CH628806A5 - Use of oxazolidines to improve the structure of damaged hair - Google Patents
Use of oxazolidines to improve the structure of damaged hair Download PDFInfo
- Publication number
- CH628806A5 CH628806A5 CH1567077A CH1567077A CH628806A5 CH 628806 A5 CH628806 A5 CH 628806A5 CH 1567077 A CH1567077 A CH 1567077A CH 1567077 A CH1567077 A CH 1567077A CH 628806 A5 CH628806 A5 CH 628806A5
- Authority
- CH
- Switzerland
- Prior art keywords
- hair
- oxazolidine
- solution
- oxazolidines
- treatment
- Prior art date
Links
- 210000004209 hair Anatomy 0.000 title claims description 38
- 150000002917 oxazolidines Chemical class 0.000 title claims description 12
- 238000011282 treatment Methods 0.000 claims description 30
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 12
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 9
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 239000004310 lactic acid Substances 0.000 claims description 6
- 235000014655 lactic acid Nutrition 0.000 claims description 6
- 239000011975 tartaric acid Substances 0.000 claims description 6
- 235000002906 tartaric acid Nutrition 0.000 claims description 6
- -1 alkyl radical Chemical class 0.000 claims description 5
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 235000015165 citric acid Nutrition 0.000 claims description 3
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 2
- 239000000834 fixative Substances 0.000 claims description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 2
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 3
- 239000000243 solution Substances 0.000 description 24
- 238000004061 bleaching Methods 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 9
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 8
- WYNCHZVNFNFDNH-UHFFFAOYSA-N Oxazolidine Chemical compound C1COCN1 WYNCHZVNFNFDNH-UHFFFAOYSA-N 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 230000002378 acidificating effect Effects 0.000 description 6
- ZOLPLBFETMHBCI-UHFFFAOYSA-N 3-ethyl-5-hexyl-1,3-oxazolidine Chemical compound C(C)N1COC(C1)CCCCCC ZOLPLBFETMHBCI-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 230000006378 damage Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- ZMXSOWGOQMFMJR-UHFFFAOYSA-N 2-(5-decyl-1,3-oxazolidin-3-yl)ethanol Chemical compound C(CCCCCCCCC)C1CN(CO1)CCO ZMXSOWGOQMFMJR-UHFFFAOYSA-N 0.000 description 3
- UXXYSKJOWOZWPP-UHFFFAOYSA-N 5,5-dimethyl-1,3-oxazolidine Chemical compound CC1(C)CNCO1 UXXYSKJOWOZWPP-UHFFFAOYSA-N 0.000 description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000005728 strengthening Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- BFHKYHMIVDBCPC-UHFFFAOYSA-N 1,3,5,7-tetrahydro-[1,3]oxazolo[3,4-c][1,3]oxazol-7a-ylmethanol Chemical compound C1OCN2COCC21CO BFHKYHMIVDBCPC-UHFFFAOYSA-N 0.000 description 2
- AOMORPLAHSIXNB-UHFFFAOYSA-N 1-(5-methyl-1,3-oxazolidin-3-yl)propan-2-ol Chemical compound CC(O)CN1COC(C)C1 AOMORPLAHSIXNB-UHFFFAOYSA-N 0.000 description 2
- BPVGGPFFTVRORQ-UHFFFAOYSA-N 6-(5-decyl-1,3-oxazolidin-3-yl)hexan-1-amine Chemical compound NCCCCCCN1COC(C1)CCCCCCCCCC BPVGGPFFTVRORQ-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 101000623895 Bos taurus Mucin-15 Proteins 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- 230000003766 combability Effects 0.000 description 2
- 239000013065 commercial product Substances 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 150000002431 hydrogen Chemical group 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- SBNYOVKCDXHDDO-UHFFFAOYSA-N 1,3-oxazolidin-4-ylmethanol Chemical compound OCC1COCN1 SBNYOVKCDXHDDO-UHFFFAOYSA-N 0.000 description 1
- YMBWJIKPLFYHOD-UHFFFAOYSA-N 1,3-oxazolidin-5-ylmethanol Chemical compound OCC1CNCO1 YMBWJIKPLFYHOD-UHFFFAOYSA-N 0.000 description 1
- KZHRNWPLAUFTDH-UHFFFAOYSA-N 1-(ethylamino)octan-2-ol Chemical compound CCCCCCC(O)CNCC KZHRNWPLAUFTDH-UHFFFAOYSA-N 0.000 description 1
- AQRSPIFEHRXMJA-UHFFFAOYSA-N 2-(4-decyl-1,3-oxazolidin-3-yl)ethanol Chemical compound C(CCCCCCCCC)C1N(COC1)CCO AQRSPIFEHRXMJA-UHFFFAOYSA-N 0.000 description 1
- DFOGEJNAYDOJTM-UHFFFAOYSA-N 2-(5-octadecyl-1,3-oxazolidin-3-yl)ethanol Chemical compound C(CCCCCCCCCCCCCCCCC)C1CN(CO1)CCO DFOGEJNAYDOJTM-UHFFFAOYSA-N 0.000 description 1
- YGRCLLQIAOXAHD-UHFFFAOYSA-N 3,5,7,7a-tetrahydro-1h-[1,3]oxazolo[3,4-c][1,3]oxazole Chemical compound C1OCC2COCN21 YGRCLLQIAOXAHD-UHFFFAOYSA-N 0.000 description 1
- XWNSFEAWWGGSKJ-UHFFFAOYSA-N 4-acetyl-4-methylheptanedinitrile Chemical compound N#CCCC(C)(C(=O)C)CCC#N XWNSFEAWWGGSKJ-UHFFFAOYSA-N 0.000 description 1
- OOTBVTALXQHTHX-UHFFFAOYSA-N 4-methyl-1,3-oxazolidine Chemical compound CC1COCN1 OOTBVTALXQHTHX-UHFFFAOYSA-N 0.000 description 1
- SGUMWGBOMHEUHE-UHFFFAOYSA-N 5-ethyl-1,3-oxazolidine Chemical compound CCC1CNCO1 SGUMWGBOMHEUHE-UHFFFAOYSA-N 0.000 description 1
- IUNVOXGEXDKMNH-UHFFFAOYSA-N 7a-decyl-1,3,5,7-tetrahydro-[1,3]oxazolo[3,4-c][1,3]oxazole Chemical compound C1OCN2COCC21CCCCCCCCCC IUNVOXGEXDKMNH-UHFFFAOYSA-N 0.000 description 1
- MNQZXJOMYWMBOU-VKHMYHEASA-N D-glyceraldehyde Chemical compound OC[C@@H](O)C=O MNQZXJOMYWMBOU-VKHMYHEASA-N 0.000 description 1
- ZNZYKNKBJPZETN-WELNAUFTSA-N Dialdehyde 11678 Chemical compound N1C2=CC=CC=C2C2=C1[C@H](C[C@H](/C(=C/O)C(=O)OC)[C@@H](C=C)C=O)NCC2 ZNZYKNKBJPZETN-WELNAUFTSA-N 0.000 description 1
- 239000004129 EU approved improving agent Substances 0.000 description 1
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 229920001744 Polyaldehyde Polymers 0.000 description 1
- 239000004153 Potassium bromate Substances 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 235000019395 ammonium persulphate Nutrition 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Inorganic materials [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 description 1
- SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical compound OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 230000003806 hair structure Effects 0.000 description 1
- 230000003699 hair surface Effects 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 235000019396 potassium bromate Nutrition 0.000 description 1
- 229940094037 potassium bromate Drugs 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 210000004761 scalp Anatomy 0.000 description 1
- 230000009528 severe injury Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/002—Preparations for repairing the hair, e.g. hair cure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19762657715 DE2657715C2 (de) | 1976-12-20 | 1976-12-20 | Verwendung von Oxazolidinen zur Strukturverbesserung geschädigter Haare |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH628806A5 true CH628806A5 (en) | 1982-03-31 |
Family
ID=5996004
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH1567077A CH628806A5 (en) | 1976-12-20 | 1977-12-20 | Use of oxazolidines to improve the structure of damaged hair |
Country Status (7)
| Country | Link |
|---|---|
| BE (1) | BE861988A (enrdf_load_stackoverflow) |
| CH (1) | CH628806A5 (enrdf_load_stackoverflow) |
| DE (1) | DE2657715C2 (enrdf_load_stackoverflow) |
| FR (1) | FR2374029A1 (enrdf_load_stackoverflow) |
| GB (1) | GB1545740A (enrdf_load_stackoverflow) |
| IT (1) | IT1091578B (enrdf_load_stackoverflow) |
| NL (1) | NL7713158A (enrdf_load_stackoverflow) |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1160680A (fr) * | 1952-08-13 | 1958-07-24 | Bohme Fettchemie Gmbh | Procédé de préparation d'oxazolidines dans lesquelles des restes d'acides sulfoniques organiques sont substitués à l'azote |
| US2987519A (en) * | 1959-11-09 | 1961-06-06 | Sterling Drug Inc | 3-alkyl-4, 4-bis (hydroxymethyl)-oxazolidines and process for the preparation thereof |
| DE2218417A1 (de) * | 1972-04-15 | 1973-10-25 | Henkel & Cie Gmbh | Verwendung substituierter oxazolidine als antimikrobielle wirkstoffe |
-
1976
- 1976-12-20 DE DE19762657715 patent/DE2657715C2/de not_active Expired
-
1977
- 1977-11-29 NL NL7713158A patent/NL7713158A/xx not_active Application Discontinuation
- 1977-12-15 GB GB5216177A patent/GB1545740A/en not_active Expired
- 1977-12-16 IT IT3082177A patent/IT1091578B/it active
- 1977-12-19 BE BE183563A patent/BE861988A/xx not_active IP Right Cessation
- 1977-12-20 FR FR7738476A patent/FR2374029A1/fr active Granted
- 1977-12-20 CH CH1567077A patent/CH628806A5/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| FR2374029B1 (enrdf_load_stackoverflow) | 1981-07-10 |
| DE2657715A1 (de) | 1978-06-29 |
| DE2657715C2 (de) | 1987-01-29 |
| IT1091578B (it) | 1985-07-06 |
| BE861988A (fr) | 1978-06-19 |
| NL7713158A (nl) | 1978-06-22 |
| GB1545740A (en) | 1979-05-16 |
| FR2374029A1 (fr) | 1978-07-13 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased | ||
| PL | Patent ceased |