JPS5925897A - シヤンプ−組成物 - Google Patents
シヤンプ−組成物Info
- Publication number
- JPS5925897A JPS5925897A JP13602582A JP13602582A JPS5925897A JP S5925897 A JPS5925897 A JP S5925897A JP 13602582 A JP13602582 A JP 13602582A JP 13602582 A JP13602582 A JP 13602582A JP S5925897 A JPS5925897 A JP S5925897A
- Authority
- JP
- Japan
- Prior art keywords
- group
- carbon atoms
- hydroxy
- methyl
- pyridone
- 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.)
- Granted
Links
- 239000002453 shampoo Substances 0.000 title claims description 21
- 239000000203 mixture Substances 0.000 title claims description 18
- 125000004432 carbon atom Chemical group C* 0.000 claims description 36
- -1 4-aminobenzoic acid ester Chemical class 0.000 claims description 30
- 125000000217 alkyl group Chemical group 0.000 claims description 14
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 11
- 239000004094 surface-active agent Substances 0.000 claims description 10
- 125000003342 alkenyl group Chemical group 0.000 claims description 7
- 239000006096 absorbing agent Substances 0.000 claims description 6
- 125000003545 alkoxy group Chemical group 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- 239000012965 benzophenone Substances 0.000 claims description 3
- 150000008366 benzophenones Chemical class 0.000 claims description 3
- 150000001768 cations Chemical class 0.000 claims description 3
- 125000002541 furyl group Chemical group 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- 229910001413 alkali metal ion Inorganic materials 0.000 claims description 2
- 229910001420 alkaline earth metal ion Inorganic materials 0.000 claims description 2
- 125000000304 alkynyl group Chemical group 0.000 claims description 2
- 229960004050 aminobenzoic acid Drugs 0.000 claims description 2
- ALYNCZNDIQEVRV-UHFFFAOYSA-N aniline-p-carboxylic acid Natural products NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 claims description 2
- 125000005018 aryl alkenyl group Chemical group 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 150000001602 bicycloalkyls Chemical group 0.000 claims description 2
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 150000007530 organic bases Chemical group 0.000 claims description 2
- AFDXODALSZRGIH-UHFFFAOYSA-N p-coumaric acid methyl ether Natural products COC1=CC=C(C=CC(O)=O)C=C1 AFDXODALSZRGIH-UHFFFAOYSA-N 0.000 claims description 2
- 150000005840 aryl radicals Chemical class 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 125000004963 sulfonylalkyl group Chemical group 0.000 claims 1
- 238000002845 discoloration Methods 0.000 description 16
- 150000003839 salts Chemical class 0.000 description 11
- 238000000034 method Methods 0.000 description 7
- 239000003945 anionic surfactant Substances 0.000 description 6
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- BLFLLBZGZJTVJG-UHFFFAOYSA-N benzocaine Chemical compound CCOC(=O)C1=CC=C(N)C=C1 BLFLLBZGZJTVJG-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 159000000000 sodium salts Chemical class 0.000 description 4
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000002280 amphoteric surfactant Substances 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000002736 nonionic surfactant Substances 0.000 description 3
- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 description 3
- 239000004711 α-olefin Substances 0.000 description 3
- AFDXODALSZRGIH-QPJJXVBHSA-N (E)-3-(4-methoxyphenyl)prop-2-enoic acid Chemical class COC1=CC=C(\C=C\C(O)=O)C=C1 AFDXODALSZRGIH-QPJJXVBHSA-N 0.000 description 2
- SNUSZUYTMHKCPM-UHFFFAOYSA-N 1-hydroxypyridin-2-one Chemical compound ON1C=CC=CC1=O SNUSZUYTMHKCPM-UHFFFAOYSA-N 0.000 description 2
- ZXDDPOHVAMWLBH-UHFFFAOYSA-N 2,4-Dihydroxybenzophenone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 ZXDDPOHVAMWLBH-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- GSPKZYJPUDYKPI-UHFFFAOYSA-N diethoxy sulfate Chemical compound CCOOS(=O)(=O)OOCC GSPKZYJPUDYKPI-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 238000005562 fading Methods 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Chemical compound O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- XDOBXTLSTUFRRP-HNNXBMFYSA-N (2s)-2-(tetradecanoylamino)propanoic acid Chemical compound CCCCCCCCCCCCCC(=O)N[C@@H](C)C(O)=O XDOBXTLSTUFRRP-HNNXBMFYSA-N 0.000 description 1
- CLXADVHCSCRADU-KRWDZBQOSA-N (2s)-4-methylsulfanyl-2-(tetradecanoylamino)butanoic acid Chemical compound CCCCCCCCCCCCCC(=O)N[C@H](C(O)=O)CCSC CLXADVHCSCRADU-KRWDZBQOSA-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
- DJOBTQHCXITUIN-UHFFFAOYSA-N 1-hydroxy-4-methyl-6-(2-phenylethenyl)pyridin-2-one Chemical compound ON1C(=O)C=C(C)C=C1C=CC1=CC=CC=C1 DJOBTQHCXITUIN-UHFFFAOYSA-N 0.000 description 1
- REBUAULUSRQVRR-UHFFFAOYSA-N 1-hydroxy-4-methyl-6-(3-methylphenyl)pyridin-2-one Chemical compound CC1=CC=CC(C=2N(C(=O)C=C(C)C=2)O)=C1 REBUAULUSRQVRR-UHFFFAOYSA-N 0.000 description 1
- CRZPSVLEBAJKMN-UHFFFAOYSA-N 1-hydroxy-4-methyl-6-(4-methylphenyl)pyridin-2-one Chemical compound C1=CC(C)=CC=C1C1=CC(C)=CC(=O)N1O CRZPSVLEBAJKMN-UHFFFAOYSA-N 0.000 description 1
- ZBIMYUJKHIXXSK-UHFFFAOYSA-N 1-hydroxy-4-methyl-6-oct-1-enylpyridin-2-one Chemical compound CCCCCCC=CC1=CC(C)=CC(=O)N1O ZBIMYUJKHIXXSK-UHFFFAOYSA-N 0.000 description 1
- 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 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
- QOWMEPRCLLJPTC-UHFFFAOYSA-N 1-hydroxy-6-methyl-4-phenylpyridin-2-one Chemical compound O=C1N(O)C(C)=CC(C=2C=CC=CC=2)=C1 QOWMEPRCLLJPTC-UHFFFAOYSA-N 0.000 description 1
- IEFRQNQEFHXQTF-UHFFFAOYSA-N 1-hydroxy-6-methylpyridin-2-one Chemical compound CC1=CC=CC(=O)N1O IEFRQNQEFHXQTF-UHFFFAOYSA-N 0.000 description 1
- OFWGTRJQCVYFBE-UHFFFAOYSA-N 1-tetradecanoylpyrrolidine-2-carboxylic acid Chemical compound CCCCCCCCCCCCCC(=O)N1CCCC1C(O)=O OFWGTRJQCVYFBE-UHFFFAOYSA-N 0.000 description 1
- MTYLJFSVEPZMIY-UHFFFAOYSA-N 2-(dodecanoylamino)-3-(1h-indol-3-yl)propanoic acid Chemical compound C1=CC=C2C(CC(NC(=O)CCCCCCCCCCC)C(O)=O)=CNC2=C1 MTYLJFSVEPZMIY-UHFFFAOYSA-N 0.000 description 1
- RKQUHHNIJVGMIG-UHFFFAOYSA-N 2-(dodecanoylamino)-3-phenylpropanoic acid Chemical compound CCCCCCCCCCCC(=O)NC(C(O)=O)CC1=CC=CC=C1 RKQUHHNIJVGMIG-UHFFFAOYSA-N 0.000 description 1
- CDOCNWRWMUMCLP-UHFFFAOYSA-N 2-(dodecanoylamino)-4-methylpentanoic acid Chemical compound CCCCCCCCCCCC(=O)NC(C(O)=O)CC(C)C CDOCNWRWMUMCLP-UHFFFAOYSA-N 0.000 description 1
- MIJDSYMOBYNHOT-UHFFFAOYSA-N 2-(ethylamino)ethanol Chemical compound CCNCCO MIJDSYMOBYNHOT-UHFFFAOYSA-N 0.000 description 1
- KKFDCBRMNNSAAW-UHFFFAOYSA-N 2-(morpholin-4-yl)ethanol Chemical compound OCCN1CCOCC1 KKFDCBRMNNSAAW-UHFFFAOYSA-N 0.000 description 1
- ZTYPCHKEXUPZEJ-UHFFFAOYSA-N 2-[2-(dodecanoylamino)ethyl-(2-hydroxyethyl)amino]acetic acid Chemical compound CCCCCCCCCCCC(=O)NCCN(CCO)CC(O)=O ZTYPCHKEXUPZEJ-UHFFFAOYSA-N 0.000 description 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
- CMDKPGRTAQVGFQ-UHFFFAOYSA-N 2-ethoxyethyl 3-(4-methoxyphenyl)prop-2-enoate Chemical compound CCOCCOC(=O)C=CC1=CC=C(OC)C=C1 CMDKPGRTAQVGFQ-UHFFFAOYSA-N 0.000 description 1
- XSZVJSCMQRJIRH-KTKRTIGZSA-N 3-[[(z)-octadec-9-enoyl]amino]propanoic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)NCCC(O)=O XSZVJSCMQRJIRH-KTKRTIGZSA-N 0.000 description 1
- KSMVBYPXNKCPAJ-UHFFFAOYSA-N 4-Methylcyclohexylamine Chemical compound CC1CCC(N)CC1 KSMVBYPXNKCPAJ-UHFFFAOYSA-N 0.000 description 1
- GAYBJDZLMVRVKL-UHFFFAOYSA-N 4-methyl-2-(tetradecanoylamino)pentanoic acid Chemical compound CCCCCCCCCCCCCC(=O)NC(C(O)=O)CC(C)C GAYBJDZLMVRVKL-UHFFFAOYSA-N 0.000 description 1
- KSGBFSAQWCOCIJ-UHFFFAOYSA-N 6-(4-chloro-3-methylphenyl)-1-hydroxy-4-methylpyridin-2-one Chemical compound ON1C(=O)C=C(C)C=C1C1=CC=C(Cl)C(C)=C1 KSGBFSAQWCOCIJ-UHFFFAOYSA-N 0.000 description 1
- MOASYRUDTPYDDJ-UHFFFAOYSA-N 6-(4-tert-butylphenyl)-1-hydroxy-4-methylpyridin-2-one Chemical compound ON1C(=O)C=C(C)C=C1C1=CC=C(C(C)(C)C)C=C1 MOASYRUDTPYDDJ-UHFFFAOYSA-N 0.000 description 1
- IIQCUCYKRFXIHP-UHFFFAOYSA-N 6-(benzenesulfonylmethyl)-1-hydroxy-4-methylpyridin-2-one Chemical compound ON1C(=O)C=C(C)C=C1CS(=O)(=O)C1=CC=CC=C1 IIQCUCYKRFXIHP-UHFFFAOYSA-N 0.000 description 1
- GRPQGRFHGIHWTA-UHFFFAOYSA-N 6-(furan-2-yl)-1-hydroxy-4-methylpyridin-2-one Chemical compound ON1C(=O)C=C(C)C=C1C1=CC=CO1 GRPQGRFHGIHWTA-UHFFFAOYSA-N 0.000 description 1
- XBRDTHCRVKZGGP-UHFFFAOYSA-N 6-[(4-bromophenoxy)methyl]-1-hydroxy-4-methylpyridin-2-one Chemical compound ON1C(=O)C=C(C)C=C1COC1=CC=C(Br)C=C1 XBRDTHCRVKZGGP-UHFFFAOYSA-N 0.000 description 1
- WCXCSGRTWNVHHT-UHFFFAOYSA-N 6-[(4-chlorophenyl)methyl]-1-hydroxy-4-methylpyridin-2-one Chemical compound ON1C(=O)C=C(C)C=C1CC1=CC=C(Cl)C=C1 WCXCSGRTWNVHHT-UHFFFAOYSA-N 0.000 description 1
- UGNNVRXABMWTSC-UHFFFAOYSA-N 6-[(4-chlorophenyl)sulfanylmethyl]-1-hydroxy-4-methylpyridin-2-one Chemical compound ON1C(=O)C=C(C)C=C1CSC1=CC=C(Cl)C=C1 UGNNVRXABMWTSC-UHFFFAOYSA-N 0.000 description 1
- 241000167854 Bourreria succulenta Species 0.000 description 1
- 241000951471 Citrus junos Species 0.000 description 1
- BWLUMTFWVZZZND-UHFFFAOYSA-N Dibenzylamine Chemical compound C=1C=CC=CC=1CNCC1=CC=CC=C1 BWLUMTFWVZZZND-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
- 239000005639 Lauric acid Substances 0.000 description 1
- 235000019501 Lemon oil Nutrition 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- CHQZBIVWDKADIA-GDWUOILNSA-N N-Oleoyl alanine Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N[C@@H](C)C(O)=O CHQZBIVWDKADIA-GDWUOILNSA-N 0.000 description 1
- NRBFOSKZAWRBJI-KRWDZBQOSA-N N-Palmitoyl alanine Chemical compound CCCCCCCCCCCCCCCC(=O)N[C@@H](C)C(O)=O NRBFOSKZAWRBJI-KRWDZBQOSA-N 0.000 description 1
- DYUGTPXLDJQBRB-UHFFFAOYSA-N N-myristoylglycine Chemical compound CCCCCCCCCCCCCC(=O)NCC(O)=O DYUGTPXLDJQBRB-UHFFFAOYSA-N 0.000 description 1
- HPFXACZRFJDURI-KTKRTIGZSA-N N-oleoylglycine Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)NCC(O)=O HPFXACZRFJDURI-KTKRTIGZSA-N 0.000 description 1
- FCVASHHBGGKTGT-IBGZPJMESA-N N-palmitoyl methionine Chemical compound CCCCCCCCCCCCCCCC(=O)N[C@H](C(O)=O)CCSC FCVASHHBGGKTGT-IBGZPJMESA-N 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- 244000273256 Phragmites communis Species 0.000 description 1
- 235000014676 Phragmites communis Nutrition 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229960002684 aminocaproic acid Drugs 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229940000635 beta-alanine Drugs 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 235000019693 cherries Nutrition 0.000 description 1
- SCKYRAXSEDYPSA-UHFFFAOYSA-N ciclopirox Chemical compound ON1C(=O)C=C(C)C=C1C1CCCCC1 SCKYRAXSEDYPSA-UHFFFAOYSA-N 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 238000004649 discoloration prevention Methods 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- SYELZBGXAIXKHU-UHFFFAOYSA-N dodecyldimethylamine N-oxide Chemical compound CCCCCCCCCCCC[N+](C)(C)[O-] SYELZBGXAIXKHU-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 235000019717 geranium oil Nutrition 0.000 description 1
- 239000010648 geranium oil Substances 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 239000010501 lemon oil Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- ONHFWHCMZAJCFB-UHFFFAOYSA-N myristamine oxide Chemical compound CCCCCCCCCCCCCC[N+](C)(C)[O-] ONHFWHCMZAJCFB-UHFFFAOYSA-N 0.000 description 1
- YWFWDNVOPHGWMX-UHFFFAOYSA-N n,n-dimethyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)C YWFWDNVOPHGWMX-UHFFFAOYSA-N 0.000 description 1
- HVAAHUDGWQAAOJ-UHFFFAOYSA-N n-benzylethanamine Chemical compound CCNCC1=CC=CC=C1 HVAAHUDGWQAAOJ-UHFFFAOYSA-N 0.000 description 1
- XANYBGJNPZKYMQ-UHFFFAOYSA-N octan-3-yl 3-(4-methoxyphenyl)prop-2-enoate Chemical compound CCCCCC(CC)OC(=O)C=CC1=CC=C(OC)C=C1 XANYBGJNPZKYMQ-UHFFFAOYSA-N 0.000 description 1
- RYNIOUSRQMXJJZ-UHFFFAOYSA-N octan-3-yl 4-(dimethylamino)benzoate Chemical compound CCCCCC(CC)OC(=O)C1=CC=C(N(C)C)C=C1 RYNIOUSRQMXJJZ-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 150000003754 zirconium Chemical class 0.000 description 1
Landscapes
- Cosmetics (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13602582A JPS5925897A (ja) | 1982-08-04 | 1982-08-04 | シヤンプ−組成物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13602582A JPS5925897A (ja) | 1982-08-04 | 1982-08-04 | シヤンプ−組成物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5925897A true JPS5925897A (ja) | 1984-02-09 |
| JPS632524B2 JPS632524B2 (enrdf_load_stackoverflow) | 1988-01-19 |
Family
ID=15165422
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13602582A Granted JPS5925897A (ja) | 1982-08-04 | 1982-08-04 | シヤンプ−組成物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5925897A (enrdf_load_stackoverflow) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63166837A (ja) * | 1986-12-23 | 1988-07-11 | ユージーン・ジェイ・ヴァン・スコット | 治療効果の増強された組成物 |
| JPS63179813A (ja) * | 1987-01-21 | 1988-07-23 | Eikoudou:Kk | 毛髪化粧料 |
| US5487884A (en) * | 1987-10-22 | 1996-01-30 | The Procter & Gamble Company | Photoprotection compositions comprising chelating agents |
| JP2011126845A (ja) * | 2009-12-21 | 2011-06-30 | Fujifilm Corp | 染毛剤 |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101945145B1 (ko) * | 2016-03-14 | 2019-02-01 | 제이엑스금속주식회사 | 산화물 소결체 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS51116785A (en) * | 1975-03-13 | 1976-10-14 | Futsudoueizu Nat Inc | Packaging device |
| JPS5774399A (en) * | 1980-10-27 | 1982-05-10 | Lion Corp | Shampoo composition |
-
1982
- 1982-08-04 JP JP13602582A patent/JPS5925897A/ja active Granted
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS51116785A (en) * | 1975-03-13 | 1976-10-14 | Futsudoueizu Nat Inc | Packaging device |
| JPS5774399A (en) * | 1980-10-27 | 1982-05-10 | Lion Corp | Shampoo composition |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63166837A (ja) * | 1986-12-23 | 1988-07-11 | ユージーン・ジェイ・ヴァン・スコット | 治療効果の増強された組成物 |
| JPS63179813A (ja) * | 1987-01-21 | 1988-07-23 | Eikoudou:Kk | 毛髪化粧料 |
| US5487884A (en) * | 1987-10-22 | 1996-01-30 | The Procter & Gamble Company | Photoprotection compositions comprising chelating agents |
| JP2011126845A (ja) * | 2009-12-21 | 2011-06-30 | Fujifilm Corp | 染毛剤 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS632524B2 (enrdf_load_stackoverflow) | 1988-01-19 |
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