ZA200508883B - Microbicidal composition - Google Patents
Microbicidal composition Download PDFInfo
- Publication number
- ZA200508883B ZA200508883B ZA200508883A ZA200508883A ZA200508883B ZA 200508883 B ZA200508883 B ZA 200508883B ZA 200508883 A ZA200508883 A ZA 200508883A ZA 200508883 A ZA200508883 A ZA 200508883A ZA 200508883 B ZA200508883 B ZA 200508883B
- Authority
- ZA
- South Africa
- Prior art keywords
- benzisothiazolin
- salts
- weight ratio
- methyl
- ppm
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 61
- 230000003641 microbiacidal effect Effects 0.000 title claims description 41
- DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 claims description 52
- 229940124561 microbicide Drugs 0.000 claims description 32
- BEGLCMHJXHIJLR-UHFFFAOYSA-N methylisothiazolinone Chemical compound CN1SC=CC1=O BEGLCMHJXHIJLR-UHFFFAOYSA-N 0.000 claims description 21
- 229940100555 2-methyl-4-isothiazolin-3-one Drugs 0.000 claims description 18
- 239000002855 microbicide agent Substances 0.000 claims description 16
- ISRLGZXSKRDKID-JXBDSQKUSA-N [3-bis[3-[dimethyl-[3-[[(9z,12z)-octadeca-9,12-dienoyl]amino]propyl]azaniumyl]-2-hydroxypropoxy]phosphoryloxy-2-hydroxypropyl]-dimethyl-[3-[[(9z,12z)-octadeca-9,12-dienoyl]amino]propyl]azanium;trichloride Chemical compound [Cl-].[Cl-].[Cl-].CCCCC\C=C/C\C=C/CCCCCCCC(=O)NCCC[N+](C)(C)CC(O)COP(=O)(OCC(O)C[N+](C)(C)CCCNC(=O)CCCCCCC\C=C/C\C=C/CCCCC)OCC(O)C[N+](C)(C)CCCNC(=O)CCCCCCC\C=C/C\C=C/CCCCC ISRLGZXSKRDKID-JXBDSQKUSA-N 0.000 claims description 15
- 150000003839 salts Chemical class 0.000 claims description 15
- AEIJTFQOBWATKX-UHFFFAOYSA-N octane-1,2-diol Chemical compound CCCCCCC(O)CO AEIJTFQOBWATKX-UHFFFAOYSA-N 0.000 claims description 11
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 claims description 10
- MXOAEAUPQDYUQM-QMMMGPOBSA-N (S)-chlorphenesin Chemical compound OC[C@H](O)COC1=CC=C(Cl)C=C1 MXOAEAUPQDYUQM-QMMMGPOBSA-N 0.000 claims description 9
- 229960003993 chlorphenesin Drugs 0.000 claims description 9
- 239000004287 Dehydroacetic acid Substances 0.000 claims description 8
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 8
- 235000019258 dehydroacetic acid Nutrition 0.000 claims description 8
- JEQRBTDTEKWZBW-UHFFFAOYSA-N dehydroacetic acid Chemical compound CC(=O)C1=C(O)OC(C)=CC1=O JEQRBTDTEKWZBW-UHFFFAOYSA-N 0.000 claims description 8
- 229940061632 dehydroacetic acid Drugs 0.000 claims description 8
- PGRHXDWITVMQBC-UHFFFAOYSA-N dehydroacetic acid Natural products CC(=O)C1C(=O)OC(C)=CC1=O PGRHXDWITVMQBC-UHFFFAOYSA-N 0.000 claims description 8
- 229940099487 linoleamidopropyl pg-dimonium chloride phosphate Drugs 0.000 claims description 8
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 claims description 8
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- SOROIESOUPGGFO-UHFFFAOYSA-N diazolidinylurea Chemical compound OCNC(=O)N(CO)C1N(CO)C(=O)N(CO)C1=O SOROIESOUPGGFO-UHFFFAOYSA-N 0.000 claims description 5
- 229960001083 diazolidinylurea Drugs 0.000 claims description 5
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- 239000004403 ethyl p-hydroxybenzoate Substances 0.000 claims description 5
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- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 claims description 5
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 claims description 5
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- DTOUUUZOYKYHEP-UHFFFAOYSA-N 1,3-bis(2-ethylhexyl)-5-methyl-1,3-diazinan-5-amine Chemical compound CCCCC(CC)CN1CN(CC(CC)CCCC)CC(C)(N)C1 DTOUUUZOYKYHEP-UHFFFAOYSA-N 0.000 claims description 4
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- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 claims description 4
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- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 238000001223 reverse osmosis Methods 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 239000011885 synergistic combination Substances 0.000 description 1
- 229960002622 triacetin Drugs 0.000 description 1
- QCRXMFTZTSTGJM-UHFFFAOYSA-N triacetyl 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound CC(=O)OC(=O)CC(O)(C(=O)OC(C)=O)CC(=O)OC(C)=O QCRXMFTZTSTGJM-UHFFFAOYSA-N 0.000 description 1
- 108010050327 trypticase-soy broth Proteins 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000012138 yeast extract Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/16—Antifouling paints; Underwater paints
- C09D5/1606—Antifouling paints; Underwater paints characterised by the anti-fouling agent
- C09D5/1612—Non-macromolecular compounds
- C09D5/1625—Non-macromolecular compounds organic
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Dentistry (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
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| US62832604P | 2004-11-16 | 2004-11-16 |
Publications (1)
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|---|---|
| ZA200508883B true ZA200508883B (en) | 2006-07-26 |
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| ZA200508883A ZA200508883B (en) | 2004-11-16 | 2005-11-02 | Microbicidal composition |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US7468384B2 (fr) |
| EP (14) | EP1820399B1 (fr) |
| JP (1) | JP4430004B2 (fr) |
| KR (13) | KR20060055324A (fr) |
| CN (4) | CN100556285C (fr) |
| AU (14) | AU2005229744B2 (fr) |
| BR (2) | BR122014003818B1 (fr) |
| DE (2) | DE602005002441T2 (fr) |
| ES (9) | ES2341134T3 (fr) |
| MX (1) | MXPA05012128A (fr) |
| TW (22) | TWI433650B (fr) |
| ZA (1) | ZA200508883B (fr) |
Families Citing this family (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9034905B2 (en) | 2003-02-05 | 2015-05-19 | Rohm And Haas Company | Synergistic microbicidal combinations |
| EP1772055A1 (fr) * | 2005-10-04 | 2007-04-11 | Rohm and Haas France SAS | Compositions microbicides synergiques comprenant une N-alkyl-1,2-benzoisothiazolin-3-one |
| GB2432119B (en) * | 2005-11-10 | 2011-03-23 | Biotech Internat Ltd | Improvements in and relating to biocidal compositions |
| US20070196301A1 (en) * | 2005-12-21 | 2007-08-23 | L'oreal | Cosmetic composition with a volumizing effect |
| WO2007098135A2 (fr) * | 2006-02-21 | 2007-08-30 | Inolex Investment Corporation | Compositions antimicrobiennes |
| US9723842B2 (en) * | 2006-05-26 | 2017-08-08 | Arch Chemicals, Inc. | Isothiazolinone biocides enhanced by zinc ions |
| DE102006045066B4 (de) * | 2006-09-21 | 2010-07-01 | Schülke & Mayr GmbH | Mikrobizide Zubereitung auf der Basis von 1,2-Benzisothiazolin-3-on mit einem Gehalt an aromatischem Alkohol |
| JP2008247751A (ja) * | 2007-03-29 | 2008-10-16 | Aquas Corp | 粒状緑藻防除剤、及び、粒状緑藻の防除方法 |
| AU2013270575B2 (en) * | 2007-07-18 | 2015-04-16 | Rohm And Haas Company | Microbicidal composition |
| JP4944843B2 (ja) * | 2007-07-18 | 2012-06-06 | ローム アンド ハース カンパニー | 殺微生物組成物 |
| US20090035340A1 (en) * | 2007-07-30 | 2009-02-05 | Kimberly-Clark Worldwide, Inc. | Preservative compositions for moist wipes |
| JP5075554B2 (ja) * | 2007-09-28 | 2012-11-21 | 富士フイルム株式会社 | 有害物質除去材及び有害物質除去方法 |
| JP2009149610A (ja) * | 2007-12-20 | 2009-07-09 | Rohm & Haas Co | 相乗的殺微生物性組成物 |
| EP2153813A1 (fr) * | 2008-08-15 | 2010-02-17 | Lonza, Inc. | Mélanges synergiques de conservateurs |
| JP5616337B2 (ja) * | 2008-06-27 | 2014-10-29 | ダウ グローバル テクノロジーズ エルエルシー | 殺生物組成物 |
| BRPI0822929B8 (pt) * | 2008-07-10 | 2021-05-25 | Symrise Ag | composição, uso de álcool 4-metilbenzílico, método para intensificação sinergística em atividade antimicrobiana e método para a conservação ou tratamento antimicrobiano de um produto perecível |
| CN102196726A (zh) * | 2008-11-04 | 2011-09-21 | 日本曹达株式会社 | 阳离子电沉积涂覆系统用缓释性杀菌·抗菌剂 |
| CN102413684B (zh) * | 2009-04-27 | 2015-01-21 | 巴斯夫欧洲公司 | 含有农药、防腐剂和未支化1,2-链烷二醇的组合物 |
| CA2760554A1 (fr) | 2009-05-01 | 2010-11-04 | Signal Investment And Management Co. | Composition antimicrobienne hydratante |
| US8106111B2 (en) | 2009-05-15 | 2012-01-31 | Eastman Chemical Company | Antimicrobial effect of cycloaliphatic diol antimicrobial agents in coating compositions |
| JP5210360B2 (ja) * | 2009-07-30 | 2013-06-12 | ローム アンド ハース カンパニー | 相乗的殺微生物組成物 |
| KR20120081160A (ko) * | 2009-09-21 | 2012-07-18 | 브리엔 홀덴 비전 인스티튜트 | 콘택트 렌즈 소독액 |
| JP5364935B2 (ja) * | 2010-11-09 | 2013-12-11 | ダウ グローバル テクノロジーズ エルエルシー | フルメツラムまたはジクロスラムとジンクピリチオンとの相乗的組み合わせ |
| JP5520272B2 (ja) | 2010-11-18 | 2014-06-11 | ダウ グローバル テクノロジーズ エルエルシー | １，２−ベンゾイソチアゾリン−３−オンとトリス（ヒドロキシメチル）ニトロメタンとの相乗的抗微生物組成物 |
| WO2012068455A1 (fr) * | 2010-11-19 | 2012-05-24 | Isp Investments Inc. | Composition de conservation stable et aqueuse concentrée d'acide déshydroacétique (dha) et de méthylisothiazolinone (mit) |
| TWI445696B (zh) * | 2010-11-29 | 2014-07-21 | Univ Nat Yang Ming | 標靶人類胸線核苷酸激酶誘導惡性腫瘤中的ｄｎａ修復毒性 |
| US9662328B2 (en) | 2010-11-29 | 2017-05-30 | National Yang-Ming University | Targeting human thymidylate kinase induces DNA repair toxicity in malignant tumor cells |
| US8317912B2 (en) * | 2011-03-28 | 2012-11-27 | Arch Chemicals, Inc. | Wet state preservation of mineral slurries |
| CN102993031B (zh) | 2011-09-19 | 2014-03-26 | 北京桑普生物化学技术有限公司 | 一种制备芳基多氧烷基季铵类化合物的方法 |
| US9089129B2 (en) * | 2011-10-07 | 2015-07-28 | American Sterilizer Company | Non-aerosol foaming alcohol hand sanitizer |
| EP2749167A1 (fr) | 2012-12-28 | 2014-07-02 | Sanitized AG | Formulation destinée à l'équipement antimicrobien de compositions à base de chlorure de polyvinyle |
| WO2014102228A1 (fr) | 2012-12-28 | 2014-07-03 | Sanitized Ag | Formulation d'apprêt antimicrobien de compositions polymériques |
| CN107920527B (zh) | 2015-09-09 | 2021-02-19 | 托尔有限公司 | 储存稳定的生物杀灭剂组合物 |
| CN105755183B (zh) * | 2016-03-25 | 2018-10-12 | 深圳市大地康恩生物科技有限公司 | 皮革浸水生物酶杀菌剂 |
| US10799433B2 (en) | 2016-04-20 | 2020-10-13 | S. C. Johnson & Son, Inc. | Foaming antimicrobial compositions |
| US20180070590A1 (en) * | 2016-09-09 | 2018-03-15 | Lonza Inc. | Enhanced Biocide Composition Containing An Isothiazolinone and a Pyrithione |
| CN106879602A (zh) * | 2017-01-11 | 2017-06-23 | 广东省微生物研究所（广东省微生物分析检测中心） | 一种协同抑细菌和抗细菌生物膜形成的组合物 |
| US11452243B2 (en) | 2017-10-12 | 2022-09-20 | Coolit Systems, Inc. | Cooling system, controllers and methods |
| CN107736357A (zh) * | 2017-11-13 | 2018-02-27 | 江苏艾津农化有限责任公司 | 一种农药悬浮剂用防腐组合物及其使用方法 |
| CN108041075A (zh) * | 2017-12-11 | 2018-05-18 | 佛山高富中石油燃料沥青有限责任公司 | 一种高效复合型杀菌剂 |
| WO2020035165A1 (fr) * | 2018-08-16 | 2020-02-20 | Thor Gmbh | Compositions biocides stables renfermant de la 1,2-benzisothiazolin-3-one et de la glycérine |
| FR3090323A1 (fr) * | 2018-12-21 | 2020-06-26 | L'oreal | Mélange antimicrobien contenant du 4-(3-éthoxy-4-hydroxyphényl)butan-2-one et un composé acide ou à base d’argent, et composition le contenant |
| CN109851440A (zh) * | 2019-04-23 | 2019-06-07 | 南京正邦园艺科技有限公司 | 一种抑制绿藻的营养液配方 |
| CN110934759B (zh) * | 2019-11-26 | 2022-06-21 | 马祥全 | 椰油酰胺丙基pg-二甲基氯化铵作为抑菌剂的应用及其作为抑菌剂在日化用品中的应用 |
| CN111000743B (zh) * | 2019-11-26 | 2022-08-12 | 马祥全 | 椰油酰胺丙基pg-二甲基氯化铵与多元醇的复配物及其应用 |
| US20230151324A1 (en) * | 2021-11-16 | 2023-05-18 | Phibro Animal Health Corporation | Preservation system for stabilizing spore-forming microbials |
Family Cites Families (59)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US611436A (en) * | 1898-09-27 | Oar-lock | ||
| US4173643A (en) | 1973-12-20 | 1979-11-06 | Rohm And Haas Company | Synergistic microbiocidal compositions |
| GB1532984A (en) | 1975-04-10 | 1978-11-22 | Ici Ltd | Method for the control of micro-organisms |
| US4209449A (en) * | 1978-11-30 | 1980-06-24 | Mona Industries | Phosphate quaternary compounds |
| US4352744A (en) | 1980-09-05 | 1982-10-05 | E. I. Du Pont De Nemours And Company | Protecting colloidal silica aquasols from bacterial degradation |
| JPS57156405A (en) | 1981-03-24 | 1982-09-27 | Yoshitomi Pharmaceut Ind Ltd | Fungicide for industrial purpose |
| US4454146A (en) | 1982-05-14 | 1984-06-12 | Lever Brothers Company | Synergistic preservative compositions |
| JPS60110793A (ja) | 1983-11-18 | 1985-06-17 | ライオン株式会社 | 液体洗浄剤組成物 |
| FI84421C (fi) | 1986-03-04 | 1991-12-10 | Sutton Lab Inc | Sammansaettningar av konserveringsaemnen och anvaendningar av desamma. |
| US4725612A (en) | 1986-08-06 | 1988-02-16 | Drew Chemical Corporation | Synergistic microbiocidal compositions containing a mixture of a bicyclic polyoxymethylene oxazolidine and a 1,2-benzisothiazolin-3-one |
| US5008150A (en) | 1987-10-02 | 1991-04-16 | Mitsubishi Paper Mills Limited | Photographic support with an undercoating layer on a resin coated base sheet |
| US4906651A (en) * | 1988-12-22 | 1990-03-06 | Rohm And Haas Company | Synergistic microbicidal combinations containing 3-isothiazolone and commercial biocides |
| US5246913A (en) * | 1988-12-22 | 1993-09-21 | Rohm And Haas Company | Synergistic microbicidal combinations containing 4-isothiazolin and commercial biocides |
| US4964892A (en) | 1988-12-22 | 1990-10-23 | Rohm And Haas Company | Synergistic microbicidal combinations containing 2-N-octyl-3-isothiazolone and certain commercial biocides |
| GB2230190A (en) | 1989-03-28 | 1990-10-17 | Ici Plc | Compositions containing an isothiazolin(thi)one derivative and a 2-mercaptopyridine-1-oxide derivative |
| GB8907298D0 (en) * | 1989-03-31 | 1989-05-17 | Ici Plc | Composition and use |
| DE3911808A1 (de) | 1989-04-11 | 1990-10-18 | Riedel De Haen Ag | Fluessiges konservierungsmittel |
| US5424324A (en) * | 1989-11-17 | 1995-06-13 | Rohm And Haas Company | Use of carbonyl stabilizers for 3-isothiazolones |
| CA2029302A1 (fr) | 1989-11-17 | 1991-05-18 | Gary L. Willingham | Stabilisateurs carbonyles pour derives d'isothiazol-3-one |
| US5125966A (en) * | 1990-12-20 | 1992-06-30 | Nalco Chemical Company | Process for de-oiling mill sludge |
| US5464850A (en) | 1991-10-04 | 1995-11-07 | Ciba Corning Diagnostics Corp. | Synergistic preservative systems for chemistry reagents |
| DE4202051A1 (de) * | 1992-01-25 | 1993-07-29 | Bayer Ag | Fliessfaehige mikrobizide mittel |
| US5294614A (en) | 1993-01-13 | 1994-03-15 | Rohm And Haas Company | Synergistic microbicidal composition comprising 3-isothiazolones and 1-methyl-3,5,7-triaza-1-azoniatricyclo(3.3.1.1)decane chloride |
| JPH06313269A (ja) | 1993-04-26 | 1994-11-08 | Toray Ind Inc | 防かび性防水布帛およびその製造方法 |
| GB9312645D0 (en) * | 1993-06-18 | 1993-08-04 | Zeneca Ltd | Stable aqueous formulation and use |
| US5444078A (en) | 1993-10-01 | 1995-08-22 | Rohm And Haas Company | Fully water-dilutable microemulsions |
| US5609432A (en) * | 1994-12-16 | 1997-03-11 | Kabushiki Kaisha Pilot | Ballpoint pen containing an aqueous ink composition |
| US5668083A (en) | 1995-06-06 | 1997-09-16 | Rohm And Haas Company | Composition containing 3-isothiazolone and stabilizer |
| US5688744A (en) * | 1995-11-03 | 1997-11-18 | Rohm And Haas Company | Antimicrobial compounds with quick speed of kill |
| DE19548710A1 (de) * | 1995-12-23 | 1997-06-26 | Riedel De Haen Ag | Konservierungsmittel, enthaltend Isothiazolinon-Derivate und Komplexbildner |
| KR19990077318A (ko) | 1996-01-16 | 1999-10-25 | 에드워드 제이. 존스 | 세제 및 소독제 제조물 |
| US6114366A (en) | 1997-02-27 | 2000-09-05 | Lonza Inc. | Broad spectrum preservative |
| AU7865598A (en) * | 1997-08-14 | 1999-02-25 | Rohm And Haas Company | Solid biocidal compositions |
| EP0900525A1 (fr) | 1997-08-20 | 1999-03-10 | Thor Chemie Gmbh | Composition biocide synergique |
| JPH1171211A (ja) | 1997-09-01 | 1999-03-16 | Takeda Chem Ind Ltd | 工業用殺菌剤および殺菌方法 |
| JPH11180806A (ja) * | 1997-12-22 | 1999-07-06 | Kurita Water Ind Ltd | 抗菌性組成物 |
| WO1999046350A1 (fr) | 1998-03-11 | 1999-09-16 | Sybron Chemical Holdings, Inc. | Composition de liquide biologique desodorisant |
| EP0980648A1 (fr) * | 1998-08-20 | 2000-02-23 | Thor Chemie Gmbh | Composition biocide synergique |
| JP3722268B2 (ja) * | 1998-09-03 | 2005-11-30 | 栗田工業株式会社 | 抗菌性組成物 |
| AU5595499A (en) * | 1998-10-19 | 2000-04-20 | Whiteley Industries Pty Ltd | A disinfectant composition |
| FR2795328B1 (fr) | 1999-06-23 | 2002-08-02 | H F F F Haut Fourneau Forges E | Procede et composition de protection contre la contamination pour articles sanitaires |
| US6255331B1 (en) * | 1999-09-14 | 2001-07-03 | Rohm And Haas Company | Stable biocidal compositions |
| US6133300A (en) | 1999-10-15 | 2000-10-17 | Troy Technology Corporation, Inc. | Antimicrobial mixtures of 1,3-bis(hydroxymethyl)-5,5-dimethylhydantoin and 1,2-benzisothiazolin-3-one |
| DE19951328C2 (de) * | 1999-10-20 | 2002-03-14 | Schuelke & Mayr Gmbh | Kältestabile Konservierungsmittel |
| EP1096310B1 (fr) * | 1999-10-26 | 2004-06-02 | Fuji Photo Film Co., Ltd. | Matériau photothermographique |
| US6511673B1 (en) | 2000-05-10 | 2003-01-28 | Rohm And Haas Company | Microbicidal composition |
| US6432433B1 (en) * | 2000-06-05 | 2002-08-13 | Isp Investments Inc. | Liquid biocidal composition of a formaldehyde adduct and an isothiazolone and method of use |
| US20020028754A1 (en) | 2000-07-21 | 2002-03-07 | Novozymes A/S | Antimicrobial compositions |
| DE10042894A1 (de) | 2000-08-31 | 2002-03-14 | Thor Chemie Gmbh | Synergistische Biozidzusammensetzung mit 2-Methylisothiazolin-3-on |
| EP1184507A1 (fr) | 2000-09-04 | 2002-03-06 | Sanitized Ag | Composition antimicrobienne comprenant 1,2-Benzisothiazolin-3-one et son utilisation dans le finissage des textiles |
| EP1206933B1 (fr) | 2000-11-16 | 2006-05-17 | Johnson & Johnson Consumer France SAS | Compositions contenant glycol de capryle et iodopropynyl butylcarbamate |
| DE10112755A1 (de) | 2001-03-16 | 2002-10-02 | Bode Chemie Gmbh & Co Kg | Synergistische biozide Wirkstoffkombinationen, Zusammensetzungen, solche Wirkstoffkombinationen enthaltend, und Verwendung solcher Zusammensetzungen als Konservierungsmittel |
| WO2003013491A1 (fr) | 2001-07-30 | 2003-02-20 | Rohm And Haas Company | Compositions microbicides synergiques |
| EP1488699B1 (fr) | 2002-01-31 | 2013-01-16 | Rohm And Haas Company | Associations microbicides synergiques |
| GB0303876D0 (en) | 2003-02-20 | 2003-03-26 | Edmunds John M | Formulation |
| AU2004201059B2 (en) * | 2003-03-26 | 2009-06-04 | Rohm And Haas Company | Microbicidal composition |
| JP2004315507A (ja) * | 2003-04-07 | 2004-11-11 | Rohm & Haas Co | 殺微生物組成物 |
| JP4026829B2 (ja) * | 2003-07-24 | 2007-12-26 | ローム アンド ハース カンパニー | 殺微生物組成物 |
| US7935732B2 (en) | 2004-04-08 | 2011-05-03 | Isp Investments Inc. | Antimicrobial compositions |
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