DE1642056A1 - Antimikrobielle Mittel - Google Patents
Antimikrobielle MittelInfo
- Publication number
- DE1642056A1 DE1642056A1 DE19671642056 DE1642056A DE1642056A1 DE 1642056 A1 DE1642056 A1 DE 1642056A1 DE 19671642056 DE19671642056 DE 19671642056 DE 1642056 A DE1642056 A DE 1642056A DE 1642056 A1 DE1642056 A1 DE 1642056A1
- Authority
- DE
- Germany
- Prior art keywords
- antimicrobial
- agent according
- methyl
- ethan
- substance
- 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.)
- Pending
Links
- 239000004599 antimicrobial Substances 0.000 title claims description 33
- 230000000845 anti-microbial effect Effects 0.000 claims description 35
- 239000008139 complexing agent Substances 0.000 claims description 35
- 239000000126 substance Substances 0.000 claims description 32
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 31
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims description 25
- 238000012360 testing method Methods 0.000 claims description 22
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 16
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 14
- 125000001931 aliphatic group Chemical group 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- 239000000460 chlorine Substances 0.000 claims description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
- 229910052801 chlorine Inorganic materials 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
- 150000007513 acids Chemical class 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 4
- GEGSSUSEWOHAFE-UHFFFAOYSA-N 2-(4-chlorphenoxy)-ethanol Chemical compound OCCOC1=CC=C(Cl)C=C1 GEGSSUSEWOHAFE-UHFFFAOYSA-N 0.000 claims description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052794 bromium Inorganic materials 0.000 claims description 3
- NLCZTXDWYTUVHI-UHFFFAOYSA-N 2-(4-bromo-3-methylphenoxy)ethanol Chemical compound CC1=CC(OCCO)=CC=C1Br NLCZTXDWYTUVHI-UHFFFAOYSA-N 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 claims description 2
- 125000001246 bromo group Chemical group Br* 0.000 claims description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 2
- BLNWTAHYTCHDJH-UHFFFAOYSA-O hydroxy(oxo)azanium Chemical compound O[NH+]=O BLNWTAHYTCHDJH-UHFFFAOYSA-O 0.000 claims description 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 150000003009 phosphonic acids Chemical class 0.000 claims description 2
- 239000011885 synergistic combination Substances 0.000 claims description 2
- ZQGKWFAIEHHYGU-UHFFFAOYSA-N 2-(4-chloro-3-methylphenoxy)ethanol Chemical compound CC1=CC(OCCO)=CC=C1Cl ZQGKWFAIEHHYGU-UHFFFAOYSA-N 0.000 claims 1
- 239000003921 oil Substances 0.000 description 21
- -1 2-chloro-phenoxy Chemical group 0.000 description 14
- 230000002401 inhibitory effect Effects 0.000 description 10
- 239000000243 solution Substances 0.000 description 5
- 235000013162 Cocos nucifera Nutrition 0.000 description 4
- 244000060011 Cocos nucifera Species 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Natural products OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 239000000645 desinfectant Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000004508 fractional distillation Methods 0.000 description 4
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 3
- 241001480035 Epidermophyton Species 0.000 description 3
- 241000233866 Fungi Species 0.000 description 3
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- 230000000844 anti-bacterial effect Effects 0.000 description 3
- 244000052616 bacterial pathogen Species 0.000 description 3
- 239000003795 chemical substances by application Substances 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
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 239000002609 medium Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 3
- ILGGYGDTPZIYSW-UHFFFAOYSA-N 1-(4-bromo-2-methylphenoxy)propan-2-ol Chemical compound CC(O)COC1=CC=C(Br)C=C1C ILGGYGDTPZIYSW-UHFFFAOYSA-N 0.000 description 2
- LBFSBWUGKQEQSK-UHFFFAOYSA-N 1-(4-iodophenoxy)propan-2-ol Chemical compound CC(O)COC1=CC=C(I)C=C1 LBFSBWUGKQEQSK-UHFFFAOYSA-N 0.000 description 2
- NOZAKUWNUGNDLI-UHFFFAOYSA-N 2-(2-phenylphenoxy)ethanol Chemical compound OCCOC1=CC=CC=C1C1=CC=CC=C1 NOZAKUWNUGNDLI-UHFFFAOYSA-N 0.000 description 2
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 241000222122 Candida albicans Species 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- XQKKWWCELHKGKB-UHFFFAOYSA-L calcium acetate monohydrate Chemical compound O.[Ca+2].CC([O-])=O.CC([O-])=O XQKKWWCELHKGKB-UHFFFAOYSA-L 0.000 description 2
- 229940095731 candida albicans Drugs 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 230000000249 desinfective effect Effects 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 2
- 229940071161 dodecylbenzenesulfonate Drugs 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 230000000855 fungicidal effect Effects 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 239000001963 growth medium Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 238000011534 incubation Methods 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 235000015097 nutrients Nutrition 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000008262 pumice Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 239000004575 stone Substances 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- 238000010626 work up procedure Methods 0.000 description 2
- GYDFVBYBCDOBFE-UHFFFAOYSA-N 1,3,5-trichloro-2-ethoxybenzene Chemical compound CCOC1=C(Cl)C=C(Cl)C=C1Cl GYDFVBYBCDOBFE-UHFFFAOYSA-N 0.000 description 1
- CGVSPABEGAOUOK-UHFFFAOYSA-N 1-(2-chloroethoxy)-2-phenylbenzene Chemical compound ClCCOC1=CC=CC=C1C1=CC=CC=C1 CGVSPABEGAOUOK-UHFFFAOYSA-N 0.000 description 1
- OIZMZUUFHOZQIT-UHFFFAOYSA-N 1-(2-chloroethoxy)-3-methylbenzene Chemical compound CC1=CC=CC(OCCCl)=C1 OIZMZUUFHOZQIT-UHFFFAOYSA-N 0.000 description 1
- JEESPINTVCBSTA-UHFFFAOYSA-N 1-(2-chlorophenoxy)propan-2-ol Chemical compound CC(O)COC1=CC=CC=C1Cl JEESPINTVCBSTA-UHFFFAOYSA-N 0.000 description 1
- XJVSFSKGXUVVHX-UHFFFAOYSA-N 1-(4-bromo-5-methyl-2-propan-2-ylphenoxy)propan-2-ol Chemical compound CC(COC1=C(C=C(C(=C1)C)Br)C(C)C)O XJVSFSKGXUVVHX-UHFFFAOYSA-N 0.000 description 1
- BYJBIUUBBIMSQO-UHFFFAOYSA-N 1-chloro-2-(2-chloroethoxy)benzene Chemical compound ClCCOC1=CC=CC=C1Cl BYJBIUUBBIMSQO-UHFFFAOYSA-N 0.000 description 1
- ZTPREVFTSTVRFB-UHFFFAOYSA-N 1-chloro-4-(2-chloroethoxy)-2-methylbenzene Chemical compound CC1=CC(OCCCl)=CC=C1Cl ZTPREVFTSTVRFB-UHFFFAOYSA-N 0.000 description 1
- SDGMUBWPXBSKCT-UHFFFAOYSA-N 1-chloro-4-methoxy-2-methylbenzene Chemical compound COC1=CC=C(Cl)C(C)=C1 SDGMUBWPXBSKCT-UHFFFAOYSA-N 0.000 description 1
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
- WGUCBRKEKIJTSN-UHFFFAOYSA-N 1-methyl-3-[2-[2-(3-methylphenoxy)propan-2-yloxy]propan-2-yloxy]benzene Chemical compound CC=1C=C(OC(C)(C)OC(C)(OC2=CC(=CC=C2)C)C)C=CC1 WGUCBRKEKIJTSN-UHFFFAOYSA-N 0.000 description 1
- AWPAAILWWGKSIF-UHFFFAOYSA-N 2,4-dichloro-1-ethoxybenzene Chemical compound CCOC1=CC=C(Cl)C=C1Cl AWPAAILWWGKSIF-UHFFFAOYSA-N 0.000 description 1
- LZTZSANFAWWCRW-UHFFFAOYSA-N 2-(2,4,6-trichlorophenoxy)ethanol Chemical compound OCCOC1=C(Cl)C=C(Cl)C=C1Cl LZTZSANFAWWCRW-UHFFFAOYSA-N 0.000 description 1
- PCCMNBRZMKANQD-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)ethanol Chemical compound OCCOC1=CC=C(Cl)C=C1Cl PCCMNBRZMKANQD-UHFFFAOYSA-N 0.000 description 1
- FDQGMCQSIVZGHW-UHFFFAOYSA-N 2-(2-chlorophenoxy)ethanol Chemical compound OCCOC1=CC=CC=C1Cl FDQGMCQSIVZGHW-UHFFFAOYSA-N 0.000 description 1
- FDBXUXVQIOQYIX-UHFFFAOYSA-N 2-(3-methylphenoxy)ethanol Chemical compound CC1=CC=CC(OCCO)=C1 FDBXUXVQIOQYIX-UHFFFAOYSA-N 0.000 description 1
- NANFKPXADIOTRP-UHFFFAOYSA-N 2-(4-iodophenoxy)ethanol Chemical compound OCCOC1=CC=C(I)C=C1 NANFKPXADIOTRP-UHFFFAOYSA-N 0.000 description 1
- YAPAEYFBLRVUMH-UHFFFAOYSA-N 2-(4-nitrophenoxy)ethanol Chemical compound OCCOC1=CC=C([N+]([O-])=O)C=C1 YAPAEYFBLRVUMH-UHFFFAOYSA-N 0.000 description 1
- CLSSBPVJCYTWNL-UHFFFAOYSA-N 2-(5-methyl-2-propan-2-ylphenoxy)ethanol Chemical compound CC(C)C1=CC=C(C)C=C1OCCO CLSSBPVJCYTWNL-UHFFFAOYSA-N 0.000 description 1
- VQUYNUJARXBNPK-UHFFFAOYSA-N 2-chloroethoxybenzene Chemical compound ClCCOC1=CC=CC=C1 VQUYNUJARXBNPK-UHFFFAOYSA-N 0.000 description 1
- QTDIEDOANJISNP-UHFFFAOYSA-N 2-dodecoxyethyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOCCOS(O)(=O)=O QTDIEDOANJISNP-UHFFFAOYSA-N 0.000 description 1
- LBLYYCQCTBFVLH-UHFFFAOYSA-M 2-methylbenzenesulfonate Chemical compound CC1=CC=CC=C1S([O-])(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-M 0.000 description 1
- BDDLHHRCDSJVKV-UHFFFAOYSA-N 7028-40-2 Chemical compound CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O BDDLHHRCDSJVKV-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000282461 Canis lupus Species 0.000 description 1
- GXGJIOMUZAGVEH-UHFFFAOYSA-N Chamazulene Chemical group CCC1=CC=C(C)C2=CC=C(C)C2=C1 GXGJIOMUZAGVEH-UHFFFAOYSA-N 0.000 description 1
- 229940120146 EDTMP Drugs 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 241000589517 Pseudomonas aeruginosa Species 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 241000191967 Staphylococcus aureus Species 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- YDONNITUKPKTIG-UHFFFAOYSA-N [Nitrilotris(methylene)]trisphosphonic acid Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CP(O)(O)=O YDONNITUKPKTIG-UHFFFAOYSA-N 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
- 235000010419 agar Nutrition 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 238000009395 breeding Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000001639 calcium acetate Substances 0.000 description 1
- 235000011092 calcium acetate Nutrition 0.000 description 1
- 229960005147 calcium acetate Drugs 0.000 description 1
- 229940067460 calcium acetate monohydrate Drugs 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- FCYRSDMGOLYDHL-UHFFFAOYSA-N chloromethoxyethane Chemical compound CCOCCl FCYRSDMGOLYDHL-UHFFFAOYSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- SMVRDGHCVNAOIN-UHFFFAOYSA-L disodium;1-dodecoxydodecane;sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC SMVRDGHCVNAOIN-UHFFFAOYSA-L 0.000 description 1
- RHPXYIKALIRNFA-UHFFFAOYSA-L disodium;2-[carboxylatomethyl(carboxymethyl)amino]acetate Chemical compound [Na+].[Na+].OC(=O)CN(CC([O-])=O)CC([O-])=O RHPXYIKALIRNFA-UHFFFAOYSA-L 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- NFDRPXJGHKJRLJ-UHFFFAOYSA-N edtmp Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CCN(CP(O)(O)=O)CP(O)(O)=O NFDRPXJGHKJRLJ-UHFFFAOYSA-N 0.000 description 1
- 229940035423 ethyl ether Drugs 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 230000002070 germicidal effect Effects 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexamethylene diamine Natural products NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
- GTTBQSNGUYHPNK-UHFFFAOYSA-N hydroxymethylphosphonic acid Chemical compound OCP(O)(O)=O GTTBQSNGUYHPNK-UHFFFAOYSA-N 0.000 description 1
- 238000001764 infiltration Methods 0.000 description 1
- 230000008595 infiltration Effects 0.000 description 1
- 238000009630 liquid culture Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 230000003158 microbiostatic effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229960003330 pentetic acid Drugs 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- LJPYJRMMPVFEKR-UHFFFAOYSA-N prop-2-ynylurea Chemical compound NC(=O)NCC#C LJPYJRMMPVFEKR-UHFFFAOYSA-N 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/48—Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE07121/68A SE364725B (en, 2012) | 1967-07-13 | 1968-05-28 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19681767426 DE1767426A1 (de) | 1968-05-09 | 1968-05-09 | Antimikrobielle Wirkstoffe enthaltende Wasch-,Waschhilfs- und Reinigungsmittel |
| DEH0063270 | 1968-06-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1642056A1 true DE1642056A1 (de) | 1971-05-06 |
Family
ID=25755457
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19671642056 Pending DE1642056A1 (de) | 1967-07-13 | 1967-07-13 | Antimikrobielle Mittel |
| DE19681767426 Pending DE1767426A1 (de) | 1967-07-13 | 1968-05-09 | Antimikrobielle Wirkstoffe enthaltende Wasch-,Waschhilfs- und Reinigungsmittel |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19681767426 Pending DE1767426A1 (de) | 1967-07-13 | 1968-05-09 | Antimikrobielle Wirkstoffe enthaltende Wasch-,Waschhilfs- und Reinigungsmittel |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3625904A (en, 2012) |
| AT (1) | AT311522B (en, 2012) |
| BE (1) | BE718023A (en, 2012) |
| CH (1) | CH525951A (en, 2012) |
| DE (2) | DE1642056A1 (en, 2012) |
| FR (2) | FR1581627A (en, 2012) |
| GB (1) | GB1239958A (en, 2012) |
| NL (1) | NL6808427A (en, 2012) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3904099C1 (en, 2012) * | 1989-02-11 | 1990-07-12 | Schuelke & Mayr Gmbh, 2000 Norderstedt, De | |
| DE19645829A1 (de) * | 1995-11-12 | 1997-05-15 | Franz Spreiter | Messer für apparative Anwendungen |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2015186A1 (de) * | 1970-03-28 | 1971-10-21 | Henkel & Cie, GmbH, 4000 Düsseldorf | Zur Verwendung in bactericiden Textilbehandlungsmitteln geeignete Aufhellerkombination |
| DE2015187A1 (en, 2012) * | 1970-03-28 | 1971-10-21 | ||
| GB1418024A (en) * | 1972-03-03 | 1975-12-17 | Unilever Ltd | Hair shampoos |
| US4289758A (en) * | 1979-09-17 | 1981-09-15 | Aquatain Partnership | Liquid biocidal compositions compriing a mixture of silver ions and sodium pectate |
| US5273896A (en) * | 1989-10-13 | 1993-12-28 | Novo Nordisk A/S | Hemopeptide having peroxidase activity for bleaching dyes |
| DE4005784C2 (de) * | 1990-02-23 | 1994-12-08 | Schuelke & Mayr Gmbh | Desinfektionsmittel-Konzentrat und dessen Verwendung als Mykobakterizid und Viruzid |
| EP0705327B1 (de) * | 1993-06-16 | 2000-04-19 | CALL, Hans-Peter Dr. | Mehrkomponentenbleichsystem |
| FR2728182B1 (fr) * | 1994-12-16 | 1997-01-24 | Coatex Sa | Procede d'obtention d'agents de broyage et/ou de dispersion par separation physico-chimique, agents obtenus et leurs utilisations |
| US5837274A (en) * | 1996-10-22 | 1998-11-17 | Kimberly Clark Corporation | Aqueous, antimicrobial liquid cleaning formulation |
| US5997847A (en) * | 1998-01-07 | 1999-12-07 | Spiesel; Sydney Z. | Ectoparasite detection method |
| US20040235680A1 (en) * | 2002-09-18 | 2004-11-25 | Ecolab Inc. | Conveyor lubricant with corrosion inhibition |
| AU2003270729A1 (en) * | 2002-09-18 | 2004-04-08 | Ecolab Inc. | Additive for use in bottle washing compositions additive |
| US9259006B2 (en) * | 2008-01-30 | 2016-02-16 | Smartwash Solutions, Llc | Antimicrobial compositions and methods of use thereof |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2868843A (en) * | 1959-01-13 | X-dichlorophenoxyalkanols | ||
| US2134001A (en) * | 1937-10-16 | 1938-10-25 | Dow Chemical Co | Mothproofing agent |
| US2289886A (en) * | 1939-05-17 | 1942-07-14 | Universal Oil Prod Co | Production of phenols |
| US2256612A (en) * | 1939-06-29 | 1941-09-23 | Standard Oil Dev Co | Manufacture of mixed phenol ethers and alkylated phenols |
| US2615823A (en) * | 1950-03-30 | 1952-10-28 | Niagara Alkali Company | Bactericidal and fungicidal composition |
| US3081224A (en) * | 1959-01-21 | 1963-03-12 | American Cyanamid Co | Methods of removing helminths employing halogenated nitrophenols and their derivatives |
| US3375199A (en) * | 1963-11-29 | 1968-03-26 | Colgate Palmolive Co | Cleaner-disinfectant composition |
-
1967
- 1967-07-13 DE DE19671642056 patent/DE1642056A1/de active Pending
-
1968
- 1968-05-09 DE DE19681767426 patent/DE1767426A1/de active Pending
- 1968-06-14 NL NL6808427A patent/NL6808427A/xx unknown
- 1968-07-02 FR FR1581627D patent/FR1581627A/fr not_active Expired
- 1968-07-08 US US743032A patent/US3625904A/en not_active Expired - Lifetime
- 1968-07-10 CH CH1023968A patent/CH525951A/de not_active IP Right Cessation
- 1968-07-12 BE BE718023D patent/BE718023A/xx unknown
- 1968-07-12 GB GB33278/68A patent/GB1239958A/en not_active Expired
- 1968-07-12 AT AT676068A patent/AT311522B/de not_active IP Right Cessation
- 1968-09-12 FR FR1580669D patent/FR1580669A/fr not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3904099C1 (en, 2012) * | 1989-02-11 | 1990-07-12 | Schuelke & Mayr Gmbh, 2000 Norderstedt, De | |
| EP0383005A1 (de) * | 1989-02-11 | 1990-08-22 | SchàLke & Mayr Gmbh | Konservierungsmittel für Systeme oder Produkte mit einer wässrigen Phase |
| DE19645829A1 (de) * | 1995-11-12 | 1997-05-15 | Franz Spreiter | Messer für apparative Anwendungen |
Also Published As
| Publication number | Publication date |
|---|---|
| FR1580669A (en, 2012) | 1969-09-05 |
| GB1239958A (en) | 1971-07-21 |
| DE1767426A1 (de) | 1971-09-02 |
| FR1581627A (en, 2012) | 1969-09-19 |
| US3625904A (en) | 1971-12-07 |
| NL6808427A (en, 2012) | 1969-01-15 |
| CH525951A (de) | 1972-07-31 |
| BE718023A (en, 2012) | 1969-01-13 |
| AT311522B (de) | 1973-11-26 |
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