IL111603A - Method for treating fungus with morpholine "Z" isomer - Google Patents

Method for treating fungus with morpholine "Z" isomer

Info

Publication number: IL111603A
Authority: IL; Israel
Prior art keywords: isomer; plants; morpholine; composition; chlorophenyl
Prior art date: 1993-11-15

Application number

IL11160394A

Other languages

English (en)

Hebrew (he)

Other versions

IL111603A0 (en

Original Assignee

Shell Int Research

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.)

1993-11-15

Filing date

1994-11-11

Publication date

1999-01-26

1994-11-11 Application filed by Shell Int Research filed Critical Shell Int Research

1995-01-24 Publication of IL111603A0 publication Critical patent/IL111603A0/xx

1999-01-26 Publication of IL111603A publication Critical patent/IL111603A/en

Links

238000000034 method Methods 0.000 title claims abstract description 23
241000233866 Fungi Species 0.000 title claims abstract description 8
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 title claims description 15
239000000203 mixture Substances 0.000 claims abstract description 40
QNBTYORWCCMPQP-JXAWBTAJSA-N (Z)-dimethomorph Chemical compound C1=C(OC)C(OC)=CC=C1C(\C=1C=CC(Cl)=CC=1)=C/C(=O)N1CCOCC1 QNBTYORWCCMPQP-JXAWBTAJSA-N 0.000 claims abstract description 20
230000000855 fungicidal effect Effects 0.000 claims abstract description 14
239000004480 active ingredient Substances 0.000 claims abstract description 13
239000000417 fungicide Substances 0.000 claims abstract description 11
230000002538 fungal effect Effects 0.000 claims abstract description 4
239000002689 soil Substances 0.000 claims description 9
238000006317 isomerization reaction Methods 0.000 claims description 8
241000233622 Phytophthora infestans Species 0.000 claims description 6
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 6
241001281803 Plasmopara viticola Species 0.000 claims description 2
238000002425 crystallisation Methods 0.000 claims description 2
238000004519 manufacturing process Methods 0.000 claims 1
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Natural products CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 29
241000196324 Embryophyta Species 0.000 description 23
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
239000005761 Dimethomorph Substances 0.000 description 11
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 10
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
239000007787 solid Substances 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
MFRIHAYPQRLWNB-UHFFFAOYSA-N sodium tert-butoxide Chemical compound [Na+].CC(C)(C)[O-] MFRIHAYPQRLWNB-UHFFFAOYSA-N 0.000 description 8
239000000243 solution Substances 0.000 description 8
201000010099 disease Diseases 0.000 description 7
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 7
-1 aliphatic amines Chemical class 0.000 description 6
230000000694 effects Effects 0.000 description 6
208000015181 infectious disease Diseases 0.000 description 6
239000003208 petroleum Substances 0.000 description 6
239000004094 surface-active agent Substances 0.000 description 6
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
241000227653 Lycopersicon Species 0.000 description 5
238000001816 cooling Methods 0.000 description 5
239000007788 liquid Substances 0.000 description 5
239000000126 substance Substances 0.000 description 5
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 4
239000000654 additive Substances 0.000 description 4
239000000969 carrier Substances 0.000 description 4
239000012141 concentrate Substances 0.000 description 4
239000002270 dispersing agent Substances 0.000 description 4
239000000706 filtrate Substances 0.000 description 4
239000008187 granular material Substances 0.000 description 4
239000003381 stabilizer Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
235000007688 Lycopersicon esculentum Nutrition 0.000 description 3
239000002253 acid Substances 0.000 description 3
235000012211 aluminium silicate Nutrition 0.000 description 3
229910000323 aluminium silicate Inorganic materials 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
239000007859 condensation product Substances 0.000 description 3
239000000839 emulsion Substances 0.000 description 3
238000009472 formulation Methods 0.000 description 3
239000012452 mother liquor Substances 0.000 description 3
239000000843 powder Substances 0.000 description 3
238000010992 reflux Methods 0.000 description 3
239000011734 sodium Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000002904 solvent Substances 0.000 description 3
238000005507 spraying Methods 0.000 description 3
239000000758 substrate Substances 0.000 description 3
238000012360 testing method Methods 0.000 description 3
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 3
QNBTYORWCCMPQP-NBVRZTHBSA-N (E)-dimethomorph Chemical compound C1=C(OC)C(OC)=CC=C1C(\C=1C=CC(Cl)=CC=1)=C\C(=O)N1CCOCC1 QNBTYORWCCMPQP-NBVRZTHBSA-N 0.000 description 2
KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 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
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
241000208125 Nicotiana Species 0.000 description 2
235000002637 Nicotiana tabacum Nutrition 0.000 description 2
241000233679 Peronosporaceae Species 0.000 description 2
241000233614 Phytophthora Species 0.000 description 2
244000061456 Solanum tuberosum Species 0.000 description 2
235000002595 Solanum tuberosum Nutrition 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
229920001577 copolymer Polymers 0.000 description 2
238000005260 corrosion Methods 0.000 description 2
230000007797 corrosion Effects 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
239000004495 emulsifiable concentrate Substances 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
239000012065 filter cake Substances 0.000 description 2
230000009969 flowable effect Effects 0.000 description 2
239000003112 inhibitor Substances 0.000 description 2
239000000463 material Substances 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
235000012015 potatoes Nutrition 0.000 description 2
239000000047 product Substances 0.000 description 2
230000000069 prophylactic effect Effects 0.000 description 2
230000001681 protective effect Effects 0.000 description 2
238000000926 separation method Methods 0.000 description 2
159000000000 sodium salts Chemical class 0.000 description 2
239000007921 spray Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
239000000725 suspension Substances 0.000 description 2
239000004546 suspension concentrate Substances 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
235000013311 vegetables Nutrition 0.000 description 2
239000004563 wettable powder Substances 0.000 description 2
UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
125000003762 3,4-dimethoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
229920000557 Nafion® Polymers 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
241000233654 Oomycetes Species 0.000 description 1
CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
241000233610 Plasmopara halstedii Species 0.000 description 1
241000233639 Pythium Species 0.000 description 1
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
239000004141 Sodium laurylsulphate Substances 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
229930006000 Sucrose Natural products 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
239000005864 Sulphur Substances 0.000 description 1
241001464837 Viridiplantae Species 0.000 description 1
238000009825 accumulation Methods 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
238000005054 agglomeration Methods 0.000 description 1
230000002776 aggregation Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
239000003513 alkali Substances 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
229910052921 ammonium sulfate Inorganic materials 0.000 description 1
239000001166 ammonium sulphate Substances 0.000 description 1
235000011130 ammonium sulphate Nutrition 0.000 description 1
239000007798 antifreeze agent Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000010426 asphalt Substances 0.000 description 1
235000013871 bee wax Nutrition 0.000 description 1
239000012166 beeswax Substances 0.000 description 1
235000019445 benzyl alcohol Nutrition 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
238000009835 boiling Methods 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
239000001175 calcium sulphate Substances 0.000 description 1
235000011132 calcium sulphate Nutrition 0.000 description 1
YYRMJZQKEFZXMX-UHFFFAOYSA-N calcium;phosphoric acid Chemical class [Ca+2].OP(O)(O)=O.OP(O)(O)=O YYRMJZQKEFZXMX-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
229920001429 chelating resin Polymers 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
239000006184 cosolvent Substances 0.000 description 1
244000038559 crop plants Species 0.000 description 1
238000009109 curative therapy Methods 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
238000007865 diluting Methods 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
QNBTYORWCCMPQP-UHFFFAOYSA-N dimethomorph Chemical compound C1=C(OC)C(OC)=CC=C1C(C=1C=CC(Cl)=CC=1)=CC(=O)N1CCOCC1 QNBTYORWCCMPQP-UHFFFAOYSA-N 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000009826 distribution Methods 0.000 description 1
YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
239000000428 dust Substances 0.000 description 1
230000002708 enhancing effect Effects 0.000 description 1
238000011067 equilibration Methods 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
238000001914 filtration Methods 0.000 description 1
231100000162 fungitoxic Toxicity 0.000 description 1
230000002464 fungitoxic effect Effects 0.000 description 1
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
230000002363 herbicidal effect Effects 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
238000000338 in vitro Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000000749 insecticidal effect Effects 0.000 description 1
239000003014 ion exchange membrane Substances 0.000 description 1
239000003456 ion exchange resin Substances 0.000 description 1
229920003303 ion-exchange polymer Polymers 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
239000000391 magnesium silicate Substances 0.000 description 1
235000012243 magnesium silicates Nutrition 0.000 description 1
239000008268 mayonnaise Substances 0.000 description 1
235000010746 mayonnaise Nutrition 0.000 description 1
238000005259 measurement Methods 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
239000012184 mineral wax Substances 0.000 description 1
239000003607 modifier Substances 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
239000000025 natural resin Substances 0.000 description 1
239000003921 oil Substances 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000004576 sand Substances 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical class [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 1
229910052814 silicon oxide Inorganic materials 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000005720 sucrose Substances 0.000 description 1
125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical class OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000002426 superphosphate Substances 0.000 description 1
239000000375 suspending agent Substances 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
230000009885 systemic effect Effects 0.000 description 1
235000012222 talc Nutrition 0.000 description 1
239000013008 thixotropic agent Substances 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 1
235000019354 vermiculite Nutrition 0.000 description 1
239000001993 wax Substances 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000008096 xylene 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
- 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
- A01N37/36—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
- A01N37/38—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system

Landscapes

Life Sciences & Earth Sciences (AREA)
Wood Science & Technology (AREA)
Environmental Sciences (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Zoology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Electrotherapy Devices (AREA)
Advance Control (AREA)
Preparation Of Compounds By Using Micro-Organisms (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pretreatment Of Seeds And Plants (AREA)
Compounds Of Unknown Constitution (AREA)

IL11160394A 1993-11-15 1994-11-11 Method for treating fungus with morpholine "Z" isomer IL111603A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
EP93118442		1993-11-15

Publications (2)

Publication Number	Publication Date
IL111603A0 IL111603A0 (en)	1995-01-24
IL111603A true IL111603A (en)	1999-01-26

Family

ID=8213417

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL11160394A IL111603A (en)	1993-11-15	1994-11-11	Method for treating fungus with morpholine "Z" isomer

Country Status (13)

Country	Link
US (1)	US5656630A (de)
EP (1)	EP0653160B1 (de)
JP (1)	JPH07196411A (de)
KR (1)	KR950013367A (de)
AT (1)	ATE152574T1 (de)
BR (1)	BR9404452A (de)
DE (1)	DE69403045T2 (de)
DK (1)	DK0653160T3 (de)
ES (1)	ES2102153T3 (de)
GR (1)	GR3024337T3 (de)
IL (1)	IL111603A (de)
RU (1)	RU2134040C1 (de)
ZA (1)	ZA949034B (de)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
RU2204248C1 (ru) *	2002-04-22	2003-05-20	Чувашский государственный университет им. И.Н.Ульянова	Средство для защиты и лечения поврежденных фруктовых и декоративных деревьев
KR101322196B1 (ko)	2006-03-29	2013-10-28	바이오-에너지가부시키가이샤	락트산 발효액으로부터의 락트산 성분의 분리 방법 및 분리장치
RU2424598C1 (ru) *	2010-03-30	2011-07-20	Общество с ограниченной ответственностью "Научно-производственный центр оптико-электронных приборов "ОПТЭЛ" (ООО "НПЦ ОЭП "ОПТЭЛ")	Светодиод зеленого свечения с применением люминофора
GB2542134B (en) *	2015-09-08	2020-05-13	Rotam Agrochem Int Co Ltd	Agent and method for reducing the E/Z isomerization of dimethomorph
CN106749104A (zh) *	2016-11-24	2017-05-31	徐韶康	一种烯酰吗啉立体异构体的制备方法和用途
US12145099B2 (en) *	2019-01-25	2024-11-19	Eurica Californiaa	Membrane-based processing for ambient water-group species captured on the moon and in space

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CS244440B2 (en)	1983-02-28	1986-07-17	Celamerck Gmbh & Co Kg	Method of acrylic acids' new amides production
DE3817711A1 (de) *	1988-05-25	1989-11-30	Shell Int Research	Verfahren zur herstellung von 3,3-diphenylacrylsaeureamiden

1994
- 1994-11-04 EP EP94308150A patent/EP0653160B1/de not_active Expired - Lifetime
- 1994-11-04 ES ES94308150T patent/ES2102153T3/es not_active Expired - Lifetime
- 1994-11-04 DE DE69403045T patent/DE69403045T2/de not_active Expired - Fee Related
- 1994-11-04 AT AT94308150T patent/ATE152574T1/de not_active IP Right Cessation
- 1994-11-04 DK DK94308150.5T patent/DK0653160T3/da active
- 1994-11-11 IL IL11160394A patent/IL111603A/en active IP Right Grant
- 1994-11-14 US US08/339,385 patent/US5656630A/en not_active Expired - Fee Related
- 1994-11-14 ZA ZA949034A patent/ZA949034B/xx unknown
- 1994-11-14 RU RU94040181A patent/RU2134040C1/ru active
- 1994-11-14 KR KR1019940029808A patent/KR950013367A/ko not_active Ceased
- 1994-11-14 BR BR9404452A patent/BR9404452A/pt not_active IP Right Cessation
- 1994-11-14 JP JP6302730A patent/JPH07196411A/ja active Pending
1997
- 1997-07-31 GR GR970401983T patent/GR3024337T3/el unknown

Also Published As

Publication number	Publication date
DK0653160T3 (da)	1997-06-02
BR9404452A (pt)	1995-06-20
RU2134040C1 (ru)	1999-08-10
KR950013367A (ko)	1995-06-15
US5656630A (en)	1997-08-12
EP0653160B1 (de)	1997-05-07
GR3024337T3 (en)	1997-10-31
EP0653160A1 (de)	1995-05-17
ZA949034B (en)	1995-07-18
ES2102153T3 (es)	1997-07-16
ATE152574T1 (de)	1997-05-15
DE69403045T2 (de)	1997-12-11
JPH07196411A (ja)	1995-08-01
RU94040181A (ru)	1996-10-10
IL111603A0 (en)	1995-01-24
DE69403045D1 (de)	1997-06-12

Legal Events

Date	Code	Title
1999-07-14	FF	Patent granted
2000-07-26	KB	Patent renewed
2000-08-31	KB	Patent renewed
2001-04-30	KB	Patent renewed

Publication	Publication Date	Title
CA1337514C (en)	1995-11-07	Fungicidal compositions
SK113198A3 (en)	2000-02-14	Fungicidal 2-methoxybenzophenones, process for the preparation thereof and compositions containing said compounds
SK281959B6 (sk)	2001-09-11	Prostriedok na ochranu rastlín a spôsob ochrany rastlín proti chorobám
US5656630A (en)	1997-08-12	Method of combating fungus
EP0008474B1 (de)	1985-10-02	Ein Carbaminsäuresulfid enthaltende pestizide Zusammensetzungen, kombiniert mit einem synthetischen Pyrethroid-Insektizid, und ihre Verwendung
US5952496A (en)	1999-09-14	Fungicidal compositions
EP0117577B1 (de)	1986-10-08	Nitromethylenderivate als Schädlingsbekämpfungsmittel
US4933328A (en)	1990-06-12	Phosphonium salts and fungicidal use
US5262414A (en)	1993-11-16	Fungicidal compositions
CZ248594A3 (en)	1995-04-12	Pesticidal agents and application method thereof
US4084952A (en)	1978-04-18	Use of alkyl(aminocarbonyl)phosphonate salts in rice culture for the control of problem herbaceous plant growth
AU612162B2 (en)	1991-07-04	Phosphonium salts
USRE35985E (en)	1998-12-08	Fungicidal compositions
US5157028A (en)	1992-10-20	Fungicidal compositions
EP0149268A2 (de)	1985-07-24	Verfahren zur Bekämpfung von Pflanzenwuchs
US4407671A (en)	1983-10-04	Use of 3-aminocyclohexadienecarboxylic acids for controlling the growth of unwanted plants
SE454399B (sv)	1988-05-02	Fungicid beredning innehallande en triazol och ett alaninderivat samt forfarande for behandling av svampinfektioner pa vexter dermed
FR2598708A1 (fr)	1987-11-20	Compositions fongicides a base de derives nicotiniques, nouveaux derives nicotiniques et leur preparation
US4356023A (en)	1982-10-26	Certain herbicidal tetrahydrofurans
SU1114319A3 (ru)	1984-09-15	Гербицидное средство
EP0013582A1 (de)	1980-07-23	Pestizide Zusammensetzungen und deren Verwendung
KR800000790B1 (ko)	1980-08-11	사이클로프로판 유도체의 제조방법
CA1162070A (en)	1984-02-14	Method of regulating the growth of soyabeans
HK1000002B (en)	1997-10-03	Fungicidal compositions
EP0078555A1 (de)	1983-05-11	Herbizide Zusammensetzung und Verfahren zur Bekämpfung unerwünschten Pflanzenwachstums