SE522685C2 - Hydroxyfenyltriaziner - Google Patents

Hydroxyfenyltriaziner

Info

Publication number: SE522685C2
Authority: SE; Sweden
Prior art keywords: alkyl; phenyl; dok; substituted; cycloalkyl
Prior art date: 1996-11-20

Application number

SE9704171A

Other languages

English (en)

Swedish (sv)

Other versions

SE9704171D0 (sv

SE9704171L (sv

Inventor

Dietmar Hueglin

Vien Van Toan

Helmut Luther

Christophe Bulliard

Gerhard Rytz

Original Assignee

Ciba Sc Holding Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1996-11-20

Filing date

1997-11-14

Publication date

2004-02-24

1997-11-14 Application filed by Ciba Sc Holding Ag filed Critical Ciba Sc Holding Ag

1997-11-14 Publication of SE9704171D0 publication Critical patent/SE9704171D0/xx

1998-05-21 Publication of SE9704171L publication Critical patent/SE9704171L/xx

2004-02-24 Publication of SE522685C2 publication Critical patent/SE522685C2/sv

Links

150000001875 compounds Chemical class 0.000 claims abstract description 135
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 93
239000003381 stabilizer Substances 0.000 claims abstract description 36
238000002360 preparation method Methods 0.000 claims abstract description 34
150000002367 halogens Chemical class 0.000 claims abstract description 33
229910052736 halogen Inorganic materials 0.000 claims abstract description 32
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims abstract description 24
239000011368 organic material Substances 0.000 claims abstract description 16
229910052760 oxygen Inorganic materials 0.000 claims abstract description 12
125000000882 C2-C6 alkenyl group Chemical group 0.000 claims abstract description 11
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 11
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 11
239000001301 oxygen Substances 0.000 claims abstract description 11
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 9
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 7
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims abstract description 6
125000004430 oxygen atom Chemical group O* 0.000 claims abstract description 5
101100516568 Caenorhabditis elegans nhr-7 gene Proteins 0.000 claims abstract 2
-1 1-adamantyl Chemical group 0.000 claims description 184
239000010410 layer Substances 0.000 claims description 126
125000000217 alkyl group Chemical group 0.000 claims description 111
239000000203 mixture Substances 0.000 claims description 98
239000000463 material Substances 0.000 claims description 88
229910052739 hydrogen Inorganic materials 0.000 claims description 48
239000006096 absorbing agent Substances 0.000 claims description 42
125000000753 cycloalkyl group Chemical group 0.000 claims description 38
239000000839 emulsion Substances 0.000 claims description 35
125000003118 aryl group Chemical group 0.000 claims description 31
238000000034 method Methods 0.000 claims description 29
239000002537 cosmetic Substances 0.000 claims description 27
239000004332 silver Substances 0.000 claims description 23
229910052709 silver Inorganic materials 0.000 claims description 23
239000001257 hydrogen Substances 0.000 claims description 22
125000003545 alkoxy group Chemical group 0.000 claims description 21
125000003342 alkenyl group Chemical group 0.000 claims description 20
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 19
239000007983 Tris buffer Substances 0.000 claims description 16
229910052799 carbon Inorganic materials 0.000 claims description 15
125000003884 phenylalkyl group Chemical group 0.000 claims description 14
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 13
239000000654 additive Substances 0.000 claims description 13
239000000758 substrate Substances 0.000 claims description 13
239000004611 light stabiliser Substances 0.000 claims description 12
239000000499 gel Substances 0.000 claims description 11
239000006210 lotion Substances 0.000 claims description 11
125000004423 acyloxy group Chemical group 0.000 claims description 9
125000004104 aryloxy group Chemical group 0.000 claims description 9
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
230000008569 process Effects 0.000 claims description 9
238000004061 bleaching Methods 0.000 claims description 8
238000001035 drying Methods 0.000 claims description 8
239000011241 protective layer Substances 0.000 claims description 8
230000000087 stabilizing effect Effects 0.000 claims description 8
125000003302 alkenyloxy group Chemical group 0.000 claims description 7
125000003710 aryl alkyl group Chemical group 0.000 claims description 7
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 7
238000004040 coloring Methods 0.000 claims description 7
150000002431 hydrogen Chemical class 0.000 claims description 7
125000002947 alkylene group Chemical group 0.000 claims description 6
239000006260 foam Substances 0.000 claims description 6
230000009931 harmful effect Effects 0.000 claims description 6
238000005303 weighing Methods 0.000 claims description 6
241001465754 Metazoa Species 0.000 claims description 5
125000000000 cycloalkoxy group Chemical group 0.000 claims description 5
125000001624 naphthyl group Chemical group 0.000 claims description 5
230000005855 radiation Effects 0.000 claims description 5
125000006727 (C1-C6) alkenyl group Chemical group 0.000 claims description 4
125000006374 C2-C10 alkenyl group Chemical group 0.000 claims description 4
239000008266 hair spray Substances 0.000 claims description 4
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
239000000546 pharmaceutical excipient Substances 0.000 claims description 4
239000002453 shampoo Substances 0.000 claims description 4
238000003860 storage Methods 0.000 claims description 4
125000006702 (C1-C18) alkyl group Chemical group 0.000 claims description 3
125000004648 C2-C8 alkenyl group Chemical group 0.000 claims description 3
241000282412 Homo Species 0.000 claims description 3
125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 claims description 3
125000005075 adamantyloxy group Chemical group C12(CC3CC(CC(C1)C3)C2)O* 0.000 claims description 3
125000004183 alkoxy alkyl group Chemical group 0.000 claims description 3
230000001680 brushing effect Effects 0.000 claims description 3
229920005613 synthetic organic polymer Polymers 0.000 claims description 3
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 3
125000003944 tolyl group Chemical group 0.000 claims description 3
125000004450 alkenylene group Chemical group 0.000 claims description 2
125000002877 alkyl aryl group Chemical group 0.000 claims description 2
125000005037 alkyl phenyl group Chemical group 0.000 claims description 2
150000001602 bicycloalkyls Chemical group 0.000 claims description 2
239000003676 hair preparation Substances 0.000 claims description 2
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 claims description 2
125000006839 xylylene group Chemical group 0.000 claims description 2
125000004399 C1-C4 alkenyl group Chemical group 0.000 claims 3
125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 1
DBBFQMCHJHMNDC-UHFFFAOYSA-N 2-[4,6-bis(4-heptoxy-2-hydroxyphenyl)-1,3,5-triazin-2-yl]-5-heptoxyphenol Chemical compound OC1=C(C=CC(=C1)OCCCCCCC)C1=NC(=NC(=N1)C1=C(C=C(C=C1)OCCCCCCC)O)C1=C(C=C(C=C1)OCCCCCCC)O DBBFQMCHJHMNDC-UHFFFAOYSA-N 0.000 claims 1
208000028257 Joubert syndrome with oculorenal defect Diseases 0.000 claims 1
239000004231 Riboflavin-5-Sodium Phosphate Substances 0.000 claims 1
125000005293 bicycloalkoxy group Chemical group 0.000 claims 1
125000004985 dialkyl amino alkyl group Chemical group 0.000 claims 1
238000004043 dyeing Methods 0.000 claims 1
125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract description 2
230000000254 damaging effect Effects 0.000 abstract 1
229910052757 nitrogen Inorganic materials 0.000 description 52
229920000642 polymer Polymers 0.000 description 49
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 47
238000000576 coating method Methods 0.000 description 31
239000002585 base Substances 0.000 description 30
229920001577 copolymer Polymers 0.000 description 30
238000006243 chemical reaction Methods 0.000 description 27
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 24
229920005989 resin Polymers 0.000 description 24
239000011347 resin Substances 0.000 description 24
108010010803 Gelatin Proteins 0.000 description 21
239000008199 coating composition Substances 0.000 description 21
239000008273 gelatin Substances 0.000 description 21
229920000159 gelatin Polymers 0.000 description 21
235000019322 gelatine Nutrition 0.000 description 21
235000011852 gelatine desserts Nutrition 0.000 description 21
229910052751 metal Inorganic materials 0.000 description 21
239000002184 metal Substances 0.000 description 21
239000003973 paint Substances 0.000 description 21
239000011248 coating agent Substances 0.000 description 20
239000012071 phase Substances 0.000 description 20
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 19
239000011230 binding agent Substances 0.000 description 19
239000003054 catalyst Substances 0.000 description 18
239000004952 Polyamide Substances 0.000 description 17
239000000975 dye Substances 0.000 description 17
229920002647 polyamide Polymers 0.000 description 17
239000004417 polycarbonate Substances 0.000 description 17
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 15
229920000728 polyester Polymers 0.000 description 15
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 14
150000002148 esters Chemical class 0.000 description 14
239000000243 solution Substances 0.000 description 14
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 13
239000004743 Polypropylene Substances 0.000 description 13
150000001412 amines Chemical class 0.000 description 13
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 13
229920001155 polypropylene Polymers 0.000 description 13
239000004814 polyurethane Substances 0.000 description 13
239000002904 solvent Substances 0.000 description 13
125000001424 substituent group Chemical group 0.000 description 13
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
239000004698 Polyethylene Substances 0.000 description 12
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 12
239000000543 intermediate Substances 0.000 description 12
229920000573 polyethylene Polymers 0.000 description 12
229920006324 polyoxymethylene Polymers 0.000 description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 11
239000004721 Polyphenylene oxide Substances 0.000 description 11
229920000515 polycarbonate Polymers 0.000 description 11
239000002253 acid Substances 0.000 description 10
150000001252 acrylic acid derivatives Chemical class 0.000 description 10
239000003921 oil Substances 0.000 description 10
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 10
239000007787 solid Substances 0.000 description 10
238000003756 stirring Methods 0.000 description 10
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 9
239000005977 Ethylene Substances 0.000 description 9
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 9
229920001971 elastomer Polymers 0.000 description 9
229920001684 low density polyethylene Polymers 0.000 description 9
239000004702 low-density polyethylene Substances 0.000 description 9
DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
239000000123 paper Substances 0.000 description 9
229920000570 polyether Polymers 0.000 description 9
229920002635 polyurethane Polymers 0.000 description 9
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 9
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 9
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 8
125000001931 aliphatic group Chemical group 0.000 description 8
KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 8
239000000460 chlorine Substances 0.000 description 8
238000001723 curing Methods 0.000 description 8
239000000047 product Substances 0.000 description 8
150000003839 salts Chemical class 0.000 description 8
229920001169 thermoplastic Polymers 0.000 description 8
239000000080 wetting agent Substances 0.000 description 8
SGZWJGRZDJCDIM-UHFFFAOYSA-N 4-[4,6-bis(2,4-dihydroxyphenyl)-1,3,5-triazin-2-yl]benzene-1,3-diol Chemical compound OC1=CC(O)=CC=C1C1=NC(C=2C(=CC(O)=CC=2)O)=NC(C=2C(=CC(O)=CC=2)O)=N1 SGZWJGRZDJCDIM-UHFFFAOYSA-N 0.000 description 7
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 7
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 7
229920000877 Melamine resin Polymers 0.000 description 7
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
239000004904 UV filter Substances 0.000 description 7
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 7
229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 7
238000001816 cooling Methods 0.000 description 7
150000001993 dienes Chemical class 0.000 description 7
125000000623 heterocyclic group Chemical group 0.000 description 7
239000000049 pigment Substances 0.000 description 7
229920002857 polybutadiene Polymers 0.000 description 7
239000004848 polyfunctional curative Substances 0.000 description 7
229920006380 polyphenylene oxide Polymers 0.000 description 7
229920000915 polyvinyl chloride Polymers 0.000 description 7
239000004800 polyvinyl chloride Substances 0.000 description 7
239000000843 powder Substances 0.000 description 7
239000007858 starting material Substances 0.000 description 7
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
229910019142 PO4 Inorganic materials 0.000 description 6
239000005062 Polybutadiene Substances 0.000 description 6
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 6
150000001298 alcohols Chemical class 0.000 description 6
230000008901 benefit Effects 0.000 description 6
239000003795 chemical substances by application Substances 0.000 description 6
238000007796 conventional method Methods 0.000 description 6
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 6
239000006185 dispersion Substances 0.000 description 6
239000000806 elastomer Substances 0.000 description 6
239000000976 ink Substances 0.000 description 6
238000007641 inkjet printing Methods 0.000 description 6
229910052740 iodine Inorganic materials 0.000 description 6
238000002156 mixing Methods 0.000 description 6
229920000058 polyacrylate Polymers 0.000 description 6
229920000647 polyepoxide Polymers 0.000 description 6
239000005056 polyisocyanate Substances 0.000 description 6
229920001228 polyisocyanate Polymers 0.000 description 6
239000002244 precipitate Substances 0.000 description 6
235000013772 propylene glycol Nutrition 0.000 description 6
229920002554 vinyl polymer Polymers 0.000 description 6
239000004925 Acrylic resin Substances 0.000 description 5
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 5
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 5
229920000180 alkyd Polymers 0.000 description 5
239000012964 benzotriazole Substances 0.000 description 5
150000001565 benzotriazoles Chemical class 0.000 description 5
150000004649 carbonic acid derivatives Chemical class 0.000 description 5
150000001991 dicarboxylic acids Chemical class 0.000 description 5
239000000835 fiber Substances 0.000 description 5
229920001903 high density polyethylene Polymers 0.000 description 5
239000004700 high-density polyethylene Substances 0.000 description 5
239000012948 isocyanate Substances 0.000 description 5
150000002739 metals Chemical class 0.000 description 5
235000021317 phosphate Nutrition 0.000 description 5
229920000139 polyethylene terephthalate Polymers 0.000 description 5
239000005020 polyethylene terephthalate Substances 0.000 description 5
229910000027 potassium carbonate Inorganic materials 0.000 description 5
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 5
239000008096 xylene Substances 0.000 description 5
DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 4
ALVZNPYWJMLXKV-UHFFFAOYSA-N 1,9-Nonanediol Chemical compound OCCCCCCCCCO ALVZNPYWJMLXKV-UHFFFAOYSA-N 0.000 description 4
HTTGVORJOBRXRJ-UHFFFAOYSA-N 2-(triazin-4-yl)phenol Chemical class OC1=CC=CC=C1C1=CC=NN=N1 HTTGVORJOBRXRJ-UHFFFAOYSA-N 0.000 description 4
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
229920002943 EPDM rubber Polymers 0.000 description 4
229920002292 Nylon 6 Polymers 0.000 description 4
YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 4
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 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
239000002250 absorbent Substances 0.000 description 4
230000002745 absorbent Effects 0.000 description 4
125000002252 acyl group Chemical group 0.000 description 4
239000000853 adhesive Substances 0.000 description 4
230000001070 adhesive effect Effects 0.000 description 4
150000008064 anhydrides Chemical class 0.000 description 4
239000003963 antioxidant agent Substances 0.000 description 4
235000006708 antioxidants Nutrition 0.000 description 4
QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 4
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 4
230000015556 catabolic process Effects 0.000 description 4
239000007795 chemical reaction product Substances 0.000 description 4
229940125904 compound 1 Drugs 0.000 description 4
239000012043 crude product Substances 0.000 description 4
238000006731 degradation reaction Methods 0.000 description 4
DENRZWYUOJLTMF-UHFFFAOYSA-N diethyl sulfate Chemical compound CCOS(=O)(=O)OCC DENRZWYUOJLTMF-UHFFFAOYSA-N 0.000 description 4
239000000539 dimer Substances 0.000 description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
239000000706 filtrate Substances 0.000 description 4
238000000227 grinding Methods 0.000 description 4
125000005842 heteroatom Chemical group 0.000 description 4
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 4
238000010348 incorporation Methods 0.000 description 4
229920000554 ionomer Polymers 0.000 description 4
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 4
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
229910052748 manganese Inorganic materials 0.000 description 4
239000011572 manganese Substances 0.000 description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
239000000178 monomer Substances 0.000 description 4
TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 4
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 4
230000001590 oxidative effect Effects 0.000 description 4
239000002245 particle Substances 0.000 description 4
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 4
150000003013 phosphoric acid derivatives Chemical class 0.000 description 4
229920003023 plastic Polymers 0.000 description 4
239000004033 plastic Substances 0.000 description 4
229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 4
229920001225 polyester resin Polymers 0.000 description 4
238000006116 polymerization reaction Methods 0.000 description 4
229920000098 polyolefin Polymers 0.000 description 4
229920001451 polypropylene glycol Polymers 0.000 description 4
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 4
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 4
239000000126 substance Substances 0.000 description 4
230000000475 sunscreen effect Effects 0.000 description 4
239000000516 sunscreening agent Substances 0.000 description 4
229920001187 thermosetting polymer Polymers 0.000 description 4
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 4
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LVZUNTGFCXNQAF-UHFFFAOYSA-N n-nonyl-n-phenylaniline Chemical class C=1C=CC=CC=1N(CCCCCCCCC)C1=CC=CC=C1 LVZUNTGFCXNQAF-UHFFFAOYSA-N 0.000 description 1
ZXGDIORKSOYRMQ-UHFFFAOYSA-N n-octadecylheptadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCCCCCCC ZXGDIORKSOYRMQ-UHFFFAOYSA-N 0.000 description 1
MCMMSXFAWOGWQE-UHFFFAOYSA-N n-octadecylhexadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCCCCCC MCMMSXFAWOGWQE-UHFFFAOYSA-N 0.000 description 1
MHJCZOMOUCUAOI-UHFFFAOYSA-N n-tert-butyl-n-phenylaniline Chemical class C=1C=CC=CC=1N(C(C)(C)C)C1=CC=CC=C1 MHJCZOMOUCUAOI-UHFFFAOYSA-N 0.000 description 1
SLYJXPKHTZCZOG-UHFFFAOYSA-N n-tetradecyltetradecan-1-imine oxide Chemical compound CCCCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCCCC SLYJXPKHTZCZOG-UHFFFAOYSA-N 0.000 description 1
125000005609 naphthenate group Chemical group 0.000 description 1
229920005615 natural polymer Polymers 0.000 description 1
229930014626 natural product Natural products 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
150000002816 nickel compounds Chemical class 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
229920001220 nitrocellulos Polymers 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
125000001400 nonyl 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])[H] 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
125000002872 norbornadienyl group Chemical group C12=C(C=C(CC1)C2)* 0.000 description 1
JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 1
125000003518 norbornenyl group Chemical group C12(C=CC(CC1)C2)* 0.000 description 1
239000002667 nucleating agent Substances 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
125000005474 octanoate group Chemical group 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
229920000620 organic polymer Polymers 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
238000010422 painting Methods 0.000 description 1
125000000913 palmityl 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])[H] 0.000 description 1
125000002958 pentadecyl 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])[H] 0.000 description 1
RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
239000002304 perfume Substances 0.000 description 1
229950000688 phenothiazine Drugs 0.000 description 1
229960000969 phenyl salicylate Drugs 0.000 description 1
ZPNJBTBYIHBSIG-UHFFFAOYSA-N phenyl-(2,2,6,6-tetramethylpiperidin-4-yl)methanone Chemical compound C1C(C)(C)NC(C)(C)CC1C(=O)C1=CC=CC=C1 ZPNJBTBYIHBSIG-UHFFFAOYSA-N 0.000 description 1
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
125000004346 phenylpentyl group Chemical group C1(=CC=CC=C1)CCCCC* 0.000 description 1
125000004344 phenylpropyl group Chemical group 0.000 description 1
150000003904 phospholipids Chemical class 0.000 description 1
150000004714 phosphonium salts Chemical group 0.000 description 1
OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
239000012994 photoredox catalyst Substances 0.000 description 1
239000003495 polar organic solvent Substances 0.000 description 1
229920001627 poly(4-methyl styrene) Polymers 0.000 description 1
229920001084 poly(chloroprene) Polymers 0.000 description 1
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
229920003055 poly(ester-imide) Polymers 0.000 description 1
229920001643 poly(ether ketone) Polymers 0.000 description 1
229920002492 poly(sulfone) Polymers 0.000 description 1
229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
229920001515 polyalkylene glycol Polymers 0.000 description 1
229920001748 polybutylene Polymers 0.000 description 1
239000004645 polyester resin Substances 0.000 description 1
229920006393 polyether sulfone Polymers 0.000 description 1
229920001601 polyetherimide Polymers 0.000 description 1
229940068886 polyethylene glycol 300 Drugs 0.000 description 1
229920001721 polyimide Polymers 0.000 description 1
229920001195 polyisoprene Polymers 0.000 description 1
229920002959 polymer blend Polymers 0.000 description 1
229920000193 polymethacrylate Polymers 0.000 description 1
229920005606 polypropylene copolymer Polymers 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
MQOCIYICOGDBSG-UHFFFAOYSA-M potassium;hexadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCC([O-])=O MQOCIYICOGDBSG-UHFFFAOYSA-M 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
239000002243 precursor Substances 0.000 description 1
VFHDDANHQLKHJQ-UHFFFAOYSA-N prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OC(=O)C=C VFHDDANHQLKHJQ-UHFFFAOYSA-N 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
DSNYFFJTZPIKFZ-UHFFFAOYSA-N propoxybenzene Chemical group CCCOC1=CC=CC=C1 DSNYFFJTZPIKFZ-UHFFFAOYSA-N 0.000 description 1
238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
238000010926 purge Methods 0.000 description 1
238000000746 purification Methods 0.000 description 1
150000003217 pyrazoles Chemical class 0.000 description 1
VNAUDIIOSMNXBA-UHFFFAOYSA-N pyrazolo[4,3-c]pyrazole Chemical class N1=NC=C2N=NC=C21 VNAUDIIOSMNXBA-UHFFFAOYSA-N 0.000 description 1
125000004076 pyridyl group Chemical group 0.000 description 1
125000000714 pyrimidinyl group Chemical group 0.000 description 1
RQGPLDBZHMVWCH-UHFFFAOYSA-N pyrrolo[3,2-b]pyrrole Chemical compound C1=NC2=CC=NC2=C1 RQGPLDBZHMVWCH-UHFFFAOYSA-N 0.000 description 1
GZTPJDLYPMPRDF-UHFFFAOYSA-N pyrrolo[3,2-c]pyrazole Chemical compound N1=NC2=CC=NC2=C1 GZTPJDLYPMPRDF-UHFFFAOYSA-N 0.000 description 1
125000000168 pyrrolyl group Chemical group 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
238000010526 radical polymerization reaction Methods 0.000 description 1
238000011110 re-filtration Methods 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000001454 recorded image Methods 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000012744 reinforcing agent Substances 0.000 description 1
230000001850 reproductive effect Effects 0.000 description 1
238000000518 rheometry Methods 0.000 description 1
229910052895 riebeckite Inorganic materials 0.000 description 1
238000007142 ring opening reaction Methods 0.000 description 1
JZWFDVDETGFGFC-UHFFFAOYSA-N salacetamide Chemical group CC(=O)NC(=O)C1=CC=CC=C1O JZWFDVDETGFGFC-UHFFFAOYSA-N 0.000 description 1
ORIHZIZPTZTNCU-YVMONPNESA-N salicylaldoxime Chemical compound O\N=C/C1=CC=CC=C1O ORIHZIZPTZTNCU-YVMONPNESA-N 0.000 description 1
239000004576 sand Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
239000002002 slurry Substances 0.000 description 1
WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
235000010234 sodium benzoate Nutrition 0.000 description 1
239000004299 sodium benzoate Substances 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
IJRHDFLHUATAOS-DPMBMXLASA-M sodium ricinoleate Chemical compound [Na+].CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O IJRHDFLHUATAOS-DPMBMXLASA-M 0.000 description 1
229940074404 sodium succinate Drugs 0.000 description 1
ZDQYSKICYIVCPN-UHFFFAOYSA-L sodium succinate (anhydrous) Chemical compound [Na+].[Na+].[O-]C(=O)CCC([O-])=O ZDQYSKICYIVCPN-UHFFFAOYSA-L 0.000 description 1
239000011343 solid material Substances 0.000 description 1
239000001593 sorbitan monooleate Substances 0.000 description 1
235000011069 sorbitan monooleate Nutrition 0.000 description 1
229940035049 sorbitan monooleate Drugs 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
230000003595 spectral effect Effects 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000009987 spinning Methods 0.000 description 1
230000002269 spontaneous effect Effects 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003892 spreading Methods 0.000 description 1
230000007480 spreading Effects 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
229920000638 styrene acrylonitrile Polymers 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
238000006277 sulfonation reaction Methods 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
229910021653 sulphate ion Inorganic materials 0.000 description 1
230000001360 synchronised effect Effects 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
MHSKRLJMQQNJNC-UHFFFAOYSA-N terephthalamide Chemical compound NC(=O)C1=CC=C(C(N)=O)C=C1 MHSKRLJMQQNJNC-UHFFFAOYSA-N 0.000 description 1
229920002803 thermoplastic polyurethane Polymers 0.000 description 1
150000003549 thiazolines Chemical class 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
125000001544 thienyl group Chemical group 0.000 description 1
230000009974 thixotropic effect Effects 0.000 description 1
235000010215 titanium dioxide Nutrition 0.000 description 1
229930003799 tocopherol Natural products 0.000 description 1
229960001295 tocopherol Drugs 0.000 description 1
235000019149 tocopherols Nutrition 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
238000005809 transesterification reaction Methods 0.000 description 1
238000012546 transfer Methods 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
125000004306 triazinyl group Chemical group 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
OHRVKCZTBPSUIK-UHFFFAOYSA-N tridodecyl phosphate Chemical compound CCCCCCCCCCCCOP(=O)(OCCCCCCCCCCCC)OCCCCCCCCCCCC OHRVKCZTBPSUIK-UHFFFAOYSA-N 0.000 description 1
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 description 1
RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical class C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 1
239000001226 triphosphate Substances 0.000 description 1
235000011178 triphosphate Nutrition 0.000 description 1
UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
AZSKHRTUXHLAHS-UHFFFAOYSA-N tris(2,4-di-tert-butylphenyl) phosphate Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(=O)(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C AZSKHRTUXHLAHS-UHFFFAOYSA-N 0.000 description 1
OOZBTDPWFHJVEK-UHFFFAOYSA-N tris(2-nonylphenyl) phosphate Chemical compound CCCCCCCCCC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC OOZBTDPWFHJVEK-UHFFFAOYSA-N 0.000 description 1
WGKLOLBTFWFKOD-UHFFFAOYSA-N tris(2-nonylphenyl) phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC WGKLOLBTFWFKOD-UHFFFAOYSA-N 0.000 description 1
229920000785 ultra high molecular weight polyethylene Polymers 0.000 description 1
229920001862 ultra low molecular weight polyethylene Polymers 0.000 description 1
238000009281 ultraviolet germicidal irradiation Methods 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
229920006337 unsaturated polyester resin Polymers 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
229940099259 vaseline Drugs 0.000 description 1
239000011709 vitamin E Substances 0.000 description 1
235000019165 vitamin E Nutrition 0.000 description 1
229940046009 vitamin E Drugs 0.000 description 1
239000007762 w/o emulsion Substances 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1
229910052724 xenon Inorganic materials 0.000 description 1
FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
238000004383 yellowing Methods 0.000 description 1
150000003751 zinc Chemical class 0.000 description 1
XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
239000002478 γ-tocopherol Substances 0.000 description 1
QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 1
QUEDXNHFTDJVIY-DQCZWYHMSA-N γ-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-DQCZWYHMSA-N 0.000 description 1

Classifications

- 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
- 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
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/14—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
- C07D251/24—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to three ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K15/00—Anti-oxidant compositions; Compositions inhibiting chemical change
- C09K15/04—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds
- C09K15/30—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing heterocyclic ring with at least one nitrogen atom as ring member
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
- G03C1/815—Photosensitive materials characterised by the base or auxiliary layers characterised by means for filtering or absorbing ultraviolet light, e.g. optical bleaching
- G03C1/8155—Organic compounds therefor

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Veterinary Medicine (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Epidemiology (AREA)
Birds (AREA)
Dermatology (AREA)
Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Plural Heterocyclic Compounds (AREA)
Compositions Of Macromolecular Compounds (AREA)
Cosmetics (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Silver Salt Photography Or Processing Solution Therefor (AREA)
Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

SE9704171A 1996-11-20 1997-11-14 Hydroxyfenyltriaziner SE522685C2 (sv)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH286496		1996-11-20

Publications (3)

Publication Number	Publication Date
SE9704171D0 SE9704171D0 (sv)	1997-11-14
SE9704171L SE9704171L (sv)	1998-05-21
SE522685C2 true SE522685C2 (sv)	2004-02-24

Family

ID=4243310

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE9704171A SE522685C2 (sv)	1996-11-20	1997-11-14	Hydroxyfenyltriaziner

Country Status (17)

Country	Link
US (2)	US6184375B1 (es)
JP (2)	JP4366670B2 (es)
CN (1)	CN1156456C (es)
AT (1)	AT410317B (es)
AU (1)	AU734952B2 (es)
BE (1)	BE1011550A3 (es)
BR (1)	BR9704843B1 (es)
CA (1)	CA2221473C (es)
DE (1)	DE19750906B4 (es)
ES (1)	ES2135347B1 (es)
FR (1)	FR2755966B1 (es)
GB (1)	GB2319523B (es)
IT (1)	IT1296467B1 (es)
NL (1)	NL1007590C2 (es)
NO (1)	NO318981B1 (es)
SE (1)	SE522685C2 (es)
TW (1)	TW546291B (es)

Families Citing this family (206)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6117997A (en) *	1997-11-19	2000-09-12	Ciba Specialty Chemicals Corporation	Hydroxyphenyltriazines
JP2000026435A (ja)	1998-05-07	2000-01-25	Ciba Specialty Chem Holding Inc	トリスレゾリシニルトリアジン
AU4425599A (en) *	1998-06-22	2000-01-10	Ciba Specialty Chemicals Holding Inc.	Trisaryl-1,3,5-triazine ultraviolet light absorbers containing hindered phenols
ID29406A (id) *	1998-11-02	2001-08-30	Ciba Sc Holding Ag	Stabilisasi produk perawatan tubuh dan produk rumah-tangga
MXPA02006120A (es)	1999-12-23	2002-12-05	Ciba Sc Holding Ag	Mezcla de estabilizador.
DE10030658C1 (de) *	2000-06-23	2002-01-03	Trespa Int Bv	Flammwidrige Harzbeschichtung
CO5231248A1 (es)	2000-07-26	2002-12-27	Ciba Sc Holding Ag	Articulos transparentes de polimero de baja consistencia
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- 1997-11-14 AU AU45207/97A patent/AU734952B2/en not_active Expired
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Publication number	Publication date
ES2135347A1 (es)	1999-10-16
GB2319523A (en)	1998-05-27
CA2221473A1 (en)	1998-05-20
DE19750906A1 (de)	1998-05-28
MX9708911A (es)	1998-09-30
NO975305D0 (no)	1997-11-19
US6284821B1 (en)	2001-09-04
CA2221473C (en)	2009-02-17
NO975305L (no)	1998-05-22
SE9704171D0 (sv)	1997-11-14
DE19750906B4 (de)	2008-06-12
ITMI972574A1 (it)	1999-05-19
FR2755966B1 (fr)	2000-10-13
SE9704171L (sv)	1998-05-21
FR2755966A1 (fr)	1998-05-22
NL1007590C2 (nl)	1998-10-27
ES2135347B1 (es)	2000-05-16
JP2009221218A (ja)	2009-10-01
NL1007590A1 (nl)	1998-05-25
US6184375B1 (en)	2001-02-06
BR9704843B1 (pt)	2009-01-13
NO318981B1 (no)	2005-05-30
GB2319523B (en)	2000-11-08
CN1183410A (zh)	1998-06-03
GB9722825D0 (en)	1997-12-24
JP4366670B2 (ja)	2009-11-18
TW546291B (en)	2003-08-11
AU734952B2 (en)	2001-06-28
JP5308914B2 (ja)	2013-10-09
BR9704843A (pt)	1998-10-27
IT1296467B1 (it)	1999-06-25
JPH10182621A (ja)	1998-07-07
CN1156456C (zh)	2004-07-07
BE1011550A3 (fr)	1999-10-05
AU4520797A (en)	1998-05-28
AT410317B (de)	2003-03-25
ATA196397A (de)	2002-08-15

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SE522685C2 (sv)	2004-02-24	Hydroxyfenyltriaziner
KR100363980B1 (ko)	2003-02-14	2,4-비스(2'-히드록시페닐)-6-아릴-1,3,5-트리아진유형의화합물및광,열및산소에의한손상으로부터안정화된유기물질
SE522822C2 (sv)	2004-03-09	Hydroxifenyltriaziner
MXPA03003474A (es)	2003-07-14	Sustancias absorbentes de luz ultravioleta constituida de triazina sustituida con ortodialquilarilo, que no amarillean.
KR20010032250A (ko)	2001-04-16	트리스아릴-1,3,5-트리아진 자외선 흡수제
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