970-04-30 | 1971-06-23 | Ciba Geigy Ag | Herbicidal compositions containing phenylureas,certain new phenylureas and their preparation |
| DE2039042A1 (de) * | 1970-08-06 | 1972-02-17 | Hoechst Ag | Herbizide Mittel |
| DE2123185A1 (de) * | 1971-05-11 | 1972-11-30 | Farbwerke Hoechst AG, vormals Meister Lucius & Brüning, 6000 Frankfurt | N-Arylharnstoffe |
| CA985523A (en) * | 1971-06-30 | 1976-03-16 | American Cyanamid Company | Inhibiting plant bud growth |
-
1973
- 1973-08-10 GB GB3794573A patent/GB1473105A/en not_active Expired
-
1974
- 1974-07-25 DE DE2435747A patent/DE2435747C2/de not_active Expired
- 1974-08-02 CS CS7400005522A patent/CS185659B2/cs unknown
- 1974-08-02 CA CA206,247A patent/CA1032362A/en not_active Expired
- 1974-08-02 BE BE147282A patent/BE818479A/xx not_active IP Right Cessation
- 1974-08-05 IL IL45404A patent/IL45404A/en unknown
- 1974-08-05 FR FR7427087A patent/FR2239941B1/fr not_active Expired
- 1974-08-07 NL NLAANVRAGE7410591,A patent/NL184935C/xx not_active IP Right Cessation
- 1974-08-07 SE SE7410118A patent/SE430014B/xx not_active IP Right Cessation
- 1974-08-08 DD DD180401A patent/DD112336A5/xx unknown
- 1974-08-08 CH CH1087774A patent/CH596755A5/xx not_active IP Right Cessation
- 1974-08-09 IT IT52547/74A patent/IT1021599B/it active
- 1974-08-09 AT AT654874A patent/AT344439B/de not_active IP Right Cessation
- 1974-08-09 JP JP49091399A patent/JPS5944285B2/ja not_active Expired
- 1974-08-09 SU SU742054979A patent/SU1243606A3/ru active
- 1974-08-09 DK DK425074AA patent/DK140741B/da not_active IP Right Cessation
- 1974-08-09 HU HU74LI00000262A patent/HU170845B/hu unknown
- 1974-08-10 PL PL1974173392A patent/PL94443B1/pl unknown
- 1974-08-10 RO RO7479721A patent/RO70571A/ro unknown
Also Published As
| Publication number | Publication date |
|---|---|
| SU1243606A3 (ru) | 1986-07-07 |
| DK425074A (el) | 1975-04-21 |
| NL184935C (nl) | 1989-12-18 |
| PL94443B1 (pl) | 1977-08-31 |
| CH596755A5 (el) | 1978-03-15 |
| CA1032362A (en) | 1978-06-06 |
| SE7410118L (el) | 1975-02-11 |
| NL184935B (nl) | 1989-07-17 |
| CS185659B2 (en) | 1978-10-31 |
| FR2239941A1 (el) | 1975-03-07 |
| BE818479A (fr) | 1975-02-03 |
| ATA654874A (de) | 1977-11-15 |
| DK140741C (el) | 1980-05-05 |
| DK140741B (da) | 1979-11-12 |
| DE2435747A1 (de) | 1975-02-13 |
| RO70571A (ro) | 1981-09-24 |
| AT344439B (de) | 1978-07-25 |
| IT1021599B (it) | 1978-02-20 |
| JPS5944285B2 (ja) | 1984-10-29 |
| HU170845B (hu) | 1977-09-28 |
| SE430014B (sv) | 1983-10-17 |
| IL45404A (en) | 1977-10-31 |
| FR2239941B1 (el) | 1976-10-22 |
| NL7410591A (nl) | 1975-02-12 |
| DD112336A5 (el) | 1975-04-12 |
| GB1473105A (el) | 1977-05-11 |
| IL45404A0 (en) | 1974-11-29 |
| JPS5069230A (el) | 1975-06-10 |
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Legal Events
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| 8128 | New person/name/address of the agent |
Representative=s name: TUERK, D., DIPL.-CHEM. DR.RER.NAT. GILLE, C., DIPL |
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| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition |