CH626534A5 - Cosmetic composition with a content of humectant for the skin - Google Patents

Cosmetic composition with a content of humectant for the skin Download PDF

Info

Publication number: CH626534A5
Authority: CH; Switzerland
Prior art keywords: skin; weight; methyl; hydroxypropyl; propyl
Prior art date: 1976-05-31

Application number

CH665777A

Other languages

German (de)

English (en)

Inventor

Hinrich Dr Moeller

Rainer Dr Osberghaus

Original Assignee

Henkel Kgaa

Priority date (The priority date 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 date listed.)

1976-05-31

Filing date

1977-05-31

Publication date

1981-11-30

1977-05-31 Application filed by Henkel Kgaa filed Critical Henkel Kgaa

1981-11-30 Publication of CH626534A5 publication Critical patent/CH626534A5/de

Links

239000000203 mixture Substances 0.000 title description 16
239000002537 cosmetic Substances 0.000 title description 8
239000003906 humectant Substances 0.000 title 1
210000003491 skin Anatomy 0.000 description 41
239000000047 product Substances 0.000 description 22
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
-1 alkyl radical Chemical class 0.000 description 18
239000006071 cream Substances 0.000 description 14
239000000126 substance Substances 0.000 description 13
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
239000004909 Moisturizer Substances 0.000 description 10
210000002615 epidermis Anatomy 0.000 description 10
230000001333 moisturizer Effects 0.000 description 10
206010016807 Fluid retention Diseases 0.000 description 9
150000001408 amides Chemical class 0.000 description 9
125000004432 carbon atom Chemical group C* 0.000 description 9
239000003921 oil Substances 0.000 description 9
235000019198 oils Nutrition 0.000 description 9
239000002304 perfume Substances 0.000 description 8
239000000344 soap Substances 0.000 description 8
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 7
150000001875 compounds Chemical class 0.000 description 6
239000003599 detergent Substances 0.000 description 6
235000014113 dietary fatty acids Nutrition 0.000 description 6
239000000194 fatty acid Substances 0.000 description 6
229930195729 fatty acid Natural products 0.000 description 6
LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 6
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Natural products OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 5
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 5
239000002904 solvent Substances 0.000 description 5
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 4
238000010521 absorption reaction Methods 0.000 description 4
239000002253 acid Substances 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
239000003995 emulsifying agent Substances 0.000 description 4
229910052739 hydrogen Inorganic materials 0.000 description 4
239000001257 hydrogen Substances 0.000 description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
230000000475 sunscreen effect Effects 0.000 description 4
239000000516 sunscreening agent Substances 0.000 description 4
238000012360 testing method Methods 0.000 description 4
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
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-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
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
239000012459 cleaning agent Substances 0.000 description 3
SASYSVUEVMOWPL-NXVVXOECSA-N decyl oleate Chemical compound CCCCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC SASYSVUEVMOWPL-NXVVXOECSA-N 0.000 description 3
238000001035 drying Methods 0.000 description 3
230000007613 environmental effect Effects 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
150000004665 fatty acids Chemical class 0.000 description 3
235000011187 glycerol Nutrition 0.000 description 3
238000010348 incorporation Methods 0.000 description 3
238000005259 measurement Methods 0.000 description 3
230000007935 neutral effect Effects 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
150000003839 salts Chemical class 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
LEACJMVNYZDSKR-UHFFFAOYSA-N 2-octyldodecan-1-ol Chemical compound CCCCCCCCCCC(CO)CCCCCCCC LEACJMVNYZDSKR-UHFFFAOYSA-N 0.000 description 2
DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
241001440269 Cutina Species 0.000 description 2
QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 2
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 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 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
150000001336 alkenes Chemical class 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
238000009835 boiling Methods 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
239000012230 colorless oil Substances 0.000 description 2
239000008271 cosmetic emulsion Substances 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
230000001815 facial effect Effects 0.000 description 2
239000003205 fragrance Substances 0.000 description 2
150000002431 hydrogen Chemical class 0.000 description 2
125000002768 hydroxyalkyl group Chemical group 0.000 description 2
WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 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
AGQSGSYOSSBGLI-UHFFFAOYSA-N n,n-bis(2-hydroxyethyl)formamide Chemical compound OCCN(C=O)CCO AGQSGSYOSSBGLI-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
XFACEAHMBQFBTP-UHFFFAOYSA-N n-(1,3-dihydroxy-2-methylpropan-2-yl)acetamide Chemical compound CC(=O)NC(C)(CO)CO XFACEAHMBQFBTP-UHFFFAOYSA-N 0.000 description 2
IOJDOGFFOQYAQB-UHFFFAOYSA-N n-(1,3-dihydroxy-2-methylpropan-2-yl)formamide Chemical compound OCC(C)(CO)NC=O IOJDOGFFOQYAQB-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
239000000419 plant extract Substances 0.000 description 2
239000003755 preservative agent Substances 0.000 description 2
230000001681 protective effect Effects 0.000 description 2
239000011734 sodium Substances 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
235000019333 sodium laurylsulphate Nutrition 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
239000004094 surface-active agent Substances 0.000 description 2
239000003760 tallow Substances 0.000 description 2
OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 2
238000005406 washing Methods 0.000 description 2
210000002268 wool Anatomy 0.000 description 2
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
ZBLSOWYBBLPLQH-UHFFFAOYSA-N 2,2-dimethyl-N-(1,3,4,5,6-pentahydroxyhexan-2-yl)propanamide Chemical compound OCC(C(C(C(CO)O)O)O)NC(C(C)(C)C)=O ZBLSOWYBBLPLQH-UHFFFAOYSA-N 0.000 description 1
LJDSTRZHPWMDPG-UHFFFAOYSA-N 2-(butylamino)ethanol Chemical compound CCCCNCCO LJDSTRZHPWMDPG-UHFFFAOYSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
TYCOIVIBOJOGEW-UHFFFAOYSA-N CCN(CC(CO)O)C(=O)C(C)(C)C Chemical compound CCN(CC(CO)O)C(=O)C(C)(C)C TYCOIVIBOJOGEW-UHFFFAOYSA-N 0.000 description 1
208000019300 CLIPPERS Diseases 0.000 description 1
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
CMBYOWLFQAFZCP-UHFFFAOYSA-N Hexyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCCCCC CMBYOWLFQAFZCP-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-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
244000302151 Myroxylon pereirae Species 0.000 description 1
JLKLYCGCRJYJIM-UHFFFAOYSA-N N,N-bis(2-hydroxypropyl)-2,2-dimethylpropanamide Chemical compound CC(O)CN(CC(C)O)C(=O)C(C)(C)C JLKLYCGCRJYJIM-UHFFFAOYSA-N 0.000 description 1
FIVJLJQPROCGNZ-UHFFFAOYSA-N N,N-bis(2-hydroxypropyl)butanamide Chemical compound CCCC(=O)N(CC(C)O)CC(C)O FIVJLJQPROCGNZ-UHFFFAOYSA-N 0.000 description 1
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
FQPVJRTZZOIRBS-UHFFFAOYSA-N N-(1,3,4,5,6-pentahydroxyhexan-2-yl)butanamide Chemical compound OCC(C(C(C(CO)O)O)O)NC(CCC)=O FQPVJRTZZOIRBS-UHFFFAOYSA-N 0.000 description 1
CWYYDECQKQNMSW-UHFFFAOYSA-N N-(1,3,4,5,6-pentahydroxyhexan-2-yl)formamide Chemical compound OCC(C(C(C(CO)O)O)O)NC=O CWYYDECQKQNMSW-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
SDLOQKCDBDWZBM-UHFFFAOYSA-N N-(2,3-dihydroxypropyl)-N-ethylformamide Chemical compound OC(CN(C=O)CC)CO SDLOQKCDBDWZBM-UHFFFAOYSA-N 0.000 description 1
KGRIBXVNEJOEOR-UHFFFAOYSA-N N-(2,3-dihydroxypropyl)-N-ethylpentanamide Chemical compound OC(CN(C(CCCC)=O)CC)CO KGRIBXVNEJOEOR-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
PBKNGGPXQAKFMN-UHFFFAOYSA-N N-(2-hydroxybutyl)pentanamide Chemical compound OC(CNC(CCCC)=O)CC PBKNGGPXQAKFMN-UHFFFAOYSA-N 0.000 description 1
PQALZXRRHANGNI-UHFFFAOYSA-N N-(2-hydroxypropyl)-N,2,2-trimethylpropanamide Chemical compound CC(O)CN(C)C(=O)C(C)(C)C PQALZXRRHANGNI-UHFFFAOYSA-N 0.000 description 1
FWHDPYPFEFNAIS-UHFFFAOYSA-N N-[1-hydroxy-2-(hydroxymethyl)butan-2-yl]butanamide Chemical compound OCC(CO)(CC)NC(CCC)=O FWHDPYPFEFNAIS-UHFFFAOYSA-N 0.000 description 1
NOPDLWYZWFKQBO-UHFFFAOYSA-N N-[1-hydroxy-2-(hydroxymethyl)butan-2-yl]formamide Chemical compound CCC(CO)(CO)NC=O NOPDLWYZWFKQBO-UHFFFAOYSA-N 0.000 description 1
AUOZSDUXQONYLT-UHFFFAOYSA-N N-[1-hydroxy-2-(hydroxymethyl)butan-2-yl]pentanamide Chemical compound OCC(CO)(CC)NC(CCCC)=O AUOZSDUXQONYLT-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
239000005662 Paraffin oil Substances 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
235000021355 Stearic acid Nutrition 0.000 description 1
ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
239000000654 additive Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
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
150000003857 carboxamides Chemical class 0.000 description 1
229960000541 cetyl alcohol Drugs 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
208000021930 chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids Diseases 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
239000000470 constituent Substances 0.000 description 1
210000004087 cornea Anatomy 0.000 description 1
235000020379 cucumber juice Nutrition 0.000 description 1
SMVRDGHCVNAOIN-UHFFFAOYSA-L disodium;1-dodecoxydodecane;sulfate Chemical group [Na+].[Na+].[O-]S([O-])(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC SMVRDGHCVNAOIN-UHFFFAOYSA-L 0.000 description 1
QVBODZPPYSSMEL-UHFFFAOYSA-N dodecyl sulfate;2-hydroxyethylazanium Chemical group NCCO.CCCCCCCCCCCCOS(O)(=O)=O QVBODZPPYSSMEL-UHFFFAOYSA-N 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000000284 extract Substances 0.000 description 1
238000000605 extraction Methods 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
238000009472 formulation Methods 0.000 description 1
125000005456 glyceride group Chemical group 0.000 description 1
210000004209 hair Anatomy 0.000 description 1
210000003128 head Anatomy 0.000 description 1
230000036074 healthy skin Effects 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
229940100463 hexyl laurate Drugs 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
230000003301 hydrolyzing effect Effects 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
150000008040 ionic compounds Chemical class 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
229940039717 lanolin Drugs 0.000 description 1
235000019388 lanolin Nutrition 0.000 description 1
238000011068 loading method Methods 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000000034 method Methods 0.000 description 1
239000001157 myroxylon pereirae klotzsch resin Substances 0.000 description 1
CZKBFNIVILPSPZ-UHFFFAOYSA-N n,n-bis(2-hydroxyethyl)-2,2-dimethylpropanamide Chemical compound CC(C)(C)C(=O)N(CCO)CCO CZKBFNIVILPSPZ-UHFFFAOYSA-N 0.000 description 1
FZALBMZJCBBKRI-UHFFFAOYSA-N n,n-bis(2-hydroxyethyl)butanamide Chemical compound CCCC(=O)N(CCO)CCO FZALBMZJCBBKRI-UHFFFAOYSA-N 0.000 description 1
RBYBLKRMFXJVST-UHFFFAOYSA-N n,n-bis(2-hydroxyethyl)pentanamide Chemical compound CCCCC(=O)N(CCO)CCO RBYBLKRMFXJVST-UHFFFAOYSA-N 0.000 description 1
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XFKBLJHKZWCBJQ-UHFFFAOYSA-N n-(1,3-dihydroxy-2-methylpropan-2-yl)-2,2-dimethylpropanamide Chemical compound CC(C)(C)C(=O)NC(C)(CO)CO XFKBLJHKZWCBJQ-UHFFFAOYSA-N 0.000 description 1
CDMCNTSAAROGLB-UHFFFAOYSA-N n-(1,3-dihydroxy-2-methylpropan-2-yl)butanamide Chemical compound CCCC(=O)NC(C)(CO)CO CDMCNTSAAROGLB-UHFFFAOYSA-N 0.000 description 1
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CXAPQWXAZIHLQI-UHFFFAOYSA-N n-(1,3-dihydroxypropan-2-yl)-2,2-dimethylpropanamide Chemical compound CC(C)(C)C(=O)NC(CO)CO CXAPQWXAZIHLQI-UHFFFAOYSA-N 0.000 description 1
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VZDYALZNRIRJNP-UHFFFAOYSA-N n-(1,3-dihydroxypropan-2-yl)butanamide Chemical compound CCCC(=O)NC(CO)CO VZDYALZNRIRJNP-UHFFFAOYSA-N 0.000 description 1
ZMUNCSIDODXWDP-UHFFFAOYSA-N n-(1,3-dihydroxypropan-2-yl)formamide Chemical compound OCC(CO)NC=O ZMUNCSIDODXWDP-UHFFFAOYSA-N 0.000 description 1
UHIOSVNTEQBUGY-UHFFFAOYSA-N n-(1,3-dihydroxypropan-2-yl)pentanamide Chemical compound CCCCC(=O)NC(CO)CO UHIOSVNTEQBUGY-UHFFFAOYSA-N 0.000 description 1
HSQLIHQKMIJWSS-UHFFFAOYSA-N n-(1,3-dihydroxypropan-2-yl)propanamide Chemical compound CCC(=O)NC(CO)CO HSQLIHQKMIJWSS-UHFFFAOYSA-N 0.000 description 1
DCKYBBYSZIOTHV-UHFFFAOYSA-N n-(1-hydroxy-2-methylpropan-2-yl)-2,2-dimethylpropanamide Chemical compound CC(C)(C)C(=O)NC(C)(C)CO DCKYBBYSZIOTHV-UHFFFAOYSA-N 0.000 description 1
WSEURCHZECZCGQ-UHFFFAOYSA-N n-(1-hydroxy-2-methylpropan-2-yl)acetamide Chemical compound CC(=O)NC(C)(C)CO WSEURCHZECZCGQ-UHFFFAOYSA-N 0.000 description 1
FUCZYUAUTVNZRS-UHFFFAOYSA-N n-(1-hydroxy-2-methylpropan-2-yl)butanamide Chemical compound CCCC(=O)NC(C)(C)CO FUCZYUAUTVNZRS-UHFFFAOYSA-N 0.000 description 1
DLFOIXQOODRPPX-UHFFFAOYSA-N n-(1-hydroxy-2-methylpropan-2-yl)formamide Chemical compound OCC(C)(C)NC=O DLFOIXQOODRPPX-UHFFFAOYSA-N 0.000 description 1
BMILLPSADVZITM-UHFFFAOYSA-N n-(1-hydroxy-2-methylpropan-2-yl)pentanamide Chemical compound CCCCC(=O)NC(C)(C)CO BMILLPSADVZITM-UHFFFAOYSA-N 0.000 description 1
QSJZKLASYBUBNS-UHFFFAOYSA-N n-(1-hydroxy-2-methylpropan-2-yl)propanamide Chemical compound CCC(=O)NC(C)(C)CO QSJZKLASYBUBNS-UHFFFAOYSA-N 0.000 description 1
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
ATOPDSQFLUQNKA-UHFFFAOYSA-N n-(2,3-dihydroxypropyl)-2,2-dimethylpropanamide Chemical compound CC(C)(C)C(=O)NCC(O)CO ATOPDSQFLUQNKA-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
FHBNPEJLQIGOPC-UHFFFAOYSA-N n-(2,3-dihydroxypropyl)acetamide Chemical compound CC(=O)NCC(O)CO FHBNPEJLQIGOPC-UHFFFAOYSA-N 0.000 description 1
LAVYZMYQWIRTEA-UHFFFAOYSA-N n-(2,3-dihydroxypropyl)butanamide Chemical compound CCCC(=O)NCC(O)CO LAVYZMYQWIRTEA-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
QJOQSNARVCFLIV-UHFFFAOYSA-N n-(2,3-dihydroxypropyl)propanamide Chemical compound CCC(=O)NCC(O)CO QJOQSNARVCFLIV-UHFFFAOYSA-N 0.000 description 1
LTKKVHOQYLMJFD-UHFFFAOYSA-N n-(2-hydroxybutyl)acetamide Chemical compound CCC(O)CNC(C)=O LTKKVHOQYLMJFD-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
ADTGZIJRMJKELC-UHFFFAOYSA-N n-(2-hydroxyethyl)-2,2-dimethylpropanamide Chemical compound CC(C)(C)C(=O)NCCO ADTGZIJRMJKELC-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
BMYBBGMVRHGUJW-UHFFFAOYSA-N n-(2-hydroxypropyl)-n-methylformamide Chemical compound CC(O)CN(C)C=O BMYBBGMVRHGUJW-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
WYRFKDCNTSFHBX-UHFFFAOYSA-N n-(3-hydroxypropyl)formamide Chemical compound OCCCNC=O WYRFKDCNTSFHBX-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
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
JGAAIGKMNGHHHI-UHFFFAOYSA-N n-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]acetamide Chemical compound CC(=O)NC(CO)(CO)CO JGAAIGKMNGHHHI-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
ZIZWZRGEIHXUGR-UHFFFAOYSA-N n-[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]formamide Chemical compound OCC(CO)(CO)NC=O ZIZWZRGEIHXUGR-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
SYJRTPKIVOIJHR-UHFFFAOYSA-N n-[1-hydroxy-2-(hydroxymethyl)butan-2-yl]-2,2-dimethylpropanamide Chemical compound CCC(CO)(CO)NC(=O)C(C)(C)C SYJRTPKIVOIJHR-UHFFFAOYSA-N 0.000 description 1
HVXXNAOQUJQTTR-UHFFFAOYSA-N n-[1-hydroxy-2-(hydroxymethyl)butan-2-yl]acetamide Chemical compound CCC(CO)(CO)NC(C)=O HVXXNAOQUJQTTR-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
BXWNKGSJHAJOGX-UHFFFAOYSA-N n-hexadecyl alcohol Natural products CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
235000016709 nutrition Nutrition 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-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
235000015277 pork Nutrition 0.000 description 1
QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 description 1
229940080818 propionamide Drugs 0.000 description 1
239000011814 protection agent Substances 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
229940100486 rice starch Drugs 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
235000011121 sodium hydroxide Nutrition 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
239000000243 solution Substances 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
239000002562 thickening agent Substances 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
150000003722 vitamin derivatives Chemical class 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000008096 xylene Substances 0.000 description 1
239000011787 zinc oxide 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)

CH665777A 1976-05-31 1977-05-31 Cosmetic composition with a content of humectant for the skin CH626534A5 (en)

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 (1)

Publication Number	Publication Date
CH626534A5 true CH626534A5 (en)	1981-11-30

Family

ID=5979386

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH665777A CH626534A5 (en)	1976-05-31	1977-05-31	Cosmetic composition with a content of humectant for the skin

Country Status (11)

Country	Link
JP (1)	JPS6055482B2 (da)
AT (1)	AT351168B (da)
BE (1)	BE855135A (da)
CH (1)	CH626534A5 (da)
DE (1)	DE2624293C2 (da)
DK (1)	DK202377A (da)
FR (1)	FR2353284A1 (da)
GB (1)	GB1554251A (da)
IT (1)	IT1085807B (da)
NL (1)	NL7705095A (da)
SE (1)	SE431398B (da)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
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
EP3408255B1 (en)	2016-01-29	2020-01-08	Nouryon Chemicals International B.V.	Method of making a composition of an alkanolamine alkylamide and a polyol
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ＮｏｕｒｙｏｎＣｈｅｍｉｃａｌｓＩｎｔｅｒｎａｔｉｏｎａｌＢ．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)

* Cited by examiner, † Cited by third party
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 NL NL7705095A patent/NL7705095A/xx not_active Application Discontinuation
- 1977-05-09 DK DK202377A patent/DK202377A/da unknown
- 1977-05-09 SE SE7705385A patent/SE431398B/xx not_active IP Right Cessation
- 1977-05-27 JP JP6128777A patent/JPS6055482B2/ja not_active Expired
- 1977-05-27 BE BE177988A patent/BE855135A/xx not_active IP Right Cessation
- 1977-05-27 IT IT2407777A patent/IT1085807B/it active
- 1977-05-27 GB GB2242877A patent/GB1554251A/en not_active Expired
- 1977-05-31 CH CH665777A patent/CH626534A5/de not_active IP Right Cessation
- 1977-05-31 AT AT382377A patent/AT351168B/de not_active IP Right Cessation
- 1977-05-31 FR FR7716541A patent/FR2353284A1/fr active Granted

Also Published As

Publication number	Publication date
SE7705385L (sv)	1977-12-01
NL7705095A (nl)	1977-12-02
DE2624293A1 (de)	1978-01-12
FR2353284A1 (fr)	1977-12-30
JPS6055482B2 (ja)	1985-12-05
ATA382377A (de)	1978-12-15
GB1554251A (en)	1979-10-17
FR2353284B1 (da)	1981-08-07
IT1085807B (it)	1985-05-28
DE2624293C2 (de)	1985-12-19
AT351168B (de)	1979-07-10
JPS52148633A (en)	1977-12-10
DK202377A (da)	1977-12-01
SE431398B (sv)	1984-02-06
BE855135A (fr)	1977-11-28

Legal Events

Date	Code	Title	Description
1989-01-31	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
DE2703185A1 (de)	1978-08-10	Kosmetische mittel mit einem gehalt an haut-feuchthaltemitteln
DE2704904A1 (de)	1978-08-10	Kosmetische mittel mit einem gehalt an haut-feuchthaltemitteln
US4143159A (en)	1979-03-06	Skin-care agents containing hydroxyalkyl carboxamides and process
DE68905770T2 (de)	1993-07-08	Topische zusammensetzung.
EP3419986B1 (de)	2025-11-05	Rhamnolipidamide zur haarduftstoff-retention
EP3419985B1 (de)	2025-04-09	Rhamnolipidester als nichtionische tenside zur kosmetischen anwendung
DE2151740C3 (de)	1975-03-13	Haarkosmetische Mittel
DE2624293C2 (de)	1985-12-19	Kosmetische Mittel mit einem Gehalt an Haut-Feuchthaltemitteln
DE68905771T2 (de)	1993-07-08	Topische zusammensetzung.
DE2404070A1 (de)	1975-08-14	Hautpflege- und hautschutzmittel mit einem gehalt an haut-feuchthaltemitteln
DE2404047A1 (de)	1975-08-14	Hautpflege- und hautschutzmittel mit einem gehalt an haut-feuchthaltemitteln
DE3633453A1 (de)	1987-04-02	Zusammensetzungen auf der basis von lysin- und argininsalzen
DE69001515T2 (de)	1993-09-09	Urethan-derivate, ihre herstellung und verwendung als hautbefeuchtendes mittel in kosmetischen und pharmazeutischen zubereitungen zur behandlung trockener haut.
DE2421638A1 (de)	1975-11-20	Hautpflege- und hautschutzmittel mit einem gehalt an haut-feuchthaltemitteln
DE4443645C2 (de)	1997-08-14	Seifenfreie kosmetische und/oder pharmazeutische Zubereitungen
DE2746650A1 (de)	1979-04-26	Kosmetische mittel mit einem gehalt an haut-feuchthaltemitteln
DE69312595T2 (de)	1997-12-04	Verwendung von Aminopolyol-carbamaten als Verdickungsmittel in Tensidlösungen
DE2421618A1 (de)	1975-11-20	Hautpflege- und hautschutzmittel mit einem gehalt an haut-feuchthaltemitteln
DE2632391A1 (de)	1978-01-26	Kosmetische mittel mit einem gehalt an haut-feuchthaltemitteln
DE2604554A1 (de)	1977-08-11	Verwendung von amiden mehrbasiger aliphatischer carbonsaeuren als haut- feuchthaltemittel
EP0075906A2 (de)	1983-04-06	Haar- und Körperreinigungsmittel mit einem Gehalt an Alkylsulfatobetainen
EP0371339B1 (de)	1993-03-03	Oberflächenaktive Mischungen
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