RU2000126395A - COSMETIC COMPOSITIONS CONTAINING VINYLEDIMETICON AND DIMETICON COPOLYMER AND SILICON ORGANIC COMPOUND, AND THEIR APPLICATION - Google Patents
COSMETIC COMPOSITIONS CONTAINING VINYLEDIMETICON AND DIMETICON COPOLYMER AND SILICON ORGANIC COMPOUND, AND THEIR APPLICATIONInfo
- Publication number
- RU2000126395A RU2000126395A RU2000126395/14A RU2000126395A RU2000126395A RU 2000126395 A RU2000126395 A RU 2000126395A RU 2000126395/14 A RU2000126395/14 A RU 2000126395/14A RU 2000126395 A RU2000126395 A RU 2000126395A RU 2000126395 A RU2000126395 A RU 2000126395A
- Authority
- RU
- Russia
- Prior art keywords
- groups
- composition according
- composition
- polydimethylsiloxane
- paragraphs
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims 40
- -1 SILICON ORGANIC COMPOUND Chemical class 0.000 title claims 33
- 239000002537 cosmetic Substances 0.000 title claims 5
- 229920001577 copolymer Polymers 0.000 title claims 4
- 229910052710 silicon Inorganic materials 0.000 title 1
- 239000010703 silicon Substances 0.000 title 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 claims 15
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims 15
- 239000004205 dimethyl polysiloxane Substances 0.000 claims 12
- 229920001296 polysiloxane Polymers 0.000 claims 11
- 150000003961 organosilicon compounds Chemical class 0.000 claims 6
- 125000004432 carbon atoms Chemical group C* 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 4
- 239000000463 material Substances 0.000 claims 4
- 102000011782 Keratins Human genes 0.000 claims 3
- 108010076876 Keratins Proteins 0.000 claims 3
- 229920002379 silicone rubber Polymers 0.000 claims 3
- 239000004094 surface-active agent Substances 0.000 claims 3
- OFHCOWSQAMBJIW-AVJTYSNKSA-N Alfacalcidol Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C\C=C1\C[C@@H](O)C[C@H](O)C1=C OFHCOWSQAMBJIW-AVJTYSNKSA-N 0.000 claims 2
- 238000007259 addition reaction Methods 0.000 claims 2
- 125000001931 aliphatic group Chemical group 0.000 claims 2
- 239000003054 catalyst Substances 0.000 claims 2
- 239000003093 cationic surfactant Substances 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 125000001453 quaternary ammonium group Chemical group 0.000 claims 2
- 229920005989 resin Polymers 0.000 claims 2
- 239000011347 resin Substances 0.000 claims 2
- 239000002453 shampoo Substances 0.000 claims 2
- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 claims 2
- 125000003396 thiol group Chemical class [H]S* 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
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- 229910004298 SiO 2 Inorganic materials 0.000 claims 1
- 229910004283 SiO 4 Inorganic materials 0.000 claims 1
- 125000005041 acyloxyalkyl 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
- 125000005376 alkyl siloxane group Chemical group 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 239000002280 amphoteric surfactant Substances 0.000 claims 1
- 125000000129 anionic group Chemical group 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 238000004061 bleaching Methods 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 238000006243 chemical reaction Methods 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
- 125000004185 ester group Chemical group 0.000 claims 1
- 125000001033 ether group Chemical group 0.000 claims 1
- 125000000524 functional group Chemical group 0.000 claims 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 1
- 238000006459 hydrosilylation reaction Methods 0.000 claims 1
- LWIGVRDDANOFTD-UHFFFAOYSA-N hydroxy(dimethyl)silane Chemical group C[SiH](C)O LWIGVRDDANOFTD-UHFFFAOYSA-N 0.000 claims 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000000962 organic group Chemical group 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Inorganic materials [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 claims 1
- 229920002050 silicone resin Polymers 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate group Chemical group S(=O)(=O)([O-])[O-] QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 claims 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
Claims (21)
(а) одним полисилоксаном формулы (I)
в которой R1 обозначает группу, способную участвовать в цепной реакции присоединения, такую как, например, атом водорода, алифатическая группа, содержащая одну ненасыщенную этиленовую связь, в частности, винил, аллил или гексенил,
группы R2 формулы (1) представляют собой алкильные группы, содержащие от 1 до 20 атомов углерода, циклоалкил, содержащий 5 или 6 атомов углерода, арил, алкиларил, содержащий от 7 до 20 атомов углерода, или гидроксил, и, кроме того, могут иметь в своем составе функциональные группы, такие как простые эфирные группы, аминогруппы, карбоксильные, гидроксильные, тиольные, сложноэфирные группы, сульфонатные группы, сульфатные группы;
n обозначает целое число, такое что полисилоксан формулы (1), предпочтительно, имеет кинематическую вязкость, составляющую от 1 до 1•106 мм2/с,
(б) и по меньшей мере одним кремнийорганическим соединением, содержащим по меньшей мере одну и не более двух групп, способных вступать в реакцию с группами R1 полисилоксана (а), при этом по меньшей мере одно из соединений типа (а) или (б) содержит алифатическую группу, содержащую ненасыщенную этиленовую связь.1. Cosmetic composition, characterized in that it contains in a cosmetically acceptable medium at least one organosilicon compound and at least one organosilicon copolymer having a viscosity in the range from 10 6 to 100 • 10 6 сP resulting from the addition reaction flowing in the presence of a catalyst, between at least
(a) one polysiloxane of formula (I)
in which R 1 denotes a group capable of participating in a chain reaction addition, such as, for example, a hydrogen atom, an aliphatic group containing one unsaturated ethylene bond, in particular, vinyl, allyl or hexyl,
R 2 groups of formula (1) are alkyl groups containing from 1 to 20 carbon atoms, cycloalkyl containing 5 or 6 carbon atoms, aryl, alkylaryl containing from 7 to 20 carbon atoms, or hydroxyl, and, in addition, they can contain functional groups, such as ether groups, amino groups, carboxyl, hydroxyl, thiol, ester groups, sulphonate groups, sulphate groups;
n is an integer such that the polysiloxane of formula (1) preferably has a kinematic viscosity of 1 to 1 x 10 6 mm 2 / s,
(b) and at least one silicone compound containing at least one and no more than two groups capable of reacting with the R 1 groups of the polysiloxane (a), with at least one of the compounds of type (a) or (b ) contains an aliphatic group containing an ethylenically unsaturated bond.
а) одним альфа, омега-дивинилполидиметилсилоксаном и
б) одним альфа, омега-дигидрополидиметилсилоксаном.4. Composition according to any one of paragraphs. 1-3, characterized in that the organosilicon copolymer is obtained by the addition reaction, proceeding in the presence of a hydrosilylation catalyst, between at least
a) one alpha, omega-divinylpolydimethylsiloxane and
b) one alpha, omega-dihydropolydimethylsiloxane.
(а) полиалкилсилоксаны выбирают среди полидиметилсилоксанов с триметилсилильными концевыми группами, полидиметилсилоксанов с диметилсиланольными концевыми группами, поли(C1-C20)-алкилсилоксанов,
(б) полиалкиларилсилоксаны выбирают среди полидиметилметилфенилсилоксанов, полидиметилдифенилсилоксанов, линейных и/или разветвленных, с вязкостью в интервале от 1•105 до 5•102 м2/c при 25oС,
(в) силиконовые каучуки выбирают среди полидиорганосилоксанов, имеющих среднечисловые молекулярные массы в интервале от 200000 до 1000000, которые используют индивидуально или в форме смеси в растворителе,
(г) смолы выбирают среди смол, состоящих из звеньев
R3SiO1/2, R2SiO2/2, RSiO3/2, SiO4/2,
в которых R обозначает углеводородную группу, содержащую от 1 до 16 атомов углерода, или фенильную группу,
д) кремнийорганические соединения, модифицированные органическими группами, выбирают среди кремнийорганических соединений, содержащих в своей структуре одну или несколько органофункциональных групп, присоединенных посредством углеводородного радикала.8. The composition according to p. 7, characterized in that
(a) polyalkylsiloxanes are selected among polydimethylsiloxanes with trimethylsilyl end groups, polydimethylsiloxanes with dimethylsilanol end groups, poly (C 1 -C 20 ) alkylsiloxanes,
(b) polyalkylaryl siloxanes are chosen from polydimethylmethylphenylsiloxanes, polydimethyldiphenylsiloxanes, linear and / or branched, with a viscosity in the range from 1 • 10 5 to 5 • 10 2 m 2 / s at 25 o С
(c) silicone rubbers are chosen from polydiorganosiloxanes having a number average molecular weight in the range from 200,000 to 1,000,000, which are used individually or in the form of a mixture in a solvent,
(g) resins are chosen from the resins consisting of links.
R 3 SiO 1/2 , R 2 SiO 2/2 , RSiO 3/2 , SiO 4/2 ,
in which R denotes a hydrocarbon group containing from 1 to 16 carbon atoms, or a phenyl group,
e) organosilicon compounds modified with organic groups are chosen from among organosilicon compounds containing in their structure one or several organofunctional groups attached by means of a hydrocarbon radical.
а) полиэтиленоксигруппы и/или полипропиленоксигруппы,
б) аминированные группы, замещенные или незамещенные,
в) тиольные группы,
г) алкоксилированные группы,
д) гидроксиалкильные группы,
е) ацилоксиалкильные группы,
ж) алкилкарбоксильные группы,
з) 2-гидроксиалкилсульфонатные группы,
и) 2-гидроксиалкилтиосульфонатные группы,
к) гидроксиациламиногруппы,
л) четвертичные аммониевые группы.10. The composition according to p. 7 or 8, characterized in that the organomodified organosilicon compounds are chosen among polyorganosiloxanes, having in its composition
a) polyethylenoxide and / or polypropylenediaxy,
b) aminirovanny groups, substituted or unsubstituted,
c) thiol groups
d) alkoxylated groups,
d) hydroxyalkyl groups,
e) acyloxyalkyl groups,
g) alkylcarboxylic groups,
h) 2-hydroxyalkylsulfonate groups,
i) 2-hydroxyalkylthiosulfonate groups,
k) hydroxyacylamino,
k) quaternary ammonium groups.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9913096 | 1999-10-20 | ||
FR9913096A FR2799969B1 (en) | 1999-10-20 | 1999-10-20 | COSMETIC COMPOSITIONS CONTAINING A VINYLDIMETHICONE / DIMETHICONE COPOLYMER AND A SILICONE AND USES THEREOF |
Publications (2)
Publication Number | Publication Date |
---|---|
RU2000126395A true RU2000126395A (en) | 2002-11-10 |
RU2212225C2 RU2212225C2 (en) | 2003-09-20 |
Family
ID=9551143
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2000126395/14A RU2212225C2 (en) | 1999-10-20 | 2000-10-19 | Cosmetic compositions containing copolymer of vinyldimethicone and dimethicone and organo- silicon compound and their using |
Country Status (16)
Country | Link |
---|---|
US (1) | US7223384B1 (en) |
EP (1) | EP1093806B1 (en) |
JP (1) | JP2001163735A (en) |
KR (1) | KR100369266B1 (en) |
CN (1) | CN1196461C (en) |
AR (1) | AR023276A1 (en) |
AT (1) | ATE314052T1 (en) |
AU (1) | AU744401B2 (en) |
BR (1) | BR0005136B1 (en) |
CA (1) | CA2323951C (en) |
DE (1) | DE60025121T2 (en) |
ES (1) | ES2255957T3 (en) |
FR (1) | FR2799969B1 (en) |
HU (1) | HUP0004104A3 (en) |
PL (1) | PL199961B1 (en) |
RU (1) | RU2212225C2 (en) |
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US6630152B2 (en) * | 1999-04-07 | 2003-10-07 | Shen Wei (Usa), Inc. | Aloe vera glove and manufacturing method |
DE20114179U1 (en) * | 2001-08-28 | 2001-10-25 | Wella Ag, 64295 Darmstadt | Colorants for keratin fibers |
DE10259291B4 (en) * | 2002-12-18 | 2006-02-23 | Rudolf Gmbh & Co. Kg Chemische Fabrik | Highly concentrated, self-emulsifying preparations containing organopolysiloxanes and alkylammonium compounds and their use in aqueous systems |
GB2412375A (en) * | 2004-03-02 | 2005-09-28 | Croda Int Plc | Ester slip agents |
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 |
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 |
FR2966351B1 (en) * | 2010-10-26 | 2015-12-18 | Oreal | COSMETIC COMPOSITION COMPRISING FATTY CHAIN ALCOXYSILANE, ANIONIC SURFACTANT AND NONIONIC, AMPHOTERIC OR ZWITTERIONIC SURFACTANT. |
US9399722B2 (en) | 2011-03-31 | 2016-07-26 | The Armor All/Stp Products Company | Compositions and methods for treating automotive surfaces |
US8591872B2 (en) | 2011-12-30 | 2013-11-26 | L'oreal | Composition and process for reducing the curl and frizziness of hair |
US8506651B2 (en) | 2011-12-30 | 2013-08-13 | L'oreal S.A. | Process for altering the appearance of hair using a composition containing dyes and non-hydroxide bases |
US8343238B1 (en) | 2011-12-30 | 2013-01-01 | L'oreal Sa. | Process for altering the appearance of hair using a composition containing dyes and non-hydroxide bases |
US8556994B2 (en) | 2011-12-30 | 2013-10-15 | L'oreal | Process for altering the appearance of hair using a composition containing direct dyes and non-hydroxide bases |
US10596100B2 (en) | 2012-12-19 | 2020-03-24 | L'oreal | Cosmetic compositions containing an alkoxysilane and a silsesquioxane resin |
US9198849B2 (en) | 2013-07-03 | 2015-12-01 | The Procter & Gamble Company | Shampoo composition comprising low viscosity emulsified silicone polymers |
WO2015047786A1 (en) | 2013-09-27 | 2015-04-02 | The Procter & Gamble Company | Hair conditioning compositions comprising low viscosity emulsified silicone polymers |
KR102369897B1 (en) * | 2020-03-12 | 2022-03-07 | 한국생산기술연구원 | Cosmetic composition in a type of porous lyophilized products comprising reactive silicone |
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-
1999
- 1999-10-20 FR FR9913096A patent/FR2799969B1/en not_active Expired - Fee Related
-
2000
- 2000-10-04 AT AT00402724T patent/ATE314052T1/en active
- 2000-10-04 EP EP00402724A patent/EP1093806B1/en not_active Expired - Lifetime
- 2000-10-04 ES ES00402724T patent/ES2255957T3/en not_active Expired - Lifetime
- 2000-10-04 DE DE60025121T patent/DE60025121T2/en not_active Expired - Lifetime
- 2000-10-11 AU AU65455/00A patent/AU744401B2/en not_active Ceased
- 2000-10-18 BR BRPI0005136-5A patent/BR0005136B1/en not_active IP Right Cessation
- 2000-10-19 CN CNB001348922A patent/CN1196461C/en not_active Expired - Fee Related
- 2000-10-19 PL PL343307A patent/PL199961B1/en not_active IP Right Cessation
- 2000-10-19 HU HU0004104A patent/HUP0004104A3/en unknown
- 2000-10-19 KR KR10-2000-0061611A patent/KR100369266B1/en not_active IP Right Cessation
- 2000-10-19 CA CA002323951A patent/CA2323951C/en not_active Expired - Fee Related
- 2000-10-19 AR ARP000105490A patent/AR023276A1/en unknown
- 2000-10-19 RU RU2000126395/14A patent/RU2212225C2/en not_active IP Right Cessation
- 2000-10-20 US US09/692,749 patent/US7223384B1/en not_active Expired - Fee Related
- 2000-10-20 JP JP2000322029A patent/JP2001163735A/en active Pending
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