JP2016539933A5 - - Google Patents
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- Publication number
- JP2016539933A5 JP2016539933A5 JP2016528133A JP2016528133A JP2016539933A5 JP 2016539933 A5 JP2016539933 A5 JP 2016539933A5 JP 2016528133 A JP2016528133 A JP 2016528133A JP 2016528133 A JP2016528133 A JP 2016528133A JP 2016539933 A5 JP2016539933 A5 JP 2016539933A5
- Authority
- JP
- Japan
- Prior art keywords
- hydrochloride
- guanidine
- hair
- acid
- straightening
- 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.)
- Pending
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- 239000000203 mixture Substances 0.000 claims 24
- ZRALSGWEFCBTJO-UHFFFAOYSA-N guanidine group Chemical group NC(=N)N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims 15
- 150000001875 compounds Chemical class 0.000 claims 14
- 239000000463 material Substances 0.000 claims 13
- -1 C b Chemical group 0.000 claims 12
- 239000000470 constituent Substances 0.000 claims 12
- 239000000835 fiber Substances 0.000 claims 12
- 239000003795 chemical substances by application Substances 0.000 claims 11
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 8
- 239000002671 adjuvant Substances 0.000 claims 7
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 claims 6
- ATHHXGZTWNVVOU-UHFFFAOYSA-N N-methylformamide Chemical compound CNC=O ATHHXGZTWNVVOU-UHFFFAOYSA-N 0.000 claims 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 5
- 229910052757 nitrogen Inorganic materials 0.000 claims 5
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 claims 4
- 229910052799 carbon Inorganic materials 0.000 claims 4
- CVSVTCORWBXHQV-UHFFFAOYSA-N creatine Chemical compound NC(=[NH2+])N(C)CC([O-])=O CVSVTCORWBXHQV-UHFFFAOYSA-N 0.000 claims 4
- DDRJAANPRJIHGJ-UHFFFAOYSA-N creatinine Chemical compound CN1CC(=O)NC1=N DDRJAANPRJIHGJ-UHFFFAOYSA-N 0.000 claims 4
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 claims 4
- 229960004198 guanidine Drugs 0.000 claims 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 4
- 150000003254 radicals Chemical class 0.000 claims 4
- FVKFHMNJTHKMRX-UHFFFAOYSA-N 3,4,6,7,8,9-hexahydro-2H-pyrimido[1,2-a]pyrimidine Chemical compound C1CCN2CCCNC2=N1 FVKFHMNJTHKMRX-UHFFFAOYSA-N 0.000 claims 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims 3
- 125000004432 carbon atom Chemical group C* 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 3
- 239000000546 pharmaceutical excipient Substances 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 claims 3
- 125000001424 substituent group Chemical group 0.000 claims 3
- 125000003396 thiol group Chemical group [H]S* 0.000 claims 3
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims 2
- YJYREIFZLKWHMM-UHFFFAOYSA-N (diaminomethylideneamino) hydrogen carbonate Chemical compound NC(N)=NOC(O)=O YJYREIFZLKWHMM-UHFFFAOYSA-N 0.000 claims 2
- FKPUYTAEIPNGRM-UHFFFAOYSA-N 1-(diaminomethylidene)guanidine;hydron;chloride Chemical compound [Cl-].N\C([NH3+])=N/C(N)=N FKPUYTAEIPNGRM-UHFFFAOYSA-N 0.000 claims 2
- KMXXSJLYVJEBHI-UHFFFAOYSA-N 3-guanidinopropanoic acid Chemical compound NC(=[NH2+])NCCC([O-])=O KMXXSJLYVJEBHI-UHFFFAOYSA-N 0.000 claims 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims 2
- ODKSFYDXXFIFQN-UHFFFAOYSA-N Arginine Chemical compound OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 claims 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims 2
- 102000011782 Keratins Human genes 0.000 claims 2
- 108010076876 Keratins Proteins 0.000 claims 2
- ODKSFYDXXFIFQN-BYPYZUCNSA-N L-arginine Chemical compound OC(=O)[C@@H](N)CCCN=C(N)N ODKSFYDXXFIFQN-BYPYZUCNSA-N 0.000 claims 2
- 229930064664 L-arginine Natural products 0.000 claims 2
- 235000014852 L-arginine Nutrition 0.000 claims 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- XDSYAIICRRZSJX-UHFFFAOYSA-N carbamimidoyl(phenyl)azanium;hydrogen carbonate Chemical compound OC(O)=O.NC(N)=NC1=CC=CC=C1 XDSYAIICRRZSJX-UHFFFAOYSA-N 0.000 claims 2
- 150000003857 carboxamides Chemical class 0.000 claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 239000011248 coating agent Substances 0.000 claims 2
- 238000000576 coating method Methods 0.000 claims 2
- 230000001143 conditioned effect Effects 0.000 claims 2
- 229960003624 creatine Drugs 0.000 claims 2
- 239000006046 creatine Substances 0.000 claims 2
- UFUWQSYRGLMLKP-UHFFFAOYSA-N creatine ethyl ester Chemical compound CCOC(=O)CN(C)C(N)=N UFUWQSYRGLMLKP-UHFFFAOYSA-N 0.000 claims 2
- 229940109239 creatinine Drugs 0.000 claims 2
- 238000001035 drying Methods 0.000 claims 2
- 229960000789 guanidine hydrochloride Drugs 0.000 claims 2
- PJJJBBJSCAKJQF-UHFFFAOYSA-N guanidinium chloride Chemical compound [Cl-].NC(N)=[NH2+] PJJJBBJSCAKJQF-UHFFFAOYSA-N 0.000 claims 2
- BPMFZUMJYQTVII-UHFFFAOYSA-N guanidinoacetic acid Chemical compound NC(=N)NCC(O)=O BPMFZUMJYQTVII-UHFFFAOYSA-N 0.000 claims 2
- 238000010438 heat treatment Methods 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 2
- KFNRNFXZFIRNEO-NSHDSACASA-N (2s)-5-(diaminomethylideneamino)-2-[(4-methylphenyl)sulfonylamino]pentanoic acid Chemical compound CC1=CC=C(S(=O)(=O)N[C@@H](CCCN=C(N)N)C(O)=O)C=C1 KFNRNFXZFIRNEO-NSHDSACASA-N 0.000 claims 1
- OTXHZHQQWQTQMW-UHFFFAOYSA-N (diaminomethylideneamino)azanium;hydrogen carbonate Chemical compound OC([O-])=O.N[NH2+]C(N)=N OTXHZHQQWQTQMW-UHFFFAOYSA-N 0.000 claims 1
- VKGQPUZNCZPZKI-UHFFFAOYSA-N (diaminomethylideneamino)azanium;sulfate Chemical compound NN=C(N)N.NN=C(N)N.OS(O)(=O)=O VKGQPUZNCZPZKI-UHFFFAOYSA-N 0.000 claims 1
- 125000003088 (fluoren-9-ylmethoxy)carbonyl group Chemical group 0.000 claims 1
- SGNLZDSZLBOVGT-UHFFFAOYSA-N (n'-benzylcarbamimidoyl)azanium;chloride Chemical compound [Cl-].[NH3+]C(=N)NCC1=CC=CC=C1 SGNLZDSZLBOVGT-UHFFFAOYSA-N 0.000 claims 1
- GVSGVBVZXJOLDD-UHFFFAOYSA-N (n'-ethylcarbamimidoyl)azanium;chloride Chemical compound [Cl-].CCN=C(N)[NH3+] GVSGVBVZXJOLDD-UHFFFAOYSA-N 0.000 claims 1
- TXYQMVROVVJZHJ-UHFFFAOYSA-N 1,1,2,3-tetramethyl-3-[8-[methyl-(n,n,n'-trimethylcarbamimidoyl)amino]naphthalen-1-yl]guanidine Chemical compound C1=CC(N(C)C(=NC)N(C)C)=C2C(N(C)C(N(C)C)=NC)=CC=CC2=C1 TXYQMVROVVJZHJ-UHFFFAOYSA-N 0.000 claims 1
- KYVBNYUBXIEUFW-UHFFFAOYSA-N 1,1,3,3-tetramethylguanidine Chemical compound CN(C)C(=N)N(C)C KYVBNYUBXIEUFW-UHFFFAOYSA-N 0.000 claims 1
- GMGZEOLIKDSQTL-UHFFFAOYSA-N 1,1,3,3-tetramethylguanidine;hydrochloride Chemical compound [Cl-].CN(C)C(N)=[N+](C)C GMGZEOLIKDSQTL-UHFFFAOYSA-N 0.000 claims 1
- NQQVLNFSVPLPII-UHFFFAOYSA-N 1,1-dimethylguanidine;hydrochloride Chemical compound [Cl-].CN(C)C([NH3+])=N NQQVLNFSVPLPII-UHFFFAOYSA-N 0.000 claims 1
- FRFFEOZSNKLMBR-UHFFFAOYSA-N 1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyrimidine Chemical compound C1CCN=C2NCCN21 FRFFEOZSNKLMBR-UHFFFAOYSA-N 0.000 claims 1
- 125000001376 1,2,4-triazolyl group Chemical group N1N=C(N=C1)* 0.000 claims 1
- OPNUROKCUBTKLF-UHFFFAOYSA-N 1,2-bis(2-methylphenyl)guanidine Chemical compound CC1=CC=CC=C1N\C(N)=N\C1=CC=CC=C1C OPNUROKCUBTKLF-UHFFFAOYSA-N 0.000 claims 1
- HAZRIBSLCUYMQP-UHFFFAOYSA-N 1,2-diaminoguanidine;hydron;chloride Chemical compound Cl.NN\C(N)=N/N HAZRIBSLCUYMQP-UHFFFAOYSA-N 0.000 claims 1
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 claims 1
- OWRCNXZUPFZXOS-UHFFFAOYSA-N 1,3-diphenylguanidine Chemical compound C=1C=CC=CC=1NC(=N)NC1=CC=CC=C1 OWRCNXZUPFZXOS-UHFFFAOYSA-N 0.000 claims 1
- SLYRGJDSFOCAAI-UHFFFAOYSA-N 1,3-thiazolidin-2-one Chemical compound O=C1NCCS1 SLYRGJDSFOCAAI-UHFFFAOYSA-N 0.000 claims 1
- FDFLJHHCXSVSNC-UHFFFAOYSA-N 1-(diaminomethylidene)-2-(2,3-dichlorophenyl)guanidine;hydrochloride Chemical compound Cl.NC(N)=NC(N)=NC1=CC=CC(Cl)=C1Cl FDFLJHHCXSVSNC-UHFFFAOYSA-N 0.000 claims 1
- OSGGBIXVZCEAHI-UHFFFAOYSA-N 1-(diaminomethylidene)-2-(2,4-dichlorophenyl)guanidine;hydrochloride Chemical compound [Cl-].NC(N)=[NH+]C(N)=NC1=CC=C(Cl)C=C1Cl OSGGBIXVZCEAHI-UHFFFAOYSA-N 0.000 claims 1
- XIUCHDFQXPAMQP-UHFFFAOYSA-N 1-(diaminomethylidene)-2-(2,4-difluorophenyl)guanidine;hydrochloride Chemical compound Cl.NC(N)=NC(N)=NC1=CC=C(F)C=C1F XIUCHDFQXPAMQP-UHFFFAOYSA-N 0.000 claims 1
- CKZRFWZMFVWDOW-UHFFFAOYSA-N 1-(diaminomethylidene)-2-(2,5-dichlorophenyl)guanidine;hydrochloride Chemical compound Cl.NC(N)=NC(N)=NC1=CC(Cl)=CC=C1Cl CKZRFWZMFVWDOW-UHFFFAOYSA-N 0.000 claims 1
- VVAARBLQYHGNAY-UHFFFAOYSA-N 1-(diaminomethylidene)-2-(2,5-difluorophenyl)guanidine;hydrochloride Chemical compound [Cl-].NC([NH3+])=NC(N)=NC1=CC(F)=CC=C1F VVAARBLQYHGNAY-UHFFFAOYSA-N 0.000 claims 1
- PZRVKJZVIPUVQH-UHFFFAOYSA-N 1-(diaminomethylidene)-2-(2,6-dichlorophenyl)guanidine;hydrochloride Chemical compound Cl.NC(N)=NC(N)=NC1=C(Cl)C=CC=C1Cl PZRVKJZVIPUVQH-UHFFFAOYSA-N 0.000 claims 1
- SQZCAOHYQSOZCE-UHFFFAOYSA-N 1-(diaminomethylidene)-2-(2-methylphenyl)guanidine Chemical compound CC1=CC=CC=C1N=C(N)N=C(N)N SQZCAOHYQSOZCE-UHFFFAOYSA-N 0.000 claims 1
- MGZOKKDDBDONAF-UHFFFAOYSA-N 1-(diaminomethylidene)-2-(3,5-dichlorophenyl)guanidine;hydrochloride Chemical compound Cl.NC(N)=NC(N)=NC1=CC(Cl)=CC(Cl)=C1 MGZOKKDDBDONAF-UHFFFAOYSA-N 0.000 claims 1
- IWYOYHXLNBELKJ-UHFFFAOYSA-N 1-(diaminomethylidene)-2-(3-fluorophenyl)guanidine;hydrochloride Chemical compound Cl.NC(N)=NC(N)=NC1=CC=CC(F)=C1 IWYOYHXLNBELKJ-UHFFFAOYSA-N 0.000 claims 1
- HBYJTLZNKNUTCP-UHFFFAOYSA-N 1-(diaminomethylidene)-2-(4-fluorophenyl)guanidine;hydrochloride Chemical compound [Cl-].N\C([NH3+])=N/C(N)=NC1=CC=C(F)C=C1 HBYJTLZNKNUTCP-UHFFFAOYSA-N 0.000 claims 1
- VAWGZGSCMHDUCU-UHFFFAOYSA-N 1-(diaminomethylidene)-2-[4-(trifluoromethoxy)phenyl]guanidine;hydrochloride Chemical compound Cl.NC(=N)NC(=N)NC1=CC=C(OC(F)(F)F)C=C1 VAWGZGSCMHDUCU-UHFFFAOYSA-N 0.000 claims 1
- RTSKKAJVUWUZDF-UHFFFAOYSA-N 1-(diaminomethylidene)-2-[4-(trifluoromethyl)phenyl]guanidine;hydrochloride Chemical compound Cl.NC(N)=NC(N)=NC1=CC=C(C(F)(F)F)C=C1 RTSKKAJVUWUZDF-UHFFFAOYSA-N 0.000 claims 1
- HGRYADBWOJPLHK-UHFFFAOYSA-N 1-(diaminomethylidene)-2-propylguanidine;hydrochloride Chemical compound [Cl-].CCC[NH2+]\C(N)=N\C(N)=N HGRYADBWOJPLHK-UHFFFAOYSA-N 0.000 claims 1
- VJQCNCOGZPSOQZ-UHFFFAOYSA-N 1-Methylguanidine hydrochloride Chemical compound [Cl-].C[NH2+]C(N)=N VJQCNCOGZPSOQZ-UHFFFAOYSA-N 0.000 claims 1
- HRUWBAUPQXBXBY-UHFFFAOYSA-N 1-benzyl-1-methylguanidine Chemical compound NC(=N)N(C)CC1=CC=CC=C1 HRUWBAUPQXBXBY-UHFFFAOYSA-N 0.000 claims 1
- IDCPFAYURAQKDZ-UHFFFAOYSA-N 1-nitroguanidine Chemical compound NC(=N)N[N+]([O-])=O IDCPFAYURAQKDZ-UHFFFAOYSA-N 0.000 claims 1
- MMGJNINGVUMRFI-UHFFFAOYSA-N 15686-38-1 Chemical compound C1CC2(C3=C(C4=CC=CC=C4N3)C3)CCCCC2C3N1CC1CC1 MMGJNINGVUMRFI-UHFFFAOYSA-N 0.000 claims 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims 1
- RBZRMBCLZMEYEH-UHFFFAOYSA-N 1h-pyrazol-1-ium-1-carboximidamide;chloride Chemical compound Cl.NC(=N)N1C=CC=N1 RBZRMBCLZMEYEH-UHFFFAOYSA-N 0.000 claims 1
- HBWDWJSRXYGILY-UHFFFAOYSA-N 2,3,5,6,7,8-hexahydro-1h-imidazo[1,2-a][1,3]diazepine Chemical compound C1CCCNC2=NCCN21 HBWDWJSRXYGILY-UHFFFAOYSA-N 0.000 claims 1
- ROYYTESGJKJHTH-UHFFFAOYSA-N 2,3,5,6-tetrahydro-1h-imidazo[1,2-a]imidazole Chemical compound C1CN=C2NCCN21 ROYYTESGJKJHTH-UHFFFAOYSA-N 0.000 claims 1
- QMHWARSFUCGBJK-UHFFFAOYSA-N 2-(1,3-benzothiazol-2-yl)guanidine Chemical compound C1=CC=C2SC(N=C(N)N)=NC2=C1 QMHWARSFUCGBJK-UHFFFAOYSA-N 0.000 claims 1
- FNGZREDJXWXRBW-UHFFFAOYSA-N 2-(1,3-benzoxazol-2-yl)guanidine Chemical compound C1=CC=C2OC(N=C(N)N)=NC2=C1 FNGZREDJXWXRBW-UHFFFAOYSA-N 0.000 claims 1
- AMHZIUVRYRVYBA-UHFFFAOYSA-N 2-(2-amino-4,5-dihydroimidazol-1-yl)acetic acid Chemical compound NC1=NCCN1CC(O)=O AMHZIUVRYRVYBA-UHFFFAOYSA-N 0.000 claims 1
- DHEWEVVTYBEELC-UHFFFAOYSA-N 2-(2-hydroxyethyl)guanidine Chemical compound NC(=N)NCCO DHEWEVVTYBEELC-UHFFFAOYSA-N 0.000 claims 1
- DLLQSZUCBVOQDX-UHFFFAOYSA-N 2-(3-chloro-4-fluorophenyl)-1-(diaminomethylidene)guanidine;hydrochloride Chemical compound Cl.NC(N)=NC(N)=NC1=CC=C(F)C(Cl)=C1 DLLQSZUCBVOQDX-UHFFFAOYSA-N 0.000 claims 1
- JDXXTKLHHZMVIO-UHFFFAOYSA-N 2-(3-hydroxypropyl)guanidine Chemical compound NC(=N)NCCCO JDXXTKLHHZMVIO-UHFFFAOYSA-N 0.000 claims 1
- JJWCTKUQWXYIIU-UHFFFAOYSA-N 2-Benzimidazolylguanidine Chemical compound C1=CC=C2NC(N=C(N)N)=NC2=C1 JJWCTKUQWXYIIU-UHFFFAOYSA-N 0.000 claims 1
- MEJYXFHCRXAUIL-UHFFFAOYSA-N 2-[carbamimidoyl(methyl)amino]acetic acid;hydrate Chemical compound O.NC(=N)N(C)CC(O)=O MEJYXFHCRXAUIL-UHFFFAOYSA-N 0.000 claims 1
- LWYWAUJJEVGBLG-UHFFFAOYSA-N 2-[carbamimidoyl(methyl)amino]propanoic acid Chemical compound OC(=O)C(C)N(C)C(N)=N LWYWAUJJEVGBLG-UHFFFAOYSA-N 0.000 claims 1
- UBDZFAGVPPMTIT-UHFFFAOYSA-N 2-aminoguanidine;hydron;chloride Chemical compound [Cl-].NC(N)=N[NH3+] UBDZFAGVPPMTIT-UHFFFAOYSA-N 0.000 claims 1
- GBIXFNRDUMTIPS-UHFFFAOYSA-N 2-chloro-n-(diaminomethylidene)acetamide;hydrochloride Chemical compound Cl.NC(=N)NC(=O)CCl GBIXFNRDUMTIPS-UHFFFAOYSA-N 0.000 claims 1
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims 1
- RYNCIRCAXCMTCY-UHFFFAOYSA-N 2-cyclohexylguanidine;hydrochloride Chemical compound Cl.NC(N)=NC1CCCCC1 RYNCIRCAXCMTCY-UHFFFAOYSA-N 0.000 claims 1
- UKQVDMIAGTYDFN-UHFFFAOYSA-N 2-ethylguanidine;sulfuric acid Chemical compound OS(O)(=O)=O.CCN=C(N)N.CCN=C(N)N UKQVDMIAGTYDFN-UHFFFAOYSA-N 0.000 claims 1
- XCXKNNGWSDYMMS-UHFFFAOYSA-N 2-methyl-1-nitroguanidine Chemical compound CNC(N)=N[N+]([O-])=O XCXKNNGWSDYMMS-UHFFFAOYSA-N 0.000 claims 1
- DTTVLDRWEFQROK-UHFFFAOYSA-N 2-octylguanidine;sulfuric acid Chemical compound OS(O)(=O)=O.CCCCCCCCN=C(N)N.CCCCCCCCN=C(N)N DTTVLDRWEFQROK-UHFFFAOYSA-N 0.000 claims 1
- YQHJFPFNGVDEDT-UHFFFAOYSA-N 2-tert-butyl-1,1,3,3-tetramethylguanidine Chemical compound CN(C)C(N(C)C)=NC(C)(C)C YQHJFPFNGVDEDT-UHFFFAOYSA-N 0.000 claims 1
- UGYHWCOMWQWLNR-UHFFFAOYSA-N 3,3,7,7-tetramethyl-2,4,6,8-tetrahydro-1H-pyrimido[1,2-b]pyridazine Chemical compound CC1(C)CNC2=CCC(C)(C)NN2C1 UGYHWCOMWQWLNR-UHFFFAOYSA-N 0.000 claims 1
- SZPBWJYIVIJVEX-UHFFFAOYSA-N 3,5-diamino-1,2,4-triazole-1-carboximidamide;hydrochloride Chemical compound Cl.NC(=N)N1N=C(N)N=C1N SZPBWJYIVIJVEX-UHFFFAOYSA-N 0.000 claims 1
- LSJOKOWBJOVVQP-UHFFFAOYSA-N 3-[carbamimidoyl(methyl)amino]propanoic acid Chemical compound NC(=N)N(C)CCC(O)=O LSJOKOWBJOVVQP-UHFFFAOYSA-N 0.000 claims 1
- GYYCWERYJWNAKZ-UHFFFAOYSA-N 4-(diaminomethylideneamino)-2-methoxybenzoic acid Chemical compound COC1=CC(N=C(N)N)=CC=C1C(O)=O GYYCWERYJWNAKZ-UHFFFAOYSA-N 0.000 claims 1
- BAKYASSDAXQKKY-UHFFFAOYSA-N 4-Hydroxy-3-methylbenzaldehyde Chemical compound CC1=CC(C=O)=CC=C1O BAKYASSDAXQKKY-UHFFFAOYSA-N 0.000 claims 1
- PTAYFGHRDOMJGC-UHFFFAOYSA-N 4-aminobutyl(diaminomethylidene)azanium;hydrogen sulfate Chemical compound OS(O)(=O)=O.NCCCCN=C(N)N PTAYFGHRDOMJGC-UHFFFAOYSA-N 0.000 claims 1
- LWFBRHSTNWMMGN-UHFFFAOYSA-N 4-phenylpyrrolidin-1-ium-2-carboxylic acid;chloride Chemical compound Cl.C1NC(C(=O)O)CC1C1=CC=CC=C1 LWFBRHSTNWMMGN-UHFFFAOYSA-N 0.000 claims 1
- DKBBZKXYIJUCDD-UHFFFAOYSA-N 5-methyl-3-oxo-1h-pyrazole-2-carboximidamide Chemical compound CC1=CC(=O)N(C(N)=N)N1 DKBBZKXYIJUCDD-UHFFFAOYSA-N 0.000 claims 1
- QYPPJABKJHAVHS-UHFFFAOYSA-N Agmatine Natural products NCCCCNC(N)=N QYPPJABKJHAVHS-UHFFFAOYSA-N 0.000 claims 1
- BMFMQGXDDJALKQ-BYPYZUCNSA-N Argininic acid Chemical compound NC(N)=NCCC[C@H](O)C(O)=O BMFMQGXDDJALKQ-BYPYZUCNSA-N 0.000 claims 1
- WJLVQTJZDCGNJN-UHFFFAOYSA-N Chlorhexidine hydrochloride Chemical compound Cl.Cl.C=1C=C(Cl)C=CC=1NC(N)=NC(N)=NCCCCCCN=C(N)N=C(N)NC1=CC=C(Cl)C=C1 WJLVQTJZDCGNJN-UHFFFAOYSA-N 0.000 claims 1
- CPXOBCDOVSGADW-UHFFFAOYSA-N Cl.COC(=O)C1=CC=C(NC(N)=N)C=C1OC Chemical compound Cl.COC(=O)C1=CC=C(NC(N)=N)C=C1OC CPXOBCDOVSGADW-UHFFFAOYSA-N 0.000 claims 1
- ODKSFYDXXFIFQN-SCSAIBSYSA-N D-arginine Chemical compound OC(=O)[C@H](N)CCCNC(N)=N ODKSFYDXXFIFQN-SCSAIBSYSA-N 0.000 claims 1
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- AMMSXYWPWHREDJ-UHFFFAOYSA-N [(z)-n'-[n'-(3,4-dichlorophenyl)carbamimidoyl]carbamimidoyl]azanium;chloride Chemical compound Cl.NC(N)=NC(N)=NC1=CC=C(Cl)C(Cl)=C1 AMMSXYWPWHREDJ-UHFFFAOYSA-N 0.000 claims 1
- KKLWSPPIRBIEOV-UHFFFAOYSA-N [n'-(n'-butylcarbamimidoyl)carbamimidoyl]azanium;chloride Chemical compound Cl.CCCCN=C(N)N=C(N)N KKLWSPPIRBIEOV-UHFFFAOYSA-N 0.000 claims 1
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- NAFSLMFLGYXGIF-UHFFFAOYSA-N [n'-[n'-(4-chlorophenyl)carbamimidoyl]carbamimidoyl]azanium;chloride Chemical compound Cl.NC(N)=NC(N)=NC1=CC=C(Cl)C=C1 NAFSLMFLGYXGIF-UHFFFAOYSA-N 0.000 claims 1
- QYPPJABKJHAVHS-UHFFFAOYSA-P agmatinium(2+) Chemical compound NC(=[NH2+])NCCCC[NH3+] QYPPJABKJHAVHS-UHFFFAOYSA-P 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- HAMNKKUPIHEESI-UHFFFAOYSA-N aminoguanidine Chemical compound NNC(N)=N HAMNKKUPIHEESI-UHFFFAOYSA-N 0.000 claims 1
- 239000012752 auxiliary agent Substances 0.000 claims 1
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims 1
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims 1
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims 1
- 125000002619 bicyclic group Chemical group 0.000 claims 1
- 125000003739 carbamimidoyl group Chemical group C(N)(=N)* 0.000 claims 1
- STIAPHVBRDNOAJ-UHFFFAOYSA-N carbamimidoylazanium;carbonate Chemical compound NC(N)=N.NC(N)=N.OC(O)=O STIAPHVBRDNOAJ-UHFFFAOYSA-N 0.000 claims 1
- CEDDGDWODCGBFQ-UHFFFAOYSA-N carbamimidoylazanium;hydron;phosphate Chemical compound NC(N)=N.OP(O)(O)=O CEDDGDWODCGBFQ-UHFFFAOYSA-N 0.000 claims 1
- LNEUSAPFBRDCPM-UHFFFAOYSA-N carbamimidoylazanium;sulfamate Chemical compound NC(N)=N.NS(O)(=O)=O LNEUSAPFBRDCPM-UHFFFAOYSA-N 0.000 claims 1
- RTPXJJIYLVIRAD-UHFFFAOYSA-N carbonic acid 1-(diaminomethylidene)-2-phenylguanidine Chemical compound OC(O)=O.NC(=N)NC(=N)Nc1ccccc1 RTPXJJIYLVIRAD-UHFFFAOYSA-N 0.000 claims 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 claims 1
- 125000000473 carbonimidoyl group Chemical group [H]\N=C(/*)* 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 125000002668 chloroacetyl group Chemical group ClCC(=O)* 0.000 claims 1
- 239000004035 construction material Substances 0.000 claims 1
- 229960004826 creatine monohydrate Drugs 0.000 claims 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- UURSXESKOOOTOV-UHFFFAOYSA-N dec-5-ene Chemical compound CCCCC=CCCCC UURSXESKOOOTOV-UHFFFAOYSA-N 0.000 claims 1
- UKUBCVAQGIZRHL-UHFFFAOYSA-N delta-Guanidinovaleric acid Chemical compound NC(N)=NCCCCC(O)=O UKUBCVAQGIZRHL-UHFFFAOYSA-N 0.000 claims 1
- ACPFLXJEPKOPGF-UHFFFAOYSA-N diaminomethylidene(dimethyl)azanium;hydrogen sulfate Chemical compound [O-]S([O-])(=O)=O.C[NH+](C)C([NH3+])=N ACPFLXJEPKOPGF-UHFFFAOYSA-N 0.000 claims 1
- ZZTURJAZCMUWEP-UHFFFAOYSA-N diaminomethylideneazanium;hydrogen sulfate Chemical compound NC(N)=N.OS(O)(=O)=O ZZTURJAZCMUWEP-UHFFFAOYSA-N 0.000 claims 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 claims 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 1
- 229940110377 dl- arginine Drugs 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- TUHVEAJXIMEOSA-UHFFFAOYSA-N gamma-guanidinobutyric acid Natural products NC(=[NH2+])NCCCC([O-])=O TUHVEAJXIMEOSA-UHFFFAOYSA-N 0.000 claims 1
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- DXTIKTAIYCJTII-UHFFFAOYSA-N guanidine acetate Chemical compound CC([O-])=O.NC([NH3+])=N DXTIKTAIYCJTII-UHFFFAOYSA-N 0.000 claims 1
- NDEMNVPZDAFUKN-UHFFFAOYSA-N guanidine;nitric acid Chemical compound NC(N)=N.O[N+]([O-])=O.O[N+]([O-])=O NDEMNVPZDAFUKN-UHFFFAOYSA-N 0.000 claims 1
- 150000002357 guanidines Chemical class 0.000 claims 1
- 229940083094 guanine derivative acting on arteriolar smooth muscle Drugs 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- OETHQSJEHLVLGH-UHFFFAOYSA-N metformin hydrochloride Chemical compound Cl.CN(C)C(=N)N=C(N)N OETHQSJEHLVLGH-UHFFFAOYSA-N 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- GTCAXTIRRLKXRU-UHFFFAOYSA-N methyl carbamate Chemical compound COC(N)=O GTCAXTIRRLKXRU-UHFFFAOYSA-N 0.000 claims 1
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- 229910052760 oxygen Inorganic materials 0.000 claims 1
- CUQCMXFWIMOWRP-UHFFFAOYSA-N phenyl biguanide Chemical compound NC(N)=NC(N)=NC1=CC=CC=C1 CUQCMXFWIMOWRP-UHFFFAOYSA-N 0.000 claims 1
- 235000019260 propionic acid Nutrition 0.000 claims 1
- 230000002040 relaxant effect Effects 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- JKLRIMRKZBSSED-UHFFFAOYSA-N taurocyamine Chemical compound NC(=[NH2+])NCCS([O-])(=O)=O JKLRIMRKZBSSED-UHFFFAOYSA-N 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- XZGNHTJSFCBWHG-UHFFFAOYSA-N tert-butyl n-[bis[(2-methylpropan-2-yl)oxycarbonylamino]methylidene]carbamate Chemical compound CC(C)(C)OC(=O)NC(NC(=O)OC(C)(C)C)=NC(=O)OC(C)(C)C XZGNHTJSFCBWHG-UHFFFAOYSA-N 0.000 claims 1
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 claims 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 1
- APIBROGXENTUGB-ZUQRMPMESA-M triphenyl-[(e)-3-phenylprop-2-enyl]phosphanium;bromide Chemical compound [Br-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C\C=C\C1=CC=CC=C1 APIBROGXENTUGB-ZUQRMPMESA-M 0.000 claims 1
- 238000005406 washing Methods 0.000 claims 1
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| PCT/US2014/064217 WO2015069823A1 (en) | 2013-11-08 | 2014-11-06 | Semi-permanent hair straightening composition and method |
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| WO (1) | WO2015069823A1 (OSRAM) |
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| WO2015094759A1 (en) | 2013-12-19 | 2015-06-25 | The Procter & Gamble Company | Shaping keratin fibres using an active agent comprising at least two functional groups selected from: -c(oh)- and -c(=o)oh |
| EP3082733A1 (en) | 2013-12-19 | 2016-10-26 | The Procter & Gamble Company | Shaping keratin fibres using an active agent comprising a functional group selected from the group consisting of: -c(=o)-, -c(=o)-h, and -c(=o)-o- |
| WO2015094757A1 (en) | 2013-12-19 | 2015-06-25 | The Procter & Gamble Company | Shaping keratin fibres using a sugar |
| MX376963B (es) | 2013-12-19 | 2025-03-07 | Procter & Gamble | Modelado de fibras de queratina mediante el uso de éster de carbonato. |
| WO2015094760A1 (en) | 2013-12-19 | 2015-06-25 | The Procter & Gamble Company | Shaping keratin fibres using carbonate ester |
| WO2015094838A1 (en) | 2013-12-19 | 2015-06-25 | The Procter & Gamble Company | Shaping keratin fibres using a reducing composition and a fixing composition |
| EP3082736B1 (en) | 2013-12-19 | 2018-08-08 | The Procter and Gamble Company | Shaping keratin fibres using 2-hydroxypropane-1,2,3-tricarboxylic acid and/or 1,2,3,4-butanetetracarboxylic acid |
| US11129784B2 (en) | 2013-12-19 | 2021-09-28 | The Procter And Gamble Company | Shaping keratin fibres using oxoethanoic acid and/or derivatives thereof |
| EP3297731A1 (en) | 2014-12-19 | 2018-03-28 | The Procter and Gamble Company | Shaping keratin fibres using arabinose and ethylene carbonate |
| EP3297730A1 (en) | 2014-12-19 | 2018-03-28 | The Procter and Gamble Company | Method of shaping keratin fibres |
| KR20210082277A (ko) | 2015-05-01 | 2021-07-02 | 로레알 | 화학적 처리 중 활성제의 용도 |
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| JP2017218394A (ja) * | 2016-06-03 | 2017-12-14 | 花王株式会社 | 毛髪化粧料 |
| US11135150B2 (en) | 2016-11-21 | 2021-10-05 | L'oreal | Compositions and methods for improving the quality of chemically treated hair |
| FR3060265B1 (fr) * | 2016-12-15 | 2021-06-18 | Oreal | Recharge de produit cosmetique pour dispositif de traitement de la chevelure |
| EP3573493A1 (en) | 2017-01-26 | 2019-12-04 | Lubrizol Advanced Materials, Inc. | Hair styling appliances and methods of operating same |
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| EP4011355A1 (en) | 2017-12-29 | 2022-06-15 | L'oreal | Compositions for altering the color of hair |
| AU2019251493A1 (en) * | 2018-04-12 | 2020-10-29 | Lubrizol Advanced Materials, Inc. | Hair modification composition and method therefor |
| JP6541118B1 (ja) * | 2018-04-27 | 2019-07-10 | 株式会社成和化成 | 化粧品基材および該化粧品基材を含有する毛髪用化粧品、美白剤 |
| DE102018209894A1 (de) * | 2018-06-19 | 2019-12-19 | Henkel Ag & Co. Kgaa | Oxidatives Haaraufhell- oder Haarfärbemittel mit verbesserten Anwendungseigenschaften |
| US11090249B2 (en) | 2018-10-31 | 2021-08-17 | L'oreal | Hair treatment compositions, methods, and kits for treating hair |
| EP3662887A1 (en) * | 2018-12-06 | 2020-06-10 | Kao Germany GmbH | Process for reshaping keratin fibers |
| JP7353754B2 (ja) * | 2018-12-14 | 2023-10-02 | ロレアル | ケラチン繊維の矯正法 |
| US11419809B2 (en) | 2019-06-27 | 2022-08-23 | L'oreal | Hair treatment compositions and methods for treating hair |
| US20220218578A1 (en) * | 2019-08-29 | 2022-07-14 | Kao Corporation | Composition, process and kit for semi-permanent straightening and curling of keratin fibers |
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| CN119816290A (zh) * | 2022-07-13 | 2025-04-11 | 威娜德国有限责任公司 | 用于角蛋白纤维的半永久性变形的化妆品组合物 |
| CN117064776B (zh) * | 2023-10-16 | 2024-01-02 | 济南萨科睿德生物技术有限公司 | 邻甲苯基双胍或其组合物在制备护理产品中的应用 |
| KR102836313B1 (ko) * | 2024-10-16 | 2025-07-21 | 배기연 | 컬의 고정력과 지속성을 향상시킨 펌 시술 방법 |
| KR102836317B1 (ko) * | 2024-10-16 | 2025-07-21 | 배기연 | 천연 잔류 물질 제거제를 이용한 펌 시술 방법 |
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| JP4370479B2 (ja) * | 2006-11-21 | 2009-11-25 | 山栄化学株式会社 | 炭酸アルキレン希釈液及びパーマネントウェーブ１剤 |
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| US8513200B2 (en) * | 2008-10-29 | 2013-08-20 | L'oreal | Process for relaxing or straightening hair, using weak dicarboxylic acids with heat |
-
2014
- 2014-11-06 US US15/035,049 patent/US20160296449A1/en not_active Abandoned
- 2014-11-06 WO PCT/US2014/064217 patent/WO2015069823A1/en not_active Ceased
- 2014-11-06 JP JP2016528133A patent/JP2016539933A/ja active Pending
- 2014-11-06 KR KR1020167015143A patent/KR20160077206A/ko not_active Withdrawn
- 2014-11-06 CN CN201480072400.1A patent/CN105916556A/zh active Pending
- 2014-11-06 EP EP14802559.6A patent/EP3065831A1/en not_active Withdrawn
- 2014-11-07 TW TW103138711A patent/TW201601770A/zh unknown
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