SU701517A3 - Fungicidic composition - Google Patents
Fungicidic compositionInfo
- Publication number
- SU701517A3 SU701517A3 SU752102879A SU2102879A SU701517A3 SU 701517 A3 SU701517 A3 SU 701517A3 SU 752102879 A SU752102879 A SU 752102879A SU 2102879 A SU2102879 A SU 2102879A SU 701517 A3 SU701517 A3 SU 701517A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- cultivated
- fungicidic
- composition
- percentage
- healthy
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title description 2
- 230000000855 fungicidal effect Effects 0.000 description 7
- 240000008067 Cucumis sativus Species 0.000 description 5
- 239000002689 soil Substances 0.000 description 5
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 4
- 235000006140 Raphanus sativus var sativus Nutrition 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 230000001717 pathogenic effect Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 241000220259 Raphanus Species 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 201000010099 disease Diseases 0.000 description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
- 239000000417 fungicide Substances 0.000 description 3
- -1 2, 4, 6-trisubstituted phenol Chemical class 0.000 description 2
- 241000102542 Kara Species 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000004495 emulsifiable concentrate Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 1
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 235000009849 Cucumis sativus Nutrition 0.000 description 1
- 241000223218 Fusarium Species 0.000 description 1
- 235000005733 Raphanus sativus var niger Nutrition 0.000 description 1
- 240000001970 Raphanus sativus var. sativus Species 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical class OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- LKPLKUMXSAEKID-UHFFFAOYSA-N pentachloronitrobenzene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LKPLKUMXSAEKID-UHFFFAOYSA-N 0.000 description 1
- 239000004476 plant protection product Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000243 solution 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
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
- C07F9/18—Esters of thiophosphoric acids with hydroxyaryl compounds
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/14—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing aromatic radicals
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
Изобретение относитс к химически средствам защиты растений, а именно к использованию фунгицидной композиции на основе сложного эфира тиофосфорной кислоты. Известен фунгицид,действующим началом которого вл етс 0-2, 4 5 Трихлорфенил-О-мети .п-изопропи.пфос фат 1 . Однако он не эффективен против болезней, развивarami-ixcH в почве. Известен также почвенный фунгицид пентахлорнитробензол, обладающий недостаточной фунгицидной активностью 2 . Более близким по технической стр туре к предлагаемому вл ютс биолог чески активные соединени , в качест ве действующих веществ которых испол syioT 0-2, 4,6-трихлорфенил-О,О-диалки тиоФосФаты.Однако они обладают антипараэитарной активностью 3. С целью изыскани новой фунгицид ной композиции-, обладающей высокой фунгицидной активностью предлагают использовать соединени общей формулы CИ,,0 сн,о где R и Rj - каждый атом хлора или брома; . метильна или этильна группа, как актирное вещество в количестве от 0,1 до, 90 вес.%. Сложные эфиры тиофосфорной кислйть4 могут быть получены взаимодействием 2, 4, 6-трехзамещенного фенола с 0,0-диметилтиофосфорилхлоридом ,предпочтительно в присутствии св зываюр(его кислоту агента,или взаимодействием соли 2,4, 6-трехз.амещенного фенола с 0,0-диметилтиофосфорилхлоридом, Указанна реакци проводитс почтительно в инертном органическом растворителе при температуре от 70 до 100°С. химические структуры.и физические константы предложенных соедииений представлены в табл..This invention relates to chemical plant protection products, namely, the use of a fungicidal composition based on thiophosphoric ester. A fungicide is known, the active principle of which is 0-2, 4 5 Trichlorophenyl-O-methi.p-isopropylphosphate 1. However, it is not effective against diseases that develop parami-ixcH in soil. Also known is the soil fungicide pentachloronitrobenzene, which has insufficient fungicidal activity 2. More technically closest to the proposed are biologically active compounds, the active substances of which are used syioT 0-2, 4,6-trichlorophenyl-O, O-dialkio thioPhosphates. However, they have antiparathyritic activity 3. With the aim of finding A new fungicidal composition- with a high fungicidal activity suggests using compounds of the general formula CI, 0 Cn, where R and Rj are each atom of chlorine or bromine; . methyl or ethyl group, as an active substance in the amount of from 0.1 to 90 wt.%. Thiophosphoric acid4 esters can be obtained by reacting 2, 4, 6-trisubstituted phenol with 0,0-dimethylthiophosphoryl chloride, preferably in the presence of a binder (its acid agent, or by reacting a salt of 2,4, 6-trisubstituted phenol with 0.0 -dimethylthiophosphoryl chloride, This reaction is conducted respectfully in an inert organic solvent at a temperature of from 70 to 100 ° C. chemical structures. and physical constants of the proposed compounds are presented in the table.
Соеди-I Compound-i
Соеди-I Химическа структура нение нениеCompound-I Chemical Structure
-«4-0-/ Vert,- "4-0- / Vert,
сНзОSNO
С1C1
ВД..„ ,WA .. „,
СНзО SNZO
Таблица 1Table 1
Физическа константаPhysical constant
Т,пл.79-79,5°СT, pl.79-79,5 °
Т.пл.73-74°СMp 73-74 ° C
снзО..,.АЛsnzO ..,. AL
СНзО SNZO
С1 :C1:
СНзО. SNSO.
CHjoJo
//Л f у-СгНз// Л f у-СгНз
/ 5 / five
с,н,c, n,
Формы применени препаратов обыч ные. В этих формах действующие вещества содержатс в количестве от 0,1 до 90 вес.%, предпочтительно от 5 до 60 вес.%. Пример 1. Борьба с выпрева нием огурцов (испытание в горшке). Возделанна земл была равномерно засыпана в цветочном горшке диаме ром 9 см. На поверхность названной земли было засыпано и инокулировано 10 МП на горгасж патогенной земли, в которой была культивирована Ризоктони солани {Rhizoctonla solani). Затем каждый из водных растворов испытательных хигдакалий в виде эмуль гируемых концентратов был залит в 1О аботаниуто таким образом землю в The form of use of drugs is normal. In these forms, the active substances are contained in an amount of from 0.1 to 90% by weight, preferably from 5 to 60% by weight. Example 1. Fight against the cucumber vybrovanie (test in a pot). The cultivated land was evenly filled in a flower pot with a diameter of 9 cm. On the surface of the named land, 10 MP were filled and inoculated on a Gorgaszh pathogenic land, in which Risoctoni solani {Rhizoctonla solani) was cultivated. Then, each of the aqueous solutions of test digdakaliums in the form of emulsifiable concentrates was poured into 100
т,пл.81-83 сt, square 81-83 s
п1 1,5500P1 1,5500
9090
п 1,5620p 1.5620
20 h;j3 1,5672 количестве 15 мл на горшок. По исте .чении 2 ч в каждый горшок было посе ;но 10 штук сем н огурца сорта Kara Аонагафушинари (Kog-q Ачопада ustiinofi ) ;И через 5 дней было произведено исследование состо ни болезни се нцев огурцов дл подсчета процентов здоровых се нцев. количество здоров1лх Процентсе нцев на обработанздоровых се нцев количество посе нных сем н на необработанном и неокулированном , участке Результаты испытаний представлены в табл.2.20 h; j3 1,5672 amount of 15 ml per pot. At the end of 2 hours, each pot was planted, but 10 pieces of cucumber seeds of the Kara Aonagafushinari variety (Kog-q Achopada ustiinofi); And after 5 days, the disease of cucumber seedlings was studied to calculate the percentage of healthy seedlings. the number of healthy percent of patients on healthy seedlings, the number of seeds sown on untreated and non-cultivated, plot The results of the tests are presented in table 2.
Концентраци активного ингредиента , части на мил250 125 62,5Concentration of the active ingredient, parts per mil250 125 62.5
250 125 62,5250 125 62.5
250 125 62,5250 125 62.5
250 125 62,5 125 62,5250 125 62.5 125 62.5
61256125
СНзО/ .250CiHjOSNSO / .250CiHjO
CHjO. Н // CHjO. H //
.Р-0-// Vci 250 .Р-0 - // Vci 250
();();
-Р-0-R-0
Вг СНзVG SNZ
(CHjOl.-P-O-fJV-KOz 250 СН,- ЗСНз(CHjOl.-P-O-fJV-KOz 250 CH, - ZSNz
.Таблица 2.Table 2
Процент здоровых се нцев, % лионThe percentage of healthy seedlings,% Lyon
100 100 90100 100 90
100 100 70100 100 70
100 100 60100 100 60
100 100 80100 100 80
100100
250 250
8080
6060
100100
9090
5050
62,562.5
Неинокулированный, необработанныйUninoculated, unprocessed
Примечаг-гие: Известные соединени 1.Note: Known compounds 1.
Имеющийс 3 продаже почвенный 3 soil sales available
Пример 2. Борьба с выпреванием огурцйв (испытани в бочонiKax ) .. Example 2. Fighting the crumble of cucumbers (tested in iKax barrels) ..
Возделанна земл была засыпана is пластиковые, бочонки размерогл 0,1 м , Л.х поверхность названной земли была равномерно засыпана и икокулирйвана патогенна земл , вThe cultivated land was filled up with plastic, the barrels were sized 0.1 m, L.x. the surface of the named earth was evenly covered and the pathogenic soil was icoculified,
которой была культивигювана PJJBOKтони .солани (Bh-izootonia sobani ) И патогенна земл была в достаточной степени перемешана с возделанной Землей, на глубину от 3 до 5 см от по верхности. Зат.ем каждый из водныхwhich was cultivated by PJJBOK toni of solani (Bh-izootonia sobani) and the pathogenic earth was sufficiently mixed with the cultivated earth to a depth of 3 to 5 cm from the surface. Then each of the water
Соединение1 2 3 4 5 6Connection1 2 3 4 5 6
ОABOUT
II II
I-C1 : Р - ОI-C1: P - O
II
(СгН50)г Р-ЗСНз(CgN50) g R-ZSNz
Продолжение табл.2Continuation of table 2
100 фунгицид (те же самые обозначени примен ютс и ниже).100 fungicide (the same designations are used below).
растворов, испытательных хи ликалий в виде эмульгируемых концентратов был залит в эту -обработанную землю из расчета 300 мл на бочонок.solutions, test chlorides in the form of emulsifiable concentrates were poured into this treated soil at the rate of 300 ml per barrel.
Через 2 ч в каждый боченок было посажено по 30 штук сем н огурца сорта Kara Аонагафушинари (Kag-Ql Aondo-aiustiinaH ) и через мес ц было иссследовано состо ние болезни се нцев огурцов дл вычислени. процента здоровых се нцев, Этот процент подсчитывалс по примеру 1.After 2 hours, 30 pieces of Kara variety Aonagafushinari (Kag Ql Aondo aiustiinaH) were planted in each barrel and after a month, the disease state of the cucumber seedlings was examined for calculation. % of healthy sleepers. This percentage was calculated in Example 1.
Результаты испытаний представлены в табл.Д-..,The test results are presented in the table. D. - ..,
Т & б л и ц а 3T & B l and c a 3
Процент здоровых се нцев,The percentage of healthy sunbeds
33
98 98 97 97 97 9598 98 97 97 97 95
200200
200200
О II РAbout II P
CLCL
СН-О- /CH-O- /
ОABOUT
С1C1
С1C1
С1 - у- N0,C1 - y - N0,
С1 --Инокулированный гриб, необработанныйC1 - Inoculated Mushroom, Untreated
йеинокулированный, необработанныйraw, untreated
Пример 3. Борьба с сухой гнилью фузариозными вилтами понской редиски :(испытани в бочонках).Example 3. Fighting dry rot of Japanese radish with dry rot: (tested in barrels).
Возделанна земл была засыпана в пластмассовые бочонки размером 0,1 м . Затем патогенна земл , в которой была культивирована Фузариум оксиспорум ф.рафани ( Fusar-iuni ox sporum f. i-apViani) была смЪшана и инокулирована с возделанной землей на глубину 5 см от поверхности , в обработанную таким образом землю было посажено по 30 штук сем н на каждый горшок понской редискиCultivated land was poured into plastic kegs 0.1 m in size. Then, the pathogenic land in which Fusarium oxiforum F. rafani (Fusar-iuni ox sporum f. I-apViani) was cultivated was smashed and inoculated with cultivated land 5 cm from the surface, 30 seeds of this type were planted in the ground thus treated. n per pot of donskoy radishes
Продолжение .S -,Continued .S -,
200200
200200
Вг-Тн.Vr-Tn.
200200
3636
9898
сорта Вайз - 40 ничи (jyase-4о nictii ) и семена были присыпаны землей. Через 3 ч каждый из водных растворов испытательных химикалий был залит в землю в количестве 300 мл на бочонок. После вызревани редиски в течение одного мес ца в теплице с регулируемым подводом воздуха при 26-28 С было исследовано состо ние болёзнисе нцев редиски дл подсчета процента здоровых се нцев. Процент подсчитывали по примеру 1.Vise varieties - 40 nichi (jyase-4o nictii) and seeds were covered with earth. After 3 hours, each of the aqueous solutions of test chemicals was poured into the ground in an amount of 300 ml per barrel. After the radish had ripened for one month in a greenhouse with an adjustable air supply at 26–28 ° C, the condition of radish patients was examined to calculate the percentage of healthy seedlings. The percentage was calculated according to example 1.
Результаты проведенных испытаний . представлены в табл.4.The results of the tests. presented in table 4.
Таблица 4Table 4
Продолжение табл.4Continuation of table 4
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP740074A JPS5120571B2 (en) | 1974-01-14 | 1974-01-14 | |
JP5153074A JPS5133970B2 (en) | 1974-05-08 | 1974-05-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
SU701517A3 true SU701517A3 (en) | 1979-11-30 |
Family
ID=26341686
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU752102879A SU701517A3 (en) | 1974-01-14 | 1975-01-13 | Fungicidic composition |
Country Status (15)
Country | Link |
---|---|
AR (1) | AR209290A1 (en) |
CA (1) | CA1049547A (en) |
CH (1) | CH612943A5 (en) |
CS (1) | CS181284B2 (en) |
DK (1) | DK137761C (en) |
ES (1) | ES433737A1 (en) |
FR (1) | FR2257598B1 (en) |
GB (1) | GB1467561A (en) |
HU (1) | HU172092B (en) |
IL (1) | IL46427A (en) |
IT (1) | IT1036863B (en) |
NL (1) | NL157309B (en) |
PL (1) | PL94954B1 (en) |
SU (1) | SU701517A3 (en) |
TR (1) | TR18202A (en) |
Families Citing this family (25)
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IE56044B1 (en) * | 1982-09-22 | 1991-03-27 | Schering Agrochemicals Ltd | Fungicidal mixtures |
JPS59122404A (en) * | 1982-12-15 | 1984-07-14 | Sumitomo Chem Co Ltd | Fungicidal composition for agriculture and horticulture |
JPS59210006A (en) * | 1983-05-13 | 1984-11-28 | Sumitomo Chem Co Ltd | Agricultural and horticultural fungicidal composition |
JPS6097907A (en) * | 1983-11-01 | 1985-05-31 | Sumitomo Chem Co Ltd | Agricultural and horticultural fungicidal composition |
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CN107075712A (en) | 2014-10-24 | 2017-08-18 | 巴斯夫欧洲公司 | Change solid particle surface charge non-both sexes, can quaternary and water-soluble polymer |
-
1975
- 1975-01-10 NL NL7500293.A patent/NL157309B/en not_active IP Right Cessation
- 1975-01-11 ES ES433737A patent/ES433737A1/en not_active Expired
- 1975-01-13 CA CA217,814A patent/CA1049547A/en not_active Expired
- 1975-01-13 AR AR257272A patent/AR209290A1/en active
- 1975-01-13 FR FR7500860A patent/FR2257598B1/fr not_active Expired
- 1975-01-13 SU SU752102879A patent/SU701517A3/en active
- 1975-01-13 GB GB139875A patent/GB1467561A/en not_active Expired
- 1975-01-13 DK DK5675A patent/DK137761C/en not_active IP Right Cessation
- 1975-01-13 IL IL46427A patent/IL46427A/en unknown
- 1975-01-13 CH CH35675A patent/CH612943A5/en not_active IP Right Cessation
- 1975-01-13 IT IT47658/75A patent/IT1036863B/en active
- 1975-01-13 CS CS7500000230A patent/CS181284B2/en unknown
- 1975-01-13 HU HU75SU00000886A patent/HU172092B/en unknown
- 1975-01-14 TR TR18202A patent/TR18202A/en unknown
- 1975-01-14 PL PL1975177339A patent/PL94954B1/pl unknown
Also Published As
Publication number | Publication date |
---|---|
NL157309B (en) | 1978-07-17 |
PL94954B1 (en) | 1977-09-30 |
CA1049547A (en) | 1979-02-27 |
DK137761C (en) | 1978-10-09 |
AR209290A1 (en) | 1977-04-15 |
IL46427A (en) | 1977-07-31 |
DK137761B (en) | 1978-05-01 |
ES433737A1 (en) | 1976-12-16 |
IL46427A0 (en) | 1975-04-25 |
CS181284B2 (en) | 1978-03-31 |
GB1467561A (en) | 1977-03-16 |
DE2501040B2 (en) | 1976-07-08 |
TR18202A (en) | 1976-11-25 |
DK5675A (en) | 1975-09-15 |
CH612943A5 (en) | 1979-08-31 |
IT1036863B (en) | 1979-10-30 |
FR2257598B1 (en) | 1978-02-03 |
FR2257598A1 (en) | 1975-08-08 |
DE2501040A1 (en) | 1975-07-17 |
NL7500293A (en) | 1975-07-16 |
HU172092B (en) | 1978-05-28 |
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