RU2656592C2 - Гетероциклические противомикробные соединения, предназначенные для применения в содержащих воду системах - Google Patents
Гетероциклические противомикробные соединения, предназначенные для применения в содержащих воду системах Download PDFInfo
- Publication number
- RU2656592C2 RU2656592C2 RU2014153679A RU2014153679A RU2656592C2 RU 2656592 C2 RU2656592 C2 RU 2656592C2 RU 2014153679 A RU2014153679 A RU 2014153679A RU 2014153679 A RU2014153679 A RU 2014153679A RU 2656592 C2 RU2656592 C2 RU 2656592C2
- Authority
- RU
- Russia
- Prior art keywords
- water
- glutaraldehyde
- oxazolo
- pyridine
- tetrahydro
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims abstract description 48
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 37
- 230000000845 anti-microbial effect Effects 0.000 title description 4
- 125000000623 heterocyclic group Chemical group 0.000 title 1
- 244000005700 microbiome Species 0.000 claims abstract description 23
- HOYUUPHKURKGKU-UHFFFAOYSA-N 2-butyl-3-ethyl-3,7,8,8a-tetrahydro-2H-[1,3]oxazolo[3,2-a]pyridine Chemical compound CCCCC1OC2CCC=CN2C1CC HOYUUPHKURKGKU-UHFFFAOYSA-N 0.000 claims abstract description 4
- VDEVQYAWDDJMMR-UHFFFAOYSA-N 2,3-dimethyl-3,7,8,8a-tetrahydro-2H-[1,3]oxazolo[3,2-a]pyridine Chemical compound CC1OC2CCC=CN2C1C VDEVQYAWDDJMMR-UHFFFAOYSA-N 0.000 claims abstract description 3
- JOSKBROZGUSOGM-UHFFFAOYSA-N 2-ethyl-2,3,4,8,9,9a-hexahydro-1H-pyrido[1,2-a]pyrimidine Chemical compound CCC1CCN2C=CCCC2N1 JOSKBROZGUSOGM-UHFFFAOYSA-N 0.000 claims abstract description 3
- ZFLTXZOXWZTJJJ-UHFFFAOYSA-N 2-heptan-3-yl-3-methyl-3,7,8,8a-tetrahydro-2H-[1,3]oxazolo[3,2-a]pyridine Chemical compound CCCCC(CC)C1OC2CCC=CN2C1C ZFLTXZOXWZTJJJ-UHFFFAOYSA-N 0.000 claims abstract description 3
- WDLXYSDSOHEMHO-UHFFFAOYSA-N 3,3-dimethyl-2,7,8,8a-tetrahydro-[1,3]oxazolo[3,2-a]pyridine Chemical compound CC1(C)COC2CCC=CN12 WDLXYSDSOHEMHO-UHFFFAOYSA-N 0.000 claims abstract description 3
- 238000000034 method Methods 0.000 claims description 9
- 239000000126 substance Substances 0.000 abstract description 15
- 230000000694 effects Effects 0.000 abstract description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 63
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 37
- 239000011541 reaction mixture Substances 0.000 description 29
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 20
- 241000894006 Bacteria Species 0.000 description 13
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 12
- 229910052757 nitrogen Inorganic materials 0.000 description 10
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 8
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 7
- 238000001816 cooling Methods 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 150000001412 amines Chemical class 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 239000010410 layer Substances 0.000 description 6
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 6
- 235000019341 magnesium sulphate Nutrition 0.000 description 6
- 230000014759 maintenance of location Effects 0.000 description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 239000012044 organic layer Substances 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 description 5
- 241001148470 aerobic bacillus Species 0.000 description 5
- 230000003115 biocidal effect Effects 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 238000011109 contamination Methods 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 230000000813 microbial effect Effects 0.000 description 5
- 150000001299 aldehydes Chemical class 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 238000000262 chemical ionisation mass spectrometry Methods 0.000 description 4
- 229940125904 compound 1 Drugs 0.000 description 4
- 239000012535 impurity Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 230000001580 bacterial effect Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 125000000753 cycloalkyl group Chemical group 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- LOKCTEFSRHRXRJ-UHFFFAOYSA-I dipotassium trisodium dihydrogen phosphate hydrogen phosphate dichloride Chemical compound P(=O)(O)(O)[O-].[K+].P(=O)(O)([O-])[O-].[Na+].[Na+].[Cl-].[K+].[Cl-].[Na+] LOKCTEFSRHRXRJ-UHFFFAOYSA-I 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 239000003345 natural gas Substances 0.000 description 3
- 239000002953 phosphate buffered saline Substances 0.000 description 3
- AHYITDFVMVPOTB-UHFFFAOYSA-N 2,3,4,8,9,9a-hexahydropyrido[2,1-b][1,3]oxazine Chemical compound C1CC=CN2CCCOC21 AHYITDFVMVPOTB-UHFFFAOYSA-N 0.000 description 2
- FERWBXLFSBWTDE-UHFFFAOYSA-N 3-aminobutan-2-ol Chemical compound CC(N)C(C)O FERWBXLFSBWTDE-UHFFFAOYSA-N 0.000 description 2
- AHZILZSKKSPIKM-UHFFFAOYSA-N 3-aminooctan-4-ol Chemical compound CCCCC(O)C(N)CC AHZILZSKKSPIKM-UHFFFAOYSA-N 0.000 description 2
- 241000203069 Archaea Species 0.000 description 2
- WUGQZFFCHPXWKQ-UHFFFAOYSA-N Propanolamine Chemical compound NCCCO WUGQZFFCHPXWKQ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 239000013058 crude material Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- WTSXICLFTPPDTL-UHFFFAOYSA-N pentane-1,3-diamine Chemical compound CCC(N)CCN WTSXICLFTPPDTL-UHFFFAOYSA-N 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000004659 sterilization and disinfection Methods 0.000 description 2
- 230000001629 suppression Effects 0.000 description 2
- 238000007725 thermal activation Methods 0.000 description 2
- 241001148471 unidentified anaerobic bacterium Species 0.000 description 2
- VDPLLINNMXFNQX-UHFFFAOYSA-N (1-aminocyclohexyl)methanol Chemical compound OCC1(N)CCCCC1 VDPLLINNMXFNQX-UHFFFAOYSA-N 0.000 description 1
- DFMNUVOZLQPWTG-UHFFFAOYSA-N (3-aminocyclohexyl)methanol Chemical compound NC1CCCC(CO)C1 DFMNUVOZLQPWTG-UHFFFAOYSA-N 0.000 description 1
- MEKOFIRRDATTAG-UHFFFAOYSA-N 2,2,5,8-tetramethyl-3,4-dihydrochromen-6-ol Chemical compound C1CC(C)(C)OC2=C1C(C)=C(O)C=C2C MEKOFIRRDATTAG-UHFFFAOYSA-N 0.000 description 1
- YPQYWQXZLFLCRZ-UHFFFAOYSA-N 2-amino-4-propan-2-ylheptan-3-ol Chemical compound CCCC(C(C)C)C(O)C(C)N YPQYWQXZLFLCRZ-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- 241000605775 Desulfovibrio longus Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 229940123973 Oxygen scavenger Drugs 0.000 description 1
- PLXBWHJQWKZRKG-UHFFFAOYSA-N Resazurin Chemical compound C1=CC(=O)C=C2OC3=CC(O)=CC=C3[N+]([O-])=C21 PLXBWHJQWKZRKG-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 241000589499 Thermus thermophilus Species 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- -1 but not limited to Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000000451 chemical ionisation Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000001332 colony forming effect Effects 0.000 description 1
- 229940125782 compound 2 Drugs 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 239000002173 cutting fluid Substances 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000004851 dishwashing Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229960000587 glutaral Drugs 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000005098 hot rolling Methods 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 150000002506 iron compounds Chemical class 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 150000002826 nitrites Chemical class 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000012545 processing 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
- 238000004064 recycling Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000002455 scale inhibitor Substances 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 239000011345 viscous material Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/10—Spiro-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261661518P | 2012-06-19 | 2012-06-19 | |
| US61/661,518 | 2012-06-19 | ||
| PCT/US2013/045418 WO2013191988A1 (en) | 2012-06-19 | 2013-06-12 | Heterocyclic antimicrobial compounds for use in water - containing systems |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2014153679A RU2014153679A (ru) | 2016-08-10 |
| RU2656592C2 true RU2656592C2 (ru) | 2018-06-06 |
Family
ID=48692677
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2014153679A RU2656592C2 (ru) | 2012-06-19 | 2013-06-12 | Гетероциклические противомикробные соединения, предназначенные для применения в содержащих воду системах |
Country Status (12)
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU733504A3 (ru) * | 1972-09-11 | 1980-05-05 | Руссель-Юклаф (Фирма) | Инсектицидный состав |
| WO2004071412A2 (en) * | 2003-02-04 | 2004-08-26 | Isp Investments Inc. | Antimicrobial oxazolidine/iodopropynyl-butyl carbamate composition containing less than 0.1wt% free formaldehyde |
| WO2008003606A1 (en) * | 2006-07-05 | 2008-01-10 | Ciba Holding Inc. | Dihalogeno-hydroxydiphenylether as antimicrobials in water treatment |
| WO2010039923A2 (en) * | 2008-10-01 | 2010-04-08 | Dow Global Technologies Inc. | Biocidal compositions and methods of use |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5480643A (en) | 1991-10-16 | 1996-01-02 | Ecolab Inc. | Stable antimicrobial dialdehyde composition and methods of use |
| US6034138A (en) | 1995-11-21 | 2000-03-07 | Block Drug Company, Inc. | Disinfectant composition |
| US7319131B2 (en) | 2003-03-07 | 2008-01-15 | Angus Chemical Company | Phenolic resins |
| EP2629608B1 (en) | 2010-12-17 | 2016-07-13 | Dow Global Technologies LLC | Protected antimicrobial compounds for high temperature applications |
| US8741928B2 (en) | 2010-12-17 | 2014-06-03 | Dow Global Technologies Llc | Protected antimicrobial compounds for high temperature applications |
-
2013
- 2013-06-12 WO PCT/US2013/045418 patent/WO2013191988A1/en active Application Filing
- 2013-06-12 IN IN10069DEN2014 patent/IN2014DN10069A/en unknown
- 2013-06-12 JP JP2015518452A patent/JP6250656B2/ja active Active
- 2013-06-12 PL PL13731226.0T patent/PL2861592T3/pl unknown
- 2013-06-12 RU RU2014153679A patent/RU2656592C2/ru active
- 2013-06-12 EP EP13731226.0A patent/EP2861592B1/en active Active
- 2013-06-12 BR BR112014030571-4A patent/BR112014030571B1/pt active IP Right Grant
- 2013-06-12 AU AU2013277511A patent/AU2013277511B2/en not_active Ceased
- 2013-06-12 CN CN201380032241.8A patent/CN104603135B/zh active Active
- 2013-06-12 US US14/565,867 patent/US9617278B2/en active Active
- 2013-06-12 CA CA2876015A patent/CA2876015C/en active Active
- 2013-06-14 AR ARP130102105 patent/AR091452A1/es active IP Right Grant
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU733504A3 (ru) * | 1972-09-11 | 1980-05-05 | Руссель-Юклаф (Фирма) | Инсектицидный состав |
| WO2004071412A2 (en) * | 2003-02-04 | 2004-08-26 | Isp Investments Inc. | Antimicrobial oxazolidine/iodopropynyl-butyl carbamate composition containing less than 0.1wt% free formaldehyde |
| WO2008003606A1 (en) * | 2006-07-05 | 2008-01-10 | Ciba Holding Inc. | Dihalogeno-hydroxydiphenylether as antimicrobials in water treatment |
| WO2010039923A2 (en) * | 2008-10-01 | 2010-04-08 | Dow Global Technologies Inc. | Biocidal compositions and methods of use |
Non-Patent Citations (3)
| Title |
|---|
| Langdale-Smith R. A., Facile synthesis of new heterocycles from glutaraldehyde, The Journal of Organic Chemistry, т. 36, n. 1, стр.:226 - 227, 1971. * |
| Langdale-Smith R. A., Facile synthesis of new heterocycles from glutaraldehyde, The Journal of Organic Chemistry, т. 36, n. 1, стр.:226 - 227, 1971. Yung-Sing Wong et al. Pyridine-Derived Oxazolidines as Chiral 3-Alkyl-4,5-dihydropyridinium and 3-Alkyl-3,4,5,6-tetrahydropyridinium Salt Equivalents, The Journal of Organic Chemistry, т. 62, n. 3, стр.:729 - 733, 1997. * |
| Yung-Sing Wong et al. Pyridine-Derived Oxazolidines as Chiral 3-Alkyl-4,5-dihydropyridinium and 3-Alkyl-3,4,5,6-tetrahydropyridinium Salt Equivalents, The Journal of Organic Chemistry, т. 62, n. 3, стр.:729 - 733, 1997. * |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2013277511B2 (en) | 2017-05-18 |
| RU2014153679A (ru) | 2016-08-10 |
| BR112014030571B1 (pt) | 2019-04-16 |
| PL2861592T3 (pl) | 2016-09-30 |
| US9617278B2 (en) | 2017-04-11 |
| CA2876015C (en) | 2020-01-07 |
| AR091452A1 (es) | 2015-02-04 |
| JP6250656B2 (ja) | 2017-12-20 |
| EP2861592B1 (en) | 2016-04-06 |
| BR112014030571A2 (pt) | 2017-07-25 |
| EP2861592A1 (en) | 2015-04-22 |
| CA2876015A1 (en) | 2013-12-27 |
| US20150336983A1 (en) | 2015-11-26 |
| CN104603135A (zh) | 2015-05-06 |
| IN2014DN10069A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 2015-08-14 |
| WO2013191988A1 (en) | 2013-12-27 |
| AU2013277511A1 (en) | 2015-01-15 |
| CN104603135B (zh) | 2016-10-05 |
| JP2015523358A (ja) | 2015-08-13 |
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