NL1007121C2 - Hard PVC, gestabiliseerd met N,N-dimethyl-6-aminouracillen. - Google Patents
Hard PVC, gestabiliseerd met N,N-dimethyl-6-aminouracillen. Download PDFInfo
- Publication number
- NL1007121C2 NL1007121C2 NL1007121A NL1007121A NL1007121C2 NL 1007121 C2 NL1007121 C2 NL 1007121C2 NL 1007121 A NL1007121 A NL 1007121A NL 1007121 A NL1007121 A NL 1007121A NL 1007121 C2 NL1007121 C2 NL 1007121C2
- Authority
- NL
- Netherlands
- Prior art keywords
- tert
- butyl
- acid
- bis
- pvc
- Prior art date
Links
- 229910052757 nitrogen Inorganic materials 0.000 title description 6
- 239000000203 mixture Substances 0.000 description 70
- -1 polydihydropyridines Chemical class 0.000 description 69
- 150000001875 compounds Chemical class 0.000 description 34
- 150000002148 esters Chemical class 0.000 description 17
- 229920001577 copolymer Polymers 0.000 description 16
- 239000004014 plasticizer Substances 0.000 description 16
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 15
- 239000007983 Tris buffer Substances 0.000 description 14
- 229920000642 polymer Polymers 0.000 description 14
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 229910052751 metal Inorganic materials 0.000 description 12
- 239000002184 metal Substances 0.000 description 12
- 239000003381 stabilizer Substances 0.000 description 12
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 11
- 229910052725 zinc Inorganic materials 0.000 description 11
- 239000011701 zinc Substances 0.000 description 11
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 10
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 10
- 239000002253 acid Substances 0.000 description 10
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 10
- 235000014113 dietary fatty acids Nutrition 0.000 description 9
- 239000000194 fatty acid Substances 0.000 description 9
- 229930195729 fatty acid Natural products 0.000 description 9
- 239000000049 pigment Substances 0.000 description 9
- 239000000344 soap Substances 0.000 description 9
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 8
- 239000000654 additive Substances 0.000 description 8
- 239000011575 calcium Substances 0.000 description 8
- 235000012424 soybean oil Nutrition 0.000 description 8
- 239000003549 soybean oil Substances 0.000 description 8
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 7
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 7
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 7
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 7
- 239000011777 magnesium Substances 0.000 description 7
- 239000004800 polyvinyl chloride Substances 0.000 description 7
- 229920000915 polyvinyl chloride Polymers 0.000 description 7
- 229910052717 sulfur Inorganic materials 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
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000003963 antioxidant agent Substances 0.000 description 6
- 235000006708 antioxidants Nutrition 0.000 description 6
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 6
- 229910052791 calcium Inorganic materials 0.000 description 6
- 229910052749 magnesium Inorganic materials 0.000 description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 6
- 230000006641 stabilisation Effects 0.000 description 6
- 238000011105 stabilization Methods 0.000 description 6
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 6
- 239000001993 wax Substances 0.000 description 6
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 5
- 230000000996 additive effect Effects 0.000 description 5
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical class [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 5
- 150000007942 carboxylates Chemical class 0.000 description 5
- 150000001735 carboxylic acids Chemical class 0.000 description 5
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 5
- 239000000314 lubricant Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 5
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 5
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 5
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 5
- 229920003023 plastic Polymers 0.000 description 5
- 239000004033 plastic Substances 0.000 description 5
- 239000000047 product 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
- BPXVHIRIPLPOPT-UHFFFAOYSA-N 1,3,5-tris(2-hydroxyethyl)-1,3,5-triazinane-2,4,6-trione Chemical compound OCCN1C(=O)N(CCO)C(=O)N(CCO)C1=O BPXVHIRIPLPOPT-UHFFFAOYSA-N 0.000 description 4
- ALVZNPYWJMLXKV-UHFFFAOYSA-N 1,9-Nonanediol Chemical compound OCCCCCCCCCO ALVZNPYWJMLXKV-UHFFFAOYSA-N 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 4
- 239000004803 Di-2ethylhexylphthalate Substances 0.000 description 4
- KCXZNSGUUQJJTR-UHFFFAOYSA-N Di-n-hexyl phthalate Chemical compound CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCC KCXZNSGUUQJJTR-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 4
- 239000006057 Non-nutritive feed additive Substances 0.000 description 4
- 229910019142 PO4 Inorganic materials 0.000 description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical class OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 4
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 4
- 239000012964 benzotriazole Substances 0.000 description 4
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 4
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 4
- 239000011888 foil Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 4
- 150000002815 nickel Chemical class 0.000 description 4
- 235000021317 phosphate Nutrition 0.000 description 4
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 4
- 235000013772 propylene glycol Nutrition 0.000 description 4
- 150000005846 sugar alcohols Polymers 0.000 description 4
- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 4
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 4
- 125000005591 trimellitate group Chemical group 0.000 description 4
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 4
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 3
- ZPIRWAHWDCHWLM-UHFFFAOYSA-N 2-dodecylsulfanylethanol Chemical compound CCCCCCCCCCCCSCCO ZPIRWAHWDCHWLM-UHFFFAOYSA-N 0.000 description 3
- CKPKHTKLLYPGFM-UHFFFAOYSA-N 6,6-dimethylheptane-1,1-diol Chemical compound CC(CCCCC(O)O)(C)C CKPKHTKLLYPGFM-UHFFFAOYSA-N 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- 239000004604 Blowing Agent Substances 0.000 description 3
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 3
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
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- 150000001340 alkali metals Chemical class 0.000 description 3
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- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 description 3
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
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- 238000002360 preparation method Methods 0.000 description 3
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- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 3
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- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
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- 229960001147 triclofos Drugs 0.000 description 1
- IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
- GRAKJTASWCEOQI-UHFFFAOYSA-N tridodecylphosphane Chemical compound CCCCCCCCCCCCP(CCCCCCCCCCCC)CCCCCCCCCCCC GRAKJTASWCEOQI-UHFFFAOYSA-N 0.000 description 1
- 150000005691 triesters Chemical class 0.000 description 1
- JNXDCMUUZNIWPQ-UHFFFAOYSA-N trioctyl benzene-1,2,4-tricarboxylate Chemical compound CCCCCCCCOC(=O)C1=CC=C(C(=O)OCCCCCCCC)C(C(=O)OCCCCCCCC)=C1 JNXDCMUUZNIWPQ-UHFFFAOYSA-N 0.000 description 1
- QOQNJVLFFRMJTQ-UHFFFAOYSA-N trioctyl phosphite Chemical compound CCCCCCCCOP(OCCCCCCCC)OCCCCCCCC QOQNJVLFFRMJTQ-UHFFFAOYSA-N 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-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
- WDRCVXGINNJWPH-UHFFFAOYSA-N tris(6-methylheptyl) benzene-1,2,4-tricarboxylate Chemical compound CC(C)CCCCCOC(=O)C1=CC=C(C(=O)OCCCCCC(C)C)C(C(=O)OCCCCCC(C)C)=C1 WDRCVXGINNJWPH-UHFFFAOYSA-N 0.000 description 1
- QQBLOZGVRHAYGT-UHFFFAOYSA-N tris-decyl phosphite Chemical compound CCCCCCCCCCOP(OCCCCCCCCCC)OCCCCCCCCCC QQBLOZGVRHAYGT-UHFFFAOYSA-N 0.000 description 1
- IRELFWHHEKNWEC-UHFFFAOYSA-N tritetradecyl phosphite Chemical compound CCCCCCCCCCCCCCOP(OCCCCCCCCCCCCCC)OCCCCCCCCCCCCCC IRELFWHHEKNWEC-UHFFFAOYSA-N 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 229940005605 valeric acid Drugs 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- FUSUHKVFWTUUBE-UHFFFAOYSA-N vinyl methyl ketone Natural products CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 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
- 239000002351 wastewater Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- NAWDYIZEMPQZHO-UHFFFAOYSA-N ytterbium Chemical compound [Yb] NAWDYIZEMPQZHO-UHFFFAOYSA-N 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 150000003752 zinc compounds Chemical class 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
- CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical compound [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3442—Heterocyclic compounds having nitrogen in the ring having two nitrogen atoms in the ring
- C08K5/3462—Six-membered 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/005—Stabilisers against oxidation, heat, light, ozone
-
- 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
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
-
- 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
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/37—Thiols
- C08K5/378—Thiols containing heterocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/04—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08L27/06—Homopolymers or copolymers of vinyl chloride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/18—Applications used for pipes
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH234496 | 1996-09-25 | ||
| CH234496 | 1996-09-25 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NL1007121A1 NL1007121A1 (nl) | 1998-03-31 |
| NL1007121C2 true NL1007121C2 (nl) | 1998-05-18 |
Family
ID=4231613
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL1007121A NL1007121C2 (nl) | 1996-09-25 | 1997-09-25 | Hard PVC, gestabiliseerd met N,N-dimethyl-6-aminouracillen. |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US5859100A (de) |
| JP (1) | JPH10158454A (de) |
| KR (1) | KR19980024864A (de) |
| AT (1) | AT407395B (de) |
| AU (1) | AU715135B2 (de) |
| BE (1) | BE1011371A3 (de) |
| BR (1) | BR9704856A (de) |
| CA (1) | CA2216141A1 (de) |
| DE (1) | DE19741778A1 (de) |
| DK (1) | DK106297A (de) |
| ES (1) | ES2131017B1 (de) |
| FI (1) | FI973734A7 (de) |
| FR (1) | FR2753709B1 (de) |
| GB (1) | GB2318118B (de) |
| IT (1) | IT1295058B1 (de) |
| MY (1) | MY114466A (de) |
| NL (1) | NL1007121C2 (de) |
| NO (1) | NO315165B1 (de) |
| SE (1) | SE9703423L (de) |
| TW (1) | TW404964B (de) |
| ZA (1) | ZA978531B (de) |
Families Citing this family (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0967209B1 (de) * | 1998-06-26 | 2003-01-08 | Crompton Vinyl Additives GmbH | Neue NH2-modifizierte 6-Aminouracile als Stabilisatoren für halogenhaltige Polymere |
| DE59902320D1 (de) * | 1998-06-26 | 2002-09-19 | Crompton Vinyl Additives Gmbh | In 5-Stellung substituierte 6-Aminouracile als Stabilisatoren für halogen-haltige Polymere |
| DE19915388A1 (de) | 1999-04-06 | 2000-10-12 | Witco Vinyl Additives Gmbh | 4-Aminopyrimidinone und Oxazolidino-4-amino-pyrimidinone, Verfahren zu deren Herstellung und ihre Verwendung zum Stabilisieren von halogenhaltigen Polymeren |
| US6498240B1 (en) | 1999-09-17 | 2002-12-24 | Millipore Corporation | Method for sequencing reaction cleanup by constant pressure diffential ultrafiltration |
| JP4516650B2 (ja) * | 2000-01-21 | 2010-08-04 | 水澤化学工業株式会社 | 塩素含有重合体用安定剤組成物 |
| MXPA01008705A (es) | 2000-09-03 | 2004-08-12 | Rohm & Haas | Sistemas de aditivos polimericos multiples: composiciones, procesos y productos derivados. |
| MXPA01008706A (es) | 2000-09-03 | 2004-08-12 | Rohm & Haas | Sistemas aditivos polimericos altos en solidos: composiciones, procesos y productos de los mismos. |
| CN1315926C (zh) | 2001-02-16 | 2007-05-16 | 克罗姆普顿乙烯添加剂有限公司 | 用于稳定含卤聚合物的新稳定剂体系 |
| DE10132836A1 (de) * | 2001-07-06 | 2003-01-16 | Cognis Deutschland Gmbh | Verwendung von Aminouracilen zur Stabilisierung von antistatisch ausgerüsteten halogenhaltigen organischen Kunststoffen |
| DE10159344A1 (de) | 2001-12-04 | 2003-06-12 | Crompton Vinyl Additives Gmbh | Prestabilisierung von halogenhaltigen Polymeren |
| MXPA02011789A (es) | 2001-12-06 | 2005-08-26 | Rohm & Haas | Composicion estabilizada de polimero, que contiene halogeno. |
| TW200303887A (en) | 2002-03-07 | 2003-09-16 | Rohm & Haas | Organic based thermal stabilizers and heat stabilized polymer compositions |
| US20050159515A1 (en) * | 2002-03-28 | 2005-07-21 | Jens-Peter Wiegner | Compounds useful for reducing acetaldehyde content of polyethylene terephthalate, their use and products resulting therefrom |
| ITVA20020058A1 (it) * | 2002-11-15 | 2004-05-16 | Lamberti Spa | Composizioni di pvc stabili al calore. |
| DE10301675A1 (de) * | 2003-01-17 | 2004-07-29 | Crompton Vinyl Additives Gmbh | Stabilisatorsystem zur PVC-Stabilisierung |
| DE10317870A1 (de) * | 2003-04-17 | 2004-11-04 | Crompton Vinyl Additives Gmbh | Neues Stabilisatorsystem zur Stabilisierung von halogenhaltigen Polymeren |
| DE10318910A1 (de) * | 2003-04-26 | 2004-11-11 | Crompton Vinyl Additives Gmbh | Stabilisatorsystem zur Stabilisierung halogenhaltiger Polymere |
| JP2007529606A (ja) * | 2004-03-15 | 2007-10-25 | ハネウェル・インターナショナル・インコーポレーテッド | セルロース強化樹脂組成物 |
| DE102004037369A1 (de) | 2004-07-30 | 2006-03-23 | Artemis Research Gmbh & Co. Kg | Stabilisatorsystem für halogenhaltige Polymere |
| KR20090009799A (ko) * | 2006-05-02 | 2009-01-23 | 시바 홀딩 인코포레이티드 | 난연제로서 피리미딘의 유도체 |
| CN101437886B (zh) * | 2006-05-02 | 2011-11-09 | 西巴控股有限公司 | 作为阻燃剂的嘧啶衍生物 |
| ES2533863T3 (es) * | 2007-06-29 | 2015-04-15 | Korea Research Institute Of Chemical Technology | Inhibidores novedosos de la transcriptasa inversa de VIH |
| WO2009005693A1 (en) * | 2007-06-29 | 2009-01-08 | Gilead Sciences, Inc. | Novel hiv reverse transcriptase inhibitors |
| DE102007037795A1 (de) | 2007-08-10 | 2009-02-12 | Nabaltec Ag | Stabilisatorsysteme für halogenhaltige Polymere |
| DE202007017631U1 (de) * | 2007-12-14 | 2008-04-10 | Baukulit Handelsgesellschaft Mbh | Kunststoffextrusionsteile für den Innen- und Außenausbau von Gebäuden |
| WO2009085797A1 (en) * | 2007-12-21 | 2009-07-09 | Gilead Sciences, Inc. | Processes for preparing hiv reverse transcriptase inhibitors |
| DE102008018872A1 (de) | 2008-04-14 | 2009-10-15 | Ika Innovative Kunststoffaufbereitung Gmbh & Co. Kg | Stabilisatorsystem für halogenhaltige Polymere |
| DE102008020203A1 (de) | 2008-04-22 | 2009-10-29 | Catena Additives Gmbh & Co. Kg | Lösemittelfreie High Solids (One-Pack)-Stabilisatoren für halogenhaltige Polymere |
| US8012539B2 (en) | 2008-05-09 | 2011-09-06 | Kraton Polymers U.S. Llc | Method for making sulfonated block copolymers, method for making membranes from such block copolymers and membrane structures |
| EP3495000A1 (de) * | 2009-02-17 | 2019-06-12 | Cornell Research Foundation, Inc. | Verfahren und kits zur diagnose von krebs und vorhersage des therapeutischen werts |
| US8263713B2 (en) | 2009-10-13 | 2012-09-11 | Kraton Polymers U.S. Llc | Amine neutralized sulfonated block copolymers and method for making same |
| US8337987B2 (en) * | 2009-12-29 | 2012-12-25 | Nesbitt Jeffrey E | Exterior UV-cured coatings and coating systems and methods of forming exterior UV-cured coating systems |
| DE102010020486A1 (de) | 2010-05-14 | 2011-11-17 | Catena Additives Gmbh & Co. Kg | Flammgeschützte halogenhaltige Polymere mit verbesserter Thermostabilität |
| US9394414B2 (en) | 2010-09-29 | 2016-07-19 | Kraton Polymers U.S. Llc | Elastic, moisture-vapor permeable films, their preparation and their use |
| US9429366B2 (en) | 2010-09-29 | 2016-08-30 | Kraton Polymers U.S. Llc | Energy recovery ventilation sulfonated block copolymer laminate membrane |
| WO2012054325A1 (en) | 2010-10-18 | 2012-04-26 | Kraton Polymers U.S. Llc | Method for producing a sulfonated block copolymer composition |
| WO2012143794A1 (en) | 2011-04-18 | 2012-10-26 | Galata Chemicals Gmbh | Polymer stabilizer system for polymers containing halogen |
| US9861941B2 (en) | 2011-07-12 | 2018-01-09 | Kraton Polymers U.S. Llc | Modified sulfonated block copolymers and the preparation thereof |
| FR2986003B1 (fr) | 2012-01-24 | 2015-01-16 | Arkema France | Procede de preparation de polymeres halogenes |
| WO2016085785A1 (en) * | 2014-11-24 | 2016-06-02 | Lubrizol Advanced Materials, Inc. | Novel coupled uracil compound for vinyl chloride polymer resins |
| KR102046264B1 (ko) * | 2018-11-27 | 2019-11-19 | 노우준 | 재생 폴리염화비닐 컴파운드 조성물 및 이의 제조방법 |
| US20230105189A1 (en) * | 2020-03-24 | 2023-04-06 | Zeon Corporation | Vinyl chloride resin composition, vinyl chloride resin molded product, and laminate |
| US20260028468A1 (en) | 2024-07-29 | 2026-01-29 | Galata Chemicals, Llc | Heat stabilizers for cpvc |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE687294A (de) * | 1966-02-12 | 1967-03-01 | ||
| FR2010134A1 (de) * | 1968-06-04 | 1970-02-13 | Asahi Chemical Ind | |
| EP0041479A1 (de) * | 1980-06-02 | 1981-12-09 | Ciba-Geigy Ag | Mit Amino-thiouracilen stabilisierte chlorhaltige Thermoplasten |
| EP0065934A1 (de) * | 1981-05-26 | 1982-12-01 | Ciba-Geigy Ag | Mit Aminouracilen stabilisierte chlorhaltige Thermoplaste |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4656209A (en) * | 1982-05-26 | 1987-04-07 | Ciba-Geigy Corporation | Chlorinated thermoplastics stabilized with aminouracils |
| DE58908208D1 (de) * | 1988-07-29 | 1994-09-22 | Ciba Geigy Ag | Thiouracile als Stabilisatoren für chlorhaltige Polymerisate. |
| DE59610885D1 (de) * | 1995-10-13 | 2004-02-05 | Crompton Vinyl Additives Gmbh | Stabilisatorkombinationen für chlorhaltige Polymere |
-
1997
- 1997-09-12 MY MYPI97004236A patent/MY114466A/en unknown
- 1997-09-16 DK DK106297A patent/DK106297A/da not_active Application Discontinuation
- 1997-09-18 AU AU38345/97A patent/AU715135B2/en not_active Ceased
- 1997-09-19 FI FI973734A patent/FI973734A7/fi unknown
- 1997-09-22 DE DE19741778A patent/DE19741778A1/de not_active Ceased
- 1997-09-22 ES ES009701977A patent/ES2131017B1/es not_active Expired - Lifetime
- 1997-09-22 US US08/934,986 patent/US5859100A/en not_active Expired - Fee Related
- 1997-09-23 CA CA002216141A patent/CA2216141A1/en not_active Abandoned
- 1997-09-23 FR FR9711792A patent/FR2753709B1/fr not_active Expired - Fee Related
- 1997-09-23 GB GB9720124A patent/GB2318118B/en not_active Expired - Fee Related
- 1997-09-23 TW TW086113802A patent/TW404964B/zh not_active IP Right Cessation
- 1997-09-23 KR KR1019970048183A patent/KR19980024864A/ko not_active Ceased
- 1997-09-23 ZA ZA9708531A patent/ZA978531B/xx unknown
- 1997-09-23 BE BE9700771A patent/BE1011371A3/fr not_active IP Right Cessation
- 1997-09-23 SE SE9703423A patent/SE9703423L/xx unknown
- 1997-09-24 BR BR9704856A patent/BR9704856A/pt not_active Application Discontinuation
- 1997-09-24 NO NO19974416A patent/NO315165B1/no unknown
- 1997-09-24 AT AT0162497A patent/AT407395B/de not_active IP Right Cessation
- 1997-09-24 IT IT97MI002161A patent/IT1295058B1/it active IP Right Grant
- 1997-09-25 JP JP9299289A patent/JPH10158454A/ja active Pending
- 1997-09-25 NL NL1007121A patent/NL1007121C2/nl not_active IP Right Cessation
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE687294A (de) * | 1966-02-12 | 1967-03-01 | ||
| FR2010134A1 (de) * | 1968-06-04 | 1970-02-13 | Asahi Chemical Ind | |
| EP0041479A1 (de) * | 1980-06-02 | 1981-12-09 | Ciba-Geigy Ag | Mit Amino-thiouracilen stabilisierte chlorhaltige Thermoplasten |
| EP0065934A1 (de) * | 1981-05-26 | 1982-12-01 | Ciba-Geigy Ag | Mit Aminouracilen stabilisierte chlorhaltige Thermoplaste |
Also Published As
| Publication number | Publication date |
|---|---|
| NO315165B1 (no) | 2003-07-21 |
| FI973734A7 (fi) | 1998-03-26 |
| IT1295058B1 (it) | 1999-04-27 |
| MY114466A (en) | 2002-10-31 |
| GB9720124D0 (en) | 1997-11-19 |
| NO974416L (no) | 1998-03-26 |
| KR19980024864A (ko) | 1998-07-06 |
| GB2318118B (en) | 2000-12-27 |
| ES2131017B1 (es) | 2000-03-01 |
| BE1011371A3 (fr) | 1999-08-03 |
| DK106297A (da) | 1998-03-26 |
| US5859100A (en) | 1999-01-12 |
| ES2131017A1 (es) | 1999-07-01 |
| AT407395B (de) | 2001-02-26 |
| ZA978531B (en) | 1998-03-25 |
| CA2216141A1 (en) | 1998-03-25 |
| ATA162497A (de) | 2000-07-15 |
| FR2753709B1 (fr) | 1998-11-27 |
| FR2753709A1 (fr) | 1998-03-27 |
| MX9707314A (es) | 1998-08-30 |
| GB2318118A (en) | 1998-04-15 |
| FI973734A0 (fi) | 1997-09-19 |
| JPH10158454A (ja) | 1998-06-16 |
| ITMI972161A1 (it) | 1999-03-24 |
| AU715135B2 (en) | 2000-01-20 |
| BR9704856A (pt) | 1998-12-29 |
| SE9703423L (sv) | 1998-03-26 |
| NL1007121A1 (nl) | 1998-03-31 |
| AU3834597A (en) | 1998-04-02 |
| NO974416D0 (no) | 1997-09-24 |
| SE9703423D0 (sv) | 1997-09-23 |
| DE19741778A1 (de) | 1998-03-26 |
| TW404964B (en) | 2000-09-11 |
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| AD1B | A search report has been drawn up | ||
| PD2B | A search report has been drawn up | ||
| SD | Assignments of patents |
Owner name: WILCO VINYL ADDITIVES GMBH |
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| TD | Modifications of names of proprietors of patents |
Owner name: CROMPTON VINYL ADDITIVES GMBH Owner name: CK WITCO VINYL ADDITIVES GMBH |
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| VD1 | Lapsed due to non-payment of the annual fee |
Effective date: 20040401 |