JPWO2020166678A5 - - Google Patents
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- JPWO2020166678A5 JPWO2020166678A5 JP2020572320A JP2020572320A JPWO2020166678A5 JP WO2020166678 A5 JPWO2020166678 A5 JP WO2020166678A5 JP 2020572320 A JP2020572320 A JP 2020572320A JP 2020572320 A JP2020572320 A JP 2020572320A JP WO2020166678 A5 JPWO2020166678 A5 JP WO2020166678A5
- Authority
- JP
- Japan
- Prior art keywords
- cosmetic
- group
- carbon atoms
- linear
- compounding agent
- 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
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- 239000002537 cosmetic Substances 0.000 claims description 56
- -1 carboxylic acid anion Chemical class 0.000 claims description 51
- 125000000217 alkyl group Chemical group 0.000 claims description 42
- 125000004432 carbon atom Chemical group C* 0.000 claims description 33
- 239000003795 chemical substances by application Substances 0.000 claims description 31
- 238000013329 compounding Methods 0.000 claims description 29
- 150000001450 anions Chemical class 0.000 claims description 28
- 150000001768 cations Chemical class 0.000 claims description 13
- 125000000524 functional group Chemical group 0.000 claims description 13
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
- 239000002253 acid Substances 0.000 claims description 10
- 150000003863 ammonium salts Chemical class 0.000 claims description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 20
- 125000004430 oxygen atom Chemical group O* 0.000 claims 15
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 12
- 238000004519 manufacturing process Methods 0.000 claims 12
- 239000000203 mixture Substances 0.000 claims 10
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 8
- 125000004181 carboxyalkyl group Chemical group 0.000 claims 5
- 150000008064 anhydrides Chemical class 0.000 claims 3
- 238000009472 formulation Methods 0.000 claims 3
- 239000007788 liquid Substances 0.000 claims 3
- 239000002994 raw material Substances 0.000 claims 3
- 150000007942 carboxylates Chemical group 0.000 claims 2
- 238000000034 method Methods 0.000 claims 1
- 238000002156 mixing Methods 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 239000007983 Tris buffer Substances 0.000 description 9
- UXFQFBNBSPQBJW-UHFFFAOYSA-N 2-amino-2-methylpropane-1,3-diol Chemical compound OCC(N)(C)CO UXFQFBNBSPQBJW-UHFFFAOYSA-N 0.000 description 4
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 description 4
- AEMRFAOFKBGASW-UHFFFAOYSA-M Glycolate Chemical compound OCC([O-])=O AEMRFAOFKBGASW-UHFFFAOYSA-M 0.000 description 3
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- 229960001231 choline Drugs 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 229940049918 linoleate Drugs 0.000 description 3
- BJEPYKJPYRNKOW-UHFFFAOYSA-L malate(2-) Chemical compound [O-]C(=O)C(O)CC([O-])=O BJEPYKJPYRNKOW-UHFFFAOYSA-L 0.000 description 3
- LGRLWUINFJPLSH-UHFFFAOYSA-N methanide Chemical compound [CH3-] LGRLWUINFJPLSH-UHFFFAOYSA-N 0.000 description 3
- 229940049964 oleate Drugs 0.000 description 3
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
- FUOOLUPWFVMBKG-UHFFFAOYSA-N 2-Aminoisobutyric acid Chemical compound CC(C)(N)C(O)=O FUOOLUPWFVMBKG-UHFFFAOYSA-N 0.000 description 2
- OYHQOLUKZRVURQ-HZJYTTRNSA-M 9-cis,12-cis-Octadecadienoate Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC([O-])=O OYHQOLUKZRVURQ-HZJYTTRNSA-M 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- DATAGRPVKZEWHA-YFKPBYRVSA-N N(5)-ethyl-L-glutamine Chemical compound CCNC(=O)CC[C@H]([NH3+])C([O-])=O DATAGRPVKZEWHA-YFKPBYRVSA-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
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- OIPILFWXSMYKGL-UHFFFAOYSA-N acetylcholine Chemical compound CC(=O)OCC[N+](C)(C)C OIPILFWXSMYKGL-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical group 0.000 description 2
- 229940024606 amino acid Drugs 0.000 description 2
- 235000001014 amino acid Nutrition 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- CVSVTCORWBXHQV-UHFFFAOYSA-N creatine Chemical compound NC(=[NH2+])N(C)CC([O-])=O CVSVTCORWBXHQV-UHFFFAOYSA-N 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 description 2
- 229940001447 lactate Drugs 0.000 description 2
- 229940049920 malate Drugs 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 125000000962 organic group Chemical group 0.000 description 2
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 2
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 2
- 229940095064 tartrate Drugs 0.000 description 2
- LKVXWHZRROVPHG-UHFFFAOYSA-N (2-amino-2-methylpropyl) 2-hydroxypropanoate Chemical compound CC(O)C(=O)OCC(C)(C)N LKVXWHZRROVPHG-UHFFFAOYSA-N 0.000 description 1
- QCGCFRQMXTUPBV-UHFFFAOYSA-N (2-amino-3-hydroxy-2-methylpropyl) 2-hydroxyacetate Chemical compound OCC(N)(C)COC(=O)CO QCGCFRQMXTUPBV-UHFFFAOYSA-N 0.000 description 1
- TTXDSCZJTRWBJI-UHFFFAOYSA-N (2-amino-3-hydroxy-2-methylpropyl) 2-hydroxypropanoate Chemical compound C(C(O)C)(=O)OCC(CO)(C)N TTXDSCZJTRWBJI-UHFFFAOYSA-N 0.000 description 1
- UGVKUMQSPZUXIJ-UHFFFAOYSA-N (2-amino-3-hydroxy-2-methylpropyl) acetate Chemical compound CC(=O)OCC(C)(N)CO UGVKUMQSPZUXIJ-UHFFFAOYSA-N 0.000 description 1
- KAKNXRDMTXKKSE-UHFFFAOYSA-N (2-amino-3-hydroxypropyl) 2-hydroxyacetate Chemical compound C(CO)(=O)OCC(CO)N KAKNXRDMTXKKSE-UHFFFAOYSA-N 0.000 description 1
- DGXIACAAKYDLLH-UHFFFAOYSA-N (2-amino-3-hydroxypropyl) 2-hydroxypropanoate Chemical compound C(C(O)C)(=O)OCC(CO)N DGXIACAAKYDLLH-UHFFFAOYSA-N 0.000 description 1
- PLNKLNFRKMRPIU-UHFFFAOYSA-N (2-amino-3-hydroxypropyl) acetate Chemical compound CC(=O)OCC(N)CO PLNKLNFRKMRPIU-UHFFFAOYSA-N 0.000 description 1
- BCFXYENGYYGIPA-BTVCFUMJSA-N (2R,3R,4R,5S)-6-aminohexane-1,2,3,4,5-pentol 2-hydroxypropanoic acid Chemical compound CC(O)C(O)=O.NC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO BCFXYENGYYGIPA-BTVCFUMJSA-N 0.000 description 1
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 description 1
- FSJVVVCZSRCTBM-RXSVEWSESA-N (2S)-2-[(2R)-3,4-dihydroxy-5-oxo-2H-furan-2-yl]-2-hydroxyethanolate 2-hydroxyethyl(trimethyl)azanium Chemical compound C[N+](C)(C)CCO.O[C@@H](C[O-])[C@H]1OC(=O)C(O)=C1O FSJVVVCZSRCTBM-RXSVEWSESA-N 0.000 description 1
- IRJCBFDCFXCWGO-BYPYZUCNSA-N (2s)-2-amino-2-(3-oxo-1,2-oxazol-5-yl)acetic acid Chemical compound OC(=O)[C@@H](N)C1=CC(=O)NO1 IRJCBFDCFXCWGO-BYPYZUCNSA-N 0.000 description 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- PBMCNXWCDKJXRU-UHFFFAOYSA-N 1-[bis(1,1,2,2,2-pentafluoroethylsulfonyl)methylsulfonyl]-1,1,2,2,2-pentafluoroethane Chemical compound FC(F)(F)C(F)(F)S(=O)(=O)[C-](S(=O)(=O)C(F)(F)C(F)(F)F)S(=O)(=O)C(F)(F)C(F)(F)F PBMCNXWCDKJXRU-UHFFFAOYSA-N 0.000 description 1
- LXFQSRIDYRFTJW-UHFFFAOYSA-M 2,4,6-trimethylbenzenesulfonate Chemical compound CC1=CC(C)=C(S([O-])(=O)=O)C(C)=C1 LXFQSRIDYRFTJW-UHFFFAOYSA-M 0.000 description 1
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 description 1
- QHXBZNOJMIQGER-UHFFFAOYSA-N 2-[bis(2-hydroxyethyl)amino]ethanol;2-hydroxypropane-1,2,3-tricarboxylic acid Chemical compound OCCN(CCO)CCO.OC(=O)CC(O)(C(O)=O)CC(O)=O QHXBZNOJMIQGER-UHFFFAOYSA-N 0.000 description 1
- CFJZQNZZGQDONE-UHFFFAOYSA-N 2-amino-2-(hydroxymethyl)propane-1,3-diol;butanedioic acid Chemical compound OCC(N)(CO)CO.OCC(N)(CO)CO.OC(=O)CCC(O)=O CFJZQNZZGQDONE-UHFFFAOYSA-N 0.000 description 1
- NOTWBODAGCEHCE-WLHGVMLRSA-N 2-amino-2-methylpropane-1,3-diol (E)-but-2-enedioic acid Chemical compound C(\C=C\C(=O)O)(=O)O.NC(CO)(CO)C NOTWBODAGCEHCE-WLHGVMLRSA-N 0.000 description 1
- WXFRGPMXIYLZJM-UHFFFAOYSA-N 2-amino-2-methylpropane-1,3-diol 2,3-dihydroxybutanedioic acid Chemical compound C(=O)(O)C(O)C(O)C(=O)O.NC(CO)(CO)C WXFRGPMXIYLZJM-UHFFFAOYSA-N 0.000 description 1
- OGZDGWAIPAWFGR-UHFFFAOYSA-N 2-amino-2-methylpropane-1,3-diol butanedioic acid Chemical compound C(CCC(=O)O)(=O)O.NC(CO)(CO)C OGZDGWAIPAWFGR-UHFFFAOYSA-N 0.000 description 1
- AKVBCGQVQXPRLD-UHFFFAOYSA-N 2-aminooctanoic acid Chemical compound CCCCCCC(N)C(O)=O AKVBCGQVQXPRLD-UHFFFAOYSA-N 0.000 description 1
- DREIFJIGWKGWQN-UHFFFAOYSA-N 2-aminopropane-1,3-diol 2-hydroxypropane-1,2,3-tricarboxylic acid Chemical compound C(CC(O)(C(=O)O)CC(=O)O)(=O)O.NC(CO)CO DREIFJIGWKGWQN-UHFFFAOYSA-N 0.000 description 1
- SQYGRSULPGJSBP-UHFFFAOYSA-N 2-aminopropane-1,3-diol butanedioic acid Chemical compound C(CCC(=O)O)(=O)O.NC(CO)CO SQYGRSULPGJSBP-UHFFFAOYSA-N 0.000 description 1
- PQJDLYIRTTVMCS-UHFFFAOYSA-N 2-hydroxyacetate;tris(2-hydroxyethyl)azanium Chemical compound OCC(O)=O.OCCN(CCO)CCO PQJDLYIRTTVMCS-UHFFFAOYSA-N 0.000 description 1
- NNUCMTORCZUCNA-UHFFFAOYSA-N 2-hydroxyacetic acid;2-(2-hydroxyethylamino)ethanol Chemical compound OCC(O)=O.OCCNCCO NNUCMTORCZUCNA-UHFFFAOYSA-N 0.000 description 1
- QWJSAWXRUVVRLH-LREBCSMRSA-M 2-hydroxyethyl(trimethyl)azanium;(2r,3r)-2,3,4-trihydroxy-4-oxobutanoate Chemical compound C[N+](C)(C)CCO.OC(=O)[C@H](O)[C@@H](O)C([O-])=O QWJSAWXRUVVRLH-LREBCSMRSA-M 0.000 description 1
- MIFGTXFTLQVWJW-UHFFFAOYSA-M 2-hydroxyethyl(trimethyl)azanium;2-hydroxypropanoate Chemical compound CC(O)C([O-])=O.C[N+](C)(C)CCO MIFGTXFTLQVWJW-UHFFFAOYSA-M 0.000 description 1
- NEQXUPRFDXNNTA-UHFFFAOYSA-N 2-hydroxyethylazanium;2-hydroxypropanoate Chemical compound [NH3+]CCO.CC(O)C([O-])=O NEQXUPRFDXNNTA-UHFFFAOYSA-N 0.000 description 1
- RJQQOKKINHMXIM-UHFFFAOYSA-N 2-hydroxypropanoate;tris(2-hydroxyethyl)azanium Chemical compound CC(O)C(O)=O.OCCN(CCO)CCO RJQQOKKINHMXIM-UHFFFAOYSA-N 0.000 description 1
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
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- KFNGWPXYNSJXOP-UHFFFAOYSA-N 3-(2-methylprop-2-enoyloxy)propane-1-sulfonic acid Chemical compound CC(=C)C(=O)OCCCS(O)(=O)=O KFNGWPXYNSJXOP-UHFFFAOYSA-N 0.000 description 1
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- WEQPBCSPRXFQQS-UHFFFAOYSA-N 4,5-dihydro-1,2-oxazole Chemical compound C1CC=NO1 WEQPBCSPRXFQQS-UHFFFAOYSA-N 0.000 description 1
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| US7659234B2 (en) | 2006-03-07 | 2010-02-09 | Conopco, Inc. | Personal care compositions containing quaternary ammonium trihydroxy substituted dipropyl ether |
| JP5117732B2 (ja) * | 2007-01-29 | 2013-01-16 | 株式会社 メドレックス | 外用剤用の低刺激性溶解助剤 |
| ES2482190T3 (es) * | 2007-03-30 | 2014-08-01 | Laccure Ab | Uso de oligómeros de ácido láctico en el tratamiento de infecciones ginecológicas |
| US8221731B2 (en) * | 2008-05-30 | 2012-07-17 | Aveda Corporation | Continuous moisturization compositions |
| CA2643784A1 (en) * | 2008-11-12 | 2009-02-05 | The Procter & Gamble Company | Personal care compositions comprising ionic liquids |
| WO2010136104A2 (en) * | 2009-05-28 | 2010-12-02 | Merck Patent Gmbh | Anti-dandruff agents |
| JP5887065B2 (ja) | 2010-06-29 | 2016-03-16 | ミヨシ油脂株式会社 | 親水性イオン液体 |
| JP5936319B2 (ja) | 2011-08-19 | 2016-06-22 | 株式会社マンダム | 多剤式毛髪処理剤、並びに該処理剤による毛髪処理方法 |
| JP5550056B2 (ja) * | 2012-09-05 | 2014-07-16 | 株式会社 メドレックス | 外用剤用の低刺激性溶解助剤 |
| JP6559394B2 (ja) | 2012-12-05 | 2019-08-14 | ミヨシ油脂株式会社 | 親水性室温イオン液体とその用途 |
| JP6378475B2 (ja) * | 2012-12-05 | 2018-08-22 | ミヨシ油脂株式会社 | 親水性室温イオン液体とその用途 |
| JP2014136678A (ja) | 2013-01-15 | 2014-07-28 | Kaigen Pharma Co Ltd | 保湿化粧品素材およびその製造方法 |
| JP2014151015A (ja) | 2013-02-08 | 2014-08-25 | Nippon Telegr & Teleph Corp <Ntt> | 体表面設置型電極、生体信号の測定方法、及び生体信号測定装置 |
| JP6081515B2 (ja) * | 2014-04-10 | 2017-02-15 | ミヨシ油脂株式会社 | イオン液体を用いた生体触媒溶液および生体触媒用溶媒を使用する方法 |
| JP7129767B2 (ja) * | 2016-08-22 | 2022-09-02 | ミヨシ油脂株式会社 | 生体触媒用反応溶媒とそれを用いた基質と生体触媒との反応方法 |
| US11166895B2 (en) * | 2016-10-03 | 2021-11-09 | L'oreal | Hair care compositions comprising thiolactic acid-based ionic liquids or thiolactic acid-based ionic mixtures |
| JP2018136893A (ja) | 2017-02-24 | 2018-08-30 | 富士通株式会社 | ストレージ制御装置、ストレージ制御プログラム、及びストレージ制御方法 |
| JP7138502B2 (ja) * | 2017-07-21 | 2022-09-16 | ミヨシ油脂株式会社 | 保水・保湿剤 |
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2020
- 2020-02-13 CN CN202080013660.7A patent/CN113423470B/zh active Active
- 2020-02-13 KR KR1020217021712A patent/KR102792818B1/ko active Active
- 2020-02-13 JP JP2020572320A patent/JP7490581B2/ja active Active
- 2020-02-13 WO PCT/JP2020/005669 patent/WO2020166678A1/ja not_active Ceased
- 2020-02-13 EP EP20755453.6A patent/EP3925671A4/en active Pending
- 2020-02-13 US US17/420,960 patent/US20220096349A1/en not_active Abandoned
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2024
- 2024-11-13 US US18/946,484 patent/US20250090437A1/en active Pending
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