Herbicidal preparation
专利摘要:
公开号:SU978713A3 申请号:SU813260553 申请日:1981-03-05 公开日:1982-11-30 发明作者:Ширмер Ульрих;Беккер Райнер;Вюрцер Бруно;Ретцлафф Гюнтер 申请人:Басф Аг (Фирма); IPC主号:
专利说明:
(5) HERBICID MEANS -. V. This invention relates to chemical complexes to combat undesirable vegetation, namely, a herbicidal agent based on carbamic acid derivatives. A herbicidal agent containing .5-methyl M-chlorophenoxy) is known. phenyl thiocarbamate and inert carrier JV. However, this tool is not enough effective and phytotoxic. A herbicidal agent containing 5-methyl-M-4 - (- chlorophenoxy) -3-chlorophenyl thiocarbamate and carrier 2. However, its activity is not always satisfactory. The purpose of the invention is the enhancement of herbicidal activity. This target is achieved using a herbicidal agent containing an active principle based on carbamic acid derivative of general formula where X is hydrogen, fluorine, bromine, C-Cdalkyl, cyclohexyl, C-C -al10 coxy, difluoromethoxy, 1-chloro-1-fluoro-2, 2-difluoroethox, and. 1,1,2,3,3,3-hexafto | e-n-propoxy, phenyl, benzyloxy; 15 Y - hydrogen, chlorine, methoxy; Z - hydrogen, chlorine, fluorine; A - oxygen, sulfur; Q - oxygen, sulfur, 13 as a carrier is sodium lignosulfone; sodium at a weight ratio of 80:20, respectively. A herbicidal agent is prepared by simply mixing the ingredients. i-С, and-СзН О n-СзН О 3-СНзО С1 95-98 66-68 85-88 68-70 108-110 90-92 106-109 123-125 : Example 2. The experiment was carried out in a greenhouse. Seeds of experimental plants, separately for varieties, are shallowly sown in flower plastic pots with a capacity of 300 cm, filled with clay sand with 1.5 humus as a substrate. The plants are allowed to grow to cm and then treated with a water treatment of the herbicidal agent consisting of 80 wt. active substance specified in tael. 2-6, and 20 wt.% Sodium lignosulfonate. Pots with experimental plants 50 inserted into a greenhouse and stored at different: 978713 8 continuation of the table. one temperatures of 2 weeks, while plants loving heat are stored at 20–30 ° C, and plants loving moderate climate are stored at 10–20 ° C. During storage, plants are cared for and their response to treatment is determined herbicide. The assessment is made on a scale from 0 to 100. At the same time, O means that there was no damage, and 100 did not completely kill at least the above-ground parts of the shoots. The active substances, plants and the results of the experiments are given in Table. 2-6. 978713 10 Table eleven 12 978713 Table 7s ten 80 ten Note. Amount of active substance 3.0 kg / ha. Example 2. Example 1 is repeated, with the difference that the plants are subjected to pre-emergence treatment with a herbicidal agent in an amount of 3.0 kg, where X is hydrogen, fluorine, bromine, alkyl, cyclohexyl, 1 alkoxy, difluoromethoxy, 1-chloro-1-fluorine -2, 2-difluoroethoxy 1,1,2,3,3,3, -hexafluoro-n-propoxy, phenyl, benzyloxy15 97871316 Y - hydrogen, chlorine, methoxy; Sources of information, Z - hydrogen, chlorine, fluorine; taken into account during excertize A - oxygen, sulfur; 1. US patent No. 39716 19, Q - oxygen, sulfur, cl. C 07 C 155/02, published 1976. : and as carrier, lignosulfo-5 2. US patent No. 3976 70, no sodium at weight ratio. C. U7 C 155/02, published 1976 80:20 respectively. 1 (PrototiN).
权利要求:
Claims (3) [1] Claim A herbicidal agent containing an active principle based on a carbamic acid derivative and a carrier, characterized in that, in order to enhance the herbicidal activity, it contains a compound of the general formula as a carbamic acid derivative Note. [2] The amount of active substance [3] 3.0 kg / ha. / / '^ -NHCOaCHs where Example 2. Repeat example 1 with the difference that the plants are pre-emergent treatment with a herbicidal agent in an amount of 3.0 kg AK55 X is hydrogen, fluoro, bromo, C ^ - ^ alkyl, cyclohexyl, alkoxy, difluoromethoxy, 1-chloro-1-fluoro-2,2-difluoroethoxy 1,1, 2,3,3,3, -hexafluoro-n- propoxy, phenyl, benzyloxy; 9787U
类似技术:
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同族专利:
公开号 | 公开日 PL126239B2|1983-07-30| JPS56139449A|1981-10-30| DD156665A5|1982-09-15| CS226423B2|1984-03-19| IL62094A|1984-12-31| AT2518T|1983-03-15| CA1172260A|1984-08-07| AR231436A1|1984-11-30| PL230021A2|1981-12-23| DE3160069D1|1983-03-24| ZA811502B|1982-04-28| BR8101208A|1981-09-08| DK101681A|1981-09-09| US4396418A|1983-08-02| AU6814081A|1981-09-17| EP0035712A1|1981-09-16| IL62094D0|1981-03-31| EP0035712B1|1983-02-16| DE3008985A1|1981-10-01| HU185861B|1985-04-28|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 US3976470A|1975-07-23|1976-08-24|Stauffer Chemical Company|Diphenyl ether amides| US3971649A|1975-07-23|1976-07-27|Stauffer Chemical Company|S-methyl-N-[4-phenyl] thiolcarbamate|DE3238079A1|1982-10-14|1984-04-19|Basf Ag, 6700 Ludwigshafen|ANILINE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR CONTROLLING UNWANTED PLANT GROWTH| JP3142638B2|1991-06-21|2001-03-07|三井化学株式会社|Thermal recording materials and phenolic compounds| US5643853A|1995-02-28|1997-07-01|Purdue Research Foundation|Thiol activation of cytotoxic and auxin-herbicidal agents and root formation stimulation| US6599942B1|1999-03-29|2003-07-29|Novartis Ag|Thyromimetic organic compounds| US6790978B2|1999-03-29|2004-09-14|Novartis Ag|Thyromimetic organic compounds| US7030109B2|1999-07-19|2006-04-18|Pharmacia & Upjohn Company|1,2,3,4,5,6-Hexahydroazepino[4,5-b]indoles containing arylsulfones at the 9-position| MY122278A|1999-07-19|2006-04-29|Upjohn Co|1,2,3,4,5,6-hexahydroazepino[4,5-b]indoles containing arylsulfones at the 9-position|
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申请号 | 申请日 | 专利标题 DE19803008985|DE3008985A1|1980-03-08|1980-03-08|N-ARYLCARBAMATE, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR CONTROLLING UNWANTED PLANT GROWTH| 相关专利
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