JPS5840397A - シヤンプ−組成物 - Google Patents
シヤンプ−組成物Info
- Publication number
- JPS5840397A JPS5840397A JP13935481A JP13935481A JPS5840397A JP S5840397 A JPS5840397 A JP S5840397A JP 13935481 A JP13935481 A JP 13935481A JP 13935481 A JP13935481 A JP 13935481A JP S5840397 A JPS5840397 A JP S5840397A
- Authority
- JP
- Japan
- Prior art keywords
- group
- carbon atoms
- methyl
- alkyl group
- hydroxy
- 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 description 14
- 239000000203 mixture Substances 0.000 title description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 33
- 125000000217 alkyl group Chemical group 0.000 claims description 24
- -1 benzhydryl group Chemical group 0.000 claims description 15
- 239000003093 cationic surfactant Substances 0.000 claims description 12
- 239000003945 anionic surfactant Substances 0.000 claims description 11
- 125000003342 alkenyl group Chemical group 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 150000001412 amines Chemical group 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
- 125000005160 aryl oxy alkyl group Chemical group 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 150000001602 bicycloalkyls Chemical group 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 2
- 125000002541 furyl group Chemical group 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 238000000034 method Methods 0.000 description 8
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- SNUSZUYTMHKCPM-UHFFFAOYSA-N 1-hydroxypyridin-2-one Chemical class ON1C=CC=CC1=O SNUSZUYTMHKCPM-UHFFFAOYSA-N 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 230000003750 conditioning effect Effects 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- 238000005187 foaming Methods 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
- 159000000000 sodium salts Chemical class 0.000 description 3
- 125000004079 stearyl group Chemical group [H]C([*])([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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000004711 α-olefin Substances 0.000 description 3
- 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
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-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
- 150000001336 alkenes Chemical class 0.000 description 2
- 239000002280 amphoteric surfactant Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000004140 cleaning 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
- 150000002148 esters Chemical class 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
- 159000000003 magnesium salts Chemical class 0.000 description 2
- 239000002075 main ingredient Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Chemical compound O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 description 2
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 description 1
- NJYFRQQXXXRJHK-UHFFFAOYSA-N (4-aminophenyl) thiocyanate Chemical group NC1=CC=C(SC#N)C=C1 NJYFRQQXXXRJHK-UHFFFAOYSA-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
- VBAHGZFODNVOAQ-UHFFFAOYSA-N 1-hydroxy-4,6-diphenylpyridin-2-one Chemical compound C=1C(=O)N(O)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 VBAHGZFODNVOAQ-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
- 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
- CBAIZBBKYBHCLT-UHFFFAOYSA-N 1-hydroxy-4-methyl-6-(phenoxymethyl)pyridin-2-one Chemical compound ON1C(=O)C=C(C)C=C1COC1=CC=CC=C1 CBAIZBBKYBHCLT-UHFFFAOYSA-N 0.000 description 1
- XFJMASHZLCWQOQ-UHFFFAOYSA-N 1-hydroxy-4-methyl-6-[(2,4,5-trichlorophenoxy)methyl]pyridin-2-one Chemical compound ON1C(=O)C=C(C)C=C1COC1=CC(Cl)=C(Cl)C=C1Cl XFJMASHZLCWQOQ-UHFFFAOYSA-N 0.000 description 1
- OWEMAELSDQIDCG-UHFFFAOYSA-N 1-hydroxy-4-methyl-6-[(3-methylphenoxy)methyl]pyridin-2-one Chemical compound CC1=CC=CC(OCC=2N(C(=O)C=C(C)C=2)O)=C1 OWEMAELSDQIDCG-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
- 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
- WLMZUANPXHJWCH-UHFFFAOYSA-N 2-[bis(2-hydroxyethyl)amino]ethanol;dodecanoic acid Chemical compound OCCN(CCO)CCO.CCCCCCCCCCCC(O)=O WLMZUANPXHJWCH-UHFFFAOYSA-N 0.000 description 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
- PYSGFFTXMUWEOT-UHFFFAOYSA-N 3-(dimethylamino)propan-1-ol Chemical compound CN(C)CCCO PYSGFFTXMUWEOT-UHFFFAOYSA-N 0.000 description 1
- KSMVBYPXNKCPAJ-UHFFFAOYSA-N 4-Methylcyclohexylamine Chemical compound CC1CCC(N)CC1 KSMVBYPXNKCPAJ-UHFFFAOYSA-N 0.000 description 1
- HSYBITQOTFCWAZ-UHFFFAOYSA-N 6-(2-butylhex-1-enyl)-1-hydroxy-4-methylpyridin-2-one Chemical compound CCCCC(CCCC)=CC1=CC(C)=CC(=O)N1O HSYBITQOTFCWAZ-UHFFFAOYSA-N 0.000 description 1
- ZRSSUJPAKAOGBP-UHFFFAOYSA-N 6-(3,5-dichlorophenyl)-1-hydroxy-4-methylpyridin-2-one Chemical compound ON1C(=O)C=C(C)C=C1C1=CC(Cl)=CC(Cl)=C1 ZRSSUJPAKAOGBP-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
- 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
- QKOQVNBLIREPBG-UHFFFAOYSA-N 6-[(2-chlorophenyl)methyl]-1-hydroxy-4-methylpyridin-2-one Chemical compound ON1C(=O)C=C(C)C=C1CC1=CC=CC=C1Cl QKOQVNBLIREPBG-UHFFFAOYSA-N 0.000 description 1
- 201000004384 Alopecia Diseases 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
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- AVLZAVSZOAQKRC-UHFFFAOYSA-N SYC-435 Chemical compound ON1C(=O)C=C(C)C=C1CC1=CC=CC=C1 AVLZAVSZOAQKRC-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 125000005526 alkyl sulfate group Chemical group 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- SCKYRAXSEDYPSA-UHFFFAOYSA-N ciclopirox Chemical compound ON1C(=O)C=C(C)C=C1C1CCCCC1 SCKYRAXSEDYPSA-UHFFFAOYSA-N 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- NAPSCFZYZVSQHF-UHFFFAOYSA-N dimantine Chemical compound CCCCCCCCCCCCCCCCCCN(C)C NAPSCFZYZVSQHF-UHFFFAOYSA-N 0.000 description 1
- 229950010007 dimantine Drugs 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 208000024963 hair loss Diseases 0.000 description 1
- 230000003676 hair loss Effects 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- HVAAHUDGWQAAOJ-UHFFFAOYSA-N n-benzylethanamine Chemical compound CCNCC1=CC=CC=C1 HVAAHUDGWQAAOJ-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 210000001732 sebaceous gland Anatomy 0.000 description 1
- 210000002374 sebum Anatomy 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Cosmetics (AREA)
- Detergent Compositions (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13935481A JPS5840397A (ja) | 1981-09-04 | 1981-09-04 | シヤンプ−組成物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13935481A JPS5840397A (ja) | 1981-09-04 | 1981-09-04 | シヤンプ−組成物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5840397A true JPS5840397A (ja) | 1983-03-09 |
| JPS632407B2 JPS632407B2 (enrdf_load_stackoverflow) | 1988-01-19 |
Family
ID=15243369
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13935481A Granted JPS5840397A (ja) | 1981-09-04 | 1981-09-04 | シヤンプ−組成物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5840397A (enrdf_load_stackoverflow) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01170699A (ja) * | 1987-11-26 | 1989-07-05 | Unilever Nv | 皿洗い機用洗剤組成物 |
| JP2011131137A (ja) * | 2009-12-22 | 2011-07-07 | Tokyo Univ Of Science | カチオン界面活性剤、アニオン界面活性剤／カチオン界面活性剤混合組成物、及び毛髪用化粧料 |
| CN113930226A (zh) * | 2020-07-14 | 2022-01-14 | 中国石油化工股份有限公司 | 含聚醚季铵盐的表面活性剂组合物及其制备和提高油气产量的方法 |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6317603A (ja) * | 1986-07-10 | 1988-01-25 | 小橋工業株式会社 | アツプカツト耕うん装置のロ−タリカバ− |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4950142A (enrdf_load_stackoverflow) * | 1972-07-11 | 1974-05-15 | ||
| JPS5543138A (en) * | 1978-09-21 | 1980-03-26 | Lion Fat Oil Co Ltd | Shampoo composition |
-
1981
- 1981-09-04 JP JP13935481A patent/JPS5840397A/ja active Granted
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4950142A (enrdf_load_stackoverflow) * | 1972-07-11 | 1974-05-15 | ||
| JPS5543138A (en) * | 1978-09-21 | 1980-03-26 | Lion Fat Oil Co Ltd | Shampoo composition |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01170699A (ja) * | 1987-11-26 | 1989-07-05 | Unilever Nv | 皿洗い機用洗剤組成物 |
| JP2011131137A (ja) * | 2009-12-22 | 2011-07-07 | Tokyo Univ Of Science | カチオン界面活性剤、アニオン界面活性剤／カチオン界面活性剤混合組成物、及び毛髪用化粧料 |
| CN113930226A (zh) * | 2020-07-14 | 2022-01-14 | 中国石油化工股份有限公司 | 含聚醚季铵盐的表面活性剂组合物及其制备和提高油气产量的方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS632407B2 (enrdf_load_stackoverflow) | 1988-01-19 |
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