LT3180B - Agrochemical compositins and methods employing 3-hydroxy-5-methylisoxazole - Google Patents
Agrochemical compositins and methods employing 3-hydroxy-5-methylisoxazole Download PDFInfo
- Publication number
- LT3180B LT3180B LTIP508A LTIP508A LT3180B LT 3180 B LT3180 B LT 3180B LT IP508 A LTIP508 A LT IP508A LT IP508 A LTIP508 A LT IP508A LT 3180 B LT3180 B LT 3180B
- Authority
- LT
- Lithuania
- Prior art keywords
- hydroxy
- methylisoxazole
- parts
- salt
- calcium
- Prior art date
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- KGVPNLBXJKTABS-UHFFFAOYSA-N hymexazol Chemical compound CC1=CC(O)=NO1 KGVPNLBXJKTABS-UHFFFAOYSA-N 0.000 title claims description 83
- 238000000034 method Methods 0.000 title claims description 39
- 239000003905 agrochemical Substances 0.000 title description 7
- 150000001875 compounds Chemical class 0.000 claims abstract description 115
- 239000004599 antimicrobial Substances 0.000 claims abstract description 25
- 230000000855 fungicidal effect Effects 0.000 claims abstract description 10
- 239000000203 mixture Substances 0.000 claims description 52
- -1 1,2-benzisothiazolin-3-yl Chemical group 0.000 claims description 50
- 150000003839 salts Chemical class 0.000 claims description 45
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 43
- 239000002689 soil Substances 0.000 claims description 36
- 159000000007 calcium salts Chemical class 0.000 claims description 34
- 239000011734 sodium Substances 0.000 claims description 21
- 229910052708 sodium Inorganic materials 0.000 claims description 21
- 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 description 20
- ARLZGEXVMUDUQZ-UHFFFAOYSA-N O.O.[Ca] Chemical compound O.O.[Ca] ARLZGEXVMUDUQZ-UHFFFAOYSA-N 0.000 claims description 20
- 238000002360 preparation method Methods 0.000 claims description 15
- DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 claims description 14
- 150000004683 dihydrates Chemical class 0.000 claims description 12
- 239000013078 crystal Substances 0.000 claims description 8
- 239000011575 calcium Substances 0.000 claims description 7
- 229910052791 calcium Inorganic materials 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 6
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 6
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 claims description 6
- 229910052700 potassium Inorganic materials 0.000 claims description 6
- 239000011591 potassium Substances 0.000 claims description 6
- WLCRJRAVOKFOMT-UHFFFAOYSA-N 5-methyl-1,2-oxazol-3-one;dihydrate Chemical compound O.O.CC1=CC(O)=NO1 WLCRJRAVOKFOMT-UHFFFAOYSA-N 0.000 claims description 5
- 230000015572 biosynthetic process Effects 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims description 4
- 239000000920 calcium hydroxide Substances 0.000 claims description 4
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims description 4
- 239000000706 filtrate Substances 0.000 claims description 4
- RHPUJHQBPORFGV-UHFFFAOYSA-N 4-chloro-2-methylphenol Chemical compound CC1=CC(Cl)=CC=C1O RHPUJHQBPORFGV-UHFFFAOYSA-N 0.000 claims description 3
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 claims description 3
- 239000005750 Copper hydroxide Substances 0.000 claims description 3
- 229910001956 copper hydroxide Inorganic materials 0.000 claims description 3
- 229940015043 glyoxal Drugs 0.000 claims description 3
- 230000008569 process Effects 0.000 claims description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 2
- 229960001716 benzalkonium Drugs 0.000 claims description 2
- 229940043430 calcium compound Drugs 0.000 claims description 2
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- OLFHCCLYTJITAW-UHFFFAOYSA-N CC1=CN(OO1)O Chemical class CC1=CN(OO1)O OLFHCCLYTJITAW-UHFFFAOYSA-N 0.000 claims 2
- 241000233866 Fungi Species 0.000 claims 2
- FTLRYZCLQBMXQU-UHFFFAOYSA-N 3-hydroxy-5-methyl-2H-1,3-oxazole Chemical compound CC1=CN(O)CO1 FTLRYZCLQBMXQU-UHFFFAOYSA-N 0.000 claims 1
- OBNZPZAOTISUNM-UHFFFAOYSA-N 4-chloro-1,6-dimethylcyclohexa-2,4-dien-1-ol Chemical compound ClC1=CC(C(C=C1)(C)O)C OBNZPZAOTISUNM-UHFFFAOYSA-N 0.000 claims 1
- 239000012872 agrochemical composition Substances 0.000 claims 1
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- CYDRXTMLKJDRQH-UHFFFAOYSA-N benzododecinium Chemical compound CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 CYDRXTMLKJDRQH-UHFFFAOYSA-N 0.000 claims 1
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- UHGIMQLJWRAPLT-UHFFFAOYSA-N octadecyl dihydrogen phosphate Chemical compound CCCCCCCCCCCCCCCCCCOP(O)(O)=O UHGIMQLJWRAPLT-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- UWVQIROCRJWDKL-UHFFFAOYSA-N oxadixyl Chemical compound CC=1C=CC=C(C)C=1N(C(=O)COC)N1CCOC1=O UWVQIROCRJWDKL-UHFFFAOYSA-N 0.000 description 1
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- 230000001717 pathogenic effect Effects 0.000 description 1
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
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- 239000010452 phosphate Substances 0.000 description 1
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- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 description 1
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Chemical class COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 208000005687 scabies Diseases 0.000 description 1
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- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- IXYACKYHUWCLAM-UHFFFAOYSA-M sodium;2-ethylhex-1-ene-1-sulfonate Chemical compound [Na+].CCCCC(CC)=CS([O-])(=O)=O IXYACKYHUWCLAM-UHFFFAOYSA-M 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
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- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000012086 standard solution Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000003890 succinate salts Chemical class 0.000 description 1
- 239000001959 sucrose esters of fatty acids Substances 0.000 description 1
- 235000010965 sucrose esters of fatty acids Nutrition 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 150000007979 thiazole derivatives Chemical class 0.000 description 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical group COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 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
- 239000013008 thixotropic agent Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more 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
- C07D261/12—Oxygen 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
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)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11480892 | 1992-05-07 | ||
| JP4252393 | 1993-03-03 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| LTIP508A LTIP508A (lt) | 1994-08-25 |
| LT3180B true LT3180B (en) | 1995-02-27 |
Family
ID=26382231
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LTIP508A LT3180B (en) | 1992-05-07 | 1993-05-03 | Agrochemical compositins and methods employing 3-hydroxy-5-methylisoxazole |
Country Status (23)
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2174484A1 (en) * | 1995-04-20 | 1996-10-21 | Masaki Hashimoto | Cut flower preservative slurry composition |
| AU7728498A (en) * | 1997-06-09 | 1998-12-30 | Dustin Investments Cc | A composition for use as a pharmaceutical and in specific agricultural and industrial applications |
| EP1145621B8 (en) * | 1998-11-06 | 2008-10-15 | Mebiol Inc. | Water-holding carriers for plants and water-holding materials for growing plants |
| JP3182648B2 (ja) * | 1999-05-12 | 2001-07-03 | ティーディーケイ株式会社 | セラミック成形体の成形用のセラミック顆粒、その製造または処理方法、セラミック成形体およびその製造方法 |
| DE10001548A1 (de) * | 2000-01-14 | 2001-07-19 | Innovation Pro Terra Gmbh & Co | Pflanzsubstrate |
| DE10042894A1 (de) * | 2000-08-31 | 2002-03-14 | Thor Chemie Gmbh | Synergistische Biozidzusammensetzung mit 2-Methylisothiazolin-3-on |
| UA74713C2 (en) * | 2004-04-29 | 2006-01-16 | Inst Of System Innovations Sal | Using a calcium salt in easily soluble form as an adaptogen to hydrothermal meteostresses in the period of plant vegetation and a multipurpose fungicidal preparation on basis thereof |
| US7977119B2 (en) * | 2004-12-08 | 2011-07-12 | Agilent Technologies, Inc. | Chemical arrays and methods of using the same |
| US20070207927A1 (en) * | 2006-03-01 | 2007-09-06 | Rosa Fred C | Polymer based seed coating |
| EA014222B1 (ru) * | 2010-01-11 | 2010-10-29 | Виктор Валентинович МОХОВ | Биоорганический препарат для обработки растений (варианты) |
| CN105248450A (zh) * | 2011-01-28 | 2016-01-20 | 迪帕克·普兰吉万达斯·沙阿 | 包括硫、杀虫剂和农业化学赋形剂的杀虫剂组合物 |
| CN102516190B (zh) * | 2011-12-06 | 2014-04-09 | 西北农林科技大学 | 噁唑喹啉类有机铜化合物及其制备方法、制剂及在防治农业植物病害中的用途 |
| CN102516189B (zh) * | 2011-12-06 | 2014-04-09 | 西北农林科技大学 | 噁唑类有机铜化合物及其制备方法、制剂及在防治农业植物病害中的用途 |
| HK1215355A1 (zh) * | 2012-12-31 | 2016-08-26 | Dow Agrosciences Llc | 調節由雙二硫代氨基甲酸鹽殺真菌劑生產亞乙基雙異硫氰酸酯硫化物的生產率的組合物和方法 |
| WO2020203963A1 (ja) * | 2019-04-05 | 2020-10-08 | 三井化学アグロ株式会社 | 効力の増強された農薬組成物 |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1113618A (en) | 1964-09-14 | 1968-05-15 | Sankyo Co | 3-hydroxyisoazole derivatives |
| JPH05108798A (ja) | 1991-10-17 | 1993-04-30 | Shinko Electric Ind Co Ltd | 画像処理方法と画像処理装置 |
| JP3973380B2 (ja) | 2001-07-25 | 2007-09-12 | シャープ株式会社 | 液晶表示装置 |
| JP4529263B2 (ja) | 2000-09-18 | 2010-08-25 | 沖電気工業株式会社 | アイリス認識装置 |
| JP4538953B2 (ja) | 1997-12-26 | 2010-09-08 | 日本ゼオン株式会社 | −ｃｈ２−ｃｈｆ−基を有する化合物の製造方法 |
| JP4572625B2 (ja) | 2004-08-25 | 2010-11-04 | 三菱マテリアルシ−エムアイ株式会社 | モータ |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1199737A (en) * | 1967-08-18 | 1970-07-22 | Sankyo Co | Process for the preparation of 3-Hydroxyisoxazole Compounds and Alkali Metal Salts thereof |
| GB1256835A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1969-07-03 | 1971-12-15 | ||
| JPS4838148B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1970-05-07 | 1973-11-15 | ||
| JPS4940933B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1970-08-19 | 1974-11-06 | ||
| JPS4838148A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1971-09-10 | 1973-06-05 | ||
| JPS5710083B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1972-04-25 | 1982-02-24 | ||
| JPS4922821A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1972-06-20 | 1974-02-28 | ||
| JPS5430097B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1972-06-29 | 1979-09-28 | ||
| JPS4940933A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1972-08-25 | 1974-04-17 | ||
| JPS5679605A (en) * | 1979-12-04 | 1981-06-30 | Sankyo Co Ltd | Preventing agent against damping-off of rice plant |
| JPS5687506A (en) * | 1979-12-19 | 1981-07-16 | Sankyo Co Ltd | Preventing agent against damping-off of rice plant |
| US4663364A (en) * | 1984-09-05 | 1987-05-05 | Kao Corporation | Biocidal fine powder, its manufacturing method and a suspension for agricultural use containing the above powder |
| JPS61151650A (ja) * | 1984-12-26 | 1986-07-10 | Konishiroku Photo Ind Co Ltd | ハロゲン化銀カラ−写真感光材料の処理方法 |
| DE3609939A1 (de) * | 1986-03-24 | 1987-10-01 | Cassella Ag | Fluessige zubereitung von 1,2-benzisothiazolin-3-on, ihre herstellung und verwendung |
| US5219875A (en) * | 1990-11-27 | 1993-06-15 | Rohm And Haas Company | Antimicrobial compositions comprising iodopropargyl butylcarbamate and 1,2-benzisothiazolin-3-one and methods of controlling microbes |
-
1993
- 1993-04-30 IL IL105577A patent/IL105577A/xx not_active IP Right Cessation
- 1993-05-03 LT LTIP508A patent/LT3180B/lt unknown
- 1993-05-04 DK DK93303446T patent/DK0569210T3/da active
- 1993-05-04 TW TW082103499A patent/TW272115B/zh active
- 1993-05-04 AT AT93303446T patent/ATE162046T1/de not_active IP Right Cessation
- 1993-05-04 ES ES93303446T patent/ES2114001T3/es not_active Expired - Lifetime
- 1993-05-04 DE DE69316262T patent/DE69316262T2/de not_active Expired - Fee Related
- 1993-05-04 EP EP93303446A patent/EP0569210B1/en not_active Expired - Lifetime
- 1993-05-06 PL PL93298838A patent/PL171674B1/pl not_active IP Right Cessation
- 1993-05-06 PL PL93315290A patent/PL172320B1/pl not_active IP Right Cessation
- 1993-05-06 HU HU9301315A patent/HU215381B/hu not_active IP Right Cessation
- 1993-05-06 RU RU93005331/04A patent/RU2091024C1/ru not_active IP Right Cessation
- 1993-05-06 UY UY23579A patent/UY23579A1/es not_active IP Right Cessation
- 1993-05-06 CA CA002095658A patent/CA2095658C/en not_active Expired - Fee Related
- 1993-05-07 SK SK447-93A patent/SK280972B6/sk unknown
- 1993-05-07 KR KR1019930007867A patent/KR100278876B1/ko not_active Expired - Fee Related
- 1993-05-07 CZ CZ1993840A patent/CZ287192B6/cs not_active IP Right Cessation
- 1993-05-07 LV LVP-93-300A patent/LV10447B/en unknown
- 1993-05-07 FI FI932070A patent/FI106525B/fi active
- 1993-05-07 CN CN93107075A patent/CN1070022C/zh not_active Expired - Fee Related
-
1994
- 1994-07-06 US US08/271,264 patent/US5472972A/en not_active Expired - Lifetime
- 1994-07-12 EE EE9400019A patent/EE03133B1/xx not_active IP Right Cessation
-
1995
- 1995-05-04 US US08/433,834 patent/US5554391A/en not_active Expired - Lifetime
-
1998
- 1998-03-13 GR GR980400545T patent/GR3026360T3/el unknown
- 1998-04-08 HK HK98102958A patent/HK1003820A1/en not_active IP Right Cessation
-
2000
- 2000-12-12 CN CNB001307959A patent/CN1149927C/zh not_active Expired - Fee Related
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1113618A (en) | 1964-09-14 | 1968-05-15 | Sankyo Co | 3-hydroxyisoazole derivatives |
| JPH05108798A (ja) | 1991-10-17 | 1993-04-30 | Shinko Electric Ind Co Ltd | 画像処理方法と画像処理装置 |
| JP4538953B2 (ja) | 1997-12-26 | 2010-09-08 | 日本ゼオン株式会社 | −ｃｈ２−ｃｈｆ−基を有する化合物の製造方法 |
| JP4529263B2 (ja) | 2000-09-18 | 2010-08-25 | 沖電気工業株式会社 | アイリス認識装置 |
| JP3973380B2 (ja) | 2001-07-25 | 2007-09-12 | シャープ株式会社 | 液晶表示装置 |
| JP4572625B2 (ja) | 2004-08-25 | 2010-11-04 | 三菱マテリアルシ−エムアイ株式会社 | モータ |
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