HU176859B - Fungicide preparation containing 1,3,4-oxadiazolin-2-one derivatives as active material - Google Patents
Fungicide preparation containing 1,3,4-oxadiazolin-2-one derivatives as active material Download PDFInfo
- Publication number
- HU176859B HU176859B HU76PI533A HUPI000533A HU176859B HU 176859 B HU176859 B HU 176859B HU 76PI533 A HU76PI533 A HU 76PI533A HU PI000533 A HUPI000533 A HU PI000533A HU 176859 B HU176859 B HU 176859B
- Authority
- HU
- Hungary
- Prior art keywords
- weight
- oxadiazolin
- active ingredient
- hydroxyphenyl
- dichloro
- Prior art date
Links
- 230000000855 fungicidal effect Effects 0.000 title claims abstract description 8
- 239000000417 fungicide Substances 0.000 title claims abstract description 7
- 238000002360 preparation method Methods 0.000 title description 3
- XLUWNAXYGUQQJL-UHFFFAOYSA-N 2h-1,3,4-oxadiazol-5-one Chemical class O=C1OCN=N1 XLUWNAXYGUQQJL-UHFFFAOYSA-N 0.000 title 1
- 239000011149 active material Substances 0.000 title 1
- YQENSQLEOLRRBD-UHFFFAOYSA-N 5-tert-butyl-3-(2,4-dichloro-5-hydroxyphenyl)-1,3,4-oxadiazol-2-one Chemical compound O=C1OC(C(C)(C)C)=NN1C1=CC(O)=C(Cl)C=C1Cl YQENSQLEOLRRBD-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000004480 active ingredient Substances 0.000 claims description 16
- 239000007788 liquid Substances 0.000 claims description 5
- 239000005995 Aluminium silicate Substances 0.000 claims description 4
- 235000012211 aluminium silicate Nutrition 0.000 claims description 4
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- 239000002563 ionic surfactant Substances 0.000 claims 1
- 239000002736 nonionic surfactant Substances 0.000 claims 1
- 241000813090 Rhizoctonia solani Species 0.000 abstract description 2
- 238000003898 horticulture Methods 0.000 abstract 1
- ZVTQYRVARPYRRE-UHFFFAOYSA-N oxadiazol-4-one Chemical class O=C1CON=N1 ZVTQYRVARPYRRE-UHFFFAOYSA-N 0.000 abstract 1
- -1 3- (2,4-dichloro-5-hydroxyphenyl) -5-tert-butyl-1,3,4-oxadiazole Chemical compound 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000000203 mixture Substances 0.000 description 7
- 241000233866 Fungi Species 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000000080 wetting agent Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000004495 emulsifiable concentrate Substances 0.000 description 4
- 230000002538 fungal effect Effects 0.000 description 4
- 239000000546 pharmaceutical excipient Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 241000894007 species Species 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 230000003373 anti-fouling effect Effects 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 230000003071 parasitic effect Effects 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000004546 suspension concentrate Substances 0.000 description 2
- 230000009974 thixotropic effect Effects 0.000 description 2
- 239000004563 wettable powder Substances 0.000 description 2
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 1
- 235000017060 Arachis glabrata Nutrition 0.000 description 1
- 241001553178 Arachis glabrata Species 0.000 description 1
- 235000010777 Arachis hypogaea Nutrition 0.000 description 1
- 235000018262 Arachis monticola Nutrition 0.000 description 1
- 241000228245 Aspergillus niger Species 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 241000123650 Botrytis cinerea Species 0.000 description 1
- 241000222122 Candida albicans Species 0.000 description 1
- 239000001692 EU approved anti-caking agent Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 241000223221 Fusarium oxysporum Species 0.000 description 1
- 241000896246 Golovinomyces cichoracearum Species 0.000 description 1
- 241001507673 Penicillium digitatum Species 0.000 description 1
- 241000221300 Puccinia Species 0.000 description 1
- 239000006159 Sabouraud's agar Substances 0.000 description 1
- 241001123227 Saccharomyces pastorianus Species 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 241001045770 Trichophyton mentagrophytes Species 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000002519 antifouling agent Substances 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229940095731 candida albicans Drugs 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 235000008504 concentrate Nutrition 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
- 229940071161 dodecylbenzenesulfonate Drugs 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000010871 livestock manure Substances 0.000 description 1
- 239000008268 mayonnaise Substances 0.000 description 1
- 235000010746 mayonnaise Nutrition 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000017066 negative regulation of growth Effects 0.000 description 1
- 239000012875 nonionic emulsifier Substances 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 235000014483 powder concentrate Nutrition 0.000 description 1
- ARENMZZMCSLORU-UHFFFAOYSA-N propan-2-yl naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)OC(C)C)=CC=CC2=C1 ARENMZZMCSLORU-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000012449 sabouraud dextrose agar Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- FGDMJJQHQDFUCP-UHFFFAOYSA-M sodium;2-propan-2-ylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=CC2=C(S([O-])(=O)=O)C(C(C)C)=CC=C21 FGDMJJQHQDFUCP-UHFFFAOYSA-M 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000001993 wax 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
- 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
- A01N43/82—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 three ring hetero atoms
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)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7525210A FR2320701A1 (fr) | 1975-08-13 | 1975-08-13 | Nouvelles compositions fongicides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HU176859B true HU176859B (en) | 1981-05-28 |
Family
ID=9159050
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU76PI533A HU176859B (en) | 1975-08-13 | 1976-08-12 | Fungicide preparation containing 1,3,4-oxadiazolin-2-one derivatives as active material |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US4078069A (enExample) |
| JP (1) | JPS6026763B2 (enExample) |
| AR (1) | AR217060A1 (enExample) |
| BR (1) | BR7605303A (enExample) |
| ES (1) | ES450685A1 (enExample) |
| FR (1) | FR2320701A1 (enExample) |
| GB (1) | GB1504477A (enExample) |
| HU (1) | HU176859B (enExample) |
| IT (1) | IT1068317B (enExample) |
| PH (1) | PH12799A (enExample) |
| PT (1) | PT65472B (enExample) |
| SU (1) | SU677628A3 (enExample) |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE740213C (de) * | 1939-02-28 | 1943-10-19 | Chem Fab In Billwaerder Vorm H | Schaedlingsbekaempfungsmittel fuer Pflanzen |
| US3385862A (en) * | 1963-12-13 | 1968-05-28 | Rhone Poulenc Sa | 5-t-butyl-3-phenyl-2-oxadiazolones |
| FR1394774A (fr) * | 1963-12-13 | 1965-04-09 | Rhone Poulenc Sa | Nouveaux dérivés de l'oxadiazolone et leur préparation |
| US3641045A (en) * | 1969-06-11 | 1972-02-08 | Ferro Corp | Hydroxy-phenyl oxadiazoles |
| US3876413A (en) * | 1971-06-02 | 1975-04-08 | Rhone Poulenc Sa | Herbicidal oxadiazolone derivatives |
-
1975
- 1975-08-13 FR FR7525210A patent/FR2320701A1/fr active Granted
-
1976
- 1976-08-03 US US05/711,367 patent/US4078069A/en not_active Expired - Lifetime
- 1976-08-11 SU SU762386748A patent/SU677628A3/ru active
- 1976-08-12 PT PT65472A patent/PT65472B/pt unknown
- 1976-08-12 JP JP51096876A patent/JPS6026763B2/ja not_active Expired
- 1976-08-12 BR BR7605303A patent/BR7605303A/pt unknown
- 1976-08-12 GB GB33664/76A patent/GB1504477A/en not_active Expired
- 1976-08-12 HU HU76PI533A patent/HU176859B/hu unknown
- 1976-08-12 AR AR264313A patent/AR217060A1/es active
- 1976-08-12 PH PH18779A patent/PH12799A/en unknown
- 1976-08-13 ES ES450685A patent/ES450685A1/es not_active Expired
- 1976-08-13 IT IT26280/76A patent/IT1068317B/it active
Also Published As
| Publication number | Publication date |
|---|---|
| PH12799A (en) | 1979-08-23 |
| ES450685A1 (es) | 1977-08-01 |
| AR217060A1 (es) | 1980-02-29 |
| BR7605303A (pt) | 1977-08-09 |
| JPS5225029A (en) | 1977-02-24 |
| PT65472A (en) | 1976-09-01 |
| IT1068317B (it) | 1985-03-21 |
| JPS6026763B2 (ja) | 1985-06-25 |
| PT65472B (en) | 1978-07-04 |
| FR2320701A1 (fr) | 1977-03-11 |
| FR2320701B1 (enExample) | 1977-12-16 |
| GB1504477A (en) | 1978-03-22 |
| US4078069A (en) | 1978-03-07 |
| SU677628A3 (ru) | 1979-07-30 |
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