NO327962B1 - Fremgangsmate for fremstilling av en steril gjenstand. - Google Patents
Fremgangsmate for fremstilling av en steril gjenstand. Download PDFInfo
- Publication number
- NO327962B1 NO327962B1 NO20030886A NO20030886A NO327962B1 NO 327962 B1 NO327962 B1 NO 327962B1 NO 20030886 A NO20030886 A NO 20030886A NO 20030886 A NO20030886 A NO 20030886A NO 327962 B1 NO327962 B1 NO 327962B1
- Authority
- NO
- Norway
- Prior art keywords
- stabilizer
- independently selected
- general formula
- och2
- article
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 13
- 239000003381 stabilizer Substances 0.000 claims abstract description 48
- 229920000642 polymer Polymers 0.000 claims abstract description 26
- 238000000034 method Methods 0.000 claims abstract description 22
- 125000005591 trimellitate group Chemical group 0.000 claims abstract description 14
- GSQPHYUVUWFHDE-XIJIAEDBSA-N (2s)-1-[(4r,7s,10s,16s,19r)-19-[[2-[[2-[(2-aminoacetyl)amino]acetyl]amino]acetyl]amino]-7-(2-amino-2-oxoethyl)-10-(3-amino-3-oxopropyl)-13-[(2s)-butan-2-yl]-16-[(4-hydroxyphenyl)methyl]-6,9,12,15,18-pentaoxo-1,2-dithia-5,8,11,14,17-pentazacycloicosane-4-c Chemical compound C([C@H]1C(=O)NC(C(N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CSSC[C@@H](C(=O)N1)NC(=O)CNC(=O)CNC(=O)CN)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CC(C)C)C(=O)NCC(N)=O)=O)[C@@H](C)CC)C1=CC=C(O)C=C1 GSQPHYUVUWFHDE-XIJIAEDBSA-N 0.000 claims abstract description 5
- 125000003118 aryl group Chemical group 0.000 claims abstract description 5
- 108700016471 tri-Gly- oxytocin Proteins 0.000 claims abstract description 5
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 4
- 150000002367 halogens Chemical class 0.000 claims abstract description 4
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 4
- -1 poly(vinyl chloride) Polymers 0.000 claims description 35
- 239000004800 polyvinyl chloride Substances 0.000 claims description 20
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 19
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 230000001954 sterilising effect Effects 0.000 claims description 6
- 150000002431 hydrogen Chemical group 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 125000006539 C12 alkyl group Chemical group [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])* 0.000 claims description 3
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 230000005865 ionizing radiation Effects 0.000 claims description 2
- 125000001033 ether group Chemical group 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 230000005855 radiation Effects 0.000 abstract description 6
- 125000002947 alkylene group Chemical group 0.000 abstract description 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 229920001451 polypropylene glycol Polymers 0.000 description 18
- 229920001223 polyethylene glycol Polymers 0.000 description 14
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 8
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 6
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 150000002170 ethers Chemical class 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- WCLDITPGPXSPGV-UHFFFAOYSA-N tricamba Chemical compound COC1=C(Cl)C=C(Cl)C(Cl)=C1C(O)=O WCLDITPGPXSPGV-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 125000005498 phthalate group Chemical class 0.000 description 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 3
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000004659 sterilization and disinfection Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 150000003606 tin compounds Chemical class 0.000 description 3
- QWOZZTWBWQMEPD-UHFFFAOYSA-N 1-(2-ethoxypropoxy)propan-2-ol Chemical compound CCOC(C)COCC(C)O QWOZZTWBWQMEPD-UHFFFAOYSA-N 0.000 description 2
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 2
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 2
- FMVOPJLFZGSYOS-UHFFFAOYSA-N 2-[2-(2-ethoxypropoxy)propoxy]propan-1-ol Chemical compound CCOC(C)COC(C)COC(C)CO FMVOPJLFZGSYOS-UHFFFAOYSA-N 0.000 description 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 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 2
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 2
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 2
- IBNUFHUVKKZWLH-UHFFFAOYSA-N tris[2-(2-methoxyethoxy)ethyl] phosphite Chemical compound COCCOCCOP(OCCOCCOC)OCCOCCOC IBNUFHUVKKZWLH-UHFFFAOYSA-N 0.000 description 2
- CFFLFIVJXKFMDC-UHFFFAOYSA-N tris[2-[2-(2-methoxyethoxy)ethoxy]ethyl] phosphate Chemical compound COCCOCCOCCOP(=O)(OCCOCCOCCOC)OCCOCCOCCOC CFFLFIVJXKFMDC-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 238000004383 yellowing Methods 0.000 description 2
- REISVQFGJQBRRN-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethyl 2-sulfanylacetate Chemical compound COCCOCCOC(=O)CS REISVQFGJQBRRN-UHFFFAOYSA-N 0.000 description 1
- WFSMVVDJSNMRAR-UHFFFAOYSA-N 2-[2-(2-ethoxyethoxy)ethoxy]ethanol Chemical compound CCOCCOCCOCCO WFSMVVDJSNMRAR-UHFFFAOYSA-N 0.000 description 1
- ZRLPFXHOMOOIDH-UHFFFAOYSA-N 2-[2-(2-ethoxyethoxy)ethoxy]ethyl 2-sulfanylacetate Chemical compound CCOCCOCCOCCOC(=O)CS ZRLPFXHOMOOIDH-UHFFFAOYSA-N 0.000 description 1
- KPMHESUMRCNTCN-UHFFFAOYSA-N 2-[2-(2-methoxyethoxy)ethoxy]ethyl 2-sulfanylacetate Chemical compound COCCOCCOCCOC(=O)CS KPMHESUMRCNTCN-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
- MAUHZCDENMEPBR-UHFFFAOYSA-N C(CS)(=O)OCC(OCC(C)OCC)C Chemical compound C(CS)(=O)OCC(OCC(C)OCC)C MAUHZCDENMEPBR-UHFFFAOYSA-N 0.000 description 1
- UTHZTKGAHRDIBC-UHFFFAOYSA-N CCOC(C)COC(C)COC(C)COC(=O)CS Chemical compound CCOC(C)COC(C)COC(C)COC(=O)CS UTHZTKGAHRDIBC-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- 239000008037 PVC plasticizer Substances 0.000 description 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- HSUIVCLOAAJSRE-UHFFFAOYSA-N bis(2-methoxyethyl) benzene-1,2-dicarboxylate Chemical compound COCCOC(=O)C1=CC=CC=C1C(=O)OCCOC HSUIVCLOAAJSRE-UHFFFAOYSA-N 0.000 description 1
- WLWJCDRYISWVCV-UHFFFAOYSA-N bis[2-[2-(2-ethoxyethoxy)ethoxy]ethyl] benzene-1,2-dicarboxylate Chemical compound CCOCCOCCOCCOC(=O)C1=CC=CC=C1C(=O)OCCOCCOCCOCC WLWJCDRYISWVCV-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- MROCJMGDEKINLD-UHFFFAOYSA-N dichlorosilane Chemical compound Cl[SiH2]Cl MROCJMGDEKINLD-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000007580 dry-mixing Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- KKHUSADXXDNRPW-UHFFFAOYSA-N malonic anhydride Chemical compound O=C1CC(=O)O1 KKHUSADXXDNRPW-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- XKHUUPWVDVIRHM-UHFFFAOYSA-N methylsulfinylmethane;propan-2-ol Chemical compound CC(C)O.CS(C)=O XKHUUPWVDVIRHM-UHFFFAOYSA-N 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000003017 thermal stabilizer Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 229940071127 thioglycolate Drugs 0.000 description 1
- QLNUSZCPEUTHBS-UHFFFAOYSA-N tris(2-methoxyethyl) phosphate Chemical compound COCCOP(=O)(OCCOC)OCCOC QLNUSZCPEUTHBS-UHFFFAOYSA-N 0.000 description 1
- ARZWPIKXHHNGCT-UHFFFAOYSA-N tris(2-methoxyethyl) phosphite Chemical compound COCCOP(OCCOC)OCCOC ARZWPIKXHHNGCT-UHFFFAOYSA-N 0.000 description 1
- SLGQVJRIDXVTLE-UHFFFAOYSA-N tris[2-(2-ethoxyethoxy)ethyl] phosphite Chemical compound CCOCCOCCOP(OCCOCCOCC)OCCOCCOCC SLGQVJRIDXVTLE-UHFFFAOYSA-N 0.000 description 1
- MWIGYZRZXFMGFN-UHFFFAOYSA-N tris[2-(2-methoxyethoxy)ethyl] phosphate Chemical compound COCCOCCOP(=O)(OCCOCCOC)OCCOCCOC MWIGYZRZXFMGFN-UHFFFAOYSA-N 0.000 description 1
- JNUDHPJKPDJVCM-UHFFFAOYSA-N tris[2-[2-(2-ethoxyethoxy)ethoxy]ethyl] phosphate Chemical compound CCOCCOCCOCCOP(=O)(OCCOCCOCCOCC)OCCOCCOCCOCC JNUDHPJKPDJVCM-UHFFFAOYSA-N 0.000 description 1
- ZGQZCZWUBFFTQF-UHFFFAOYSA-N tris[2-[2-(2-ethoxyethoxy)ethoxy]ethyl] phosphite Chemical compound CCOCCOCCOCCOP(OCCOCCOCCOCC)OCCOCCOCCOCC ZGQZCZWUBFFTQF-UHFFFAOYSA-N 0.000 description 1
- VMYZCQMZFCZXMM-UHFFFAOYSA-N tris[2-[2-(2-methoxyethoxy)ethoxy]ethyl] phosphite Chemical compound COCCOCCOCCOP(OCCOCCOCCOC)OCCOCCOCCOC VMYZCQMZFCZXMM-UHFFFAOYSA-N 0.000 description 1
- WDWGBVJDFUMTHW-UHFFFAOYSA-N tris[3-(3-ethoxypropoxy)propyl] phosphate Chemical compound CCOCCCOCCCOP(=O)(OCCCOCCCOCC)OCCCOCCCOCC WDWGBVJDFUMTHW-UHFFFAOYSA-N 0.000 description 1
- RYKXHIHFCPYFRR-UHFFFAOYSA-N tris[3-(3-ethoxypropoxy)propyl] phosphite Chemical compound CCOCCCOCCCOP(OCCCOCCCOCC)OCCCOCCCOCC RYKXHIHFCPYFRR-UHFFFAOYSA-N 0.000 description 1
- NFAPAKBYGNFWCU-UHFFFAOYSA-N tris[3-(3-methoxypropoxy)propyl] phosphate Chemical compound COCCCOCCCOP(=O)(OCCCOCCCOC)OCCCOCCCOC NFAPAKBYGNFWCU-UHFFFAOYSA-N 0.000 description 1
- UVXDDXDGGBZYLC-UHFFFAOYSA-N tris[3-(3-methoxypropoxy)propyl] phosphite Chemical compound COCCCOCCCOP(OCCCOCCCOC)OCCCOCCCOC UVXDDXDGGBZYLC-UHFFFAOYSA-N 0.000 description 1
- RBYACWNVMZBNCE-UHFFFAOYSA-N tris[3-[3-(3-ethoxypropoxy)propoxy]propyl] phosphate Chemical compound CCOCCCOCCCOCCCOP(=O)(OCCCOCCCOCCCOCC)OCCCOCCCOCCCOCC RBYACWNVMZBNCE-UHFFFAOYSA-N 0.000 description 1
- RUGMXNXSMPGPTR-UHFFFAOYSA-N tris[3-[3-(3-ethoxypropoxy)propoxy]propyl] phosphite Chemical compound CCOCCCOCCCOCCCOP(OCCCOCCCOCCCOCC)OCCCOCCCOCCCOCC RUGMXNXSMPGPTR-UHFFFAOYSA-N 0.000 description 1
- KXGWHMUUJSHTMX-UHFFFAOYSA-N tris[3-[3-(3-methoxypropoxy)propoxy]propyl] phosphate Chemical compound COCCCOCCCOCCCOP(=O)(OCCCOCCCOCCCOC)OCCCOCCCOCCCOC KXGWHMUUJSHTMX-UHFFFAOYSA-N 0.000 description 1
- GLIVZKIMTCTLLS-UHFFFAOYSA-N tris[3-[3-(3-methoxypropoxy)propoxy]propyl] phosphite Chemical compound COCCCOCCCOCCCOP(OCCCOCCCOCCCOC)OCCCOCCCOCCCOC GLIVZKIMTCTLLS-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/02—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using physical phenomena
- A61L2/08—Radiation
- A61L2/081—Gamma radiation
-
- 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
-
- 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
- C08K5/10—Esters; Ether-esters
- C08K5/12—Esters; Ether-esters of cyclic polycarboxylic acids
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2202/00—Aspects relating to methods or apparatus for disinfecting or sterilising materials or objects
- A61L2202/20—Targets to be treated
- A61L2202/24—Medical instruments, e.g. endoscopes, catheters, sharps
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/02—Polyalkylene oxides
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Apparatus For Disinfection Or Sterilisation (AREA)
- Polyesters Or Polycarbonates (AREA)
- Silicon Polymers (AREA)
- Materials For Medical Uses (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/654,359 US6348517B1 (en) | 2000-09-01 | 2000-09-01 | Preparing sterile articles from polymers containing a stabilizer based on a poly(oxyalkylene) |
| PCT/GB2001/003889 WO2002017972A2 (en) | 2000-09-01 | 2001-08-30 | Preparing sterile articles from polymers containing a stabiliser based on a poly(oxyalkylene) |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO20030886D0 NO20030886D0 (no) | 2003-02-25 |
| NO20030886L NO20030886L (no) | 2003-02-25 |
| NO327962B1 true NO327962B1 (no) | 2009-10-26 |
Family
ID=24624537
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20030886A NO327962B1 (no) | 2000-09-01 | 2003-02-25 | Fremgangsmate for fremstilling av en steril gjenstand. |
Country Status (18)
| Country | Link |
|---|---|
| US (2) | US6348517B1 (ko) |
| EP (2) | EP1818361B1 (ko) |
| JP (1) | JP2004507583A (ko) |
| KR (1) | KR100743554B1 (ko) |
| CN (2) | CN101775030B (ko) |
| AT (1) | ATE365187T1 (ko) |
| AU (2) | AU2001284209B2 (ko) |
| CA (1) | CA2420858C (ko) |
| CZ (1) | CZ304395B6 (ko) |
| DE (1) | DE60129027T2 (ko) |
| DK (2) | DK1313802T3 (ko) |
| ES (2) | ES2288981T3 (ko) |
| IL (2) | IL154653A0 (ko) |
| MX (1) | MXPA03001519A (ko) |
| NO (1) | NO327962B1 (ko) |
| PT (2) | PT1818361E (ko) |
| SK (1) | SK287053B6 (ko) |
| WO (1) | WO2002017972A2 (ko) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7282527B2 (en) * | 2003-08-19 | 2007-10-16 | Crompton Corporation | Stabilization system for halogen-containing polymers |
| JP5374154B2 (ja) * | 2006-09-11 | 2013-12-25 | 株式会社カネカ | 医療用樹脂組成物、樹脂ペレット及び医療用部品 |
| TWI689538B (zh) | 2018-11-12 | 2020-04-01 | 南亞塑膠工業股份有限公司 | 一種用於含鹵素聚合物之安定劑及其用途 |
| FR3107278A1 (fr) * | 2020-02-14 | 2021-08-20 | Arkema France | Composition bitumineuse contenant une huile époxydée |
Family Cites Families (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1326387A (en) * | 1969-08-16 | 1973-08-08 | Toho Chem Ind Co Ltd | Lubricating composition for synthetic fibres |
| US3976616A (en) * | 1972-06-13 | 1976-08-24 | Ciba-Geigy Corporation | Bis(phosphate) plasticizers and plasticized compositions |
| DE2656927C2 (de) * | 1976-12-16 | 1983-03-03 | Akzo Gmbh, 5600 Wuppertal | Gleitmittel aus Polyalkylenoxiden für die formgebende Verarbeitung von Kunststoffen |
| EP0000976B1 (en) * | 1977-07-26 | 1982-05-19 | The Malaysian Rubber Producers' Research Association | A method of forming graft copolymers by attaching pre-polymerised side chains to an unsaturated natural or synthetic rubber backbone, and the resulting graft copolymers |
| US4159681A (en) * | 1977-10-03 | 1979-07-03 | Vandament Daniel D | Reinforced, light-weight pallet |
| SU956459A1 (ru) * | 1978-03-21 | 1982-09-07 | Уфимский Нефтяной Институт | Способ получени пластификатора |
| JPS5661448A (en) * | 1979-10-25 | 1981-05-26 | Mitsubishi Plastics Ind Ltd | Vinyl resin composition having good gamma radiation resistance |
| FR2491871A1 (fr) * | 1980-10-10 | 1982-04-16 | Ato Chimie | Perfectionnement a la sterilisation d'objets en polymeres halogeno-vinyliques par des rayonnements ionisants, et resines pour sa realisation |
| US4478961A (en) * | 1981-11-18 | 1984-10-23 | Toyo Boseki Kabushika Kaisha | Polyvinyl chloride composition |
| JPS59109548A (ja) * | 1982-12-16 | 1984-06-25 | Sanyo Chem Ind Ltd | 重合体組成物 |
| US4569953A (en) * | 1984-02-28 | 1986-02-11 | Minnesota Mining And Manufacturing Company | Photoactivated polymerization of vinyl monomers by polysilanes |
| US4710532A (en) * | 1985-03-13 | 1987-12-01 | Morflex Chemical Company, Inc. | Medical article and method |
| JPS6153237A (ja) * | 1984-08-24 | 1986-03-17 | Human Ind Corp | ポリヒドロキシ化合物の改質方法 |
| US4698111A (en) * | 1985-07-15 | 1987-10-06 | W. R. Grace & Co., Cryovac Div. | Vinylidene chloride composition and film made therefrom |
| US4686148A (en) * | 1985-07-15 | 1987-08-11 | W. R. Grace & Co., Cryovac Div. | Vinylidene chloride composition and film made therefrom |
| NZ217159A (en) * | 1985-08-26 | 1989-04-26 | Goodrich Co B F | Clear polyvinyl chloride compositions |
| US5011660A (en) * | 1987-04-10 | 1991-04-30 | Huls America Inc. | Method of sterilizing medical grade film |
| PH25823A (en) * | 1987-07-22 | 1991-11-05 | Sherex Chem | Anti-stat for polyvinyl chloride polymers |
| US4906681A (en) * | 1987-07-22 | 1990-03-06 | Sherex Chemical Company, Inc. | Anti-stat for polyvinyl chloride polymers |
| JPS6443551A (en) * | 1987-08-10 | 1989-02-15 | Sekisui Chemical Co Ltd | Antistatic plasticizer |
| JPS6466257A (en) * | 1987-09-07 | 1989-03-13 | Nitto Kasei Co Ltd | One-pack stabilizer for halogen-containing resin |
| FR2625506B1 (fr) * | 1987-12-31 | 1992-02-21 | Bp Chimie Sa | Procede et appareillage de fabrication de polymeres controlee a l'aide d'un systeme de regulation comprenant un spectrophotometre infrarouge |
| US5077331A (en) * | 1988-01-15 | 1991-12-31 | Lonza Inc. | Polyvinyl chloride lubricant |
| JPH04356441A (ja) * | 1991-06-03 | 1992-12-10 | Satoru Matsumoto | エ−テルエステル複合エステル |
| US5830937A (en) * | 1992-02-04 | 1998-11-03 | Congoleum Corporation | Coating and wearlayer compositions for surface coverings |
| JPH0657131A (ja) * | 1992-08-14 | 1994-03-01 | Mitsubishi Petrochem Co Ltd | 熱可塑性樹脂組成物 |
| CA2110209A1 (en) * | 1992-11-30 | 1994-05-31 | Tadashi Amano | Process for preparing vinyl chloride polymers |
| JPH07292235A (ja) * | 1994-04-20 | 1995-11-07 | Sanyo Chem Ind Ltd | 耐寒性可塑剤 |
| US5948838A (en) * | 1996-03-06 | 1999-09-07 | Mitsubishi Engineering-Plastics Corp. | Polycarbonate resin composition |
| US5710199A (en) * | 1996-06-19 | 1998-01-20 | Hubert; James F. | Automotive additives and sealants containing waste powder prime |
| US5686147A (en) * | 1996-11-18 | 1997-11-11 | The Goodyear Tire & Rubber Company | Plastisol composition |
| JPH1121205A (ja) * | 1997-07-03 | 1999-01-26 | Mitsui Chem Inc | 塩化ビニル樹脂成形用組成物 |
-
2000
- 2000-09-01 US US09/654,359 patent/US6348517B1/en not_active Expired - Lifetime
-
2001
- 2001-08-30 CA CA2420858A patent/CA2420858C/en not_active Expired - Lifetime
- 2001-08-30 ES ES01963176T patent/ES2288981T3/es not_active Expired - Lifetime
- 2001-08-30 SK SK240-2003A patent/SK287053B6/sk not_active IP Right Cessation
- 2001-08-30 JP JP2002522945A patent/JP2004507583A/ja active Pending
- 2001-08-30 AT AT01963176T patent/ATE365187T1/de not_active IP Right Cessation
- 2001-08-30 PT PT70106380T patent/PT1818361E/pt unknown
- 2001-08-30 EP EP07010638.0A patent/EP1818361B1/en not_active Expired - Lifetime
- 2001-08-30 AU AU2001284209A patent/AU2001284209B2/en not_active Ceased
- 2001-08-30 EP EP01963176A patent/EP1313802B1/en not_active Expired - Lifetime
- 2001-08-30 CZ CZ2003-575A patent/CZ304395B6/cs not_active IP Right Cessation
- 2001-08-30 CN CN200910174606.6A patent/CN101775030B/zh not_active Expired - Fee Related
- 2001-08-30 DE DE60129027T patent/DE60129027T2/de not_active Expired - Lifetime
- 2001-08-30 IL IL15465301A patent/IL154653A0/xx active IP Right Grant
- 2001-08-30 CN CNB018148751A patent/CN100558803C/zh not_active Expired - Fee Related
- 2001-08-30 MX MXPA03001519A patent/MXPA03001519A/es active IP Right Grant
- 2001-08-30 AU AU8420901A patent/AU8420901A/xx active Pending
- 2001-08-30 KR KR1020037003055A patent/KR100743554B1/ko active IP Right Grant
- 2001-08-30 WO PCT/GB2001/003889 patent/WO2002017972A2/en active IP Right Grant
- 2001-08-30 PT PT01963176T patent/PT1313802E/pt unknown
- 2001-08-30 DK DK01963176T patent/DK1313802T3/da active
- 2001-08-30 DK DK07010638.0T patent/DK1818361T3/da active
- 2001-08-30 ES ES07010638T patent/ES2432362T3/es not_active Expired - Lifetime
- 2001-10-09 US US09/973,566 patent/US6451904B1/en not_active Expired - Lifetime
-
2003
- 2003-02-25 NO NO20030886A patent/NO327962B1/no not_active IP Right Cessation
- 2003-02-27 IL IL154653A patent/IL154653A/en unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES2252042T3 (es) | Compuestos de glicerol acilado especificos para plastificantes en polimeros. | |
| US4808649A (en) | Beta-ketoester substituted diorganopolysiloxanes and PVC stabilzers comprised thereof | |
| US4122057A (en) | Mixed-terminated polyester plasticizers | |
| KR101419062B1 (ko) | 신규한 폴리염화비닐수지 가소제 | |
| KR20100132253A (ko) | 신규한 폴리염화비닐수지 가소제 | |
| NO327962B1 (no) | Fremgangsmate for fremstilling av en steril gjenstand. | |
| EP1169380B1 (en) | Stabilization of polymers after exposure to oxidation | |
| AU2001284209A1 (en) | Preparing sterile articles from polymers containing a stabiliser based on a poly(oxyalkylene) | |
| US3546162A (en) | Ortho-ester stabilized polyvinylchloride resins | |
| US3356630A (en) | Stabilizer for vinyl chloride polymers | |
| US3068193A (en) | Esters of epoxy fatty acids and 2, 4-dihydroxy benzophenone | |
| US5225467A (en) | Cellulose ester resin stabilizer and cellulose ester resin compositions stabilized therewith | |
| CA1264163A (en) | Citrate esters and methods | |
| JPS62246373A (ja) | 医療用塩化ビニル樹脂組成物 | |
| JPS5920342A (ja) | 塩化ビニル樹脂組成物 | |
| US2936299A (en) | Organo-tin compounds | |
| WO2002017973A2 (en) | Preparing sterile articles from certain polymers | |
| JPS5811538A (ja) | 農業用ポリ塩化ビニルフイルム | |
| JPH0220543A (ja) | ガンマ線照射に対し、すぐれた安定性を有する塩化ビニル樹脂組成物 | |
| JPH10330566A (ja) | 耐電子線性にすぐれるハロゲン含有樹脂組成物 | |
| JPS6340824B2 (ko) | ||
| JPH02200270A (ja) | 医療用具用組成物 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM1K | Lapsed by not paying the annual fees |