Abstract:
Described is the use of benzotropolone and their derivatives, especially the compounds of formula (1); wherein R2, R3, R4, R5 and R6 independently of one another are hydrogen; OH; C1-C30alkyl, C2-C30al- kenyl, C1-C30alkoxy, C3-C12cycloalkyl or C1C30hydroxyalkyl, which may be substituted by one or more E and/or interrupted by one or more D; C6-C20aryl, which may be substitu¬ ted by one or more G; C4-C20heteroaryl, which may be substituted by one or more G, C2- C18alkenyl, C2-C18alkynyl, C7-C25aralkyl, CN, or -CO-R17; C1-C30mono- or dialkylamino; COR9; COOR9; CONR9R10; CN; SO2R9; OCOOR9; OCOR9; NHCOOR9; NR9COR10; NH2; *-(CO)-NH-(CH2)n1-(PO)-(OR11)2; -(CO)-O-(CH2)n1-(PO)-(OR11)2; sulphate; sulphonate; phosphate; phosphonate; -(CH2)n2-[O-(SO2)]n3-OR11; -O-(CH2)n4(CO)n5-R11; -(O)n6-(CH2)n7-(PO)-(OR9)2; -(O)n6-(CH2)n7-SO2-OR9; halogen; organosilanyl; organo- siloxanyl; or a sugar residue linked directly in an a- or ß-mode via the anomeric oxygen to the benzotropolone system or via a linear or branched alkylene, alkenylene, alkadiene or alkatriene spacer (sugar- (CH2)n-(X1)1 or 0 -benzotropolone system, wherein n = 1 -10 and X1 = -0-; -(CO)-; -0-C0-; -COO-, -NH-; -S-; -SO2-); R1, R7 and R8 independently of one another are hydrogen; C1C12alkyl or C3-C12-cycloalkyl, which may be substituted by one or more E and/or interrupted by one or more D; C6- C20aryl, which may be substituted by one or more G; C4-C20heteroaryl, which may be substituted by one or more G, C2-C18alkenyl, C2-C18alkynyl, C7-C25aralkyl, or COOR9; COR9; CONR9R10; SO3R9; SO2R9; PO3(R9)2; PO2(R9)2; organosilanyl; organosiloxanyl; or a sugar residue linked directly in an a- or ß-mode via the anomeric oxygen to the benzotropolone system or via a linear or branched alkylene, alkenylene, alkadiene or alkatriene spacer (sugar-(CH2)n-(X2)1 or 0-*, wherein n = 1 -10 and X2 = -C(=0)-; -0-C0-*); R9 and R10 independently from each other are hydrogen; C1C18alkyl or C3-C12-cycloalkyl which may be substituted by one or more E and/or interrupted by one or more D; C6- C20aryl, which may be substituted by one or more G; C4-C20heteroaryl, which may be substituted by one or more G; organosilanyl; organosiloxanyl; or a sugar residue linked directly in an a- or ß-mode via the anomeric oxygen or via a linear or branched alkylene, alkenylene, alkadiene or alkatriene spacer (sugar- (CH2)n-*, wherein n = 1 -10); or R9 and R10 together form a five or six membered ring, R11 is hydrogen; or C1-C5alkyl; n1, n2, n4 and n7 independently from each other are a number from 1 to 5; n3, n5 and n6 independently from each other are a 0; or 1; D is -CO-; -COO-; -S-; -SO-; -SO2-; -O-; -NR14-; -S1R19R20-; -POR11-; -CR12=CR13-; or -C=C-; and E is -0R18; -SR18; -NR14R15; -NR14COR15; -C0R17; -COOR16; -CONR14R15; -CN; halogen; Or SO3R18; SO2R18; PO3(R18)2; PO2(R18)2; organosilanyl; organosiloxanyl; or a sugar residue linked directly in an a- or ß-mode via the anomeric oxygen or via a linear or branched alkylene, alkenylene, alkadiene or alkatriene spacer (sugar- (CH2)n-(X1)1 or 0-*, wherein n = 1 -10 and X1 = -0-; -C(=0)-; -0-C0-; -COO-; -NH-; -S-; -SO2-); G is E; C1-C18alkyl, which is optionally interrupted by D; C1-C18perfluoroalkyl; C1-C18alkoxy, which is optionally substituted by E and/or interrupted by D; wherein R12, R13, R14 and R15 independently of each other are hydrogen; C6-C18aryl which is optionally substituted by OH, C1-C18alkyl or C1-C18alkoxy; C1-C18alkyl, which is optionally interrupted by -O-; or Ri4 and Ri5 together form a five or six membered ring, Ri6 is hydrogen; C6-Ci8aryl which is optionally substituted by OH, C1-C18alkyl or d- C18alkoxy; C1-C18alkyl which is optionally interrupted by -O-; R17 is H; C6-C18aryl which is optionally substituted by OH, C1-C18alkyl or C1-C18alkoxy; or d- C18alkyl which is optionally interrupted by -O-; R18 is hydrogen; C6-C18aryl, which is optionally substituted by OH, C1-C18alkyl or d- C18alkoxy; C1-C18alkyl, which is optionally interrupted by -O-; R19 and R20 independently of each other are hydrogen; C1-C18alkyl; C6-C18aryl which is optionally substituted by C1-C18alkyl; and R21 is C1-C18alkyl; or C6-C18aryl, which is substituted by C1-C18alkyl; * means, that this radical is directed to the benzotropolone moiety; for the protection of human and animal hair and skin against UV radiation.
Abstract:
Disclosed is the use of benzylidene malonates of formula (1), wherein R1 is methyl; ethyl; propyl; or n-butyl; if R1 is methyl, then R is tert. butyl; formula (A); a radical of formula (1a); or a radical of formula (1b); wherein R2 and R3, independently from each other are hydrogen; or methyl; R4 is methyl; ethyl; or n-propyl; R5 and R6 independently from each other are hydrogen; or C1-C3alkyl; if R1 is ethyl; propyl; or n-butyl, then R is isopropyl; for the protection of human and animal hair and skin against UV radiation.
Abstract:
Disclosed is the use of oleogels (a) for increasing the sun protection factor of sunscreens comprising at least one organic or inorganic UV filter (b).
Abstract:
The instant invention refers to the use of a concentrated aqueous polymer dispersion with an average particle size of less than 1000 nm comprising (a) a polymer carrier prepared by heterophase radical polymerization of at least one ethylenically unsaturated monomer in the presence of (b) an oil-soluble organic UV absorber selected from the class of p-aminobenzoic acid derivatives; salicylic acid derivatives; benzophenone derivatives; diphenyl acrylate derivatives; benzofuran derivatives; polymeric UV absorbers, comprising one or more organosilicon radicals; cinnamic acid derivatives; camphor derivatives; s-triazine derivatives; trianilino-s-triazine derivatives; menthyl anthranilates; and benzotriazole derivatives; wherein the weight ratio of the oil-soluble organic UV absorber (b) to polymer carrier (a) is greater than 50 parts UV absorber per 100 parts of carrier; for the protection of human and animal hair and skin against the damaging effect of UV radiation. The concentrated aqueous polymer dispersions show unexpectedly high sunscreen effects and a positive skin feeling.
Abstract:
Disclosed is the Use of UV absorbers selected from (a1) diphenylacrylates; and (a2) specific hydroxyphenyl triazines for stabilizing cosmetic compositions comprising an organic UV absorber selected from (b1) a specific benzophenone derivative, (b2) a specific benzotriazole derivative and (b3) a specific triazine derivative and UV filters selected from (c1) cinnamic acid derivatives; and (c2) dibenzoylmethane derivatives.
Abstract:
uso de misturas. é divulgado o uso de misturas que compreendem pelo menos dois derivados de bis(bifenil)triazina da fórmula x é hidrogênio; alquila c~1 ~ - c~50 ~ que pode ser não interrompido ou interrompido por um ou mais átomos de oxigênio e/ou substituído por um ou mais grupos r~8 ~; cicloalquila c~3 ~ - c~12 ~ que é substituído por r~8 ~; ch((ch~2 ~)~p ~- r~8 ~)-co-o-(ch~2 ~)~m ~ - r~9 ~; -ch((ch~2 ~)~p ~ - r~8 ~)-co-(nr~10 ~)-(ch~2 ~)~m ~ - r~9 ~; -co-(ch~2 ~)~p ~ - r~8 ~; -co-o(ch~2 ~)p-r~8 ~; -ch~2 ~ch(-o(co)-r~8 ~)-r~9 ~; -co-(nr~10 ~) - (ch~2 ~)~p ~ - r~8 ~;arila c~6 ~ - c~20 ~; alila; alquenila c~4 ~ - c~50 ~ que é não interrompido ou é interrompido por um ou mais átomos de oxigênio; cicloalquila c~3~ - c~12 ~ que é não interrompido ou interrompido por um ou mais átomos de oxigênio; alquinila c~3 ~- c~20 ~; cicloalquinila c~6 ~ - c~12 ~; r~1 ~ é hidrogênio; alquila c~1 ~- c~12 ~ não substituído ou substituído; cicloalquila c~3 ~ - c~12 ~ não substituído ou substituído; arila c~6 ~ - c~20 ~ não substituído ou substituído, alquinila c~2 ~ - c~20 ~ não substituído ou substituído; or~7 ~; oh; sr~8 ~; sor~7 ~;so~2 ~r~7 ~; so~3 ~m ou um radical da fórmula r~2 ~, r~3 ~, r~4 ~, r~5 ~ e r~6 ~ independentemente um do outro são hidrogênio; hidroxila; -cn; alquila c~1 ~ - c~20 ~ não substituído ou substituído ; fenilalquila c~7 ~ - c~20 ~; halogênio; halo-alquila c~1 ~ - c~5 ~; sulfonila; carboxila; acilamino; acilóxi; alcóxi c~1 ~ - c~12 ~ carbonila; aminocarbonila; r~7 ~ é alquila c ~1 ~ - c~18 ~ substituído ou não substituido; cicloalquila c~3 ~ - c~12 ~ não substituido ou substituido; arila c~6 ~ - c~20 ~ não substituido ou substituido; alqulina c~2 ~ - c~20 ~ não substituído ou substituído ou fenilalquila c~7 ~ - c~20 ~; m é metal alcalino; r~8 ~ - r~9 ~ independentemente um do outro são r~x ~ se ligado a um átomo de carbono e são r~y ~ se ligados a um átomo de oxigênio; p é 0 a 20, m é 0 a 20; r~x ~ é hidrogênio; hidroxila; alquila c~1 ~ - c~30 ~; cicloalquila c~3 ~ - c~12 ~ ou cicloalcóxi c~1 ~ - c~30 ~; cicloalcóxi c~3 ~ - c~12 ~ ou cicloalquila c~3 ~ - c~12 ~ ou cicloalcóxi c~3 ~ - c~12 ~ que é interrompido por um ou mais átomos de oxigênio; arila c~6 ~12; ; heteroarila c~3 ~ - c~12 ~; or~z ~; nhr~z ~; r~z ~; conr~10 ~r~11 ~; so~3 ~h; so~3 ~m; oso~3 ~h~2 ~; alila, alquenila c~2 ~ - c~30 ~; cicloalquinila c~4 ~ - c~12 ~ que é não interrompido ou interrompido por ou mais átomos de oxigênio; alquinila c~3 ~ - c~20 ~ou cicloalquinila c~6 ~ - c~12 ~; r~y ~ é hidrogênio; alquila c~1 ~ - c~30 ~; cicloalquila c~3 ~ - c~12 ~ que é não interrompido ou interrompido por um ou mais átomos de oxigênio; arila c~6 ~ - c~12 ~ ; hetero-arila c~3 ~ - c~12 ~; r~z ~; alila, alquenila c~2 ~ - c~30 ~; cicloalquenila c~4 ~ - c~12 ~ que é não interrompido ou interrompido por um ou mais átomos de oxigênio; alquinila c~3 ~ - c~20 ~ ou cicloalquinila c~6 ~ - c~12 ~; r~z ~é -cir~10 ~; -coor~10 ~; -conr~10 ~r~11 ~; -co-ch=ch~2 ~; -co-c(ch~3 ~)=ch~2 ~; r~10 ~ e r~11 ~ independentemente um do outro são hidrogênio; alquila c~1 ~ - c~30 ~; alquila c~1 ~ - c~20 ~ que é interrompido por uma ou mais átomos de oxigênio; cicloalquila c~3 ~ - c~12 ~que é não interrompido ou interrompido por um ou mais átomos de oxigênio; alquenila c~2 ~ - c~20 ~ que é não interrompido ou é interrompido por um ou mais átomos de oxigênio ou arila c~6 ~ - c~12 ~ ou r~10 e r~11 ~ juntos formam um anel de cinco ou seis membros; como absorvedores de uv para aumentar o fator de proteção contra uva de composições cosméticas ou dermatológicas.
Abstract:
Disclosed is the use of UV absorbers selected from(a) hydroxyphenyl triazines of formulain whichR, Rand Rindependently of one another, are C-Calkyl; and(a) benzotriazole derivatives of formulawhereinRis a random statistical mixture of at least three isomeric branched secondary alkyl groups each having 8 to 30 carbon atoms and having the formulaEis a straight-chain C-Calkyl;Eis a straight-chain C-Calkyl; wherein the total number of carbon atoms in Eplus Eis from 7 to 29; andRis C-Calkyl;for stabilizing cosmetic compositions against photodegradation comprising(b)symmetrical triazine derivatives of formulawhereinA is a radical of formulaRand Rindependently from each other are hydrogen; C-Calkyl; or C-Caryl;R, Rand Rindependently from each other are hydrogen; or a radical of formulawherein, in formula (3a), at least one of the radicals R, Rand Rare a radical of formula (3c);R, R, Rand Rindependently from each other are hydrogen; hydroxy; halogen; C-Calkyl; C-Calkoxy; C-Caryl; biphenylyl; C-Caryloxy; C-Calkylthio; carboxy; -COOM; C-C-alkylcarboxyl; aminocarbonyl; mono- or di-C-Calkylamino; C-Cacylamino; or -COOH;M is an alkali metal ion;x is 1 or 2; andy is a number from 2 to 10;and a UV-absorber selected from(c) cinnamic acid derivatives; and(c) dibenzoylmethane derivatives.