CH634720A5 - Alcoholic disinfectant having a sporicidal action - Google Patents

Alcoholic disinfectant having a sporicidal action Download PDF

Info

Publication number: CH634720A5
Authority: CH; Switzerland
Prior art keywords: acid; alcoholic; solution; percarboxylic; alcohol
Prior art date: 1977-06-03

Application number

CH1388377A

Other languages

German (de)

English (en)

Inventor

Heinz Dr Eggensperger

Wolfgang Dr Beilfuss

Wolfgang Zerling

Original Assignee

Schuelke & Mayr Gmbh

Priority date (The priority date 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 date listed.)

1977-06-03

Filing date

1977-11-14

Publication date

1983-02-28

1977-11-14 Application filed by Schuelke & Mayr Gmbh filed Critical Schuelke & Mayr Gmbh

1983-02-28 Publication of CH634720A5 publication Critical patent/CH634720A5/de

Links

230000001476 alcoholic effect Effects 0.000 title description 33
239000000645 desinfectant Substances 0.000 title description 27
230000003330 sporicidal effect Effects 0.000 title description 10
239000002253 acid Substances 0.000 description 44
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 40
150000007513 acids Chemical class 0.000 description 27
SCKXCAADGDQQCS-UHFFFAOYSA-N Performic acid Chemical compound OOC=O SCKXCAADGDQQCS-UHFFFAOYSA-N 0.000 description 19
150000001298 alcohols Chemical class 0.000 description 15
KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 14
239000000126 substance Substances 0.000 description 14
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 12
IAPQCQCJCOIPGG-UHFFFAOYSA-N 4-methoxybenzenecarboperoxoic acid Chemical compound COC1=CC=C(C(=O)OO)C=C1 IAPQCQCJCOIPGG-UHFFFAOYSA-N 0.000 description 9
239000000203 mixture Substances 0.000 description 9
210000004215 spore Anatomy 0.000 description 8
238000004659 sterilization and disinfection Methods 0.000 description 8
-1 alkyl radical Chemical class 0.000 description 7
244000005700 microbiome Species 0.000 description 7
230000000694 effects Effects 0.000 description 6
230000002401 inhibitory effect Effects 0.000 description 6
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
241000894006 Bacteria Species 0.000 description 5
150000001735 carboxylic acids Chemical class 0.000 description 5
239000000463 material Substances 0.000 description 5
238000000034 method Methods 0.000 description 5
238000012360 testing method Methods 0.000 description 5
239000003513 alkali Substances 0.000 description 4
244000052616 bacterial pathogen Species 0.000 description 4
125000004432 carbon atom Chemical group C* 0.000 description 4
230000009965 odorless effect Effects 0.000 description 4
QSOVSKMNRYAVJR-UHFFFAOYSA-N 2-benzoyloxybenzoic acid Chemical compound OC(=O)C1=CC=CC=C1OC(=O)C1=CC=CC=C1 QSOVSKMNRYAVJR-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
YGSDEFSMJLZEOE-UHFFFAOYSA-N Salicylic acid Natural products OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 3
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 3
239000004480 active ingredient Substances 0.000 description 3
150000001244 carboxylic acid anhydrides Chemical class 0.000 description 3
150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
150000001733 carboxylic acid esters Chemical class 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
238000005260 corrosion Methods 0.000 description 3
230000007797 corrosion Effects 0.000 description 3
150000002989 phenols Chemical class 0.000 description 3
239000007787 solid Substances 0.000 description 3
230000001954 sterilising effect Effects 0.000 description 3
239000000080 wetting agent Substances 0.000 description 3
FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 2
YNJSNEKCXVFDKW-UHFFFAOYSA-N 3-(5-amino-1h-indol-3-yl)-2-azaniumylpropanoate Chemical compound C1=C(N)C=C2C(CC(N)C(O)=O)=CNC2=C1 YNJSNEKCXVFDKW-UHFFFAOYSA-N 0.000 description 2
235000001674 Agaricus brunnescens Nutrition 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
235000014469 Bacillus subtilis Nutrition 0.000 description 2
ZNZYKNKBJPZETN-WELNAUFTSA-N Dialdehyde 11678 Chemical compound N1C2=CC=CC=C2C2=C1[C@H](C[C@H](/C(=C/O)C(=O)OC)[C@@H](C=C)C=O)NCC2 ZNZYKNKBJPZETN-WELNAUFTSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
241000233866 Fungi Species 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
239000013543 active substance Substances 0.000 description 2
150000001299 aldehydes Chemical class 0.000 description 2
150000008064 anhydrides Chemical class 0.000 description 2
230000000845 anti-microbial effect Effects 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
150000003857 carboxamides Chemical class 0.000 description 2
239000008139 complexing agent Substances 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
238000011109 contamination Methods 0.000 description 2
238000000354 decomposition reaction Methods 0.000 description 2
239000003599 detergent Substances 0.000 description 2
VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
230000002070 germicidal effect Effects 0.000 description 2
LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
230000007774 longterm Effects 0.000 description 2
238000007254 oxidation reaction Methods 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
239000003380 propellant Substances 0.000 description 2
229960004889 salicylic acid Drugs 0.000 description 2
LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
229940045872 sodium percarbonate Drugs 0.000 description 2
229910052938 sodium sulfate Inorganic materials 0.000 description 2
235000011152 sodium sulphate Nutrition 0.000 description 2
239000002904 solvent Substances 0.000 description 2
239000007921 spray Substances 0.000 description 2
239000003381 stabilizer Substances 0.000 description 2
229940014800 succinic anhydride Drugs 0.000 description 2
AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 2
KDFRADWZKMRRPJ-UHFFFAOYSA-N (4-methoxybenzoyl) 4-methoxybenzenecarboperoxoate Chemical compound C1=CC(OC)=CC=C1C(=O)OOC(=O)C1=CC=C(OC)C=C1 KDFRADWZKMRRPJ-UHFFFAOYSA-N 0.000 description 1
YGMHIBLUWGDWKP-UHFFFAOYSA-N (4-methoxybenzoyl) 4-methoxybenzoate Chemical compound C1=CC(OC)=CC=C1C(=O)OC(=O)C1=CC=C(OC)C=C1 YGMHIBLUWGDWKP-UHFFFAOYSA-N 0.000 description 1
RERBZZQPFKUWQP-UHFFFAOYSA-N (4-tert-butylbenzoyl) 4-tert-butylbenzenecarboperoxoate Chemical compound C1=CC(C(C)(C)C)=CC=C1C(=O)OOC(=O)C1=CC=C(C(C)(C)C)C=C1 RERBZZQPFKUWQP-UHFFFAOYSA-N 0.000 description 1
DZKRDHLYQRTDBU-UPHRSURJSA-N (z)-but-2-enediperoxoic acid Chemical compound OOC(=O)\C=C/C(=O)OO DZKRDHLYQRTDBU-UPHRSURJSA-N 0.000 description 1
PIYNUZCGMLCXKJ-UHFFFAOYSA-N 1,4-dioxane-2,6-dione Chemical compound O=C1COCC(=O)O1 PIYNUZCGMLCXKJ-UHFFFAOYSA-N 0.000 description 1
IQJVXCIYYQAIKL-UHFFFAOYSA-N 1-(4-bromophenyl)-3,3-bis(methylsulfanyl)prop-2-en-1-one Chemical compound CSC(SC)=CC(=O)C1=CC=C(Br)C=C1 IQJVXCIYYQAIKL-UHFFFAOYSA-N 0.000 description 1
NOGFHTGYPKWWRX-UHFFFAOYSA-N 2,2,6,6-tetramethyloxan-4-one Chemical compound CC1(C)CC(=O)CC(C)(C)O1 NOGFHTGYPKWWRX-UHFFFAOYSA-N 0.000 description 1
GGHUPYLTAYIGHK-UHFFFAOYSA-N 2-benzoyloxypropanoic acid Chemical compound OC(=O)C(C)OC(=O)C1=CC=CC=C1 GGHUPYLTAYIGHK-UHFFFAOYSA-N 0.000 description 1
GLVYLTSKTCWWJR-UHFFFAOYSA-N 2-carbonoperoxoylbenzoic acid Chemical compound OOC(=O)C1=CC=CC=C1C(O)=O GLVYLTSKTCWWJR-UHFFFAOYSA-N 0.000 description 1
LODHFNUFVRVKTH-ZHACJKMWSA-N 2-hydroxy-n'-[(e)-3-phenylprop-2-enoyl]benzohydrazide Chemical compound OC1=CC=CC=C1C(=O)NNC(=O)\C=C\C1=CC=CC=C1 LODHFNUFVRVKTH-ZHACJKMWSA-N 0.000 description 1
WQIAKSRYDHIZDB-UHFFFAOYSA-N 2-hydroxybenzenecarboperoxoic acid Chemical compound OOC(=O)C1=CC=CC=C1O WQIAKSRYDHIZDB-UHFFFAOYSA-N 0.000 description 1
GCDIHXGIRSXGQZ-UHFFFAOYSA-N 3-(trifluoromethyl)benzenecarboperoxoic acid Chemical compound OOC(=O)C1=CC=CC(C(F)(F)F)=C1 GCDIHXGIRSXGQZ-UHFFFAOYSA-N 0.000 description 1
MEUAICCVSAZKMX-UHFFFAOYSA-N 3-benzoyloxybenzoic acid Chemical compound OC(=O)C1=CC=CC(OC(=O)C=2C=CC=CC=2)=C1 MEUAICCVSAZKMX-UHFFFAOYSA-N 0.000 description 1
NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 1
MEUAVGJWGDPTLF-UHFFFAOYSA-N 4-(5-benzenesulfonylamino-1-methyl-1h-benzoimidazol-2-ylmethyl)-benzamidine Chemical compound N=1C2=CC(NS(=O)(=O)C=3C=CC=CC=3)=CC=C2N(C)C=1CC1=CC=C(C(N)=N)C=C1 MEUAVGJWGDPTLF-UHFFFAOYSA-N 0.000 description 1
QUTZOZQUKYTDGN-UHFFFAOYSA-N 4-hydroxybenzenecarboperoxoic acid Chemical compound OOC(=O)C1=CC=C(O)C=C1 QUTZOZQUKYTDGN-UHFFFAOYSA-N 0.000 description 1
TZAJCDOWOPBMKD-UHFFFAOYSA-N 4-tert-butylbenzenecarboperoxoic acid Chemical compound CC(C)(C)C1=CC=C(C(=O)OO)C=C1 TZAJCDOWOPBMKD-UHFFFAOYSA-N 0.000 description 1
229920001817 Agar Polymers 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
239000004342 Benzoyl peroxide Substances 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 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
SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 1
LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
241000588769 Proteus <enterobacteria> Species 0.000 description 1
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
239000000654 additive Substances 0.000 description 1
239000008272 agar Substances 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000001447 alkali salts Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
239000004599 antimicrobial Substances 0.000 description 1
239000003443 antiviral agent Substances 0.000 description 1
230000001580 bacterial effect Effects 0.000 description 1
210000004666 bacterial spore Anatomy 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
239000012964 benzotriazole Substances 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
VEZXCJBBBCKRPI-UHFFFAOYSA-N beta-propiolactone Chemical compound O=C1CCO1 VEZXCJBBBCKRPI-UHFFFAOYSA-N 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
150000001728 carbonyl compounds Chemical class 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
239000003518 caustics Substances 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Substances OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
238000012937 correction Methods 0.000 description 1
230000000368 destabilizing effect Effects 0.000 description 1
239000012933 diacyl peroxide Substances 0.000 description 1
PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000000975 dye Substances 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
238000011049 filling Methods 0.000 description 1
239000010419 fine particle Substances 0.000 description 1
239000003205 fragrance Substances 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000008103 glucose Substances 0.000 description 1
235000011187 glycerol Nutrition 0.000 description 1
229940015043 glyoxal Drugs 0.000 description 1
239000008187 granular material Substances 0.000 description 1
239000001963 growth medium Substances 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
229910001385 heavy metal Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
JJTUDXZGHPGLLC-UHFFFAOYSA-N lactide Chemical compound CC1OC(=O)C(C)OC1=O JJTUDXZGHPGLLC-UHFFFAOYSA-N 0.000 description 1
150000002632 lipids Chemical class 0.000 description 1
239000007788 liquid Substances 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
229910017464 nitrogen compound Inorganic materials 0.000 description 1
150000002830 nitrogen compounds Chemical class 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
239000002304 perfume Substances 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
125000005385 peroxodisulfate group Chemical group 0.000 description 1
150000004965 peroxy acids Chemical class 0.000 description 1
125000005342 perphosphate group Chemical group 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
229960000380 propiolactone Drugs 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
235000010288 sodium nitrite Nutrition 0.000 description 1
229960001922 sodium perborate Drugs 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
239000002422 sporicide Substances 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
238000011146 sterile filtration Methods 0.000 description 1
239000001384 succinic acid Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
239000003826 tablet Substances 0.000 description 1
239000010409 thin film Substances 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000002110 toxicologic effect Effects 0.000 description 1
231100000027 toxicology Toxicity 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
- 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
- A01N37/16—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 containing the group; Thio analogues thereof
- 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
- A01N37/36—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 containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
- A01N37/38—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 containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
- A01N37/40—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 containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (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)
Agricultural Chemicals And Associated Chemicals (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

CH1388377A 1977-06-03 1977-11-14 Alcoholic disinfectant having a sporicidal action CH634720A5 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19772725067 DE2725067A1 (de)	1977-06-03	1977-06-03	Alkohlisches desinfektionsmittel mit sporizider wirkung

Publications (1)

Publication Number	Publication Date
CH634720A5 true CH634720A5 (en)	1983-02-28

Family

ID=6010613

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH1388377A CH634720A5 (en)	1977-06-03	1977-11-14	Alcoholic disinfectant having a sporicidal action

Country Status (13)

Country	Link
AT (1)	ATA714277A (da)
BE (1)	BE861024A (da)
CH (1)	CH634720A5 (da)
DE (1)	DE2725067A1 (da)
DK (1)	DK29978A (da)
FI (1)	FI64265C (da)
FR (1)	FR2392676A1 (da)
GB (1)	GB1577396A (da)
IE (1)	IE46453B1 (da)
LU (1)	LU78568A1 (da)
NL (1)	NL7801851A (da)
NO (1)	NO149232C (da)
SE (1)	SE7714474L (da)

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GB8500108D0 (en) *	1985-01-03	1985-02-13	Unilever Plc	Disinfectant compositions
EP0267175B1 (en) *	1986-11-03	1993-10-13	Monsanto Company	Sulfone peroxycarboxylic acids
US5004558A (en) *	1986-11-03	1991-04-02	Monsanto Company	Sulfone peroxycarboxylic acids
US4758369A (en) *	1986-11-03	1988-07-19	Monsanto Company	Sulfone peroxycarboxylic acids
US5039447A (en) *	1988-12-12	1991-08-13	Monsanto Company	Pourable sulfone peracid compositions
US5200189A (en) *	1991-07-23	1993-04-06	Ecolab Inc.	Peroxyacid antimicrobial composition
DE4225795C2 (de) *	1992-07-31	1994-09-01	Schuelke & Mayr Gmbh	Desinfektionsmittel auf Carbonsäurebasis
US6010729A (en)	1998-08-20	2000-01-04	Ecolab Inc.	Treatment of animal carcasses
DE10106444C2 (de) *	2000-02-11	2002-12-12	Kesla Forschung U Service Kg	Mittel zur viruziden Händedesinfektion
US7150884B1 (en)	2000-07-12	2006-12-19	Ecolab Inc.	Composition for inhibition of microbial growth
US6479454B1 (en)	2000-10-05	2002-11-12	Ecolab Inc.	Antimicrobial compositions and methods containing hydrogen peroxide and octyl amine oxide
US6627593B2 (en)	2001-07-13	2003-09-30	Ecolab Inc.	High concentration monoester peroxy dicarboxylic acid compositions, use solutions, and methods employing them
GB2378136A (en) *	2001-08-01	2003-02-05	Thomas David White	Disinfectant formulation and method for determining sporicidal activity
US7771737B2 (en)	2004-01-09	2010-08-10	Ecolab Inc.	Medium chain peroxycarboxylic acid compositions
WO2005070205A1 (en)	2004-01-09	2005-08-04	Ecolab Inc.	Medium chain peroxycarboxylic acid compositions
US7887641B2 (en)	2004-01-09	2011-02-15	Ecolab Usa Inc.	Neutral or alkaline medium chain peroxycarboxylic acid compositions and methods employing them
DE102005024001A1 (de) *	2005-05-25	2006-11-30	Schneiders, Josef	Desinfektions- und Entkeimungsmittel
US7754670B2 (en)	2005-07-06	2010-07-13	Ecolab Inc.	Surfactant peroxycarboxylic acid compositions
US7547421B2 (en)	2006-10-18	2009-06-16	Ecolab Inc.	Apparatus and method for making a peroxycarboxylic acid
US8075857B2 (en)	2006-10-18	2011-12-13	Ecolab Usa Inc.	Apparatus and method for making a peroxycarboxylic acid
DE102006062616A1 (de) *	2006-12-29	2008-07-03	Anovis Biotech Gmbh	Kontaktlinsenreiniger
EP2724614A1 (de) *	2012-10-24	2014-04-30	Wesso Ag	Verwendung einer Reinigungszusammensetzung, insbesondere zur Desinfektion und/oder Keimreduzierung, von Eiern und Verfahren
DE102016220253B4 (de) *	2016-10-17	2025-08-21	Bayerische Motoren Werke Aktiengesellschaft	Kraftfahrzeug mit Desinfektionsvorrichtung
AU2019222696B2 (en)	2018-02-14	2024-02-29	Ecolab Usa Inc.	Compositions and methods for the reduction of biofilm and spores from membranes
EP4097082B1 (en)	2020-01-31	2024-04-24	Ecolab USA Inc.	Generation of peroxyhydroxycarboxylic acid and the use thereof
US11739058B2 (en)	2021-01-29	2023-08-29	Ecolab Usa Inc.	Solid peroxyalphahydroxycarboxylic acid generation compositions and the use thereof

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Publication number	Priority date	Publication date	Assignee	Title
FR319248A (fr) *	1902-03-03	1902-11-07	Page	Perfectionnements dans les compositions antiseptiques et les procédés pour les produire
BE587389A (da) *	1959-02-11
GB1269677A (en) *	1969-12-11	1972-04-06	Procter & Gamble Ltd	Bleaching composition
GB1538744A (en) *	1975-05-13	1979-01-24	Interox Chemicals Ltd	Bleaching composition containing diacyl peroxides

1977
- 1977-06-03 DE DE19772725067 patent/DE2725067A1/de not_active Withdrawn
- 1977-10-06 AT AT714277A patent/ATA714277A/de unknown
- 1977-11-14 CH CH1388377A patent/CH634720A5/de not_active IP Right Cessation
- 1977-11-21 BE BE182788A patent/BE861024A/xx not_active IP Right Cessation
- 1977-11-22 LU LU78568A patent/LU78568A1/xx unknown
- 1977-11-30 FR FR7736034A patent/FR2392676A1/fr active Granted
- 1977-12-20 SE SE7714474A patent/SE7714474L/xx not_active Application Discontinuation
- 1977-12-29 FI FI773961A patent/FI64265C/fi not_active IP Right Cessation
1978
- 1978-01-16 NO NO780154A patent/NO149232C/no unknown
- 1978-01-20 DK DK29978A patent/DK29978A/da not_active Application Discontinuation
- 1978-02-03 GB GB4389/78A patent/GB1577396A/en not_active Expired
- 1978-02-08 IE IE277/78A patent/IE46453B1/en unknown
- 1978-02-17 NL NL7801851A patent/NL7801851A/xx not_active Application Discontinuation

Also Published As

Publication number	Publication date
FI64265B (fi)	1983-07-29
NO780154L (no)	1978-12-05
NO149232C (no)	1984-03-14
LU78568A1 (da)	1978-04-20
FI64265C (fi)	1983-11-10
FR2392676B1 (da)	1980-08-22
IE780277L (en)	1978-12-03
ATA714277A (de)	1981-01-15
NL7801851A (nl)	1978-12-05
DK29978A (da)	1978-12-04
NO149232B (no)	1983-12-05
FI773961A7 (fi)	1978-12-04
IE46453B1 (en)	1983-06-15
BE861024A (fr)	1978-03-16
SE7714474L (sv)	1978-12-04
GB1577396A (en)	1980-10-22
DE2725067A1 (de)	1978-12-14
FR2392676A1 (fr)	1978-12-29

Legal Events

Date	Code	Title	Description
1984-07-31	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
CH634720A5 (en)	1983-02-28	Alcoholic disinfectant having a sporicidal action
DE69418305T2 (de)	1999-11-25	Zusammensetzungen und verwendungen davon
KR101608109B1 (ko)	2016-03-31	알파-케토 과산 및 이의 제조 및 사용 방법
DE69508939T2 (de)	1999-11-11	Persauerstoffverbindung enthaltende zusammensetzung
AU2017238050B2 (en)	2021-03-04	Non-alpha substituted peroxy acids and uses thereof
DE3543500A1 (de)	1987-06-11	Waessrige loesung aromatischer percarbonsaeuren und deren verwendung
DE60311486T2 (de)	2007-11-08	Stabile synergistische antimikrobielle zusammensetzungen aus aldehyddonatoren und deshydroessigsüure mit niedrigem gehalt an freiem formaldehyd
DE2554587C2 (de)	1983-09-01	Desinfektionsmittel
DE69728911T2 (de)	2005-04-28	Verfahren zur bekämpfung von mikroorganismen
DE1297813B (de)	1969-06-19	Antimikrobielle Mittel
DE2312280A1 (de)	1974-09-26	Verwendung von beta-hydroxycarbonsaeuren als antimikrobielle substanzen
DE69906070T2 (de)	2003-12-04	Desinfizierende zubereitung, die chlor in alkohol enthält
DE19642127A1 (de)	1998-04-16	Verfahren zur Desinfektion und Mittel zu seiner Durchführung
DE2320415C3 (de)	1980-04-24	Verfahren zur Verhinderung der Schleimbildung in wäßrigen Zellstoffsuspensionen durch Anwendung keimtötender Mittel
DE68903510T2 (de)	1993-04-01	Wasserstoffperoxid enthaltende desinfektionsmittel.
DE69032220T2 (de)	1998-12-17	Zusammensetzung und Verfahren zur Sterilisierung der Pathogene in Gegenwart von Wasser
DE2538771A1 (de)	1977-03-17	Antimikrobielle mittel
DE102011120076A1 (de)	2013-06-06	Desinfektions- und Entkeimungsmittel auf Percarbonsäurebasis
DE2516922C3 (de)	1980-09-11	Desinfektionsmittel
DE2433836A1 (de)	1976-01-29	Desinfektionsmittel mit sporicider wirkung
EP0668014A1 (de)	1995-08-23	Wässriges Desinfektionsmittelkonzentrat und Desinfektionsmittel auf Aldehyd- und Alkoholbasis und deren Verwendung
DE2817942A1 (de)	1979-10-25	Verfahren zum herstellen einer verbindung mit keimtoetender wirkung sowie verwendung der verbindung als keimtoetungsmittel
EP0017011A1 (de)	1980-10-15	Mikrobizides Mittel und seine Verwendung
DE2349058A1 (de)	1975-04-03	Verwendung von beta-hydroxycarbonsaeuren in kombination mit formaldehyd als antimikrobielle mittel
DE10121625A1 (de)	2002-11-07	Neuartige Mischungen von Alkali- oder Erdalkalibromiden mit Salzen der Monoperphtalsäure