NO812580L - Mikrobicid middel til beskyttelse av tekniske materialer - Google Patents

Mikrobicid middel til beskyttelse av tekniske materialer

Info

Publication number: NO812580L
Authority: NO; Norway
Prior art keywords: nitroso; pyrazoles; protection; nitro; substituted
Prior art date: 1980-08-09

Application number

NO812580A

Other languages

English (en)

Norwegian (no)

Inventor

Fritz Maurer

Hans-Jochem Riebel

Wilfried Paulus

Hermann Genth

Original Assignee

Bayer Ag

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.)

1980-08-09

Filing date

1981-07-28

Publication date

1982-02-10

1981-07-28 Application filed by Bayer Ag filed Critical Bayer Ag

1982-02-10 Publication of NO812580L publication Critical patent/NO812580L/no

Links

239000000463 material Substances 0.000 title claims description 14
-1 nitro, methoxy Chemical group 0.000 claims description 16
OCXDFFKDFIZMRC-UHFFFAOYSA-N 4-nitroso-1h-pyrazole Chemical class O=NC=1C=NNC=1 OCXDFFKDFIZMRC-UHFFFAOYSA-N 0.000 claims description 15
239000002855 microbicide agent Substances 0.000 claims description 10
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims description 8
125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 claims description 7
125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims description 5
125000004432 carbon atom Chemical group C* 0.000 claims description 5
125000004966 cyanoalkyl group Chemical group 0.000 claims description 5
125000000623 heterocyclic group Chemical group 0.000 claims description 5
125000004433 nitrogen atom Chemical group N* 0.000 claims description 5
125000000714 pyrimidinyl group Chemical group 0.000 claims description 5
229910052717 sulfur Inorganic materials 0.000 claims description 5
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
125000004434 sulfur atom Chemical group 0.000 claims description 4
229910052736 halogen Inorganic materials 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
125000004076 pyridyl group Chemical group 0.000 claims description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
239000013543 active substance Substances 0.000 description 12
239000000243 solution Substances 0.000 description 11
150000002429 hydrazines Chemical class 0.000 description 8
239000005068 cooling lubricant Substances 0.000 description 7
BMFNDMNRYPFUPF-HWKANZROSA-N (E)-4-hydroxy-3-nitrosopent-3-en-2-one Chemical compound C\C(O)=C(/N=O)C(C)=O BMFNDMNRYPFUPF-HWKANZROSA-N 0.000 description 6
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
125000000753 cycloalkyl group Chemical group 0.000 description 5
244000005700 microbiome Species 0.000 description 5
235000015097 nutrients Nutrition 0.000 description 5
238000003756 stirring Methods 0.000 description 5
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
241000894006 Bacteria Species 0.000 description 4
150000001875 compounds Chemical class 0.000 description 4
239000013078 crystal Substances 0.000 description 4
230000000694 effects Effects 0.000 description 4
238000004519 manufacturing process Methods 0.000 description 4
238000000034 method Methods 0.000 description 4
YAOCUJFREWDKRQ-UHFFFAOYSA-N 1-benzyl-3,5-dimethyl-4-nitrosopyrazole Chemical compound CC1=C(N=O)C(C)=NN1CC1=CC=CC=C1 YAOCUJFREWDKRQ-UHFFFAOYSA-N 0.000 description 3
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 3
229920001817 Agar Polymers 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
239000008272 agar Substances 0.000 description 3
125000003545 alkoxy group Chemical group 0.000 description 3
125000000217 alkyl group Chemical group 0.000 description 3
238000011109 contamination Methods 0.000 description 3
150000002430 hydrocarbons Chemical group 0.000 description 3
239000000203 mixture Substances 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
241000223600 Alternaria Species 0.000 description 2
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
241000588724 Escherichia coli Species 0.000 description 2
241000233866 Fungi Species 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
241000191967 Staphylococcus aureus Species 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
230000000844 anti-bacterial effect Effects 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
244000052616 bacterial pathogen Species 0.000 description 2
IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
NHOWLEZFTHYCTP-UHFFFAOYSA-N benzylhydrazine Chemical compound NNCC1=CC=CC=C1 NHOWLEZFTHYCTP-UHFFFAOYSA-N 0.000 description 2
LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 2
230000015556 catabolic process Effects 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
125000004093 cyano group Chemical group *C#N 0.000 description 2
238000010790 dilution Methods 0.000 description 2
239000012895 dilution Substances 0.000 description 2
JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
230000000855 fungicidal effect Effects 0.000 description 2
239000007788 liquid Substances 0.000 description 2
GTCAXTIRRLKXRU-UHFFFAOYSA-N methyl carbamate Chemical compound COC(N)=O GTCAXTIRRLKXRU-UHFFFAOYSA-N 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
230000000813 microbial effect Effects 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
239000000047 product Substances 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
239000000126 substance Substances 0.000 description 2
NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 description 1
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
LKLLNYWECKEQIB-UHFFFAOYSA-N 1,3,5-triazinane Chemical class C1NCNCN1 LKLLNYWECKEQIB-UHFFFAOYSA-N 0.000 description 1
DWKNOLCXIFYNFV-HSZRJFAPSA-N 2-[[(2r)-1-[1-[(4-chloro-3-methylphenyl)methyl]piperidin-4-yl]-5-oxopyrrolidine-2-carbonyl]amino]-n,n,6-trimethylpyridine-4-carboxamide Chemical compound CN(C)C(=O)C1=CC(C)=NC(NC(=O)[C@@H]2N(C(=O)CC2)C2CCN(CC=3C=C(C)C(Cl)=CC=3)CC2)=C1 DWKNOLCXIFYNFV-HSZRJFAPSA-N 0.000 description 1
229940061334 2-phenylphenol Drugs 0.000 description 1
UUECYTLJOJGWJK-UHFFFAOYSA-N 3,5-dimethyl-4-nitroso-1-propan-2-ylpyrazole Chemical compound CC(C)N1N=C(C)C(N=O)=C1C UUECYTLJOJGWJK-UHFFFAOYSA-N 0.000 description 1
FBBRXPZJCWMPIF-UHFFFAOYSA-N 3-(3,5-dimethyl-4-nitrosopyrazol-1-yl)propanenitrile Chemical compound CC1=NN(CCC#N)C(C)=C1N=O FBBRXPZJCWMPIF-UHFFFAOYSA-N 0.000 description 1
CFKMVGJGLGKFKI-UHFFFAOYSA-N 4-chloro-m-cresol Chemical compound CC1=CC(O)=CC=C1Cl CFKMVGJGLGKFKI-UHFFFAOYSA-N 0.000 description 1
NOBWYVALEWRNEZ-UHFFFAOYSA-N 5-nitroso-1h-pyrazole Chemical class O=NC=1C=CNN=1 NOBWYVALEWRNEZ-UHFFFAOYSA-N 0.000 description 1
RQCLKJICDPMGDH-UHFFFAOYSA-N 7-(dichloromethyl)-2-fluoro-3-sulfanylideneisoindol-1-one Chemical compound S=C1N(F)C(=O)C2=C1C=CC=C2C(Cl)Cl RQCLKJICDPMGDH-UHFFFAOYSA-N 0.000 description 1
241000228212 Aspergillus Species 0.000 description 1
241000228245 Aspergillus niger Species 0.000 description 1
241000223678 Aureobasidium pullulans Species 0.000 description 1
QPTPOVJDVBMDDH-UHFFFAOYSA-N CC1=CC=C(C=C1)C2=C(C=NN2)N=O Chemical compound CC1=CC=C(C=C1)C2=C(C=NN2)N=O QPTPOVJDVBMDDH-UHFFFAOYSA-N 0.000 description 1
UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
241001600093 Coniophora Species 0.000 description 1
241001626940 Coniophora cerebella Species 0.000 description 1
241000195493 Cryptophyta Species 0.000 description 1
241000588722 Escherichia Species 0.000 description 1
229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
241000222418 Lentinus Species 0.000 description 1
241000222451 Lentinus tigrinus Species 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
241000228143 Penicillium Species 0.000 description 1
241001123663 Penicillium expansum Species 0.000 description 1
239000001888 Peptone Substances 0.000 description 1
108010080698 Peptones Proteins 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
241000222640 Polyporus Species 0.000 description 1
241000589516 Pseudomonas Species 0.000 description 1
241000589517 Pseudomonas aeruginosa Species 0.000 description 1
240000004808 Saccharomyces cerevisiae Species 0.000 description 1
239000004902 Softening Agent Substances 0.000 description 1
241000191940 Staphylococcus Species 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
241000907561 Sydowia polyspora Species 0.000 description 1
241000222355 Trametes versicolor Species 0.000 description 1
241000223259 Trichoderma Species 0.000 description 1
241000223261 Trichoderma viride Species 0.000 description 1
241000700605 Viruses Species 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
235000019270 ammonium chloride Nutrition 0.000 description 1
230000000845 anti-microbial effect Effects 0.000 description 1
235000013405 beer Nutrition 0.000 description 1
125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 1
MSJHOJKVMMEMNX-UHFFFAOYSA-N benzylhydrazine;hydron;dichloride Chemical compound Cl.Cl.NNCC1=CC=CC=C1 MSJHOJKVMMEMNX-UHFFFAOYSA-N 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000001110 calcium chloride Substances 0.000 description 1
229910001628 calcium chloride Inorganic materials 0.000 description 1
239000011111 cardboard Substances 0.000 description 1
239000000969 carrier Substances 0.000 description 1
239000003638 chemical reducing agent Substances 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
239000000498 cooling water Substances 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
230000006378 damage Effects 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
150000008049 diazo compounds Chemical class 0.000 description 1
ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical compound [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
239000012259 ether extract Substances 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
239000000284 extract Substances 0.000 description 1
238000000605 extraction Methods 0.000 description 1
238000009472 formulation Methods 0.000 description 1
244000053095 fungal pathogen Species 0.000 description 1
239000003292 glue Substances 0.000 description 1
239000008187 granular material Substances 0.000 description 1
IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
125000002510 isobutoxy group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])O* 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
238000002955 isolation Methods 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000010985 leather Substances 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
230000003641 microbiacidal effect Effects 0.000 description 1
229940124561 microbicide Drugs 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
238000002156 mixing Methods 0.000 description 1
210000003097 mucus Anatomy 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
150000002832 nitroso derivatives Chemical class 0.000 description 1
235000010292 orthophenyl phenol Nutrition 0.000 description 1
150000002917 oxazolidines Chemical class 0.000 description 1
229940070805 p-chloro-m-cresol Drugs 0.000 description 1
239000011087 paperboard Substances 0.000 description 1
239000006072 paste Substances 0.000 description 1
235000019319 peptone Nutrition 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
230000008659 phytopathology Effects 0.000 description 1
239000011505 plaster Substances 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000002243 precursor Substances 0.000 description 1
238000004321 preservation Methods 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
238000000926 separation method Methods 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
235000010344 sodium nitrate Nutrition 0.000 description 1
239000004317 sodium nitrate Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000008223 sterile water Substances 0.000 description 1
125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000004557 technical material Substances 0.000 description 1
239000004753 textile Substances 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
229960002447 thiram Drugs 0.000 description 1
230000007306 turnover Effects 0.000 description 1
239000002023 wood Substances 0.000 description 1
238000010626 work up procedure Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/38—Nitrogen atoms
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Plural Heterocyclic Compounds (AREA)

NO812580A 1980-08-09 1981-07-28 Mikrobicid middel til beskyttelse av tekniske materialer NO812580L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19803030192 DE3030192A1 (de)	1980-08-09	1980-08-09	Neue mikrobizide zum schutz technischer materialien

Publications (1)

Publication Number	Publication Date
NO812580L true NO812580L (no)	1982-02-10

Family

ID=6109263

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO812580A NO812580L (no)	1980-08-09	1981-07-28	Mikrobicid middel til beskyttelse av tekniske materialer

Country Status (7)

Country	Link
EP (1)	EP0047850B1 (da)
JP (1)	JPS5759870A (da)
CA (1)	CA1188856A (da)
DE (2)	DE3030192A1 (da)
DK (1)	DK352181A (da)
FI (1)	FI65359C (da)
NO (1)	NO812580L (da)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2745469B1 (fr) *	1996-03-04	1998-09-18	Rhone Poulenc Agrochimie	Pyrazoles fongicides
RU2198165C2 (ru) *	2000-01-10	2003-02-10	Пермский государственный университет	5(3)-фенил-4-фенилазо-3(5)-пиразолкарбоновая кислота, проявляющая антимикробную активность
RU2471785C1 (ru) *	2011-04-27	2013-01-10	Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Сибирский государственный технологический университет" ("СибГТУ")	1-(1-адамантил)-4-нитрозопиразолы

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2510724A (en) *	1947-02-12	1950-06-06	Us Rubber Co	Germicidal composition comprising a 3, 5-dimethyl-4-nitrosopyrazole
US2751395A (en) *	1954-10-19	1956-06-19	May & Baker Ltd	Isomeric nitroso-1-phenyl pyrazoles
GB786753A (en) *	1955-02-12	1957-11-27	May & Baker Ltd	Improvements in or relating to pyrazole compounds and compositions containing them
GB791688A (en) *	1955-05-12	1958-03-12	May & Baker Ltd	Improvements in or relating to pyrazole derivatives
NL91061C (da) *	1955-08-15

1980
- 1980-08-09 DE DE19803030192 patent/DE3030192A1/de not_active Withdrawn
1981
- 1981-07-28 NO NO812580A patent/NO812580L/no unknown
- 1981-07-30 EP EP81105995A patent/EP0047850B1/de not_active Expired
- 1981-07-30 DE DE8181105995T patent/DE3166032D1/de not_active Expired
- 1981-08-06 FI FI812438A patent/FI65359C/fi not_active IP Right Cessation
- 1981-08-07 CA CA000383441A patent/CA1188856A/en not_active Expired
- 1981-08-07 DK DK352181A patent/DK352181A/da not_active Application Discontinuation
- 1981-08-07 JP JP56123163A patent/JPS5759870A/ja active Pending

Also Published As

Publication number	Publication date
JPS5759870A (en)	1982-04-10
FI65359C (fi)	1984-05-10
EP0047850A3 (en)	1982-04-21
FI812438L (fi)	1982-02-10
EP0047850A2 (de)	1982-03-24
EP0047850B1 (de)	1984-09-12
DK352181A (da)	1982-02-10
DE3030192A1 (de)	1982-03-18
FI65359B (fi)	1984-01-31
CA1188856A (en)	1985-06-18
DE3166032D1 (de)	1984-10-18

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KR100988904B1 (ko)	2010-10-20	살균 방법
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