SU534172A3 - Herbicide - Google Patents
HerbicideInfo
- Publication number
- SU534172A3 SU534172A3 SU1704918A SU1704918A SU534172A3 SU 534172 A3 SU534172 A3 SU 534172A3 SU 1704918 A SU1704918 A SU 1704918A SU 1704918 A SU1704918 A SU 1704918A SU 534172 A3 SU534172 A3 SU 534172A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- compounds
- alkyl
- methyl
- hydrogen
- herbicidal
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title claims description 8
- 230000002363 herbicidal effect Effects 0.000 title claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 11
- 230000002070 germicidal effect Effects 0.000 claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 3
- 239000013543 active substance Substances 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 239000002270 dispersing agent Substances 0.000 claims description 2
- 239000003995 emulsifying agent Substances 0.000 claims description 2
- 239000000945 filler Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 230000000694 effects Effects 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000002689 soil Substances 0.000 description 5
- 241000196324 Embryophyta Species 0.000 description 4
- 240000007594 Oryza sativa Species 0.000 description 4
- 235000007164 Oryza sativa Nutrition 0.000 description 3
- 235000009566 rice Nutrition 0.000 description 3
- -1 ether amide Chemical class 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 1
- 244000000626 Daucus carota Species 0.000 description 1
- 235000002767 Daucus carota Nutrition 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 244000299507 Gossypium hirsutum Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 231100000674 Phytotoxicity Toxicity 0.000 description 1
- 244000088415 Raphanus sativus Species 0.000 description 1
- 235000006140 Raphanus sativus var sativus Nutrition 0.000 description 1
- 244000062793 Sorghum vulgare Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical class CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 230000005080 plant death Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/22—Amides of acids of phosphorus
- C07F9/24—Esteramides
- C07F9/2404—Esteramides the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/242—Esteramides the ester moiety containing a substituent or a structure which is considered as characteristic of hydroxyaryl compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
(54) ГЕРБИЦИДНОЕ СРЕДСТВО(54) HERBICID MEANS
Изобретение относитс к химическим средства.м борьбы с сорной растительностью в посевах возделываемых культур, а именно к средствам на основе производных тионфосфорной кислоты.The invention relates to chemical means of weed control in crops of cultivated crops, namely to means based on derivatives of thionophosphoric acid.
Известен целый р д соединений - эфироамидов тиомфосфорной кислоты, обладающих гербицидной активностью. Например, описаны гербицидные средства, содержащие в качестве действующего .вещест1ва О-алкил-О-2нитpo-4-aлкил-фeнил-N - изопропиламидотиофосфат или 0-алкил-О-2-нитрофенил-Ы-изопропиламидотиофосфат .A number of compounds are known — thiophosphoric acid esters of amide having herbicidal activity. For example, herbicidal agents containing O-alkyl-O-2nitpo-4-alkyl-phenyl-N - isopropylamidothiophosphate or 0-alkyl-O-2-nitrophenyl-N-isopropylamidothiophosphate as acting.
Однако известные гер бицидные средства этой -группы недостаточно эффективны.However, the well-known germicidal agents of this group are not effective enough.
Целью изобретени вл етс новое гербицищное средство .на основе эфнроамидов тионфосфориой кдаслоты.The aim of the invention is a new herbicidal agent based on the efnroamidov thionphosphoria kdislot.
Эта цель достигаетс тем, что в качестве действующего вещества в предлагаемом гербнцидно .м средстве использованы соединени общей формулы (I)This goal is achieved by the use of compounds of general formula (I) as the active substance in the proposed herbicidal agent.
NOzNoz
X - водород или метил;X is hydrogen or methyl;
причем содержание действующего вещества в гер.бицидном средстве находитс в пределах от 2 до 80 вес. %.moreover, the content of the active substance in the germicidal agent is in the range from 2 to 80 weight. %
Помимо действующего вещества общей формулы (I) гербицидное средство согласно изобретению содержит вспомогательные компоненты ИЗ числа растворителей, наполнителей , эмульгаторов, диспергаторов и т. д.In addition to the active ingredient of general formula (I), the herbicidal agent according to the invention contains auxiliary components FROM the number of solvents, fillers, emulsifiers, dispersants, etc.
Формы применени средства обычные - растворы, эмульсии, порощки, пасты, гранул ты и т. д. Их .готов т общ еизвестными спосббами .The usual forms of application are solutions, emulsions, powders, pastes, granules, etc. They are prepared by well known sposbbs.
Предлагаемое гербицидное средство вл етс избирательным. Эффективно подавл рост сорных растений, оно не наносит вреда таким культурным растени м, как рис, редис, соевые бобы, фасоль, морковь и хлопчатник.The proposed herbicidal agent is selective. Effectively suppressed the growth of weeds, it does not harm such cultivated plants as rice, radish, soybeans, beans, carrots and cotton.
Способ получени соединений общей формулы (I) основан на реакции эфироамидохлортиофосфатов с соответствующими 2-нитро-5-:метилфенолами в присутствии акцептора хлористого водорода.The method of producing compounds of general formula (I) is based on the reaction of ether amide hydrochlorothiophosphates with the corresponding 2-nitro-5-: methylphenols in the presence of a hydrogen chloride acceptor.
Таблица 1Table 1
Во Воех примерах, испытыва соединени общей форМулы (I) на гербицидную активность , дл сравнени используют -известные соединени , обладающие гер.бицидной активностью:In Voye examples, having tested compounds of general form (I) for herbicidal activity, for comparison, well-known compounds with germicidal activity are used:
О-метил - О-2,4-дихлорфенил - N - изопропиламидотиофосфат (соединение Л) и 0-метил-О2-нитрофенил - N - изопропиламидотиофосфат (соединение В).O-methyl - O-2,4-dichlorophenyl - N - isopropylamidothiophosphate (compound L) and 0-methyl-O2-nitrophenyl - N - isopropylamidothiophosphate (compound B).
Пример I. Семена опытных растений высевают в цветочные горщки и прикрывают семена почвой. После этого почву обрабатывают соединени ми согласно изобретению в форме эмульгируемых концентратов. Через 20 дней после обработки оценивают гербицидный эффект по п тибалльной шкале: О- отсутствие повреждений, 5 - полна гибель растений.Example I. Seeds of experimental plants are sown in flower pods and cover the seeds with soil. Thereafter, the soil is treated with compounds according to the invention in the form of emulsifiable concentrates. 20 days after the treatment, the herbicidal effect is evaluated on a five-point scale: O means no damage, 5 is full of plant death.
Результаты опыта представлены в табл. 2 (номера соединений соответствуют номерам в таблице 1).The results of the experiment are presented in table. 2 (numbers of compounds correspond to the numbers in table 1).
Таблица 2table 2
Пример 2. В горшочки Ва.гнера диаметром 14 см помещают почву с рисовых полей в количестве 1,5 кг и довод т ее до состо ни рисового пол . После этого в горшочки высаживают рассаду риса иа стадии развити трех листков, затем высевают семеиа куриного проса, прикрывают их землей и расПродолжение табл. 2Example 2. The soil from a paddy field in an amount of 1.5 kg is placed in Ba.gner pots with a diameter of 14 cm and brought to the state of a rice floor. After that, rice seedlings are planted in the pots and the development stage of three leaves, then the millet family is sown, covered with soil and continued. 2
т т в теплице. На второй день после посева на почву, покрытую водой, нанос т указанные в табл. 3 количества соединений.t t in the greenhouse. On the second day after sowing, the following are applied to the soil covered with water. 3 numbers of compounds.
Через 25 дней определ ют гербицидный эффект по 5-балльной шкале и фитотоксичность по отношению к растени м риса. Результаты приведены в табл. 3.After 25 days, the herbicidal effect is determined on a 5-point scale and phytotoxicity with respect to rice plants. The results are shown in Table. 3
Таблица 3Table 3
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8443270 | 1970-09-25 | ||
JP12902170 | 1970-12-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
SU534172A3 true SU534172A3 (en) | 1976-10-30 |
Family
ID=26425474
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU1704918A SU534172A3 (en) | 1970-09-25 | 1971-09-24 | Herbicide |
Country Status (12)
Country | Link |
---|---|
AR (1) | AR194464A1 (en) |
AU (1) | AU443186B2 (en) |
CA (1) | CA1011341A (en) |
CH (1) | CH570110A5 (en) |
CS (1) | CS172931B2 (en) |
DE (1) | DE2147873C2 (en) |
ES (1) | ES395352A1 (en) |
FR (1) | FR2107999B1 (en) |
GB (1) | GB1359727A (en) |
IT (1) | IT943617B (en) |
NL (1) | NL7113173A (en) |
SU (1) | SU534172A3 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1007241A (en) * | 1972-12-15 | 1977-03-22 | Sumitomo Chemical Company | Organo phosphorus herbicides |
EP0089191A3 (en) * | 1982-03-15 | 1983-11-02 | Sumitomo Chemical Company, Limited | Fungicidal composition comprising phosphoramidothionates |
EP2052611A1 (en) | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Herbicide combination |
DE102008037626A1 (en) | 2008-08-14 | 2010-02-18 | Bayer Cropscience Ag | Herbicide combination with dimethoxytriazinyl-substituted difluoromethanesulfonylanilides |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1245952B (en) * | 1965-12-08 | Farbenfabriken Bayer Aktienge Seilschaft Leverkusen | Ver drive for the production of an O alkyl N alkvlamido thionophosphoric acid ester | |
BG15528A3 (en) * | 1968-05-14 | 1976-05-25 | Gerhard Schrader | HERBICIDE |
JPS4818462B1 (en) * | 1969-02-08 | 1973-06-06 | ||
JPS4818809B1 (en) * | 1969-02-14 | 1973-06-08 | ||
DE2001773A1 (en) * | 1969-02-27 | 1970-09-24 | Bayer Ag | Herbicides |
DE2167007C3 (en) * | 1970-09-25 | 1979-05-03 | Sumitomo Chemical Co., Ltd., Osaka (Japan) | Phosphorus dinamidate with herbicidal effect |
-
1971
- 1971-09-22 CH CH1386271A patent/CH570110A5/xx not_active IP Right Cessation
- 1971-09-22 IT IT269271A patent/IT943617B/en active
- 1971-09-23 AR AR23814071A patent/AR194464A1/en active
- 1971-09-23 CS CS677271A patent/CS172931B2/cs unknown
- 1971-09-23 AU AU33825/71A patent/AU443186B2/en not_active Expired
- 1971-09-23 ES ES395352A patent/ES395352A1/en not_active Expired
- 1971-09-24 FR FR7134554A patent/FR2107999B1/fr not_active Expired
- 1971-09-24 GB GB4474371A patent/GB1359727A/en not_active Expired
- 1971-09-24 DE DE19712147873 patent/DE2147873C2/en not_active Expired
- 1971-09-24 NL NL7113173A patent/NL7113173A/xx unknown
- 1971-09-24 SU SU1704918A patent/SU534172A3/en active
- 1971-09-27 CA CA123,711A patent/CA1011341A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
CA1011341A (en) | 1977-05-31 |
CS172931B2 (en) | 1977-01-28 |
DE2147873C2 (en) | 1984-05-17 |
FR2107999A1 (en) | 1972-05-12 |
AU443186B2 (en) | 1973-12-13 |
IT943617B (en) | 1973-04-10 |
AU3382571A (en) | 1973-03-29 |
FR2107999B1 (en) | 1974-05-31 |
CH570110A5 (en) | 1975-12-15 |
DE2147873A1 (en) | 1972-03-30 |
NL7113173A (en) | 1972-03-28 |
ES395352A1 (en) | 1974-12-16 |
GB1359727A (en) | 1974-07-10 |
AR194464A1 (en) | 1973-07-23 |
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