KR102661331B1 - 릴렉싱된 헤어의 처리 방법 - Google Patents
릴렉싱된 헤어의 처리 방법 Download PDFInfo
- Publication number
- KR102661331B1 KR102661331B1 KR1020177033786A KR20177033786A KR102661331B1 KR 102661331 B1 KR102661331 B1 KR 102661331B1 KR 1020177033786 A KR1020177033786 A KR 1020177033786A KR 20177033786 A KR20177033786 A KR 20177033786A KR 102661331 B1 KR102661331 B1 KR 102661331B1
- Authority
- KR
- South Korea
- Prior art keywords
- hair
- group
- relaxing
- formulation
- active 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.)
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- 210000004209 hair Anatomy 0.000 title claims abstract description 203
- 239000000203 mixture Substances 0.000 claims abstract description 227
- 238000009472 formulation Methods 0.000 claims abstract description 203
- 230000002040 relaxant effect Effects 0.000 claims abstract description 144
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 91
- 239000012190 activator Substances 0.000 claims abstract description 74
- 238000000034 method Methods 0.000 claims abstract description 62
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims abstract description 29
- 239000013543 active substance Substances 0.000 claims description 109
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 93
- 125000000217 alkyl group Chemical group 0.000 claims description 38
- 230000014759 maintenance of location Effects 0.000 claims description 35
- 125000003118 aryl group Chemical group 0.000 claims description 27
- 125000003396 thiol group Chemical class [H]S* 0.000 claims description 27
- 230000008569 process Effects 0.000 claims description 26
- 125000000524 functional group Chemical group 0.000 claims description 21
- 125000001072 heteroaryl group Chemical group 0.000 claims description 20
- 125000001424 substituent group Chemical group 0.000 claims description 16
- 229920000642 polymer Polymers 0.000 claims description 15
- 230000003750 conditioning effect Effects 0.000 claims description 14
- 229910052760 oxygen Inorganic materials 0.000 claims description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims description 13
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 12
- 125000003342 alkenyl group Chemical group 0.000 claims description 12
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 12
- 229910052717 sulfur Inorganic materials 0.000 claims description 12
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 11
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 11
- 229910052799 carbon Inorganic materials 0.000 claims description 11
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 11
- 239000001257 hydrogen Substances 0.000 claims description 11
- 239000001301 oxygen Substances 0.000 claims description 11
- 239000011593 sulfur Substances 0.000 claims description 11
- 125000000304 alkynyl group Chemical group 0.000 claims description 10
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- 229910052783 alkali metal Inorganic materials 0.000 claims description 7
- 150000001340 alkali metals Chemical class 0.000 claims description 7
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 7
- 239000012038 nucleophile Substances 0.000 claims description 7
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 claims description 6
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical group OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 6
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical group NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical group OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 4
- AFOSIXZFDONLBT-UHFFFAOYSA-N divinyl sulfone Chemical compound C=CS(=O)(=O)C=C AFOSIXZFDONLBT-UHFFFAOYSA-N 0.000 claims description 4
- 125000003010 ionic group Chemical group 0.000 claims description 4
- LVHBHZANLOWSRM-UHFFFAOYSA-N itaconic acid Chemical group OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 4
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical group CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 4
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- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 4
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- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 2
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- 238000011282 treatment Methods 0.000 abstract description 27
- -1 hydroxide ions Chemical class 0.000 description 50
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- 125000005647 linker group Chemical group 0.000 description 25
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 21
- 150000001875 compounds Chemical class 0.000 description 19
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical group [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 15
- 239000006071 cream Substances 0.000 description 14
- 125000005842 heteroatom Chemical group 0.000 description 13
- 239000007788 liquid Substances 0.000 description 13
- 125000000623 heterocyclic group Chemical group 0.000 description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 11
- 230000001143 conditioned effect Effects 0.000 description 11
- 239000002453 shampoo Substances 0.000 description 11
- 239000004094 surface-active agent Substances 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 125000003545 alkoxy group Chemical group 0.000 description 10
- 150000002978 peroxides Chemical class 0.000 description 10
- 239000000546 pharmaceutical excipient Substances 0.000 description 10
- 150000001412 amines Chemical class 0.000 description 9
- 125000004432 carbon atom Chemical group C* 0.000 description 9
- 229910052736 halogen Inorganic materials 0.000 description 9
- 150000002367 halogens Chemical class 0.000 description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 9
- 239000000370 acceptor Substances 0.000 description 8
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- 231100000640 hair analysis Toxicity 0.000 description 8
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- 239000003995 emulsifying agent Substances 0.000 description 7
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- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 125000003368 amide group Chemical group 0.000 description 6
- 150000001413 amino acids Chemical class 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 125000000392 cycloalkenyl group Chemical group 0.000 description 6
- 229940008099 dimethicone Drugs 0.000 description 6
- 239000004205 dimethyl polysiloxane Substances 0.000 description 6
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 6
- 239000003974 emollient agent Substances 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 6
- XMSXQFUHVRWGNA-UHFFFAOYSA-N Decamethylcyclopentasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 XMSXQFUHVRWGNA-UHFFFAOYSA-N 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 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 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 5
- 239000006210 lotion Substances 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
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- 229940083542 sodium Drugs 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- HQQTZCPKNZVLFF-UHFFFAOYSA-N 4h-1,2-benzoxazin-3-one Chemical class C1=CC=C2ONC(=O)CC2=C1 HQQTZCPKNZVLFF-UHFFFAOYSA-N 0.000 description 4
- 244000144725 Amygdalus communis Species 0.000 description 4
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- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 4
- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 4
- 206010044625 Trichorrhexis Diseases 0.000 description 4
- 125000004414 alkyl thio group Chemical group 0.000 description 4
- 125000003277 amino group Chemical group 0.000 description 4
- 229960003237 betaine Drugs 0.000 description 4
- JHRWWRDRBPCWTF-OLQVQODUSA-N captafol Chemical group C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)C(Cl)Cl)C(=O)[C@H]21 JHRWWRDRBPCWTF-OLQVQODUSA-N 0.000 description 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 4
- 239000003085 diluting agent Substances 0.000 description 4
- 125000004185 ester group Chemical group 0.000 description 4
- 230000000737 periodic effect Effects 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
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- 125000004076 pyridyl group Chemical group 0.000 description 4
- 125000000714 pyrimidinyl group Chemical group 0.000 description 4
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- 125000006413 ring segment Chemical group 0.000 description 4
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- 150000003573 thiols Chemical class 0.000 description 4
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 3
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 3
- 201000004384 Alopecia Diseases 0.000 description 3
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- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
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- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
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Landscapes
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562152220P | 2015-04-24 | 2015-04-24 | |
| US62/152,220 | 2015-04-24 | ||
| PCT/US2016/029215 WO2016172708A1 (en) | 2015-04-24 | 2016-04-25 | Methods for treating relaxed hair |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20180008513A KR20180008513A (ko) | 2018-01-24 |
| KR102661331B1 true KR102661331B1 (ko) | 2024-04-30 |
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| KR1020177033786A Active KR102661331B1 (ko) | 2015-04-24 | 2016-04-25 | 릴렉싱된 헤어의 처리 방법 |
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| EP (1) | EP3285733B1 (enExample) |
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| WO (1) | WO2016172708A1 (enExample) |
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| US12233289B2 (en) | 2013-08-01 | 2025-02-25 | Olaplex, Inc. | Methods for fixing hair and skin |
| US20230201632A1 (en) * | 2013-08-01 | 2023-06-29 | Olaplex, Inc. | Methods for fixing hair and skin |
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|---|---|
| US12251456B2 (en) | 2025-03-18 |
| JP2018513181A (ja) | 2018-05-24 |
| EP3285733A1 (en) | 2018-02-28 |
| US11191707B2 (en) | 2021-12-07 |
| US20160310394A1 (en) | 2016-10-27 |
| WO2016172708A1 (en) | 2016-10-27 |
| US20180125768A1 (en) | 2018-05-10 |
| US9597273B2 (en) | 2017-03-21 |
| US9717668B2 (en) | 2017-08-01 |
| US20220323327A1 (en) | 2022-10-13 |
| US20200009035A1 (en) | 2020-01-09 |
| JP7338949B2 (ja) | 2023-09-05 |
| KR20180008513A (ko) | 2018-01-24 |
| US20170071838A1 (en) | 2017-03-16 |
| EP3285733B1 (en) | 2019-10-23 |
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