DE2752253B2 - Konservierung^- und Desinfektionsmittel - Google Patents
Konservierung^- und DesinfektionsmittelInfo
- Publication number
- DE2752253B2 DE2752253B2 DE19772752253 DE2752253A DE2752253B2 DE 2752253 B2 DE2752253 B2 DE 2752253B2 DE 19772752253 DE19772752253 DE 19772752253 DE 2752253 A DE2752253 A DE 2752253A DE 2752253 B2 DE2752253 B2 DE 2752253B2
- Authority
- DE
- Germany
- Prior art keywords
- ether
- aminomethyl
- thioether
- benzyl
- ethyl
- 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.)
- Granted
Links
- 239000000645 desinfectant Substances 0.000 title claims description 5
- 238000004321 preservation Methods 0.000 title description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 20
- 239000003755 preservative agent Substances 0.000 claims description 5
- 150000001298 alcohols Chemical class 0.000 claims description 4
- 239000007859 condensation product Substances 0.000 claims description 4
- 150000003335 secondary amines Chemical class 0.000 claims description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 74
- 150000003568 thioethers Chemical class 0.000 description 65
- -1 Di- (n-propyl) aminomethyl-n-propyl Chemical group 0.000 description 57
- 229940035423 ethyl ether Drugs 0.000 description 25
- GQKZBCPTCWJTAS-UHFFFAOYSA-N methoxymethylbenzene Chemical compound COCC1=CC=CC=C1 GQKZBCPTCWJTAS-UHFFFAOYSA-N 0.000 description 23
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical compound C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 description 17
- VLGUBUHHNFCMKI-UHFFFAOYSA-N aminomethoxymethanamine Chemical compound NCOCN VLGUBUHHNFCMKI-UHFFFAOYSA-N 0.000 description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 6
- 230000000845 anti-microbial effect Effects 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 125000006264 diethylaminomethyl group Chemical group [H]C([H])([H])C([H])([H])N(C([H])([H])*)C([H])([H])C([H])([H])[H] 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- 230000002335 preservative effect Effects 0.000 description 6
- 229910052717 sulfur Chemical group 0.000 description 6
- 239000011593 sulfur Chemical group 0.000 description 6
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 5
- 241000588724 Escherichia coli Species 0.000 description 5
- 244000052616 bacterial pathogen Species 0.000 description 5
- 239000002537 cosmetic Substances 0.000 description 5
- POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 description 5
- 238000011081 inoculation Methods 0.000 description 5
- 125000001064 morpholinomethyl group Chemical group [H]C([H])(*)N1C([H])([H])C([H])([H])OC([H])([H])C1([H])[H] 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical compound C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 description 4
- KNQMOJDREHVDAF-UHFFFAOYSA-N 4-(ethoxymethyl)morpholine Chemical compound CCOCN1CCOCC1 KNQMOJDREHVDAF-UHFFFAOYSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- XOBKSJJDNFUZPF-UHFFFAOYSA-N Methoxyethane Chemical compound CCOC XOBKSJJDNFUZPF-UHFFFAOYSA-N 0.000 description 4
- 241000589517 Pseudomonas aeruginosa Species 0.000 description 4
- 241000191967 Staphylococcus aureus Species 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 4
- MJYMHNHBVQDKOW-UHFFFAOYSA-N aminomethylsulfanylmethanamine Chemical compound NCSCN MJYMHNHBVQDKOW-UHFFFAOYSA-N 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- RMGHERXMTMUMMV-UHFFFAOYSA-N 2-methoxypropane Chemical compound COC(C)C RMGHERXMTMUMMV-UHFFFAOYSA-N 0.000 description 3
- 241000228245 Aspergillus niger Species 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- LUFPJJNWMYZRQE-UHFFFAOYSA-N benzylsulfanylmethylbenzene Chemical compound C=1C=CC=CC=1CSCC1=CC=CC=C1 LUFPJJNWMYZRQE-UHFFFAOYSA-N 0.000 description 3
- 239000005068 cooling lubricant Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- 244000005700 microbiome Species 0.000 description 3
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 3
- FKWUBBCUJLXTFR-UHFFFAOYSA-N n-(ethoxymethyl)-n-ethylethanamine Chemical compound CCOCN(CC)CC FKWUBBCUJLXTFR-UHFFFAOYSA-N 0.000 description 3
- WJUUTHFUYZOIDV-UHFFFAOYSA-N n-ethyl-n-(phenylmethoxymethyl)ethanamine Chemical compound CCN(CC)COCC1=CC=CC=C1 WJUUTHFUYZOIDV-UHFFFAOYSA-N 0.000 description 3
- DYDOBQCNGFPQDY-UHFFFAOYSA-N n-ethyl-n-(propan-2-yloxymethyl)ethanamine Chemical compound CCN(CC)COC(C)C DYDOBQCNGFPQDY-UHFFFAOYSA-N 0.000 description 3
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- JHMKKNJCOSITDU-UHFFFAOYSA-N 1-(phenylmethoxymethyl)pyrrolidine Chemical class C1CCCN1COCC1=CC=CC=C1 JHMKKNJCOSITDU-UHFFFAOYSA-N 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- XAAOTQNLODOGKL-UHFFFAOYSA-N 1-methyl-4-phenylmethoxypiperazine Chemical compound C1CN(C)CCN1OCC1=CC=CC=C1 XAAOTQNLODOGKL-UHFFFAOYSA-N 0.000 description 2
- UWNADWZGEHDQAB-UHFFFAOYSA-N 2,5-dimethylhexane Chemical group CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 2
- CQLYXIUHVFRXLT-UHFFFAOYSA-N 2-methoxyethylbenzene Chemical compound COCCC1=CC=CC=C1 CQLYXIUHVFRXLT-UHFFFAOYSA-N 0.000 description 2
- ODQNOERFLDQRSB-UHFFFAOYSA-N 4-(propan-2-yloxymethyl)morpholine Chemical compound CC(C)OCN1CCOCC1 ODQNOERFLDQRSB-UHFFFAOYSA-N 0.000 description 2
- ZTFUILMRJBMTGK-UHFFFAOYSA-N 5-ethoxynonan-5-amine Chemical compound CCCCC(N)(OCC)CCCC ZTFUILMRJBMTGK-UHFFFAOYSA-N 0.000 description 2
- MVKDDSRNHPHLRE-UHFFFAOYSA-N CCC=COCN Chemical compound CCC=COCN MVKDDSRNHPHLRE-UHFFFAOYSA-N 0.000 description 2
- KFDSBQOOMUQNTF-UHFFFAOYSA-N CCOC(CC(C)C)(CC(C)C)N Chemical compound CCOC(CC(C)C)(CC(C)C)N KFDSBQOOMUQNTF-UHFFFAOYSA-N 0.000 description 2
- 241000222120 Candida <Saccharomycetales> Species 0.000 description 2
- 241000222122 Candida albicans Species 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- 241000588767 Proteus vulgaris Species 0.000 description 2
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 2
- OCDXZFSOHJRGIL-UHFFFAOYSA-N cyclohexyloxycyclohexane Chemical compound C1CCCCC1OC1CCCCC1 OCDXZFSOHJRGIL-UHFFFAOYSA-N 0.000 description 2
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000005553 drilling Methods 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 159000000011 group IA salts Chemical class 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 230000007794 irritation Effects 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- 230000002147 killing effect Effects 0.000 description 2
- 239000006210 lotion Substances 0.000 description 2
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
- 210000004400 mucous membrane Anatomy 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 239000006916 nutrient agar Substances 0.000 description 2
- FEHPATFOJAWXIY-UHFFFAOYSA-N phenylmethoxymethanamine Chemical compound NCOCC1=CC=CC=C1 FEHPATFOJAWXIY-UHFFFAOYSA-N 0.000 description 2
- 125000003367 polycyclic group Chemical group 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229940007042 proteus vulgaris Drugs 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- OYWRDHBGMCXGFY-UHFFFAOYSA-N 1,2,3-triazinane Chemical class C1CNNNC1 OYWRDHBGMCXGFY-UHFFFAOYSA-N 0.000 description 1
- FZWRUVFZORCTLX-UHFFFAOYSA-N 1-(ethoxymethyl)-4-methylpiperazine Chemical compound CCOCN1CCN(C)CC1 FZWRUVFZORCTLX-UHFFFAOYSA-N 0.000 description 1
- IHQZMTASTVTDLX-UHFFFAOYSA-N 1-(ethoxymethyl)piperidine Chemical compound CCOCN1CCCCC1 IHQZMTASTVTDLX-UHFFFAOYSA-N 0.000 description 1
- FQQLPHRTYNPTLT-UHFFFAOYSA-N 1-(ethoxymethyl)pyrrolidine Chemical compound CCOCN1CCCC1 FQQLPHRTYNPTLT-UHFFFAOYSA-N 0.000 description 1
- FXXKSWOIMQOWHF-UHFFFAOYSA-N 1-(phenylmethoxymethyl)piperidine Chemical compound C1CCCCN1COCC1=CC=CC=C1 FXXKSWOIMQOWHF-UHFFFAOYSA-N 0.000 description 1
- VMHRXXKNCRAKNN-UHFFFAOYSA-N 1-(propan-2-yloxymethyl)piperidine Chemical compound CC(C)OCN1CCCCC1 VMHRXXKNCRAKNN-UHFFFAOYSA-N 0.000 description 1
- KBJKKOQVRMZFNO-UHFFFAOYSA-N 1-(propan-2-yloxymethyl)pyrrolidine Chemical compound C(C)(C)OCN1CCCC1 KBJKKOQVRMZFNO-UHFFFAOYSA-N 0.000 description 1
- AQTCZOBQVQCQKR-UHFFFAOYSA-N 1-(propoxymethyl)pyrrolidine Chemical compound CCCOCN1CCCC1 AQTCZOBQVQCQKR-UHFFFAOYSA-N 0.000 description 1
- ZELAUPRECLNAEE-UHFFFAOYSA-N 1-ethoxy-4-methylpiperazine Chemical compound CCON1CCN(C)CC1 ZELAUPRECLNAEE-UHFFFAOYSA-N 0.000 description 1
- NZLCDJADEWGUAX-UHFFFAOYSA-N 1-ethylsulfanyl-2-(2-ethylsulfanylethoxy)ethane Chemical compound CCSCCOCCSCC NZLCDJADEWGUAX-UHFFFAOYSA-N 0.000 description 1
- BPIUIOXAFBGMNB-UHFFFAOYSA-N 1-hexoxyhexane Chemical compound CCCCCCOCCCCCC BPIUIOXAFBGMNB-UHFFFAOYSA-N 0.000 description 1
- YFTNTMQKPLVKFQ-UHFFFAOYSA-N 1-methoxy-n,n-dimethylmethanamine Chemical compound COCN(C)C YFTNTMQKPLVKFQ-UHFFFAOYSA-N 0.000 description 1
- 125000002817 1-piperidinomethyl group Chemical group [H]C([H])([*])N1C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- GXVUZYLYWKWJIM-UHFFFAOYSA-N 2-(2-aminoethoxy)ethanamine Chemical compound NCCOCCN GXVUZYLYWKWJIM-UHFFFAOYSA-N 0.000 description 1
- AMOYMEBHYUTMKJ-UHFFFAOYSA-N 2-(2-phenylethoxy)ethylbenzene Chemical compound C=1C=CC=CC=1CCOCCC1=CC=CC=C1 AMOYMEBHYUTMKJ-UHFFFAOYSA-N 0.000 description 1
- KLGHJDHDVMDMDO-UHFFFAOYSA-N 2-ethoxypropylbenzene Chemical compound CCOC(C)CC1=CC=CC=C1 KLGHJDHDVMDMDO-UHFFFAOYSA-N 0.000 description 1
- SEJCKRBOUBURBN-UHFFFAOYSA-N 3-(aminomethoxy)propanenitrile Chemical compound C(#N)CCOCN SEJCKRBOUBURBN-UHFFFAOYSA-N 0.000 description 1
- XVYVLFQAFDDTQM-UHFFFAOYSA-N 4-(phenylmethoxymethyl)morpholine Chemical compound C1COCCN1COCC1=CC=CC=C1 XVYVLFQAFDDTQM-UHFFFAOYSA-N 0.000 description 1
- 241000228212 Aspergillus Species 0.000 description 1
- 244000063299 Bacillus subtilis Species 0.000 description 1
- 235000014469 Bacillus subtilis Nutrition 0.000 description 1
- LDOJMFVLUBNMLC-UHFFFAOYSA-N C(COCN1CCCCC1)C1=CC=CC=C1 Chemical compound C(COCN1CCCCC1)C1=CC=CC=C1 LDOJMFVLUBNMLC-UHFFFAOYSA-N 0.000 description 1
- SRHIGTNODPWAFL-UHFFFAOYSA-N CC(C)C(C(C)C)(N)OC(C)C Chemical compound CC(C)C(C(C)C)(N)OC(C)C SRHIGTNODPWAFL-UHFFFAOYSA-N 0.000 description 1
- USNZYZDQGAJSQH-UHFFFAOYSA-N CC(C)C(C(C)C)(N)OCC1=CC=CC=C1 Chemical compound CC(C)C(C(C)C)(N)OCC1=CC=CC=C1 USNZYZDQGAJSQH-UHFFFAOYSA-N 0.000 description 1
- JLOJQQTUKNKJBE-UHFFFAOYSA-N CC(C)CC(CC(C)C)(N)OC(C)C Chemical compound CC(C)CC(CC(C)C)(N)OC(C)C JLOJQQTUKNKJBE-UHFFFAOYSA-N 0.000 description 1
- VLDSVVFOXMSERC-UHFFFAOYSA-N CC(C)CC(CC(C)C)(N)OCC(C)C Chemical compound CC(C)CC(CC(C)C)(N)OCC(C)C VLDSVVFOXMSERC-UHFFFAOYSA-N 0.000 description 1
- BDKGWNUUMLFPGQ-UHFFFAOYSA-N CC(C)CC1=CC=CC(C(C)(N)OC(C)(C2=C(CC(C)C)C(CC(C)C)=CC=C2)N)=C1CC(C)C Chemical compound CC(C)CC1=CC=CC(C(C)(N)OC(C)(C2=C(CC(C)C)C(CC(C)C)=CC=C2)N)=C1CC(C)C BDKGWNUUMLFPGQ-UHFFFAOYSA-N 0.000 description 1
- PAXXMDPZKXBOPN-UHFFFAOYSA-N CC(C)CN(CC(C)C)COCC1=CC=CC=C1 Chemical compound CC(C)CN(CC(C)C)COCC1=CC=CC=C1 PAXXMDPZKXBOPN-UHFFFAOYSA-N 0.000 description 1
- XBDUEORLOQAYPH-UHFFFAOYSA-N CC(C)N(C(C)C)COCC1=CC=CC=C1 Chemical compound CC(C)N(C(C)C)COCC1=CC=CC=C1 XBDUEORLOQAYPH-UHFFFAOYSA-N 0.000 description 1
- DPYYRDFXLAUREB-UHFFFAOYSA-N CC(C1=C(CCOC)C(CCOC)=CC=C1)(N)OC(C)(C1=C(CCOC)C(CCOC)=CC=C1)N Chemical compound CC(C1=C(CCOC)C(CCOC)=CC=C1)(N)OC(C)(C1=C(CCOC)C(CCOC)=CC=C1)N DPYYRDFXLAUREB-UHFFFAOYSA-N 0.000 description 1
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- LNWAOPXGCVQIGM-UHFFFAOYSA-N CC(CN1CCC(C)CC1)OC(C)CN1CCC(C)CC1 Chemical compound CC(CN1CCC(C)CC1)OC(C)CN1CCC(C)CC1 LNWAOPXGCVQIGM-UHFFFAOYSA-N 0.000 description 1
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- CNDOGXQVNHHJFH-UHFFFAOYSA-N CCCC(CCC)(N)OC(C)C Chemical compound CCCC(CCC)(N)OC(C)C CNDOGXQVNHHJFH-UHFFFAOYSA-N 0.000 description 1
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- KYLJYRURWFSVAE-UHFFFAOYSA-N COCCC(CCOC)(N)OCC1=CC=CC=C1 Chemical compound COCCC(CCOC)(N)OCC1=CC=CC=C1 KYLJYRURWFSVAE-UHFFFAOYSA-N 0.000 description 1
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- UBJVUCKUDDKUJF-UHFFFAOYSA-N Diallyl sulfide Chemical compound C=CCSCC=C UBJVUCKUDDKUJF-UHFFFAOYSA-N 0.000 description 1
- 241000321713 Dromus Species 0.000 description 1
- 241001154435 Escherichia coli PS Species 0.000 description 1
- 241000223221 Fusarium oxysporum Species 0.000 description 1
- 241000588915 Klebsiella aerogenes Species 0.000 description 1
- 150000001204 N-oxides Chemical class 0.000 description 1
- GDAYAVDFKQREDW-UHFFFAOYSA-N NC(C1CCCC1)(C1CCCC1)OC1CCCCC1 Chemical compound NC(C1CCCC1)(C1CCCC1)OC1CCCCC1 GDAYAVDFKQREDW-UHFFFAOYSA-N 0.000 description 1
- KZKMTFUQFJPWER-UHFFFAOYSA-N NC(C1CCCCC1)(C1CCCCC1)OC1CCCCC1 Chemical compound NC(C1CCCCC1)(C1CCCCC1)OC1CCCCC1 KZKMTFUQFJPWER-UHFFFAOYSA-N 0.000 description 1
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- 241001123663 Penicillium expansum Species 0.000 description 1
- 241001045770 Trichophyton mentagrophytes Species 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000002353 algacidal effect Effects 0.000 description 1
- 150000007854 aminals Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 230000001580 bacterial effect Effects 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
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 239000007853 buffer solution Substances 0.000 description 1
- 229940095731 candida albicans Drugs 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000001332 colony forming effect Effects 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- PBYJDXLFADJPJF-UHFFFAOYSA-N cyclopentyloxymethanamine Chemical compound NCOC1CCCC1 PBYJDXLFADJPJF-UHFFFAOYSA-N 0.000 description 1
- 230000000249 desinfective effect Effects 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- QSCNLGHKALSYKF-UHFFFAOYSA-N ethoxymethanamine Chemical compound CCOCN QSCNLGHKALSYKF-UHFFFAOYSA-N 0.000 description 1
- JXBPSENIJJPTCI-UHFFFAOYSA-N ethyl cyanate Chemical compound CCOC#N JXBPSENIJJPTCI-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002366 halogen compounds Chemical class 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 231100000086 high toxicity Toxicity 0.000 description 1
- 230000036512 infertility Effects 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- KZGFTKAJCVXVJI-UHFFFAOYSA-N n-(ethoxymethyl)-n-propylpropan-1-amine Chemical compound CCCN(CCC)COCC KZGFTKAJCVXVJI-UHFFFAOYSA-N 0.000 description 1
- WXDCTXTWTOEIJM-UHFFFAOYSA-N n-(phenylmethoxymethyl)-n-propylpropan-1-amine Chemical compound CCCN(CCC)COCC1=CC=CC=C1 WXDCTXTWTOEIJM-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- GBTIKYSUNDICQH-UHFFFAOYSA-N n-butyl-n-(ethoxymethyl)butan-1-amine Chemical compound CCCCN(CCCC)COCC GBTIKYSUNDICQH-UHFFFAOYSA-N 0.000 description 1
- MGNHVQPGXLYHAZ-UHFFFAOYSA-N n-butyl-n-(phenylmethoxymethyl)butan-1-amine Chemical compound CCCCN(CCCC)COCC1=CC=CC=C1 MGNHVQPGXLYHAZ-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000004893 oxazines Chemical class 0.000 description 1
- 150000002917 oxazolidines Chemical class 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229940113115 polyethylene glycol 200 Drugs 0.000 description 1
- 229960004063 propylene glycol Drugs 0.000 description 1
- WHMDPDGBKYUEMW-UHFFFAOYSA-N pyridine-2-thiol Chemical compound SC1=CC=CC=N1 WHMDPDGBKYUEMW-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000013207 serial dilution Methods 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 229960005486 vaccine Drugs 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
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical at least one of the bonds to hetero atoms is to nitrogen
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19772752253 DE2752253B2 (de) | 1977-11-23 | 1977-11-23 | Konservierung^- und Desinfektionsmittel |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19772752253 DE2752253B2 (de) | 1977-11-23 | 1977-11-23 | Konservierung^- und Desinfektionsmittel |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2752253A1 DE2752253A1 (de) | 1979-05-31 |
| DE2752253B2 true DE2752253B2 (de) | 1980-05-29 |
| DE2752253C3 DE2752253C3 (enExample) | 1981-02-05 |
Family
ID=6024416
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19772752253 Granted DE2752253B2 (de) | 1977-11-23 | 1977-11-23 | Konservierung^- und Desinfektionsmittel |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE2752253B2 (enExample) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2953720B1 (fr) * | 2009-12-11 | 2012-05-11 | Oreal | Utilisation de derives de benzyloxy-ethylamines comme conservateur, |
-
1977
- 1977-11-23 DE DE19772752253 patent/DE2752253B2/de active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| DE2752253C3 (enExample) | 1981-02-05 |
| DE2752253A1 (de) | 1979-05-31 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OAP | Request for examination filed | ||
| OD | Request for examination | ||
| OI | Miscellaneous see part 1 | ||
| C3 | Grant after two publication steps (3rd publication) | ||
| 8339 | Ceased/non-payment of the annual fee |