MXPA02004723A - Uso de absorbentes de uv de benzotriazol. - Google Patents
Uso de absorbentes de uv de benzotriazol.Info
- Publication number
- MXPA02004723A MXPA02004723A MXPA02004723A MXPA02004723A MXPA02004723A MX PA02004723 A MXPA02004723 A MX PA02004723A MX PA02004723 A MXPA02004723 A MX PA02004723A MX PA02004723 A MXPA02004723 A MX PA02004723A MX PA02004723 A MXPA02004723 A MX PA02004723A
- Authority
- MX
- Mexico
- Prior art keywords
- formula
- compound
- hair
- alkyl
- radical
- Prior art date
Links
- 239000006096 absorbing agent Substances 0.000 title claims abstract description 35
- 239000012964 benzotriazole Substances 0.000 title claims abstract description 24
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 title claims abstract description 23
- 210000004209 hair Anatomy 0.000 claims abstract description 51
- 239000002537 cosmetic Substances 0.000 claims abstract description 25
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 19
- 150000003254 radicals Chemical class 0.000 claims abstract description 19
- 239000001257 hydrogen Substances 0.000 claims abstract description 18
- 150000002431 hydrogen Chemical class 0.000 claims abstract description 13
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 11
- 150000002367 halogens Chemical class 0.000 claims abstract description 11
- 230000005855 radiation Effects 0.000 claims abstract description 11
- 238000011282 treatment Methods 0.000 claims abstract description 10
- 230000004224 protection Effects 0.000 claims abstract description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 5
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 claims abstract description 4
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims abstract description 4
- 229940095064 tartrate Drugs 0.000 claims abstract description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 claims abstract 3
- 229910019142 PO4 Inorganic materials 0.000 claims abstract 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims abstract 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims abstract 3
- 239000010452 phosphate Substances 0.000 claims abstract 3
- 238000002360 preparation method Methods 0.000 claims description 81
- 150000001875 compounds Chemical class 0.000 claims description 76
- 239000000203 mixture Substances 0.000 claims description 42
- -1 ester compound Chemical class 0.000 claims description 33
- 238000000034 method Methods 0.000 claims description 23
- 239000002657 fibrous material Substances 0.000 claims description 19
- 239000000499 gel Substances 0.000 claims description 18
- 239000006210 lotion Substances 0.000 claims description 16
- 150000001412 amines Chemical class 0.000 claims description 13
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 13
- 239000004753 textile Substances 0.000 claims description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 239000006260 foam Substances 0.000 claims description 12
- 239000002453 shampoo Substances 0.000 claims description 12
- 230000037072 sun protection Effects 0.000 claims description 9
- 239000000839 emulsion Substances 0.000 claims description 8
- 239000002671 adjuvant Substances 0.000 claims description 7
- 238000004040 coloring Methods 0.000 claims description 7
- 230000006641 stabilisation Effects 0.000 claims description 7
- 238000011105 stabilization Methods 0.000 claims description 7
- 239000008266 hair spray Substances 0.000 claims description 6
- 230000000845 anti-microbial effect Effects 0.000 claims description 5
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 claims description 4
- 238000004043 dyeing Methods 0.000 claims description 4
- 230000037308 hair color Effects 0.000 claims description 4
- 230000001476 alcoholic effect Effects 0.000 claims description 3
- 239000007864 aqueous solution Substances 0.000 claims description 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 3
- 239000003755 preservative agent Substances 0.000 claims description 3
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 claims description 2
- 239000004599 antimicrobial Substances 0.000 claims description 2
- 230000001680 brushing effect Effects 0.000 claims description 2
- 239000000969 carrier Substances 0.000 claims description 2
- 239000011087 paperboard Substances 0.000 claims description 2
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims 2
- 239000002152 aqueous-organic solution Substances 0.000 claims 1
- 239000011111 cardboard Substances 0.000 claims 1
- 239000003676 hair preparation Substances 0.000 claims 1
- 230000002335 preservative effect Effects 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 description 76
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 35
- 239000003921 oil Substances 0.000 description 17
- 238000005481 NMR spectroscopy Methods 0.000 description 16
- 239000006071 cream Substances 0.000 description 16
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 12
- 125000004005 formimidoyl group Chemical group [H]\N=C(/[H])* 0.000 description 12
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 12
- 239000000243 solution Substances 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- 229910052757 nitrogen Inorganic materials 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- 238000009472 formulation Methods 0.000 description 9
- 150000002148 esters Chemical class 0.000 description 8
- 101150041968 CDC13 gene Proteins 0.000 description 7
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 7
- 239000013078 crystal Substances 0.000 description 7
- 239000002781 deodorant agent Substances 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 239000002304 perfume Substances 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 7
- 239000000344 soap Substances 0.000 description 7
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 6
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 239000000975 dye Substances 0.000 description 6
- 239000000835 fiber Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 5
- 230000029936 alkylation Effects 0.000 description 5
- 238000005804 alkylation reaction Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000006072 paste Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 238000005956 quaternization reaction Methods 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 4
- ZFOZVQLOBQUTQQ-UHFFFAOYSA-N Tributyl citrate Chemical compound CCCCOC(=O)CC(O)(C(=O)OCCCC)CC(=O)OCCCC ZFOZVQLOBQUTQQ-UHFFFAOYSA-N 0.000 description 4
- 230000006750 UV protection Effects 0.000 description 4
- 239000002168 alkylating agent Substances 0.000 description 4
- 229940100198 alkylating agent Drugs 0.000 description 4
- 230000009435 amidation Effects 0.000 description 4
- 238000007112 amidation reaction Methods 0.000 description 4
- 150000001565 benzotriazoles Chemical class 0.000 description 4
- 238000004061 bleaching Methods 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 239000003205 fragrance Substances 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 239000000123 paper Substances 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- 230000003711 photoprotective effect Effects 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- NPSJHQMIVNJLNN-UHFFFAOYSA-N 2-ethylhexyl 4-nitrobenzoate Chemical compound CCCCC(CC)COC(=O)C1=CC=C([N+]([O-])=O)C=C1 NPSJHQMIVNJLNN-UHFFFAOYSA-N 0.000 description 3
- 239000004808 2-ethylhexylester Substances 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 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
- 230000001166 anti-perspirative effect Effects 0.000 description 3
- 239000003213 antiperspirant Substances 0.000 description 3
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 3
- 239000002324 mouth wash Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 230000001681 protective effect Effects 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical class OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 2
- VMKOFRJSULQZRM-UHFFFAOYSA-N 1-bromooctane Chemical compound CCCCCCCCBr VMKOFRJSULQZRM-UHFFFAOYSA-N 0.000 description 2
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 241000186245 Corynebacterium xerosis Species 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-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
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
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- 239000004952 Polyamide Substances 0.000 description 2
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 239000002250 absorbent Substances 0.000 description 2
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- 150000001768 cations Chemical class 0.000 description 2
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- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
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- QOHMWDJIBGVPIF-UHFFFAOYSA-N n',n'-diethylpropane-1,3-diamine Chemical compound CCN(CC)CCCN QOHMWDJIBGVPIF-UHFFFAOYSA-N 0.000 description 2
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- OIQXFRANQVWXJF-ACCUITESSA-N (2e)-2-benzylidene-4,7,7-trimethylbicyclo[2.2.1]heptan-3-one Chemical compound CC1(C)C2CCC1(C)C(=O)\C2=C\C1=CC=CC=C1 OIQXFRANQVWXJF-ACCUITESSA-N 0.000 description 1
- CUNWUEBNSZSNRX-RKGWDQTMSA-N (2r,3r,4r,5s)-hexane-1,2,3,4,5,6-hexol;(z)-octadec-9-enoic acid Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O CUNWUEBNSZSNRX-RKGWDQTMSA-N 0.000 description 1
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- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
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- JLCTUGNTSLBAND-UHFFFAOYSA-N 2-[4-(2-hydroxy-4-octoxyphenyl)-6-(4-methoxyphenyl)-1,3,5-triazin-2-yl]-5-octoxyphenol Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C1=NC(C=2C=CC(OC)=CC=2)=NC(C=2C(=CC(OCCCCCCCC)=CC=2)O)=N1 JLCTUGNTSLBAND-UHFFFAOYSA-N 0.000 description 1
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- 125000006176 2-ethylbutyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(C([H])([H])*)C([H])([H])C([H])([H])[H] 0.000 description 1
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- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- 239000001027 temporary hair color Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 235000015961 tonic Nutrition 0.000 description 1
- 230000001256 tonic effect Effects 0.000 description 1
- 229960000716 tonics Drugs 0.000 description 1
- 125000002889 tridecyl 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])[H] 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl 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])[H] 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- LOIYMIARKYCTBW-UHFFFAOYSA-N urocanic acid Chemical compound OC(=O)C=CC1=CNC=N1 LOIYMIARKYCTBW-UHFFFAOYSA-N 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3472—Five-membered rings
- C08K5/3475—Five-membered rings condensed with carbocyclic rings
-
- 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
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A61K8/4966—Triazines or their condensed derivatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/16—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
- C07D249/18—Benzotriazoles
- C07D249/20—Benzotriazoles with aryl radicals directly attached in position 2
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Cosmetics (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Paper (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP99811053 | 1999-11-16 | ||
| PCT/EP2000/010969 WO2001036396A1 (en) | 1999-11-16 | 2000-11-07 | Use of benzotriazole uv absorbers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA02004723A true MXPA02004723A (es) | 2002-08-30 |
Family
ID=8243144
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA02004723A MXPA02004723A (es) | 1999-11-16 | 2000-11-07 | Uso de absorbentes de uv de benzotriazol. |
Country Status (12)
| Country | Link |
|---|---|
| US (3) | US7066184B1 (enExample) |
| EP (1) | EP1232148B1 (enExample) |
| JP (1) | JP2003514805A (enExample) |
| CN (1) | CN1198808C (enExample) |
| AT (1) | ATE294784T1 (enExample) |
| AU (1) | AU779934B2 (enExample) |
| BR (1) | BR0015619A (enExample) |
| DE (1) | DE60019959T2 (enExample) |
| ES (1) | ES2241669T3 (enExample) |
| IL (1) | IL149342A0 (enExample) |
| MX (1) | MXPA02004723A (enExample) |
| WO (1) | WO2001036396A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2004020530A1 (en) | 2002-08-30 | 2004-03-11 | Ciba Specialty Chemicals Holding Inc. | Coloured gloss pigments having at least one coating of siox, with x=0.03 to 0.95 for use in cosmetic and personal care formulations |
| WO2005042828A2 (en) * | 2003-11-03 | 2005-05-12 | Ciba Specialty Chemicals Holding Inc. | Stabilized body care products, household products, textiles and fabrics |
| DE602005015749D1 (de) * | 2004-11-09 | 2009-09-10 | Ciba Holding Inc | Antimikrobielle polymerzusammensetzungen mit verbesserter verfärbungsbeständigkeit |
| EP1893697B1 (en) | 2005-06-23 | 2014-04-23 | Basf Se | Nitrosulfide dyes |
| JP5204766B2 (ja) | 2006-06-13 | 2013-06-05 | チバ ホールディング インコーポレーテッド | トリカチオン性染料 |
| EP1992659B1 (de) * | 2007-05-16 | 2016-07-20 | EMS-Patent AG | Polyamidformmassen-Schmelze zur Herstellung von transparenten Formteilen |
| JP5875576B2 (ja) * | 2012-12-26 | 2016-03-02 | シプロ化成株式会社 | ベンゾトリアゾール化合物及びこれを用いた化粧用紫外線吸収剤と皮膚外用剤 |
| WO2015059368A1 (fr) | 2013-09-02 | 2015-04-30 | L'oreal | Procede de coloration des fibres keratiniques a partir de colorants cationiques styryles disulfures, et composition comprenant lesdits colorants |
| CN105155338A (zh) * | 2015-09-10 | 2015-12-16 | 上海晶华胶粘新材料股份有限公司 | 抗uv水性纸张浸渍剂及其制备方法 |
| CN106279051A (zh) * | 2016-08-11 | 2017-01-04 | 重庆大学 | 一类水性的含查耳酮‑苯并三氮唑二联体的可见光光敏剂 |
| CN108947920B (zh) * | 2018-07-19 | 2021-05-25 | 浙江理工大学上虞工业技术研究院有限公司 | 反应性紫外线吸收剂及其制备方法 |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL126588C (enExample) | 1961-06-16 | |||
| NL6809017A (enExample) * | 1967-07-01 | 1969-01-03 | ||
| CA1006165A (en) | 1971-04-06 | 1977-03-01 | Eastman Kodak Company | Ballasted color photographic couplers |
| JPS50121178A (enExample) | 1974-03-12 | 1975-09-22 | ||
| DE2434934B2 (de) | 1974-07-19 | 1977-05-26 | Presseinrichtung zum beidseitigen oberflaechenvergueten von flaechigen werkstoffen durch aufpressen von waermehaertbaren kunstharzen | |
| EP0133164B1 (de) | 1983-07-26 | 1988-12-14 | Ciba-Geigy Ag | Copolymerisierbare Verbindungen |
| JPS61192781A (ja) * | 1985-02-21 | 1986-08-27 | Toyota Central Res & Dev Lab Inc | 水溶性紫外線吸収剤 |
| US4937349A (en) * | 1987-10-29 | 1990-06-26 | Ciba-Geigy Corporation | Process for the preparation of 3-[2'H-benzotriazol-(2')-yl]-4-hydroxy-benzenesulfonic acids and the salts thereof |
| US5096781A (en) * | 1988-12-19 | 1992-03-17 | Ciba-Geigy Corporation | Water-soluble compounds as light stabilizers |
| US5280124A (en) * | 1991-02-12 | 1994-01-18 | Ciba-Geigy Corporation | 5-sulfonyl-substituted benzotriazole UV-absorbers |
| JPH06305938A (ja) * | 1993-03-08 | 1994-11-01 | Lion Corp | 毛髪化粧料 |
| JPH07228510A (ja) * | 1994-02-17 | 1995-08-29 | Lion Corp | 毛髪化粧料 |
| TW332827B (en) * | 1994-02-24 | 1998-06-01 | Ciba Sc Holding Ag | UV absorber |
| JPH09268183A (ja) * | 1996-03-30 | 1997-10-14 | Oji Paper Co Ltd | ベンゾトリアゾール化合物、及びこれを用いた感熱記録体 |
| DE19748658B4 (de) | 1996-11-07 | 2015-08-20 | Ciba Holding Inc. | Benzotriazol-UV-Absorptionsmittel mit erhöhter Haltbarkeit |
| IL129705A (en) * | 1996-11-22 | 2003-10-31 | Ciba Sc Holding Ag | Use of selected benzotriazole derivatives for protecting human and animal skin and hair from the harmful effects of uv radiation |
| JPH11254812A (ja) * | 1998-03-13 | 1999-09-21 | Oji Paper Co Ltd | インクジェット記録体 |
| EP1135093B1 (en) * | 1998-11-02 | 2010-07-07 | Basf Se | Stabilization of body-care and household products |
| JP2000141874A (ja) * | 1998-11-10 | 2000-05-23 | Oji Paper Co Ltd | インクジェット記録用シート |
-
2000
- 2000-11-07 DE DE60019959T patent/DE60019959T2/de not_active Expired - Lifetime
- 2000-11-07 JP JP2001538885A patent/JP2003514805A/ja active Pending
- 2000-11-07 EP EP00976009A patent/EP1232148B1/en not_active Expired - Lifetime
- 2000-11-07 BR BR0015619-1A patent/BR0015619A/pt not_active IP Right Cessation
- 2000-11-07 AT AT00976009T patent/ATE294784T1/de not_active IP Right Cessation
- 2000-11-07 AU AU13927/01A patent/AU779934B2/en not_active Ceased
- 2000-11-07 ES ES00976009T patent/ES2241669T3/es not_active Expired - Lifetime
- 2000-11-07 IL IL14934200A patent/IL149342A0/xx unknown
- 2000-11-07 MX MXPA02004723A patent/MXPA02004723A/es active IP Right Grant
- 2000-11-07 WO PCT/EP2000/010969 patent/WO2001036396A1/en not_active Ceased
- 2000-11-07 US US10/130,235 patent/US7066184B1/en not_active Expired - Fee Related
- 2000-11-07 CN CNB008157642A patent/CN1198808C/zh not_active Expired - Fee Related
-
2005
- 2005-01-31 US US11/046,913 patent/US7179924B2/en not_active Expired - Fee Related
- 2005-06-30 US US11/171,309 patent/US7129198B1/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JP2003514805A (ja) | 2003-04-22 |
| IL149342A0 (en) | 2002-11-10 |
| CN1198808C (zh) | 2005-04-27 |
| WO2001036396A1 (en) | 2001-05-25 |
| AU1392701A (en) | 2001-05-30 |
| US20050158255A1 (en) | 2005-07-21 |
| US7066184B1 (en) | 2006-06-27 |
| ATE294784T1 (de) | 2005-05-15 |
| ES2241669T3 (es) | 2005-11-01 |
| BR0015619A (pt) | 2002-07-16 |
| DE60019959T2 (de) | 2005-11-17 |
| AU779934B2 (en) | 2005-02-17 |
| EP1232148B1 (en) | 2005-05-04 |
| CN1390209A (zh) | 2003-01-08 |
| EP1232148A1 (en) | 2002-08-21 |
| DE60019959D1 (de) | 2005-06-09 |
| US7129198B1 (en) | 2006-10-31 |
| US7179924B2 (en) | 2007-02-20 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant or registration |