PL112622B1 - Fungicide - Google Patents

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Publication number
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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formula
compound
active substances
weight
substances
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PL1978216611A
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Polish (pl)
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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N47/00Biocides, 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
    • A01N47/08Biocides, 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
    • A01N47/10Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/18Carbamic 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
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N57/00Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/10Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
    • A01N57/12Biocides, 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

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  • 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)

1.Zastrzezenia patentowe Zwiazek 0 wzorze 1 Zwiazek 0 wzorze 2 Srodek lub srodki powierzchniowo 4 czynne Srodek zgeszczajacy ^ Srodek przeciw zamarzaniu Srodek konserwujacy Srodek przeciwpienny Woda % wagowy 0,1—8 20^52 0—15 0—3 0—20 0-^1 0—0,5 do 100 55 60 1. Srodek grzybobójczy zawierajacy substancje czynne i jeden lub kilka obojetnych, niefitotok- sycznych nosników, znamienny tym, ze jako jed¬ na substancje czynna grzybobójcza zawiera po¬ chodna triazyny o wzorze 1 a jako druga sub¬ stancje czynna grzybobójczo zawiera benzimidazol o wzorze 2.1. Patent claims Compound 0 formula 1 Compound 0 formula 2 Surfactant or agents 4 Thickener ^ Antifreeze Preservative Antifoam Water % by weight 0.1—8 20^52 0—15 0—3 0—20 0- ^1 0-0.5 to 100 55 60 1. A fungicide containing active substances and one or more inert, non-phytotoxic carriers, characterized in that one of the active fungicidal substances is a triazine derivative of the formula I. the second fungicidally active substance contains benzimidazole of formula 2. 2. Srodek wedlug zastrz. 1, znamienny tym, ze zawiera 0,5—90% wagowych substancji czynnych.112 622 Cl N—n ^^0-CH-CO-C (CH3)3 MzOr N NT H o ^ C-NH-C-OCH3 Ncór 2 PL PL PL2. The agent according to claim 1, characterized in that it contains 0.5-90% by weight of active substances. 112 622 Cl N—n ^^0-CH-CO-C (CH3)3 MzOr N NT H o ^ C-NH-C-OCH3 Ncór 2 PL PL PL
PL1978216611A 1977-03-28 1978-03-24 Fungicide PL112622B1 (en)

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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

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AR227124A1 (en) 1982-09-30
SE7803184L (en) 1978-09-29
FR2390099A1 (en) 1978-12-08
IE780588L (en) 1978-09-28
PL112286B1 (en) 1980-10-31
ATA203678A (en) 1980-09-15
HU179506B (en) 1982-10-28
HU188701B (en) 1986-05-28
CS198292B2 (en) 1980-05-30
SE8703224D0 (en) 1987-08-19
DD135031A5 (en) 1979-04-11
BR7801746A (en) 1978-12-19
DK149442C (en) 1986-11-17
IL54318A0 (en) 1978-06-15
BG30165A4 (en) 1981-04-15
CS198290B2 (en) 1980-05-30
SE8703223L (en) 1987-08-19
FR2390098A1 (en) 1978-12-08
NO821513L (en) 1978-09-29
NL7803064A (en) 1978-10-02
CS198289B2 (en) 1980-05-30
SE8602470L (en) 1986-05-30
ZA781700B (en) 1979-03-28
FR2390098B1 (en) 1980-07-11
RO78260A (en) 1982-04-12
PL108903B1 (en) 1980-05-31
PL205555A1 (en) 1978-12-04
AT362195B (en) 1981-04-27
DE2812287A1 (en) 1978-10-05
FR2390097A1 (en) 1978-12-08
FR2390096A1 (en) 1978-12-08
NO147260C (en) 1983-03-09
JPS6259081B2 (en) 1987-12-09
BG30167A4 (en) 1981-04-15
SE454398B (en) 1988-05-02
RO78273A (en) 1982-04-12
BG29863A3 (en) 1981-02-16
DE2812287C2 (en) 1986-12-11
NO148241C (en) 1983-09-07
NO148622B (en) 1983-08-08
AR225793A1 (en) 1982-04-30
LU79285A1 (en) 1978-06-29
FR2390099B1 (en) 1980-07-11
CH629363A5 (en) 1982-04-30
PL112146B1 (en) 1980-09-30
RO73042A (en) 1981-11-24
SE8703224L (en) 1987-08-19
DK149442B (en) 1986-06-16
MX5640E (en) 1983-11-23
FR2390096B1 (en) 1980-06-06
CA1108046A (en) 1981-09-01
PT67801A (en) 1978-04-01
IE46690B1 (en) 1983-08-24
SU1409119A3 (en) 1988-07-07
FR2390097B1 (en) 1980-07-11
TR20072A (en) 1980-07-08
GR64791B (en) 1980-06-02
BG30166A4 (en) 1981-04-15
IL54318A (en) 1983-06-15
NO148622C (en) 1983-11-16
GB1596380A (en) 1981-08-26
IT7848444A0 (en) 1978-03-15
NO148241B (en) 1983-05-30
IT1105157B (en) 1985-10-28
SE8703223D0 (en) 1987-08-19
SE8301606L (en) 1983-03-23
NZ186757A (en) 1980-11-14
ES468098A1 (en) 1979-09-01
NO821512L (en) 1978-09-29
JPS53121932A (en) 1978-10-24
SE8602470D0 (en) 1986-05-30
NO148621C (en) 1983-11-16
NO147260B (en) 1982-11-29
SE8301606D0 (en) 1983-03-23
DK127978A (en) 1978-09-29
SE447783B (en) 1986-12-15
AU3443078A (en) 1979-09-27
IN147690B (en) 1980-05-31
CS198291B2 (en) 1980-05-30
NO148621B (en) 1983-08-08
BE865215A (en) 1978-09-22
DE2858350C2 (en) 1988-06-16
RO78274A (en) 1982-04-12
NO821514L (en) 1978-09-29
NO781040L (en) 1978-09-29
AU515204B2 (en) 1981-03-19

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