DD217960A3 - Mittel zur bekaempfung phytopathogener pilze und bakterien - Google Patents

Mittel zur bekaempfung phytopathogener pilze und bakterien

Info

Publication number: DD217960A3
Authority: DD; German Democratic Republic
Prior art keywords: methyl; weight; chlorine; hydrogen; bromine
Prior art date: 1981-11-20

Application number

DD23501981A

Other languages

German (de)

English (en)

Inventor

Lothar Adam

Ulrich Burth

Axel Kramer

Rainer Mueller

Wolfgang Weuffen

Original Assignee

Adl D Ddr Inst F Pfl Schutzfor

Priority date (The priority date 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 date listed.)

1981-11-20

Filing date

1981-11-20

Publication date

1985-01-23

1981-11-20 Application filed by Adl D Ddr Inst F Pfl Schutzfor filed Critical Adl D Ddr Inst F Pfl Schutzfor

1981-11-20 Priority to DD23501981A priority Critical patent/DD217960A3/de

1982-06-22 Priority to FI822238A priority patent/FI68498C/fi

1982-06-23 Priority to DK281182A priority patent/DK281182A/da

1982-06-24 Priority to DE8282105548T priority patent/DE3269609D1/de

1982-06-24 Priority to EP82105548A priority patent/EP0068442B1/de

1982-06-24 Priority to AT82105548T priority patent/ATE18332T1/de

1982-08-17 Priority to US06/408,582 priority patent/US4593040A/en

1982-09-09 Priority to CS826529A priority patent/CS652982A1/cs

1982-09-13 Priority to BG5794382A priority patent/BG46166A1/xx

1985-01-23 Publication of DD217960A3 publication Critical patent/DD217960A3/de

Links

241000894006 Bacteria Species 0.000 title claims abstract description 7
239000000203 mixture Substances 0.000 claims abstract description 36
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 17
229910052794 bromium Inorganic materials 0.000 claims abstract description 17
239000000460 chlorine Substances 0.000 claims abstract description 17
229910052801 chlorine Inorganic materials 0.000 claims abstract description 17
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 16
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 15
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 15
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 8
239000001257 hydrogen Substances 0.000 claims abstract description 8
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 7
241000233866 Fungi Species 0.000 claims abstract description 6
230000003032 phytopathogenic effect Effects 0.000 claims abstract description 6
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims abstract description 4
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims abstract description 4
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 claims abstract description 4
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims abstract description 4
229910052788 barium Inorganic materials 0.000 claims abstract description 4
DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims abstract description 4
239000011575 calcium Substances 0.000 claims abstract description 4
229910052791 calcium Inorganic materials 0.000 claims abstract description 4
239000011591 potassium Substances 0.000 claims abstract description 4
229910052700 potassium Inorganic materials 0.000 claims abstract description 4
239000011734 sodium Substances 0.000 claims abstract description 4
229910052708 sodium Inorganic materials 0.000 claims abstract description 4
125000000217 alkyl group Chemical group 0.000 claims abstract description 3
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 3
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract 2
230000000855 fungicidal effect Effects 0.000 claims description 17
239000000417 fungicide Substances 0.000 claims description 14
-1 viricides Substances 0.000 claims description 14
ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 claims description 10
239000005807 Metalaxyl Substances 0.000 claims description 9
230000001580 bacterial effect Effects 0.000 claims description 7
241000196324 Embryophyta Species 0.000 claims description 6
235000002595 Solanum tuberosum Nutrition 0.000 claims description 4
244000061456 Solanum tuberosum Species 0.000 claims description 4
230000000844 anti-bacterial effect Effects 0.000 claims description 4
229910052500 inorganic mineral Inorganic materials 0.000 claims description 4
239000011707 mineral Substances 0.000 claims description 4
235000010755 mineral Nutrition 0.000 claims description 4
235000013311 vegetables Nutrition 0.000 claims description 4
208000003322 Coinfection Diseases 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
239000003899 bactericide agent Substances 0.000 claims description 3
230000031018 biological processes and functions Effects 0.000 claims description 3
235000013339 cereals Nutrition 0.000 claims description 3
239000012990 dithiocarbamate Substances 0.000 claims description 3
150000004659 dithiocarbamates Chemical class 0.000 claims description 3
235000013399 edible fruits Nutrition 0.000 claims description 3
230000002538 fungal effect Effects 0.000 claims description 3
150000002431 hydrogen Chemical group 0.000 claims description 3
239000002917 insecticide Substances 0.000 claims description 3
150000002989 phenols Chemical class 0.000 claims description 3
239000011573 trace mineral Substances 0.000 claims description 3
235000013619 trace mineral Nutrition 0.000 claims description 3
239000004009 herbicide Substances 0.000 claims description 2
230000002195 synergetic effect Effects 0.000 abstract description 5
125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 2
239000002316 fumigant Substances 0.000 abstract 1
TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 18
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 15
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 15
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 13
239000003795 chemical substances by application Substances 0.000 description 11
150000001875 compounds Chemical class 0.000 description 10
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
239000006013 carbendazim Substances 0.000 description 7
229920000151 polyglycol Polymers 0.000 description 7
239000010695 polyglycol Substances 0.000 description 7
UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
241000223218 Fusarium Species 0.000 description 6
125000005037 alkyl phenyl group Chemical group 0.000 description 6
238000009472 formulation Methods 0.000 description 6
239000000843 powder Substances 0.000 description 6
238000012360 testing method Methods 0.000 description 6
230000000694 effects Effects 0.000 description 5
239000000377 silicon dioxide Substances 0.000 description 5
239000005995 Aluminium silicate Substances 0.000 description 4
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
241000722921 Tulipa gesneriana Species 0.000 description 4
235000012211 aluminium silicate Nutrition 0.000 description 4
150000002170 ethers Chemical class 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
239000011593 sulfur Substances 0.000 description 4
229910052717 sulfur Inorganic materials 0.000 description 4
LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 description 3
241001465180 Botrytis Species 0.000 description 3
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 3
239000005745 Captan Substances 0.000 description 3
241000588698 Erwinia Species 0.000 description 3
206010061217 Infestation Diseases 0.000 description 3
208000031888 Mycoses Diseases 0.000 description 3
231100000674 Phytotoxicity Toxicity 0.000 description 3
230000000845 anti-microbial effect Effects 0.000 description 3
229940117949 captan Drugs 0.000 description 3
239000000969 carrier Substances 0.000 description 3
239000010949 copper Substances 0.000 description 3
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 3
208000015181 infectious disease Diseases 0.000 description 3
235000012239 silicon dioxide Nutrition 0.000 description 3
239000000126 substance Substances 0.000 description 3
239000000725 suspension Substances 0.000 description 3
ZNNPQQQAYCQFHP-UHFFFAOYSA-N 4-benzyl-2-chloro-6-methylphenol Chemical compound ClC1=C(O)C(C)=CC(CC=2C=CC=CC=2)=C1 ZNNPQQQAYCQFHP-UHFFFAOYSA-N 0.000 description 2
CFKMVGJGLGKFKI-UHFFFAOYSA-N 4-chloro-m-cresol Chemical compound CC1=CC(O)=CC=C1Cl CFKMVGJGLGKFKI-UHFFFAOYSA-N 0.000 description 2
241000221785 Erysiphales Species 0.000 description 2
239000005909 Kieselgur Substances 0.000 description 2
235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
239000005802 Mancozeb Substances 0.000 description 2
241001465754 Metazoa Species 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
241000233622 Phytophthora infestans Species 0.000 description 2
239000013543 active substance Substances 0.000 description 2
239000000654 additive Substances 0.000 description 2
FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 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
238000002474 experimental method Methods 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 description 2
229920000940 maneb Polymers 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
231100000324 minimal toxicity Toxicity 0.000 description 2
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
239000003921 oil Substances 0.000 description 2
IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
229920005552 sodium lignosulfonate Polymers 0.000 description 2
GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
230000009885 systemic effect Effects 0.000 description 2
239000004308 thiabendazole Substances 0.000 description 2
WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 2
235000010296 thiabendazole Nutrition 0.000 description 2
229960004546 thiabendazole Drugs 0.000 description 2
MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 2
URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 2
239000002699 waste material Substances 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
SODQFLRLAOALCF-UHFFFAOYSA-N 1lambda3-bromacyclohexa-1,3,5-triene Chemical compound Br1=CC=CC=C1 SODQFLRLAOALCF-UHFFFAOYSA-N 0.000 description 1
YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 description 1
ZAMOVMHWSVVCQD-UHFFFAOYSA-N 2-benzyl-3-chlorophenol Chemical compound OC1=CC=CC(Cl)=C1CC1=CC=CC=C1 ZAMOVMHWSVVCQD-UHFFFAOYSA-N 0.000 description 1
CDMGNVWZXRKJNS-UHFFFAOYSA-N 2-benzylphenol Chemical compound OC1=CC=CC=C1CC1=CC=CC=C1 CDMGNVWZXRKJNS-UHFFFAOYSA-N 0.000 description 1
ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 1
WUXQWIPGTRQTSY-UHFFFAOYSA-N 4-benzyl-2-bromo-6-methylphenol Chemical compound BrC1=C(O)C(C)=CC(CC=2C=CC=CC=2)=C1 WUXQWIPGTRQTSY-UHFFFAOYSA-N 0.000 description 1
102000009027 Albumins Human genes 0.000 description 1
108010088751 Albumins Proteins 0.000 description 1
208000035143 Bacterial infection Diseases 0.000 description 1
241001480061 Blumeria graminis Species 0.000 description 1
239000004375 Dextrin Substances 0.000 description 1
229920001353 Dextrin Polymers 0.000 description 1
IIUZTXTZRGLYTI-UHFFFAOYSA-N Dihydrogriseofulvin Natural products COC1CC(=O)CC(C)C11C(=O)C(C(OC)=CC(OC)=C2Cl)=C2O1 IIUZTXTZRGLYTI-UHFFFAOYSA-N 0.000 description 1
239000005791 Fuberidazole Substances 0.000 description 1
UXWOXTQWVMFRSE-UHFFFAOYSA-N Griseoviridin Natural products O=C1OC(C)CC=C(C(NCC=CC=CC(O)CC(O)C2)=O)SCC1NC(=O)C1=COC2=N1 UXWOXTQWVMFRSE-UHFFFAOYSA-N 0.000 description 1
229920001732 Lignosulfonate Polymers 0.000 description 1
241000227653 Lycopersicon Species 0.000 description 1
DDUHZTYCFQRHIY-UHFFFAOYSA-N Negwer: 6874 Natural products COC1=CC(=O)CC(C)C11C(=O)C(C(OC)=CC(OC)=C2Cl)=C2O1 DDUHZTYCFQRHIY-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
239000004113 Sepiolite Substances 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
240000003768 Solanum lycopersicum Species 0.000 description 1
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241000209140 Triticum Species 0.000 description 1
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PUQDNLJWZWZQFI-UHFFFAOYSA-M [Cu+]=O.[Cl-] Chemical compound [Cu+]=O.[Cl-] PUQDNLJWZWZQFI-UHFFFAOYSA-M 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
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RIOXQFHNBCKOKP-UHFFFAOYSA-N benomyl Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 RIOXQFHNBCKOKP-UHFFFAOYSA-N 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
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SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
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MITFXPHMIHQXPI-UHFFFAOYSA-N benzoxaprofen Natural products N=1C2=CC(C(C(O)=O)C)=CC=C2OC=1C1=CC=C(Cl)C=C1 MITFXPHMIHQXPI-UHFFFAOYSA-N 0.000 description 1
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JHRWWRDRBPCWTF-OLQVQODUSA-N captafol Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)C(Cl)Cl)C(=O)[C@H]21 JHRWWRDRBPCWTF-OLQVQODUSA-N 0.000 description 1
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UYJUZNLFJAWNEZ-UHFFFAOYSA-N fuberidazole Chemical compound C1=COC(C=2NC3=CC=CC=C3N=2)=C1 UYJUZNLFJAWNEZ-UHFFFAOYSA-N 0.000 description 1
239000001087 glyceryl triacetate Substances 0.000 description 1
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DDUHZTYCFQRHIY-RBHXEPJQSA-N griseofulvin Chemical compound COC1=CC(=O)C[C@@H](C)[C@@]11C(=O)C(C(OC)=CC(OC)=C2Cl)=C2O1 DDUHZTYCFQRHIY-RBHXEPJQSA-N 0.000 description 1
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230000002363 herbicidal effect Effects 0.000 description 1
GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
238000011835 investigation Methods 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
238000009533 lab test Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
238000000034 method Methods 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
239000000025 natural resin Substances 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
239000002420 orchard Substances 0.000 description 1
LKPLKUMXSAEKID-UHFFFAOYSA-N pentachloronitrobenzene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LKPLKUMXSAEKID-UHFFFAOYSA-N 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
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235000019422 polyvinyl alcohol Nutrition 0.000 description 1
230000003389 potentiating effect Effects 0.000 description 1
239000011814 protection agent Substances 0.000 description 1
239000010453 quartz Substances 0.000 description 1
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150000004760 silicates Chemical class 0.000 description 1
208000017520 skin disease Diseases 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
235000017550 sodium carbonate Nutrition 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
239000001488 sodium phosphate Substances 0.000 description 1
235000011008 sodium phosphates Nutrition 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
235000010265 sodium sulphite Nutrition 0.000 description 1
AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
235000019345 sodium thiosulphate Nutrition 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000007921 spray Substances 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
208000024891 symptom Diseases 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
229960000790 thymol Drugs 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
239000003053 toxin Substances 0.000 description 1
231100000765 toxin Toxicity 0.000 description 1
229960002622 triacetin Drugs 0.000 description 1
150000003626 triacylglycerols Chemical class 0.000 description 1
239000012178 vegetable wax Substances 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
239000002351 wastewater Substances 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Landscapes

Agricultural Chemicals And Associated Chemicals (AREA)

DD23501981A 1981-06-25 1981-11-20 Mittel zur bekaempfung phytopathogener pilze und bakterien DD217960A3 (de)

Priority Applications (9)

Application Number	Priority Date	Filing Date	Title
DD23501981A DD217960A3 (de)	1981-11-20	1981-11-20	Mittel zur bekaempfung phytopathogener pilze und bakterien
FI822238A FI68498C (fi)	1981-06-25	1982-06-22	Blandning foer bekaempning av fytopatogeniska svampar och bakterier
DK281182A DK281182A (da)	1981-06-25	1982-06-23	Middel til bekaempelse af phytopatogene sampe og bakterier
DE8282105548T DE3269609D1 (en)	1981-06-25	1982-06-24	Agent, its application and process for combating phytopathogenic fungi and bacteria
EP82105548A EP0068442B1 (de)	1981-06-25	1982-06-24	Mittel, dessen Verwendung und Verfahren zur Bekämpfung phytopathogener Pilze und Bakterien
AT82105548T ATE18332T1 (de)	1981-06-25	1982-06-24	Mittel, dessen verwendung und verfahren zur bekaempfung phytopathogener pilze und bakterien.
US06/408,582 US4593040A (en)	1981-06-25	1982-08-17	Compositions for combatting phytopathogenical fungi and bacteria employing mixtures of benzyl phenol derivatives and carbendazin
CS826529A CS652982A1 (en)	1981-11-20	1982-09-09	Prostredek k potirani fytopatogennich hub a bakterii
BG5794382A BG46166A1 (en)	1981-11-20	1982-09-13	Remedy for phytopathogenic fungi and bacteria control

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DD23501981A DD217960A3 (de)	1981-11-20	1981-11-20	Mittel zur bekaempfung phytopathogener pilze und bakterien

Publications (1)

Publication Number	Publication Date
DD217960A3 true DD217960A3 (de)	1985-01-23

Family

ID=5534833

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD23501981A DD217960A3 (de)	1981-06-25	1981-11-20	Mittel zur bekaempfung phytopathogener pilze und bakterien

Country Status (3)

Country	Link
BG (1)	BG46166A1 (cs)
CS (1)	CS652982A1 (cs)
DD (1)	DD217960A3 (cs)

1981
- 1981-11-20 DD DD23501981A patent/DD217960A3/de not_active IP Right Cessation
1982
- 1982-09-09 CS CS826529A patent/CS652982A1/cs unknown
- 1982-09-13 BG BG5794382A patent/BG46166A1/xx unknown

Also Published As

Publication number	Publication date
BG46166A1 (en)	1989-11-15
CS652982A1 (en)	1985-04-16

Legal Events

Date	Code	Title	Description
1999-08-26	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
DE68920851T2 (de)	1995-08-31	Biozide Mischungen.
DE69033037T3 (de)	2002-08-01	Synergetische mikrobizide Kombinationen
WO2004000021A1 (de)	2003-12-31	Fungizide wirkstoffkombinationen
WO2004000020A1 (de)	2003-12-31	Fungizide wirkstoffkombinationen
DE10333373A1 (de)	2005-02-10	Fungizide Wirkstoffkombinationen
DE10333371A1 (de)	2005-02-10	Fungizide Wirkstoffkombinationen
EP0383005A1 (de)	1990-08-22	Konservierungsmittel für Systeme oder Produkte mit einer wässrigen Phase
EP0068442B1 (de)	1986-03-05	Mittel, dessen Verwendung und Verfahren zur Bekämpfung phytopathogener Pilze und Bakterien
EP1962594A1 (de)	2008-09-03	Insektizide zusammensetzungen mit verbesserter wirkung
EP0495748A1 (de)	1992-07-22	Akarizide Mittel
EP0043802B1 (de)	1984-02-22	Synergistisches Mittel und Verfahren zur selektiven Unkrautbekämpfung, insbesondere in Getreide
DD217960A3 (de)	1985-01-23	Mittel zur bekaempfung phytopathogener pilze und bakterien
DE2516670A1 (de)	1976-10-28	Desinfektionsmittel auf der basis von aldehyden
DE2311666C3 (de)	1981-07-09	Desinfektions- und Konservierungsmittel
DE2736892A1 (de)	1978-05-03	Fungizides mittel und dessen verwendung
WO2002043495A1 (de)	2002-06-06	Fungizide wirkstoffkombinationen
EP0075249B1 (de)	1985-02-13	Herbizide Mittel
EP0043349A1 (de)	1982-01-06	Synergistisches Mittel und Verfahren zur selektiven Unkrautbekämpfung, insbesondere in Getreide und Sojabohnenkulturen
DD160576A3 (de)	1983-11-02	Mittel zur bekaempfung phytopathogener pilze und bakterien
DE1903169C (de)	1973-05-24	Fungizides Mittel
DE937497C (de)	1956-01-05	Behandlung von Pflanzen zwecks Bekaempfung von Krankheitserregern
DD208451A3 (de)	1984-05-02	Mittel zur bekaempfung phytopathogener pilze und bakterien
DD248500A1 (de)	1987-08-12	Mittel zur behandlung von saat- und pflanzgut
DE2354873B2 (de)	1978-11-23	Fungizide Mittel auf Basis von bicyclischen Dicarbonsäurederivaten
DE2005256C3 (de)	1976-07-15	Substituierte Derivate von 1,1-Dichloralken-(i)