CA1145261A - Preparation orale contenant un derive polyoxyethylenique d'un alcool gras - Google Patents

Preparation orale contenant un derive polyoxyethylenique d'un alcool gras

Info

Publication number: CA1145261A
Authority: CA; Canada
Prior art keywords: weight; percent; oil; mouthwash; surfactant
Prior art date: 1980-12-15
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.): Expired

Application number

CA000366823A

Other languages

English (en)

Inventor

Irving R. Schmolka

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 Corp

Original Assignee

BASF Wyandotte Corp

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.)

1980-12-15

Filing date

1980-12-15

Publication date

1983-04-26

1980-12-15 Application filed by BASF Wyandotte Corp filed Critical BASF Wyandotte Corp

1980-12-15 Priority to CA000366823A priority Critical patent/CA1145261A/fr

1983-04-26 Application granted granted Critical

1983-04-26 Publication of CA1145261A publication Critical patent/CA1145261A/fr

Status Expired legal-status Critical Current

Links

-1 polyoxyethylene Polymers 0.000 title claims abstract description 24
150000002191 fatty alcohols Chemical class 0.000 title claims abstract description 11
229920003171 Poly (ethylene oxide) Polymers 0.000 title claims abstract description 7
238000002360 preparation method Methods 0.000 title description 5
239000002736 nonionic surfactant Substances 0.000 claims abstract description 34
239000002324 mouth wash Substances 0.000 claims abstract description 33
229940051866 mouthwash Drugs 0.000 claims abstract description 31
239000004094 surface-active agent Substances 0.000 claims abstract description 30
239000001525 mentha piperita l. herb oil Substances 0.000 claims abstract description 16
235000019477 peppermint oil Nutrition 0.000 claims abstract description 16
239000013588 oral product Substances 0.000 claims abstract description 15
229940023486 oral product Drugs 0.000 claims abstract description 10
239000006071 cream Substances 0.000 claims abstract description 9
235000019640 taste Nutrition 0.000 claims abstract description 8
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 20
239000003921 oil Substances 0.000 claims description 18
235000019198 oils Nutrition 0.000 claims description 18
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 16
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 15
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
239000003795 chemical substances by application Substances 0.000 claims description 9
239000003906 humectant Substances 0.000 claims description 8
238000005498 polishing Methods 0.000 claims description 7
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 6
235000011187 glycerol Nutrition 0.000 claims description 6
239000000600 sorbitol Substances 0.000 claims description 6
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 5
231100000252 nontoxic Toxicity 0.000 claims description 5
230000003000 nontoxic effect Effects 0.000 claims description 5
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
244000246386 Mentha pulegium Species 0.000 claims description 4
235000016257 Mentha pulegium Nutrition 0.000 claims description 4
235000004357 Mentha x piperita Nutrition 0.000 claims description 4
239000003086 colorant Substances 0.000 claims description 4
235000001050 hortel pimenta Nutrition 0.000 claims description 4
239000003349 gelling agent Substances 0.000 claims description 3
239000000377 silicon dioxide Substances 0.000 claims 1
239000002562 thickening agent Substances 0.000 claims 1
239000000203 mixture Substances 0.000 abstract description 50
239000000551 dentifrice Substances 0.000 abstract description 24
239000000796 flavoring agent Substances 0.000 abstract description 2
235000019634 flavors Nutrition 0.000 abstract description 2
125000006353 oxyethylene group Chemical group 0.000 abstract 1
239000000306 component Substances 0.000 description 14
235000019441 ethanol Nutrition 0.000 description 12
239000000463 material Substances 0.000 description 9
239000004615 ingredient Substances 0.000 description 7
235000019658 bitter taste Nutrition 0.000 description 6
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 5
235000003599 food sweetener Nutrition 0.000 description 5
CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 5
239000011734 sodium Substances 0.000 description 5
229910052708 sodium Inorganic materials 0.000 description 5
239000003765 sweetening agent Substances 0.000 description 5
239000003242 anti bacterial agent Substances 0.000 description 4
230000003139 buffering effect Effects 0.000 description 4
235000014113 dietary fatty acids Nutrition 0.000 description 4
239000000194 fatty acid Substances 0.000 description 4
229930195729 fatty acid Natural products 0.000 description 4
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 3
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
239000002671 adjuvant Substances 0.000 description 3
229910052783 alkali metal Inorganic materials 0.000 description 3
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
230000000694 effects Effects 0.000 description 3
150000004665 fatty acids Chemical class 0.000 description 3
238000009472 formulation Methods 0.000 description 3
238000002156 mixing Methods 0.000 description 3
239000001509 sodium citrate Substances 0.000 description 3
NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 3
230000003381 solubilizing effect Effects 0.000 description 3
NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 2
229910002012 Aerosil® Inorganic materials 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 2
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
125000000129 anionic group Chemical group 0.000 description 2
HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
UREZNYTWGJKWBI-UHFFFAOYSA-M benzethonium chloride Chemical compound [Cl-].C1=CC(C(C)(C)CC(C)(C)C)=CC=C1OCCOCC[N+](C)(C)CC1=CC=CC=C1 UREZNYTWGJKWBI-UHFFFAOYSA-M 0.000 description 2
150000001720 carbohydrates Chemical class 0.000 description 2
230000015556 catabolic process Effects 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
238000001816 cooling Methods 0.000 description 2
229940041616 menthol Drugs 0.000 description 2
150000002924 oxiranes Chemical class 0.000 description 2
ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
229940081974 saccharin Drugs 0.000 description 2
235000019204 saccharin Nutrition 0.000 description 2
239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 2
108700004121 sarkosyl Proteins 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
239000000243 solution Substances 0.000 description 2
230000009967 tasteless effect Effects 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
230000000007 visual effect Effects 0.000 description 2
239000004711 α-olefin Substances 0.000 description 2
JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
KJPRLNWUNMBNBZ-QPJJXVBHSA-N (E)-cinnamaldehyde Chemical compound O=C\C=C\C1=CC=CC=C1 KJPRLNWUNMBNBZ-QPJJXVBHSA-N 0.000 description 1
DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
WEEGYLXZBRQIMU-UHFFFAOYSA-N 1,8-cineole Natural products C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 description 1
OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
LFJJOPDNPVFCNZ-UHFFFAOYSA-N 2-[hexadecanoyl(methyl)amino]acetic acid Chemical compound CCCCCCCCCCCCCCCC(=O)N(C)CC(O)=O LFJJOPDNPVFCNZ-UHFFFAOYSA-N 0.000 description 1
NGOZDSMNMIRDFP-UHFFFAOYSA-N 2-[methyl(tetradecanoyl)amino]acetic acid Chemical group CCCCCCCCCCCCCC(=O)N(C)CC(O)=O NGOZDSMNMIRDFP-UHFFFAOYSA-N 0.000 description 1
WLAMNBDJUVNPJU-UHFFFAOYSA-N 2-methylbutyric acid Chemical compound CCC(C)C(O)=O WLAMNBDJUVNPJU-UHFFFAOYSA-N 0.000 description 1
HOSGXJWQVBHGLT-UHFFFAOYSA-N 6-hydroxy-3,4-dihydro-1h-quinolin-2-one Chemical group N1C(=O)CCC2=CC(O)=CC=C21 HOSGXJWQVBHGLT-UHFFFAOYSA-N 0.000 description 1
GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
241000416162 Astragalus gummifer Species 0.000 description 1
241000723346 Cinnamomum camphora Species 0.000 description 1
239000005696 Diammonium phosphate Substances 0.000 description 1
101100536354 Drosophila melanogaster tant gene Proteins 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
WEEGYLXZBRQIMU-WAAGHKOSSA-N Eucalyptol Chemical compound C1C[C@H]2CC[C@]1(C)OC2(C)C WEEGYLXZBRQIMU-WAAGHKOSSA-N 0.000 description 1
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
BACYUWVYYTXETD-UHFFFAOYSA-N N-Lauroylsarcosine Chemical compound CCCCCCCCCCCC(=O)N(C)CC(O)=O BACYUWVYYTXETD-UHFFFAOYSA-N 0.000 description 1
235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
235000011613 Pinus brutia Nutrition 0.000 description 1
241000018646 Pinus brutia Species 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
206010037660 Pyrexia Diseases 0.000 description 1
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
229930006000 Sucrose Natural products 0.000 description 1
239000005844 Thymol Substances 0.000 description 1
229920001615 Tragacanth Polymers 0.000 description 1
AXMVYSVVTMKQSL-UHFFFAOYSA-N UNPD142122 Natural products OC1=CC=C(C=CC=O)C=C1O AXMVYSVVTMKQSL-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
230000002411 adverse Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
ZOJBYZNEUISWFT-UHFFFAOYSA-N allyl isothiocyanate Chemical compound C=CCN=C=S ZOJBYZNEUISWFT-UHFFFAOYSA-N 0.000 description 1
150000003868 ammonium compounds Chemical class 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
239000010617 anise oil Substances 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 1
229960001950 benzethonium chloride Drugs 0.000 description 1
GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
229960000846 camphor Drugs 0.000 description 1
229930008380 camphor Natural products 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
239000003093 cationic surfactant Substances 0.000 description 1
229940119201 cedar leaf oil Drugs 0.000 description 1
DVBJBNKEBPCGSY-UHFFFAOYSA-M cetylpyridinium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 DVBJBNKEBPCGSY-UHFFFAOYSA-M 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical class C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 1
229960005233 cineole Drugs 0.000 description 1
229940117916 cinnamic aldehyde Drugs 0.000 description 1
KJPRLNWUNMBNBZ-UHFFFAOYSA-N cinnamic aldehyde Natural products O=CC=CC1=CC=CC=C1 KJPRLNWUNMBNBZ-UHFFFAOYSA-N 0.000 description 1
239000010630 cinnamon oil Substances 0.000 description 1
239000010632 citronella oil Substances 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000010634 clove oil Substances 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
239000003398 denaturant Substances 0.000 description 1
208000002925 dental caries Diseases 0.000 description 1
MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
229910000388 diammonium phosphate Inorganic materials 0.000 description 1
235000019838 diammonium phosphate Nutrition 0.000 description 1
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical class CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
150000002169 ethanolamines Chemical class 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
235000013355 food flavoring agent Nutrition 0.000 description 1
229910021485 fumed silica Inorganic materials 0.000 description 1
150000002460 imidazoles Chemical class 0.000 description 1
230000001939 inductive effect Effects 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 description 1
239000008101 lactose Substances 0.000 description 1
239000001683 mentha spicata herb oil Substances 0.000 description 1
238000000034 method Methods 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
210000000214 mouth Anatomy 0.000 description 1
239000008164 mustard oil Substances 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
239000002245 particle Substances 0.000 description 1
229960000969 phenyl salicylate Drugs 0.000 description 1
239000010665 pine oil Substances 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
KYKNRZGSIGMXFH-ZVGUSBNCSA-M potassium bitartrate Chemical compound [K+].OC(=O)[C@H](O)[C@@H](O)C([O-])=O KYKNRZGSIGMXFH-ZVGUSBNCSA-M 0.000 description 1
229940111695 potassium tartrate Drugs 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
239000001327 prunus amygdalus amara l. extract Substances 0.000 description 1
238000009877 rendering Methods 0.000 description 1
239000010668 rosemary oil Substances 0.000 description 1
229940058206 rosemary oil Drugs 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical class C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 1
239000010672 sassafras oil Substances 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000344 soap Substances 0.000 description 1
WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
239000004299 sodium benzoate Substances 0.000 description 1
235000010234 sodium benzoate Nutrition 0.000 description 1
235000011083 sodium citrates Nutrition 0.000 description 1
229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
KSAVQLQVUXSOCR-UHFFFAOYSA-M sodium lauroyl sarcosinate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O KSAVQLQVUXSOCR-UHFFFAOYSA-M 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
239000001488 sodium phosphate Substances 0.000 description 1
229910000162 sodium phosphate Inorganic materials 0.000 description 1
235000011008 sodium phosphates Nutrition 0.000 description 1
239000001476 sodium potassium tartrate Substances 0.000 description 1
235000011006 sodium potassium tartrate Nutrition 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000001587 sorbitan monostearate Substances 0.000 description 1
235000011076 sorbitan monostearate Nutrition 0.000 description 1
229940035048 sorbitan monostearate Drugs 0.000 description 1
235000019721 spearmint oil Nutrition 0.000 description 1
239000005720 sucrose Substances 0.000 description 1
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
230000008719 thickening Effects 0.000 description 1
239000001789 thuja occidentalis l. leaf oil Substances 0.000 description 1
239000010678 thyme oil Substances 0.000 description 1
229960000790 thymol Drugs 0.000 description 1
RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
239000009637 wintergreen oil Substances 0.000 description 1

Landscapes

Cosmetics (AREA)

CA000366823A 1980-12-15 1980-12-15 Preparation orale contenant un derive polyoxyethylenique d'un alcool gras Expired CA1145261A (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA000366823A CA1145261A (fr)	1980-12-15	1980-12-15	Preparation orale contenant un derive polyoxyethylenique d'un alcool gras

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CA000366823A CA1145261A (fr)	1980-12-15	1980-12-15	Preparation orale contenant un derive polyoxyethylenique d'un alcool gras

Publications (1)

Publication Number	Publication Date
CA1145261A true CA1145261A (fr)	1983-04-26

Family

ID=4118705

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000366823A Expired CA1145261A (fr)	1980-12-15	1980-12-15	Preparation orale contenant un derive polyoxyethylenique d'un alcool gras

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CA (1)	CA1145261A (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4923685A (en) *	1987-07-30	1990-05-08	Henkel Kommanditgesellschaft Auf Aktien	Antimicrobial flavored compositions having particular utility as mouth washes
JP2013133280A (ja) *	2011-12-26	2013-07-08	Lion Corp	口腔用組成物

1980
- 1980-12-15 CA CA000366823A patent/CA1145261A/fr not_active Expired

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4923685A (en) *	1987-07-30	1990-05-08	Henkel Kommanditgesellschaft Auf Aktien	Antimicrobial flavored compositions having particular utility as mouth washes
JP2013133280A (ja) *	2011-12-26	2013-07-08	Lion Corp	口腔用組成物

Legal Events

Date	Code	Title	Description
2000-04-26	MKEX	Expiry

Publication	Publication Date	Title
US4465661A (en)	1984-08-14	Oral product having improved taste
US4476107A (en)	1984-10-09	Mouthwash composition
US3947570A (en)	1976-03-30	Oral product
CA2146635C (fr)	1999-12-28	Rince-bouche concentre pour la liberation efficace d'agents antimicrobiens
US4937066A (en)	1990-06-26	Zinc containing oral compositions
US3864472A (en)	1975-02-04	Clear lemon-flavored mouthwash
US5945088A (en)	1999-08-31	Taste masking of phenolics using citrus flavors
US5165914A (en)	1992-11-24	Oral compositions containing zinc lactate complexes
US4469674A (en)	1984-09-04	Stable oral compositions containing zinc and fluoride compounds
JP3446214B2 (ja)	2003-09-16	液状透明口腔用組成物
KR0169139B1 (ko)	1999-01-15	미각을 보존하는, 온화한 경구 위생용 조성물
CA1327531C (fr)	1994-03-08	Dentifrice anti-plaque stable a base d'exetidine, de sel de zinc et de fluorure
US5094845A (en)	1992-03-10	Oral compositions containing zinc gluconate complexes
WO2012064339A1 (fr)	2012-05-18	Produit de soin buccal et procédés d'utilisation et de fabrication de celui-ci
US4256730A (en)	1981-03-17	Oral compositions
CA1288358C (fr)	1991-09-03	Dentifrice contenant un tensio-actif non ionique poly(hydroxypropylether) et un sel d'un derive specifique d'un produit de degradation des proteines
JP5842565B2 (ja)	2016-01-13	洗口剤組成物及び洗口剤組成物における変色抑制方法
WO1996016633A1 (fr)	1996-06-06	Bain de bouche a teneur reduite en alcool
CA1145261A (fr)	1983-04-26	Preparation orale contenant un derive polyoxyethylenique d'un alcool gras
JP2627709B2 (ja)	1997-07-09	口腔用組成物
JPH0774139B2 (ja)	1995-08-09	口腔用組成物
CA1254149A (fr)	1989-05-16	Stabilisation de parfums renfermant de l'aldehyde cinnamique grace a des terpenes, des sesquiterpenes, du propyleneglycol et du dipropyleneglycol
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KR910003554B1 (ko)	1991-06-05	거품 및 불소안정성이 향상된 안정한 앤티플래크 치약
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CA1145261A - Preparation orale contenant un derive polyoxyethylenique d'un alcool gras - Google Patents

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ID=4118705

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