JPS6212201B2 - - Google Patents
Info
- Publication number
- JPS6212201B2 JPS6212201B2 JP53119063A JP11906378A JPS6212201B2 JP S6212201 B2 JPS6212201 B2 JP S6212201B2 JP 53119063 A JP53119063 A JP 53119063A JP 11906378 A JP11906378 A JP 11906378A JP S6212201 B2 JPS6212201 B2 JP S6212201B2
- Authority
- JP
- Japan
- Prior art keywords
- compound
- test
- chloride
- methyl
- efficacy
- 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
- 239000013543 active substance Substances 0.000 claims description 5
- OOKUTCYPKPJYFV-UHFFFAOYSA-N 1-methyl-1h-imidazol-1-ium;bromide Chemical compound [Br-].CN1C=C[NH+]=C1 OOKUTCYPKPJYFV-UHFFFAOYSA-N 0.000 claims description 4
- GJYWPRKIEORZLX-UHFFFAOYSA-M 1,3-didecyl-2-methylimidazol-1-ium;chloride Chemical compound [Cl-].CCCCCCCCCCN1C=C[N+](CCCCCCCCCC)=C1C GJYWPRKIEORZLX-UHFFFAOYSA-M 0.000 claims description 3
- 239000000417 fungicide Substances 0.000 claims description 3
- 230000000855 fungicidal effect Effects 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 23
- 125000000217 alkyl group Chemical group 0.000 description 8
- 241000195493 Cryptophyta Species 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- 239000000725 suspension Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 244000286779 Hansenula anomala Species 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 241000894006 Bacteria Species 0.000 description 4
- 241000233866 Fungi Species 0.000 description 4
- 239000012153 distilled water Substances 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- ZTEHOZMYMCEYRM-UHFFFAOYSA-N 1-chlorodecane Chemical compound CCCCCCCCCCCl ZTEHOZMYMCEYRM-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- NBXYZCPGZXOGTN-UHFFFAOYSA-M [Cl-].C(CCCCCCC)[N+]1=C(N(C=C1)CCCCCCCC)C Chemical compound [Cl-].C(CCCCCCC)[N+]1=C(N(C=C1)CCCCCCCC)C NBXYZCPGZXOGTN-UHFFFAOYSA-M 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- -1 compounds 1,3 - Di-n-decyl-2-methyl-imidazolium chloride Chemical class 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 230000002906 microbiologic effect Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- 240000001817 Cereus hexagonus Species 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 241000588724 Escherichia coli Species 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 241000588767 Proteus vulgaris Species 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 230000002353 algacidal effect Effects 0.000 description 2
- 239000003619 algicide Substances 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 230000000844 anti-bacterial effect Effects 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 239000002798 polar solvent Substances 0.000 description 2
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 2
- 229920000053 polysorbate 80 Polymers 0.000 description 2
- 229940007042 proteus vulgaris Drugs 0.000 description 2
- 239000013049 sediment Substances 0.000 description 2
- 239000008399 tap water Substances 0.000 description 2
- 235000020679 tap water Nutrition 0.000 description 2
- 239000012085 test solution Substances 0.000 description 2
- ONVPFSYQVOTHPK-UHFFFAOYSA-M 1,3-didodecyl-2-methylimidazol-1-ium;chloride Chemical compound [Cl-].CCCCCCCCCCCCN1C=C[N+](CCCCCCCCCCCC)=C1C ONVPFSYQVOTHPK-UHFFFAOYSA-M 0.000 description 1
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- YZPNFYQRPJKWFJ-UHFFFAOYSA-N 2-methyl-1h-imidazol-1-ium;chloride Chemical compound Cl.CC1=NC=CN1 YZPNFYQRPJKWFJ-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 241000228197 Aspergillus flavus Species 0.000 description 1
- 241000193830 Bacillus <bacterium> Species 0.000 description 1
- 241000193755 Bacillus cereus Species 0.000 description 1
- 244000063299 Bacillus subtilis Species 0.000 description 1
- 235000014469 Bacillus subtilis Nutrition 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 241000222122 Candida albicans Species 0.000 description 1
- 244000249214 Chlorella pyrenoidosa Species 0.000 description 1
- 235000007091 Chlorella pyrenoidosa Nutrition 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 244000168141 Geotrichum candidum Species 0.000 description 1
- 235000017388 Geotrichum candidum Nutrition 0.000 description 1
- 235000014683 Hansenula anomala Nutrition 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical group Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
- 241001123663 Penicillium expansum Species 0.000 description 1
- 241000589517 Pseudomonas aeruginosa Species 0.000 description 1
- 241000191967 Staphylococcus aureus Species 0.000 description 1
- 241001045770 Trichophyton mentagrophytes Species 0.000 description 1
- FAYKZUNZJQUVIO-UHFFFAOYSA-M [Cl-].CCCCCCCCCCCC[N+]1=C(C)N(CCCCCCCC)C=C1 Chemical compound [Cl-].CCCCCCCCCCCC[N+]1=C(C)N(CCCCCCCC)C=C1 FAYKZUNZJQUVIO-UHFFFAOYSA-M 0.000 description 1
- 238000001720 action spectrum Methods 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 150000001449 anionic compounds Chemical class 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 229940027983 antiseptic and disinfectant quaternary ammonium compound Drugs 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical class [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229940095731 candida albicans Drugs 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 229960001927 cetylpyridinium chloride Drugs 0.000 description 1
- YMKDRGPMQRFJGP-UHFFFAOYSA-M cetylpyridinium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 YMKDRGPMQRFJGP-UHFFFAOYSA-M 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 150000004693 imidazolium salts Chemical class 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000036962 time dependent Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16D—COUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
- F16D65/00—Parts or details
- F16D65/02—Braking members; Mounting thereof
- F16D65/12—Discs; Drums for disc brakes
- F16D65/123—Discs; Drums for disc brakes comprising an annular disc secured to a hub member; Discs characterised by means for mounting
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16D—COUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
- F16D65/00—Parts or details
- F16D65/02—Braking members; Mounting thereof
- F16D2065/13—Parts or details of discs or drums
- F16D2065/1304—Structure
- F16D2065/1316—Structure radially segmented
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16D—COUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
- F16D65/00—Parts or details
- F16D65/02—Braking members; Mounting thereof
- F16D2065/13—Parts or details of discs or drums
- F16D2065/1304—Structure
- F16D2065/1328—Structure internal cavities, e.g. cooling channels
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16D—COUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
- F16D65/00—Parts or details
- F16D65/02—Braking members; Mounting thereof
- F16D2065/13—Parts or details of discs or drums
- F16D2065/134—Connection
- F16D2065/1356—Connection interlocking
- F16D2065/136—Connection interlocking with relative movement radially
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16D—COUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
- F16D65/00—Parts or details
- F16D65/02—Braking members; Mounting thereof
- F16D2065/13—Parts or details of discs or drums
- F16D2065/134—Connection
- F16D2065/1392—Connection elements
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- General Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Environmental Sciences (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Oncology (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Communicable Diseases (AREA)
- Mechanical Engineering (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2829137A DE2829137C2 (de) | 1978-07-03 | 1978-07-03 | Verwendung von 1.3-Di-n-decyl-2-methyl-imidazoliumchlorid oder -bromid als Mikrobicide |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5522652A JPS5522652A (en) | 1980-02-18 |
| JPS6212201B2 true JPS6212201B2 (US07655688-20100202-C00109.png) | 1987-03-17 |
Family
ID=6043404
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11906378A Granted JPS5522652A (en) | 1978-07-03 | 1978-09-27 | Bactericidal composition |
Country Status (13)
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0376312U (US07655688-20100202-C00109.png) * | 1989-11-27 | 1991-07-31 |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58161181U (ja) * | 1982-04-21 | 1983-10-27 | 日本電子株式会社 | クライオポンプ装置 |
| DE3617069A1 (de) * | 1986-05-21 | 1987-11-26 | Basf Ag | Verfahren zur herstellung von 3-methyl-1-vinyl-imidazoliumchloriden und ihre verwendung zur herstellung von polymerisaten |
| MX9504271A (es) * | 1994-02-10 | 1997-04-30 | Bp Chem Int Ltd | Liquidos ionicos. |
| ATE266008T1 (de) * | 2000-10-27 | 2004-05-15 | Centre Nat Rech Scient | Imidazolium-salze und die verwendung dieser ionischen flüssigkeiten als lösungsmittel und als katalysator |
| US20040077519A1 (en) * | 2002-06-28 | 2004-04-22 | The Procter & Gamble Co. | Ionic liquid based products and method of using the same |
| US7776810B2 (en) * | 2004-11-01 | 2010-08-17 | The Procter & Gamble Company | Compositions containing ionic liquid actives |
| US7737102B2 (en) * | 2004-11-01 | 2010-06-15 | The Procter & Gamble Company | Ionic liquids derived from functionalized anionic surfactants |
| US20060094616A1 (en) * | 2004-11-01 | 2006-05-04 | Hecht Stacie E | Ionic liquids derived from surfactants |
| US20060090271A1 (en) * | 2004-11-01 | 2006-05-04 | Price Kenneth N | Processes for modifying textiles using ionic liquids |
| US7939485B2 (en) * | 2004-11-01 | 2011-05-10 | The Procter & Gamble Company | Benefit agent delivery system comprising ionic liquid |
| US20060094621A1 (en) * | 2004-11-01 | 2006-05-04 | Jordan Glenn T Iv | Process for improving processability of a concentrate and compositions made by the same |
| US20060090777A1 (en) * | 2004-11-01 | 2006-05-04 | Hecht Stacie E | Multiphase cleaning compositions having ionic liquid phase |
| US7786065B2 (en) * | 2005-02-18 | 2010-08-31 | The Procter & Gamble Company | Ionic liquids derived from peracid anions |
| BRPI0713591A2 (pt) * | 2006-06-14 | 2012-11-06 | Ciba Holding Inc | composições antimicrobianas |
| JP4993443B2 (ja) * | 2006-07-28 | 2012-08-08 | 日本エンバイロケミカルズ株式会社 | 工業用殺菌剤およびそれを用いた殺菌方法 |
| GB0803026D0 (en) * | 2008-02-20 | 2008-03-26 | Enviroquest Group Ltd | External surface treatment system |
| US8303818B2 (en) * | 2010-06-24 | 2012-11-06 | Streamline Automation, Llc | Method and apparatus using an active ionic liquid for algae biofuel harvest and extraction |
| US8450111B2 (en) | 2010-03-02 | 2013-05-28 | Streamline Automation, Llc | Lipid extraction from microalgae using a single ionic liquid |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1521259A (fr) * | 1966-05-04 | 1968-04-12 | Shell Int Research | Procédé de préparation de n-alcoylimidazoles ou de n-alcénylimidazoles |
| DE2508420A1 (de) * | 1975-02-27 | 1976-09-09 | Goldschmidt Ag Th | Quaternaere imidazoliumverbindungen |
| DE2510525C3 (de) * | 1975-03-11 | 1978-03-30 | Th. Goldschmidt Ag, 4300 Essen | Quartäre 2-Alkylimidazoliumsalze |
-
1978
- 1978-07-03 DE DE2829137A patent/DE2829137C2/de not_active Expired
- 1978-09-27 JP JP11906378A patent/JPS5522652A/ja active Granted
- 1978-10-06 AT AT720978A patent/AT361137B/de not_active IP Right Cessation
- 1978-10-12 NL NLAANVRAGE7810275,A patent/NL173401C/xx not_active IP Right Cessation
- 1978-10-19 CH CH1080578A patent/CH637942A5/de not_active IP Right Cessation
- 1978-11-09 US US05/959,020 patent/US4189311A/en not_active Expired - Lifetime
- 1978-12-04 BE BE192120A patent/BE872502R/xx not_active IP Right Cessation
- 1978-12-06 GB GB7847431A patent/GB2024805B/en not_active Expired
- 1978-12-13 IT IT52279/78A patent/IT1107982B/it active
- 1978-12-15 SE SE7812918A patent/SE443976B/sv not_active IP Right Cessation
- 1978-12-20 AU AU42741/78A patent/AU519753B2/en not_active Expired
-
1979
- 1979-01-05 ES ES476626A patent/ES476626A2/es not_active Expired
- 1979-02-12 FR FR7903483A patent/FR2434156A2/fr active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0376312U (US07655688-20100202-C00109.png) * | 1989-11-27 | 1991-07-31 |
Also Published As
| Publication number | Publication date |
|---|---|
| NL173401C (nl) | 1984-01-16 |
| ES476626A2 (es) | 1979-07-01 |
| SE443976B (sv) | 1986-03-17 |
| JPS5522652A (en) | 1980-02-18 |
| GB2024805B (en) | 1982-09-08 |
| AT361137B (de) | 1981-02-25 |
| GB2024805A (en) | 1980-01-16 |
| ATA720978A (de) | 1980-07-15 |
| CH637942A5 (de) | 1983-08-31 |
| SE7812918L (sv) | 1980-01-04 |
| US4189311A (en) | 1980-02-19 |
| IT1107982B (it) | 1985-12-02 |
| IT7852279A0 (it) | 1978-12-13 |
| FR2434156B2 (US07655688-20100202-C00109.png) | 1983-04-01 |
| BE872502R (fr) | 1979-03-30 |
| AU4274178A (en) | 1980-03-20 |
| NL173401B (nl) | 1983-08-16 |
| AU519753B2 (en) | 1981-12-17 |
| DE2829137C2 (de) | 1982-09-16 |
| FR2434156A2 (fr) | 1980-03-21 |
| NL7810275A (nl) | 1980-01-07 |
| DE2829137A1 (de) | 1980-01-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPS6212201B2 (US07655688-20100202-C00109.png) | ||
| JPS6128668B2 (US07655688-20100202-C00109.png) | ||
| US4264604A (en) | Quinolonecarboxylic acid derivatives as bactericides | |
| US5073570A (en) | Mono-iodopropargyl esters of dicarboxylic anhydrides and their use as antimicrobial agents | |
| DE2510525C3 (de) | Quartäre 2-Alkylimidazoliumsalze | |
| JPS61291584A (ja) | 殺菌剤組成物および第３アミン化合物 | |
| US4386103A (en) | Dichloroamino acid derivatives useful as potent germicidal and fungicidal agents | |
| CA1113944A (en) | 2,3-substituted-1,2-isothiazolium salt antimicrobials | |
| US4535088A (en) | Propynylaminothiazole derivatives | |
| US4073926A (en) | Mono-quaternary ammonium salts of hydantoin and compositions thereof | |
| US4210645A (en) | (1,4)Dithiino(2,3-b)(1,2,5)-thiadiazole(3,4-e)pyrazine-6,7-dicarbonitrile | |
| US4207326A (en) | Antimicrobial quaternary pyrazole derivatives | |
| US4339453A (en) | Antimicrobial aminopyrimidinium salts | |
| DE3815700A1 (de) | Substituierte pyridyl(3)-alkanole, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel | |
| US4199581A (en) | 1,4-Dithiino pyrazine tetracarbonitriles | |
| US4481211A (en) | Microbiocidal substituted benzylimidazolium salts | |
| US4172133A (en) | (1,4)Dithiino(2,3-b)(1,3)thiazole-(4,5-e)pyrazine-6,7-dicarbonitriles | |
| US3467752A (en) | Preservation of organic materials from microbial attack with halogenated uracils | |
| JPH02231487A (ja) | 置換グアニジン及びアミジン化合物，並びにその製造方法 | |
| US4613620A (en) | Novel oxiodinium and thiaiodinium compounds | |
| US5334603A (en) | Composition and use of 3-phenyl-5-thiocyano-methylthio-1,3,4-thiadiazole-2(3h)thione | |
| US5155119A (en) | 3-(2-pyridinylthio)-N-oxide, 2-halo-2-propenenitrile compounds useful as antimicrobials | |
| US5180740A (en) | Composition and use of dimercapto-substituted dinitriles as an antimicrobial | |
| JP3459086B2 (ja) | 殺菌殺藻剤 | |
| US3873550A (en) | Antimicrobial bis(dihalonitro-methyl)pyridines |
