NL1005608C2 - 4-acylamidopiperidine-verbindingen in stabilisatorcombinaties voor chloor-houdende polymeren. - Google Patents

4-acylamidopiperidine-verbindingen in stabilisatorcombinaties voor chloor-houdende polymeren. Download PDF

Info

Publication number: NL1005608C2
Authority: NL; Netherlands
Prior art keywords: alkyl; acid; tert; butyl; compounds
Prior art date: 1996-03-22

Application number

NL1005608A

Other languages

English (en)

Dutch (nl)

Other versions

NL1005608A1 (nl

Inventor

Karl Josef Kuhn

Wolfgang Wehner

Gerhard Rytz

Horst Zinke

Valerio Borzatta

Original Assignee

Witco Vinyl Additives Gmbh

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.)

1996-03-22

Filing date

1997-03-21

Publication date

2000-05-22

1997-03-21 Application filed by Witco Vinyl Additives Gmbh filed Critical Witco Vinyl Additives Gmbh

1997-09-23 Publication of NL1005608A1 publication Critical patent/NL1005608A1/xx

2000-05-22 Application granted granted Critical

2000-05-22 Publication of NL1005608C2 publication Critical patent/NL1005608C2/nl

Links

229920000642 polymer Polymers 0.000 title claims description 53
239000003381 stabilizer Substances 0.000 title claims description 37
150000001875 compounds Chemical class 0.000 title claims description 32
239000000460 chlorine Substances 0.000 title description 16
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 title description 15
229910052801 chlorine Inorganic materials 0.000 title description 15
-1 zinc carboxylate Chemical class 0.000 claims description 98
239000010457 zeolite Substances 0.000 claims description 51
239000000203 mixture Substances 0.000 claims description 50
125000000217 alkyl group Chemical group 0.000 claims description 31
239000011701 zinc Substances 0.000 claims description 22
229910052725 zinc Inorganic materials 0.000 claims description 20
239000011575 calcium Substances 0.000 claims description 15
229910052739 hydrogen Inorganic materials 0.000 claims description 14
229910052799 carbon Inorganic materials 0.000 claims description 11
229910052736 halogen Inorganic materials 0.000 claims description 11
150000002367 halogens Chemical class 0.000 claims description 11
229910052791 calcium Inorganic materials 0.000 claims description 10
AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 claims description 9
125000003342 alkenyl group Chemical group 0.000 claims description 8
229910052782 aluminium Inorganic materials 0.000 claims description 8
VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical class OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 8
125000000753 cycloalkyl group Chemical group 0.000 claims description 7
235000014113 dietary fatty acids Nutrition 0.000 claims description 7
239000000194 fatty acid Substances 0.000 claims description 7
229930195729 fatty acid Natural products 0.000 claims description 7
238000000034 method Methods 0.000 claims description 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
239000000126 substance Substances 0.000 claims description 6
RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical class OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 claims description 5
239000003513 alkali Substances 0.000 claims description 5
229910052783 alkali metal Inorganic materials 0.000 claims description 5
150000001340 alkali metals Chemical class 0.000 claims description 5
239000003963 antioxidant agent Substances 0.000 claims description 5
229920005862 polyol Polymers 0.000 claims description 5
150000001341 alkaline earth metal compounds Chemical class 0.000 claims description 4
AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims description 4
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
HDFRDWFLWVCOGP-UHFFFAOYSA-N carbonothioic O,S-acid Chemical class OC(S)=O HDFRDWFLWVCOGP-UHFFFAOYSA-N 0.000 claims description 4
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 4
125000004925 dihydropyridyl group Chemical group N1(CC=CC=C1)* 0.000 claims description 4
150000003077 polyols Chemical class 0.000 claims description 4
239000006096 absorbing agent Substances 0.000 claims description 3
125000003545 alkoxy group Chemical group 0.000 claims description 3
229910052760 oxygen Inorganic materials 0.000 claims description 3
125000003884 phenylalkyl group Chemical group 0.000 claims description 3
230000000087 stabilizing effect Effects 0.000 claims description 3
125000004209 (C1-C8) alkyl group Chemical group 0.000 claims 2
150000001339 alkali metal compounds Chemical class 0.000 claims 1
150000002118 epoxides Chemical class 0.000 claims 1
239000003223 protective agent Substances 0.000 claims 1
229910021536 Zeolite Inorganic materials 0.000 description 36
HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 36
239000004800 polyvinyl chloride Substances 0.000 description 21
229920000915 polyvinyl chloride Polymers 0.000 description 21
239000011734 sodium Substances 0.000 description 17
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 15
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 15
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 15
150000002148 esters Chemical class 0.000 description 15
229910052757 nitrogen Inorganic materials 0.000 description 15
229910052700 potassium Inorganic materials 0.000 description 13
229910052708 sodium Inorganic materials 0.000 description 13
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 11
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 10
239000000654 additive Substances 0.000 description 10
229920001577 copolymer Polymers 0.000 description 10
239000004014 plasticizer Substances 0.000 description 10
229910052717 sulfur Inorganic materials 0.000 description 10
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 9
239000002253 acid Substances 0.000 description 9
239000011777 magnesium Substances 0.000 description 9
239000000049 pigment Substances 0.000 description 9
KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 8
229910052784 alkaline earth metal Inorganic materials 0.000 description 8
239000007983 Tris buffer Substances 0.000 description 7
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 7
229910052749 magnesium Inorganic materials 0.000 description 7
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 6
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 6
150000001342 alkaline earth metals Chemical class 0.000 description 6
QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 6
239000012964 benzotriazole Substances 0.000 description 6
229910052593 corundum Inorganic materials 0.000 description 6
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 6
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 6
238000002360 preparation method Methods 0.000 description 6
229910001845 yogo sapphire Inorganic materials 0.000 description 6
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 5
CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 5
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-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
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical group CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 5
150000007942 carboxylates Chemical class 0.000 description 5
229910052681 coesite Inorganic materials 0.000 description 5
239000007859 condensation product Substances 0.000 description 5
229910052906 cristobalite Inorganic materials 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
229910052751 metal Inorganic materials 0.000 description 5
239000002184 metal Substances 0.000 description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 5
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 5
229910052682 stishovite Inorganic materials 0.000 description 5
229910052905 tridymite Inorganic materials 0.000 description 5
229940113165 trimethylolpropane Drugs 0.000 description 5
150000003752 zinc compounds Chemical class 0.000 description 5
DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 4
RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidine Chemical compound CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 4
ZPIRWAHWDCHWLM-UHFFFAOYSA-N 2-dodecylsulfanylethanol Chemical compound CCCCCCCCCCCCSCCO ZPIRWAHWDCHWLM-UHFFFAOYSA-N 0.000 description 4
FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 4
CKPKHTKLLYPGFM-UHFFFAOYSA-N 6,6-dimethylheptane-1,1-diol Chemical compound CC(CCCCC(O)O)(C)C CKPKHTKLLYPGFM-UHFFFAOYSA-N 0.000 description 4
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
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 4
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 4
229910019142 PO4 Inorganic materials 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 4
235000006708 antioxidants Nutrition 0.000 description 4
229910052788 barium Inorganic materials 0.000 description 4
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical group OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 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
PGRHXDWITVMQBC-UHFFFAOYSA-N dehydroacetic acid Chemical compound CC(=O)C1C(=O)OC(C)=CC1=O PGRHXDWITVMQBC-UHFFFAOYSA-N 0.000 description 4
229910052744 lithium Inorganic materials 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
FPQJEXTVQZHURJ-UHFFFAOYSA-N n,n'-bis(2-hydroxyethyl)oxamide Chemical compound OCCNC(=O)C(=O)NCCO FPQJEXTVQZHURJ-UHFFFAOYSA-N 0.000 description 4
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
150000002815 nickel Chemical class 0.000 description 4
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 4
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 4
239000010452 phosphate Substances 0.000 description 4
235000021317 phosphate Nutrition 0.000 description 4
238000012545 processing Methods 0.000 description 4
235000013772 propylene glycol Nutrition 0.000 description 4
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 4
150000003839 salts Chemical class 0.000 description 4
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 4
239000000377 silicon dioxide Substances 0.000 description 4
235000012239 silicon dioxide Nutrition 0.000 description 4
230000006641 stabilisation Effects 0.000 description 4
238000011105 stabilization Methods 0.000 description 4
229910052712 strontium Inorganic materials 0.000 description 4
150000005846 sugar alcohols Polymers 0.000 description 4
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
238000012360 testing method Methods 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
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 3
ALVZNPYWJMLXKV-UHFFFAOYSA-N 1,9-Nonanediol Chemical compound OCCCCCCCCCO ALVZNPYWJMLXKV-UHFFFAOYSA-N 0.000 description 3
IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical group CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 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
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
YIKSCQDJHCMVMK-UHFFFAOYSA-N Oxamide Chemical compound NC(=O)C(N)=O YIKSCQDJHCMVMK-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
125000001931 aliphatic group Chemical group 0.000 description 3
229910000272 alkali metal oxide Inorganic materials 0.000 description 3
OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
239000004305 biphenyl Substances 0.000 description 3
235000010290 biphenyl Nutrition 0.000 description 3
239000001273 butane Substances 0.000 description 3
150000001735 carboxylic acids Chemical class 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical group CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
125000004494 ethyl ester group Chemical group 0.000 description 3
239000000945 filler Substances 0.000 description 3
239000006260 foam Substances 0.000 description 3
238000009472 formulation Methods 0.000 description 3
229910052500 inorganic mineral Inorganic materials 0.000 description 3
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
239000000395 magnesium oxide Substances 0.000 description 3
239000011707 mineral Substances 0.000 description 3
235000010755 mineral Nutrition 0.000 description 3
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 3
150000002924 oxiranes Chemical class 0.000 description 3
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 3
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
239000000047 product Substances 0.000 description 3
235000019260 propionic acid Nutrition 0.000 description 3
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
239000000344 soap Substances 0.000 description 3
239000003549 soybean oil Substances 0.000 description 3
235000012424 soybean oil Nutrition 0.000 description 3
239000000725 suspension Substances 0.000 description 3
210000003462 vein Anatomy 0.000 description 3
239000008096 xylene Substances 0.000 description 3
JWZZKOKVBUJMES-UHFFFAOYSA-N (+-)-Isoprenaline Chemical compound CC(C)NCC(O)C1=CC=C(O)C(O)=C1 JWZZKOKVBUJMES-UHFFFAOYSA-N 0.000 description 2
DXALOGXSFLZLLN-WTZPKTTFSA-N (3s,4s,5r)-1,3,4,6-tetrahydroxy-5-[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhexan-2-one Chemical compound OCC(=O)[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O DXALOGXSFLZLLN-WTZPKTTFSA-N 0.000 description 2
GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 2
FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 2
150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 2
LIKQHVGPOUBDTG-UHFFFAOYSA-N 1,4-diphenylbutane-1,3-dione Chemical compound C=1C=CC=CC=1CC(=O)CC(=O)C1=CC=CC=C1 LIKQHVGPOUBDTG-UHFFFAOYSA-N 0.000 description 2
CVBUKMMMRLOKQR-UHFFFAOYSA-N 1-phenylbutane-1,3-dione Chemical compound CC(=O)CC(=O)C1=CC=CC=C1 CVBUKMMMRLOKQR-UHFFFAOYSA-N 0.000 description 2
ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 description 2
XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 2
KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 2
FTVFPPFZRRKJIH-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-4-amine Chemical compound CC1(C)CC(N)CC(C)(C)N1 FTVFPPFZRRKJIH-UHFFFAOYSA-N 0.000 description 2
SLUKQUGVTITNSY-UHFFFAOYSA-N 2,6-di-tert-butyl-4-methoxyphenol Chemical compound COC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SLUKQUGVTITNSY-UHFFFAOYSA-N 0.000 description 2
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
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239000012266 salt solution Substances 0.000 description 1
238000007789 sealing 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
150000003330 sebacic acids Chemical class 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
229910052711 selenium Inorganic materials 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
229910052665 sodalite Inorganic materials 0.000 description 1
239000004334 sorbic acid Substances 0.000 description 1
235000010199 sorbic acid Nutrition 0.000 description 1
229940075582 sorbic acid Drugs 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
229960002920 sorbitol Drugs 0.000 description 1
229910052566 spinel group Inorganic materials 0.000 description 1
238000009987 spinning Methods 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
150000003440 styrenes Chemical class 0.000 description 1
TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000000758 substrate Substances 0.000 description 1
239000011593 sulfur Chemical group 0.000 description 1
239000002600 sunflower oil Substances 0.000 description 1
229920003051 synthetic elastomer Polymers 0.000 description 1
239000005061 synthetic rubber Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000003760 tallow Substances 0.000 description 1
239000011975 tartaric acid Substances 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
229940072958 tetrahydrofurfuryl oleate Drugs 0.000 description 1
NQRYJNQNLNOLGT-UHFFFAOYSA-N tetrahydropyridine hydrochloride Natural products C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 1
239000004753 textile Substances 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
NJRXVEJTAYWCQJ-UHFFFAOYSA-N thiomalic acid Chemical compound OC(=O)CC(S)C(O)=O NJRXVEJTAYWCQJ-UHFFFAOYSA-N 0.000 description 1
ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
NBOMNTLFRHMDEZ-UHFFFAOYSA-N thiosalicylic acid Chemical class OC(=O)C1=CC=CC=C1S NBOMNTLFRHMDEZ-UHFFFAOYSA-N 0.000 description 1
DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 1
210000001685 thyroid gland Anatomy 0.000 description 1
229910052718 tin Inorganic materials 0.000 description 1
AOBORMOPSGHCAX-DGHZZKTQSA-N tocofersolan Chemical compound OCCOC(=O)CCC(=O)OC1=C(C)C(C)=C2O[C@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C AOBORMOPSGHCAX-DGHZZKTQSA-N 0.000 description 1
229960000984 tocofersolan Drugs 0.000 description 1
229930003799 tocopherol Natural products 0.000 description 1
229960001295 tocopherol Drugs 0.000 description 1
235000019149 tocopherols Nutrition 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
238000005809 transesterification reaction Methods 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
FICPQAZLPKLOLH-UHFFFAOYSA-N tricyclohexyl phosphite Chemical compound C1CCCCC1OP(OC1CCCCC1)OC1CCCCC1 FICPQAZLPKLOLH-UHFFFAOYSA-N 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
150000005691 triesters Chemical class 0.000 description 1
125000005591 trimellitate group Chemical group 0.000 description 1
QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-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
229960004418 trolamine Drugs 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
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
UIYCHXAGWOYNNA-UHFFFAOYSA-N vinyl sulfide Chemical group C=CSC=C UIYCHXAGWOYNNA-UHFFFAOYSA-N 0.000 description 1
239000011709 vitamin E Substances 0.000 description 1
235000019165 vitamin E Nutrition 0.000 description 1
229940046009 vitamin E Drugs 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
239000010456 wollastonite Substances 0.000 description 1
229910052882 wollastonite Inorganic materials 0.000 description 1
238000010626 work up procedure Methods 0.000 description 1
238000004383 yellowing Methods 0.000 description 1
239000011667 zinc carbonate Substances 0.000 description 1
235000004416 zinc carbonate Nutrition 0.000 description 1
229910000010 zinc carbonate 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
UGZADUVQMDAIAO-UHFFFAOYSA-L zinc hydroxide Chemical compound [OH-].[OH-].[Zn+2] UGZADUVQMDAIAO-UHFFFAOYSA-L 0.000 description 1
229910021511 zinc hydroxide Inorganic materials 0.000 description 1
229940007718 zinc hydroxide Drugs 0.000 description 1
239000011787 zinc oxide Substances 0.000 description 1
229910052984 zinc sulfide Inorganic materials 0.000 description 1
RBEYUVZBFYVXEX-UHFFFAOYSA-L zinc;2-sulfanylacetate Chemical compound [Zn+2].[O-]C(=O)CS.[O-]C(=O)CS RBEYUVZBFYVXEX-UHFFFAOYSA-L 0.000 description 1
JIXJDKNPPOUBJH-UHFFFAOYSA-L zinc;2-sulfanylbenzoate Chemical compound [Zn+2].[O-]C(=O)C1=CC=CC=C1S.[O-]C(=O)C1=CC=CC=C1S JIXJDKNPPOUBJH-UHFFFAOYSA-L 0.000 description 1
YCFZZALTCSESPA-UHFFFAOYSA-L zinc;2-sulfanylbutanedioate Chemical compound [Zn+2].[O-]C(=O)CC(S)C([O-])=O YCFZZALTCSESPA-UHFFFAOYSA-L 0.000 description 1
YMTQMTSQMKJKPX-UHFFFAOYSA-L zinc;diphenoxide Chemical class [Zn+2].[O-]C1=CC=CC=C1.[O-]C1=CC=CC=C1 YMTQMTSQMKJKPX-UHFFFAOYSA-L 0.000 description 1
PCHQDTOLHOFHHK-UHFFFAOYSA-L zinc;hydrogen carbonate Chemical compound [Zn+2].OC([O-])=O.OC([O-])=O PCHQDTOLHOFHHK-UHFFFAOYSA-L 0.000 description 1
DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
239000002076 α-tocopherol Substances 0.000 description 1
235000004835 α-tocopherol Nutrition 0.000 description 1
235000007680 β-tocopherol Nutrition 0.000 description 1
239000011590 β-tocopherol Substances 0.000 description 1
239000002478 γ-tocopherol Substances 0.000 description 1
QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 1
QUEDXNHFTDJVIY-DQCZWYHMSA-N γ-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-DQCZWYHMSA-N 0.000 description 1

Classifications

- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/13—Phenols; Phenolates
- C08K5/138—Phenolates
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3432—Six-membered rings
- C08K5/3435—Piperidines

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)

NL1005608A 1996-03-22 1997-03-21 4-acylamidopiperidine-verbindingen in stabilisatorcombinaties voor chloor-houdende polymeren. NL1005608C2 (nl)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
CH75196		1996-03-22
CH75196		1996-03-22

Publications (2)

Publication Number	Publication Date
NL1005608A1 NL1005608A1 (nl)	1997-09-23
NL1005608C2 true NL1005608C2 (nl)	2000-05-22

Family

ID=4194353

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL1005608A NL1005608C2 (nl)	1996-03-22	1997-03-21	4-acylamidopiperidine-verbindingen in stabilisatorcombinaties voor chloor-houdende polymeren.

Country Status (16)

Country	Link
JP (1)	JPH1045983A (de)
AT (1)	AT413210B (de)
BE (1)	BE1012198A5 (de)
BR (1)	BR9701422A (de)
CA (1)	CA2200536A1 (de)
DE (1)	DE19711690A1 (de)
DK (1)	DK29697A (de)
ES (1)	ES2147078B1 (de)
FR (1)	FR2746405A1 (de)
GB (1)	GB2311292B (de)
IT (1)	IT1290431B1 (de)
NL (1)	NL1005608C2 (de)
NO (1)	NO971335L (de)
SE (1)	SE9701011L (de)
TW (1)	TW354800B (de)
ZA (1)	ZA972426B (de)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE19752481A1 (de) *	1997-11-27	1999-06-02	Cit Alcatel	Isoliermaterial auf der Basis von Polyvinylchlorid
JP2000273254A (ja) *	1999-03-19	2000-10-03	Mitsubishi Chem Mkv Co	熱可塑性エラストマー及びその製造方法
JP2000273248A (ja) *	1999-03-19	2000-10-03	Mitsubishi Chem Mkv Co	熱可塑性エラストマー及びその製造方法
GB0219260D0 (en)	2002-08-19	2002-09-25	Clariant Gmbh	Improvements in or relating to organic compounds
DE502008002175D1 (de)	2007-08-28	2011-02-10	Basf Se	Stabilisatormischung
CN103554009B (zh) *	2013-10-22	2016-05-04	山西省化工研究所（有限公司）	一种尼龙多功能稳定剂的制备方法
CN118812417A (zh) *	2024-06-21	2024-10-22	福建帝盛科技股份有限公司	N,n-双(2,2,6,6-四甲基哌啶基)-1,4-乙二酰胺的制备方法

Citations (7)

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Publication number	Priority date	Publication date	Assignee	Title
FR2074871A5 (de) *	1970-01-08	1971-10-08	Sankyo Co
EP0421933A1 (de) *	1989-10-06	1991-04-10	Ciba-Geigy Ag	Stabilisierte chlorhaltige Polymerzusammensetzungen
EP0432096A1 (de) *	1989-12-06	1991-06-12	Ciba-Geigy Ag	Stabilisierte chlorhaltige Zusammensetzung
EP0446171A2 (de) *	1990-03-08	1991-09-11	Ciba-Geigy Ag	Stabilisierte chlorhaltige Polymerzusammensetzungen
EP0488951A1 (de) *	1990-11-30	1992-06-03	Ciba-Geigy Ag	Stabilisierte chlorhaltige Polymere
EP0488950A1 (de) *	1990-11-30	1992-06-03	Ciba-Geigy Ag	Stabilisierte chlorhaltige Polymere
EP0570337A2 (de) *	1992-05-13	1993-11-18	Ciba-Geigy Ag	Stabilisierte chlorhaltige Polymerzusammensetzungen

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Publication number	Priority date	Publication date	Assignee	Title
US5283273A (en) *	1990-11-30	1994-02-01	Ciba-Geigy Corporation	Stabilized chlorine-containing polymers
ATE312874T1 (de) *	1996-03-22	2005-12-15	Wolfgang Wehner	Stabilisatorkombination für chlorhaltige polymere

1997
- 1997-03-17 DK DK029697A patent/DK29697A/da not_active Application Discontinuation
- 1997-03-19 SE SE9701011A patent/SE9701011L/xx not_active Application Discontinuation
- 1997-03-20 DE DE19711690A patent/DE19711690A1/de not_active Withdrawn
- 1997-03-20 CA CA002200536A patent/CA2200536A1/en not_active Abandoned
- 1997-03-20 FR FR9703402A patent/FR2746405A1/fr not_active Withdrawn
- 1997-03-20 ZA ZA9702426A patent/ZA972426B/xx unknown
- 1997-03-21 NO NO971335A patent/NO971335L/no not_active Application Discontinuation
- 1997-03-21 JP JP9108012A patent/JPH1045983A/ja active Pending
- 1997-03-21 GB GB9705846A patent/GB2311292B/en not_active Expired - Fee Related
- 1997-03-21 IT IT97MI000662A patent/IT1290431B1/it active IP Right Grant
- 1997-03-21 ES ES009700618A patent/ES2147078B1/es not_active Expired - Fee Related
- 1997-03-21 NL NL1005608A patent/NL1005608C2/nl not_active IP Right Cessation
- 1997-03-21 TW TW086103573A patent/TW354800B/zh active
- 1997-03-21 AT AT0050297A patent/AT413210B/de not_active IP Right Cessation
- 1997-03-21 BE BE9700251A patent/BE1012198A5/fr not_active IP Right Cessation
- 1997-03-21 BR BR9701422A patent/BR9701422A/pt not_active Application Discontinuation

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2074871A5 (de) *	1970-01-08	1971-10-08	Sankyo Co
EP0421933A1 (de) *	1989-10-06	1991-04-10	Ciba-Geigy Ag	Stabilisierte chlorhaltige Polymerzusammensetzungen
EP0432096A1 (de) *	1989-12-06	1991-06-12	Ciba-Geigy Ag	Stabilisierte chlorhaltige Zusammensetzung
EP0446171A2 (de) *	1990-03-08	1991-09-11	Ciba-Geigy Ag	Stabilisierte chlorhaltige Polymerzusammensetzungen
EP0488951A1 (de) *	1990-11-30	1992-06-03	Ciba-Geigy Ag	Stabilisierte chlorhaltige Polymere
EP0488950A1 (de) *	1990-11-30	1992-06-03	Ciba-Geigy Ag	Stabilisierte chlorhaltige Polymere
EP0570337A2 (de) *	1992-05-13	1993-11-18	Ciba-Geigy Ag	Stabilisierte chlorhaltige Polymerzusammensetzungen

Also Published As

Publication number	Publication date
FR2746405A1 (fr)	1997-09-26
GB2311292A (en)	1997-09-24
GB9705846D0 (en)	1997-05-07
TW354800B (en)	1999-03-21
IT1290431B1 (it)	1998-12-03
NL1005608A1 (nl)	1997-09-23
ES2147078A1 (es)	2000-08-16
CA2200536A1 (en)	1997-09-22
NO971335D0 (no)	1997-03-21
DE19711690A1 (de)	1997-11-06
ES2147078B1 (es)	2001-04-01
ATA50297A (de)	2005-05-15
BE1012198A5 (fr)	2000-07-04
SE9701011L (sv)	1997-09-23
ZA972426B (en)	1997-09-22
AT413210B (de)	2005-12-15
DK29697A (da)	1997-09-23
ITMI970662A1 (it)	1998-09-21
BR9701422A (pt)	1998-11-10
SE9701011D0 (sv)	1997-03-19
JPH1045983A (ja)	1998-02-17
NO971335L (no)	1997-09-23
GB2311292B (en)	2000-10-04

Legal Events

Date	Code	Title	Description
1997-11-03	AD1A	A request for search or an international type search has been filed
1999-02-01	CD	Transfer of rights (laid open patent application)	Free format text: WILCO VINYL ADDITIVES GMBH
2000-03-01	RD2N	Patents in respect of which a decision has been taken or a report has been made (novelty report)	Effective date: 19991222
2000-08-01	PD2B	A search report has been drawn up
2002-12-02	VD1	Lapsed due to non-payment of the annual fee	Effective date: 20021001

Publication	Publication Date	Title
CA2216170C (en)	2006-08-29	Monomeric and oligomeric bisphosphites as stabilisers for polyvinyl chloride
ES2246023T3 (es)	2006-02-01	Combinaciones de estabilizantes para polimeros clorados.
AU696696B2 (en)	1998-09-17	Stabilized polyvinyl chloride
NO309942B1 (no)	2001-04-23	Stabilisert polyvinylklorid-blanding, fremgangsmÕte for fremstilling av stabilisert PVC, anvendelse av denne PVC samt anvendelse av et perklorat for stabilisering av PVC
US6013703A (en)	2000-01-11	Stabilizer combination for chlorine-containing polymers
NO309941B1 (no)	2001-04-23	Stabilisert myk-PVC-blanding, dens fremstilling og anvendelse
CN100467517C (zh)	2009-03-11	用于含卤聚合物的稳定剂组合物
NL1005608C2 (nl)	2000-05-22	4-acylamidopiperidine-verbindingen in stabilisatorcombinaties voor chloor-houdende polymeren.
NL1005609C2 (nl)	2000-06-06	Monomere N-piperidinylmelaminen als stabilisatoren voor chloor-houdende polymeren.
JPH1053571A (ja)	1998-02-24	塩素含有ポリマーのための安定剤
NL1007102C2 (nl)	2000-11-14	Monomere en oligomere bisfosfieten als stabilisatoren voor polyvinylchloride.
JPH07300544A (ja)	1995-11-14	安定化ハロゲン含有ポリマー
GB2345696A (en)	2000-07-19	Stabilizer combinations for halogen-containing polymers
AU2003203276B2 (en)	2005-02-24	Stabiliser combinations for chlorine-containing polymers
AU7257200A (en)	2001-04-05	Stabiliser combinations for chlorine-containing polymers