DD294022A5 - Piperidintriazinverbindungen zum einsatz als stabilisatoren fuer organische materialien - Google Patents

Piperidintriazinverbindungen zum einsatz als stabilisatoren fuer organische materialien Download PDF

Info

Publication number: DD294022A5
Authority: DD; German Democratic Republic
Prior art keywords: alkyl; formula; group; different; hydrogen
Prior art date: 1989-04-27

Application number

DD90340155A

Other languages

German (de)

English (en)

Inventor

Valerio Borzatta

Franca Masina

Original Assignee

��`��@��k��

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.)

1989-04-27

Filing date

1990-04-26

Publication date

1991-09-19

1990-04-26 Application filed by ��`��@��k�� filed Critical ��`��@��k��

1991-09-19 Publication of DD294022A5 publication Critical patent/DD294022A5/de

Links

150000001875 compounds Chemical class 0.000 title claims abstract description 71
239000011368 organic material Substances 0.000 title claims abstract description 14
239000003381 stabilizer Substances 0.000 title abstract description 17
-1 * or * represent Chemical compound 0.000 claims abstract description 130
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 68
239000001257 hydrogen Substances 0.000 claims abstract description 67
150000002431 hydrogen Chemical class 0.000 claims abstract description 40
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 abstract description 25
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 24
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 24
230000003647 oxidation Effects 0.000 claims abstract description 8
238000007254 oxidation reaction Methods 0.000 claims abstract description 8
239000000203 mixture Substances 0.000 claims description 29
125000000217 alkyl group Chemical group 0.000 claims description 23
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 18
125000004430 oxygen atom Chemical group O* 0.000 claims description 17
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 17
CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims description 14
239000004743 Polypropylene Substances 0.000 claims description 11
125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 11
125000002947 alkylene group Chemical group 0.000 claims description 10
229920001155 polypropylene Polymers 0.000 claims description 7
229920001059 synthetic polymer Polymers 0.000 claims description 7
125000006839 xylylene group Chemical group 0.000 claims description 7
239000004698 Polyethylene Substances 0.000 claims description 6
229920000573 polyethylene Polymers 0.000 claims description 6
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
239000000654 additive Substances 0.000 claims description 5
125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 claims description 5
125000003161 (C1-C6) alkylene group Chemical group 0.000 claims description 4
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 4
125000003545 alkoxy group Chemical group 0.000 claims description 4
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 4
125000000623 heterocyclic group Chemical group 0.000 claims description 4
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 4
230000015556 catabolic process Effects 0.000 claims description 3
125000000000 cycloalkoxy group Chemical group 0.000 claims description 3
125000000753 cycloalkyl group Chemical group 0.000 claims description 3
125000004956 cyclohexylene group Chemical group 0.000 claims description 3
238000006731 degradation reaction Methods 0.000 claims description 3
125000002147 dimethylamino group Chemical class [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 3
229920000098 polyolefin Polymers 0.000 claims description 3
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 2
SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims 3
125000006832 (C1-C10) alkylene group Chemical group 0.000 claims 1
241000854350 Enicospilus group Species 0.000 claims 1
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims 1
125000005936 piperidyl group Chemical group 0.000 claims 1
239000004611 light stabiliser Substances 0.000 abstract description 7
239000012760 heat stabilizer Substances 0.000 abstract description 3
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 29
239000010410 layer Substances 0.000 description 28
239000000463 material Substances 0.000 description 27
229920001577 copolymer Polymers 0.000 description 19
238000000034 method Methods 0.000 description 19
229920000642 polymer Polymers 0.000 description 19
229910052757 nitrogen Inorganic materials 0.000 description 17
239000000975 dye Substances 0.000 description 15
239000000976 ink Substances 0.000 description 14
HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 14
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
239000000243 solution Substances 0.000 description 12
230000008569 process Effects 0.000 description 11
239000000047 product Substances 0.000 description 11
238000006243 chemical reaction Methods 0.000 description 10
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239000005062 Polybutadiene Substances 0.000 description 8
125000003118 aryl group Chemical group 0.000 description 8
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VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 7
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239000004800 polyvinyl chloride Substances 0.000 description 7
229920000915 polyvinyl chloride Polymers 0.000 description 7
239000002904 solvent Substances 0.000 description 7
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 7
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 6
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
229920001684 low density polyethylene Polymers 0.000 description 6
239000004702 low-density polyethylene Substances 0.000 description 6
239000004814 polyurethane Substances 0.000 description 6
229910052709 silver Inorganic materials 0.000 description 6
239000004332 silver Substances 0.000 description 6
125000001424 substituent group Chemical group 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
239000008096 xylene Substances 0.000 description 6
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 5
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 5
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
229910052736 halogen Inorganic materials 0.000 description 5
150000002367 halogens Chemical class 0.000 description 5
229920001903 high density polyethylene Polymers 0.000 description 5
239000004700 high-density polyethylene Substances 0.000 description 5
150000002815 nickel Chemical class 0.000 description 5
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239000000843 powder Substances 0.000 description 5
150000003839 salts Chemical class 0.000 description 5
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
229920002292 Nylon 6 Polymers 0.000 description 4
239000004721 Polyphenylene oxide Substances 0.000 description 4
150000001252 acrylic acid derivatives Chemical class 0.000 description 4
229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 4
238000007792 addition Methods 0.000 description 4
KJCVRFUGPWSIIH-UHFFFAOYSA-N alpha-naphthol Natural products C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 4
150000001412 amines Chemical class 0.000 description 4
239000000945 filler Substances 0.000 description 4
238000002844 melting Methods 0.000 description 4
230000008018 melting Effects 0.000 description 4
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 4
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 4
229920000515 polycarbonate Polymers 0.000 description 4
229920000647 polyepoxide Polymers 0.000 description 4
229920000570 polyether Polymers 0.000 description 4
150000005846 sugar alcohols Polymers 0.000 description 4
HWCKGOZZJDHMNC-UHFFFAOYSA-M tetraethylammonium bromide Chemical compound [Br-].CC[N+](CC)(CC)CC HWCKGOZZJDHMNC-UHFFFAOYSA-M 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
229920002943 EPDM rubber Polymers 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
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 3
229920000877 Melamine resin Polymers 0.000 description 3
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
229920002396 Polyurea Polymers 0.000 description 3
239000004372 Polyvinyl alcohol Substances 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 3
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000007983 Tris buffer Substances 0.000 description 3
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
125000004442 acylamino group Chemical group 0.000 description 3
125000001931 aliphatic group Chemical group 0.000 description 3
125000004453 alkoxycarbonyl group Chemical group 0.000 description 3
XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 3
125000003368 amide group Chemical group 0.000 description 3
238000004458 analytical method Methods 0.000 description 3
239000008346 aqueous phase Substances 0.000 description 3
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 3
125000004432 carbon atom Chemical group C* 0.000 description 3
239000004927 clay Substances 0.000 description 3
MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 3
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239000006185 dispersion Substances 0.000 description 3
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235000019256 formaldehyde Nutrition 0.000 description 3
229960004279 formaldehyde Drugs 0.000 description 3
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
238000007641 inkjet printing Methods 0.000 description 3
ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 3
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239000002243 precursor Substances 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
MCSKRVKAXABJLX-UHFFFAOYSA-N pyrazolo[3,4-d]triazole Chemical class N1=NN=C2N=NC=C21 MCSKRVKAXABJLX-UHFFFAOYSA-N 0.000 description 3
229920005989 resin Polymers 0.000 description 3
239000011347 resin Substances 0.000 description 3
239000011734 sodium Substances 0.000 description 3
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238000012546 transfer Methods 0.000 description 3
PFTAWBLQPZVEMU-DZGCQCFKSA-N (+)-catechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-DZGCQCFKSA-N 0.000 description 2
FYGHSUNMUKGBRK-UHFFFAOYSA-N 1,2,3-trimethylbenzene Chemical compound CC1=CC=CC(C)=C1C FYGHSUNMUKGBRK-UHFFFAOYSA-N 0.000 description 2
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
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YHMYGUUIMTVXNW-UHFFFAOYSA-N 1,3-dihydrobenzimidazole-2-thione Chemical compound C1=CC=C2NC(S)=NC2=C1 YHMYGUUIMTVXNW-UHFFFAOYSA-N 0.000 description 2
KJUGUADJHNHALS-UHFFFAOYSA-N 1H-tetrazole Substances C=1N=NNN=1 KJUGUADJHNHALS-UHFFFAOYSA-N 0.000 description 2
ONTODYXHFBKCDK-UHFFFAOYSA-N 2-(2,4-dimethylphenyl)-1,3,5-triazine Chemical compound CC1=CC(C)=CC=C1C1=NC=NC=N1 ONTODYXHFBKCDK-UHFFFAOYSA-N 0.000 description 2
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 2
125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 2
JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
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CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
235000013539 calcium stearate Nutrition 0.000 description 2
239000008116 calcium stearate Substances 0.000 description 2
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 2
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125000001887 cyclopentyloxy group Chemical group C1(CCCC1)O* 0.000 description 2
NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
150000004985 diamines Chemical class 0.000 description 2
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KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 1
125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
239000011241 protective layer Substances 0.000 description 1
150000003217 pyrazoles Chemical class 0.000 description 1
YRJYANBGTAMXRQ-UHFFFAOYSA-N pyrazolo[3,4-h]quinazolin-2-one Chemical compound C1=C2N=NC=C2C2=NC(=O)N=CC2=C1 YRJYANBGTAMXRQ-UHFFFAOYSA-N 0.000 description 1
229940079877 pyrogallol Drugs 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
229920005604 random copolymer Polymers 0.000 description 1
239000012744 reinforcing agent Substances 0.000 description 1
PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
WBHHMMIMDMUBKC-QJWNTBNXSA-M ricinoleate Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O WBHHMMIMDMUBKC-QJWNTBNXSA-M 0.000 description 1
229940066675 ricinoleate Drugs 0.000 description 1
229910052895 riebeckite Inorganic materials 0.000 description 1
239000005060 rubber Substances 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
229940058287 salicylic acid derivative anticestodals Drugs 0.000 description 1
150000003872 salicylic acid derivatives Chemical class 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
238000007650 screen-printing Methods 0.000 description 1
229940116351 sebacate Drugs 0.000 description 1
CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
238000000926 separation method Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
AQRYNYUOKMNDDV-UHFFFAOYSA-M silver behenate Chemical compound [Ag+].CCCCCCCCCCCCCCCCCCCCCC([O-])=O AQRYNYUOKMNDDV-UHFFFAOYSA-M 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
239000000992 solvent dye Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
150000003413 spiro compounds Chemical class 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
230000003068 static effect Effects 0.000 description 1
229920003048 styrene butadiene rubber Polymers 0.000 description 1
229920000468 styrene butadiene styrene block copolymer Polymers 0.000 description 1
150000003440 styrenes Chemical class 0.000 description 1
238000000859 sublimation Methods 0.000 description 1
230000008022 sublimation Effects 0.000 description 1
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
229940124530 sulfonamide Drugs 0.000 description 1
150000003456 sulfonamides Chemical class 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
230000000475 sunscreen effect Effects 0.000 description 1
239000000516 sunscreening agent Substances 0.000 description 1
229920003051 synthetic elastomer Polymers 0.000 description 1
239000005061 synthetic rubber Substances 0.000 description 1
125000006488 t-butyl benzyl group Chemical group 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 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
239000004753 textile Substances 0.000 description 1
150000004897 thiazines Chemical class 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
229960000790 thymol Drugs 0.000 description 1
125000003944 tolyl group Chemical group 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
238000011282 treatment Methods 0.000 description 1
150000003918 triazines Chemical class 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
230000001960 triggered effect Effects 0.000 description 1
125000005591 trimellitate group Chemical group 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
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
125000003774 valeryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
235000019871 vegetable fat Nutrition 0.000 description 1
PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
238000010792 warming Methods 0.000 description 1
125000001834 xanthenyl group Chemical class C1=CC=CC=2OC3=CC=CC=C3C(C12)* 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
BOXSVZNGTQTENJ-UHFFFAOYSA-L zinc dibutyldithiocarbamate Chemical compound [Zn+2].CCCCN(C([S-])=S)CCCC.CCCCN(C([S-])=S)CCCC BOXSVZNGTQTENJ-UHFFFAOYSA-L 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
239000004711 α-olefin Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
- 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
- C08K5/34926—Triazines also containing heterocyclic groups other than triazine groups
- 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
- 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
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/392—Additives
- G03C7/39208—Organic compounds
- G03C7/3924—Heterocyclic
- G03C7/39244—Heterocyclic the nucleus containing only nitrogen as hetero atoms
- G03C7/3926—Heterocyclic the nucleus containing only nitrogen as hetero atoms four or more nitrogen atoms

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Chemical Kinetics & Catalysis (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Health & Medical Sciences (AREA)
Spectroscopy & Molecular Physics (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Compositions Of Macromolecular Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Hydrogenated Pyridines (AREA)
Detergent Compositions (AREA)
Thermal Transfer Or Thermal Recording In General (AREA)

DD90340155A 1989-04-27 1990-04-26 Piperidintriazinverbindungen zum einsatz als stabilisatoren fuer organische materialien DD294022A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
IT8920285A IT1230091B (it)	1989-04-27	1989-04-27	Composti piperidin-triazinici atti all'impiego come stabilizzanti per materiali organici.

Publications (1)

Publication Number	Publication Date
DD294022A5 true DD294022A5 (de)	1991-09-19

Family

ID=11165434

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD90340155A DD294022A5 (de)	1989-04-27	1990-04-26	Piperidintriazinverbindungen zum einsatz als stabilisatoren fuer organische materialien

Country Status (8)

Country	Link
US (1)	US5171855A (fr)
EP (1)	EP0395584B1 (fr)
JP (1)	JP2926351B2 (fr)
BR (1)	BR9001947A (fr)
CA (1)	CA2015436A1 (fr)
DD (1)	DD294022A5 (fr)
DE (1)	DE69027556T2 (fr)
IT (1)	IT1230091B (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5216156A (en) *	1992-05-05	1993-06-01	Ciba-Geigy Corporation	Non-migrating 1-hydrocarbyloxy-2,2,6,6-tetramethylpiperidine 1,3,5-triazine derivatives
EP0595771B1 (fr) *	1992-10-30	1996-11-27	Ciba-Geigy Ag	Additifs pour lubrifiants exempts de phosphore
IT1256636B (it) *	1992-12-10	1995-12-12	Ciba Geigy Spa	Processo per la preparazione di 2,2,6,6-tetrametil-4- piperidilossi-1,3,5-triazine contenenti due o piu' anelli triazinici
US6046304A (en) *	1995-12-04	2000-04-04	Ciba Specialty Chemicals Corporation	Block oligomers containing 2,2,6,6-tetramethyl-4-piperidyl groups as stabilizers for organic materials

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1393551A (en) *	1972-04-21	1975-05-07	Ciba Geigy Ag	Piperidine derivatives
IT1060458B (it) *	1975-12-18	1982-08-20	Chimosa Chimica Organica Spa	Composti piperidil triazinici adatti per la stabilizzazione di polimeri sintetici e procedimento per la loro preparazione
DE2944729A1 (de) *	1979-11-06	1981-05-14	Hoechst Ag, 6000 Frankfurt	Neue triazinstabilisatoren
JPS59122487A (ja) *	1982-12-28	1984-07-14	Sankyo Co Ltd	ピペリジル−トリアジン−トリアミン誘導体及び高分子材料用安定剤
IT1193659B (it) *	1983-02-04	1988-07-21	Chimosa Chimica Organica Spa	Composti piperidinil-triazinici utili come stabilizzanti per polimeri sintetici
JPS6181441A (ja) *	1984-09-28	1986-04-25	Adeka Argus Chem Co Ltd	高分子材料組成物
JPS6218444A (ja) *	1985-07-16	1987-01-27	Adeka Argus Chem Co Ltd	安定化された高分子材料組成物
IT1222049B (it) *	1987-07-16	1990-08-31	Ciba Geygi Spa	Composti piperidin triazinici utilizzabili come stabilizzanti per polimeri sintetici

1989
- 1989-04-27 IT IT8920285A patent/IT1230091B/it active
1990
- 1990-04-18 DE DE69027556T patent/DE69027556T2/de not_active Expired - Fee Related
- 1990-04-18 EP EP90810309A patent/EP0395584B1/fr not_active Expired - Lifetime
- 1990-04-19 US US07/511,143 patent/US5171855A/en not_active Expired - Fee Related
- 1990-04-25 CA CA002015436A patent/CA2015436A1/fr not_active Abandoned
- 1990-04-26 BR BR909001947A patent/BR9001947A/pt not_active IP Right Cessation
- 1990-04-26 DD DD90340155A patent/DD294022A5/de not_active IP Right Cessation
- 1990-04-27 JP JP2114952A patent/JP2926351B2/ja not_active Expired - Lifetime

Also Published As

Publication number	Publication date
CA2015436A1 (fr)	1990-10-27
DE69027556D1 (de)	1996-08-01
EP0395584A2 (fr)	1990-10-31
JPH02306972A (ja)	1990-12-20
US5171855A (en)	1992-12-15
BR9001947A (pt)	1991-07-30
EP0395584A3 (fr)	1991-10-16
IT8920285A0 (it)	1989-04-27
JP2926351B2 (ja)	1999-07-28
DE69027556T2 (de)	1997-01-09
IT1230091B (it)	1991-10-05
EP0395584B1 (fr)	1996-06-26

Legal Events

Date	Code	Title	Description
1998-02-12	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
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EP0323408B1 (fr)	1994-04-06	Dérivés de l'(hydroxy-2 phényl)-2 benzotriazole
US5096781A (en)	1992-03-17	Water-soluble compounds as light stabilizers
DE60112892T2 (de)	2006-02-09	Ausblühungsfreie uv absorber benzotriazole und damit stabilisierte zusammensetzungen
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TW419497B (en)	2001-01-21	Novel 2-(2-hudroxy-3-<alpha>-cumyl-5-alkylphenyl)-2H-benzotriazoles
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DE60107874T2 (de)	2005-05-19	Substituierte 5-aryl- und 5-heteroaryl-2-(2-hydroxyphenyl)-2h-benzotriazolderivate als uv-absorbierende substanzen
TW512160B (en)	2002-12-01	N, N', N'''-tris{2,4-bis[(1-hydrocarbyloxy-2,2,6,6-tetra- methylpiperidin-4-yl)alkylamino]-s-triazin-6-yl}-3,3'- ethylenediiminodipropylamines, their isomers and bridged derivatives and polymer compositions stabilized therewith
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DE60026177T2 (de)	2006-08-03	Stabilisatormischung
JP2004534009A (ja)	2004-11-11	ベンゾトリアゾール類及び紫外線安定剤としてのそれらの用途
IT8922293A1 (it)	1991-05-07	Stabilizzanti polimerici contenenti gruppi amminici impediti e gruppi idrossilamminici
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DE4416809A1 (de)	1994-11-24	Gegen Schädigung durch Licht, Wärme und Sauerstoff stabilisierte Überzugsmittel
DD294022A5 (de)	1991-09-19	Piperidintriazinverbindungen zum einsatz als stabilisatoren fuer organische materialien
DE68927787T2 (de)	1997-08-28	Substituierte Piperidinverbindungen und ihrer Verwendung als Stabilisatoren für organische Materialien
DE69109937T2 (de)	1995-11-02	Neue Piperidintriazin-Cooligomere zur Verwendung als Stabilisatoren für organische Materialien.
EP0328024B1 (fr)	1994-12-28	Tétraméthylpipéridino-s-triazine
EP0399953A2 (fr)	1990-11-28	Composés pipéridine-triazine et leur utilisation comme stabilisants pour des matériaux organiques
DE3809628A1 (de)	1988-10-27	Sich von 2,2,6,6-tetramethylpiperidin ableitende triazin-verbindungen
US5118736A (en)	1992-06-02	N,N-bis(1-hydrocarbyloxy-2,2,6,6-tetramethylpiperidin-4-yl)amino triazines and stabilized compositions
DE69008406T2 (de)	1994-08-25	N-Hydroxycarbyloxy-Derivate von s-Triazinen mit gehinderter Aminogruppe.
US5194466A (en)	1993-03-16	Piperidine-triazine compounds for use as stabilizers for organic materials
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