NO320324B1 - Polymerer og monomerer og anvendelse derav samt fremgangsmate for fremstilling av polymerer og begroingshindrende maling inneholdende polymerer - Google Patents
Polymerer og monomerer og anvendelse derav samt fremgangsmate for fremstilling av polymerer og begroingshindrende maling inneholdende polymerer Download PDFInfo
- Publication number
- NO320324B1 NO320324B1 NO20021491A NO20021491A NO320324B1 NO 320324 B1 NO320324 B1 NO 320324B1 NO 20021491 A NO20021491 A NO 20021491A NO 20021491 A NO20021491 A NO 20021491A NO 320324 B1 NO320324 B1 NO 320324B1
- Authority
- NO
- Norway
- Prior art keywords
- acrylate
- meth
- chloride
- substituted
- alcohol
- Prior art date
Links
- 239000000178 monomer Substances 0.000 title claims abstract description 73
- 229920000642 polymer Polymers 0.000 title claims abstract description 65
- 230000003373 anti-fouling effect Effects 0.000 title claims abstract description 34
- 239000003973 paint Substances 0.000 title claims abstract description 34
- 238000000034 method Methods 0.000 title claims description 9
- 125000003118 aryl group Chemical group 0.000 claims abstract description 37
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 36
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 23
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims abstract description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 19
- 150000002367 halogens Chemical class 0.000 claims abstract description 17
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 17
- 125000004104 aryloxy group Chemical group 0.000 claims abstract description 16
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 13
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims abstract description 13
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 13
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims abstract description 10
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 10
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 9
- 125000003860 C1-C20 alkoxy group Chemical group 0.000 claims abstract description 9
- 125000002861 (C1-C4) alkanoyl group Chemical group 0.000 claims abstract description 7
- -1 triethylsilyl Chemical group 0.000 claims description 1014
- 150000001875 compounds Chemical class 0.000 claims description 44
- 238000004519 manufacturing process Methods 0.000 claims description 20
- 238000005498 polishing Methods 0.000 claims description 17
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 16
- 238000000576 coating method Methods 0.000 claims description 14
- 229920001577 copolymer Polymers 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 14
- 125000003545 alkoxy group Chemical group 0.000 claims description 12
- 238000006116 polymerization reaction Methods 0.000 claims description 9
- 238000006243 chemical reaction Methods 0.000 claims description 8
- 239000003999 initiator Substances 0.000 claims description 8
- 238000002360 preparation method Methods 0.000 claims description 6
- 239000012442 inert solvent Substances 0.000 claims description 4
- 125000002252 acyl group Chemical group 0.000 claims description 3
- 239000011248 coating agent Substances 0.000 claims description 3
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 3
- ILMRJRBKQSSXGY-UHFFFAOYSA-N tert-butyl(dimethyl)silicon Chemical group C[Si](C)C(C)(C)C ILMRJRBKQSSXGY-UHFFFAOYSA-N 0.000 claims description 3
- 125000002306 tributylsilyl group Chemical group C(CCC)[Si](CCCC)(CCCC)* 0.000 claims description 3
- 125000000025 triisopropylsilyl group Chemical group C(C)(C)[Si](C(C)C)(C(C)C)* 0.000 claims description 3
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- 230000003115 biocidal effect Effects 0.000 claims description 2
- 239000003139 biocide Substances 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 2
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims 1
- 125000004423 acyloxy group Chemical group 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 238000012512 characterization method Methods 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 abstract description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 512
- 235000019441 ethanol Nutrition 0.000 description 187
- LRHPLDYGYMQRHN-UHFFFAOYSA-N butyl alcohol Substances CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 119
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Natural products CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 113
- BDERNNFJNOPAEC-UHFFFAOYSA-N n-propyl alcohol Natural products CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 111
- 239000011230 binding agent Substances 0.000 description 22
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 16
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 13
- 239000002904 solvent Substances 0.000 description 13
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- 150000002148 esters Chemical class 0.000 description 12
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 12
- 229920005989 resin Polymers 0.000 description 12
- 239000011347 resin Substances 0.000 description 12
- SNMVRZFUUCLYTO-UHFFFAOYSA-N n-propyl chloride Chemical compound CCCCl SNMVRZFUUCLYTO-UHFFFAOYSA-N 0.000 description 10
- 239000000049 pigment Substances 0.000 description 10
- FPCPOLLWTJARLO-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)acetic acid Chemical compound CC(=C)C(=O)OCC(O)=O FPCPOLLWTJARLO-UHFFFAOYSA-N 0.000 description 9
- SBWOBTUYQXLKSS-UHFFFAOYSA-N 3-(2-methylprop-2-enoyloxy)propanoic acid Chemical compound CC(=C)C(=O)OCCC(O)=O SBWOBTUYQXLKSS-UHFFFAOYSA-N 0.000 description 9
- CYUZOYPRAQASLN-UHFFFAOYSA-N 3-prop-2-enoyloxypropanoic acid Chemical compound OC(=O)CCOC(=O)C=C CYUZOYPRAQASLN-UHFFFAOYSA-N 0.000 description 9
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 9
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- VFWCMGCRMGJXDK-UHFFFAOYSA-N 1-chlorobutane Chemical compound CCCCCl VFWCMGCRMGJXDK-UHFFFAOYSA-N 0.000 description 8
- JYSWMLAADBQAQX-UHFFFAOYSA-N 2-prop-2-enoyloxyacetic acid Chemical compound OC(=O)COC(=O)C=C JYSWMLAADBQAQX-UHFFFAOYSA-N 0.000 description 8
- FWGJQLNEEMJIRO-UHFFFAOYSA-N 5-(2-methylprop-2-enoyloxy)pentanoic acid Chemical compound CC(=C)C(=O)OCCCCC(O)=O FWGJQLNEEMJIRO-UHFFFAOYSA-N 0.000 description 8
- WCPPBOCOQZELQO-UHFFFAOYSA-N 5-prop-2-enoyloxypentanoic acid Chemical compound OC(=O)CCCCOC(=O)C=C WCPPBOCOQZELQO-UHFFFAOYSA-N 0.000 description 8
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 8
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 8
- 239000000945 filler Substances 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 229960004419 dimethyl fumarate Drugs 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 6
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- DTJGMNVTTPUVFY-UHFFFAOYSA-N 4-(2-methylprop-2-enoyloxy)butanoic acid Chemical compound CC(=C)C(=O)OCCCC(O)=O DTJGMNVTTPUVFY-UHFFFAOYSA-N 0.000 description 6
- HEMYIEDNNZJZSV-UHFFFAOYSA-N 4-prop-2-enoyloxybutanoic acid Chemical compound OC(=O)CCCOC(=O)C=C HEMYIEDNNZJZSV-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 6
- 229960003750 ethyl chloride Drugs 0.000 description 6
- 239000000835 fiber Substances 0.000 description 6
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical class OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 150000001408 amides Chemical class 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 239000000460 chlorine Substances 0.000 description 5
- 229910052802 copper Inorganic materials 0.000 description 5
- 239000010949 copper Substances 0.000 description 5
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 5
- 125000002524 organometallic group Chemical group 0.000 description 5
- 150000003254 radicals Chemical class 0.000 description 5
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 4
- XLLIQLLCWZCATF-UHFFFAOYSA-N 2-methoxyethyl acetate Chemical compound COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N acrylic acid methyl ester Natural products COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- KQIADDMXRMTWHZ-UHFFFAOYSA-N chloro-tri(propan-2-yl)silane Chemical compound CC(C)[Si](Cl)(C(C)C)C(C)C KQIADDMXRMTWHZ-UHFFFAOYSA-N 0.000 description 4
- 239000012043 crude product Substances 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- RWRIWBAIICGTTQ-UHFFFAOYSA-N difluoromethane Chemical compound FCF RWRIWBAIICGTTQ-UHFFFAOYSA-N 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- 125000004185 ester group Chemical group 0.000 description 4
- XLYMOEINVGRTEX-UHFFFAOYSA-N fumaric acid monoethyl ester Natural products CCOC(=O)C=CC(O)=O XLYMOEINVGRTEX-UHFFFAOYSA-N 0.000 description 4
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 4
- 235000019341 magnesium sulphate Nutrition 0.000 description 4
- HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 description 4
- 239000012074 organic phase Substances 0.000 description 4
- 238000001953 recrystallisation Methods 0.000 description 4
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- XLYMOEINVGRTEX-ONEGZZNKSA-N (e)-4-ethoxy-4-oxobut-2-enoic acid Chemical compound CCOC(=O)\C=C\C(O)=O XLYMOEINVGRTEX-ONEGZZNKSA-N 0.000 description 3
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 3
- XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 3
- 239000005751 Copper oxide Substances 0.000 description 3
- IEPRKVQEAMIZSS-UHFFFAOYSA-N Di-Et ester-Fumaric acid Natural products CCOC(=O)C=CC(=O)OCC IEPRKVQEAMIZSS-UHFFFAOYSA-N 0.000 description 3
- IEPRKVQEAMIZSS-WAYWQWQTSA-N Diethyl maleate Chemical compound CCOC(=O)\C=C/C(=O)OCC IEPRKVQEAMIZSS-WAYWQWQTSA-N 0.000 description 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 3
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 3
- 150000008064 anhydrides Chemical group 0.000 description 3
- 235000019445 benzyl alcohol Nutrition 0.000 description 3
- 239000004359 castor oil Substances 0.000 description 3
- 235000019438 castor oil Nutrition 0.000 description 3
- 229910000431 copper oxide Inorganic materials 0.000 description 3
- BQVVSSAWECGTRN-UHFFFAOYSA-L copper;dithiocyanate Chemical compound [Cu+2].[S-]C#N.[S-]C#N BQVVSSAWECGTRN-UHFFFAOYSA-L 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 239000000543 intermediate Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 150000002978 peroxides Chemical class 0.000 description 3
- 238000001556 precipitation Methods 0.000 description 3
- 239000013535 sea water Substances 0.000 description 3
- 239000013049 sediment Substances 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 150000003751 zinc Chemical class 0.000 description 3
- VYBIZBGDHYRFBW-OWBHPGMISA-N (Z)-2-methyl-3-[4-oxo-4-(3-phenylpropanoyloxy)butyl]but-2-enedioic acid Chemical compound OC(=O)C(/C)=C(C(O)=O)/CCCC(=O)OC(=O)CCC1=CC=CC=C1 VYBIZBGDHYRFBW-OWBHPGMISA-N 0.000 description 2
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 description 2
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 2
- UJPMYEOUBPIPHQ-UHFFFAOYSA-N 1,1,1-trifluoroethane Chemical compound CC(F)(F)F UJPMYEOUBPIPHQ-UHFFFAOYSA-N 0.000 description 2
- NPNPZTNLOVBDOC-UHFFFAOYSA-N 1,1-difluoroethane Chemical compound CC(F)F NPNPZTNLOVBDOC-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- CLMOTGBOOYXUAE-UHFFFAOYSA-N 1,4-dichloro-1,1-diphenylbutane-2,3-dione Chemical compound C=1C=CC=CC=1C(Cl)(C(=O)C(=O)CCl)C1=CC=CC=C1 CLMOTGBOOYXUAE-UHFFFAOYSA-N 0.000 description 2
- YAJOYOBJPNAYHH-UHFFFAOYSA-N 1,4-dichloro-1-phenylbutane-2,3-dione Chemical compound ClCC(=O)C(=O)C(Cl)C1=CC=CC=C1 YAJOYOBJPNAYHH-UHFFFAOYSA-N 0.000 description 2
- HVSHJFFGLQTUHX-UHFFFAOYSA-N 1,5-dichloro-1,1-diphenylpentane-2,3-dione Chemical compound C=1C=CC=CC=1C(Cl)(C(=O)C(=O)CCCl)C1=CC=CC=C1 HVSHJFFGLQTUHX-UHFFFAOYSA-N 0.000 description 2
- NHBPTRUUPJUTNG-UHFFFAOYSA-N 1,5-dichloro-1-phenylpentane-2,3-dione Chemical compound ClCCC(=O)C(=O)C(Cl)C1=CC=CC=C1 NHBPTRUUPJUTNG-UHFFFAOYSA-N 0.000 description 2
- PVQXKWYRDXIWFJ-UHFFFAOYSA-N 1,6-dichloro-1,1-diphenylhexane-2,3-dione Chemical compound C=1C=CC=CC=1C(Cl)(C(=O)C(=O)CCCCl)C1=CC=CC=C1 PVQXKWYRDXIWFJ-UHFFFAOYSA-N 0.000 description 2
- QKQQEWDWKPZVKC-UHFFFAOYSA-N 1,6-dichloro-1-phenylhexane-2,3-dione Chemical compound ClCCCC(=O)C(=O)C(Cl)C1=CC=CC=C1 QKQQEWDWKPZVKC-UHFFFAOYSA-N 0.000 description 2
- JFESQDALZVWHCT-UHFFFAOYSA-N 1,7-dichloro-1,1-diphenylheptane-2,3-dione Chemical compound C=1C=CC=CC=1C(Cl)(C(=O)C(=O)CCCCCl)C1=CC=CC=C1 JFESQDALZVWHCT-UHFFFAOYSA-N 0.000 description 2
- CKFKRNPRPGNLLV-UHFFFAOYSA-N 1,7-dichloro-1-phenylheptane-2,3-dione Chemical compound ClCCCCC(=O)C(=O)C(Cl)C1=CC=CC=C1 CKFKRNPRPGNLLV-UHFFFAOYSA-N 0.000 description 2
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 2
- MWTFOYVPAQSMKR-UHFFFAOYSA-N 1-chloro-4-(4-methoxyphenyl)butane-2,3-dione Chemical compound COC1=CC=C(CC(=O)C(=O)CCl)C=C1 MWTFOYVPAQSMKR-UHFFFAOYSA-N 0.000 description 2
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 2
- BSWWXRFVMJHFBN-UHFFFAOYSA-N 2,4,6-tribromophenol Chemical compound OC1=C(Br)C=C(Br)C=C1Br BSWWXRFVMJHFBN-UHFFFAOYSA-N 0.000 description 2
- MNVMYTVDDOXZLS-UHFFFAOYSA-N 2,4-dimethoxyphenol Chemical compound COC1=CC=C(O)C(OC)=C1 MNVMYTVDDOXZLS-UHFFFAOYSA-N 0.000 description 2
- CXJOONIFSVSFAD-UHFFFAOYSA-N 2-(4-methoxyphenyl)acetyl chloride Chemical compound COC1=CC=C(CC(Cl)=O)C=C1 CXJOONIFSVSFAD-UHFFFAOYSA-N 0.000 description 2
- HCLJOFJIQIJXHS-UHFFFAOYSA-N 2-[2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOCCOC(=O)C=C HCLJOFJIQIJXHS-UHFFFAOYSA-N 0.000 description 2
- ATEBGNALLCMSGS-UHFFFAOYSA-N 2-chloro-1,1-difluoroethane Chemical compound FC(F)CCl ATEBGNALLCMSGS-UHFFFAOYSA-N 0.000 description 2
- NFHKZAUDRWRXMZ-UHFFFAOYSA-N 2-chloro-2,2-diphenylacetyl chloride Chemical compound C=1C=CC=CC=1C(Cl)(C(=O)Cl)C1=CC=CC=C1 NFHKZAUDRWRXMZ-UHFFFAOYSA-N 0.000 description 2
- FGEAOSXMQZWHIQ-UHFFFAOYSA-N 2-chloro-2-phenylacetyl chloride Chemical compound ClC(=O)C(Cl)C1=CC=CC=C1 FGEAOSXMQZWHIQ-UHFFFAOYSA-N 0.000 description 2
- PORQOHRXAJJKGK-UHFFFAOYSA-N 4,5-dichloro-2-n-octyl-3(2H)-isothiazolone Chemical compound CCCCCCCCN1SC(Cl)=C(Cl)C1=O PORQOHRXAJJKGK-UHFFFAOYSA-N 0.000 description 2
- LKVFCSWBKOVHAH-UHFFFAOYSA-N 4-Ethoxyphenol Chemical compound CCOC1=CC=C(O)C=C1 LKVFCSWBKOVHAH-UHFFFAOYSA-N 0.000 description 2
- RGHHSNMVTDWUBI-UHFFFAOYSA-N 4-hydroxybenzaldehyde Chemical compound OC1=CC=C(C=O)C=C1 RGHHSNMVTDWUBI-UHFFFAOYSA-N 0.000 description 2
- NQJXQCTULPPHLO-SEYXRHQNSA-N 4-o-[2-(2,2-diphenylacetyl)oxy-2-oxoethyl] 1-o-methyl (z)-but-2-enedioate Chemical compound C=1C=CC=CC=1C(C(=O)OC(=O)COC(=O)\C=C/C(=O)OC)C1=CC=CC=C1 NQJXQCTULPPHLO-SEYXRHQNSA-N 0.000 description 2
- PQHZYSPLEJIMBR-UHFFFAOYSA-N 5-chloro-1-(4-methoxyphenyl)pentane-2,3-dione Chemical compound COC1=CC=C(CC(=O)C(=O)CCCl)C=C1 PQHZYSPLEJIMBR-UHFFFAOYSA-N 0.000 description 2
- RKIJSJXSQIQGCH-UHFFFAOYSA-N 6-chloro-1-(4-methoxyphenyl)hexane-2,3-dione Chemical compound COC1=CC=C(CC(=O)C(=O)CCCCl)C=C1 RKIJSJXSQIQGCH-UHFFFAOYSA-N 0.000 description 2
- BVHWDWJVXWTFLC-UHFFFAOYSA-N 7-chloro-1-(4-methoxyphenyl)heptane-2,3-dione Chemical compound COC1=CC=C(CC(=O)C(=O)CCCCCl)C=C1 BVHWDWJVXWTFLC-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- XWCDCDSDNJVCLO-UHFFFAOYSA-N Chlorofluoromethane Chemical compound FCCl XWCDCDSDNJVCLO-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 235000006708 antioxidants Nutrition 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 2
- 229960002836 biphenylol Drugs 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 2
- 150000001805 chlorine compounds Chemical class 0.000 description 2
- DCFKHNIGBAHNSS-UHFFFAOYSA-N chloro(triethyl)silane Chemical compound CC[Si](Cl)(CC)CC DCFKHNIGBAHNSS-UHFFFAOYSA-N 0.000 description 2
- 239000003240 coconut oil Substances 0.000 description 2
- 235000019864 coconut oil Nutrition 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 239000002274 desiccant Substances 0.000 description 2
- 230000006866 deterioration Effects 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
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- LHGVFZTZFXWLCP-UHFFFAOYSA-N guaiacol Chemical compound COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 150000002484 inorganic compounds Chemical class 0.000 description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 239000000944 linseed oil Substances 0.000 description 2
- 235000021388 linseed oil Nutrition 0.000 description 2
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 150000002688 maleic acid derivatives Chemical class 0.000 description 2
- 125000005395 methacrylic acid group Chemical group 0.000 description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 2
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
- QULYNCCPRWKEMF-UHFFFAOYSA-N parachlorobenzotrifluoride Chemical compound FC(F)(F)C1=CC=C(Cl)C=C1 QULYNCCPRWKEMF-UHFFFAOYSA-N 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- 239000003505 polymerization initiator Substances 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 229960004889 salicylic acid Drugs 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- WMOVHXAZOJBABW-UHFFFAOYSA-N tert-butyl acetate Chemical compound CC(=O)OC(C)(C)C WMOVHXAZOJBABW-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 150000003672 ureas Chemical class 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- PICXIOQBANWBIZ-UHFFFAOYSA-N zinc;1-oxidopyridine-2-thione Chemical compound [Zn+2].[O-]N1C=CC=CC1=S.[O-]N1C=CC=CC1=S PICXIOQBANWBIZ-UHFFFAOYSA-N 0.000 description 2
- BCXVDCGENUQTPC-UHFFFAOYSA-N (1,4-dimethoxycyclohexa-2,4-dien-1-yl) 3-chloropropanoate Chemical compound COC1=CCC(OC)(OC(=O)CCCl)C=C1 BCXVDCGENUQTPC-UHFFFAOYSA-N 0.000 description 1
- VUMXVJIMZWDJTK-UHFFFAOYSA-N (1,4-dimethoxycyclohexa-2,4-dien-1-yl) 4-chlorobutanoate Chemical compound COC1=CCC(OC)(OC(=O)CCCCl)C=C1 VUMXVJIMZWDJTK-UHFFFAOYSA-N 0.000 description 1
- DHDZIFRXQQMLRY-UHFFFAOYSA-N (1,4-dimethoxycyclohexa-2,4-dien-1-yl) 5-chloropentanoate Chemical compound COC1=CCC(OC)(OC(=O)CCCCCl)C=C1 DHDZIFRXQQMLRY-UHFFFAOYSA-N 0.000 description 1
- RLOFWHYMZGNWQG-UHFFFAOYSA-N (2,4,6-tribromophenyl) 3-chloropropanoate Chemical compound ClCCC(=O)OC1=C(Br)C=C(Br)C=C1Br RLOFWHYMZGNWQG-UHFFFAOYSA-N 0.000 description 1
- HZMCPGBOTPQRMT-UHFFFAOYSA-N (2,4,6-tribromophenyl) 4-chlorobutanoate Chemical compound ClCCCC(=O)OC1=C(Br)C=C(Br)C=C1Br HZMCPGBOTPQRMT-UHFFFAOYSA-N 0.000 description 1
- HMUINHLGGABBHY-UHFFFAOYSA-N (2,4,6-tribromophenyl) 5-chloropentanoate Chemical compound ClCCCCC(=O)OC1=C(Br)C=C(Br)C=C1Br HMUINHLGGABBHY-UHFFFAOYSA-N 0.000 description 1
- WUSGUUFHBIXQHD-UHFFFAOYSA-N (2,4,6-trichlorophenyl) 3-chloropropanoate Chemical compound ClCCC(=O)OC1=C(Cl)C=C(Cl)C=C1Cl WUSGUUFHBIXQHD-UHFFFAOYSA-N 0.000 description 1
- GNQAFLXDOXYSDZ-UHFFFAOYSA-N (2,4,6-trichlorophenyl) 4-chlorobutanoate Chemical compound ClCCCC(=O)OC1=C(Cl)C=C(Cl)C=C1Cl GNQAFLXDOXYSDZ-UHFFFAOYSA-N 0.000 description 1
- FWIVNVNWXVVGFZ-UHFFFAOYSA-N (2,4,6-trichlorophenyl) 5-chloropentanoate Chemical compound ClCCCCC(=O)OC1=C(Cl)C=C(Cl)C=C1Cl FWIVNVNWXVVGFZ-UHFFFAOYSA-N 0.000 description 1
- WAWDAHSPNVQIJB-UHFFFAOYSA-N (2,4-dibromo-6-chlorophenyl) 3-chloropropanoate Chemical compound ClCCC(=O)OC1=C(Cl)C=C(Br)C=C1Br WAWDAHSPNVQIJB-UHFFFAOYSA-N 0.000 description 1
- VCSSPECWDUXQHO-UHFFFAOYSA-N (2,4-dibromo-6-chlorophenyl) 5-chloropentanoate Chemical compound ClCCCCC(=O)OC1=C(Cl)C=C(Br)C=C1Br VCSSPECWDUXQHO-UHFFFAOYSA-N 0.000 description 1
- CJEOTGQSFGPVJV-UHFFFAOYSA-N (2,4-dibromo-6-formylphenyl) 3-chloropropanoate Chemical compound ClCCC(=O)OC1=C(Br)C=C(Br)C=C1C=O CJEOTGQSFGPVJV-UHFFFAOYSA-N 0.000 description 1
- RGLSHLAQRRGXMW-UHFFFAOYSA-N (2,4-dibromo-6-formylphenyl) 4-chlorobutanoate Chemical compound ClCCCC(=O)OC1=C(Br)C=C(Br)C=C1C=O RGLSHLAQRRGXMW-UHFFFAOYSA-N 0.000 description 1
- KLCVSWJIMRYGMV-UHFFFAOYSA-N (2,4-dibromo-6-formylphenyl) 5-chloropentanoate Chemical compound ClCCCCC(=O)OC1=C(Br)C=C(Br)C=C1C=O KLCVSWJIMRYGMV-UHFFFAOYSA-N 0.000 description 1
- RZMMKMDXQZANFU-UHFFFAOYSA-N (2,4-dichloro-6-iodophenyl) 3-chloropropanoate Chemical compound ClCCC(=O)OC1=C(Cl)C=C(Cl)C=C1I RZMMKMDXQZANFU-UHFFFAOYSA-N 0.000 description 1
- ZTLBTHVQNHFXFO-UHFFFAOYSA-N (2,4-dichloro-6-iodophenyl) 4-chlorobutanoate Chemical compound ClCCCC(=O)OC1=C(Cl)C=C(Cl)C=C1I ZTLBTHVQNHFXFO-UHFFFAOYSA-N 0.000 description 1
- IXPLPRXZYUPEOA-UHFFFAOYSA-N (2,4-dichloro-6-iodophenyl) 5-chloropentanoate Chemical compound ClCCCCC(=O)OC1=C(Cl)C=C(Cl)C=C1I IXPLPRXZYUPEOA-UHFFFAOYSA-N 0.000 description 1
- RSCAJFFCYHAVRZ-UHFFFAOYSA-N (2,4-dimethoxyphenyl) 3-chloropropanoate Chemical compound COC1=CC=C(OC(=O)CCCl)C(OC)=C1 RSCAJFFCYHAVRZ-UHFFFAOYSA-N 0.000 description 1
- WOYBVLPGNKUMKE-UHFFFAOYSA-N (2,4-dimethoxyphenyl) 4-chlorobutanoate Chemical compound COC1=CC=C(OC(=O)CCCCl)C(OC)=C1 WOYBVLPGNKUMKE-UHFFFAOYSA-N 0.000 description 1
- UTMLIGWRHFKUCM-UHFFFAOYSA-N (2,4-dimethoxyphenyl) 5-chloropentanoate Chemical compound COC1=CC=C(OC(=O)CCCCCl)C(OC)=C1 UTMLIGWRHFKUCM-UHFFFAOYSA-N 0.000 description 1
- HZDNNJABYXNPPV-UHFFFAOYSA-N (2-chloro-2-oxoethyl) acetate Chemical compound CC(=O)OCC(Cl)=O HZDNNJABYXNPPV-UHFFFAOYSA-N 0.000 description 1
- YDMKYDWSFUWXON-UHFFFAOYSA-N (2-chloro-5-methoxyphenyl) 3-chloropropanoate Chemical compound COC1=CC=C(Cl)C(OC(=O)CCCl)=C1 YDMKYDWSFUWXON-UHFFFAOYSA-N 0.000 description 1
- ZDCSKOSDMQLZFX-UHFFFAOYSA-N (2-chloro-5-methoxyphenyl) 4-chlorobutanoate Chemical compound COC1=CC=C(Cl)C(OC(=O)CCCCl)=C1 ZDCSKOSDMQLZFX-UHFFFAOYSA-N 0.000 description 1
- PDJSQRUVDUOYJM-UHFFFAOYSA-N (2-chloro-5-methoxyphenyl) 5-chloropentanoate Chemical compound COC1=CC=C(Cl)C(OC(=O)CCCCCl)=C1 PDJSQRUVDUOYJM-UHFFFAOYSA-N 0.000 description 1
- VAOMWULWMQDHMK-UHFFFAOYSA-N (2-ethoxy-6-formylphenyl) 3-chloropropanoate Chemical compound CCOC1=CC=CC(C=O)=C1OC(=O)CCCl VAOMWULWMQDHMK-UHFFFAOYSA-N 0.000 description 1
- ZSHQHZQZUUJOBC-UHFFFAOYSA-N (2-ethoxy-6-formylphenyl) 5-chloropentanoate Chemical compound CCOC1=CC=CC(C=O)=C1OC(=O)CCCCCl ZSHQHZQZUUJOBC-UHFFFAOYSA-N 0.000 description 1
- SAFKSSVDVUVHES-UHFFFAOYSA-N (2-fluoro-6-formylphenyl) 3-chloropropanoate Chemical compound FC1=CC=CC(C=O)=C1OC(=O)CCCl SAFKSSVDVUVHES-UHFFFAOYSA-N 0.000 description 1
- FTKNUUUHZKBQBO-UHFFFAOYSA-N (2-fluoro-6-formylphenyl) 4-chlorobutanoate Chemical compound FC1=CC=CC(C=O)=C1OC(=O)CCCCl FTKNUUUHZKBQBO-UHFFFAOYSA-N 0.000 description 1
- AHHGADKGKNFILT-UHFFFAOYSA-N (2-fluoro-6-formylphenyl) 5-chloropentanoate Chemical compound FC1=CC=CC(C=O)=C1OC(=O)CCCCCl AHHGADKGKNFILT-UHFFFAOYSA-N 0.000 description 1
- WDNGPSIZPGOSIL-UHFFFAOYSA-N (2-formyl-4-methoxyphenyl) 3-chloropropanoate Chemical compound COC1=CC=C(OC(=O)CCCl)C(C=O)=C1 WDNGPSIZPGOSIL-UHFFFAOYSA-N 0.000 description 1
- VBHDFWFASATRGL-UHFFFAOYSA-N (2-formyl-4-methoxyphenyl) 4-chlorobutanoate Chemical compound COC1=CC=C(OC(=O)CCCCl)C(C=O)=C1 VBHDFWFASATRGL-UHFFFAOYSA-N 0.000 description 1
- SGXZDQFADUZKTI-UHFFFAOYSA-N (2-formyl-4-methoxyphenyl) 5-chloropentanoate Chemical compound COC1=CC=C(OC(=O)CCCCCl)C(C=O)=C1 SGXZDQFADUZKTI-UHFFFAOYSA-N 0.000 description 1
- NGYSKFLMRAEOHP-UHFFFAOYSA-N (2-formyl-6-hydroxyphenyl) 3-chloropropanoate Chemical compound OC1=CC=CC(C=O)=C1OC(=O)CCCl NGYSKFLMRAEOHP-UHFFFAOYSA-N 0.000 description 1
- NEYYHHQJQBGQQQ-UHFFFAOYSA-N (2-formyl-6-hydroxyphenyl) 4-chlorobutanoate Chemical compound OC1=CC=CC(C=O)=C1OC(=O)CCCCl NEYYHHQJQBGQQQ-UHFFFAOYSA-N 0.000 description 1
- ZEHPTKAUKUGNNN-UHFFFAOYSA-N (2-formyl-6-hydroxyphenyl) 5-chloropentanoate Chemical compound OC1=CC=CC(C=O)=C1OC(=O)CCCCCl ZEHPTKAUKUGNNN-UHFFFAOYSA-N 0.000 description 1
- VYKSGOIMRFSVED-UHFFFAOYSA-N (2-formyl-6-methoxyphenyl) 3-chloropropanoate Chemical compound COC1=CC=CC(C=O)=C1OC(=O)CCCl VYKSGOIMRFSVED-UHFFFAOYSA-N 0.000 description 1
- RIPYOMUVGDRHHH-UHFFFAOYSA-N (2-formyl-6-methoxyphenyl) 4-chlorobutanoate Chemical compound COC1=CC=CC(C=O)=C1OC(=O)CCCCl RIPYOMUVGDRHHH-UHFFFAOYSA-N 0.000 description 1
- DLYMJEPHROHWQV-UHFFFAOYSA-N (2-formyl-6-methoxyphenyl) 5-chloropentanoate Chemical compound COC1=CC=CC(C=O)=C1OC(=O)CCCCCl DLYMJEPHROHWQV-UHFFFAOYSA-N 0.000 description 1
- YPVZDHUHPYKFPL-UHFFFAOYSA-N (2-formylphenyl) 3-chloropropanoate Chemical compound ClCCC(=O)OC1=CC=CC=C1C=O YPVZDHUHPYKFPL-UHFFFAOYSA-N 0.000 description 1
- PMMLTWIHDHDRPX-UHFFFAOYSA-N (2-formylphenyl) 4-chlorobutanoate Chemical compound ClCCCC(=O)OC1=CC=CC=C1C=O PMMLTWIHDHDRPX-UHFFFAOYSA-N 0.000 description 1
- JXSRXJZPVYJOHF-UHFFFAOYSA-N (2-formylphenyl) 5-chloropentanoate Chemical compound ClCCCCC(=O)OC1=CC=CC=C1C=O JXSRXJZPVYJOHF-UHFFFAOYSA-N 0.000 description 1
- DWDWZRCYWKGDJI-UHFFFAOYSA-N (2-hydroxyphenyl) 3-chloropropanoate Chemical compound OC1=CC=CC=C1OC(=O)CCCl DWDWZRCYWKGDJI-UHFFFAOYSA-N 0.000 description 1
- KOQBKAQXCCFBNQ-UHFFFAOYSA-N (2-hydroxyphenyl) 4-chlorobutanoate Chemical compound OC1=CC=CC=C1OC(=O)CCCCl KOQBKAQXCCFBNQ-UHFFFAOYSA-N 0.000 description 1
- ZFLTYGVBPJUIBL-UHFFFAOYSA-N (2-hydroxyphenyl) 5-chloropentanoate Chemical compound OC1=CC=CC=C1OC(=O)CCCCCl ZFLTYGVBPJUIBL-UHFFFAOYSA-N 0.000 description 1
- BICBSZSOQRDEOD-UHFFFAOYSA-N (2-methoxyphenyl) 3-chloropropanoate Chemical compound COC1=CC=CC=C1OC(=O)CCCl BICBSZSOQRDEOD-UHFFFAOYSA-N 0.000 description 1
- ZMSSMKCWVJORDV-UHFFFAOYSA-N (2-methoxyphenyl) 4-chlorobutanoate Chemical compound COC1=CC=CC=C1OC(=O)CCCCl ZMSSMKCWVJORDV-UHFFFAOYSA-N 0.000 description 1
- VRRZQBMILSCUCK-UHFFFAOYSA-N (2-methoxyphenyl) 5-chloropentanoate Chemical compound COC1=CC=CC=C1OC(=O)CCCCCl VRRZQBMILSCUCK-UHFFFAOYSA-N 0.000 description 1
- HGXJDMCMYLEZMJ-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOOC(=O)C(C)(C)C HGXJDMCMYLEZMJ-UHFFFAOYSA-N 0.000 description 1
- UUIPAJHTKDSSOK-UHFFFAOYSA-N (2-nonylphenyl) dihydrogen phosphate Chemical compound CCCCCCCCCC1=CC=CC=C1OP(O)(O)=O UUIPAJHTKDSSOK-UHFFFAOYSA-N 0.000 description 1
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- UZRYPNUZVXDOLM-UHFFFAOYSA-N (3,5-diethoxyphenyl) 3-chloropropanoate Chemical compound CCOC1=CC(OCC)=CC(OC(=O)CCCl)=C1 UZRYPNUZVXDOLM-UHFFFAOYSA-N 0.000 description 1
- FVWUHJLYPPCDDF-UHFFFAOYSA-N (3,5-diethoxyphenyl) 4-chlorobutanoate Chemical compound CCOC1=CC(OCC)=CC(OC(=O)CCCCl)=C1 FVWUHJLYPPCDDF-UHFFFAOYSA-N 0.000 description 1
- FNCQORKBAKSJPH-UHFFFAOYSA-N (3,5-diethoxyphenyl) 5-chloropentanoate Chemical compound CCOC1=CC(OCC)=CC(OC(=O)CCCCCl)=C1 FNCQORKBAKSJPH-UHFFFAOYSA-N 0.000 description 1
- BSNLWTDIYOCAMO-UHFFFAOYSA-N (3,5-dihydroxyphenyl) 3-chloropropanoate Chemical compound OC1=CC(O)=CC(OC(=O)CCCl)=C1 BSNLWTDIYOCAMO-UHFFFAOYSA-N 0.000 description 1
- MFJYXVITOLXZQY-UHFFFAOYSA-N (3,5-dihydroxyphenyl) 4-chlorobutanoate Chemical compound OC1=CC(O)=CC(OC(=O)CCCCl)=C1 MFJYXVITOLXZQY-UHFFFAOYSA-N 0.000 description 1
- OUSJFCZAKKAAKX-UHFFFAOYSA-N (3,5-dihydroxyphenyl) 5-chloropentanoate Chemical compound OC1=CC(O)=CC(OC(=O)CCCCCl)=C1 OUSJFCZAKKAAKX-UHFFFAOYSA-N 0.000 description 1
- YCINZASPXREBEF-UHFFFAOYSA-N (3-chloro-4-formylphenyl) 3-chloropropanoate Chemical compound ClCCC(=O)OC1=CC=C(C=O)C(Cl)=C1 YCINZASPXREBEF-UHFFFAOYSA-N 0.000 description 1
- DUHIKVNSMCHUPD-UHFFFAOYSA-N (3-chloro-4-formylphenyl) 4-chlorobutanoate Chemical compound ClCCCC(=O)OC1=CC=C(C=O)C(Cl)=C1 DUHIKVNSMCHUPD-UHFFFAOYSA-N 0.000 description 1
- BJQPLXHVWOKBDA-UHFFFAOYSA-N (3-chloro-4-formylphenyl) 5-chloropentanoate Chemical compound ClCCCCC(=O)OC1=CC=C(C=O)C(Cl)=C1 BJQPLXHVWOKBDA-UHFFFAOYSA-N 0.000 description 1
- XWNUOCFPPCRJRI-UHFFFAOYSA-N (3-formylphenyl) 3-chloropropanoate Chemical compound ClCCC(=O)OC1=CC=CC(C=O)=C1 XWNUOCFPPCRJRI-UHFFFAOYSA-N 0.000 description 1
- MGDZOQIPTFBKSE-UHFFFAOYSA-N (3-formylphenyl) 4-chlorobutanoate Chemical compound ClCCCC(=O)OC1=CC=CC(C=O)=C1 MGDZOQIPTFBKSE-UHFFFAOYSA-N 0.000 description 1
- NSFDRHCMCSFIRN-UHFFFAOYSA-N (3-formylphenyl) 5-chloropentanoate Chemical compound ClCCCCC(=O)OC1=CC=CC(C=O)=C1 NSFDRHCMCSFIRN-UHFFFAOYSA-N 0.000 description 1
- DAFHKNAQFPVRKR-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylpropanoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)C DAFHKNAQFPVRKR-UHFFFAOYSA-N 0.000 description 1
- XLJRTCRMXBVCCX-UHFFFAOYSA-N (3-hydroxy-2,5-dimethoxyphenyl) 3-chloropropanoate Chemical compound COC1=CC(O)=C(OC)C(OC(=O)CCCl)=C1 XLJRTCRMXBVCCX-UHFFFAOYSA-N 0.000 description 1
- IVXFYEAVPWEPEQ-UHFFFAOYSA-N (3-hydroxy-2,5-dimethoxyphenyl) 4-chlorobutanoate Chemical compound COC1=CC(O)=C(OC)C(OC(=O)CCCCl)=C1 IVXFYEAVPWEPEQ-UHFFFAOYSA-N 0.000 description 1
- UITTZYHMNBCALA-UHFFFAOYSA-N (3-hydroxy-2,5-dimethoxyphenyl) 5-chloropentanoate Chemical compound COC1=CC(O)=C(OC)C(OC(=O)CCCCCl)=C1 UITTZYHMNBCALA-UHFFFAOYSA-N 0.000 description 1
- YFPDXCGEZAVGIB-UHFFFAOYSA-N (3-hydroxyphenyl) 3-chloropropanoate Chemical compound OC1=CC=CC(OC(=O)CCCl)=C1 YFPDXCGEZAVGIB-UHFFFAOYSA-N 0.000 description 1
- YEOJVVGJGQQYBB-UHFFFAOYSA-N (3-hydroxyphenyl) 4-chlorobutanoate Chemical compound OC1=CC=CC(OC(=O)CCCCl)=C1 YEOJVVGJGQQYBB-UHFFFAOYSA-N 0.000 description 1
- GLRZPRUSFWFWLP-UHFFFAOYSA-N (3-hydroxyphenyl) 5-chloropentanoate Chemical compound OC1=CC=CC(OC(=O)CCCCCl)=C1 GLRZPRUSFWFWLP-UHFFFAOYSA-N 0.000 description 1
- DTHMNZAKAPZZJS-UHFFFAOYSA-N (4-bromo-2,6-dichlorophenyl) 3-chloropropanoate Chemical compound ClCCC(=O)OC1=C(Cl)C=C(Br)C=C1Cl DTHMNZAKAPZZJS-UHFFFAOYSA-N 0.000 description 1
- XDVJHPOHMIMNQE-UHFFFAOYSA-N (4-bromo-2-formylphenyl) 3-chloropropanoate Chemical compound ClCCC(=O)OC1=CC=C(Br)C=C1C=O XDVJHPOHMIMNQE-UHFFFAOYSA-N 0.000 description 1
- HNBPYZMAFBJWIB-UHFFFAOYSA-N (4-bromo-2-formylphenyl) 4-chlorobutanoate Chemical compound ClCCCC(=O)OC1=CC=C(Br)C=C1C=O HNBPYZMAFBJWIB-UHFFFAOYSA-N 0.000 description 1
- SLUNNQPMPMQBFK-UHFFFAOYSA-N (4-bromo-2-formylphenyl) 5-chloropentanoate Chemical compound ClCCCCC(=O)OC1=CC=C(Br)C=C1C=O SLUNNQPMPMQBFK-UHFFFAOYSA-N 0.000 description 1
- WKBOFYCEQNKJEW-UHFFFAOYSA-N (4-bromophenyl) 3-chloropropanoate Chemical compound ClCCC(=O)OC1=CC=C(Br)C=C1 WKBOFYCEQNKJEW-UHFFFAOYSA-N 0.000 description 1
- NBYYNONQXADLAB-UHFFFAOYSA-N (4-bromophenyl) 4-chlorobutanoate Chemical compound ClCCCC(=O)OC1=CC=C(Br)C=C1 NBYYNONQXADLAB-UHFFFAOYSA-N 0.000 description 1
- FNBORIYOPDFXSR-UHFFFAOYSA-N (4-bromophenyl) 5-chloropentanoate Chemical compound ClCCCCC(=O)OC1=CC=C(Br)C=C1 FNBORIYOPDFXSR-UHFFFAOYSA-N 0.000 description 1
- AQDPPDLQTFRFCQ-UHFFFAOYSA-N (4-chloro-2,3-dioxobutyl) acetate Chemical compound CC(=O)OCC(=O)C(=O)CCl AQDPPDLQTFRFCQ-UHFFFAOYSA-N 0.000 description 1
- HKQRZYURMVEBBX-UHFFFAOYSA-N (4-ethoxyphenyl) 3-chloropropanoate Chemical compound CCOC1=CC=C(OC(=O)CCCl)C=C1 HKQRZYURMVEBBX-UHFFFAOYSA-N 0.000 description 1
- LONQQTFTUKSRNH-UHFFFAOYSA-N (4-ethoxyphenyl) 4-chlorobutanoate Chemical compound CCOC1=CC=C(OC(=O)CCCCl)C=C1 LONQQTFTUKSRNH-UHFFFAOYSA-N 0.000 description 1
- WZZPRNQSFDFTIS-UHFFFAOYSA-N (4-ethoxyphenyl) 5-chloropentanoate Chemical compound CCOC1=CC=C(OC(=O)CCCCCl)C=C1 WZZPRNQSFDFTIS-UHFFFAOYSA-N 0.000 description 1
- UUBBBGFZXHDWDS-UHFFFAOYSA-N (4-formyl-2,5-dimethylphenyl) 3-chloropropanoate Chemical compound CC1=CC(C=O)=C(C)C=C1OC(=O)CCCl UUBBBGFZXHDWDS-UHFFFAOYSA-N 0.000 description 1
- PUVXHQKKJCUQAA-UHFFFAOYSA-N (4-formyl-2,5-dimethylphenyl) 5-chloropentanoate Chemical compound CC1=CC(C=O)=C(C)C=C1OC(=O)CCCCCl PUVXHQKKJCUQAA-UHFFFAOYSA-N 0.000 description 1
- SHZKKYDASMJIIC-UHFFFAOYSA-N (4-formyl-2-methoxyphenyl) 3-chloropropanoate Chemical compound COC1=CC(C=O)=CC=C1OC(=O)CCCl SHZKKYDASMJIIC-UHFFFAOYSA-N 0.000 description 1
- HVDVYRKWSBHZCU-UHFFFAOYSA-N (4-formyl-2-methoxyphenyl) 4-chlorobutanoate Chemical compound COC1=CC(C=O)=CC=C1OC(=O)CCCCl HVDVYRKWSBHZCU-UHFFFAOYSA-N 0.000 description 1
- DWYDGSBLFNUDIT-UHFFFAOYSA-N (4-formyl-2-methoxyphenyl) 5-chloropentanoate Chemical compound COC1=CC(C=O)=CC=C1OC(=O)CCCCCl DWYDGSBLFNUDIT-UHFFFAOYSA-N 0.000 description 1
- PIMQAJFQUADIDQ-UHFFFAOYSA-N (4-formyl-2-methylphenyl) 3-chloropropanoate Chemical compound CC1=CC(C=O)=CC=C1OC(=O)CCCl PIMQAJFQUADIDQ-UHFFFAOYSA-N 0.000 description 1
- QCPNMYGQZIIGJW-UHFFFAOYSA-N (4-formyl-2-methylphenyl) 5-chloropentanoate Chemical compound CC1=CC(C=O)=CC=C1OC(=O)CCCCCl QCPNMYGQZIIGJW-UHFFFAOYSA-N 0.000 description 1
- PRZIBFKHEPMWAQ-UHFFFAOYSA-N (4-formyl-2-nitrophenyl) 3-chloropropanoate Chemical compound [O-][N+](=O)C1=CC(C=O)=CC=C1OC(=O)CCCl PRZIBFKHEPMWAQ-UHFFFAOYSA-N 0.000 description 1
- UHYGQVMAQAMYED-UHFFFAOYSA-N (4-formyl-2-nitrophenyl) 5-chloropentanoate Chemical compound [O-][N+](=O)C1=CC(C=O)=CC=C1OC(=O)CCCCCl UHYGQVMAQAMYED-UHFFFAOYSA-N 0.000 description 1
- VQPFPCLBOGBYSZ-UHFFFAOYSA-N (4-formylphenyl) 3-chloropropanoate Chemical compound ClCCC(=O)OC1=CC=C(C=O)C=C1 VQPFPCLBOGBYSZ-UHFFFAOYSA-N 0.000 description 1
- NCRIUSUHKQWMRE-UHFFFAOYSA-N (4-formylphenyl) 4-chlorobutanoate Chemical compound ClCCCC(=O)OC1=CC=C(C=O)C=C1 NCRIUSUHKQWMRE-UHFFFAOYSA-N 0.000 description 1
- TVZCEUWAEJCSQB-UHFFFAOYSA-N (4-formylphenyl) 5-chloropentanoate Chemical compound ClCCCCC(=O)OC1=CC=C(C=O)C=C1 TVZCEUWAEJCSQB-UHFFFAOYSA-N 0.000 description 1
- JEGWZIUIJMPGNB-UHFFFAOYSA-N (4-hydroxyphenyl) 3-chloropropanoate Chemical compound OC1=CC=C(OC(=O)CCCl)C=C1 JEGWZIUIJMPGNB-UHFFFAOYSA-N 0.000 description 1
- CJIUVLDHMQGFRQ-UHFFFAOYSA-N (4-hydroxyphenyl) 4-chlorobutanoate Chemical compound OC1=CC=C(OC(=O)CCCCl)C=C1 CJIUVLDHMQGFRQ-UHFFFAOYSA-N 0.000 description 1
- SIUDVMLRWRSEFM-UHFFFAOYSA-N (4-hydroxyphenyl) 5-chloropentanoate Chemical compound OC1=CC=C(OC(=O)CCCCCl)C=C1 SIUDVMLRWRSEFM-UHFFFAOYSA-N 0.000 description 1
- YIDZNXNGEIAZTM-UHFFFAOYSA-N (4-methoxyphenyl) 3-chloropropanoate Chemical compound COC1=CC=C(OC(=O)CCCl)C=C1 YIDZNXNGEIAZTM-UHFFFAOYSA-N 0.000 description 1
- JBOBRZWEFOHJFK-UHFFFAOYSA-N (4-methoxyphenyl) 4-chlorobutanoate Chemical compound COC1=CC=C(OC(=O)CCCCl)C=C1 JBOBRZWEFOHJFK-UHFFFAOYSA-N 0.000 description 1
- KGAVHPXSHLZLNB-UHFFFAOYSA-N (4-methoxyphenyl) 5-chloropentanoate Chemical compound COC1=CC=C(OC(=O)CCCCCl)C=C1 KGAVHPXSHLZLNB-UHFFFAOYSA-N 0.000 description 1
- DNDIFUCPEJYESR-UHFFFAOYSA-N (5-chloro-2,3-dioxopentyl) acetate Chemical compound CC(=O)OCC(=O)C(=O)CCCl DNDIFUCPEJYESR-UHFFFAOYSA-N 0.000 description 1
- PWVWLCUQMWDGKG-UHFFFAOYSA-N (6-chloro-2,3-dioxohexyl) acetate Chemical compound CC(=O)OCC(=O)C(=O)CCCCl PWVWLCUQMWDGKG-UHFFFAOYSA-N 0.000 description 1
- BYEYXCLZDLDVGO-UHFFFAOYSA-N (7-chloro-2,3-dioxoheptyl) acetate Chemical compound CC(=O)OCC(=O)C(=O)CCCCCl BYEYXCLZDLDVGO-UHFFFAOYSA-N 0.000 description 1
- NGULBISQWGMRGK-AATRIKPKSA-N (E)-hex-1-ene-1,2,6-tricarboxylic acid Chemical class C(=O)(O)CCCC/C(/C(=O)O)=C\C(=O)O NGULBISQWGMRGK-AATRIKPKSA-N 0.000 description 1
- VVMPRJKWDFCPGY-UHFFFAOYSA-N 1,1,1,4-tetrachlorobutane-2,3-dione Chemical compound ClCC(=O)C(=O)C(Cl)(Cl)Cl VVMPRJKWDFCPGY-UHFFFAOYSA-N 0.000 description 1
- NBVQBSOYBKANFS-UHFFFAOYSA-N 1,1,1,5-tetrachloropentane-2,3-dione Chemical compound ClCCC(=O)C(=O)C(Cl)(Cl)Cl NBVQBSOYBKANFS-UHFFFAOYSA-N 0.000 description 1
- GLDHOLGKSYUVQQ-UHFFFAOYSA-N 1,1,1,6-tetrachlorohexane-2,3-dione Chemical compound ClCCCC(=O)C(=O)C(Cl)(Cl)Cl GLDHOLGKSYUVQQ-UHFFFAOYSA-N 0.000 description 1
- CXWLSZAPNCADBY-UHFFFAOYSA-N 1,1,1,7-tetrachloroheptane-2,3-dione Chemical compound ClCCCCC(=O)C(=O)C(Cl)(Cl)Cl CXWLSZAPNCADBY-UHFFFAOYSA-N 0.000 description 1
- MYONHZRDCJXWMO-UHFFFAOYSA-N 1,1,1-tribromo-4-chlorobutane-2,3-dione Chemical compound ClCC(=O)C(=O)C(Br)(Br)Br MYONHZRDCJXWMO-UHFFFAOYSA-N 0.000 description 1
- UZZAKUIOOQEJOE-UHFFFAOYSA-N 1,1,1-tribromo-5-chloropentane-2,3-dione Chemical compound ClCCC(=O)C(=O)C(Br)(Br)Br UZZAKUIOOQEJOE-UHFFFAOYSA-N 0.000 description 1
- OMPWUUGTIFRBQV-UHFFFAOYSA-N 1,1,1-tribromo-6-chlorohexane-2,3-dione Chemical compound ClCCCC(=O)C(=O)C(Br)(Br)Br OMPWUUGTIFRBQV-UHFFFAOYSA-N 0.000 description 1
- HRVYWMBFYJJDGO-UHFFFAOYSA-N 1,1,1-tribromo-7-chloroheptane-2,3-dione Chemical compound ClCCCCC(=O)C(=O)C(Br)(Br)Br HRVYWMBFYJJDGO-UHFFFAOYSA-N 0.000 description 1
- ZQAOGJYTPASPOU-UHFFFAOYSA-N 1,1,4-trichlorobutane-2,3-dione Chemical compound ClCC(=O)C(=O)C(Cl)Cl ZQAOGJYTPASPOU-UHFFFAOYSA-N 0.000 description 1
- WUSBKYSYSWOACU-UHFFFAOYSA-N 1,1,5-trichloropentane-2,3-dione Chemical compound ClCCC(=O)C(=O)C(Cl)Cl WUSBKYSYSWOACU-UHFFFAOYSA-N 0.000 description 1
- VJDPPHXPCKXVMX-UHFFFAOYSA-N 1,1,6-trichlorohexane-2,3-dione Chemical compound ClCCCC(=O)C(=O)C(Cl)Cl VJDPPHXPCKXVMX-UHFFFAOYSA-N 0.000 description 1
- GRIRIQSGLAOPQI-UHFFFAOYSA-N 1,1,7-trichloroheptane-2,3-dione Chemical compound ClCCCCC(=O)C(=O)C(Cl)Cl GRIRIQSGLAOPQI-UHFFFAOYSA-N 0.000 description 1
- QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 description 1
- MYWOJODOMFBVCB-UHFFFAOYSA-N 1,2,6-trimethylphenanthrene Chemical compound CC1=CC=C2C3=CC(C)=CC=C3C=CC2=C1C MYWOJODOMFBVCB-UHFFFAOYSA-N 0.000 description 1
- VDYWHVQKENANGY-UHFFFAOYSA-N 1,3-Butyleneglycol dimethacrylate Chemical compound CC(=C)C(=O)OC(C)CCOC(=O)C(C)=C VDYWHVQKENANGY-UHFFFAOYSA-N 0.000 description 1
- TUBQDCKAWGHZPF-UHFFFAOYSA-N 1,3-benzothiazol-2-ylsulfanylmethyl thiocyanate Chemical compound C1=CC=C2SC(SCSC#N)=NC2=C1 TUBQDCKAWGHZPF-UHFFFAOYSA-N 0.000 description 1
- OHJTUHYSPQZBDY-UHFFFAOYSA-N 1,4-dichlorobutane-2,3-dione Chemical compound ClCC(=O)C(=O)CCl OHJTUHYSPQZBDY-UHFFFAOYSA-N 0.000 description 1
- LCNPOYCRKPEWDH-UHFFFAOYSA-N 1,4-dimethoxycyclohexa-2,4-dien-1-ol Chemical compound COC1=CCC(O)(OC)C=C1 LCNPOYCRKPEWDH-UHFFFAOYSA-N 0.000 description 1
- WXAKZHHTJHCTPK-UHFFFAOYSA-N 1,5-dichloropentane-2,3-dione Chemical compound ClCCC(=O)C(=O)CCl WXAKZHHTJHCTPK-UHFFFAOYSA-N 0.000 description 1
- KAEWZDJLVGCGKF-UHFFFAOYSA-N 1,6-dichlorohexane-2,3-dione Chemical compound ClCCCC(=O)C(=O)CCl KAEWZDJLVGCGKF-UHFFFAOYSA-N 0.000 description 1
- GRBLYDSIVYOUCQ-UHFFFAOYSA-N 1-(2-bromo-4,5-dimethoxyphenyl)-4-chlorobutane-2,3-dione Chemical compound COC1=CC(Br)=C(CC(=O)C(=O)CCl)C=C1OC GRBLYDSIVYOUCQ-UHFFFAOYSA-N 0.000 description 1
- UCSWCKRDCKSPMS-UHFFFAOYSA-N 1-(2-bromo-4,5-dimethoxyphenyl)-5-chloropentane-2,3-dione Chemical compound COC1=CC(Br)=C(CC(=O)C(=O)CCCl)C=C1OC UCSWCKRDCKSPMS-UHFFFAOYSA-N 0.000 description 1
- BBLLCUPKUMYWMK-UHFFFAOYSA-N 1-(2-bromo-4,5-dimethoxyphenyl)-6-chlorohexane-2,3-dione Chemical compound COC1=CC(Br)=C(CC(=O)C(=O)CCCCl)C=C1OC BBLLCUPKUMYWMK-UHFFFAOYSA-N 0.000 description 1
- DILHKKLRPACQRT-UHFFFAOYSA-N 1-(2-bromophenyl)-4-chlorobutane-2,3-dione Chemical compound ClCC(=O)C(=O)CC1=CC=CC=C1Br DILHKKLRPACQRT-UHFFFAOYSA-N 0.000 description 1
- JXEKIVRBFBAWBC-UHFFFAOYSA-N 1-(2-bromophenyl)-5-chloropentane-2,3-dione Chemical compound ClCCC(=O)C(=O)CC1=CC=CC=C1Br JXEKIVRBFBAWBC-UHFFFAOYSA-N 0.000 description 1
- XZVOERLWSLWTJO-UHFFFAOYSA-N 1-(2-bromophenyl)-6-chlorohexane-2,3-dione Chemical compound ClCCCC(=O)C(=O)CC1=CC=CC=C1Br XZVOERLWSLWTJO-UHFFFAOYSA-N 0.000 description 1
- CABPTXFNFCPXAK-UHFFFAOYSA-N 1-(2-bromophenyl)-7-chloroheptane-2,3-dione Chemical compound ClCCCCC(=O)C(=O)CC1=CC=CC=C1Br CABPTXFNFCPXAK-UHFFFAOYSA-N 0.000 description 1
- XOILGBPDXMVFIP-UHFFFAOYSA-N 1-(diiodomethylsulfonyl)-4-methylbenzene Chemical compound CC1=CC=C(S(=O)(=O)C(I)I)C=C1 XOILGBPDXMVFIP-UHFFFAOYSA-N 0.000 description 1
- ZDQNWDNMNKSMHI-UHFFFAOYSA-N 1-[2-(2-prop-2-enoyloxypropoxy)propoxy]propan-2-yl prop-2-enoate Chemical compound C=CC(=O)OC(C)COC(C)COCC(C)OC(=O)C=C ZDQNWDNMNKSMHI-UHFFFAOYSA-N 0.000 description 1
- ZULMJJCZPOPPGF-UHFFFAOYSA-N 1-bromo-4-chlorobutane-2,3-dione Chemical compound ClCC(=O)C(=O)CBr ZULMJJCZPOPPGF-UHFFFAOYSA-N 0.000 description 1
- PTUIQPDFBFVNJB-UHFFFAOYSA-N 1-bromo-5-chloropentane-2,3-dione Chemical compound ClCCC(=O)C(=O)CBr PTUIQPDFBFVNJB-UHFFFAOYSA-N 0.000 description 1
- MQAGYJHNSGVONY-UHFFFAOYSA-N 1-bromo-6-chlorohexane-2,3-dione Chemical compound ClCCCC(=O)C(=O)CBr MQAGYJHNSGVONY-UHFFFAOYSA-N 0.000 description 1
- WKEXQQFYWDNHKC-UHFFFAOYSA-N 1-bromo-7-chloroheptane-2,3-dione Chemical compound ClCCCCC(=O)C(=O)CBr WKEXQQFYWDNHKC-UHFFFAOYSA-N 0.000 description 1
- MKVJZNVNFCFXPM-UHFFFAOYSA-N 1-chloro-4,4-dimethylpentane-2,3-dione Chemical compound CC(C)(C)C(=O)C(=O)CCl MKVJZNVNFCFXPM-UHFFFAOYSA-N 0.000 description 1
- ZEXFJYKPRHFUIS-UHFFFAOYSA-N 1-chloro-4-(2,4,5-trichlorophenoxy)butane-2,3-dione Chemical compound ClCC(=O)C(=O)COC1=CC(Cl)=C(Cl)C=C1Cl ZEXFJYKPRHFUIS-UHFFFAOYSA-N 0.000 description 1
- KBGJMDOMXSTYIO-UHFFFAOYSA-N 1-chloro-4-(2,5-dimethoxyphenyl)butane-2,3-dione Chemical compound COC1=CC=C(OC)C(CC(=O)C(=O)CCl)=C1 KBGJMDOMXSTYIO-UHFFFAOYSA-N 0.000 description 1
- ZZUDTHXEXRJOIR-UHFFFAOYSA-N 1-chloro-4-(3,4-dimethoxyphenyl)butane-2,3-dione Chemical compound COC1=CC=C(CC(=O)C(=O)CCl)C=C1OC ZZUDTHXEXRJOIR-UHFFFAOYSA-N 0.000 description 1
- MWLLVYLCYTXIFD-UHFFFAOYSA-N 1-chloro-4-(4-chlorophenyl)butane-2,3-dione Chemical compound ClCC(=O)C(=O)CC1=CC=C(Cl)C=C1 MWLLVYLCYTXIFD-UHFFFAOYSA-N 0.000 description 1
- LXVLRZKNRTXPLH-UHFFFAOYSA-N 1-chloro-4-(4-fluorophenoxy)butane-2,3-dione Chemical compound FC1=CC=C(OCC(=O)C(=O)CCl)C=C1 LXVLRZKNRTXPLH-UHFFFAOYSA-N 0.000 description 1
- XTYJOYUKAVSARJ-UHFFFAOYSA-N 1-chloro-4-(4-fluorophenyl)butane-2,3-dione Chemical compound FC1=CC=C(CC(=O)C(=O)CCl)C=C1 XTYJOYUKAVSARJ-UHFFFAOYSA-N 0.000 description 1
- DGBWEEMXXWDAJS-UHFFFAOYSA-N 1-chloro-4-cyclopentylbutane-2,3-dione Chemical compound ClCC(=O)C(=O)CC1CCCC1 DGBWEEMXXWDAJS-UHFFFAOYSA-N 0.000 description 1
- SVGGIOCROPHCAY-UHFFFAOYSA-N 1-chloro-4-methoxybutane-2,3-dione Chemical compound COCC(=O)C(=O)CCl SVGGIOCROPHCAY-UHFFFAOYSA-N 0.000 description 1
- NATFDEMDTDGKQS-UHFFFAOYSA-N 1-chloro-4-phenoxybutane-2,3-dione Chemical compound ClCC(=O)C(=O)COC1=CC=CC=C1 NATFDEMDTDGKQS-UHFFFAOYSA-N 0.000 description 1
- QXBHJBFUGZSJBT-UHFFFAOYSA-N 1-chloro-4-phenylbutane-2,3-dione Chemical compound ClCC(=O)C(=O)CC1=CC=CC=C1 QXBHJBFUGZSJBT-UHFFFAOYSA-N 0.000 description 1
- FICCTWBRADGBME-UHFFFAOYSA-N 1-chloro-4-phenylmethoxybutane-2,3-dione Chemical compound ClCC(=O)C(=O)COCC1=CC=CC=C1 FICCTWBRADGBME-UHFFFAOYSA-N 0.000 description 1
- BHKKEWYLGBPLGN-UHFFFAOYSA-N 1-chloro-5,5-dimethylhexane-3,4-dione Chemical compound CC(C)(C)C(=O)C(=O)CCCl BHKKEWYLGBPLGN-UHFFFAOYSA-N 0.000 description 1
- QYAYWFHHRPNPDU-UHFFFAOYSA-N 1-chloro-6,6-dimethylheptane-3,4-dione Chemical compound CC(C)(C)CC(=O)C(=O)CCCl QYAYWFHHRPNPDU-UHFFFAOYSA-N 0.000 description 1
- QCQWAFSQGWGHCM-UHFFFAOYSA-N 1-chloro-7,7-dimethyloctane-4,5-dione Chemical compound CC(C)(C)CC(=O)C(=O)CCCCl QCQWAFSQGWGHCM-UHFFFAOYSA-N 0.000 description 1
- LGJCFVYMIJLQJO-UHFFFAOYSA-N 1-dodecylperoxydodecane Chemical compound CCCCCCCCCCCCOOCCCCCCCCCCCC LGJCFVYMIJLQJO-UHFFFAOYSA-N 0.000 description 1
- ITUNZCVRYICLQM-UHFFFAOYSA-N 1-ethenyl-1,2,4-triazole Chemical compound C=CN1C=NC=N1 ITUNZCVRYICLQM-UHFFFAOYSA-N 0.000 description 1
- JWYVGKFDLWWQJX-UHFFFAOYSA-N 1-ethenylazepan-2-one Chemical compound C=CN1CCCCCC1=O JWYVGKFDLWWQJX-UHFFFAOYSA-N 0.000 description 1
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 description 1
- LEWNYOKWUAYXPI-UHFFFAOYSA-N 1-ethenylpiperidine Chemical compound C=CN1CCCCC1 LEWNYOKWUAYXPI-UHFFFAOYSA-N 0.000 description 1
- PZNPLUBHRSSFHT-RRHRGVEJSA-N 1-hexadecanoyl-2-octadecanoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCCCC(=O)O[C@@H](COP([O-])(=O)OCC[N+](C)(C)C)COC(=O)CCCCCCCCCCCCCCC PZNPLUBHRSSFHT-RRHRGVEJSA-N 0.000 description 1
- PUAGYGYUGZRRSQ-KTKRTIGZSA-N 1-o-ethyl 4-o-(2-oxo-2-triethylsilyloxyethyl) (z)-but-2-enedioate Chemical compound CCOC(=O)\C=C/C(=O)OCC(=O)O[Si](CC)(CC)CC PUAGYGYUGZRRSQ-KTKRTIGZSA-N 0.000 description 1
- GRZGONNNNBHJOJ-MDZDMXLPSA-N 1-o-ethyl 4-o-(3-oxo-3-triethylsilyloxypropyl) (e)-but-2-enedioate Chemical compound CCOC(=O)\C=C\C(=O)OCCC(=O)O[Si](CC)(CC)CC GRZGONNNNBHJOJ-MDZDMXLPSA-N 0.000 description 1
- GRZGONNNNBHJOJ-KTKRTIGZSA-N 1-o-ethyl 4-o-(3-oxo-3-triethylsilyloxypropyl) (z)-but-2-enedioate Chemical compound CCOC(=O)\C=C/C(=O)OCCC(=O)O[Si](CC)(CC)CC GRZGONNNNBHJOJ-KTKRTIGZSA-N 0.000 description 1
- FMDGCGNNHAEJJP-QXMHVHEDSA-N 1-o-ethyl 4-o-(4-oxo-4-triethylsilyloxybutyl) (z)-but-2-enedioate Chemical compound CCOC(=O)\C=C/C(=O)OCCCC(=O)O[Si](CC)(CC)CC FMDGCGNNHAEJJP-QXMHVHEDSA-N 0.000 description 1
- AIPTUSVBCAQPJY-SEYXRHQNSA-N 1-o-ethyl 4-o-(5-oxo-5-triethylsilyloxypentyl) (z)-but-2-enedioate Chemical compound CCOC(=O)\C=C/C(=O)OCCCCC(=O)O[Si](CC)(CC)CC AIPTUSVBCAQPJY-SEYXRHQNSA-N 0.000 description 1
- CTGZQEPLEKEFPM-CMDGGOBGSA-N 1-o-ethyl 4-o-[3-oxo-3-(2-phenylacetyl)oxypropyl] (e)-but-2-enedioate Chemical compound CCOC(=O)\C=C\C(=O)OCCC(=O)OC(=O)CC1=CC=CC=C1 CTGZQEPLEKEFPM-CMDGGOBGSA-N 0.000 description 1
- WAXBWNWMNNCMLH-KHPPLWFESA-N 1-o-ethyl 4-o-[3-oxo-3-(3-phenylpropanoyloxy)propyl] (z)-but-2-enedioate Chemical compound CCOC(=O)\C=C/C(=O)OCCC(=O)OC(=O)CCC1=CC=CC=C1 WAXBWNWMNNCMLH-KHPPLWFESA-N 0.000 description 1
- FAQPWLGCKDICQM-VOTSOKGWSA-N 1-o-ethyl 4-o-[4-(2-methoxyacetyl)oxy-4-oxobutyl] (e)-but-2-enedioate Chemical compound CCOC(=O)\C=C\C(=O)OCCCC(=O)OC(=O)COC FAQPWLGCKDICQM-VOTSOKGWSA-N 0.000 description 1
- SQBJTVSAXGXOCQ-ZHACJKMWSA-N 1-o-ethyl 4-o-[4-oxo-4-(2-phenylacetyl)oxybutyl] (e)-but-2-enedioate Chemical compound CCOC(=O)\C=C\C(=O)OCCCC(=O)OC(=O)CC1=CC=CC=C1 SQBJTVSAXGXOCQ-ZHACJKMWSA-N 0.000 description 1
- AZEKSFNJZOVNRW-WAYWQWQTSA-N 1-o-methyl 4-o-(2-oxo-2-trimethylsilyloxyethyl) (z)-but-2-enedioate Chemical compound COC(=O)\C=C/C(=O)OCC(=O)O[Si](C)(C)C AZEKSFNJZOVNRW-WAYWQWQTSA-N 0.000 description 1
- YQIKLFCMJFIBCM-AATRIKPKSA-N 1-o-methyl 4-o-(3-oxo-3-trimethylsilyloxypropyl) (e)-but-2-enedioate Chemical compound COC(=O)\C=C\C(=O)OCCC(=O)O[Si](C)(C)C YQIKLFCMJFIBCM-AATRIKPKSA-N 0.000 description 1
- YQIKLFCMJFIBCM-WAYWQWQTSA-N 1-o-methyl 4-o-(3-oxo-3-trimethylsilyloxypropyl) (z)-but-2-enedioate Chemical compound COC(=O)\C=C/C(=O)OCCC(=O)O[Si](C)(C)C YQIKLFCMJFIBCM-WAYWQWQTSA-N 0.000 description 1
- BREWXYAJERIFFT-FPLPWBNLSA-N 1-o-methyl 4-o-(4-oxo-4-trimethylsilyloxybutyl) (z)-but-2-enedioate Chemical compound COC(=O)\C=C/C(=O)OCCCC(=O)O[Si](C)(C)C BREWXYAJERIFFT-FPLPWBNLSA-N 0.000 description 1
- IUSOFPCDAOTTQD-HJWRWDBZSA-N 1-o-methyl 4-o-(5-oxo-5-trimethylsilyloxypentyl) (z)-but-2-enedioate Chemical compound COC(=O)\C=C/C(=O)OCCCCC(=O)O[Si](C)(C)C IUSOFPCDAOTTQD-HJWRWDBZSA-N 0.000 description 1
- IHCMGNIZNVTZGZ-BQYQJAHWSA-N 1-o-methyl 4-o-[2-oxo-2-(2-phenylacetyl)oxyethyl] (e)-but-2-enedioate Chemical compound COC(=O)\C=C\C(=O)OCC(=O)OC(=O)CC1=CC=CC=C1 IHCMGNIZNVTZGZ-BQYQJAHWSA-N 0.000 description 1
- IHCMGNIZNVTZGZ-FPLPWBNLSA-N 1-o-methyl 4-o-[2-oxo-2-(2-phenylacetyl)oxyethyl] (z)-but-2-enedioate Chemical compound COC(=O)\C=C/C(=O)OCC(=O)OC(=O)CC1=CC=CC=C1 IHCMGNIZNVTZGZ-FPLPWBNLSA-N 0.000 description 1
- VIKYUWIIJVURNN-BQYQJAHWSA-N 1-o-methyl 4-o-[3-oxo-3-(2-phenylacetyl)oxypropyl] (e)-but-2-enedioate Chemical compound COC(=O)\C=C\C(=O)OCCC(=O)OC(=O)CC1=CC=CC=C1 VIKYUWIIJVURNN-BQYQJAHWSA-N 0.000 description 1
- VIKYUWIIJVURNN-FPLPWBNLSA-N 1-o-methyl 4-o-[3-oxo-3-(2-phenylacetyl)oxypropyl] (z)-but-2-enedioate Chemical compound COC(=O)\C=C/C(=O)OCCC(=O)OC(=O)CC1=CC=CC=C1 VIKYUWIIJVURNN-FPLPWBNLSA-N 0.000 description 1
- NMRHUEJMHGMKTH-KTKRTIGZSA-N 1-o-methyl 4-o-[4-oxo-4-(2-phenylacetyl)oxybutyl] (z)-but-2-enedioate Chemical compound COC(=O)\C=C/C(=O)OCCCC(=O)OC(=O)CC1=CC=CC=C1 NMRHUEJMHGMKTH-KTKRTIGZSA-N 0.000 description 1
- MHNFGYOLCDLJOL-KHPPLWFESA-N 1-o-methyl 4-o-[5-oxo-5-(2-phenylacetyl)oxypentyl] (z)-but-2-enedioate Chemical compound COC(=O)\C=C/C(=O)OCCCCC(=O)OC(=O)CC1=CC=CC=C1 MHNFGYOLCDLJOL-KHPPLWFESA-N 0.000 description 1
- VOBUAPTXJKMNCT-UHFFFAOYSA-N 1-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound CCCCCC(OC(=O)C=C)OC(=O)C=C VOBUAPTXJKMNCT-UHFFFAOYSA-N 0.000 description 1
- RDBMNMVDVKRYKW-UHFFFAOYSA-N 2,2,2-tribromoacetyl chloride Chemical compound ClC(=O)C(Br)(Br)Br RDBMNMVDVKRYKW-UHFFFAOYSA-N 0.000 description 1
- UOZBNMMELVBICG-UHFFFAOYSA-N 2,2,2-triphenylacetyl chloride Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(C(=O)Cl)C1=CC=CC=C1 UOZBNMMELVBICG-UHFFFAOYSA-N 0.000 description 1
- JVSFQJZRHXAUGT-UHFFFAOYSA-N 2,2-dimethylpropanoyl chloride Chemical compound CC(C)(C)C(Cl)=O JVSFQJZRHXAUGT-UHFFFAOYSA-N 0.000 description 1
- MSYLETHDEIJMAF-UHFFFAOYSA-N 2,2-diphenylacetyl chloride Chemical compound C=1C=CC=CC=1C(C(=O)Cl)C1=CC=CC=C1 MSYLETHDEIJMAF-UHFFFAOYSA-N 0.000 description 1
- IXWOUPGDGMCKGT-UHFFFAOYSA-N 2,3-dihydroxybenzaldehyde Chemical compound OC1=CC=CC(C=O)=C1O IXWOUPGDGMCKGT-UHFFFAOYSA-N 0.000 description 1
- LINPIYWFGCPVIE-UHFFFAOYSA-N 2,4,6-trichlorophenol Chemical compound OC1=C(Cl)C=C(Cl)C=C1Cl LINPIYWFGCPVIE-UHFFFAOYSA-N 0.000 description 1
- MQSIWVCWTVYFDP-UHFFFAOYSA-N 2,4-dibromo-6-chlorophenol Chemical compound OC1=C(Cl)C=C(Br)C=C1Br MQSIWVCWTVYFDP-UHFFFAOYSA-N 0.000 description 1
- KTKJDGDFMSJUQQ-UHFFFAOYSA-N 2,4-dibutyl-6-(5-chlorobenzotriazol-2-yl)phenol Chemical compound CCCCC1=CC(CCCC)=C(O)C(N2N=C3C=C(Cl)C=CC3=N2)=C1 KTKJDGDFMSJUQQ-UHFFFAOYSA-N 0.000 description 1
- UMDKVOOEGYNMEB-UHFFFAOYSA-N 2,4-dichloro-6-iodophenol Chemical compound OC1=C(Cl)C=C(Cl)C=C1I UMDKVOOEGYNMEB-UHFFFAOYSA-N 0.000 description 1
- VQMRYJZWLGXFLR-UHFFFAOYSA-N 2,5-dimethoxybenzene-1,3-diol Chemical compound COC1=CC(O)=C(OC)C(O)=C1 VQMRYJZWLGXFLR-UHFFFAOYSA-N 0.000 description 1
- UWNADWZGEHDQAB-UHFFFAOYSA-N 2,5-dimethylhexane Chemical group CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 1
- AZFAIOQVEYTPKD-UHFFFAOYSA-N 2-(2,4,5-trichlorophenoxy)acetyl chloride Chemical compound ClC(=O)COC1=CC(Cl)=C(Cl)C=C1Cl AZFAIOQVEYTPKD-UHFFFAOYSA-N 0.000 description 1
- RAPIPBRHRYSAHQ-UHFFFAOYSA-N 2-(2,5-dimethoxyphenyl)acetyl chloride Chemical compound COC1=CC=C(OC)C(CC(Cl)=O)=C1 RAPIPBRHRYSAHQ-UHFFFAOYSA-N 0.000 description 1
- VAFRAGGSHGIDGS-UHFFFAOYSA-N 2-(2-bromo-4,5-dimethoxyphenyl)acetyl chloride Chemical compound COC1=CC(Br)=C(CC(Cl)=O)C=C1OC VAFRAGGSHGIDGS-UHFFFAOYSA-N 0.000 description 1
- RFPBUXOVSZEMSW-UHFFFAOYSA-N 2-(2-bromophenyl)acetyl chloride Chemical compound ClC(=O)CC1=CC=CC=C1Br RFPBUXOVSZEMSW-UHFFFAOYSA-N 0.000 description 1
- AVTLBBWTUPQRAY-UHFFFAOYSA-N 2-(2-cyanobutan-2-yldiazenyl)-2-methylbutanenitrile Chemical compound CCC(C)(C#N)N=NC(C)(CC)C#N AVTLBBWTUPQRAY-UHFFFAOYSA-N 0.000 description 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 1
- PTDJGJIYBSUQLM-UHFFFAOYSA-N 2-(2-methylpropoxy)ethyl 2-methylprop-2-enoate Chemical compound CC(C)COCCOC(=O)C(C)=C PTDJGJIYBSUQLM-UHFFFAOYSA-N 0.000 description 1
- BHNHCQUVVRPWPB-UHFFFAOYSA-N 2-(2-methylpropoxy)ethyl prop-2-enoate Chemical compound CC(C)COCCOC(=O)C=C BHNHCQUVVRPWPB-UHFFFAOYSA-N 0.000 description 1
- QBJIMTPENIGDOG-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)acetyl chloride Chemical compound COC1=CC=C(CC(Cl)=O)C=C1OC QBJIMTPENIGDOG-UHFFFAOYSA-N 0.000 description 1
- MVPWJPAZDHEKQN-UHFFFAOYSA-N 2-(4-bromophenyl)-2-chloroacetic acid Chemical compound OC(=O)C(Cl)C1=CC=C(Br)C=C1 MVPWJPAZDHEKQN-UHFFFAOYSA-N 0.000 description 1
- UMQUIRYNOVNYPA-UHFFFAOYSA-N 2-(4-chlorophenyl)acetyl chloride Chemical compound ClC(=O)CC1=CC=C(Cl)C=C1 UMQUIRYNOVNYPA-UHFFFAOYSA-N 0.000 description 1
- VNOMNADZORCTGC-UHFFFAOYSA-N 2-(4-fluorophenoxy)acetyl chloride Chemical compound FC1=CC=C(OCC(Cl)=O)C=C1 VNOMNADZORCTGC-UHFFFAOYSA-N 0.000 description 1
- SIOJFYRPBYGHOO-UHFFFAOYSA-N 2-(4-fluorophenyl)acetyl chloride Chemical compound FC1=CC=C(CC(Cl)=O)C=C1 SIOJFYRPBYGHOO-UHFFFAOYSA-N 0.000 description 1
- FLKHVLRENDBIDB-UHFFFAOYSA-N 2-(butylcarbamoyloxy)ethyl prop-2-enoate Chemical compound CCCCNC(=O)OCCOC(=O)C=C FLKHVLRENDBIDB-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- FDSUVTROAWLVJA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OCC(CO)(CO)COCC(CO)(CO)CO FDSUVTROAWLVJA-UHFFFAOYSA-N 0.000 description 1
- NCDBYAPSWOPDRN-UHFFFAOYSA-N 2-[dichloro(fluoro)methyl]sulfanylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)F)C(=O)C2=C1 NCDBYAPSWOPDRN-UHFFFAOYSA-N 0.000 description 1
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
- KWIPUXXIFQQMKN-UHFFFAOYSA-N 2-azaniumyl-3-(4-cyanophenyl)propanoate Chemical compound OC(=O)C(N)CC1=CC=C(C#N)C=C1 KWIPUXXIFQQMKN-UHFFFAOYSA-N 0.000 description 1
- SYZRZLUNWVNNNV-UHFFFAOYSA-N 2-bromoacetyl chloride Chemical compound ClC(=O)CBr SYZRZLUNWVNNNV-UHFFFAOYSA-N 0.000 description 1
- DJKKWVGWYCKUFC-UHFFFAOYSA-N 2-butoxyethyl 2-methylprop-2-enoate Chemical compound CCCCOCCOC(=O)C(C)=C DJKKWVGWYCKUFC-UHFFFAOYSA-N 0.000 description 1
- PTJDGKYFJYEAOK-UHFFFAOYSA-N 2-butoxyethyl prop-2-enoate Chemical compound CCCCOCCOC(=O)C=C PTJDGKYFJYEAOK-UHFFFAOYSA-N 0.000 description 1
- YAUCKEPYKXHCFF-UHFFFAOYSA-N 2-carbamothioylsulfanylethyl carbamodithioate;manganese Chemical compound [Mn].NC(=S)SCCSC(N)=S YAUCKEPYKXHCFF-UHFFFAOYSA-N 0.000 description 1
- FWEDGEVOINBOOZ-UHFFFAOYSA-N 2-chloro-2-(2,4,6-trichlorophenyl)acetic acid Chemical compound OC(C(C(C(Cl)=CC(Cl)=C1)=C1Cl)Cl)=O FWEDGEVOINBOOZ-UHFFFAOYSA-N 0.000 description 1
- ACBUXEHGBMMHRR-UHFFFAOYSA-N 2-chloro-2-(2-methoxyphenyl)acetic acid Chemical compound COC1=CC=CC=C1C(Cl)C(O)=O ACBUXEHGBMMHRR-UHFFFAOYSA-N 0.000 description 1
- MEQYRPOUEGMLOV-UHFFFAOYSA-N 2-chloro-2-(3-hydroxyphenyl)acetic acid Chemical compound ClC(C(=O)O)C1=CC=CC(=C1)O MEQYRPOUEGMLOV-UHFFFAOYSA-N 0.000 description 1
- PKEYFIKVMQUYSM-UHFFFAOYSA-N 2-chloro-2-(4-ethoxyphenyl)acetic acid Chemical compound CCOC1=CC=C(C(Cl)C(O)=O)C=C1 PKEYFIKVMQUYSM-UHFFFAOYSA-N 0.000 description 1
- MLTHQBJVZAHFFC-UHFFFAOYSA-N 2-chloro-2-(4-hydroxyphenyl)acetic acid Chemical compound OC(=O)C(Cl)C1=CC=C(O)C=C1 MLTHQBJVZAHFFC-UHFFFAOYSA-N 0.000 description 1
- UTNSTTZHNMPBEE-UHFFFAOYSA-N 2-chloro-2-hydroxy-2-phenylacetic acid Chemical compound OC(=O)C(O)(Cl)C1=CC=CC=C1 UTNSTTZHNMPBEE-UHFFFAOYSA-N 0.000 description 1
- ZMOMCILMBYEGLD-UHFFFAOYSA-N 2-chloro-4-hydroxybenzaldehyde Chemical compound OC1=CC=C(C=O)C(Cl)=C1 ZMOMCILMBYEGLD-UHFFFAOYSA-N 0.000 description 1
- KULSVCANYQIOFD-UHFFFAOYSA-N 2-chloro-5-methoxyphenol Chemical compound COC1=CC=C(Cl)C(O)=C1 KULSVCANYQIOFD-UHFFFAOYSA-N 0.000 description 1
- NILLIUYSJFTTRH-UHFFFAOYSA-N 2-cyclopentylacetyl chloride Chemical compound ClC(=O)CC1CCCC1 NILLIUYSJFTTRH-UHFFFAOYSA-N 0.000 description 1
- WHKKNVAGWPTSRS-UHFFFAOYSA-N 2-dodecylnaphthalene-1-sulfonic acid Chemical class C1=CC=CC2=C(S(O)(=O)=O)C(CCCCCCCCCCCC)=CC=C21 WHKKNVAGWPTSRS-UHFFFAOYSA-N 0.000 description 1
- KKBHSBATGOQADJ-UHFFFAOYSA-N 2-ethenyl-1,3-dioxolane Chemical compound C=CC1OCCO1 KKBHSBATGOQADJ-UHFFFAOYSA-N 0.000 description 1
- FWWXYLGCHHIKNY-UHFFFAOYSA-N 2-ethoxyethyl prop-2-enoate Chemical compound CCOCCOC(=O)C=C FWWXYLGCHHIKNY-UHFFFAOYSA-N 0.000 description 1
- ACBOBKJKSFYJML-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;2-sulfanylpropanoic acid Chemical compound CC(S)C(O)=O.CC(S)C(O)=O.CC(S)C(O)=O.CCC(CO)(CO)CO ACBOBKJKSFYJML-UHFFFAOYSA-N 0.000 description 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 1
- WQUZBERVMUEJTD-UHFFFAOYSA-N 2-hydroxy-5-(trifluoromethoxy)benzaldehyde Chemical compound OC1=CC=C(OC(F)(F)F)C=C1C=O WQUZBERVMUEJTD-UHFFFAOYSA-N 0.000 description 1
- DRIGZYJEJBTAII-UHFFFAOYSA-N 2-hydroxyethyl 2-methylprop-2-enoate;2-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCO.CC(O)COC(=O)C(C)=C DRIGZYJEJBTAII-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- GWZMWHWAWHPNHN-UHFFFAOYSA-N 2-hydroxypropyl prop-2-enoate Chemical compound CC(O)COC(=O)C=C GWZMWHWAWHPNHN-UHFFFAOYSA-N 0.000 description 1
- JJKWHOSQTYYFAE-UHFFFAOYSA-N 2-methoxyacetyl chloride Chemical compound COCC(Cl)=O JJKWHOSQTYYFAE-UHFFFAOYSA-N 0.000 description 1
- YXYJVFYWCLAXHO-UHFFFAOYSA-N 2-methoxyethyl 2-methylprop-2-enoate Chemical compound COCCOC(=O)C(C)=C YXYJVFYWCLAXHO-UHFFFAOYSA-N 0.000 description 1
- HFCUBKYHMMPGBY-UHFFFAOYSA-N 2-methoxyethyl prop-2-enoate Chemical compound COCCOC(=O)C=C HFCUBKYHMMPGBY-UHFFFAOYSA-N 0.000 description 1
- IFXDUNDBQDXPQZ-UHFFFAOYSA-N 2-methylbutan-2-yl 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)CC IFXDUNDBQDXPQZ-UHFFFAOYSA-N 0.000 description 1
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
- GIPHORSWWWLUQX-UHFFFAOYSA-N 2-oxo-3-phenoxypropanoyl chloride Chemical compound ClC(=O)C(=O)COC1=CC=CC=C1 GIPHORSWWWLUQX-UHFFFAOYSA-N 0.000 description 1
- CEXQWAAGPPNOQF-UHFFFAOYSA-N 2-phenoxyethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOC1=CC=CC=C1 CEXQWAAGPPNOQF-UHFFFAOYSA-N 0.000 description 1
- RZVINYQDSSQUKO-UHFFFAOYSA-N 2-phenoxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC1=CC=CC=C1 RZVINYQDSSQUKO-UHFFFAOYSA-N 0.000 description 1
- VMZCDNSFRSVYKQ-UHFFFAOYSA-N 2-phenylacetyl chloride Chemical compound ClC(=O)CC1=CC=CC=C1 VMZCDNSFRSVYKQ-UHFFFAOYSA-N 0.000 description 1
- QISAUDWTBBNJIR-UHFFFAOYSA-N 2-phenylmethoxyacetyl chloride Chemical compound ClC(=O)COCC1=CC=CC=C1 QISAUDWTBBNJIR-UHFFFAOYSA-N 0.000 description 1
- NSIWGZFZGMIPEC-UHFFFAOYSA-N 2-propoxyethyl 2-methylprop-2-enoate Chemical compound CCCOCCOC(=O)C(C)=C NSIWGZFZGMIPEC-UHFFFAOYSA-N 0.000 description 1
- ACHWNFGWACZQHU-UHFFFAOYSA-N 2-propoxyethyl prop-2-enoate Chemical compound CCCOCCOC(=O)C=C ACHWNFGWACZQHU-UHFFFAOYSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- BUTKIHRNYUEGKB-UHFFFAOYSA-N 3,3-dimethylbutanoyl chloride Chemical compound CC(C)(C)CC(Cl)=O BUTKIHRNYUEGKB-UHFFFAOYSA-N 0.000 description 1
- FIXKCCRANLATRP-UHFFFAOYSA-N 3,5,5-trimethylhexyl prop-2-enoate Chemical compound CC(C)(C)CC(C)CCOC(=O)C=C FIXKCCRANLATRP-UHFFFAOYSA-N 0.000 description 1
- JHZOXYGFQMROFJ-UHFFFAOYSA-N 3,5-dibromo-2-hydroxybenzaldehyde Chemical compound OC1=C(Br)C=C(Br)C=C1C=O JHZOXYGFQMROFJ-UHFFFAOYSA-N 0.000 description 1
- YLMYXAAUQOWAOK-UHFFFAOYSA-N 3,5-diethoxyphenol Chemical compound CCOC1=CC(O)=CC(OCC)=C1 YLMYXAAUQOWAOK-UHFFFAOYSA-N 0.000 description 1
- ASVKKRLMJCWVQF-UHFFFAOYSA-N 3-buten-1-amine Chemical compound NCCC=C ASVKKRLMJCWVQF-UHFFFAOYSA-N 0.000 description 1
- OFQBYHLLIJGMNP-UHFFFAOYSA-N 3-ethoxy-2-hydroxybenzaldehyde Chemical compound CCOC1=CC=CC(C=O)=C1O OFQBYHLLIJGMNP-UHFFFAOYSA-N 0.000 description 1
- QKOGQKOMPJPHIZ-UHFFFAOYSA-N 3-ethoxypropyl 2-methylprop-2-enoate Chemical compound CCOCCCOC(=O)C(C)=C QKOGQKOMPJPHIZ-UHFFFAOYSA-N 0.000 description 1
- UACBZRBYLSMNGV-UHFFFAOYSA-N 3-ethoxypropyl prop-2-enoate Chemical compound CCOCCCOC(=O)C=C UACBZRBYLSMNGV-UHFFFAOYSA-N 0.000 description 1
- NWDHTEIVMDYWQJ-UHFFFAOYSA-N 3-fluoro-2-hydroxybenzaldehyde Chemical compound OC1=C(F)C=CC=C1C=O NWDHTEIVMDYWQJ-UHFFFAOYSA-N 0.000 description 1
- IAVREABSGIHHMO-UHFFFAOYSA-N 3-hydroxybenzaldehyde Chemical compound OC1=CC=CC(C=O)=C1 IAVREABSGIHHMO-UHFFFAOYSA-N 0.000 description 1
- WYVVKGNFXHOCQV-UHFFFAOYSA-N 3-iodoprop-2-yn-1-yl butylcarbamate Chemical compound CCCCNC(=O)OCC#CI WYVVKGNFXHOCQV-UHFFFAOYSA-N 0.000 description 1
- LHEKBWMWMVRJMO-UHFFFAOYSA-N 3-methoxypropyl prop-2-enoate Chemical compound COCCCOC(=O)C=C LHEKBWMWMVRJMO-UHFFFAOYSA-N 0.000 description 1
- FQMIAEWUVYWVNB-UHFFFAOYSA-N 3-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OC(C)CCOC(=O)C=C FQMIAEWUVYWVNB-UHFFFAOYSA-N 0.000 description 1
- XOJWAAUYNWGQAU-UHFFFAOYSA-N 4-(2-methylprop-2-enoyloxy)butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCOC(=O)C(C)=C XOJWAAUYNWGQAU-UHFFFAOYSA-N 0.000 description 1
- BAKYASSDAXQKKY-UHFFFAOYSA-N 4-Hydroxy-3-methylbenzaldehyde Chemical compound CC1=CC(C=O)=CC=C1O BAKYASSDAXQKKY-UHFFFAOYSA-N 0.000 description 1
- XYASJCIGVBJXPS-PFONDFGASA-N 4-O-[4-(2,2-diphenylacetyl)oxy-4-oxobutyl] 1-O-methyl (Z)-but-2-enedioate Chemical compound c1ccccc1C(C(=O)OC(=O)CCCOC(=O)\C=C/C(=O)OC)c1ccccc1 XYASJCIGVBJXPS-PFONDFGASA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- KGURSDWHGSLAPP-UHFFFAOYSA-N 4-bromo-2,6-dichlorophenol Chemical compound OC1=C(Cl)C=C(Br)C=C1Cl KGURSDWHGSLAPP-UHFFFAOYSA-N 0.000 description 1
- GZFGOTFRPZRKDS-UHFFFAOYSA-N 4-bromophenol Chemical compound OC1=CC=C(Br)C=C1 GZFGOTFRPZRKDS-UHFFFAOYSA-N 0.000 description 1
- UWJBCVMXUZVMFM-UHFFFAOYSA-N 4-chloro-1,1,1-trifluorobutane-2,3-dione Chemical compound FC(F)(F)C(=O)C(=O)CCl UWJBCVMXUZVMFM-UHFFFAOYSA-N 0.000 description 1
- MZZOGXHCICZWLE-UHFFFAOYSA-N 4-chloro-1,1,1-triphenylbutane-2,3-dione Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(C(=O)C(=O)CCl)C1=CC=CC=C1 MZZOGXHCICZWLE-UHFFFAOYSA-N 0.000 description 1
- CPWINGLAUBVORM-UHFFFAOYSA-N 4-chloro-1,1-diphenylbutane-2,3-dione Chemical compound C=1C=CC=CC=1C(C(=O)C(=O)CCl)C1=CC=CC=C1 CPWINGLAUBVORM-UHFFFAOYSA-N 0.000 description 1
- KFDVPJUYSDEJTH-UHFFFAOYSA-N 4-ethenylpyridine Chemical compound C=CC1=CC=NC=C1 KFDVPJUYSDEJTH-UHFFFAOYSA-N 0.000 description 1
- XLIMLVMYIYSMIQ-UHFFFAOYSA-N 4-hydroxy-2,5-dimethylbenzaldehyde Chemical compound CC1=CC(C=O)=C(C)C=C1O XLIMLVMYIYSMIQ-UHFFFAOYSA-N 0.000 description 1
- YTHJCZRFJGXPTL-UHFFFAOYSA-N 4-hydroxy-3-nitrobenzaldehyde Chemical compound OC1=CC=C(C=O)C=C1[N+]([O-])=O YTHJCZRFJGXPTL-UHFFFAOYSA-N 0.000 description 1
- NDWUBGAGUCISDV-UHFFFAOYSA-N 4-hydroxybutyl prop-2-enoate Chemical compound OCCCCOC(=O)C=C NDWUBGAGUCISDV-UHFFFAOYSA-N 0.000 description 1
- PRSVECUCHRJOPM-WAYWQWQTSA-N 4-o-[2-(2,2-dimethylpropanoyloxy)-2-oxoethyl] 1-o-methyl (z)-but-2-enedioate Chemical compound COC(=O)\C=C/C(=O)OCC(=O)OC(=O)C(C)(C)C PRSVECUCHRJOPM-WAYWQWQTSA-N 0.000 description 1
- VQAMKCYBTLNYPN-BUHFOSPRSA-N 4-o-[2-(2,2-diphenylacetyl)oxy-2-oxoethyl] 1-o-ethyl (e)-but-2-enedioate Chemical compound C=1C=CC=CC=1C(C(=O)OC(=O)COC(=O)/C=C/C(=O)OCC)C1=CC=CC=C1 VQAMKCYBTLNYPN-BUHFOSPRSA-N 0.000 description 1
- NQJXQCTULPPHLO-OUKQBFOZSA-N 4-o-[2-(2,2-diphenylacetyl)oxy-2-oxoethyl] 1-o-methyl (e)-but-2-enedioate Chemical compound C=1C=CC=CC=1C(C(=O)OC(=O)COC(=O)/C=C/C(=O)OC)C1=CC=CC=C1 NQJXQCTULPPHLO-OUKQBFOZSA-N 0.000 description 1
- XALFFNNPDYPSJT-ARJAWSKDSA-N 4-o-[2-(2-bromoacetyl)oxy-2-oxoethyl] 1-o-ethyl (z)-but-2-enedioate Chemical compound CCOC(=O)\C=C/C(=O)OCC(=O)OC(=O)CBr XALFFNNPDYPSJT-ARJAWSKDSA-N 0.000 description 1
- AKIGGEVOJALOBU-IHWYPQMZSA-N 4-o-[2-(2-bromoacetyl)oxy-2-oxoethyl] 1-o-methyl (z)-but-2-enedioate Chemical compound COC(=O)\C=C/C(=O)OCC(=O)OC(=O)CBr AKIGGEVOJALOBU-IHWYPQMZSA-N 0.000 description 1
- PHWITBNEMFGDTD-BUHFOSPRSA-N 4-o-[2-(2-chloro-2,2-diphenylacetyl)oxy-2-oxoethyl] 1-o-ethyl (e)-but-2-enedioate Chemical compound C=1C=CC=CC=1C(Cl)(C(=O)OC(=O)COC(=O)/C=C/C(=O)OCC)C1=CC=CC=C1 PHWITBNEMFGDTD-BUHFOSPRSA-N 0.000 description 1
- SLGNLIUYSRUYST-OUKQBFOZSA-N 4-o-[2-(2-chloro-2,2-diphenylacetyl)oxy-2-oxoethyl] 1-o-methyl (e)-but-2-enedioate Chemical compound C=1C=CC=CC=1C(Cl)(C(=O)OC(=O)COC(=O)/C=C/C(=O)OC)C1=CC=CC=C1 SLGNLIUYSRUYST-OUKQBFOZSA-N 0.000 description 1
- SLGNLIUYSRUYST-SEYXRHQNSA-N 4-o-[2-(2-chloro-2,2-diphenylacetyl)oxy-2-oxoethyl] 1-o-methyl (z)-but-2-enedioate Chemical compound C=1C=CC=CC=1C(Cl)(C(=O)OC(=O)COC(=O)\C=C/C(=O)OC)C1=CC=CC=C1 SLGNLIUYSRUYST-SEYXRHQNSA-N 0.000 description 1
- NHTCDWCKVKHLFR-SREVYHEPSA-N 4-o-[2-(3,3-dimethylbutanoyloxy)-2-oxoethyl] 1-o-ethyl (z)-but-2-enedioate Chemical compound CCOC(=O)\C=C/C(=O)OCC(=O)OC(=O)CC(C)(C)C NHTCDWCKVKHLFR-SREVYHEPSA-N 0.000 description 1
- DAISGCCPHSJHIS-BQYQJAHWSA-N 4-o-[2-[2-(4-methoxyphenyl)acetyl]oxy-2-oxoethyl] 1-o-methyl (e)-but-2-enedioate Chemical compound COC(=O)\C=C\C(=O)OCC(=O)OC(=O)CC1=CC=C(OC)C=C1 DAISGCCPHSJHIS-BQYQJAHWSA-N 0.000 description 1
- DAISGCCPHSJHIS-FPLPWBNLSA-N 4-o-[2-[2-(4-methoxyphenyl)acetyl]oxy-2-oxoethyl] 1-o-methyl (z)-but-2-enedioate Chemical compound COC(=O)\C=C/C(=O)OCC(=O)OC(=O)CC1=CC=C(OC)C=C1 DAISGCCPHSJHIS-FPLPWBNLSA-N 0.000 description 1
- OOKXSJUWRMEVDD-SREVYHEPSA-N 4-o-[3-(2,2-dimethylpropanoyloxy)-3-oxopropyl] 1-o-ethyl (z)-but-2-enedioate Chemical compound CCOC(=O)\C=C/C(=O)OCCC(=O)OC(=O)C(C)(C)C OOKXSJUWRMEVDD-SREVYHEPSA-N 0.000 description 1
- ZAFAVLIYAMXXEW-WAYWQWQTSA-N 4-o-[3-(2,2-dimethylpropanoyloxy)-3-oxopropyl] 1-o-methyl (z)-but-2-enedioate Chemical compound COC(=O)\C=C/C(=O)OCCC(=O)OC(=O)C(C)(C)C ZAFAVLIYAMXXEW-WAYWQWQTSA-N 0.000 description 1
- FISIZWQDAUIBCI-BUHFOSPRSA-N 4-o-[3-(2,2-diphenylacetyl)oxy-3-oxopropyl] 1-o-ethyl (e)-but-2-enedioate Chemical compound C=1C=CC=CC=1C(C(=O)OC(=O)CCOC(=O)/C=C/C(=O)OCC)C1=CC=CC=C1 FISIZWQDAUIBCI-BUHFOSPRSA-N 0.000 description 1
- CKACNMHUCFHUQI-ONEGZZNKSA-N 4-o-[3-(2-bromoacetyl)oxy-3-oxopropyl] 1-o-ethyl (e)-but-2-enedioate Chemical compound CCOC(=O)\C=C\C(=O)OCCC(=O)OC(=O)CBr CKACNMHUCFHUQI-ONEGZZNKSA-N 0.000 description 1
- CKACNMHUCFHUQI-ARJAWSKDSA-N 4-o-[3-(2-bromoacetyl)oxy-3-oxopropyl] 1-o-ethyl (z)-but-2-enedioate Chemical compound CCOC(=O)\C=C/C(=O)OCCC(=O)OC(=O)CBr CKACNMHUCFHUQI-ARJAWSKDSA-N 0.000 description 1
- OXHGDEQMQYXPSD-NSCUHMNNSA-N 4-o-[3-(2-bromoacetyl)oxy-3-oxopropyl] 1-o-methyl (e)-but-2-enedioate Chemical compound COC(=O)\C=C\C(=O)OCCC(=O)OC(=O)CBr OXHGDEQMQYXPSD-NSCUHMNNSA-N 0.000 description 1
- OXHGDEQMQYXPSD-IHWYPQMZSA-N 4-o-[3-(2-bromoacetyl)oxy-3-oxopropyl] 1-o-methyl (z)-but-2-enedioate Chemical compound COC(=O)\C=C/C(=O)OCCC(=O)OC(=O)CBr OXHGDEQMQYXPSD-IHWYPQMZSA-N 0.000 description 1
- BCLVUFNEQPPIFD-BQYQJAHWSA-N 4-o-[3-(2-cyclopentylacetyl)oxy-3-oxopropyl] 1-o-ethyl (e)-but-2-enedioate Chemical compound CCOC(=O)\C=C\C(=O)OCCC(=O)OC(=O)CC1CCCC1 BCLVUFNEQPPIFD-BQYQJAHWSA-N 0.000 description 1
- BCLVUFNEQPPIFD-FPLPWBNLSA-N 4-o-[3-(2-cyclopentylacetyl)oxy-3-oxopropyl] 1-o-ethyl (z)-but-2-enedioate Chemical compound CCOC(=O)\C=C/C(=O)OCCC(=O)OC(=O)CC1CCCC1 BCLVUFNEQPPIFD-FPLPWBNLSA-N 0.000 description 1
- SJTKSVLBOZNUSI-VOTSOKGWSA-N 4-o-[3-(2-cyclopentylacetyl)oxy-3-oxopropyl] 1-o-methyl (e)-but-2-enedioate Chemical compound COC(=O)\C=C\C(=O)OCCC(=O)OC(=O)CC1CCCC1 SJTKSVLBOZNUSI-VOTSOKGWSA-N 0.000 description 1
- SJTKSVLBOZNUSI-SREVYHEPSA-N 4-o-[3-(2-cyclopentylacetyl)oxy-3-oxopropyl] 1-o-methyl (z)-but-2-enedioate Chemical compound COC(=O)\C=C/C(=O)OCCC(=O)OC(=O)CC1CCCC1 SJTKSVLBOZNUSI-SREVYHEPSA-N 0.000 description 1
- BQDSOMVWELGAGB-SREVYHEPSA-N 4-o-[3-(3,3-dimethylbutanoyloxy)-3-oxopropyl] 1-o-ethyl (z)-but-2-enedioate Chemical compound CCOC(=O)\C=C/C(=O)OCCC(=O)OC(=O)CC(C)(C)C BQDSOMVWELGAGB-SREVYHEPSA-N 0.000 description 1
- ONXJUQBDNZJJSU-WAYWQWQTSA-N 4-o-[3-(3,3-dimethylbutanoyloxy)-3-oxopropyl] 1-o-methyl (z)-but-2-enedioate Chemical compound COC(=O)\C=C/C(=O)OCCC(=O)OC(=O)CC(C)(C)C ONXJUQBDNZJJSU-WAYWQWQTSA-N 0.000 description 1
- ZHVQJFOKFHGAKS-BQYQJAHWSA-N 4-o-[3-[2-(4-methoxyphenyl)acetyl]oxy-3-oxopropyl] 1-o-methyl (e)-but-2-enedioate Chemical compound COC(=O)\C=C\C(=O)OCCC(=O)OC(=O)CC1=CC=C(OC)C=C1 ZHVQJFOKFHGAKS-BQYQJAHWSA-N 0.000 description 1
- ZHVQJFOKFHGAKS-FPLPWBNLSA-N 4-o-[3-[2-(4-methoxyphenyl)acetyl]oxy-3-oxopropyl] 1-o-methyl (z)-but-2-enedioate Chemical compound COC(=O)\C=C/C(=O)OCCC(=O)OC(=O)CC1=CC=C(OC)C=C1 ZHVQJFOKFHGAKS-FPLPWBNLSA-N 0.000 description 1
- XIRFCZJZALYTNF-AATRIKPKSA-N 4-o-[4-(2-methoxyacetyl)oxy-4-oxobutyl] 1-o-methyl (e)-but-2-enedioate Chemical compound COCC(=O)OC(=O)CCCOC(=O)\C=C\C(=O)OC XIRFCZJZALYTNF-AATRIKPKSA-N 0.000 description 1
- XIRFCZJZALYTNF-WAYWQWQTSA-N 4-o-[4-(2-methoxyacetyl)oxy-4-oxobutyl] 1-o-methyl (z)-but-2-enedioate Chemical compound COCC(=O)OC(=O)CCCOC(=O)\C=C/C(=O)OC XIRFCZJZALYTNF-WAYWQWQTSA-N 0.000 description 1
- IQUOMUNNWMUEGX-MDZDMXLPSA-N 4-o-[5-(2,2-dimethylpropanoyloxy)-5-oxopentyl] 1-o-ethyl (e)-but-2-enedioate Chemical compound CCOC(=O)\C=C\C(=O)OCCCCC(=O)OC(=O)C(C)(C)C IQUOMUNNWMUEGX-MDZDMXLPSA-N 0.000 description 1
- IQUOMUNNWMUEGX-KTKRTIGZSA-N 4-o-[5-(2,2-dimethylpropanoyloxy)-5-oxopentyl] 1-o-ethyl (z)-but-2-enedioate Chemical compound CCOC(=O)\C=C/C(=O)OCCCCC(=O)OC(=O)C(C)(C)C IQUOMUNNWMUEGX-KTKRTIGZSA-N 0.000 description 1
- XSGOCMFXJFSCKB-CMDGGOBGSA-N 4-o-[5-(2,2-dimethylpropanoyloxy)-5-oxopentyl] 1-o-methyl (e)-but-2-enedioate Chemical compound COC(=O)\C=C\C(=O)OCCCCC(=O)OC(=O)C(C)(C)C XSGOCMFXJFSCKB-CMDGGOBGSA-N 0.000 description 1
- XSGOCMFXJFSCKB-HJWRWDBZSA-N 4-o-[5-(2,2-dimethylpropanoyloxy)-5-oxopentyl] 1-o-methyl (z)-but-2-enedioate Chemical compound COC(=O)\C=C/C(=O)OCCCCC(=O)OC(=O)C(C)(C)C XSGOCMFXJFSCKB-HJWRWDBZSA-N 0.000 description 1
- CRIBVPVWYGYOJW-CMDGGOBGSA-N 4-o-[5-(3,3-dimethylbutanoyloxy)-5-oxopentyl] 1-o-methyl (e)-but-2-enedioate Chemical compound COC(=O)\C=C\C(=O)OCCCCC(=O)OC(=O)CC(C)(C)C CRIBVPVWYGYOJW-CMDGGOBGSA-N 0.000 description 1
- WNCLCGHAPDJYPA-ZHACJKMWSA-N 4-o-[5-[2-(2-bromophenyl)acetyl]oxy-5-oxopentyl] 1-o-ethyl (e)-but-2-enedioate Chemical compound CCOC(=O)\C=C\C(=O)OCCCCC(=O)OC(=O)CC1=CC=CC=C1Br WNCLCGHAPDJYPA-ZHACJKMWSA-N 0.000 description 1
- YLNWYKBMXWWGMF-MDZDMXLPSA-N 4-o-[5-[2-(2-bromophenyl)acetyl]oxy-5-oxopentyl] 1-o-methyl (e)-but-2-enedioate Chemical compound COC(=O)\C=C\C(=O)OCCCCC(=O)OC(=O)CC1=CC=CC=C1Br YLNWYKBMXWWGMF-MDZDMXLPSA-N 0.000 description 1
- YLNWYKBMXWWGMF-KTKRTIGZSA-N 4-o-[5-[2-(2-bromophenyl)acetyl]oxy-5-oxopentyl] 1-o-methyl (z)-but-2-enedioate Chemical compound COC(=O)\C=C/C(=O)OCCCCC(=O)OC(=O)CC1=CC=CC=C1Br YLNWYKBMXWWGMF-KTKRTIGZSA-N 0.000 description 1
- JHWGFJBTMHEZME-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCOC(=O)C=C JHWGFJBTMHEZME-UHFFFAOYSA-N 0.000 description 1
- MKKSTJKBKNCMRV-UHFFFAOYSA-N 5-bromo-2-hydroxybenzaldehyde Chemical compound OC1=CC=C(Br)C=C1C=O MKKSTJKBKNCMRV-UHFFFAOYSA-N 0.000 description 1
- HUVJDNKUSVGGSY-UHFFFAOYSA-N 5-chloro-1,1,1-trifluoropentane-2,3-dione Chemical compound FC(F)(F)C(=O)C(=O)CCCl HUVJDNKUSVGGSY-UHFFFAOYSA-N 0.000 description 1
- DVDCROOVCKMLOW-UHFFFAOYSA-N 5-chloro-1,1,1-triphenylpentane-2,3-dione Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(C(=O)C(=O)CCCl)C1=CC=CC=C1 DVDCROOVCKMLOW-UHFFFAOYSA-N 0.000 description 1
- WIPVBDHCKGDSOV-UHFFFAOYSA-N 5-chloro-1,1-diphenylpentane-2,3-dione Chemical compound C=1C=CC=CC=1C(C(=O)C(=O)CCCl)C1=CC=CC=C1 WIPVBDHCKGDSOV-UHFFFAOYSA-N 0.000 description 1
- FFHQUTPIQLCVOY-UHFFFAOYSA-N 5-chloro-1-(2,4,5-trichlorophenoxy)pentane-2,3-dione Chemical compound ClCCC(=O)C(=O)COC1=CC(Cl)=C(Cl)C=C1Cl FFHQUTPIQLCVOY-UHFFFAOYSA-N 0.000 description 1
- OOXJEPJUBFWYFZ-UHFFFAOYSA-N 5-chloro-1-(2,5-dimethoxyphenyl)pentane-2,3-dione Chemical compound COC1=CC=C(OC)C(CC(=O)C(=O)CCCl)=C1 OOXJEPJUBFWYFZ-UHFFFAOYSA-N 0.000 description 1
- NQTWPSPERLGCDK-UHFFFAOYSA-N 5-chloro-1-(3,4-dimethoxyphenyl)pentane-2,3-dione Chemical compound COC1=CC=C(CC(=O)C(=O)CCCl)C=C1OC NQTWPSPERLGCDK-UHFFFAOYSA-N 0.000 description 1
- NHQQULFCWWOATR-UHFFFAOYSA-N 5-chloro-1-(4-chlorophenyl)pentane-2,3-dione Chemical compound ClCCC(=O)C(=O)CC1=CC=C(Cl)C=C1 NHQQULFCWWOATR-UHFFFAOYSA-N 0.000 description 1
- XRXLXJZOGNGOJR-UHFFFAOYSA-N 5-chloro-1-(4-fluorophenoxy)pentane-2,3-dione Chemical compound FC1=CC=C(OCC(=O)C(=O)CCCl)C=C1 XRXLXJZOGNGOJR-UHFFFAOYSA-N 0.000 description 1
- JLSSRIGTFDKPKQ-UHFFFAOYSA-N 5-chloro-1-(4-fluorophenyl)pentane-2,3-dione Chemical compound FC1=CC=C(CC(=O)C(=O)CCCl)C=C1 JLSSRIGTFDKPKQ-UHFFFAOYSA-N 0.000 description 1
- GUFAKGIRMKCXSB-UHFFFAOYSA-N 5-chloro-1-cyclopentylpentane-2,3-dione Chemical compound ClCCC(=O)C(=O)CC1CCCC1 GUFAKGIRMKCXSB-UHFFFAOYSA-N 0.000 description 1
- UFLIUSXYWJGWAU-UHFFFAOYSA-N 5-chloro-1-phenoxypentane-2,3-dione Chemical compound ClCCC(=O)C(=O)COC1=CC=CC=C1 UFLIUSXYWJGWAU-UHFFFAOYSA-N 0.000 description 1
- VIDJMGNYTXXHIZ-UHFFFAOYSA-N 5-chloro-1-phenylmethoxypentane-2,3-dione Chemical compound ClCCC(=O)C(=O)COCC1=CC=CC=C1 VIDJMGNYTXXHIZ-UHFFFAOYSA-N 0.000 description 1
- VELQZPNHZWKXED-UHFFFAOYSA-N 5-chloro-1-phenylpentane-2,3-dione Chemical compound ClCCC(=O)C(=O)CC1=CC=CC=C1 VELQZPNHZWKXED-UHFFFAOYSA-N 0.000 description 1
- FZHSPPYCNDYIKD-UHFFFAOYSA-N 5-methoxysalicylaldehyde Chemical compound COC1=CC=C(O)C(C=O)=C1 FZHSPPYCNDYIKD-UHFFFAOYSA-N 0.000 description 1
- NBDAHKQJXVLAID-UHFFFAOYSA-N 5-nitroisophthalic acid Chemical class OC(=O)C1=CC(C(O)=O)=CC([N+]([O-])=O)=C1 NBDAHKQJXVLAID-UHFFFAOYSA-N 0.000 description 1
- NUXLDNTZFXDNBA-UHFFFAOYSA-N 6-bromo-2-methyl-4h-1,4-benzoxazin-3-one Chemical compound C1=C(Br)C=C2NC(=O)C(C)OC2=C1 NUXLDNTZFXDNBA-UHFFFAOYSA-N 0.000 description 1
- PRIHJYOOSYFAHW-UHFFFAOYSA-N 6-chloro-1,1,1-trifluorohexane-2,3-dione Chemical compound FC(F)(F)C(=O)C(=O)CCCCl PRIHJYOOSYFAHW-UHFFFAOYSA-N 0.000 description 1
- UHASHOVJFMVVFS-UHFFFAOYSA-N 6-chloro-1,1,1-triphenylhexane-2,3-dione Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(C(=O)C(=O)CCCCl)C1=CC=CC=C1 UHASHOVJFMVVFS-UHFFFAOYSA-N 0.000 description 1
- UQIVFEILPUQAKX-UHFFFAOYSA-N 6-chloro-1,1-diphenylhexane-2,3-dione Chemical compound C=1C=CC=CC=1C(C(=O)C(=O)CCCCl)C1=CC=CC=C1 UQIVFEILPUQAKX-UHFFFAOYSA-N 0.000 description 1
- ABLRPGMYXLUXSG-UHFFFAOYSA-N 6-chloro-1-(2,4,5-trichlorophenoxy)hexane-2,3-dione Chemical compound ClCCCC(=O)C(=O)COC1=CC(Cl)=C(Cl)C=C1Cl ABLRPGMYXLUXSG-UHFFFAOYSA-N 0.000 description 1
- PJJNBVSJNXVQOT-UHFFFAOYSA-N 6-chloro-1-(3,4-dimethoxyphenyl)hexane-2,3-dione Chemical compound COC1=CC=C(CC(=O)C(=O)CCCCl)C=C1OC PJJNBVSJNXVQOT-UHFFFAOYSA-N 0.000 description 1
- MRDZVIFCHLNFRD-UHFFFAOYSA-N 6-chloro-1-(4-chlorophenyl)hexane-2,3-dione Chemical compound ClCCCC(=O)C(=O)CC1=CC=C(Cl)C=C1 MRDZVIFCHLNFRD-UHFFFAOYSA-N 0.000 description 1
- WSHVYMZFQFBTTH-UHFFFAOYSA-N 6-chloro-1-(4-fluorophenoxy)hexane-2,3-dione Chemical compound FC1=CC=C(OCC(=O)C(=O)CCCCl)C=C1 WSHVYMZFQFBTTH-UHFFFAOYSA-N 0.000 description 1
- DZWVGZSSDIXSFC-UHFFFAOYSA-N 6-chloro-1-(4-fluorophenyl)hexane-2,3-dione Chemical compound FC1=CC=C(CC(=O)C(=O)CCCCl)C=C1 DZWVGZSSDIXSFC-UHFFFAOYSA-N 0.000 description 1
- MGWNJXOCGBJCNV-UHFFFAOYSA-N 6-chloro-1-cyclopentylhexane-2,3-dione Chemical compound ClCCCC(=O)C(=O)CC1CCCC1 MGWNJXOCGBJCNV-UHFFFAOYSA-N 0.000 description 1
- HUPYSBGFBNMAOX-UHFFFAOYSA-N 6-chloro-1-phenoxyhexane-2,3-dione Chemical compound ClCCCC(=O)C(=O)COC1=CC=CC=C1 HUPYSBGFBNMAOX-UHFFFAOYSA-N 0.000 description 1
- DEMYGTQNUMREOD-UHFFFAOYSA-N 6-chloro-1-phenylhexane-2,3-dione Chemical compound ClCCCC(=O)C(=O)CC1=CC=CC=C1 DEMYGTQNUMREOD-UHFFFAOYSA-N 0.000 description 1
- LGEBWCHXRDOWMA-UHFFFAOYSA-N 6-chloro-1-phenylmethoxyhexane-2,3-dione Chemical compound ClCCCC(=O)C(=O)COCC1=CC=CC=C1 LGEBWCHXRDOWMA-UHFFFAOYSA-N 0.000 description 1
- HNMZZHZBUORISK-UHFFFAOYSA-N 6-chlorohexyl(dimethyl)silane Chemical compound C[SiH](C)CCCCCCCl HNMZZHZBUORISK-UHFFFAOYSA-N 0.000 description 1
- JTHZUSWLNCPZLX-UHFFFAOYSA-N 6-fluoro-3-methyl-2h-indazole Chemical compound FC1=CC=C2C(C)=NNC2=C1 JTHZUSWLNCPZLX-UHFFFAOYSA-N 0.000 description 1
- RQINQJTUMGQYOB-UHFFFAOYSA-N 6-methylheptyl dihydrogen phosphate Chemical compound CC(C)CCCCCOP(O)(O)=O RQINQJTUMGQYOB-UHFFFAOYSA-N 0.000 description 1
- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 description 1
- GRHPVBLUKWSRRG-UHFFFAOYSA-N 7-chloro-1,1,1-trifluoroheptane-2,3-dione Chemical compound FC(F)(F)C(=O)C(=O)CCCCCl GRHPVBLUKWSRRG-UHFFFAOYSA-N 0.000 description 1
- XMADONYIKXLJJI-UHFFFAOYSA-N 7-chloro-1,1,1-triphenylheptane-2,3-dione Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(C(=O)C(=O)CCCCCl)C1=CC=CC=C1 XMADONYIKXLJJI-UHFFFAOYSA-N 0.000 description 1
- ADTDWJPQLDBPTG-UHFFFAOYSA-N 7-chloro-1,1-diphenylheptane-2,3-dione Chemical compound C=1C=CC=CC=1C(C(=O)C(=O)CCCCCl)C1=CC=CC=C1 ADTDWJPQLDBPTG-UHFFFAOYSA-N 0.000 description 1
- JHPWHXXZQWRBLC-UHFFFAOYSA-N 7-chloro-1-(2,4,5-trichlorophenoxy)heptane-2,3-dione Chemical compound ClCCCCC(=O)C(=O)COC1=CC(Cl)=C(Cl)C=C1Cl JHPWHXXZQWRBLC-UHFFFAOYSA-N 0.000 description 1
- MYYQLWDPDHJHQR-UHFFFAOYSA-N 7-chloro-1-(2,5-dimethoxyphenyl)heptane-2,3-dione Chemical compound COC1=CC=C(OC)C(CC(=O)C(=O)CCCCCl)=C1 MYYQLWDPDHJHQR-UHFFFAOYSA-N 0.000 description 1
- CXQLAYAOOFQSGH-UHFFFAOYSA-N 7-chloro-1-(3,4-dimethoxyphenyl)heptane-2,3-dione Chemical compound COC1=CC=C(CC(=O)C(=O)CCCCCl)C=C1OC CXQLAYAOOFQSGH-UHFFFAOYSA-N 0.000 description 1
- SBPFWKKXWKHVBK-UHFFFAOYSA-N 7-chloro-1-(4-chlorophenyl)heptane-2,3-dione Chemical compound ClCCCCC(=O)C(=O)CC1=CC=C(Cl)C=C1 SBPFWKKXWKHVBK-UHFFFAOYSA-N 0.000 description 1
- LQSMVNGJPBPJQX-UHFFFAOYSA-N 7-chloro-1-(4-fluorophenoxy)heptane-2,3-dione Chemical compound FC1=CC=C(OCC(=O)C(=O)CCCCCl)C=C1 LQSMVNGJPBPJQX-UHFFFAOYSA-N 0.000 description 1
- BSDUIYGEQIMRNH-UHFFFAOYSA-N 7-chloro-1-(4-fluorophenyl)heptane-2,3-dione Chemical compound FC1=CC=C(CC(=O)C(=O)CCCCCl)C=C1 BSDUIYGEQIMRNH-UHFFFAOYSA-N 0.000 description 1
- ZTXRKSXONFANJK-UHFFFAOYSA-N 7-chloro-1-phenoxyheptane-2,3-dione Chemical compound ClCCCCC(=O)C(=O)COC1=CC=CC=C1 ZTXRKSXONFANJK-UHFFFAOYSA-N 0.000 description 1
- WREFLDOKLBLCMC-UHFFFAOYSA-N 7-chloro-1-phenylheptane-2,3-dione Chemical compound ClCCCCC(=O)C(=O)CC1=CC=CC=C1 WREFLDOKLBLCMC-UHFFFAOYSA-N 0.000 description 1
- FUVVBEMYTASAEA-UHFFFAOYSA-N 7-chloro-1-phenylmethoxyheptane-2,3-dione Chemical compound ClCCCCC(=O)C(=O)COCC1=CC=CC=C1 FUVVBEMYTASAEA-UHFFFAOYSA-N 0.000 description 1
- VOMQVJCZGOBKLW-UHFFFAOYSA-N 7-chloro-2,2-dimethylheptane-3,4-dione Chemical compound CC(C)(C)C(=O)C(=O)CCCCl VOMQVJCZGOBKLW-UHFFFAOYSA-N 0.000 description 1
- IWDFIMPAUAWJEI-UHFFFAOYSA-N 8-chloro-2,2-dimethyloctane-3,4-dione Chemical compound CC(C)(C)C(=O)C(=O)CCCCCl IWDFIMPAUAWJEI-UHFFFAOYSA-N 0.000 description 1
- UNQOAYVVXVJLBM-UHFFFAOYSA-N 9-chloro-2,2-dimethylnonane-4,5-dione Chemical compound CC(C)(C)CC(=O)C(=O)CCCCCl UNQOAYVVXVJLBM-UHFFFAOYSA-N 0.000 description 1
- LHTHJEKMSNYGHT-UHFFFAOYSA-N 9-octylheptadecan-9-amine Chemical compound CCCCCCCCC(N)(CCCCCCCC)CCCCCCCC LHTHJEKMSNYGHT-UHFFFAOYSA-N 0.000 description 1
- 235000007173 Abies balsamea Nutrition 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 229920002972 Acrylic fiber Polymers 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241000512259 Ascophyllum nodosum Species 0.000 description 1
- 239000004857 Balsam Substances 0.000 description 1
- 239000004255 Butylated hydroxyanisole Substances 0.000 description 1
- WXZASCSXAMHFCX-SNAWJCMRSA-N C(=O)(O)CCC/C(/C(=O)O)=C\C(=O)O Chemical class C(=O)(O)CCC/C(/C(=O)O)=C\C(=O)O WXZASCSXAMHFCX-SNAWJCMRSA-N 0.000 description 1
- AFXWWSFYTDBJTG-VOTSOKGWSA-N C/C(=C(/CC(=O)OC(=O)C(C)(C)C)\C(=O)O)/C(=O)O Chemical compound C/C(=C(/CC(=O)OC(=O)C(C)(C)C)\C(=O)O)/C(=O)O AFXWWSFYTDBJTG-VOTSOKGWSA-N 0.000 description 1
- ZYFSVEBNXQTWRF-SNAWJCMRSA-N C/C(=C(/CC(=O)OC(=O)CBr)\C(=O)O)/C(=O)O Chemical compound C/C(=C(/CC(=O)OC(=O)CBr)\C(=O)O)/C(=O)O ZYFSVEBNXQTWRF-SNAWJCMRSA-N 0.000 description 1
- IBWMWJWMYPKIAK-BQYQJAHWSA-N C/C(=C(/CC(=O)OC(=O)CC(C)(C)C)\C(=O)O)/C(=O)O Chemical compound C/C(=C(/CC(=O)OC(=O)CC(C)(C)C)\C(=O)O)/C(=O)O IBWMWJWMYPKIAK-BQYQJAHWSA-N 0.000 description 1
- OBDKQGVRENQCAX-CSKARUKUSA-N C/C(=C(/CC(=O)OC(=O)CC1CCCC1)\C(=O)O)/C(=O)O Chemical compound C/C(=C(/CC(=O)OC(=O)CC1CCCC1)\C(=O)O)/C(=O)O OBDKQGVRENQCAX-CSKARUKUSA-N 0.000 description 1
- NNRPPNPZGUWKGT-OBGWFSINSA-N C/C(=C(/CCCC(=O)OC(=O)C(C1=CC=CC=C1)C2=CC=CC=C2)\C(=O)O)/C(=O)O Chemical compound C/C(=C(/CCCC(=O)OC(=O)C(C1=CC=CC=C1)C2=CC=CC=C2)\C(=O)O)/C(=O)O NNRPPNPZGUWKGT-OBGWFSINSA-N 0.000 description 1
- NEXYKRRBJIDGNR-CMDGGOBGSA-N C/C(=C(/CCCC(=O)O[Si](C)(C)C)\C(=O)O)/C(=O)O Chemical compound C/C(=C(/CCCC(=O)O[Si](C)(C)C)\C(=O)O)/C(=O)O NEXYKRRBJIDGNR-CMDGGOBGSA-N 0.000 description 1
- KWBZLMLBVRRPMF-WYMLVPIESA-N C/C(=C(/CCCCC(=O)OC(=O)CC1=CC=CC=C1)\C(=O)O)/C(=O)O Chemical compound C/C(=C(/CCCCC(=O)OC(=O)CC1=CC=CC=C1)\C(=O)O)/C(=O)O KWBZLMLBVRRPMF-WYMLVPIESA-N 0.000 description 1
- RKDRPXQRVYKUAW-MDZDMXLPSA-N C/C(=C(/CCCCC(=O)O[Si](C)(C)C)\C(=O)O)/C(=O)O Chemical compound C/C(=C(/CCCCC(=O)O[Si](C)(C)C)\C(=O)O)/C(=O)O RKDRPXQRVYKUAW-MDZDMXLPSA-N 0.000 description 1
- PFFKSCCZBRBVAP-UHFFFAOYSA-N CC(C)[SiH](OC(=O)CCCCCl)C(C)C Chemical compound CC(C)[SiH](OC(=O)CCCCCl)C(C)C PFFKSCCZBRBVAP-UHFFFAOYSA-N 0.000 description 1
- KXDQPCNVFHHXBP-SEYXRHQNSA-N CC(CC(=O)OC(=O)C(C1=CC=CC=C1)(C2=CC=CC=C2)Cl)OC(=O)/C=C\C(=O)O Chemical compound CC(CC(=O)OC(=O)C(C1=CC=CC=C1)(C2=CC=CC=C2)Cl)OC(=O)/C=C\C(=O)O KXDQPCNVFHHXBP-SEYXRHQNSA-N 0.000 description 1
- UOICVLCSIWWVAK-FPLPWBNLSA-N CC(CC(=O)OC(=O)CC1=CC=C(C=C1)OC)OC(=O)/C=C\C(=O)O Chemical compound CC(CC(=O)OC(=O)CC1=CC=C(C=C1)OC)OC(=O)/C=C\C(=O)O UOICVLCSIWWVAK-FPLPWBNLSA-N 0.000 description 1
- YQJPOCMWBCMMSP-SQFISAMPSA-N CC(CCC(=O)OC(=O)C(C1=CC=CC=C1)C2=CC=CC=C2)OC(=O)/C=C\C(=O)O Chemical compound CC(CCC(=O)OC(=O)C(C1=CC=CC=C1)C2=CC=CC=C2)OC(=O)/C=C\C(=O)O YQJPOCMWBCMMSP-SQFISAMPSA-N 0.000 description 1
- PSYKWULYGLWVGQ-NTMALXAHSA-N CC(CCC(=O)OC(=O)CC1=CC=C(C=C1)OC)OC(=O)/C=C\C(=O)O Chemical compound CC(CCC(=O)OC(=O)CC1=CC=C(C=C1)OC)OC(=O)/C=C\C(=O)O PSYKWULYGLWVGQ-NTMALXAHSA-N 0.000 description 1
- LYDWSTVPJUCPCW-NTMALXAHSA-N CC(CCC(=O)OC(=O)CC1=CC=CC=C1)OC(=O)/C=C\C(=O)O Chemical compound CC(CCC(=O)OC(=O)CC1=CC=CC=C1)OC(=O)/C=C\C(=O)O LYDWSTVPJUCPCW-NTMALXAHSA-N 0.000 description 1
- YBUBAFYUIHMTSF-NXVVXOECSA-N CC(CCCC(=O)OC(=O)C(C1=CC=CC=C1)C2=CC=CC=C2)OC(=O)/C=C\C(=O)O Chemical compound CC(CCCC(=O)OC(=O)C(C1=CC=CC=C1)C2=CC=CC=C2)OC(=O)/C=C\C(=O)O YBUBAFYUIHMTSF-NXVVXOECSA-N 0.000 description 1
- UXBBRWQXPBNOEW-KHPPLWFESA-N CC(CCCC(=O)OC(=O)CC1=CC=CC=C1)OC(=O)/C=C\C(=O)O Chemical compound CC(CCCC(=O)OC(=O)CC1=CC=CC=C1)OC(=O)/C=C\C(=O)O UXBBRWQXPBNOEW-KHPPLWFESA-N 0.000 description 1
- SHZAJFRQTVYTCW-KHPPLWFESA-N CC(CCCCC(=O)OC(=O)CC1=CC=CC=C1Br)OC(=O)/C=C\C(=O)O Chemical compound CC(CCCCC(=O)OC(=O)CC1=CC=CC=C1Br)OC(=O)/C=C\C(=O)O SHZAJFRQTVYTCW-KHPPLWFESA-N 0.000 description 1
- NJKRGLXVPIPBJZ-BQYQJAHWSA-N CC/C(=C(/CC(=O)OC(=O)C(C)(C)C)\C(=O)O)/C(=O)O Chemical compound CC/C(=C(/CC(=O)OC(=O)C(C)(C)C)\C(=O)O)/C(=O)O NJKRGLXVPIPBJZ-BQYQJAHWSA-N 0.000 description 1
- XMONMLPLBUHJDC-OUKQBFOZSA-N CC/C(=C(/CCCC(=O)O[Si](CC)(CC)CC)\C(=O)O)/C(=O)O Chemical compound CC/C(=C(/CCCC(=O)O[Si](CC)(CC)CC)\C(=O)O)/C(=O)O XMONMLPLBUHJDC-OUKQBFOZSA-N 0.000 description 1
- AIHHGIQPWVCUPX-BUHFOSPRSA-N CC/C(=C(/CCCCC(=O)O[Si](CC)(CC)CC)\C(=O)O)/C(=O)O Chemical compound CC/C(=C(/CCCCC(=O)O[Si](CC)(CC)CC)\C(=O)O)/C(=O)O AIHHGIQPWVCUPX-BUHFOSPRSA-N 0.000 description 1
- YWLIQAKSSDDFKC-VOTSOKGWSA-N COC1=CC=C(C=C1)CC(=O)OC(=O)CCOC(=O)/C=C/C(=O)O Chemical compound COC1=CC=C(C=C1)CC(=O)OC(=O)CCOC(=O)/C=C/C(=O)O YWLIQAKSSDDFKC-VOTSOKGWSA-N 0.000 description 1
- 229910021532 Calcite Inorganic materials 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 241000195628 Chlorophyta Species 0.000 description 1
- 239000005046 Chlorosilane Substances 0.000 description 1
- 239000005749 Copper compound Substances 0.000 description 1
- 241000548230 Crassostrea angulata Species 0.000 description 1
- 229910000570 Cupronickel Inorganic materials 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- RDOFJDLLWVCMRU-UHFFFAOYSA-N Diisobutyl adipate Chemical compound CC(C)COC(=O)CCCCC(=O)OCC(C)C RDOFJDLLWVCMRU-UHFFFAOYSA-N 0.000 description 1
- ZVFDTKUVRCTHQE-UHFFFAOYSA-N Diisodecyl phthalate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC(C)C ZVFDTKUVRCTHQE-UHFFFAOYSA-N 0.000 description 1
- 239000005510 Diuron Substances 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- MWAYRGBWOVHDDZ-UHFFFAOYSA-N Ethyl vanillate Chemical compound CCOC(=O)C1=CC=C(O)C(OC)=C1 MWAYRGBWOVHDDZ-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 239000013032 Hydrocarbon resin Substances 0.000 description 1
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 1
- 244000018716 Impatiens biflora Species 0.000 description 1
- CMHMMKSPYOOVGI-UHFFFAOYSA-N Isopropylparaben Chemical compound CC(C)OC(=O)C1=CC=C(O)C=C1 CMHMMKSPYOOVGI-UHFFFAOYSA-N 0.000 description 1
- 239000002211 L-ascorbic acid Substances 0.000 description 1
- 235000000069 L-ascorbic acid Nutrition 0.000 description 1
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 1
- NPPQSCRMBWNHMW-UHFFFAOYSA-N Meprobamate Chemical group NC(=O)OCC(C)(CCC)COC(N)=O NPPQSCRMBWNHMW-UHFFFAOYSA-N 0.000 description 1
- 229920000914 Metallic fiber Polymers 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- BVBSGGBDFJUSIH-UHFFFAOYSA-N Methyl (2-hydroxyphenyl)acetate Chemical compound COC(=O)CC1=CC=CC=C1O BVBSGGBDFJUSIH-UHFFFAOYSA-N 0.000 description 1
- WCQZCKUNZVMBDC-UHFFFAOYSA-N Methyl 2,6-dihydroxybenzoate Chemical compound COC(=O)C1=C(O)C=CC=C1O WCQZCKUNZVMBDC-UHFFFAOYSA-N 0.000 description 1
- 241000237536 Mytilus edulis Species 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 241000500459 Nucella lapillus Species 0.000 description 1
- CGSLYBDCEGBZCG-UHFFFAOYSA-N Octicizer Chemical compound C=1C=CC=CC=1OP(=O)(OCC(CC)CCCC)OC1=CC=CC=C1 CGSLYBDCEGBZCG-UHFFFAOYSA-N 0.000 description 1
- 241000237502 Ostreidae Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 241000199919 Phaeophyceae Species 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- YNPNZTXNASCQKK-UHFFFAOYSA-N Phenanthrene Natural products C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical class CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 241000131858 Siboglinidae Species 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 1
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 1
- FMRLDPWIRHBCCC-UHFFFAOYSA-L Zinc carbonate Chemical compound [Zn+2].[O-]C([O-])=O FMRLDPWIRHBCCC-UHFFFAOYSA-L 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 description 1
- NETCJUNYJCNILL-UHFFFAOYSA-N [2-(2-methoxy-2-oxoethyl)phenyl] 3-chloropropanoate Chemical compound COC(=O)CC1=CC=CC=C1OC(=O)CCCl NETCJUNYJCNILL-UHFFFAOYSA-N 0.000 description 1
- SRKHECKWHLZVOJ-UHFFFAOYSA-N [2-(2-methoxy-2-oxoethyl)phenyl] 4-chlorobutanoate Chemical compound COC(=O)CC1=CC=CC=C1OC(=O)CCCCl SRKHECKWHLZVOJ-UHFFFAOYSA-N 0.000 description 1
- UOIYLUUQRVGBGN-UHFFFAOYSA-N [2-(2-methoxy-2-oxoethyl)phenyl] 5-chloropentanoate Chemical compound COC(=O)CC1=CC=CC=C1OC(=O)CCCCCl UOIYLUUQRVGBGN-UHFFFAOYSA-N 0.000 description 1
- RYIHVCKWWPHXMZ-UHFFFAOYSA-N [2-(hydroxymethyl)-3-(2-sulfanylacetyl)oxy-2-[(2-sulfanylacetyl)oxymethyl]propyl] 2-sulfanylacetate Chemical compound SCC(=O)OCC(CO)(COC(=O)CS)COC(=O)CS RYIHVCKWWPHXMZ-UHFFFAOYSA-N 0.000 description 1
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 description 1
- XRMBQHTWUBGQDN-UHFFFAOYSA-N [2-[2,2-bis(prop-2-enoyloxymethyl)butoxymethyl]-2-(prop-2-enoyloxymethyl)butyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(CC)COCC(CC)(COC(=O)C=C)COC(=O)C=C XRMBQHTWUBGQDN-UHFFFAOYSA-N 0.000 description 1
- VPQCPOIHKPTTPP-UHFFFAOYSA-N [2-formyl-4-(trifluoromethoxy)phenyl] 3-chloropropanoate Chemical compound FC(F)(F)OC1=CC=C(OC(=O)CCCl)C(C=O)=C1 VPQCPOIHKPTTPP-UHFFFAOYSA-N 0.000 description 1
- LBJFOOCLZYBQFT-UHFFFAOYSA-N [2-formyl-4-(trifluoromethoxy)phenyl] 4-chlorobutanoate Chemical compound FC(F)(F)OC1=CC=C(OC(=O)CCCCl)C(C=O)=C1 LBJFOOCLZYBQFT-UHFFFAOYSA-N 0.000 description 1
- RUDUCNPHDIMQCY-UHFFFAOYSA-N [3-(2-sulfanylacetyl)oxy-2,2-bis[(2-sulfanylacetyl)oxymethyl]propyl] 2-sulfanylacetate Chemical compound SCC(=O)OCC(COC(=O)CS)(COC(=O)CS)COC(=O)CS RUDUCNPHDIMQCY-UHFFFAOYSA-N 0.000 description 1
- JOBBTVPTPXRUBP-UHFFFAOYSA-N [3-(3-sulfanylpropanoyloxy)-2,2-bis(3-sulfanylpropanoyloxymethyl)propyl] 3-sulfanylpropanoate Chemical compound SCCC(=O)OCC(COC(=O)CCS)(COC(=O)CCS)COC(=O)CCS JOBBTVPTPXRUBP-UHFFFAOYSA-N 0.000 description 1
- MYYXDCNEQIODGY-UHFFFAOYSA-N [4-(3-ethoxy-3-oxopropyl)-2-nitrophenyl] 4-chlorobutanoate Chemical compound CCOC(=O)CCC1=CC=C(OC(=O)CCCCl)C([N+]([O-])=O)=C1 MYYXDCNEQIODGY-UHFFFAOYSA-N 0.000 description 1
- FXEKREJNXULXRV-UHFFFAOYSA-N [4-(3-ethoxy-3-oxopropyl)-2-nitrophenyl] 5-chloropentanoate Chemical compound CCOC(=O)CCC1=CC=C(OC(=O)CCCCCl)C([N+]([O-])=O)=C1 FXEKREJNXULXRV-UHFFFAOYSA-N 0.000 description 1
- JUIBLDFFVYKUAC-UHFFFAOYSA-N [5-(2-ethylhexanoylperoxy)-2,5-dimethylhexan-2-yl] 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)CCC(C)(C)OOC(=O)C(CC)CCCC JUIBLDFFVYKUAC-UHFFFAOYSA-N 0.000 description 1
- GJHKYCKMHAMZKM-UHFFFAOYSA-N [butyl(dimethyl)silyl] 3-chloropropanoate Chemical compound CCCC[Si](C)(C)OC(=O)CCCl GJHKYCKMHAMZKM-UHFFFAOYSA-N 0.000 description 1
- DVVOEVQHSNXGBO-UHFFFAOYSA-N [butyl(dimethyl)silyl] 4-chlorobutanoate Chemical compound CCCC[Si](C)(C)OC(=O)CCCCl DVVOEVQHSNXGBO-UHFFFAOYSA-N 0.000 description 1
- PENZPMPQLNZKRB-UHFFFAOYSA-N [butyl(dimethyl)silyl] 5-chloropentanoate Chemical compound CCCC[Si](C)(C)OC(=O)CCCCCl PENZPMPQLNZKRB-UHFFFAOYSA-N 0.000 description 1
- CGQRMHRBKQHPGM-UHFFFAOYSA-N [ethyl(dimethyl)silyl] 3-chloropropanoate Chemical compound CC[Si](C)(C)OC(=O)CCCl CGQRMHRBKQHPGM-UHFFFAOYSA-N 0.000 description 1
- SGZOXNHECFEHCY-UHFFFAOYSA-N [ethyl(dimethyl)silyl] 4-chlorobutanoate Chemical compound CC[Si](C)(C)OC(=O)CCCCl SGZOXNHECFEHCY-UHFFFAOYSA-N 0.000 description 1
- BMQWRINKGRDAJP-UHFFFAOYSA-N [ethyl(dimethyl)silyl] 5-chloropentanoate Chemical compound CC[Si](C)(C)OC(=O)CCCCCl BMQWRINKGRDAJP-UHFFFAOYSA-N 0.000 description 1
- HVGHATJZFBLPJX-UHFFFAOYSA-N [tert-butyl(diphenyl)silyl] 2-chloroacetate Chemical compound C=1C=CC=CC=1[Si](OC(=O)CCl)(C(C)(C)C)C1=CC=CC=C1 HVGHATJZFBLPJX-UHFFFAOYSA-N 0.000 description 1
- QNYSVGIHPMVLHO-UHFFFAOYSA-N [tert-butyl(diphenyl)silyl] 3-chloropropanoate Chemical compound C=1C=CC=CC=1[Si](OC(=O)CCCl)(C(C)(C)C)C1=CC=CC=C1 QNYSVGIHPMVLHO-UHFFFAOYSA-N 0.000 description 1
- UCLBTHNJCXQMRG-UHFFFAOYSA-N [tert-butyl(diphenyl)silyl] 4-chlorobutanoate Chemical compound C=1C=CC=CC=1[Si](OC(=O)CCCCl)(C(C)(C)C)C1=CC=CC=C1 UCLBTHNJCXQMRG-UHFFFAOYSA-N 0.000 description 1
- YMUSNNRHLFOQAE-UHFFFAOYSA-N [tert-butyl(diphenyl)silyl] 5-chloropentanoate Chemical compound C=1C=CC=CC=1[Si](OC(=O)CCCCCl)(C(C)(C)C)C1=CC=CC=C1 YMUSNNRHLFOQAE-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical class OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 1
- 150000001279 adipic acids Chemical class 0.000 description 1
- 239000011717 all-trans-retinol Substances 0.000 description 1
- 235000019169 all-trans-retinol Nutrition 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 1
- 229940090948 ammonium benzoate Drugs 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- QBLDFAIABQKINO-UHFFFAOYSA-N barium borate Chemical compound [Ba+2].[O-]B=O.[O-]B=O QBLDFAIABQKINO-UHFFFAOYSA-N 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- FHCIILYMWWRNIZ-UHFFFAOYSA-N benzhydryl(chloro)silane Chemical compound C=1C=CC=CC=1C([SiH2]Cl)C1=CC=CC=C1 FHCIILYMWWRNIZ-UHFFFAOYSA-N 0.000 description 1
- DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical group OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- AOJOEFVRHOZDFN-UHFFFAOYSA-N benzyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC1=CC=CC=C1 AOJOEFVRHOZDFN-UHFFFAOYSA-N 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- SAOKZLXYCUGLFA-UHFFFAOYSA-N bis(2-ethylhexyl) adipate Chemical compound CCCCC(CC)COC(=O)CCCCC(=O)OCC(CC)CCCC SAOKZLXYCUGLFA-UHFFFAOYSA-N 0.000 description 1
- 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 1
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- OCWYEMOEOGEQAN-UHFFFAOYSA-N bumetrizole Chemical compound CC(C)(C)C1=CC(C)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O OCWYEMOEOGEQAN-UHFFFAOYSA-N 0.000 description 1
- BJYPZFUWWJSAKC-ARJAWSKDSA-N but-1-ene-1,2,4-tricarboxylic acid Chemical class OC(=O)CC\C(C(O)=O)=C\C(O)=O BJYPZFUWWJSAKC-ARJAWSKDSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- KDLWFURXIWRTJT-UHFFFAOYSA-N butyl-chloro-di(propan-2-yl)silane Chemical compound CCCC[Si](Cl)(C(C)C)C(C)C KDLWFURXIWRTJT-UHFFFAOYSA-N 0.000 description 1
- MXOSTENCGSDMRE-UHFFFAOYSA-N butyl-chloro-dimethylsilane Chemical compound CCCC[Si](C)(C)Cl MXOSTENCGSDMRE-UHFFFAOYSA-N 0.000 description 1
- 235000019282 butylated hydroxyanisole Nutrition 0.000 description 1
- 229940043253 butylated hydroxyanisole Drugs 0.000 description 1
- CZBZUDVBLSSABA-UHFFFAOYSA-N butylated hydroxyanisole Chemical compound COC1=CC=C(O)C(C(C)(C)C)=C1.COC1=CC=C(O)C=C1C(C)(C)C CZBZUDVBLSSABA-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- 229910001634 calcium fluoride Inorganic materials 0.000 description 1
- FUFJGUQYACFECW-UHFFFAOYSA-L calcium hydrogenphosphate Chemical compound [Ca+2].OP([O-])([O-])=O FUFJGUQYACFECW-UHFFFAOYSA-L 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- 235000012241 calcium silicate Nutrition 0.000 description 1
- DWPDSISGRAWLLV-JHZYRPMRSA-L calcium;(1r,4ar,4br,10ar)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate Chemical compound [Ca+2].C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C([O-])=O.C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C([O-])=O DWPDSISGRAWLLV-JHZYRPMRSA-L 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- WZQSBCHNVPAYOC-UHFFFAOYSA-N chloro(trihexyl)silane Chemical compound CCCCCC[Si](Cl)(CCCCCC)CCCCCC WZQSBCHNVPAYOC-UHFFFAOYSA-N 0.000 description 1
- ZTDOOLPLGSINJS-UHFFFAOYSA-N chloro(tripentyl)silane Chemical compound CCCCC[Si](Cl)(CCCCC)CCCCC ZTDOOLPLGSINJS-UHFFFAOYSA-N 0.000 description 1
- MNKYQPOFRKPUAE-UHFFFAOYSA-N chloro(triphenyl)silane Chemical compound C=1C=CC=CC=1[Si](C=1C=CC=CC=1)(Cl)C1=CC=CC=C1 MNKYQPOFRKPUAE-UHFFFAOYSA-N 0.000 description 1
- ACTAPAGNZPZLEF-UHFFFAOYSA-N chloro(tripropyl)silane Chemical compound CCC[Si](Cl)(CCC)CCC ACTAPAGNZPZLEF-UHFFFAOYSA-N 0.000 description 1
- ITKVLPYNJQOCPW-UHFFFAOYSA-N chloro-(chloromethyl)-dimethylsilane Chemical compound C[Si](C)(Cl)CCl ITKVLPYNJQOCPW-UHFFFAOYSA-N 0.000 description 1
- OIAGZBIVESSKBU-UHFFFAOYSA-N chloro-dicyclohexyl-phenylsilane Chemical compound C1CCCCC1[Si](C=1C=CC=CC=1)(Cl)C1CCCCC1 OIAGZBIVESSKBU-UHFFFAOYSA-N 0.000 description 1
- PQRFRTCWNCVQHI-UHFFFAOYSA-N chloro-dimethyl-(2,3,4,5,6-pentafluorophenyl)silane Chemical compound C[Si](C)(Cl)C1=C(F)C(F)=C(F)C(F)=C1F PQRFRTCWNCVQHI-UHFFFAOYSA-N 0.000 description 1
- WLLRGLQEXSPNJJ-UHFFFAOYSA-N chloro-dimethyl-(4-phenylphenyl)silane Chemical compound C1=CC([Si](C)(Cl)C)=CC=C1C1=CC=CC=C1 WLLRGLQEXSPNJJ-UHFFFAOYSA-N 0.000 description 1
- GZGREZWGCWVAEE-UHFFFAOYSA-N chloro-dimethyl-octadecylsilane Chemical compound CCCCCCCCCCCCCCCCCC[Si](C)(C)Cl GZGREZWGCWVAEE-UHFFFAOYSA-N 0.000 description 1
- KWYZNESIGBQHJK-UHFFFAOYSA-N chloro-dimethyl-phenylsilane Chemical compound C[Si](C)(Cl)C1=CC=CC=C1 KWYZNESIGBQHJK-UHFFFAOYSA-N 0.000 description 1
- AVDUEHWPPXIAEB-UHFFFAOYSA-N chloro-ethyl-dimethylsilane Chemical compound CC[Si](C)(C)Cl AVDUEHWPPXIAEB-UHFFFAOYSA-N 0.000 description 1
- TZPZCTBZJKZFGY-UHFFFAOYSA-N chloro-tris(2-methylpropyl)silane Chemical compound CC(C)C[Si](Cl)(CC(C)C)CC(C)C TZPZCTBZJKZFGY-UHFFFAOYSA-N 0.000 description 1
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 1
- GTZCVFVGUGFEME-IWQZZHSRSA-N cis-aconitic acid Chemical class OC(=O)C\C(C(O)=O)=C\C(O)=O GTZCVFVGUGFEME-IWQZZHSRSA-N 0.000 description 1
- WXZASCSXAMHFCX-PLNGDYQASA-N cis-dihomoaconitic acid Chemical class OC(=O)CCC\C(C(O)=O)=C\C(O)=O WXZASCSXAMHFCX-PLNGDYQASA-N 0.000 description 1
- NGULBISQWGMRGK-WAYWQWQTSA-N cis-trihomoaconitic acid Chemical class OC(=O)CCCC\C(C(O)=O)=C\C(O)=O NGULBISQWGMRGK-WAYWQWQTSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000012718 coordination polymerization Methods 0.000 description 1
- 150000001880 copper compounds Chemical class 0.000 description 1
- 229940120693 copper naphthenate Drugs 0.000 description 1
- YOCUPQPZWBBYIX-UHFFFAOYSA-N copper nickel Chemical compound [Ni].[Cu] YOCUPQPZWBBYIX-UHFFFAOYSA-N 0.000 description 1
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 description 1
- QHNCWVQDOPICKC-UHFFFAOYSA-N copper;1-hydroxypyridine-2-thione Chemical compound [Cu].ON1C=CC=CC1=S.ON1C=CC=CC1=S QHNCWVQDOPICKC-UHFFFAOYSA-N 0.000 description 1
- XDUPUJNNHFTMQS-UHFFFAOYSA-N copper;1-oxidopyridine-2-thione Chemical compound [Cu+2].[O-]N1C=CC=CC1=S.[O-]N1C=CC=CC1=S XDUPUJNNHFTMQS-UHFFFAOYSA-N 0.000 description 1
- RCYPBTYYGICSND-UHFFFAOYSA-L copper;2,3,4,5,6-pentachlorophenolate Chemical compound [Cu+2].[O-]C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl.[O-]C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl RCYPBTYYGICSND-UHFFFAOYSA-L 0.000 description 1
- CSFHHDBCKILMMF-UHFFFAOYSA-N copper;2-nonylphenol Chemical compound [Cu].CCCCCCCCCC1=CC=CC=C1O CSFHHDBCKILMMF-UHFFFAOYSA-N 0.000 description 1
- SEVNKWFHTNVOLD-UHFFFAOYSA-L copper;3-(4-ethylcyclohexyl)propanoate;3-(3-ethylcyclopentyl)propanoate Chemical compound [Cu+2].CCC1CCC(CCC([O-])=O)C1.CCC1CCC(CCC([O-])=O)CC1 SEVNKWFHTNVOLD-UHFFFAOYSA-L 0.000 description 1
- OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 description 1
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 1
- NMCCNOZOBBWFMN-UHFFFAOYSA-N davicil Chemical compound CS(=O)(=O)C1=C(Cl)C(Cl)=NC(Cl)=C1Cl NMCCNOZOBBWFMN-UHFFFAOYSA-N 0.000 description 1
- 125000002704 decyl 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])* 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- AFJWRTVSCGQUON-UHFFFAOYSA-N di(propan-2-yl)silyl 2-chloroacetate Chemical compound CC(C)[SiH](OC(=O)CCl)C(C)C AFJWRTVSCGQUON-UHFFFAOYSA-N 0.000 description 1
- WJXLWOJZWCBOPH-UHFFFAOYSA-N di(propan-2-yl)silyl 3-chloropropanoate Chemical compound CC(C)[SiH](OC(=O)CCCl)C(C)C WJXLWOJZWCBOPH-UHFFFAOYSA-N 0.000 description 1
- CQCXONHEAXVRCF-UHFFFAOYSA-N di(propan-2-yl)silyl 4-chlorobutanoate Chemical compound CC(C)[SiH](OC(=O)CCCCl)C(C)C CQCXONHEAXVRCF-UHFFFAOYSA-N 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- SHFGJEQAOUMGJM-UHFFFAOYSA-N dialuminum dipotassium disodium dioxosilane iron(3+) oxocalcium oxomagnesium oxygen(2-) Chemical compound [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[Na+].[Na+].[Al+3].[Al+3].[K+].[K+].[Fe+3].[Fe+3].O=[Mg].O=[Ca].O=[Si]=O SHFGJEQAOUMGJM-UHFFFAOYSA-N 0.000 description 1
- 229960002380 dibutyl phthalate Drugs 0.000 description 1
- 235000019700 dicalcium phosphate Nutrition 0.000 description 1
- FBCCMZVIWNDFMO-UHFFFAOYSA-N dichloroacetyl chloride Chemical compound ClC(Cl)C(Cl)=O FBCCMZVIWNDFMO-UHFFFAOYSA-N 0.000 description 1
- UGMCXQCYOVCMTB-UHFFFAOYSA-K dihydroxy(stearato)aluminium Chemical compound CCCCCCCCCCCCCCCCCC(=O)O[Al](O)O UGMCXQCYOVCMTB-UHFFFAOYSA-K 0.000 description 1
- 229940031769 diisobutyl adipate Drugs 0.000 description 1
- CXLDEBSPHFAHOR-UHFFFAOYSA-N dimethylsilyl 2-chlorobutanoate Chemical compound C(C)C(C(=O)O[SiH](C)C)Cl CXLDEBSPHFAHOR-UHFFFAOYSA-N 0.000 description 1
- YNSQGRLOSACKGB-UHFFFAOYSA-N dimethylsilyl 2-chlorohexanoate Chemical compound C(CCC)C(C(=O)O[SiH](C)C)Cl YNSQGRLOSACKGB-UHFFFAOYSA-N 0.000 description 1
- DROMNWUQASBTFM-UHFFFAOYSA-N dinonyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCC DROMNWUQASBTFM-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000003974 emollient agent Substances 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical class NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 description 1
- BLCTWBJQROOONQ-UHFFFAOYSA-N ethenyl prop-2-enoate Chemical compound C=COC(=O)C=C BLCTWBJQROOONQ-UHFFFAOYSA-N 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- KBPUBCVJHFXPOC-UHFFFAOYSA-N ethyl 3,4-dihydroxybenzoate Chemical compound CCOC(=O)C1=CC=C(O)C(O)=C1 KBPUBCVJHFXPOC-UHFFFAOYSA-N 0.000 description 1
- VHQUFYWRLCBLRS-UHFFFAOYSA-N ethyl 3-(4-chlorobutanoyloxy)-4-hydroxybenzoate Chemical compound CCOC(=O)C1=CC=C(O)C(OC(=O)CCCCl)=C1 VHQUFYWRLCBLRS-UHFFFAOYSA-N 0.000 description 1
- MBGHJGVNPBUZSI-UHFFFAOYSA-N ethyl 3-(4-hydroxy-3-nitrophenyl)propanoate Chemical compound CCOC(=O)CCC1=CC=C(O)C([N+]([O-])=O)=C1 MBGHJGVNPBUZSI-UHFFFAOYSA-N 0.000 description 1
- OSUFVKHZABKAPS-UHFFFAOYSA-N ethyl 3-(5-chloropentanoyloxy)-4-hydroxybenzoate Chemical compound CCOC(=O)C1=CC=C(O)C(OC(=O)CCCCCl)=C1 OSUFVKHZABKAPS-UHFFFAOYSA-N 0.000 description 1
- UGJCKZNQBKHYEV-UHFFFAOYSA-N ethyl 3-[4-(3-chloropropanoyloxy)-3-nitrophenyl]propanoate Chemical compound CCOC(=O)CCC1=CC=C(OC(=O)CCCl)C([N+]([O-])=O)=C1 UGJCKZNQBKHYEV-UHFFFAOYSA-N 0.000 description 1
- MOJIORPJBWMKKV-UHFFFAOYSA-N ethyl 4-(3-chloropropanoyloxy)-3-methoxybenzoate Chemical compound CCOC(=O)C1=CC=C(OC(=O)CCCl)C(OC)=C1 MOJIORPJBWMKKV-UHFFFAOYSA-N 0.000 description 1
- BRNNDSGTLVMMTO-UHFFFAOYSA-N ethyl 4-(4-chlorobutanoyloxy)-3-methoxybenzoate Chemical compound CCOC(=O)C1=CC=C(OC(=O)CCCCl)C(OC)=C1 BRNNDSGTLVMMTO-UHFFFAOYSA-N 0.000 description 1
- PTQPGPNBIHYHRS-UHFFFAOYSA-N ethyl 4-(5-chloropentanoyloxy)-3-methoxybenzoate Chemical compound CCOC(=O)C1=CC=C(OC(=O)CCCCCl)C(OC)=C1 PTQPGPNBIHYHRS-UHFFFAOYSA-N 0.000 description 1
- ZJXZSIYSNXKHEA-UHFFFAOYSA-N ethyl dihydrogen phosphate Chemical compound CCOP(O)(O)=O ZJXZSIYSNXKHEA-UHFFFAOYSA-N 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- RAQDACVRFCEPDA-UHFFFAOYSA-L ferrous carbonate Chemical compound [Fe+2].[O-]C([O-])=O RAQDACVRFCEPDA-UHFFFAOYSA-L 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 150000002311 glutaric acids Chemical class 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 229960001867 guaiacol Drugs 0.000 description 1
- 150000002357 guanidines Chemical class 0.000 description 1
- 229940083094 guanine derivative acting on arteriolar smooth muscle Drugs 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- PZDUWXKXFAIFOR-UHFFFAOYSA-N hexadecyl prop-2-enoate Chemical compound CCCCCCCCCCCCCCCCOC(=O)C=C PZDUWXKXFAIFOR-UHFFFAOYSA-N 0.000 description 1
- LNCPIMCVTKXXOY-UHFFFAOYSA-N hexyl 2-methylprop-2-enoate Chemical compound CCCCCCOC(=O)C(C)=C LNCPIMCVTKXXOY-UHFFFAOYSA-N 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- LNMQRPPRQDGUDR-UHFFFAOYSA-N hexyl prop-2-enoate Chemical compound CCCCCCOC(=O)C=C LNMQRPPRQDGUDR-UHFFFAOYSA-N 0.000 description 1
- 229920006270 hydrocarbon resin Polymers 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 238000012690 ionic polymerization Methods 0.000 description 1
- HDHLIWCXDDZUFH-UHFFFAOYSA-N irgarol 1051 Chemical compound CC(C)(C)NC1=NC(SC)=NC(NC2CC2)=N1 HDHLIWCXDDZUFH-UHFFFAOYSA-N 0.000 description 1
- 229940087654 iron carbonyl Drugs 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical class OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 230000001665 lethal effect Effects 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 description 1
- 239000011656 manganese carbonate Substances 0.000 description 1
- 235000006748 manganese carbonate Nutrition 0.000 description 1
- 229940093474 manganese carbonate Drugs 0.000 description 1
- 150000002697 manganese compounds Chemical class 0.000 description 1
- 229910000016 manganese(II) carbonate Inorganic materials 0.000 description 1
- XMWCXZJXESXBBY-UHFFFAOYSA-L manganese(ii) carbonate Chemical compound [Mn+2].[O-]C([O-])=O XMWCXZJXESXBBY-UHFFFAOYSA-L 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- LZZSGTBHLJJLPU-UHFFFAOYSA-N methyl 2-(3-chloropropanoyloxy)benzoate Chemical compound COC(=O)C1=CC=CC=C1OC(=O)CCCl LZZSGTBHLJJLPU-UHFFFAOYSA-N 0.000 description 1
- GZCVEZGVAJVHSL-UHFFFAOYSA-N methyl 2-(4-chlorobutanoyloxy)-6-hydroxybenzoate Chemical compound COC(=O)C1=C(O)C=CC=C1OC(=O)CCCCl GZCVEZGVAJVHSL-UHFFFAOYSA-N 0.000 description 1
- SLXZLZBPKLCCMQ-UHFFFAOYSA-N methyl 2-(4-chlorobutanoyloxy)benzoate Chemical compound COC(=O)C1=CC=CC=C1OC(=O)CCCCl SLXZLZBPKLCCMQ-UHFFFAOYSA-N 0.000 description 1
- PFYFRADYAUSFGQ-UHFFFAOYSA-N methyl 2-(5-chloropentanoyloxy)-6-hydroxybenzoate Chemical compound COC(=O)C1=C(O)C=CC=C1OC(=O)CCCCCl PFYFRADYAUSFGQ-UHFFFAOYSA-N 0.000 description 1
- BZAKTFKDXOUMHG-UHFFFAOYSA-N methyl 2-(5-chloropentanoyloxy)benzoate Chemical compound COC(=O)C1=CC=CC=C1OC(=O)CCCCCl BZAKTFKDXOUMHG-UHFFFAOYSA-N 0.000 description 1
- VAVJIMJRVMZXGD-UHFFFAOYSA-N methyl 4-(3-chloropropanoyloxy)-3-nitrobenzoate Chemical compound COC(=O)C1=CC=C(OC(=O)CCCl)C([N+]([O-])=O)=C1 VAVJIMJRVMZXGD-UHFFFAOYSA-N 0.000 description 1
- FAQACBXNWOYGNK-UHFFFAOYSA-N methyl 4-(3-chloropropanoyloxy)benzoate Chemical compound COC(=O)C1=CC=C(OC(=O)CCCl)C=C1 FAQACBXNWOYGNK-UHFFFAOYSA-N 0.000 description 1
- ZOOPRPVHGDHFQI-UHFFFAOYSA-N methyl 4-(4-chlorobutanoyloxy)benzoate Chemical compound COC(=O)C1=CC=C(OC(=O)CCCCl)C=C1 ZOOPRPVHGDHFQI-UHFFFAOYSA-N 0.000 description 1
- PSOBOTNGIGYKIF-UHFFFAOYSA-N methyl 4-(5-chloropentanoyloxy)benzoate Chemical compound COC(=O)C1=CC=C(OC(=O)CCCCCl)C=C1 PSOBOTNGIGYKIF-UHFFFAOYSA-N 0.000 description 1
- GNCWCTBHZCBXGL-UHFFFAOYSA-N methyl 4-hydroxy-3-nitrobenzoate Chemical compound COC(=O)C1=CC=C(O)C([N+]([O-])=O)=C1 GNCWCTBHZCBXGL-UHFFFAOYSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 1
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000002557 mineral fiber Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 235000020638 mussel Nutrition 0.000 description 1
- ZQXSMRAEXCEDJD-UHFFFAOYSA-N n-ethenylformamide Chemical compound C=CNC=O ZQXSMRAEXCEDJD-UHFFFAOYSA-N 0.000 description 1
- SWPMNMYLORDLJE-UHFFFAOYSA-N n-ethylprop-2-enamide Chemical compound CCNC(=O)C=C SWPMNMYLORDLJE-UHFFFAOYSA-N 0.000 description 1
- YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 description 1
- WDFKEEALECCKTJ-UHFFFAOYSA-N n-propylprop-2-enamide Chemical compound CCCNC(=O)C=C WDFKEEALECCKTJ-UHFFFAOYSA-N 0.000 description 1
- 125000005609 naphthenate group Chemical group 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 231100001160 nonlethal Toxicity 0.000 description 1
- 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 1
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 1
- 125000005474 octanoate group Chemical group 0.000 description 1
- 125000002347 octyl 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])[H] 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- JJVNINGBHGBWJH-UHFFFAOYSA-N ortho-vanillin Chemical compound COC1=CC=CC(C=O)=C1O JJVNINGBHGBWJH-UHFFFAOYSA-N 0.000 description 1
- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 description 1
- 235000020636 oyster Nutrition 0.000 description 1
- UVBBCQLPTZEDHT-UHFFFAOYSA-N pent-4-en-1-amine Chemical compound NCCCC=C UVBBCQLPTZEDHT-UHFFFAOYSA-N 0.000 description 1
- GYDSPAVLTMAXHT-UHFFFAOYSA-N pentyl 2-methylprop-2-enoate Chemical compound CCCCCOC(=O)C(C)=C GYDSPAVLTMAXHT-UHFFFAOYSA-N 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- ULDDEWDFUNBUCM-UHFFFAOYSA-N pentyl prop-2-enoate Chemical compound CCCCCOC(=O)C=C ULDDEWDFUNBUCM-UHFFFAOYSA-N 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- QIWKUEJZZCOPFV-UHFFFAOYSA-N phenyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1=CC=CC=C1 QIWKUEJZZCOPFV-UHFFFAOYSA-N 0.000 description 1
- WRAQQYDMVSCOTE-UHFFFAOYSA-N phenyl prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1 WRAQQYDMVSCOTE-UHFFFAOYSA-N 0.000 description 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical compound CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 description 1
- MWTVMRXEOFAHOP-UHFFFAOYSA-N propan-2-yl 4-(4-chlorobutanoyloxy)benzoate Chemical compound CC(C)OC(=O)C1=CC=C(OC(=O)CCCCl)C=C1 MWTVMRXEOFAHOP-UHFFFAOYSA-N 0.000 description 1
- XRJCXQVSAMZHKQ-UHFFFAOYSA-N propan-2-yl 4-(5-chloropentanoyloxy)benzoate Chemical compound CC(C)OC(=O)C1=CC=C(OC(=O)CCCCCl)C=C1 XRJCXQVSAMZHKQ-UHFFFAOYSA-N 0.000 description 1
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
- FOKZHJCFBNVOAV-UHFFFAOYSA-N propyl 2-hydroxy-3-phenoxyprop-2-enoate Chemical compound CCCOC(=O)C(O)=COC1=CC=CC=C1 FOKZHJCFBNVOAV-UHFFFAOYSA-N 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- DHMFBGFMKCGMKL-UHFFFAOYSA-N propyl 4-(3-chloropropanoyloxy)benzoate Chemical compound CCCOC(=O)C1=CC=C(OC(=O)CCCl)C=C1 DHMFBGFMKCGMKL-UHFFFAOYSA-N 0.000 description 1
- KBBBOQGIMVSZIU-UHFFFAOYSA-N propyl 4-(4-chlorobutanoyloxy)benzoate Chemical compound CCCOC(=O)C1=CC=C(OC(=O)CCCCl)C=C1 KBBBOQGIMVSZIU-UHFFFAOYSA-N 0.000 description 1
- HFTGQIZHMVZYKM-UHFFFAOYSA-N propyl 4-(5-chloropentanoyloxy)benzoate Chemical compound CCCOC(=O)C1=CC=C(OC(=O)CCCCCl)C=C1 HFTGQIZHMVZYKM-UHFFFAOYSA-N 0.000 description 1
- 239000000473 propyl gallate Substances 0.000 description 1
- 235000010388 propyl gallate Nutrition 0.000 description 1
- 229940075579 propyl gallate Drugs 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 1
- WJSXSXUHWBSPEP-UHFFFAOYSA-N pyridine;triphenylborane Chemical compound C1=CC=NC=C1.C1=CC=CC=C1B(C=1C=CC=CC=1)C1=CC=CC=C1 WJSXSXUHWBSPEP-UHFFFAOYSA-N 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 1
- SMQUZDBALVYZAC-UHFFFAOYSA-N salicylaldehyde Chemical compound OC1=CC=CC=C1C=O SMQUZDBALVYZAC-UHFFFAOYSA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 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
- 230000035945 sensitivity Effects 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 229910001923 silver oxide Inorganic materials 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- SONHXMAHPHADTF-UHFFFAOYSA-M sodium;2-methylprop-2-enoate Chemical compound [Na+].CC(=C)C([O-])=O SONHXMAHPHADTF-UHFFFAOYSA-M 0.000 description 1
- 239000008347 soybean phospholipid Substances 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 235000011044 succinic acid Nutrition 0.000 description 1
- 150000003444 succinic acids Chemical class 0.000 description 1
- NVBFHJWHLNUMCV-UHFFFAOYSA-N sulfamide Chemical compound NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 description 1
- 150000003450 sulfenic acids Chemical class 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- KXYJPVZMZBJJBZ-UHFFFAOYSA-N tert-butyl 2-ethylbutaneperoxoate Chemical compound CCC(CC)C(=O)OOC(C)(C)C KXYJPVZMZBJJBZ-UHFFFAOYSA-N 0.000 description 1
- WYKYCHHWIJXDAO-UHFFFAOYSA-N tert-butyl 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)C WYKYCHHWIJXDAO-UHFFFAOYSA-N 0.000 description 1
- SJMYWORNLPSJQO-UHFFFAOYSA-N tert-butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)(C)C SJMYWORNLPSJQO-UHFFFAOYSA-N 0.000 description 1
- RJSZFSOFYVMDIC-UHFFFAOYSA-N tert-butyl n,n-dimethylcarbamate Chemical compound CN(C)C(=O)OC(C)(C)C RJSZFSOFYVMDIC-UHFFFAOYSA-N 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- MHYGQXWCZAYSLJ-UHFFFAOYSA-N tert-butyl-chloro-diphenylsilane Chemical compound C=1C=CC=CC=1[Si](Cl)(C(C)(C)C)C1=CC=CC=C1 MHYGQXWCZAYSLJ-UHFFFAOYSA-N 0.000 description 1
- BCNZYOJHNLTNEZ-UHFFFAOYSA-N tert-butyldimethylsilyl chloride Chemical compound CC(C)(C)[Si](C)(C)Cl BCNZYOJHNLTNEZ-UHFFFAOYSA-N 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 235000019149 tocopherols Nutrition 0.000 description 1
- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 description 1
- GTZCVFVGUGFEME-HNQUOIGGSA-N trans-aconitic acid Chemical class OC(=O)C\C(C(O)=O)=C/C(O)=O GTZCVFVGUGFEME-HNQUOIGGSA-N 0.000 description 1
- DOVSWWRKFANNHT-UHFFFAOYSA-N tri(butan-2-yl)-chlorosilane Chemical compound CCC(C)[Si](Cl)(C(C)CC)C(C)CC DOVSWWRKFANNHT-UHFFFAOYSA-N 0.000 description 1
- VYCNEZZEYGLYMC-UHFFFAOYSA-N tri(butan-2-yl)silyl 3-chloropropanoate Chemical compound CCC(C)[Si](C(C)CC)(C(C)CC)OC(=O)CCCl VYCNEZZEYGLYMC-UHFFFAOYSA-N 0.000 description 1
- CNKRMIWEJYVMQG-UHFFFAOYSA-N tri(butan-2-yl)silyl 4-chlorobutanoate Chemical compound CCC(C)[Si](C(C)CC)(C(C)CC)OC(=O)CCCCl CNKRMIWEJYVMQG-UHFFFAOYSA-N 0.000 description 1
- MPQGCILYACORHR-UHFFFAOYSA-N tri(butan-2-yl)silyl 5-chloropentanoate Chemical compound CCC(C)[Si](C(C)CC)(C(C)CC)OC(=O)CCCCCl MPQGCILYACORHR-UHFFFAOYSA-N 0.000 description 1
- GQEGXEQSUSXNIL-UHFFFAOYSA-N tri(propan-2-yl)silyl 3-chloropropanoate Chemical compound CC(C)[Si](C(C)C)(C(C)C)OC(=O)CCCl GQEGXEQSUSXNIL-UHFFFAOYSA-N 0.000 description 1
- NOQBGTVRGVVWRS-UHFFFAOYSA-N tri(propan-2-yl)silyl 4-chlorobutanoate Chemical compound CC(C)[Si](C(C)C)(C(C)C)OC(=O)CCCCl NOQBGTVRGVVWRS-UHFFFAOYSA-N 0.000 description 1
- NKCFAUQQNVZRSI-UHFFFAOYSA-N tri(propan-2-yl)silyl 5-chloropentanoate Chemical compound CC(C)[Si](C(C)C)(C(C)C)OC(=O)CCCCCl NKCFAUQQNVZRSI-UHFFFAOYSA-N 0.000 description 1
- UTXPCJHKADAFBB-UHFFFAOYSA-N tribenzyl(chloro)silane Chemical compound C=1C=CC=CC=1C[Si](CC=1C=CC=CC=1)(Cl)CC1=CC=CC=C1 UTXPCJHKADAFBB-UHFFFAOYSA-N 0.000 description 1
- MHBZWBDYKJYQIB-UHFFFAOYSA-N tribenzylsilyl 3-chloropropanoate Chemical compound C=1C=CC=CC=1C[Si](CC=1C=CC=CC=1)(OC(=O)CCCl)CC1=CC=CC=C1 MHBZWBDYKJYQIB-UHFFFAOYSA-N 0.000 description 1
- AKIAUQPQNDVOID-UHFFFAOYSA-N tribenzylsilyl 5-chloropentanoate Chemical compound C=1C=CC=CC=1C[Si](CC=1C=CC=CC=1)(OC(=O)CCCCCl)CC1=CC=CC=C1 AKIAUQPQNDVOID-UHFFFAOYSA-N 0.000 description 1
- JSQJUDVTRRCSRU-UHFFFAOYSA-N tributyl(chloro)silane Chemical compound CCCC[Si](Cl)(CCCC)CCCC JSQJUDVTRRCSRU-UHFFFAOYSA-N 0.000 description 1
- OBUTZZMHCYDDKC-UHFFFAOYSA-N tributylsilyl 3-chloropropanoate Chemical compound CCCC[Si](CCCC)(CCCC)OC(=O)CCCl OBUTZZMHCYDDKC-UHFFFAOYSA-N 0.000 description 1
- HPMNSBGNJZWFQO-UHFFFAOYSA-N tributylsilyl 4-chlorobutanoate Chemical compound CCCC[Si](CCCC)(CCCC)OC(=O)CCCCl HPMNSBGNJZWFQO-UHFFFAOYSA-N 0.000 description 1
- YULWNPBXUOXGFC-UHFFFAOYSA-N tributylsilyl 5-chloropentanoate Chemical compound CCCC[Si](CCCC)(CCCC)OC(=O)CCCCCl YULWNPBXUOXGFC-UHFFFAOYSA-N 0.000 description 1
- PIILXFBHQILWPS-UHFFFAOYSA-N tributyltin Chemical compound CCCC[Sn](CCCC)CCCC PIILXFBHQILWPS-UHFFFAOYSA-N 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- PVFOMCVHYWHZJE-UHFFFAOYSA-N trichloroacetyl chloride Chemical compound ClC(=O)C(Cl)(Cl)Cl PVFOMCVHYWHZJE-UHFFFAOYSA-N 0.000 description 1
- KEROTHRUZYBWCY-UHFFFAOYSA-N tridecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCOC(=O)C(C)=C KEROTHRUZYBWCY-UHFFFAOYSA-N 0.000 description 1
- DQWPFSLDHJDLRL-UHFFFAOYSA-N triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 description 1
- PNFCORTXCSHISC-UHFFFAOYSA-N triethylsilyl 3-chloropropanoate Chemical compound CC[Si](CC)(CC)OC(=O)CCCl PNFCORTXCSHISC-UHFFFAOYSA-N 0.000 description 1
- BXPORHIGYLCNAO-UHFFFAOYSA-N triethylsilyl 4-chlorobutanoate Chemical compound CC[Si](CC)(CC)OC(=O)CCCCl BXPORHIGYLCNAO-UHFFFAOYSA-N 0.000 description 1
- BDKLXDPWYFBKRO-UHFFFAOYSA-N triethylsilyl 5-chloropentanoate Chemical compound CC[Si](CC)(CC)OC(=O)CCCCCl BDKLXDPWYFBKRO-UHFFFAOYSA-N 0.000 description 1
- PNQBEPDZQUOCNY-UHFFFAOYSA-N trifluoroacetyl chloride Chemical compound FC(F)(F)C(Cl)=O PNQBEPDZQUOCNY-UHFFFAOYSA-N 0.000 description 1
- SKSAIOTZDFGRPS-UHFFFAOYSA-N trihexylsilyl 3-chloropropanoate Chemical compound CCCCCC[Si](CCCCCC)(CCCCCC)OC(=O)CCCl SKSAIOTZDFGRPS-UHFFFAOYSA-N 0.000 description 1
- CWXRXVOILYJOKW-UHFFFAOYSA-N trihexylsilyl 4-chlorobutanoate Chemical compound CCCCCC[Si](CCCCCC)(CCCCCC)OC(=O)CCCCl CWXRXVOILYJOKW-UHFFFAOYSA-N 0.000 description 1
- JUNPGQVDQNBHHU-UHFFFAOYSA-N trihexylsilyl 5-chloropentanoate Chemical compound CCCCCC[Si](CCCCCC)(CCCCCC)OC(=O)CCCCCl JUNPGQVDQNBHHU-UHFFFAOYSA-N 0.000 description 1
- 229940096522 trimethylolpropane triacrylate Drugs 0.000 description 1
- GMRJMUHIFLXPBH-UHFFFAOYSA-N trimethylsilyl 3-chloropropanoate Chemical compound C[Si](C)(C)OC(=O)CCCl GMRJMUHIFLXPBH-UHFFFAOYSA-N 0.000 description 1
- JUNDFMYCRYPIIW-UHFFFAOYSA-N trimethylsilyl 4-chlorobutanoate Chemical compound C[Si](C)(C)OC(=O)CCCCl JUNDFMYCRYPIIW-UHFFFAOYSA-N 0.000 description 1
- ZCEGENDZAOAARN-UHFFFAOYSA-N trimethylsilyl 5-chloropentanoate Chemical compound C[Si](C)(C)OC(=O)CCCCCl ZCEGENDZAOAARN-UHFFFAOYSA-N 0.000 description 1
- FRLSTDQHYQGLQR-UHFFFAOYSA-N trioctylsilyl 2-chloroacetate Chemical compound CCCCCCCC[Si](CCCCCCCC)(CCCCCCCC)OC(=O)CCl FRLSTDQHYQGLQR-UHFFFAOYSA-N 0.000 description 1
- WYBRDPFQNLRWQR-UHFFFAOYSA-N trioctylsilyl 4-chlorobutanoate Chemical compound CCCCCCCC[Si](CCCCCCCC)(CCCCCCCC)OC(=O)CCCCl WYBRDPFQNLRWQR-UHFFFAOYSA-N 0.000 description 1
- NTMVQXUJGMRKOX-UHFFFAOYSA-N trioctylsilyl 5-chloropentanoate Chemical compound CCCCCCCC[Si](CCCCCCCC)(CCCCCCCC)OC(=O)CCCCCl NTMVQXUJGMRKOX-UHFFFAOYSA-N 0.000 description 1
- DOQRZCPSLCGPJQ-UHFFFAOYSA-N tripentylsilyl 3-chloropropanoate Chemical compound CCCCC[Si](CCCCC)(CCCCC)OC(=O)CCCl DOQRZCPSLCGPJQ-UHFFFAOYSA-N 0.000 description 1
- PKYXJIKDINJWIP-UHFFFAOYSA-N tripentylsilyl 4-chlorobutanoate Chemical compound CCCCC[Si](CCCCC)(CCCCC)OC(=O)CCCCl PKYXJIKDINJWIP-UHFFFAOYSA-N 0.000 description 1
- QOUKYAPPBUVQGG-UHFFFAOYSA-N tripentylsilyl 5-chloropentanoate Chemical compound CCCCC[Si](CCCCC)(CCCCC)OC(=O)CCCCCl QOUKYAPPBUVQGG-UHFFFAOYSA-N 0.000 description 1
- LNWMJYACVPQWES-UHFFFAOYSA-N triphenylsilyl 2-chloroacetate Chemical compound C=1C=CC=CC=1[Si](C=1C=CC=CC=1)(OC(=O)CCl)C1=CC=CC=C1 LNWMJYACVPQWES-UHFFFAOYSA-N 0.000 description 1
- FPBJFPOCVTWZHM-UHFFFAOYSA-N triphenylsilyl 3-chloropropanoate Chemical compound C=1C=CC=CC=1[Si](C=1C=CC=CC=1)(OC(=O)CCCl)C1=CC=CC=C1 FPBJFPOCVTWZHM-UHFFFAOYSA-N 0.000 description 1
- ICRWCXGYCJPMET-UHFFFAOYSA-N triphenylsilyl 4-chlorobutanoate Chemical compound C=1C=CC=CC=1[Si](C=1C=CC=CC=1)(OC(=O)CCCCl)C1=CC=CC=C1 ICRWCXGYCJPMET-UHFFFAOYSA-N 0.000 description 1
- USPMKDKTFOZZQH-UHFFFAOYSA-N triphenylsilyl 5-chloropentanoate Chemical compound C=1C=CC=CC=1[Si](C=1C=CC=CC=1)(OC(=O)CCCCCl)C1=CC=CC=C1 USPMKDKTFOZZQH-UHFFFAOYSA-N 0.000 description 1
- PXNHFAOATHAJJQ-UHFFFAOYSA-N tripropylsilyl 4-chlorobutanoate Chemical compound CCC[Si](CCC)(CCC)OC(=O)CCCCl PXNHFAOATHAJJQ-UHFFFAOYSA-N 0.000 description 1
- CZAVRTZRQWOGAC-UHFFFAOYSA-N tripropylsilyl 5-chloropentanoate Chemical compound CCC[Si](CCC)(CCC)OC(=O)CCCCCl CZAVRTZRQWOGAC-UHFFFAOYSA-N 0.000 description 1
- WTLBZVNBAKMVDP-UHFFFAOYSA-N tris(2-butoxyethyl) phosphate Chemical compound CCCCOCCOP(=O)(OCCOCCCC)OCCOCCCC WTLBZVNBAKMVDP-UHFFFAOYSA-N 0.000 description 1
- HWAFFSIUXMYZKB-UHFFFAOYSA-N tris(2-methylpropyl)silyl 3-chloropropanoate Chemical compound CC(C)C[Si](CC(C)C)(CC(C)C)OC(=O)CCCl HWAFFSIUXMYZKB-UHFFFAOYSA-N 0.000 description 1
- KRSLTEQJLPSDST-UHFFFAOYSA-N tris(2-methylpropyl)silyl 5-chloropentanoate Chemical compound CC(C)C[Si](CC(C)C)(CC(C)C)OC(=O)CCCCCl KRSLTEQJLPSDST-UHFFFAOYSA-N 0.000 description 1
- ZTAUIWXDRLLHJK-UHFFFAOYSA-N tris(3-methylbutyl)silyl 3-chloropropanoate Chemical compound CC(C)CC[Si](CCC(C)C)(CCC(C)C)OC(=O)CCCl ZTAUIWXDRLLHJK-UHFFFAOYSA-N 0.000 description 1
- RDWUMFKSKLTLDX-UHFFFAOYSA-N tris(3-methylbutyl)silyl 4-chlorobutanoate Chemical compound CC(C)CC[Si](CCC(C)C)(CCC(C)C)OC(=O)CCCCl RDWUMFKSKLTLDX-UHFFFAOYSA-N 0.000 description 1
- GZWKQHNJAUJYTC-UHFFFAOYSA-N tris(3-methylbutyl)silyl 5-chloropentanoate Chemical compound CC(C)CC[Si](CCC(C)C)(CCC(C)C)OC(=O)CCCCCl GZWKQHNJAUJYTC-UHFFFAOYSA-N 0.000 description 1
- DJECDCLXTNZYDL-UHFFFAOYSA-N tritert-butyl(chloro)silane Chemical compound CC(C)(C)[Si](Cl)(C(C)(C)C)C(C)(C)C DJECDCLXTNZYDL-UHFFFAOYSA-N 0.000 description 1
- LDWABGLTLCAXKI-UHFFFAOYSA-N tritert-butylsilyl 4-chlorobutanoate Chemical compound CC(C)(C)[Si](C(C)(C)C)(C(C)(C)C)OC(=O)CCCCl LDWABGLTLCAXKI-UHFFFAOYSA-N 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 235000010493 xanthan gum Nutrition 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
- 239000011787 zinc oxide Substances 0.000 description 1
- 229940043810 zinc pyrithione Drugs 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- NDKWCCLKSWNDBG-UHFFFAOYSA-N zinc;dioxido(dioxo)chromium Chemical compound [Zn+2].[O-][Cr]([O-])(=O)=O NDKWCCLKSWNDBG-UHFFFAOYSA-N 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/16—Antifouling paints; Underwater paints
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1896—Compounds having one or more Si-O-acyl linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/52—Esters of acyclic unsaturated carboxylic acids having the esterified carboxyl group bound to an acyclic carbon atom
- C07C69/533—Monocarboxylic acid esters having only one carbon-to-carbon double bond
- C07C69/54—Acrylic acid esters; Methacrylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/67—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/14—Methyl esters, e.g. methyl (meth)acrylate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D133/00—Coating compositions based on 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 only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D143/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing boron, silicon, phosphorus, selenium, tellurium, or a metal; Coating compositions based on derivatives of such polymers
- C09D143/04—Homopolymers or copolymers of monomers containing silicon
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/16—Antifouling paints; Underwater paints
- C09D5/1656—Antifouling paints; Underwater paints characterised by the film-forming substance
- C09D5/1662—Synthetic film-forming substance
- C09D5/1668—Vinyl-type polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F220/28—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
- C08F220/281—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety and containing only one oxygen, e.g. furfuryl (meth)acrylate or 2-methoxyethyl (meth)acrylate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F220/28—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
- C08F220/283—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety and containing one or more carboxylic moiety in the chain, e.g. acetoacetoxyethyl(meth)acrylate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L43/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing boron, silicon, phosphorus, selenium, tellurium or a metal; Compositions of derivatives of such polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Paints Or Removers (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Adhesive Tapes (AREA)
Abstract
Vannuløselig, vanneroderbar, filmdannende polymer for begroingshindrende maling som omfatter gjentatte enheter svarende til monomerer A og B: A) 2-95 mol% monomerer med formelen hvor n er et heltall fra 1 til 4, X er H eller CH, Y er H eller eventuelt forestret COOH gruppe, Rer Ph(R)-C(0)Reller -Si(R), m er et heltall fra 1 til 3, R, som er like eller forskjellige, er valgt fra -C(0)H, C(0)R, COOR, CH2COOR7 d.alkyl, Calkanoyl, halogen, nitro, OH og OR, Rer valgt fra substituert eller usubstituert alkyl, aryl, aralkyl og heterocyklyl, 4R ,som er like eller forskjellige, er valgt fra substituert eller usubstituert C_alkyl, C.aryl, Ci_20 alkoksy og C.aryloksy, og R,,og Rer uavhengig valgt fra substituert eller usubstituert Ci_2oalkyl og C5.2o aryl, og B) 5-98 mol% andre vinyl polymeriserbare monomerer.
Description
Bakgrunn
Overflater som er nedsenket i sjøvann begros av marine organismer som grønnalger, brunalger, rur, blåskjell, rørormer og liknende. På marine konstruksjoner som skip, oljeplattformer, bøyer osv. kan denne begroing medføre økt belastning og akselerert korrosjon. På fartøyer vil begroing føre til redusert manøvrerbarhet samt gi økt friksjon som igjen medfører redusert hastighet og økt drivstofforbruk.
For å forhindre avsetning og vekst av slike marine organismer brukes belegg
kjent som begroingshindrende malinger. Disse malingene består vanligvis av et filmdannende bindemiddel med eller uten biologisk aktivitet sammen med ulike komponenter som for eksempel pigmenter, fyllstoffer, løsningsmidler og biologisk aktive stoffer.
Av de begroingshindrende malingtypene som har vært i bruk de senere år er selvpolerende begroingshindrende malinger som inneholder organotinnpolymerer blitt anvendt i stor utstrekning. Denne typer malinger er for eksempel beskrevet i GB1457590 og GB2152947. Suksessen til de selvpolerende triorganotinnholdige malingene skyldes at organotinnpolymeren i malingoverflaten hydrolyserer i sjøvann og dermed frigjøres triorganotinnforbindelser som er meget effektive biologisk aktive forbindelser. Den gjenværende polymeren på overflaten blir hydrofil og dermed eroderbar slik at den blir selvpolerende. Denne selvpolerende effekten gir kontrollert utlekking av den biologisk aktive forbindelsen og bidrar til å gi en jevn overflate som medfører redusert friksjon mellom skip (marin konstruksjon) og vann.
Det har i de senere år vært fokusert på miljøeffektene ved bruk av triorganotinnforbindelser. Man har sett at organotinn-gruppene som frigis ved hydrolyse, spesielt tribulyltinn, brytes langsomt ned og det fører til en akkumulering i sedimentene i lokaliserte områder. I tillegg har man sett at noen organismer har vist ekstrem følsomhet overfor disse forbindelsene, og dette har ført til flere ikke-dødelige effekter som imposex i sneglen Nucella lapillus og økt tykkelse på østers skall som for eksempel hos Crassostrea gigas.
International Maritime Organization (IMO) har vedtatt en konvensjon som forbyr påføring av tinn-holdig bunnstoff fra 1. januar 2003 og tilstedeværelse av slike bunnstoffer på skipene fra 1. januar 2008. Forbudet omfatter tributyltinn og andre tinnorganiske forbindelser.
Som en følge av dette er det utviklet og introdusert flere tinnfrie
begroingshindrende systemer. Disse malingene er for eksempel beskrevet i
WO8402915, EP646630, EP802243, WO9606870 som beskriver selvpolerende begroingshindrende malinger hvor det i stedet for å inkorporere organotinn-grupper i den anvendte polymer er inkorporert organosilyl grupper eller organiske syrer bundet til metallatomer. Karakteristisk også for disse selvpolerende tinnfrie begroingshindrende systemene er at de består av polymere med hydrolyserbare grupper som sikrer den kontrollerte oppløsningen av polymerene og dermed frigivelse av begroingshindrende forbindelser.
IW09641841 og W09641842 er det beskrevet polymerer av akrylsyre- eller metakrylsyreestere, som hydrolyserer i kontakt med sjøvann og dermed gir et selvpolerende system. Erfaring viser imidlertid at disse systemene ofte ikke innehar den ønskede hydrolysehastigheten som er nødvendig for å oppnå tilstrekkelig polering og begroingshindrende effekt. Monomerer som er meget lik monomerne ifølge ovennevnte W09641842, benyttes i EP 0841380 A1 sammen med tinnholdige monomerer for å fremstille polymerer for anvendelse som bindemiddel i skipsmåling. Foreliggende oppfinnelse har imidlertid vist at visse modifikasjoner i akrylsyre- eller metakrylsyre-strukturen gir polymersystemer som innehar en rask hydrolyse og dermed forbedrede selvpolerende egenskaper.
W09641842 og EP 0841380 A1 beskriver generelt monomerer som har en viss likhet med monomerene som benyttes i foreliggende oppfinnelse, men de monomere som beskrives spesifikt i de to nevnte søknader, er vesentlig forskjellige fra de essensielle monomerer som benyttes ifølge foreliggende oppfinnelse. EP 0841380 A1 beskriver dessuten, som nevnte ovenfor, tinnholdige polymerer, mens polymerene ifølge foreliggende oppfinnelse er tinnf rie.
I JP63215780 har forbindelsen med formel III en annen kjemisk struktur enn monomer A i foreliggende oppfinnelse slik det fremgår av de nedenfor viste strukturformlene. Formel III er en vinylalkohol med forlenget sidekjede;
I motsetning til det er formel I i foreliggende oppfinnelse en umettet syre (for eksempel metakylsyre, akrylsyre, maleinsyre) med forlenget sidekjede:
Tilsvarende gjelder for polymerene som er beskrevet i EP-A-1016681. Disse kan ikke få den forlengede alkylkjeden -[CH2]n- i sidekjeden, selv ikke i det tilfellet der polymeren inneholder strukturene (I) og (II) ved siden av hverandre i kjeden. Ettersom det er den forlengede sidekjeden ved gruppen -[CH2]n- som gir polymerene ifølge foreliggende oppfinnelse de spesielle og fordelaktige hydrolyseringsegenskapene, er de påpekte forskjellene vesentlige for den oppnåelige tekniske effekten.
Foreliggende oppfinnelse angår tinn-frie, hydrolyserbare polymerer for anvendelse i begroingshindrende belegg og en fremgangsmåte for fremstilling av tinn-frie, polymeriserbare monomerer som kan anvendes til fremstilling av bindemiddélsystemer for begroingshindrende belegg for å beskytte flater under vann mot vekst av marine organismer, anvendelse av polymerene og monomerene, fremstilling av polymerene og maling inneholdende disse.
Foreliggende oppfinnelse angår vannuløselig, vanneroderbar, filmdannende polymer, kjennetegnet ved at den omfatter gjentatte enheter svarende til monomerer A ogB:
A) monomerer med formelen
n er et heltall fra 1 til 4,
X er H eller CH3,
Y er H eller eventuelt forestret COOH gruppe,
R<1> er Ph(R<2>)m,-C(0)R<3> eller-Si(R<4>)3)
m er et heltall fra 1 til 3,
R<2>, som er like eller forskjellige, er valgt fra -C(0)H, COOR<5>, CH2COOR<6>, Ci^alkyl, halogen, nitro, C^alkanoyl, OH og OR<7>,
R<3> er substituert eller usubstituert alkyl, aryl, aralkyl eller heterocyklyl,
R<4>, som er like eller forskjellige, er valgt fra substituert eller usubstituert C1.20 alkyl, C5.2o aryl, d-20 alkoksy og C5-20 aryloksy, og
R<5>, R6 og R7 er uavhengig valgt fra substituert eller usubstituert Ci-2oalkyl og C5-2oaryl; som er tilstede i en mengde på 2-95 mol-%; og
B) andre vinyl-polymeriserbare monomerer
som er tilstede i en mengde på 5-98 mol-%.
Enheter av A-monomerer er normalt tilstede i en mengde på 2-95 mol%, fortrinnsvis 5-80 mol%, særlig 10-70 mol%. Enheter av B-monomerer er normalt tilstede i en mengde på 5-98 mol%, fortrinnsvis 20-95 mol%, særlig 30-90 mol%.
I polymeren over kan R<4> i triorganosilylgruppen, Si(R<4>)3, være valgt fra gruppen bestående av trimetylsilyl, trietylsilyl, tri-n-propylsilyl, tri-iso-propylsilyl, tri-n-butylsilyl, tri-fert-butylsilyl, tri-iso-butylsilyl, tri-n-pentylsilyl, tri-n-heksylsilyl, tri-fenylsilyl, tri-benzylsilyl, etyldimetylsilyl, n-butyldimetylsilyl, diisopropyl-n-butylsilyl, dicykloheksylfenylsilyl, t-butyldifenylsilyl, t-butyldimetylsilyl, dimetylfenylsilyl, bifenyldimetylsilyl, bifenyldiisopropylsilyl, difenylmetylsilyl, dimetylheksylsilyl.
I polymeren kan videre R<5>, R<6> og/eller R<7> være substituert med halogen.
Oppfinnelsen angår videre monomerer kjennetegnet ved formelen
hvor
n er et heltall fra 1 til 4,
X er H eller CH3,
Y er H eller eventuelt forestret COOH gruppe,
R1 er-C(0)R3 eller-Si(R4)3,
m er et heltall fra 1 til 3,
R<2>, som er like eller forskjellige, er valgt fra -C(0)H, COOR<5>, CH2COOR<6>, Ci-4alkyl, halogen, nitro, Ci^alkanoyl, OH og OR<7>,
R<3> er substituert eller usubstituert alkyl, aryl, aralkyl eller heterocyklyl,
R<4>, som er like eller forskjellige, er valgt fra substituert eller usubstituert C1-20 alkyl, C5-20 aryl, C-|.2o alkoksy og Cs-2o aryloksy, og
R<5>, R<6> og R7 er uavhengig valgt fra substituert eller usubstituert Ci-20alkyl og C5-2oaryl. Substituentene kan være videre substituert som tidligere angitt.
Oppfinnelsen angår videre fremgangsmåte for fremstilling av polymerer ved homopolymerisasjon eller kopolymerisasjon av polymeriserbare monomerer kjennetegnet ved polymerisering av en blanding bestående av
A) 2-95 mol-% av en eller flere monomerer med formelen
hvor
n er et heltall fra 1 til 4,
X er H eller CH3,
Y er H eller eventuelt forestret COOH gruppe,
R<1> er Ph(R<2>)m, -C(0)R3 eller -Si(R4)3,
m er et heltall fra 1 til 3,
R<2>, som er like eller forskjellige, er valgt fra -C(0)H, COOR<5>, CH2COOR<6>, Ci-4alkyl, halogen, nitro, CMalkanoyl, OH og OR<7>,
R<3> er substituert eller usubstituert alkyl, aryl, aralkyl eller heterocyklyl,
R<4>, som er like eller forskjellige, er valgt fra substituert eller usubstituert C1-20 alkyl, C5-20 aryl, C1.20 alkoksy og C5-20 aryloksy, og
R<5>, R6 og R<7> er uavhengig valgt fra substituert eller usubstituert Ci.20alky! og C5-20aryl; og
B) 5-98 mol-% av andre vinyl-polymeriserbare monomerer,
i nærvær av radikal- eller ionedannende initiatorer og inerte løsningsmidler.
Oppfinnelsen angår dessuten fremgangsmåte for fremstilling av polymerer ved homopolymerisasjon eller kopolymerisasjon av polymeriserbare monomerer, kjennetegnet ved polymerisering av en blanding bestående av
C) 2-95 mol-% av én eller flere monomerer med formelen
og
D) 5-98 mol-% av andre vinyl polymeriserbare monomere,
i nærvær av radikal eller ionedannende initiatorer og inerte løsningsmidler,
og deretter, ved en polymer-analog reaksjon, omsetning av de oppnådde kopolymerer med én eller flere forbindelser med den generelle formelen
hvor
n er et heltall fra 1 til 4,
XerHellerCH3,
Y er H eller eventuelt forestret COOH gruppe,
Z<1> er Cl eller OH
Z2 er grupper som er reaktive med Z<1>, såsom OH eller Cl
R<1> er Ph(R<2>)m,-C(0)R<3> eller-Si(R<4>)3,
m er et heltall fra 1 til 3,
R<2>, som er like eller forskjellige, er valgt fra -C(0)H, COOR<5>, CH2COOR<6>, Ci^alkyl, halogen, nitro, Ci-4alkanoyl, OH og OR<7>,
R3 er substituert eller usubstituert alkyl, aryl, aralkyl eller heterocyklyl,
R<4>, som er like eller forskjellige, er valgt fra substituert eller usubstituert C1-20 alkyl, C5.20 aryl, C1-20 alkoksy og C5-20 aryloksy, og
R<5>, R6 og R<7> er uavhengig valgt fra substituert eller usubstituert Ci-2oalkyl og
Cs-2oaryl.
Videre angår oppfinnelsen fremgangsmåte for fremstilling av polymerer ved homopolymerisasjon eller kopolymerisasjon av polymeriserbare monomerer, kjennetegnet ved polymerisering av en blanding bestående av
E) 2-95 mol-% av én eller flere monomerer med formelen
og
F) 5-98 mol-% av andre vinyl polymeriserbare monomerer,
i nærvær av radikal- eller ionedannende initiatorer,
og i en polymer-analog reaksjon omsetning av de oppnådde kopolymerer med én eller flere forbindelser med den generelle formelen
hvor
n er et heltall fra 1 til 4,
X er H eller CH3,
Y er H eller eventuelt forestret COOH gruppe,
Z<1> er Cl eller OH
Z<2> er grupper som er reaktive med Z<1>, såsom OH eller Cl
R<1> er Ph(R<2>)m, -C(0)R<3> eller -Si(R<4>)3,
m er et heltall fra 1 til 3,
R<2>, som er like eller forskjellige, er valgt fra -C(0)H, COOR5, CH2COOR6, Ci^alkyl, halogen, nitro, Ci-4alkanoyl, OH og OR<7>,
R3 er substituert eller usubstituert alkyl, aryl, aralkyl eller heterocyklyl,
R<4>, som er like eller forskjellige, er valgt fra substituert eller usubstituert C1-20 alkyl, C5.20 aryl, C1-20 alkoksy og C5-20 aryloksy, og
R<5>, R6 og R7 er uavhengig valgt fra substituert eller usubstituert Ci-2oalkyl og C^oaryl
Oppfinnelsen angår videre begroingshindrende maling, kjennetegnet ved at den inneholder en polymer som tidligere angitt, og dessuten et biocid og eventuelt andre komponenter som er hensiktsmessige i marin maling.
Oppfinnelsen angår videre anvendelse av en polymer som tidligere angitt som komponent i en marin maling for å oppnå belegg med selvpolerende egenskaper i vann.
Videre angår oppfinnelsen anvendelse av monomerer, kjennetegnet ved den generelle formelen
hvor
n er et heltall fra 1 til 4,
X er H eller CH3,
Y er H eller eventuelt forestret COOH gruppe,
R<1> er Ph(R<2>)m, -C(0)R3 eller -Si(R<4>)3,
m er et heltall fra 1 til 3,
R2, som er like eller forskjellige, er valgt fra -C(0)H, COOR<5>, ChfeCOOR<6>, Ci^alkyl, halogen, nitro, Ci^alkanoyl, OH <p>g OR<7>,
R<3> er substituert eller usubstituert alkyl, aryl, aralkyl eller heterocyklyl,
R<4>, som er like eller forskjellige, er valgt fra substituert eller usubstituert C1-20 alkyl, C5-20 aryl, C1-20 alkoksy og C5-20 aryloksy, og
R<5>, R6 og R<7> er uavhengig valgt fra substituert eller usubstituert Ci-20alkyl og Cs^oatyl,
for fremstilling av polymerer for begroingshindrende maling.
Alkyl- og alkoksygruppene nevnt ovenfor er fortrinnsvis C1.12 særlig C14, og aryl-og aryloksygruppene er fortrinnsvis C5.12, særlig Cs*.
Eksempler på monomerer som kan anvendes som komponent A for fremstilling av bindemidler for begroingshindrende belegg inneholdende fenylestergrupper definert ved strukturen I omfatter: formyl-substituerte fenylestre av karboksymetylakrylat og karboksymetylmetakrylat såsom 3-formylfenylkarboksymetyl(met)akrylat, 4-formylfenylkarboksymetyl(met)akrylat, 6-fluor-2-formylfenylkarboksymetyl(met)akrylat, 2-formylfenylkarboksymetyl(met)akrylat, 2- formyl-6-metoksyfenylkarboksymetyl(met)akrylat, 6-etoksy-2-formylfenylkarbbksymetyl(met)akrylat, 2-formyl-6-hydroksyfenylkarboksymetyl(met)akrylat, 4-formyl-2-metylfenylkarboksymetyl(met)åkrylat, 4-formyl-3-klorfenylkarboksymetyl(met)akrylat, 4-brom-2-formylfenylkarboksymetyl(met)akrylat, 2-formyl-4-metoksyfenylkarboksymetyl(met)akrylat, 4-formyl-2-metoksyfenylkarboksymetyl(met)akrylat, 2-formyl-4-(trifluormetoksy) fenylkarboksymetyl(met)akrylat, 4-formyl-2-nitrofenylkarboksymetyl(met)akrylat, 4,6-dibrom-2-formyl-fenylkarboksymetyl(met)akrylat og 2,5-dimetyl-4-formylfenylkarboksymetyi(met)akrylat og 2-formyl- 4-acetylfenylkarboksymetyl(met)akrylat;
formyl-substituerte fenylestre av karboksyetylakrylat og karboksyetylmetakrylat såsom 3-foirnylfenylkarboksyetyl(met)akrylat, 4-formylfeny|karboksyetyl(met)akrylat, 6-fluor-2-
formylfenylkarboksyetyl(met)akrylat, 2-formylfenylkarboksyetyl(met)akrylat, 2-formyl-6-metoksyfenylkarboksyetyl(met)akrylat, 6-etoksy-2-formylfenylkarboksyetyl(met)akrylat, 2-formyl-6-hydroksyfenylkarboksyetyl(met)akrylat, 4-formyl-2-metylfenylkarboksyetyl(met)akrylat, 4-formyl-3-klorfenylkarboksyetyl(met)akrylat, 4-brom-2-formylfenylkarboksyetyl(met)akrylat, 2-formyl-4-metoksyfenylkarboksyetyl(met)akrylat, 4-formyl-2-metoksyfenylkarboksyetyl(met)akrylat, 2-formyl-4-(trifluormetoksy) fenylkarboksyetyl(met)akrylat, 4-formyl-2-nitrofenylkarboksyetyl(met)akrylat, 4,6-dibrom-2-formyl-fenylkarboksyetyl(met)akrylat og 2,5-dimetyl-4-formylfenylkarboksyetyl(met)akrylat og 2-formyl- 4-acetylfenylkarboksyetyl(met)akrylat;
formyl-substituerte fenylestre av karboksypropylakrylat og karboksypropylmetakrylat såsom 3-formylfenylkarboksypropyl(met)akrylat, 4-formylfenylkarboksypropyl(met)akrylat, 6-fluor-2-formylfenylkarboksypropyl(met)akrylat, 2-formylfenylkarboksypropyl(met)akrylat, 2-formyl-6-metoksyfenylkarboksypropyl(met)akrylat, 6-etoksy-2-formylfenylkarboksypropyl(met)akrylat, 2-formyl-6-hydroksyfenylkarboksypropyl(met)akrylat, 4-formyl-2-metylfenylkarboksypropyl(met)akrylat, 4-formyl-3-klorfenylkarboksypropyl(met)akrylat, 4-brom-2-formylfenylkarboksypropyl(met)akrylat, 2-formyl-4-metoksyfenylkarboksypropyl(met)akrylat, 4-formyl-2-metoksyfenylkarboksypropyl(met)akrylat, 2-formyl-4-(trifluormetoksy) fenylkarboksypropyl(met)akrylat, 4-formyl-2-nitrofenylkarboksypropyl(met)akrylat, 4,6-dibrom-2-formyl-fenylkarboksypropyl(met)akrylat og 2,5-dimetyl-4-formylfenylkarboksypropyl(met)akrylat og 2-formyl- 4-acetylfenylkarboksypropyl(met)akrylat;
formyl-substituerte fenylestre av karboksybutylakrylat og karboksybutylmetakrylat såsom 3-formylfenylkarboksybutyl(met)akrylat, 4-formylfenylkarboksybutyl(met)akrylat, 6-fluor-2-formylfenylkarboksybutyl(met)akrylat, 2-formylfenylkarboksybutyl(met)akrylat, 2-formyl-6-metoksyfenylkarboksybutyl(met)akrylat, 6-etoksy-2-formylfenylkarboksybutyl(met)akrylat, 2-formyl-6-hydroksyfenylkarboksybutyl(met)akrylat, 4-formyl-2-metylfenylkarboksybutyl(met)akrylat, 4-formyl-3-klorfenylkarboksybutyl(met)akrylat, 4-
brom-2-foiTnylfenylkarboksybutyl(met)akrylat, 2-formyl-4-metoksyfenylkarboksybutyl(met)akrylat, 4-formyl-2-metoksyfenylkarboksybutyl(met)akrylat, 2-formyl-4-(trifluormetoksy) fenylkarboksybutyl(met)akrylat, 4-formyl-2-nitrofenylkarboksybutyl(met)akrylat, 4,6-dibrom-2-formyl-fenylkarboksybutyl(met)akrylat og 2,5-dimetyl-4-formylfenylkarboksybutyl(met)akrylat og 2-formyl- 4-acetylfenylkarboksybutyl(met)akrylat;
ester-substituerte fenylestre av karboksymetylakrylat og karboksymetylmetakrylat såsom 4-metoksykarbonylfenylkarboksymetyl(met)akrylat, 4-propoksykarbonylfenylkarboksymetyl(met)akrylat, 4-isopropoksykarbonylfenylkarboksymetyl(met)akrylat, 2-metoksykarbonylfenylkarboksymetyl(met)akrylat, 4-metoksykarbonyl-2-nitrofenylkarboksymetyl(met)akrylat, 4-etoksykarbonyl-2-metoksyfenylkarboksymetyl(met)akrylat, 5-etoksykarbonyl-2-hydroksyfenylkarboksymetyl(met)akrylat, 3-hydroksy-2
metoksykarbonylfenylkarboksymetyl(met)akrylat, 2-metoksykarbonylmetylfenylkarboksymetyl (met)akrylat og 4-etoksykarbonyl-2-nitro-etylfenylkarboksymetyl(met)akrylat;
ester-substituerte fenylestre av karboksyetylakrylat og karboksyetylmetakrylat såsom 4-metoksykarbonylfenylkarboksyetyl(met)akrylat, 4-propoksykarbonylfenylkarboksyetyl(met)akrylat, 4-isopropoksykarbonylfenylkarboksyetyl(met)akrylat, 2-metoksykarbonylfenylkarboksyetyl(met)akrylat, 4-metoksykarbonyl-2-nitrofenylkarboksyetyl(met)akrylat, 4-etoksykarbonyl-2-metoksyfenylkarboksyetyl(met)akrylat, 5-etoksykarbonyl-2-hydroksyfenylkarboksyetyl(met)akrylat, 3-hydroksy-2
metoksykarbonylfenylkarboksyetyl(met)akrylat, 2-metoksykarbonylmetylfenylkarboksyetyl (met)akrylat og 4-etoksykarbonyl-2-nitro-etylfenylkarboksyetyl(met)akrylat;
ester-substituerte fenylestre av karboksypropylakrylat og karboksypropylmetakrylat såsom 4-metoksykarbonylfenylkarboksypropyl(met)akrylat, 4-
propoksykarbonylfenylkarboksypropyl(met)akrylat, 4-isopropoksykarbonylfenylkarboksypropyl(met)akrylat, 2-metoksykarbonylfenylkarboksypropyl(met)akrylat, 4-metoksykarbonyl-2-nitrofenylkarboksypropyl(met)akrylat, 4-etoksykarbonyl-2-metoksyfenylkarboksypropyl(met)akrylat, 5-etoksykarbonyl-2-hydroksyfenylkarboksypropyl(met)akrylat, 3-hydroksy-2
metoksykartoonylfenylkarboksypropyl(met)akrylat, 2-metoksykarbonylmetylfenylkarboksypropyl(met)akrylat og 4-etoksykarbonyl-2-nitro-etylfenylkarboksypropyl(met)akrylat;
ester-substituerte fenylestre av karboksybutylakrylat og karboksybutylmetakrylat såsom 4-metoksykarbonylfenylkarboksybutyl(met)akrylat, 4-propoksykarbonylfenylkarboksybutyl(met)akrylat, 4-isopropoksykarbonylfenylkarboksybutyl(met)akrylat, 2-metoksykarbonylfenylkarboksybutyl(met)akrylat, 4-metoksykarbonyl-2-nitrofenylkarboksybutyl(met)akrylat, 4-etoksykarbonyl-2-metoksyfenylkarboksybutyl(met)akrylat, 5-etoksykarbonyl-2-hydroksyfenylkarboksybutyl(met)akrylat, 3-hydroksy-2
metoksykarbonylfenylkarboksybutyl(met)akrylat, 2-metoksykarbonylmetylfenylkarboksybutyl(met)akrylat og 4-etoksykarbonyl-2-nitro-etylfenylkarboksybutyl(met)akrylat;
alkoksy-substituerte fenylestre av karboksymetylakrylat og karboksymetylmetakrylat såsom 2-metoksyfenylkarboksymetyl(met)akrylat, 4-metoksyfenylkarboksymetyl(met)akrylat, 4-etoksyfenylkarboksymetyl(met)akrylat, 1,4-dimetoksyfenylkarboksymetyl(met)akrylat, 2,4-dimetoksyfenylkarboksymetyl(met)akrylat, 2-klor-5-metoksyfenylkarboksymetyl(met)akrylat, 3,5-dietoksyfenylkarboksybutyl(met)akrylat og 2,5-dimetoksy-3-hydroksyfenylkarboksymetyl(met)akrylat;
alkoksy-substituerte fenylestre av karboksyetylakrylat og karboksyetylmetakrylat såsom 2-metoksyfenylkarboksyetyl(met)akrylat, 4-metoksyfenylkarboksyetyl(met)akrylat, 4-etoksyfenylkarboksyetyl(met)akrylat, 1,4-dimetoksyfenylkarboksyetyl(met)akrylat, 2,4-dimetoksyfenylkarboksyetyl(met)akrylat, 2-klor-5-metoksyfenylkarboksyetyl(met)akrylat,
3,5-dietoksyfenylkarboksyetyl(met)akrylat og 2,5-dimetoksy-3-hydroksyfenylkarboksyetyl(met)akrylat;
alkoksy-substituerte fenylestre av karboksypropylakrylat og karboksypropylmetakrylat såsom 2-metoksyfenylkarboksypropyl(met)akrylat, 4-metoksyfenylkarboksypropyl(met)akrylat, 4-etoksyfenylkarboksypropyl(met)akrylat, 1,4-dimetoksyfenylkarboksypropyl(met)akrylat, 2,4-dimetoksyfenylkarboksypropyl(met)akrylat, 2-klor-5-metoksyfenylkarboksypropyl(met)akrylat, 3,5-dietoksyfenylkarboksypropyl(met)akrylat og 2,5-dimetoksy-3-hydroksyfenylkarboksypropyl(met)akrylat;
alkoksy-substituerte fenylestre av karboksybutylakrylat og karboksybutylmetakrylat såsom 2-metoksyfenylkarboksybutyl(met)akrylat, 4-metoksyfenylkarboksybutyl(met)akrylat, 4-etoksyfenylkarboksybutyl(met)akrylat, 1,4-dimetoksyfenylkarboksybutyl(met)akrylat, 2,4-dimetoksyfenylkarboksybutyl(met)akrylat, 2-klor-5-metoksyfenylkarboksybutyl(met)akrylat, 3,5-dietoksyfenylkarboksybutyl(met)akrylat og 2,5-dimetoksy-3-hydroksyfenylkarboksybutylmetakrylat;
hydroksy-substituerte fenylestre av karboksymetylakrylat og karboksymetylmetakrylat såsom 2-hydroksyfenylkarboksymetyl(met)akrylat, 3-hydroksyfenylkarboksymetyl(met)akrylat, 4-hydroksyfenylkarboksymetyl(met)akrylat, 3,5-dihydroksyfenylkarboksymetyl(met)akrylat;
hydroksy-substituerte fenylestre av karboksyetylakrylat og karboksyetylmetakrylat såsom 2-hydroksyfenylkarboksyetyl(met)akrylat, 3-hydroksyfenylkarboksyetyl(met)akrylat, 4-hydroksyfenylkarboksyetyl(met)akrylat, 3,5-dihydroksyfenylkarboksyetyl(met)akrylat;
hydroksy-substituerte fenylestre av karboksypropylmetylakrylat og karboksypropylmetylmetakrylat såsom 2-hydroksyfenylkarboksypropyl(met)akrylat, 3-hydroksyfenylkarboksypropyl(met)akrylat, 4-hydroksyfenylkarboksypropyl(met)akrylat, 3,5-dihydroksyfenylkarboksypropyl(met)akrylat;
hydroksy-substituerte fenylestre av karboksybutylakrylat og karboksybutylmetakrylat såsom 2-hydroksyfenylkarboksybutyl(met)akrylat, 3-hydroksyfenylkarboksybutyl(met)akrylat, 4-hydroksyfenylkarboksybutyl(met)akrylat, 3,5-dihydroksyfenylkarboksybutyl(met)akrylat;
halogen-substituerte fenylestre av karboksymetylakrylat og karboksymetylmetakrylat såsom 4-bromfenylkarboksymetyl(met)akrylat, 2,4,6-tribromfenylkarboksymetyl(met)akrylat, 2,4,6-triklorfenylkarboksymetyl(met)akrylat, 4-brom-2,6-diklorfenylkarboksymetyl(met)akrylat, 6-jod-2,4-diklorfenylkarboksymetyl(met)akrylat, 4,6-dibrom-2-klor-fenylkarboksymetyl(met)akrylat;
halogen-substituerte fenylestre av karboksyetylakrylat og karboksyetylmetakrylat såsom 4-bromfenylkarboksyetyl(met)akrylat, 2,4,6-tribromfenylkarboksyetyl(met)akrylat, 2,4,6-triklorfenyikarboksyetyl(met)akrylat, 4-brom-2,6-diklorfenylkarboksyetyl(met)akrylat6-jod-, 2,4-diklorfenylkarboksyetyl(met)akrylat, 4,6-dibrom-2-klor-fenylkarboksyetyl(met)akrylat;
halogen-substituerte fenylestre av karboksypropylmetylakrylat og
karboksypropylmetylmetakrylat såsom 4-bromfenylkarboksypropyl(met)akrylat, 2,4,6-tribromfenylkarboksypropyl(met)akrylat, 2,4,6-triklorfenylkarboksypropyl(met)akrylat, 4-brom-2,6-diklorfenylkarboksypropyl(met)akrylat, 6-jod-2,4-diklorfenylkarboksypropyl(met)akrylat, 4,6-dibrom-2-klor-fenylkarboksypropyl(met)akrylat;
halogen-substituerte fenylestre av karboksybutylakrylat og karboksybutylmetakrylat såsom 4-bromfenylkarboksybutyl(met)akrylat, 2,4,6-tribromfenylkarboksybutyl(met)akrylat, 2,4,6-triklorfenylkarboksybutyl(met)akrylat, 4-brom-2,6-diklorfenylkarboksybutyl(met)akrylat, 6-jodr2,4-diklorfenylkarboksybutyl(met)akrylat, 4,6-dibrom-2-klor-fenylkarboksybutyl(met)akrylat;
og andre flersubstituerte fenylestre av karboksyetylakrylat og karboksyetylmetakrylat;
derivater av maleinsyreestere såsom 4-formylfenylkarboksymetyl-metylmaleat, 2-formylfenylkarboksymetyl-metylmaleat, 4-brom-2-formylfenylkarboksymetyl-
metylmaleat, 4-brom-3-formylfenylkarboksymetyl-metylmaleat, 2-formyl-6-metoksyfenylkarboksymetyl-metylmaleat, 4-foirnyl-6-metoksyfenylkarboksymetyl-metylmaleat, 4-formylfenylkarboksypropyl-metylmåleat, 2-formylfenylkarboksypropyl-metylmaleat, 4-brom-2-formylfenylkarboksypropyl-metylmaleat, 4-brom-3-formylfenylkarooksypropyl-metylmaleat, 2-formyl-6-metoksyfenylkarboksypropyl-metylmaleat, 4-formyl-6-metoksyfenylkarboksypropyl-metylmaleat, 4-metoksykarbonylfenylkaoroksymetyl-metylmaleat, 4-metoksykarbonyl-2-nitrofenylkarboksymetyl-metylmaleat, 2-metoksyfenylkarboksymetyl-metylmaleat, 4-metoksyfenylkarboksymetyl-metylmaleat, 4-etoksyfenylkarooksymetyl-metylmaleat, 4-metoksyfenylkarboksyetyl-metylmaleat, 2-metoksyfenylkarboksypropyl-metylmaleat, 4-metoksyfenylkarboksypropyl-metylmaleat, 2-hydroksyfenylkarboksymetyl-metylmaleat, 3-hydroksyfenylkarboksymetyl-metylmaleat, 4-hydroksyfenylkarboksymetyl-metylmaleat, 3,5-dihydroksyfenylkaoroksymetyl-metylmaleat, 3-hydroksyfenylkarboksyetyl-metylmaleat, 4-hydroksyfenylkarboksypropyl-metylmaleat, 3-hydroksyfenylkarboksypropyl-metylmaleat, 3,5-dihydroksyfenylkarboksypropyl-metylmaleat, 4-hydroksyfenylkarboksybutyl-metylmaleat, 4-bromfenylkarboksymetyl-metylmaleat, 2-4-6-tribromfenylkarooksymetyl-metylmaleat, 2-4-6-triklorfenylkarooksymetyl-metylmaleat, 4-bromfenylkarboksyetyl-metylmaleat, 4-bromfenylkarboksypropyl-metylmaleat, 2-formylfenylkarboksymetyl-etylmaleat, 4-brom-2- formylfenylkarboksymetyl-etylmaleat, 2-formylfenylkarboksypropyl-etylmaleat, 4-brom-3- formylfenylkarboksypropyl-etylmaleat, 4-metoksykarbonylfenylkarboksymetyl-etylmaleat, 4-metoksyfenylkarboksymetyl-etylmaleat, 4-metoksyfenylkarboksypropyl-etylmaleat, 3-hydroksyfenylkarboksymetyl-etylmaleat, 4-hydroksyfenylkarboksymetyl-etylmaleat, 3-hydroksyfenylkarboksypropyl-etylmaleat, 4-hydroksyfenylkarboksypropyl-etylmaleat, 3,5-dihydroksyfenylkarboksypropyl-etylmaleat, 4-.
hydroksyfenylkarboksybutyl-etylmaleat, 4-bromfenylkarboksymetyl-etylmaleat, 4-bromfenylkarboksymetyl-etylmaleat, 4-bromfenylkarboksyetyl-etylmaleat, 4-bromfenylkarboksypropyl-etylmaleat;
derivater av fumarsyreestere såsom 4-formylfenylkarboksymetyl-metylfumarat, 2-formylfenylkarboksymetyl-metylfumarat, 4-brom-2-formylfenylkarboksymetyl-metylfumarat, 4-brom-3-formylfenylkarboksymetyl-metylfumarat, 2-formyl-6-metoksyfenylkarboksymetyl-metylfumarat, 4-formyl-6-metoksyfenylkarboksymetyl-metylfumarat, 4-formylfenylkarboksypropyl-metylfumarat, 2-formylfenylkarboksypropyl-
metylfumarat, 4-brom-2-formylfenylkarboksypropyl-metylfumarat, 4-brom-3-formylfenylkarboksypropyl-metylfumarat, 2-formyl-6-metoksyfenylkarboksypropyl-metylfumarat, 4-fom<y>l-6-metoks<y>fen<y>lkarboks<y>pro<p>yl-met<y>lfumarat, 4-metoksykarbonylfenylkarboksymetyl-metylfumarat, 4-metoksykarbonyl-2-nitrofenylkarboksymetyl-metylfumarat, 2-metoksyfenylkarboksymetyl-metylfumarat, 4-metoksyfenylkarboksymetyl-metylfumarat, 4-etoksyfenylkarboksymetyl-metylfumarat, 4-metoksyfenylkarboksyetyl-metylfumarat, 2-metoksyfenylkarboksypropyl-metylfumarat, 4-metoksyfenylkarboksypropyl-metylfumarat, 2-hydroksyfenylkarboksymetyl-metylfumarat, 3-hydroksyfenylkarboksymetyl-metylfumarat, 4-hydroksyfenylkarboksymetyl-metylfumarat, 3,5-dihydroksyfenylkarboksymetyl-metylfumarat, 3-hydroksyfenylkarboksyetyl-metylfumarat, 4-hydroksyfenylkarboksypropyl-metylfumarat, 3-hydroksyfenylkarboksypropyl-metylfumarat, 3,5-dihydroksyfenylkarboksypropyl-metylfumarat, 4-hydroksyfenylkarboksybutyl-metylfumarat, 4-bromfenylkarboksymetyl-metylfumarat, 2-4-6-tribromfenylkarboksymetyl-metylfumarat, 2-4-6-triklorfenylkarboksymetyl-metylfumarat, 4-bromfenylkarboksyetyl-metylfumarat, 4-bromfenylkarboksypropyl-metylfumarat, 2-formylfenylkarboksymetyl-etylfumarat, 4-brom-2-formylfenylkarboksymetyl-etylfumarat, 2-formylfenylkarboksypropyl-etylfumarat, 4-brom-3-formylfenylkarboksypropyl-etylfumarat, 4-metoksykarbonylfenylkarboksymetyl-etylfumarat, 4-metoksyfenylkarboksymetyl-etylfumarat, 4-metoksyfenylkarboksypropyl-etylfumarat, 3-hydroksyfenylkarboksymetyl-ety!fumarat, 4-hydroksyfenylkarboksymetyl-etylfumarat, 3-hydroksyfenylkarboksypropyl-etylfumarat, 4-hydroksyfenylkarboksypropyl-etylfumarat, 3,5-dihydroksyfenylkarboksypropyl-etylfumarat, 4-hydroksyfenylkarboksybutyl-etylfumarat, 4-bromfenylkarboksymetyl-etylfumarat, 4-bromfenylkarboksymetyl-etylfumarat, 4-bromfenylkarboksyetyl-
etylfumarat, 4-bromfenylkarboksypropyl-etylfumarat;
Foretrukne eksempler på monomerer som kan anvendes som komponent A for fremstilling av bindemidler for begroingshindrende belegg inneholdende fenylestergrupper definert ved strukturen I inkluderer 4-formylfenylkarboksymetyl(met)akrylat, 2-formylfenylkarboksymetyl(met)akrylat, 4-brom-2-formylfenylkarboksymetyl(met)akrylat, 4-brom-3-
formylfenylkarboksymetyl(met)akrylat, 2-formyl-6-metoksyfenylkarboksymetyl(met)akrylat, 4 formyl-6-metoksyfenylkarboksymetyl(met)akrylat, 4-formylfenylkarboksypropyl(met)akrylat, 2-
formylfenylkarboksypropyl(met)akrylat, 4-brom-2-formylfenylkarboksypropyl(met)akrylat, 4-brom-3-formylfenylkarboksypropyl(met)akrylat, 2-formyl-6-metoksyfenylkarboksypropyKmetJakrylat, 4 formyl-6-metoksyfenylkarboksypropyKmetJakrylat, 4-metoksykarbonyifenylkarboksymetyl(met)akrylat, 4-metoksykarbonyl-2-nitrofenylkarboksymetyl(met)akrylat, 2-metoksyfenylkarooksymetyl(met)akrylat, 4-metoksyfenylkarboksymetyl(met)akrylat, 4-etoksyfenylkarboksymetyl(met)akrylat, 4-metoksyfenylkarboksyetyl(met)akrylat, 2-metoksyfenylkarboksypropyl(met)akrylat) 4-metoksyfenylkarboksypropyl(met)akrylat, 2-hydroksyfenylkarboksymetyl(met)akrylat, 3-hydroksyfenylkarboksymetyl(met)akrylat, 4-hydroksyfenylkarboksymetyl(met)akrylat, 3,5-dihydroksyfenylkarboksymetyl(met)akrylat, 3-hydroksyfenylkarboksyetyl(met)akrylat, 4-hydroksyfenylkarboksypropyl(met)akrylat, 3-hydroksyfenylkarboksypropyl(met)akrylat, 3,5-dihydroksyfenylkarboksypropyl(met)akrylat, 4-hydroksyfenylkarboksybutyKmetJakrylat, 4-bromfenylkarboksymetyl(met)akrylat, 2-4-6-tribromfenylkarboksymetyl(met)akrylat) 2-4-6-triklorfenylkarboksymetyl(met)akrylat, 4-bromfenylkarboksyetyl(met)akrylat og 4-bromfenylkarboksypropyl(met)akrylat.
Spesielt foretrukne eksempler på monomerer som kan anvendes som komponent A for fremstilling av bindemidler for begroingshindrende belegg inneholdende fenylestergrupper definert ved strukturen I inkluderer 2-formylfenylkarboksymetyl(met)akrylat, 4-brom-2-formylfenylkarboksymetyl(met)akrylat, 2-formylfenylkarboksypropyl(met)akrylat, 4-brom-3-formylfenylkarboksypropyl(met)akrylat, 4-metoksykarbonylfenylkarboksymetyl(met)akrylat, 4-metoksyfenylkarboksymetyl(mét)akrylat, 4-metoksyfenylkarboksypropyl(met)akrylat, 3-hydroksyfenylkarboksymetyl(met)akrylat, 4-hydroksyfenylkarboksymetyl(met)akrylat, 3-hydroksyfenylkarboksypropyl(met)akrylat, 4-hydroksyfenylkarboksypropyl(met)akrylat, 3,5-dihydroksyfenylkarboksypropyl(met)akrylat, 4-hydroksyfenylkarboksybutyl(met)akrylat, 4-bromfenylkarboksymetyl(met)akrylat, 4-bromfenylkarboksymetyl(met)akrylat, 4-bromfenylkarboksyetyl(met)akrylat og 4-bromfenylkarboksypropyl(met)akrylat.
Eksempler på monomerer som kan anvendes som komponent A for fremstilling av bindemidler for begroingshindrende belegg inneholdende anhydrid grupper definert ved strukturen I omfatter: ikke-aromatiske anhydrider av karboksymetylakrylat og karboksymetylmetakrylat såsom trimetylacetoksykarbonylmetyl(met)akrylat, metoksyacetoksykarbonylmetyl(met)akrylat, fe/t-butylacetoksykarbonylmetyKmetJakrylat, acetoksyacetylkarbonylmetyl(met)akrylat, bromacetoksykarbonylmetyl(met)akrylat, kloracetoksykarbonylmetyl(met)akrylat, cyklopentylacetoksykarbonylmetyl(met)akrylat, dikloracetoksykarbonylmetyl(met)akrylat, tribromacetoksykarbonylmetyl(met)akrylat, trikloracetoksykarbonylmetyl(met)akrylat og trifluoracetoksykarbonylmetyl(met)akrylat;
ikke-aromatiske anhydrider av karboksyetylakrylat og karboksyetylmetakrylat såsom trimetylacetoksykarbonyletyl(met)akrylat, metoksyacetoksykarbonyletyl(met)akrylat, tert-butylacetoksykarbonyletyl(met)akrylat, acetoksyacetylkarbonyletyl(met)akrylat, bromacetoksykarbonyletyl(met)akrylat, kloracetoksykarbonyletyl(met)akrylat, cyklopentylacetoksykarbonyletyl(met)akrylat, dikloracetoksykarbonyletyl(met)akrylat, tribromacetoksykarbonyletyl(met)akrylat, trikioracetoksykarbonyletyl(met)akrylat og trifluoracetoksykarbonyletyl(met)akrylat;
ikke-aromatiske anhydrider av karboksypropylakrylat og karboksypropylmetakrylat såsom trimetylacetoksykarbonylpropyl(met)akrylat,
metoksyacetoksykarbonylpropyl(met)akrylat, tert-butylacetoksykarbonylpropyl(met)akrylat, acetoksyacetylkarbonylpropyl(met)akrylat, bromacetoksykarbonylpropyl(met)akrylat, kloracetoksykarbonylpropyl(met)akrylat, cyklopentylacetoksykarbonylpropyl(met)akrylat,
dikloracetoksykarbonylpropyl(met)akrylat, tribromacetoksykarbonylpropyl(met)akrylat, trikloracetoksykarbonylpropyl(met)akrylat og trifluoracetoksykarbonylpropyl(met)akrylat;
ikke-aromatiske anhydrider av karboksybutylakrylat og karboksybutylmetakrylat såsom trimetylacetoksykarbonylbutyl(met)akrylat, metoksyacetoksykarbonylbutyl(met)akrylat, fert-butylacetoksykarbonylbutyl(met)akrylat, acetoksyacetylkarbonylbutyl(met)akrylat, bromacetoksykarbonylbutyl(met)akrylat, kloracetoksykarbonylbutyl(met)akrylat, cyklopentylacetoksykarbonylbutyl(met)akrylat, dikloracetoksykarbonylbutyl(met)akrylat, tribromacetoksykarbonylbutyl(met)akrylat, trikloracetoksykarbonylbutyl(met)akrylat og trifluoracetoksykarbonylbutyl(met)akrylat;
aromatiske anhydrider av karboksymetylakrylat og karboksymetylmetakrylat såsom fenylacetoksykarbonylmetyl(met)akrylat, 2,2-difenylacetoksykarbonylmetyl(met)akrylat, 2,2,2-trifenylacetoksykarbonylmety!(met)akrylat, 4-metoksyfenylacetoksykarbonylmetyl(met)akrylat, 3,4-dimetoksyfenylacetoksykarbonylmetyl(met)akrylat, 2,5-dimetoksyfenylacetoksykarbonylmetyl(met)akrylat, 2-bromfenylacetoksykarbonylmetyl(met)akrylat, 2-brom-4,5-dimetoksyfenylacetoksykarbonylmetyl(met)akrylat, 4-klorfenylacetoksykarbonylmetyl(met)akrylat, 2-fenyl-2-klor-acetoksykarbonylmetyl(met)akrylat, 2-klor-2,2-difenylacetoksykarbonylmetyl(met)akrylat, 4-fluorfenylacetoksykarbonylmetyl(met)akrylat, 4-metoksyfenylacetoksykarbonylmetyl(met)akrylat,
fenoksyacetoksykarbonylmetyl(met)akrylat, 4-fluorfenoksyacetoksykarbonylmetyl(met)akrylat,
benzyloksyacetoksykarbonylmetyl(met)akrylat, 2-klor-2-fenylacetoksykarbonylmetyl(met)akrylat, 2,2-difenyl-2-klor-acetoksykarbonylmetyl(met)akrylat, 2-(2,4,5-triklorfenoksy)-acetoksykarbonylmetyl(met)akrylat, benzylacetoksykarbonylmetyl(met)akrylat, benzoyloksykarbonylmetyl(met)akrylat, og
nikotinoyloksykarbonylmetyl(met)akrylat;
aromatiske anhydrider av karboksyetylakrylat og karboksyetylmetakrylat såsom fenylacetoksykarbonyletyl(met)akrylat, 2,2-difenylacetoksykarbonyletyl(met)akrylat, 2,2,2-trifenylacetoksykarbonyletyl(met)akrylat, 4-metoksyfenylacetoksykarbOnyletyl(met)akrylat, 3,4-dimetoksyfenylacetoksykarbonyletyl(met)akrylat, 2,5-dimetoksyfenylacetoksykarbonyletyl(met)akrylat, 2-bromfenylacetoksykarbonyletyl(met)akrylat, 2-brom-4,5-dimetoksyfenylacetoksykarbonyletyl(met)akrylat, 4-klorfenylacetoksykarbonyletyl(met)akrylat, 2-fenyl-2-klor-acetoksykarbonyletyl(met)akrylat, 2-klor-2,2-difenylacetoksykarbonyletyl(met)akrylat, 4-fluorfenylacetoksykarbonyletyl(met)akrylat, 4-metoksyfenylacetoksykarbonyletyl(met)akrylat,
fenoksyacetoksykarbonyletyl(met)akrylat, 4-fluorfenoksyacetoksykarbonyletyl(met)akrylat,
benzyloksyacetoksykarbonyletyl(met)akrylat, 2-fenyl-2-klor-acetoksykarbonyletyl(met)akrylat, 2-klor-2,2-difenyl acetoksykarbonyletyl(met)akrylat, 2-(2,4,5-triklorfenoksy) acetoksykarbonyletyl(met)akrylat,
benzylacetoksykarbonyletyl(met)akrylat,
benzoyloksykarbonyletyl(met)akrylat, og
nikotinoyloksykarbonyletyl(met)akrylat;
aromatiske anhydrider av karboksypropylakrylat og karboksypropylmetakrylat såsom fenylacetoksykarbonylpropyl(met)akrylat, 2,2-difenylacetoksykarbonylpropyl(met)akrylat, 2,2,2-trifenylacetoksykarbonylpropyl(met)akrylat, 4-metoksyfenylacetoksykarbonylpropyl(met)akrylat, 3,4-dimetoksyfenyiacetoksykarbonylpropyl(met)akrylat, 2,5-dimetoksyfenylacetoksykarbonylpropyl(met)akrylat, 2-bromfenylacetoksykarbonylpropyl(met)akrylat, 2-brom-4,5-dimetoksyfenylacetoksykarbonylpropyl(met)akrylat, 4-klorfenylacetoksykarbonylpropyl(met)akrylat, 2-klor-2-fenylacetoksykarbonylpropyl(met)akrylat, 2,2-difenyl-2-klor-acetoksykarbonylpropyl(met)akrylat, 4-fluorfenylacetoksykarbonylpropyl(met)akrylat, 4-metoksyfenylacetoksykarbonylpropyl(met)akrylat,
fenoksyacetoksykarbonylpropyl(met)akrylat, 4-fluorfenoksyacetoksykarbonylpropyi(met)akrylat,
benzyloksyacetoksykarbonylpropyl(met)akrylat, 2-fenyl-2-klor-acetoksykarbonylpropyl(met)akrylat, 2-klor-2,2-difenylacetoksykarbonylpropyl(met)akrylat, 2-(2,4,5-triklorfenoksy)-acetoksykarbonylpropyl(met)akrylat, benzylacetoksykarbonylpropyl(met)akrylat, benzoyloksykarbonylpropyl(met)akrylat, og
nikotinoyloksykarbonylpropyl(met)akrylat;
aromatiske anhydrider av karboksybutylakrylat og karboksybutylmetakrylat såsom fenylacetoksykarbonylbutyl(met)akrylat, 2,2-difenylacetoksykarbonylbutyl(met)akrylat, 2,2,2-trifenylacetoksykarbonylbutyl(met)akrylat, 4-
metoksyfenylacetoksykarbonylbutyl(met)akrylat, 3,4-dimetoksyfenylacetoksykarbonylbutyl(met)akrylat, 2,5-dimetoksyfenylacetoksykarbonylbutyl(met)akrylat, 2-bromfenylacetoksykarbonylbutyl(met)akrylat, 2-brom-4,5-dimetoksyfenylacetoksykarbonylbutyl(met)akrylat, 4-klorfenylacetoksykarbonylbutyl(met)akrylat, 2-fenyl-2-klor-acetoksykarbonylbutyl(met)akrylat, 2-klor-2,2-difenylacetoksykarbonylbutyl(met)akrylat, 4-fluorfenylacetoksykarbonylbutyl(met)akrylat, 4-metoksyfenylacetoksykarbortylbutyl(met)akrylat,
fenoksyacetoksykarbonylbutyl(met)akrylat, 4-fluorfenoksyacetoksykarbonylbutyl(met)akrylat,
benzyloksyacetoksykarbonylbutyl(met)akrylat, 2-klor-2-fenylacetoksykarbonylbutyl(met)akrylat, 2,2-difenyl-2-klor-acetoksykarbonylbutyl(met)akrylat, 2-(2,4,5-triklorfenoksy)acetoksykarbonylbutyl(met)akrylat,
benzylacetoksykarbonylbutyl(met)akrylat,
benzoyloksykarbonylbutyl(met)akrylat, og
nikotinoyloksykarbonylbutyl(met)akrylat;
derivater av maleinsyreestere såsom trimetylacetoksykarbonylmetyl-metylmaleat, tert-butyiacetoksykarbonylmetyl-metylmaleat, cyklopentylacetoksykarbonylmetyl-metylmaleat, bromacetoksykarbonylmetyl-metylmaleat, trimetylacetoksykarbonyletyl-metylmaleat, fert-butylacetoksykarbonyletyl-metylmaleat,
cyklopentylacetoksykarbonyletyl-metylmaleat, bromacetoksykarbonyletyl-metylmaleat, trimetylacetoksykarbonylbutyl-metylmaleat, fe/t-butylacetoksykarbonylbutyl-metylmaleat, metoksyacetoksykarbonylpropyl-metylmaleat,
fenylacetoksykarbonylmetyl-metylmaleat, 2,2-difenylacetoksykarbonylmetyl-metylmaleat, 4-metoksyfenylacetoksykarbonylmetyl-metylmaleat, 2-bromfenylacetoksykarbonylbutyl-metylmaleat, 2,2-difenyl-2-klor-acetoksykarbonylmetyl-metylmaleat, fenylacetoksykarbonyletyl-metylmaleat, 2,2-difenylacetoksykarbonyletyl-metylmaleat, 4-metoksyfenylacetoksykarbonyletyl-metylmaleat,
fenylacetoksykarbonylpropyl-metylmaleat, 2,2-difenylacetoksykarbonylpropyl-metylmaleat, fenylacetoksykarbonylbutyl-metylmaleat, trimetyiacetoksykarbonylmetyl-etylmaleat, ferf-butylacetoksykarbonylmetyl-etylmaleat,
cyklopentylacetoksykarbonylmetyl-etylmaleat, bromacetoksykarbonylmetyl-etylmaleat, trimetylacetoksykarbonyletyl-etylmaleat, fert-butylacetoksykarbonyletyl-etylmaleat, cyklopentylacetoksykarbonyletyl-etylmaleat, bromacetoksykarbonyletyl-etylmaleat, trimetylacetoksykarbonylbutyl-etylmaleat, fe^-butylacetoksykarbonylbutyl-etylmaleat, metoksyacetoksykarbonylpropyl-etylmaleat, fenylacetoksykarbonylmetyl-etylmaleat, 2,2-difenylacetoksykaoronylmetyl-etylmaleat, 4-metoksyfenylacetoksykarbonylmetyl-etylmaleat, 2-bromfenylacetoksykarbonylbutyl-etylmaleat, 2,2-difenyl-2-kloracetoksykarbonylmetyl-etylmaleat, fenylacetoksykarbonyletyl-etylmaleat, 2,2-difenylacetoksykarbonyletyl-etylmaleat, 4-metoksyfenylacetoksykarbonyletyl-etylmaleat, fenylacetoksykarbonylpropyl-etylmaleat, 2,2-difenylacetoksykarbonylpropyl-etylmaleat, fenylacetoksykarbonylbutyl-etylmaleat, benzylacetoksykarbonylmetyl-etylmaleat, benzylacetoksykarbonyletyl-etylmaleat og benzylacetoksykarbonylpropyl-metylmaleat;
derivater av fumarsyreestere såsom trimetylacetoksykarbonylmetyl-metylfumarat, tert-butylacetoksykarbonylmetyl-metylfumarat, cyklopentylacetoksykarbonylmetyl-metylfumarat, bromacetoksykarbonylmetyl-metylfumarat, trimetylacetoksykarbonyletyl-metylfumarat, fe/t-butylacetoksykarbonyletyl-metylfumarat,
cyklopentylacetoksykarbonyletyl-metylfumarat, bromacetoksykarbonyletyl-metylfumarat, trimetylacetoksykarbonylbutyl-metylfumarat, fert-butylacetoksykarbonylbutyl-metylfumarat, metoksyacetoksykarbonylpropyl-metylfumarat,
fenylacetoksykarbonylmetyl-metylfumarat, 2,2-difenylacetoksykarbonylmetyl-metylfumarat, 4-metoksyfenylacetoksykarbonylmetyl-metylfumarat, 2-bromfenylacetoksykarbonylbutyl-metylfumarat, 2,2-difenyl-2-klor-acetoksykarbonylmetyl-metylfumarat, fenylacetoksykarbonyletyl-metylfumarat, 2,2-difenylacetoksykarbonyletyl-metylfumarat, 4-metoksyfenylacetoksykarbonyletyl-metylfumarat, fenylacetoksykarbonylpropyl-metylfumarat, 2,2-difenylacetoksykarbonylpropyl-metylfumarat, fenylacetoksykarbonylbutyl-metylfumarat, trimetylacetoksykarbonylmetyl-etylfumarat, ferf-butylacetoksykarbonylmetyl-etylfumarat, cyklopentylacetoksykarbonylmetyl-etylfumarat, bromacetoksykarbonylmetyl-etylfumarat, trimetylacetoksykarbonyletyl-etylfumarat, fe/t-butylacetoksykarbonyletyl-etylfumarat, cyklopentylacetoksykarbonyletyl-etylfumarat, bromacetoksykarbonyletyl-etylfumarat, trimetylacetoksykarbonylbutyl-etylfumarat, ferl-butylacetoksykarbonylbutyl-etylfumarat, metoksyacetoksykarbonylpropyl-etylfumarat, fenylacetoksykarbonylmetyl-etylfumarat, 2,2-difenylacetoksykarbonylmetyl-etylfumarat, 4-metoksyfenylacetoksykarbonylmetyl-
etylfumarat, 2-bromfenylacetoksykarbonylbutyl-etylfumarat, 2,2-difenyl-2-klor-acetoksykarbonylmetyl-etylfumarat, fenylacetoksykarbonyletyl-etylfumarat, 2,2-difenylacetoksykarbonyletyl-etylfumarat, 4-metoksyfenylacetoksykarbonyletyl-etylfumarat, fenylacetoksykarbonylpropyl-etylfumarat, 2,2-difenylacetoksykarbonylpropyl-etylfumarat, benzylacetoksykarbonylmetyl-etylfumarat, benzylacetoksykarbonyletyl-etylfumarat, benzylacetoksykarbonylpropyl-metylfumarat og fenylacetoksykarbonylbutyl-etylfumarat.
Foretrukne eksempler på monomerer som kan anvendes som komponent A for fremstilling av bindemidler for begroingshindrende belegg inneholdende anhydrid-grupper definert ved strukturen I inkluderer trimetylacetoksykarbonylmetyl(met)akrylat, fert-butylacetoksykarbonylmetyl(met)akrylat, cyklopentylacetoksykarbonylmetyl(met)akrylat, bromacetoksykarbonylmetyl(met)akrylat, trimetylacetoksykarbonyletyl(met)akrylat, ferf-butylacetoksykarbonyletyl(met)akrylat, cyklopentylacetoksykarbonyletyl(met)akrylat, bromacetoksykarbonyletyl(met)akrylat, trimetylacetoksykarbonylbutyl(met)akrylat, fert-butylacetoksykarbonylbutyl(met)akry1at, metoksyacetoksykarbonylpropyl(met)akrylat, fenylacetoksykarbonylmetyl(met)akrylat, benzylacetoksykarbonylmetyl(met)akrylat, benzylacetoksykarbonyletyl-etylmaleat og benzylacetoksykarbonylpropylmetylmaleat;2,2-difenylacetoksykarbonylmetyl(met)akrylat, 4-metoksyfenylacetoksykarbonylmetyl(met)akrylat, 2-bromfenylacetoksykarbonylbutyl(met)akrylat, 2,2-difenyl-2-klor-acetoksykarbonylmetyl(met)akrylat, fenylacetoksykarbonyletyl(met)akrylat, 2,2-difenylacetoksykarbonyletyl(met)akrylat, 4-metoksyfenylacetoksykarbonyletyl(met)akrylat, benzylacetoksykarbonyletyl(met)akrylat, fenylacetoksykarbonylpropyl(met)akrylat, 2,2-difenylacetoksykarbonylpropyl(met)akrylat, benzylacetoksykarbonylbutyl(met)akrylat og fenylacetoksykarbonylbutyl(met)akrylat.
Spesielt foretrukne eksempler på monomerer som kan anvendes som komponent A for fremstilling av bindemidler for begroingshindrende belegg inneholdende anhydrid grupper definert ved strukturen I inkluderer trimetylacetoksykarbonylmetyl(met)akrylat, ferf-butylacetoksykarbonylmetyl(met)akrylat, trimetylacetoksykarbonyletyl(met)akrylat, terf-butylacetoksykarbonyletyl(met)akrylat, trimetylacetoksykarbonylbutyl(met)akrylat, fe/t-butylacetoksykarbonylbutyl(met)akrylat, benzylacetoksykarbonylmetyl(met)akrylat, fenylacetoksykarbonylmetyl(met)akrylat, 2,2-difenylacetoksykarbonylmetyl(met)akrylat, 4-metoksyfenylacetoksykarbonylmetyl(met)akrylat, fenylacetoksykarbonyletyl(met)akrylat, 2,2-difenylacetoksykarbonyletyl(met)akrylatI 4-metoksyfenylacetoksykarbonyletyl(met)akrylat, fenylacetoksykarbonylpropyl(met)akrylat og benzylacetoksykarbonylpropyl(met)akrylat.
For monomerer som kan anvendes som komponent A for fremstilling av bindemidler for begroingshindrende belegg inneholdende organosilyl gruppen bestående av -Si(R4)3 definert i I, kan substituentene R4 være like eller forskjellige, med alkyl grupper med opp til 20 C atomer, fortrinnsvis opp til 12 C atomer, spesielt opp til 8 C atomer, som for eksempel metyl, etyl, propyl, butyl, pentyl, heksyl, heptyl, oktyl, nonyl, dekyl, iso-propyl, fe/t-butyl, iso-butyl, sec-butyl, cykloheksyl og substituert cykloheksyl, aryl grupper med opp til 20 C atomer, fortinnsvis opp til 12 C atomer, som for eksempel aryl og naftyl og substituerte aryl grupper der minst en substituent er hentet fra gruppen av fluor, klor, brom, iod, nitro, cyano, amino, hydroksy osv.
Eksempler på triorganosilylgrupper -Si(R4), er trimetylsilyl, trietylsilyl, tri-n-propylsilyl, tri-iso-propylsilyl, tri-n-butylsilyl, tri-fert-butylsilyl, tri-iso-butylsilyl, tri-s-butylsilyl, tri-n-pentylsilyl, tri-n-heksylsilyl, tri-fenylsilyl, tri-benzylsilyl, etyldimetylsilyl, n-butyldimetylsilyl, diisopropyl-n-butylsilyl, dicykloheksylfenylsilyl, t-butyldifenylsilyl, t-butyldimetylsilyl, dimetylfenylsilyl, bifenyldimetylsilyl, bifenyldiisopropylsilyl, difenylmetylsilyl, dimetyloktadesylsilyl, dimetyloktylsilyl, dimetylcykloheksylsilyl, dimetylheksylsilyl, klormetyldimetylsilyl og pentafluorfenyldimetylsilyl.
Eksempler på monomerer som kan anvendes som komponent A for fremstilling av bindemidler for begroingshindrende belegg inneholdende organosilylester grupper definert ved strukturen I omfatter: silylestre av karboksymetylakrylat og karboksymetylmetakrylat såsom trimetylsilyloksykarbonylmetyl(met)akrylat, trietylsilyloksykarbonylmetyl(met)akrylat, tri-n-propylsilyloksykarbonylmetyl(met)akrylat, triisopropylsilyloksykarbonylmetyl(met)akrylat, tri-n-butylsilyloksykarbonylmetyl(met)akrylat, triisobutylsilyloksykarbonylmetyl(met)akrylat, tri-fert-butylsilyloksykarbonylmetyl(met)akrylat, tri-s-butylsilyloksykarbonylmetyl(met)akrylat, tri-n-pentylsilyloksykarbonylmetyl(met)akrylat, triisopentylsilyloksykarbonylmetyl(met)akrylat, tri-n-heksylsilyloksykarbonylmetyl(met)akrylat, tri-n-oktylsilyloksykarbonylmetyl(met)akrylat, trifenylsilyloksykarbonylmetyl(met)akrylat, tri-p-metylfenylsilyloksykarbonylmetyl(met)akrylat,
tribenzylsilyloksykarbonylmetyl(met)akrylat,
etyldimetylsilyloksykarbonylmetyl(met)akrylat, n-butyldimetylsilyloksykarbonylmetyl(met)akrylat,
diisopropylsilyloksykarbonylmetyl(met)akrylat og t-butyldifenylsilyloksykarbonylmetyl(mét)akrylat;
silylestre av karboksyetylakrylat og karboksyetylmetakrylat såsom trimetylsilyloksykarbonyletyl(met)akrylat, triet<y>lsil<y>loks<y>karbon<y>letyl(met)akrylat, tri-n-propylsilyloksykarbonyletyl(met)akrylat, triisopropylsilyloksykarbonyletyl(met)akrylat, tri-n-butylsilyloksykarbonyletyl(met)akrylat, triisobutylsilyloksykarbonyletyl(met)akrylat, tri-fert-butylsilyloksykarbonyletyl(met)akrylat, tri-s-butylsilyloksykarbonyletyl(met)akrylat, tri-n-pentylsilyloksykarbonyletyl(met)akrylat, triisopentylsilyloksykarbonyletyl(met)akrylat, tri-n-heksylsilyloksykarbonyletyl(met)akrylat, tri-n-oktylsilyloksykarbonyletyl(met)akrylat, trifenylsilyloksykarbonyletyl(met)akrylat, tri-p-metylfenylsilyloksykarbonyletyl(met)akrylat, tribenzylsilyloksykarbonyletyl(met)akrylat, etyldimetylsilyloksykarbonyletyl(met)akrylat, ri-butyldimetylsilyloksykarbonyletyl(met)akrylat,
diisopropylsilyloksykarbonyletyl(met)akrylat og t-butyldifenylsilyloksykarbonyletyl(met)akrylat;
silylestre av karboksypropylakrylat og karboksypropylmetakrylat såsom trimetylsilyloksykarbonylpropyl(met)akrylat, trietylsilyloksykarbonylpropyl(met)akrylat, tri-n-propylsilyloksykarbonylpropyl(met)akrylat,
triisopropylsilyloksykarbonylpropyl(met)akrylat, tri-n-butylsilyloksykarbonylpropyl(met)akrylat, triisobutylsilyloksykarbonylpropyl(met)akrylat, tri-fe/t-butylsilyloksykarbonylpropyl(met)akrylat, tri-s-butylsilyloksykarbonylpropyl(met)akrylat, tri-n-pentylsilyloksykarbonylpropyl(met)akrylat, triisopentylsilyloksykarbonylpropyl(met)akrylat, tri-n-heksylsilyloksykarbonylpropyl(met)akrylat, tri-n-oktylsilyloksykarbonylpropyl(met)akrylat, trifenylsilyloksykarbonylpropyl(met)akrylat, tri-p-metylfenylsilyloksykarbonylpropyl(met)akrylat,
tribenzylsilyloksykarbonylpropyl(met)akrylat,
etyldimetylsilyloksykarbonylpropyl(met)akrylat, n-butyldimetylsilyloksykarbonylpropyl(met)akrylat,
diisopropylsilyloksykarbonylpropyl(met)akrylat og t-butyldifenylsilyloksykarbonylpropyl(met)akrylat;
silylestre av karboksybutylakrylat og karboksybutylmetakrylat såsom trimetylsilyloksykarbonylbutyl(met)akrylat, trietylsilyloksykarbonylbutyl(met)akrylat, tri-n-propylsilyloksykarbonylbutyl(met)akrylat, triisopropylsilyloksykarbonylbutyl(met)akrylat, tri-n-butylsilyloksykarbonylbutyl(met)akrylat,
triisobutylsilyloksykarbonylbutyl(met)akrylat, tri-ferf-butylsilyloksykarbonylbutyl(met)akrylat, tri-s-butylsilyloksykarbonylbutyl(met)akrylat, tri-n-pentylsilyloksykarbonylbutyl(met)akrylat, triisopentylsilyloksykarbonylbutyl(met)akrylat, tri-n-heksylsilyloksykarbonylbutyl(met)akrylat, tri-n-oktylsilyloksykarbonylbutyl(met)akrylat, trifenylsilyloksykarbonylbutyl(met)akrylat, tri-p-metylfenylsilyloksykarbonylbutyl(met)akrylat, tribenzylsilyloksykarbonylbutyl(met)akrylat, etyldimetylsilyloksykarbonylbutyl(met)akrylat, n-butyldimetylsilyloksykarbonylbutyl(met)akrylat,
diisopropylsilyloksykarbonylbutyl(met)akrylat og t-butyldifenylsilyloksykarbonylbutyl(met)akrylat;
silylestre av karboksymetyl maleinsyreestere såsom trimetylsilyloksykarbonylmetyl-metylmaleat, trietylsilyloksykarbonylmetyl-etylmaleat, tri-n-propylsilyloksykarbonylmetyl-n-propylmaleat, triisopropylsilyloksykarbonylmetyl-metylmaleat, tri-n-butylsilyloksykarbonylmetyl-n-butylmaleat og tri-n-heksylsilyloksykarbonylmetyl-n-heksylmaleat;
silylestre av karboksyetyl maleinsyreestere såsom trimetylsilyloksykarbonyletyl-metylmaleat, trietylsilyloksykarbonyletyl-etylmaleat, tri-n-propylsilyloksykarbonyletyl-n-propylmaleat, triisopropylsilyloksykarbonyletyl-metylmaleat, tri-n-butylsilyloksykarbonyletyl-n-butylmaleat og tri-n-heksylsilyloksykarbonyletyl-n-heksylmaleat;
silylestre av karboksypropyl maleinsyreestere såsom trimetylsilyloksykarbonylpropyl-metylmaleat, trietylsilyloksykarbonylpropyl-etylmaleat, tri-n-
propylsilyloksykarbonylpropyl-n-propylmaleat, triisopropylsilyloksykarbonylpropyl-metylmaleat, tri-n-butylsilyloksykarbonylpropyl-n-butylmaleat og tri-n-heksylsilyloksykarbonylpropyl-n-heksylmaleat;
silylestre av karboksybutyl maleinsyreestere såsom trimetylsilyloksykarbonylbutyl-metylmaleat, trietylsilyloksykarbonylbutyl-etylmaleat, tri-n-propylsilyloksykarbonylbutyl-n-propylmaleat, triisopropylsilyloksykarbpnylbutyl-metylmaleat, tri-n-butylsilyloksykarbonylbutyl-n-butylmaleat og tri-n-heksylsilyloksykarbonylbutyl-n-heksylmaleat;
silylestre av karboksymetyl fumarsyreestere såsom trimetylsilyloksykarbonylmetyl-metylfumarat, trietylsilyloksykarbonylmetyl-etylfumarat, tri-n-propylsilyloksykarbonylmetyl-n-propylfumarat, triisopropylsilyloksykarbonylmetyl-metylfumarat, tri-n-butylsilyloksykarbonylmetyl-n-butylfumarat og tri-n-heksylsilyloksykarbonylmetyl-n-heksylfumarat;
silylestre-avkarboksyetylfumarsyreestere såsom trimetylsilyloksykarbonyletyl-metylfumarat, trietylsilyloksykarbonyletyl-etylf umarat, tri-n-propylsilyloksykarbonyletyl-n-propylfumarat, triisopropylsilyloksykarbonyletyl-metylfumarat, tri-n-butylsilyloksykarbonyletyl-n-butylfumarat og tri-n-heksylsilyloksykarbonyletyl-n-heksylfumarat;
silylestre av karboksypropyl fumarsyreestere såsom trimetylsilyloksykarbonylpropyl-metylfumarat, trietylsilyloksykarbonylpropyl-etylfumarat, tri-n-propylsilyloksykarbonylpropyl-n-propylfumarat, triisopropylsilyloksykarbonylpropyl-metylfumarat, tri-n-butylsilyloksykarbonylpropyl-n-butylfumarat og tri-n-heksylsilyloksykarbonylpropyl-n-heksylfumarat;
silylestre av karboksybutyl fumarsyreestere såsom trimetylsilyloksykarbonylbutyl-metylfumarat, trietylsilyloksykarbonylbutyl-etylfumarat, tri-n-propylsilyloksykarbonylbutyl-n-propylfumarat, triisopropylsilyloksykarbonylbutyl-metylfumarat, tri-n-butylsilyloksykarbonylbutyl-n-butylfumarat og tri-n-heksylsilyloksykarbonylbutyl-n-heksylfumarat;
I foreliggende oppfinnelse kopolymeriseres minst en monomer A, C eller E, definert ved strukturen I, II eller IV, med en eller flere andre vinyl polymeriserbare monomerer B, D eller F.
Eksempler på slike vinyl polymeriserbare monomerer B, D og F er akrylsyre og estere av akrylsyre som metylakrylat, etylakrylat, n-propylakrylat, isopropylakrylat, n-butylakrylat, iso-butylakrylat, fert-butylakrylat, butyletylakrylat, pentylakrylat, heksylakrylat, cykloheksylakrylat, fenylakrylat, n-oktylakrylat, isooktylakrylat, 2-etylheksylakrylat, 3,5,5-trimetylheksylakrylat, laurylakrylat, cetylakrylat, stearylakrylat, 2-hydroksyetylakrylat, 2-hydroksypropylakrylat, 4-hydroksybutylakrylat, 3-fenoksy-2-hydroksypropylakrylat, 2-metoksyetylakrylat, metoksypropylakrylat, 2-etoksyetylakrylat, etoksypropylakrylat, propoksyetylakrylat, butoksyetylakrylat, isobutoksyetyiakrylat, fenoksyetylakrylat;
metakrylsyre og estere av metakrylsyre som metylmetakrylat, etylmetakrylat, propylmetakrylat, isopropylmetakrylat, n-butylmetakrylat, iso-butylmetakrylat, tert-butylmetakrylat, pentylmetakrylat, heksylmetakrylat, cykloheksylmetakrylat, fenylmetakrylat, benzylmetakrylat, tridesylmetakrylat, laurylmetakrylat, stearylmetakrylat, 2-etylheksylmetakrylat, 2-hydroksyetylmetakrylat, 2-hydroksypropylmetakrylat, metoksyetylmetakrylat, 2-etoksyetylmetakrylat, etoksypropylmetakrylat, propoksyetylmetakrylat, 2-butoksyetylmetakrylat, isobutoksyetylmetakrylat, isobutoksybutyldiglykolmetakrylat, fenoksyetylmetakrylat;
amider som for eksempel akrylamid, metakrylamid, N-metylakrylamid, N-etylacrylamid, N-propylakrylamid, maleimid;
aminofunksjonelle akrylater og metakrylater som for eksempel 2-aminoetyl(met)akrylat, dimetylaminoetyl(met)akrylat, 2-dietylamionoetyl(met)akrylat, 3-aminopropyl(met)akrylat, 2-butylaminoetyl(met)akrylat, tertbutylaminoetyl(met)akrylat;
N-vinyl-amider som N-vinylformamid, N-vinyletylamid, N-vinylpropylamid og andre som beskrevet i WO0162811;
N-vinyl-lactamer som for eksempel N-vinylpyrrolidon, N-vinylpiperidin, N-vinylcaprolactam og andre som beskrevet i EP1127902;
hetrocyklisk substituerte akrylater og metakrylater som furfuryl(met)akrylat og tetrahydrofurfuryl(met)akrylat;
hetrocyklisk substituerte vinyl monomerer som vinylimidazol, 2-vinylpyridin, 4-vinylpyridin, 1 -vinyl-1,2,4-triazol, 2-vinyl-1,3-dioxolan;
funksjonelle karbonyloksy etyl(met)akrylater som 2-(metakrylkarbonyloksy)etyl acetoacetat, 2-(((butylamino)karbonyl)oksy)etyl akrylat;
alifatiske og hetrocyklisk substituerte akrylater og metakrylater som 1-/so-butoksyetyl(met)akrylat, 1-etoksyetyl(met)akrylat, 1-propoksyetyl(met)akrylat, 1-(2-etylheksyloksy)etyl(met)akrylat, 2-tetrahydrofuranyl(met)akrylat, 2-tetrahydropyranyl(met)akrylat og andre som beskrevet i JP4103671;
flerfunksjonene akrylater og metakrylater som tetraetylenglykol diakrylat, tripropylenglykol diakrylat, 1,3-butandiol diakrylat, 1,4-butandiol diakrylat, 1,3-butandiol-dimetakrylat, 1,4-butandiol-dimetakrylat, heksandiol-diakrylat, etylenglykol-dimetakrylat, trimetylolpropan-triakrylat, trimetylolpropan-trimetakrylat, di-(trimetylolpropan)-tetraakrylat, pentaerytritol-triakrylat, pentaerytritol-tetraakrylat, dipentaerytritol-pentaakrylat, vinylakrylat.
Eksempler på forbindelser som kan anvendes som komponent C for fremstilling av bindemidler for begroingshindrende maling i henhold til oppfinnelsen omfatter: akrylater og metakrylater såsom karboksymetyl(met)akrylat, karboksyetyl(met)akrylat, karboksypropyl(met)akrylat, karboksybutyl(met)akrylat;
syreklorider såsom karboksylsyreklorid substituerte metylestere av (met)akrylsyre, 2-karboksylsyreklorid substituerte etylestere av (met)akrylsyre, 3-karboksylsyreklorid substituerte propylestere av (met)akrylsyre og 4-karboksylsyreklorid substituerte butylestere av (met)akrylsyre.
Eksempler på komponenter med den generelle formel III reaktive med komponent C omfatter: fenylsubstituerte aromatiske alkoholer såsom 3-formylfenol, 4-formylfenol, 6-fluor-2-formylfenol, 2-formylfenol, 2-formyl-6-metoksyfenol, 6-etoksy-2-formylfenol, 2-formyl-6-hydroksyfenol, 4-formyl-2-metylfenol, 4-formyl-3-klorfenol, 4-brom-2-formylfenol, 2-formyl-4-metoksyfenol, 4-formyl-2-metoksyfenol, 4-(trifluormetoksy)-2-formylfenol, 4-formyl-2-nitrofenol, 4,6-dibrom-2-foimylfenol og 4-formyl-2,5-dimetylfenol;
estersubstituerte aromatiske alkoholer såsom 4-metoksykarbonylfenol, 4-propoksykarbonylfenol, 4-isopropoksykarbonylfenol, 2-metoksykarbonylfenol, 4-metoksykarbonyl-2-nitrofenol, 4-etoksykarbonyl-2-metoksyfenol, 5-etoksykarbonyl-2-hydroksyfenol, 3-hydroksy-2-metoksykarbonylfenol, 2-metoksykarbonylmetylfenol og 4-etoksykarbonyletyl-2-nitrofenol;
alkoksysubstituerte aromatiske alkoholer såsom 2-metoksyfenol, 4-metoksyfenol, 4-etoksyfenol, 1,4-dimetoksyfenol, 2,4-dimetoksyfenol, 2-klor-5-metoksyfenol, 3,5-dietoksyfenol og 3-hydroksy-2,5-dimetoksyfenol;
hydroksysubstituerte aromatiske alkoholer såsom 2-hydroksyfenol, 3-hydroksyfenol, 4-hydroksyfenol, 3,5-dihydroksyfenol;
halogensubstituerte aromatiske alkoholer såsom 4-bromfenol, 2,4,6-tribromfenol, 2,4,6-triklorfenol, 4-brom-2,6-diklorfenol, 2,4-diklor-6-jodfenol, 4,6-dibrom-2-klorfenol;
aromatiske acetylklorider såsom benskarbonylklorid, fenylacetyiklorid, 2,2-difenylacetylklorid, 2,2,2-trifenylacetylklorid, 4-metoksyfenylacetylklorid, 3,4-dimetoksyfenylacetylklorid, 2,5-dimetoksyfenylacetylklorid, 2-bromfenylacetylklorid, 2-brom-4,5-dimetoksyfenylacetylklorid, 4-klorfenylacetylklorid, 2-fenyl-2-kloracetylklorid, 2,2-difenyl-2-kloracetylklorid, 4-fluorfenylacetylklorid, 4-metoksyfenylacetylklorid, fenoksyacetyikarbonylklorid, 4-fluorfenoksyacetylklorid, benzyloksyacetylklorid, 2-fenyl-2-kloracetylklorid, 2,2-difenyl-2-kloracetylklorid og 2-(2,4,5-triklorfenoksy)acetylklorid;
alifatiske acetylklorider såsom trimetylacetylklorid, metoksyacetylklorid, tert-butylacetylklorid, acetoksyacetylklorid, bromoacetylklorid, kioracetylklorid, cyklopentylacetylklorid, dikloracetylklorid, tribromacetylklorid, trikloracetyiklorid og trifluoracetylklorid;
aromatiske eller alifatiske silylklorider såsom trimetylsilylklorid, trietylsilylklorid, tri-n-propylsilylklorid, tri-iso-propylsilylklorid, tri-n-butylsilylklorid, tri-ferf-butylsilylklorid, tri-iso-butylsilylklorid, tri-s-butylsilylklorid, tri-n-pentylsilylklorid, tri-n-heksylsilylklorid, tri-fenylsilylklorid, tri-benzylsilylklorid, etyldimetylsilylklorid, n-butyldimetylsilylklorid, diisopropyl-n-butylsilylklorid, dicykloheksylfenylsilylklorid, t-butyldifenylsilylklorid, t-butyldimetylsilylklorid, dimetylfenylsilylklorid, bifenyldimetylsilylklorid, bifenyldiisopropylsiiylklorid, difenylmetylsilylklorid, dimetyloktadesylsilylklorid, dimetyloktylsilylklorid, dimetylcykloheksylsilylklorid, dimetylheksylsilylklorid, klormetyldimetylsilylklorid og pentafluorfenyldimetylsilylklorid.
Eksempler på forbindelser som kan anvendes som komponent E for fremstilling av bindemidler for begroingshindrende maling i henhold til oppfinnelsen omfatter akrylsyre, metakrylsyre, akrylkarbonylklorid og metakrylkarbonylklorid.
Eksempler på komponenter med den generelle formel V reaktive med komponent E omfatter: formylsubstituerte metylalkoholforbindelser såsom 3-formylfenylkarboksymetylalkohol, 4-formylfenylkarboksymetylalkohol, 2-formylfenylkarboksymetylalkohol, 6-fluor-2-formylfenylkarboksymetylalkohol, 2-formyl-6-metoksyfenylkarboksymetylalkohol, 6-etoksy-2-formylfenylkarboksymetylalkohol, 2-formyl-6-hydroksyfenylkarboksymetylalkohol, 4-formyl-2-metylfenylkarboksymetylalkohol, 4-formyl-3-klorfenylkarboksymetylalkohol, 2-formyl-4-bromfenylkarboksymetylalkohol, 2-formyl-4-metoksyfenylkarboksymetylalkohol, 4-formyl-2-metoksyfenylkarboksymetylalkohol, 2-formyl-4-(trifluormetoksy) fenylkarboksymetylalkohol, 4-formyl-2-nitrofenylkarboksymetylalkohol, 4,6-dibrom-2-formylfenylkarboksymetylalkohol og 4-formyl-2,5-dimetylfenylkarboksymetylalkohol;
formylsubstituerte etylalkoholforbindelser såsom 2-(3-formylfenylkarboksy)etylalkohol, 2-(4-formylfenylkarboksy)etylalkohol, 2-(2-formylfenylkarboksy)etylalkohol, 2-(6-fluor-2-formylfenylkarboksy)etylalkohol, 2-(2-formyl-6-metoksyfenylkarboksy)etylalkohol, 2-(6-etoksy-2-formylfenylkarboksy)etylalkohol, 2-(2-formyl-6-hydroksyfenylkarboksy)etylalkohol, 2-(4-formyl-2-metylfenylkarboksy)etylalkohol, 2-(4-formyl-3-klorfenylkarboksy)etylalkohol, 2-(4-brom-2-formylfenylkarboksy)etylalkohol, 2-(2-formyl-4-metoksyfenylkarboksy)etylalkohol, 2-(4-formyl-2-
metoksyfenylkarboksy}etylalkohol, 2-(2-formyl-4-(trtfluormetoksy)
feny!karboksy)etylalkohol, 2-(4-formyl-2-nitrofenylkarboksy)etylalkohol, 2-(4,6-dtbrom-2-formylfenylkarboksy)ety!alkohol og 2-(4-fomiyl-2,5-dirnetylfenylkarboksy)etylalkohol;
formylsubstituerte propylalkoholforbindelser såsom 3-(3-formylfenylkarboksy)propylalkohol, 3-(4-formylfenylkarboksy)propylalkohol, 3-(2-formylfenylkarboksy)propylalkohol, 3-(6-fluor-2-formylfenylkarboksy)propylalkohol, 3-(2-formyl-6-metoksyfenylkarboksy)propylalkohol, 3-(6-etoksy-2-formylfenylkarboksy)propylalkohol, 3-(2-foirnyi-6-hydroksyfenylkarboksy)propylalkohol, 3-(4-formyl-2-metylfenylkarboksy)propylalkohol, 3-{4-formyl-3-klorfenylkarboksy)propy!alkohol, 3-(4-brom-2-formylfenylkarboksy)propylalkohol, 3-(2-formyl-4-metoksyfenylkarboksy)propylalkohol, 3-(4-formyl-2-metoksyfenylkarboksy)propylalkohol, 3-(2-formyl-4-(trif luormetoksy) fenylkarboksy)propylalkohol, 3-{4-formyl-2-nitrofenylkarboksy)propylalkohol, 3-(4,6-dibrom-2-formylfenylkarboksy)propylalkohol og 3-(4-formyl-2,5-dimetylfenylkarboksy)propylalkohol;
formylsubstituerte butylalkohofforbindelser såsom 4-{3-formylfenylkarboksy)butylalkohol, 4-{4-formylfenylkarboksy)butylalkohol, 4-(2-formylfenylkarboksy)butylalkohol, 4-(6-fluor-2-formylfenylkarboksy)butylalkohol, 4-(2-formyl-6-metoksyfenylkarboksy)butylalkohol, 4-(6-etoksy-2-formylfenylkarboksy)butylalkohol, 4-(2-formyl-6-hydroksyfenylkarboksy)butylalkohol, 4-(4-formyl-2-metylfenylkarboksy)butylalkohol, 4-(4-formyl-3-klorfenylkarboksy)butylalkohol, 4-(4-brom-2-formylfenytkarboksy)butylalkohol, 4-{2-formyl-4-metoksyfenylkarboksy)butylalkohol, 4-(4-formyl-2-
metoksyfenylkarboksy)butylalkohol, 4-(2-formyl-4-(trifluormetoksy) fenylkarboksy)butylalkohol, 4-(4-formy!-2-nitrofenylkarboksy)butylalkohol, 4-(4,6-dibrom-2-formytfenylkarboksy)butylalkohol og 4-(4-formyl-2,5-dimetylfenylkarboksy)butylalkohol;
estersubstituerte metylalkoholforbindelser såsom 4-metoksykarbonylfenylkarboksymetylalkohol, 4-propoksykarbonylfenylkarboksymetylalkohol, 4-isopropoksykarbonylfenylkarboksymetylalkohol, 2-
metoksykarbonylfenylkarboksymetylalkohol, 2-nitro-4-metoksykarbonylfenylkarboksymetylalkohol, 4-etoksykarbonyl-2-metoksyfenylkarboksymetylalkohol, 5-etoksykarbonyl-2-hydroksyfenylkarboksymetylalkohol, 3-hydroksy-2-metoksykarbonylfenylkarboksymetylalkohol, 2-metoksykarbonylmetylfenylkarboksymetyl alkohol og 4-etoksykarbonyletyl-2-nitrofenylkarboksymetylalkohol;
estersubstituerte etylalkoholforbindelser såsom 2-(4-metoksykarbonylfenylkarboksy)etylalkohol, 2-(4-propoksykarbonylfenylkarboksy)etylalkohol, 2-(4-isopropoksykarbonylfenylkarboksy)etylalkohol, 2-(2-metoksykarbonylfenylkarboksy)etylalkohol, 2-(2-nitro-4-metoksykarbonylfenylkarboksy)etylalkohol, 2-(4-etoksykarbonyl-2-metoksyfenylkarboksy)etylalkohol, 2-(5-etoksykarbonyl-2-hydroksyfenylkarboksy)etylalkohol, 2-(3-hydroksy-2 -metoksykarbonylfenylkarboksy)etylalkohol, 2-(2-metoksykarbonylmetylfenylkarboksy)etylalkohol og 2-(4-etoksykarbonyletyl-2-nitrofenylkarboksy)etylalkohol;
estersubstituerte propylalkoholforbindelser såsom 3-(4-metoksykarbonylfenylkarboksy)propylalkohol, 3-(4-propoksykarbonylfenylkarboksy)propylalkohol, 3-(4-isopropoksykarbonylfenylkarboksy)propylalkohol, 3-(2-metoksykarbonylfenylkarboksy)propylalkohol, 3-(2-nitro-4-metoksykarbonylfenylkarboksy)propylalkohol, 3-(4-etoksykarbonyl-2-metoksyfenylkarboksy)propylalkohol, 3-(5-etoksykarbonyl-2-hydroksyfenylkarboksy)propylalkohol, 3-(3-hydroksy-2
metoksykarbonylfenylkarboksy)propylalkohol, 3-(2-metoksykarbonylmetylfenylkarboksy)propylalkohol og 3-(4-etoksykarbonyletyl-2-nitrofenylkarboksy)propylalkohol;
estersubstituerte butylalkoholforbindelser såsom 4-(4-metoksykarbonylfenylkarboksy)butylalkohol, 4-(4-
propoksykarbonylfenylkarboksy)butylalkohol, 4-(4-isopropoksykarbonylfenylkarboksy)butylalkohol, 4-(2-metoksykarbonylfenylkarboksy)butylalkohol, 4-(2-nitro-4-metoksykarbonylfenylkarboksy)butylalkohol, 4-(4-etoksykarbonyl-2-metoksyfenylkarboksy)butylalkohol, 4-(5-etoksykarbonyl-2-hydroksyfenylkarboksy)butylalkohol, 4-(3-hydroksy-2
metoksykarbonylfenylkarboksy)butylalkohol, 4-(2-metoksykarbonylmetylfenylkarboksy)butylalkohol og 4-(4-etoksykarbonyletyl-2-nitrofenylkarboksy)butylalkohol;
alkoksysubstituerte metylalkoholforbindelser såsom 2-metoksyfenylkarboksymetylalkohol, 4-metoksyfenylkarboksymetylalkohol, 4 etoksyfenylkarboksymetylalkohol, 1,4-dimetoksyfenylkarboksymetylalkohol, 2,4-dimetoksyfenylkarboksymetylalkohol, 2-klor-5-metoksyfenylkarboksymetylalkohol, 3,5-dietoksyfenylkarboksymetylalkohol og 3-hydroksy-2,5-dimetoksyfenylkarboksymetylalkohol;
alkoksysubstituerte etylalkoholforbindelser såsom 2-(2-metoksyfenylkarboksy)etylalkohol, 2-(4-metoksyfenylkarboksy)etylalkohol, 2-(4 etoksyfenylkarboksy)etylalkohol, 2-(1,4-dimetoksyfenylkarboksy)etylalkohol, 2-(2,4-dimetoksyfenylkarboksy)etylalkohol, 2-(2-klor-5-metoksyfenylkarboksy)etylalkohol, 2-(3,5-dietoksyfenylkarboksy)etylalkohol og 2-(3-hydroksy-2,5-dimetoksyfenylkarboksy)etylalkohol;
alkoksysubstituerte propylalkoholforbindelser såsom 3-(2-metoksyfenylkarboksy)propylalkohol, 3-(4-metoksyfenylkarboksy)propylalkohol, 3-(4 etoksyfenylkarboksy)propylalkohol, 3-(1,4-dimetoksyfenyikarboksy)propylalkohol, 3-(2,4-dimetoksyfenylkarboksy)propylalkohol, 3-(2-klor-5-metoksyfenylkarboksy)propylalkohol, 3-(3,5-dietoksyfenylkarboksy)propylalkohol og 3-(3-hydroksy-2,5-dimetoksyfenylkarboksy)propylalkohol;
alkoksysubstituerte butylalkoholforbindelser såsom 4-(2-metoksyfenylkarboksy)butylalkohol, 4-(4-metoksyfenylkarboksy)butylalkohol, 4-(4 etoksyfenylkarboksy)butylalkohol, 4-(1,4-dimetoksyfenylkarboksy)butylalkohol, 4-(2,4-
dimetoksyfenylkarboksy)butylalkohol, 4-(2-klor-5-metoksyfenylkarboksy)butylalkohol, 4-(3,5-dietoksyfenylkarboksy)butylalkohol og 4-(3-hydroksy-2,5-dimetoksyfenylkarboksy)butylalkohol;
hydroksysubstituerte metylalkoholforbindelser såsom 2-hydroksyfenylkarboksymetylalkohol, 3-hydroksyfenylkarboksymetylalkohol, 4-hydroksyfenylkarboksymetylalkohol og 3,5-dihydroksyfenylkarboksymetylalkohol;
hydroksysubstituerte etyialkoholforbindelser såsom 2-(2-hydroksyfenylkarboksy)etylalkohol, 2-(3-hydroksyfenylkarboksy)etylalkohol, 2-(4-hydroksyfenylkarboksy)etylalkohol og 2-(3,5-dihydroksyfenylkarboksy)etylalkohol;
hydroksysubstituerte propylalkoholforbindelser såsom 3-(2-hydroksyfenylkarboksy)propylalkohol, 3-(3-hydroksyfenylkarboksy)propylalkohol, 3-(4-hydroksyfenylkarboksy)propylalkohol og 3-(3,5-dihydroksyfenylkarboksy)propylalkohol;
hydroksysubstituerte butylalkoholforbindelser såsom 4-(2-hydroksyfenylkarboksy)butylalkohol, 4-(3-hydroksyfenylkarboksy)butylalkohol, 4-(4-hydroksyfenylkarboksy)butylalkohol og 4-(3,5-dihydroksyfenylkarboksy)butylalkohol;
halogensubstituerte metylalkoholforbindelser såsom 4-bromfenylkarboksymetylalkohol, 2,4,6-tribromfenylkarboksymetylalkohol, 2,4,6-triklorfenylkarboksymetylalkohol, 4-brom-2,6-diklorfenylkarboksymetylalkohol, 6-jod-2,4-diklorfenylkarboksymetylalkohol, 4,6-dibrom-2-klorfenylkarboksymetylalkohol;
halogensubstituerte etyialkoholforbindelser såsom 2-(4-bromfenylkarbpksy)etylalkohol, 2-(2,4,6-tribromfenylkarboksy)etylalkohol, 2-(2,4,6-triklorfenylkarboksy)etylalkohol, 2-(4-brom-2,6-diklorfenylkarboksy)etylalkohol, 2-(6-jod-2,4-diklorfenylkarboksy)etylalkohol, 2-(4,6-dibrom-2-klorfenylkarboksy)etylalkohol;
halogensubstituerte propylalkoholforbindelser såsom 3-(4-bromfenylkarboksy)propylalkohol, 3-(2,4,6-tribromfenylkarboksy)propylalkohol, 3-(2,4,6-triklorfenylkarboksy)propylalkohol, 3-(4-brom-2,6-diklorfenylkarboksy)propylalkohol, 3-
(6-jod-2J4-diklorfenylkarboksy)propylalkohol, 3-(4,6-dibrom-2-klorfenylkarboksy)propylalkohol;
halogensubstituerte butylalkoholforbindelser såsom 4-(4-bromfenylkarboksy)butylalkohol, 4-(2,4)6-tribromfenylkarboksy)butylalkohol, 4-(2,4,6-triklorfenylkarboksy)butylalkohol, 4-(4-brom-2,6-diklorfenylkarboksy)butylalkohol, 4-(6-jod-2,4-diklorfenylkarboksy)butylalkohol, 4-(4,6-dibrom-2-klorfenylkarboksy)butylalkohol;
substituerte acetylkarbonylmetylalkoholforbindelser såsom
trimetylacetylkarbonylmetylalkohol, metoksyacetylkarbonylmetylalkohol, tert-butylacetylkarbonylmetylalkohol, acetoksyacetylkarbonylmetylalkohol, bromoacetylkarbonylmetylalkohol, kloracetylkarbonylmetylalkohol, ccyklopentylacetylkarbonylmetylalkohol, dikloracetylkarbonylmetylalkohol, tribromacetylkarbonylmetylalkohol, trikloracetylkarbonylmetylalkohol og trifluoracetylkarbonylmetylalkohol,
substituerte acetylkarbonyletylalkoholforbindelser såsom 2-(trimetylacetylkarbonyl)etylalkohol, metoksyacetylkarbonyl)etylalkohol, 2-( tert-butylacetylkarbonyl)etylalkohol, 2-(acetoksyacétylkarbonyl)etylalkohol, 2-(bromoacetylkarbonyl)etylalkohol, 2-(kloracetylkarbonyl)etylalkohol, 2-(cyklopentylacetylkarbonyl)etylalkohol, 2-(dikloracetylkarbonyl)etylalkohol, 2-(tribromacetylkarbonyl)etylalkohol, 2-(trikloracetylkarbonyl)etylalkohol og 2-(trifluoracetylkarbonyl)etylalkohol;
substituerte acetylkarbonylpropylalkoholforbindelser såsom 3-(trimetylacetylkarbonyl)propylalkohol, metoksyacetylkarbonyl)propylalkohol, 3-{ tert-butylacetylkarbonyl)propylalkohol, 3-(acetoksyacetylkarbonyl)propylalkohol, 3-(bromoacetylkarbonyl)propylalkohol, 3-(kloracetylkarbonyl)propylalkohol, 3-(cyklopentylacetylkarbonyl)propylalkohol, 3-(dikloracetylkarbonyl)propylalkohol, 3-(tribromacetylkarbonyl)propylalkohol, 3-(trikloracetylkarbonyl)propylalkohol og 3-(trifluoracetylkarbonyl)propylalkohol;
substituerte acetylkarbonylbutylalkoholforbindelser såsom 4-(trimetylacetylkarbonyl)butylalkohol, metoksyacetylkarbonyl)butylalkohol, 4-(ferf-
butylacetylkarbonyl)butylalkohol, 4-(acetoksyacetylkarbonyl)butylalkohol, 4-(bromoacetylkarbonyl)butylalkohol, 4-(kloracetylkarbonyl)butylalkohol, 4-(cyklopentylacetylkarbonyl)butylalkohol, 4-(dikloracetylkarbonyl)butylalkohol, 4-(tribromacetylkarbonyl)butylalkohol, 4-(trikloracetylkarbonyl)butylalkohol og 4-(trifluoracetylkarbonyl)butylalkohol;
substituerte acetylkarbonyimetylalkoholforbindelser såsom
fenylacetylkarbonylmetylalkohol, 2,2-difenylacetylkarbonylmetylalkohol, 2,2,2-trifenylacetylkarbonylmetylalkohol, 4-metoksyfenylacetylkarbonylmetylalkohol, 3,4-dimetoksyfenylacetylkarbonylmetylalkohol, 2,5-
dimetoksyfenylacetylkarbonylmetylalkohol, 2-bromfenylacetylkarbonylmetylalkohol, 2-brom-4,5-dimetoksyfenylacetylkarbonylmetylalkohol, 4-klorfenylacetylkarbonylmetylalkohol, 2-klor-2-fenylacetylkarbonylmetylalkohol, 2,2-difenyl-2-kloracetylkarbonylmetylalkohol, 4-fluorfenylacetylkarbonylmetylalkohol, 4-metoksyfenylacetylkarbonylmetylalkohol, fenoksyacetylkarbonylmetylalkohol, 4-fluorfenoksyacetylkarbonylmetylalkohol, benzyloksyacetylkarbonylmetylalkohol, 2-fenyl-2-kloracetylkarbonylmetylalkohol, 2,2-difenyl-2-kloracetylkarbonylmetylalkohol og 2-(2,4,5-triklorfenoksy)acetylkarbonylmetylalkohol;
substituerte acetylkarbonyletylalkoholforbindelser såsom 2-(fenylacetylkarbonyl)etylalkohol, 2-(2,2-difenylacetylkarbonyl)etylalkohol, 2-(2,2,2-trifenylacetylkarbonyl)etylalkohol, 2-(4-metoksyfenylacetylkarbonyl)etylalkohol, 2-(3,4-dimetoksyfenylacetylkarbonyl)etylalkohol, 2-(2,5-dimetoksyfenylacetylkarbonyl)etylalkohol, 2-(2-bromfenylacetylkarbonyl)etylalkohol, 2-(2-brom-4,5-dimetoksyfenylacetylkarbonyl)etylalkohol, 2-(4-klorfenylacetylkarbonyl)etylalkohol, 2-(2-fenyl-2-kloracetylkarbonyl)etylalkohol, 2-(2,2-difenyl-2-kloracetylkarbonyl)etylalkohol, 2-(4-fluorfenylacetylkarbonyl)etylalkohol, 2-(4-metoksyfenylacetylkarbonyl)etylalkohol, 2-(fenoksyacetylkarbonyl)etylalkohol, 2-(4-fluorfenoksyacetylkarbonyl)etylalkohol, 2-(benzyloksyacetylkarbonyl)etylalkohol, 2-(2-fenyl-2-kloracetylkarbonyl)etylalkohol, 2-(2,2-difenyl-2-kloracetylkarbonyl)etylalkohol og 2-(2-(2,4,5-triklorfenoksy)acetylkarbonyl)etylalkohol;
substituerte acetylkarbonylpropylalkoholforbindelser såsom 3-(fenylacetylkarbonyl)propylalkohol, 3-(2,2-difenylacetylkarbonyl)propylalkohol, 3-(2,2,2-
trifenylacetylkarbonyl)propylalkohol, 3-(4-metoksyfenylacetylkarbonyl)propylalkohol, 3-(3,4- dimetoksyfenylacetylkarbonyl)propylalkohol, 3-(2,5-dimetoksyfenylacetylkarbonyl)propylalkohol, 3-(2-bromfenylacetylkarbonyl)propylalkohol, 3-(2-brom-4,5-dimetoksyfenylacetylkarbonyOpropylalkohol, 3-(4-klorfenylacetylkarbonyl)propylalkohol, 3- (2-fenyl-2-kloracetylkarbonyljpropylalkohol, 3-(2,2-difenyl-2-kloracetylkarbonyl)propylalkohol, 3-(4-fluorfenylacetylkarbonyl)propylalkohol, 3-(4-metoksyfenylacetylkarbonyl)propylalkohol, 3-(fenoksyacetylkarbonyl)propylalkohol, 3-(4-fluorfenoksyacetylkarbonyl)propylalkohol, 3-(benzyloksyacetylkarbonyl)propylalkohol, 3-(2-fenyl-2-kloracetylkarbonyl)propylalkohol, 3-(2,2-difenyl-2-kloracetylkarbonyl)propylalkohol og 3-(2-(2,4,5-triklorfenoksy)acetylkarbonyl)propylalkohol;
substituerte acetylkarbonylbutylalkoholforbindelser såsom 4-(fenylacetylkarbonyl)butylalkohol, 4-(2,2-difenylacetylkarbonyl)butylalkohol, 4-(2,2,2-trifenylacetylkarbonyl)butylalkohol, 4-(4-metoksyfenylacetylkarbonyl)butylalkohol, 4-(3,4-dimetoksyfenyiacetylkarbonyl)butylalkohol, 4-(2,5-dimetoksyfenylacetylkarbonyl)butylalkohol, 4-(2-bromfenylacetylkarbonyl)butylalkohol, 4- (2-brom-4,5-dimetoksyfenylacetylkarbonyl)butylalkohol, 4-(4-klorfenylacetylkarbonyl)butylalkohol, 4-(2-fenyl-2-kloracetylkarbonyl)butylalkohol, 4-(2,2-difenyl-2-kloracetylkarbonyl)butylalkohol, 4-(4-fluorfenylacetylkarbonyl)butylalkohol, 4-(4-metoksyfenylacetylkarbonyl)butylalkohol, 4-(fenoksyacetylkarbonyl)butylalkohol, 4-(4-fluorfenoksyacetylkarbonyl)butylalkohol, 4-(benzyloksyacetylkarbonyl)butylalkohol, 4-(2-fenyl-2-kloracetylkarbonyl)butylalkohol, 4-(2,2-difenyl-2-kloracetylkarbonyl)butylalkohol og 4-(2-(2,4,5-triklorfenoksy)acetylkarbonyi)butylalkohol;
substituerte silyloksykarbonyimetylalkoholforbindelser såsom
trimetylsilyloksykarbonylmetylalkohol, trietylsilyloksykarbonylmetylalkohol, tri-n-propylsilyloksykarbonylmetylaikohol, triisopropylsilyloksykarbonylmetylalkohol, tri-n-butylsilyloksykarbonylmetylalkohol, triisobutylsilyloksykarbonylmetylalkohol, Xr'\- tert-butylsilyloksykarbonylmetylalkohol, tri-s-butylsilyloksykarbonylmetylalkohol, tri-n-pentyisilyloksykarbonylmetylalkohol, triisopentylsilyloksykarbonylmetylalkohol, tri-n-heksylsilyloksykarbonylmetylalkohol, tri-n-oktylsilyloksykarbonylmetylalkohol, trifenylsilyloksykarbonylmetylalkohol, tri-p-metylfenylsilyloksykarbonylmetylalkohol,
tribenzylsilyloksykarbonylmetylalkohol, etyldimetylsilyloksykarbonylmetylalkohol, n-butyldimetylsilyloksykarbonylmetylalkohol, diisopropylsilyloksykarbonylmetylalkohol og t-butyldifenylsilyloksykarbonylmetylalkohol;
substituerte silyloksykarbonyletylalkoholforbindelser såsom 2-(trimetylsilyloksykarbonyl)etylalkohol, 2-(trietylsilyloksykarbonyl)etylalkoholJ 2-(tri-n-propylsilyloksykarbonyl)etylalkohol, 2-(triisopropylsiiyloksykarbonyl)etylalkohol, 2-(tri-n-butylsiiyloksykarbonyl)etylalkohol, 2-(triisobutylsilyloksykarbonyl)etylalkoholf 2-(tri-fert-butylsilyloksykarbonyl)etylalkohol, 2-(tri-s-butylsilyloksykarbonyl)etylalkohol, 2-(tri-n-pentylsilyloksykarbonyl)etylalkohol, 2-(triisopentylsilyloksykarbonyl)etylalkohol, 2-(tri-n-heksylsilyloksykarbonyl)etylalkohol, 2-(tri-n-oktylsilyloksykarbonyl)etylalkohol, 2-(trifenylsilyloksykarbonyl)etylalkohol, 2-(tri-p-metylfenylsilyloksykarbonyl)etylalkohol, 2-(tribenzylsilyloksykarbonyl)etylalkohol, 2-(etyldimetylsilyloksykarbonyl)etylalkohol, 2-(n-butyldimetylsilyloksykarbonyl)etyialkohol, 2-(diisopropylsilyloksykarbonyl)etylalkohol og 2- (t-butyldifenylsilyloksykarbonyl)etylalkohoi;
substituerte silyloksykarbonylpropylalkoholforbindelser såsom 3-(trimetylsilyloksykarbonyl)propylalkohol, 3-(trietylsilyloksykarbonyl)propylalkohol, 3-(tri-n-propylsilyloksykarbonyl)propylalkohol, 3-(triisopropylsilyloksykarbonyl)propylalkohol, 3- (tri-n-butylsilyloksykarbonyl)propyialkohol, 3-(triisobutylsilyloksykarbonyl)propylalkohol, 3-(tri-te/t-butylsilyloksykarbonyl)propylalkohol, 3-(tri-s-butylsilyloksykarbonyl)propylalkohol, 3-(tri-n-pentylsilyloksykarbonyl)prbpylalkohol, 3-(triisopentylsilyloksykarbonyl)propylalkohol, 3-(tri-n-heksylsilyloksykarbonyl)propylalkohol, 3-(tri-n-oktylsilyloksykarbonyl)propylalkohol, 3-(trifenylsilyloksykarbonyl)propylalkohol, 3-(tri-p-metylfenylsilyloksykarbonyl)propylalkohol, S^tribenzylsilyloksykarbonyljpropylalkohol, 3-(etyldimetylsilyloksykarbonyl)propylalkohol, 3-(n-butyldimetylsilyloksykarbonyl)propylalkohol, 3-(diisopropylsilyloksykarbonyl)propylalkohol og 3-(t-butyldifenylsilyioksykarbonyl)propylalkohol;
substituerte silyloksykarbonylbutylalkoholforbindelser såsom 4-(trimetylsilyloksykarbonyl)butylalkohol, 4-(trietylsilyloksykarbonyl)butylalkohol, 4-(tri-n-propylsilyloksykarbonyl)butylalkohol, 4-(triisopropylsilyloksykarbonyl)butylalkohol, 4-(tri-
n-butylsilyloksykarbonyl)butylalkohol, 4-(triisobutylsilyloksykarbonyl)butylalkohol, 4-(tri-fe/t-butylsilyloksykarbonyl)butylaikohol, 4-(tri-s-butylsilyloksykarbonyl)butylalkohol, 4-(tri-n-pentylsilyloksykarbonyl)butylalkohol, 4-(triisopentylsilyloksykarbonyl)butylalkohol, 4-(tri-n-heksylsilyloksykarbonyl)butylalkohol, 4-(tri-n-oktylsilyloksykarbonyl)butylalkohol, 4-(trifenylsilyloksykarbonyl)butylalkohol, 4-(tri-p-metylfenylsilyloksykarbonyl)butylalkohol, 4-(tribenzylsilyloksykarbonyl)butylalkohol, 4-(etyldimetylsilyloksykarbonyl)butylalkohol, 4-(n-butyldimetylsilyloksykarbonyl)butylalkohol, 4-(diisopropylsilyloksykarbonyl)butylalkohol og 4-(t-butyldifenylsilyloksykarbonyl)butylalkohol;
formylsubstituerte metylhalogener såsom 3-formylfenylkarboksymetylklorid, 4-formylfenylkarboksymetylklorid, 2-formylfenylkarboksymetylklorid, 6-fluor-2-formylfenylkarboksymetylklorid, 2-formyl-6-metoksyfenylkarboksymetylklorid, 6-etoksy-2-formylfenylkarboksymetylklorid, 2'formyl-6-hydroksyfenylkarboksymetylklorid, 4-formyl-2-metylfenylkarboksymetylklorid, 4-formyl-3-klorfenylkarboksymetylklorid4-brom-, 2-formylfenylkarboksymetylklorid, 2-formyl-4-metoksyfenylkarboksymetylklorid, 4-formyl-2-metoksyfenylkarboksymetylklorid, 2-formyl-4-(trifluormetoksy) fenylkarboksymetylklorid, 4-formyl-2-nitrofenylkarboksymetylklorid, 4,6-dibrom-2-formylfenylkarboksymetylklorid og 4-formyl-2,5-dimetylfenylkarboksymetylklorid;
formylsubstituerte etylhalogener såsom 2-(3-formylfenylkarboksy)etylklorid, 2-(4-formylfenylkarbbksy)etylklorid, 2-(2-formylfenylkarboksy)etylklorid, 2-(6-fluor-2-formylfenylkarboksy)etylklorid, 2-(2-formyl-6-metoksyfenylkarboksy)etylk|orid, 2-(6-etoksy-2-formylfenylkarboksy)etylklorid, 2-(2-formyl-6-hydroksyfenylkarboksy)etylklorid, 2-(4-formyl-2-metylfenylkarboksy)etylklorid, 2-(4-formyl-3-klorfenylkarboksy)etylklorid, 2-(4-brom-2-formylfenylkarboksy)etylklorid, 2-(2-formyl-4-metoksyfenylkarboksy)etylklorid, 2-(4-formyl-2-metoksyfenylkarboksy)etylklorid, 2-(2-formyl-4-(trifluormetoksy)fenylkarboksy)etylklorid, 2-(4-formyl-2-nitrofenylkarboksy)etylklorid, 2-(4,6-dibrom-2-formylfenylkarboksy)etylklorid og 2-(4-formyl-2,5-dimetylfenylkarboksy)etylklorid;
formylsubstituerte propylhalogener såsom 3-(3-formylfenylkarboksy)propylklorid, 3-(4-formylfenylkarboksy)propylklorid, 3-(2-formylfenylkarboksy)propylklorid, 3-(6-fluor-2-formylfenylkarboksy)propylklorid, 3-(2-formyl-6-metoksyfenylkarboksy)propylklorid, 3-(6-
etoksy-2-formylfenylkarboksy)propylklorid, 3-(2-formyl-6-hydroksyfenylkarboksy)propylklorid, 3-(4-forrriyl-2-metylfenylkarboksy)propylklorid, 3-(4-formyl-3-klorfenylkarboksy)propylklorid, 3-(4-brom-2-formylfenylkarboksy)propylklorid, 3- (2-formyl-4-metoksyfenylkarboksy)propylklorid, 3-(4-formyl-2-metoksyfenylkarboksy)propylklorid, 3-(2-formyl-4-(trifluormetoksy)fenylkarboksy)propylklorid, 3-(4-formyl-2-
nitrofenylkarboksy)propylklorid, 3-(4,6-dibrom-2-formylfenylkarboksy)propylklorid og 3-(4-forrnyl-2,5-dimetylfenylkarboksy)propylklorid;
formylsubstituerte butylhalogener såsom 4-(3-formylfenylkarboksy)butylklorid, 4-(4-formylfenylkarboksy)butylklorid, 4-(2-formylfenylkarboksy)butylklorid, 4-(6-fluor-2-formylfenylkarboksy)butylklorid, 4-(2-formyl-6-metoksyfenylkarboksy)butylklorid, 4-(6-etoksy-2-formylfenylkarboksy)butylklorid, 4-(2-formyl-6-hydroksyfenylkarboksy)butylklorid, 4-(4-formyl-2-metylfenylkarboksy)butylklorid, 4-(4-formyl-3-klorfenylkarboksy)butylklorid, 4-(4-brom-2-formylfenylkarboksy)butylklorid, 4-(2-formyl-4-metoksyfenylkarboksy)butylklorid, 4-(4-formyl-2-metoksyfenylkarboksy)butylklorid, 4i(2-formyl-4-(trifluormetoksy)fenylkarboksy)butylklorid, 4-(4-formyl-2-nitrofenylkarboksy)butylklorid, 4- (4,6-dibrom-2-formylfenylkarboksy)butylklorid og 4-(4-formyl-2,5-dimetylfenylkarboksy)butylklorid;
estersubstituerte metylhalogener såsom 4-metoksykarbonylfenylkarboksymetylklorid, 4-propoksykarbonylfenylkarboksymetylklorid, 4-isopropoksykarbonylfenylkarboksymetylklorid, 2-metoksykarbonylfenylkarboksymetylklorid, 2-nitro-4-metoksykarbonylfenylkarboksymetylklorid, 4-etoksykarbonyl-2-metoksyfenylkarboksymetylklorid, 5-etoksykarbonyl-2-
hydroksyfenylkarboksymetylklorid, 3-hydroksy-2-metoksykarbonylfenylkarboksymetylklorid, 2-metoksykarbonylmetylfenylkarboksymetylklorid og 4-etoksykarbonyletyl-2-nitrofenylkarboksymetylklorid;
estersubstituerte etylhalogener såsom 2-(4-metoksykarbonylfenylkarboksy)etylklorid, 2-(4-propoksykarbonylfenylkarboksy)etylklorid, 2-(4-
isopropoksykarbonylfenylkarboksy)etylklorid, 2-(2-metoksykarbonylfenylkarboksy)etylklorid, 2-(2-nitro-4-metoksykarbonylfenylkarboksy)etylklorid, 2-(4-etoksykarbonyl-2-metoksyfenylkarboksy)etylklorid, 2-(5-etoksykarbonyl-2-hydroksyfenylkarboksy)etylklorid, 2-(3-hydroksy-2-metoksykarbonylfenylkarboksyjetylklorid, 2-(2-metoksykarbonylmetylfenylkarboksy)etylklorid og 2-(4-etoksykarbonyletyl-2-nitrofenylkarboksy)etylklorid;
estersubstituerte propylhalogener såsom 3-(4-metoksykarbonylfenylkarboksy)propylklorid, 3-(4-propoksykarbonylfenylkarboksy)propylklorid, 3-(4-isopropoksykarbonylfenylkarboksy)propylklorid, 3-(2-metoksykarbonylfenylkarboksy)propylklorid, 3-(2-nitro-4-metoksykarbonylfenylkarboksy)propylklorid, 3-(4-etoksykarbonyl-2-metoksyfenylkarboksy)propylklorid, 3-(5-etoksykarbonyl-2-hydroksyfenylkarboksy)propylklorid, 3-(3-hydroksy-2-metoksykarbonylfenylkarboksy)propylklorid, 3-(2-metoksykarbonylmetylfenylkarboksy)propylklorid og 3-(4-etoksykarbonyletyl-2-nitrofenylkarboksy)propylklorid;
estersubstituerte butylhalogener såsom 4-(4-metoksykarbonylfenylkarboksy)butylklorid, 4-(4-propoksykarbonylfenylkarboksy)butylklorid, 4-(4-isopropoksykarbonylfenylkarboksy)butylklorid, 4-(2-metoksykarbonylfenylkarboksy)butylklorid, 4-(2-nitro-4-metoksykarbonylfenylkarboksy)butylklorid, 4-(4-etoksykarbonyl-2-metoksyfenylkarboksy)butylklorid, 4-(5-etoksykarbonyl-2-hydroksyfenylkarboksy)butylklorid, 4-(3-hydroksy-2-metoksykarbonylfenylkarboksy)butylklorid, 4-(2-metoksykarbonylmetylfenylkarboksy)butylklorid og 4-(4-etoksykarbonyletyl-2-nitrofenylkarboksy)butylklorid;
alkoksysubstituerte metylhalogener såsom 2-metoksyfenylkarboksymetylklorid, 4-metoksyfenylkarboksymetylklorid, 4 etoksyfenylkarboksymetylklorid, 1,4-
dimetoksyfenylkarboksymetylklorid, 2,4-dimetoksyfenylkarboksymetylklorid, 2-klor-5-metoksyfenylkarboksymetylklorid, 3,5-dietoksyfenylkarboksymetylklorid 3-hydroksy- og 2,5-dimetoksyfenylkarboksymetylklorid;
alkoksysubstituerte etylhalogener såsom 2-(2-metoksyfenylkarboksy)etylklorid, 2-(4-metoksyfenylkarboksy)etylklorid, 2-(4 etoksyfenylkarboksy)etylklorid, 2-(1,4-dimetoksyfenylkarboksy)etylklorid, 2-(2,4-dimetoksyfenylkarboksy)etylklorid, 2-(2-klor-5-metoksyfenylkarboksy)etylklorid, 2-(3,5-dietoksyfenylkarboksy)etylklorid og 2-(3-hydroksy-2,5-dimetoksyfenylkarboksy)etylklorid;
alkoksysubstituerte propylhalogener såsom 3-(2-metoksyfenylkarboksy)propylklorid, 3-(4-metoksyfenylkarboksy)propylklorid, 3-(4 etoksyfenylkarboksy)propylklorid, 3-(1,4-dimetoksyfenylkarboksy)propylklorid, 3-(2,4-dimetoksyfenylkarboksy)propylklorid, 3-(2-klor-5-metoksyfenylkarboksy)propylklorid, 3-(3,5-dietoksyfenylkarboksy)propylklorid og 3-(3-hydroksy-2,5-dimetoksyfenylkarboksy)propylklorid;
alkoksysubstituerte butylhalogener såsom 4-(2-metoksyfenylkarboksy)butylklorid, 4-(4-metoksyfenylkarboksy)butylklorid, 4-(4 etoksyfenylkarboksy)butylklorid, 4-(1,4-dimetoksyfenylkarboksy)butylklorid, 4-(2,4-dimetoksyfenylkarboksy)butylklorid, 4-(2-klor-5-metoksyfenylkarboksy)butylklorid, 4-(3,5-dietoksyfenylkarboksy)butylklorid og 4-(3-hydroksy-2,5-dimetoksyfenylkarboksy)butylklorid;
hydroksysubstituerte metylhalogener såsom 2-hydroksyfenylkarboksymetylklorid, 3-hydroksyfenylkarboksymetylklorid, 4-hydroksyfenylkarboksymetylklorid og 3,5-dihydroksyfenylkarboksymetylklorid;
hydroksysubstituerte etylhalogener såsom 2-(2-hydroksyfenylkarboksy)etylklorid, 2-(3-hydroksyfenylkarboksy)etylklorid, 2-(4-hydroksyfenylkarboksy)etylklorid og 2-(3,5-dihydroksyfenylkarboksy)etylklorid;
hydroksysubstituerte propylhalogener såsom 3-(2-hydroksyfenylkarboksy)propylklorid, 3-(3-hydroksyfenylkarboksy)propylklorid, 3-(4-hydroksyfenylkarboksy)propylklorid og 3-(3,5-dihydroksyfenylkarboksy)propylklorid;
hydroksysubstituerte butylhalogener såsom 4-(2-hydroksyfenylkarboksy)butylklorid, 4-(3-hydroksyfenylkarboksy)butylklorid, 4-(4-hydroksyfenylkarboksy)butylklorid og 4-(3,5-dihydroksyfenylkarboksy)butylklorid;
halogensubstituerte forbindelser såsom 4-bromfenylkarboksymetylklorid, 2,4,6-tribromfenylkarboksymetylklorid, 2,4,6-triklorfenylkarboksymetylkiorid, 4-brom-2,6-diklorfenylkarboksymetylklorid, 6-jod-2,4-diklorfenylkarboksymetylklorid, 4,6-dibrom-2-klorfenylkarboksymetylklorid;
halogensubstituerte forbindelser såsom 2-(4-bromfenylkarboksy)etylklorid, 2-(2,4,6-tribromfenylkarboksy)etylklorid, 2-(2,4,6-triklorfenylkarboksy)etylk!orid, 2-(4-brom-2,6-dikiorfenylkarboksy)etylklorid, 2-(6-jod-2,4-diklorfenylkarboksy)etylklorid, 2-(4,6-dibrom-2-klorfenylkarboksy)etylklorid;
halogensubstituerte forbindelser såsom 3-(4-bromfenylkarboksy)propylklorid, 3-(2,4,6-tribromfenylkarboksy)propylklorid, 3-(2,4,6-triklorfenylkarboksy)propylklorid, 3-(4-brom-"2;6-diklorfenylkarboksy)propylklorid, 3-(6-jod-2,4-diklorfenylkarboksy)propylklorid, 34,6-dibrom~(2-klorfenylkarboksy)propylklorid;
halogensubstituerte forbindelser såsom 4-(4-bromfenylkarboksy)butylklorid, 4-(2,4,6-tribromfenylkarboksy)butylklorid, 4-(2,4,6-triklorfenylkarboksy)butylklorid, 4-(4-brom-2,6-diklorfenylkarboksy)butylklorid, 4-(6-jod-2,4-diklorfenylkarboksy)butylklorid, 4-(4,6-dibrom-2-klorfenylkarboksy)butylklorid;
halogensubstituerte acetylkarbonylforbindelser såsom trimetylacetylkarbonylmetylklorid, metoksyacetylkarbonylmetylklorid, te/t-butylacetylkarbonylmetylklorid, acetoksyacetylkarbonylmetylklorid, bromoacetylkarbonylmetylklorid, kloracetylkarbonylmetylklorid, cyklopentylacetylkarbonylmetylklorid, dikloracetylkarbonylmetylklorid, tribromacetylkarbonylmetylklorid, trikloracetylkarbonylmetylklorid og trifluoracetylkarbonylmetylklorid,
halogensubstituerte acetylkarbonylforbindelser såsom 2-(trimetylacetylkarbonyl)etylklorid, metoksyacetylkarbonyl)etylklorid, 2-( tert-butylacetylkarbonyl)etylklorid, 2-(acetoksyacetylkarbonyl)etylklorid, 2-
(bromoacetylkarbonyl)etyiklorid, 2-(kloracetylkarbonyl)etylklorid, 2-(cyklopentylacetylkarbonyl)etylklorid, 2-(dikloracetylkarbonyl)etylklorid, 2-(tribromacetylkarbonyl)etylklorid, 2-(trikloracetylkarbonyl)etylklorid og 2-(trifluoracetylkarbonyl)etylklorid;
halogensubstituerte acetylkarbonylforbindelser såsom 3-(trimetylacetylkarbonyl)propylklorid, metoksyacetylkarbonyl)propylklorid, 3-( tert-butylacetylkarbonyl)propylklorid, 3-(acetoksyacetylkarbonyl)propylklorid, 3-(bromoacetylkarbonyl)propylklorid, 3-(kloracetylkarbonyl)propylklorid, 3-(cyklopentylacetylkarbonyl)propylklorid, 3-(dikloracetylkarbonyl)propylklorid, 3-(tribromacetylkarbonyl)propylklorid, 3-(trikloracetylkarbonyl)propylklorid og 3-(trifluoracetylkarbonyl)propylklorid;
halogensubstituerte acetylkarbonylforbindelser såsom 4-(trimetylacetylkarbonyl)butylklorid, metoksyacetylkarbonyl)butylklorid, 4-{ tert-butylacetylkarbonyl)butylklorid, 4-(acetoksyacetylkarbonyl)butylklorid, 4-(bromoacetylkarbonyl)butylklorid, "4-(kloracetylkarbonyl)butylklorid, 4-(cyklopentylacetylkarbonyl)butylklorid, 4-(dikloracetylkarbonyl)butylklorid, 4-(tribromacetylkarbonyl)butylklorid, 4-(trikloracetylkarbonyl)butylklorid og 4-(trifluoracetylkarbonyl)butylklorid;
halogensubstituerte acetylkarbonylforbindelser såsom fenylacetylkarbonylmetylklorid, 2,2-difenylacetylkarbonylmetylklorid, 2,2,2-trifenylacetylkarbonylmetylklorid, 4-metoksyfenylacetylkarbonylmetylklorid, 3,4-dimetoksyfenylacetylkarbonylmetylklorid, 2,5-dimetoksyfenylacetylkarbonylmetylklorid, 2-bromfenylacetylkarbonylmetylklorid, 2-brom-4,5-dimetoksyfenylacetylkarbonylmetylklorid, 4-klorfenylacetylkarbonylmetylklorid, 2-fenyl-2-k|oracetylkarbonylmetylklorid, 2,2-difenyl-2-kloracetylkarbonylmetylklorid, 4-fluorfenylacetylkarbonylmetylklorid, 4-metoksyfenylacetylkarbonylmetylklorid, fenoksyacetylkarbonylmetylklorid, 4-fluorfenoksyacetylkarbonylmetylklorid, benzyloksyacetylkarbonylmetylklorid, 2-fenyl-2-kloracetylkarbonylmetylklorid, 2,2-difenyl-2-kloracetylkarbonylmetylklorid og 2-(2,4,5-triklorfenoksy) acetylkarbonylmetylklorid;
halogensubstituerte acetylkarbonylforbindelser såsom 2-(fenylacetylkarbonyl)etylklorid, 2-(2,2-difenylacetylkarbonyl)etylklorid, 2-(2,2,2-trifenylacetylkarbonyl)etylklorid, 2-(4-metoksyfenylacetylkarbonyl)etylklorid, 2-(3,4-dimetoksyfenylacetylkarbonyl)etylklorid, 2-(2,5-dimetoksyfenylacetylkarbonyl)etylklorid, 2-(2-bromfenylacetylkarbonyl)etylklorid, 2-(2-brom-4,5-dimetoksyfenylacetylkarbonyl)etylklorid, 2-(4-klorfenylacetylkarbonyl)etylklorid, 2-(2-fenyl-2-kloracetylkarbonyl)etylklorid, 2-(2,2-difenyl-2-kloracetylkarbonyl)etylklorid, 2-(4-fluorfenylacetylkarbonyl)etylklorid, 2-(4-metoksyfenylacetylkarbonyl)etylklorid, 2-(fenoksyacetylkarbonyl)etylklorid, 2-(4-fluorfenoksyacetylkarbonyl)etylklorid, 2-(benzyloksyacetylkarbonyl)etylklorid, 2-(2-fenyl-2-kloracetylkarbonyl)etylklorid, 2-(2,2-difenyl-2-kloracetylkarbonyl)etylklorid og 2-(2-(2,4,5-triklorfenoksy) acetylkarbonyl)etylklorid;
halogensubstituerte acetylkarbonylforbindelser såsom 3-(fenylacetylkarbonyl)propylklorid, 3-(2,2-difenylacetylkarbonyl)prdpylklorid, 3-(2,2,2-trifenylacetylkarbonyl)propylklorid, 3-(4-metoksyfenylacetylkarbonyl)propylklorid, 3-(3,4-dimetoksyfenylacetylkarbonyl)propylklorid, 3-(2,5-"dimetoksyfenyiacetylkarbonyOpropylklorid, 3-(2-bromfenylacetylkarbonyl)propylklorid, 3-(2-brom-4,5-dimetoksyfenylacetylkarbonyl)propylklorid, 3-(4-klorfenylacetylkarbonyl)propylklorid, 3-(2-fenyl-2-kloracetylkarbonyl)propylklorid, 3-(2,2-difenyl-2-kloracetylkarbonyl)propylklorid, 3-(4-fluorfenylacetylkarbonyl)propylklorid, 3-(4-metoksyfenylacetylkarbonyl)propylklorid, 3-(fenoksyacetylkarbonyl)propylklorid, 3-(4-fluorfenoksyacetylkarbonyl)propylklorid, 3-(benzyloksyacetylkarbonyl)propylklorid, 3-(2-fenyl-2-kloracetylkarbonyl)propylklorid, 3-(2,2-difenyl-2-kloracetylkarbonyl)propylklorid og 3-(2-(2,4,5-triklorfenoksy) acetylkarbonyl)propylklorid;
halogensubstituerte acetylkarbonylforbindelser såsom 4-(fenylacetylkarbonyl)butylklorid, 4-(2,2-difenylacetylkarbonyl)butylklorid, 4-(2,2,2-trifenylacetylkarbonyl)butylklorid, 4-(4-metoksyfenylacetylkarbonyl)butylklorid, 4-(3,4-dimetoksyfenylacetylkarbonyl)butylklorid, 4-(2,5-dimetoksyfehylacetylkarbonyl)butylklorid, 4-(2-bromfenylacetylkarbonyl)butylklorid, 4-(2-brom-4,5-
dimetoksyfenylacetylkarbonyl)butylklorid, 4-(4-klorfenylacetylkarbonyl)butylklorid, 4-(2-fenyl-2-kloracetylkarbonyl)butylklorid, 4-(2,2-difenyl-2-kloracetylkarbonyl)butylklorid, 4-(4-fluorfenylacetylkarbonyl)butylklorid, 4-(4-metoksyfenylacetylkarbonyl)butylklorid, 4-(fenoksyacetylkarbonyl)butylklorid, 4-(4-fluorfenoksyacetylkarbonyl)butylklorid, 4-
(benzyloksyacetylkarbonyl)butylklorid, 4-(2-fenyl-2-kloracetylkarbonyl)butylklorid, 4-(2,2-difenyl-2-kloracetylkarbonyl)butylklorid og 4-(2-(2,4,5-triklorfenoksy) acetylkarbonyl)butylklorid;
silyisubstituerte metylhalogener såsom trimetylsilyloksykarbonylmetylklorid, trietylsilyloksykarbonylmetylklorid, tri-n-propylsilyloksykarbonylmetylklorid, triisopropylsilyloksykarbonylmetylklorid, tri-n-butylsilyloksykarbonylmetylklorid, triisobutylsilyloksykarbonylmetylklorid, tri-fe/t-butylsilyloksykarbonylmetylklorid, tri-s-butylsilyloksykarbonylmetylklorid, tri-n-pentylsilyloksykarbonylmetylklorid, triisopentylsilyloksykarbonylmetylklorid, tri-n-heksylsilyloksykarbonylmetylklorid, tri-n-oktylsilyloksykarbonylmetylklorid, trifenylsilyloksykarbonylmetylklorid, tri-p-metylfenylsilyloksykarbonylmetylklorid, tribenzylsilyloksykarbonylmetylklorid, etyldimetylsilyloksykarbonylmetylklorid, n-butyldimetylsilyloksykarbonylmetylklorid, diisopropylsilyloksykarbonylmetylklorid og t-butyldifenylsilyloksykarbonylmetylklorid;
silyisubstituerte etylhalogener såsom 2-(trimetylsilyloksykarbonyl)etylklorid, 2--(trietylsilyloksykarbonyl)etylklorid, 2-(tri;n-propylsilyloksykarbonyl)etylklorid, 2-(triisopropylsilyloksykarbonyl)etylklorid, 2-(tri-n-butylsilyloksykarbonyl)etylklorid, 2-(triisobutylsilyloksykarbonyl)etylklorid, 2-(tri-?ert-butylsilyloksykarbonyl)etylklorid, 2-(tri-s-butylsilyloksykarbonyl)etylklorid, 2-(tri-n-pentylsilyloksykarbonyl)etylklorid, 2-(triisopentylsilyloksykarbonyl)etylklorid, 2-(tri-n-heksylsilyloksykarbonyl)etylklorid, 2-(tri- . n-oktylsilyloksykarbonyl)etylklorid, 2-(trifenylsilyloksykarbonyl)etylklorid, 2-(tri-p-metylfenylsilyloksykarbonyl)etylklorid, 2-(tribenzylsilyloksykarbonyl)etylklorid, 2-(etyldimetylsilyloksykarbonyl)etylklorid, 2-(n-butyldimetylsilyloksykarbonyl)etylklorid, 2-(diisopropylsilyloksykarbonyl)etylklorid og 2-(t-butyldifenylsilyloksykarbonyl)etylklorid;
silyisubstituerte propylhalogener såsom 3-(trimetylsilyloksykarbonyl)propylklorid, 3-(trietylsilyloksykarbonyl)propylklorid, 3-(tri-n-propylsilyloksykarbonyl)propylklorid, 3-(triisopropylsilyloksykarbonyl)propylklorid, 3-(tri-n-butylsilyloksykarbonyl)propylklorid, 3-(triisobutylsilyloksykarbonyl)propylklorid, 3-(tri-fert-butylsilyloksykarbonyl)propylklorid, 3-(tri-s-butylsilyloksykarbonyl)propylklorid, 3-(tri-n-pentylsilyloksykarbonyl)propylklorid, 3^
(triisopentylsilyloksykarbonyl)propylklorid, 3-(tri-n-heksylsilyloksykarbonyl)propylklorid, 3-(tri-n-oktylsilyloksykarbonyl)propylklorid, 3-(trifenylsilyloksykarbonyl)propylklorid, 3-(tri-p-metylfenylsilyloksykarbonyl)propylklorid, 3-(tribenzylsilyloksykarbonyl)propylklorid, 3-
(etyldimetylsilyloksykarbonyl)propylklorid, 3-(n-butyldimetylsilyloksykarbonyl)propylklorid, 3-(diisopropylsilyloksykarbonyl)propylklorid og 3-(t-butyldifenylsilyloksykarbonyl)propylklorid;
silyisubstituerte butylhalogener såsom 4-(trimetylsilyloksykarbonyl)butylklorid, 4-(trietylsilyloksykarbonyl)butylklorid, 4-(tri-n-propylsilyloksykarbonyl)butylklorid, 4-(triisopropylsilyloksykarbonyl)butylklorid, 4-(tri-n-butylsilyloksykarbonyl)butylklorid, 4-(triisobutylsilyloksykarbonyl)butylklorid, 4-(tri-fe/t-butylsilyloksykarbonyl)butylklorid, 4-(tri-s-butylsilyloksykarbonyl)butylklorid, 4-(tri-n-pentylsilyloksykarbonyl)butylklorid, 4-(triisopentylsilyloksykarbonyl)butylklorid, 4-(tri-n-heksylsilyloksykarbonyl)butylklorid, 4-(tri-n-oktylsilyloksykarbonyl)butylklorid, 4-(trifenylsilyloksykarbonyl)butylklorid, 4-(tri-p-metylfenylsilyloksykarbonyl)butylklorid, 4-(tribenzylsilyloksykarbonyl)butylklorid, 4-(etyldimetylsilyloksykarbonyl)butylklorid, 4-(n-butyldimetylsilyloksykarbonyl)butylklorid, 4-(diisopropylsilyloksykarbonyl)butylklorid og 4-(t-butyldifenylsilyloksykarbonyl)butylklorid.
Kopolymeren i foreliggende oppfinnelse kan fremstilles ved å polymerisere minst en monomer med strukturerrdefinert ved I, II eller IV, og minsfen annen vinyl-polymeriserbar monomer ved bruk av en passende polymerisasjonsinitiator i en passende polymerisasjonsmetode.
Passende polymerisasjonsmetoder inkluderer radikal- eller ionisk polymerisasjon i for eksempel løsningspolymerisasjon, bulkpolymerisasjon, semibatch-polymerisasjon, koordinasjonspolymerisasjon, supensjonspolymerisasjon eller
emulsjonspolymerisasjon.
Polymerisasjon i egnet løsningsmiddel omfatter bruk av for eksempel vann;
aromatiske hydrokarboner såsom xylen, white spirit, toluen; ålifatiske hydrokarboner som heksan og heptan; klorerte hydrokarboner som diklormetan, trikloretan, tetrakloretan, fluorerte hydrokarboner som difluormetan, difluoretan, trifluoretan, tetrafluoretan; fluorklor ålifatiske og aromatiske hydrokarboner som klorfluormetan, klordifluoretan, paraklorbenzotrifluorid; ketoner såsom aceton, metyletylketon, metylisobutylketon, cykloheksanon; estere såsom metylacetat, etylacetat, butylacetat, te/t-butylacetat, etylenglykolmetyleteracetat; etere såsom etylenglykoldimetyleter, dietylenglykoldimetyleter, dibutyleter, dioksan, tetrahydrofuran, alkoholer som metanol, etanol, propanol, isopropanol, butanol, benzylalkohol; eter alkoholer som butoksyetanol, propylenglykol-monometyleter, amider som N-metylpyrrolidon,
dimetylformamid eller løsningsmidler såsom dimetylsulfoksid; eventuelt blandinger av ovenfor nevnte løsningsmidler.
Passende radikalinitiatorer inkluderer peroksider som for eksempel benzoyl-
peroksid, diferf-butyl-peroksid, didekanoyl-peroksid og dilaurylperoksid, ferf-butyl-peroksy-2-etylheksanoat, fert-butyl-peroksypivalat, fert-butyl-peroksydietylacetat, tert-amyl-peroksy-2-etylheksanoat og 2,5-dimetyl-2,5-di(2-etylheksanoylperoksy)heksan og azoforbindelser som for eksempel 2,2'azobis(isobutyronitril) og 2,2'azobis(2-metylbutyronitril), vanligvis i konsentrasjoner på 0,01 til 5 vekt% av den anvendte monomerblanding.
Kopolymeren i foreliggende oppfinnelse, kan også fremstilles ved å polymerisere minst en monomer definert ved strukturen I, II eller IV og minst en annen vinyl polymeriserbar monomer ved bruk av en passende polymerisasjonsinitiator og et passende kjedeoverføringsreagens. Ved bruk av kjedeoverføringsreagenser oppnås det
en forgrenet eller stjerneformet struktur hvor polymermolekylene har 3 eller flere polymerkjeder ut fra forgreningspunktet.
Passende kjedeoverføringsreagenser inkluderer flerfunksjonene merkaptaner somforeksempel pentaerytritol-tetra(3-merkaptopropionat)7 trimetylolpropan-tri(merkaptopropionat), pentaerytritol-tetra(tioglykolat), pentaerytritol-tri(tioglykolat) eller andre som beskrevet i WO9603465.
Kopolymeren i foreliggende oppfinnelese som er fremstilt fra minst en monomer definert ved strukturen I, II eller IV, har fortrinnsvis en vektgjennomsnitt molekylvekt
(Mw) fra 1000 til 200000 g/mol.
En typisk begroingshindrende maling i henhold til oppfinnelsen består av
bindemidler og en eller flere andre komponenter. Disse bindemidlene kan være
polymeren beskrevet ovenfor, eventuelt blandinger av flere polymere av typen som beskrevet ovenfor, og andre bindemidler.
En typisk begroingshindrende maling i henhold til oppfinnelsen kan også bestå
av polymeren beskrevet ovenfor i blanding med andre polymere som beskrevet i
NO2002 0846.
En typisk begroingshindrende maling i henhold til oppfinnelsen kan også bestå
av polymeren beskrevet ovenfor i blanding med andre polymere som beskrevet i EP1127925.
Det vil forstås av de som er kjent med slike formuleringer, at bindemiddelfasen også kan inneholde andre kobindemidler som for eksempel harpiks, mykningsmidler eller andre som eksemplifisert nedenfor.
Eksempler på kobindemidler omfatter harpiks, harpiksderivater og metallsalter av harpiks som for eksempel talloljeharpiks, balsamharpiks, treharpiks, hydrogenert harpiks, fumarsyre-harpiksester, maleinsyre-harpiksester, polymerisert harpiks, dimerisert harpiks, sinkrosinat, kobberrosinat, kalsiumrosinat, kaliumrosinat eller andre som beskrevet i WO9744401 og W09615198;
andre kobindemidler som lakserolje og derivater av lakserolje, linfrøolje og derivater av linfrøolje, soyaolje og derivater av soyaolje, kokosolje og derivater av kokosolje;
vinylklorid og kopolymerer av vinylklorid;
styrenkopolymerer som styren/(met)akrylat-kopoylymerer; mettede polyestere som polyvinylacetat; alkyder og modifiserte alkyder; hydrokarbon-harpikser som ~p~etroleumfraksjon=kondensater.
Eksempler på mykningsmidler inkluderer klorerte parafiner;
ftalater som dibutylftalat og benzylbutylftalat, dioktylftalat, dinonylftalat og diisodesylftalat;
fosfatestere som for eksempel trikresylfosfat, nonylfenylfosfat,
oktyloksypoly(etylenoksy)etylfosfat, tributoksyetylfosfat, isooktylfosfat og 2-etylheksyl-difenylfosfat;
sulfonamider som for eksempel H-etyl-para-toluen-sulfonamid og alkyl-para-toluen-sulfonamid;
adipater som for eksempel bis(2-etylheksyl)adipat, diisobutyladipat og dioktyladipat; og andre som for eksempel fosforsyre-trietylester, butylstearat, sorbitantriolat og epoksydert soya(bønne)olje.
De andre komponentene som inngår i malingen kan være biologisk aktive stoffer, pigmenter og fyllstoffer, surfaktanter, fuktemidler og dispergeringsmidler, tørkestoffer, aktivatorer, skumdempere, stabilisatorer, antioksidanter, korrosjonsinhibitorer, koalesceringsmidler, fortykningsmidler og antibunnfallsmidler, fibrer og løsningsmidler.
Den totale bindemiddelsammensetningen gir malingen de nødvendige selvpolerende og brede mekaniske egenskapene. I tillegg er det nødvendig med bruk av ulike forbindelser for å kontrollere befesting og vekst av begroingsorganismer. Disse biologisk aktive forbindelsene kan i store trekk deles inn i to grupper, nemlig uorganiske og organiske forbindelser.
Uorganiske biologisk aktive forbindelser inkluderer ulike kobberforbindelser inklusive oksider, salter, metaller og legeringer enten brukt alene eller flere i kombinasjon. Spesifikke eksempler er kobberoksid, kobbertiocyanat, metallisk kobber og metallisk kobber-nikkel. Denne kategorien inkluderer også barium metaborat.
De organiske biologisk aktive forbindelsene inkluderer både rene organiske og metallorganiske stoffer som er mye brukt i begroingshindrende teknologi i dag eller som blir evaluert for denne teknologien. Disse blir generelt brukt i kombinasjon med uorganiske forbindelser for å gi forbedret ytelse, men kan også brukes i maling som ikke inneholder disse. De mest utbredte benyttede forbindelsene av denne typen i dag er tilgjengelige under de kommmersielle navnene Copper Omadine, Zinc Omdine/Zinc-Pyrion, Sea-Nine 211, Irgarol 1051, Preventol A4, Preventol A5, Preventol A6/Diuron, Zineb og PK. Disse og andre er listet opp av The European Council of the Paint, Printing Ink and Artists Colours Industri (CEPE)'s liste over begroingshindrende forbindelser som var tilgjengelige på det europeiske markedet i 1998 (Utilisation of more "Environmentally Friendly" Antifouling Products, EC project No96/559/3040/DEB/E2, Final Report, July 1999) og disse er herved inkludert som referanse.
Metallorganiske forbindelser inkluderer organokobber-, sink- og mangan-forbindelser.
Eksempler på organokobberforbindelser inkluderer kobberpyrition, oxin-kobber, kobber nonylfenolsulfonat, kobber-naftenat, kobber-acetat, kobber-bis(etylendiamin)bisdodesylbenzensuifonat og kobber bis(pentaklorfenolat).
Eksempler på organosinkforbindelsere inkluderer sink-pyrition, sink-dimetylditiokarbamat, sink-etylen-bis(ditiokarbamat) og mangan-etylen-bis(ditiokarbamat)polymer kompleksert med sinksalt. Et eksempel på organomanganforbindelse er mangan-etylenbis(ditiokarbamat)polymer.
Eksempler på heterocykliske nitrogenholdige forbindelser inkluderer 2-metyltio-4-ferf43utylamino-6-cyklopropylamino-triazin, 2,3,5,6-tetraklor-4-(metylsulfonyl)pyridin og pyridintrifenylboran.
Eksempler på heterocykliske svovelholdige forbindelser inkluderer 4,5-diklor-2-oktyl-3(2H)-isotiazolon, 1,2-bensisotiazolin-3-on og 2-(tiocyanometyltio)-benzotiazol.
Eksempler på ureaderivater inkluderer 3-(3,4-diklorfenyl)-1,1 -dimetylurea.
Eksempler på amider og imider av karboksylsyrer, sulfoniske og sulfeniske syrer inkluderer N-(diklorfluormetyltio)ftalimid, N,N-dimetyl-N-fenyl-(diklorfluorometyltio)-sulfamid og 1,1-diklor-N-((dimetylamino)sulfonyl)-1-fluor-N-(4-metylfenyl)metan-sulfenamid.
Eksempler på salter eller estere av karboksylsyrer inkluderer 2-((3-jod-2-propynyl)okso)-etanolfenylkarbamat og 3-jod-2-propynyl N-butylkarbamat.
Eksempler på aminer inkluderer dehydroabetylaminer og kokodimetylamin.
Eksempler på substituert benzen inkluderer 2,4,5,6-tetrakloM ,3-benzendikarbonitril og 1-((dijodmetyl)sulfonyl)-4-metylbenzen.
Andre eksempler kan være tetraalkylfosfoniumhalogenider og guanidinderivater.
Ved bruk av de organiske og metallorganiske aktive forbindelsene i kombinasjon med uorganiske aktive forbindelser som for eksempel kobberoksid, kobbertiocyanat og metallisk kobber, blir mengdene av organiske og metallorganiske aktive forbindelser
typisk lavere enn når disse benyttes alene.
Disse organiske og metallorganiske aktive forbindelser kan også brukes i kombinasjon med andre organiske og metallorganiske aktive forbindelser i fravær av uorganiske aktive forbindelser.
I mange begroingshindrende malinger representerer de biologisk aktive forbindelsene hoveddelen av pigmentene. I tillegg kan ulike forbindelser inkluderes. Disse forbindelsene betegnes enten som pigmenter eller som fyllstoffer avhengig av deres brytningsindeks.
En viktig egenskap til pigmentene eller fyllstoffene er graden av vannløselighet. Dette gjelder spesielt når man ser på selvpolerende begroingshindrende malinger basert på et hydrolyserende bindemiddel. Pigmenter eller fyllstoffer kan deles inn i de som er følsomme for vann eller løselige i vann og de som ikke er følsomme for vann eller uløselige i vann. Den første kategorien inkluderer pigmenter eller fyllstoffer som er biologisk aktive nevnt tidligere. Eksempler på disse inkluderer kobberoksid og kobbertiocyanat. Andre pigmenter eller fyllstoffer i denne kategorien inkluderer sinkoksid, sølvklorid, sølvoksid, kalsiumfluorid, kalsiumhydrogenfosfat, kalsiumfosfat, kalsiumsilikat, jernkarbonat, jernkarbonyl, magnesiumhydroksyd, magnesiumdihydroksyd, magnesiumkarbonat, mangankarbonat, sinkkromat, sinkkarbonat, sinksulfid. I selvpolerende systemer, som er beskrevet her, kan slike stoffer brukes til å justere poleringshastigheten til malingen. Disse komponentene kan bli brukt alene eller i kombinasjon.
De vannuløselige pigmentene eller fyllstoffene i denne gruppen er omfattende og når disse blir brukt i selvpolerende systemer, som er beskrevet i dette patentet, kan de redusere poleringshastigheten til malingen. Eksempler på disse inkluderer talkum, dolomitter, kalsiumkarbonat, glimmer, bariumsulfat, kaolin, silika, perlit, magnesiumoksid, kalsitt og kvartsmel. Andre vannuløselige pigmenter inkluderer titandioksid, jernoksid, grafitt og sot. Disse blir generelt brukt i kombinasjon med vannløselige komponenter.
Eksempler på surfaktanter inkluderer derivater av propylenoksid og etylenoksid som alkylfenol-etylenoksid-kondensater; etoksylerte monoetanolamider av umettede fettsyrer som etoksylerte monoetanolamider av linolensyre; og andre som for eksempel natriumdodesylsulfat, alkylfenoletoksylater og soya-lecitin.
Eksempler på fuktemidler og dispergeringsmidler inkluderer de som er detaljert beskrevet i M. Ash og I. Asn., Handbook of Paint and Coating Raw Materials, Vol. 1, 1996, Gower Publ. Ltd., Great Britain, s. 821 -823, 849-851.
Eksempler på tørkestoffer inkluderer metalloktoater og metallnaftenater;
Eksempler på aktivatorer inkluderer salicylsyre og benzylalkohol;
Eksempler på skumdempere inkluderer silikonoljer og aromatiske eller ålifatiske
mineraloljer;
Eksempler på stabilisatorer for å forebygge forringelse både på grunn av lys og varme inkluderer HALS forbindelser som 2-hydroksy-4-metoksybenzofenon, 2-(5-klor-(2H)-benzotriazol-2-yl)-4-metyl-6-(fetr-butyl)fenol og 2,4-difert-butyl-6-(5-klorbenzotriazol-2-yl)fenol; stabilisatorer for å forebygge forringelse på grunn av fuktighet inkluderer molekylsikter og vannabsorbere;
Eksempler på antioksidater inkluderer butylert hydroksyanisol, butylert hydroksy-
toluen, propyl-gallat, tocoferoler, 2,5-di-fe/f-butyl-hydrokinon, L-askorbinsyre;
Eksempler på korrosjonsinhibitorer inkluderer aminokarboksylater og metallsalter av disse, kalsiumsilikafosfat, ammoniumbenzoat, barium-, kalsium-, sink og magnesiumsalter av alkylnaftalen, sulfonsyrer, sinksalter av cyanursyre og 5-nitroisoftalsyrer, sinksalter av dodesylnaftalen sulfonsyre, sink- og aminkomplekser av toluylpropan syre;
Eksempler på koalesceringsmidler inkluderer glykoler, 2-butoksy-etanol, 2,2,4-trimetyl-1,3-pentandiol-monoisobutyrat, diisobutylestere av adipin-, glutar- og ravsyre;
Eksempler på fortykningsmidler og antibunnfallsmidler inkluderer kolloidal silika, hydratisert aluminiumsilikat, aluminiumtristearat, aluminiummonostearat, xantangummi, salisylsyre, krysolitt, fumed silika, umettet og hydrogenert lakserolje, organomodifisert leire, polyhydroksykarboksylsyreamider, modifiserte urea- og polyamid-harpikser.
Eksempler på fibre inkluderer naturlige og syntetiske uorganiske fibre som silikonholdige fibre, metallfibre, oksidfibre, mineralfibre; naturlige og syntetiske organiske fibre som celiulosefibre, gummifibre, akrylfibre; eller andre som beskrevet i WO0077102.
Eksempler på løsningsmidler inkluderer vann; aromatiske hydrokarboner så som
xylen, white spirit, Solvesso, toluen; ålifatiske hydrokarboner som heksan og heptan;
klorerte hydrokarboner som diklormetan, trikloretan, tetrakloretan, fluorerte hydrokarboner som difluormetan, difluoretan, trifluoretan, tetrafluoretan; fluorklor-
alifatiske og -aromatiske hydrokarboner som klorfluormetan, klordifluoretan, paraklorbenzotrifluorid; ketoner så som aceton, metyletylketon, metylisobutylketon, cykloheksanon; estere så som metylacetat, etylacetat, butylacetat, fert-butylacetat, etylenglykoimetyleteracetat; etere så som etylenglykoldimetyleter, dietylenglykoldimetyleter, dibutyleter, dioksan, tetrahydrofuran, alkoholer som metanol,
etanol, propanol, isopropanol, butanol, benzylalkohol; eter alkoholer som butoksyetanol, propylenglykolmonometyleter, amider som N-metylpyrrolidon, dimetylformamid eller løsningsmidler så som dimetylsulfoksid; eventuelt blandinger av ovenfor nevnte løsningsmidler.
Foreliggende oppfinnelse er beskrevet mer detaljert i de følgende eksempler.
Eksempler
Eksempel 1
Generelle synteseinstruksjoner for fremstilling av intermediater
En løsning av utgangsforbindelsen med OH-gruppe (100 mmol) i aceton (100 ml) kjølt til 20°C tilsettes Jones' reagens (150mmol) sakte ved omrøring. Etter fullført tilsetning omrøres i ytterligere 10 timer før aceton dekanteres av. Bunnfallet vaskes med eter og eteren drives av ved hjelp av vakuum. Vannfasen gjøres basisk med vandig natriumkarbonatløsning, vaskes med dietyleter og surgjøres med saltsyre før ekstrahering med etylacetat. Den organiske fasen vaskes med vann og tørkes med magnesiumsulfat før løsningsmidlet drives av ved hjelp av vakuum. Råproduktet kan renses ved destillasjon eller omkrystallisering.
Eksempel 2
Generelle synteseinstruksjoner for fremstilling av intermediater
En løsning av utgangsforbindelsene med fenoliske OH-grupper (lOOmmol) og med klorsubstituerte syreklorider (1 OOmmol) i diklormetan (1 OOml) tilsettes trietylamin (lOOmmol) ved hjelp av dråpetrakt under omrøring. Etter ytterligere 5 timer omrøring filtreres det utfelte salt fra og den organiske løsningen vaskes med vann. Den organiske fasen tørkes med magnesiumsulfat før løsningsmidlet drives av ved hjelp av vakuum. Råproduktet kan renses ved destillasjon eller omkrystallisering.
Eksempel 3
Generelle synteseinstruksjoner for fremstilling av monomerer
Den syrefunksjonelle utgangsforbindelsen (1 mol) løses i diklormetan sammen med trietylamin (1mol). Til blandingen tilsettes den ønskede klorsilanforbindelse (1 mol) ved hjelp av dråpetrakt ved omrøring. Omrøringen fortsettes i 5 timer før utfelt salt filtreres fra og den organiske fasen vaskes en gang med en mettet natriomkarbonatløsning og to ganger med vann før det tørkes på magnesiumsulfat og løsningsmidlet drives av ved hjelp av vakuum. Råproduktet kan renses ved destillasjon eller omkrystallisering.
Eksempel 4
Generelle synteseinstruksjoner for fremstilling av monomer
En løsning av klorert utgangsforbindelse (100 mmol) og natriummetakrylat (150mmol) i acetonitril tilsettes trioktylmetylamin (5 mol-%) og reflukseres i 4 timer. Den organiske fasen vaskes med vann før den tørkes på magnesiumsulfat og løsningsmidlet drives av ved hjelp av vakuum. Råproduktet kan renses ved destillasjon eller omkrystallisering.
Eksempel 5
Generelle synteseinstruksjoner for fremstilling av polymerer
Mengden av de ønskede monomere tilsvarende ønsket monomersammensetning overføres til reaksjonskolbe sammen med initiator og løsningsmiddel til ønsket tørrstoffinnhold. Kolben med nitrogenatmosfære varmes til 80°C og kopolymeriseres i 3 timer før avkjøling. Kopolymeren kan renses ved utfelling i heksan eller vann.
Eksempel 6
Polymer-analog reaksjon;
Syntese av kopolymer: Metylmetakrylat/tri-isopropylsilyloksykarbonylmetylmetakrylat
Metylmetakrylat (400 mmol) og karboksymetylmetakrylat (lOOmmol) kopolymeriseres i følge eksempel 5. Kopolymeren tilsettes dråpevis først tri-isopropylsilylklorid (150 mmol) og så trietylamin (150 mmol) under omrøring. Omrøringen fortsettes ytterligere 12 timer ved romtemperatur før utfelt salt filtreres fra. Kopolymeren kan renses ved utfelling i heksan eller vann.
En oversikt over syntiserte intermediater og monomere er gitt i tabell 1.
En oversikt over polymere er gitt i tabell 2.
Claims (26)
1. Vannuløselig, vanneroderbar,filmdannendepolymer, karakterisert ved at den omfatter gjentatte enheter svarende til monomerer A og B: A) monomerer med formelen
hvor
n er et heltall fra 1 til 4,
XerHellerCH3,
Y er H eller eventuelt forestret COOH gruppe,
R1 er Ph(R<2>)m, -C(0)R3 eller -Si(R4)3,
m er et heltall fra 1 til 3,
R<2>, som er like eller forskjellige, er valgt fra -C(0)H, COOR<5>, CH2COOR<6>, Ci-4alkyl, halogen, nitro, Ci-4alkanoyl, OH og OR<7>,
R<3> er substituert eller usubstituert alkyl, aryl, aralkyl eller heterocyklyl, R<4>, som er like eller forskjellige, er valgt fra substituert eller usubstituert C1.20 alkyl, C5-20 aryl, C1.20 alkoksy og C5-20 aryloksy, og
R<5>, R<6> og R7 er uavhengig valgt fra substituert eller usubstituert Ci-2oalkyl og C5-2oaryl; som er tilstede i en mengde på 2-95 mol-%; og B) andre vinyl-polymeriserbare monomerer
som er tilstede i en mengde på 5-98 mol-%.
2. Polymer i følge krav 1,karakterisert
ved at enheter av monomerer A er tilstede i en mengde på 5-80 mol-%, og enheter av monomer B er tilstede i en mengde på 20-95 mol-%.
3. Polymer i følge krav 1,karakterisert
ved at enheter av monomerer A er tilstede i en mengde på 10-70 mol-%, og enheter av monomer B er tilstede i en mengde på 30-90 mol-%.
4. Polymer i følge et av kravene 1-3, karakterisert
ved at R<1>erSi(R<4>)3.
5. Polymer i følge krav 4, karakterisert
ved at R4 gruppene er like eller forskjellige og er uavhengig valgt fra substituert eller usubstituert Ci-i2alkyl, C5-i2aryl, CM2alkoksy og Cs-^aryloksy.
6. Polymer i følge krav 5, karakterisert
ved at R4 gruppene er like eller forskjellige og er uavhengig valgt fra substituert eller usubstituert Ci-8alkyl, C5-8aryl, Ci-8alkoksy og C5.8aryloksy.
7. Polymer i følge krav 4, karakterisert
ved at R4 på triorganosilylgruppen, Si(R<4>)3, er valgt fra gruppen bestående av trimetylsilyl, trietylsilyl, tri-n-propylsilyl, tri-iso-propylsilyl, tri-n-butylsilyl, tri-ferf-butylsilyl, tri-iso-butylsilyl, tri-n-pentylsilyl, tri-n-heksylsilyl, tri-fenylsilyl, tri-benzylsilyl, etyldimetylsilyl, n-butyldimetylsilyl, diisopropyl-n-butylsilyl, dicykloheksylfenylsilyl, t-butyldifenylsilyl, t-butyldimetylsilyl, dimetylfenylsilyl, bifenyldimetylsilyl, bifenyldiisopropylsilyl, difenylmetylsilyl, dimetylheksylsilyl.
8. Polymer i følge et av kravene 1-3, karakterisert
ved at R1 er Ph(R<2>)m.
9. Polymer ifølge krav 8, karakterisert
ved at R2 er valgt f ra COOR<5>, CH2COOR<6> og OR<7>.
10. Polymer ifølge krav 9, karakterisert
ved at R5, R6 og R<7> uavhengig er valgt fra usubstituert eller substituert Ci-12-alkyl og C5-i2aryl.
11. Polymer ifølge krav 10, karakterisert
ved at R5, R6 og R7 uavhengig er valgt fra usubstituert eller substituert Ci-8-alkyl og C5-i2aryl.
12. Polymer ifølge et av kravene 10og 11, karakterisert ved at R5, R6 og/eller R7 er substituert med halogen.
13. Polymer i følge krav 8, karakterisert
ved at R2 gruppene er like eller forskjellige og er uavhengig valgt fra formyl, Ci-4alkoksy og halogen.
14. Polymer i følge krav 13, k a rå kt e ri s e rt
ved at R2 gruppene er like eller forskjellige og er uavhengig valgt fra formyl, metoksy og brom.
15. Polymer i følge et av kravene 1-3, karakterisert
ved atR<1>er-C(0)R<3>.
16. Polymer ifølge krav 15, karakterisert
ved at R3 er fenyl eller Ci 6alkyl, som kan være substituert med fenoksy eller fenyl, idet nevnte fenyl-, alkyl- og fenoksygruppe kan være substituert med halogen, C-i-4alkoksy, C4.6cykloalkyl eller Ci^alkanoyloksy.
17. Polymer i følge krav 16, karakterisert
ved at R<3> gruppen er fenyl, benzyl, fert-butyl eller fe/f-amyl.
18. Monomerer, karakterisert ved formelen
hvor n er et heltall fra 1 til 4, XerHellerCHg,
Y er H eller eventuelt forestret COOH gruppe,
R1 er-C(0)R3 eller-Si(R4)3,
m er et heltall fra 1 til 3,
R<2>, som er like eller forskjellige, er valgt fra -C(0)H, COOR<5>, CH2COOR<6>, Ci-4alkyl, halogen, nitro, C1.4alkanoyl, OH og OR<7>,
R3 er substituert eller usubstituert alkyl, aryl, aralkyl eller heterocyklyl, R<4>, som er like eller forskjellige, er valgt fra substituert eller usubstituert C1-20 alkyl, C5.2o aryl, Ci-2o alkoksy og C5-20 aryloksy, og
R<5>, R<6> og R7 er uavhengig valgt fra substituert eller usubstituert Ci-20alkyl og C5.2oaryl.
19. Monomer ifølge krav 18, karakterisert
ved at R<1> er -Si(R<4>)3, hvor R4 er som angitt i et av kravene 6-8.
20. Monomer i følge krav 18, karakterisert
ved at R<1> er -C(0)R3, hvor R3 er som angitt i et av kravene 16 og 17.
21. Fremgangsmåte for fremstilling av polymerer ved homopolymerisasjon eller kopolymerisasjon av polymeriserbare monomerer,
karakterisert ved polymerisering av en blanding av A) 2-95 mol-% av en eller flere monomerer med formelen
hvor
n er et heltall fra 1 til 4,
XerHellerCH3,
Y er H eller eventuelt forestret COOH gruppe,
R<1> er Ph(R<2>)m, -C(0)R<3> eller -Si(R<4>)3,
m er et heltall fra 1 til 3,
R<2>, som er like eller forskjellige, er valgt fra -C(0)H, COOR<5>, CH2COOR<6>, Ci^alkyl, halogen, nitro, Ci^alkanoyl, OH og OR<7>,
R<3> er substituert eller usubstituert alkyl, aryl, aralkyl eller heterocyklyl, R<4>, som er like eller forskjellige, er valgt fra substituert eller usubstituert C1-20 alkyl, C5.2o aryl, C1-20 alkoksy og C5-20 aryloksy, og
R<5>, R<6> og R<7> er uavhengig valgt fra substituert eller usubstituert Ci-2oalkyl og C5.2oar<y>l; og B) 5-98 mol-% av andre vinyl-polymeriserbare monomerer.
i nærvær av radikal- eller ionedannende initiatorer og inerte løsningsmidler.
22. Fremgangsmåte for fremstilling av polymerer ved homopolymerisasjon eller kopolymerisasjon av polymeriserbare monomerer,
karakterisert ved polymerisering av en blanding av C) 2-95 mol-% av én eller flere monomerer med formelen
og D) 5-98 mol-% av andre vinyl polymeriserbare monomere,
i nærvær av radikal eller ionedannende initiatorer og inerte løsningsmidler,
og deretter, ved en polymer-analog reaksjon, omsetning av de oppnådde kopolymerer med én eller flere forbindelser med den generelle formelen
hvor n er et heltall fra 1 til 4, X er H eller CH3,
Y er H eller eventuelt forestret COOH gruppe,
Z<1> er Cl eller OH
Z<2> er grupper som er reaktive med Z<1>, såsom OH eller Cl
R<1> er Ph(R<2>)m, -C(0)R<3> eller -Si(R<4>)3,
m er et heltall fra 1 til 3,
R<2>, som er like eller forskjellige, er valgt fra -C(0)H, COOR<5>, CH2COOR<6>, C14alkyl, halogen, nitro, Ci^alkanoyl, OH og OR7,
R<3> er substituert eller usubstituert alkyl, aryl, aralkyl eller heterocyklyl, R<4>, som er like eller forskjellige, er valgt fra substituert eller usubstituert C1-20 alkyl, C5.2o aryl, C1-29 alkoksy og C5-2o aryloksy, og
R<5>, R<6> og R7 er uavhengig valgt fra substituert eller usubstituert Ci-20alkyl og C5-2oaryl.
23. Fremgangsmåte for fremstilling av polymerer ved homopolymerisasjon eller kopolymerisasjon av polymeriserbare monomerer,
karakterisert ved polymerisering av en blanding av E) 2-95 mol-% av én eller flere monomerer med formelen
og F) 5-98 mol-% av andre vinyl polymeriserbare monomerer,
i nærvær av radikal- eller ionedannende initiatorer,
og i en polymer-analog reaksjon omsetning av de oppnådde kopolymerer med én eller flere forbindelser med den generelle formelen
hvor
n er et heltall fra 1 til 4,
X er H eller CH3,
Y er H eller eventuelt forestret COOH gruppe,
Z<1> er Cl eller OH
Z<2> er grupper som er reaktive med Z<1>, såsom OH eller Cl
R<1> er Ph(R2)m,-C(0)R3 eller-Si(R4)3,
m er et heltall fra 1 til 3,
R<2>, som er like eller forskjellige, er valgt fra -C(0)H, COOR<5>, CH2COOR<6>, Ci^alkyl, halogen, nitro, Ci-4alkanoyl, OH og OR<7>,
R3 er substituert eller usubstituert alkyl, aryl, aralkyl eller heterocyklyl, R<4>, som er like eller forskjellige, er valgt fra substituert eller usubstituert Ci-2o alkyl, C5.2o aryl, Ci-2o alkoksy og C5-2o aryloksy, og
R<5>, R<6> og R<7> er uavhengig valgt fra substituert eller usubstituert Ci-20alkyl og C5.2oaryl
24. Begroingshindrende maling, karakterisert
ved at den inneholder en polymer ifølge et av kravene 1-17, og dessuten et biocid og eventuelt andre komponenter som er hensiktsmessige i marin maling.
25. Anvendelse av en polymer ifølge et av kravene 1-17 som komponent i en marin maling for å oppnå belegg med selvpolerende egenskaper i vann.
26. Anvendelse av monomerer med den generelle formelen
hvor
n er et heltall fra 1 til 4,
XerHellerCH3l
Y er H eller eventuelt forestret COOH gruppe,
R<1> er Ph(R<2>)m, -C(0)R3 eller -Si(R<4>)3,
m er et heltall fra 1 til 3,
R<2>, som er like eller forskjellige, er valgt fra -C(0)H, COOR<5>, CH2COOR<6>, Ci^alkyl, halogen, nitro, Ci-4alkanoyl, OH og OR<7>,
R<3> er substituert eller usubstituert alkyl, aryl, aralkyl eller heterocyklyl, R<4>, som er like eller forskjellige, er valgt fra substituert eller usubstituert Ci-2o alkyl, C5-20 aryl, Ci-20 alkoksy og C5-2o aryloksy, og
R<5>, R<6> og R7 er uavhengig valgt fra substituert eller usubstituert Ci-2oalkyl og C5-2oaryl, for fremstilling av polymerer for begroingshindrende maling.
Priority Applications (10)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NO20021491A NO320324B1 (no) | 2002-03-26 | 2002-03-26 | Polymerer og monomerer og anvendelse derav samt fremgangsmate for fremstilling av polymerer og begroingshindrende maling inneholdende polymerer |
PT03745039T PT1487928E (pt) | 2002-03-26 | 2003-03-20 | Polímero que forma filmes e tinta antivegetativa |
EP03745039A EP1487928B1 (en) | 2002-03-26 | 2003-03-20 | Film-forming polymer and antifouling paint |
PCT/NO2003/000095 WO2003080747A1 (en) | 2002-03-26 | 2003-03-20 | Film-forming polymer and antifouling paint |
AT03745039T ATE404642T1 (de) | 2002-03-26 | 2003-03-20 | Filmbildendes polymer und bewuchsverhindernder anstrichstoff |
KR1020047015466A KR101015264B1 (ko) | 2002-03-26 | 2003-03-20 | 필름 형성 폴리머 및 방오 페인트 |
DE60322853T DE60322853D1 (de) | 2002-03-26 | 2003-03-20 | Filmbildendes polymer und bewuchsverhindernder anstrichstoff |
JP2003578484A JP4468702B2 (ja) | 2002-03-26 | 2003-03-20 | 皮膜形成性ポリマーと防汚塗料 |
CNB038069261A CN100519671C (zh) | 2002-03-26 | 2003-03-20 | 成膜聚合物和防污漆 |
AU2003225433A AU2003225433A1 (en) | 2002-03-26 | 2003-03-20 | Film-forming polymer and antifouling paint |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NO20021491A NO320324B1 (no) | 2002-03-26 | 2002-03-26 | Polymerer og monomerer og anvendelse derav samt fremgangsmate for fremstilling av polymerer og begroingshindrende maling inneholdende polymerer |
Publications (3)
Publication Number | Publication Date |
---|---|
NO20021491D0 NO20021491D0 (no) | 2002-03-26 |
NO20021491L NO20021491L (no) | 2003-09-29 |
NO320324B1 true NO320324B1 (no) | 2005-11-21 |
Family
ID=19913471
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20021491A NO320324B1 (no) | 2002-03-26 | 2002-03-26 | Polymerer og monomerer og anvendelse derav samt fremgangsmate for fremstilling av polymerer og begroingshindrende maling inneholdende polymerer |
Country Status (10)
Country | Link |
---|---|
EP (1) | EP1487928B1 (no) |
JP (1) | JP4468702B2 (no) |
KR (1) | KR101015264B1 (no) |
CN (1) | CN100519671C (no) |
AT (1) | ATE404642T1 (no) |
AU (1) | AU2003225433A1 (no) |
DE (1) | DE60322853D1 (no) |
NO (1) | NO320324B1 (no) |
PT (1) | PT1487928E (no) |
WO (1) | WO2003080747A1 (no) |
Families Citing this family (34)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009076722A1 (en) * | 2007-12-19 | 2009-06-25 | The University Of Melbourne | Method of protecting a surface from biological fouling |
NO328788B1 (no) * | 2008-03-14 | 2010-05-18 | Jotun As | Bindemiddel til lufttørkende maling |
US20100135949A1 (en) | 2008-12-01 | 2010-06-03 | Becton, Dickinson And Company | Antimicrobial compositions |
EP2348077B1 (en) | 2010-01-26 | 2013-04-03 | Jotun A/S | Antifouling composition |
KR20130131277A (ko) | 2010-06-04 | 2013-12-03 | 요툰 에이/에스 | 오염방지용 코팅 |
US9352119B2 (en) | 2012-05-15 | 2016-05-31 | Becton, Dickinson And Company | Blood control IV catheter with antimicrobial properties |
US9579486B2 (en) | 2012-08-22 | 2017-02-28 | Becton, Dickinson And Company | Blood control IV catheter with antimicrobial properties |
EP2708594A1 (en) | 2012-09-18 | 2014-03-19 | Jotun A/S | Cleaning process |
EP2725073B1 (en) | 2012-10-23 | 2016-08-03 | Jotun A/S | Antifouling coating composition |
EP2912120B1 (en) | 2012-10-23 | 2017-12-20 | Jotun A/S | Antifouling coating composition |
WO2014096102A1 (en) | 2012-12-19 | 2014-06-26 | Jotun A/S | Silyl ester copolymer |
US9695323B2 (en) | 2013-02-13 | 2017-07-04 | Becton, Dickinson And Company | UV curable solventless antimicrobial compositions |
US9750928B2 (en) | 2013-02-13 | 2017-09-05 | Becton, Dickinson And Company | Blood control IV catheter with stationary septum activator |
EP2902453A1 (en) | 2014-01-31 | 2015-08-05 | Jotun A/S | Antifouling Composition |
EP2902452A1 (en) | 2014-01-31 | 2015-08-05 | Jotun A/S | Antifouling composition |
US9789279B2 (en) | 2014-04-23 | 2017-10-17 | Becton, Dickinson And Company | Antimicrobial obturator for use with vascular access devices |
US9675793B2 (en) | 2014-04-23 | 2017-06-13 | Becton, Dickinson And Company | Catheter tubing with extraluminal antimicrobial coating |
US10376686B2 (en) | 2014-04-23 | 2019-08-13 | Becton, Dickinson And Company | Antimicrobial caps for medical connectors |
US10232088B2 (en) | 2014-07-08 | 2019-03-19 | Becton, Dickinson And Company | Antimicrobial coating forming kink resistant feature on a vascular access device |
CN106047173B (zh) | 2015-04-09 | 2020-12-11 | 佐敦集团 | 防污组合物 |
KR20180030999A (ko) | 2015-07-13 | 2018-03-27 | 에보니크 데구사 게엠베하 | 가수분해가능한 결합제 |
US10493244B2 (en) | 2015-10-28 | 2019-12-03 | Becton, Dickinson And Company | Extension tubing strain relief |
CN106221344A (zh) * | 2016-07-28 | 2016-12-14 | 江苏昌悦重工科技有限公司 | 一种耐腐蚀光伏箱 |
JP7161845B2 (ja) | 2016-11-11 | 2022-10-27 | ヨトゥン アーエス | 防汚組成物 |
WO2018086670A1 (en) | 2016-11-11 | 2018-05-17 | Hempel A/S | An antifouling coating composition comprising novel carbon-based hydrolysable polymers |
JP7178167B2 (ja) | 2016-11-11 | 2022-11-25 | ヨトゥン アーエス | 防汚組成物 |
CN109983083B (zh) | 2016-11-11 | 2021-08-17 | 佐敦有限公司 | 防污组合物 |
WO2018134291A1 (en) | 2017-01-19 | 2018-07-26 | Jotun A/S | Antifouling composition |
ES2968849T3 (es) | 2018-08-29 | 2024-05-14 | Nitto Kasei Co Ltd | Composición de material de recubrimiento antiincrustante |
DE102018129419A1 (de) * | 2018-11-22 | 2020-05-28 | Johannes Gutenberg-Universität Mainz | Acrylat-Copolymer für galenische Anwendungen |
JPWO2022102492A1 (no) * | 2020-11-10 | 2022-05-19 | ||
CN117440997A (zh) * | 2021-05-12 | 2024-01-23 | 日东化成株式会社 | 防污涂料组合物 |
KR102473773B1 (ko) | 2021-05-17 | 2022-12-02 | 한국신발피혁연구원 | 해수 저항성이 우수한 방오점착테이프용 아크릴 점착제 조성물 |
WO2023145634A1 (ja) * | 2022-01-26 | 2023-08-03 | 日東化成株式会社 | 防汚塗料組成物 |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5847066A (ja) * | 1981-09-16 | 1983-03-18 | Nippon Oil & Fats Co Ltd | 防汚塗料 |
JPS63215780A (ja) * | 1987-03-04 | 1988-09-08 | Dainippon Ink & Chem Inc | 防汚塗料用樹脂 |
JP2514217B2 (ja) * | 1987-12-04 | 1996-07-10 | 東芝シリコーン株式会社 | 防汚コ―ティング材 |
JPH0820778A (ja) * | 1994-07-06 | 1996-01-23 | Kawasaki Steel Corp | コークス炉の炉壁補修用仮炉蓋 |
MY115462A (en) * | 1995-06-01 | 2003-06-30 | Chugoku Marine Paints | Antifouling coating composition, coating film formed from said antifouling coating composition, antifouling method using said antifouling coating composition and hull or underwater structure coated with said coating film |
NO952329D0 (no) * | 1995-06-13 | 1995-06-13 | Jotun As | Polymerer for grohemmende maling og fremgangsmåte for fremstilling derav |
PL200670B1 (pl) * | 1998-12-28 | 2009-01-30 | Chugoku Marine Paints | Kopolimer sililo(met)akrylanowy, sposób jego wytwarzania, przeciwporostowa kompozycja do malowania zawierająca kopolimer sililo(met)akrylanowy oraz jej zastosowanie |
US6992120B2 (en) * | 2001-11-13 | 2006-01-31 | Arkema Inc. | Coating compositions |
DE60212225T2 (de) * | 2001-03-06 | 2007-05-03 | Shin-Etsu Chemical Co., Ltd. | Silyl(meth)acrylate mit sterisch anspruchsvollen Substituenten und Verfahren zur Herstellung dieser Verbindungen |
EP1295888A1 (en) * | 2001-09-21 | 2003-03-26 | Sigma Coatings B.V. | Process for the preparation of trialkylsilylated carboxylate monomers, the obtained trialkylsilylated carboxylate monomers and their use in antifouling coatings |
ATE345347T1 (de) * | 2001-09-21 | 2006-12-15 | Sigma Coatings Bv | Verfahren zur herstellung von organosilylkarboxylatmonomeren, und deren verwendung als anwuchsverhindernde überzüge |
-
2002
- 2002-03-26 NO NO20021491A patent/NO320324B1/no not_active IP Right Cessation
-
2003
- 2003-03-20 JP JP2003578484A patent/JP4468702B2/ja not_active Expired - Fee Related
- 2003-03-20 AU AU2003225433A patent/AU2003225433A1/en not_active Abandoned
- 2003-03-20 EP EP03745039A patent/EP1487928B1/en not_active Expired - Lifetime
- 2003-03-20 KR KR1020047015466A patent/KR101015264B1/ko not_active IP Right Cessation
- 2003-03-20 DE DE60322853T patent/DE60322853D1/de not_active Expired - Lifetime
- 2003-03-20 PT PT03745039T patent/PT1487928E/pt unknown
- 2003-03-20 CN CNB038069261A patent/CN100519671C/zh not_active Expired - Fee Related
- 2003-03-20 AT AT03745039T patent/ATE404642T1/de not_active IP Right Cessation
- 2003-03-20 WO PCT/NO2003/000095 patent/WO2003080747A1/en active Application Filing
Also Published As
Publication number | Publication date |
---|---|
JP4468702B2 (ja) | 2010-05-26 |
AU2003225433A1 (en) | 2003-10-08 |
KR20050016323A (ko) | 2005-02-21 |
NO20021491L (no) | 2003-09-29 |
PT1487928E (pt) | 2008-11-14 |
ATE404642T1 (de) | 2008-08-15 |
KR101015264B1 (ko) | 2011-02-18 |
JP2005520912A (ja) | 2005-07-14 |
NO20021491D0 (no) | 2002-03-26 |
CN1643085A (zh) | 2005-07-20 |
CN100519671C (zh) | 2009-07-29 |
WO2003080747A1 (en) | 2003-10-02 |
EP1487928B1 (en) | 2008-08-13 |
EP1487928A1 (en) | 2004-12-22 |
DE60322853D1 (de) | 2008-09-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
NO320324B1 (no) | Polymerer og monomerer og anvendelse derav samt fremgangsmate for fremstilling av polymerer og begroingshindrende maling inneholdende polymerer | |
JP4330449B2 (ja) | 自己研磨性防汚塗料 | |
AU2005211439B2 (en) | Antifouling compositions comprising a polymer with salt groups | |
KR101045922B1 (ko) | 산-캡핑된 4차 중합체 및 이 중합체를 포함하는 조성물 | |
KR100193215B1 (ko) | 방오 코팅 조성물 | |
NO339571B1 (no) | Akrylharpiks og antibegroingsbelegg | |
DK1603979T3 (en) | ANTI-BREAKING PAINTING COMPOSITION | |
EP0204444B1 (en) | Binder for anti-fouling paints | |
JP6765149B2 (ja) | 共重合体と防汚薬剤を含有する防汚塗料組成物を用いて船舶の表面に防汚塗膜を形成する方法 | |
EP0833870B1 (en) | Polymers for antifouling coatings and a process for the preparation thereof | |
EP1288234A1 (en) | Binders with low content in hydrolysable monomer suitable for selfpolishing antifouling paints | |
US5891935A (en) | Process for preparing polymeric binders and their use for antifouling paint systems | |
ZA200206510B (en) | Improved marine paint compositions. | |
NO316385B1 (no) | Selvpolerende grohindrende maling | |
CN111886304A (zh) | 防污涂料组合物 | |
KR101994061B1 (ko) | 적층 방오 도막, 방오 기재 및 선박 | |
US20030225230A1 (en) | Polymers for antifouling coatings and a process for the preparation thereof | |
EP3783073A1 (en) | Antifouling coating composition | |
JPH0577712B2 (no) | ||
KR950012765B1 (ko) | 방오도료 바인더용 가수분해성 모너머 및 이의 제조방법 및 이 모너머를 이용한 방오도료용 바인더의 제조방법 | |
KR19980042147A (ko) | 중합체 결합제의 제조 방법 및 그의 오염방지 페인트 계를 위한용도 | |
JPH04227770A (ja) | 防汚塗料用樹脂組成物及び防汚塗料 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM1K | Lapsed by not paying the annual fees |