CA1102502A - Germicidal agent - Google Patents
Germicidal agentInfo
- Publication number
- CA1102502A CA1102502A CA280,024A CA280024A CA1102502A CA 1102502 A CA1102502 A CA 1102502A CA 280024 A CA280024 A CA 280024A CA 1102502 A CA1102502 A CA 1102502A
- Authority
- CA
- Canada
- Prior art keywords
- germicidal agent
- agent
- germicidal
- acid
- hydroxybenzoic acid
- 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
- 230000002070 germicidal effect Effects 0.000 title claims abstract description 57
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 72
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims abstract description 55
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims abstract description 19
- 230000002195 synergetic effect Effects 0.000 claims abstract description 17
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 claims abstract description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 10
- 150000003839 salts Chemical class 0.000 claims abstract description 10
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 8
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical compound NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 claims abstract description 8
- 125000005907 alkyl ester group Chemical group 0.000 claims abstract description 7
- -1 p-hydroxybenzoic acid compound Chemical class 0.000 claims abstract description 7
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 4
- 239000001257 hydrogen Substances 0.000 claims abstract description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 4
- 238000006243 chemical reaction Methods 0.000 claims abstract description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract 10
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract 9
- 239000004615 ingredient Substances 0.000 claims abstract 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 3
- WJJMNDUMQPNECX-UHFFFAOYSA-N dipicolinic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=N1 WJJMNDUMQPNECX-UHFFFAOYSA-N 0.000 claims description 10
- 239000000243 solution Substances 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 5
- 230000007797 corrosion Effects 0.000 claims description 5
- 238000005260 corrosion Methods 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 4
- 239000011707 mineral Substances 0.000 claims description 4
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 claims description 4
- 150000001491 aromatic compounds Chemical class 0.000 claims description 3
- 239000003112 inhibitor Substances 0.000 claims description 3
- 239000003381 stabilizer Substances 0.000 claims description 3
- LVPMIMZXDYBCDF-UHFFFAOYSA-N isocinchomeronic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)N=C1 LVPMIMZXDYBCDF-UHFFFAOYSA-N 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
- GJAWHXHKYYXBSV-UHFFFAOYSA-N pyridinedicarboxylic acid Natural products OC(=O)C1=CC=CN=C1C(O)=O GJAWHXHKYYXBSV-UHFFFAOYSA-N 0.000 claims description 2
- 239000007864 aqueous solution Substances 0.000 claims 2
- 239000005725 8-Hydroxyquinoline Substances 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 229960003540 oxyquinoline Drugs 0.000 claims 1
- 238000009877 rendering Methods 0.000 claims 1
- 229960002163 hydrogen peroxide Drugs 0.000 description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 239000013543 active substance Substances 0.000 description 11
- 239000000203 mixture Substances 0.000 description 10
- 238000007792 addition Methods 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- 244000052616 bacterial pathogen Species 0.000 description 5
- 244000005700 microbiome Species 0.000 description 5
- 239000002351 wastewater Substances 0.000 description 5
- 239000000654 additive Substances 0.000 description 4
- 239000000306 component Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000004659 sterilization and disinfection Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000011282 treatment Methods 0.000 description 4
- GEHMBYLTCISYNY-UHFFFAOYSA-N Ammonium sulfamate Chemical compound [NH4+].NS([O-])(=O)=O GEHMBYLTCISYNY-UHFFFAOYSA-N 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 235000010755 mineral Nutrition 0.000 description 3
- 150000002978 peroxides Chemical class 0.000 description 3
- 230000009182 swimming Effects 0.000 description 3
- 231100000331 toxic Toxicity 0.000 description 3
- 230000002588 toxic effect Effects 0.000 description 3
- FJNCXZZQNBKEJT-UHFFFAOYSA-N 8beta-hydroxymarrubiin Natural products O1C(=O)C2(C)CCCC3(C)C2C1CC(C)(O)C3(O)CCC=1C=COC=1 FJNCXZZQNBKEJT-UHFFFAOYSA-N 0.000 description 2
- 244000026610 Cynodon dactylon var. affinis Species 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000005352 clarification Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- NUVBSKCKDOMJSU-UHFFFAOYSA-N ethylparaben Chemical compound CCOC(=O)C1=CC=C(O)C=C1 NUVBSKCKDOMJSU-UHFFFAOYSA-N 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 235000015097 nutrients Nutrition 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000012266 salt solution Substances 0.000 description 2
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 2
- 229940048086 sodium pyrophosphate Drugs 0.000 description 2
- 230000001954 sterilising effect Effects 0.000 description 2
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 2
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- LDXJRKWFNNFDSA-UHFFFAOYSA-N 2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound C1CN(CC2=NNN=C21)CC(=O)N3CCN(CC3)C4=CN=C(N=C4)NCC5=CC(=CC=C5)OC(F)(F)F LDXJRKWFNNFDSA-UHFFFAOYSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- YLZOPXRUQYQQID-UHFFFAOYSA-N 3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]propan-1-one Chemical compound N1N=NC=2CN(CCC=21)CCC(=O)N1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F YLZOPXRUQYQQID-UHFFFAOYSA-N 0.000 description 1
- DFGKGUXTPFWHIX-UHFFFAOYSA-N 6-[2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]acetyl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)C1=CC2=C(NC(O2)=O)C=C1 DFGKGUXTPFWHIX-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 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 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000001741 anti-phlogistic effect Effects 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 238000003287 bathing Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229940041514 candida albicans extract Drugs 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000007857 degradation product Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000001877 deodorizing effect Effects 0.000 description 1
- 229910000396 dipotassium phosphate Inorganic materials 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- PJDVOLYULHZZAG-UHFFFAOYSA-N ethylmercury Chemical compound CC[Hg] PJDVOLYULHZZAG-UHFFFAOYSA-N 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000005452 food preservative Substances 0.000 description 1
- 235000019249 food preservative Nutrition 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 230000001408 fungistatic effect Effects 0.000 description 1
- 239000003864 humus Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- 239000000644 isotonic solution Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229940041669 mercury Drugs 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- DCNLOVYDMCVNRZ-UHFFFAOYSA-N phenylmercury(.) Chemical class [Hg]C1=CC=CC=C1 DCNLOVYDMCVNRZ-UHFFFAOYSA-N 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000003134 recirculating effect Effects 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Inorganic materials [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 239000012138 yeast extract Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/72—Treatment of water, waste water, or sewage by oxidation
- C02F1/722—Oxidation by peroxides
-
- 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
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/50—Treatment of water, waste water, or sewage by addition or application of a germicide or by oligodynamic treatment
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Hydrology & Water Resources (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2629081A DE2629081C2 (de) | 1976-06-29 | 1976-06-29 | Verwendung eines germiziden Mittels aus H↓2↓O↓2↓ und p-Hydroxybenzoesäurederivaten |
| DEP2629081.3 | 1976-06-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1102502A true CA1102502A (en) | 1981-06-09 |
Family
ID=5981700
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA280,024A Expired CA1102502A (en) | 1976-06-29 | 1977-06-07 | Germicidal agent |
Country Status (12)
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7354604B2 (en) | 2002-11-15 | 2008-04-08 | Virox Technologies Inc. | Hydrogen peroxide disinfectant containing a cyclic carboxylic acid and/or aromatic alcohol |
| US7632523B2 (en) | 2002-02-12 | 2009-12-15 | Virox Technologies Inc. | Enhanced activity hydrogen peroxide disinfectant |
| US8808755B2 (en) | 2004-05-14 | 2014-08-19 | Virox Technologies Inc. | Hydrogen peroxide-based skin disinfectant |
| US9233180B2 (en) | 2002-11-15 | 2016-01-12 | Virox Technologies Inc. | Hydrogen peroxide disinfectant containing a cyclic carboxylic acid and/or aromatic alcohol |
| US10450535B2 (en) | 2017-10-18 | 2019-10-22 | Virox Technologies Inc. | Shelf-stable hydrogen peroxide antimicrobial compositions |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3109070A1 (de) * | 1981-03-10 | 1982-09-30 | Bayrol Chemische Fabrik Gmbh, 8033 Planegg | Verfahren zur chemischen aufbereitung und entkeimung von waessern und wassersystemen |
| DE3625280A1 (de) * | 1986-07-25 | 1988-02-04 | Feldmann Hagen | Reiniger fuer trinkwasseranlagen |
| CA1321137C (en) * | 1988-08-08 | 1993-08-10 | Raymond C. Kralovic | Anti-microbial composition |
| ES2025018A6 (es) * | 1991-02-18 | 1992-03-01 | Bueno Flamarique Luis Miguel | Liquido limpiador de protesis dentales removibles. |
| DE4142319A1 (de) * | 1991-12-20 | 1993-06-24 | Henkel Kgaa | Wundantiseptikum |
| FR2748267B1 (fr) * | 1996-04-19 | 1999-04-23 | Assche Charles Jacques Van | Nouveaux procedes de traitements biocides des eaux industrielles et de baignade par application de substances inductrices de mortalite a la lumiere |
| DE19837068A1 (de) | 1998-08-17 | 2000-02-24 | Bayer Ag | Mittel zur Wasserbehandlung |
| US12203056B2 (en) | 2008-03-28 | 2025-01-21 | Ecolab Usa Inc. | Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents |
| US8809392B2 (en) | 2008-03-28 | 2014-08-19 | Ecolab Usa Inc. | Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents |
| US8871807B2 (en) | 2008-03-28 | 2014-10-28 | Ecolab Usa Inc. | Detergents capable of cleaning, bleaching, sanitizing and/or disinfecting textiles including sulfoperoxycarboxylic acids |
| CN102105443B (zh) | 2008-03-28 | 2014-05-28 | 埃科莱布有限公司 | 磺基过氧羧酸、它们的制备和用作漂白剂和抗微生物剂的方法 |
| FR2979243B1 (fr) * | 2011-08-25 | 2013-12-20 | Arkema France | Stabilisation de peroxyde d'hydrogene dans une composition de desinfection pour emballage |
| US9321664B2 (en) | 2011-12-20 | 2016-04-26 | Ecolab Usa Inc. | Stable percarboxylic acid compositions and uses thereof |
| FR2988088B1 (fr) * | 2012-03-16 | 2014-11-07 | Rhodia Operations | Procede de traitement d'effluents de production d'un compose aromatique derive de benzene dihydroxyle. |
| CN104254496B (zh) | 2012-03-30 | 2016-10-26 | 艺康美国股份有限公司 | 过乙酸/过氧化氢和过氧化物还原剂用于处理钻井液、压裂液、回流水和排放水的用途 |
| US8822719B1 (en) | 2013-03-05 | 2014-09-02 | Ecolab Usa Inc. | Peroxycarboxylic acid compositions suitable for inline optical or conductivity monitoring |
| US10165774B2 (en) | 2013-03-05 | 2019-01-01 | Ecolab Usa Inc. | Defoamer useful in a peracid composition with anionic surfactants |
| US20140256811A1 (en) | 2013-03-05 | 2014-09-11 | Ecolab Usa Inc. | Efficient stabilizer in controlling self accelerated decomposition temperature of peroxycarboxylic acid compositions with mineral acids |
| EP3841059A1 (en) | 2018-08-22 | 2021-06-30 | Ecolab USA Inc. | Hydrogen peroxide and peracid stabilization with molecules based on a pyridine carboxylic acid at c-3, -4 or -5 |
| US12096768B2 (en) | 2019-08-07 | 2024-09-24 | Ecolab Usa Inc. | Polymeric and solid-supported chelators for stabilization of peracid-containing compositions |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE807122C (de) * | 1950-02-04 | 1951-06-25 | Krisp Kg Kukirol | Verfahren zur Herstellung stark wirksamer bakterizider und desinfizierender Mittel |
| GB669612A (en) * | 1950-02-24 | 1952-04-02 | Ethan Allan Brown | Improvements in or relating to antiseptics of the peroxide type |
| CH310644A (de) * | 1950-08-16 | 1955-10-31 | Mueller Otto | Verfahren zur Herstellung eines Keime und Mikroorganismen abtötenden Mittels. |
| FR1347436A (fr) * | 1963-02-05 | 1963-12-27 | Heilmittelwerke Wien Gmbh | Procédé pour l'obtention de liquides exempts de germes et de produits de désinfection |
| SE401448B (sv) * | 1970-05-29 | 1978-05-16 | Henkel Kgaa | Vattenlosningar av ett desinfektionsmedel for desinfektion av medicinska redskap och instrument pa basis av aktivt syre |
| DE2235539A1 (de) * | 1972-07-20 | 1974-02-07 | Degussa | Verfahren zum entkeimen und entalgen von waessern und wassersystemen |
| ZA74799B (en) * | 1973-03-21 | 1974-12-24 | American Cyanamid Co | Substituted halotriazine derivatives as peroxygen bleach activators |
| US3948795A (en) * | 1973-12-21 | 1976-04-06 | Tokai Denka Kogyo Kabushiki Kaisha | Method of low-temperature activation of peroxides |
-
1976
- 1976-06-29 DE DE2629081A patent/DE2629081C2/de not_active Expired
-
1977
- 1977-06-07 CA CA280,024A patent/CA1102502A/en not_active Expired
- 1977-06-15 IT IT68394/77A patent/IT1083432B/it active
- 1977-06-20 SE SE7707117A patent/SE440849B/xx not_active IP Right Cessation
- 1977-06-21 NL NL7706807A patent/NL7706807A/xx not_active Application Discontinuation
- 1977-06-27 BE BE1008226A patent/BE856132A/xx not_active IP Right Cessation
- 1977-06-27 FR FR7719898A patent/FR2356600A1/fr active Granted
- 1977-06-28 FI FI772018A patent/FI66722C/fi not_active IP Right Cessation
- 1977-06-28 BR BR7704208A patent/BR7704208A/pt unknown
- 1977-06-28 DK DK287377A patent/DK152324C/da not_active IP Right Cessation
- 1977-06-29 JP JP7770677A patent/JPS533525A/ja active Pending
- 1977-06-29 GB GB27165/77A patent/GB1584170A/en not_active Expired
-
1985
- 1985-10-11 JP JP60225015A patent/JPS61218505A/ja active Granted
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7632523B2 (en) | 2002-02-12 | 2009-12-15 | Virox Technologies Inc. | Enhanced activity hydrogen peroxide disinfectant |
| US8637085B2 (en) | 2002-02-12 | 2014-01-28 | Virox Technologies Inc. | Enhanced activity hydrogen peroxide disinfectant |
| US8999400B2 (en) | 2002-02-12 | 2015-04-07 | Virox Technologies Inc. | Enhanced activity hydrogen peroxide disinfectant |
| US7354604B2 (en) | 2002-11-15 | 2008-04-08 | Virox Technologies Inc. | Hydrogen peroxide disinfectant containing a cyclic carboxylic acid and/or aromatic alcohol |
| US9233180B2 (en) | 2002-11-15 | 2016-01-12 | Virox Technologies Inc. | Hydrogen peroxide disinfectant containing a cyclic carboxylic acid and/or aromatic alcohol |
| US8808755B2 (en) | 2004-05-14 | 2014-08-19 | Virox Technologies Inc. | Hydrogen peroxide-based skin disinfectant |
| US9198935B2 (en) | 2004-05-14 | 2015-12-01 | Virox Technologies Inc. | Hydrogen peroxide-based skin disinfectant |
| US10450535B2 (en) | 2017-10-18 | 2019-10-22 | Virox Technologies Inc. | Shelf-stable hydrogen peroxide antimicrobial compositions |
| US10968417B2 (en) | 2017-10-18 | 2021-04-06 | Diversey, Inc. | Shelf-stable hydrogen peroxide antimicrobial compositions |
Also Published As
| Publication number | Publication date |
|---|---|
| BE856132A (fr) | 1977-12-27 |
| JPS6332326B2 (enrdf_load_stackoverflow) | 1988-06-29 |
| DK152324B (da) | 1988-02-22 |
| BR7704208A (pt) | 1978-03-21 |
| DK287377A (da) | 1977-12-30 |
| FR2356600A1 (fr) | 1978-01-27 |
| FI66722C (fi) | 1984-12-10 |
| GB1584170A (en) | 1981-02-11 |
| FI772018A7 (enrdf_load_stackoverflow) | 1977-12-30 |
| SE7707117L (sv) | 1977-12-30 |
| JPS533525A (en) | 1978-01-13 |
| JPS61218505A (ja) | 1986-09-29 |
| FI66722B (fi) | 1984-08-31 |
| DK152324C (da) | 1988-08-15 |
| FR2356600B1 (enrdf_load_stackoverflow) | 1982-06-04 |
| DE2629081A1 (de) | 1978-01-12 |
| IT1083432B (it) | 1985-05-21 |
| SE440849B (sv) | 1985-08-26 |
| DE2629081C2 (de) | 1987-01-15 |
| NL7706807A (nl) | 1978-01-02 |
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