RU2277329C1 - Method for protection of vegetative sunflower plants from damage action of 2,4-d - Google Patents
Method for protection of vegetative sunflower plants from damage action of 2,4-d Download PDFInfo
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- RU2277329C1 RU2277329C1 RU2005102858/15A RU2005102858A RU2277329C1 RU 2277329 C1 RU2277329 C1 RU 2277329C1 RU 2005102858/15 A RU2005102858/15 A RU 2005102858/15A RU 2005102858 A RU2005102858 A RU 2005102858A RU 2277329 C1 RU2277329 C1 RU 2277329C1
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- Prior art keywords
- antidote
- herbicide
- sunflower plants
- protection
- damage action
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- 241000208818 Helianthus Species 0.000 title claims abstract description 9
- 238000000034 method Methods 0.000 title claims abstract description 6
- 239000004009 herbicide Substances 0.000 claims abstract description 17
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 15
- UQMRAFJOBWOFNS-UHFFFAOYSA-N butyl 2-(2,4-dichlorophenoxy)acetate Chemical compound CCCCOC(=O)COC1=CC=C(Cl)C=C1Cl UQMRAFJOBWOFNS-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000000729 antidote Substances 0.000 claims description 21
- 230000000254 damaging effect Effects 0.000 claims description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 2
- -1 N- (2-methoxyphenyl) -2,6-dichloro-4-methylnicotinoylamide Chemical compound 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 8
- 241000196324 Embryophyta Species 0.000 abstract description 5
- 239000000126 substance Substances 0.000 abstract 1
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 235000003222 Helianthus annuus Nutrition 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- AVVMTRZWAZYOBR-UHFFFAOYSA-N 2,6-dichloro-4-methylpyridine-3-carbonyl chloride Chemical compound CC1=CC(Cl)=NC(Cl)=C1C(Cl)=O AVVMTRZWAZYOBR-UHFFFAOYSA-N 0.000 description 1
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 description 1
- SXKLOQCGXUTBNP-UHFFFAOYSA-N 4-methylpyridine-3-carboxamide Chemical compound CC1=CC=NC=C1C(N)=O SXKLOQCGXUTBNP-UHFFFAOYSA-N 0.000 description 1
- 238000000692 Student's t-test Methods 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 229940075522 antidotes Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- VMPITZXILSNTON-UHFFFAOYSA-N o-anisidine Chemical compound COC1=CC=CC=C1N VMPITZXILSNTON-UHFFFAOYSA-N 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 229960000468 sulfalene Drugs 0.000 description 1
- KXRZBTAEDBELFD-UHFFFAOYSA-N sulfamethopyrazine Chemical compound COC1=NC=CN=C1NS(=O)(=O)C1=CC=C(N)C=C1 KXRZBTAEDBELFD-UHFFFAOYSA-N 0.000 description 1
- 235000020238 sunflower seed Nutrition 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
Изобретение относится к технологии защиты культурных растений от повреждающего действия гербицидов.The invention relates to a technology for the protection of cultivated plants from the damaging effects of herbicides.
Известен способ защиты вегетирующих культурных растений от повреждающего действия гербицидов, предусматривающий их обработку антидотом после использования гербицида (Питина М.Р. и др., Современный уровень и перспективные направления защиты сельскохозяйственных культур от нежелательных последствий применения гербицидов // Агрохимия, 1986, №4, с.107-136).A known method of protecting vegetative crops from the damaging effects of herbicides, providing for their treatment with an antidote after using the herbicide (Pitina M.R. et al., The current level and promising areas of crop protection from undesirable effects of the use of herbicides // Agrochemistry, 1986, No. 4, p. 107-136).
Задачей изобретения является расширение арсенала антидотов подсолнечника от повреждающего действия 2,4-Д.The objective of the invention is to expand the arsenal of antidotes of sunflower from the damaging effects of 2,4-D.
Техническим результатом изобретения является защита вегетирующих растений подсолнечника от повреждающего действия 2,4-Д, выражающаяся в повышении урожайности по сравнению с обработанным гербицидом контролем.The technical result of the invention is the protection of vegetative sunflower plants from the damaging effects of 2,4-D, which is expressed in an increase in yield compared to a herbicide-treated control.
Этот результат достигается тем, что в способе защиты вегетирующих растений подсолнечника от повреждающего действия 2,4-Д, предусматривающем их обработку антидотом после использования гербицида, согласно изобретению, в качестве антидота используют N-(2-метоксифенил)-2,6-дихлор-4-метилникотиноиламид в количестве 200 г/га через 5 суток после использования гербицида.This result is achieved by the fact that in the method of protecting vegetative sunflower plants from the damaging effects of 2,4-D, providing for their treatment with an antidote after using the herbicide according to the invention, N- (2-methoxyphenyl) -2,6-dichloro- is used as an antidote 4-methylnicotinoylamide in an amount of 200 g / ha 5 days after using the herbicide.
Синтез антидота впервые осуществлен авторами по схеме:The synthesis of the antidote was first carried out by the authors according to the scheme:
Методика синтезаSynthesis Method
Смешивали раствор 2,1 г (10 ммоль) 2,6-дихлор-4-метилникотиноилхлорида в 15 мл абсолютного толуола и 1,35 г (11 ммоль) 2-метоксианилина, добавляли 1,1 г (10 ммоль) триэтиламина в 15 мл абсолютного толуола и нагревали при кипении 8 ч. Из охлажденной реакционной массы отфильтровывали осадок, промывали его водой, сушили. Реакционный раствор упаривали досуха, остаток объединяли с осадком и перекристаллизовывали из ацетона, сушили. Получено 2,27 г (76% теор.) целевого продукта с Тпл.=132-133°С.A solution of 2.1 g (10 mmol) of 2,6-dichloro-4-methylnicotinoyl chloride in 15 ml of absolute toluene and 1.35 g (11 mmol) of 2-methoxyaniline were mixed, 1.1 g (10 mmol) of triethylamine in 15 ml was added. absolute toluene and heated at boiling for 8 hours. The precipitate was filtered from the cooled reaction mass, washed with water, and dried. The reaction solution was evaporated to dryness, the residue was combined with the precipitate and recrystallized from acetone, dried. Received 2.27 g (76% of theory.) Of the target product with T pl. = 132-133 ° C.
Оценку антидотной активности полученного соединения на растениях подсолнечника проводили на экспериментальном поле ВНИИБЗР. В качестве эталона использовали известный антидот 2,4-Д - сульфален (Список пестицидов и агрохимикатов, разрешенных к использованию на территории РФ. Приложение к журналу "Защита и карантин растений", 2002, №6). Эталон использовали в рекомендованном для подсолнечника количестве 200 г/га при расходе рабочей жидкости 300 л/га. Испытания проводили по следующей методике.The antidote activity of the obtained compound in sunflower plants was evaluated in the experimental field of VNIIBZR. The known antidote 2,4-D, sulfalene, was used as a reference (List of pesticides and agrochemicals permitted for use in the Russian Federation. Appendix to the journal "Plant Protection and Quarantine", 2002, No. 6). The standard was used in the recommended amount for sunflower 200 g / ha at a flow rate of 300 l / ha. The tests were carried out according to the following procedure.
В полевых условиях растения подсолнечника сорта ВНИИМК-8883 в фазу 10-16 листьев обрабатывали бутиловым эфиром 2,4-дихлорфеноксиуксусной кислоты в дозе 18 г/га и через 5 сут наносили раствор полученного соединения в дозе 200 г/га с нормой расхода рабочей жидкосто 300 л/га.In the field, sunflower plants of the VNIIMK-8883 variety in the 10-16 leaf phase were treated with 2,4-dichlorophenoxyacetic acid butyl ether at a dose of 18 g / ha and after 5 days a solution of the obtained compound was applied at a dose of 200 g / ha with a working fluid flow rate of 300 l / ha.
В опыте предусмотрены следующие варианты:In the experiment, the following options are provided:
1. Гербицид (контроль)1. Herbicide (control)
2. Гербицид + антидот (заявляемый)2. Herbicide + antidote (claimed)
3. Гербицид + антидот (эталон)3. Herbicide + antidote (standard)
4. Контроль (необработанные растения)4. Control (untreated plants)
Опыты проводили на делянках площадью 3 м2, повторность пятикратная. Уборку урожая подсолнечника проводили в момент полного созревания семян.The experiments were carried out on plots with an area of 3 m 2 , five repetition. Harvesting of sunflower seeds was carried out at the time of complete ripening of seeds.
Антидотный эффект синтезированного соединения и эталона определяли по абсолютной величине прибавки к гербицидному контролю и в процентах по формуле:The antidote effect of the synthesized compound and the standard was determined by the absolute value of the addition to the herbicidal control and in percentage by the formula:
Ax - антидотный эффект, %;A x - antidote effect,%;
А - урожай в варианте антидот + гербицид;A - crop in the variant antidote + herbicide;
Э - урожай в варианте эталон (гербицид).E - crop in the standard version (herbicide).
Полученные данные статистически обработаны с использованием t -критерия Стьюдента.The data obtained are statistically processed using student t-test.
Результаты испытаний представлены в таблице 1.The test results are presented in table 1.
Антидотная активность в отношении 2,4-Д синтезированного соединения.Table 1
Antidote activity against 2,4-D synthesized compounds.
антидота, г/гаDose
antidote, g / ha
ц/гаproductivity
c / ha
ц/гаproductivity
c / ha
Р=0,90* The differences between the options "antidote + herbicide" and "herbicide (control)" are significant when
P = 0.90
Таким образом, предлагаемое изобретение позволяет обеспечить антидотный эффект на уровне 52,1%, против 18,8% у эталона.Thus, the present invention allows to provide an antidote effect at the level of 52.1%, against 18.8% of the standard.
Claims (1)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| RU2005102858/15A RU2277329C1 (en) | 2005-02-07 | 2005-02-07 | Method for protection of vegetative sunflower plants from damage action of 2,4-d |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| RU2005102858/15A RU2277329C1 (en) | 2005-02-07 | 2005-02-07 | Method for protection of vegetative sunflower plants from damage action of 2,4-d |
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| Publication Number | Publication Date |
|---|---|
| RU2277329C1 true RU2277329C1 (en) | 2006-06-10 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2005102858/15A RU2277329C1 (en) | 2005-02-07 | 2005-02-07 | Method for protection of vegetative sunflower plants from damage action of 2,4-d |
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| RU (1) | RU2277329C1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2408582C1 (en) * | 2009-07-01 | 2011-01-10 | Федеральное государственное образовательное учреждение высшего профессионального образования Кубанский государственный аграрный университет | N-benzyl-n-phenyl-4,6-dimethyl-2-chloropyridyl-3-carboxamide, having growth-regulating activity |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2093029C1 (en) * | 1987-08-13 | 1997-10-20 | Монсанто Компани | Oxazolidine dihaloacetamide compounds and a method of herbicide phytotoxic effect decrease |
| RU2182423C2 (en) * | 1996-05-29 | 2002-05-20 | Хехст Шеринг Агрево ГмбХ | Agent for protection of cultured plants from phytotoxic adverse effect of herbicides, n- acylsulfonamides |
| RU2202184C2 (en) * | 1994-11-11 | 2003-04-20 | Хехст Шеринг Агрево ГмбХ | Combinations of phenylsulfonylurea herbicides with antidotes and method of protection of cultured plants from adverse phytotoxic effects of phenylsulfonylurea herbicides |
-
2005
- 2005-02-07 RU RU2005102858/15A patent/RU2277329C1/en not_active IP Right Cessation
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2093029C1 (en) * | 1987-08-13 | 1997-10-20 | Монсанто Компани | Oxazolidine dihaloacetamide compounds and a method of herbicide phytotoxic effect decrease |
| RU2202184C2 (en) * | 1994-11-11 | 2003-04-20 | Хехст Шеринг Агрево ГмбХ | Combinations of phenylsulfonylurea herbicides with antidotes and method of protection of cultured plants from adverse phytotoxic effects of phenylsulfonylurea herbicides |
| RU2182423C2 (en) * | 1996-05-29 | 2002-05-20 | Хехст Шеринг Агрево ГмбХ | Agent for protection of cultured plants from phytotoxic adverse effect of herbicides, n- acylsulfonamides |
Non-Patent Citations (1)
| Title |
|---|
| ПИТИНА М.Р. и др. Современный уровень и перспективные направления защиты сельскохозяйственных культур от нежелательных последствий применения гербицидов. Агрохимия, 1986, №4, с.107-136. * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2408582C1 (en) * | 2009-07-01 | 2011-01-10 | Федеральное государственное образовательное учреждение высшего профессионального образования Кубанский государственный аграрный университет | N-benzyl-n-phenyl-4,6-dimethyl-2-chloropyridyl-3-carboxamide, having growth-regulating activity |
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