NO300523B1 - Vandig blanding omfattende polymert biguanid og anvendelse derav - Google Patents
Vandig blanding omfattende polymert biguanid og anvendelse derav Download PDFInfo
- Publication number
- NO300523B1 NO300523B1 NO914327A NO914327A NO300523B1 NO 300523 B1 NO300523 B1 NO 300523B1 NO 914327 A NO914327 A NO 914327A NO 914327 A NO914327 A NO 914327A NO 300523 B1 NO300523 B1 NO 300523B1
- Authority
- NO
- Norway
- Prior art keywords
- biguanide
- mixture
- aqueous
- polymeric biguanide
- aqueous mixture
- Prior art date
Links
- 229940123208 Biguanide Drugs 0.000 title claims abstract description 43
- XNCOSPRUTUOJCJ-UHFFFAOYSA-N Biguanide Chemical compound NC(N)=NC(N)=N XNCOSPRUTUOJCJ-UHFFFAOYSA-N 0.000 title claims abstract description 31
- 239000000203 mixture Substances 0.000 title claims description 60
- VAZJLPXFVQHDFB-UHFFFAOYSA-N 1-(diaminomethylidene)-2-hexylguanidine Polymers CCCCCCN=C(N)N=C(N)N VAZJLPXFVQHDFB-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229920000642 polymer Polymers 0.000 claims description 11
- 244000005700 microbiome Species 0.000 claims description 5
- 239000007864 aqueous solution Substances 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- 230000002401 inhibitory effect Effects 0.000 claims description 3
- QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 claims description 2
- AAQCEEMRPKWTMP-UHFFFAOYSA-N [Br].CC1=CC=CC=C1O Chemical group [Br].CC1=CC=CC=C1O AAQCEEMRPKWTMP-UHFFFAOYSA-N 0.000 claims 1
- 238000003860 storage Methods 0.000 abstract description 6
- 239000002609 medium Substances 0.000 abstract description 5
- 239000012736 aqueous medium Substances 0.000 abstract description 4
- 239000003139 biocide Substances 0.000 abstract description 2
- 230000003115 biocidal effect Effects 0.000 abstract 1
- 230000000845 anti-microbial effect Effects 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 10
- 239000000463 material Substances 0.000 description 10
- 150000004283 biguanides Chemical class 0.000 description 9
- -1 biguanide compound Chemical class 0.000 description 7
- 239000011521 glass Substances 0.000 description 7
- FRPHFZCDPYBUAU-UHFFFAOYSA-N Bromocresolgreen Chemical compound CC1=C(Br)C(O)=C(Br)C=C1C1(C=2C(=C(Br)C(O)=C(Br)C=2)C)C2=CC=CC=C2S(=O)(=O)O1 FRPHFZCDPYBUAU-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- 239000000243 solution Substances 0.000 description 5
- 125000001183 hydrocarbyl group Chemical group 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 2
- 229920002413 Polyhexanide Polymers 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 239000004599 antimicrobial Substances 0.000 description 2
- 230000001580 bacterial effect Effects 0.000 description 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical class OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 2
- TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000000645 desinfectant Substances 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- FDZZZRQASAIRJF-UHFFFAOYSA-M malachite green Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 FDZZZRQASAIRJF-UHFFFAOYSA-M 0.000 description 2
- 229940107698 malachite green Drugs 0.000 description 2
- 230000000813 microbial effect Effects 0.000 description 2
- 230000002906 microbiologic effect Effects 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- YGKOYVNJPRSSRX-UHFFFAOYSA-M (4-dodecylphenyl)methyl-trimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCC1=CC=C(C[N+](C)(C)C)C=C1 YGKOYVNJPRSSRX-UHFFFAOYSA-M 0.000 description 1
- QAGFPFWZCJWYRP-UHFFFAOYSA-N 1,1-bis(hydroxymethyl)urea Chemical compound NC(=O)N(CO)CO QAGFPFWZCJWYRP-UHFFFAOYSA-N 0.000 description 1
- OYWRDHBGMCXGFY-UHFFFAOYSA-N 1,2,3-triazinane Chemical compound C1CNNNC1 OYWRDHBGMCXGFY-UHFFFAOYSA-N 0.000 description 1
- TUBQDCKAWGHZPF-UHFFFAOYSA-N 1,3-benzothiazol-2-ylsulfanylmethyl thiocyanate Chemical compound C1=CC=C2SC(SCSC#N)=NC2=C1 TUBQDCKAWGHZPF-UHFFFAOYSA-N 0.000 description 1
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 1
- DTOUUUZOYKYHEP-UHFFFAOYSA-N 1,3-bis(2-ethylhexyl)-5-methyl-1,3-diazinan-5-amine Chemical compound CCCCC(CC)CN1CN(CC(CC)CCCC)CC(C)(N)C1 DTOUUUZOYKYHEP-UHFFFAOYSA-N 0.000 description 1
- XOILGBPDXMVFIP-UHFFFAOYSA-N 1-(diiodomethylsulfonyl)-4-methylbenzene Chemical compound CC1=CC=C(S(=O)(=O)C(I)I)C=C1 XOILGBPDXMVFIP-UHFFFAOYSA-N 0.000 description 1
- SIQZJFKTROUNPI-UHFFFAOYSA-N 1-(hydroxymethyl)-5,5-dimethylhydantoin Chemical compound CC1(C)N(CO)C(=O)NC1=O SIQZJFKTROUNPI-UHFFFAOYSA-N 0.000 description 1
- PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 description 1
- GKQHIYSTBXDYNQ-UHFFFAOYSA-M 1-dodecylpyridin-1-ium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+]1=CC=CC=C1 GKQHIYSTBXDYNQ-UHFFFAOYSA-M 0.000 description 1
- IQDVXXOBJULTFE-UHFFFAOYSA-M 1-dodecylpyridin-1-ium;hydron;sulfate Chemical compound OS([O-])(=O)=O.CCCCCCCCCCCC[N+]1=CC=CC=C1 IQDVXXOBJULTFE-UHFFFAOYSA-M 0.000 description 1
- OLQJQHSAWMFDJE-UHFFFAOYSA-N 2-(hydroxymethyl)-2-nitropropane-1,3-diol Chemical compound OCC(CO)(CO)[N+]([O-])=O OLQJQHSAWMFDJE-UHFFFAOYSA-N 0.000 description 1
- NWPCFCBFUXXJIE-UHFFFAOYSA-N 2-(hydroxymethylamino)ethanol Chemical compound OCCNCO NWPCFCBFUXXJIE-UHFFFAOYSA-N 0.000 description 1
- RXGSAYBOEDPICZ-UHFFFAOYSA-N 2-[6-[[amino-(diaminomethylideneamino)methylidene]amino]hexyl]-1-(diaminomethylidene)guanidine Chemical compound NC(N)=NC(N)=NCCCCCCN=C(N)N=C(N)N RXGSAYBOEDPICZ-UHFFFAOYSA-N 0.000 description 1
- DHVLDKHFGIVEIP-UHFFFAOYSA-N 2-bromo-2-(bromomethyl)pentanedinitrile Chemical compound BrCC(Br)(C#N)CCC#N DHVLDKHFGIVEIP-UHFFFAOYSA-N 0.000 description 1
- OIMQLXQDHOFORS-UHFFFAOYSA-N 2-chloro-2-(chloromethyl)pentanedinitrile Chemical compound ClCC(Cl)(C#N)CCC#N OIMQLXQDHOFORS-UHFFFAOYSA-N 0.000 description 1
- SXVFGEJOKLTATI-UHFFFAOYSA-N 2-chloro-n,n-bis(hydroxymethyl)acetamide Chemical compound OCN(CO)C(=O)CCl SXVFGEJOKLTATI-UHFFFAOYSA-N 0.000 description 1
- TXNSZCSYBXHETP-UHFFFAOYSA-N 2-chloro-n-(hydroxymethyl)acetamide Chemical compound OCNC(=O)CCl TXNSZCSYBXHETP-UHFFFAOYSA-N 0.000 description 1
- PUSPAPGHKSLKKH-UHFFFAOYSA-N 2-methyl-1,2-thiazolidin-3-one Chemical compound CN1SCCC1=O PUSPAPGHKSLKKH-UHFFFAOYSA-N 0.000 description 1
- PZOGAKOZVSTZSO-UHFFFAOYSA-N 2-methyl-5,6-dihydro-4h-cyclopenta[d][1,2]thiazol-3-one Chemical compound C1CCC2=C1SN(C)C2=O PZOGAKOZVSTZSO-UHFFFAOYSA-N 0.000 description 1
- 229940061334 2-phenylphenol Drugs 0.000 description 1
- 229940099451 3-iodo-2-propynylbutylcarbamate Drugs 0.000 description 1
- WYVVKGNFXHOCQV-UHFFFAOYSA-N 3-iodoprop-2-yn-1-yl butylcarbamate Chemical compound CCCCNC(=O)OCC#CI WYVVKGNFXHOCQV-UHFFFAOYSA-N 0.000 description 1
- KWFFEQXPFFDJER-UHFFFAOYSA-N 4-[3-(4-aminophenoxy)propoxy]aniline Chemical compound C1=CC(N)=CC=C1OCCCOC1=CC=C(N)C=C1 KWFFEQXPFFDJER-UHFFFAOYSA-N 0.000 description 1
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 description 1
- 229940046305 5-bromo-5-nitro-1,3-dioxane Drugs 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- LVDKZNITIUWNER-UHFFFAOYSA-N Bronopol Chemical compound OCC(Br)(CO)[N+]([O-])=O LVDKZNITIUWNER-UHFFFAOYSA-N 0.000 description 1
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 1
- RGHNJXZEOKUKBD-SQOUGZDYSA-M D-gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O RGHNJXZEOKUKBD-SQOUGZDYSA-M 0.000 description 1
- RUPBZQFQVRMKDG-UHFFFAOYSA-M Didecyldimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCC[N+](C)(C)CCCCCCCCCC RUPBZQFQVRMKDG-UHFFFAOYSA-M 0.000 description 1
- 241000588724 Escherichia coli Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 description 1
- WYNCHZVNFNFDNH-UHFFFAOYSA-N Oxazolidine Chemical compound C1COCN1 WYNCHZVNFNFDNH-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 241001061127 Thione Species 0.000 description 1
- XEFQLINVKFYRCS-UHFFFAOYSA-N Triclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1Cl XEFQLINVKFYRCS-UHFFFAOYSA-N 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229940053991 aldehydes and derivative Drugs 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 230000001098 anti-algal effect Effects 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000000843 anti-fungal effect Effects 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 229940027987 antiseptic and disinfectant phenol and derivative Drugs 0.000 description 1
- 229940027983 antiseptic and disinfectant quaternary ammonium compound Drugs 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 description 1
- JBIROUFYLSSYDX-UHFFFAOYSA-M benzododecinium chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 JBIROUFYLSSYDX-UHFFFAOYSA-M 0.000 description 1
- UUSQFLGKGQEVCM-UHFFFAOYSA-M benzoxonium chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](CCO)(CCO)CC1=CC=CC=C1 UUSQFLGKGQEVCM-UHFFFAOYSA-M 0.000 description 1
- PEJWCDZMACRFHF-UHFFFAOYSA-M benzyl-(1,1-dichlorododecyl)-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC(Cl)(Cl)[N+](C)(C)CC1=CC=CC=C1 PEJWCDZMACRFHF-UHFFFAOYSA-M 0.000 description 1
- FADYGXGJTNYCHZ-UHFFFAOYSA-M benzyl-dodecyl-diethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](CC)(CC)CC1=CC=CC=C1 FADYGXGJTNYCHZ-UHFFFAOYSA-M 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- XVBRCOKDZVQYAY-UHFFFAOYSA-N bronidox Chemical compound [O-][N+](=O)C1(Br)COCOC1 XVBRCOKDZVQYAY-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- SXPWTBGAZSPLHA-UHFFFAOYSA-M cetalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SXPWTBGAZSPLHA-UHFFFAOYSA-M 0.000 description 1
- 229960000228 cetalkonium chloride Drugs 0.000 description 1
- DVBJBNKEBPCGSY-UHFFFAOYSA-M cetylpyridinium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 DVBJBNKEBPCGSY-UHFFFAOYSA-M 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
- VXIVSQZSERGHQP-UHFFFAOYSA-N chloroacetamide Chemical compound NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 0.000 description 1
- DHNRXBZYEKSXIM-UHFFFAOYSA-N chloromethylisothiazolinone Chemical compound CN1SC(Cl)=CC1=O DHNRXBZYEKSXIM-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- QWJNFFYFEKXZBF-UHFFFAOYSA-N cyanocyanamide Chemical compound N#CNC#N QWJNFFYFEKXZBF-UHFFFAOYSA-N 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- NMCCNOZOBBWFMN-UHFFFAOYSA-N davicil Chemical compound CS(=O)(=O)C1=C(Cl)C(Cl)=NC(Cl)=C1Cl NMCCNOZOBBWFMN-UHFFFAOYSA-N 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- WLCFKPHMRNPAFZ-UHFFFAOYSA-M didodecyl(dimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCC WLCFKPHMRNPAFZ-UHFFFAOYSA-M 0.000 description 1
- 238000003113 dilution method Methods 0.000 description 1
- VZVNXHMIKPHKHV-UHFFFAOYSA-M dimethyl-octadecyl-(2-phenylpropan-2-yl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C(C)(C)C1=CC=CC=C1 VZVNXHMIKPHKHV-UHFFFAOYSA-M 0.000 description 1
- WSDISUOETYTPRL-UHFFFAOYSA-N dmdm hydantoin Chemical compound CC1(C)N(CO)C(=O)N(CO)C1=O WSDISUOETYTPRL-UHFFFAOYSA-N 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 229940050410 gluconate Drugs 0.000 description 1
- 229960000587 glutaral Drugs 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- 239000013529 heat transfer fluid Substances 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 1
- 239000004312 hexamethylene tetramine Substances 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- ZCTXEAQXZGPWFG-UHFFFAOYSA-N imidurea Chemical compound O=C1NC(=O)N(CO)C1NC(=O)NCNC(=O)NC1C(=O)NC(=O)N1CO ZCTXEAQXZGPWFG-UHFFFAOYSA-N 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 239000002054 inoculum Substances 0.000 description 1
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 description 1
- 125000002346 iodo group Chemical group I* 0.000 description 1
- MGIYRDNGCNKGJU-UHFFFAOYSA-N isothiazolinone Chemical compound O=C1C=CSN1 MGIYRDNGCNKGJU-UHFFFAOYSA-N 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000005555 metalworking Methods 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000006916 nutrient agar Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 235000010292 orthophenyl phenol Nutrition 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000007793 ph indicator Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 150000007979 thiazole derivatives Chemical class 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- YBNLWIZAWPBUKQ-UHFFFAOYSA-N trichloro(trichloromethylsulfonyl)methane Chemical compound ClC(Cl)(Cl)S(=O)(=O)C(Cl)(Cl)Cl YBNLWIZAWPBUKQ-UHFFFAOYSA-N 0.000 description 1
- CEYYIKYYFSTQRU-UHFFFAOYSA-M trimethyl(tetradecyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCC[N+](C)(C)C CEYYIKYYFSTQRU-UHFFFAOYSA-M 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 238000011179 visual inspection Methods 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
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/04—Nitrogen directly attached to aliphatic or cycloaliphatic 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides
- A01N47/42—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides containing —N=CX2 groups, e.g. isothiourea
- A01N47/44—Guanidine; Derivatives thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Developing Agents For Electrophotography (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Luminescent Compositions (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB909024133A GB9024133D0 (en) | 1990-11-06 | 1990-11-06 | Aqueous composition |
Publications (3)
Publication Number | Publication Date |
---|---|
NO914327D0 NO914327D0 (no) | 1991-11-05 |
NO914327L NO914327L (no) | 1992-05-07 |
NO300523B1 true NO300523B1 (no) | 1997-06-16 |
Family
ID=10684960
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO914327A NO300523B1 (no) | 1990-11-06 | 1991-11-05 | Vandig blanding omfattende polymert biguanid og anvendelse derav |
Country Status (19)
Country | Link |
---|---|
US (1) | US5990174A (zh) |
EP (1) | EP0485079B2 (zh) |
JP (1) | JP3232348B2 (zh) |
KR (1) | KR100216859B1 (zh) |
AT (1) | ATE155647T1 (zh) |
AU (1) | AU646097B2 (zh) |
CA (1) | CA2054300C (zh) |
DE (1) | DE69126945T3 (zh) |
DK (1) | DK0485079T4 (zh) |
ES (1) | ES2103784T5 (zh) |
FI (1) | FI915209A (zh) |
GB (2) | GB9024133D0 (zh) |
GR (2) | GR3024741T3 (zh) |
IE (1) | IE913645A1 (zh) |
NO (1) | NO300523B1 (zh) |
NZ (1) | NZ240295A (zh) |
PT (1) | PT99425B (zh) |
TW (1) | TW221371B (zh) |
ZA (1) | ZA918386B (zh) |
Families Citing this family (34)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR960004500B1 (ko) * | 1992-10-20 | 1996-04-06 | 주식회사유공 | 살균조성물 및 이를 함유하는 비누 |
EP0696353A4 (en) * | 1993-04-28 | 1998-01-21 | Environmental Test Systems | METHOD AND METHOD FOR DETERMINING POLYMER BIGUANIDES IN AQUEOUS LIQUIDS |
GB9322132D0 (en) * | 1993-10-27 | 1993-12-15 | Zeneca Ltd | Antimicrobial treatment of textile materials |
US5668084A (en) * | 1995-08-01 | 1997-09-16 | Zeneca Inc. | Polyhexamethylene biguanide and surfactant composition and method for preventing waterline residue |
DE19604475A1 (de) * | 1996-02-08 | 1997-08-14 | Fresenius Ag | Verwendung von PHMB zur Behandlung von durch sich intrazellulär vermehrende Erreger verursachten Infektionen |
GB9827884D0 (en) | 1998-12-18 | 1999-02-10 | Zeneca Ltd | Process |
WO2000037258A1 (en) * | 1998-12-18 | 2000-06-29 | Avecia Limited | Ink-jet printing process using polymeric biguanides |
US8806549B1 (en) * | 1999-10-13 | 2014-08-12 | Starz Entertainment, Llc | Pre-storing a portion of a program to allow user control of playback |
US7122505B1 (en) | 1999-10-21 | 2006-10-17 | Arch Chemicals Inc. | Composition for controlling the growth of algae, fungi and pathogenic organisms in water |
JP3883763B2 (ja) * | 1999-11-18 | 2007-02-21 | 花王株式会社 | 繊維製品防臭処理剤 |
MXPA01008719A (es) * | 2000-09-06 | 2002-04-10 | Air Products Polymers Lp | Conservacion de emulsiones polimericas usando compuestos cationicos. |
GB0124860D0 (en) * | 2001-10-17 | 2001-12-05 | Avecia Ltd | Composition and media |
AU2003210557A1 (en) * | 2002-01-17 | 2003-09-02 | Verichem, Inc. | Synergistic mixtures of o-phenylphenol and other microbiocides |
US20100160445A1 (en) * | 2002-01-17 | 2010-06-24 | Carlson Paul E | Synergistic Mixtures of OPP and DGH |
GB0207655D0 (en) | 2002-04-02 | 2002-05-15 | Avecia Ltd | Compositions and processes |
US8100872B2 (en) | 2002-10-23 | 2012-01-24 | Tyco Healthcare Group Lp | Medical dressing containing antimicrobial agent |
US20060073185A1 (en) * | 2002-12-13 | 2006-04-06 | Bausch & Lomb Incorporated | Method and composition for contact lenses |
US7619017B2 (en) | 2003-05-19 | 2009-11-17 | Wacker Chemical Corporation | Polymer emulsions resistant to biodeterioration |
US20050118058A1 (en) * | 2003-12-01 | 2005-06-02 | Erning Xia | Gentle preservative compositions for self-preserving solutions |
US20050118128A1 (en) * | 2003-12-01 | 2005-06-02 | Borazjani Roya N. | Disinfection efficacy of lens care regimen |
US20050119221A1 (en) * | 2003-12-01 | 2005-06-02 | Erning Xia | Use of a cationic polysaccharide to enhance biocidal efficacies |
US20050119141A1 (en) * | 2003-12-01 | 2005-06-02 | Irene Quenville | Stability enhancement of solutions containing antimicrobial agents |
US20050118129A1 (en) * | 2003-12-01 | 2005-06-02 | Erning Xia | Gentle and enhanced preservative systems |
US20050266095A1 (en) * | 2004-06-01 | 2005-12-01 | Erning Xia | Gentle preservative compositions |
DE102005017845A1 (de) * | 2005-04-18 | 2006-10-19 | Lohmann & Rauscher Gmbh & Co. Kg | Autosterile, antiseptische Kollagenzubereitungen, ihre Verwendung und Verfahren zu ihrer Herstellung |
US20060292105A1 (en) * | 2005-06-28 | 2006-12-28 | Lever O W Jr | Topical preservative compositions |
US20070149428A1 (en) * | 2005-12-14 | 2007-06-28 | Bausch & Lomb Incorporated | Method of Packaging a Lens |
US20070203039A1 (en) * | 2005-12-21 | 2007-08-30 | Roya Borazjani | Method for cleaning and maintaining contact lenses and related system and kit |
US20070142321A1 (en) * | 2005-12-21 | 2007-06-21 | Roya Borazjani | Method for preventing growth of bacteria on contact lenses with eye drops |
US20070196329A1 (en) * | 2006-01-20 | 2007-08-23 | Erning Xia | Disinfection efficacy of lens care regimen for rigid gas permeable contact lenses |
GB0903375D0 (en) * | 2009-02-27 | 2009-04-08 | Bio Technics Ltd | Disinfectant composition comprising a biguanide compound |
US8829053B2 (en) | 2011-12-07 | 2014-09-09 | Rochal Industries Llp | Biocidal compositions and methods of using the same |
WO2015161860A1 (en) * | 2014-04-25 | 2015-10-29 | Frank Flechsig | Improved biocide compositions based on calcium fluoride as well as uses thereof |
KR102479429B1 (ko) * | 2021-05-14 | 2022-12-19 | 유상선 | 연속적 수거가 가능한 친환경 선택형 대용량 재활용품 분리수거함 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB702268A (en) * | 1949-08-22 | 1954-01-13 | Francis Leslie Rose | Polymeric diguanides |
GB1114155A (en) * | 1964-08-24 | 1968-05-15 | Evans Medical Ltd | Guanidino derivatives |
GB1152243A (en) * | 1965-11-26 | 1969-05-14 | Ici Ltd | Process for the Manufacture of Polymeric Diguanides |
FR2517208A1 (fr) † | 1981-12-02 | 1983-06-03 | Pos Lab | Composition pour le nettoyage et la sterilisation de protheses oculaires et auriculaires |
GB2133689A (en) * | 1982-10-29 | 1984-08-01 | Procter & Gamble | Plaque-inhibiting oral compositions containing carboxylic acids |
CA1259542A (en) † | 1984-09-28 | 1989-09-19 | Francis X. Smith | Disinfecting and preserving solutions for contact lenses and methods of use |
DE3439519A1 (de) * | 1984-10-29 | 1986-04-30 | Henkel KGaA, 4000 Düsseldorf | Verfahren zur verbesserung des korrosionsverhaltens von desinfektionsmittelloesungen |
DE3542516A1 (de) * | 1985-12-02 | 1987-06-04 | Henkel Kgaa | Desinfektionsmittel |
GB8604986D0 (en) * | 1986-02-28 | 1986-04-09 | Unilever Plc | Disinfectant compositions |
DE3723976A1 (de) * | 1986-07-23 | 1988-02-04 | Ciba Geigy Ag | Desinfektionsmittel mit virucider wirkung |
GB8625103D0 (en) † | 1986-10-20 | 1986-11-26 | Unilever Plc | Disinfectant compositions |
EP0324211A1 (en) * | 1988-01-12 | 1989-07-19 | Bosshardt-Chemie AG | Use of compositions for odour removal |
US5008030A (en) * | 1989-01-17 | 1991-04-16 | Colgate-Palmolive Co. | Acidic disinfectant all-purpose liquid cleaning composition |
-
1990
- 1990-11-06 GB GB909024133A patent/GB9024133D0/en active Pending
-
1991
- 1991-10-15 GB GB919121871A patent/GB9121871D0/en active Pending
- 1991-10-16 ES ES91309508T patent/ES2103784T5/es not_active Expired - Lifetime
- 1991-10-16 EP EP91309508A patent/EP0485079B2/en not_active Expired - Lifetime
- 1991-10-16 DE DE69126945T patent/DE69126945T3/de not_active Expired - Lifetime
- 1991-10-16 DK DK91309508T patent/DK0485079T4/da active
- 1991-10-16 AT AT91309508T patent/ATE155647T1/de not_active IP Right Cessation
- 1991-10-17 IE IE364591A patent/IE913645A1/en unknown
- 1991-10-21 NZ NZ240295A patent/NZ240295A/xx not_active IP Right Cessation
- 1991-10-21 ZA ZA918386A patent/ZA918386B/xx unknown
- 1991-10-22 AU AU86048/91A patent/AU646097B2/en not_active Expired
- 1991-10-25 CA CA002054300A patent/CA2054300C/en not_active Expired - Lifetime
- 1991-11-05 FI FI915209A patent/FI915209A/fi unknown
- 1991-11-05 NO NO914327A patent/NO300523B1/no not_active IP Right Cessation
- 1991-11-05 TW TW080108705A patent/TW221371B/zh active
- 1991-11-05 PT PT99425A patent/PT99425B/pt not_active IP Right Cessation
- 1991-11-06 JP JP28981391A patent/JP3232348B2/ja not_active Expired - Lifetime
- 1991-11-06 KR KR1019910019631A patent/KR100216859B1/ko not_active IP Right Cessation
-
1993
- 1993-05-19 US US08/063,330 patent/US5990174A/en not_active Expired - Lifetime
-
1997
- 1997-09-17 GR GR970402386T patent/GR3024741T3/el unknown
-
2001
- 2001-04-20 GR GR20010400614T patent/GR3035766T3/el not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
KR920009293A (ko) | 1992-06-25 |
CA2054300C (en) | 2002-08-27 |
EP0485079A1 (en) | 1992-05-13 |
PT99425B (pt) | 1997-09-30 |
EP0485079B1 (en) | 1997-07-23 |
US5990174A (en) | 1999-11-23 |
IE913645A1 (en) | 1992-05-22 |
ES2103784T3 (es) | 1997-10-01 |
DE69126945T2 (de) | 1997-11-27 |
EP0485079B2 (en) | 2001-02-28 |
NO914327L (no) | 1992-05-07 |
KR100216859B1 (ko) | 1999-10-01 |
TW221371B (zh) | 1994-03-01 |
GB9024133D0 (en) | 1990-12-19 |
FI915209A0 (fi) | 1991-11-05 |
ATE155647T1 (de) | 1997-08-15 |
JPH04264009A (ja) | 1992-09-18 |
FI915209A (fi) | 1992-05-07 |
GB9121871D0 (en) | 1991-11-27 |
AU646097B2 (en) | 1994-02-10 |
DK0485079T4 (da) | 2001-06-18 |
DE69126945T3 (de) | 2001-07-19 |
DK0485079T3 (da) | 1998-02-02 |
ES2103784T5 (es) | 2001-05-01 |
NZ240295A (en) | 1993-09-27 |
PT99425A (pt) | 1992-11-30 |
DE69126945D1 (de) | 1997-08-28 |
ZA918386B (en) | 1992-08-26 |
NO914327D0 (no) | 1991-11-05 |
GR3024741T3 (en) | 1997-12-31 |
GR3035766T3 (en) | 2001-07-31 |
JP3232348B2 (ja) | 2001-11-26 |
CA2054300A1 (en) | 1992-05-07 |
AU8604891A (en) | 1992-05-14 |
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Legal Events
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MM1K | Lapsed by not paying the annual fees |
Free format text: LAPSED IN MAY 2002 |