JPS5839805B2 - フケボウシザイ - Google Patents
フケボウシザイInfo
- Publication number
- JPS5839805B2 JPS5839805B2 JP48077564A JP7756473A JPS5839805B2 JP S5839805 B2 JPS5839805 B2 JP S5839805B2 JP 48077564 A JP48077564 A JP 48077564A JP 7756473 A JP7756473 A JP 7756473A JP S5839805 B2 JPS5839805 B2 JP S5839805B2
- Authority
- JP
- Japan
- Prior art keywords
- hair
- hydroxy
- pyridone
- methyl
- alkyl
- 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.)
- Expired
Links
- 208000001840 Dandruff Diseases 0.000 title description 2
- 150000003839 salts Chemical class 0.000 claims description 24
- 206010053615 Thermal burn Diseases 0.000 claims description 19
- 239000004480 active ingredient Substances 0.000 claims description 6
- SNUSZUYTMHKCPM-UHFFFAOYSA-N 1-hydroxypyridin-2-one Chemical compound ON1C=CC=CC1=O SNUSZUYTMHKCPM-UHFFFAOYSA-N 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 description 40
- -1 furobil Chemical group 0.000 description 30
- 239000002453 shampoo Substances 0.000 description 28
- 150000001875 compounds Chemical class 0.000 description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 26
- 235000002639 sodium chloride Nutrition 0.000 description 25
- 239000002304 perfume Substances 0.000 description 23
- 239000013543 active substance Substances 0.000 description 22
- 239000003921 oil Substances 0.000 description 21
- 235000019198 oils Nutrition 0.000 description 21
- 239000000194 fatty acid Substances 0.000 description 19
- 235000014113 dietary fatty acids Nutrition 0.000 description 18
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 18
- 229930195729 fatty acid Natural products 0.000 description 18
- 150000004665 fatty acids Chemical class 0.000 description 17
- 239000002537 cosmetic Substances 0.000 description 15
- 239000000126 substance Substances 0.000 description 15
- 229920001577 copolymer Polymers 0.000 description 14
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 13
- 239000003795 chemical substances by application Substances 0.000 description 13
- 239000000975 dye Substances 0.000 description 13
- 239000000203 mixture Substances 0.000 description 13
- 239000000243 solution Substances 0.000 description 12
- 229920000151 polyglycol Polymers 0.000 description 11
- 239000010695 polyglycol Substances 0.000 description 11
- 210000004761 scalp Anatomy 0.000 description 11
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 10
- 150000003751 zinc Chemical class 0.000 description 10
- 238000004140 cleaning Methods 0.000 description 9
- 239000003240 coconut oil Substances 0.000 description 9
- 235000019864 coconut oil Nutrition 0.000 description 9
- 206010067723 Skin plaque Diseases 0.000 description 8
- 239000003755 preservative agent Substances 0.000 description 8
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 238000009472 formulation Methods 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 239000012071 phase Substances 0.000 description 7
- YBBJKCMMCRQZMA-UHFFFAOYSA-N pyrithione Chemical compound ON1C=CC=CC1=S YBBJKCMMCRQZMA-UHFFFAOYSA-N 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- 238000005406 washing Methods 0.000 description 7
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 6
- 239000002202 Polyethylene glycol Substances 0.000 description 6
- 239000006071 cream Substances 0.000 description 6
- 150000002191 fatty alcohols Chemical class 0.000 description 6
- 239000000499 gel Substances 0.000 description 6
- 229920001223 polyethylene glycol Polymers 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 5
- 239000000443 aerosol Substances 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 5
- 150000002169 ethanolamines Chemical class 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 5
- 239000003205 fragrance Substances 0.000 description 5
- 210000003128 head Anatomy 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 159000000000 sodium salts Chemical class 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 239000004166 Lanolin Chemical class 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 4
- 229960001040 ammonium chloride Drugs 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 239000007859 condensation product Substances 0.000 description 4
- 230000003750 conditioning effect Effects 0.000 description 4
- 239000008266 hair spray Substances 0.000 description 4
- 229940039717 lanolin Drugs 0.000 description 4
- 235000019388 lanolin Nutrition 0.000 description 4
- 239000006210 lotion Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- LVWZTYCIRDMTEY-UHFFFAOYSA-N metamizole Chemical compound O=C1C(N(CS(O)(=O)=O)C)=C(C)N(C)N1C1=CC=CC=C1 LVWZTYCIRDMTEY-UHFFFAOYSA-N 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 125000002252 acyl group Chemical group 0.000 description 3
- 125000005907 alkyl ester group Chemical group 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- 239000007795 chemical reaction product Substances 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
- 230000000052 comparative effect Effects 0.000 description 3
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 3
- SMVRDGHCVNAOIN-UHFFFAOYSA-L disodium;1-dodecoxydodecane;sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC SMVRDGHCVNAOIN-UHFFFAOYSA-L 0.000 description 3
- 239000006185 dispersion Chemical class 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000001556 precipitation Methods 0.000 description 3
- 230000002335 preservative effect Effects 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 150000004671 saturated fatty acids Chemical class 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 230000001988 toxicity Effects 0.000 description 3
- 231100000419 toxicity Toxicity 0.000 description 3
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 3
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 2
- QVWDCUMRWIBGJX-UHFFFAOYSA-N 1-hydroxy-4,6-dimethylpyridin-2-one Chemical compound CC=1C=C(C)N(O)C(=O)C=1 QVWDCUMRWIBGJX-UHFFFAOYSA-N 0.000 description 2
- QHCSPVRVAUBWQV-UHFFFAOYSA-N 1-hydroxy-4-methyl-6-undecylpyridin-2-one Chemical compound CCCCCCCCCCCC1=CC(C)=CC(=O)N1O QHCSPVRVAUBWQV-UHFFFAOYSA-N 0.000 description 2
- MIJDSYMOBYNHOT-UHFFFAOYSA-N 2-(ethylamino)ethanol Chemical compound CCNCCO MIJDSYMOBYNHOT-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- NSDAFIXBLIOQQP-UHFFFAOYSA-N 3-cyclohexyl-1h-pyridin-2-one Chemical compound O=C1NC=CC=C1C1CCCCC1 NSDAFIXBLIOQQP-UHFFFAOYSA-N 0.000 description 2
- ZZUKZMLPCBPVED-UHFFFAOYSA-N 6-cyclohexyl-3-methyl-1H-pyridin-2-one Chemical compound CC=1C(NC(=CC1)C1CCCCC1)=O ZZUKZMLPCBPVED-UHFFFAOYSA-N 0.000 description 2
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 229940124091 Keratolytic Drugs 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- SUZRRICLUFMAQD-UHFFFAOYSA-N N-Methyltaurine Chemical compound CNCCS(O)(=O)=O SUZRRICLUFMAQD-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 239000005662 Paraffin oil Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 108010009736 Protein Hydrolysates Proteins 0.000 description 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 150000003973 alkyl amines Chemical class 0.000 description 2
- 235000019270 ammonium chloride Nutrition 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 150000001767 cationic compounds Chemical class 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 description 2
- SCKYRAXSEDYPSA-UHFFFAOYSA-N ciclopirox Chemical compound ON1C(=O)C=C(C)C=C1C1CCCCC1 SCKYRAXSEDYPSA-UHFFFAOYSA-N 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 2
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 2
- JMGZBMRVDHKMKB-UHFFFAOYSA-L disodium;2-sulfobutanedioate Chemical compound [Na+].[Na+].OS(=O)(=O)C(C([O-])=O)CC([O-])=O JMGZBMRVDHKMKB-UHFFFAOYSA-L 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 229910001411 inorganic cation Inorganic materials 0.000 description 2
- 230000001530 keratinolytic effect Effects 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- ISTASGAHDLTQRU-UHFFFAOYSA-N n-(2-hydroxyethyl)undec-10-enamide Chemical compound OCCNC(=O)CCCCCCCCC=C ISTASGAHDLTQRU-UHFFFAOYSA-N 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 229940055577 oleyl alcohol Drugs 0.000 description 2
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 2
- 150000007530 organic bases Chemical class 0.000 description 2
- QJFMCHRSDOLMHA-UHFFFAOYSA-N phenylmethanamine;hydrobromide Chemical compound Br.NCC1=CC=CC=C1 QJFMCHRSDOLMHA-UHFFFAOYSA-N 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 229920000191 poly(N-vinyl pyrrolidone) Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000003380 propellant Substances 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical compound OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 description 2
- 230000001172 regenerating effect Effects 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 2
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 2
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 229940043810 zinc pyrithione Drugs 0.000 description 2
- PICXIOQBANWBIZ-UHFFFAOYSA-N zinc;1-oxidopyridine-2-thione Chemical compound [Zn+2].[O-]N1C=CC=CC1=S.[O-]N1C=CC=CC1=S PICXIOQBANWBIZ-UHFFFAOYSA-N 0.000 description 2
- JNBVLGDICHLLTN-DZUOILHNSA-N (2s)-2-acetamido-n-[(2s,3s)-4-[[[(2s)-2-acetamido-3-methylbutanoyl]amino]-(cyclohexylmethyl)amino]-3-hydroxy-1-phenylbutan-2-yl]-3-methylbutanamide Chemical compound C([C@H](NC(=O)[C@@H](NC(C)=O)C(C)C)[C@@H](O)CN(CC1CCCCC1)NC(=O)[C@@H](NC(C)=O)C(C)C)C1=CC=CC=C1 JNBVLGDICHLLTN-DZUOILHNSA-N 0.000 description 1
- QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 description 1
- PVOAHINGSUIXLS-UHFFFAOYSA-N 1-Methylpiperazine Chemical compound CN1CCNCC1 PVOAHINGSUIXLS-UHFFFAOYSA-N 0.000 description 1
- SNHWDNDKRMTYNV-UHFFFAOYSA-N 1-hydroxy-4-methyl-6-(1-methylcyclohexyl)pyridin-2-one Chemical compound ON1C(=O)C=C(C)C=C1C1(C)CCCCC1 SNHWDNDKRMTYNV-UHFFFAOYSA-N 0.000 description 1
- HZXAUBYEALZPGG-UHFFFAOYSA-N 1-hydroxy-4-methyl-6-(4-methylcyclohexyl)pyridin-2-one Chemical compound C1CC(C)CCC1C1=CC(C)=CC(=O)N1O HZXAUBYEALZPGG-UHFFFAOYSA-N 0.000 description 1
- AFXHVMLWGXYZJA-UHFFFAOYSA-N 1-hydroxy-4-methylpyridin-2-one Chemical compound CC=1C=CN(O)C(=O)C=1 AFXHVMLWGXYZJA-UHFFFAOYSA-N 0.000 description 1
- DLNPJWYSCKUGHI-UHFFFAOYSA-N 1-hydroxypyridine-2-thione;sodium Chemical compound [Na].ON1C=CC=CC1=S DLNPJWYSCKUGHI-UHFFFAOYSA-N 0.000 description 1
- VOHCMATXIKWIKC-UHFFFAOYSA-N 1-hydroxypyridine-2-thione;zinc Chemical compound [Zn].ON1C=CC=CC1=S VOHCMATXIKWIKC-UHFFFAOYSA-N 0.000 description 1
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical class CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- KKFDCBRMNNSAAW-UHFFFAOYSA-N 2-(morpholin-4-yl)ethanol Chemical compound OCCN1CCOCC1 KKFDCBRMNNSAAW-UHFFFAOYSA-N 0.000 description 1
- BQJLEQAXRYBKPQ-UHFFFAOYSA-N 2-amino-2-methylpropane-1,1-diol Chemical compound CC(C)(N)C(O)O BQJLEQAXRYBKPQ-UHFFFAOYSA-N 0.000 description 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
- MARYDOMJDFATPK-UHFFFAOYSA-N 3-hydroxy-1h-pyridine-2-thione Chemical compound OC1=CC=CN=C1S MARYDOMJDFATPK-UHFFFAOYSA-N 0.000 description 1
- FSPIBFKGESGOLU-UHFFFAOYSA-N 4,6-dimethyl-1h-pyridin-2-one Chemical compound CC1=CC(C)=NC(O)=C1 FSPIBFKGESGOLU-UHFFFAOYSA-N 0.000 description 1
- KSMVBYPXNKCPAJ-UHFFFAOYSA-N 4-Methylcyclohexylamine Chemical compound CC1CCC(N)CC1 KSMVBYPXNKCPAJ-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
- A61Q5/00—Preparations for care of the hair
- A61Q5/006—Antidandruff preparations
-
- 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
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
- A61K8/4926—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having six membered rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/08—Antiseborrheics
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S424/00—Drug, bio-affecting and body treating compositions
- Y10S424/01—Aerosol hair preparation
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S424/00—Drug, bio-affecting and body treating compositions
- Y10S424/02—Resin hair settings
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S424/00—Drug, bio-affecting and body treating compositions
- Y10S424/04—Dandruff
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- 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)
- Birds (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Dermatology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2234009A DE2234009C3 (de) | 1972-07-11 | 1972-07-11 | Kosmetische Zubereitungen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS4950142A JPS4950142A (en, 2012) | 1974-05-15 |
| JPS5839805B2 true JPS5839805B2 (ja) | 1983-09-01 |
Family
ID=5850316
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP48077564A Expired JPS5839805B2 (ja) | 1972-07-11 | 1973-07-11 | フケボウシザイ |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US4711775A (en, 2012) |
| JP (1) | JPS5839805B2 (en, 2012) |
| AR (1) | AR222133A1 (en, 2012) |
| AT (1) | AT329187B (en, 2012) |
| BE (1) | BE802208A (en, 2012) |
| BR (1) | BR7305186D0 (en, 2012) |
| CA (1) | CA1013675A (en, 2012) |
| CH (1) | CH584033A5 (en, 2012) |
| CS (1) | CS220304B2 (en, 2012) |
| DD (1) | DD105391A5 (en, 2012) |
| DE (1) | DE2234009C3 (en, 2012) |
| DK (1) | DK135362C (en, 2012) |
| FR (1) | FR2191904B1 (en, 2012) |
| GB (1) | GB1440975A (en, 2012) |
| HU (1) | HU166867B (en, 2012) |
| IT (1) | IT1043856B (en, 2012) |
| LU (1) | LU67973A1 (en, 2012) |
| NL (1) | NL175259C (en, 2012) |
| NO (1) | NO139074C (en, 2012) |
| SE (1) | SE401978B (en, 2012) |
| SU (1) | SU580806A3 (en, 2012) |
| ZA (1) | ZA734620B (en, 2012) |
Families Citing this family (78)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5421416B2 (en, 2012) * | 1973-04-09 | 1979-07-30 | ||
| DE2931379A1 (de) * | 1979-08-02 | 1981-02-26 | Rewo Chemische Werke Gmbh | Kosmetisches mittel |
| JPS6032678B2 (ja) * | 1980-10-27 | 1985-07-29 | ライオン株式会社 | 液体洗浄剤組成物 |
| JPS5827800A (ja) * | 1981-08-12 | 1983-02-18 | ライオン株式会社 | シヤンプ−組成物 |
| JPS5832813A (ja) * | 1981-08-21 | 1983-02-25 | Lion Corp | 毛髪化粧料 |
| JPS5832814A (ja) * | 1981-08-21 | 1983-02-25 | Lion Corp | 毛髪化粧料 |
| JPS5832812A (ja) * | 1981-08-21 | 1983-02-25 | Lion Corp | 毛髪化粧料 |
| JPS5840397A (ja) * | 1981-09-04 | 1983-03-09 | ライオン株式会社 | シヤンプ−組成物 |
| JPS58113300A (ja) * | 1981-12-26 | 1983-07-06 | ライオン株式会社 | シヤンプ−組成物 |
| JPS58113299A (ja) * | 1981-12-26 | 1983-07-06 | ライオン株式会社 | シヤンプ−組成物 |
| JPS58180415A (ja) * | 1982-04-15 | 1983-10-21 | Lion Corp | 毛髪化粧料 |
| JPS58185699A (ja) * | 1982-04-24 | 1983-10-29 | ライオン株式会社 | シヤンプ−組成物 |
| JPS58198413A (ja) * | 1982-05-13 | 1983-11-18 | Lion Corp | 頭髪化粧料 |
| JPS58198412A (ja) * | 1982-05-13 | 1983-11-18 | Lion Corp | 頭髪化粧料 |
| JPS5910509A (ja) * | 1982-07-09 | 1984-01-20 | Lion Corp | 整髪料 |
| JPS5939817A (ja) * | 1982-08-31 | 1984-03-05 | Lion Corp | 毛髪化粧料 |
| JPS59135300A (ja) * | 1982-10-13 | 1984-08-03 | ザ，プロクタ−，エンド，ギヤンブル，カンパニ− | シヤンプ−組成物の製造法 |
| JPS5988411A (ja) * | 1982-11-12 | 1984-05-22 | Lion Corp | 毛髪化粧料 |
| GB8407999D0 (en) * | 1984-03-28 | 1984-05-10 | Procter & Gamble Ltd | Hair care compositions |
| GB8524508D0 (en) * | 1985-10-04 | 1985-11-06 | Beecham Group Plc | Composition |
| AR242187A1 (es) * | 1986-04-18 | 1993-03-31 | Hoechst Ag | Procedimiento para la preparacion de 1-hidroxi-2-piridonas, obtencion de medicamentos que las contienen, e intermediarios utiles en dicho procedimiento. |
| LU86944A1 (fr) * | 1987-07-17 | 1989-03-08 | Oreal | Composition a base de derives d'hydroxypyridone pour diminuer la chute des cheveux |
| GB8814296D0 (en) * | 1988-06-16 | 1988-07-20 | Unilever Plc | Shampoo composition |
| US5053218A (en) * | 1989-07-17 | 1991-10-01 | Cosmosol, Ltd. | Pressurized hair spray composition |
| JPH0372413A (ja) * | 1989-08-10 | 1991-03-27 | Japan Happy:Kk | 毛髪のコールドパーマネントウエーブ処理剤と染毛剤 |
| JPH0623087B2 (ja) * | 1989-10-09 | 1994-03-30 | 花王株式会社 | 洗浄剤組成物 |
| US5104645A (en) * | 1990-02-02 | 1992-04-14 | The Proctor & Gamble Company | Antidandruff shampoo compositions |
| GB2245279B (en) * | 1990-06-20 | 1993-04-07 | Unilever Plc | Shampoo composition |
| FR2685867B1 (fr) * | 1992-01-07 | 1995-06-09 | Thorel Jean | Compositions contre la desquamation de l'epiderme et du cuir chevelu. |
| DE4333893A1 (de) * | 1993-10-05 | 1995-04-06 | Hoechst Ag | Kosmetische Zubereitungen |
| JP3200723B2 (ja) * | 1993-08-18 | 2001-08-20 | 日本農薬株式会社 | 育毛剤 |
| US5424435A (en) * | 1993-10-18 | 1995-06-13 | Olin Corporation | 1-hydroxy-6-substituted-2-pyridones |
| FR2740685B1 (fr) * | 1995-11-08 | 1998-01-23 | Pf Medicament | Composition pharmaceutique topique moussante pour le traitement des dermatoses, induites par pityrosporum ovale |
| US5846984A (en) * | 1996-01-19 | 1998-12-08 | The Trustees Of Columbia University In The City Of New York | Use of ciclopirox or a pharmaceutically acceptable salt thereof for inhibiting neuronal cell damage or neuronal cell death |
| GB2311995B (en) * | 1996-04-12 | 1999-12-15 | Unilever Plc | Antimicrobial hair treatment composition |
| US20040039030A1 (en) * | 1996-09-27 | 2004-02-26 | Hoechst Akeengesellschaft | Use of 1-hydroxy-2-pyridones for the treatment of seborrheic dermatitis |
| DE19639818A1 (de) * | 1996-09-27 | 1998-04-02 | Hoechst Ag | Verwendung von 1-Hydroxy-2-pyridonen zur Behandlung der Seborrhoischen Dermatitis |
| JP2002537307A (ja) * | 1999-02-19 | 2002-11-05 | ベー・エル・アー・ハー・エム・エス・ディアグノスティカ・ゲーエムベーハー | 甲状腺機能亢進症の治療におけるブロッキング抗ｔｓｈレセプター抗体の使用およびかかる使用のためのモノクローナル抗体 |
| DE50015912D1 (de) | 1999-07-15 | 2010-06-10 | Clariant Produkte Deutschland | Wasserlösliche Polymere und ihre Verwendung in kosmetischen und pharmazeutischen Mitteln |
| DE19961256A1 (de) * | 1999-12-18 | 2001-06-21 | Clariant Gmbh | Kosmetische Zubereitungen |
| US6730641B2 (en) * | 2002-03-26 | 2004-05-04 | Alberto-Culver Company | Hair conditioning composition |
| US20050095215A1 (en) * | 2003-11-03 | 2005-05-05 | Popp Karl F. | Antimicrobial shampoo compositions |
| US8877234B2 (en) | 2005-02-03 | 2014-11-04 | Clariant Finance (Bvi) Limited | Preservatives |
| DE102009022445A1 (de) | 2009-05-23 | 2009-12-24 | Clariant International Limited | Zusammensetzung enthaltend Sorbitanmonocaprylat und Alkohol |
| WO2011153197A1 (en) | 2010-06-01 | 2011-12-08 | Biotheryx, Inc. | Hydroxypyridone derivatives, pharmaceutical compositions thereof, and their therapeutic use for treating proliferative diseases |
| DE102010054865A1 (de) | 2010-12-17 | 2011-08-18 | Clariant International Ltd. | Verwendung von Hydroxypyridonen oder deren Salzen zur Stabilisierung von Wasserstoffperoxid oder Wasserstoffperoxid freisetzenden Substanzen |
| MX2013001095A (es) | 2010-07-27 | 2013-03-12 | Clariant Finance Bvi Ltd | Composiciones que comprenden peroxido de hidrogeno o sustancias donadoras de peroxido de hidrogeno. |
| DE102010054918A1 (de) | 2010-12-17 | 2011-06-30 | Clariant International Ltd. | Zusammensetzungen enthaltend Wasserstoffperoxid oder Wasserstoffperoxid freisetzende Substanzen |
| WO2012019689A2 (de) | 2010-07-27 | 2012-02-16 | Clariant International Ltd | Verwendung von hydroxypyridonen oder deren salzen zur stabilisierung von wasserstoffperoxid oder wasserstoffperoxid freisetzenden substanzen |
| DE102010054866A1 (de) | 2010-12-17 | 2011-08-18 | Clariant International Ltd. | Zusammensetzungen enthaltend Wasserstoffperoxid oder Wasserstoffperoxid freisetzende Substanzen |
| JP6027112B2 (ja) | 2011-08-04 | 2016-11-16 | クラリアント・インターナシヨナル・リミテツド | 抗菌作用物質としてのイソソルビドモノエステルの使用 |
| ES2610236T3 (es) | 2011-08-04 | 2017-04-26 | Clariant International Ltd. | Composición que contiene monoésteres de isosorbida y diésteres de isosorbida |
| BR112014002612B1 (pt) | 2011-08-04 | 2020-02-27 | Clariant International Ltd. | Composições compreendendo monoésteres de isossorbida e hidroxipiridonas e seus usos |
| BR112014002594A2 (pt) | 2011-08-04 | 2017-04-11 | Clariant Int Ltd | uso de diésteres de isossorbida como espessantes |
| BR112014002600B1 (pt) | 2011-08-04 | 2020-04-22 | Clariant Int Ltd | composições compreendendo monoésteres e álcoois de isosorbida compreendendo pelo menos um grupo aromático e uso das mesmas |
| CN103717064B (zh) | 2011-08-04 | 2016-08-17 | 克拉里安特国际有限公司 | 异山梨醇单酯作为增稠剂的用途 |
| US11235020B2 (en) | 2013-03-13 | 2022-02-01 | Abraham Palmer | Methods and compositions for inhibiting glyoxalase 1 (GLO1) |
| US10555884B2 (en) | 2017-06-30 | 2020-02-11 | The Procter & Gamble Company | 2-pyridinol-N-oxide deodorant and antiperspirant compositions |
| EP3644951B1 (en) | 2017-06-30 | 2025-06-11 | The Procter & Gamble Company | Hair care compositions comprising a 2-pyridinol-n-oxide material and an iron chelator |
| US10543164B2 (en) | 2017-06-30 | 2020-01-28 | The Procter & Gamble Company | Deodorant compositions |
| WO2019228988A1 (en) | 2018-05-30 | 2019-12-05 | Clariant International Ltd | Process for forming 2-hydroxypyridine-1-oxide or derivatives thereof |
| EP3647303B1 (en) | 2018-10-31 | 2022-08-31 | Clariant International Ltd | Process for preparing fatty acid chlorides and n-acyl amino acid salts |
| ES2988078T3 (es) | 2019-02-19 | 2024-11-19 | Clariant Int Ltd | Recristalización de piroctonaolamina |
| WO2020216676A1 (en) | 2019-04-26 | 2020-10-29 | Clariant International Ltd | Emulsion comprising piroctone olamine |
| BR112021024645A2 (pt) | 2019-07-31 | 2022-02-08 | Clariant Int Ltd | Processo para a fabricação de grânulos de piroctona olamina |
| EP3944852A1 (en) | 2020-07-28 | 2022-02-02 | Clariant International Ltd | Use of a booster to enhance the anti-dandruff or preservative activity of piroctone olamine |
| WO2022094450A1 (en) * | 2020-11-02 | 2022-05-05 | The Board Of Regents Of The University Of Texas System | Compounds, compositions thereof, and methods for treating er+ breast cancer |
| WO2022096286A1 (en) | 2020-11-05 | 2022-05-12 | Clariant International Ltd | Process for making piroctone olamine agglomerate particles |
| EP3818972A3 (en) | 2021-01-29 | 2021-09-08 | Clariant International Ltd | Piroctone olamine granules for use in cosmetic compositions |
| CN115590780A (zh) * | 2021-06-28 | 2023-01-13 | 南京华狮新材料有限公司（Cn） | 一种毛发用杀菌去屑组合物及其制备方法 |
| EP4122918A1 (en) | 2021-07-19 | 2023-01-25 | Clariant International Ltd | Process for the preparation of n-hydroxypyridone compounds |
| WO2022238590A2 (en) | 2021-07-19 | 2022-11-17 | Clariant International Ltd | Piroctone particles for use in cosmetic compositions |
| EP4091675A1 (en) | 2021-07-19 | 2022-11-23 | Clariant International Ltd | Cosmetic composition comprising piroctone and a fragrance |
| WO2023164938A1 (en) * | 2022-03-04 | 2023-09-07 | Clariant International Ltd. | Compositions comprising piroctone olamine |
| WO2024104987A2 (en) | 2022-11-16 | 2024-05-23 | Clariant International Ltd | Process for the crystallization or precipitation of piroctone |
| CN120225505A (zh) | 2022-11-28 | 2025-06-27 | 科莱恩国际有限公司 | 制备n-羟基吡啶酮化合物的方法 |
| WO2024189119A1 (en) | 2023-03-16 | 2024-09-19 | Clariant International Ltd | Bio-based n-hydroxypyridone compounds |
| CN116987030B (zh) * | 2023-08-03 | 2024-05-03 | 济宁科友新材料有限公司 | 一种吡啶酮乙醇胺盐的制备方法 |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2748142A (en) * | 1956-05-29 | - process of production | ||
| US2540218A (en) * | 1947-08-25 | 1951-02-06 | Squibb & Sons Inc | 2-hydroxy-pyridine-n-oxide and process for preparing same |
| US2742393A (en) * | 1953-05-19 | 1956-04-17 | Olin Mathieson | Derivatives of 2-mercaptopyridine-1-oxide |
| US2809971A (en) * | 1955-11-22 | 1957-10-15 | Olin Mathieson | Heavy-metal derivatives of 1-hydroxy-2-pyridinethiones and method of preparing same |
| US2922793A (en) * | 1958-01-06 | 1960-01-26 | Olin Mathieson | 2-allylic thio pyridine n-oxides |
| CA671117A (en) * | 1961-10-17 | 1963-09-24 | S. Karsten Kenneth | Germicidal detergent compositions |
| US3235455A (en) * | 1962-02-09 | 1966-02-15 | Procter & Gamble | Synergistic antibacterial compositions |
| FR3691M (fr) * | 1963-05-06 | 1965-11-15 | Olin Mathieson | Nouvelle composition pharmaceutique utile en tant que fongicide. |
| US3236733A (en) * | 1963-09-05 | 1966-02-22 | Vanderbilt Co R T | Method of combatting dandruff with pyridinethiones metal salts detergent compositions |
| US3968118A (en) * | 1968-08-31 | 1976-07-06 | Hoechst Aktiengesellschaft | Process for the manufacture of 1-hydroxy-2-pyridones |
| US3883545A (en) * | 1968-08-31 | 1975-05-13 | Hoechst Ag | Certain 1-hydroxy-2-pyridones |
| NL156397B (nl) * | 1968-08-31 | 1978-04-17 | Hoechst Ag | Werkwijze voor het bereiden van preparaten tegen schimmelaandoeningen, gevormde preparaten, alsmede werkwijze voor het bereiden van daarvoor geschikte actieve stoffen. |
| US3583999A (en) * | 1968-11-01 | 1971-06-08 | Procter & Gamble | Process for preparing 2-pyridinethiol n-oxides and derivatives thereof |
| US3644626A (en) * | 1969-11-25 | 1972-02-22 | Merck & Co Inc | Novel pyridones in compositions and methods for treating inflammation pain and fever |
| US3655897A (en) * | 1971-01-25 | 1972-04-11 | Merck & Co Inc | Anti-inflammatory agents |
| US3972888A (en) * | 1972-03-25 | 1976-08-03 | Hoechst Aktiengesellschaft | Process for the preparation of 1-hydroxy-pyridones |
-
1972
- 1972-07-11 DE DE2234009A patent/DE2234009C3/de not_active Expired
-
1973
- 1973-07-06 NL NLAANVRAGE7309506,A patent/NL175259C/xx not_active IP Right Cessation
- 1973-07-06 CH CH988373A patent/CH584033A5/xx not_active IP Right Cessation
- 1973-07-09 LU LU67973A patent/LU67973A1/xx unknown
- 1973-07-09 IT IT26375/73A patent/IT1043856B/it active
- 1973-07-09 CA CA176,021A patent/CA1013675A/en not_active Expired
- 1973-07-10 NO NO2824/73A patent/NO139074C/no unknown
- 1973-07-10 HU HUHO1592A patent/HU166867B/hu unknown
- 1973-07-10 ZA ZA734620A patent/ZA734620B/xx unknown
- 1973-07-10 DK DK383473A patent/DK135362C/da not_active IP Right Cessation
- 1973-07-10 GB GB3285373A patent/GB1440975A/en not_active Expired
- 1973-07-10 CS CS734959A patent/CS220304B2/cs unknown
- 1973-07-10 AT AT605273A patent/AT329187B/de active
- 1973-07-10 AR AR249012A patent/AR222133A1/es active
- 1973-07-10 DD DD172191A patent/DD105391A5/xx unknown
- 1973-07-11 SE SE7309705A patent/SE401978B/xx unknown
- 1973-07-11 FR FR7325464A patent/FR2191904B1/fr not_active Expired
- 1973-07-11 BE BE133365A patent/BE802208A/xx not_active IP Right Cessation
- 1973-07-11 BR BR5186/73A patent/BR7305186D0/pt unknown
- 1973-07-11 SU SU7301951651A patent/SU580806A3/ru active
- 1973-07-11 JP JP48077564A patent/JPS5839805B2/ja not_active Expired
-
1984
- 1984-12-04 US US06/677,891 patent/US4711775A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| SE401978B (sv) | 1978-06-12 |
| NL7309506A (en, 2012) | 1974-01-15 |
| NO139074C (no) | 1979-01-10 |
| DE2234009B2 (de) | 1977-03-17 |
| JPS4950142A (en, 2012) | 1974-05-15 |
| SU580806A3 (ru) | 1977-11-15 |
| ATA605273A (de) | 1975-07-15 |
| BE802208A (fr) | 1974-01-11 |
| CS220304B2 (en) | 1983-03-25 |
| LU67973A1 (en, 2012) | 1975-04-11 |
| DK135362B (da) | 1977-04-18 |
| HU166867B (en, 2012) | 1975-06-28 |
| DD105391A5 (en, 2012) | 1974-04-20 |
| AT329187B (de) | 1976-04-26 |
| GB1440975A (en) | 1976-06-30 |
| FR2191904B1 (en, 2012) | 1977-07-15 |
| AU5788173A (en) | 1975-01-09 |
| US4711775A (en) | 1987-12-08 |
| NO139074B (no) | 1978-09-25 |
| DE2234009A1 (de) | 1974-01-24 |
| NL175259C (nl) | 1984-10-16 |
| CH584033A5 (en, 2012) | 1977-01-31 |
| AR222133A1 (es) | 1981-04-30 |
| CA1013675A (en) | 1977-07-12 |
| BR7305186D0 (pt) | 1974-08-29 |
| ZA734620B (en) | 1974-06-26 |
| IT1043856B (it) | 1980-02-29 |
| FR2191904A1 (en, 2012) | 1974-02-08 |
| DE2234009C3 (de) | 1979-01-11 |
| DK135362C (da) | 1977-10-03 |
| NL175259B (nl) | 1984-05-16 |
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