CA1232706A - Antimicrobial compositions - Google Patents
Antimicrobial compositionsInfo
- Publication number
- CA1232706A CA1232706A CA000467210A CA467210A CA1232706A CA 1232706 A CA1232706 A CA 1232706A CA 000467210 A CA000467210 A CA 000467210A CA 467210 A CA467210 A CA 467210A CA 1232706 A CA1232706 A CA 1232706A
- Authority
- CA
- Canada
- Prior art keywords
- solvent
- mixture
- phenoxyarsine
- antimicrobial
- plasticizer
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 230000000845 anti-microbial effect Effects 0.000 title claims abstract description 19
- 239000000203 mixture Substances 0.000 title claims description 42
- 239000002904 solvent Substances 0.000 claims abstract description 24
- AVKUWNUBPFREQI-UHFFFAOYSA-N phenoxyarsenic Chemical compound [As]OC1=CC=CC=C1 AVKUWNUBPFREQI-UHFFFAOYSA-N 0.000 claims abstract description 22
- 229920002994 synthetic fiber Polymers 0.000 claims abstract description 20
- 239000004599 antimicrobial Substances 0.000 claims abstract description 10
- 150000001875 compounds Chemical class 0.000 claims abstract description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
- 239000001257 hydrogen Substances 0.000 claims abstract description 3
- 125000000217 alkyl group Chemical group 0.000 claims abstract 2
- 239000004014 plasticizer Substances 0.000 claims description 20
- VCRZAKVGPJFABU-UHFFFAOYSA-N 10-phenoxarsinin-10-yloxyphenoxarsinine Chemical compound C12=CC=CC=C2OC2=CC=CC=C2[As]1O[As]1C2=CC=CC=C2OC2=CC=CC=C21 VCRZAKVGPJFABU-UHFFFAOYSA-N 0.000 claims description 12
- 238000004519 manufacturing process Methods 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 10
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 8
- 229920002554 vinyl polymer Polymers 0.000 claims description 8
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 7
- 239000004800 polyvinyl chloride Substances 0.000 claims description 7
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical group OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 claims description 6
- 229920005989 resin Polymers 0.000 claims description 4
- 239000011347 resin Substances 0.000 claims description 4
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical group OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 claims description 2
- 229960005323 phenoxyethanol Drugs 0.000 claims description 2
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical group OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims 3
- 235000019445 benzyl alcohol Nutrition 0.000 claims 1
- 239000000126 substance Substances 0.000 abstract description 3
- 239000003795 chemical substances by application Substances 0.000 abstract description 2
- 101100188540 Candida albicans (strain SC5314 / ATCC MYA-2876) OBPA gene Proteins 0.000 description 7
- -1 aliphatic alcohols Chemical class 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000012141 concentrate Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 4
- VYKJIKQKGQORET-UHFFFAOYSA-N phenoxyarsane Chemical class [AsH2]OC1=CC=CC=C1 VYKJIKQKGQORET-UHFFFAOYSA-N 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 2
- 208000037062 Polyps Diseases 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 235000019987 cider Nutrition 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000002118 epoxides Chemical class 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- NMRPBPVERJPACX-UHFFFAOYSA-N octan-3-ol Chemical compound CCCCCC(O)CC NMRPBPVERJPACX-UHFFFAOYSA-N 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- FEXBEKLLSUWSIM-UHFFFAOYSA-N 2-Butyl-4-methylphenol Chemical compound CCCCC1=CC(C)=CC=C1O FEXBEKLLSUWSIM-UHFFFAOYSA-N 0.000 description 1
- PLLBRTOLHQQAQQ-UHFFFAOYSA-N 8-methylnonan-1-ol Chemical compound CC(C)CCCCCCCO PLLBRTOLHQQAQQ-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- GHKOFFNLGXMVNJ-UHFFFAOYSA-N Didodecyl thiobispropanoate Chemical compound CCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCC GHKOFFNLGXMVNJ-UHFFFAOYSA-N 0.000 description 1
- ZVFDTKUVRCTHQE-UHFFFAOYSA-N Diisodecyl phthalate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC(C)C ZVFDTKUVRCTHQE-UHFFFAOYSA-N 0.000 description 1
- 239000003508 Dilauryl thiodipropionate Substances 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 239000004440 Isodecyl alcohol Substances 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 235000019304 dilauryl thiodipropionate Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 230000001408 fungistatic effect Effects 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- YJOMWQQKPKLUBO-UHFFFAOYSA-L lead(2+);phthalate Chemical compound [Pb+2].[O-]C(=O)C1=CC=CC=C1C([O-])=O YJOMWQQKPKLUBO-UHFFFAOYSA-L 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 235000019645 odor Nutrition 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000723 toxicological property Toxicity 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/59—Arsenic- or antimony-containing compounds
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
-
- 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
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
- A01N55/02—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur containing metal atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0058—Biocides
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Toxicology (AREA)
- Biodiversity & Conservation Biology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH618483 | 1983-11-17 | ||
| CH6184/83 | 1983-11-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1232706A true CA1232706A (en) | 1988-02-16 |
Family
ID=4305584
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000467210A Expired CA1232706A (en) | 1983-11-17 | 1984-11-07 | Antimicrobial compositions |
Country Status (9)
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4891391A (en) * | 1985-01-03 | 1990-01-02 | Morton Thiokol, Inc. | Compositions containing antimicrobial agents in combination with stabilizers |
Families Citing this family (50)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0144726B2 (de) * | 1983-11-17 | 1995-05-24 | Akzo Nobel N.V. | Antimikrobielle Mischungen |
| US4663077A (en) * | 1984-06-11 | 1987-05-05 | Morton Thiokol Inc. | Microbiocidal compositions comprising an aryl alkanol and a microbiocidal compound dissolved therein |
| US4683080A (en) * | 1984-06-11 | 1987-07-28 | Morton Thiokol, Inc. | Microbiocidal compositions comprising an aryl alkanol and a microbiocidal compound dissolved therein |
| US4624679A (en) * | 1985-01-03 | 1986-11-25 | Morton Thiokol, Inc. | Compositions containing antimicorbial agents in combination with stabilizers |
| DE3629010A1 (de) * | 1986-08-27 | 1988-03-03 | Siemens Ag | Keimarme dentalausruestung |
| BE1003042A3 (fr) * | 1989-03-29 | 1991-11-05 | Hamon Sobelco Sa | Feuilles de ruissellement resistantes a l'encrassement biologique. |
| CA2037282C (en) * | 1990-04-02 | 1997-01-28 | Nuno M. Rei | Microbicides immobilized in water-soluble thermoplastic polymeric resins and aqueous dispersions of microbicides prepared therefrom |
| US5554373A (en) * | 1993-11-05 | 1996-09-10 | Seabrook; Samuel G. | Compositions containing anti-microbial agents and methods for making and using same |
| US5906825A (en) * | 1997-10-20 | 1999-05-25 | Magellan Companies, Inc. | Polymers containing antimicrobial agents and methods for making and using same |
| US6627676B1 (en) | 1999-08-27 | 2003-09-30 | Richard George | Antimicrobial biocidic fiber-plastic composite and method of making same |
| US6444737B1 (en) | 2000-04-05 | 2002-09-03 | 3M Innovative Properties Company | Water-dispersed polymer stabilizer |
| CA2463908A1 (en) * | 2001-10-18 | 2003-04-24 | Bristol-Myers Squibb Company | Human glucagon-like-peptide-1 mimics and their use in the treatment of diabetes and related conditions |
| EP1447066B1 (en) | 2003-02-12 | 2008-10-01 | The Procter & Gamble Company | Comfortable diaper |
| EP2177188B1 (en) | 2003-02-12 | 2015-11-04 | The Procter and Gamble Company | Absorbent Core For An Absorbent Article |
| US7323044B1 (en) | 2007-01-22 | 2008-01-29 | Troy Corporation | Biocidal compositions |
| GB2460727B (en) | 2007-06-18 | 2012-04-11 | Procter & Gamble | Disposable absorbent article with substantially continously distributed absorbent particulate polymer material and method |
| JP5259705B2 (ja) | 2007-06-18 | 2013-08-07 | ザ プロクター アンド ギャンブル カンパニー | ほぼ連続的に分布した吸収性粒子状ポリマー材料を含む封止された吸収性コアを備える使い捨て吸収性物品 |
| CN102014826A (zh) | 2008-04-29 | 2011-04-13 | 宝洁公司 | 制造具有抗应变芯覆盖件的吸收芯的方法 |
| EP2329803B1 (en) | 2009-12-02 | 2019-06-19 | The Procter & Gamble Company | Apparatus and method for transferring particulate material |
| PL3338750T5 (pl) | 2011-06-10 | 2023-10-09 | The Procter & Gamble Company | Struktura chłonna do wyrobów chłonnych |
| PL2532332T5 (pl) | 2011-06-10 | 2018-07-31 | The Procter And Gamble Company | Pieluszka jednorazowego użytku o zredukowanym połączeniu pomiędzy wkładem chłonnym a warstwą spodnią |
| RU2013156991A (ru) | 2011-06-10 | 2015-07-20 | Дзе Проктер Энд Гэмбл Компани | Абсорбирующая сердцевина для одноразовых абсорбирующих изделий |
| EP2532329B1 (en) | 2011-06-10 | 2018-09-19 | The Procter and Gamble Company | Method and apparatus for making absorbent structures with absorbent material |
| ES2459724T3 (es) | 2011-06-10 | 2014-05-12 | The Procter & Gamble Company | Método y aparato para hacer estructuras absorbentes con material absorbente |
| PH12013502575A1 (en) | 2011-06-10 | 2014-02-10 | Procter & Gamble | Absorbent structure for absorbent articles |
| DE202012013585U1 (de) | 2011-06-10 | 2018-01-17 | The Procter & Gamble Company | Einwegwindel |
| CN107550648A (zh) | 2012-11-13 | 2018-01-09 | 宝洁公司 | 具有通道和标志的吸收制品 |
| PL2740452T3 (pl) | 2012-12-10 | 2022-01-31 | The Procter & Gamble Company | Wyrób chłonny o wysokiej zawartości materiału chłonnego |
| EP2740450A1 (en) | 2012-12-10 | 2014-06-11 | The Procter & Gamble Company | Absorbent core with high superabsorbent material content |
| US10639215B2 (en) | 2012-12-10 | 2020-05-05 | The Procter & Gamble Company | Absorbent articles with channels and/or pockets |
| PL2740449T3 (pl) | 2012-12-10 | 2019-07-31 | The Procter & Gamble Company | Artykuł chłonny o wysokiej zawartości materiału chłonnego |
| US8979815B2 (en) | 2012-12-10 | 2015-03-17 | The Procter & Gamble Company | Absorbent articles with channels |
| US9216116B2 (en) | 2012-12-10 | 2015-12-22 | The Procter & Gamble Company | Absorbent articles with channels |
| US9216118B2 (en) | 2012-12-10 | 2015-12-22 | The Procter & Gamble Company | Absorbent articles with channels and/or pockets |
| EP2813201B1 (en) | 2013-06-14 | 2017-11-01 | The Procter and Gamble Company | Absorbent article and absorbent core forming channels when wet |
| WO2015031229A1 (en) | 2013-08-27 | 2015-03-05 | The Procter & Gamble Company | Absorbent articles with channels |
| US9987176B2 (en) | 2013-08-27 | 2018-06-05 | The Procter & Gamble Company | Absorbent articles with channels |
| RU2636366C2 (ru) | 2013-09-16 | 2017-11-22 | Дзе Проктер Энд Гэмбл Компани | Абсорбирующие изделия с каналами и индицирующими элементами |
| US11207220B2 (en) | 2013-09-16 | 2021-12-28 | The Procter & Gamble Company | Absorbent articles with channels and signals |
| EP3351225B1 (en) | 2013-09-19 | 2021-12-29 | The Procter & Gamble Company | Absorbent cores having material free areas |
| US9789009B2 (en) | 2013-12-19 | 2017-10-17 | The Procter & Gamble Company | Absorbent articles having channel-forming areas and wetness indicator |
| EP2886092B1 (en) | 2013-12-19 | 2016-09-14 | The Procter and Gamble Company | Absorbent cores having channel-forming areas and c-wrap seals |
| EP2905001B1 (en) | 2014-02-11 | 2017-01-04 | The Procter and Gamble Company | Method and apparatus for making an absorbent structure comprising channels |
| EP2949300B1 (en) | 2014-05-27 | 2017-08-02 | The Procter and Gamble Company | Absorbent core with absorbent material pattern |
| RU2017133027A (ru) | 2015-03-16 | 2019-04-16 | Дзе Проктер Энд Гэмбл Компани | Абсорбирующие изделия повышенной прочности |
| JP6542390B2 (ja) | 2015-05-12 | 2019-07-10 | ザ プロクター アンド ギャンブル カンパニーＴｈｅ Ｐｒｏｃｔｅｒ ＆ Ｇａｍｂｌｅ Ｃｏｍｐａｎｙ | 改善されたコア−バックシート接着を有する吸収性物品 |
| CN107683126A (zh) | 2015-05-29 | 2018-02-09 | 宝洁公司 | 具有槽和润湿指示标记的吸收制品 |
| EP3167859B1 (en) | 2015-11-16 | 2020-05-06 | The Procter and Gamble Company | Absorbent cores having material free areas |
| EP3238678B1 (en) | 2016-04-29 | 2019-02-27 | The Procter and Gamble Company | Absorbent core with transversal folding lines |
| EP3238676B1 (en) | 2016-04-29 | 2019-01-02 | The Procter and Gamble Company | Absorbent core with profiled distribution of absorbent material |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3228830A (en) * | 1962-11-05 | 1966-01-11 | Dow Chemical Co | Biocidally-active phenoxarsine-containing polymeric materials |
| USRE29409E (en) * | 1965-03-15 | 1977-09-20 | Ventron Corporation | Phenoxarsine compounds incorporated into resins with phenols |
| US3288674A (en) * | 1965-03-15 | 1966-11-29 | Scient Chemicals Inc | Phenoxarsine compounds incorporated into resins with phenols |
| GB1085970A (en) * | 1966-09-12 | 1967-10-04 | Scient Chemicals Inc | Vinyl resin compositions |
| US3544610A (en) * | 1969-01-23 | 1970-12-01 | Dow Chemical Co | Phenoxy- and substituted phenoxy-phenoxarsine compounds |
| US3660353A (en) * | 1970-04-01 | 1972-05-02 | Dow Chemical Co | Monomers and polymers of 10-(alkenyl) oxyphenoxarsines |
| US3636024A (en) * | 1970-05-04 | 1972-01-18 | Dow Chemical Co | Halogenated-10 10'-riphenoxarsines |
| US3689449A (en) * | 1971-04-01 | 1972-09-05 | Ventron Corp | Composition for imparting anti-bacterial characteristics to vinyl resins |
| US4049822A (en) * | 1975-08-04 | 1977-09-20 | Ventron Corporation | Microbiocidal compositions comprising a solution of a phenoxarsine compound |
| EP0144726B2 (de) * | 1983-11-17 | 1995-05-24 | Akzo Nobel N.V. | Antimikrobielle Mischungen |
| US4683080A (en) * | 1984-06-11 | 1987-07-28 | Morton Thiokol, Inc. | Microbiocidal compositions comprising an aryl alkanol and a microbiocidal compound dissolved therein |
-
1984
- 1984-11-02 EP EP84113170A patent/EP0144726B2/de not_active Expired - Lifetime
- 1984-11-02 DE DE8484113170T patent/DE3478387D1/de not_active Expired
- 1984-11-02 AT AT84113170T patent/ATE43471T1/de not_active IP Right Cessation
- 1984-11-07 ZA ZA848714A patent/ZA848714B/xx unknown
- 1984-11-07 DK DK530384A patent/DK165960C/da not_active IP Right Cessation
- 1984-11-07 CA CA000467210A patent/CA1232706A/en not_active Expired
- 1984-11-15 NO NO844569A patent/NO164574C/no not_active IP Right Cessation
- 1984-11-15 JP JP59241572A patent/JPS60116614A/ja active Granted
-
1986
- 1986-04-28 US US06/859,189 patent/US5488065A/en not_active Expired - Lifetime
-
1996
- 1996-01-25 US US08/591,326 patent/US5629342A/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4891391A (en) * | 1985-01-03 | 1990-01-02 | Morton Thiokol, Inc. | Compositions containing antimicrobial agents in combination with stabilizers |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0144726B2 (de) | 1995-05-24 |
| NO844569L (no) | 1985-05-20 |
| DE3478387D1 (en) | 1989-07-06 |
| NO164574C (no) | 1990-10-24 |
| JPS60116614A (ja) | 1985-06-24 |
| JPH0553765B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1993-08-10 |
| EP0144726A3 (en) | 1985-07-10 |
| DK165960B (da) | 1993-02-22 |
| US5629342A (en) | 1997-05-13 |
| NO164574B (no) | 1990-07-16 |
| DK530384A (da) | 1985-05-18 |
| ZA848714B (en) | 1985-07-31 |
| DK165960C (da) | 1993-07-26 |
| US5488065A (en) | 1996-01-30 |
| ATE43471T1 (de) | 1989-06-15 |
| EP0144726B1 (de) | 1989-05-31 |
| DK530384D0 (da) | 1984-11-07 |
| EP0144726A2 (de) | 1985-06-19 |
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Legal Events
| Date | Code | Title | Description |
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| MKEX | Expiry |