SU1780673A1 - Fungicide agent - Google Patents
Fungicide agent Download PDFInfo
- Publication number
- SU1780673A1 SU1780673A1 SU914929593A SU4929593A SU1780673A1 SU 1780673 A1 SU1780673 A1 SU 1780673A1 SU 914929593 A SU914929593 A SU 914929593A SU 4929593 A SU4929593 A SU 4929593A SU 1780673 A1 SU1780673 A1 SU 1780673A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- dimethyl
- ammonium chloride
- fungicidal
- formula
- properties
- Prior art date
Links
Description
Изобретение относится к сельскому хозяйству, конкретно к Ь1,М-диметил-М-децилацетат-М-этилметакрилат аммоний хлориду формулыThe invention relates to agriculture, specifically to b1, M-dimethyl-M-decyl acetate-M-ethyl methacrylate ammonium chloride of the formula
СН-ι гн=с CH2-COOC10HW •2? 4-1 сьцCH-ι gn = s CH 2 -COOC 10 H W • 2? 4-1 sc
C00-CH,CH<N<C00-CH, CH <N <
1 СНз / ег -который обладает фунгицидным действием в отношении патогенных грибов микрофлоры инфекционных болезней тутового шелкопряда и шелковицы, и может быть использован в шелководстве. 1 CH3 / er - which has a fungicidal effect against pathogenic fungi of the microflora of the infectious diseases of the silkworm and mulberry, and can be used in sericulture.
N, N-ди метил-ГФдецил а цетат-И-этил ме такрилэт аммоний хлорид ранее использовался в качестве мономера для получения высокомолекулярных соединений и как поверхностно-активное вещество (Егоров В., Ксенофонтова О. Б., Батракова Е. В.. Зубов Ε. П., Влияние природы противоиона на коллоидно-химические свойства поверхностноактивных мономеров, Коллоиды, ж., том I, вып. 4, 1988, с. 821 -824).N, N-di-methyl-HFdecyl a cetate-I-ethyl methacrylate ammonium chloride was previously used as a monomer to obtain high molecular weight compounds and as a surfactant (Egorov V., Ksenofontova O. B., Batrakova E. V. .. Zubov П.. P., Effect of the nature of the counterion on the colloidal chemical properties of surface active monomers, Colloids, J., Volume I, issue 4, 1988, pp. 821-824).
Наиболее близким к предлагаемому изобретению является диэтиламиноётилметакрилат, который входит в состав атмосферостойкой, ударопрочной композиции, которую прессуют в листы, имеющие высокую прочность при растяжении и высокую ударную прочность (Патент Японии № 49 23821, 1974, РЖХим, 1975, 9С410).Closest to the proposed invention is diethylaminoethyl methacrylate, which is part of a weather-resistant, impact-resistant composition, which is pressed into sheets having high tensile strength and high impact strength (Japan Patent No. 49 23821, 1974, RZhKhim, 1975, 9C410).
Сравнение свойств ГфМ-диметил-ГФдецилацетаг-М-этилметакрилат аммоний хлорида и диэтиламиноэтилметакрилата приведены в табл. 1.A comparison of the properties of HfM-dimethyl-HFdecylacetag-M-ethyl methacrylate of ammonium chloride and diethylaminoethyl methacrylate is given in table. 1.
1780673 А11780673 A1
Как видно из табл. 1. Ν,Ν-диметил- N-децилацетат-Й-этилметакрилат аммоний хло- :As can be seen from the table. 1. Ν, Ν-dimethyl-N-decyl acetate-Y-ethyl methacrylate ammonium chloro-:
рид отличается от аналога по структуре рядом полезных свойств, как, фунгицидные и пенообразующие свойства. 5Rid differs from the analogue in structure in a number of useful properties, such as fungicidal and foaming properties. 5
В шелководстве в качестве фунгицида используют тетраметил-тиурамдисульфид (ТМТД)(Н. И. Мельников, К. В. Новожилов, Т. Н. Пылова, Химические средства защиты растений, Справочник, М., Химия, 1980, с. 10 260; А. А. Кравцов, Η. М. Голышин, Препараты для защиты растений, Справочник, М., Колос, 1984, с. 97 - 99). Известное вещество в виде водного раствора в присутствии смачивателя применяют для подавления роста 15 грибов. ТМТД токсичен, трудно поддается разложению и имеет способность накапливаться в организме. Кроме того, концентрированные водные растворы ТМТД вызывают раздражение слизистых покро- 20 вов и имеют побочные действия при попаданий в глаза. 'In sericulture, tetramethyl-thiuramdisulfide (TMTD) is used as a fungicide (N. I. Melnikov, K. V. Novozhilov, T. N. Pylova, Chemical plant protection products, Directory, M., Chemistry, 1980, p. 10 260; A. A. Kravtsov, Η. M. Golyshin, Preparations for the protection of plants, Handbook, M., Kolos, 1984, pp. 97 - 99). The known substance in the form of an aqueous solution in the presence of a wetting agent is used to inhibit the growth of 15 fungi. TMTD is toxic, difficult to decompose, and has the ability to accumulate in the body. In addition, concentrated aqueous solutions of TMTD cause irritation of the mucous membranes of 20 and have side effects in contact with the eyes. ''
Указанные недостатки могут быть устранены при использовании водных растворов 1Ч,1М-диметил-М-деци.лацетат-Й-этилметак- 25 рилат аммоний хлорида, который имеет малую токсичность и не имеет побочных действий, а также относится к веществам легкой биоразлагаемости.These disadvantages can be eliminated by using aqueous solutions of 1CH, 1M-dimethyl-M-dec. Acetate-Y-ethylmethac-25 ammonium chloride rilate, which has low toxicity and no side effects, and also relates to substances of easy biodegradability.
Цель изобретения - выявление нового 30 вида действия Ν,Ν-диметил-М-децилацетатN-этилметакрилат аммоний хлорида, а также снижение токсичности фунгицидов.The purpose of the invention is the identification of a new 30 type of action of Ν, Ν-dimethyl-M-decyl acetate N-ethyl methacrylate of ammonium chloride, as well as reducing the toxicity of fungicides.
Поставленная цель, достигается тем, что в качестве фунгицида используют вод- 35 ные растворы МИ-диметил-Ы-децилацетатN-этилметакрилат аммоний хлорида. Препарат эффективен при концентрации 0,3- 10%. Предложенное соединение хорошо растворимо в воде, из-за наличия слож- 40 ноэфирных групп, легко подвергается разложению и относится к малотоксичным соединениям.This goal is achieved by the fact that as a fungicide, aqueous solutions of MI-dimethyl-Y-decyl acetate N-ethyl methacrylate of ammonium chloride are used. The drug is effective at a concentration of 0.3-10%. The proposed compound is readily soluble in water, due to the presence of complex 40-ester groups, it is easily decomposed and is a low-toxic compound.
/ Пример (конкретное выполнение). Фунгицидное действие Ν,Ν-диметил-И-де- 45 цилацетат-М-этилметакрилат аммоний хлорида проводилось методом наложения дисков, пропитанных растворами препарата в концентрациях от 0,3 до 10% на газон тест культур. Фунгицидные свойства ука- 50 занного препарата излучались на следующих грибах Vertlcilllum dahllal, Aspterglllus flavus, Aspergillus nlger, Fusarium monlllforme, Stachybotrys alternans, выделенных из больных хлорозом шелковицы и гусеницы тутового шелкопряда. Тест культурами засевали газон-питательную среду Чапека в чашках Петри. Засеянные чашки, после наложения дисков, инкубировали в термостате при 298 К в течение 48 ч. Контролем служили диски^ропитанные стерильной водой./ Example (specific implementation). The fungicidal effect of Ν, Ν-dimethyl-I-de-45-ethyl acetate-M-ethyl methacrylate of ammonium chloride was carried out by the method of applying discs impregnated with solutions of the drug in concentrations from 0.3 to 10% on the lawn test cultures. The fungicidal properties of the indicated preparation were emitted on the following fungi Vertlcilllum dahllal, Aspterglllus flavus, Aspergillus nlger, Fusarium monlllforme, Stachybotrys alternans isolated from mulberry chlorosis and silkworm caterpillars. Test cultures were seeded with Chapek's lawn-nutrient medium in Petri dishes. Sown plates, after applying discs, were incubated in a thermostat at 298 K for 48 hours. Disks soaked with sterile water served as a control.
Фунгицидную активность Ν,Ν-диметилN-децилацетат-М-этилметакрилат аммоний хлорида оценивали путем сравнения его свойств с известным фунгицидом - ТМТД (табл. 2).The fungicidal activity of Ν, Ν-dimethylN-decyl acetate-M-ethylmethacrylate of ammonium chloride was evaluated by comparing its properties with the well-known fungicide - TMTD (Table 2).
В результате проведенных испытаний установлено, что водные растворы N-N-диметил-М-децилацетат-М-этил метакрилат аммоний хлорида проявляют фунгицидную активность на патогеннук? микрофлору при концентрации от 0,3 до 10%. Это соединение особенно эффективно при низких концентрациях, т. е. 0,3%. При этих концентрациях известных фунгицид ТМТД - малоэффективен.As a result of the tests, it was found that aqueous solutions of N-N-dimethyl-M-decyl acetate-M-ethyl ammonium chloride methacrylate exhibit fungicidal activity on the pathogen? microflora at a concentration of from 0.3 to 10%. This compound is especially effective at low concentrations, i.e. 0.3%. At these concentrations, the known fungicide TMTD is ineffective.
Ν,Ν-диметил-М-децилацетат-М-этилметакрилат аммоний хлорида является поверхностно-активным, малотоксичным, безвредным для организма человека и животных, что имеет важное значение для использования его в качестве фунгицида в шелководстве. ( Ammonium chloride Ν, Ν-dimethyl-M-decyl acetate-M-ethyl methacrylate is surface-active, low-toxic, harmless to humans and animals, which is important for using it as a fungicide in sericulture. (
На основе изложенных данных следует, что ММ-диметил-М-децилацетат-М-этилметакрилат аммоний хлорид может быть рекомендован в качестве фунгицида в шелководстве против патогенных грибов микрофлоры тутового шелкопряда и шелко вицы.Based on the data presented, it follows that MM-dimethyl-M-decyl acetate-M-ethyl methacrylate ammonium chloride can be recommended as a fungicide in silkworm against pathogenic fungi of silkworm and silkworm microflora.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU914929593A SU1780673A1 (en) | 1991-04-19 | 1991-04-19 | Fungicide agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU914929593A SU1780673A1 (en) | 1991-04-19 | 1991-04-19 | Fungicide agent |
Publications (1)
Publication Number | Publication Date |
---|---|
SU1780673A1 true SU1780673A1 (en) | 1992-12-15 |
Family
ID=21570921
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU914929593A SU1780673A1 (en) | 1991-04-19 | 1991-04-19 | Fungicide agent |
Country Status (1)
Country | Link |
---|---|
SU (1) | SU1780673A1 (en) |
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2225331A4 (en) * | 2007-11-19 | 2010-12-01 | Univ Washington | Marine coatings |
US8268301B2 (en) | 2007-11-19 | 2012-09-18 | University Of Washington | Cationic betaine precursors to zwitterionic betaines having controlled biological properties |
US8545983B2 (en) | 2005-08-25 | 2013-10-01 | University Of Washington | Super-low fouling sulfobetaine materials and related methods |
US8617592B2 (en) | 2009-11-06 | 2013-12-31 | University Of Washington Through Its Center For Commercialization | Self-assembled particles from zwitterionic polymers and related methods |
US8658192B2 (en) | 2007-11-19 | 2014-02-25 | University Of Washington | Integrated antimicrobial and low fouling materials |
US8835144B2 (en) | 2006-12-29 | 2014-09-16 | University Of Washington | Dual-functional nonfouling surfaces comprising target binding partner covalently coupled to polymer attached to substrate |
US8870372B2 (en) | 2011-12-14 | 2014-10-28 | Semprus Biosciences Corporation | Silicone hydrogel contact lens modified using lanthanide or transition metal oxidants |
US8877172B2 (en) | 2009-11-06 | 2014-11-04 | University Of Washington Through Its Center For Commercialization | Zwitterionic polymer bioconjugates and related methods |
US9000063B2 (en) | 2011-12-14 | 2015-04-07 | Semprus Biosciences Corporation | Multistep UV process to create surface modified contact lenses |
US9006359B2 (en) | 2011-12-14 | 2015-04-14 | Semprus Biosciences Corporation | Imbibing process for contact lens surface modification |
US9004682B2 (en) | 2011-12-14 | 2015-04-14 | Semprus Biosciences Corporation | Surface modified contact lenses |
US9045576B2 (en) | 2006-08-07 | 2015-06-02 | University Of Washington | Mixed charge copolymers and hydrogels |
US9255929B2 (en) | 2009-09-25 | 2016-02-09 | University Of Washington | Zwitterionic polymers having biomimetic adhesive linkages |
US9358326B2 (en) | 2008-12-05 | 2016-06-07 | Arrow International, Inc. | Layered non-fouling, antimicrobial antithrombogenic coatings |
US9533006B2 (en) | 2007-11-19 | 2017-01-03 | University Of Washington | Marine coatings |
US9599613B2 (en) | 2011-07-20 | 2017-03-21 | University Of Washington Through Its Center For Commercialization | Photonic blood typing |
US9598544B2 (en) | 2005-08-25 | 2017-03-21 | University Of Washington Through Its Center For Commercialization | Particles coated with zwitterionic polymers comprising sulfobetaine or carboxybetaine |
US10031138B2 (en) | 2012-01-20 | 2018-07-24 | University Of Washington Through Its Center For Commercialization | Hierarchical films having ultra low fouling and high recognition element loading properties |
-
1991
- 1991-04-19 SU SU914929593A patent/SU1780673A1/en active
Cited By (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8545983B2 (en) | 2005-08-25 | 2013-10-01 | University Of Washington | Super-low fouling sulfobetaine materials and related methods |
US9598544B2 (en) | 2005-08-25 | 2017-03-21 | University Of Washington Through Its Center For Commercialization | Particles coated with zwitterionic polymers comprising sulfobetaine or carboxybetaine |
US9045576B2 (en) | 2006-08-07 | 2015-06-02 | University Of Washington | Mixed charge copolymers and hydrogels |
US10301413B2 (en) | 2006-08-07 | 2019-05-28 | University Of Washington | Mixed charge copolymers and hydrogels |
US10060918B2 (en) | 2006-12-29 | 2018-08-28 | University Of Washington | Dual-functional nonfouling surfaces comprising target binding partner covalently coupled to polymer attached to substrate |
US8835144B2 (en) | 2006-12-29 | 2014-09-16 | University Of Washington | Dual-functional nonfouling surfaces comprising target binding partner covalently coupled to polymer attached to substrate |
US9535062B2 (en) | 2006-12-29 | 2017-01-03 | University Of Washington | Dual-functional nonfouling surfaces comprising target binding partner covalently coupled to polymer attached to substrate |
US10544312B2 (en) | 2007-11-19 | 2020-01-28 | University Of Washington | Marine coatings |
US8658192B2 (en) | 2007-11-19 | 2014-02-25 | University Of Washington | Integrated antimicrobial and low fouling materials |
US8268301B2 (en) | 2007-11-19 | 2012-09-18 | University Of Washington | Cationic betaine precursors to zwitterionic betaines having controlled biological properties |
US9533006B2 (en) | 2007-11-19 | 2017-01-03 | University Of Washington | Marine coatings |
EP2225331A4 (en) * | 2007-11-19 | 2010-12-01 | Univ Washington | Marine coatings |
US9358326B2 (en) | 2008-12-05 | 2016-06-07 | Arrow International, Inc. | Layered non-fouling, antimicrobial antithrombogenic coatings |
US9255929B2 (en) | 2009-09-25 | 2016-02-09 | University Of Washington | Zwitterionic polymers having biomimetic adhesive linkages |
US8877172B2 (en) | 2009-11-06 | 2014-11-04 | University Of Washington Through Its Center For Commercialization | Zwitterionic polymer bioconjugates and related methods |
US10130716B2 (en) | 2009-11-06 | 2018-11-20 | University Of Washington Through Its Center For Commercialization | Zwitterionic polymer bioconjugates and related methods |
US8617592B2 (en) | 2009-11-06 | 2013-12-31 | University Of Washington Through Its Center For Commercialization | Self-assembled particles from zwitterionic polymers and related methods |
US9599613B2 (en) | 2011-07-20 | 2017-03-21 | University Of Washington Through Its Center For Commercialization | Photonic blood typing |
US11105820B2 (en) | 2011-07-20 | 2021-08-31 | University Of Washington Through Its Center For Commercialization | Photonic pathogen detection |
US10794921B2 (en) | 2011-07-20 | 2020-10-06 | University Of Washington | Photonic blood typing |
US10073102B2 (en) | 2011-07-20 | 2018-09-11 | University Of Washington Through Its Center For Commercialization | Photonic blood typing |
US8870372B2 (en) | 2011-12-14 | 2014-10-28 | Semprus Biosciences Corporation | Silicone hydrogel contact lens modified using lanthanide or transition metal oxidants |
US9004682B2 (en) | 2011-12-14 | 2015-04-14 | Semprus Biosciences Corporation | Surface modified contact lenses |
US9006359B2 (en) | 2011-12-14 | 2015-04-14 | Semprus Biosciences Corporation | Imbibing process for contact lens surface modification |
US9000063B2 (en) | 2011-12-14 | 2015-04-07 | Semprus Biosciences Corporation | Multistep UV process to create surface modified contact lenses |
US10031138B2 (en) | 2012-01-20 | 2018-07-24 | University Of Washington Through Its Center For Commercialization | Hierarchical films having ultra low fouling and high recognition element loading properties |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
SU1780673A1 (en) | Fungicide agent | |
PT778731E (en) | IONENE POLYMERS CONTAINING BIOLOGICALLY ACTIVE ANTIES | |
JPH0228589B2 (en) | ||
US3291683A (en) | Controlling fungi and bacteria with alkoxy or alkylthio alkylamine ethers | |
DE2133056A1 (en) | Fungicidal guanidines - for combatting mildew and grey mould | |
US3085931A (en) | Plant virus growth inhibitors | |
US3899585A (en) | Fungicidal method for protecting a plant | |
CA1263648A (en) | .beta.-CYCLODEXTRINE COMPLEX OF BENZENE SULPHONYL UREA DERIVATIVES | |
EP0230698A1 (en) | Use of an ester compound as a temporary microbicide | |
US4251545A (en) | Fungicidal process using 1-(alkoxyaroyl)guanidines | |
US4075327A (en) | Method for the treatment of trees subject to Dutch elm disease | |
US4251544A (en) | Fungicidal process using 1-(alkylacyl) guanidines | |
US4094986A (en) | 2-r-substituted-1,2,5-thiadiazole-3-one antimicrobials | |
DE1025203B (en) | Combating plant parasites | |
US4241083A (en) | Germicidal composition for agriculture and horticulture | |
DD278053A1 (en) | MEANS FOR CONTROLLING PLANT PATHOGENS | |
US3002882A (en) | Systemically working agent for combating micro-organisms | |
CA1123732A (en) | Fungicidal process using (1-alkyl-acyl) guanidines | |
US3245874A (en) | Cyanine dyes as an agricultural bactericide | |
US5470869A (en) | Pyrazolium fungicidal compositions | |
Smith et al. | Investigations on fungitoxic derivatives of salicylaldehyde: I. The 3‐, 5‐and 3, 5‐chlorinated derivatives of salicylanilide and salicyl‐para‐chloroanilide | |
DE921180C (en) | Pest repellants | |
PT632957E (en) | PROCESS TO KILL HARMFUL INSECTS | |
US3238095A (en) | Fungicides derived from dibenzoylmethane | |
DE1134855B (en) | Fungicidal pesticides |