CS209494B2 - Desinfectant - Google Patents

Desinfectant Download PDF

Info

Publication number: CS209494B2
Authority: CS; Czechoslovakia
Prior art keywords: carbon atoms; alkyl; chlorinated; formula; mixture
Prior art date: 1976-04-15

Application number

CS772459A

Other languages

Czech (cs)

English (en)

Inventor

Ulrich Cuntze

Wolfgang Raether

Bernhard Reul

Gerhard Ross

Original Assignee

Hoechst Ag

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.)

1976-04-15

Filing date

1977-04-14

Publication date

1981-12-31

1977-04-14 Application filed by Hoechst Ag filed Critical Hoechst Ag

1981-12-31 Publication of CS209494B2 publication Critical patent/CS209494B2/cs

Links

239000000645 desinfectant Substances 0.000 title claims abstract description 20
239000000203 mixture Substances 0.000 claims abstract description 48
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 20
150000001875 compounds Chemical class 0.000 claims abstract description 20
125000000217 alkyl group Chemical group 0.000 claims abstract description 18
150000004945 aromatic hydrocarbons Chemical class 0.000 claims abstract description 12
150000008280 chlorinated hydrocarbons Chemical class 0.000 claims abstract description 11
125000003342 alkenyl group Chemical group 0.000 claims abstract description 10
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 8
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 5
229910052739 hydrogen Inorganic materials 0.000 claims description 8
239000001257 hydrogen Substances 0.000 claims description 8
150000001335 aliphatic alkanes Chemical class 0.000 claims description 5
229930195733 hydrocarbon Natural products 0.000 claims description 5
150000002430 hydrocarbons Chemical class 0.000 claims description 5
239000003995 emulsifying agent Substances 0.000 claims description 4
239000004215 Carbon black (E152) Substances 0.000 claims description 3
150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 2
HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 claims 1
229910052799 carbon Inorganic materials 0.000 claims 1
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 12
210000003250 oocyst Anatomy 0.000 description 11
235000013162 Cocos nucifera Nutrition 0.000 description 10
244000060011 Cocos nucifera Species 0.000 description 10
235000019197 fats Nutrition 0.000 description 10
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 8
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 8
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 8
235000014113 dietary fatty acids Nutrition 0.000 description 7
239000000194 fatty acid Substances 0.000 description 7
229930195729 fatty acid Natural products 0.000 description 7
238000009472 formulation Methods 0.000 description 7
-1 lysium Chemical compound 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 6
150000004665 fatty acids Chemical group 0.000 description 6
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
241001465754 Metazoa Species 0.000 description 5
239000004359 castor oil Substances 0.000 description 5
235000019438 castor oil Nutrition 0.000 description 5
230000000694 effects Effects 0.000 description 5
210000003608 fece Anatomy 0.000 description 5
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 5
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 4
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 4
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 4
241000224483 Coccidia Species 0.000 description 4
239000005639 Lauric acid Substances 0.000 description 4
239000005642 Oleic acid Substances 0.000 description 4
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 4
150000001336 alkenes Chemical class 0.000 description 4
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 4
230000000052 comparative effect Effects 0.000 description 4
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 4
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 4
239000000126 substance Substances 0.000 description 4
239000003760 tallow Substances 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
241000287828 Gallus gallus Species 0.000 description 3
206010061218 Inflammation Diseases 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 3
235000013330 chicken meat Nutrition 0.000 description 3
230000004054 inflammatory process Effects 0.000 description 3
OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 3
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical group CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 3
239000000344 soap Substances 0.000 description 3
UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 2
QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
GBDZXPJXOMHESU-UHFFFAOYSA-N 1,2,3,4-tetrachlorobenzene Chemical compound ClC1=CC=C(Cl)C(Cl)=C1Cl GBDZXPJXOMHESU-UHFFFAOYSA-N 0.000 description 2
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 2
FQHUDZKKDCTQET-UHFFFAOYSA-N 2-undecyl-4,5-dihydro-1h-imidazole Chemical compound CCCCCCCCCCCC1=NCCN1 FQHUDZKKDCTQET-UHFFFAOYSA-N 0.000 description 2
241000894006 Bacteria Species 0.000 description 2
241000252983 Caecum Species 0.000 description 2
241000223932 Eimeria tenella Species 0.000 description 2
241000233866 Fungi Species 0.000 description 2
208000032843 Hemorrhage Diseases 0.000 description 2
CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 2
241000700605 Viruses Species 0.000 description 2
150000007824 aliphatic compounds Chemical class 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
150000001491 aromatic compounds Chemical class 0.000 description 2
230000000740 bleeding effect Effects 0.000 description 2
239000008280 blood Substances 0.000 description 2
210000004369 blood Anatomy 0.000 description 2
210000004534 cecum Anatomy 0.000 description 2
229930003836 cresol Natural products 0.000 description 2
235000013601 eggs Nutrition 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
239000007970 homogeneous dispersion Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
238000007127 saponification reaction Methods 0.000 description 2
239000008149 soap solution Substances 0.000 description 2
230000000087 stabilizing effect Effects 0.000 description 2
238000004659 sterilization and disinfection Methods 0.000 description 2
229950011008 tetrachloroethylene Drugs 0.000 description 2
RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-N 0.000 description 1
OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
VGVRPFIJEJYOFN-UHFFFAOYSA-N 2,3,4,6-tetrachlorophenol Chemical class OC1=C(Cl)C=C(Cl)C(Cl)=C1Cl VGVRPFIJEJYOFN-UHFFFAOYSA-N 0.000 description 1
QSTMCYGOOQYONB-UHFFFAOYSA-N 2-(2-undecyl-1,3-diazinan-1-yl)ethanol Chemical compound CCCCCCCCCCCC1NCCCN1CCO QSTMCYGOOQYONB-UHFFFAOYSA-N 0.000 description 1
MOZMMIQDWCAKPB-UHFFFAOYSA-N 2-(2-undecylimidazolidin-1-yl)ethanol Chemical compound CCCCCCCCCCCC1NCCN1CCO MOZMMIQDWCAKPB-UHFFFAOYSA-N 0.000 description 1
QULUVEPNTKJBMR-KTKRTIGZSA-N 2-[(z)-octadec-9-enyl]-4,5-dihydro-1h-imidazole Chemical compound CCCCCCCC\C=C/CCCCCCCCC1=NCCN1 QULUVEPNTKJBMR-KTKRTIGZSA-N 0.000 description 1
YTWBFUCJVWKCCK-UHFFFAOYSA-N 2-heptadecyl-1h-imidazole Chemical compound CCCCCCCCCCCCCCCCCC1=NC=CN1 YTWBFUCJVWKCCK-UHFFFAOYSA-N 0.000 description 1
DNBBBVUQNUFZPZ-UHFFFAOYSA-N 2-heptadecyl-5-methyl-4,5-dihydro-1h-imidazole Chemical compound CCCCCCCCCCCCCCCCCC1=NC(C)CN1 DNBBBVUQNUFZPZ-UHFFFAOYSA-N 0.000 description 1
AFLPLRHYPOBJKP-UHFFFAOYSA-N 2-undecyl-1,2,3,4-tetrahydropyrimidine Chemical compound CCCCCCCCCCCC1NCC=CN1 AFLPLRHYPOBJKP-UHFFFAOYSA-N 0.000 description 1
WADQOGCINABPRT-UHFFFAOYSA-N 3-chloro-2-methylphenol Chemical class CC1=C(O)C=CC=C1Cl WADQOGCINABPRT-UHFFFAOYSA-N 0.000 description 1
KFZXVMNBUMVKLN-UHFFFAOYSA-N 4-chloro-5-methyl-2-propan-2-ylphenol Chemical compound CC(C)C1=CC(Cl)=C(C)C=C1O KFZXVMNBUMVKLN-UHFFFAOYSA-N 0.000 description 1
FWZWHBIVRBXYRE-KHPPLWFESA-N 5-methyl-2-[(z)-octadec-9-enyl]-4,5-dihydro-1h-imidazole Chemical compound CCCCCCCC\C=C/CCCCCCCCC1=NC(C)CN1 FWZWHBIVRBXYRE-KHPPLWFESA-N 0.000 description 1
YWPDAKSNPWIZOX-UHFFFAOYSA-N 5-methyl-2-undecyl-4,5-dihydro-1h-imidazole Chemical compound CCCCCCCCCCCC1=NCC(C)N1 YWPDAKSNPWIZOX-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
206010003011 Appendicitis Diseases 0.000 description 1
241000271566 Aves Species 0.000 description 1
241000283690 Bos taurus Species 0.000 description 1
DRSHXJFUUPIBHX-UHFFFAOYSA-N COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 Chemical compound COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 DRSHXJFUUPIBHX-UHFFFAOYSA-N 0.000 description 1
241000282472 Canis lupus familiaris Species 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
235000008733 Citrus aurantifolia Nutrition 0.000 description 1
208000003495 Coccidiosis Diseases 0.000 description 1
241000282326 Felis catus Species 0.000 description 1
206010023076 Isosporiasis Diseases 0.000 description 1
102000011782 Keratins Human genes 0.000 description 1
108010076876 Keratins Proteins 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
241000283973 Oryctolagus cuniculus Species 0.000 description 1
241001494479 Pecora Species 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
206010037549 Purpura Diseases 0.000 description 1
239000005708 Sodium hypochlorite Substances 0.000 description 1
235000011941 Tilia x europaea Nutrition 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
239000013543 active substance Substances 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000004996 alkyl benzenes Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
235000021053 average weight gain Nutrition 0.000 description 1
238000005422 blasting Methods 0.000 description 1
208000003836 bluetongue Diseases 0.000 description 1
238000009395 breeding Methods 0.000 description 1
230000001488 breeding effect Effects 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000011280 coal tar Substances 0.000 description 1
239000003240 coconut oil Substances 0.000 description 1
235000019864 coconut oil Nutrition 0.000 description 1
150000001896 cresols Chemical class 0.000 description 1
230000006378 damage Effects 0.000 description 1
230000000249 desinfective effect Effects 0.000 description 1
229940117389 dichlorobenzene Drugs 0.000 description 1
238000007865 diluting Methods 0.000 description 1
231100000676 disease causative agent Toxicity 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 1
230000029142 excretion Effects 0.000 description 1
239000002360 explosive Substances 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
230000001976 improved effect Effects 0.000 description 1
210000004347 intestinal mucosa Anatomy 0.000 description 1
210000000936 intestine Anatomy 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
239000011630 iodine Substances 0.000 description 1
235000015110 jellies Nutrition 0.000 description 1
239000008274 jelly Substances 0.000 description 1
239000004571 lime Substances 0.000 description 1
210000004877 mucosa Anatomy 0.000 description 1
QCENGKPIBJNODL-UHFFFAOYSA-N n'-dodecylethane-1,2-diamine Chemical compound CCCCCCCCCCCCNCCN QCENGKPIBJNODL-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000019198 oils Nutrition 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
231100000915 pathological change Toxicity 0.000 description 1
230000036285 pathological change Effects 0.000 description 1
230000001575 pathological effect Effects 0.000 description 1
239000008188 pellet Substances 0.000 description 1
CETWGWHVAKIHPW-UHFFFAOYSA-N pentadecane-2,3-diamine Chemical compound CCCCCCCCCCCCC(N)C(C)N CETWGWHVAKIHPW-UHFFFAOYSA-N 0.000 description 1
230000002085 persistent effect Effects 0.000 description 1
206010034754 petechiae Diseases 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
244000144977 poultry Species 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000007704 transition Effects 0.000 description 1
230000004580 weight loss Effects 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/01—Deodorant compositions
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/141—Esters of phosphorous acids
- C07F9/1411—Esters of phosphorous acids with hydroxyalkyl compounds with further substituents on alkyl

Landscapes

Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
General Health & Medical Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
Animal Behavior & Ethology (AREA)
Molecular Biology (AREA)
Biochemistry (AREA)
Epidemiology (AREA)
Pharmacology & Pharmacy (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Medicinal Chemistry (AREA)
Tropical Medicine & Parasitology (AREA)
General Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

CS772459A 1976-04-15 1977-04-14 Desinfectant CS209494B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19762616713 DE2616713A1 (de)	1976-04-15	1976-04-15	Desinfektionsmittel

Publications (1)

Publication Number	Publication Date
CS209494B2 true CS209494B2 (en)	1981-12-31

Family

ID=5975491

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS772459A CS209494B2 (en)	1976-04-15	1977-04-14	Desinfectant

Country Status (20)

Country	Link
US (1)	US4185098A (de)
JP (1)	JPS52128224A (de)
AR (1)	AR212760A1 (de)
AT (1)	AT361136B (de)
AU (1)	AU511838B2 (de)
BE (1)	BE853665R (de)
BR (1)	BR7702352A (de)
CA (1)	CA1086641A (de)
CH (1)	CH608715A5 (de)
CS (1)	CS209494B2 (de)
DD (1)	DD132233A5 (de)
DE (1)	DE2616713A1 (de)
DK (1)	DK165977A (de)
FR (1)	FR2347935A2 (de)
GB (1)	GB1569373A (de)
HU (1)	HU181440B (de)
IT (1)	IT1113556B (de)
NL (1)	NL7703888A (de)
SE (1)	SE7704246L (de)
ZA (1)	ZA772281B (de)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4128977A (en) *	1973-11-05	1978-12-12	Schubeis Ewald I E	Door frame, especially for fireproof doors
AU6667894A (en) *	1993-04-28	1994-11-21	Alcon Laboratories, Inc.	Diamines as antimicrobial agents and use thereof in ophthalmic composition
US5573726A (en) *	1993-09-22	1996-11-12	Alcon Laboratories, Inc.	Use of amidoamines in ophthalmic compositions
US5631005A (en) *	1994-09-21	1997-05-20	Alcon Laboratories, Inc.	Use of amidoamines in ophthalmic compositions
US5393491A (en) *	1993-09-22	1995-02-28	Alcon Laboratories, Inc.	Use of amidoamines in ophthalmic compositions
FR2926954B1 (fr) *	2008-02-05	2012-03-23	Cid Lines Nv	Utilisation d'une composition pour le traitement des surfaces des batiments d'elevage et/ou de leur materiel
AU2011323841B2 (en)	2010-10-25	2016-08-25	Stepan Company	Fatty amines, amidoamines, and their derivatives from natural oil metathesis

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2459062A (en) *	1944-02-08	1949-01-11	American Cyanamid Co	Quaternary ammonium compounds
GB783882A (en)	1954-04-05	1957-10-02	Shell Res Ltd	Pesticidal compositions
NL7310890A (de) *	1972-08-12	1974-02-14
AR208061A1 (es) *	1973-04-14	1976-11-30	Hoechst Ag	Una composicion desinfectante en base a esteres de acido alquilo alquenil-amonio-alquilen fosforico

1976
- 1976-04-15 DE DE19762616713 patent/DE2616713A1/de not_active Withdrawn
1977
- 1977-04-07 NL NL7703888A patent/NL7703888A/xx not_active Application Discontinuation
- 1977-04-12 CH CH774508A patent/CH608715A5/xx not_active IP Right Cessation
- 1977-04-13 DD DD7700198380A patent/DD132233A5/de unknown
- 1977-04-13 SE SE7704246A patent/SE7704246L/xx not_active Application Discontinuation
- 1977-04-13 AR AR267199A patent/AR212760A1/es active
- 1977-04-13 US US05/787,205 patent/US4185098A/en not_active Expired - Lifetime
- 1977-04-13 IT IT22436/77A patent/IT1113556B/it active
- 1977-04-14 CS CS772459A patent/CS209494B2/cs unknown
- 1977-04-14 BR BR7702352A patent/BR7702352A/pt unknown
- 1977-04-14 ZA ZA00772281A patent/ZA772281B/xx unknown
- 1977-04-14 AU AU24268/77A patent/AU511838B2/en not_active Expired
- 1977-04-14 HU HU77HO1974A patent/HU181440B/hu unknown
- 1977-04-14 DK DK165977A patent/DK165977A/da not_active IP Right Cessation
- 1977-04-14 AT AT262577A patent/AT361136B/de not_active IP Right Cessation
- 1977-04-15 GB GB15780A patent/GB1569373A/en not_active Expired
- 1977-04-15 FR FR7711476A patent/FR2347935A2/fr active Granted
- 1977-04-15 JP JP4272377A patent/JPS52128224A/ja active Pending
- 1977-04-15 CA CA276,302A patent/CA1086641A/en not_active Expired
- 1977-04-15 BE BE176775A patent/BE853665R/xx active

Also Published As

Publication number	Publication date
CH608715A5 (de)	1979-01-31
AT361136B (de)	1981-02-25
DD132233A5 (de)	1978-09-13
SE7704246L (sv)	1977-10-16
IT1113556B (it)	1986-01-20
BR7702352A (pt)	1978-05-09
JPS52128224A (en)	1977-10-27
BE853665R (fr)	1977-10-17
DK165977A (da)	1977-10-16
AU511838B2 (en)	1980-09-11
ATA262577A (de)	1980-07-15
NL7703888A (nl)	1977-10-18
AU2426877A (en)	1978-10-19
AR212760A1 (es)	1978-09-29
GB1569373A (en)	1980-06-11
ZA772281B (en)	1978-03-29
FR2347935A2 (fr)	1977-11-10
DE2616713A1 (de)	1977-11-03
HU181440B (en)	1983-07-28
CA1086641A (en)	1980-09-30
US4185098A (en)	1980-01-22
FR2347935B2 (de)	1980-10-10

Publication	Publication Date	Title
ES2632265T3 (es)	2017-09-12	Azinas sustituidas como plaguicidas
JPH06192128A (ja)	1994-07-12	魚類寄生虫の駆除
KR102341812B1 (ko)	2021-12-21	구충제로서의 신규 술포닐아미노벤즈아미드 화합물
US4185098A (en)	1980-01-22	Disinfectant
KR20170018915A (ko)	2017-02-20	신규 술포닐아미노벤즈아미드 화합물
Lauten et al.	1992	Efficacies of novel N-halamine disinfectants against Salmonella and Pseudomonas species
CS208761B2 (en)	1981-09-15	Fungicide means
US3702360A (en)	1972-11-07	Method of controlling insects on animals with organotin compounds
JPH06500565A (ja)	1994-01-20	軟体動物の抑制および低減方法
Soll	1989	Use of ivermectin in laboratory and exotic mammals and in birds, fish, and reptiles
EP1246624B1 (de)	2005-06-29	Triazinonverbindungen zur behandlung von durch den befall mit parasitischen protozoen bedingten krankheiten
JP2598774B2 (ja)	1997-04-09	動物のコクシジウム症予防殺菌消毒剤
PT99669B (pt)	1998-01-30	Processo para a preparacao de composicoes nematodicidas contendo como ingrediente activo 2r,5r-di-hidroximetil-3r,4r-di-hidroxipirrolidina (dmdp) como ingrediente activo
DE2319045C3 (de)	1976-04-01	Desinfektionsmittel
JP2010510285A (ja)	2010-04-02	寄生虫の駆除および阻止用組成物
ATE26832T1 (de)	1987-05-15	Isothioharnstoffe.
KUTSUMI et al.	1965	Effect of thiabendazole as an ovicide on helminth eggs in nightsoil
US5585403A (en)	1996-12-17	Sterilizing agent for preventing coccidiosis in animals
DE10136397A1 (de)	2003-02-13	Mittel zum Abtöten oder Auflösen von Kokzidien und Oozysten
GB2052988A (en)	1981-02-04	Compositions for the control of parasites in warm-blooded animals
DE2260763C3 (de)	1979-11-29	Bekämpfung von schädlichen Organismen mit Dihalogenpropansulfonsäureesterderivaten
Richards et al.	1987	Anthelmintic efficacy of netobimin against naturally acquired gastrointestinal nematodes in yearling heifers
JPS58128321A (ja)	1983-07-30	動物のコクシジウム症予防剤
DE2319045A1 (de)	1974-10-31	Desinfektionsmittel
US3386881A (en)	1968-06-04	Chlorinated hydrocarbon insecticides synergized with aliphastic amines