DE2812287A1 - Fungizides mittel - Google Patents
Fungizides mittelInfo
- Publication number
- DE2812287A1 DE2812287A1 DE19782812287 DE2812287A DE2812287A1 DE 2812287 A1 DE2812287 A1 DE 2812287A1 DE 19782812287 DE19782812287 DE 19782812287 DE 2812287 A DE2812287 A DE 2812287A DE 2812287 A1 DE2812287 A1 DE 2812287A1
- Authority
- DE
- Germany
- Prior art keywords
- formula
- compound
- agent according
- weight ratio
- fungicidal agent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000417 fungicide Substances 0.000 title claims description 18
- 150000001875 compounds Chemical class 0.000 claims description 37
- 239000004480 active ingredient Substances 0.000 claims description 12
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical group 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 claims description 12
- 206010017533 Fungal infection Diseases 0.000 claims description 7
- 208000031888 Mycoses Diseases 0.000 claims description 7
- 235000013339 cereals Nutrition 0.000 claims description 6
- 229910052801 chlorine Inorganic materials 0.000 claims description 6
- 239000000460 chlorine Substances 0.000 claims description 6
- 238000011282 treatment Methods 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 229910052731 fluorine Chemical group 0.000 claims description 5
- 239000011737 fluorine Chemical group 0.000 claims description 5
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 4
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims description 4
- 239000000969 carrier Substances 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 3
- 239000006185 dispersion Substances 0.000 claims description 3
- 231100001184 nonphytotoxic Toxicity 0.000 claims description 3
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims description 2
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims 2
- 238000011321 prophylaxis Methods 0.000 claims 2
- 241000233679 Peronosporaceae Species 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- -1 pyrimidine compound Chemical class 0.000 claims 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 claims 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000000080 wetting agent Substances 0.000 description 8
- 241000196324 Embryophyta Species 0.000 description 7
- 239000000843 powder Substances 0.000 description 6
- 239000007900 aqueous suspension Substances 0.000 description 5
- 239000002562 thickening agent Substances 0.000 description 5
- 239000005995 Aluminium silicate Substances 0.000 description 4
- 235000012211 aluminium silicate Nutrition 0.000 description 4
- 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 4
- 230000000855 fungicidal effect Effects 0.000 description 4
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 4
- 239000003755 preservative agent Substances 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 235000012239 silicon dioxide Nutrition 0.000 description 4
- 241000221785 Erysiphales Species 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 239000005909 Kieselgur Substances 0.000 description 3
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 3
- 239000002518 antifoaming agent Substances 0.000 description 3
- 201000010099 disease Diseases 0.000 description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920000847 nonoxynol Polymers 0.000 description 3
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 3
- 229920005552 sodium lignosulfonate Polymers 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 239000005789 Folpet Substances 0.000 description 2
- 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 2
- 229920001732 Lignosulfonate Polymers 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000007798 antifreeze agent Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 229960000892 attapulgite Drugs 0.000 description 2
- 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 2
- 239000012895 dilution Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 2
- YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 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
- 208000015181 infectious disease Diseases 0.000 description 2
- 235000019357 lignosulphonate Nutrition 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052901 montmorillonite Inorganic materials 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
- 229910052625 palygorskite Inorganic materials 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 230000002335 preservative effect Effects 0.000 description 2
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- DRSHXJFUUPIBHX-UHFFFAOYSA-N COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 Chemical compound COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 DRSHXJFUUPIBHX-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 239000005802 Mancozeb Substances 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
- 239000004141 Sodium laurylsulphate Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- RLUDBKMUNGUSSY-UHFFFAOYSA-N [Si](=O)=O.[Na] Chemical compound [Si](=O)=O.[Na] RLUDBKMUNGUSSY-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000002528 anti-freeze Effects 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000003899 bactericide agent 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
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- JYIMWRSJCRRYNK-UHFFFAOYSA-N dialuminum;disodium;oxygen(2-);silicon(4+);hydrate Chemical class O.[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Na+].[Na+].[Al+3].[Al+3].[Si+4] JYIMWRSJCRRYNK-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 210000005069 ears Anatomy 0.000 description 1
- ZUNGGJHBMLMRFJ-UHFFFAOYSA-O ethoxy-hydroxy-oxophosphanium Chemical compound CCO[P+](O)=O ZUNGGJHBMLMRFJ-UHFFFAOYSA-O 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 208000010801 foot rot Diseases 0.000 description 1
- KKZZGMRPRQOZID-UHFFFAOYSA-N formaldehyde propane-1,2-diol Chemical compound C=O.C(C(C)O)O KKZZGMRPRQOZID-UHFFFAOYSA-N 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 229920003063 hydroxymethyl cellulose Polymers 0.000 description 1
- 229940031574 hydroxymethyl cellulose Drugs 0.000 description 1
- 239000011872 intimate mixture Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000035800 maturation Effects 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- HQCFDOOSGDZRII-UHFFFAOYSA-M sodium;tridecyl sulfate Chemical compound [Na+].CCCCCCCCCCCCCOS([O-])(=O)=O HQCFDOOSGDZRII-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000003890 succinate salts Chemical class 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 150000003871 sulfonates Chemical class 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
- 244000045561 useful plants Species 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 235000010493 xanthan gum Nutrition 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)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (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)
Description
Henrietta House, Henrietta Place
London W.1., England
gekennzeichnet ist, daß es als einen fungizid wirksamen Bestandteil eine Triazin- oder Pyriraidinverbindung der allgemeinen Formel
wässrige Suspensionen gemäß der Erfindung sind folgende:
| (U | CCPM | Gew.% |
| AEP | 0,5 | |
| Natriumdioctylsulfosucpinat | 50,0 | |
| äthoxyliertes Nonylphenol | 2,0 | |
| Natriumligninsulfonat | 2,0 | |
| Siliziumdioxid | 3,0 | |
| Kaolinton auf | 6,0 | |
| 100,0 |
| CFPM | • | 2812287 | 1 | |
| (2) | AEP | Gew.% | ||
| Natriumlaury!sulfat | 1,0 | |||
| sulfoniertes Lignin | 50,0 | |||
| Diatomenerde auf | 3,0 | |||
| 2,0 | ||||
| CTDB | 100,0 | |||
| (3) | AEP | Gew.% | ||
| Natriumalkylathersulfat | 0,5 | |||
| Sulfitlaugepulver | 37,5 | |||
| Siliziumdioxid | 5,0 | |||
| Talk auf | 3,0 | |||
| 4,0 | ||||
| CCPM | 100,0 | |||
| (4) | MBC | Gew.% | ||
| Natriumdioctylsulfosuccinat | 5,0 | |||
| Natriumligninsulfonat | 50,0 | |||
| ausgefälltes Siliziumdioxid | 4,0 | |||
| Attapulgit auf | 1/5 | |||
| 2,5 | ||||
| CFPM | 100,0 | |||
| (5) | MBC | Gew.% | ||
| Natriumalkylnaphthalinsulfonat | 3,0 | |||
| Diatomenerde | 45,0 | |||
| Montmorillonit auf | 8,0 | |||
| 6,0 | ||||
| CTDB | 100,0 | |||
| (6) | MBC | Gew.% | ||
| Natriumsalz von kondensierten | 12,0 | |||
| Naphthalinsulfonsäuren | 60,0 | |||
| Natriumtridecylsulfat ^" | ||||
| Siliziumdioxid | 5,0 | |||
| Kaolin auf | 2,0 | |||
| 5,0 | ||||
| 100,0 | ||||
| 40 | 121 | CCPM | (8) | CTDB | 2812287 | Gew.% | '· | Es wurden die folgenden wässrigen Suspensionen hergestellt: | CFPM ^. | Gew.% |
| AEP | AEP | 1/0 | I | (9) | MBC | 4,0 | ||||
| Folpet | Maneοζeb | 30,0 | Polyoxyäthylenpolyoxypropylen- | 40,0 | ||||||
| Natriumlaurylsulfat | äthoxyliertes Nonylphenol | 15,0 | Blockcopolymeres | |||||||
| Natriumlignirisulfonat | Natriumdioctylsulfosuccinat | "2,5 | Xanthangummi | 2,0 | ||||||
| ausgefälltes Siliziumdioxid | Natriumligninsulfonat | 4,0 | Siliconantischaummittel | 0,4 | ||||||
| Kaolin auf | hydriertes Natriumsilicoaluminat | 8,0 ! | Wasser auf | 0/1 | ||||||
| Talk auf | 100,0 ; | 100,0 | ||||||||
| In jedem Beispiel wurden die Wirkstoffe | Gew.% I | |||||||||
| 2,0 j | ||||||||||
| 40,0 j | ||||||||||
| 20,0 j | ||||||||||
| 2,0 | ||||||||||
| 2,0 | ||||||||||
| 3,0 | ||||||||||
| 7,5 | ||||||||||
| 100,0 | ||||||||||
| mit den angegebenen | ||||||||||
| Streckmitteln in herkömmlichen Mischeinrichtungen sorgfältig : | ||||||||||
| vermengt. Das Gemisch wurde weiterhin in einer Fluidenergiemühle | ||||||||||
| zum Größenbereich von 1 bis 10 μπι weiter vermählen. Schließlich | ||||||||||
| wurde das Gemisch erneut vermischt und vor dem Abpacken entlüf- ■ | ||||||||||
| tet. | ||||||||||
| Beispiele 9 bis 11 |
| (10) | CTDB | (11) | CCPM | Gew.% |
| MBC | MBC | 2,5 | ||
| Natriumlaurylsulfat | äthoxyliertes Nonylphenol | 50,0 | ||
| Bentonit | Hydroxymethylcellulose | 3,0 | ||
| Äthylenglykol | Siliconantischaummittel | 3,0 | ||
| Formaldehyd | Propylenglykol | 5,0 | ||
| Wasser auf | Wasser auf | 0,2 | ||
| 100,0 | ||||
| Gew.% | ||||
| 5.0 | ||||
| 40,0 | ||||
| 4,0 | ||||
| 2,0 | ||||
| 0,15 | ||||
| 6,0 | ||||
| 100,0 |
aufnehmen gelassen. Schließlich wurde das Produkt mit Wasser auf
das entsprechende Volumen verdünnt.
Claims (9)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB12972/77A GB1596380A (en) | 1977-03-28 | 1977-03-28 | Fungicidal combinations |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2812287A1 true DE2812287A1 (de) | 1978-10-05 |
| DE2812287C2 DE2812287C2 (de) | 1986-12-11 |
Family
ID=10014480
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2812287A Expired DE2812287C2 (de) | 1977-03-28 | 1978-03-21 | Fungizides Mittel und dessen Verwendung zur Behandlung von Pilzinfektionen bei Kulturpflanzen |
| DE2858350A Expired DE2858350C2 (de) | 1977-03-28 | 1978-03-21 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2858350A Expired DE2858350C2 (de) | 1977-03-28 | 1978-03-21 |
Country Status (34)
| Country | Link |
|---|---|
| JP (1) | JPS53121932A (de) |
| AR (2) | AR227124A1 (de) |
| AT (1) | AT362195B (de) |
| AU (1) | AU515204B2 (de) |
| BE (1) | BE865215A (de) |
| BG (4) | BG30167A4 (de) |
| BR (1) | BR7801746A (de) |
| CA (1) | CA1108046A (de) |
| CH (1) | CH629363A5 (de) |
| CS (4) | CS198291B2 (de) |
| DD (1) | DD135031A5 (de) |
| DE (2) | DE2812287C2 (de) |
| DK (1) | DK149442C (de) |
| ES (1) | ES468098A1 (de) |
| FR (4) | FR2390096A1 (de) |
| GB (1) | GB1596380A (de) |
| GR (1) | GR64791B (de) |
| HU (2) | HU188701B (de) |
| IE (1) | IE46690B1 (de) |
| IL (1) | IL54318A (de) |
| IN (1) | IN147690B (de) |
| IT (1) | IT1105157B (de) |
| LU (1) | LU79285A1 (de) |
| MX (1) | MX5640E (de) |
| NL (1) | NL7803064A (de) |
| NO (4) | NO147260C (de) |
| NZ (1) | NZ186757A (de) |
| PL (4) | PL112622B1 (de) |
| PT (1) | PT67801A (de) |
| RO (4) | RO78273A (de) |
| SE (5) | SE447783B (de) |
| SU (1) | SU1409119A3 (de) |
| TR (1) | TR20072A (de) |
| ZA (1) | ZA781700B (de) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2852121A1 (de) * | 1977-12-01 | 1979-06-07 | Sipcam | Fungizide pflanzenschutzmittel |
| EP0010691A1 (de) * | 1978-10-23 | 1980-05-14 | BASF Aktiengesellschaft | Neue 1,2,4-Triazolderivate Verfahren zu ihrer Herstellung, ihre Verwendung zur Herstellung von Pflanzenschutzmitteln, Verfahren zur Herstellung von Fungiziden und Verfahren zur Bekämpfung von Fungi sowie fungizide Mittel |
| EP0088256A1 (de) * | 1982-03-06 | 1983-09-14 | Bayer Ag | Fungizide Mittel |
| AT393437B (de) * | 1986-12-09 | 1991-10-25 | Sandoz Ag | Verfahren zur bekaempfung von pilzkrankheiten von pflanzen und fungizides mittel |
| FR2732191A1 (fr) * | 1995-03-30 | 1996-10-04 | Rhone Poulenc Agrochimie | Procede de traitement antifongique des bananiers |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2552967A1 (de) * | 1975-11-26 | 1977-06-08 | Bayer Ag | Fungizide mittel |
| FR2524261A1 (fr) * | 1982-04-01 | 1983-10-07 | Rhone Poulenc Agrochimie | Composition fongicide en poudre a base de fenarimol |
| JPH01167287U (de) * | 1988-05-16 | 1989-11-24 | ||
| DE3818903A1 (de) * | 1988-06-03 | 1989-12-14 | Stama Maschinenfabrik Gmbh | Bohr- und fraeswerk |
| JPH0274094U (de) * | 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 |
| GB0811079D0 (en) * | 2008-06-17 | 2008-07-23 | Syngenta Participations Ag | Herbicide formulation |
| CN105028419B (zh) * | 2012-08-17 | 2017-06-16 | 陕西美邦农药有限公司 | 一种含氯苯嘧啶醇的杀菌组合物 |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1218623A (en) | 1967-04-27 | 1971-01-06 | Lilly Co Eli | Susbtituted-5-pyrimidine compounds |
| 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 |
| US3869454A (en) | 1971-06-04 | 1975-03-04 | Oreal | Novel diazamerocyanines and their use for dyeing keratinous fibers |
| DE2456627A1 (de) * | 1973-12-14 | 1975-06-19 | Pepro | Fungizide auf alkylphosphit-basis |
| DE2354467A1 (de) | 1973-10-31 | 1975-07-17 | Hoechst Ag | Fungizide dispersionen |
| DE2552967A1 (de) * | 1975-11-26 | 1977-06-08 | Bayer Ag | Fungizide mittel |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3912752A (en) * | 1972-01-11 | 1975-10-14 | Bayer Ag | 1-Substituted-1,2,4-triazoles |
| DE2303757A1 (de) * | 1973-01-26 | 1974-08-15 | Hoechst Ag | Fungizide mittel |
| FR2254276B1 (de) * | 1973-12-14 | 1977-03-04 | Philagro Sa | |
| FR2279331A1 (fr) * | 1974-07-24 | 1976-02-20 | Hoechst Ag | Agents fongicides a base de carbamates derivant du benzimidazole et leur preparation |
-
1977
- 1977-03-28 GB GB12972/77A patent/GB1596380A/en not_active Expired
-
1978
- 1978-03-15 IT IT48444/78A patent/IT1105157B/it active
- 1978-03-20 FR FR7807978A patent/FR2390096A1/fr active Granted
- 1978-03-20 PT PT67801A patent/PT67801A/pt unknown
- 1978-03-20 SE SE7803184A patent/SE447783B/sv not_active IP Right Cessation
- 1978-03-20 CA CA299,331A patent/CA1108046A/en not_active Expired
- 1978-03-20 IN IN295/CAL/78A patent/IN147690B/en unknown
- 1978-03-20 MX MX786944U patent/MX5640E/es unknown
- 1978-03-21 GR GR55758A patent/GR64791B/el unknown
- 1978-03-21 ES ES468098A patent/ES468098A1/es not_active Expired
- 1978-03-21 RO RO7899323A patent/RO78273A/ro unknown
- 1978-03-21 CH CH306178A patent/CH629363A5/fr not_active IP Right Cessation
- 1978-03-21 RO RO7899324A patent/RO78274A/ro unknown
- 1978-03-21 IL IL54318A patent/IL54318A/xx unknown
- 1978-03-21 RO RO7899325A patent/RO78260A/ro unknown
- 1978-03-21 BR BR7801746A patent/BR7801746A/pt unknown
- 1978-03-21 RO RO7893574A patent/RO73042A/ro unknown
- 1978-03-21 DE DE2812287A patent/DE2812287C2/de not_active Expired
- 1978-03-21 DE DE2858350A patent/DE2858350C2/de not_active Expired
- 1978-03-21 DK DK127978A patent/DK149442C/da not_active IP Right Cessation
- 1978-03-21 AR AR271494A patent/AR227124A1/es active
- 1978-03-22 DD DD78204345A patent/DD135031A5/de unknown
- 1978-03-22 BG BG041508A patent/BG30167A4/xx unknown
- 1978-03-22 BG BG041507A patent/BG30166A4/xx unknown
- 1978-03-22 AT AT203678A patent/AT362195B/de not_active IP Right Cessation
- 1978-03-22 BG BG041506A patent/BG30165A4/xx unknown
- 1978-03-22 NL NL7803064A patent/NL7803064A/xx not_active Application Discontinuation
- 1978-03-22 NO NO781040A patent/NO147260C/no unknown
- 1978-03-22 LU LU79285A patent/LU79285A1/xx unknown
- 1978-03-22 AU AU34430/78A patent/AU515204B2/en not_active Expired
- 1978-03-22 NZ NZ186757A patent/NZ186757A/xx unknown
- 1978-03-22 BG BG039128A patent/BG29863A3/xx unknown
- 1978-03-22 BE BE6046404A patent/BE865215A/xx not_active IP Right Cessation
- 1978-03-23 HU HU812978A patent/HU188701B/hu unknown
- 1978-03-23 ZA ZA00781700A patent/ZA781700B/xx unknown
- 1978-03-23 TR TR20072A patent/TR20072A/xx unknown
- 1978-03-23 IE IE588/78A patent/IE46690B1/en unknown
- 1978-03-23 HU HU78LI322A patent/HU179506B/hu unknown
- 1978-03-24 PL PL1978216611A patent/PL112622B1/pl unknown
- 1978-03-24 CS CS789184A patent/CS198291B2/cs unknown
- 1978-03-24 CS CS789185A patent/CS198292B2/cs unknown
- 1978-03-24 CS CS781922A patent/CS198289B2/cs unknown
- 1978-03-24 SU SU782594402A patent/SU1409119A3/ru active
- 1978-03-24 JP JP3402678A patent/JPS53121932A/ja active Granted
- 1978-03-24 PL PL1978216610A patent/PL112146B1/pl unknown
- 1978-03-24 CS CS789183A patent/CS198290B2/cs unknown
- 1978-03-24 PL PL1978216612A patent/PL112286B1/pl unknown
- 1978-03-24 PL PL1978205555A patent/PL108903B1/pl unknown
- 1978-09-08 FR FR7825894A patent/FR2390098A1/fr active Granted
- 1978-09-08 FR FR7825895A patent/FR2390099B1/fr not_active Expired
- 1978-09-08 FR FR7825893A patent/FR2390097A1/fr active Granted
-
1981
- 1981-02-02 AR AR284171A patent/AR225793A1/es active
-
1982
- 1982-05-07 NO NO821514A patent/NO148621C/no unknown
- 1982-05-07 NO NO821512A patent/NO148622C/no unknown
- 1982-05-07 NO NO821513A patent/NO148241C/no unknown
-
1983
- 1983-03-23 SE SE8301606A patent/SE454398B/sv not_active IP Right Cessation
-
1986
- 1986-05-30 SE SE8602470A patent/SE8602470L/xx not_active Application Discontinuation
-
1987
- 1987-08-19 SE SE8703224A patent/SE8703224L/xx not_active Application Discontinuation
- 1987-08-19 SE SE8703223A patent/SE8703223L/xx not_active Application Discontinuation
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1218623A (en) | 1967-04-27 | 1971-01-06 | Lilly Co Eli | Susbtituted-5-pyrimidine compounds |
| US3869454A (en) | 1971-06-04 | 1975-03-04 | Oreal | Novel diazamerocyanines and their use for dyeing keratinous fibers |
| 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 |
| DE2354467A1 (de) | 1973-10-31 | 1975-07-17 | Hoechst Ag | Fungizide dispersionen |
| DE2456627A1 (de) * | 1973-12-14 | 1975-06-19 | Pepro | Fungizide auf alkylphosphit-basis |
| DE2552967A1 (de) * | 1975-11-26 | 1977-06-08 | Bayer Ag | Fungizide mittel |
Non-Patent Citations (4)
| Title |
|---|
| Chemie der Pflanzenschutz und Schädlingsbekämpfungsmittel, WEGLER, R.: Bd. 4, Springer-Verlag Berlin, 1977, S.214 |
| Providence Agricole, Buide des Traitements, Januier 1977 * |
| Weeds, 15, 1967, 20-22 |
| Zeitschrift für Pflanzenkrankheiten und Pflanzenschutz, H. 11, 1974, Bd. 81, S.711-716 |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2852121A1 (de) * | 1977-12-01 | 1979-06-07 | Sipcam | Fungizide pflanzenschutzmittel |
| EP0010691A1 (de) * | 1978-10-23 | 1980-05-14 | BASF Aktiengesellschaft | Neue 1,2,4-Triazolderivate Verfahren zu ihrer Herstellung, ihre Verwendung zur Herstellung von Pflanzenschutzmitteln, Verfahren zur Herstellung von Fungiziden und Verfahren zur Bekämpfung von Fungi sowie fungizide Mittel |
| EP0088256A1 (de) * | 1982-03-06 | 1983-09-14 | Bayer Ag | Fungizide Mittel |
| AT393437B (de) * | 1986-12-09 | 1991-10-25 | Sandoz Ag | Verfahren zur bekaempfung von pilzkrankheiten von pflanzen und fungizides mittel |
| FR2732191A1 (fr) * | 1995-03-30 | 1996-10-04 | Rhone Poulenc Agrochimie | Procede de traitement antifongique des bananiers |
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