AU742600B2 - Composition for use in personal care - Google Patents
Composition for use in personal care Download PDFInfo
- Publication number
- AU742600B2 AU742600B2 AU79192/98A AU7919298A AU742600B2 AU 742600 B2 AU742600 B2 AU 742600B2 AU 79192/98 A AU79192/98 A AU 79192/98A AU 7919298 A AU7919298 A AU 7919298A AU 742600 B2 AU742600 B2 AU 742600B2
- Authority
- AU
- Australia
- Prior art keywords
- composition
- formula
- composition according
- biguanide
- polymeric biguanide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
- 239000000203 mixture Substances 0.000 title claims description 50
- 229940123208 Biguanide Drugs 0.000 claims description 23
- XNCOSPRUTUOJCJ-UHFFFAOYSA-N Biguanide Chemical compound NC(N)=NC(N)=N XNCOSPRUTUOJCJ-UHFFFAOYSA-N 0.000 claims description 20
- 150000007524 organic acids Chemical class 0.000 claims description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims description 13
- 150000003839 salts Chemical class 0.000 claims description 11
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 10
- 238000009472 formulation Methods 0.000 claims description 9
- 239000002781 deodorant agent Substances 0.000 claims description 5
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- 235000021355 Stearic acid Nutrition 0.000 claims description 3
- 230000001166 anti-perspirative effect Effects 0.000 claims description 3
- 239000003213 antiperspirant Substances 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 239000012458 free base Substances 0.000 claims description 3
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims description 3
- 239000008117 stearic acid Substances 0.000 claims description 3
- 150000001559 benzoic acids Chemical class 0.000 claims description 2
- 239000002537 cosmetic Substances 0.000 claims description 2
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid group Chemical group C(CCCCC)(=O)O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims description 2
- 150000005165 hydroxybenzoic acids Chemical class 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
- 150000003330 sebacic acids Chemical class 0.000 claims description 2
- 150000003504 terephthalic acids Chemical class 0.000 claims description 2
- 239000004599 antimicrobial Substances 0.000 claims 1
- 150000004283 biguanides Chemical class 0.000 description 19
- 229920002413 Polyhexanide Polymers 0.000 description 15
- -1 organic acid salts Chemical class 0.000 description 12
- 239000003974 emollient agent Substances 0.000 description 8
- VAZJLPXFVQHDFB-UHFFFAOYSA-N 1-(diaminomethylidene)-2-hexylguanidine Polymers CCCCCCN=C(N)N=C(N)N VAZJLPXFVQHDFB-UHFFFAOYSA-N 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 125000001183 hydrocarbyl group Chemical group 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 description 5
- 125000001931 aliphatic group Chemical group 0.000 description 5
- 239000006071 cream Substances 0.000 description 5
- 125000001424 substituent group Chemical group 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 4
- 125000004122 cyclic group Chemical group 0.000 description 4
- 239000006210 lotion Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 230000002906 microbiologic effect Effects 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 239000001993 wax Substances 0.000 description 3
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- QTDIEDOANJISNP-UHFFFAOYSA-N 2-dodecoxyethyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOCCOS(O)(=O)=O QTDIEDOANJISNP-UHFFFAOYSA-N 0.000 description 2
- 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 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
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 230000000844 anti-bacterial effect Effects 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 150000004287 bisbiguanides Chemical class 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000001815 facial effect Effects 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 239000002453 shampoo Substances 0.000 description 2
- 230000000475 sunscreen effect Effects 0.000 description 2
- 239000000516 sunscreening agent Substances 0.000 description 2
- WCOXQTXVACYMLM-UHFFFAOYSA-N 2,3-bis(12-hydroxyoctadecanoyloxy)propyl 12-hydroxyoctadecanoate Chemical compound CCCCCCC(O)CCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCC(O)CCCCCC)COC(=O)CCCCCCCCCCC(O)CCCCCC WCOXQTXVACYMLM-UHFFFAOYSA-N 0.000 description 1
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229910002016 Aerosil® 200 Inorganic materials 0.000 description 1
- 241001237961 Amanita rubescens Species 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- 241000195940 Bryophyta Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- RGHNJXZEOKUKBD-SQOUGZDYSA-M D-gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O RGHNJXZEOKUKBD-SQOUGZDYSA-M 0.000 description 1
- 229920004511 Dow Corning® 200 Fluid Polymers 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920002565 Polyethylene Glycol 400 Polymers 0.000 description 1
- 229920002582 Polyethylene Glycol 600 Polymers 0.000 description 1
- 239000004146 Propane-1,2-diol Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 206010040904 Skin odour abnormal Diseases 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 229940022663 acetate Drugs 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- LFVVNPBBFUSSHL-UHFFFAOYSA-N alexidine Chemical compound CCCCC(CC)CNC(=N)NC(=N)NCCCCCCNC(=N)NC(=N)NCC(CC)CCCC LFVVNPBBFUSSHL-UHFFFAOYSA-N 0.000 description 1
- 229950010221 alexidine Drugs 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000000845 anti-microbial effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000004104 aryloxy group Chemical group 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- UKMSUNONTOPOIO-UHFFFAOYSA-M behenate Chemical compound CCCCCCCCCCCCCCCCCCCCCC([O-])=O UKMSUNONTOPOIO-UHFFFAOYSA-M 0.000 description 1
- 229940116224 behenate Drugs 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 235000013736 caramel Nutrition 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- MRUAUOIMASANKQ-UHFFFAOYSA-O carboxymethyl-[3-(dodecanoylamino)propyl]-dimethylazanium Chemical compound CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC(O)=O MRUAUOIMASANKQ-UHFFFAOYSA-O 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229960003260 chlorhexidine Drugs 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 229940050410 gluconate Drugs 0.000 description 1
- YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 1
- SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 229940094522 laponite Drugs 0.000 description 1
- XCOBTUNSZUJCDH-UHFFFAOYSA-B lithium magnesium sodium silicate Chemical compound [Li+].[Li+].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 XCOBTUNSZUJCDH-UHFFFAOYSA-B 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 239000003750 molluscacide Substances 0.000 description 1
- 230000002013 molluscicidal effect Effects 0.000 description 1
- 235000011929 mousse Nutrition 0.000 description 1
- 239000002324 mouth wash Substances 0.000 description 1
- 229940051866 mouthwash Drugs 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 229960004063 propylene glycol Drugs 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000001012 protector Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000000606 toothpaste Substances 0.000 description 1
- 229940034610 toothpaste Drugs 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides
- A01N47/42—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides containing —N=CX2 groups, e.g. isothiourea
- A01N47/44—Guanidine; Derivatives thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Environmental Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Cosmetics (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9712317 | 1997-06-13 | ||
| GBGB9712317.8A GB9712317D0 (en) | 1997-06-13 | 1997-06-13 | Composition, compound and use |
| PCT/EP1998/003492 WO1998056252A1 (en) | 1997-06-13 | 1998-06-03 | Composition for use in personal care |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU7919298A AU7919298A (en) | 1998-12-30 |
| AU742600B2 true AU742600B2 (en) | 2002-01-10 |
Family
ID=10814094
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU79192/98A Ceased AU742600B2 (en) | 1997-06-13 | 1998-06-03 | Composition for use in personal care |
| AU77825/98A Abandoned AU7782598A (en) | 1997-06-13 | 1998-06-05 | Biocidal organic acid salts of a polymeric biguanide |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU77825/98A Abandoned AU7782598A (en) | 1997-06-13 | 1998-06-05 | Biocidal organic acid salts of a polymeric biguanide |
Country Status (22)
| Country | Link |
|---|---|
| US (2) | US20020142020A1 (enEXAMPLES) |
| EP (2) | EP0987947B1 (enEXAMPLES) |
| JP (2) | JP4308331B2 (enEXAMPLES) |
| KR (1) | KR20010013704A (enEXAMPLES) |
| CN (2) | CN100577142C (enEXAMPLES) |
| AR (2) | AR012965A1 (enEXAMPLES) |
| AT (1) | ATE227932T1 (enEXAMPLES) |
| AU (2) | AU742600B2 (enEXAMPLES) |
| BR (2) | BR9810435B1 (enEXAMPLES) |
| CA (2) | CA2295012A1 (enEXAMPLES) |
| DE (2) | DE69817564T2 (enEXAMPLES) |
| ES (1) | ES2205509T3 (enEXAMPLES) |
| GB (1) | GB9712317D0 (enEXAMPLES) |
| HU (1) | HUP0003065A3 (enEXAMPLES) |
| ID (1) | ID24652A (enEXAMPLES) |
| IN (1) | IN190655B (enEXAMPLES) |
| NO (1) | NO996042D0 (enEXAMPLES) |
| NZ (1) | NZ501740A (enEXAMPLES) |
| PL (1) | PL188771B1 (enEXAMPLES) |
| RU (1) | RU2209620C2 (enEXAMPLES) |
| WO (2) | WO1998056252A1 (enEXAMPLES) |
| ZA (2) | ZA985030B (enEXAMPLES) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030147925A1 (en) * | 1998-09-11 | 2003-08-07 | Samuel P. Sawan | Topical dermal antimicrobial compositions, methods for generating same, and monitoring methods utilizing same |
| US6294163B1 (en) | 1998-10-02 | 2001-09-25 | Geltex Pharmaceuticals, Inc. | Polymers containing guanidinium groups as bile acid sequestrants |
| FR2827507B1 (fr) * | 2001-07-18 | 2005-07-01 | Oreal | Compose derive de polyguanidine et utilisation d'un tel compose pour la protection et/ou le soin des fibres keratiniques |
| MXPA04003308A (es) | 2001-10-09 | 2004-07-23 | Procter & Gamble | Toallita prehumedecida que contiene biguanida polimerica para tratar superficies. |
| FR2830442B1 (fr) * | 2001-10-09 | 2004-02-06 | Oreal | Utilisation d'un compose de polyguanidine pour le traitement ou la mise en forme des cheveux, notamment le defrisage ou la permanente |
| FR2841778B1 (fr) * | 2002-07-05 | 2004-10-01 | Oreal | Utilisation d'un compose derive de polyguanidine dans un traitement de coloration |
| US8795638B1 (en) * | 2003-08-26 | 2014-08-05 | Nevada Naturals Inc. | Compositions for dental care |
| FR2860158A1 (fr) * | 2003-09-30 | 2005-04-01 | Oreal | Composition moussante contenant un derive de polyguanidine, et ses utilisations notamment cosmetiques |
| RU2256439C1 (ru) * | 2004-04-08 | 2005-07-20 | Генкин Дмитрий Дмитриевич | Композиция для умывания кожи лица |
| DE102004037598A1 (de) * | 2004-08-03 | 2006-02-23 | Prontomed Gmbh | Mundspüllösung |
| US20060269498A1 (en) * | 2005-05-17 | 2006-11-30 | Gerard Malle | Hair shaping composition comprising at least one polyguanidine other than hydroxide |
| FR2885902B1 (fr) * | 2005-05-17 | 2008-05-09 | Oreal | Composition de defrisage des cheveux comprenant au moins une multiguanidine hors hydroxyde |
| FR2885800B1 (fr) * | 2005-05-17 | 2008-05-09 | Oreal | Composition de mise en forme des cheveux comprenant au moins une multiguanidine hors hydroxyde |
| US20060272107A1 (en) * | 2005-05-17 | 2006-12-07 | Gerard Malle | Hair relaxing composition comprising at least one non-hydroxide polyguanidine |
| ES2348645T3 (es) * | 2005-09-15 | 2010-12-10 | Aesculap Ag | Material de sutura antimicrobiano biocompatible. |
| BRPI0716325A2 (pt) * | 2006-10-27 | 2014-03-04 | 3M Innovative Properties Co | Composição antimicrobianas |
| CN101951779A (zh) | 2007-12-31 | 2011-01-19 | 3M创新有限公司 | 抗微生物组合物 |
| US8685379B2 (en) * | 2008-01-29 | 2014-04-01 | International Art And Science Group, Inc. | Functional material and delivery gel composition and method for manufacturing |
| EP3255085B1 (en) * | 2008-09-19 | 2020-06-10 | 3M Innovative Properties Co. | Ligand graft functionalized substrates |
| TW201138843A (en) | 2009-12-18 | 2011-11-16 | Colgate Palmolive Co | Biguanide preservation of precipitated calcium carbonate |
| EP2386589A1 (en) | 2010-04-23 | 2011-11-16 | Centre National de la Recherche Scientifique (C.N.R.S) | Novel antimicrobial composition, use and preparation thereof |
| EP2524705B1 (de) * | 2011-05-19 | 2014-04-23 | Lohmann & Rauscher GmbH & Co. KG | Sterile Wundauflage mit einem synthethischen Dreiblock-Elastomer und einem hydrophorbierten polymeren Biguanid |
| US10289412B2 (en) * | 2012-02-09 | 2019-05-14 | Qualcomm Incorporated | Floating point constant generation instruction |
| WO2013121407A1 (en) * | 2012-02-17 | 2013-08-22 | Budhi Haryanto | The composition of malodor removing aerosol for daily worn objects or items |
| CN105315459B (zh) * | 2014-10-29 | 2017-09-26 | 吉林云飞医药有限公司 | 一种聚己二酸基胍盐酸盐的制备方法 |
| WO2018081059A1 (en) | 2016-10-24 | 2018-05-03 | Colgate-Palmolive Company | Oral care compositions and methods of use |
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|---|---|---|---|---|
| GB843676A (en) * | 1957-12-31 | 1960-08-10 | Ici Ltd | New biguanide salts |
| BE698595A (enEXAMPLES) * | 1966-05-23 | 1967-11-17 | ||
| US4478821A (en) * | 1982-01-26 | 1984-10-23 | The Gillette Company | Inhibition of body odor |
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| GB1434040A (en) * | 1973-08-06 | 1976-04-28 | Ici Ltd | Process for combating fungi and bacteria |
| GB1464005A (en) * | 1974-04-22 | 1977-02-09 | Ici Ltd | Method for the destruction of aquatic molluscs |
| LU74539A1 (enEXAMPLES) * | 1976-03-12 | 1977-09-27 | ||
| JP2544388B2 (ja) * | 1986-09-04 | 1996-10-16 | 株式会社 上野製薬応用研究所 | ウイルス不活化剤 |
| WO1990000055A1 (en) * | 1988-06-30 | 1990-01-11 | Davis Michael H | Method of inhibiting the activity of human immunodeficiency virus (hiv) in vivo |
| US4954636A (en) * | 1989-07-03 | 1990-09-04 | Gaf Chemicals Corporation | Antimicrobial polymeric bisbiguanides |
| US5268168A (en) * | 1990-02-19 | 1993-12-07 | Sakai Engineering Co., Ltd. | Antibacterial and deodorant processing agent and processing method using same |
| US5708023A (en) * | 1994-03-28 | 1998-01-13 | The Trustees Of Columbia University In The City Of New York | Zinc gluconate gel compositions |
| JPH08119878A (ja) * | 1994-10-19 | 1996-05-14 | Lion Corp | 殺菌剤及びその製造方法 |
| GB9726132D0 (en) | 1997-12-10 | 1998-02-11 | Unilever Plc | Deodorant composition |
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1997
- 1997-06-13 GB GBGB9712317.8A patent/GB9712317D0/en active Pending
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1998
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- 1998-06-03 DE DE69817564T patent/DE69817564T2/de not_active Expired - Lifetime
- 1998-06-03 JP JP50160199A patent/JP4308331B2/ja not_active Expired - Fee Related
- 1998-06-03 NZ NZ501740A patent/NZ501740A/en not_active IP Right Cessation
- 1998-06-03 WO PCT/EP1998/003492 patent/WO1998056252A1/en active IP Right Grant
- 1998-06-03 RU RU2000100989/14A patent/RU2209620C2/ru not_active IP Right Cessation
- 1998-06-03 PL PL98337277A patent/PL188771B1/pl unknown
- 1998-06-03 HU HU0003065A patent/HUP0003065A3/hu unknown
- 1998-06-03 BR BRPI9810435-7A patent/BR9810435B1/pt not_active IP Right Cessation
- 1998-06-03 EP EP98929439A patent/EP0987947B1/en not_active Expired - Lifetime
- 1998-06-03 CA CA002295012A patent/CA2295012A1/en not_active Abandoned
- 1998-06-03 ES ES98929439T patent/ES2205509T3/es not_active Expired - Lifetime
- 1998-06-03 AU AU79192/98A patent/AU742600B2/en not_active Ceased
- 1998-06-03 CN CN98808095A patent/CN100577142C/zh not_active Expired - Fee Related
- 1998-06-05 CN CN98806103A patent/CN1259846A/zh active Pending
- 1998-06-05 KR KR1019997011719A patent/KR20010013704A/ko not_active Withdrawn
- 1998-06-05 JP JP50187899A patent/JP2002505695A/ja active Pending
- 1998-06-05 CA CA002293558A patent/CA2293558A1/en not_active Abandoned
- 1998-06-05 AT AT98925853T patent/ATE227932T1/de not_active IP Right Cessation
- 1998-06-05 EP EP98925853A patent/EP0987946B1/en not_active Expired - Lifetime
- 1998-06-05 AU AU77825/98A patent/AU7782598A/en not_active Abandoned
- 1998-06-05 DE DE69809548T patent/DE69809548T2/de not_active Expired - Lifetime
- 1998-06-05 US US09/445,765 patent/US20020142020A1/en not_active Abandoned
- 1998-06-05 BR BR9810251-6A patent/BR9810251A/pt not_active IP Right Cessation
- 1998-06-05 WO PCT/GB1998/001662 patent/WO1998056253A1/en not_active Application Discontinuation
- 1998-06-09 US US09/094,324 patent/US6509022B2/en not_active Expired - Lifetime
- 1998-06-10 AR ARP980102760A patent/AR012965A1/es unknown
- 1998-06-10 ZA ZA9805030A patent/ZA985030B/xx unknown
- 1998-06-11 ZA ZA985096A patent/ZA985096B/xx unknown
- 1998-06-11 IN IN359BO1998 patent/IN190655B/en unknown
- 1998-06-12 AR ARP980102797A patent/AR015884A1/es active IP Right Grant
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1999
- 1999-12-08 NO NO996042A patent/NO996042D0/no not_active Application Discontinuation
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| GB843676A (en) * | 1957-12-31 | 1960-08-10 | Ici Ltd | New biguanide salts |
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| TH | Corrigenda |
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