SU683601A3 - Method of controlling undesired plants - Google Patents
Method of controlling undesired plantsInfo
- Publication number
- SU683601A3 SU683601A3 SU762354750A SU2354750A SU683601A3 SU 683601 A3 SU683601 A3 SU 683601A3 SU 762354750 A SU762354750 A SU 762354750A SU 2354750 A SU2354750 A SU 2354750A SU 683601 A3 SU683601 A3 SU 683601A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- plants
- weeks
- herbicidal activity
- controlling undesired
- undesired plants
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
- C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/782—Ketones containing a keto group bound to a six-membered aromatic ring polycyclic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/782—Ketones containing a keto group bound to a six-membered aromatic ring polycyclic
- C07C49/784—Ketones containing a keto group bound to a six-membered aromatic ring polycyclic with all keto groups bound to a non-condensed ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/794—Ketones containing a keto group bound to a six-membered aromatic ring having unsaturation outside an aromatic ring
- C07C49/796—Ketones containing a keto group bound to a six-membered aromatic ring having unsaturation outside an aromatic ring polycyclic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F1/00—Compounds containing elements of Groups 1 or 11 of the Periodic System
- C07F1/04—Sodium compounds
Description
(54) СПОСОБ БОРЬБЫ С НЕЖЕЛАТЕЛЬНОЙ РАСТИТЕЛЬНОСТЬЮ Пример 1. Предвсходова активность соединени по иредлагаемому способу установлена в соответствии со следующими испытани ми, при которых смесь ацетона и воды (50:50 - по объему) и достаточного количества испытуемого соединени , обеспечивающего указанные в табл. 1 количества указанного соединени в расчете на гектар , вносили в горшочки, засаженные семенами или ростками испытуемых видов растений . Горщочки готовили дл гербицидной обработки следующим образом: на дно каждого пластмассового горщочка насыпались 100 мл почвы, затем на это одно высевали семена вьюнка пурпурного и овсюга и покрывали 50 мл почвы (от 1 до 1,37 см). Семена других восьми видов растений, указанных ниже, раздельно смещивали с почвой и эту смесь добавл лись в горшочек в количестве 50 мл. Горшочки затем слегка утрамбовывали дл выравнивани почвы и перед гербицидной обработкой почву увлажн ли водой. Такое предварительное увлажнение гарантировало равномерное распределение гербицидного раствора по поверхности почвы в горшочке и защищало семена сорн ков от повреждени ацетоном. Каждый из 10 сорн ков помещали в отШкала оценок О-нет действи 1-возможное действие 2-слабое действие 3-умеренное действие 5-четкое повреждение 6-гербицидное действие 7- хорошее гербицидное действие 8-приближение к полному уничтоже 9-полное уничтожение 4-ненормальный рост, т. е. определен логическое уродство, но полное меньше, чем в случае оценки 5 оценок. Примечание: На основании меров, силы, х растени .(54) METHOD OF FIGHTING AGAINST UNDESIRABLE VEGETATION Example 1. The pre-emergence activity of a compound according to the proposed method was established in accordance with the following tests, in which a mixture of acetone and water (50:50 by volume) and a sufficient amount of the test compound providing the values shown in table. 1 amounts of the compound indicated per hectare were put in pots planted with seeds or sprouts of test species of plants. Potholes were prepared for herbicidal treatment as follows: 100 ml of soil were poured at the bottom of each plastic pod, then purple bindweed and oat seed were sown and covered with 50 ml of soil (from 1 to 1.37 cm). The seeds of the other eight plant species listed below were separately biased with the soil and this mixture was added to the pot in an amount of 50 ml. The pots were then lightly tamped down to level the soil and moistened with water before the herbicidal treatment. Such pre-moistening guaranteed a uniform distribution of the herbicidal solution over the soil surface in the pot and protected the weed seeds from damage by acetone. Each of the 10 weeds was placed on the scale of assessments. O-no action 1-possible effect 2-weak effect 3-moderate action 5-clear damage 6-herbicidal action 7- good herbicidal effect 8-approximation to full, 9-complete destruction 4- abnormal growth, i.e., a logical deformity is determined, but the total is less than in the case of an assessment of 5 estimates. Note: Based on measures, strength, x plants.
Пример 2. Следующими опытами определ ли послевсходовую гербицидную активность соединений по предлагаемому способу . Монокотиледонные и дикотиледонные растени обрабатывали испытуемыми соединени ми , диспергированными в водно - ацетоновой смеси. В этих экспериментах во временных щиках в течение двух недель выращивали рассаду растений. Испытуемые соединени диспергировали в смес х ацетона и воды (50:50) по объему, содержащих 0,5% твина 20, полиоксиэтилен (2) сорбитаимонолаурата в качестве поверхностно-активного соединени .Example 2. The following experiments determined the post-emergence herbicidal activity of the compounds according to the proposed method. Monocotyledonic and dicotyledonic plants were treated with test compounds dispersed in an aqueous-acetone mixture. In these experiments, seedlings were grown in temporary boxes for two weeks. Test compounds were dispersed in mixtures of acetone and water (50:50) by volume, containing 0.5% Tween 20, polyoxyethylene (2) sorbitol-monolaurate as a surfactant.
Количество диспергированных испытуемых соединений брали из расчета получени определенных в табл. 2 количеств активного соединени , отнесенного к одному гектару, при распылении на растени через сопло, действующее под давлением 2,8 кг/см, в течение заданного промежутка времени. После опрыскивани растени помещали на полки теплицы и за ними ухаживали, как обычно, в соответствии с существующей практикой дл выращивани растений в теплицах. Через две недели после обработки ростки растений за исключением овсюгов, которые выращивали дельный горшочек. Горшочки перед химической обработкой устанавливали на поддоны размером 25,4X30,4 см. Засе нные горшочки обрабатывали 5 мл испытуемого раствора и затем помещали на полках в теплице. Горщочки после обработки поливали по мере необходимости и выдерживали в теплице в течение трех недель . В табл. 1 приведены полученные результаты . Виды растений, использованные при оценке предвсходовой гербицидной активности . Название Сокращение Лебеда бела ЛВ Дика горчица Марь Абрози Вьюнок пурпурный Просо куриное Росичка кров на Щетинник зеленый Овсюги Лимнохарис Пщеница Рис Ниже приведена система оценки, используема в указанных экспериментах. Отличие в росте от контрольных опытов, % изиоствие кале льного определени Состо ни , разза , уродства роста и внешнего вида The amount of dispersed test compounds was taken from the calculation for the preparation of the table. 2 quantities of active compound per hectare when sprayed onto plants through a nozzle operating under a pressure of 2.8 kg / cm for a given period of time. After spraying, the plants were placed on the shelves of the greenhouse and cared for, as usual, in accordance with current practice for growing plants in greenhouses. Two weeks after the treatment, the plant sprouts, with the exception of the wild oats, which grew a pot. Before chemical treatment, the pots were placed on pallets 25.4X30.4 cm in size. Sown pots were treated with 5 ml of the test solution and then placed on shelves in a greenhouse. After treatment, the pods were watered as needed and kept in the greenhouse for three weeks. In tab. 1 shows the results obtained. Plant species used in the assessment of pre-emergence herbicidal activity. Name Abbreviation Cygnus white LV Dick mustard Mar Abrosi Convolvulus purple Millet chicken Rosicka shelter on Bristles green Ovsyugi Limnokharis Wheat Rice Below is the rating system used in these experiments. Difference in growth from control experiments,% isostvia kal lennogo determining State, time, deformity of growth and appearance
, Предвсходова гербицидна активность пиразолиевых солейPre-emergence herbicidal activity of pyrazolium salts
в течение 5 недель, осматривали и оценивали в соответствии с приведенной в примере 1 шкалой оценок.for 5 weeks, examined and evaluated in accordance with the scale of estimates given in example 1.
В этом эксперименте использовали те же виды растений, что в опытах по определению предвсходовой гербицидной активности в примере 1.In this experiment, the same plant species were used as in the experiments for determining the pre-emergence herbicidal activity in Example 1.
Полученные результаты представлены в табл. 2.The results are presented in Table. 2
Пример 3. Предвсходова обработка.Example 3. Pre-emergence treatment.
Семена опытных растений высевали в подготовленную почву в специальных горшочках и после этого почву обрабатывали водно-ацетоновыми растворами действующих вешеств. После этого горшочки помещали в теплицу и поливали по мере необходимости . Результаты опыта оценивали через три недели после обработки. Шкала оценки аналогична примеру 1.The seeds of the experimental plants were sown in prepared soil in special pots and then the soil was treated with water-acetone solutions of active substances. After that, the pots were placed in a greenhouse and watered as needed. The results of the experiment were evaluated three weeks after treatment. The rating scale is similar to example 1.
Результаты опыта представлены в табл. 3.The results of the experiment are presented in table. 3
Пример 4. Послевсходова гербицидна активность предлагаемых соединений была показана с помощью следующих тестов , в которых различные однодольные и двудольные растени обрабатывали испытуемыми соединени ми, диспергированными в водно-ацетоновой смеси. В этих тестах се нцы растений выращивали в поддонахExample 4. The post-emergence herbicidal activity of the proposed compounds was shown by the following tests, in which various monocotyledonous and dicotyledonous plants were treated with the test compounds dispersed in a water-acetone mixture. In these tests, plant seedlings were grown in trays.
в течение примерно 2 недель. Испытуемые соединени диспергируют в смес х 50/50 вода - ацетон (объем/объем), содержащих 0,5% твина 20, полиоксиэтилен (20), сорбитанмонолаурат - поверхностно активное вещество, в количестве, достаточном дл обеспечени такого количества на гектар предлагаемого соединени , которое указано в табл. 4, когда нанос т на растени с помощью распылительного сопла, работа под давлением 2,8 кг/см в течение заранее определенного времени. После опрыскивани растени помещали на скамьи теплицы и ухаживали за ними обычным образом,for about 2 weeks. Test compounds are dispersed in 50/50 water-acetone (v / v) mixtures containing 0.5% Tween 20, polyoxyethylene (20), sorbitan monolaurate is a surfactant in an amount sufficient to provide such amount per hectare of the proposed compound, which is indicated in the table. 4, when applied to the plants with a spray nozzle, working under a pressure of 2.8 kg / cm for a predetermined time. After spraying the plants were placed on the benches of the greenhouse and cared for them in the usual way.
руководству сь обычной практикой работы в теплицах. Через 2 недели после обработки се нцы растений, за нсключением овсюга , который оценивали через 5 недель, исследовали и оценивали в соответствии сmanagement of the usual practice of working in greenhouses. After 2 weeks after treatment, the plant seedlings, after the oats, which was evaluated after 5 weeks, were examined and evaluated in accordance with
оценочной системой, приведенной в примере 1.evaluation system described in example 1.
Результаты опыта представлены в табл. 4. Пример 5. По методике примера 3The results of the experiment are presented in table. 4. Example 5. According to the method of example 3
испытывали предлагаемые соединени в сравнении с известным соединением, обладающим гербицидной активностью 1.Compounds of the present invention were tested against a known compound having a herbicidal activity 1.
Результаты опыта представлены в табл. 5.The results of the experiment are presented in table. five.
Послевсходова гербицидна активность пиразолиевых солейPost-emergence herbicidal activity of pyrazolium salts
Предвсходова гербицидна активность 4-замещенных пиразолиевых солей Послевсходова гербицидна активность 4-заиещенных Pre-emergence herbicidal activity of 4-substituted pyrazolium salts. Post-emergence herbicidal activity of 4-zaischennyh
Предвсходова гербицидна активностьPre-emergence herbicidal activity
Таблица 3 Table 3
Таблица 5 Таблица4 пиразолиевых солейTable 5 Table4 pyrazolium salts
11eleven
Claims (2)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US05/574,067 US3958001A (en) | 1975-05-02 | 1975-05-02 | 4-Alkyl-1,2-dimethyl-3,5-diphenylpyrazolium salts and derivatives thereof as fungicidal agents |
US05/574,068 US4017298A (en) | 1975-05-02 | 1975-05-02 | 1,2,4-Trialkyl-3,5-diphenylpyrazolium salts as herbicides |
Publications (1)
Publication Number | Publication Date |
---|---|
SU683601A3 true SU683601A3 (en) | 1979-08-30 |
Family
ID=27076277
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU762354750A SU683601A3 (en) | 1975-05-02 | 1976-04-30 | Method of controlling undesired plants |
Country Status (19)
Country | Link |
---|---|
JP (1) | JPS51133265A (en) |
AR (1) | AR217400A1 (en) |
AU (1) | AU503523B2 (en) |
CA (1) | CA1078850A (en) |
CS (1) | CS191170B2 (en) |
DD (1) | DD127656A5 (en) |
DE (1) | DE2618421A1 (en) |
DK (1) | DK194476A (en) |
ES (1) | ES447515A1 (en) |
FI (1) | FI761159A (en) |
FR (1) | FR2309539A1 (en) |
GB (1) | GB1543338A (en) |
IL (1) | IL49410A (en) |
IT (1) | IT1060500B (en) |
NL (1) | NL7604597A (en) |
PL (1) | PL107282B1 (en) |
SE (1) | SE7605011L (en) |
SU (1) | SU683601A3 (en) |
TR (1) | TR18655A (en) |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3818096A (en) * | 1972-04-12 | 1974-06-18 | Schering Corp | Compositions of 1,2-dilower alkyl arylpyrazolium quaternary salts and method of lowering blood sugar levels with same |
DE2404795C2 (en) * | 1974-02-01 | 1983-03-24 | Basf Ag, 6700 Ludwigshafen | 1,2-Dimethyl-3,5-diphenylpyrazolium salts and their use as herbicides |
DE2524853A1 (en) * | 1975-06-04 | 1976-12-09 | Vulkan Werk Gmbh | PROCESS AND DEVICE FOR PRODUCING POLES, IN PARTICULAR LIGHTING POLES |
-
1976
- 1976-04-13 IL IL49410A patent/IL49410A/en unknown
- 1976-04-14 AU AU12987/76A patent/AU503523B2/en not_active Expired
- 1976-04-21 CA CA250,620A patent/CA1078850A/en not_active Expired
- 1976-04-22 GB GB16439/76A patent/GB1543338A/en not_active Expired
- 1976-04-22 AR AR262970A patent/AR217400A1/en active
- 1976-04-27 DE DE19762618421 patent/DE2618421A1/en not_active Withdrawn
- 1976-04-27 FI FI761159A patent/FI761159A/fi not_active Application Discontinuation
- 1976-04-29 NL NL7604597A patent/NL7604597A/en not_active Application Discontinuation
- 1976-04-29 FR FR7612809A patent/FR2309539A1/en not_active Withdrawn
- 1976-04-29 TR TR18655A patent/TR18655A/en unknown
- 1976-04-29 CS CS762833A patent/CS191170B2/en unknown
- 1976-04-30 SU SU762354750A patent/SU683601A3/en active
- 1976-04-30 PL PL1976189201A patent/PL107282B1/en unknown
- 1976-04-30 SE SE7605011A patent/SE7605011L/en unknown
- 1976-04-30 DD DD192622A patent/DD127656A5/xx unknown
- 1976-04-30 IT IT49288/76A patent/IT1060500B/en active
- 1976-04-30 ES ES447515A patent/ES447515A1/en not_active Expired
- 1976-04-30 DK DK194476A patent/DK194476A/en unknown
- 1976-05-04 JP JP51050052A patent/JPS51133265A/en active Pending
Also Published As
Publication number | Publication date |
---|---|
FR2309539A1 (en) | 1976-11-26 |
CS191170B2 (en) | 1979-06-29 |
TR18655A (en) | 1977-06-23 |
ES447515A1 (en) | 1977-11-01 |
IT1060500B (en) | 1982-08-20 |
PL107282B1 (en) | 1980-02-29 |
JPS51133265A (en) | 1976-11-18 |
AR217400A1 (en) | 1980-03-31 |
IL49410A (en) | 1980-06-30 |
FI761159A (en) | 1976-11-03 |
IL49410A0 (en) | 1976-06-30 |
SE7605011L (en) | 1976-11-03 |
NL7604597A (en) | 1976-11-04 |
DK194476A (en) | 1976-11-03 |
AU503523B2 (en) | 1979-09-06 |
GB1543338A (en) | 1979-04-04 |
DE2618421A1 (en) | 1976-11-18 |
DD127656A5 (en) | 1977-10-05 |
AU1298776A (en) | 1977-10-20 |
CA1078850A (en) | 1980-06-03 |
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