DE2329752A1 - Verfahren und zusammensetzung zur zahnbehandlung - Google Patents
Verfahren und zusammensetzung zur zahnbehandlungInfo
- Publication number
- DE2329752A1 DE2329752A1 DE2329752A DE2329752A DE2329752A1 DE 2329752 A1 DE2329752 A1 DE 2329752A1 DE 2329752 A DE2329752 A DE 2329752A DE 2329752 A DE2329752 A DE 2329752A DE 2329752 A1 DE2329752 A1 DE 2329752A1
- Authority
- DE
- Germany
- Prior art keywords
- acid
- group
- solution
- halogen
- teeth
- 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.)
- Withdrawn
Links
- 238000000034 method Methods 0.000 title claims description 23
- 239000000203 mixture Substances 0.000 title claims description 9
- 239000000243 solution Substances 0.000 claims description 50
- 239000002253 acid Substances 0.000 claims description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 8
- 239000007864 aqueous solution Substances 0.000 claims description 7
- 239000002324 mouth wash Substances 0.000 claims description 7
- 229940051866 mouthwash Drugs 0.000 claims description 7
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims description 6
- 239000007853 buffer solution Substances 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052794 bromium Inorganic materials 0.000 claims description 3
- 125000002843 carboxylic acid group Chemical group 0.000 claims description 3
- 239000000460 chlorine Substances 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 229940098779 methanesulfonic acid Drugs 0.000 claims description 3
- 229910017464 nitrogen compound Inorganic materials 0.000 claims description 3
- 235000015927 pasta Nutrition 0.000 claims description 3
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 3
- FEGLDXXHCNIVFP-UHFFFAOYSA-N 2-(bromoamino)acetic acid Chemical compound OC(=O)CNBr FEGLDXXHCNIVFP-UHFFFAOYSA-N 0.000 claims description 2
- YKCPTPSKQFNDHL-UHFFFAOYSA-N 2-(chloroamino)acetic acid Chemical group OC(=O)CNCl YKCPTPSKQFNDHL-UHFFFAOYSA-N 0.000 claims description 2
- YEDWGVWMZXICSQ-UHFFFAOYSA-N 2-(iodoamino)acetic acid Chemical compound OC(=O)CNI YEDWGVWMZXICSQ-UHFFFAOYSA-N 0.000 claims description 2
- 208000006558 Dental Calculus Diseases 0.000 claims description 2
- 235000019738 Limestone Nutrition 0.000 claims description 2
- 239000006028 limestone Substances 0.000 claims description 2
- 150000002830 nitrogen compounds Chemical class 0.000 claims description 2
- 239000002562 thickening agent Substances 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims 2
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 claims 2
- 210000000214 mouth Anatomy 0.000 claims 2
- 229910000019 calcium carbonate Inorganic materials 0.000 claims 1
- 229940125782 compound 2 Drugs 0.000 claims 1
- 235000011837 pasties Nutrition 0.000 claims 1
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 38
- 239000004471 Glycine Substances 0.000 description 19
- -1 Beta-aanine Chemical compound 0.000 description 14
- 208000002925 dental caries Diseases 0.000 description 13
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 11
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 10
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 9
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Inorganic materials [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 9
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 8
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 7
- 230000002087 whitening effect Effects 0.000 description 7
- 208000002064 Dental Plaque Diseases 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 5
- 239000005708 Sodium hypochlorite Substances 0.000 description 5
- 239000011575 calcium Substances 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 239000011780 sodium chloride Substances 0.000 description 5
- 229960003080 taurine Drugs 0.000 description 5
- HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 description 4
- 229910019093 NaOCl Inorganic materials 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000004140 cleaning Methods 0.000 description 4
- 230000008030 elimination Effects 0.000 description 4
- 238000003379 elimination reaction Methods 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 4
- XALVEISOOLUDJW-UHFFFAOYSA-N 2-[chloro(methyl)amino]acetic acid Chemical compound CN(Cl)CC(O)=O XALVEISOOLUDJW-UHFFFAOYSA-N 0.000 description 3
- CNPURSDMOWDNOQ-UHFFFAOYSA-N 4-methoxy-7h-pyrrolo[2,3-d]pyrimidin-2-amine Chemical compound COC1=NC(N)=NC2=C1C=CN2 CNPURSDMOWDNOQ-UHFFFAOYSA-N 0.000 description 3
- LEVWYRKDKASIDU-IMJSIDKUSA-N L-cystine Chemical compound [O-]C(=O)[C@@H]([NH3+])CSSC[C@H]([NH3+])C([O-])=O LEVWYRKDKASIDU-IMJSIDKUSA-N 0.000 description 3
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 description 3
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 description 3
- 108010077895 Sarcosine Proteins 0.000 description 3
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 description 3
- 229940043230 sarcosine Drugs 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 229940034610 toothpaste Drugs 0.000 description 3
- 239000000606 toothpaste Substances 0.000 description 3
- NMMHHSLZJLPMEG-UHFFFAOYSA-N 2-(chloroamino)ethanesulfonic acid Chemical compound OS(=O)(=O)CCNCl NMMHHSLZJLPMEG-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- QNAYBMKLOCPYGJ-UHFFFAOYSA-N Alanine Chemical compound CC([NH3+])C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- CKLJMWTZIZZHCS-UHFFFAOYSA-N Aspartic acid Chemical compound OC(=O)C(N)CC(O)=O CKLJMWTZIZZHCS-UHFFFAOYSA-N 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- PMMYEEVYMWASQN-DMTCNVIQSA-N Hydroxyproline Chemical compound O[C@H]1CN[C@H](C(O)=O)C1 PMMYEEVYMWASQN-DMTCNVIQSA-N 0.000 description 2
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 description 2
- DCXYFEDJOCDNAF-REOHCLBHSA-N L-asparagine Chemical compound OC(=O)[C@@H](N)CC(N)=O DCXYFEDJOCDNAF-REOHCLBHSA-N 0.000 description 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 2
- ZDXPYRJPNDTMRX-VKHMYHEASA-N L-glutamine Chemical compound OC(=O)[C@@H](N)CCC(N)=O ZDXPYRJPNDTMRX-VKHMYHEASA-N 0.000 description 2
- AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 description 2
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 2
- 239000004472 Lysine Substances 0.000 description 2
- OKJIRPAQVSHGFK-UHFFFAOYSA-N N-acetylglycine Chemical compound CC(=O)NCC(O)=O OKJIRPAQVSHGFK-UHFFFAOYSA-N 0.000 description 2
- AHLPHDHHMVZTML-UHFFFAOYSA-N Orn-delta-NH2 Natural products NCCCC(N)C(O)=O AHLPHDHHMVZTML-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 description 2
- 235000011941 Tilia x europaea Nutrition 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000012459 cleaning agent Substances 0.000 description 2
- 229960003067 cystine Drugs 0.000 description 2
- 210000003298 dental enamel Anatomy 0.000 description 2
- 210000004268 dentin Anatomy 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- PMMYEEVYMWASQN-UHFFFAOYSA-N dl-hydroxyproline Natural products OC1C[NH2+]C(C([O-])=O)C1 PMMYEEVYMWASQN-UHFFFAOYSA-N 0.000 description 2
- 230000003628 erosive effect Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 229960002743 glutamine Drugs 0.000 description 2
- XKUKSGPZAADMRA-UHFFFAOYSA-N glycyl-glycyl-glycine Chemical compound NCC(=O)NCC(=O)NCC(O)=O XKUKSGPZAADMRA-UHFFFAOYSA-N 0.000 description 2
- YMAWOPBAYDPSLA-UHFFFAOYSA-N glycylglycine Chemical compound [NH3+]CC(=O)NCC([O-])=O YMAWOPBAYDPSLA-UHFFFAOYSA-N 0.000 description 2
- 230000009931 harmful effect Effects 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 229960002885 histidine Drugs 0.000 description 2
- 229960002591 hydroxyproline Drugs 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229930182817 methionine Natural products 0.000 description 2
- 235000006109 methionine Nutrition 0.000 description 2
- ORQYPOUSZINNCB-UHFFFAOYSA-N potassium;hypobromite Chemical compound [K+].Br[O-] ORQYPOUSZINNCB-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 150000003388 sodium compounds Chemical class 0.000 description 2
- 229950000244 sulfanilic acid Drugs 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 238000004448 titration Methods 0.000 description 2
- 229960004295 valine Drugs 0.000 description 2
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 description 1
- BICAZEGHQUHWMD-REOHCLBHSA-N (2r)-2-(chloroamino)-3-sulfanylpropanoic acid Chemical compound OC(=O)[C@H](CS)NCl BICAZEGHQUHWMD-REOHCLBHSA-N 0.000 description 1
- FGBFBQULHKUDQV-IMJSIDKUSA-N (2r)-2-amino-3-[[(2r)-2-carboxy-2-(chloroamino)ethyl]disulfanyl]propanoic acid Chemical compound OC(=O)[C@@H](N)CSSC[C@H](NCl)C(O)=O FGBFBQULHKUDQV-IMJSIDKUSA-N 0.000 description 1
- OBRKOYNVXRUADL-BYPYZUCNSA-N (2s)-1-chloropyrrolidine-2-carboxylic acid Chemical compound OC(=O)[C@@H]1CCCN1Cl OBRKOYNVXRUADL-BYPYZUCNSA-N 0.000 description 1
- IRHTVZIUGVMYDI-BYPYZUCNSA-N (2s)-1-iodopyrrolidine-2-carboxylic acid Chemical compound OC(=O)[C@@H]1CCCN1I IRHTVZIUGVMYDI-BYPYZUCNSA-N 0.000 description 1
- RLRYVSYUAHQYLS-QMMMGPOBSA-N (2s)-2-(bromoamino)-3-(4-hydroxyphenyl)propanoic acid Chemical compound OC(=O)[C@@H](NBr)CC1=CC=C(O)C=C1 RLRYVSYUAHQYLS-QMMMGPOBSA-N 0.000 description 1
- RPPLPTLNPSOPSB-REOHCLBHSA-N (2s)-2-(bromoamino)-3-hydroxypropanoic acid Chemical compound OC[C@H](NBr)C(O)=O RPPLPTLNPSOPSB-REOHCLBHSA-N 0.000 description 1
- DOSWGDLXZCTKIX-YFKPBYRVSA-N (2s)-2-(bromoamino)-4-methylpentanoic acid Chemical compound CC(C)C[C@H](NBr)C(O)=O DOSWGDLXZCTKIX-YFKPBYRVSA-N 0.000 description 1
- BGGDKMFFFDGBOP-REOHCLBHSA-N (2s)-2-(bromoamino)butanedioic acid Chemical compound OC(=O)C[C@H](NBr)C(O)=O BGGDKMFFFDGBOP-REOHCLBHSA-N 0.000 description 1
- ARNDBMMDZPKHMA-YFKPBYRVSA-N (2s)-2-(chloroamino)-3-(1h-imidazol-5-yl)propanoic acid Chemical compound OC(=O)[C@@H](NCl)CC1=CNC=N1 ARNDBMMDZPKHMA-YFKPBYRVSA-N 0.000 description 1
- HKDIYFPRGVYHOI-QMMMGPOBSA-N (2s)-2-(chloroamino)-3-(4-hydroxyphenyl)propanoic acid Chemical compound OC(=O)[C@@H](NCl)CC1=CC=C(O)C=C1 HKDIYFPRGVYHOI-QMMMGPOBSA-N 0.000 description 1
- QRCAHEGWUXJKMU-REOHCLBHSA-N (2s)-2-(chloroamino)-3-hydroxypropanoic acid Chemical compound OC[C@H](NCl)C(O)=O QRCAHEGWUXJKMU-REOHCLBHSA-N 0.000 description 1
- YQYBDANXQKBAKJ-BYPYZUCNSA-N (2s)-2-(chloroamino)-3-methylbutanoic acid Chemical compound CC(C)[C@H](NCl)C(O)=O YQYBDANXQKBAKJ-BYPYZUCNSA-N 0.000 description 1
- ASVRUJBTDNHQMI-YFKPBYRVSA-N (2s)-2-(chloroamino)-4-methylpentanoic acid Chemical compound CC(C)C[C@H](NCl)C(O)=O ASVRUJBTDNHQMI-YFKPBYRVSA-N 0.000 description 1
- NZCZCNKLNYYFBC-BYPYZUCNSA-N (2s)-2-(chloroamino)-4-methylsulfanylbutanoic acid Chemical compound CSCC[C@H](NCl)C(O)=O NZCZCNKLNYYFBC-BYPYZUCNSA-N 0.000 description 1
- LPNDDEGGEFXQQV-BYPYZUCNSA-N (2s)-2-(chloroamino)-5-(diaminomethylideneamino)pentanoic acid Chemical compound NC(=N)NCCC[C@H](NCl)C(O)=O LPNDDEGGEFXQQV-BYPYZUCNSA-N 0.000 description 1
- VMLMULDNFDPOMM-REOHCLBHSA-N (2s)-2-(chloroamino)butanedioic acid Chemical compound OC(=O)C[C@H](NCl)C(O)=O VMLMULDNFDPOMM-REOHCLBHSA-N 0.000 description 1
- BZOMFDPEVFVFHI-BYPYZUCNSA-N (2s)-2-(chloroamino)pentanoic acid Chemical compound CCC[C@H](NCl)C(O)=O BZOMFDPEVFVFHI-BYPYZUCNSA-N 0.000 description 1
- OULUARVWFSHZJQ-VKHMYHEASA-N (2s)-2-(iodoamino)pentanedioic acid Chemical compound OC(=O)CC[C@H](NI)C(O)=O OULUARVWFSHZJQ-VKHMYHEASA-N 0.000 description 1
- GQAKENMGEKUHDM-VKHMYHEASA-N (2s)-5-amino-2-(bromoamino)-5-oxopentanoic acid Chemical compound NC(=O)CC[C@H](NBr)C(O)=O GQAKENMGEKUHDM-VKHMYHEASA-N 0.000 description 1
- WUNZCSWDOYZOPR-VKHMYHEASA-N (2s)-5-amino-2-(chloroamino)-5-oxopentanoic acid Chemical compound NC(=O)CC[C@H](NCl)C(O)=O WUNZCSWDOYZOPR-VKHMYHEASA-N 0.000 description 1
- BSOXJTXLPLIVAG-YFKPBYRVSA-N (2s)-6-amino-2-(chloroamino)hexanoic acid Chemical compound NCCCC[C@H](NCl)C(O)=O BSOXJTXLPLIVAG-YFKPBYRVSA-N 0.000 description 1
- CPEGVQVQEKOVGU-GBXIJSLDSA-N (2s,3r)-2-(chloroamino)-3-hydroxybutanoic acid Chemical compound C[C@@H](O)[C@H](NCl)C(O)=O CPEGVQVQEKOVGU-GBXIJSLDSA-N 0.000 description 1
- QVJWPWBERRGLTN-WHFBIAKZSA-N (2s,3s)-2-(chloroamino)-3-methylpentanoic acid Chemical compound CC[C@H](C)[C@H](NCl)C(O)=O QVJWPWBERRGLTN-WHFBIAKZSA-N 0.000 description 1
- DLGAUVSRZXNATA-DHYYHALDSA-N (2s,3s)-2-amino-3-methylpentanoic acid;(2s)-pyrrolidine-2-carboxylic acid Chemical compound OC(=O)[C@@H]1CCCN1.CC[C@H](C)[C@H](N)C(O)=O DLGAUVSRZXNATA-DHYYHALDSA-N 0.000 description 1
- KHDXVKDLWMZLFM-DMTCNVIQSA-N (2s,4r)-1-chloro-4-hydroxypyrrolidine-2-carboxylic acid Chemical compound O[C@@H]1C[C@@H](C(O)=O)N(Cl)C1 KHDXVKDLWMZLFM-DMTCNVIQSA-N 0.000 description 1
- YTVCTVCDMNUZOH-UHNVWZDZSA-N (2s,5r)-6-amino-2-(chloroamino)-5-hydroxyhexanoic acid Chemical compound NC[C@H](O)CC[C@H](NCl)C(O)=O YTVCTVCDMNUZOH-UHNVWZDZSA-N 0.000 description 1
- USAWSWBIFACPGD-UHFFFAOYSA-N 2-(bromoamino)ethanesulfonic acid Chemical compound OS(=O)(=O)CCNBr USAWSWBIFACPGD-UHFFFAOYSA-N 0.000 description 1
- BIECFEMCDBQPTL-UHFFFAOYSA-N 2-(chloroamino)benzoic acid Chemical compound OC(=O)C1=CC=CC=C1NCl BIECFEMCDBQPTL-UHFFFAOYSA-N 0.000 description 1
- ZUUHDGNAOZSRRB-UHFFFAOYSA-N 2-(chloroamino)ethanol Chemical compound OCCNCl ZUUHDGNAOZSRRB-UHFFFAOYSA-N 0.000 description 1
- XUGMGYUIGNYMJQ-UHFFFAOYSA-N 2-(iodoamino)ethanesulfonic acid Chemical compound OS(=O)(=O)CCNI XUGMGYUIGNYMJQ-UHFFFAOYSA-N 0.000 description 1
- MNHBIAPEEQWPIZ-UHFFFAOYSA-N 2-(iodoamino)ethanol Chemical compound OCCNI MNHBIAPEEQWPIZ-UHFFFAOYSA-N 0.000 description 1
- HFYFQWAWAXTQMX-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]ethyl-(carboxymethyl)amino]acetate;bis(2-hydroxyethyl)azanium Chemical compound OCCNCCO.OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O HFYFQWAWAXTQMX-UHFFFAOYSA-N 0.000 description 1
- ZVYADCOTSRZJFI-UHFFFAOYSA-N 2-[acetyl(bromo)amino]acetic acid Chemical compound CC(=O)N(Br)CC(O)=O ZVYADCOTSRZJFI-UHFFFAOYSA-N 0.000 description 1
- QGLFALHOWWFKJO-UHFFFAOYSA-N 2-[acetyl(chloro)amino]acetic acid Chemical compound CC(=O)N(Cl)CC(O)=O QGLFALHOWWFKJO-UHFFFAOYSA-N 0.000 description 1
- ZPGAQMYKMUKMOV-UHFFFAOYSA-N 2-[bromo(methyl)amino]acetic acid Chemical compound CN(Br)CC(O)=O ZPGAQMYKMUKMOV-UHFFFAOYSA-N 0.000 description 1
- ZTWGZWADDCUMHM-UHFFFAOYSA-N 2-[iodo(methyl)amino]acetic acid Chemical compound CN(I)CC(O)=O ZTWGZWADDCUMHM-UHFFFAOYSA-N 0.000 description 1
- DZUMFNGQHXQAFZ-UHFFFAOYSA-N 2-amino-1-bromoethanol Chemical compound NCC(O)Br DZUMFNGQHXQAFZ-UHFFFAOYSA-N 0.000 description 1
- ZMCHBSMFKQYNKA-UHFFFAOYSA-N 2-aminobenzenesulfonic acid Chemical compound NC1=CC=CC=C1S(O)(=O)=O ZMCHBSMFKQYNKA-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q11/00—Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61C—DENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
- A61C17/00—Devices for cleaning, polishing, rinsing or drying teeth, teeth cavities or prostheses; Saliva removers; Dental appliances for receiving spittle
- A61C17/02—Rinsing or air-blowing devices, e.g. using fluid jets or comprising liquid medication
- A61C17/028—Rinsing or air-blowing devices, e.g. using fluid jets or comprising liquid medication with intermittent liquid flow
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/20—Protective coatings for natural or artificial teeth, e.g. sealings, dye coatings or varnish
-
- 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
- A61K2800/22—Gas releasing
- A61K2800/222—Effervescent
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Chemical & Material Sciences (AREA)
- Dentistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Birds (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- Cosmetics (AREA)
- Dental Preparations (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2744372A GB1468144A (en) | 1972-06-12 | 1972-06-12 | Dental method composition |
| GB3061172 | 1972-06-29 | ||
| GB3958872 | 1972-08-24 | ||
| GB3958972 | 1972-08-24 | ||
| US30114172A | 1972-10-26 | 1972-10-26 | |
| US05/301,163 US3932605A (en) | 1972-06-12 | 1972-10-26 | Dental treatment |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2329752A1 true DE2329752A1 (de) | 1974-01-31 |
Family
ID=27546708
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2329752A Withdrawn DE2329752A1 (de) | 1972-06-12 | 1973-06-12 | Verfahren und zusammensetzung zur zahnbehandlung |
Country Status (4)
| Country | Link |
|---|---|
| JP (1) | JPS6018642B2 (enrdf_load_stackoverflow) |
| CA (1) | CA995586A (enrdf_load_stackoverflow) |
| DE (1) | DE2329752A1 (enrdf_load_stackoverflow) |
| FR (1) | FR2187289A1 (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997021419A1 (en) * | 1995-12-08 | 1997-06-19 | Colgate-Palmolive Company | Dual component tooth whitening dentifrice |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04273813A (ja) * | 1991-02-28 | 1992-09-30 | Kanebo Ltd | 口腔用組成物 |
| AU2020273162C1 (en) * | 2019-04-10 | 2024-09-19 | Black Tulip Management, Inc. | Oral rinse compositions for reducing pathogens underlying and for treating periodontal disease and oral malodor in the canine |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE569397A (enrdf_load_stackoverflow) * | 1957-07-13 | |||
| NL239622A (enrdf_load_stackoverflow) * | 1958-05-29 | |||
| US3277118A (en) * | 1958-05-29 | 1966-10-04 | Gaba Ag | Quaternary ammonium fluorides |
-
1973
- 1973-06-08 CA CA173,632A patent/CA995586A/en not_active Expired
- 1973-06-12 DE DE2329752A patent/DE2329752A1/de not_active Withdrawn
- 1973-06-12 FR FR7321264A patent/FR2187289A1/fr active Granted
- 1973-06-12 JP JP48066279A patent/JPS6018642B2/ja not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997021419A1 (en) * | 1995-12-08 | 1997-06-19 | Colgate-Palmolive Company | Dual component tooth whitening dentifrice |
Also Published As
| Publication number | Publication date |
|---|---|
| AU5665273A (en) | 1974-12-12 |
| FR2187289A1 (en) | 1974-01-18 |
| FR2187289B1 (enrdf_load_stackoverflow) | 1976-11-12 |
| JPS6018642B2 (ja) | 1985-05-11 |
| JPS4948848A (enrdf_load_stackoverflow) | 1974-05-11 |
| CA995586A (en) | 1976-08-24 |
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