DD257378A5 - Pflanzenmikrobizides mittel - Google Patents

Pflanzenmikrobizides mittel Download PDF

Info

Publication number: DD257378A5
Authority: DD; German Democratic Republic
Prior art keywords: phosphite; composition according; formula; active ingredient; component
Prior art date: 1985-12-16

Application number

DD86297630A

Other languages

German (de)

English (en)

Inventor

Theodor Staub

Robert J Williams

Paul Margot

Original Assignee

��@��@��k��

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.)

1985-12-16

Filing date

1986-12-15

Publication date

1988-06-15

1986-12-15 Application filed by ��@��@��k�� filed Critical ��@��@��k��

1988-06-15 Publication of DD257378A5 publication Critical patent/DD257378A5/de

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229940124561 microbicide Drugs 0.000 title 1
239000004480 active ingredient Substances 0.000 claims abstract description 43
239000000417 fungicide Substances 0.000 claims abstract description 11
230000001681 protective effect Effects 0.000 claims abstract description 11
230000000855 fungicidal effect Effects 0.000 claims abstract description 9
239000000460 chlorine Chemical group 0.000 claims abstract description 8
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 7
229910052801 chlorine Inorganic materials 0.000 claims abstract description 5
239000002855 microbicide agent Substances 0.000 claims abstract description 4
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 3
125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 claims abstract description 3
125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 claims abstract description 3
125000000623 heterocyclic group Chemical group 0.000 claims abstract description 3
125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims abstract description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 3
239000000203 mixture Substances 0.000 claims description 52
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 23
239000005807 Metalaxyl Substances 0.000 claims description 21
-1 2-tetrahydrofuryl Chemical group 0.000 claims description 20
150000001875 compounds Chemical class 0.000 claims description 19
239000013543 active substance Substances 0.000 claims description 11
201000010099 disease Diseases 0.000 claims description 9
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 9
OWDLFBLNMPCXSD-UHFFFAOYSA-N 2-chloro-N-(2,6-dimethylphenyl)-N-(2-oxotetrahydrofuran-3-yl)acetamide Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)C1C(=O)OCC1 OWDLFBLNMPCXSD-UHFFFAOYSA-N 0.000 claims description 8
239000010949 copper Substances 0.000 claims description 8
UWVQIROCRJWDKL-UHFFFAOYSA-N oxadixyl Chemical compound CC=1C=CC=C(C)C=1N(C(=O)COC)N1CCOC1=O UWVQIROCRJWDKL-UHFFFAOYSA-N 0.000 claims description 8
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 6
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 claims description 6
PYZSVQVRHDXQSL-UHFFFAOYSA-N dithianon Chemical compound S1C(C#N)=C(C#N)SC2=C1C(=O)C1=CC=CC=C1C2=O PYZSVQVRHDXQSL-UHFFFAOYSA-N 0.000 claims description 6
HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 claims description 6
238000000034 method Methods 0.000 claims description 6
OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims description 6
ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims description 6
239000005789 Folpet Substances 0.000 claims description 5
150000003863 ammonium salts Chemical class 0.000 claims description 5
CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 claims description 5
CIEXPHRYOLIQQD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-2-furoylalaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)C1=CC=CO1 CIEXPHRYOLIQQD-UHFFFAOYSA-N 0.000 claims description 5
XWKBMOUUGHARTI-UHFFFAOYSA-N tricalcium;diphosphite Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])[O-].[O-]P([O-])[O-] XWKBMOUUGHARTI-UHFFFAOYSA-N 0.000 claims description 5
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 claims description 4
239000005745 Captan Substances 0.000 claims description 4
239000005747 Chlorothalonil Substances 0.000 claims description 4
KRZUZYJEQBXUIN-UHFFFAOYSA-N Cyprofuram Chemical compound ClC1=CC=CC(N(C2C(OCC2)=O)C(=O)C2CC2)=C1 KRZUZYJEQBXUIN-UHFFFAOYSA-N 0.000 claims description 4
239000005802 Mancozeb Substances 0.000 claims description 4
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 4
239000003513 alkali Substances 0.000 claims description 4
FAARTQSZKSBAOS-UHFFFAOYSA-N barium(2+);diphosphite Chemical compound [Ba+2].[Ba+2].[Ba+2].[O-]P([O-])[O-].[O-]P([O-])[O-] FAARTQSZKSBAOS-UHFFFAOYSA-N 0.000 claims description 4
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 claims description 4
229940117949 captan Drugs 0.000 claims description 4
229910052802 copper Inorganic materials 0.000 claims description 4
WURGXGVFSMYFCG-UHFFFAOYSA-N dichlofluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=CC=C1 WURGXGVFSMYFCG-UHFFFAOYSA-N 0.000 claims description 4
KGVPNLBXJKTABS-UHFFFAOYSA-N hymexazol Chemical compound CC1=CC(O)=NO1 KGVPNLBXJKTABS-UHFFFAOYSA-N 0.000 claims description 4
CJPQIRJHIZUAQP-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(phenylacetyl)alaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-UHFFFAOYSA-N 0.000 claims description 4
KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 claims description 4
239000005734 Benalaxyl Substances 0.000 claims description 3
239000005764 Dithianon Substances 0.000 claims description 3
239000005823 Propineb Substances 0.000 claims description 3
239000011717 all-trans-retinol Substances 0.000 claims description 3
235000019169 all-trans-retinol Nutrition 0.000 claims description 3
PFIADAMVCJPXSF-UHFFFAOYSA-N chloroneb Chemical compound COC1=CC(Cl)=C(OC)C=C1Cl PFIADAMVCJPXSF-UHFFFAOYSA-N 0.000 claims description 3
IIRVGTWONXBBAW-UHFFFAOYSA-M disodium;dioxido(oxo)phosphanium Chemical compound [Na+].[Na+].[O-][P+]([O-])=O IIRVGTWONXBBAW-UHFFFAOYSA-M 0.000 claims description 3
YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 claims description 3
229920000940 maneb Polymers 0.000 claims description 3
125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 claims description 2
YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical group O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims description 2
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
NHQSYENHCTXNIG-UHFFFAOYSA-N [Cu+3].[O-]P([O-])[O-] Chemical compound [Cu+3].[O-]P([O-])[O-] NHQSYENHCTXNIG-UHFFFAOYSA-N 0.000 claims description 2
125000003277 amino group Chemical group 0.000 claims description 2
NDGSBJSAXJUQTE-UHFFFAOYSA-N azane;phosphorous acid Chemical compound N.OP(O)O NDGSBJSAXJUQTE-UHFFFAOYSA-N 0.000 claims description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
125000001309 chloro group Chemical group Cl* 0.000 claims description 2
HKMOPYJWSFRURD-UHFFFAOYSA-N chloro hypochlorite;copper Chemical compound [Cu].ClOCl HKMOPYJWSFRURD-UHFFFAOYSA-N 0.000 claims description 2
229910000365 copper sulfate Inorganic materials 0.000 claims description 2
ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 claims description 2
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 2
YXXXKCDYKKSZHL-UHFFFAOYSA-M dipotassium;dioxido(oxo)phosphanium Chemical compound [K+].[K+].[O-][P+]([O-])=O YXXXKCDYKKSZHL-UHFFFAOYSA-M 0.000 claims description 2
208000015181 infectious disease Diseases 0.000 claims description 2
150000002696 manganese Chemical class 0.000 claims description 2
239000000463 material Substances 0.000 claims description 2
BZHCGFBZBPVRFE-UHFFFAOYSA-N monopotassium phosphite Chemical compound [K+].OP(O)[O-] BZHCGFBZBPVRFE-UHFFFAOYSA-N 0.000 claims description 2
229910052759 nickel Inorganic materials 0.000 claims description 2
AQMNWCRSESPIJM-UHFFFAOYSA-N sodium;phosphenic acid Chemical compound [Na+].O[P+]([O-])=O AQMNWCRSESPIJM-UHFFFAOYSA-N 0.000 claims description 2
QBTOMQRTTGQPIB-UHFFFAOYSA-N tricopper;diphosphite Chemical compound [Cu+2].[Cu+2].[Cu+2].[O-]P([O-])[O-].[O-]P([O-])[O-] QBTOMQRTTGQPIB-UHFFFAOYSA-N 0.000 claims description 2
AUTOISGCBLBLBA-UHFFFAOYSA-N trizinc;diphosphite Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])[O-].[O-]P([O-])[O-] AUTOISGCBLBLBA-UHFFFAOYSA-N 0.000 claims description 2
239000011701 zinc Substances 0.000 claims description 2
229910052725 zinc Inorganic materials 0.000 claims description 2
125000000842 isoxazolyl group Chemical group 0.000 claims 1
GVALZJMUIHGIMD-UHFFFAOYSA-H magnesium phosphate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O GVALZJMUIHGIMD-UHFFFAOYSA-H 0.000 claims 1
239000004137 magnesium phosphate Substances 0.000 claims 1
229960002261 magnesium phosphate Drugs 0.000 claims 1
229910000157 magnesium phosphate Inorganic materials 0.000 claims 1
235000010994 magnesium phosphates Nutrition 0.000 claims 1
150000003839 salts Chemical class 0.000 abstract description 21
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 abstract 1
241000196324 Embryophyta Species 0.000 description 31
239000011734 sodium Substances 0.000 description 13
238000002360 preparation method Methods 0.000 description 11
230000000694 effects Effects 0.000 description 10
206010061217 Infestation Diseases 0.000 description 8
238000002156 mixing Methods 0.000 description 8
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
239000007921 spray Substances 0.000 description 7
239000005995 Aluminium silicate Substances 0.000 description 6
235000012211 aluminium silicate Nutrition 0.000 description 6
230000002538 fungal effect Effects 0.000 description 6
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 6
239000002689 soil Substances 0.000 description 6
241001281803 Plasmopara viticola Species 0.000 description 5
239000000654 additive Substances 0.000 description 5
239000003814 drug Substances 0.000 description 5
229940079593 drug Drugs 0.000 description 5
238000009472 formulation Methods 0.000 description 5
239000008187 granular material Substances 0.000 description 5
239000000126 substance Substances 0.000 description 5
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
241000233866 Fungi Species 0.000 description 4
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
239000002202 Polyethylene glycol Substances 0.000 description 4
239000000969 carrier Substances 0.000 description 4
235000013339 cereals Nutrition 0.000 description 4
238000005520 cutting process Methods 0.000 description 4
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
239000000839 emulsion Substances 0.000 description 4
238000011081 inoculation Methods 0.000 description 4
AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 4
229920001223 polyethylene glycol Polymers 0.000 description 4
239000000843 powder Substances 0.000 description 4
230000003449 preventive effect Effects 0.000 description 4
239000007787 solid Substances 0.000 description 4
239000000725 suspension Substances 0.000 description 4
230000009885 systemic effect Effects 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 3
208000031888 Mycoses Diseases 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
231100000674 Phytotoxicity Toxicity 0.000 description 3
235000014787 Vitis vinifera Nutrition 0.000 description 3
240000006365 Vitis vinifera Species 0.000 description 3
150000001768 cations Chemical group 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
239000011248 coating agent Substances 0.000 description 3
238000000576 coating method Methods 0.000 description 3
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239000012141 concentrate Substances 0.000 description 3
238000011161 development Methods 0.000 description 3
235000013399 edible fruits Nutrition 0.000 description 3
238000005516 engineering process Methods 0.000 description 3
230000002349 favourable effect Effects 0.000 description 3
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229910052748 manganese Inorganic materials 0.000 description 3
239000011572 manganese Substances 0.000 description 3
244000005700 microbiome Species 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
239000002904 solvent Substances 0.000 description 3
239000004094 surface-active agent Substances 0.000 description 3
244000105624 Arachis hypogaea Species 0.000 description 2
235000016068 Berberis vulgaris Nutrition 0.000 description 2
241000335053 Beta vulgaris Species 0.000 description 2
229910021532 Calcite Inorganic materials 0.000 description 2
240000008067 Cucumis sativus Species 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
206010017533 Fungal infection Diseases 0.000 description 2
235000010469 Glycine max Nutrition 0.000 description 2
244000068988 Glycine max Species 0.000 description 2
229920001732 Lignosulfonate Polymers 0.000 description 2
241001465754 Metazoa Species 0.000 description 2
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
241000233654 Oomycetes Species 0.000 description 2
QNAYBMKLOCPYGJ-UHFFFAOYSA-M alaninate Chemical compound CC(N)C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-M 0.000 description 2
229910000147 aluminium phosphate Inorganic materials 0.000 description 2
230000002238 attenuated effect Effects 0.000 description 2
239000011575 calcium Substances 0.000 description 2
210000004027 cell Anatomy 0.000 description 2
244000038559 crop plants Species 0.000 description 2
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
239000003337 fertilizer Substances 0.000 description 2
238000000227 grinding Methods 0.000 description 2
238000011534 incubation Methods 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
239000011777 magnesium Substances 0.000 description 2
239000011707 mineral Substances 0.000 description 2
235000020232 peanut Nutrition 0.000 description 2
150000003904 phospholipids Chemical class 0.000 description 2
230000003032 phytopathogenic effect Effects 0.000 description 2
230000035945 sensitivity Effects 0.000 description 2
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
235000012239 silicon dioxide Nutrition 0.000 description 2
238000002791 soaking Methods 0.000 description 2
235000020354 squash Nutrition 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
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238000012360 testing method Methods 0.000 description 2
239000004563 wettable powder Substances 0.000 description 2
239000008096 xylene Substances 0.000 description 2
ASWBNKHCZGQVJV-UHFFFAOYSA-N (3-hexadecanoyloxy-2-hydroxypropyl) 2-(trimethylazaniumyl)ethyl phosphate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(O)COP([O-])(=O)OCC[N+](C)(C)C ASWBNKHCZGQVJV-UHFFFAOYSA-N 0.000 description 1
DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
KILNVBDSWZSGLL-KXQOOQHDSA-N 1,2-dihexadecanoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCCCC KILNVBDSWZSGLL-KXQOOQHDSA-N 0.000 description 1
TZCPCKNHXULUIY-RGULYWFUSA-N 1,2-distearoyl-sn-glycero-3-phosphoserine Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(=O)OC[C@H](N)C(O)=O)OC(=O)CCCCCCCCCCCCCCCCC TZCPCKNHXULUIY-RGULYWFUSA-N 0.000 description 1
KBLAMUYRMZPYLS-UHFFFAOYSA-N 2,3-bis(2-methylpropyl)naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(O)(=O)=O)=C(CC(C)C)C(CC(C)C)=CC2=C1 KBLAMUYRMZPYLS-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical group COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 description 1
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 1
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244000025254 Cannabis sativa Species 0.000 description 1
235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
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MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
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PHJJWPXKTFKKPD-UHFFFAOYSA-N [Ni+3].[O-]P([O-])[O-] Chemical compound [Ni+3].[O-]P([O-])[O-] PHJJWPXKTFKKPD-UHFFFAOYSA-N 0.000 description 1
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MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
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239000000835 fiber Substances 0.000 description 1
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ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
210000002216 heart Anatomy 0.000 description 1
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150000002500 ions Chemical class 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000000787 lecithin Substances 0.000 description 1
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229910052744 lithium Inorganic materials 0.000 description 1
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239000010695 polyglycol Substances 0.000 description 1
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235000012424 soybean oil Nutrition 0.000 description 1
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235000013616 tea Nutrition 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
VMFOHNMEJNFJAE-UHFFFAOYSA-N trimagnesium;diphosphite Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])[O-].[O-]P([O-])[O-] VMFOHNMEJNFJAE-UHFFFAOYSA-N 0.000 description 1
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239000000080 wetting agent Substances 0.000 description 1
150000003738 xylenes Chemical class 0.000 description 1
229910052727 yttrium Inorganic materials 0.000 description 1
AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
- 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
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
- A01N59/26—Phosphorus; Compounds thereof

Landscapes

Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Inorganic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

DD86297630A 1985-12-16 1986-12-15 Pflanzenmikrobizides mittel DD257378A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH540685		1985-12-16

Publications (1)

Publication Number	Publication Date
DD257378A5 true DD257378A5 (de)	1988-06-15

Family

ID=4293050

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD86297630A DD257378A5 (de)	1985-12-16	1986-12-15	Pflanzenmikrobizides mittel

Country Status (16)

Country	Link
US (1)	US4849219A (da)
EP (1)	EP0230209A3 (da)
JP (1)	JPS62148412A (da)
KR (1)	KR870005579A (da)
CN (1)	CN86108526A (da)
AU (1)	AU6652586A (da)
BR (1)	BR8606200A (da)
CA (1)	CA1259255A (da)
DD (1)	DD257378A5 (da)
DK (1)	DK603386A (da)
IL (1)	IL80993A0 (da)
PL (1)	PL263003A1 (da)
PT (1)	PT83931B (da)
TR (1)	TR23009A (da)
ZA (1)	ZA869379B (da)
ZW (1)	ZW24586A1 (da)

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US5601847A (en) *	1993-04-01	1997-02-11	Ciba-Geigy Corporation	Microbicides
FR2706736B1 (da) *	1993-06-23	1995-08-25	Rhone Poulenc Agrochimie
FR2708415B1 (fr) *	1993-06-23	1996-08-30	Rhone Poulenc Agrochimie	Traitement de semences à l'aide d'acide phosphoreux ou un de ses sels, et semences ainsi traitées.
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US6338860B1 (en)	1996-08-30	2002-01-15	Foliar Nutrients, Inc.	Compositions for plants containing phosphonate and phosphate salts, and derivatives thereof
US5736164A (en) *	1996-08-30	1998-04-07	Taylor; John B.	Fungicidal compositions for plants containing phosphonate and phosphate salts, and derivatives thereof
US5800837A (en) *	1996-08-30	1998-09-01	Foliar Nutrients, Inc.	Plant fertilizer compositions containing phosphonate and phosphate salts and derivatives thereof
CN1067213C (zh) *	1998-07-24	2001-06-20	陈守利	杀菌组合物
FR2819991B1 (fr) *	2001-01-31	2005-11-11	Jean Louis Soyez	Composition fongicide a base de phosphite acide de potassium pour lutter contre les maladies cryptogamiques des plantes et procede de traitement
FR2819992B1 (fr) *	2001-01-31	2007-05-11	Jean Louis Soyez	Composition fongicide a base de phosphite acide de potassium pour la lutte contre les maladies cryptomatiques des plantes, et procede de traitement
WO2002076215A1 (fr) *	2001-03-19	2002-10-03	Sankyo Company,Limited	Compositions agricoles/horticoles
UA77507C2 (en) *	2002-03-21	2006-12-15	Basf Ag	Fungicidal mixture
ITMI20022516A1 (it) *	2002-11-27	2004-05-28	Isagro Spa	Composizioni fungicide.
WO2004049805A1 (ja) *	2002-12-04	2004-06-17	Sankyo Agro Company, Limited	麦類のマイコトキシン汚染抑制方法
US20100068299A1 (en) *	2003-01-27	2010-03-18	Van Der Krieken Wilhelmus Maria	Lignosulfonate compositions for control of plant pathogens
US20060084573A1 (en) *	2004-10-12	2006-04-20	Biagro Western Sales, Inc.	High calcium fertilizer composition
EP1885665A4 (en) *	2005-05-23	2012-05-02	Plant Protectants Llc	FORMULATIONS OF DITHIOCARBAMATES AND PHOSPHITE
ITMI20051019A1 (it) *	2005-05-31	2006-12-01	Isagro Spa	Composizioni fungicide sinergiche
AU2006260959B2 (en) *	2005-06-21	2011-11-24	Bayer Intellectual Property Gmbh	Fungicide composition comprising a phosphorous acid derivative, a mandelamide type compound and a further fungicide compound
ITMI20051558A1 (it) *	2005-08-09	2007-02-10	Isagro Spa	Miscele e-o composizioni sinergiche cin elevata attivita'fungicida
BRPI0615849B1 (pt) *	2005-09-13	2015-12-01	Basf Se	método de proteção de uma planta contra um fitopatógeno, uso de um composto, e, composição para tratar semente de uma planta para protegê-la contra um fitopatógeno
EP2099301B1 (en) *	2006-12-08	2010-09-29	DSM IP Assets B.V.	Post-harvest treatment of fruits with an antifungal composition
PE20091532A1 (es) *	2007-12-19	2009-10-03	Dsm Ip Assets Bv	Tratamiento de plantas de platano y papa con una nueva composicion antifungica
US20110052720A1 (en) *	2007-12-20	2011-03-03	Wim Van Der Krieken	Compositions for the control of plant pathogens and for use as plant fertilizer
US20110105323A1 (en) *	2008-06-12	2011-05-05	Basf Se	Calcium Salts of Phosphorous Acid for Increasing the Effect of Fungicides
US8795736B2 (en) *	2009-12-15	2014-08-05	Don M. Huber	Composition and method for control of plant pathogenic bacteria and endophytic microorganisms using copper phosphite and nutrient-halo-phosphite compounds
CN102204550B (zh) *	2011-04-06	2013-09-25	江苏宝灵化工股份有限公司	一种含有精甲霜灵的杀菌组合物及其用途
CN103380784B (zh) *	2013-06-21	2015-04-22	李萍	一种杀菌除味剂
CN104012529B (zh) *	2014-06-19	2016-03-23	江苏金万禾农业科技有限公司	一种植物杀菌剂及其制备方法
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OA04979A (fr) *	1974-04-09	1980-11-30	Ciba Geigy	Nouveaux dérivés de l'aniline utiles comme agents microbicides et leur procédé de préparation.
FR2377155A1 (fr) *	1977-01-14	1978-08-11	Philagro Sa	Compositions fongicides a base d'alcoylphosphites
DE2913459A1 (de) *	1979-04-04	1980-11-13	Bayer Ag	N-dichloracetyl-n-phenyl-alanin (thiol)ester, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide
IT8220198A0 (it) *	1981-03-24	1982-03-16	Rhone Poulenc Agrochimie	Derivati fosforosi e loro composizioni antifunghi a base di applicazione per la protezione dei vegetali.
CH654979A5 (de) *	1982-01-26	1986-03-27	Sandoz Ag	Fungizide und ihre verwendung.
GB2114002B (en) *	1982-01-26	1985-02-13	Sandoz Ltd	Improvements in or relating to fungicides

1986
- 1986-12-10 EP EP86810580A patent/EP0230209A3/de not_active Withdrawn
- 1986-12-12 CA CA000525159A patent/CA1259255A/en not_active Expired
- 1986-12-12 ZA ZA869379A patent/ZA869379B/xx unknown
- 1986-12-15 PT PT83931A patent/PT83931B/pt unknown
- 1986-12-15 BR BR8606200A patent/BR8606200A/pt unknown
- 1986-12-15 AU AU66525/86A patent/AU6652586A/en not_active Abandoned
- 1986-12-15 PL PL1986263003A patent/PL263003A1/xx unknown
- 1986-12-15 DK DK603386A patent/DK603386A/da unknown
- 1986-12-15 TR TR701/80A patent/TR23009A/xx unknown
- 1986-12-15 ZW ZW245/86A patent/ZW24586A1/xx unknown
- 1986-12-15 DD DD86297630A patent/DD257378A5/de not_active IP Right Cessation
- 1986-12-16 JP JP61299828A patent/JPS62148412A/ja active Pending
- 1986-12-16 IL IL80993A patent/IL80993A0/xx unknown
- 1986-12-16 CN CN198686108526A patent/CN86108526A/zh active Pending
- 1986-12-16 KR KR860010857A patent/KR870005579A/ko not_active Ceased
1988
- 1988-04-27 US US07/188,108 patent/US4849219A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
TR23009A (tr)	1989-01-10
PT83931A (en)	1987-01-01
EP0230209A3 (de)	1987-08-12
PT83931B (en)	1988-12-20
US4849219A (en)	1989-07-18
IL80993A0 (en)	1987-03-31
BR8606200A (pt)	1987-09-29
ZW24586A1 (en)	1987-09-23
KR870005579A (ko)	1987-07-06
DK603386A (da)	1987-06-17
ZA869379B (en)	1987-09-30
CA1259255A (en)	1989-09-12
EP0230209A2 (de)	1987-07-29
CN86108526A (zh)	1987-07-01
AU6652586A (en)	1987-06-18
JPS62148412A (ja)	1987-07-02
PL263003A1 (en)	1988-07-21
DK603386D0 (da)	1986-12-15

Legal Events

Date	Code	Title	Description
1995-11-09	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
EP0230209A2 (de)	1987-07-29	Mikrobizide
EP1023838B1 (de)	2003-09-10	Mikrobizide
DE69618953T2 (de)	2002-06-20	Mikrobizide zusammensetzungen
DE60202132T2 (de)	2005-11-10	Fungizide Zusammensetzungen suf der Basis von Pyridylmethylbenzamid-Derivaten und mindestens einer den Komplex III hemmenden Verbindung
DE69603944T2 (de)	1999-12-23	Pflanzenschutzmittel
DE69613843T2 (de)	2002-04-04	Pflanzenschutzmitteln
DE4422776A1 (de)	1995-01-12	Mikrobizide
EP0779030B1 (de)	2001-07-18	Pflanzenschutzmittel
EP1276375B1 (de)	2005-07-20	Fungizide wirkstoffkombinationen
EP0235082B1 (de)	1989-07-26	Mikrobizide
EP0818144B1 (de)	2000-08-30	Mikrobizide
EP0627164B2 (de)	2001-08-22	Mikrobizide Mischungen die Prochloraz und Cyprodinil enthalten
DD283912A5 (de)	1990-10-31	Pflanzenmikrobizides mittel
DD257575A5 (de)	1988-06-22	Fungizide mittel
DE10349503A1 (de)	2005-05-25	Fungizide Wirkstoffkombinationen
US6358938B1 (en)	2002-03-19	Synergistic fungicidal composition
ES2231671T3 (es)	2005-05-16	Composiciones fungicidas basadas en derivados de piridilmetilbenzamida y de propamocarb.
DE3605551A1 (de)	1987-09-10	Fungizide mittel
EP0975221A1 (de)	2000-02-02	Fungizide wirkstoffkombinationen
DE19845407B4 (de)	2012-06-28	Selektive Herbizide auf Basis eines substituierten Phenylsulfonylaminocarbonyl-triazolinons
DE69904955T2 (de)	2003-09-04	Fungizide zusammensetzungen
DE69805808T2 (de)	2003-03-06	Verfahren zum pflanzenschutz
EP0487451A1 (de)	1992-05-27	Mikrobizide Mittel
EP1247452A2 (de)	2002-10-09	Fungizide Wirkstoffkombinationen
CH669088A5 (de)	1989-02-28	Mikrobizides mittel.