PT99734B - Processo para a preparacao de composicoes solidas estaveis antimicrobianas contendo 3-isotiazolonas - Google Patents
Processo para a preparacao de composicoes solidas estaveis antimicrobianas contendo 3-isotiazolonas Download PDFInfo
- Publication number
- PT99734B PT99734B PT99734A PT9973491A PT99734B PT 99734 B PT99734 B PT 99734B PT 99734 A PT99734 A PT 99734A PT 9973491 A PT9973491 A PT 9973491A PT 99734 B PT99734 B PT 99734B
- Authority
- PT
- Portugal
- Prior art keywords
- isothiazolone
- vehicle
- polymers
- process according
- alkyl
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 20
- 238000000034 method Methods 0.000 title claims description 15
- 238000002360 preparation method Methods 0.000 title claims description 3
- 239000007787 solid Substances 0.000 title abstract description 9
- 230000000845 anti-microbial effect Effects 0.000 title description 4
- 230000003068 static effect Effects 0.000 title 1
- MGIYRDNGCNKGJU-UHFFFAOYSA-N isothiazolinone Chemical class O=C1C=CSN1 MGIYRDNGCNKGJU-UHFFFAOYSA-N 0.000 claims abstract description 19
- 229920000642 polymer Polymers 0.000 claims abstract description 18
- 239000001913 cellulose Substances 0.000 claims abstract description 7
- 229920002678 cellulose Polymers 0.000 claims abstract description 7
- 229920002635 polyurethane Polymers 0.000 claims abstract description 7
- 239000004814 polyurethane Substances 0.000 claims abstract description 7
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims abstract description 4
- 150000004676 glycans Chemical class 0.000 claims abstract description 4
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229920001282 polysaccharide Polymers 0.000 claims abstract description 4
- 239000005017 polysaccharide Substances 0.000 claims abstract description 4
- 229920002845 Poly(methacrylic acid) Polymers 0.000 claims abstract description 3
- 229920001577 copolymer Polymers 0.000 claims abstract description 3
- 230000002209 hydrophobic effect Effects 0.000 claims abstract description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000012141 concentrate Substances 0.000 claims abstract 2
- JLHMJWHSBYZWJJ-UHFFFAOYSA-N 1,2-thiazole 1-oxide Chemical compound O=S1C=CC=N1 JLHMJWHSBYZWJJ-UHFFFAOYSA-N 0.000 claims description 14
- 125000005843 halogen group Chemical group 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 6
- 239000003381 stabilizer Substances 0.000 claims description 5
- -1 carbalcoxy Chemical group 0.000 claims description 4
- 150000003839 salts Chemical group 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 239000004599 antimicrobial Substances 0.000 claims description 3
- 238000001704 evaporation Methods 0.000 claims description 3
- 230000008020 evaporation Effects 0.000 claims description 3
- 230000000087 stabilizing effect Effects 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- 241000894006 Bacteria Species 0.000 claims description 2
- 241000195493 Cryptophyta Species 0.000 claims description 2
- 241000233866 Fungi Species 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- 125000003282 alkyl amino group Chemical group 0.000 claims description 2
- 125000004414 alkyl thio group Chemical group 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000001769 aryl amino group Chemical group 0.000 claims description 2
- 125000004104 aryloxy group Chemical group 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 230000006835 compression Effects 0.000 claims description 2
- 238000007906 compression Methods 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 230000001877 deodorizing effect Effects 0.000 claims description 2
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 2
- 239000002270 dispersing agent Substances 0.000 claims description 2
- 238000001125 extrusion Methods 0.000 claims description 2
- 230000004927 fusion Effects 0.000 claims description 2
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 230000014759 maintenance of location Effects 0.000 claims description 2
- 238000000465 moulding Methods 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 239000004094 surface-active agent Substances 0.000 claims description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims 3
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 238000004040 coloring Methods 0.000 claims 1
- 238000000354 decomposition reaction Methods 0.000 claims 1
- 125000001786 isothiazolyl group Chemical group 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 230000001737 promoting effect Effects 0.000 claims 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- 238000001694 spray drying Methods 0.000 claims 1
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 claims 1
- 239000000725 suspension Substances 0.000 claims 1
- 238000002144 chemical decomposition reaction Methods 0.000 abstract description 4
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 abstract description 2
- 230000003641 microbiacidal effect Effects 0.000 abstract description 2
- SQAINHDHICKHLX-UHFFFAOYSA-N 1-naphthaldehyde Chemical compound C1=CC=C2C(C=O)=CC=CC2=C1 SQAINHDHICKHLX-UHFFFAOYSA-N 0.000 abstract 1
- 229940124561 microbicide Drugs 0.000 abstract 1
- 239000002855 microbicide agent Substances 0.000 abstract 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- OQMBBFQZGJFLBU-UHFFFAOYSA-N Oxyfluorfen Chemical compound C1=C([N+]([O-])=O)C(OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 OQMBBFQZGJFLBU-UHFFFAOYSA-N 0.000 description 3
- 239000005590 Oxyfluorfen Substances 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- BEGLCMHJXHIJLR-UHFFFAOYSA-N methylisothiazolinone Chemical compound CN1SC=CC1=O BEGLCMHJXHIJLR-UHFFFAOYSA-N 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 239000008247 solid mixture Substances 0.000 description 2
- YVWZBMHCQCVNFR-UHFFFAOYSA-N 4-chloro-2-methyl-1,2-thiazol-3-one Chemical compound CN1SC=C(Cl)C1=O YVWZBMHCQCVNFR-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 229920003105 Methocel™ A15 LV Polymers 0.000 description 1
- 229920003094 Methocel™ K4M Polymers 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 125000004442 acylamino group Chemical group 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- DHNRXBZYEKSXIM-UHFFFAOYSA-N chloromethylisothiazolinone Chemical compound CN1SC(Cl)=CC1=O DHNRXBZYEKSXIM-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- CBYZIWCZNMOEAV-UHFFFAOYSA-N formaldehyde;naphthalene Chemical compound O=C.C1=CC=CC2=CC=CC=C21 CBYZIWCZNMOEAV-UHFFFAOYSA-N 0.000 description 1
- UPBDXRPQPOWRKR-UHFFFAOYSA-N furan-2,5-dione;methoxyethene Chemical compound COC=C.O=C1OC(=O)C=C1 UPBDXRPQPOWRKR-UHFFFAOYSA-N 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000012768 molten material Substances 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 1
- 231100000344 non-irritating Toxicity 0.000 description 1
- JPMIIZHYYWMHDT-UHFFFAOYSA-N octhilinone Chemical compound CCCCCCCCN1SC=CC1=O JPMIIZHYYWMHDT-UHFFFAOYSA-N 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000000737 potassium alginate Substances 0.000 description 1
- 235000010408 potassium alginate Nutrition 0.000 description 1
- MZYRDLHIWXQJCQ-YZOKENDUSA-L potassium alginate Chemical compound [K+].[K+].O1[C@@H](C([O-])=O)[C@@H](OC)[C@H](O)[C@H](O)[C@@H]1O[C@@H]1[C@@H](C([O-])=O)O[C@@H](O)[C@@H](O)[C@H]1O MZYRDLHIWXQJCQ-YZOKENDUSA-L 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 229920001059 synthetic polymer Polymers 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
- 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
- A01N43/74—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 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
-
- 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
- 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)
- Paints Or Removers (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US62526590A | 1990-12-10 | 1990-12-10 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| PT99734A PT99734A (pt) | 1992-11-30 |
| PT99734B true PT99734B (pt) | 1999-05-31 |
Family
ID=24505286
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PT99734A PT99734B (pt) | 1990-12-10 | 1991-12-09 | Processo para a preparacao de composicoes solidas estaveis antimicrobianas contendo 3-isotiazolonas |
Country Status (22)
| Country | Link |
|---|---|
| US (2) | US5703105A (OSRAM) |
| EP (1) | EP0492843B1 (OSRAM) |
| JP (1) | JP3248589B2 (OSRAM) |
| KR (1) | KR100225270B1 (OSRAM) |
| CN (1) | CN1038979C (OSRAM) |
| AT (1) | ATE126419T1 (OSRAM) |
| AU (1) | AU656746B2 (OSRAM) |
| BR (1) | BR9105131A (OSRAM) |
| CA (1) | CA2055380A1 (OSRAM) |
| DE (1) | DE69112193T2 (OSRAM) |
| DK (1) | DK0492843T3 (OSRAM) |
| ES (1) | ES2077185T3 (OSRAM) |
| FI (1) | FI97268C (OSRAM) |
| GR (1) | GR3017149T3 (OSRAM) |
| HU (1) | HU207786B (OSRAM) |
| IE (1) | IE68952B1 (OSRAM) |
| IL (1) | IL100291A (OSRAM) |
| MX (1) | MX9102485A (OSRAM) |
| NO (1) | NO179962C (OSRAM) |
| NZ (1) | NZ240893A (OSRAM) |
| PT (1) | PT99734B (OSRAM) |
| TW (1) | TW212749B (OSRAM) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5430046A (en) * | 1994-03-11 | 1995-07-04 | Rohm And Haas Company | Solid 3-isothiazolone biocidal concentrates |
| JP2587582B2 (ja) * | 1994-03-22 | 1997-03-05 | 株式会社日本アルミ | ヒートシンク及びその製造方法 |
| GB9504630D0 (en) * | 1995-03-08 | 1995-04-26 | Kodak Ltd | A material and method for inhibiting bacterial growth in an aqueous medium |
| US6093387A (en) * | 1997-04-29 | 2000-07-25 | United Technologies Corporation | Extended-release chemical formulation in tablet form for urine pretreatment |
| US5910503A (en) * | 1997-10-28 | 1999-06-08 | Rohm And Haas Company | Stable microbicide formulation |
| US6270786B1 (en) * | 1998-07-09 | 2001-08-07 | Eastman Kodak Company | Method of preparing a biocidal material |
| US6069142A (en) * | 1998-12-23 | 2000-05-30 | Calgon Corporation | Synergistic antimicrobial combination of 4,5-dichloro-2-N-octyl-4-isothiazolin-3-one and a mixture of a chlorinated isocyanurate and a bromide compound and methods of using same |
| FR2801767B1 (fr) * | 1999-12-01 | 2002-09-13 | Eastman Kodak Co | Materiau biocide ayant une activite amelioree |
| US6437020B1 (en) * | 1999-12-21 | 2002-08-20 | Amick David Richard | Polymer stabilization |
| KR100615571B1 (ko) * | 1999-12-31 | 2006-08-25 | 에스케이케미칼주식회사 | 스케일 및 미생물 억제 수처리제 조성물 |
| KR100383098B1 (ko) * | 2000-05-10 | 2003-05-12 | 에스케이케미칼주식회사 | 이소티아졸론 용액의 침전형성 방지방법 및 그 조성물 |
| GB0019296D0 (en) * | 2000-08-07 | 2000-09-27 | Nipa Lab Limited | Treatment for part processed leather |
| AUPR040600A0 (en) * | 2000-09-27 | 2000-10-19 | Chemeq Ltd | Polymeric formulation |
| KR100817136B1 (ko) * | 2001-03-07 | 2008-03-27 | 롬 앤드 하스 캄파니 | 수지 고정된 살균제 |
| DE102004026274A1 (de) * | 2004-05-05 | 2006-02-16 | Ecs Environment Care Systems Gmbh | Wasserlösliche Folie zur Freisetzung von Wirkstoffen |
| EP2207416B1 (en) * | 2007-10-02 | 2018-11-07 | Imerys Filtration Minerals, Inc. | Enhanced retention capabilities through methods comprising surface treatment of functional particulate carrier materials, and functional particulate carrier materials made therefrom |
| CN101952525A (zh) * | 2007-10-30 | 2011-01-19 | 世界矿物公司 | 改性的基于矿物的填料 |
| EP2744328A2 (en) * | 2011-08-15 | 2014-06-25 | Medivators Inc. | Water soluble antimicrobial composition |
| WO2024248969A1 (en) * | 2023-05-30 | 2024-12-05 | Rohm And Haas Company | Method for deactivating 1,2-benzisothiazolin-3-one in a latex |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1223172A (en) * | 1982-09-23 | 1987-06-23 | Sidney Melamed | Encapsulated solid microbiocidal article |
| BR8304987A (pt) * | 1982-09-23 | 1984-09-04 | Rohm & Haas | Composicao microbiocida,metodo para controlar microorganismos vivos em um sistema aquosos e metodo de proteger isotiazolonas microbiocidas |
| US4542169A (en) * | 1983-12-12 | 1985-09-17 | Rohm And Haas Company | Biomedical devices containing isothiazolones to control bacteria growth |
| US4552591A (en) * | 1984-05-15 | 1985-11-12 | Petrolite Corporation | Oil field biocide composition |
| CA1334824C (en) * | 1987-02-11 | 1995-03-21 | Stewart Nelson Paul | Biocide protectors |
| CA1328175C (en) * | 1988-05-16 | 1994-04-05 | John Robert Mattox | Epoxide stabilizers for biocidal compositions |
| GB8913513D0 (en) * | 1989-06-13 | 1989-08-02 | Ici Plc | Composition |
-
1991
- 1991-10-11 TW TW080108003A patent/TW212749B/zh active
- 1991-10-30 US US07/784,852 patent/US5703105A/en not_active Expired - Lifetime
- 1991-11-13 CA CA002055380A patent/CA2055380A1/en not_active Abandoned
- 1991-11-26 BR BR919105131A patent/BR9105131A/pt not_active IP Right Cessation
- 1991-12-04 NO NO914754A patent/NO179962C/no unknown
- 1991-12-04 DK DK91311279.3T patent/DK0492843T3/da active
- 1991-12-04 ES ES91311279T patent/ES2077185T3/es not_active Expired - Lifetime
- 1991-12-04 DE DE69112193T patent/DE69112193T2/de not_active Expired - Lifetime
- 1991-12-04 EP EP91311279A patent/EP0492843B1/en not_active Expired - Lifetime
- 1991-12-04 AT AT91311279T patent/ATE126419T1/de not_active IP Right Cessation
- 1991-12-06 AU AU88891/91A patent/AU656746B2/en not_active Ceased
- 1991-12-06 NZ NZ240893A patent/NZ240893A/en unknown
- 1991-12-09 IE IE427091A patent/IE68952B1/en not_active IP Right Cessation
- 1991-12-09 FI FI915784A patent/FI97268C/fi not_active IP Right Cessation
- 1991-12-09 PT PT99734A patent/PT99734B/pt not_active IP Right Cessation
- 1991-12-09 IL IL10029191A patent/IL100291A/en not_active IP Right Cessation
- 1991-12-10 KR KR1019910022537A patent/KR100225270B1/ko not_active Expired - Lifetime
- 1991-12-10 JP JP35004391A patent/JP3248589B2/ja not_active Expired - Lifetime
- 1991-12-10 HU HU913879A patent/HU207786B/hu not_active IP Right Cessation
- 1991-12-10 CN CN91111562A patent/CN1038979C/zh not_active Expired - Lifetime
- 1991-12-10 MX MX9102485A patent/MX9102485A/es unknown
-
1995
- 1995-06-06 US US08/471,888 patent/US5648086A/en not_active Expired - Lifetime
- 1995-08-17 GR GR950402080T patent/GR3017149T3/el unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| PT99734B (pt) | Processo para a preparacao de composicoes solidas estaveis antimicrobianas contendo 3-isotiazolonas | |
| US5529770A (en) | Viscous liquid conditioning topical germicides | |
| JPS6350322B2 (OSRAM) | ||
| PT84761B (pt) | Processo para a preparacao de composicoes fungicidas contendo ditiocarbamatos com estabilidade melhorada relativamente a accao da chuva | |
| JP3805014B2 (ja) | ３−イソチアゾロン化合物のマイクロエマルション組成物 | |
| JP2003511471A (ja) | 低温安定防腐剤 | |
| US6121302A (en) | Stabilization of isothiazolone | |
| EP0332336B1 (en) | Antimicrobial composition | |
| EP0604906B1 (en) | Water dispersible granular herbicidal compositions | |
| JP2014510109A (ja) | 低界面活性剤のヨウ素系局所殺菌剤 | |
| JPH0544441B2 (OSRAM) | ||
| US20030039580A1 (en) | Stable preservative formulations comprising halopropynyl compounds and butoxydiglycol solvent | |
| JPS6032701A (ja) | 水性懸濁殺生剤組成物 | |
| JPH02164803A (ja) | 安定な殺菌組成物 | |
| EP4017266A1 (en) | Crystallisation-free, highly concentrated suspension concentrates of metribuzin and diflufenican | |
| JPH07145013A (ja) | 農芸化学において特に有用なホスフェート化ポリアルコキシル化トリスチリルフェノール誘導体を含有する流体状濃厚処方物 | |
| BR112021001501B1 (pt) | Composições aquosas para proteção de colheita, e seus usos | |
| CA2112040C (en) | Water dispersible granular herbicidal compositions | |
| EP3829297A1 (en) | Surfactant combination for agrochemical formulations | |
| LT3395B (en) | Stable and water-soluble veterinary composition and process for preparing thereof | |
| IL111895A (en) | Water dispersible granular herbicidal compositions comprising dinitroanaline derivatives together with imidazolinone and their preparation |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| BB1A | Laying open of patent application |
Effective date: 19920713 |
|
| FG3A | Patent granted, date of granting |
Effective date: 19990218 |
|
| MM3A | Annulment or lapse |
Free format text: LAPSE DUE TO NON-PAYMENT OF FEES Effective date: 20000831 |