RU1795879C - Бактерицидна композици дл защиты растений - Google Patents
Бактерицидна композици дл защиты растенийInfo
- Publication number
- RU1795879C RU1795879C SU853915002A SU3915002A RU1795879C RU 1795879 C RU1795879 C RU 1795879C SU 853915002 A SU853915002 A SU 853915002A SU 3915002 A SU3915002 A SU 3915002A RU 1795879 C RU1795879 C RU 1795879C
- Authority
- RU
- Russia
- Prior art keywords
- plant protection
- bactericidal composition
- bactericidal
- composition
- active ingredient
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 22
- 230000000844 anti-bacterial effect Effects 0.000 title claims abstract description 12
- 239000000654 additive Substances 0.000 claims abstract 3
- 239000004480 active ingredient Substances 0.000 claims description 7
- FUBFWTUFPGFHOJ-UHFFFAOYSA-N 2-nitrofuran Chemical class [O-][N+](=O)C1=CC=CO1 FUBFWTUFPGFHOJ-UHFFFAOYSA-N 0.000 claims description 4
- 239000000243 solution Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 2
- -1 phosphoric acid diester Chemical class 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- GBHCABUWWQUMAJ-UHFFFAOYSA-N 2-hydrazinoethanol Chemical compound NNCCO GBHCABUWWQUMAJ-UHFFFAOYSA-N 0.000 description 1
- SXINBFXPADXIEY-UHFFFAOYSA-N 5-Nitrofurfural Chemical compound [O-][N+](=O)C1=CC=C(C=O)O1 SXINBFXPADXIEY-UHFFFAOYSA-N 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 description 1
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
- YDEXUEFDPVHGHE-GGMCWBHBSA-L disodium;(2r)-3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Na+].[Na+].COC1=CC=CC(C[C@H](CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O YDEXUEFDPVHGHE-GGMCWBHBSA-L 0.000 description 1
- YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002240 furans Chemical class 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- UYDLBVPAAFVANX-UHFFFAOYSA-N octylphenoxy polyethoxyethanol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCOCCO)C=C1 UYDLBVPAAFVANX-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- 239000004476 plant protection product Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/26—Oxidation products of dithiocarbamic acid derivatives, e.g. thiuram sulfides
-
- 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
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
-
- 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
- A01N43/76—1,3-Oxazoles; Hydrogenated 1,3-oxazoles
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
- A01N47/04—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom containing >N—S—C≡(Hal)3 groups
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
- A01N47/14—Di-thio analogues 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/18—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
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)
Abstract
Использование: сельское хоз йство, бактерицидна композици . Сущность изобретени : композици содержит производное 5-нитрофурфулиден-3-амино-2- оксазолидон в количестве 25,9-80 мас.%, остальное целевые добавки. 1 табл.
Description
Изобретение относитс к химическим средствам защиты растений, конкретно, к бактерицидной композиции дл защиты растений на основе производного 5-нитро- фурана.
Известна бактерицидна композици дл защиты растений на основе производного фурана.
Более близкой к за вленной бактерицидной композиции вл етс бактерицидна композици на основе производного 5-нитрофурана.
Однако указанные бактерицидные композиции обладают недостаточной активностью при малых концентраци х.
Целью изобретени вл етс увеличение бактерицидной активности композиций .
Пример 1. Получение 5-нитрофурфу- лиден-З-амино-2-оксазолидона.
Раствор ют 1,8 г натри в 25 мл безводного метанола и к полученному раствору
прибавл ют 46 г 2-гидроксиэтилгидразина в 90 мл диэтилкарбоната. Полученный раствор перемешивают в течение 3 часов и охлаждают до комнатной температуры. Затем добавл ют 375 мл спирта и 25 мл концентрированной с 6л и ной кислоты. Полученный раствор приливают при перемешивании к 75 г 5-нитро-2-фурфурола в 750 мл спирта, Образующуюс смесь перемешиваютччв течение часа, а затем фильтруют. Желтый осадок промывают водой, а потом спиртом. После сушки и перекристаллизации из N.N- диметилформамида получают продукт с температурой плавлени 25б-257°С.
Пример 2,
100 кг активного ингредиента, 3 кг диок- тилсульфосукцината натри , 5 кгтетраэтил- родэмина, 41 кг мела и 1 кг натриевой соли карбоксиметилцеллюлозы загружают через измельчающий гранул тор в 600 литровую мешалку и перемешивают в течение 10 минут . Затем измельчают в мельнице имеюVI
О
ел
00
3
w
щей производительность 200 кг/час и гомогенизируют в 300 литровой мешалке. Получают композицию с содержанием активного ингредиента 66,7%.
Пример 3. Приготовление композиции осуществл ют в соответствии с методикой примера 2. При этом используют следующие вещества:
Активный ингредиент160кг Карбонат кальци 20 кг Натриева соль карбо- ксиметилцеллюлозы 1 кг Алкилполигликол т натри 2 кг Алкилнафталинсуль- фонат натри 6 кг Лигнинсульфонат натри 10 кг Синтетическа кремнева кислота . 1 кг Получают композицию с содержанием активного ингредиента 80%.
Пример 4, 183,35 г воды смешивают с 55 г этиленгликол . В полученной смеси раствор ют при 40° 16,5 г смеси додецил- бензолсульфоната кальци с (Сэ-С12)-алкил- фенолполиэтиленгликоль-полипропиленг - ликолевым эфиром и 16,5 г смеси моно.-и диэфира фосфорной кислоты с Св-Сэ-алкил- фенолполиэтиленгликолевым эфиром. В полученном растворе с помощью ультра мешалки диспергируют 143 г активного ингредиента . К суспензии при дальнейшем диспергирующем перемешивании добавл ют 99 г парафинового масла и 11 г октилфе- ноксиполиэтоксиэтанола. Перемешивание продолжают до получени гомогенной системы и при перемешивании добавл ют 27,5 г полисахарида (2% водный раствор). Смесь перемешивают до образовани гомогенной
массы и добавл ют 1,1 г масл ной эмульсии. Получают композицию с содержанием активного ингредиента 25,9 мае. %.
П р и м е р 5. Бактерицидна активность за вленных композиций.
Клубни картофел разрезают на две части . В них проделывают по п ть отверстий (глубина 15 мм, диаметр 10 мм) примерно на равном рассто нии друг от друга, 0,1 мл водной суспензии, содержащей Erwlnia carotovore разновидности atroseptica закапывают в эти отверсти (0,1 мл в каждое отверстие). Испытываемую композицию ввод т в отверсти , предваритель- но обработанные бактери ми, с помощью микропипетки через полчаса. Обработанные и зараженные клубни выдерживают в увлажнительной камере в течение трех дней, после чего производитс оценка. От- версти разрезаютс на две части, перпендикул рно первоначальной плоскости разреза. Частицы м гкой гнили выскребывают и взвешивают. Эффективность обработки оценивают сравнением с необработанным контрольным материалом по следующей шкале: 1 6-10% 2 11 -25% 3 25-50%
. 4 выше50 %Y
Указанные величины в процентах выражают вес выстребанного материала, пекто- лизированного Erwlnia carotovore относительно веса контрольного материала. Данные представлены в таблице 1.
Таким образом, за вленные композиции обладают высокой бактерицидной активностью при небольших концентраци х.
Claims (1)
- Формула изобретени Бактерицидна композици дл защиты растений, содержаща активный ингредиент-производное 5-нитрофурана и целевые добавки, отличающа с тем, что, сцелью увеличени бактерицидной активности , она содержит в качестве производного 5-нитрофурана 5-нитрофурфулиден-З-ами- но-2-оксазолидон в количестве 25,9-80 мас.%, целевые добавки - остальное.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU842454A HU199443B (en) | 1984-06-25 | 1984-06-25 | Bactericidal and/or fungicidal synergic plant protective comprising nitrofuran derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
RU1795879C true RU1795879C (ru) | 1993-02-15 |
Family
ID=10959447
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU853915002A RU1795879C (ru) | 1984-06-25 | 1985-06-25 | Бактерицидна композици дл защиты растений |
SU874355054A RU1834636C (ru) | 1984-06-25 | 1987-01-22 | Бактерицидна композици |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU874355054A RU1834636C (ru) | 1984-06-25 | 1987-01-22 | Бактерицидна композици |
Country Status (11)
Country | Link |
---|---|
US (1) | US4943678A (ru) |
EP (1) | EP0170395B1 (ru) |
JP (1) | JPS6144805A (ru) |
BR (1) | BR8503019A (ru) |
CS (1) | CS252485B2 (ru) |
DD (1) | DD232807A5 (ru) |
DE (1) | DE3584648D1 (ru) |
HU (1) | HU199443B (ru) |
IL (1) | IL75552A (ru) |
PL (1) | PL144541B1 (ru) |
RU (2) | RU1795879C (ru) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2886446B2 (ja) * | 1994-03-03 | 1999-04-26 | 関西ペイント株式会社 | 塗膜保護用シート |
DE4432404C1 (de) * | 1994-08-30 | 1995-11-30 | Exner Heinrich Dr Med Vet | Mittel zur Bekämpfung der Naßfäule und Schwarzbeinigkeit von Pflanzkartoffeln |
US5719103A (en) * | 1996-05-02 | 1998-02-17 | Uniroyal Chemical Company, Inc. | Powder formulation useful for seed treatment and foliar treatment of plants |
US7569692B2 (en) | 2003-06-02 | 2009-08-04 | Fujifilm Corporation | Organic electroluminescent devices and metal complex compounds |
JP2014131979A (ja) * | 2012-12-06 | 2014-07-17 | Ishihara Sangyo Kaisha Ltd | 油性懸濁状有害生物防除剤組成物 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2742462A (en) * | 1952-02-28 | 1956-04-17 | Norwich Pharma Co | New n-(5-nitro-2-furfurylidene)-3-amino-2-oxazolidones |
US2759932A (en) * | 1953-08-10 | 1956-08-21 | Norwich Pharma Co | Series of new n-(5-nitro-2-furfurylidene)-3-amino-2-iminooxazolidines |
US2924554A (en) * | 1957-07-10 | 1960-02-09 | Virginia Carolina Chem Corp | Method of repelling rodents with furan compounds |
NL108055C (ru) * | 1958-06-19 | |||
US3154543A (en) * | 1961-09-18 | 1964-10-27 | Norwich Pharma Co | Preparation of 5-aminofurans |
-
1984
- 1984-06-25 HU HU842454A patent/HU199443B/hu not_active IP Right Cessation
-
1985
- 1985-06-18 IL IL75552A patent/IL75552A/xx not_active IP Right Cessation
- 1985-06-24 BR BR8503019A patent/BR8503019A/pt not_active IP Right Cessation
- 1985-06-24 JP JP60136210A patent/JPS6144805A/ja active Pending
- 1985-06-25 US US06/748,740 patent/US4943678A/en not_active Expired - Fee Related
- 1985-06-25 DE DE8585304528T patent/DE3584648D1/de not_active Expired - Fee Related
- 1985-06-25 DD DD85277744A patent/DD232807A5/de not_active IP Right Cessation
- 1985-06-25 RU SU853915002A patent/RU1795879C/ru active
- 1985-06-25 EP EP85304528A patent/EP0170395B1/en not_active Expired
- 1985-06-25 CS CS854667A patent/CS252485B2/cs unknown
- 1985-06-25 PL PL1985254159A patent/PL144541B1/pl unknown
-
1987
- 1987-01-22 RU SU874355054A patent/RU1834636C/ru active
Non-Patent Citations (1)
Title |
---|
Патент GB № 1263125, кл. С 2 С, опублик. 1972. Патент Чехословакии N 169550 кл. А 01 N 9/28, опублик. 1977. * |
Also Published As
Publication number | Publication date |
---|---|
CS252485B2 (en) | 1987-09-17 |
IL75552A (en) | 1988-11-30 |
DE3584648D1 (de) | 1991-12-19 |
DD232807A5 (de) | 1986-02-12 |
BR8503019A (pt) | 1986-03-11 |
EP0170395B1 (en) | 1991-11-13 |
JPS6144805A (ja) | 1986-03-04 |
RU1834636C (ru) | 1993-08-15 |
US4943678A (en) | 1990-07-24 |
EP0170395A1 (en) | 1986-02-05 |
HU199443B (en) | 1990-02-28 |
HUT39171A (en) | 1986-08-28 |
PL254159A1 (en) | 1987-02-23 |
PL144541B1 (en) | 1988-06-30 |
CS466785A2 (en) | 1987-01-15 |
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