CS198290B2 - Fungicide - Google Patents
Fungicide Download PDFInfo
- Publication number
- CS198290B2 CS198290B2 CS789183A CS918378A CS198290B2 CS 198290 B2 CS198290 B2 CS 198290B2 CS 789183 A CS789183 A CS 789183A CS 918378 A CS918378 A CS 918378A CS 198290 B2 CS198290 B2 CS 198290B2
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- Czechoslovakia
- Prior art keywords
- formula
- compound
- compounds
- fungicidal composition
- active ingredient
- Prior art date
Links
- 230000000855 fungicidal effect Effects 0.000 title claims description 7
- 239000000417 fungicide Substances 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 15
- 239000004480 active ingredient Substances 0.000 claims description 10
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- 229910052731 fluorine Chemical group 0.000 claims description 4
- 125000001153 fluoro group Chemical group F* 0.000 claims description 4
- -1 pyrimidine compound Chemical class 0.000 claims description 4
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims description 3
- 231100001184 nonphytotoxic Toxicity 0.000 claims description 2
- 239000000843 powder Substances 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 239000007900 aqueous suspension Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 241000219094 Vitaceae Species 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 235000021021 grapes Nutrition 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 3
- 239000005995 Aluminium silicate Substances 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 239000005789 Folpet Substances 0.000 description 2
- 206010017533 Fungal infection Diseases 0.000 description 2
- 208000031888 Mycoses Diseases 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- LRAJHPGSGBRUJN-OMIVUECESA-N cefepime hydrochloride Chemical compound O.Cl.[Cl-].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 LRAJHPGSGBRUJN-OMIVUECESA-N 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- 150000003871 sulfonates Chemical class 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 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
- 108010053481 Antifreeze Proteins Proteins 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 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
- 239000005909 Kieselgur Substances 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 230000002528 anti-freeze Effects 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000007798 antifreeze agent Substances 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 210000000481 breast Anatomy 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- RZHBMYQXKIDANM-UHFFFAOYSA-N dioctyl butanedioate;sodium Chemical compound [Na].CCCCCCCCOC(=O)CCC(=O)OCCCCCCCC RZHBMYQXKIDANM-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 235000019357 lignosulphonate Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229920001206 natural gum Polymers 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229920005552 sodium lignosulfonate Polymers 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000000080 wetting agent 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
- 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)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
Description
Vynález se týká fungicidního prostředku.The invention relates to a fungicidal composition.
Podstata fungicidního prostředku podle vynálezu je v tom, že jako jednu fungicídně účinnou složku obsahuje pyrimidinovou sloučeninu obecného vzorce IThe fungicidal composition according to the invention is characterized in that it contains as a fungicidally active ingredient a pyrimidine compound of the formula I
/I/ kde X značí atom chloru nebo atom fluoru, a jako druhou fungicídně účinnou složku hlinitou sůl vzorce II r H(I) wherein X represents a chlorine atom or a fluorine atom, and the second fungicidally active ingredient is an aluminum salt of the formula II r H
C1H5—P—OH C1H5 — P — O H
II oII o
AI /II/ v kombinaci s alespoň jedním nefytoxickým nosičem, přičemž účinné látky I а II tvoříAl (II) in combination with at least one non-phytoxic carrier, wherein the active ingredients I and II form
0,5 až 90 % hmotnostních fungicidního prostředku a jsou přítomny v hmotnostním poměru0.5 to 90% by weight of the fungicidal composition and are present in a weight ratio
1:10 až I:100.1:10 to I: 100.
Výše uvedené sloučeniny jsou známé a lze je připravovat metodami dobře známými z literatury. Kombinace účinných složek, vymezených ve výše uvedeném prostředku, jsou nové aThe above compounds are known and can be prepared by methods well known in the literature. Combinations of the active ingredients as defined in the above formulation are novel and
1982 90.1982 90.
bylo zjištěno, že jeou.překvapivě účinné . při potlačování nebo při boji proti houbovým infekcím pěst°vaných rostlin, přičernž tobiuu Blouíeniny vzorce I а II je především po°uitelná při potlačování plíeňových infekcí hroznů.has been found to be surprisingly effective. in the control or in combating fungal infections in a fist and n ° H Yc plants, eg ičernž Tobiume B l y ouíenin а formula I II, j e e d ev BC SIM along with readable ° in suppressing infections plíeňových grapes.
Pro8tředek podle vynálezu se výhodně aplikuje na Ksty v období po vzejjtí dilí až do 8klizně, pHtaž rnnnožSvi a četn°st aplUace je dána závažností nebo očekávanou eávažno' pLi^í^n^ové choroby. Chaarateri8tcckým znakem vynálezu a zvláštní výhodou vyplývející z . p^i^u^ivání výše uvrdrnýca ^^i-naci je snížená črtoo8t ošetření, poetačuúící ' k dos^^í účinku, například jenom . ^ždá _dva až W týdny při potlačování MísSc^ých Uf^cí ^o^ů, Ш se d°- sáhne značného snížení pracovních nákladů.Pro8t ředek according VYN AL Cutting is preferably a pl also h a e on Ksty post vzejjtí Delhi to 8 to L and from them, p Htaž RNN CTMR vi p e tn ° st aplUace bring them to the severity n eb oo awaits bath ávažno e 'p L i ^ i ^ n ^ o ve C horoby. Cha ara c teri 8 t ym c k from NAK em y n Alez and also special advantages in plývející from you. p ^ i ^ u ^ i tion with the above rdrný C ^^ i-tion is reduced No. O8 t RTO treatment oetačuúící p 'to dos ^^ also learning ge, n, and p of manufacture example Jeno m. ^ _ whether two or yd T W in suppressing MísSc ny ^ ACTIVE compounding Uf ^ o ^ s, Ш the d ° - reaches a considerable reduction of labor costs.
Výhodný pyrimidin vzorce I pro pouští při ošetřování hroznů je ten, kde X značí atom chloru, zatímco sloučenina vzorce I, kde X značí atom fluoru, má přednost pro pouuití ve spoottosti s plísňovýoi infekcemi o^íLoIo.A preferred pyrimidine of the formula I for the desert treatment of grapes is one where X is a chlorine atom, while a compound of the formula I where X is a fluorine atom is preferred for use in conjunction with fungal infections of 10-10.
Složky prostředku podle vynálezu Lze aplikovat na ošetřovanou rostlinu po sobě nebo současně, přičemž poslednímu způsobu se dává přednnet. Sloučeniny obecného vzorce I se appikují s výhodou v mnnžesví 10 až 100 g, nejvýhodnOJi od 10 až 30' g na hektar při ošetřování hroznů, zatímco sL^oučeniny vzorce II se appi^í s výhodou v množsSvíca od 100 do 3 000 g na hektar. Poměr sloučenin vzorce I ke sloučeninám vzorce II v kombinacích podle vynálezu ' se tedy může pohybovat od 1:10 do 1:100, vyjádřenoThe components of the composition according to the invention can be applied to the plant to be treated sequentially or simultaneously, the latter method being pre-treated. The compounds of the formula I are preferably applied in an amount of 10 to 100 g, most preferably from 10 to 30 g per hectare in the treatment of grapes, while the compounds of the formula II are preferably applied in an amount of 100 to 3000 g per hectare. . Thus, the ratio of the compounds of formula I to the compounds of formula II in the combinations according to the invention may range from 1:10 to 1: 100, expressed as
Sloučenina vzorce II, hlinitá sůl dy^^^tu /AEEP, se užívá s' výhodou v kombinaci s dalším fungicidem, například mancozebeo nebo popřípadě s folpetem, 2-£/t^chlormety1/-. -thioi“^! H-isoiodol-1,3/2H/-dionem . /viz. ΡΗ^ί^^ Phytopharmoaie . /.197,7/.7.The compound of formula (II), the aluminum salt of dimethyl (AEEP), is preferably used in combination with another fungicide, for example mancose or optionally with folpet, 2- (chloromethyl) -. -thioi “^! H-isoiodol-1,3 (2H) -dione. / viz. Yt ^ ί ^^ Phytopharmoaie. /.197,7/.7.
Za účelem zjednodušení výroby, skladováni a transportu se kombinace sloučenin vzorce I a sloučenin vzorce . II obvykle vyráběl ve formě koncentrátu určeného k ředění vodou na požadovanou Сопо€гOraai. Takové konaentrované prostředky mohou obsahovat 0,5 až 90 Z, s výhodou 5 . až . 90 Z hod. aktivních složek, doplněných jedním nebo více netečnými nefytnxickýoi . takové prostředky budou obvykle ve formě somá^e^ého prášku, popra-še· 'nebo vodná suspenze, i když vodné suspenze AEP . maaí sklon k nestálosti v důsledku poměrně krátkého poločasu. /přibližně 100 dní/.AEP.ve vodných.prostředcích. . KonocnOráty jsou určeny pro přiměřené. ředění vodou před použitím. . Vodné disperze lze připravovat v obvyklých rozprašovacích tancích vhodných . k . účelu.. · ,In order to simplify production, storage and transport, a combination of compounds of formula I and compounds of formula I is used. II was usually produced in the form of a concentrate intended to be diluted with water to the desired Snaproaai. Such concentrate compositions may contain 0.5 to 90 Z, preferably 5. to. 90 Of the active ingredients, supplemented with one or more inert non-phytotoxic agents. such compositions will generally be in the form of a dry powder, dust or aqueous suspension, although aqueous AEP suspensions. has a tendency to instability due to the relatively short half-life. (about 100 days) .AEP.in aqueous media. . CONNECTORS are designed to be adequate. dilution with water before use. . Aqueous dispersions can be prepared in conventional spray tanks suitable. k. purpose .. ·,
SinOáčtelné prášky nebo. ' popraše. obsahuuí.dokonalou směs aktivních složek, jeden.nebo více netečných nosičů . a vhodné povrchově. aktivní Látky. . Netečný nosič lze voUt в attapuugitových altort', oooOnorillonitovýia altort, iifu8nrio>výca hlinek, kaolinů, .talků a čištěných silikátů. Účinné povrchově aktivní látky Lze oalézt mezi sulnonovanýot ligniny, oaftaLm sulfonáty a ;; kondenzovanými . oaftaLro8ulfnoáty, altyl8ut.ciiáty,' aLtyLirizensuufonáty, a^yy-sultáty a ietonogriiíoi povrchově aktivními látkami, například etylenoxódovýoi adukty fenolu. Pro názornost jsou dále uvedeny smáčitrlné prášky spadajcí do rozsahu vynálezu; maaíoááleduujci složení:Sinable powders or. dusts. containing a perfect mixture of the active ingredients, one or more inert carriers. and suitable surface. Active Substances. . The inert carrier can be used in attapuugite altorts, oornorillonite altorts, aluminum, kaolins, talc and purified silicates. Active Surfactants Can be found between sulfonated lignins, oaftal sulfonates and ;; condensed. oaftaol sulfonates, allyl sulfates, allyl sulfizuufonates, allyl sulfates and ionic surfactants, for example ethylene oxide adducts of phenol. For illustrative purposes, wettable powders falling within the scope of the invention are set forth below; maaíoááfollowing composition:
SmOčiielné prášky . . Z hmonnnnSních sloučenina vzorce I sloučenina vzorce IISpecial purpose powders. . Among the compounds of formula I, the compound of formula II
8o0ččr0Ό/a/ disperzní činidLo protispékavé čtoi0ln netečnýýé/ ο^^/^(A) dispersing agent (s) Anti-caking agent (s) inert (ο ^^ / ^)
0,25 až 100.25 to 10
10,00 až 8010.00 to 80
0,00 až 100.00 to 10
0,00 až 100.00 to 10
0,00 až 10 do 1000.00 to 10 to 100
Vodné roztoky a suspenze obsahиui aktivní složky suspendované nebo rozpuštěné ve vodě nebo ve vhodných rnzpouUtt0lrch spolu s.krerýokkli požadovanými povrchově aktivními látkami, zahuuřovadly, přísadami proti zamrzání . nebo konzervačními prostředky. Vhodné povrchově aktivní Látky mohou být voleny z těch, které byly uvedeny výše v souuve 1 osti se somái^lnýoi prášky. PolUívV-lt se zahu Utnvador, volí se obvykle z vhodných celulóz<)výca maatriálů a přirozených gum, zatímco glykolů se používá obecně jako přísad .proti zamr^O. Konozrvační prostředky mohou být vybírány ze široké palety mami^^Lů, například z an^ba^e^á-oich látek na bázi parabenu, fenolu, n-ialnrtre8olu, dusičnanu friyLrtutiatéan a formaH^y^.Aqueous solutions and suspensions containing the active ingredient suspended or dissolved in water or in a suitable solution together with the desired surfactants, thickeners, antifreeze agents. or preservatives. Suitable surfactants may be selected from those mentioned above in relation to the separate powders. The polymers are selected from suitable celluloses, in particular maize materials and natural gums, while glycols are generally used as additives against ice. Preservatives may be selected from a wide variety of mamma, for example, paraben, phenol, n-allyltrole, nitrile, lututate and nitrate formulations.
Typickými příklady vodných suspenzí spadajících do rozsahu vynálezu jsou:Typical examples of aqueous suspensions within the scope of the invention are:
Vodné suspenze /tekuté/Aqueous suspensions (liquid)
Z hmotnostníchFrom weight
Zatímco předchozí obecné příklady dostatečně ilustrují odborníkům typy koncentrovaných přípravků používaných v tomto vynálezu, následující neomezující příklady slouží к další ilustrací prostředků podle tohoto vynálezu.While the foregoing general examples sufficiently illustrate to those skilled in the art the types of concentrated formulations used in this invention, the following non-limiting examples serve to further illustrate the compositions of the invention.
Název CCPM” v těchto příkladech značí sloučeninu obecného vzorce I, ve kterém X značí atom chloru, zatímco příbuzná sloučenina, ve které X značí atom fluoru, je označena písmeny ?CFPM”. Podobně sloučenina vzorce II je označena symbolem ”AEP”.The name CCPM ”in these examples denotes a compound of formula I in which X represents a chlorine atom, while a related compound in which X represents a fluorine atom is denoted by the letters? CFPM." Similarly, the compound of formula II is indicated by the symbol "AEP".
PříkladyExamples
Byly připraveny následující smáčítelné prášky:The following wettable powders were prepared:
Z hmotnostníchFrom weight
Aktivní složky v každém příkladu byly pečlivě smíchány se specifickými pomocnými látka mi v obvyklém míchacím zařízení. Směs byla potom dále mleta ve fluidním mlýnu na velikost částic řádu od 1 do 10^um a nakonec byla směs znovu promíchána a před balením byla odvzdušněna.The active ingredients in each example were carefully mixed with the specific excipients in a conventional mixer. The mixture was then further milled in a fluid mill to a particle size of the order of 1 to 10 µm and finally mixed again and vented before packing.
Claims (1)
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 |
---|---|
CS198290B2 true CS198290B2 (en) | 1980-05-30 |
Family
ID=10014480
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CS789183A CS198290B2 (en) | 1977-03-28 | 1978-03-24 | Fungicide |
CS789184A CS198291B2 (en) | 1977-03-28 | 1978-03-24 | Fungicide |
CS789185A CS198292B2 (en) | 1977-03-28 | 1978-03-24 | Fungicide |
CS781922A CS198289B2 (en) | 1977-03-28 | 1978-03-24 | Fungicide |
Family Applications After (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CS789184A CS198291B2 (en) | 1977-03-28 | 1978-03-24 | Fungicide |
CS789185A CS198292B2 (en) | 1977-03-28 | 1978-03-24 | Fungicide |
CS781922A CS198289B2 (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) | HU179506B (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) | PL108903B1 (en) |
PT (1) | PT67801A (en) |
RO (4) | RO78273A (en) |
SE (5) | SE447783B (en) |
SU (1) | SU1409119A3 (en) |
TR (1) | TR20072A (en) |
ZA (1) | ZA781700B (en) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2560510C2 (en) * | 1975-11-26 | 1989-02-16 | Bayer Ag, 5090 Leverkusen, De | |
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 | ||
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 |
CN103583541B (en) * | 2012-08-17 | 2015-11-11 | 陕西美邦农药有限公司 | A kind of bactericidal composition containing pyrimidine alcohol |
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 |
US3868244A (en) | 1972-03-13 | 1975-02-25 | Lilly Co Eli | Plant growth regulation |
US3869456A (en) | 1972-03-13 | 1975-03-04 | Lilly Co Eli | Synthesis of 5-pyrimidinecarbinols |
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 |
FR2254276B1 (en) * | 1973-12-14 | 1977-03-04 | Philagro Sa | |
DE2463046C2 (en) * | 1973-12-14 | 1984-05-03 | PEPRO - Société pour le Développement et la Vente de Spécialités Chimiques, Lyon | Ammonium phosphonate-based fungicidal agents |
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 |
DE2560510C2 (en) * | 1975-11-26 | 1989-02-16 | Bayer Ag, 5090 Leverkusen, De |
-
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 SE SE7803184A patent/SE447783B/en not_active IP Right Cessation
- 1978-03-20 IN IN295/CAL/78A patent/IN147690B/en unknown
- 1978-03-20 CA CA299,331A patent/CA1108046A/en not_active Expired
- 1978-03-20 PT PT67801A patent/PT67801A/en unknown
- 1978-03-20 FR FR7807978A patent/FR2390096A1/en active Granted
- 1978-03-20 MX MX786944U patent/MX5640E/en unknown
- 1978-03-21 RO RO7899323A patent/RO78273A/en unknown
- 1978-03-21 AR AR271494A patent/AR227124A1/en active
- 1978-03-21 DK DK127978A patent/DK149442C/en not_active IP Right Cessation
- 1978-03-21 DE DE2812287A patent/DE2812287C2/en not_active Expired
- 1978-03-21 RO RO7893574A patent/RO73042A/en unknown
- 1978-03-21 RO RO7899325A patent/RO78260A/en unknown
- 1978-03-21 GR GR55758A patent/GR64791B/en unknown
- 1978-03-21 IL IL54318A patent/IL54318A/en unknown
- 1978-03-21 ES ES468098A patent/ES468098A1/en not_active Expired
- 1978-03-21 CH CH306178A patent/CH629363A5/en not_active IP Right Cessation
- 1978-03-21 BR BR7801746A patent/BR7801746A/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 NL NL7803064A patent/NL7803064A/en not_active Application Discontinuation
- 1978-03-22 BG BG041508A patent/BG30167A4/en unknown
- 1978-03-22 NO NO781040A patent/NO147260C/en unknown
- 1978-03-22 BG BG039128A patent/BG29863A3/en unknown
- 1978-03-22 BG BG041507A patent/BG30166A4/en unknown
- 1978-03-22 AU AU34430/78A patent/AU515204B2/en not_active Expired
- 1978-03-22 NZ NZ186757A patent/NZ186757A/en unknown
- 1978-03-22 DD DD78204345A patent/DD135031A5/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 BE BE6046404A patent/BE865215A/en not_active IP Right Cessation
- 1978-03-22 BG BG041506A patent/BG30165A4/en unknown
- 1978-03-23 HU HU78LI322A patent/HU179506B/en unknown
- 1978-03-23 IE IE588/78A patent/IE46690B1/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
- 1978-03-24 CS CS789183A patent/CS198290B2/en unknown
- 1978-03-24 PL PL1978205555A patent/PL108903B1/en unknown
- 1978-03-24 CS CS789184A patent/CS198291B2/en unknown
- 1978-03-24 SU SU782594402A patent/SU1409119A3/en active
- 1978-03-24 CS CS789185A patent/CS198292B2/en unknown
- 1978-03-24 PL PL1978216612A patent/PL112286B1/en unknown
- 1978-03-24 CS CS781922A patent/CS198289B2/en unknown
- 1978-03-24 PL PL1978216610A patent/PL112146B1/en unknown
- 1978-03-24 JP JP3402678A patent/JPS53121932A/en active Granted
- 1978-03-24 PL PL1978216611A patent/PL112622B1/en unknown
- 1978-09-08 FR FR7825893A patent/FR2390097A1/en active Granted
- 1978-09-08 FR FR7825894A patent/FR2390098A1/en active Granted
- 1978-09-08 FR FR7825895A patent/FR2390099B1/fr not_active Expired
-
1981
- 1981-02-02 AR AR284171A patent/AR225793A1/en active
-
1982
- 1982-05-07 NO NO821514A patent/NO148621C/en unknown
- 1982-05-07 NO NO821513A patent/NO148241C/en unknown
- 1982-05-07 NO NO821512A patent/NO148622C/en unknown
-
1983
- 1983-03-23 SE SE8301606A patent/SE454398B/en not_active IP Right Cessation
-
1986
- 1986-05-30 SE SE8602470A patent/SE8602470L/en not_active Application Discontinuation
-
1987
- 1987-08-19 SE SE8703223A patent/SE8703223L/en not_active Application Discontinuation
- 1987-08-19 SE SE8703224A patent/SE8703224L/en not_active Application Discontinuation
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