SU550104A3 - Herbicidal composition - Google Patents
Herbicidal compositionInfo
- Publication number
- SU550104A3 SU550104A3 SU2139078A SU2139078A SU550104A3 SU 550104 A3 SU550104 A3 SU 550104A3 SU 2139078 A SU2139078 A SU 2139078A SU 2139078 A SU2139078 A SU 2139078A SU 550104 A3 SU550104 A3 SU 550104A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- herbicidal composition
- composition
- dichlorophenoxy
- derivatives
- weed
- Prior art date
Links
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
- 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
- A01N43/34—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
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)
Description
(54) ГЕРБИЦИДНЫЙ СОСТАВ(54) HERBICIDE STRUCTURE
Изобретение относитс к химическим средствам дли борьбы с сорной растительностью , а именно к гербицидным составам содержащим синергитические смеси органических веществ. Известны гербицидные составы на осно ве двухкомпонентных синергитических смесей , например состав, содержащий об -(2, 4-дихлорфенокси)пропионовую кислоту или ее производные (соли, эфиры) и двуокись З-алкил-2,1,3-бензотиадиазинона 1. Однако такие гербицидные составы или недостаточно эффективны против сорных растений, или малоизбирательны в отнощении культурных растений. Цель изобретени - эффективное подавле ние роста устойчивых сорных растег-тй и избирательное действие по отношению к культурным растени м. Это достигаетс гербицидным составом на основе двухкомпонентной синерГитической смеси, содержащей об -(2,4-дихлорфенокси ) пропионовую кислоту или ее произ водные (соли или эфиры) и 3,6-дихлорпико липовую кислоту или ее производные (соли или эфиры). Предлагаемый гербицидный состав содержит 3,6-дихлорпиколиновую -кислоту или ее производные и об -(2,4-дихлорфенокси)пропионовую кислоту или ее производные в весовом соотношении от 1:6 до 1:1ОО соответственно , в пересчете на кислотные эквиваленты . Данный состав эффективно подавл ет рост таких устойчивых сорных растений, как ромашка пахуча , трехреберник и мокрица. Он избирателен в отношении пщеницы, чмен и некоторых трав нистых культурных растений . Формы применени состава обычные: растворы , пасты, эмульсии, порошки, суспензии, гранул ты и т.д. Их готов т общеизвестными способами. Содержание действующих веществ в этих формах может значительно колебатьс и находитьс в пределах от 0,1 - 95 вес.% (предпочтительно 0,1 - 6О вес,%). Состав имеет совместимость с другими органическими пестицидами и удобрени ми. 55 3 Синергитический эффект смесей о6-(2, 4,-дихлорфенокси) пропионовой и 3,6-дихлор пиколиновой кислот или их производных рассчитывали по известной методике (Weeds 1967, 5О, стр. 20-22). Ниже представлены примеры, подтверждающие наличие синергизма рассматриваемой смеси и иллкх;трирующие гербидидное действие предлагаемого состава. Пример 1. Сорное растение (мокрицу ) выращивали в песчано-суглинистой почве в услови х теплицы при температуре 18°С. Растени выращивали в противн х (по три растени на каждом) до стадии 48 листиков, затем опрыскивали предлагаемым гербицидным составом и отдельными компонентами состава. Через 14 дней после обработки определ ли гербицидное действие состава в сравнении с действием отдельных компонентов. Шкала оценки: О - отсутствие эффекта 5 - полна гибель растений.This invention relates to chemical means for controlling weed vegetation, namely, to herbicidal compositions containing synergistic mixtures of organic substances. Herbicidal compositions based on two-component synergistic mixtures are known, for example, a composition containing about - (2, 4-dichlorophenoxy) propionic acid or its derivatives (salts, esters) and 3-alkyl-2,1-benzothiadiazinone dioxide 1. However herbicidal compositions are either not sufficiently effective against weeds, or are low-selective in relation to cultivated plants. The purpose of the invention is the effective suppression of the growth of resistant weed spreads and selective action with respect to cultivated plants. This is achieved by a herbicidal composition based on a two-component synergistic mixture containing ob - (2,4-dichlorophenoxy) propionic acid or its derivatives (salts or esters) and 3,6-dichloropyco-lipic acid or its derivatives (salts or esters). The proposed herbicidal composition contains 3,6-dichloropicolinic -acid or its derivatives and about - (2,4-dichlorophenoxy) propionic acid or its derivatives in a weight ratio of from 1: 6 to 1: 1OO, respectively, in terms of acid equivalents. This compound effectively inhibits the growth of such resistant weeds as chamomile, trichoptera and woodlouse. It is selective for wheat, barley, and some grassy cultivated plants. The form of application of the composition of the usual: solutions, pastes, emulsions, powders, suspensions, granules, etc. They are prepared in well-known ways. The content of active substances in these forms can vary considerably and range from 0.1 to 95% by weight (preferably 0.1 to 6O by weight,%). The formulation is compatible with other organic pesticides and fertilizers. 55 3 The synergistic effect of mixtures of o6- (2, 4, -dichlorophenoxy) propionic and 3,6-dichloric picolinic acids or their derivatives was calculated by the known method (Weeds 1967, 5O, pp. 20-22). Below are examples confirming the presence of synergism of the mixture and illkh; triaming herbidid action of the proposed composition. Example 1. Weed plant (wood lice) was grown in sandy-loamy soil under greenhouse conditions at a temperature of 18 ° C. Plants were grown in opposites (three plants each) to a stage of 48 leaves, then sprayed with the proposed herbicidal composition and individual components of the composition. 14 days after treatment, the herbicidal effect of the composition was determined in comparison with the action of the individual components. Rating scale: O - no effect 5 - full of plant death.
Степень поражени зародышей сорн ка (в %) при использованииThe degree of infestation of weed germs (in%) when using
(5б-(2,4-дихлорфенокси)пропионова кислота. (5b- (2,4-dichlorophenoxy) propionic acid.
Таблица 2 4 опыта представлены в таблиРезультаты 1. це Пример 2. Участок озимого чмен , зараженный трехреберником, обрабатывали водными растворами этаноламинных солей 3,6-дихлорпиколиновой и сС -(2,4-ди- хлорфенокси) пропионовой кислот. Сорн к к этому времени имел стадию развити 612 листков. Степень поражени сорного растени оценивали через 12 недель после обработки . В таблице 2 приведены наблюдени наблюдаемой степени поражени (О) и ожидаемой (Е), причем последн рассчитана по известному методу (Weedg, 1967, 50 стр. 20-22). Из таблицы видно, что эффект синергизма особенно отчетливо наблюдаетс при использовании сравнительно низких доз смеси. Таблица 1Table 2 4 of the experiment are presented in Table 1. Results Example 2. A plot of winter barley infected with trinity, was treated with aqueous solutions of ethanolamine salts of 3,6-dichloropicolinic and cC - (2,4-dichlorophenoxy) propionic acids. By this time, the weed had a stage of development of 612 leaves. The degree of damage to the weed was evaluated 12 weeks after treatment. Table 2 shows the observed degree of damage (O) and expected (E), the latter being calculated by a known method (Weedg, 1967, 50 pp. 20-22). From the table it can be seen that the synergistic effect is especially clearly observed when using relatively low doses of the mixture. Table 1
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB25018/74A GB1494205A (en) | 1974-06-05 | 1974-06-05 | Herbicidal compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
SU550104A3 true SU550104A3 (en) | 1977-03-05 |
Family
ID=10220899
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU2139078A SU550104A3 (en) | 1974-06-05 | 1975-06-04 | Herbicidal composition |
SU752146726A SU596149A3 (en) | 1974-06-05 | 1975-06-04 | Herbicide composition |
SU752141754A SU587836A3 (en) | 1974-06-05 | 1975-06-04 | Herbicidal composition |
SU752143831A SU603313A3 (en) | 1974-06-05 | 1975-06-05 | Herbicide |
Family Applications After (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU752146726A SU596149A3 (en) | 1974-06-05 | 1975-06-04 | Herbicide composition |
SU752141754A SU587836A3 (en) | 1974-06-05 | 1975-06-04 | Herbicidal composition |
SU752143831A SU603313A3 (en) | 1974-06-05 | 1975-06-05 | Herbicide |
Country Status (12)
Country | Link |
---|---|
BE (4) | BE829874A (en) |
CA (3) | CA1024769A (en) |
CS (4) | CS187477B2 (en) |
DE (4) | DE2524880A1 (en) |
DK (4) | DK138032B (en) |
FR (4) | FR2273475A1 (en) |
GB (1) | GB1494205A (en) |
IT (3) | IT1036910B (en) |
NL (4) | NL180971C (en) |
PL (3) | PL94094B1 (en) |
SE (4) | SE419025B (en) |
SU (4) | SU550104A3 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1518672A (en) * | 1974-09-17 | 1978-07-19 | Boots Co Ltd | Herbicidal composition |
IT1115383B (en) * | 1977-08-04 | 1986-02-03 | Sipcam Spa | HERBICIDE COMPOSITIONS FOR THE FIGHT AGAINST DICOTYLEDON WEEDS IN CEREAL FIELDS AND PREPARATION AND USE PROCEDURES |
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1974
- 1974-06-05 GB GB25018/74A patent/GB1494205A/en not_active Expired
-
1975
- 1975-05-30 NL NLAANVRAGE7506460,A patent/NL180971C/en not_active IP Right Cessation
- 1975-05-30 NL NLAANVRAGE7506459,A patent/NL181393C/en not_active IP Right Cessation
- 1975-05-30 NL NL7506442A patent/NL7506442A/en not_active Application Discontinuation
- 1975-05-30 NL NLAANVRAGE7506451,A patent/NL181392C/en not_active IP Right Cessation
- 1975-06-03 IT IT49882/75A patent/IT1036910B/en active
- 1975-06-03 IT IT49881/75A patent/IT1036909B/en active
- 1975-06-03 IT IT49884/75A patent/IT1036911B/en active
- 1975-06-04 PL PL1975180891A patent/PL94094B1/pl unknown
- 1975-06-04 BE BE157040A patent/BE829874A/en unknown
- 1975-06-04 DE DE19752524880 patent/DE2524880A1/en active Pending
- 1975-06-04 FR FR7517474A patent/FR2273475A1/en active Granted
- 1975-06-04 DE DE19752524879 patent/DE2524879A1/en active Pending
- 1975-06-04 SU SU2139078A patent/SU550104A3/en active
- 1975-06-04 PL PL1975180890A patent/PL94093B1/pl unknown
- 1975-06-04 SE SE7506418A patent/SE419025B/en not_active IP Right Cessation
- 1975-06-04 PL PL1975180892A patent/PL94044B1/xx unknown
- 1975-06-04 BE BE157041A patent/BE829875A/en not_active IP Right Cessation
- 1975-06-04 SE SE7506417A patent/SE419024B/en not_active IP Right Cessation
- 1975-06-04 DK DK253675AA patent/DK138032B/en not_active IP Right Cessation
- 1975-06-04 SE SE7506419A patent/SE425539B/en not_active IP Right Cessation
- 1975-06-04 DE DE19752524878 patent/DE2524878A1/en active Pending
- 1975-06-04 SU SU752146726A patent/SU596149A3/en active
- 1975-06-04 CA CA228,524A patent/CA1024769A/en not_active Expired
- 1975-06-04 FR FR7517472A patent/FR2273473A1/en active Granted
- 1975-06-04 DE DE19752524881 patent/DE2524881A1/en active Pending
- 1975-06-04 BE BE157038A patent/BE829872A/en not_active IP Right Cessation
- 1975-06-04 CA CA228,459A patent/CA1024768A/en not_active Expired
- 1975-06-04 DK DK253575AA patent/DK138031B/en not_active IP Right Cessation
- 1975-06-04 SE SE7506420A patent/SE419026B/en not_active IP Right Cessation
- 1975-06-04 FR FR7517471A patent/FR2273472A1/en active Granted
- 1975-06-04 DK DK253875AA patent/DK138034B/en not_active IP Right Cessation
- 1975-06-04 BE BE157039A patent/BE829873A/en not_active IP Right Cessation
- 1975-06-04 DK DK253775AA patent/DK138033B/en unknown
- 1975-06-04 SU SU752141754A patent/SU587836A3/en active
- 1975-06-04 CA CA228,458A patent/CA1026964A/en not_active Expired
- 1975-06-04 FR FR7517473A patent/FR2273474A1/en active Granted
- 1975-06-05 CS CS753950A patent/CS187477B2/en unknown
- 1975-06-05 CS CS753949A patent/CS187476B2/en unknown
- 1975-06-05 CS CS753952A patent/CS187479B2/en unknown
- 1975-06-05 SU SU752143831A patent/SU603313A3/en active
- 1975-06-05 CS CS753951A patent/CS187478B2/en unknown
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