DE2624293C2 - Kosmetische Mittel mit einem Gehalt an Haut-Feuchthaltemitteln - Google Patents
Kosmetische Mittel mit einem Gehalt an Haut-FeuchthaltemittelnInfo
- Publication number
- DE2624293C2 DE2624293C2 DE19762624293 DE2624293A DE2624293C2 DE 2624293 C2 DE2624293 C2 DE 2624293C2 DE 19762624293 DE19762624293 DE 19762624293 DE 2624293 A DE2624293 A DE 2624293A DE 2624293 C2 DE2624293 C2 DE 2624293C2
- Authority
- DE
- Germany
- Prior art keywords
- weight
- parts
- skin
- methyl
- hydroxypropyl
- 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.)
- Expired
Links
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- 239000004909 Moisturizer Substances 0.000 title description 8
- 230000001333 moisturizer Effects 0.000 title description 8
- 238000002360 preparation method Methods 0.000 title description 4
- 150000001408 amides Chemical class 0.000 claims description 14
- 239000000126 substance Substances 0.000 claims description 12
- 239000003599 detergent Substances 0.000 claims description 9
- 239000002904 solvent Substances 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 239000003205 fragrance Substances 0.000 claims description 4
- 239000003995 emulsifying agent Substances 0.000 claims description 3
- 239000004615 ingredient Substances 0.000 claims description 3
- 239000000419 plant extract Substances 0.000 claims description 3
- 239000003755 preservative agent Substances 0.000 claims description 3
- 239000004094 surface-active agent Substances 0.000 claims description 3
- 239000002562 thickening agent Substances 0.000 claims description 2
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- -1 alkyl radical Chemical class 0.000 description 22
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- 239000000203 mixture Substances 0.000 description 17
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- 210000002615 epidermis Anatomy 0.000 description 11
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- 125000004432 carbon atom Chemical group C* 0.000 description 9
- 239000000344 soap Substances 0.000 description 8
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- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 7
- 239000002304 perfume Substances 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 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
- 150000001875 compounds Chemical class 0.000 description 6
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- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 4
- 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 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- LEACJMVNYZDSKR-UHFFFAOYSA-N 2-octyldodecan-1-ol Chemical compound CCCCCCCCCCC(CO)CCCCCCCC LEACJMVNYZDSKR-UHFFFAOYSA-N 0.000 description 3
- 244000060011 Cocos nucifera Species 0.000 description 3
- 235000013162 Cocos nucifera Nutrition 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- PVCJKHHOXFKFRP-UHFFFAOYSA-N N-acetylethanolamine Chemical compound CC(=O)NCCO PVCJKHHOXFKFRP-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 3
- 239000004327 boric acid Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 239000003925 fat Substances 0.000 description 3
- 150000002191 fatty alcohols Chemical class 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 229960002216 methylparaben Drugs 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
- XIPFMBOWZXULIA-UHFFFAOYSA-N pivalamide Chemical compound CC(C)(C)C(N)=O XIPFMBOWZXULIA-UHFFFAOYSA-N 0.000 description 3
- 229940080818 propionamide Drugs 0.000 description 3
- 230000001681 protective effect Effects 0.000 description 3
- 230000037072 sun protection Effects 0.000 description 3
- 235000015112 vegetable and seed oil Nutrition 0.000 description 3
- 239000008158 vegetable oil Substances 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 2
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 241000282887 Suidae Species 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- DNSISZSEWVHGLH-UHFFFAOYSA-N butanamide Chemical compound CCCC(N)=O DNSISZSEWVHGLH-UHFFFAOYSA-N 0.000 description 2
- 239000012230 colorless oil Substances 0.000 description 2
- 239000008271 cosmetic emulsion Substances 0.000 description 2
- 229950001902 dimevamide Drugs 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- CSSWCWIUAZSBHV-UHFFFAOYSA-N n,n-bis(2-hydroxyethyl)acetamide Chemical compound OCCN(C(=O)C)CCO CSSWCWIUAZSBHV-UHFFFAOYSA-N 0.000 description 2
- SULYJQSYRRJOEC-UHFFFAOYSA-N n,n-bis(2-hydroxypropyl)formamide Chemical compound CC(O)CN(C=O)CC(C)O SULYJQSYRRJOEC-UHFFFAOYSA-N 0.000 description 2
- KAAWNSDZHZIGQT-UHFFFAOYSA-N n-(1,3-dihydroxy-2-methylpropan-2-yl)propanamide Chemical compound CCC(=O)NC(C)(CO)CO KAAWNSDZHZIGQT-UHFFFAOYSA-N 0.000 description 2
- GQKLTNAIFDFUDN-UHFFFAOYSA-N n-(2-hydroxyethyl)propanamide Chemical compound CCC(=O)NCCO GQKLTNAIFDFUDN-UHFFFAOYSA-N 0.000 description 2
- YKDZEZDQPMEHGB-UHFFFAOYSA-N n-(2-hydroxypropyl)acetamide Chemical compound CC(O)CNC(C)=O YKDZEZDQPMEHGB-UHFFFAOYSA-N 0.000 description 2
- INCAHTRUJOJBBB-UHFFFAOYSA-N n-(2-hydroxypropyl)propanamide Chemical compound CCC(=O)NCC(C)O INCAHTRUJOJBBB-UHFFFAOYSA-N 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- IPWFJLQDVFKJDU-UHFFFAOYSA-N pentanamide Chemical compound CCCCC(N)=O IPWFJLQDVFKJDU-UHFFFAOYSA-N 0.000 description 2
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Chemical compound O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 description 2
- 239000003760 tallow Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- LPMBTLLQQJBUOO-KTKRTIGZSA-N (z)-n,n-bis(2-hydroxyethyl)octadec-9-enamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(CCO)CCO LPMBTLLQQJBUOO-KTKRTIGZSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- GBBANOPMWWQLET-UHFFFAOYSA-N CCN(CC(O)CO)C(C)=O Chemical compound CCN(CC(O)CO)C(C)=O GBBANOPMWWQLET-UHFFFAOYSA-N 0.000 description 1
- 208000019300 CLIPPERS Diseases 0.000 description 1
- CMBYOWLFQAFZCP-UHFFFAOYSA-N Hexyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCCCCC CMBYOWLFQAFZCP-UHFFFAOYSA-N 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 235000014150 Myroxylon pereirae Nutrition 0.000 description 1
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- PDUBWAUQNYDCJS-UHFFFAOYSA-N N,N-bis(2-hydroxypropyl)pentanamide Chemical compound OC(CN(C(CCCC)=O)CC(C)O)C PDUBWAUQNYDCJS-UHFFFAOYSA-N 0.000 description 1
- HTAYYAMDMUCVCG-UHFFFAOYSA-N N-(1,3,4,5,6-pentahydroxyhexan-2-yl)pentanamide Chemical compound OCC(C(C(C(CO)O)O)O)NC(CCCC)=O HTAYYAMDMUCVCG-UHFFFAOYSA-N 0.000 description 1
- HTHLOHQBAKKHLE-UHFFFAOYSA-N N-(2-hydroxybutyl)-2,2-dimethylpropanamide Chemical compound OC(CNC(C(C)(C)C)=O)CC HTHLOHQBAKKHLE-UHFFFAOYSA-N 0.000 description 1
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- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
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- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000007098 aminolysis reaction Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- RERVRRLGFUNERS-UHFFFAOYSA-N boron;propane-1,2,3-triol Chemical compound [B].OCC(O)CO RERVRRLGFUNERS-UHFFFAOYSA-N 0.000 description 1
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- 229940082500 cetostearyl alcohol Drugs 0.000 description 1
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- 208000021930 chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids Diseases 0.000 description 1
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- 230000000694 effects Effects 0.000 description 1
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- ASXCJONOVQSZRF-UHFFFAOYSA-N n-(2,3,4,5,6-pentahydroxyhexyl)acetamide Chemical compound CC(=O)NCC(O)C(O)C(O)C(O)CO ASXCJONOVQSZRF-UHFFFAOYSA-N 0.000 description 1
- GVKHAMKBQJSGQI-UHFFFAOYSA-N n-(2,3,4,5,6-pentahydroxyhexyl)butanamide Chemical compound CCCC(=O)NCC(O)C(O)C(O)C(O)CO GVKHAMKBQJSGQI-UHFFFAOYSA-N 0.000 description 1
- ILXGPMLOFSWMBU-UHFFFAOYSA-N n-(2,3,4,5,6-pentahydroxyhexyl)formamide Chemical compound OCC(O)C(O)C(O)C(O)CNC=O ILXGPMLOFSWMBU-UHFFFAOYSA-N 0.000 description 1
- MFYNLBVJDOLIMH-UHFFFAOYSA-N n-(2,3,4,5,6-pentahydroxyhexyl)propanamide Chemical compound CCC(=O)NCC(O)C(O)C(O)C(O)CO MFYNLBVJDOLIMH-UHFFFAOYSA-N 0.000 description 1
- APAXTUKBJOASEI-UHFFFAOYSA-N n-(2,3-dihydroxypropyl)-n-ethylpropanamide Chemical compound CCC(=O)N(CC)CC(O)CO APAXTUKBJOASEI-UHFFFAOYSA-N 0.000 description 1
- BLWTXDTUYUHPEN-UHFFFAOYSA-N n-(2,3-dihydroxypropyl)formamide Chemical compound OCC(O)CNC=O BLWTXDTUYUHPEN-UHFFFAOYSA-N 0.000 description 1
- JKPJOQBNMGVZEH-UHFFFAOYSA-N n-(2,3-dihydroxypropyl)pentanamide Chemical compound CCCCC(=O)NCC(O)CO JKPJOQBNMGVZEH-UHFFFAOYSA-N 0.000 description 1
- WCOKSBOKLHVDPT-UHFFFAOYSA-N n-(2-hydroxybutyl)butanamide Chemical compound CCCC(=O)NCC(O)CC WCOKSBOKLHVDPT-UHFFFAOYSA-N 0.000 description 1
- BBUOPHQPUSGSSU-UHFFFAOYSA-N n-(2-hydroxybutyl)formamide Chemical compound CCC(O)CNC=O BBUOPHQPUSGSSU-UHFFFAOYSA-N 0.000 description 1
- YQPJOSJJQYTSDL-UHFFFAOYSA-N n-(2-hydroxybutyl)propanamide Chemical compound CCC(O)CNC(=O)CC YQPJOSJJQYTSDL-UHFFFAOYSA-N 0.000 description 1
- AVWUHZZARFAVLF-UHFFFAOYSA-N n-(2-hydroxyethyl)-n,2,2-trimethylpropanamide Chemical compound OCCN(C)C(=O)C(C)(C)C AVWUHZZARFAVLF-UHFFFAOYSA-N 0.000 description 1
- OBSKGKGKPGOOTB-UHFFFAOYSA-N n-(2-hydroxyethyl)-n-methylacetamide Chemical compound CC(=O)N(C)CCO OBSKGKGKPGOOTB-UHFFFAOYSA-N 0.000 description 1
- DVABXBSMVJVVKK-UHFFFAOYSA-N n-(2-hydroxyethyl)-n-methylbutanamide Chemical compound CCCC(=O)N(C)CCO DVABXBSMVJVVKK-UHFFFAOYSA-N 0.000 description 1
- ZFEJGMDGENZPMS-UHFFFAOYSA-N n-(2-hydroxyethyl)-n-methylformamide Chemical compound O=CN(C)CCO ZFEJGMDGENZPMS-UHFFFAOYSA-N 0.000 description 1
- YFILUQPERUNTEN-UHFFFAOYSA-N n-(2-hydroxyethyl)-n-methylpentanamide Chemical compound CCCCC(=O)N(C)CCO YFILUQPERUNTEN-UHFFFAOYSA-N 0.000 description 1
- RKJFTBDHQJNVGT-UHFFFAOYSA-N n-(2-hydroxyethyl)-n-methylpropanamide Chemical compound CCC(=O)N(C)CCO RKJFTBDHQJNVGT-UHFFFAOYSA-N 0.000 description 1
- BAMUPQJDKBGDPU-UHFFFAOYSA-N n-(2-hydroxyethyl)formamide Chemical compound OCCNC=O BAMUPQJDKBGDPU-UHFFFAOYSA-N 0.000 description 1
- NURPOXDFZKXLRW-UHFFFAOYSA-N n-(2-hydroxyethyl)pentanamide Chemical compound CCCCC(=O)NCCO NURPOXDFZKXLRW-UHFFFAOYSA-N 0.000 description 1
- VKKRLNYESYPMRO-UHFFFAOYSA-N n-(2-hydroxypropyl)-2,2-dimethylpropanamide Chemical compound CC(O)CNC(=O)C(C)(C)C VKKRLNYESYPMRO-UHFFFAOYSA-N 0.000 description 1
- SUOVZMUZQGZAQM-UHFFFAOYSA-N n-(2-hydroxypropyl)-n-methylacetamide Chemical compound CC(O)CN(C)C(C)=O SUOVZMUZQGZAQM-UHFFFAOYSA-N 0.000 description 1
- KRBOTEWRLNGRCL-UHFFFAOYSA-N n-(2-hydroxypropyl)-n-methylbutanamide Chemical compound CCCC(=O)N(C)CC(C)O KRBOTEWRLNGRCL-UHFFFAOYSA-N 0.000 description 1
- JIIUUNVXFYVXOW-UHFFFAOYSA-N n-(2-hydroxypropyl)-n-methylpentanamide Chemical compound CCCCC(=O)N(C)CC(C)O JIIUUNVXFYVXOW-UHFFFAOYSA-N 0.000 description 1
- XXIZNALCXBZFBC-UHFFFAOYSA-N n-(2-hydroxypropyl)-n-methylpropanamide Chemical compound CCC(=O)N(C)CC(C)O XXIZNALCXBZFBC-UHFFFAOYSA-N 0.000 description 1
- MUULCPJUUOCRAT-UHFFFAOYSA-N n-(2-hydroxypropyl)butanamide Chemical compound CCCC(=O)NCC(C)O MUULCPJUUOCRAT-UHFFFAOYSA-N 0.000 description 1
- SIVVBLSNZZQDNV-UHFFFAOYSA-N n-(2-hydroxypropyl)formamide Chemical compound CC(O)CNC=O SIVVBLSNZZQDNV-UHFFFAOYSA-N 0.000 description 1
- QIQAATBNBKVGNT-UHFFFAOYSA-N n-(2-hydroxypropyl)pentanamide Chemical compound CCCCC(=O)NCC(C)O QIQAATBNBKVGNT-UHFFFAOYSA-N 0.000 description 1
- KAIQZAZSOJBMMK-UHFFFAOYSA-N n-(3-hydroxypropyl)-2,2-dimethylpropanamide Chemical compound CC(C)(C)C(=O)NCCCO KAIQZAZSOJBMMK-UHFFFAOYSA-N 0.000 description 1
- LEICDYOVJNQLTN-UHFFFAOYSA-N n-(3-hydroxypropyl)acetamide Chemical compound CC(=O)NCCCO LEICDYOVJNQLTN-UHFFFAOYSA-N 0.000 description 1
- BXZXQTXKLQAOEF-UHFFFAOYSA-N n-(3-hydroxypropyl)butanamide Chemical compound CCCC(=O)NCCCO BXZXQTXKLQAOEF-UHFFFAOYSA-N 0.000 description 1
- XEBPQQOPQNUSAD-UHFFFAOYSA-N n-(3-hydroxypropyl)pentanamide Chemical compound CCCCC(=O)NCCCO XEBPQQOPQNUSAD-UHFFFAOYSA-N 0.000 description 1
- ZSSOONKGCDIKMO-UHFFFAOYSA-N n-(3-hydroxypropyl)propanamide Chemical compound CCC(=O)NCCCO ZSSOONKGCDIKMO-UHFFFAOYSA-N 0.000 description 1
- OLKOIWQNCSVBCU-UHFFFAOYSA-N n-(4-hydroxybutyl)acetamide Chemical compound CC(=O)NCCCCO OLKOIWQNCSVBCU-UHFFFAOYSA-N 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- CYVOZVLWADJEEB-UHFFFAOYSA-N n-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]-2,2-dimethylpropanamide Chemical compound CC(C)(C)C(=O)NC(CO)(CO)CO CYVOZVLWADJEEB-UHFFFAOYSA-N 0.000 description 1
- WEOXHUOXXPRLMU-UHFFFAOYSA-N n-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]butanamide Chemical compound CCCC(=O)NC(CO)(CO)CO WEOXHUOXXPRLMU-UHFFFAOYSA-N 0.000 description 1
- ZDBLHSGGSPNJSV-UHFFFAOYSA-N n-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]pentanamide Chemical compound CCCCC(=O)NC(CO)(CO)CO ZDBLHSGGSPNJSV-UHFFFAOYSA-N 0.000 description 1
- PRXNVVSTKRKFNS-UHFFFAOYSA-N n-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]propanamide Chemical compound CCC(=O)NC(CO)(CO)CO PRXNVVSTKRKFNS-UHFFFAOYSA-N 0.000 description 1
- NSAFFMANMNCZCA-UHFFFAOYSA-N n-[1-hydroxy-2-(hydroxymethyl)butan-2-yl]propanamide Chemical compound CCC(=O)NC(CC)(CO)CO NSAFFMANMNCZCA-UHFFFAOYSA-N 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- FWFGVMYFCODZRD-UHFFFAOYSA-N oxidanium;hydrogen sulfate Chemical compound O.OS(O)(=O)=O FWFGVMYFCODZRD-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940100486 rice starch Drugs 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000002884 skin cream Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontyl alcohol Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
- 230000001256 tonic effect Effects 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 230000004584 weight gain Effects 0.000 description 1
- 235000019786 weight gain Nutrition 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0212—Face masks
-
- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/42—Amides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/005—Preparations for sensitive skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q9/00—Preparations for removing hair or for aiding hair removal
- A61Q9/02—Shaving preparations
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)
- Dermatology (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19762624293 DE2624293C2 (de) | 1976-05-31 | 1976-05-31 | Kosmetische Mittel mit einem Gehalt an Haut-Feuchthaltemitteln |
| DK202377A DK202377A (da) | 1976-05-31 | 1977-05-09 | Kosmetisk middel med et indholt af hudfugtighedsbevarende middel |
| SE7705385A SE431398B (sv) | 1976-05-31 | 1977-05-09 | Kosmetiska medel som innehaller n-hydroxialkylalkansyraamider som hudfuktighetsbevarande komponent |
| NL7705095A NL7705095A (nl) | 1976-05-31 | 1977-05-09 | Werkwijze voor de bereiding van cosmetische preparaten met een gehalte aan middelen die de huid vochtig houden. |
| GB2242877A GB1554251A (en) | 1976-05-31 | 1977-05-27 | Cosmetic compositions having a content of agents for keeping the skin moist |
| IT2407777A IT1085807B (it) | 1976-05-31 | 1977-05-27 | Prodotto cosmetico con un contenuto di agenti umettanti per la cute |
| JP6128777A JPS6055482B2 (ja) | 1976-05-31 | 1977-05-27 | 皮フ−湿潤剤を含有する化粧料 |
| BE177988A BE855135A (fr) | 1976-05-31 | 1977-05-27 | Produits cosmetiques contenant des n-hydroxyalkylamides d'acides alcanoiques comme agents hydratants de la peau |
| FR7716541A FR2353284A1 (fr) | 1976-05-31 | 1977-05-31 | Produits cosmetiques contenant des n-hydroxyalkylamides d'acides alcanoiques comme agents hydratants de la peau |
| CH665777A CH626534A5 (en) | 1976-05-31 | 1977-05-31 | Cosmetic composition with a content of humectant for the skin |
| AT382377A AT351168B (de) | 1976-05-31 | 1977-05-31 | Kosmetische mittel mit einem gehalt an haut- feuchthaltefaktor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19762624293 DE2624293C2 (de) | 1976-05-31 | 1976-05-31 | Kosmetische Mittel mit einem Gehalt an Haut-Feuchthaltemitteln |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2624293A1 DE2624293A1 (de) | 1978-01-12 |
| DE2624293C2 true DE2624293C2 (de) | 1985-12-19 |
Family
ID=5979386
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19762624293 Expired DE2624293C2 (de) | 1976-05-31 | 1976-05-31 | Kosmetische Mittel mit einem Gehalt an Haut-Feuchthaltemitteln |
Country Status (11)
| Country | Link |
|---|---|
| JP (1) | JPS6055482B2 (cg-RX-API-DMAC10.html) |
| AT (1) | AT351168B (cg-RX-API-DMAC10.html) |
| BE (1) | BE855135A (cg-RX-API-DMAC10.html) |
| CH (1) | CH626534A5 (cg-RX-API-DMAC10.html) |
| DE (1) | DE2624293C2 (cg-RX-API-DMAC10.html) |
| DK (1) | DK202377A (cg-RX-API-DMAC10.html) |
| FR (1) | FR2353284A1 (cg-RX-API-DMAC10.html) |
| GB (1) | GB1554251A (cg-RX-API-DMAC10.html) |
| IT (1) | IT1085807B (cg-RX-API-DMAC10.html) |
| NL (1) | NL7705095A (cg-RX-API-DMAC10.html) |
| SE (1) | SE431398B (cg-RX-API-DMAC10.html) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR840000045B1 (ko) * | 1979-05-11 | 1984-01-28 | 콤베인 코오포레이팃드 | 섬유물의 염색용 조성물 |
| FR2499852A1 (fr) * | 1981-02-19 | 1982-08-20 | Rocador Sa | Medicament a base de n-hydroxyethylacetamide pour le traitement des affections occasionnees par la seborrhee sur le cuir chevelu humain |
| DE3233638A1 (de) * | 1982-09-10 | 1984-03-15 | Thilo & Co Gmbh Dr | Dermatologische zubereitung |
| DE3318789C2 (de) * | 1983-05-24 | 1987-04-02 | Eduard Gerlach GmbH Chemische Fabrik, 4990 Lübbecke | Deodorant |
| DE3600664A1 (de) * | 1986-01-13 | 1987-07-16 | Nattermann A & Cie | Pflanzenbehandlungsmittel |
| JPH0686373B2 (ja) * | 1987-02-05 | 1994-11-02 | 花王株式会社 | 化粧料 |
| EP0620000A3 (de) * | 1992-12-18 | 1994-11-02 | Rhone-Poulenc Rorer Gmbh | Kosmetische und/oder pharmazeutische Verwendung von N-Acylalkanolaminen |
| RU2121341C1 (ru) * | 1996-03-28 | 1998-11-10 | Валерий Николаевич Коновалов | Лечебно-косметический крем |
| DE19624455C2 (de) * | 1996-06-20 | 1998-08-27 | Henkel Kgaa | Sonnenschutzmittel in Form von O/W-Mikroemulsionen |
| CN108602759B (zh) * | 2016-01-29 | 2023-10-27 | 阿克苏诺贝尔化学品国际有限公司 | 制备烷醇胺烷基酰胺和多元醇的组合物的方法 |
| JP6628890B2 (ja) | 2016-01-29 | 2020-01-15 | ヌーリオン ケミカルズ インターナショナル ベスローテン フェノーツハップＮｏｕｒｙｏｎ Ｃｈｅｍｉｃａｌｓ Ｉｎｔｅｒｎａｔｉｏｎａｌ Ｂ．Ｖ． | アルカノールアミンアルキルアミドと他の湿潤剤との相乗効果 |
| CN108495615B (zh) | 2016-01-29 | 2021-07-06 | 阿克苏诺贝尔化学品国际有限公司 | 链烷醇胺烷基酰胺作为保湿剂的用途 |
| JP6247340B2 (ja) * | 2016-06-08 | 2017-12-13 | 高級アルコール工業株式会社 | アミドアルコールを含む化粧用基剤および化粧品 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1015261A (en) * | 1960-11-18 | 1965-12-31 | Kenneth Richard Dutton | Compositions based on short-chain substituted fatty acid amides and on amine complexes thereof, and exhibiting activity against micro-organisms |
-
1976
- 1976-05-31 DE DE19762624293 patent/DE2624293C2/de not_active Expired
-
1977
- 1977-05-09 SE SE7705385A patent/SE431398B/xx not_active IP Right Cessation
- 1977-05-09 NL NL7705095A patent/NL7705095A/xx not_active Application Discontinuation
- 1977-05-09 DK DK202377A patent/DK202377A/da unknown
- 1977-05-27 GB GB2242877A patent/GB1554251A/en not_active Expired
- 1977-05-27 IT IT2407777A patent/IT1085807B/it active
- 1977-05-27 BE BE177988A patent/BE855135A/xx not_active IP Right Cessation
- 1977-05-27 JP JP6128777A patent/JPS6055482B2/ja not_active Expired
- 1977-05-31 FR FR7716541A patent/FR2353284A1/fr active Granted
- 1977-05-31 AT AT382377A patent/AT351168B/de not_active IP Right Cessation
- 1977-05-31 CH CH665777A patent/CH626534A5/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| IT1085807B (it) | 1985-05-28 |
| JPS6055482B2 (ja) | 1985-12-05 |
| AT351168B (de) | 1979-07-10 |
| NL7705095A (nl) | 1977-12-02 |
| ATA382377A (de) | 1978-12-15 |
| GB1554251A (en) | 1979-10-17 |
| SE7705385L (sv) | 1977-12-01 |
| SE431398B (sv) | 1984-02-06 |
| CH626534A5 (en) | 1981-11-30 |
| FR2353284A1 (fr) | 1977-12-30 |
| JPS52148633A (en) | 1977-12-10 |
| BE855135A (fr) | 1977-11-28 |
| FR2353284B1 (cg-RX-API-DMAC10.html) | 1981-08-07 |
| DK202377A (da) | 1977-12-01 |
| DE2624293A1 (de) | 1978-01-12 |
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