BE1012428A3 - Hydroxyphenyltriazines et compositions de polymeres organiques stabilisees par des hydroxyphenyltriazines. - Google Patents

Hydroxyphenyltriazines et compositions de polymeres organiques stabilisees par des hydroxyphenyltriazines. Download PDF

Info

Publication number: BE1012428A3
Authority: BE; Belgium
Prior art keywords: sep; alkyl; phenyl; residue; formula
Prior art date: 1996-03-26

Application number

BE9700253A

Other languages

English (en)

French (fr)

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.)

1996-03-26

Filing date

1997-03-21

Publication date

2000-11-07

1997-03-21 Application filed by Ciba Sc Holding Ag filed Critical Ciba Sc Holding Ag

2000-11-07 Application granted granted Critical

2000-11-07 Publication of BE1012428A3 publication Critical patent/BE1012428A3/fr

Links

239000000203 mixture Substances 0.000 title claims abstract description 84
VMRIVYANZGSGRV-UHFFFAOYSA-N 4-phenyl-2h-triazin-5-one Chemical class OC1=CN=NN=C1C1=CC=CC=C1 VMRIVYANZGSGRV-UHFFFAOYSA-N 0.000 title description 4
229920000620 organic polymer Polymers 0.000 title description 3
150000001875 compounds Chemical class 0.000 claims abstract description 145
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 18
229910052760 oxygen Inorganic materials 0.000 claims abstract description 18
239000001301 oxygen Substances 0.000 claims abstract description 18
229920005613 synthetic organic polymer Polymers 0.000 claims abstract description 11
230000009931 harmful effect Effects 0.000 claims abstract description 6
-1 alkyl radical Chemical class 0.000 claims description 164
125000000217 alkyl group Chemical group 0.000 claims description 85
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 70
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 69
239000003381 stabilizer Substances 0.000 claims description 37
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 35
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 27
125000003342 alkenyl group Chemical group 0.000 claims description 26
238000000034 method Methods 0.000 claims description 23
125000003884 phenylalkyl group Chemical group 0.000 claims description 23
150000001412 amines Chemical class 0.000 claims description 20
125000002947 alkylene group Chemical group 0.000 claims description 19
239000011230 binding agent Substances 0.000 claims description 19
238000000576 coating method Methods 0.000 claims description 19
125000003302 alkenyloxy group Chemical group 0.000 claims description 17
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 17
125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims description 15
125000003545 alkoxy group Chemical group 0.000 claims description 13
239000000470 constituent Substances 0.000 claims description 10
239000004611 light stabiliser Substances 0.000 claims description 10
150000001602 bicycloalkyls Chemical group 0.000 claims description 9
125000004093 cyano group Chemical group *C#N 0.000 claims description 9
229920001169 thermoplastic Polymers 0.000 claims description 9
125000004400 (C1-C12) alkyl group Chemical group 0.000 claims description 8
125000006702 (C1-C18) alkyl group Chemical group 0.000 claims description 8
125000000753 cycloalkyl group Chemical group 0.000 claims description 8
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 7
229910052799 carbon Inorganic materials 0.000 claims description 7
125000002933 cyclohexyloxy group Chemical group C1(CCCCC1)O* 0.000 claims description 7
239000000654 additive Substances 0.000 claims description 6
230000015556 catabolic process Effects 0.000 claims description 6
125000000000 cycloalkoxy group Chemical group 0.000 claims description 6
238000006731 degradation reaction Methods 0.000 claims description 6
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 5
125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 5
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 5
125000003547 cyclohexylalkoxy group Chemical group 0.000 claims description 5
239000011368 organic material Substances 0.000 claims description 5
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 5
230000006641 stabilisation Effects 0.000 claims description 5
238000011105 stabilization Methods 0.000 claims description 5
230000000087 stabilizing effect Effects 0.000 claims description 5
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 5
230000009471 action Effects 0.000 claims description 4
125000005037 alkyl phenyl group Chemical group 0.000 claims description 4
125000002071 phenylalkoxy group Chemical group 0.000 claims description 4
125000006732 (C1-C15) alkyl group Chemical group 0.000 claims description 3
HWRLEEPNFJNTOP-UHFFFAOYSA-N 2-(1,3,5-triazin-2-yl)phenol Chemical compound OC1=CC=CC=C1C1=NC=NC=N1 HWRLEEPNFJNTOP-UHFFFAOYSA-N 0.000 claims description 2
MHPIFHORTBEEEF-UHFFFAOYSA-N 2-[4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-(2-hydroxycyclohexyl)oxyphenol Chemical compound CC1=C(C=CC(=C1)C)C1=NC(=NC(=N1)C1=C(C=C(C=C1)C)C)C1=C(C=C(C=C1)OC1C(CCCC1)O)O MHPIFHORTBEEEF-UHFFFAOYSA-N 0.000 claims description 2
RIOZSIUZXTUMAM-UHFFFAOYSA-N 5-(2-hydroxycyclohexyl)oxy-2-[4-[2-hydroxy-4-(2-hydroxycyclohexyl)oxyphenyl]-6-phenyl-1,3,5-triazin-2-yl]phenol Chemical compound C1(=CC=CC=C1)C1=NC(=NC(=N1)C1=C(C=C(C=C1)OC1C(CCCC1)O)O)C1=C(C=C(C=C1)OC1C(CCCC1)O)O RIOZSIUZXTUMAM-UHFFFAOYSA-N 0.000 claims description 2
229910052736 halogen Inorganic materials 0.000 claims description 2
150000002367 halogens Chemical class 0.000 claims description 2
125000003518 norbornenyl group Chemical group C12(C=CC(CC1)C2)* 0.000 claims description 2
125000001475 halogen functional group Chemical group 0.000 claims 3
125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 2
125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 1
125000004209 (C1-C8) alkyl group Chemical group 0.000 claims 1
NUENSZMSNYAUJH-UHFFFAOYSA-N 2-(4,6-diphenyl-1,3,5-triazin-2-yl)-5-(2-hydroxycyclohexyl)oxyphenol Chemical compound OC1CCCCC1Oc1ccc(c(O)c1)-c1nc(nc(n1)-c1ccccc1)-c1ccccc1 NUENSZMSNYAUJH-UHFFFAOYSA-N 0.000 claims 1
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 50
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 47
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 42
239000002966 varnish Substances 0.000 description 41
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IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 12
239000005977 Ethylene Substances 0.000 description 12
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 12
150000002148 esters Chemical group 0.000 description 12
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 11
239000004952 Polyamide Substances 0.000 description 11
239000003973 paint Substances 0.000 description 11
229920002647 polyamide Polymers 0.000 description 11
239000000243 solution Substances 0.000 description 11
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XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
229920000877 Melamine resin Polymers 0.000 description 9
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 9
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239000011248 coating agent Substances 0.000 description 9
150000004820 halides Chemical class 0.000 description 9
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239000004702 low-density polyethylene Substances 0.000 description 9
238000002844 melting Methods 0.000 description 9
230000008018 melting Effects 0.000 description 9
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
229920002857 polybutadiene Polymers 0.000 description 9
KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 9
FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 8
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 8
239000005062 Polybutadiene Substances 0.000 description 8
125000005843 halogen group Chemical group 0.000 description 8
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 8
239000004417 polycarbonate Substances 0.000 description 8
230000008569 process Effects 0.000 description 8
239000008096 xylene Substances 0.000 description 8
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
239000002253 acid Substances 0.000 description 7
229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 7
125000001309 chloro group Chemical group Cl* 0.000 description 7
239000012043 crude product Substances 0.000 description 7
150000001993 dienes Chemical class 0.000 description 7
229920001971 elastomer Polymers 0.000 description 7
229920001903 high density polyethylene Polymers 0.000 description 7
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239000007787 solid Substances 0.000 description 7
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WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
150000001252 acrylic acid derivatives Chemical class 0.000 description 6
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 6
125000001931 aliphatic group Chemical group 0.000 description 6
229910052782 aluminium Inorganic materials 0.000 description 6
KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 6
238000004440 column chromatography Methods 0.000 description 6
238000001816 cooling Methods 0.000 description 6
SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 6
230000000694 effects Effects 0.000 description 6
229910052739 hydrogen Inorganic materials 0.000 description 6
150000002739 metals Chemical class 0.000 description 6
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 6
150000002989 phenols Chemical class 0.000 description 6
229920000058 polyacrylate Polymers 0.000 description 6
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239000005056 polyisocyanate Substances 0.000 description 6
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239000004800 polyvinyl chloride Substances 0.000 description 6
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 6
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 6
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XVMSFILGAMDHEY-UHFFFAOYSA-N 6-(4-aminophenyl)sulfonylpyridin-3-amine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=N1 XVMSFILGAMDHEY-UHFFFAOYSA-N 0.000 description 5
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QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 5
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TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
238000010422 painting Methods 0.000 description 1
210000002741 palatine tonsil Anatomy 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
239000002245 particle Substances 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
150000002978 peroxides Chemical class 0.000 description 1
229950000688 phenothiazine Drugs 0.000 description 1
229960000969 phenyl salicylate Drugs 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 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
150000004714 phosphonium salts Chemical group 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
150000003018 phosphorus compounds Chemical class 0.000 description 1
239000012994 photoredox catalyst Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920001603 poly (alkyl acrylates) Polymers 0.000 description 1
229920001627 poly(4-methyl styrene) Polymers 0.000 description 1
229920001084 poly(chloroprene) Polymers 0.000 description 1
229920003055 poly(ester-imide) Polymers 0.000 description 1
229920001643 poly(ether ketone) Polymers 0.000 description 1
229920000889 poly(m-phenylene isophthalamide) 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
229920002480 polybenzimidazole 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
229920001223 polyethylene glycol Polymers 0.000 description 1
229940068886 polyethylene glycol 300 Drugs 0.000 description 1
239000004848 polyfunctional curative Substances 0.000 description 1
229920001721 polyimide Polymers 0.000 description 1
229920001195 polyisoprene Polymers 0.000 description 1
229920000193 polymethacrylate Polymers 0.000 description 1
229920000306 polymethylpentene Polymers 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
229920005749 polyurethane resin 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
229920002620 polyvinyl fluoride Polymers 0.000 description 1
229920002981 polyvinylidene fluoride 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
235000011181 potassium carbonates Nutrition 0.000 description 1
MQOCIYICOGDBSG-UHFFFAOYSA-M potassium;hexadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCC([O-])=O MQOCIYICOGDBSG-UHFFFAOYSA-M 0.000 description 1
239000002243 precursor Substances 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
KOODSCBKXPPKHE-UHFFFAOYSA-N propanethioic s-acid Chemical compound CCC(S)=O KOODSCBKXPPKHE-UHFFFAOYSA-N 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
238000005510 radiation hardening Methods 0.000 description 1
230000001869 rapid Effects 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000012744 reinforcing agent Substances 0.000 description 1
229910052895 riebeckite Inorganic materials 0.000 description 1
WWYDYZMNFQIYPT-UHFFFAOYSA-N ru78191 Chemical compound OC(=O)C(C(O)=O)C1=CC=CC=C1 WWYDYZMNFQIYPT-UHFFFAOYSA-N 0.000 description 1
SMQUZDBALVYZAC-UHFFFAOYSA-N salicylaldehyde Chemical compound OC1=CC=CC=C1C=O SMQUZDBALVYZAC-UHFFFAOYSA-N 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
229910052814 silicon oxide Inorganic materials 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
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
230000003595 spectral effect Effects 0.000 description 1
238000009987 spinning Methods 0.000 description 1
238000005507 spraying Methods 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
KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000000725 suspension Substances 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
239000012209 synthetic fiber Substances 0.000 description 1
WHRNULOCNSKMGB-UHFFFAOYSA-N tetrahydrofuran thf Chemical compound C1CCOC1.C1CCOC1 WHRNULOCNSKMGB-UHFFFAOYSA-N 0.000 description 1
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
229920002803 thermoplastic polyurethane Polymers 0.000 description 1
235000019303 thiodipropionic acid Nutrition 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
239000013008 thixotropic agent Substances 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
235000010215 titanium dioxide Nutrition 0.000 description 1
YONPGGFAJWQGJC-UHFFFAOYSA-K titanium(iii) chloride Chemical compound Cl[Ti](Cl)Cl YONPGGFAJWQGJC-UHFFFAOYSA-K 0.000 description 1
229930003799 tocopherol Natural products 0.000 description 1
235000019149 tocopherols Nutrition 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
150000003918 triazines Chemical class 0.000 description 1
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
CNUJLMSKURPSHE-UHFFFAOYSA-N trioctadecyl phosphite Chemical compound CCCCCCCCCCCCCCCCCCOP(OCCCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCCCC CNUJLMSKURPSHE-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
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
150000003672 ureas Chemical class 0.000 description 1
229920001866 very low density polyethylene Polymers 0.000 description 1
235000019154 vitamin C Nutrition 0.000 description 1
239000011718 vitamin C Substances 0.000 description 1
235000019165 vitamin E Nutrition 0.000 description 1
239000011709 vitamin E Substances 0.000 description 1
229940046009 vitamin E Drugs 0.000 description 1
239000001993 wax Substances 0.000 description 1
239000002023 wood Substances 0.000 description 1
125000005023 xylyl group Chemical group 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
HEPBQSXQJMTVFI-UHFFFAOYSA-N zinc;butane Chemical compound [Zn+2].CCC[CH2-].CCC[CH2-] HEPBQSXQJMTVFI-UHFFFAOYSA-N 0.000 description 1
GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 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

Classifications

- 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
- 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
- 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
- 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
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Compositions Of Macromolecular Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Paints Or Removers (AREA)
Printing Methods (AREA)

BE9700253A 1996-03-26 1997-03-21 Hydroxyphenyltriazines et compositions de polymeres organiques stabilisees par des hydroxyphenyltriazines. BE1012428A3 (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH78396		1996-03-26

Publications (1)

Publication Number	Publication Date
BE1012428A3 true BE1012428A3 (fr)	2000-11-07

Family

ID=4195088

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
BE9700253A BE1012428A3 (fr)	1996-03-26	1997-03-21	Hydroxyphenyltriazines et compositions de polymeres organiques stabilisees par des hydroxyphenyltriazines.

Country Status (18)

Country	Link
US (1)	US5959008A (2)
JP (1)	JP4332819B2 (2)
KR (1)	KR100448332B1 (2)
CN (1)	CN1104476C (2)
AU (1)	AU731977B2 (2)
BE (1)	BE1012428A3 (2)
BR (1)	BR9701462B1 (2)
CA (1)	CA2200807C (2)
CH (1)	CH692739A5 (2)
DE (1)	DE19712277B4 (2)
ES (1)	ES2130985B1 (2)
FR (1)	FR2747122B1 (2)
GB (1)	GB2312210B (2)
IT (1)	IT1290823B1 (2)
NL (1)	NL1005651C2 (2)
SE (1)	SE523139C2 (2)
TW (1)	TW449610B (2)
ZA (1)	ZA975233B (2)

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ES2632783T3 (es)	2014-12-19	2017-09-15	Evonik Degussa Gmbh	Sistemas de redes de cubierta para láminas de encapsulación que comprenden compuestos de bis-(alquenilamidas)
KR102580043B1 (ko)	2015-07-20	2023-09-20	바스프 에스이	난연성 폴리올레핀 물품
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1997
- 1997-03-17 CH CH00638/97A patent/CH692739A5/de not_active IP Right Cessation
- 1997-03-19 SE SE9701012A patent/SE523139C2/sv not_active IP Right Cessation
- 1997-03-20 AU AU16441/97A patent/AU731977B2/en not_active Expired
- 1997-03-21 BE BE9700253A patent/BE1012428A3/fr active
- 1997-03-21 GB GB9705854A patent/GB2312210B/en not_active Expired - Lifetime
- 1997-03-21 US US08/828,200 patent/US5959008A/en not_active Expired - Lifetime
- 1997-03-24 CA CA002200807A patent/CA2200807C/en not_active Expired - Lifetime
- 1997-03-24 DE DE19712277.9A patent/DE19712277B4/de not_active Expired - Lifetime
- 1997-03-25 BR BRPI9701462-1A patent/BR9701462B1/pt not_active IP Right Cessation
- 1997-03-25 ES ES009700638A patent/ES2130985B1/es not_active Expired - Fee Related
- 1997-03-25 ZA ZA9702533A patent/ZA975233B/xx unknown
- 1997-03-25 IT IT97MI000689A patent/IT1290823B1/it active IP Right Grant
- 1997-03-25 TW TW086103743A patent/TW449610B/zh not_active IP Right Cessation
- 1997-03-25 CN CN97109694A patent/CN1104476C/zh not_active Expired - Lifetime
- 1997-03-25 FR FR9703596A patent/FR2747122B1/fr not_active Expired - Lifetime
- 1997-03-26 NL NL1005651A patent/NL1005651C2/nl not_active IP Right Cessation
- 1997-03-26 JP JP11329997A patent/JP4332819B2/ja not_active Expired - Lifetime
- 1997-03-26 KR KR1019970010541A patent/KR100448332B1/ko not_active Expired - Lifetime

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Also Published As

Publication number	Publication date
BR9701462B1 (pt)	2008-11-18
GB2312210A (en)	1997-10-22
FR2747122A1 (fr)	1997-10-10
DE19712277A1 (de)	1997-10-30
ES2130985B1 (es)	2000-03-01
FR2747122B1 (fr)	2003-01-17
KR100448332B1 (ko)	2004-12-04
CN1104476C (zh)	2003-04-02
ITMI970689A1 (it)	1998-09-25
ZA975233B (en)	1997-09-26
BR9701462A (pt)	1998-08-25
SE9701012L (sv)	1997-11-04
DE19712277B4 (de)	2014-11-06
CA2200807C (en)	2007-04-17
NL1005651A1 (nl)	1997-09-30
NL1005651C2 (nl)	2000-06-19
US5959008A (en)	1999-09-28
TW449610B (en)	2001-08-11
KR970065611A (ko)	1997-10-13
SE523139C2 (sv)	2004-03-30
CH692739A5 (de)	2002-10-15
IT1290823B1 (it)	1998-12-11
AU731977B2 (en)	2001-04-12
ES2130985A1 (es)	1999-07-01
AU1644197A (en)	1997-10-02
JP4332819B2 (ja)	2009-09-16
CA2200807A1 (en)	1997-09-26
GB2312210B (en)	1998-08-19
MX9702211A (es)	1998-05-31
SE9701012D0 (sv)	1997-03-19
CN1171422A (zh)	1998-01-28
GB9705854D0 (en)	1997-05-07
JPH1045729A (ja)	1998-02-17

Publication	Publication Date	Title
BE1012428A3 (fr)	2000-11-07	Hydroxyphenyltriazines et compositions de polymeres organiques stabilisees par des hydroxyphenyltriazines.
BE1012529A3 (fr)	2000-12-05	Melange de triaryltriazines et son utilisation pour la stabilisation de materiaux organiques.
BE1011451A5 (fr)	1999-09-07	Hydroxyphenyltriazines comme agents stabilisants de matieres organiques.
BE1012526A5 (fr)	2000-12-05	Melange stabilisant, composition le contenant et procede l'utilisant pour stabiliser une matiere organique.
BE1009461A3 (fr)	1997-04-01	Combinaison de stabilisants contenant des mono- et bis- resorcinyltriazines.
KR100576982B1 (ko)	2006-05-10	모폴리논 유도체, 이를 포함하는 조성물, 이를 사용하여 유기 물질을 안정화시키는 방법 및 이를 제조하기 위한 중간체
BE1014990A5 (fr)	2004-08-03	Procede de preparation d'ethers d'amine a empechement sterique, composes de cette classe et leur utilisation pour stabiliser une matiere organique.
JP5497077B2 (ja)	2014-05-21	トリスレゾリシニルトリアジン
US20060252857A1 (en)	2006-11-09	Aminoaryl-1-3-5-triazines and their use as uv absorbers
RU2418791C2 (ru)	2011-05-20	Гидроксифенилтриазины, содержащие ароматическую карбоциклическую конденсированную кольцевую систему
EP0750011B1 (de)	2001-11-07	Polysiloxane als Lichtschutzmittel
CN1413199A (zh)	2003-04-23	稳定剂混合物
BE1014206A3 (fr)	2003-06-03	Melanges de stabilisants.
BE1012760A3 (fr)	2001-03-06	Composition stabilisee, compose contenu dans celle-ci comme stabilisant et utilisation de ce compose.
BE1011972A3 (fr)	2000-03-07	Compose stabilisant, composition le contenant et son utilisation.
MXPA97002211A (en)	1998-10-23	Hidroxifenil triazi