RU2000126397A - COSMETIC COMPOSITIONS CONTAINING VINYLDYMETICON AND DIMETICON COPOLYMER AND AIR CONDITIONING AGENT, AND ALSO THE APPLICATION OF THESE COMPOSITIONS - Google Patents
COSMETIC COMPOSITIONS CONTAINING VINYLDYMETICON AND DIMETICON COPOLYMER AND AIR CONDITIONING AGENT, AND ALSO THE APPLICATION OF THESE COMPOSITIONSInfo
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- RU2000126397A RU2000126397A RU2000126397/14A RU2000126397A RU2000126397A RU 2000126397 A RU2000126397 A RU 2000126397A RU 2000126397/14 A RU2000126397/14 A RU 2000126397/14A RU 2000126397 A RU2000126397 A RU 2000126397A RU 2000126397 A RU2000126397 A RU 2000126397A
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- 239000000203 mixture Substances 0.000 title claims 31
- 239000003795 chemical substances by application Substances 0.000 title claims 5
- 239000002537 cosmetic Substances 0.000 title claims 4
- 238000004378 air conditioning Methods 0.000 title 1
- 229920001577 copolymer Polymers 0.000 title 1
- 229920001296 polysiloxane Polymers 0.000 claims 14
- -1 sulfo-galactosyl Chemical group 0.000 claims 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 8
- 239000001993 wax Substances 0.000 claims 8
- 150000001875 compounds Chemical class 0.000 claims 6
- 125000004432 carbon atoms Chemical group C* 0.000 claims 5
- 239000003921 oil Substances 0.000 claims 5
- 235000019198 oils Nutrition 0.000 claims 5
- 229940106189 Ceramides Drugs 0.000 claims 4
- 239000010775 animal oil Substances 0.000 claims 4
- 150000001783 ceramides Chemical class 0.000 claims 4
- 239000004094 surface-active agent Substances 0.000 claims 4
- 239000008158 vegetable oil Substances 0.000 claims 4
- 238000007259 addition reaction Methods 0.000 claims 3
- 125000002091 cationic group Chemical group 0.000 claims 3
- 230000003750 conditioning Effects 0.000 claims 3
- 235000014113 dietary fatty acids Nutrition 0.000 claims 3
- 239000000194 fatty acid Substances 0.000 claims 3
- 150000004665 fatty acids Chemical class 0.000 claims 3
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 3
- 239000000463 material Substances 0.000 claims 3
- 235000015112 vegetable and seed oil Nutrition 0.000 claims 3
- 239000004215 Carbon black (E152) Substances 0.000 claims 2
- 102000011782 Keratins Human genes 0.000 claims 2
- 108010076876 Keratins Proteins 0.000 claims 2
- 244000165082 Lavanda vera Species 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 125000001931 aliphatic group Chemical group 0.000 claims 2
- 125000000129 anionic group Chemical group 0.000 claims 2
- 239000003054 catalyst Substances 0.000 claims 2
- 125000002519 galactosyl group Chemical group C1([C@H](O)[C@@H](O)[C@@H](O)[C@H](O1)CO)* 0.000 claims 2
- 125000003147 glycosyl group Chemical group 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 229920000098 polyolefin Polymers 0.000 claims 2
- 239000002453 shampoo Substances 0.000 claims 2
- 238000005406 washing Methods 0.000 claims 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 1
- 240000006054 Agastache cana Species 0.000 claims 1
- 235000007639 Anthemis cotula Nutrition 0.000 claims 1
- 235000000832 Ayote Nutrition 0.000 claims 1
- 240000003538 Chamaemelum nobile Species 0.000 claims 1
- 235000007866 Chamaemelum nobile Nutrition 0.000 claims 1
- 244000223760 Cinnamomum zeylanicum Species 0.000 claims 1
- 235000004310 Cinnamomum zeylanicum Nutrition 0.000 claims 1
- 235000005979 Citrus limon Nutrition 0.000 claims 1
- 240000002268 Citrus limon Species 0.000 claims 1
- 240000009226 Corylus americana Species 0.000 claims 1
- 235000001543 Corylus americana Nutrition 0.000 claims 1
- 235000007466 Corylus avellana Nutrition 0.000 claims 1
- 240000004244 Cucurbita moschata Species 0.000 claims 1
- 235000009854 Cucurbita moschata Nutrition 0.000 claims 1
- 235000009804 Cucurbita pepo subsp pepo Nutrition 0.000 claims 1
- SNPLKNRPJHDVJA-ZETCQYMHSA-N D-panthenol Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCCO SNPLKNRPJHDVJA-ZETCQYMHSA-N 0.000 claims 1
- AFFLGGQVNFXPEV-UHFFFAOYSA-N Decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- 229940044949 Eucalyptus oil Drugs 0.000 claims 1
- 241001553290 Euphorbia antisyphilitica Species 0.000 claims 1
- 239000005792 Geraniol Substances 0.000 claims 1
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 claims 1
- 235000010469 Glycine max Nutrition 0.000 claims 1
- 240000007842 Glycine max Species 0.000 claims 1
- 240000006669 Helianthus annuus Species 0.000 claims 1
- 235000003222 Helianthus annuus Nutrition 0.000 claims 1
- 235000010650 Hyssopus officinalis Nutrition 0.000 claims 1
- 241000592238 Juniperus communis Species 0.000 claims 1
- 235000010701 Lavanda vera Nutrition 0.000 claims 1
- 235000002997 Lavandula Nutrition 0.000 claims 1
- 235000003515 Lavandula officinalis Nutrition 0.000 claims 1
- 235000007232 Matricaria chamomilla Nutrition 0.000 claims 1
- 235000009421 Myristica fragrans Nutrition 0.000 claims 1
- 240000006984 Myristica fragrans Species 0.000 claims 1
- VODZWWMEJITOND-OWWNRXNESA-N N-Stearoylsphingosine Chemical compound CCCCCCCCCCCCCCCCCC(=O)NC(CO)C(O)\C=C\CCCCCCCCCCCCC VODZWWMEJITOND-OWWNRXNESA-N 0.000 claims 1
- 240000007817 Olea europaea Species 0.000 claims 1
- 240000007594 Oryza sativa Species 0.000 claims 1
- 235000007164 Oryza sativa Nutrition 0.000 claims 1
- 229940101267 Panthenol Drugs 0.000 claims 1
- 240000008426 Persea americana Species 0.000 claims 1
- 229920001083 Polybutene Polymers 0.000 claims 1
- 239000004698 Polyethylene (PE) Substances 0.000 claims 1
- 240000004926 Ribes cereum Species 0.000 claims 1
- 235000006402 Ribes cereum var cereum Nutrition 0.000 claims 1
- 235000006398 Ribes cereum var colubrinum Nutrition 0.000 claims 1
- 240000003136 Rosmarinus officinalis Species 0.000 claims 1
- 240000000513 Santalum album Species 0.000 claims 1
- 235000008632 Santalum album Nutrition 0.000 claims 1
- 235000003434 Sesamum indicum Nutrition 0.000 claims 1
- 240000003670 Sesamum indicum Species 0.000 claims 1
- 244000044822 Simmondsia californica Species 0.000 claims 1
- 235000004433 Simmondsia californica Nutrition 0.000 claims 1
- 235000007303 Thymus vulgaris Nutrition 0.000 claims 1
- 240000002657 Thymus vulgaris Species 0.000 claims 1
- 229940029983 VITAMINS Drugs 0.000 claims 1
- 229940021016 Vitamin IV solution additives Drugs 0.000 claims 1
- 240000006365 Vitis vinifera Species 0.000 claims 1
- 235000014787 Vitis vinifera Nutrition 0.000 claims 1
- 240000008042 Zea mays Species 0.000 claims 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive Effects 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000002877 alkyl aryl group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000005466 alkylenyl group Chemical group 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 239000002280 amphoteric surfactant Substances 0.000 claims 1
- 239000012164 animal wax Substances 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 235000013871 bee wax Nutrition 0.000 claims 1
- 239000012166 beeswax Substances 0.000 claims 1
- 238000004061 bleaching Methods 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 235000001544 chamomile Nutrition 0.000 claims 1
- 235000017803 cinnamon Nutrition 0.000 claims 1
- 239000001926 citrus aurantium l. subsp. bergamia wright et arn. oil Substances 0.000 claims 1
- 239000003086 colorant Substances 0.000 claims 1
- 235000005822 corn Nutrition 0.000 claims 1
- 235000005824 corn Nutrition 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 238000004043 dyeing Methods 0.000 claims 1
- 239000000839 emulsion Substances 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- 239000010642 eucalyptus oil Substances 0.000 claims 1
- 235000021323 fish oil Nutrition 0.000 claims 1
- 239000003205 fragrance Substances 0.000 claims 1
- 125000000524 functional group Chemical group 0.000 claims 1
- 229940113087 geraniol Drugs 0.000 claims 1
- 229930008393 geraniol Natural products 0.000 claims 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 1
- 235000011187 glycerol Nutrition 0.000 claims 1
- 235000009754 grape Nutrition 0.000 claims 1
- 235000012333 grape Nutrition 0.000 claims 1
- 125000006038 hexenyl group Chemical group 0.000 claims 1
- 150000002430 hydrocarbons Chemical group 0.000 claims 1
- 238000006459 hydrosilylation reaction Methods 0.000 claims 1
- 150000001261 hydroxy acids Chemical class 0.000 claims 1
- 229920000831 ionic polymer Polymers 0.000 claims 1
- 229940119170 jojoba wax Drugs 0.000 claims 1
- 239000001102 lavandula vera Substances 0.000 claims 1
- 235000018219 lavender Nutrition 0.000 claims 1
- 239000001702 nutmeg Substances 0.000 claims 1
- 239000012186 ozocerite Substances 0.000 claims 1
- 235000020957 pantothenol Nutrition 0.000 claims 1
- 239000011619 pantothenol Substances 0.000 claims 1
- 239000012188 paraffin wax Substances 0.000 claims 1
- 235000005426 persea americana Nutrition 0.000 claims 1
- 239000001161 piper cubeba l. fruit oil Substances 0.000 claims 1
- 229920000573 polyethylene Polymers 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 230000002335 preservative Effects 0.000 claims 1
- 239000003755 preservative agent Substances 0.000 claims 1
- 239000003531 protein hydrolysate Substances 0.000 claims 1
- 102000004169 proteins and genes Human genes 0.000 claims 1
- 108090000623 proteins and genes Proteins 0.000 claims 1
- 235000015136 pumpkin Nutrition 0.000 claims 1
- 235000009566 rice Nutrition 0.000 claims 1
- 150000003871 sulfonates Chemical class 0.000 claims 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims 1
- 239000002562 thickening agent Substances 0.000 claims 1
- 150000003573 thiols Chemical class 0.000 claims 1
- 239000001585 thymus vulgaris Substances 0.000 claims 1
- 239000012178 vegetable wax Substances 0.000 claims 1
- 239000010679 vetiver oil Substances 0.000 claims 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
- 239000011782 vitamin Substances 0.000 claims 1
- 235000013343 vitamin Nutrition 0.000 claims 1
- 229930003231 vitamins Natural products 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- GLZPCOQZEFWAFX-JXMROGBWSA-N β-Geraniol Chemical compound CC(C)=CCC\C(C)=C\CO GLZPCOQZEFWAFX-JXMROGBWSA-N 0.000 claims 1
- 0 CC(C(*)CI)N Chemical compound CC(C(*)CI)N 0.000 description 3
Claims (20)
синтетических масел,
животных или растительных масел,
фторированных и перфторированных масел,
природных или синтетических восков,
керамидов приведенной ниже формулы I
в которой R1 обозначает насыщенный или ненасыщенный, нормальный или разветвленный алкильный радикал, являющийся производным от жирных С14-С30-кислот, который может быть замещен гидроксильной группой в положении α или гидроксильной группой в положении ω, эстерифицированной насыщенной или ненасыщенной жирной С16-С30-кислотой;
R2 обозначает атом водорода или радикал (гликозил)n, (галактозил)mили сульфогалактозил, в которых n является целым числом от 1 до 4 и m является целым числом от 1 до 8;
R3 обозначает насыщенный или ненасыщенный С15-С26-углеводородный радикал в положении α, который может быть замещен одним или несколькими С1-С14-алкильными радикалами,
при условии, что в случае природных керамидов или гликокерамидов, R3 может также обозначать α-гидрокси-С15-С26-алкильный радикал, в котором гидроксильная группа может быть эстерифицирована С16-С30-α-гидроксикислотой,
и по меньшей мере один силиконовый сополимер с вязкостью от 106 до 100•106 сПз, образующийся в результате реакции присоединения в присутствии катализатора по меньшей мере
(а) одного полисилоксана формулы I
в которой R1 обозначает группу, способную участвовать в реакции присоединения цепи, такую, например, как атом водорода, алифатическая группа, имеющая этиленовую ненасыщенность, в частности винил, аллил или гексенил;
группы R2 в формуле I обозначают алкил, имеющий 1-20 атомов углерода, циклоалкил, имеющий 5 или 6 атомов углерода, арил, алкиларил, имеющий 7-20 атомов углерода, или гидроксил и могут, кроме того, содержать функциональные группы, такие как группы простых эфиров, аминов, карбоксильные, гидроксильные, тиоловые, группы сложных эфиров, сульфонатов, сульфатов;
n является целым числом, при котором полисилоксан формулы I имеет кинематическую вязкость, преимущественно составляющую от 1 до 1•106 мм2/c;
(b) и по меньшей мере одного силиконового соединения, содержащего по меньшей мере одну или самое большее две группы, способные реагировать с группами R1 полисилоксана (а), причем по крайней мере одно из соединений типа (а) или (b) содержит алифатическую группу, имеющую этиленовую ненасыщенность.1. Cosmetic composition, characterized in that it contains in a cosmetically acceptable medium at least one conditioning agent selected from
synthetic oils
animal or vegetable oils
fluorinated and perfluorinated oils,
natural or synthetic waxes
ceramides of formula I below
in which R 1 denotes a saturated or unsaturated, normal or branched alkyl radical derived from C 14 -C 30 fatty acids, which can be substituted by a hydroxyl group in the α position or a hydroxyl group in the ω position, esterified with a saturated or unsaturated fatty C 16 - With 30 - acid;
R 2 denotes a hydrogen atom or a radical (glycosyl) n , (galactosyl) m or sulfo-galactosyl, in which n is an integer from 1 to 4 and m is an integer from 1 to 8;
R 3 denotes a saturated or unsaturated C 15 -C 26 -hydrocarbon radical in the α position, which may be substituted by one or more C 1 -C 14 -alkyl radicals,
with the proviso that in the case of natural ceramides or glycoceramides, R 3 can also denote an α-hydroxy-C 15 -C 26 -alkyl radical, in which a hydroxyl group can be esterified with C 16 -C 30 -α-hydroxy acid,
and at least one silicone copolymer with a viscosity of from 10 6 to 100 • 10 6 cPz, resulting from the addition reaction in the presence of a catalyst, at least
(a) one polysiloxane of formula I
in which R 1 denotes a group capable of participating in a chain addition reaction, such as, for example, a hydrogen atom, an aliphatic group having ethylene unsaturation, in particular vinyl, allyl or hexenyl;
the R 2 groups in formula I are alkyl having 1-20 carbon atoms, cycloalkyl having 5 or 6 carbon atoms, aryl, alkylaryl having 7-20 carbon atoms, or hydroxyl and may, in addition, contain functional groups such as groups of ethers, amines, carboxyl, hydroxyl, thiol, groups of esters, sulfonates, sulfates;
n is an integer such that the polysiloxane of formula I has a kinematic viscosity, preferably between 1 and 1 × 10 6 mm 2 / s;
(b) and at least one silicone compound containing at least one or at most two groups capable of reacting with R 1 groups of the polysiloxane (a), and at least one of the compounds of type (a) or (b) contains aliphatic group having ethylenic unsaturation.
(a) одного α, ω-дивинилполидиметилсилоксана и
(b) одного α, ω-дигидрополидиметилсилоксана.4. Composition according to any one of paragraphs. 1-3, characterized in that the silicone copolymer is obtained by the addition reaction in the presence of a hydrosilylation catalyst at least
(a) one α, ω-divinylpolydimethylsiloxane and
(b) single α, ω-dihydropolydimethylsiloxane.
2-N-линолеиламинооктадекан-1,3-диол,
2-N-олеиламинооктадекан-1, 3-диол,
2-N-пальмитиламинооктадекан-1,3-диол,
2-N-стеариламинооктадекан-1,3-диол,
2-N-бегениламинооктадекан-1,3-диол,
2-N-[2-гидроксипальмитил] аминооктадекан-1,3-диол,
2-N-стеариламино-октадекан-1,3,4-триол и, в частности,
N-стеарилфитосфингозин,
2-N-пальмитиламиногексадекан-1,3-диол,
или смеси этих соединений.10. Composition according to any one of paragraphs. 1-6, characterized in that the compounds of ceramide type are chosen from the following compounds
2-N-linoleyl-aminooctadecan-1,3-diol,
2-N-oleylaminoctadecan-1, 3-diol,
2-N-palmitylaminooctadecan-1,3-diol,
2-N-stearylamino-octadecan-1,3-diol,
2-N-behenylamino-octadecan-1,3-diol,
2-N- [2-hydroxypalmityl] aminooctadecan-1,3-diol,
2-N-stearylamino-octadecan-1,3,4-triol and, in particular,
N-stearyl Fitosphingosine,
2-N-palmitylaminohexadecane-1,3-diol,
or mixtures of these compounds.
синтетических масел,
животных или растительных масел,
фторированных и перфторированных масел,
природных или синтетических восков,
керамидов приведенной ниже формулы I
в которой R1 обозначает насыщенный или ненасыщенный, нормальный или разветвленный алкильный радикал, являющийся производным жирных С14-С30-кислот, который может быть замещен гидроксильной группой в положении α или гидроксильной группой в положении ω, эстерифицированной насыщенной или ненасыщенной жирной С16-С30-кислотой;
R2 обозначает атом водорода или радикал (гликозил)n, (галактозил)m или сульфогалактозил, в которых n является целым числом от 1 до 4 и m является целым числом от 1 до 8;
R3 обозначает насыщенный или ненасыщенный С15-С26-углеводородный радикал в положении α, который может быть замещен одним или несколькими С1-С14-алкильными радикалами,
при условии, что в случае природных керамидов или гликокерамидов, R3 может также обозначать α-гидрокси-С15-С2б-алкильный радикал, в котором гидроксильная группа может быть эстерифицирована С16-С30-α-гидроксикислотой.20. Application of silicone copolymer, as defined in paragraphs. 1-5 in or for the preparation of a cosmetic composition containing a conditioning agent selected from:
synthetic oils
animal or vegetable oils
fluorinated and perfluorinated oils,
natural or synthetic waxes
ceramides of formula I below
in which R 1 denotes a saturated or unsaturated, normal or branched alkyl radical derived from C 14 -C 30 fatty acids, which can be substituted with a hydroxyl group in the α position or a hydroxyl group in the ω position, esterified with a saturated or unsaturated C 16 - esterified With 30 -acid;
R 2 denotes a hydrogen atom or a radical (glycosyl) n , (galactosyl) m or sulfo-galactosyl, in which n is an integer from 1 to 4 and m is an integer from 1 to 8;
R 3 denotes a saturated or unsaturated C 15 -C 26 -hydrocarbon radical in the α position, which may be substituted by one or more C 1 -C 14 -alkyl radicals,
provided that in the case of natural ceramides or glycoceramides, R 3 can also denote an α-hydroxy-C 15 -C 2b- alkyl radical, in which a hydroxyl group can be esterified with C 16 -C 30 -α-hydroxy-acid.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9913097A FR2799970B1 (en) | 1999-10-20 | 1999-10-20 | COSMETIC COMPOSITIONS CONTAINING A VINYLDIMETHICONE / DIMETHICONE COPOLYMER AND A CONDITIONING AGENT AND USES THEREOF |
FR9913097 | 1999-10-20 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU2000126397A true RU2000126397A (en) | 2002-12-20 |
RU2212226C2 RU2212226C2 (en) | 2003-09-20 |
Family
ID=9551144
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2000126397/14A RU2212226C2 (en) | 1999-10-20 | 2000-10-19 | Cosmetic composition containing copolymer of vinyldimethicone and dimethicone and conditioning agent and usage of these compositions |
Country Status (16)
Country | Link |
---|---|
US (1) | US20060120984A1 (en) |
EP (1) | EP1093809B1 (en) |
JP (1) | JP2001139418A (en) |
KR (1) | KR100369267B1 (en) |
CN (1) | CN1202800C (en) |
AR (1) | AR023277A1 (en) |
AT (1) | ATE343373T1 (en) |
AU (1) | AU745458B2 (en) |
BR (1) | BR0005084B1 (en) |
CA (1) | CA2323945C (en) |
DE (1) | DE60031494T2 (en) |
ES (1) | ES2273655T3 (en) |
FR (1) | FR2799970B1 (en) |
HU (1) | HUP0004107A3 (en) |
PL (1) | PL343338A1 (en) |
RU (1) | RU2212226C2 (en) |
Families Citing this family (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2799971B1 (en) * | 1999-10-20 | 2001-12-07 | Oreal | COSMETIC COMPOSITIONS CONTAINING A VINYLDIMETHICONE / DIMETHICONE COPOLYMER AND A CATIONIC POLYMER AND USES THEREOF |
JP4738680B2 (en) * | 2001-09-26 | 2011-08-03 | ホーユー株式会社 | Hair dye composition and hair dyeing article |
AU2003297001A1 (en) * | 2002-09-10 | 2004-04-30 | Dow Corning S.A. | Compositions comprising silicone-in-water emulsions and fragrances and hair care preparations comprising such compositions |
FR2848828B1 (en) * | 2002-12-19 | 2005-01-28 | Oreal | COSMETIC COMPOSITION CONTAINING AMPHOTERIC SURFACTANT AND USES THEREOF |
EP1677753B1 (en) * | 2003-10-27 | 2009-08-12 | Unilever PLC | Hair care composition |
GB2412375A (en) * | 2004-03-02 | 2005-09-28 | Croda Int Plc | Ester slip agents |
US20060083704A1 (en) * | 2004-10-19 | 2006-04-20 | Torgerson Peter M | Hair conditioning composition comprising high internal phase viscosity silicone copolymer emulsions |
US8252271B2 (en) | 2006-03-03 | 2012-08-28 | L'oreal S.A. | Hair styling compositions containing a silicone elastomer and a non-aqueous polar solvent |
US20070286837A1 (en) * | 2006-05-17 | 2007-12-13 | Torgerson Peter M | Hair care composition comprising an aminosilicone and a high viscosity silicone copolymer emulsion |
FR2910311B1 (en) | 2006-12-20 | 2009-02-13 | Oreal | COMPOSITION COMPRISING A SILICONE COMPOUND AND A PARTICULAR ORGANOSILANE |
FR2910312A1 (en) | 2006-12-20 | 2008-06-27 | Oreal | Treating hair, to form shampoo-resistant sheaths in situ on the hair, by applying silicone-based components reacting by hydrosilylation |
KR100890454B1 (en) * | 2008-07-21 | 2009-03-26 | 손영순 | Hair growth promoting composition |
EP2161016A1 (en) | 2008-09-05 | 2010-03-10 | KPSS-Kao Professional Salon Services GmbH | Conditioning composition for hair |
EP2161018A1 (en) | 2008-09-05 | 2010-03-10 | KPSS-Kao Professional Salon Services GmbH | Cleansing composition |
FR2954154B1 (en) | 2009-12-23 | 2012-02-24 | Oreal | COSMETIC COMPOSITION COMPRISING AT LEAST ONE VOLATILE LINEAR ALKANE, AT LEAST ONE SILICONE AND AT LEAST ONE FAT BODY IN A PARTICULAR BODY / SILICONE RATIO |
DE102010063787A1 (en) * | 2010-12-21 | 2012-06-21 | Henkel Ag & Co. Kgaa | Single-phase hair cure with increased proportion of silicone |
WO2013019969A2 (en) * | 2011-08-03 | 2013-02-07 | Melaleuca, Inc. | Hair care compositions |
US8987180B2 (en) * | 2012-12-18 | 2015-03-24 | Kimberly-Clark Worldwide, Inc. | Wet wipes including silicone reactive amino containing dimethicone copolyols |
US9198849B2 (en) | 2013-07-03 | 2015-12-01 | The Procter & Gamble Company | Shampoo composition comprising low viscosity emulsified silicone polymers |
MX363628B (en) | 2013-09-27 | 2019-03-28 | Procter & Gamble | Hair conditioning compositions comprising low viscosity emulsified silicone polymers. |
CN107058040A (en) * | 2016-11-30 | 2017-08-18 | 佛山市芊茹化妆品有限公司 | A kind of shaddock vinegar of beautifying face and moistering lotion and its application in cosmetics |
WO2018098822A1 (en) * | 2016-12-02 | 2018-06-07 | L'oreal | Method and kit for altering shape of human keratin fibres |
MY169884A (en) * | 2017-10-03 | 2019-05-31 | Kl Kepong Oleomas Sdn Bhd | A conditioning shampoo composition |
WO2019099047A1 (en) * | 2017-11-20 | 2019-05-23 | Wacker Chemie Ag | Silicone elastomer gels incorporating natural oils |
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US2528378A (en) * | 1947-09-20 | 1950-10-31 | John J Mccabe Jr | Metal salts of substituted quaternary hydroxy cycloimidinic acid metal alcoholates and process for preparation of same |
US2781354A (en) * | 1956-03-26 | 1957-02-12 | John J Mccabe Jr | Imidazoline derivatives and process |
US4183917A (en) * | 1976-12-25 | 1980-01-15 | The Lion Dentifrice Co., Ltd. | Emulsion-type hair conditioner composition |
US5690920A (en) * | 1990-11-15 | 1997-11-25 | L'oreal | Foamable washing composition based on selected insoluble silicones and an alkylpolyglycoside, and cosmetic and dermatological uses thereof |
US5679357A (en) * | 1991-08-01 | 1997-10-21 | L'oreal | Cationic dispersions based on ceramides and/or glycoceramides |
CA2213235A1 (en) * | 1995-02-15 | 1996-08-22 | The Procter & Gamble Company | Crystalline hydroxy waxes as oil in water stabilizers for skin cleansing liquid composition |
FR2739284B1 (en) * | 1995-09-29 | 1997-11-07 | Oreal | COMPOSITION FOR THE TREATMENT OF KERATINIC MATERIALS COMPRISING AT LEAST ONE GRAFTED SILICONE POLYMER AND AT LEAST ONE FATTY CHAIN AMIDE AND USES THEREOF |
FR2742657B1 (en) * | 1995-12-21 | 1998-01-30 | Oreal | COMPOSITIONS FOR THE TREATMENT OF KERATINIC MATERIALS COMPRISING THE ASSOCIATION OF A POLYAMPHOLYTE POLYMER AND A CATIONIC POLYMER |
US5665804A (en) * | 1996-02-05 | 1997-09-09 | Dow Corning Corporation | Silicone latex solvent thickening |
US5804207A (en) * | 1996-03-21 | 1998-09-08 | L'oreal | Detergent cosmetic compositions containing a thickening polyacrylamide |
FR2747567B1 (en) * | 1996-04-22 | 1998-05-22 | Oreal | USE OF CERAMIDE FOR THE TREATMENT OF NAILS |
FR2748392B1 (en) * | 1996-05-13 | 1998-08-07 | Oreal | COMPOSITIONS FOR THE TREATMENT OF KERATINIC MATERIALS COMPRISING THE COMBINATION OF A POLYAMPHOLYTE POLYMER AND A NON-VOLATILE AND WATER INSOLUBLE ORGANOPOLYSILOXANE |
FR2755854B1 (en) * | 1996-11-15 | 1998-12-24 | Oreal | NANOEMULSION BASED ON NON-IONIC AND CATIONIC AMPHIPHILIC LIPIDS AND USES |
GB9708182D0 (en) * | 1997-04-23 | 1997-06-11 | Dow Corning Sa | A method of making silicone in water emulsions |
US5863943A (en) * | 1997-06-03 | 1999-01-26 | The Andrew Jergens Company | Stabilized skin conditioner with alpha hydroxy acids |
FR2770523B1 (en) * | 1997-11-04 | 1999-12-31 | Oreal | CERAMID TYPE COMPOUND, PROCESS FOR PREPARATION AND USE |
-
1999
- 1999-10-20 FR FR9913097A patent/FR2799970B1/en not_active Expired - Fee Related
-
2000
- 2000-10-12 AT AT00402821T patent/ATE343373T1/en not_active IP Right Cessation
- 2000-10-12 DE DE60031494T patent/DE60031494T2/en not_active Expired - Lifetime
- 2000-10-12 ES ES00402821T patent/ES2273655T3/en not_active Expired - Lifetime
- 2000-10-12 EP EP00402821A patent/EP1093809B1/en not_active Expired - Lifetime
- 2000-10-19 CN CNB001348957A patent/CN1202800C/en not_active Expired - Fee Related
- 2000-10-19 HU HU0004107A patent/HUP0004107A3/en unknown
- 2000-10-19 RU RU2000126397/14A patent/RU2212226C2/en not_active IP Right Cessation
- 2000-10-19 AR ARP000105491A patent/AR023277A1/en unknown
- 2000-10-19 CA CA002323945A patent/CA2323945C/en not_active Expired - Fee Related
- 2000-10-20 KR KR10-2000-0061873A patent/KR100369267B1/en not_active IP Right Cessation
- 2000-10-20 AU AU66639/00A patent/AU745458B2/en not_active Ceased
- 2000-10-20 BR BRPI0005084-9A patent/BR0005084B1/en not_active IP Right Cessation
- 2000-10-20 PL PL00343338A patent/PL343338A1/en not_active Application Discontinuation
- 2000-10-20 JP JP2000322032A patent/JP2001139418A/en active Pending
-
2006
- 2006-01-23 US US11/336,852 patent/US20060120984A1/en not_active Abandoned
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