CA2196771A1 - Surface-active formulations - Google Patents

Surface-active formulations

Info

Publication number: CA2196771A1
Authority: CA; Canada
Prior art keywords: formulation according; component; weight; hydrogen; acid
Prior art date: 1994-08-25
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.): Abandoned

Application number

CA002196771A

Other languages

English (en)

French (fr)

Inventor

Laszlo Moldovanyi

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

BASF Schweiz AG

Original Assignee

Individual

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.)

1994-08-25

Filing date

1995-08-14

Publication date

1996-02-29

1995-08-14 Application filed by Individual filed Critical Individual

1996-02-29 Publication of CA2196771A1 publication Critical patent/CA2196771A1/en

Status Abandoned legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 42
238000009472 formulation Methods 0.000 title claims abstract 27
239000002253 acid Substances 0.000 claims abstract description 46
150000003839 salts Chemical class 0.000 claims abstract description 32
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 30
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 28
239000000344 soap Substances 0.000 claims abstract description 15
239000008367 deionised water Substances 0.000 claims abstract description 12
239000004094 surface-active agent Substances 0.000 claims abstract description 12
150000001298 alcohols Chemical class 0.000 claims abstract description 10
229920006395 saturated elastomer Polymers 0.000 claims abstract description 7
239000013543 active substance Substances 0.000 claims abstract description 5
235000019445 benzyl alcohol Nutrition 0.000 claims abstract description 5
239000002280 amphoteric surfactant Substances 0.000 claims abstract description 3
150000003938 benzyl alcohols Chemical class 0.000 claims abstract description 3
125000006267 biphenyl group Chemical group 0.000 claims abstract description 3
239000003795 chemical substances by application Substances 0.000 claims abstract description 3
150000002989 phenols Chemical class 0.000 claims abstract description 3
GHXZTYHSJHQHIJ-UHFFFAOYSA-N Chlorhexidine Chemical compound C=1C=C(Cl)C=CC=1NC(N)=NC(N)=NCCCCCCN=C(N)N=C(N)NC1=CC=C(Cl)C=C1 GHXZTYHSJHQHIJ-UHFFFAOYSA-N 0.000 claims abstract 3
229960003260 chlorhexidine Drugs 0.000 claims abstract 3
230000003165 hydrotropic effect Effects 0.000 claims abstract 2
230000003641 microbiacidal effect Effects 0.000 claims abstract 2
238000004659 sterilization and disinfection Methods 0.000 claims abstract 2
239000000126 substance Substances 0.000 claims abstract 2
229910052739 hydrogen Inorganic materials 0.000 claims description 35
239000001257 hydrogen Substances 0.000 claims description 35
-1 chloro, nitro, phenyl Chemical group 0.000 claims description 31
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 30
150000002431 hydrogen Chemical group 0.000 claims description 20
150000001875 compounds Chemical class 0.000 claims description 18
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 15
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
125000001309 chloro group Chemical group Cl* 0.000 claims description 9
229940079842 sodium cumenesulfonate Drugs 0.000 claims description 9
QEKATQBVVAZOAY-UHFFFAOYSA-M sodium;4-propan-2-ylbenzenesulfonate Chemical compound [Na+].CC(C)C1=CC=C(S([O-])(=O)=O)C=C1 QEKATQBVVAZOAY-UHFFFAOYSA-M 0.000 claims description 9
229910052783 alkali metal Inorganic materials 0.000 claims description 8
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 8
229910052736 halogen Chemical group 0.000 claims description 7
150000002367 halogens Chemical group 0.000 claims description 7
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
150000003871 sulfonates Chemical class 0.000 claims description 6
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 5
239000003945 anionic surfactant Substances 0.000 claims description 5
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 5
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
125000001246 bromo group Chemical group Br* 0.000 claims description 4
RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 claims description 4
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 4
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 4
150000007522 mineralic acids Chemical class 0.000 claims description 3
150000007524 organic acids Chemical class 0.000 claims description 3
DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 claims description 2
JBVOQKNLGSOPNZ-UHFFFAOYSA-N 2-propan-2-ylbenzenesulfonic acid Chemical compound CC(C)C1=CC=CC=C1S(O)(=O)=O JBVOQKNLGSOPNZ-UHFFFAOYSA-N 0.000 claims description 2
DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 claims description 2
241000723346 Cinnamomum camphora Species 0.000 claims description 2
URXZXNYJPAJJOQ-UHFFFAOYSA-N Erucic acid Natural products CCCCCCC=CCCCCCCCCCCCC(O)=O URXZXNYJPAJJOQ-UHFFFAOYSA-N 0.000 claims description 2
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
229960000846 camphor Drugs 0.000 claims description 2
229930008380 camphor Natural products 0.000 claims description 2
229940071118 cumenesulfonate Drugs 0.000 claims description 2
UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 claims description 2
DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 claims description 2
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 2
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 2
IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 claims description 2
229910052717 sulfur Inorganic materials 0.000 claims description 2
239000011593 sulfur Substances 0.000 claims description 2
150000003505 terpenes Chemical class 0.000 claims description 2
239000008096 xylene Substances 0.000 claims description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 claims 7
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 3
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 claims 2
YASYEJJMZJALEJ-UHFFFAOYSA-N Citric acid monohydrate Chemical compound O.OC(=O)CC(O)(C(O)=O)CC(O)=O YASYEJJMZJALEJ-UHFFFAOYSA-N 0.000 claims 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims 2
150000003863 ammonium salts Chemical class 0.000 claims 2
150000001491 aromatic compounds Chemical class 0.000 claims 2
229960002303 citric acid monohydrate Drugs 0.000 claims 2
FKKAGFLIPSSCHT-UHFFFAOYSA-N 1-dodecoxydodecane;sulfuric acid Chemical compound OS(O)(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC FKKAGFLIPSSCHT-UHFFFAOYSA-N 0.000 claims 1
230000000845 anti-microbial effect Effects 0.000 claims 1
239000004599 antimicrobial Substances 0.000 claims 1
MRUAUOIMASANKQ-UHFFFAOYSA-N cocamidopropyl betaine Chemical compound CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O MRUAUOIMASANKQ-UHFFFAOYSA-N 0.000 claims 1
229940073507 cocamidopropyl betaine Drugs 0.000 claims 1
150000003242 quaternary ammonium salts Chemical class 0.000 claims 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims 1
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Natural products OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 35
150000007513 acids Chemical class 0.000 description 13
229910052708 sodium Inorganic materials 0.000 description 13
239000011734 sodium Substances 0.000 description 13
239000000243 solution Substances 0.000 description 13
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 8
125000004356 hydroxy functional group Chemical group O* 0.000 description 7
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 6
230000000694 effects Effects 0.000 description 6
229910052751 metal Inorganic materials 0.000 description 6
239000002184 metal Substances 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
125000004432 carbon atom Chemical group C* 0.000 description 5
235000014113 dietary fatty acids Nutrition 0.000 description 5
239000000194 fatty acid Substances 0.000 description 5
229930195729 fatty acid Natural products 0.000 description 5
239000000843 powder Substances 0.000 description 5
241000304886 Bacilli Species 0.000 description 4
WLJVNTCWHIRURA-UHFFFAOYSA-N Heptanedioic acid Natural products OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 4
BDJRBEYXGGNYIS-UHFFFAOYSA-N Nonanedioid acid Natural products OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 4
TYFQFVWCELRYAO-UHFFFAOYSA-N Suberic acid Natural products OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 4
150000004665 fatty acids Chemical class 0.000 description 4
WNLRTRBMVRJNCN-UHFFFAOYSA-N hexanedioic acid Natural products OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 4
150000001412 amines Chemical class 0.000 description 3
239000003599 detergent Substances 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
150000003467 sulfuric acid derivatives Chemical class 0.000 description 3
OOCCDEMITAIZTP-QPJJXVBHSA-N (E)-cinnamyl alcohol Chemical compound OC\C=C\C1=CC=CC=C1 OOCCDEMITAIZTP-QPJJXVBHSA-N 0.000 description 2
ZCHHRLHTBGRGOT-SNAWJCMRSA-N (E)-hex-2-en-1-ol Chemical compound CCC\C=C\CO ZCHHRLHTBGRGOT-SNAWJCMRSA-N 0.000 description 2
BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 2
UFLHIIWVXFIJGU-ARJAWSKDSA-N (Z)-hex-3-en-1-ol Chemical compound CC\C=C/CCO UFLHIIWVXFIJGU-ARJAWSKDSA-N 0.000 description 2
KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 2
244000060011 Cocos nucifera Species 0.000 description 2
235000013162 Cocos nucifera Nutrition 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 2
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 2
125000000129 anionic group Chemical group 0.000 description 2
150000001768 cations Chemical class 0.000 description 2
MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
239000001630 malic acid Substances 0.000 description 2
235000011090 malic acid Nutrition 0.000 description 2
238000000034 method Methods 0.000 description 2
VSMOENVRRABVKN-UHFFFAOYSA-N oct-1-en-3-ol Chemical compound CCCCCC(O)C=C VSMOENVRRABVKN-UHFFFAOYSA-N 0.000 description 2
OIPPWFOQEKKFEE-UHFFFAOYSA-N orcinol Chemical compound CC1=CC(O)=CC(O)=C1 OIPPWFOQEKKFEE-UHFFFAOYSA-N 0.000 description 2
229920000151 polyglycol Polymers 0.000 description 2
239000010695 polyglycol Substances 0.000 description 2
229910052700 potassium Inorganic materials 0.000 description 2
239000011591 potassium Substances 0.000 description 2
WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 2
HFVMEOPYDLEHBR-UHFFFAOYSA-N (2-fluorophenyl)-phenylmethanol Chemical compound C=1C=CC=C(F)C=1C(O)C1=CC=CC=C1 HFVMEOPYDLEHBR-UHFFFAOYSA-N 0.000 description 1
AMXYRHBJZOVHOL-ODYTWBPASA-N (2E,6Z)-nona-2,6-dien-1-ol Chemical compound CC\C=C/CC\C=C\CO AMXYRHBJZOVHOL-ODYTWBPASA-N 0.000 description 1
NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 description 1
239000001124 (E)-prop-1-ene-1,2,3-tricarboxylic acid Substances 0.000 description 1
TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 1
VSMOENVRRABVKN-MRVPVSSYSA-N 1-Octen-3-ol Natural products CCCCC[C@H](O)C=C VSMOENVRRABVKN-MRVPVSSYSA-N 0.000 description 1
UIEVCEQLNUHDIF-UHFFFAOYSA-N 1-chloro-2,4-dimethylbenzene Chemical group CC1=CC=C(Cl)C(C)=C1 UIEVCEQLNUHDIF-UHFFFAOYSA-N 0.000 description 1
LDMOEFOXLIZJOW-UHFFFAOYSA-N 1-dodecanesulfonic acid Chemical compound CCCCCCCCCCCCS(O)(=O)=O LDMOEFOXLIZJOW-UHFFFAOYSA-N 0.000 description 1
RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
IBLKWZIFZMJLFL-UHFFFAOYSA-N 1-phenoxypropan-2-ol Chemical compound CC(O)COC1=CC=CC=C1 IBLKWZIFZMJLFL-UHFFFAOYSA-N 0.000 description 1
DBHODFSFBXJZNY-UHFFFAOYSA-N 2,4-dichlorobenzyl alcohol Chemical compound OCC1=CC=C(Cl)C=C1Cl DBHODFSFBXJZNY-UHFFFAOYSA-N 0.000 description 1
ROKSAUSPJGWCSM-UHFFFAOYSA-N 2-(7,7-dimethyl-4-bicyclo[3.1.1]hept-3-enyl)ethanol Chemical compound C1C2C(C)(C)C1CC=C2CCO ROKSAUSPJGWCSM-UHFFFAOYSA-N 0.000 description 1
YDXQPTHHAPCTPP-UHFFFAOYSA-N 3-Octen-1-ol Natural products CCCCC=CCCO YDXQPTHHAPCTPP-UHFFFAOYSA-N 0.000 description 1
OSDLLIBGSJNGJE-UHFFFAOYSA-N 4-chloro-3,5-dimethylphenol Chemical compound CC1=CC(O)=CC(C)=C1Cl OSDLLIBGSJNGJE-UHFFFAOYSA-N 0.000 description 1
CFKMVGJGLGKFKI-UHFFFAOYSA-N 4-chloro-m-cresol Chemical compound CC1=CC(O)=CC=C1Cl CFKMVGJGLGKFKI-UHFFFAOYSA-N 0.000 description 1
PXRKCOCTEMYUEG-UHFFFAOYSA-N 5-aminoisoindole-1,3-dione Chemical compound NC1=CC=C2C(=O)NC(=O)C2=C1 PXRKCOCTEMYUEG-UHFFFAOYSA-N 0.000 description 1
241000193830 Bacillus <bacterium> Species 0.000 description 1
241000894006 Bacteria Species 0.000 description 1
LSPHULWDVZXLIL-UHFFFAOYSA-N Camphoric acid Natural products CC1(C)C(C(O)=O)CCC1(C)C(O)=O LSPHULWDVZXLIL-UHFFFAOYSA-N 0.000 description 1
241000588724 Escherichia coli Species 0.000 description 1
239000001263 FEMA 3042 Substances 0.000 description 1
239000005792 Geraniol Substances 0.000 description 1
GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 description 1
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
LRBQNJMCXXYXIU-PPKXGCFTSA-N Penta-digallate-beta-D-glucose Natural products OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-PPKXGCFTSA-N 0.000 description 1
239000004721 Polyphenylene oxide Substances 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
YZCKVEUIGOORGS-IGMARMGPSA-N Protium Chemical compound [1H] YZCKVEUIGOORGS-IGMARMGPSA-N 0.000 description 1
240000004808 Saccharomyces cerevisiae Species 0.000 description 1
241000607720 Serratia Species 0.000 description 1
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
239000005844 Thymol Substances 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical group [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
239000006096 absorbing agent Substances 0.000 description 1
229940091181 aconitic acid Drugs 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
OOCCDEMITAIZTP-UHFFFAOYSA-N allylic benzylic alcohol Natural products OCC=CC1=CC=CC=C1 OOCCDEMITAIZTP-UHFFFAOYSA-N 0.000 description 1
WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 1
AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical group [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
150000001413 amino acids Chemical class 0.000 description 1
JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
230000002421 anti-septic effect Effects 0.000 description 1
229940064004 antiseptic throat preparations Drugs 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
BTFJIXJJCSYFAL-UHFFFAOYSA-N arachidyl alcohol Natural products CCCCCCCCCCCCCCCCCCCCO BTFJIXJJCSYFAL-UHFFFAOYSA-N 0.000 description 1
125000001204 arachidyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
SUMDYPCJJOFFON-UHFFFAOYSA-N beta-hydroxyethanesulfonic acid Natural products OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
239000004327 boric acid Substances 0.000 description 1
OWBTYPJTUOEWEK-UHFFFAOYSA-N butane-2,3-diol Chemical compound CC(O)C(C)O OWBTYPJTUOEWEK-UHFFFAOYSA-N 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
LSPHULWDVZXLIL-QUBYGPBYSA-N camphoric acid Chemical compound CC1(C)[C@H](C(O)=O)CC[C@]1(C)C(O)=O LSPHULWDVZXLIL-QUBYGPBYSA-N 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
RECUKUPTGUEGMW-UHFFFAOYSA-N carvacrol Chemical compound CC(C)C1=CC=C(C)C(O)=C1 RECUKUPTGUEGMW-UHFFFAOYSA-N 0.000 description 1
HHTWOMMSBMNRKP-UHFFFAOYSA-N carvacrol Natural products CC(=C)C1=CC=C(C)C(O)=C1 HHTWOMMSBMNRKP-UHFFFAOYSA-N 0.000 description 1
235000007746 carvacrol Nutrition 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
GTZCVFVGUGFEME-IWQZZHSRSA-N cis-aconitic acid Chemical compound OC(=O)C\C(C(O)=O)=C\C(O)=O GTZCVFVGUGFEME-IWQZZHSRSA-N 0.000 description 1
230000036461 convulsion Effects 0.000 description 1
150000001896 cresols Chemical class 0.000 description 1
NSFKBZXCXCJZDQ-UHFFFAOYSA-N cumene;sodium Chemical compound [Na].CC(C)C1=CC=CC=C1 NSFKBZXCXCJZDQ-UHFFFAOYSA-N 0.000 description 1
PYRZPBDTPRQYKG-UHFFFAOYSA-N cyclopentene-1-carboxylic acid Chemical compound OC(=O)C1=CCCC1 PYRZPBDTPRQYKG-UHFFFAOYSA-N 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 1
229960004698 dichlorobenzyl alcohol Drugs 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 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
229960000735 docosanol Drugs 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
229940043264 dodecyl sulfate Drugs 0.000 description 1
239000000975 dye Substances 0.000 description 1
239000003974 emollient agent Substances 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
229940113087 geraniol Drugs 0.000 description 1
UFLHIIWVXFIJGU-UHFFFAOYSA-N hex-3-en-1-ol Natural products CCC=CCCO UFLHIIWVXFIJGU-UHFFFAOYSA-N 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid group Chemical group C(CCCCC)(=O)O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
229940045996 isethionic acid Drugs 0.000 description 1
WYXXLXHHWYNKJF-UHFFFAOYSA-N isocarvacrol Natural products CC(C)C1=CC=C(O)C(C)=C1 WYXXLXHHWYNKJF-UHFFFAOYSA-N 0.000 description 1
CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 1
239000007788 liquid Substances 0.000 description 1
229910052744 lithium Inorganic materials 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
229910021645 metal ion Inorganic materials 0.000 description 1
DUNCVNHORHNONW-UHFFFAOYSA-N myrcenol Chemical compound CC(C)(O)CCCC(=C)C=C DUNCVNHORHNONW-UHFFFAOYSA-N 0.000 description 1
229930008383 myrcenol Natural products 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
238000010899 nucleation Methods 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000003921 oil Substances 0.000 description 1
XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
229940070805 p-chloro-m-cresol Drugs 0.000 description 1
150000002931 p-cresols Chemical class 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000002304 perfume Substances 0.000 description 1
WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920001184 polypeptide Polymers 0.000 description 1
159000000001 potassium salts Chemical class 0.000 description 1
102000004196 processed proteins & peptides Human genes 0.000 description 1
108090000765 processed proteins & peptides Proteins 0.000 description 1
239000000047 product Substances 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
239000011814 protection agent Substances 0.000 description 1
229940079877 pyrogallol Drugs 0.000 description 1
239000008149 soap solution Substances 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
238000003756 stirring Methods 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000000271 synthetic detergent Substances 0.000 description 1
235000015523 tannic acid Nutrition 0.000 description 1
229920002258 tannic acid Polymers 0.000 description 1
229940033123 tannic acid Drugs 0.000 description 1
235000007586 terpenes Nutrition 0.000 description 1
229940116411 terpineol Drugs 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
229960000790 thymol Drugs 0.000 description 1
GTZCVFVGUGFEME-UHFFFAOYSA-N trans-aconitic acid Natural products OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 description 1
125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000003739 xylenols Chemical class 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 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
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0063—Photo- activating compounds
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/342—Alcohols having more than seven atoms in an unbroken chain
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/347—Phenols
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/42—Amides
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/43—Guanidines
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
- A61K8/442—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof substituted by amido group(s)
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/005—Antimicrobial preparations
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Birds (AREA)
Epidemiology (AREA)
Dermatology (AREA)
Chemical & Material Sciences (AREA)
Emergency Medicine (AREA)
Engineering & Computer Science (AREA)
Organic Chemistry (AREA)
Wood Science & Technology (AREA)
Oil, Petroleum & Natural Gas (AREA)
Chemical Kinetics & Catalysis (AREA)
Detergent Compositions (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Cosmetics (AREA)

CA002196771A 1994-08-25 1995-08-14 Surface-active formulations Abandoned CA2196771A1 (en)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
CH2611/94-8		1994-08-25
CH261194		1994-08-25
PCT/EP1995/003211 WO1996006153A2 (en)	1994-08-25	1995-08-14	Surface-active formulations

Publications (1)

Publication Number	Publication Date
CA2196771A1 true CA2196771A1 (en)	1996-02-29

Family

ID=4237670

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA002196771A Abandoned CA2196771A1 (en)	1994-08-25	1995-08-14	Surface-active formulations

Country Status (12)

Country	Link
EP (1)	EP0777717A2 (cs)
JP (1)	JPH10504592A (cs)
AU (1)	AU3345295A (cs)
BG (1)	BG101308A (cs)
BR (1)	BR9508775A (cs)
CA (1)	CA2196771A1 (cs)
CZ (1)	CZ55697A3 (cs)
FI (1)	FI970742A0 (cs)
HU (1)	HUT76688A (cs)
MX (1)	MX9701416A (cs)
SK (1)	SK24497A3 (cs)
WO (1)	WO1996006153A2 (cs)

Families Citing this family (39)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6221823B1 (en) †	1995-10-25	2001-04-24	Reckitt Benckiser Inc.	Germicidal, acidic hard surface cleaning compositions
US5955408A (en) *	1996-07-10	1999-09-21	Steris Inc.	Triclosan skin wash with enhanced efficacy
JPH1071190A (ja) *	1996-08-30	1998-03-17	Tomey Technol Corp	コンタクトレンズ用液剤
US6183757B1 (en)	1997-06-04	2001-02-06	Procter & Gamble Company	Mild, rinse-off antimicrobial cleansing compositions which provide improved immediate germ reduction during washing
US6190674B1 (en)	1997-06-04	2001-02-20	Procter & Gamble Company	Liquid antimicrobial cleansing compositions
US6287577B1 (en)	1997-11-12	2001-09-11	The Procter & Gamble Company	Leave-on antimicrobial compositions which provide improved residual benefit versus gram positive bacteria
US6210695B1 (en)	1997-06-04	2001-04-03	The Procter & Gamble Company	Leave-on antimicrobial compositions
US5968539A (en) *	1997-06-04	1999-10-19	Procter & Gamble Company	Mild, rinse-off antimicrobial liquid cleansing compositions which provide residual benefit versus gram negative bacteria
US6197315B1 (en)	1997-06-04	2001-03-06	Procter & Gamble Company	Antimicrobial wipes which provide improved residual benefit versus gram negative bacteria
US6284259B1 (en)	1997-11-12	2001-09-04	The Procter & Gamble Company	Antimicrobial wipes which provide improved residual benefit versus Gram positive bacteria
US6190675B1 (en)	1997-06-04	2001-02-20	Procter & Gamble Company	Mild, rinse-off antimicrobial liquid cleansing compositions which provide improved residual benefit versus gram positive bacteria
US6214363B1 (en)	1997-11-12	2001-04-10	The Procter & Gamble Company	Liquid antimicrobial cleansing compositions which provide residual benefit versus gram negative bacteria
US6183763B1 (en)	1997-06-04	2001-02-06	Procter & Gamble Company	Antimicrobial wipes which provide improved immediate germ reduction
EP0903401B1 (de) *	1997-09-17	2003-08-06	Ciba SC Holding AG	Antimikrobieller Waschmittelzusatz
ATE246722T1 (de) *	1997-09-17	2003-08-15	Ciba Sc Holding Ag	Antimikrobieller waschmittelzusatz
US6287583B1 (en)	1997-11-12	2001-09-11	The Procter & Gamble Company	Low-pH, acid-containing personal care compositions which exhibit reduced sting
GB2331703B (en) *	1997-11-28	2002-01-23	Reckitt & Colman Inc	Disinfectant compositions
GB2331758B (en)	1997-11-28	2002-04-17	Reckitt & Colman Inc	Disinfectant compositions
EP1034245B1 (en) *	1997-11-28	2003-09-17	Reckitt Benckiser Inc.	Concentrated liquid cleaner for hard surfaces
GB2331760B (en) *	1997-11-28	2002-05-15	Reckitt & Colman Inc	Hard surface cleaning compositions
JPH11189784A (ja) *	1997-12-26	1999-07-13	Kose Corp	洗浄剤組成物
ES2191417T3 (es)	1998-03-19	2003-09-01	Bifodan As	Composicion desinfectante.
US6861397B2 (en)	1999-06-23	2005-03-01	The Dial Corporation	Compositions having enhanced deposition of a topically active compound on a surface
US6107261A (en)	1999-06-23	2000-08-22	The Dial Corporation	Compositions containing a high percent saturation concentration of antibacterial agent
EP1191843A2 (en) *	1999-06-23	2002-04-03	The Dial Corporation	Antibacterial compositions
DE19937295C2 (de) *	1999-08-06	2002-11-21	Cognis Deutschland Gmbh	Syndetseifen
US20020123440A1 (en) *	2000-04-04	2002-09-05	Hoang Minh Q.	Foamable antimicrobial formulation
AU2001249365A1 (en) *	2000-04-04	2001-10-15	Becton, Dickinson And Company	Foamable antimicrobial formulation
DE102004038104A1 (de) *	2004-08-05	2006-02-23	Henkel Kgaa	Verwendung von ortho-Phenylphenol und/oder dessen Derivaten zur Hemmung der asexuellen Vermehrung von Pilzen
US20090029896A1 (en) †	2006-02-24	2009-01-29	Andrew Paul Chapple	Fast Release Granules
JP2008106022A (ja) *	2006-10-27	2008-05-08	Miura Co Ltd	皮膚用殺菌剤
EP2727991A1 (en) *	2012-10-30	2014-05-07	The Procter & Gamble Company	Cleaning and disinfecting liquid hand dishwashing detergent compositions
JP5752220B2 (ja) *	2013-12-16	2015-07-22	花王株式会社	硬質表面用殺菌洗浄剤組成物
JP2019510037A (ja)	2016-03-31	2019-04-11	ゴジョ・インダストリーズ・インコーポレイテッド	抗菌ペプチド刺激性洗浄組成物
JP2019511505A (ja)	2016-03-31	2019-04-25	ゴジョ・インダストリーズ・インコーポレイテッド	抗菌ペプチド刺激性清浄組成物
US10874700B2 (en)	2016-03-31	2020-12-29	Gojo Industries, Inc.	Sanitizer composition with probiotic/prebiotic active ingredient
WO2018098152A1 (en)	2016-11-23	2018-05-31	Gojo Industries, Inc.	Sanitizer composition with probiotic/prebiotic active ingredient
JP2020518590A (ja)	2017-05-01	2020-06-25	ゴジョ・インダストリーズ・インコーポレイテッド	低含水洗浄組成物を含有するアルコール
JP7219583B2 (ja) *	2018-10-19	2023-02-08	大日本除蟲菊株式会社	殺菌剤組成物

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1467619A1 (de) *	1965-11-27	1969-02-13	Henkel & Cie Gmbh	Farbstabile,Desinfektionsmittel enthaltende fluessige Wasch-,Reinigungs- und Spuelmittel
GB1266060A (cs) *	1969-09-12	1972-03-08
BE768041R (fr) *	1971-06-03	1971-12-03	Ciba Geigy Ag	Composition pour combattre les
SE376928B (cs) *	1971-12-13	1975-06-16	Basf Wyandotte Corp
GB1539031A (en) *	1975-02-22	1979-01-24	Beecham Group Ltd	Pharmaceutical compositions
US4310433A (en) *	1980-09-02	1982-01-12	The Procter & Gamble Company	Superfatted liquid soap skin cleansing compositions
DE3117792C2 (de) *	1981-05-06	1990-08-23	Schülke & Mayr GmbH, 2000 Norderstedt	Die Verwendung einer wässrigen Lösung von Alkoholen, Phenolen und oberflächenaktiven Stoffen als viruzides Mittel
DE3723990A1 (de) *	1986-07-23	1988-02-04	Ciba Geigy Ag	Mikrobizide zubereitung
DE3723994A1 (de) *	1986-07-23	1988-02-04	Ciba Geigy Ag	Mikrobizide zubereitung
JPH0753657B2 (ja) *	1986-12-03	1995-06-07	ライオン株式会社	皮膚洗浄剤
BR8900685A (pt) *	1988-02-17	1989-10-10	Ciba Geigy Ag	Composicao de sabao antimicrobiana e aplicacao
US4832861A (en) *	1988-05-27	1989-05-23	Lever Brothers Company	Soap compositions of enhanced antimicrobial effectiveness
JPH03193727A (ja) *	1989-12-22	1991-08-23	Kao Corp	腋臭防止剤
JPH05279693A (ja) *	1992-04-02	1993-10-26	Shin Etsu Chem Co Ltd	抗菌性洗浄剤
NZ256543A (en) *	1992-11-09	1997-10-24	West Agro Inc	Sanitizer/biocidal dilutable concentrate comprising germicidal fatty acids

1995
- 1995-08-14 HU HU9701263A patent/HUT76688A/hu unknown
- 1995-08-14 JP JP8507758A patent/JPH10504592A/ja active Pending
- 1995-08-14 AU AU33452/95A patent/AU3345295A/en not_active Abandoned
- 1995-08-14 CZ CZ97556A patent/CZ55697A3/cs unknown
- 1995-08-14 WO PCT/EP1995/003211 patent/WO1996006153A2/en not_active Ceased
- 1995-08-14 SK SK244-97A patent/SK24497A3/sk unknown
- 1995-08-14 MX MX9701416A patent/MX9701416A/es unknown
- 1995-08-14 EP EP95929863A patent/EP0777717A2/en not_active Withdrawn
- 1995-08-14 BR BR9508775A patent/BR9508775A/pt not_active Application Discontinuation
- 1995-08-14 CA CA002196771A patent/CA2196771A1/en not_active Abandoned
1997
- 1997-02-21 FI FI970742A patent/FI970742A0/fi not_active Application Discontinuation
- 1997-03-11 BG BG101308A patent/BG101308A/xx unknown

Also Published As

Publication number	Publication date
FI970742A7 (fi)	1997-02-21
WO1996006153A2 (en)	1996-02-29
BG101308A (bg)	1997-09-30
FI970742A0 (fi)	1997-02-21
BR9508775A (pt)	1997-12-23
SK24497A3 (en)	1997-07-09
EP0777717A2 (en)	1997-06-11
JPH10504592A (ja)	1998-05-06
WO1996006153A3 (en)	1996-05-02
AU3345295A (en)	1996-03-14
MX9701416A (es)	1997-05-31
CZ55697A3 (en)	1997-06-11
HUT76688A (en)	1997-10-28

Publication	Publication Date	Title
CA2196771A1 (en)	1996-02-29	Surface-active formulations
US8232305B2 (en)	2012-07-31	Anti-microbial compositions
CA2196774A1 (en)	1996-02-29	Surface-active formulations
JP2022180512A (ja)	2022-12-06	ビタミンｄの形成のために最適化された日焼け止め製剤
ES2205509T3 (es)	2004-05-01	Composicion para uso en el cuidado personal.
KR20110002886A (ko)	2011-01-10	신규 결정질 피리치온/산화아연 복합체 및 이를 포함하는 생리/항생 활성 조성물
WO2013133091A1 (ja)	2013-09-12	揺変剤およびその製造方法
WO2022228806A1 (en)	2022-11-03	Biphasic cosmetic composition and application thereof
WO2021047905A1 (en)	2021-03-18	Topical compositions
IL145751A (en)	2010-12-30	Use of aluminum fluoride for the preparation of compositions for the treatment of acne vulgaris and folliculitis
EP2790650B1 (en)	2017-05-24	Solubilized magnolol analogs
ES2260202T3 (es)	2006-11-01	Empleo de derivados de feniletilamina para el tratamiento antimicrobiano de superficies.
EP2832345B1 (en)	2017-11-22	Cosmetic composition
JP3419124B2 (ja)	2003-06-23	口腔用組成物
JP2002326918A (ja)	2002-11-15	美白化粧料
JP2011046747A (ja)	2011-03-10	皮膚外用剤並びに皮膚外用剤の防腐抗菌方法
EP3727300B1 (en)	2022-10-26	An antimicrobial composition
CA2294345A1 (en)	1998-12-30	A skin-protective composition
EP4027791A1 (en)	2022-07-20	Microbiocidal use
EP2793823B1 (en)	2017-12-06	Suncare formulations and methods
US20140357546A1 (en)	2014-12-04	Transparent aqueous fragrance microemulsions
EP3927308B1 (en)	2022-09-21	Personal cleansing compositions comprising a preservative system
AU2011383310B2 (en)	2014-08-07	Oral care or cleanser composition comprising solubilized magnolol analogs and PPG-1 - PEG-9 lauryl glycol ether
JPS6089402A (ja)	1985-05-20	殺菌剤組成物
JP2004231561A (ja)	2004-08-19	歯周病予防歯磨剤組成物

Legal Events

Date	Code	Title	Description
2000-08-14	FZDE	Discontinued
2022-09-10	FZDE	Discontinued	Effective date: 20000814