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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| MX2009010445A (es) * | 2007-03-30 | 2010-01-29 | Laccure Ab | Uso de oligomeros de acido lactico en el tratamiento de trastornos ginecologicos. |
| 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 |
| CN102448431A (zh) * | 2009-05-28 | 2012-05-09 | 默克专利股份有限公司 | 抗头屑试剂 |
| 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 |
| EP3130670B1 (en) * | 2014-04-10 | 2020-10-21 | Miyoshi Oil & Fat Co., Ltd. | Biocatalyst solvent using ionic liquid, and biocatalyst solution containing biocatalyst and said solvent |
| 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 |
| WO2018065827A1 (en) * | 2016-10-03 | 2018-04-12 | 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 |
-
2020
- 2020-02-13 CN CN202080013660.7A patent/CN113423470B/zh active Active
- 2020-02-13 WO PCT/JP2020/005669 patent/WO2020166678A1/ja not_active Ceased
- 2020-02-13 US US17/420,960 patent/US20220096349A1/en not_active Abandoned
- 2020-02-13 EP EP20755453.6A patent/EP3925671A4/en active Pending
- 2020-02-13 KR KR1020217021712A patent/KR102792818B1/ko active Active
- 2020-02-13 JP JP2020572320A patent/JP7490581B2/ja active Active
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2024
- 2024-11-13 US US18/946,484 patent/US20250090437A1/en active Pending
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