SU294282A1 - METHOD OF OBTAINING FUNGICIDE - Google Patents
METHOD OF OBTAINING FUNGICIDEInfo
- Publication number
- SU294282A1 SU294282A1 SU1320067A SU1320067A SU294282A1 SU 294282 A1 SU294282 A1 SU 294282A1 SU 1320067 A SU1320067 A SU 1320067A SU 1320067 A SU1320067 A SU 1320067A SU 294282 A1 SU294282 A1 SU 294282A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- fungicide
- obtaining
- copper
- compositions
- fungicidal activity
- Prior art date
Links
- 230000000855 fungicidal Effects 0.000 title description 9
- 239000000417 fungicide Substances 0.000 title description 5
- 239000000203 mixture Substances 0.000 description 8
- 239000000969 carrier Substances 0.000 description 2
- 239000005725 8-Hydroxyquinoline Substances 0.000 description 1
- -1 8-hydroxyquinoline ester Chemical class 0.000 description 1
- PZZYQPZGQPZBDN-UHFFFAOYSA-N Aluminium silicate Chemical compound O=[Al]O[Si](=O)O[Al]=O PZZYQPZGQPZBDN-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 240000008529 Triticum aestivum Species 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive Effects 0.000 description 1
- 125000005024 alkenyl aryl group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 125000005518 carboxamido group Chemical group 0.000 description 1
- GYSSRZJIHXQEHQ-UHFFFAOYSA-N carboxin Chemical compound S1CCOC(C)=C1C(=O)NC1=CC=CC=C1 GYSSRZJIHXQEHQ-UHFFFAOYSA-N 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- QHECZRAGQOGJLT-UHFFFAOYSA-N copper;1H-quinolin-2-one Chemical compound [Cu].C1=CC=CC2=NC(O)=CC=C21 QHECZRAGQOGJLT-UHFFFAOYSA-N 0.000 description 1
- JJKSAEHNIHMQKQ-UHFFFAOYSA-N copper;quinoline Chemical compound [Cu].N1=CC=CC2=CC=CC=C21 JJKSAEHNIHMQKQ-UHFFFAOYSA-N 0.000 description 1
- JLOULEJYJNBUMX-UHFFFAOYSA-L copper;quinoline-2-carboxylate Chemical compound [Cu+2].C1=CC=CC2=NC(C(=O)[O-])=CC=C21.C1=CC=CC2=NC(C(=O)[O-])=CC=C21 JLOULEJYJNBUMX-UHFFFAOYSA-L 0.000 description 1
- 125000004367 cycloalkylaryl group Chemical group 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
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drugs Drugs 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 229960003540 oxyquinoline Drugs 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229920005552 sodium lignosulfonate Polymers 0.000 description 1
- 239000000021 stimulant Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 235000021307 wheat Nutrition 0.000 description 1
Description
Предлагаетс способ получени фунгицида путем смешени двух соединений, известных в качестве фунгицидов. Известно применение в качестве фунгицида оксатиина общей формулы . 0. Н/ С-СНз где X означает карбоксамидогруппу, предпочтительно , формулы / - С - N/ где R - Н, СНз; R - алкил, алкенил, циклоалкил, или замещенный арил; ,l или 2. Известно также использование в качестве фунгицида соли, например медной, или эфира 8-оксихинолина. 5 10 15 20 25 При этом фунгицидна активность смеси превышает фунгицидную активность каждого из компонентов, вз тых в отдельности. Предлагаемыми компонентами вл ютс 2,3-дигидро-5-карбоксанилидо - 6 - метил-1,4оксатиин и хинол т меди. В табл. 1 приведены данные о фунгицидной активности фунгицидной смеси при различных соотношени х компонентов. В первой группе испытаний готов т 11 дустовых композиций дл обработки сем н. Примен ют два количества карбоксанилидооксатиина (112,5 г и 56,2 г) и три количества хинолинол та меди (10, 20 и 30 г). Композиции готов т смещением препарата «Витавакс, содержащего 75 вес. о/о карбоксанилидооксатиина , технически чистого хинол та меди, каолина в качестве носител и 1 % (по весу общей смеси) лигносульфоната натри . Эти дозы примен ют дл обработки 100 кг сем н. Композиции довод т до 200 г добавлением минеральных носителей, стимул торов , клейких веществ или смачивающих агентов, совместимых с активными веществами . Композиции размалывают таким образом, чтобы получить средний размер зерен, дающий в результате полное покрытие поверхности сем н пшеницы.A method for the preparation of a fungicide is proposed by mixing two compounds known as fungicides. It is known to use oxatiin as a fungicide of the general formula. 0. H / C — CH 3 where X is a carboxamido group, preferably, of the formula / —C — N / where R is H, CH 3; R is alkyl, alkenyl, cycloalkyl, or substituted aryl; , l or 2. It is also known to use salt, for example, copper, or 8-hydroxyquinoline ester as a fungicide. 5 10 15 20 25 At the same time, the fungicidal activity of the mixture exceeds the fungicidal activity of each of the components taken separately. The proposed components are 2,3-dihydro-5-carboxanilido-6-methyl-1,4oxathiine and copper quinolate. In tab. Figure 1 shows the fungicidal activity of the fungicidal mixture at various ratios of the components. In the first group of tests, 11 dusting compositions were prepared for seed treatment. Two quantities of carboxanilidooxathiine (112.5 g and 56.2 g) and three amounts of quinolinol copper (10, 20, and 30 g) are used. Compositions are prepared by displacing the drug Vitavax containing 75 wt. carboxanilidooxatiine, technically pure quinolate copper, kaolin as carrier, and 1% (by weight of the total mixture) sodium lignosulfonate. These doses are used to treat 100 kg n. The compositions are brought to 200 g by the addition of mineral carriers, stimulants, adhesives or wetting agents compatible with the active substances. The compositions are milled in such a way as to obtain an average grain size, resulting in a complete coverage of the surface of wheat seeds.
в табл. 1 приведены результаты испытани композиции (количества в граммах).in tab. 1 shows the results of testing the composition (amount in grams).
Таблица 1Table 1
294282294282
Таблица 3Table 3
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU294282A1 true SU294282A1 (en) |
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3513241A (en) | Fungicidal and fungistatic n-(dialkylaminoalkyl) - carbamic acid and thiocarbamic acid esters | |
| HU180094B (en) | Synergetic composition for controlling growth of plants first of all for defoliation | |
| CS221820B2 (en) | Herbicide means | |
| IE54555B1 (en) | A fungicidal indanylbenzamide | |
| JPS6252743B2 (en) | ||
| SU294282A1 (en) | METHOD OF OBTAINING FUNGICIDE | |
| US3697589A (en) | N-(4-carboxy-benzylidene)amines | |
| CS241143B2 (en) | Fungicide | |
| US2557520A (en) | Pesticidal compositions comprising an alkyl aryl sulfide | |
| US4092429A (en) | (Tetrachloro-fluoro-ethyl-thio)N-phenyl sulfonamides and their use in controlling pests | |
| US3549767A (en) | Method of controlling insects and acarinae,employing certain acylated hydrazones and hydrazines | |
| US3914240A (en) | Agricultural fungicide | |
| CA1214100A (en) | Fungicide compound | |
| US2557519A (en) | Pest control compositions and process of producing them | |
| US3595963A (en) | Method of controlling the growth of fungi | |
| US3966961A (en) | Methanesulfonic acid-2-bromoethyl ester nematocide | |
| KR840001148B1 (en) | Process for preparing thiazolylidene-oxo-propionitriles | |
| IL31205A (en) | (thiono)carbamates of dithiacycloheptanone-oxime | |
| US3840538A (en) | 1-(4',6'-dichloro-s-triazin-2-ylcarbamoyl)-2-methoxycarbonylamino-benzimidazole | |
| KR20020022817A (en) | Derivatives of trifluoromethylpyri (mi)dine | |
| US4193933A (en) | N-(2-fluoro-1,1,2,2-tetrachloroethylthio)-N-phenyl methane sulfonamides and their use in controlling pests | |
| JPS5911561B2 (en) | Soil fungicide for agriculture and horticulture | |
| SU347968A1 (en) | ||
| KR830001149B1 (en) | Insecticide composition | |
| IL42626A (en) | Dichlorobenzaldehyde-oxime carbonates |