UA79082C2 - Mixtures of isomeric isononyl esters of benzoic acid, their mixtures with alkyl esters of phthalic, adipinic or cyclohexandicarboxylic acids, as well as use of these mixtures - Google Patents
Mixtures of isomeric isononyl esters of benzoic acid, their mixtures with alkyl esters of phthalic, adipinic or cyclohexandicarboxylic acids, as well as use of these mixtures Download PDFInfo
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- UA79082C2 UA79082C2 UA2003043503A UA2003043503A UA79082C2 UA 79082 C2 UA79082 C2 UA 79082C2 UA 2003043503 A UA2003043503 A UA 2003043503A UA 2003043503 A UA2003043503 A UA 2003043503A UA 79082 C2 UA79082 C2 UA 79082C2
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- esters
- temperature
- acid
- mixture
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- 239000000203 mixture Substances 0.000 title abstract description 76
- QYQADNCHXSEGJT-UHFFFAOYSA-N cyclohexane-1,1-dicarboxylate;hydron Chemical class OC(=O)C1(C(O)=O)CCCCC1 QYQADNCHXSEGJT-UHFFFAOYSA-N 0.000 title abstract description 8
- 125000005907 alkyl ester group Chemical group 0.000 title abstract description 6
- -1 isononyl Chemical class 0.000 title description 28
- 229940052296 esters of benzoic acid for local anesthesia Drugs 0.000 title description 8
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 abstract description 13
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 abstract description 11
- BBVARVTURNYWGV-UHFFFAOYSA-N 7-methyloctyl benzoate Chemical class CC(C)CCCCCCOC(=O)C1=CC=CC=C1 BBVARVTURNYWGV-UHFFFAOYSA-N 0.000 abstract description 10
- 150000002148 esters Chemical class 0.000 description 35
- 235000019441 ethanol Nutrition 0.000 description 32
- 229920001944 Plastisol Polymers 0.000 description 26
- 239000004999 plastisol Substances 0.000 description 26
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 25
- 239000003054 catalyst Substances 0.000 description 21
- 239000000047 product Substances 0.000 description 19
- 238000000034 method Methods 0.000 description 18
- 239000002253 acid Substances 0.000 description 16
- 150000001298 alcohols Chemical class 0.000 description 16
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 15
- 239000004800 polyvinyl chloride Substances 0.000 description 14
- 229920000915 polyvinyl chloride Polymers 0.000 description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
- 125000004432 carbon atom Chemical group C* 0.000 description 12
- 230000000875 corresponding effect Effects 0.000 description 11
- 239000004014 plasticizer Substances 0.000 description 11
- BODRLKRKPXBDBN-UHFFFAOYSA-N 3,5,5-Trimethyl-1-hexanol Chemical compound OCCC(C)CC(C)(C)C BODRLKRKPXBDBN-UHFFFAOYSA-N 0.000 description 10
- 125000000217 alkyl group Chemical group 0.000 description 10
- 238000004821 distillation Methods 0.000 description 10
- UADWUILHKRXHMM-UHFFFAOYSA-N 2-ethylhexyl benzoate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1 UADWUILHKRXHMM-UHFFFAOYSA-N 0.000 description 9
- 235000010233 benzoic acid Nutrition 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 9
- 230000032050 esterification Effects 0.000 description 9
- 238000005886 esterification reaction Methods 0.000 description 9
- 238000005259 measurement Methods 0.000 description 9
- 229910052751 metal Inorganic materials 0.000 description 9
- 239000002184 metal Substances 0.000 description 9
- 239000005711 Benzoic acid Substances 0.000 description 8
- 238000009835 boiling Methods 0.000 description 8
- 238000007127 saponification reaction Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 150000007513 acids Chemical class 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 7
- 230000008569 process Effects 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 7
- QDTDKYHPHANITQ-UHFFFAOYSA-N 7-methyloctan-1-ol Chemical class CC(C)CCCCCCO QDTDKYHPHANITQ-UHFFFAOYSA-N 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 238000003860 storage Methods 0.000 description 6
- 229940106004 2-ethylhexyl benzoate Drugs 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 5
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 5
- 235000011037 adipic acid Nutrition 0.000 description 5
- 239000001361 adipic acid Substances 0.000 description 5
- 150000001336 alkenes Chemical class 0.000 description 5
- UADWUILHKRXHMM-ZDUSSCGKSA-N benzoflex 181 Natural products CCCC[C@H](CC)COC(=O)C1=CC=CC=C1 UADWUILHKRXHMM-ZDUSSCGKSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 229910052703 rhodium Inorganic materials 0.000 description 5
- 239000010948 rhodium Substances 0.000 description 5
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 4
- 230000009471 action Effects 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 125000004185 ester group Chemical group 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 125000005498 phthalate group Chemical class 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 229910052718 tin Inorganic materials 0.000 description 4
- 239000010936 titanium Substances 0.000 description 4
- 229910052719 titanium Inorganic materials 0.000 description 4
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 4
- 238000005809 transesterification reaction Methods 0.000 description 4
- PQSMEVPHTJECDZ-UHFFFAOYSA-N 2,3-dimethylheptan-2-ol Chemical compound CCCCC(C)C(C)(C)O PQSMEVPHTJECDZ-UHFFFAOYSA-N 0.000 description 3
- BUWRPJINRQFQPN-UHFFFAOYSA-N 3,5,5-trimethylhexyl benzoate Chemical compound CC(C)(C)CC(C)CCOC(=O)C1=CC=CC=C1 BUWRPJINRQFQPN-UHFFFAOYSA-N 0.000 description 3
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 3
- 150000001559 benzoic acids Chemical class 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 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 3
- 238000004817 gas chromatography Methods 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- VUHMHACHBVTPMF-UHFFFAOYSA-N nonyl benzoate Chemical class CCCCCCCCCOC(=O)C1=CC=CC=C1 VUHMHACHBVTPMF-UHFFFAOYSA-N 0.000 description 3
- 125000001400 nonyl 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])[H] 0.000 description 3
- 238000006384 oligomerization reaction Methods 0.000 description 3
- 125000004430 oxygen atom Chemical group O* 0.000 description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 230000002829 reductive effect Effects 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 229910052726 zirconium Inorganic materials 0.000 description 3
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- BWDBEAQIHAEVLV-UHFFFAOYSA-N 6-methylheptan-1-ol Chemical compound CC(C)CCCCCO BWDBEAQIHAEVLV-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 229920012485 Plasticized Polyvinyl chloride Polymers 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- FPCJKVGGYOAWIZ-UHFFFAOYSA-N butan-1-ol;titanium Chemical compound [Ti].CCCCO.CCCCO.CCCCO.CCCCO FPCJKVGGYOAWIZ-UHFFFAOYSA-N 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 238000007037 hydroformylation reaction Methods 0.000 description 2
- 150000004679 hydroxides Chemical class 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- XVQUOJBERHHONY-UHFFFAOYSA-N isometheptene Chemical group CNC(C)CCC=C(C)C XVQUOJBERHHONY-UHFFFAOYSA-N 0.000 description 2
- 229940098779 methanesulfonic acid Drugs 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 230000010355 oscillation Effects 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 2
- 150000003022 phthalic acids Chemical class 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical class CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 1
- VFRRCEIJQYJSAY-UHFFFAOYSA-N 2,2,3-trimethylhexanal Chemical compound CCCC(C)C(C)(C)C=O VFRRCEIJQYJSAY-UHFFFAOYSA-N 0.000 description 1
- LXODQLXKQIJVNK-UHFFFAOYSA-N 2-(2-benzoyloxypropoxy)propyl benzoate Chemical class C=1C=CC=CC=1C(=O)OC(C)COC(C)COC(=O)C1=CC=CC=C1 LXODQLXKQIJVNK-UHFFFAOYSA-N 0.000 description 1
- JLWMMYZWEHHTFF-UHFFFAOYSA-N 2-[6-(3-carbamimidoylphenoxy)-4-[di(propan-2-yl)amino]-3,5-difluoropyridin-2-yl]oxy-5-(2-methylpropylcarbamoyl)benzoic acid Chemical compound OC(=O)C1=CC(C(=O)NCC(C)C)=CC=C1OC1=NC(OC=2C=C(C=CC=2)C(N)=N)=C(F)C(N(C(C)C)C(C)C)=C1F JLWMMYZWEHHTFF-UHFFFAOYSA-N 0.000 description 1
- LNKHFECVVLVFFE-UHFFFAOYSA-N 2-nonoxycarbonylbenzoic acid Chemical class CCCCCCCCCOC(=O)C1=CC=CC=C1C(O)=O LNKHFECVVLVFFE-UHFFFAOYSA-N 0.000 description 1
- WTPYRCJDOZVZON-UHFFFAOYSA-N 3,5,5-Trimethylhexanal Chemical compound O=CCC(C)CC(C)(C)C WTPYRCJDOZVZON-UHFFFAOYSA-N 0.000 description 1
- KZJIOVQKSAOPOP-UHFFFAOYSA-N 5,5-dimethylhex-1-ene Chemical compound CC(C)(C)CCC=C KZJIOVQKSAOPOP-UHFFFAOYSA-N 0.000 description 1
- IOFUAVGBFVXDAO-UHFFFAOYSA-N 6,6-dimethylheptan-1-ol Chemical class CC(C)(C)CCCCCO IOFUAVGBFVXDAO-UHFFFAOYSA-N 0.000 description 1
- CXEZPNICPJDTPH-UHFFFAOYSA-N 6,6-dimethylheptyl benzoate Chemical compound C(C1=CC=CC=C1)(=O)OCCCCCC(C)(C)C CXEZPNICPJDTPH-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 206010015137 Eructation Diseases 0.000 description 1
- 101000714497 Homo sapiens Carbonic anhydrase 5B, mitochondrial Proteins 0.000 description 1
- 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 1
- 206010051602 Laziness Diseases 0.000 description 1
- 102100026933 Myelin-associated neurite-outgrowth inhibitor Human genes 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 102100024245 Putative inactive carbonic anhydrase 5B-like protein Human genes 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- 229920002253 Tannate Polymers 0.000 description 1
- DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 150000000475 acetylene derivatives Chemical class 0.000 description 1
- 239000002535 acidifier Substances 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- 208000027687 belching Diseases 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- IRLQAJPIHBZROB-UHFFFAOYSA-N buta-2,3-dienenitrile Chemical compound C=C=CC#N IRLQAJPIHBZROB-UHFFFAOYSA-N 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 description 1
- BSDOQSMQCZQLDV-UHFFFAOYSA-N butan-1-olate;zirconium(4+) Chemical compound [Zr+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] BSDOQSMQCZQLDV-UHFFFAOYSA-N 0.000 description 1
- 235000013844 butane Nutrition 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- USCGTWCFKOJWOB-UHFFFAOYSA-N carboxy hydrogen carbonate;cyclohexane Chemical compound C1CCCCC1.OC(=O)OC(O)=O USCGTWCFKOJWOB-UHFFFAOYSA-N 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
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- 230000001419 dependent effect Effects 0.000 description 1
- 229960002380 dibutyl phthalate Drugs 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- DLAHAXOYRFRPFQ-UHFFFAOYSA-N dodecyl benzoate Chemical compound CCCCCCCCCCCCOC(=O)C1=CC=CC=C1 DLAHAXOYRFRPFQ-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
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- 230000022244 formylation Effects 0.000 description 1
- 238000006170 formylation reaction Methods 0.000 description 1
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- 238000001879 gelation Methods 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
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- 239000012535 impurity Substances 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
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- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 239000002649 leather substitute Substances 0.000 description 1
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- 238000004949 mass spectrometry Methods 0.000 description 1
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- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- QPJVMBTYPHYUOC-UHFFFAOYSA-N methyl benzoate Chemical compound COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 235000013379 molasses Nutrition 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical class CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- JKXONPYJVWEAEL-UHFFFAOYSA-N oxiran-2-ylmethyl acetate Chemical compound CC(=O)OCC1CO1 JKXONPYJVWEAEL-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 230000008447 perception Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 239000006041 probiotic Substances 0.000 description 1
- 235000018291 probiotics Nutrition 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000007614 solvation Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000002411 thermogravimetry Methods 0.000 description 1
- LLZRNZOLAXHGLL-UHFFFAOYSA-J titanic acid Chemical compound O[Ti](O)(O)O LLZRNZOLAXHGLL-UHFFFAOYSA-J 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 239000010913 used oil Substances 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- ZPEJZWGMHAKWNL-UHFFFAOYSA-L zinc;oxalate Chemical compound [Zn+2].[O-]C(=O)C([O-])=O ZPEJZWGMHAKWNL-UHFFFAOYSA-L 0.000 description 1
- RNWHGQJWIACOKP-UHFFFAOYSA-N zinc;oxygen(2-) Chemical compound [O-2].[Zn+2] RNWHGQJWIACOKP-UHFFFAOYSA-N 0.000 description 1
- 150000003754 zirconium Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
- C07C69/78—Benzoic acid esters
-
- 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
-
- 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
- C08K2201/00—Specific properties of additives
- C08K2201/014—Additives containing two or more different additives of the same subgroup in C08K
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Aiming, Guidance, Guns With A Light Source, Armor, Camouflage, And Targets (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Paints Or Removers (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10217186A DE10217186A1 (de) | 2002-04-18 | 2002-04-18 | Benzoesäureisononylester und deren Verwendung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA79082C2 true UA79082C2 (en) | 2007-05-25 |
Family
ID=7714379
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UA2003043503A UA79082C2 (en) | 2002-04-18 | 2003-04-17 | Mixtures of isomeric isononyl esters of benzoic acid, their mixtures with alkyl esters of phthalic, adipinic or cyclohexandicarboxylic acids, as well as use of these mixtures |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US7323588B2 (no) |
| EP (1) | EP1354867B1 (no) |
| JP (1) | JP2003335729A (no) |
| KR (1) | KR100994916B1 (no) |
| CN (1) | CN1451647A (no) |
| BR (1) | BR0300936A (no) |
| CA (1) | CA2426919C (no) |
| CZ (1) | CZ303483B6 (no) |
| DE (1) | DE10217186A1 (no) |
| DK (1) | DK1354867T3 (no) |
| ES (1) | ES2539816T3 (no) |
| HU (2) | HUE025451T2 (no) |
| MX (1) | MXPA03003360A (no) |
| NO (1) | NO339698B1 (no) |
| PL (1) | PL207719B1 (no) |
| RU (1) | RU2335489C2 (no) |
| TW (1) | TWI297680B (no) |
| UA (1) | UA79082C2 (no) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1558927A (zh) | 2001-09-25 | 2004-12-29 | ����ɭ���ڻ�ѧר����˾ | 增塑聚氯乙烯 |
| DE50211172D1 (de) * | 2001-09-26 | 2007-12-20 | Oxeno Olefinchemie Gmbh | Phthalsäurealkylestergemische mit kontrollierter viskosität |
| DE10217186A1 (de) | 2002-04-18 | 2003-11-13 | Oxeno Olefinchemie Gmbh | Benzoesäureisononylester und deren Verwendung |
| DE10336150A1 (de) * | 2003-08-07 | 2005-03-10 | Oxeno Olefinchemie Gmbh | Schäumbare Kompositionen, die Benzoesäureisononylester aufweisen |
| DE10341428A1 (de) | 2003-09-09 | 2005-03-31 | Oxeno Olefinchemie Gmbh | Verwendung von Isononylbenzoaten als Filmbildehilfsmittel |
| DE10347863A1 (de) * | 2003-10-10 | 2005-05-04 | Oxeno Olefinchemie Gmbh | Verfahren zur Herstellung von Benzoesäureestern |
| EP1846492B1 (en) * | 2005-01-18 | 2014-10-01 | ExxonMobil Chemical Patents Inc. | Improvements in or relating to plasticiser compositions |
| DE102005021075A1 (de) * | 2005-05-06 | 2006-11-09 | Oxeno Olefinchemie Gmbh | Verfahren zur Herstellung von Carbonsäureestern |
| DE102006001795A1 (de) * | 2006-01-12 | 2007-07-19 | Oxeno Olefinchemie Gmbh | Terephthalsäuredialkylester und deren Verwendung |
| US8729289B2 (en) * | 2007-03-13 | 2014-05-20 | Exxonmobil Chemical Patents Inc. | Ester production |
| DE102007055483A1 (de) | 2007-11-21 | 2009-05-28 | Evonik Goldschmidt Gmbh | Kosmetische und dermatologische Formulierungen enthaltend Isononylbenzoat |
| EP2231763B1 (en) * | 2007-12-21 | 2015-01-07 | ExxonMobil Chemical Patents Inc. | Co-plasticizer systems |
| DE102008006400A1 (de) * | 2008-01-28 | 2009-07-30 | Evonik Oxeno Gmbh | Gemische von Diisononylestern der Terephthalsäure, Verfahren zu deren Herstellung und deren Verwendung |
| US20110021680A1 (en) * | 2008-03-28 | 2011-01-27 | Colle Karla S | Polyol Ester Plasticizers and Process of Making the Same |
| DE102008001655A1 (de) * | 2008-05-08 | 2009-11-12 | Kuraray Europe Gmbh | Weichmacherhaltige Folien aus Polyvinylacetal mit Cyclohexan-1,2-dicarbon-säureestern als Weichmacher |
| US20100113664A1 (en) * | 2008-06-11 | 2010-05-06 | Ferro Corporation | Asymmetric Cyclic Diester Compounds |
| EP2354172B1 (de) * | 2010-02-08 | 2012-11-21 | LANXESS Deutschland GmbH | Phthalatfreie Isocyanuratzubereitungen |
| US8653171B2 (en) * | 2010-02-22 | 2014-02-18 | Polyone Corporation | Plastisol compositions that are essentially free of polyvinyl halides and phthalates |
| EP2404961A1 (de) | 2010-07-05 | 2012-01-11 | LANXESS Deutschland GmbH | Weichmacherzubereitungen mit guten Geliereigenschaften |
| DE102010061867A1 (de) * | 2010-11-24 | 2012-05-24 | Evonik Oxeno Gmbh | Verwendung von Di(isononyl)cyclohexansäureester (DINCH) in verschäumbaren PVC-Formulierungen |
| ES2603929T3 (es) | 2012-10-12 | 2017-03-02 | Evonik Degussa Gmbh | Bisfosfito asimétrico |
| DE102013203972A1 (de) * | 2013-03-08 | 2014-09-11 | Evonik Industries Ag | Isononylester auf Basis von Fettsäuren oder Fettsäuregemischen aus Tallöl oder Leinöl |
| PL3090023T3 (pl) | 2014-01-03 | 2023-01-16 | Tarkett Gdl | Dekoracyjne pokrycia powierzchniowe z ulepszonych bezftalanowych kompozycji plastizolu poli(chlorku winylu) |
| TW201605945A (zh) | 2014-07-08 | 2016-02-16 | 巴斯夫歐洲公司 | 包含二羧酸的酯及１，２－環己烷二羧酸的酯之模製化合物 |
| TW201609628A (zh) | 2014-07-08 | 2016-03-16 | 巴斯夫歐洲公司 | 包含脂族二羧酸二酯及對苯二甲酸二烷基酯之塑化劑組成物 |
| TW201619120A (zh) | 2014-10-09 | 2016-06-01 | 巴斯夫歐洲公司 | 包含飽和二羧酸之環烷基酯及對苯二甲酯之塑化劑組成物 |
| TW201619119A (zh) | 2014-10-09 | 2016-06-01 | 巴斯夫歐洲公司 | 包含飽和二羧酸之環烷基酯及１，２－環己烷二羧酸酯的塑化劑組成物 |
| PL3405518T3 (pl) | 2016-01-20 | 2020-05-18 | Basf Se | Kompozycja plastyfikatora, która zawiera estry alifatycznych kwasów dikarboksylowych i diestry wybrane spośród estrów kwasu 1,2-cykloheksanodikarboksylowego i estrów kwasu tereftalowego |
| EP3491054A1 (de) | 2016-08-01 | 2019-06-05 | Basf Se | Weichmacher-zusammensetzung |
| WO2018024591A1 (de) | 2016-08-01 | 2018-02-08 | Basf Se | Weichmacher-zusammensetzung |
| JP7159155B2 (ja) * | 2016-09-29 | 2022-10-24 | コーニンクレッカ フィリップス エヌ ヴェ | 動的ビームサイズ制限を有する撮像システム |
| CN109317196A (zh) * | 2018-07-18 | 2019-02-12 | 芮立 | 非酸性催化剂及基于该催化剂的增塑剂、制备方法和应用 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH274531A (de) * | 1949-03-12 | 1951-04-15 | Ici Ltd | Mindestens eine organische thermoplastische Substanz enthaltendes Material. |
| CH516608A (de) * | 1968-12-14 | 1971-12-15 | Ciba Geigy Ag | Verformbare Mischungen und deren Verwendung zur Herstellung von Folien und Überzügen |
| DE2009505A1 (de) | 1970-02-28 | 1971-09-09 | Badische Anilin & Soda Fabrik AG, 6700 Ludwigshafen | Isonananole sowie deren Verwendung in Form von Bis Isononylestern der Phthal saure oder Adipinsäure |
| HU165522B (no) | 1972-10-16 | 1974-09-28 | ||
| DE2710630A1 (de) | 1977-03-11 | 1978-09-21 | Mitsubishi Chem Ind | Verfahren zur herstellung von estern von carbonsaeure, insbesondere durch umesterung bzw. verfahren zur hydrolyse derartiger ester |
| WO1989000173A2 (en) * | 1987-07-02 | 1989-01-12 | Velsicol Chemical Corporation | Benzoic acid esters as coalescing agents for paint composition |
| US5236987A (en) | 1987-07-02 | 1993-08-17 | Velsicol Chemical Corporation | Isodecyl benzoate coalescing agents in latex compositions |
| GB9607686D0 (en) | 1996-04-12 | 1996-06-12 | Exxon Chemical Patents Inc | Plastisol compostions |
| DE19629906A1 (de) | 1996-07-24 | 1998-01-29 | Huels Chemische Werke Ag | Verfahren zur Herstellung von Butenoligomeren aus Fischer-Tropsch-Olefinen |
| DE19927978A1 (de) * | 1999-06-18 | 2000-12-21 | Basf Ag | Ausgewählte Cyclohexan-1,3- und 1,4-dicarbonsäureester |
| JP4314711B2 (ja) | 2000-01-27 | 2009-08-19 | 新日本理化株式会社 | シクロヘキサンジカルボン酸ジエステル系可塑剤、塩化ビニル系樹脂組成物及びそれを用いた塩化ビニル系樹脂成形体 |
| DE10217186A1 (de) | 2002-04-18 | 2003-11-13 | Oxeno Olefinchemie Gmbh | Benzoesäureisononylester und deren Verwendung |
| DE10336150A1 (de) * | 2003-08-07 | 2005-03-10 | Oxeno Olefinchemie Gmbh | Schäumbare Kompositionen, die Benzoesäureisononylester aufweisen |
-
2002
- 2002-04-18 DE DE10217186A patent/DE10217186A1/de not_active Withdrawn
-
2003
- 2003-04-11 DK DK03008409.9T patent/DK1354867T3/en active
- 2003-04-11 HU HUE03008409A patent/HUE025451T2/hu unknown
- 2003-04-11 EP EP03008409.9A patent/EP1354867B1/de not_active Expired - Lifetime
- 2003-04-11 ES ES03008409.9T patent/ES2539816T3/es not_active Expired - Lifetime
- 2003-04-15 MX MXPA03003360A patent/MXPA03003360A/es active IP Right Grant
- 2003-04-15 PL PL359696A patent/PL207719B1/pl unknown
- 2003-04-16 TW TW092108789A patent/TWI297680B/zh not_active IP Right Cessation
- 2003-04-16 CA CA2426919A patent/CA2426919C/en not_active Expired - Fee Related
- 2003-04-16 BR BR0300936-0A patent/BR0300936A/pt not_active Application Discontinuation
- 2003-04-16 NO NO20031777A patent/NO339698B1/no not_active IP Right Cessation
- 2003-04-17 HU HU0301063A patent/HU230644B1/hu not_active IP Right Cessation
- 2003-04-17 RU RU2003110980/04A patent/RU2335489C2/ru not_active IP Right Cessation
- 2003-04-17 UA UA2003043503A patent/UA79082C2/uk unknown
- 2003-04-17 CN CN03123121A patent/CN1451647A/zh active Pending
- 2003-04-17 CZ CZ20031097A patent/CZ303483B6/cs not_active IP Right Cessation
- 2003-04-17 JP JP2003113155A patent/JP2003335729A/ja active Pending
- 2003-04-18 US US10/418,103 patent/US7323588B2/en not_active Expired - Fee Related
- 2003-04-18 KR KR1020030024620A patent/KR100994916B1/ko not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| HU230644B1 (hu) | 2017-05-29 |
| KR20030082926A (ko) | 2003-10-23 |
| HUP0301063A2 (hu) | 2004-03-01 |
| CN1451647A (zh) | 2003-10-29 |
| MXPA03003360A (es) | 2005-11-08 |
| TWI297680B (en) | 2008-06-11 |
| BR0300936A (pt) | 2004-08-17 |
| CZ303483B6 (cs) | 2012-10-10 |
| CA2426919A1 (en) | 2003-10-18 |
| JP2003335729A (ja) | 2003-11-28 |
| PL359696A1 (en) | 2003-10-20 |
| NO20031777D0 (no) | 2003-04-16 |
| NO339698B1 (no) | 2017-01-23 |
| ES2539816T3 (es) | 2015-07-06 |
| US7323588B2 (en) | 2008-01-29 |
| PL207719B1 (pl) | 2011-01-31 |
| HUE025451T2 (hu) | 2016-04-28 |
| CZ20031097A3 (cs) | 2004-09-15 |
| US20040015007A1 (en) | 2004-01-22 |
| HUP0301063A3 (en) | 2011-05-30 |
| EP1354867A3 (de) | 2004-03-10 |
| NO20031777L (no) | 2003-10-20 |
| KR100994916B1 (ko) | 2010-11-19 |
| TW200407301A (en) | 2004-05-16 |
| RU2335489C2 (ru) | 2008-10-10 |
| EP1354867B1 (de) | 2015-04-01 |
| DK1354867T3 (en) | 2015-07-06 |
| EP1354867A2 (de) | 2003-10-22 |
| CA2426919C (en) | 2010-12-07 |
| DE10217186A1 (de) | 2003-11-13 |
| HU0301063D0 (en) | 2003-08-28 |
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