CH499319A - Composition à propriétés tensio-actives - Google Patents
Composition à propriétés tensio-activesInfo
- Publication number
- CH499319A CH499319A CH580366A CH580366A CH499319A CH 499319 A CH499319 A CH 499319A CH 580366 A CH580366 A CH 580366A CH 580366 A CH580366 A CH 580366A CH 499319 A CH499319 A CH 499319A
- Authority
- CH
- Switzerland
- Prior art keywords
- water
- hair
- solution
- formula
- rinsed
- Prior art date
Links
- 238000002360 preparation method Methods 0.000 title abstract description 4
- 150000002170 ethers Chemical class 0.000 title abstract 2
- 239000004094 surface-active agent Substances 0.000 claims abstract description 5
- 239000000203 mixture Substances 0.000 claims description 41
- 239000007864 aqueous solution Substances 0.000 claims description 19
- 150000001875 compounds Chemical class 0.000 claims description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 239000002537 cosmetic Substances 0.000 claims description 6
- 239000002453 shampoo Substances 0.000 claims description 5
- 235000013336 milk Nutrition 0.000 claims description 3
- 239000008267 milk Substances 0.000 claims description 3
- 210000004080 milk Anatomy 0.000 claims description 3
- 239000002671 adjuvant Substances 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 239000000118 hair dye Substances 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 239000002562 thickening agent Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims 4
- 239000006071 cream Substances 0.000 claims 1
- 239000003995 emulsifying agent Substances 0.000 abstract description 6
- 239000004088 foaming agent Substances 0.000 abstract description 4
- 239000000080 wetting agent Substances 0.000 abstract description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 1
- VMPVEPPRYRXYNP-UHFFFAOYSA-I antimony(5+);pentachloride Chemical compound Cl[Sb](Cl)(Cl)(Cl)Cl VMPVEPPRYRXYNP-UHFFFAOYSA-I 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 238000006068 polycondensation reaction Methods 0.000 abstract 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 40
- 239000000243 solution Substances 0.000 description 30
- 239000006260 foam Substances 0.000 description 17
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- AOMUHOFOVNGZAN-UHFFFAOYSA-N N,N-bis(2-hydroxyethyl)dodecanamide Chemical compound CCCCCCCCCCCC(=O)N(CCO)CCO AOMUHOFOVNGZAN-UHFFFAOYSA-N 0.000 description 6
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
- 235000014655 lactic acid Nutrition 0.000 description 5
- 239000004310 lactic acid Substances 0.000 description 5
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 4
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- 239000001768 carboxy methyl cellulose Substances 0.000 description 4
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 4
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 4
- 239000003599 detergent Substances 0.000 description 4
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 239000002736 nonionic surfactant Substances 0.000 description 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 4
- 235000019441 ethanol Nutrition 0.000 description 3
- 238000005187 foaming Methods 0.000 description 3
- 210000004400 mucous membrane Anatomy 0.000 description 3
- -1 quaternary ammonium halides Chemical class 0.000 description 3
- OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 description 2
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 2
- LIFHMKCDDVTICL-UHFFFAOYSA-N 6-(chloromethyl)phenanthridine Chemical compound C1=CC=C2C(CCl)=NC3=CC=CC=C3C2=C1 LIFHMKCDDVTICL-UHFFFAOYSA-N 0.000 description 2
- 235000013162 Cocos nucifera Nutrition 0.000 description 2
- 244000060011 Cocos nucifera Species 0.000 description 2
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 241000283973 Oryctolagus cuniculus Species 0.000 description 2
- 239000005662 Paraffin oil Substances 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- BTBJBAZGXNKLQC-UHFFFAOYSA-N ammonium lauryl sulfate Chemical compound [NH4+].CCCCCCCCCCCCOS([O-])(=O)=O BTBJBAZGXNKLQC-UHFFFAOYSA-N 0.000 description 2
- 229940063953 ammonium lauryl sulfate Drugs 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 229960001484 edetic acid Drugs 0.000 description 2
- YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 2
- SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241001070941 Castanea Species 0.000 description 1
- 235000014036 Castanea Nutrition 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- ZCPCLAPUXMZUCD-UHFFFAOYSA-M dihexadecyl(dimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCC ZCPCLAPUXMZUCD-UHFFFAOYSA-M 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- HWYHDWGGACRVEH-UHFFFAOYSA-N n-methyl-n-(4-pyrrolidin-1-ylbut-2-ynyl)acetamide Chemical compound CC(=O)N(C)CC#CCN1CCCC1 HWYHDWGGACRVEH-UHFFFAOYSA-N 0.000 description 1
- 231100000344 non-irritating Toxicity 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
-
- 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/39—Derivatives containing from 2 to 10 oxyalkylene groups
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
- A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
- A61Q1/06—Lipsticks
-
- 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
- A61Q5/02—Preparations for cleaning the hair
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Emergency Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Cosmetics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyethers (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| LU48458A LU48458A1 (en)) | 1965-04-23 | 1965-04-23 | |
| LU49902 | 1965-11-22 | ||
| LU50850A LU50850A1 (en)) | 1966-04-06 | 1966-04-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH499319A true CH499319A (fr) | 1970-11-30 |
Family
ID=27350597
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH580366A CH499319A (fr) | 1965-04-23 | 1966-04-21 | Composition à propriétés tensio-actives |
| CH19268A CH465888A (fr) | 1965-04-23 | 1966-04-21 | Procédé de préparation de composés tensio-actifs non ioniques |
| CH19168A CH465887A (fr) | 1965-04-23 | 1966-04-21 | Procédé de préparation de polyéthers polyhalogénés |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH19268A CH465888A (fr) | 1965-04-23 | 1966-04-21 | Procédé de préparation de composés tensio-actifs non ioniques |
| CH19168A CH465887A (fr) | 1965-04-23 | 1966-04-21 | Procédé de préparation de polyéthers polyhalogénés |
Country Status (9)
| Country | Link |
|---|---|
| JP (1) | JPS5130138B1 (en)) |
| AT (1) | AT277462B (en)) |
| BE (1) | BE679901A (en)) |
| CH (3) | CH499319A (en)) |
| DE (2) | DE1617694C3 (en)) |
| GB (2) | GB1155712A (en)) |
| IT (1) | IT951511B (en)) |
| LU (1) | LU49902A1 (en)) |
| NL (1) | NL6605468A (en)) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4217296A (en) * | 1978-07-24 | 1980-08-12 | Fmc Corporation | Alkyl glyceryl ether sulfate salts and process for their preparation |
| DE3025434C2 (de) * | 1979-07-04 | 1982-09-16 | Nisso Petrochemical Industry Co., Ltd., Tokyo | Verfahren zur Herstellung von Alkylenglykoldiäthern |
| US4298764A (en) * | 1979-07-27 | 1981-11-03 | Fmc Corporation | Preparation of alkyl glyceryl ether alcohols |
| JPS6026366B2 (ja) * | 1979-09-07 | 1985-06-24 | 花王株式会社 | 油中水型化粧料 |
| LU83911A1 (fr) * | 1982-01-29 | 1983-09-02 | Oreal | Produit nettoyant des cheveux et de la peau a base d'acylise thionates et de polymeres cationiques |
| GB2224740B (en) * | 1985-08-30 | 1990-08-22 | Minnesota Mining & Mfg | Hydroxyl-terminated polyepichlorohydrin and derivatives |
| DE3840525A1 (de) * | 1988-12-01 | 1990-06-07 | Beiersdorf Ag | Kosmetische zubereitungen |
| JPH06102615B2 (ja) * | 1990-08-28 | 1994-12-14 | 花王株式会社 | 毛髪化粧料 |
| FR2673179B1 (fr) * | 1991-02-21 | 1993-06-11 | Oreal | Ceramides, leur procede de preparation et leurs applications en cosmetique et en dermopharmacie. |
| FR2727979B1 (fr) * | 1994-12-09 | 1998-07-31 | Oreal | Compositions a base d'un systeme abrasif et d'un systeme tensio-actif |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1108677B (de) * | 1959-12-31 | 1961-06-15 | Witten Gmbh Chem Werke | Verfahren zur Herstellung von Arylalkylalkoholen |
| DE1149343B (de) * | 1960-05-04 | 1963-05-30 | Devoe & Raynolds Co | Verfahren zur Herstellung partieller Glycidaether mehrwertiger Alkohole |
-
1965
- 1965-11-22 LU LU49902D patent/LU49902A1/xx unknown
-
1966
- 1966-04-20 AT AT371666A patent/AT277462B/de not_active IP Right Cessation
- 1966-04-21 CH CH580366A patent/CH499319A/fr not_active IP Right Cessation
- 1966-04-21 CH CH19268A patent/CH465888A/fr unknown
- 1966-04-21 CH CH19168A patent/CH465887A/fr unknown
- 1966-04-22 BE BE679901D patent/BE679901A/xx not_active IP Right Cessation
- 1966-04-22 IT IT970466A patent/IT951511B/it active
- 1966-04-22 NL NL6605468A patent/NL6605468A/xx unknown
- 1966-04-23 DE DE19661617694 patent/DE1617694C3/de not_active Expired
- 1966-04-23 DE DE19661593217 patent/DE1593217C3/de not_active Expired
- 1966-04-25 GB GB1778466A patent/GB1155712A/en not_active Expired
- 1966-04-25 GB GB5613267A patent/GB1155713A/en not_active Expired
-
1971
- 1971-12-21 JP JP10401971A patent/JPS5130138B1/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5130138B1 (en)) | 1976-08-30 |
| DE1593217B2 (en)) | 1973-10-11 |
| GB1155713A (en) | 1969-06-18 |
| LU49902A1 (en)) | 1967-05-22 |
| DE1617694B2 (de) | 1974-02-07 |
| DE1617694A1 (de) | 1970-03-26 |
| DE1593217A1 (de) | 1971-11-04 |
| DE1593217C3 (de) | 1982-11-04 |
| DE1617694C3 (de) | 1982-09-02 |
| CH465888A (fr) | 1968-11-30 |
| BE679901A (en)) | 1966-10-24 |
| GB1155712A (en) | 1969-06-18 |
| IT951511B (it) | 1973-07-10 |
| AT277462B (de) | 1969-12-29 |
| CH465887A (fr) | 1968-11-30 |
| NL6605468A (en)) | 1966-10-24 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |