PL112622B1 - Fungicide - Google Patents
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- PL112622B1 PL112622B1 PL1978216611A PL21661178A PL112622B1 PL 112622 B1 PL112622 B1 PL 112622B1 PL 1978216611 A PL1978216611 A PL 1978216611A PL 21661178 A PL21661178 A PL 21661178A PL 112622 B1 PL112622 B1 PL 112622B1
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- compound
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- 230000000855 fungicidal effect Effects 0.000 title claims description 6
- 239000000417 fungicide Substances 0.000 title claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 15
- 239000013543 active substance Substances 0.000 claims description 14
- 239000003795 chemical substances by application Substances 0.000 claims description 13
- 239000004094 surface-active agent Substances 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- 239000000969 carrier Substances 0.000 claims description 5
- 239000002562 thickening agent Substances 0.000 claims description 5
- 239000003755 preservative agent Substances 0.000 claims description 4
- 230000002528 anti-freeze Effects 0.000 claims description 3
- 231100001184 nonphytotoxic Toxicity 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims description 2
- 150000003918 triazines Chemical class 0.000 claims description 2
- 239000002518 antifoaming agent Substances 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 230000002335 preservative effect Effects 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 10
- 239000007900 aqueous suspension Substances 0.000 description 6
- 241000196324 Embryophyta Species 0.000 description 5
- -1 alkyl succinates Chemical class 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 206010017533 Fungal infection Diseases 0.000 description 4
- 208000031888 Mycoses Diseases 0.000 description 4
- 235000013339 cereals Nutrition 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 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
- 238000002360 preparation method Methods 0.000 description 2
- FZZRKNVCSWWGJL-UHFFFAOYSA-N (2-methylphenyl) hypochlorite Chemical compound CC1=CC=CC=C1OCl FZZRKNVCSWWGJL-UHFFFAOYSA-N 0.000 description 1
- WPRAXAOJIODQJR-UHFFFAOYSA-N 1-(3,4-dimethylphenyl)ethanone Chemical compound CC(=O)C1=CC=C(C)C(C)=C1 WPRAXAOJIODQJR-UHFFFAOYSA-N 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 241000221785 Erysiphales Species 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 235000014787 Vitis vinifera Nutrition 0.000 description 1
- 240000006365 Vitis vinifera Species 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 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
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 208000032625 disorder of ear Diseases 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- WSKZQEYNQOLWTF-UHFFFAOYSA-N ethane-1,2-diol;formaldehyde Chemical compound O=C.OCCO WSKZQEYNQOLWTF-UHFFFAOYSA-N 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 235000019357 lignosulphonate Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- VSXGXPNADZQTGQ-UHFFFAOYSA-N oxirane;phenol Chemical class C1CO1.OC1=CC=CC=C1 VSXGXPNADZQTGQ-UHFFFAOYSA-N 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- DAJSVUQLFFJUSX-UHFFFAOYSA-M sodium;dodecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCS([O-])(=O)=O DAJSVUQLFFJUSX-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
Classifications
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- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/18—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring
-
- 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
- A01N57/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing acyclic or cycloaliphatic radicals
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)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Description
Opis patentowy opublikowano: 15.01.1982 112622 CZYTELNIA Urzedu Patentowego hlaiij l2tczrp«itiii'it Luaimj IntCl.'A01N9/02 Twórca wynalazku: —. Uprawniony z patentu: Lilly Industries Limited, Londyn (Wielka Bry¬ tania) Srodek grzybobójczy [Rrzemiotem wynalazku jest srodek grzybobój¬ czy do ochrony upraw przed zakazeniem grzy¬ bowym.Srodek grzybobójczy wedlug wynalazku zawiera substancje czynne w polaczeniu z jednym lub kil¬ koma obojetnymi i niefitotoksycznymi nosnikami.Srodek zawiera jako jedna substancje czynna grzy¬ bobójczo pochodna triazyny o wzorze 1, a jako druga substancje czynna grzybobójczo zawiera benzimidazol o wzorze 2.Oba wymienione zwiazki sa znane i mozna je otrzymac metodami opisanymi dokladnie w litera¬ turze. Okreslone polaczenie substancji czynnych wchodzacych w sklad srodka wedlug wynalazku jest nowe i, jak stwierdzono, dziala niespodziewa¬ nie skutecznie przy ograniczeniu lub zwalczaniuv zakazen upraw grzybami. Srodek zawierajacy jako substancje czynna zwiazek o wzorze 1 i zwiazek o wzorze 2 wykazuje, jak stwierdzono, szczególna skutecznosc przy zwalczaniu chorób zbóz, takich jak plesn proszkowa, zgnilizna korzeniowa i inne choroby lisci i klosów atakujace rosliny zbozowe w stadium dojrzewania.Srodek wedlug wynalazku stosuje sie przeciw zakazeniom grzybowym na rosliny, zwlaszcza na zboze i winorosle, w ilosci skutecznej grzybobójczo.Srodek stosuje sie korzystnie na liscie w dowolnym czasie, poczawszy od wykielkowania rosliny do czasu zbioru. Ilosc i czestotliwosc stosowania srod¬ ka zalezy od stwierdzonego lub spodziewanego 10 15 20 25 30 stopnia zaatakowania roslin zakazeniem grzybo¬ wym. Jednakze cecha srodka wedlug wynalazku jest to, ze szczególnie dobre dzialanie wykazuje on przy ograniczonej czestotliwosci stosowania.Przykladowo, w celu panowania nad zakazeniami winorosli plesnia, srodek stosuje sie skutecznie tyl¬ ko raz na 2—3 tygodnie, dzieki czemu ogranicza sie koszty robocizny.Skladniki srodka wedlug wynalazku mozna sto¬ sowac na rosliny kolejno lub jednoczesnie, przy czym bardziej zalecane jest stosowanie ich razem.Zwiazek o wzorze 1 stosuje sie korzystnie w ilosci 10—500 g/ha.Zwiazki o wzorze 2 stosuje sie korzystnie w ilosci 100—3000 g/ha. Tak wiec stosunek wagowy zwiaz¬ ków o wzorze 1 do zwiazków o wzorze 2 wchodza¬ cych w sklad srodka zawiera sie w zakresie 5:1 do 1:300. Korzystny stosunek wagowy zwiazku o wzo¬ rze 1 do zwiazku o wzorze 2 wynosi 2:1 do 1:25.W celu uproszczenia produkcji, magazynowania i transportu srodek przygotowuje sie zwykle w postaci koncentratu przeznaczonego do rozciencza¬ nia woda w takim stopniu, który pozwala na latwe stosowanie omawianych poprzednio dawek substan¬ cji czynnych. Koncentraty takie moga zawierac 0,5—90%, a korzystnie 5—90% wagowych substan¬ cji czynnych w polaczeniu z jednym lub kilkoma obojetnymi, niefitotoksycznymi nosnikami. Srodek taki ma zwykle ,postac zwilzalnego proszku, pylu lub zawiesiny wodnej, chociaz nalezy podkreslic, 112 622112 622 3 ze wodne zawiesiny sa nietrwale, poniewaz maja stosunkowo krótki czas polowy trwalosci {okolo 100 dni) w srodowisku wodnym. Srodek w postaci koncentratów przeznaczony jest do rozcienczania woda przed uzyciem. Zawiesiny wodne przygoto- 5 wuje sie z koncentratów w zwyklych, nadajacych x sie do tego celu zbiornikach.Zwilzalne proszki lub pyly zawieraja dokladnie zmieszane substancje czynne i jeden lub kilka obojetnych nosników oraz odpowiednie srodki po- 10 wierzchniowo czynne. Obojetny nosnik moze byc dobrany z glin atapulgitowych, glin montmoryloni- towych, ziem okrzemkowych, kaolinów, miki, tal¬ ków i oczyszczanych krzemianów. Odpowiednie srodki powierzchniowo czynne wybiera sie sposród i» sulfonowanych lignin, naftalenosulfonianów i kon- densowanych naftalenosulfonianów, bursztynianów alkilowych,' sulfonianów alkilobenzenu, sulfonia¬ nów alkilowych i niejonowych srodków powierzch¬ niowo czynnych, takich jak addukty tlenku etyle- 20 nu i fenolu. Przykladowymi zwilzalnymi proszkami wedlug wynalazku sa preparaty o nastepujacym skladzie: Zwilzalneproszki % wagowy 25 Zwiazek o wzorze 1 0,25—10 Zwiazek o wzorze 2 10—80 Srodek lub srodki powierzchniowo czyne 0—10 Srodek dyspergujacy 0—10 Srodek zapobiegajacy zbrylaniu 0—10 Obojetny nosnik lub nosniki do 100 Zawiesiny wodne i roztwory zawieraja substan¬ cje czynne zawieszone lub rozpuszczone w wodzie lub odpowiednio rozpuszczalnikach oraz dowolne srodki powierzchniowo 4 czynne, srodki zgeszczaja- ce, srodki przeciw zamarzaniu lub srodki konser¬ wujace. Odpowiednie srodki powierzchniowe czyn¬ ne mozna wybrac sposród wymienionych poprzed¬ nio w odniesieniu do zwilzalnych proszków. Srodki zgeszczajace jezeli sie je stosuje, wybiera sie z na¬ dajacych sie do tego celu materialów celulozowych i zywic naturalnych.Glikole stosuje sie zwykle jako srodek przeciw zamarzaniu o ile jest potrzebny. Srodki konser- 45 wujace mozna wybrac z wielu róznych substancji tego typu, takich jak rózne parabenowe substan¬ cje przeciwbakteryjne, fenol, O-chlorokrezol, azotan fetnylorteci i formaldehyd. Typowymi zawiesina¬ mi wodnymi sa wedlug wynalazku preparaty o na- 50 stepujacym skladzie: ^ 30 25 40 Mimo, ze podane wyzej ogólne sklady prepa¬ ratów srodka odpowiednio ilustruja fachowcom typy stosowanych zestawów, w celu dokladniej¬ szego zilustrowania wynalazku we wszystkich jego aspektach przytoczone sa nastepujace przy¬ klady: W przykladach zwiazek o wzorze 1 oznaczony jest symbolem literowym „CTDB", a zwiazek o wzorze 2 symbolem „MBC".Przyklad I. Przygotowano zwilzany proszek o nastepujacym skladzie: CTDB MBC Sól sodowa kondensowanych naftalenosulfonowych Trójdecylosulfonian sodu Krzemionka Kaolin kwasów % wagowy 12,0 60,0 5,0 2,0 5,0 do 100,0 Substancje czynne starannie mieszano z odpo¬ wiednimi rozczynnikami w zwyklym mieszalniku.Mieszanine mielono w mlynie hydraulicznie do iiziarnienia rzedu 1—10 mikronów^ korygowano sklad mieszanki i odpowietrzano ja zapakowa¬ niem. , Przyklad II. Przygotowano zawiesine wod¬ na o nastepujacym skladzie: % wagowy 2,5 50,0 3,0 3,0 5,0 0,2 do 100,0 CTDB MBC Laurylosulfonian sodu Bentonit Glikol etylenowy Formaldehyd Woda Oba skladniki czynne zmielone w zwykly spo¬ sób w razie potrzelby dyspergowano w wodzie zawierajacej srodki powierzchniowo czynne, kon¬ serwujace i czesc srodka zgeszczajacego. Uziar- nienie obu substancji czynnych zmniejszano da¬ lej przez mielenie cieczy i dodawano pozostala ilosc srodka zageszczajacego. Pozostawiano zawie¬ sine do uwodnienia i produkt rozcienczono woda do odpowiedniej objetosci. PL PL PL Patent description published: 15/01/1982 112622 READING ROOM of the Patent Office hlaiij l2tczrp«itiii'it Luaimj IntCl.'A01N9/02 Inventor: —. Patent holder: Lilly Industries Limited, London (Great Britain) Fungicide [The subject of the invention is a fungicide for the protection of crops against fungal infection. The fungicide according to the invention contains active substances in combination with one or more inert and non-phytotoxic carriers. The agent contains as one fungicidally active substance a triazine derivative of formula 1, and as a second fungicidally active substance it contains benzimidazole of formula 2. Both compounds mentioned are known and can be obtained by methods described in detail in the literature. The specific combination of active substances included in the composition according to the invention is new and has been found to be surprisingly effective in limiting or combating fungal infections of crops. The agent containing as an active substance a compound of formula 1 and a compound of formula 2 has been found to be particularly effective in combating cereal diseases such as powdery mildew, root rot and other leaf and ear diseases attacking cereal plants at the ripening stage. The agent according to the invention is used against fungal infections on plants, especially grain and vines, in a fungicidally effective amount. The agent is preferably applied to the leaves at any time, from germination of the plant to harvest. The amount and frequency of application of the agent depend on the detected or expected degree of fungal infection of the plants. However, the feature of the agent according to the invention is that it works particularly well with a limited frequency of use. For example, in order to control mold infections in grapevines, the agent is effectively used only once every 2-3 weeks, which reduces labor costs. The ingredients of the agent according to the invention can be applied to the plants successively or simultaneously, but it is more recommended to use them together. The compound of the formula 1 is preferably used in an amount of 10-500 g/ha. The compounds of the formula 2 are preferably used in an amount of 100-500 g/ha. 3000 g/ha. Thus, the weight ratio of the compounds of formula 1 to the compounds of formula 2 contained in the composition ranges from 5:1 to 1:300. The preferred weight ratio of the compound of formula 1 to the compound of formula 2 is 2:1 to 1:25. In order to simplify production, storage and transportation, the agent is usually prepared in the form of a concentrate intended for dilution with water to an extent that allows for easy use of the previously discussed doses of active substances. Such concentrates may contain 0.5-90%, preferably 5-90%, by weight of active substances in combination with one or more neutral, non-phytotoxic carriers. Such a composition is usually in the form of a wettable powder, dust or aqueous suspension, although it should be emphasized that aqueous suspensions are unstable because they have a relatively short half-life (approximately 100 days) in an aqueous environment. The product in the form of concentrates is intended to be diluted with water before use. Aqueous suspensions are prepared from concentrates in ordinary tanks suitable for this purpose. Wettable powders or dusts contain thoroughly mixed active substances and one or more inert carriers as well as suitable surfactants. The inert carrier may be selected from attapulgite clays, montmorillonite clays, diatomaceous earths, kaolins, micas, talcs and purified silicates. Suitable surfactants are selected from sulfonated lignins, naphthalene sulfonates and condensed naphthalene sulfonates, alkyl succinates, alkylbenzene sulfonates, alkyl sulfonates and non-ionic surfactants such as ethylene oxide-phenol adducts. Examples of wettable powders according to the invention are preparations with the following composition: Wettable powders % by weight 25 Compound of formula 1 0.25-10 Compound of formula 2 10-80 Surfactant or agents 0-10 Dispersant 0-10 Anti-caking agent 0-10 Inert carrier or carriers up to 100 Aqueous suspensions and solutions contain active substances suspended or dissolved in water or solvents, respectively, and any surfactants, thickeners, antifreezes or preservatives. Suitable surfactants may be selected from those mentioned above for wettable powders. Thickening agents, if used, are selected from suitable cellulosic materials and natural resins. Glycol is usually used as an antifreeze when needed. Preservatives can be selected from a wide variety of substances of this type, such as various paraben antibacterial substances, phenol, O-chlorocresol, phenylmercury nitrate and formaldehyde. Typical aqueous suspensions according to the invention are preparations with the following composition: are the following examples: In the examples, the compound of formula 1 is marked with the letter symbol "CTDB" and the compound of formula 2 with the symbol "MBC". Example I. A wetted powder with the following composition was prepared: CTDB MBC Sodium salt of condensed naphthalenesulfonic acids Sodium tridecylsulfonate Silica Kaolin acids % by weight 12.0 60.0 5.0 2.0 5.0 to 100.0 The active substances were carefully mixed with appropriate excipients in a standard mixer. The mixture was ground hydraulically in a mill to a grain size of 1-10 microns and the composition was adjusted. mixture and deaerated it by packaging, Example II. An aqueous suspension was prepared with the following composition: weight % 2.5 50.0 3.0 3.0 5.0 0.2 to 100.0 CTDB MBC Sodium lauryl sulfonate Bentonite Ethylene glycol Formaldehyde Water Both active ingredients ground in the usual manner. if necessary, they were dispersed in water containing surfactants, preservatives and part of the thickener. The particle size of both active substances was further reduced by grinding the liquid and the remaining amount of thickener was added. The suspension was allowed to hydrate and the product was diluted with water to the appropriate volume. PL PL PL
Claims (2)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB12972/77A GB1596380A (en) | 1977-03-28 | 1977-03-28 | Fungicidal combinations |
Publications (1)
Publication Number | Publication Date |
---|---|
PL112622B1 true PL112622B1 (en) | 1980-10-31 |
Family
ID=10014480
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PL1978216611A PL112622B1 (en) | 1977-03-28 | 1978-03-24 | Fungicide |
PL1978216612A PL112286B1 (en) | 1977-03-28 | 1978-03-24 | Fungicide |
PL1978216610A PL112146B1 (en) | 1977-03-28 | 1978-03-24 | Fungicide |
PL1978205555A PL108903B1 (en) | 1977-03-28 | 1978-03-24 | Fungicide |
Family Applications After (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PL1978216612A PL112286B1 (en) | 1977-03-28 | 1978-03-24 | Fungicide |
PL1978216610A PL112146B1 (en) | 1977-03-28 | 1978-03-24 | Fungicide |
PL1978205555A PL108903B1 (en) | 1977-03-28 | 1978-03-24 | Fungicide |
Country Status (34)
Country | Link |
---|---|
JP (1) | JPS53121932A (en) |
AR (2) | AR227124A1 (en) |
AT (1) | AT362195B (en) |
AU (1) | AU515204B2 (en) |
BE (1) | BE865215A (en) |
BG (4) | BG30167A4 (en) |
BR (1) | BR7801746A (en) |
CA (1) | CA1108046A (en) |
CH (1) | CH629363A5 (en) |
CS (4) | CS198290B2 (en) |
DD (1) | DD135031A5 (en) |
DE (2) | DE2812287C2 (en) |
DK (1) | DK149442C (en) |
ES (1) | ES468098A1 (en) |
FR (4) | FR2390096A1 (en) |
GB (1) | GB1596380A (en) |
GR (1) | GR64791B (en) |
HU (2) | HU188701B (en) |
IE (1) | IE46690B1 (en) |
IL (1) | IL54318A (en) |
IN (1) | IN147690B (en) |
IT (1) | IT1105157B (en) |
LU (1) | LU79285A1 (en) |
MX (1) | MX5640E (en) |
NL (1) | NL7803064A (en) |
NO (4) | NO147260C (en) |
NZ (1) | NZ186757A (en) |
PL (4) | PL112622B1 (en) |
PT (1) | PT67801A (en) |
RO (4) | RO73042A (en) |
SE (5) | SE447783B (en) |
SU (1) | SU1409119A3 (en) |
TR (1) | TR20072A (en) |
ZA (1) | ZA781700B (en) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2552967A1 (en) * | 1975-11-26 | 1977-06-08 | Bayer Ag | FUNGICIDALS |
IT1143721B (en) * | 1977-12-01 | 1986-10-22 | Sipcam Spa | FUNGICIDAL COMPOSITION FOR THE FIGHT AGAINST PLANT DISEASES |
DE2846038A1 (en) * | 1978-10-23 | 1980-05-08 | Basf Ag | 1,2,4-TRIAZOLE DERIVATIVES, THEIR PRODUCTION AND USE |
DE3208142A1 (en) * | 1982-03-06 | 1983-09-08 | Bayer Ag, 5090 Leverkusen | FUNGICIDAL AGENT |
FR2524261A1 (en) * | 1982-04-01 | 1983-10-07 | Rhone Poulenc Agrochimie | FENARIMOL FUNGICIDE POWDER COMPOSITION |
GB8629360D0 (en) * | 1986-12-09 | 1987-01-21 | Sandoz Ltd | Fungicides |
JPH01167287U (en) * | 1988-05-16 | 1989-11-24 | ||
DE3818903A1 (en) * | 1988-06-03 | 1989-12-14 | Stama Maschinenfabrik Gmbh | DRILLING AND MILLING PLANT |
JPH0274094U (en) * | 1988-11-28 | 1990-06-06 | ||
JPH071190Y2 (en) * | 1989-03-01 | 1995-01-18 | 狭山精密工業株式会社 | Spiral control mechanism in pachinko ball lifting device |
NZ260462A (en) * | 1994-05-05 | 1996-04-26 | Horticulture & Food Res Inst | Tree treatment and composition comprising phosphorous acid, a bioprecursor or a salt thereof and a triazole |
FR2732191B1 (en) * | 1995-03-30 | 2000-12-29 | Rhone Poulenc Agrochimie | ANTIFUNGAL TREATMENT OF BANANA TREES |
GB0811079D0 (en) * | 2008-06-17 | 2008-07-23 | Syngenta Participations Ag | Herbicide formulation |
CN105028419B (en) * | 2012-08-17 | 2017-06-16 | 陕西美邦农药有限公司 | A kind of bactericidal composition containing Fenarimol |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1569940A (en) * | 1967-04-27 | 1969-06-06 | ||
FR2140205B1 (en) | 1971-06-04 | 1977-12-23 | Oreal | |
US3912752A (en) * | 1972-01-11 | 1975-10-14 | Bayer Ag | 1-Substituted-1,2,4-triazoles |
US3869456A (en) | 1972-03-13 | 1975-03-04 | Lilly Co Eli | Synthesis of 5-pyrimidinecarbinols |
US3868244A (en) | 1972-03-13 | 1975-02-25 | Lilly Co Eli | Plant growth regulation |
DE2303757A1 (en) * | 1973-01-26 | 1974-08-15 | Hoechst Ag | Fungicidal wettable powders contg. benzimidazole carbamates - mixed with powdered carrier, penetrating agent, but without emulsifying agents |
DE2354467C3 (en) * | 1973-10-31 | 1981-07-30 | Hoechst Ag, 6000 Frankfurt | Fungicidal dispersions based on benzimidazole methyl carbamate |
DE2456627C2 (en) * | 1973-12-14 | 1984-05-10 | PEPRO - Société pour le Développement et la Vente de Spécialités Chimiques, Lyon | Fungicidal agents based on phosphonic acid esters |
FR2254276B1 (en) * | 1973-12-14 | 1977-03-04 | Philagro Sa | |
FR2279331A1 (en) * | 1974-07-24 | 1976-02-20 | Hoechst Ag | Fungicidal wettable powders contg. benzimidazole carbamates - mixed with powdered carrier, penetrating agent, but without emulsifying agents |
DE2552967A1 (en) * | 1975-11-26 | 1977-06-08 | Bayer Ag | FUNGICIDALS |
-
1977
- 1977-03-28 GB GB12972/77A patent/GB1596380A/en not_active Expired
-
1978
- 1978-03-15 IT IT48444/78A patent/IT1105157B/en active
- 1978-03-20 FR FR7807978A patent/FR2390096A1/en active Granted
- 1978-03-20 CA CA299,331A patent/CA1108046A/en not_active Expired
- 1978-03-20 PT PT67801A patent/PT67801A/en unknown
- 1978-03-20 SE SE7803184A patent/SE447783B/en not_active IP Right Cessation
- 1978-03-20 IN IN295/CAL/78A patent/IN147690B/en unknown
- 1978-03-20 MX MX786944U patent/MX5640E/en unknown
- 1978-03-21 ES ES468098A patent/ES468098A1/en not_active Expired
- 1978-03-21 DK DK127978A patent/DK149442C/en not_active IP Right Cessation
- 1978-03-21 CH CH306178A patent/CH629363A5/en not_active IP Right Cessation
- 1978-03-21 AR AR271494A patent/AR227124A1/en active
- 1978-03-21 RO RO7893574A patent/RO73042A/en unknown
- 1978-03-21 DE DE2812287A patent/DE2812287C2/en not_active Expired
- 1978-03-21 BR BR7801746A patent/BR7801746A/en unknown
- 1978-03-21 GR GR55758A patent/GR64791B/en unknown
- 1978-03-21 RO RO7899323A patent/RO78273A/en unknown
- 1978-03-21 IL IL54318A patent/IL54318A/en unknown
- 1978-03-21 RO RO7899325A patent/RO78260A/en unknown
- 1978-03-21 DE DE2858350A patent/DE2858350C2/de not_active Expired
- 1978-03-21 RO RO7899324A patent/RO78274A/en unknown
- 1978-03-22 AT AT203678A patent/AT362195B/en not_active IP Right Cessation
- 1978-03-22 LU LU79285A patent/LU79285A1/en unknown
- 1978-03-22 DD DD78204345A patent/DD135031A5/en unknown
- 1978-03-22 BG BG7841508A patent/BG30167A4/en unknown
- 1978-03-22 NL NL7803064A patent/NL7803064A/en not_active Application Discontinuation
- 1978-03-22 AU AU34430/78A patent/AU515204B2/en not_active Expired
- 1978-03-22 BG BG7841506A patent/BG30165A4/en unknown
- 1978-03-22 BE BE6046404A patent/BE865215A/en not_active IP Right Cessation
- 1978-03-22 BG BG7839128A patent/BG29863A3/en unknown
- 1978-03-22 NO NO781040A patent/NO147260C/en unknown
- 1978-03-22 BG BG7841507A patent/BG30166A4/en unknown
- 1978-03-22 NZ NZ186757A patent/NZ186757A/en unknown
- 1978-03-23 HU HU812978A patent/HU188701B/en unknown
- 1978-03-23 ZA ZA00781700A patent/ZA781700B/en unknown
- 1978-03-23 TR TR20072A patent/TR20072A/en unknown
- 1978-03-23 IE IE588/78A patent/IE46690B1/en unknown
- 1978-03-23 HU HU78LI322A patent/HU179506B/en unknown
- 1978-03-24 SU SU782594402A patent/SU1409119A3/en active
- 1978-03-24 CS CS789183A patent/CS198290B2/en unknown
- 1978-03-24 PL PL1978216611A patent/PL112622B1/en unknown
- 1978-03-24 PL PL1978216612A patent/PL112286B1/en unknown
- 1978-03-24 CS CS789184A patent/CS198291B2/en unknown
- 1978-03-24 CS CS781922A patent/CS198289B2/en unknown
- 1978-03-24 PL PL1978216610A patent/PL112146B1/en unknown
- 1978-03-24 PL PL1978205555A patent/PL108903B1/en unknown
- 1978-03-24 CS CS789185A patent/CS198292B2/en unknown
- 1978-03-24 JP JP3402678A patent/JPS53121932A/en active Granted
- 1978-09-08 FR FR7825893A patent/FR2390097A1/en active Granted
- 1978-09-08 FR FR7825895A patent/FR2390099B1/fr not_active Expired
- 1978-09-08 FR FR7825894A patent/FR2390098A1/en active Granted
-
1981
- 1981-02-02 AR AR284171A patent/AR225793A1/en active
-
1982
- 1982-05-07 NO NO821512A patent/NO148622C/en unknown
- 1982-05-07 NO NO821513A patent/NO148241C/en unknown
- 1982-05-07 NO NO821514A patent/NO148621C/en unknown
-
1983
- 1983-03-23 SE SE8301606A patent/SE454398B/en not_active IP Right Cessation
-
1986
- 1986-05-30 SE SE8602470A patent/SE8602470D0/en not_active Application Discontinuation
-
1987
- 1987-08-19 SE SE8703223A patent/SE8703223D0/en not_active Application Discontinuation
- 1987-08-19 SE SE8703224A patent/SE8703224L/en not_active Application Discontinuation
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