CH623990A5 - Fungicidal composition based on 2,4,5,6-tetrachloro-1,3-dicyanobenzene and pyrimidinemethanol, process for preparing it, and the use of this composition in a process of fungicidal treatment - Google Patents
Fungicidal composition based on 2,4,5,6-tetrachloro-1,3-dicyanobenzene and pyrimidinemethanol, process for preparing it, and the use of this composition in a process of fungicidal treatment Download PDFInfo
- Publication number
- CH623990A5 CH623990A5 CH1008277A CH1008277A CH623990A5 CH 623990 A5 CH623990 A5 CH 623990A5 CH 1008277 A CH1008277 A CH 1008277A CH 1008277 A CH1008277 A CH 1008277A CH 623990 A5 CH623990 A5 CH 623990A5
- Authority
- CH
- Switzerland
- Prior art keywords
- dicyanobenzene
- tetrachloro
- pyrimidinemethanol
- fungicidal
- dcb
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 27
- 230000000855 fungicidal effect Effects 0.000 title claims description 17
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 title claims description 16
- KCDACWMWSAEJNW-UHFFFAOYSA-N methanol;pyrimidine Chemical compound OC.C1=CN=CN=C1 KCDACWMWSAEJNW-UHFFFAOYSA-N 0.000 title claims description 16
- 238000000034 method Methods 0.000 title claims description 14
- 238000011282 treatment Methods 0.000 title claims description 13
- 238000004519 manufacturing process Methods 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims description 10
- 206010017533 Fungal infection Diseases 0.000 claims description 8
- 208000031888 Mycoses Diseases 0.000 claims description 8
- 239000000460 chlorine Substances 0.000 claims description 8
- 241001123569 Puccinia recondita Species 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 5
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 4
- 235000013339 cereals Nutrition 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- 239000011737 fluorine Chemical group 0.000 claims description 4
- 229910052731 fluorine Chemical group 0.000 claims description 4
- 231100001184 nonphytotoxic Toxicity 0.000 claims description 4
- -1 pyri-midinemethanol compound Chemical class 0.000 claims description 4
- 238000003306 harvesting Methods 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 15
- 241000209140 Triticum Species 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000000470 constituent Substances 0.000 description 7
- 239000004094 surface-active agent Substances 0.000 description 7
- NHOWDZOIZKMVAI-UHFFFAOYSA-N (2-chlorophenyl)(4-chlorophenyl)pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(Cl)C=C1 NHOWDZOIZKMVAI-UHFFFAOYSA-N 0.000 description 6
- SAPGTCDSBGMXCD-UHFFFAOYSA-N (2-chlorophenyl)-(4-fluorophenyl)-pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(F)C=C1 SAPGTCDSBGMXCD-UHFFFAOYSA-N 0.000 description 6
- 235000021307 Triticum Nutrition 0.000 description 6
- 239000007900 aqueous suspension Substances 0.000 description 6
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 6
- HZGCZRCZOMANHK-UHFFFAOYSA-N pyrimidin-2-ylmethanol Chemical class OCC1=NC=CC=N1 HZGCZRCZOMANHK-UHFFFAOYSA-N 0.000 description 6
- 239000000843 powder Substances 0.000 description 5
- 239000002562 thickening agent Substances 0.000 description 5
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 4
- HVFLCNVBZFFHBT-ZKDACBOMSA-N cefepime Chemical compound S([C@@H]1[C@@H](C(N1C=1C([O-])=O)=O)NC(=O)\C(=N/OC)C=2N=C(N)SC=2)CC=1C[N+]1(C)CCCC1 HVFLCNVBZFFHBT-ZKDACBOMSA-N 0.000 description 4
- 201000010099 disease Diseases 0.000 description 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 241001281805 Pseudoperonospora cubensis Species 0.000 description 3
- 239000004480 active ingredient Substances 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- 230000002195 synergetic effect Effects 0.000 description 3
- UGDWWCJKEUBONY-UHFFFAOYSA-N 6-chloro-6-methylcyclohexa-1,3-dien-1-ol Chemical compound CC1(Cl)CC=CC=C1O UGDWWCJKEUBONY-UHFFFAOYSA-N 0.000 description 2
- 239000005747 Chlorothalonil Substances 0.000 description 2
- 241000221785 Erysiphales Species 0.000 description 2
- 241000233866 Fungi Species 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 239000007798 antifreeze agent Substances 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 230000006735 deficit Effects 0.000 description 2
- 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 2
- 230000002538 fungal effect Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 2
- 229920000847 nonoxynol Polymers 0.000 description 2
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 235000012222 talc Nutrition 0.000 description 2
- 239000004563 wettable powder Substances 0.000 description 2
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical class OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241000221787 Erysiphe Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 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 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- 241001459558 Monographella nivalis Species 0.000 description 1
- 241000736122 Parastagonospora nodorum Species 0.000 description 1
- 241000221300 Puccinia Species 0.000 description 1
- 241001533598 Septoria Species 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000002528 anti-freeze Effects 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- CRPOUZQWHJYTMS-UHFFFAOYSA-N dialuminum;magnesium;disilicate Chemical compound [Mg+2].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] CRPOUZQWHJYTMS-UHFFFAOYSA-N 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000011872 intimate mixture Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 235000019357 lignosulphonate Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 229920001206 natural gum Polymers 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- PDTFCHSETJBPTR-UHFFFAOYSA-N phenylmercuric nitrate Chemical compound [O-][N+](=O)O[Hg]C1=CC=CC=C1 PDTFCHSETJBPTR-UHFFFAOYSA-N 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- TYRDEZUMAVRTEO-UHFFFAOYSA-N pyrimidin-5-ylmethanol Chemical class OCC1=CN=CN=C1 TYRDEZUMAVRTEO-UHFFFAOYSA-N 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- HIEHAIZHJZLEPQ-UHFFFAOYSA-M sodium;naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 HIEHAIZHJZLEPQ-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB34346/76A GB1581527A (en) | 1976-08-18 | 1976-08-18 | Fungicidal formulations |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH623990A5 true CH623990A5 (en) | 1981-07-15 |
Family
ID=10364511
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH1008277A CH623990A5 (en) | 1976-08-18 | 1977-08-17 | Fungicidal composition based on 2,4,5,6-tetrachloro-1,3-dicyanobenzene and pyrimidinemethanol, process for preparing it, and the use of this composition in a process of fungicidal treatment |
Country Status (36)
| Country | Link |
|---|---|
| JP (1) | JPS5324029A (en)) |
| AR (1) | AR217081A1 (en)) |
| AT (1) | AT355870B (en)) |
| AU (1) | AU518069B2 (en)) |
| BE (1) | BE857842A (en)) |
| BG (1) | BG31061A3 (en)) |
| BR (1) | BR7705434A (en)) |
| CA (1) | CA1089357A (en)) |
| CH (1) | CH623990A5 (en)) |
| CS (1) | CS193493B2 (en)) |
| CY (1) | CY1220A (en)) |
| DD (1) | DD131123A5 (en)) |
| DE (1) | DE2736892A1 (en)) |
| DK (1) | DK151001C (en)) |
| FR (1) | FR2361819A1 (en)) |
| GB (1) | GB1581527A (en)) |
| GR (1) | GR64962B (en)) |
| HK (1) | HK34984A (en)) |
| HU (1) | HU178815B (en)) |
| IE (1) | IE45657B1 (en)) |
| IL (1) | IL52736A0 (en)) |
| IT (1) | IT1079820B (en)) |
| KE (1) | KE3343A (en)) |
| MX (1) | MX4824E (en)) |
| MY (1) | MY8500289A (en)) |
| NL (1) | NL184762C (en)) |
| NZ (1) | NZ184920A (en)) |
| PH (1) | PH12365A (en)) |
| PL (1) | PL103739B1 (en)) |
| PT (1) | PT66920B (en)) |
| SE (1) | SE430116B (en)) |
| SG (1) | SG74083G (en)) |
| SU (1) | SU722459A3 (en)) |
| TR (1) | TR19719A (en)) |
| UA (1) | UA6332A1 (en)) |
| ZA (1) | ZA774949B (en)) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1114941B (it) * | 1977-12-27 | 1986-02-03 | Sipcam Spa | Fumero - studio consulenza brevetti s.n.c.via s.agnese,12 milano |
| CS217977B2 (en) * | 1978-04-01 | 1983-02-25 | Lilly Industries Ltd | Fungicide means |
| JPS56134469A (en) * | 1980-03-25 | 1981-10-21 | Matsushita Electric Ind Co Ltd | Cathode ray tube |
| TW491686B (en) * | 1997-12-18 | 2002-06-21 | Basf Ag | Fungicidal mixtures based on amide compounds and tetrachloroisophthalonitrile |
| JP6013032B2 (ja) * | 2011-07-08 | 2016-10-25 | 石原産業株式会社 | 殺菌剤組成物及び植物病害の防除方法 |
| CN105037721B (zh) * | 2015-07-30 | 2017-05-17 | 四川大学 | 含活性氢杂环化合物在制备邻苯二甲腈树脂中的应用 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1561634A (en) * | 1975-10-29 | 1980-02-27 | Lilly Industries Ltd | Fungicidal compositions |
-
1976
- 1976-08-18 GB GB34346/76A patent/GB1581527A/en not_active Expired
-
1977
- 1977-08-12 IT IT7750676A patent/IT1079820B/it active
- 1977-08-15 IL IL52736A patent/IL52736A0/xx not_active IP Right Cessation
- 1977-08-15 SE SE7709195A patent/SE430116B/xx not_active IP Right Cessation
- 1977-08-15 AU AU27901/77A patent/AU518069B2/en not_active Expired
- 1977-08-15 NZ NZ184920A patent/NZ184920A/xx unknown
- 1977-08-15 AR AR268796A patent/AR217081A1/es active
- 1977-08-16 CY CY1220A patent/CY1220A/xx unknown
- 1977-08-16 DE DE19772736892 patent/DE2736892A1/de active Granted
- 1977-08-16 JP JP9817877A patent/JPS5324029A/ja active Granted
- 1977-08-16 CS CS775374A patent/CS193493B2/cs unknown
- 1977-08-16 ZA ZA00774949A patent/ZA774949B/xx unknown
- 1977-08-16 IE IE1712/77A patent/IE45657B1/en not_active IP Right Cessation
- 1977-08-16 PT PT66920A patent/PT66920B/pt unknown
- 1977-08-16 PL PL1977200292A patent/PL103739B1/pl unknown
- 1977-08-16 GR GR54172A patent/GR64962B/el unknown
- 1977-08-16 NL NLAANVRAGE7709004,A patent/NL184762C/xx not_active IP Right Cessation
- 1977-08-16 DK DK364877A patent/DK151001C/da not_active IP Right Cessation
- 1977-08-16 FR FR7725023A patent/FR2361819A1/fr active Granted
- 1977-08-16 BR BR7705434A patent/BR7705434A/pt unknown
- 1977-08-16 AT AT592377A patent/AT355870B/de not_active IP Right Cessation
- 1977-08-16 BE BE6046114A patent/BE857842A/xx not_active IP Right Cessation
- 1977-08-16 BG BG037174A patent/BG31061A3/xx unknown
- 1977-08-17 SU SU772514251A patent/SU722459A3/ru active
- 1977-08-17 TR TR19719A patent/TR19719A/xx unknown
- 1977-08-17 HU HU77LI314A patent/HU178815B/hu unknown
- 1977-08-17 MX MX776035U patent/MX4824E/es unknown
- 1977-08-17 PH PH7720143A patent/PH12365A/en unknown
- 1977-08-17 CA CA284,870A patent/CA1089357A/en not_active Expired
- 1977-08-17 UA UA2514251A patent/UA6332A1/uk unknown
- 1977-08-17 CH CH1008277A patent/CH623990A5/fr not_active IP Right Cessation
- 1977-08-17 DD DD7700200626A patent/DD131123A5/xx not_active IP Right Cessation
-
1983
- 1983-11-15 KE KE3343A patent/KE3343A/xx unknown
- 1983-11-26 SG SG740/83A patent/SG74083G/en unknown
-
1984
- 1984-04-18 HK HK349/84A patent/HK34984A/xx unknown
-
1985
- 1985-12-30 MY MY289/85A patent/MY8500289A/xx unknown
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased | ||
| PL | Patent ceased |