PH26455A - Antimicrobial composition and method of use - Google Patents
Antimicrobial composition and method of use Download PDFInfo
- Publication number
- PH26455A PH26455A PH39303A PH39303A PH26455A PH 26455 A PH26455 A PH 26455A PH 39303 A PH39303 A PH 39303A PH 39303 A PH39303 A PH 39303A PH 26455 A PH26455 A PH 26455A
- Authority
- PH
- Philippines
- Prior art keywords
- coe
- biocide
- cee
- dibromo
- ere
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 31
- 238000000034 method Methods 0.000 title claims description 20
- 230000000845 anti-microbial effect Effects 0.000 title claims description 19
- 239000003139 biocide Substances 0.000 claims description 27
- 230000003115 biocidal effect Effects 0.000 claims description 24
- 241000894006 Bacteria Species 0.000 claims description 9
- 244000005700 microbiome Species 0.000 claims description 8
- 241000195493 Cryptophyta Species 0.000 claims description 6
- 238000012053 enzymatic serum creatinine assay Methods 0.000 claims description 6
- 230000002401 inhibitory effect Effects 0.000 claims description 5
- 230000002147 killing effect Effects 0.000 claims description 4
- 230000000813 microbial effect Effects 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 239000000498 cooling water Substances 0.000 claims description 3
- 239000012530 fluid Substances 0.000 claims description 3
- 239000002002 slurry Substances 0.000 claims description 3
- 239000003245 coal Substances 0.000 claims description 2
- JXVIIQLNUPXOII-UHFFFAOYSA-N Siduron Chemical compound CC1CCCCC1NC(=O)NC1=CC=CC=C1 JXVIIQLNUPXOII-UHFFFAOYSA-N 0.000 claims 2
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 claims 2
- WRRSFOZOETZUPG-FFHNEAJVSA-N (4r,4ar,7s,7ar,12bs)-9-methoxy-3-methyl-2,4,4a,7,7a,13-hexahydro-1h-4,12-methanobenzofuro[3,2-e]isoquinoline-7-ol;hydrate Chemical compound O.C([C@H]1[C@H](N(CC[C@@]112)C)C3)=C[C@H](O)[C@@H]1OC1=C2C3=CC=C1OC WRRSFOZOETZUPG-FFHNEAJVSA-N 0.000 claims 1
- VUZPGEIXNYGDJN-UHFFFAOYSA-N 1-nitroethanol Chemical compound CC(O)[N+]([O-])=O VUZPGEIXNYGDJN-UHFFFAOYSA-N 0.000 claims 1
- 101100332641 Caenorhabditis elegans eat-4 gene Proteins 0.000 claims 1
- 101100228200 Caenorhabditis elegans gly-5 gene Proteins 0.000 claims 1
- 101100233050 Caenorhabditis elegans ima-1 gene Proteins 0.000 claims 1
- 229920008347 Cellulose acetate propionate Polymers 0.000 claims 1
- 241000283715 Damaliscus lunatus Species 0.000 claims 1
- 241000282320 Panthera leo Species 0.000 claims 1
- 240000002834 Paulownia tomentosa Species 0.000 claims 1
- 235000010678 Paulownia tomentosa Nutrition 0.000 claims 1
- 241000568452 Sania Species 0.000 claims 1
- 241000120020 Tela Species 0.000 claims 1
- 241000607479 Yersinia pestis Species 0.000 claims 1
- 240000008042 Zea mays Species 0.000 claims 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims 1
- 230000004888 barrier function Effects 0.000 claims 1
- 235000013405 beer Nutrition 0.000 claims 1
- BBXRRTJNJCPGBU-UHFFFAOYSA-N beta-naphthyl N-acetylphenylalaninate Chemical compound C=1C=C2C=CC=CC2=CC=1OC(=O)C(NC(=O)C)CC1=CC=CC=C1 BBXRRTJNJCPGBU-UHFFFAOYSA-N 0.000 claims 1
- ONTQJDKFANPPKK-UHFFFAOYSA-L chembl3185981 Chemical compound [Na+].[Na+].CC1=CC(C)=C(S([O-])(=O)=O)C=C1N=NC1=CC(S([O-])(=O)=O)=C(C=CC=C2)C2=C1O ONTQJDKFANPPKK-UHFFFAOYSA-L 0.000 claims 1
- AGOYDEPGAOXOCK-KCBOHYOISA-N clarithromycin Chemical compound O([C@@H]1[C@@H](C)C(=O)O[C@@H]([C@@]([C@H](O)[C@@H](C)C(=O)[C@H](C)C[C@](C)([C@H](O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)N(C)C)O)[C@H]1C)OC)(C)O)CC)[C@H]1C[C@@](C)(OC)[C@@H](O)[C@H](C)O1 AGOYDEPGAOXOCK-KCBOHYOISA-N 0.000 claims 1
- 239000000571 coke Substances 0.000 claims 1
- 238000009470 controlled atmosphere packaging Methods 0.000 claims 1
- 235000005822 corn Nutrition 0.000 claims 1
- 125000000950 dibromo group Chemical group Br* 0.000 claims 1
- 239000011888 foil Substances 0.000 claims 1
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- LVDKZNITIUWNER-UHFFFAOYSA-N Bronopol Chemical compound OCC(Br)(CO)[N+]([O-])=O LVDKZNITIUWNER-UHFFFAOYSA-N 0.000 description 9
- 229960003168 bronopol Drugs 0.000 description 9
- 230000000694 effects Effects 0.000 description 8
- FMNZAHDAULEOSO-UHFFFAOYSA-N 2,2-dibromo-2-nitroethanol Chemical compound OCC(Br)(Br)[N+]([O-])=O FMNZAHDAULEOSO-UHFFFAOYSA-N 0.000 description 6
- 241000228245 Aspergillus niger Species 0.000 description 6
- 229920001817 Agar Polymers 0.000 description 5
- 239000008272 agar Substances 0.000 description 5
- 239000002054 inoculum Substances 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- 241000222122 Candida albicans Species 0.000 description 2
- 101100536354 Drosophila melanogaster tant gene Proteins 0.000 description 2
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 229940095731 candida albicans Drugs 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 230000003641 microbiacidal effect Effects 0.000 description 2
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- JSZOAYXJRCEYSX-UHFFFAOYSA-N 1-nitropropane Chemical compound CCC[N+]([O-])=O JSZOAYXJRCEYSX-UHFFFAOYSA-N 0.000 description 1
- KIPMDPDAFINLIV-UHFFFAOYSA-N 2-nitroethanol Chemical compound OCC[N+]([O-])=O KIPMDPDAFINLIV-UHFFFAOYSA-N 0.000 description 1
- XXONZJKORUUFIZ-UHFFFAOYSA-N 3-sulfanylpyridine-2-sulfonamide Chemical compound NS(=O)(=O)C1=NC=CC=C1S XXONZJKORUUFIZ-UHFFFAOYSA-N 0.000 description 1
- 101150067539 AMBP gene Proteins 0.000 description 1
- 241000238876 Acari Species 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 241000219498 Alnus glutinosa Species 0.000 description 1
- 241000428352 Amma Species 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- XUKUURHRXDUEBC-KAYWLYCHSA-N Atorvastatin Chemical compound C=1C=CC=CC=1C1=C(C=2C=CC(F)=CC=2)N(CC[C@@H](O)C[C@@H](O)CC(O)=O)C(C(C)C)=C1C(=O)NC1=CC=CC=C1 XUKUURHRXDUEBC-KAYWLYCHSA-N 0.000 description 1
- 244000276440 Betula nigra Species 0.000 description 1
- 238000009631 Broth culture Methods 0.000 description 1
- 208000032325 CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome Diseases 0.000 description 1
- 241000282994 Cervidae Species 0.000 description 1
- 241000543381 Cliftonia monophylla Species 0.000 description 1
- 206010010071 Coma Diseases 0.000 description 1
- 241000518994 Conta Species 0.000 description 1
- 241001649081 Dina Species 0.000 description 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 241000195619 Euglena gracilis Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 101001091379 Homo sapiens Kallikrein-5 Proteins 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 102100034868 Kallikrein-5 Human genes 0.000 description 1
- 101000941450 Lasioglossum laticeps Lasioglossin-1 Proteins 0.000 description 1
- 102100033356 Lecithin retinol acyltransferase Human genes 0.000 description 1
- 241000985627 Lota Species 0.000 description 1
- 241000252067 Megalops atlanticus Species 0.000 description 1
- 241001608711 Melo Species 0.000 description 1
- 241000751119 Mila <angiosperm> Species 0.000 description 1
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical class O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 241000940835 Pales Species 0.000 description 1
- 241000228143 Penicillium Species 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 229920001218 Pullulan Polymers 0.000 description 1
- 241000347485 Silurus glanis Species 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- HATRDXDCPOXQJX-UHFFFAOYSA-N Thapsigargin Natural products CCCCCCCC(=O)OC1C(OC(O)C(=C/C)C)C(=C2C3OC(=O)C(C)(O)C3(O)C(CC(C)(OC(=O)C)C12)OC(=O)CCC)C HATRDXDCPOXQJX-UHFFFAOYSA-N 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 230000031709 bromination Effects 0.000 description 1
- 238000005893 bromination reaction Methods 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 235000014121 butter Nutrition 0.000 description 1
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 239000012990 dithiocarbamate Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- -1 glutaraldehyde Chemical class 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
- KEBHLNDPKPIPLI-UHFFFAOYSA-N hydron;2-(3h-inden-4-yloxymethyl)morpholine;chloride Chemical compound Cl.C=1C=CC=2C=CCC=2C=1OCC1CNCCO1 KEBHLNDPKPIPLI-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 230000007775 late Effects 0.000 description 1
- 108010084957 lecithin-retinol acyltransferase Proteins 0.000 description 1
- 235000015250 liver sausages Nutrition 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000005007 materials handling Methods 0.000 description 1
- PSGAAPLEWMOORI-PEINSRQWSA-N medroxyprogesterone acetate Chemical compound C([C@@]12C)CC(=O)C=C1[C@@H](C)C[C@@H]1[C@@H]2CC[C@]2(C)[C@@](OC(C)=O)(C(C)=O)CC[C@H]21 PSGAAPLEWMOORI-PEINSRQWSA-N 0.000 description 1
- WABYCCJHARSRBH-UHFFFAOYSA-N metaclazepam Chemical compound C12=CC(Br)=CC=C2N(C)C(COC)CN=C1C1=CC=CC=C1Cl WABYCCJHARSRBH-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 239000010813 municipal solid waste Substances 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 239000002332 oil field water Substances 0.000 description 1
- 239000003129 oil well Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 238000000675 plasmon resonance energy transfer Methods 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 235000019423 pullulan Nutrition 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000001603 reducing effect Effects 0.000 description 1
- 210000000582 semen Anatomy 0.000 description 1
- 238000013207 serial dilution Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds containing nitrogen-to-oxygen bonds
- A01N33/18—Nitro compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/13—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups
- C07C205/26—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups and being further substituted by halogen 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/251,361 US5055493A (en) | 1988-09-30 | 1988-09-30 | Antimicrobial composition and method of use in oil well flooding |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PH26455A true PH26455A (en) | 1992-07-27 |
Family
ID=22951624
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PH39303A PH26455A (en) | 1988-09-30 | 1989-09-29 | Antimicrobial composition and method of use |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US5055493A (el) |
| EP (1) | EP0364789B1 (el) |
| JP (1) | JPH02134302A (el) |
| KR (1) | KR900004252A (el) |
| CN (1) | CN1032619C (el) |
| AR (1) | AR247068A1 (el) |
| AT (1) | ATE86435T1 (el) |
| AU (1) | AU625176B2 (el) |
| BR (1) | BR8904980A (el) |
| CA (1) | CA1321749C (el) |
| DE (1) | DE68905294T2 (el) |
| ES (1) | ES2046422T3 (el) |
| GR (1) | GR3007851T3 (el) |
| HK (1) | HK48295A (el) |
| IL (1) | IL91851A (el) |
| MX (1) | MX170951B (el) |
| MY (1) | MY104232A (el) |
| NO (1) | NO178213C (el) |
| PH (1) | PH26455A (el) |
| ZA (1) | ZA897446B (el) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5075510A (en) * | 1990-12-20 | 1991-12-24 | Great Lakes Chemical Corporation | Process for the preparation of bromonitro-alcohols |
| US5144087A (en) * | 1990-12-20 | 1992-09-01 | Great Lakes Chemical Corp. | Process for the preparation of dibromonitro-alcohols and blends with dibromonitro-alcohols |
| AU2005312894B2 (en) * | 2004-12-10 | 2011-08-18 | Bromine Compounds Ltd. | Methods, formulations and articles of manufacturing for disinfecting substances, products and structures |
| US20080196892A1 (en) * | 2007-02-20 | 2008-08-21 | Lau Philip Y | Enzyme enhanced oil recovery (EEOR) for waterflooding operations |
| IL183445A (en) | 2007-05-27 | 2013-02-28 | Bromine Compounds Ltd | Continuous process of preparing bromopicrin |
| CN101849547B (zh) * | 2010-06-04 | 2012-12-26 | 内蒙古天晨科技有限责任公司 | 一种高效杀菌剂 |
| CN103478170A (zh) * | 2013-09-18 | 2014-01-01 | 中国海洋石油总公司 | 一种适用于高氨氮高cod水质的溴类杀生剂的制法 |
| CN106572660B (zh) * | 2014-08-01 | 2020-12-22 | 巴克曼实验室国际公司 | 杀微生物剂及其用途 |
| CN108935463A (zh) * | 2018-08-15 | 2018-12-07 | 新疆水处理工程技术研究中心有限公司 | 一种油田回注水复合杀菌剂及其制作方法 |
| CN109258668A (zh) * | 2018-10-31 | 2019-01-25 | 福州盛世凌云环保科技有限公司 | 一种高效复合多菌灵杀菌灭藻剂及其制备方法 |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3024192A (en) * | 1959-11-13 | 1962-03-06 | Commerical Solvents Corp | Process for the control of bacteria in a flooding process for the recovery of petroleum oil |
| GB1057131A (en) * | 1963-02-21 | 1967-02-01 | Boots Pure Drug Co Ltd | New antibacterial and antifungal compositions |
| DE1287259B (de) * | 1967-04-26 | 1969-01-16 | Henkel & Cie Gmbh | Verwendung von Nitroalkoholen als Potenzierungsmittel in antimikrobiellen Mitteln |
| NL170411C (nl) * | 1968-07-19 | 1982-11-01 | Henkel Kgaa | Werkwijze voor het bereiden van broomnitroalcoholen. |
| BE757999A (fr) * | 1969-10-28 | 1971-04-26 | Henkel & Cie Gmbh | Procede de preparation de bromonitro-alcools. |
| JPS6054281B2 (ja) * | 1977-03-28 | 1985-11-29 | 株式会社パ−マケム・アジア | 殺菌剤 |
| JPS61289063A (ja) * | 1985-06-17 | 1986-12-19 | Paamakemu Asia:Kk | ジブロモニトロ化合物の製造法 |
| JPH07523B2 (ja) * | 1986-10-03 | 1995-01-11 | ソマ−ル株式会社 | 工業用防菌剤 |
| JPH0737424B2 (ja) * | 1986-10-09 | 1995-04-26 | 株式会社パ−マケム・アジア | 新規なニトロエ−テル誘導体及びその製造法 |
| US4732905A (en) * | 1987-03-13 | 1988-03-22 | Betz Laboratories, Inc. | Biocidal compositions and use thereof containing a synergistic mixture of 2-bromo-2-nitropropane-1,3-diol and a mixture of 5-chloro-2-methyl-4-isothiazolin-3-one and 2-methyl-4-isothiazolin-3-one |
| JPH0647524B2 (ja) * | 1987-06-19 | 1994-06-22 | ソマ−ル株式会社 | 工業用防菌剤 |
| JP2577226B2 (ja) * | 1987-07-06 | 1997-01-29 | 株式会社 パ−マケム・アジア | 製紙用スライム防除剤 |
| JP2534726B2 (ja) * | 1987-09-12 | 1996-09-18 | ソマール株式会社 | 工業用殺菌剤 |
| JPH0780727B2 (ja) * | 1987-10-15 | 1995-08-30 | ソマール株式会社 | 工業用殺菌剤 |
| JP2752106B2 (ja) * | 1987-10-26 | 1998-05-18 | 株式会社片山化学工業研究所 | 工業用殺菌剤及び殺菌方法 |
| JP2584835B2 (ja) * | 1988-08-16 | 1997-02-26 | 株式会社片山化学研究所 | 工業用殺菌剤 |
-
1988
- 1988-09-30 US US07/251,361 patent/US5055493A/en not_active Expired - Fee Related
-
1989
- 1989-09-29 AT AT89118090T patent/ATE86435T1/de not_active IP Right Cessation
- 1989-09-29 AR AR89315053A patent/AR247068A1/es active
- 1989-09-29 EP EP89118090A patent/EP0364789B1/en not_active Expired - Lifetime
- 1989-09-29 NO NO893892A patent/NO178213C/no unknown
- 1989-09-29 ZA ZA897446A patent/ZA897446B/xx unknown
- 1989-09-29 MY MYPI89001386A patent/MY104232A/en unknown
- 1989-09-29 DE DE8989118090T patent/DE68905294T2/de not_active Expired - Fee Related
- 1989-09-29 CA CA000615326A patent/CA1321749C/en not_active Expired - Fee Related
- 1989-09-29 PH PH39303A patent/PH26455A/en unknown
- 1989-09-29 MX MX017755A patent/MX170951B/es unknown
- 1989-09-29 ES ES198989118090T patent/ES2046422T3/es not_active Expired - Lifetime
- 1989-09-29 IL IL9185189A patent/IL91851A/en not_active IP Right Cessation
- 1989-09-30 KR KR1019890014082A patent/KR900004252A/ko not_active Application Discontinuation
- 1989-09-30 CN CN89108367A patent/CN1032619C/zh not_active Expired - Fee Related
- 1989-09-30 JP JP1256932A patent/JPH02134302A/ja active Pending
- 1989-10-02 BR BR898904980A patent/BR8904980A/pt not_active Application Discontinuation
- 1989-10-02 AU AU42433/89A patent/AU625176B2/en not_active Ceased
-
1993
- 1993-05-14 GR GR920403061T patent/GR3007851T3/el unknown
-
1995
- 1995-03-30 HK HK48295A patent/HK48295A/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| AU4243389A (en) | 1990-04-05 |
| DE68905294T2 (de) | 1993-06-17 |
| EP0364789A1 (en) | 1990-04-25 |
| ZA897446B (en) | 1990-07-25 |
| HK48295A (en) | 1995-04-07 |
| EP0364789B1 (en) | 1993-03-10 |
| IL91851A0 (en) | 1990-06-10 |
| CN1032619C (zh) | 1996-08-28 |
| CA1321749C (en) | 1993-08-31 |
| AU625176B2 (en) | 1992-07-02 |
| ES2046422T3 (es) | 1994-02-01 |
| NO178213C (no) | 1996-02-14 |
| KR900004252A (ko) | 1990-04-12 |
| IL91851A (en) | 1994-01-25 |
| MY104232A (en) | 1994-02-28 |
| BR8904980A (pt) | 1990-05-08 |
| AR247068A1 (es) | 1994-11-30 |
| DE68905294D1 (de) | 1993-04-15 |
| CN1041512A (zh) | 1990-04-25 |
| MX170951B (es) | 1993-09-22 |
| JPH02134302A (ja) | 1990-05-23 |
| US5055493A (en) | 1991-10-08 |
| GR3007851T3 (el) | 1993-08-31 |
| NO178213B (no) | 1995-11-06 |
| NO893892L (no) | 1990-04-02 |
| ATE86435T1 (de) | 1993-03-15 |
| NO893892D0 (no) | 1989-09-29 |
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