JP6369275B2 - 積層シート用接着剤組成物 - Google Patents
積層シート用接着剤組成物 Download PDFInfo
- Publication number
- JP6369275B2 JP6369275B2 JP2014207901A JP2014207901A JP6369275B2 JP 6369275 B2 JP6369275 B2 JP 6369275B2 JP 2014207901 A JP2014207901 A JP 2014207901A JP 2014207901 A JP2014207901 A JP 2014207901A JP 6369275 B2 JP6369275 B2 JP 6369275B2
- Authority
- JP
- Japan
- Prior art keywords
- meth
- vinyl
- acrylate
- ether
- compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 239000000853 adhesive Substances 0.000 title claims description 111
- 230000001070 adhesive effect Effects 0.000 title claims description 111
- 239000000203 mixture Substances 0.000 title claims description 98
- 150000001875 compounds Chemical class 0.000 claims description 158
- 229920001577 copolymer Polymers 0.000 claims description 80
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 44
- 239000000463 material Substances 0.000 claims description 29
- 229910000831 Steel Inorganic materials 0.000 claims description 28
- 239000010959 steel Substances 0.000 claims description 28
- 125000004018 acid anhydride group Chemical group 0.000 claims description 24
- 239000000758 substrate Substances 0.000 claims description 22
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 18
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 16
- 239000012948 isocyanate Substances 0.000 claims description 13
- 125000003700 epoxy group Chemical group 0.000 claims description 12
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 12
- 230000009477 glass transition Effects 0.000 claims description 11
- 150000002513 isocyanates Chemical class 0.000 claims description 9
- 230000000379 polymerizing effect Effects 0.000 claims description 2
- -1 b-1 Chemical class 0.000 description 262
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 166
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 85
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 85
- 239000010408 film Substances 0.000 description 55
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 49
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 38
- 229920002554 vinyl polymer Polymers 0.000 description 36
- 238000006243 chemical reaction Methods 0.000 description 34
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 30
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 28
- 239000002253 acid Substances 0.000 description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 25
- 238000000576 coating method Methods 0.000 description 24
- 238000001723 curing Methods 0.000 description 24
- 239000011248 coating agent Substances 0.000 description 23
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 22
- 230000000052 comparative effect Effects 0.000 description 22
- 239000002985 plastic film Substances 0.000 description 22
- 239000002904 solvent Substances 0.000 description 22
- 239000002585 base Substances 0.000 description 21
- NHOGGUYTANYCGQ-UHFFFAOYSA-N ethenoxybenzene Chemical compound C=COC1=CC=CC=C1 NHOGGUYTANYCGQ-UHFFFAOYSA-N 0.000 description 20
- 229910052751 metal Inorganic materials 0.000 description 20
- 239000002184 metal Substances 0.000 description 20
- 229920006255 plastic film Polymers 0.000 description 20
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 18
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 17
- 229910000576 Laminated steel Inorganic materials 0.000 description 16
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 15
- 238000000034 method Methods 0.000 description 15
- 229920001451 polypropylene glycol Polymers 0.000 description 15
- 229920005989 resin Polymers 0.000 description 14
- 239000011347 resin Substances 0.000 description 14
- 229940070710 valerate Drugs 0.000 description 13
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 12
- 230000000694 effects Effects 0.000 description 12
- 229910052757 nitrogen Inorganic materials 0.000 description 12
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 11
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 11
- 238000009835 boiling Methods 0.000 description 11
- 125000000524 functional group Chemical group 0.000 description 11
- 238000012360 testing method Methods 0.000 description 11
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical compound C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 description 10
- 230000015572 biosynthetic process Effects 0.000 description 10
- 238000011156 evaluation Methods 0.000 description 10
- 239000003960 organic solvent Substances 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 125000002947 alkylene group Chemical group 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 9
- 238000004132 cross linking Methods 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 9
- 238000002156 mixing Methods 0.000 description 9
- 239000000178 monomer Substances 0.000 description 9
- 238000006116 polymerization reaction Methods 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- 238000003786 synthesis reaction Methods 0.000 description 9
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 8
- 239000012790 adhesive layer Substances 0.000 description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 8
- 230000006872 improvement Effects 0.000 description 8
- 238000003475 lamination Methods 0.000 description 8
- 239000005056 polyisocyanate Substances 0.000 description 8
- 229920001228 polyisocyanate Polymers 0.000 description 8
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 7
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 7
- 150000003926 acrylamides Chemical class 0.000 description 7
- 239000002981 blocking agent Substances 0.000 description 7
- 238000013461 design Methods 0.000 description 7
- AZDCYKCDXXPQIK-UHFFFAOYSA-N ethenoxymethylbenzene Chemical compound C=COCC1=CC=CC=C1 AZDCYKCDXXPQIK-UHFFFAOYSA-N 0.000 description 7
- 125000004433 nitrogen atom Chemical group N* 0.000 description 7
- 230000009257 reactivity Effects 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- 238000003860 storage Methods 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 229960000834 vinyl ether Drugs 0.000 description 7
- OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical compound C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 description 6
- 239000004925 Acrylic resin Substances 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 125000001931 aliphatic group Chemical group 0.000 description 6
- 125000003277 amino group Chemical group 0.000 description 6
- 230000007423 decrease Effects 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 125000000623 heterocyclic group Chemical group 0.000 description 6
- RISDDVKHYROMNH-UHFFFAOYSA-N prop-1-en-2-yloxybenzene Chemical compound CC(=C)OC1=CC=CC=C1 RISDDVKHYROMNH-UHFFFAOYSA-N 0.000 description 6
- FIPBXQBXPNTQAA-UHFFFAOYSA-N 1-ethenyl-2-ethoxybenzene Chemical compound CCOC1=CC=CC=C1C=C FIPBXQBXPNTQAA-UHFFFAOYSA-N 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 5
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 5
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 5
- 150000003863 ammonium salts Chemical class 0.000 description 5
- 125000003118 aryl group Chemical group 0.000 description 5
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 5
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 5
- 125000004122 cyclic group Chemical group 0.000 description 5
- 239000003822 epoxy resin Substances 0.000 description 5
- 235000019439 ethyl acetate Nutrition 0.000 description 5
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 5
- 229920001519 homopolymer Polymers 0.000 description 5
- 230000003993 interaction Effects 0.000 description 5
- 229910052742 iron Inorganic materials 0.000 description 5
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Natural products OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 5
- 150000002923 oximes Chemical class 0.000 description 5
- 229920000647 polyepoxide Polymers 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 239000003505 polymerization initiator Substances 0.000 description 5
- 229920005862 polyol Polymers 0.000 description 5
- 150000003077 polyols Chemical class 0.000 description 5
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 229910001335 Galvanized steel Inorganic materials 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 4
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 4
- 150000008065 acid anhydrides Chemical class 0.000 description 4
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 4
- 125000002252 acyl group Chemical group 0.000 description 4
- 230000001476 alcoholic effect Effects 0.000 description 4
- 125000003342 alkenyl group Chemical group 0.000 description 4
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 4
- 239000012298 atmosphere Substances 0.000 description 4
- VPKDCDLSJZCGKE-UHFFFAOYSA-N carbodiimide group Chemical group N=C=N VPKDCDLSJZCGKE-UHFFFAOYSA-N 0.000 description 4
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 4
- 239000004205 dimethyl polysiloxane Substances 0.000 description 4
- 238000010494 dissociation reaction Methods 0.000 description 4
- 230000005593 dissociations Effects 0.000 description 4
- 238000009826 distribution Methods 0.000 description 4
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 4
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 4
- 239000008397 galvanized steel Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- 239000004800 polyvinyl chloride Substances 0.000 description 4
- 229920000915 polyvinyl chloride Polymers 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- ZIFHFFOAEFKJJL-UHFFFAOYSA-N prop-1-en-2-yloxymethylbenzene Chemical compound CC(=C)OCC1=CC=CC=C1 ZIFHFFOAEFKJJL-UHFFFAOYSA-N 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- 150000003606 tin compounds Chemical class 0.000 description 4
- 230000000007 visual effect Effects 0.000 description 4
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 3
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 3
- 229940035437 1,3-propanediol Drugs 0.000 description 3
- XHYCSVZWIGEZAS-UHFFFAOYSA-N 1-ethenyl-2h-quinoline Chemical compound C1=CC=C2N(C=C)CC=CC2=C1 XHYCSVZWIGEZAS-UHFFFAOYSA-N 0.000 description 3
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 3
- 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 3
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 3
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 description 3
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 3
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 3
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 3
- YUCOVHFIYPJDDN-UHFFFAOYSA-N 4-prop-1-en-2-ylbenzoic acid Chemical compound CC(=C)C1=CC=C(C(O)=O)C=C1 YUCOVHFIYPJDDN-UHFFFAOYSA-N 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 3
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- 239000006087 Silane Coupling Agent Substances 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000002518 antifoaming agent Substances 0.000 description 3
- 125000001204 arachidyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 3
- 150000001735 carboxylic acids Chemical class 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 229930016911 cinnamic acid Natural products 0.000 description 3
- 235000013985 cinnamic acid Nutrition 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 239000012975 dibutyltin dilaurate Substances 0.000 description 3
- 238000004049 embossing Methods 0.000 description 3
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 3
- 238000005227 gel permeation chromatography Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 150000003951 lactams Chemical class 0.000 description 3
- 238000010030 laminating Methods 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- QYZFTMMPKCOTAN-UHFFFAOYSA-N n-[2-(2-hydroxyethylamino)ethyl]-2-[[1-[2-(2-hydroxyethylamino)ethylamino]-2-methyl-1-oxopropan-2-yl]diazenyl]-2-methylpropanamide Chemical compound OCCNCCNC(=O)C(C)(C)N=NC(C)(C)C(=O)NCCNCCO QYZFTMMPKCOTAN-UHFFFAOYSA-N 0.000 description 3
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 3
- 125000004430 oxygen atom Chemical group O* 0.000 description 3
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 3
- 238000007747 plating Methods 0.000 description 3
- 229920006267 polyester film Polymers 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
- 238000007142 ring opening reaction Methods 0.000 description 3
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 3
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 3
- WYKYCHHWIJXDAO-UHFFFAOYSA-N tert-butyl 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)C WYKYCHHWIJXDAO-UHFFFAOYSA-N 0.000 description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- 125000001302 tertiary amino group Chemical group 0.000 description 3
- 239000013638 trimer Substances 0.000 description 3
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- 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 2
- GQLGFBRMCCVQLU-XCGJVMPOSA-N (6r)-7-amino-3-ethenyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid Chemical compound S1CC(C=C)=C(C(O)=O)N2C(=O)C(N)[C@H]21 GQLGFBRMCCVQLU-XCGJVMPOSA-N 0.000 description 2
- SKYXLDSRLNRAPS-UHFFFAOYSA-N 1,2,4-trifluoro-5-methoxybenzene Chemical compound COC1=CC(F)=C(F)C=C1F SKYXLDSRLNRAPS-UHFFFAOYSA-N 0.000 description 2
- MBQIGVLDESBKFG-UHFFFAOYSA-N 1-(2-ethenoxyethoxy)-2-methoxyethane Chemical compound COCCOCCOC=C MBQIGVLDESBKFG-UHFFFAOYSA-N 0.000 description 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 2
- CZAVRNDQSIORTH-UHFFFAOYSA-N 1-ethenoxy-2,2-bis(ethenoxymethyl)butane Chemical compound C=COCC(CC)(COC=C)COC=C CZAVRNDQSIORTH-UHFFFAOYSA-N 0.000 description 2
- SAMJGBVVQUEMGC-UHFFFAOYSA-N 1-ethenoxy-2-(2-ethenoxyethoxy)ethane Chemical compound C=COCCOCCOC=C SAMJGBVVQUEMGC-UHFFFAOYSA-N 0.000 description 2
- OZCMOJQQLBXBKI-UHFFFAOYSA-N 1-ethenoxy-2-methylpropane Chemical compound CC(C)COC=C OZCMOJQQLBXBKI-UHFFFAOYSA-N 0.000 description 2
- XXCVIFJHBFNFBO-UHFFFAOYSA-N 1-ethenoxyoctane Chemical compound CCCCCCCCOC=C XXCVIFJHBFNFBO-UHFFFAOYSA-N 0.000 description 2
- KBICSUODQLDGFE-UHFFFAOYSA-N 1-ethenylbenzimidazole Chemical compound C1=CC=C2N(C=C)C=NC2=C1 KBICSUODQLDGFE-UHFFFAOYSA-N 0.000 description 2
- PLWOURZNEOAFHE-UHFFFAOYSA-N 1-ethenylindazole Chemical compound C1=CC=C2N(C=C)N=CC2=C1 PLWOURZNEOAFHE-UHFFFAOYSA-N 0.000 description 2
- GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 2
- QWDQYHPOSSHSAW-UHFFFAOYSA-N 1-isocyanatooctadecane Chemical compound CCCCCCCCCCCCCCCCCCN=C=O QWDQYHPOSSHSAW-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
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 2
- JCTXKRPTIMZBJT-UHFFFAOYSA-N 2,2,4-trimethylpentane-1,3-diol Chemical compound CC(C)C(O)C(C)(C)CO JCTXKRPTIMZBJT-UHFFFAOYSA-N 0.000 description 2
- FCMUPMSEVHVOSE-UHFFFAOYSA-N 2,3-bis(ethenyl)pyridine Chemical compound C=CC1=CC=CN=C1C=C FCMUPMSEVHVOSE-UHFFFAOYSA-N 0.000 description 2
- KQSMCAVKSJWMSI-UHFFFAOYSA-N 2,4-dimethyl-1-n,1-n,3-n,3-n-tetrakis(oxiran-2-ylmethyl)benzene-1,3-diamine Chemical compound CC1=C(N(CC2OC2)CC2OC2)C(C)=CC=C1N(CC1OC1)CC1CO1 KQSMCAVKSJWMSI-UHFFFAOYSA-N 0.000 description 2
- DBTGFWMBFZBBEF-UHFFFAOYSA-N 2,4-dimethylpentane-2,4-diol Chemical compound CC(C)(O)CC(C)(C)O DBTGFWMBFZBBEF-UHFFFAOYSA-N 0.000 description 2
- ZWNMRZQYWRLGMM-UHFFFAOYSA-N 2,5-dimethylhexane-2,5-diol Chemical compound CC(C)(O)CCC(C)(C)O ZWNMRZQYWRLGMM-UHFFFAOYSA-N 0.000 description 2
- RKYJPYDJNQXILT-UHFFFAOYSA-N 2-(2-prop-2-enoyloxyethoxycarbonyl)benzoic acid Chemical compound OC(=O)C1=CC=CC=C1C(=O)OCCOC(=O)C=C RKYJPYDJNQXILT-UHFFFAOYSA-N 0.000 description 2
- UECGJSXCVLTIMQ-UHFFFAOYSA-N 2-(2-prop-2-enoyloxyethoxycarbonyl)cyclohexane-1-carboxylic acid Chemical compound OC(=O)C1CCCCC1C(=O)OCCOC(=O)C=C UECGJSXCVLTIMQ-UHFFFAOYSA-N 0.000 description 2
- ITPZSEHIQWKKAE-UHFFFAOYSA-N 2-(4-prop-2-enoyloxybutoxycarbonyl)benzoic acid Chemical compound OC(=O)C1=CC=CC=C1C(=O)OCCCCOC(=O)C=C ITPZSEHIQWKKAE-UHFFFAOYSA-N 0.000 description 2
- KZXOOWGVLDEHDT-UHFFFAOYSA-N 2-Ethenyl-6-methylpyrazine Chemical compound CC1=CN=CC(C=C)=N1 KZXOOWGVLDEHDT-UHFFFAOYSA-N 0.000 description 2
- JASFBLBUHWKFBZ-UHFFFAOYSA-N 2-Methyl-5-vinylpyrazine Chemical compound CC1=CN=C(C=C)C=N1 JASFBLBUHWKFBZ-UHFFFAOYSA-N 0.000 description 2
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 2
- DSKYSDCYIODJPC-UHFFFAOYSA-N 2-butyl-2-ethylpropane-1,3-diol Chemical compound CCCCC(CC)(CO)CO DSKYSDCYIODJPC-UHFFFAOYSA-N 0.000 description 2
- XUDBVJCTLZTSDC-UHFFFAOYSA-N 2-ethenylbenzoic acid Chemical compound OC(=O)C1=CC=CC=C1C=C XUDBVJCTLZTSDC-UHFFFAOYSA-N 0.000 description 2
- KANZWHBYRHQMKZ-UHFFFAOYSA-N 2-ethenylpyrazine Chemical compound C=CC1=CN=CC=N1 KANZWHBYRHQMKZ-UHFFFAOYSA-N 0.000 description 2
- JRMAQQQTXDJDNC-UHFFFAOYSA-M 2-ethoxy-2-oxoacetate Chemical compound CCOC(=O)C([O-])=O JRMAQQQTXDJDNC-UHFFFAOYSA-M 0.000 description 2
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 2
- AKRNPYKLZFDTPP-UHFFFAOYSA-N 2-heptylpropane-1,3-diol Chemical compound CCCCCCCC(CO)CO AKRNPYKLZFDTPP-UHFFFAOYSA-N 0.000 description 2
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 2
- RTEZVHMDMFEURJ-UHFFFAOYSA-N 2-methylpentan-2-yl 2,2-dimethylpropaneperoxoate Chemical compound CCCC(C)(C)OOC(=O)C(C)(C)C RTEZVHMDMFEURJ-UHFFFAOYSA-N 0.000 description 2
- UDWIZRDPCQAYRF-UHFFFAOYSA-N 3-[diethoxy(methyl)silyl]propyl prop-2-enoate Chemical compound CCO[Si](C)(OCC)CCCOC(=O)C=C UDWIZRDPCQAYRF-UHFFFAOYSA-N 0.000 description 2
- MCDBEBOBROAQSH-UHFFFAOYSA-N 3-[dimethoxy(methyl)silyl]propyl prop-2-enoate Chemical compound CO[Si](C)(OC)CCCOC(=O)C=C MCDBEBOBROAQSH-UHFFFAOYSA-N 0.000 description 2
- PRNMXSACOXQQRF-UHFFFAOYSA-N 3-amino-3-oxoprop-1-ene-2-sulfonic acid Chemical compound NC(=O)C(=C)S(O)(=O)=O PRNMXSACOXQQRF-UHFFFAOYSA-N 0.000 description 2
- UJTRCPVECIHPBG-UHFFFAOYSA-N 3-cyclohexylpyrrole-2,5-dione Chemical compound O=C1NC(=O)C(C2CCCCC2)=C1 UJTRCPVECIHPBG-UHFFFAOYSA-N 0.000 description 2
- OJXVWULQHYTXRF-UHFFFAOYSA-N 3-ethenoxypropan-1-ol Chemical compound OCCCOC=C OJXVWULQHYTXRF-UHFFFAOYSA-N 0.000 description 2
- JLPZQZIYSREPPU-UHFFFAOYSA-N 3-ethenyl-2,5-dimethylpyrazine Chemical compound CC1=CN=C(C)C(C=C)=N1 JLPZQZIYSREPPU-UHFFFAOYSA-N 0.000 description 2
- VWXZFDWVWMQRQR-UHFFFAOYSA-N 3-ethenylbenzoic acid Chemical compound OC(=O)C1=CC=CC(C=C)=C1 VWXZFDWVWMQRQR-UHFFFAOYSA-N 0.000 description 2
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 2
- HMBNQNDUEFFFNZ-UHFFFAOYSA-N 4-ethenoxybutan-1-ol Chemical compound OCCCCOC=C HMBNQNDUEFFFNZ-UHFFFAOYSA-N 0.000 description 2
- SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-UHFFFAOYSA-N 0.000 description 2
- NDWUBGAGUCISDV-UHFFFAOYSA-N 4-hydroxybutyl prop-2-enoate Chemical compound OCCCCOC(=O)C=C NDWUBGAGUCISDV-UHFFFAOYSA-N 0.000 description 2
- INYHZQLKOKTDAI-UHFFFAOYSA-N 5-ethenylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(C=C)CC1C=C2 INYHZQLKOKTDAI-UHFFFAOYSA-N 0.000 description 2
- ASPUDHDPXIBNAP-UHFFFAOYSA-N 6-ethenoxyhexan-1-ol Chemical compound OCCCCCCOC=C ASPUDHDPXIBNAP-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- UIERETOOQGIECD-UHFFFAOYSA-N Angelic acid Natural products CC=C(C)C(O)=O UIERETOOQGIECD-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- PCCSDBPHBFQBAY-UHFFFAOYSA-N C(=C)N1CN=CC2=CC=CC=C12 Chemical compound C(=C)N1CN=CC2=CC=CC=C12 PCCSDBPHBFQBAY-UHFFFAOYSA-N 0.000 description 2
- OSEBHEIFCSZTCU-UHFFFAOYSA-N C(=C)N1NC=CC2=CC=CC=C12 Chemical compound C(=C)N1NC=CC2=CC=CC=C12 OSEBHEIFCSZTCU-UHFFFAOYSA-N 0.000 description 2
- JDWDRCWQPJBXSJ-UHFFFAOYSA-N C=CC(=O)OCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)O Chemical compound C=CC(=O)OCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)O JDWDRCWQPJBXSJ-UHFFFAOYSA-N 0.000 description 2
- MKNHYEZJYYMSQF-UHFFFAOYSA-N C=CC(=O)OCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)O Chemical compound C=CC(=O)OCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)O MKNHYEZJYYMSQF-UHFFFAOYSA-N 0.000 description 2
- MZZDYPRFXNXEOG-UHFFFAOYSA-N CC1(C(C=CC=C1)S(=O)(=O)O)OC=CC Chemical compound CC1(C(C=CC=C1)S(=O)(=O)O)OC=CC MZZDYPRFXNXEOG-UHFFFAOYSA-N 0.000 description 2
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-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
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 229920002873 Polyethylenimine Polymers 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 2
- JJSCUXAFAJEQGB-MRVPVSSYSA-N [(1r)-1-isocyanatoethyl]benzene Chemical compound O=C=N[C@H](C)C1=CC=CC=C1 JJSCUXAFAJEQGB-MRVPVSSYSA-N 0.000 description 2
- IAXXETNIOYFMLW-COPLHBTASA-N [(1s,3s,4s)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] 2-methylprop-2-enoate Chemical compound C1C[C@]2(C)[C@@H](OC(=O)C(=C)C)C[C@H]1C2(C)C IAXXETNIOYFMLW-COPLHBTASA-N 0.000 description 2
- MZVQCMJNVPIDEA-UHFFFAOYSA-N [CH2]CN(CC)CC Chemical group [CH2]CN(CC)CC MZVQCMJNVPIDEA-UHFFFAOYSA-N 0.000 description 2
- 238000010306 acid treatment Methods 0.000 description 2
- 125000005396 acrylic acid ester group Chemical group 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000005370 alkoxysilyl group Chemical group 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- YBPOEDKYWDVVTP-UHFFFAOYSA-N azanium;2-methylprop-2-ene-1-sulfonate Chemical compound [NH4+].CC(=C)CS([O-])(=O)=O YBPOEDKYWDVVTP-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 230000001588 bifunctional effect Effects 0.000 description 2
- QNRMTGGDHLBXQZ-UHFFFAOYSA-N buta-1,2-diene Chemical compound CC=C=C QNRMTGGDHLBXQZ-UHFFFAOYSA-N 0.000 description 2
- YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 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
- GJWSUKYXUMVMGX-UHFFFAOYSA-N citronellic acid Chemical compound OC(=O)CC(C)CCC=C(C)C GJWSUKYXUMVMGX-UHFFFAOYSA-N 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 230000008602 contraction Effects 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 description 2
- ZQMIGQNCOMNODD-UHFFFAOYSA-N diacetyl peroxide Chemical compound CC(=O)OOC(C)=O ZQMIGQNCOMNODD-UHFFFAOYSA-N 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- 150000001993 dienes Chemical class 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 125000005442 diisocyanate group Chemical group 0.000 description 2
- 229950001467 docosil Drugs 0.000 description 2
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 2
- WMRDPJYQERQCEP-UHFFFAOYSA-N dotriacont-1-ene Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC=C WMRDPJYQERQCEP-UHFFFAOYSA-N 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 2
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- WOLATMHLPFJRGC-UHFFFAOYSA-N furan-2,5-dione;styrene Chemical compound O=C1OC(=O)C=C1.C=CC1=CC=CC=C1 WOLATMHLPFJRGC-UHFFFAOYSA-N 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 2
- GJBXIPOYHVMPQJ-UHFFFAOYSA-N hexadecane-1,16-diol Chemical compound OCCCCCCCCCCCCCCCCO GJBXIPOYHVMPQJ-UHFFFAOYSA-N 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 125000004464 hydroxyphenyl group Chemical group 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 229940119545 isobornyl methacrylate Drugs 0.000 description 2
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 238000005304 joining Methods 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- CCCMONHAUSKTEQ-UHFFFAOYSA-N octadec-1-ene Chemical compound CCCCCCCCCCCCCCCCC=C CCCMONHAUSKTEQ-UHFFFAOYSA-N 0.000 description 2
- SRSFOMHQIATOFV-UHFFFAOYSA-N octanoyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(=O)CCCCCCC SRSFOMHQIATOFV-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 150000002902 organometallic compounds Chemical class 0.000 description 2
- KJFMBFZCATUALV-UHFFFAOYSA-N phenolphthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C(=O)O1 KJFMBFZCATUALV-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920005749 polyurethane resin Polymers 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000011342 resin composition Substances 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- 150000003460 sulfonic acids Chemical class 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 2
- WMZHDICSCDKPFS-UHFFFAOYSA-N triacont-1-ene Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCC=C WMZHDICSCDKPFS-UHFFFAOYSA-N 0.000 description 2
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 2
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 2
- 229920001567 vinyl ester resin Polymers 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 229910052726 zirconium Inorganic materials 0.000 description 2
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- DWANEFRJKWXRSG-UHFFFAOYSA-N (+-)-Tetradecan-1,2-diol Natural products CCCCCCCCCCCCC(O)CO DWANEFRJKWXRSG-UHFFFAOYSA-N 0.000 description 1
- CJCGDEYGAIPAEN-UHFFFAOYSA-N (1-methylcyclohexyl) prop-2-enoate Chemical compound C=CC(=O)OC1(C)CCCCC1 CJCGDEYGAIPAEN-UHFFFAOYSA-N 0.000 description 1
- KIFAKLJJKSLDBP-UHFFFAOYSA-N (2,2,3,3-tetramethylpiperidin-1-yl) prop-2-enoate Chemical compound CC1(C)CCCN(OC(=O)C=C)C1(C)C KIFAKLJJKSLDBP-UHFFFAOYSA-N 0.000 description 1
- MZXAKZZMAPICNW-UHFFFAOYSA-N (2-hydroxy-3-phenoxydecyl) prop-2-enoate Chemical compound C(C=C)(=O)OCC(C(CCCCCCC)OC1=CC=CC=C1)O MZXAKZZMAPICNW-UHFFFAOYSA-N 0.000 description 1
- JDCBWJCUHSVVMN-SCSAIBSYSA-N (2r)-but-3-en-2-amine Chemical compound C[C@@H](N)C=C JDCBWJCUHSVVMN-SCSAIBSYSA-N 0.000 description 1
- ZINGPVGWKVTAAC-IAROGAJJSA-N (2z,4e)-2-chlorohexa-2,4-dienoic acid Chemical compound C\C=C\C=C(/Cl)C(O)=O ZINGPVGWKVTAAC-IAROGAJJSA-N 0.000 description 1
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 1
- VKNLVLNOHCTKII-ONEGZZNKSA-N (e)-1,1,1-trichloro-4-ethoxybut-3-en-2-one Chemical compound CCO\C=C\C(=O)C(Cl)(Cl)Cl VKNLVLNOHCTKII-ONEGZZNKSA-N 0.000 description 1
- INMSLZIWGZNXRL-VQHVLOKHSA-N (e)-2,3-bis(furan-2-yl)prop-2-enamide Chemical compound C=1C=COC=1/C(C(=O)N)=C\C1=CC=CO1 INMSLZIWGZNXRL-VQHVLOKHSA-N 0.000 description 1
- NCNYEGJDGNOYJX-NSCUHMNNSA-N (e)-2,3-dibromo-4-oxobut-2-enoic acid Chemical compound OC(=O)C(\Br)=C(/Br)C=O NCNYEGJDGNOYJX-NSCUHMNNSA-N 0.000 description 1
- LUMLZKVIXLWTCI-NSCUHMNNSA-N (e)-2,3-dichloro-4-oxobut-2-enoic acid Chemical compound OC(=O)C(\Cl)=C(/Cl)C=O LUMLZKVIXLWTCI-NSCUHMNNSA-N 0.000 description 1
- BSSNZUFKXJJCBG-OWOJBTEDSA-N (e)-but-2-enediamide Chemical compound NC(=O)\C=C\C(N)=O BSSNZUFKXJJCBG-OWOJBTEDSA-N 0.000 description 1
- KYPOHTVBFVELTG-OWOJBTEDSA-N (e)-but-2-enedinitrile Chemical compound N#C\C=C\C#N KYPOHTVBFVELTG-OWOJBTEDSA-N 0.000 description 1
- GWENLLRIMBJBRA-IHWYPQMZSA-N (z)-4-amino-3-methyl-4-oxobut-2-enoic acid Chemical compound NC(=O)C(/C)=C\C(O)=O GWENLLRIMBJBRA-IHWYPQMZSA-N 0.000 description 1
- ORTVZLZNOYNASJ-UPHRSURJSA-N (z)-but-2-ene-1,4-diol Chemical compound OC\C=C/CO ORTVZLZNOYNASJ-UPHRSURJSA-N 0.000 description 1
- KHXKESCWFMPTFT-UHFFFAOYSA-N 1,1,1,2,2,3,3-heptafluoro-3-(1,2,2-trifluoroethenoxy)propane Chemical compound FC(F)=C(F)OC(F)(F)C(F)(F)C(F)(F)F KHXKESCWFMPTFT-UHFFFAOYSA-N 0.000 description 1
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
- GPHWXFINOWXMDN-UHFFFAOYSA-N 1,1-bis(ethenoxy)hexane Chemical compound CCCCCC(OC=C)OC=C GPHWXFINOWXMDN-UHFFFAOYSA-N 0.000 description 1
- WTBVSWPUNJVDHW-UHFFFAOYSA-N 1,1-bis(ethenoxy)nonane Chemical compound CCCCCCCCC(OC=C)OC=C WTBVSWPUNJVDHW-UHFFFAOYSA-N 0.000 description 1
- GHLKSLMMWAKNBM-UHFFFAOYSA-N 1,12-Dodecanediol Natural products OCCCCCCCCCCCCO GHLKSLMMWAKNBM-UHFFFAOYSA-N 0.000 description 1
- FYADHXFMURLYQI-UHFFFAOYSA-N 1,2,4-triazine Chemical compound C1=CN=NC=N1 FYADHXFMURLYQI-UHFFFAOYSA-N 0.000 description 1
- CYIGRWUIQAVBFG-UHFFFAOYSA-N 1,2-bis(2-ethenoxyethoxy)ethane Chemical compound C=COCCOCCOCCOC=C CYIGRWUIQAVBFG-UHFFFAOYSA-N 0.000 description 1
- ZXHDVRATSGZISC-UHFFFAOYSA-N 1,2-bis(ethenoxy)ethane Chemical compound C=COCCOC=C ZXHDVRATSGZISC-UHFFFAOYSA-N 0.000 description 1
- LXSVCBDMOGLGFA-UHFFFAOYSA-N 1,2-bis(ethenoxy)propane Chemical compound C=COC(C)COC=C LXSVCBDMOGLGFA-UHFFFAOYSA-N 0.000 description 1
- ZGDSDWSIFQBAJS-UHFFFAOYSA-N 1,2-diisocyanatopropane Chemical compound O=C=NC(C)CN=C=O ZGDSDWSIFQBAJS-UHFFFAOYSA-N 0.000 description 1
- BTOOAFQCTJZDRC-UHFFFAOYSA-N 1,2-hexadecanediol Chemical compound CCCCCCCCCCCCCCC(O)CO BTOOAFQCTJZDRC-UHFFFAOYSA-N 0.000 description 1
- 229940015975 1,2-hexanediol Drugs 0.000 description 1
- 229940031723 1,2-octanediol Drugs 0.000 description 1
- IFPMZBBHBZQTOV-UHFFFAOYSA-N 1,3,5-trinitro-2-(2,4,6-trinitrophenyl)-4-[2,4,6-trinitro-3-(2,4,6-trinitrophenyl)phenyl]benzene Chemical compound [O-][N+](=O)C1=CC([N+](=O)[O-])=CC([N+]([O-])=O)=C1C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C(C=2C(=C(C=3C(=CC(=CC=3[N+]([O-])=O)[N+]([O-])=O)[N+]([O-])=O)C(=CC=2[N+]([O-])=O)[N+]([O-])=O)[N+]([O-])=O)=C1[N+]([O-])=O IFPMZBBHBZQTOV-UHFFFAOYSA-N 0.000 description 1
- KCZQSKKNAGZQSZ-UHFFFAOYSA-N 1,3,5-tris(6-isocyanatohexyl)-1,3,5-triazin-2,4,6-trione Chemical compound O=C=NCCCCCCN1C(=O)N(CCCCCCN=C=O)C(=O)N(CCCCCCN=C=O)C1=O KCZQSKKNAGZQSZ-UHFFFAOYSA-N 0.000 description 1
- XDWRKTULOHXYGN-UHFFFAOYSA-N 1,3-bis(ethenoxy)-2,2-bis(ethenoxymethyl)propane Chemical compound C=COCC(COC=C)(COC=C)COC=C XDWRKTULOHXYGN-UHFFFAOYSA-N 0.000 description 1
- AITKNDQVEUUYHE-UHFFFAOYSA-N 1,3-bis(ethenoxy)-2,2-dimethylpropane Chemical compound C=COCC(C)(C)COC=C AITKNDQVEUUYHE-UHFFFAOYSA-N 0.000 description 1
- RTTZISZSHSCFRH-UHFFFAOYSA-N 1,3-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC(CN=C=O)=C1 RTTZISZSHSCFRH-UHFFFAOYSA-N 0.000 description 1
- PCHXZXKMYCGVFA-UHFFFAOYSA-N 1,3-diazetidine-2,4-dione Chemical group O=C1NC(=O)N1 PCHXZXKMYCGVFA-UHFFFAOYSA-N 0.000 description 1
- VGHSXKTVMPXHNG-UHFFFAOYSA-N 1,3-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC(N=C=O)=C1 VGHSXKTVMPXHNG-UHFFFAOYSA-N 0.000 description 1
- UFXYYTWJETZVHG-UHFFFAOYSA-N 1,3-diisocyanatobutane Chemical compound O=C=NC(C)CCN=C=O UFXYYTWJETZVHG-UHFFFAOYSA-N 0.000 description 1
- IKYNWXNXXHWHLL-UHFFFAOYSA-N 1,3-diisocyanatopropane Chemical compound O=C=NCCCN=C=O IKYNWXNXXHWHLL-UHFFFAOYSA-N 0.000 description 1
- NALISUVNCITOCO-UHFFFAOYSA-N 1,4-bis(ethenoxy)benzene Chemical compound C=COC1=CC=C(OC=C)C=C1 NALISUVNCITOCO-UHFFFAOYSA-N 0.000 description 1
- MWZJGRDWJVHRDV-UHFFFAOYSA-N 1,4-bis(ethenoxy)butane Chemical compound C=COCCCCOC=C MWZJGRDWJVHRDV-UHFFFAOYSA-N 0.000 description 1
- CGHMMUAOPPRRMX-UHFFFAOYSA-N 1,4-bis(ethenoxy)cyclohexane Chemical compound C=COC1CCC(OC=C)CC1 CGHMMUAOPPRRMX-UHFFFAOYSA-N 0.000 description 1
- ALQLPWJFHRMHIU-UHFFFAOYSA-N 1,4-diisocyanatobenzene Chemical compound O=C=NC1=CC=C(N=C=O)C=C1 ALQLPWJFHRMHIU-UHFFFAOYSA-N 0.000 description 1
- OVBFMUAFNIIQAL-UHFFFAOYSA-N 1,4-diisocyanatobutane Chemical compound O=C=NCCCCN=C=O OVBFMUAFNIIQAL-UHFFFAOYSA-N 0.000 description 1
- UNVGBIALRHLALK-UHFFFAOYSA-N 1,5-Hexanediol Natural products CC(O)CCCCO UNVGBIALRHLALK-UHFFFAOYSA-N 0.000 description 1
- DFPJRUKWEPYFJT-UHFFFAOYSA-N 1,5-diisocyanatopentane Chemical compound O=C=NCCCCCN=C=O DFPJRUKWEPYFJT-UHFFFAOYSA-N 0.000 description 1
- QGLRLXLDMZCFBP-UHFFFAOYSA-N 1,6-diisocyanato-2,4,4-trimethylhexane Chemical compound O=C=NCC(C)CC(C)(C)CCN=C=O QGLRLXLDMZCFBP-UHFFFAOYSA-N 0.000 description 1
- ALVZNPYWJMLXKV-UHFFFAOYSA-N 1,9-Nonanediol Chemical compound OCCCCCCCCCO ALVZNPYWJMLXKV-UHFFFAOYSA-N 0.000 description 1
- UWFRVQVNYNPBEF-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)propan-1-one Chemical compound CCC(=O)C1=CC=C(C)C=C1C UWFRVQVNYNPBEF-UHFFFAOYSA-N 0.000 description 1
- UEIPWOFSKAZYJO-UHFFFAOYSA-N 1-(2-ethenoxyethoxy)-2-[2-(2-ethenoxyethoxy)ethoxy]ethane Chemical compound C=COCCOCCOCCOCCOC=C UEIPWOFSKAZYJO-UHFFFAOYSA-N 0.000 description 1
- AYMDJPGTQFHDSA-UHFFFAOYSA-N 1-(2-ethenoxyethoxy)-2-ethoxyethane Chemical compound CCOCCOCCOC=C AYMDJPGTQFHDSA-UHFFFAOYSA-N 0.000 description 1
- UNMYKPSSIFZORM-UHFFFAOYSA-N 1-(2-ethenoxyethoxy)butane Chemical compound CCCCOCCOC=C UNMYKPSSIFZORM-UHFFFAOYSA-N 0.000 description 1
- IZYHCUTTWJQLSK-UHFFFAOYSA-N 1-(2-methylbutan-2-yloxy)-4-prop-1-en-2-ylbenzene Chemical compound CCC(C)(C)OC1=CC=C(C(C)=C)C=C1 IZYHCUTTWJQLSK-UHFFFAOYSA-N 0.000 description 1
- LQDGDDQWVWZDCS-UHFFFAOYSA-N 1-[(2-methylpropan-2-yl)oxy]-4-prop-1-en-2-ylbenzene Chemical compound CC(=C)C1=CC=C(OC(C)(C)C)C=C1 LQDGDDQWVWZDCS-UHFFFAOYSA-N 0.000 description 1
- RRNNPMNWSGRGBH-UHFFFAOYSA-N 1-[2-(2-ethenoxyethoxy)ethoxy]butane Chemical compound CCCCOCCOCCOC=C RRNNPMNWSGRGBH-UHFFFAOYSA-N 0.000 description 1
- HASUCEDGKYJBDC-UHFFFAOYSA-N 1-[3-[[bis(oxiran-2-ylmethyl)amino]methyl]cyclohexyl]-n,n-bis(oxiran-2-ylmethyl)methanamine Chemical compound C1OC1CN(CC1CC(CN(CC2OC2)CC2OC2)CCC1)CC1CO1 HASUCEDGKYJBDC-UHFFFAOYSA-N 0.000 description 1
- CSBPEICMQGBFID-UHFFFAOYSA-N 1-[4-(2-hydroxypropyl)phenyl]propan-2-ol Chemical compound CC(O)CC1=CC=C(CC(C)O)C=C1 CSBPEICMQGBFID-UHFFFAOYSA-N 0.000 description 1
- ODEIZNBPYITUTO-UHFFFAOYSA-N 1-[diethoxy(propyl)silyl]oxyethyl prop-2-enoate Chemical compound CCC[Si](OCC)(OCC)OC(C)OC(=O)C=C ODEIZNBPYITUTO-UHFFFAOYSA-N 0.000 description 1
- MNCMBBIFTVWHIP-UHFFFAOYSA-N 1-anthracen-9-yl-2,2,2-trifluoroethanone Chemical group C1=CC=C2C(C(=O)C(F)(F)F)=C(C=CC=C3)C3=CC2=C1 MNCMBBIFTVWHIP-UHFFFAOYSA-N 0.000 description 1
- UAQUKNKEWMASMM-UHFFFAOYSA-N 1-benzyl-2-ethenylpiperazine Chemical compound C=CC1CNCCN1CC1=CC=CC=C1 UAQUKNKEWMASMM-UHFFFAOYSA-N 0.000 description 1
- BFYGMFJYMANSGU-UHFFFAOYSA-N 1-benzyl-3-ethenylpiperazine Chemical compound C1CNC(C=C)CN1CC1=CC=CC=C1 BFYGMFJYMANSGU-UHFFFAOYSA-N 0.000 description 1
- WERBWSLPTVDMMJ-UHFFFAOYSA-N 1-butoxyprop-2-enylbenzene Chemical compound CCCCOC(C=C)C1=CC=CC=C1 WERBWSLPTVDMMJ-UHFFFAOYSA-N 0.000 description 1
- CVMYEWFFFUKQEF-UHFFFAOYSA-N 1-chloro-2-(2-chloroethenoxy)ethene Chemical compound ClC=COC=CCl CVMYEWFFFUKQEF-UHFFFAOYSA-N 0.000 description 1
- BCMYXYHEMGPZJN-UHFFFAOYSA-N 1-chloro-2-isocyanatoethane Chemical compound ClCCN=C=O BCMYXYHEMGPZJN-UHFFFAOYSA-N 0.000 description 1
- ADAKRBAJFHTIEW-UHFFFAOYSA-N 1-chloro-4-isocyanatobenzene Chemical compound ClC1=CC=C(N=C=O)C=C1 ADAKRBAJFHTIEW-UHFFFAOYSA-N 0.000 description 1
- WQDGTJOEMPEHHL-UHFFFAOYSA-N 1-chloro-4-prop-1-en-2-ylbenzene Chemical compound CC(=C)C1=CC=C(Cl)C=C1 WQDGTJOEMPEHHL-UHFFFAOYSA-N 0.000 description 1
- CCHIBVWJTVVHRO-UHFFFAOYSA-N 1-decoxy-2-ethenylbenzene Chemical compound CCCCCCCCCCOC1=CC=CC=C1C=C CCHIBVWJTVVHRO-UHFFFAOYSA-N 0.000 description 1
- XMSXHNOJGOTTPP-UHFFFAOYSA-N 1-dodecoxyprop-2-enylbenzene Chemical compound CCCCCCCCCCCCOC(C=C)C1=CC=CC=C1 XMSXHNOJGOTTPP-UHFFFAOYSA-N 0.000 description 1
- RQJCIXUNHZZFMB-UHFFFAOYSA-N 1-ethenoxy-2-(2-ethenoxypropoxy)propane Chemical compound C=COCC(C)OCC(C)OC=C RQJCIXUNHZZFMB-UHFFFAOYSA-N 0.000 description 1
- FOWNZLLMQHBVQT-UHFFFAOYSA-N 1-ethenoxy-2-[2-(2-ethenoxypropoxy)propoxy]propane Chemical compound C=COCC(C)OCC(C)OCC(C)OC=C FOWNZLLMQHBVQT-UHFFFAOYSA-N 0.000 description 1
- HWCLMKDWXUGDKL-UHFFFAOYSA-N 1-ethenoxy-2-ethoxyethane Chemical compound CCOCCOC=C HWCLMKDWXUGDKL-UHFFFAOYSA-N 0.000 description 1
- GXZPMXGRNUXGHN-UHFFFAOYSA-N 1-ethenoxy-2-methoxyethane Chemical compound COCCOC=C GXZPMXGRNUXGHN-UHFFFAOYSA-N 0.000 description 1
- QIUCYKBVFAPWRR-UHFFFAOYSA-N 1-ethenoxy-3-methylbutane Chemical compound CC(C)CCOC=C QIUCYKBVFAPWRR-UHFFFAOYSA-N 0.000 description 1
- BNWLJBLIQDSPHJ-UHFFFAOYSA-N 1-ethenoxy-4-ethoxybutane Chemical compound CCOCCCCOC=C BNWLJBLIQDSPHJ-UHFFFAOYSA-N 0.000 description 1
- XMJQCVMNFPEJLN-UHFFFAOYSA-N 1-ethenoxy-4-methylpentane Chemical compound CC(C)CCCOC=C XMJQCVMNFPEJLN-UHFFFAOYSA-N 0.000 description 1
- SHHYVKSJGBTTLX-UHFFFAOYSA-N 1-ethenoxy-6-methylheptane Chemical compound CC(C)CCCCCOC=C SHHYVKSJGBTTLX-UHFFFAOYSA-N 0.000 description 1
- MFKVIGSGQLMCIG-UHFFFAOYSA-N 1-ethenoxyadamantane Chemical compound C1C(C2)CC3CC2CC1(OC=C)C3 MFKVIGSGQLMCIG-UHFFFAOYSA-N 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N 1-ethenoxybutane Chemical compound CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- NSOAQRMLVFRWIT-UHFFFAOYSA-N 1-ethenoxydecane Chemical compound CCCCCCCCCCOC=C NSOAQRMLVFRWIT-UHFFFAOYSA-N 0.000 description 1
- LAYAKLSFVAPMEL-UHFFFAOYSA-N 1-ethenoxydodecane Chemical compound CCCCCCCCCCCCOC=C LAYAKLSFVAPMEL-UHFFFAOYSA-N 0.000 description 1
- SWZSKZZXXULJHU-UHFFFAOYSA-N 1-ethenoxyheptane Chemical compound CCCCCCCOC=C SWZSKZZXXULJHU-UHFFFAOYSA-N 0.000 description 1
- YAOJJEJGPZRYJF-UHFFFAOYSA-N 1-ethenoxyhexane Chemical compound CCCCCCOC=C YAOJJEJGPZRYJF-UHFFFAOYSA-N 0.000 description 1
- OHSFPBQPZFLOKE-UHFFFAOYSA-N 1-ethenoxynaphthalene Chemical compound C1=CC=C2C(OC=C)=CC=CC2=C1 OHSFPBQPZFLOKE-UHFFFAOYSA-N 0.000 description 1
- MIMKRVLJPMYKID-UHFFFAOYSA-N 1-ethenoxynonane Chemical compound CCCCCCCCCOC=C MIMKRVLJPMYKID-UHFFFAOYSA-N 0.000 description 1
- IOSXLUZXMXORMX-UHFFFAOYSA-N 1-ethenoxypentane Chemical compound CCCCCOC=C IOSXLUZXMXORMX-UHFFFAOYSA-N 0.000 description 1
- OVGRCEFMXPHEBL-UHFFFAOYSA-N 1-ethenoxypropane Chemical compound CCCOC=C OVGRCEFMXPHEBL-UHFFFAOYSA-N 0.000 description 1
- ICHUDCIOYDOHEF-UHFFFAOYSA-N 1-ethenyl-2-heptoxybenzene Chemical compound CCCCCCCOC1=CC=CC=C1C=C ICHUDCIOYDOHEF-UHFFFAOYSA-N 0.000 description 1
- RFMCWCQLHUQQHW-UHFFFAOYSA-N 1-ethenyl-2-hexoxybenzene Chemical compound CCCCCCOC1=CC=CC=C1C=C RFMCWCQLHUQQHW-UHFFFAOYSA-N 0.000 description 1
- VDSAXHBDVIUOGV-UHFFFAOYSA-N 1-ethenyl-2-methyl-4,5-dihydroimidazole Chemical compound CC1=NCCN1C=C VDSAXHBDVIUOGV-UHFFFAOYSA-N 0.000 description 1
- NVZWEEGUWXZOKI-UHFFFAOYSA-N 1-ethenyl-2-methylbenzene Chemical compound CC1=CC=CC=C1C=C NVZWEEGUWXZOKI-UHFFFAOYSA-N 0.000 description 1
- CCRAQNXKHZFYJM-UHFFFAOYSA-N 1-ethenyl-2-methylindole Chemical compound C1=CC=C2N(C=C)C(C)=CC2=C1 CCRAQNXKHZFYJM-UHFFFAOYSA-N 0.000 description 1
- UVXQFKDPMTZCJQ-UHFFFAOYSA-N 1-ethenyl-2-nonoxybenzene Chemical compound CCCCCCCCCOC1=CC=CC=C1C=C UVXQFKDPMTZCJQ-UHFFFAOYSA-N 0.000 description 1
- ZKBHNWBIDLLNJL-UHFFFAOYSA-N 1-ethenyl-2-octoxybenzene Chemical compound CCCCCCCCOC1=CC=CC=C1C=C ZKBHNWBIDLLNJL-UHFFFAOYSA-N 0.000 description 1
- FCTGEMDIBOJIOF-UHFFFAOYSA-N 1-ethenyl-2-pentoxybenzene Chemical compound CCCCCOC1=CC=CC=C1C=C FCTGEMDIBOJIOF-UHFFFAOYSA-N 0.000 description 1
- SAURBKQRKDFBCJ-UHFFFAOYSA-N 1-ethenyl-2h-isoindole Chemical compound C1=CC=CC2=C(C=C)NC=C21 SAURBKQRKDFBCJ-UHFFFAOYSA-N 0.000 description 1
- PWHCXMAJNAYEOR-UHFFFAOYSA-N 1-ethenyl-3,5-dimethylpyrazole Chemical compound CC=1C=C(C)N(C=C)N=1 PWHCXMAJNAYEOR-UHFFFAOYSA-N 0.000 description 1
- PECUPOXPPBBFLU-UHFFFAOYSA-N 1-ethenyl-3-methoxybenzene Chemical compound COC1=CC=CC(C=C)=C1 PECUPOXPPBBFLU-UHFFFAOYSA-N 0.000 description 1
- SBTDKABWZAAKMI-UHFFFAOYSA-N 1-ethenyl-3-methyl-5-phenylpyrazole Chemical compound C=CN1N=C(C)C=C1C1=CC=CC=C1 SBTDKABWZAAKMI-UHFFFAOYSA-N 0.000 description 1
- JZHGRUMIRATHIU-UHFFFAOYSA-N 1-ethenyl-3-methylbenzene Chemical compound CC1=CC=CC(C=C)=C1 JZHGRUMIRATHIU-UHFFFAOYSA-N 0.000 description 1
- HXVJQEGYAYABRY-UHFFFAOYSA-N 1-ethenyl-4,5-dihydroimidazole Chemical compound C=CN1CCN=C1 HXVJQEGYAYABRY-UHFFFAOYSA-N 0.000 description 1
- DTNCNFLLRLHPNJ-UHFFFAOYSA-N 1-ethenyl-4-(1-ethoxyethoxy)benzene Chemical compound CCOC(C)OC1=CC=C(C=C)C=C1 DTNCNFLLRLHPNJ-UHFFFAOYSA-N 0.000 description 1
- KTCTUVAYZCVCDP-UHFFFAOYSA-N 1-ethenyl-4-(2-methylbutan-2-yloxy)benzene Chemical compound CCC(C)(C)OC1=CC=C(C=C)C=C1 KTCTUVAYZCVCDP-UHFFFAOYSA-N 0.000 description 1
- GRFNSWBVXHLTCI-UHFFFAOYSA-N 1-ethenyl-4-[(2-methylpropan-2-yl)oxy]benzene Chemical compound CC(C)(C)OC1=CC=C(C=C)C=C1 GRFNSWBVXHLTCI-UHFFFAOYSA-N 0.000 description 1
- UAJRSHJHFRVGMG-UHFFFAOYSA-N 1-ethenyl-4-methoxybenzene Chemical compound COC1=CC=C(C=C)C=C1 UAJRSHJHFRVGMG-UHFFFAOYSA-N 0.000 description 1
- VHOOEHAVNHNUPK-UHFFFAOYSA-N 1-ethenyl-5,6-dimethylbenzimidazole Chemical compound C1=C(C)C(C)=CC2=C1N(C=C)C=N2 VHOOEHAVNHNUPK-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
- RCSKFKICHQAKEZ-UHFFFAOYSA-N 1-ethenylindole Chemical compound C1=CC=C2N(C=C)C=CC2=C1 RCSKFKICHQAKEZ-UHFFFAOYSA-N 0.000 description 1
- ZCYXFITUYVYSJW-UHFFFAOYSA-N 1-ethenylisoquinoline Chemical compound C1=CC=C2C(C=C)=NC=CC2=C1 ZCYXFITUYVYSJW-UHFFFAOYSA-N 0.000 description 1
- DCRYNQTXGUTACA-UHFFFAOYSA-N 1-ethenylpiperazine Chemical compound C=CN1CCNCC1 DCRYNQTXGUTACA-UHFFFAOYSA-N 0.000 description 1
- NWHSSMRWECHZEP-UHFFFAOYSA-N 1-ethenylpyrazole Chemical compound C=CN1C=CC=N1 NWHSSMRWECHZEP-UHFFFAOYSA-N 0.000 description 1
- NFPLJTNXOKFJRO-UHFFFAOYSA-N 1-ethenylpyridin-2-one Chemical compound C=CN1C=CC=CC1=O NFPLJTNXOKFJRO-UHFFFAOYSA-N 0.000 description 1
- CTXUTPWZJZHRJC-UHFFFAOYSA-N 1-ethenylpyrrole Chemical compound C=CN1C=CC=C1 CTXUTPWZJZHRJC-UHFFFAOYSA-N 0.000 description 1
- HMNZROFMBSUMAB-UHFFFAOYSA-N 1-ethoxybutan-1-ol Chemical compound CCCC(O)OCC HMNZROFMBSUMAB-UHFFFAOYSA-N 0.000 description 1
- DZZWVFPWASTIBP-UHFFFAOYSA-N 1-hexoxyprop-2-enylbenzene Chemical compound CCCCCCOC(C=C)C1=CC=CC=C1 DZZWVFPWASTIBP-UHFFFAOYSA-N 0.000 description 1
- GFNKTLQTQSALEJ-UHFFFAOYSA-N 1-isocyanato-4-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=C(N=C=O)C=C1 GFNKTLQTQSALEJ-UHFFFAOYSA-N 0.000 description 1
- XFEWMFDVBLLXFE-UHFFFAOYSA-N 1-isocyanatodecane Chemical compound CCCCCCCCCCN=C=O XFEWMFDVBLLXFE-UHFFFAOYSA-N 0.000 description 1
- DYQFCTCUULUMTQ-UHFFFAOYSA-N 1-isocyanatooctane Chemical compound CCCCCCCCN=C=O DYQFCTCUULUMTQ-UHFFFAOYSA-N 0.000 description 1
- OQURWGJAWSLGQG-UHFFFAOYSA-N 1-isocyanatopropane Chemical compound CCCN=C=O OQURWGJAWSLGQG-UHFFFAOYSA-N 0.000 description 1
- XLPJNCYCZORXHG-UHFFFAOYSA-N 1-morpholin-4-ylprop-2-en-1-one Chemical compound C=CC(=O)N1CCOCC1 XLPJNCYCZORXHG-UHFFFAOYSA-N 0.000 description 1
- UTMOWRSIAHMBDH-UHFFFAOYSA-N 1-octoxyprop-2-enylbenzene Chemical compound CCCCCCCCOC(C=C)C1=CC=CC=C1 UTMOWRSIAHMBDH-UHFFFAOYSA-N 0.000 description 1
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- GTTBINDPHWHJKF-UHFFFAOYSA-N 1-prop-2-enyladamantane Chemical compound C1C(C2)CC3CC2CC1(CC=C)C3 GTTBINDPHWHJKF-UHFFFAOYSA-N 0.000 description 1
- ZWAQJGHGPPDZSF-UHFFFAOYSA-N 1-prop-2-enylpiperazine Chemical compound C=CCN1CCNCC1 ZWAQJGHGPPDZSF-UHFFFAOYSA-N 0.000 description 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
- VAWQANAQMBEQFM-UHFFFAOYSA-N 10-ethenoxydecan-1-ol Chemical compound OCCCCCCCCCCOC=C VAWQANAQMBEQFM-UHFFFAOYSA-N 0.000 description 1
- TXRVDLRXTLMRMS-UHFFFAOYSA-N 12-ethenoxydodecan-1-ol Chemical compound OCCCCCCCCCCCCOC=C TXRVDLRXTLMRMS-UHFFFAOYSA-N 0.000 description 1
- SJLHMYREZLMHBA-UHFFFAOYSA-N 18-ethenoxyoctadecan-1-ol Chemical compound C(=C)OCCCCCCCCCCCCCCCCCCO SJLHMYREZLMHBA-UHFFFAOYSA-N 0.000 description 1
- GRNOZCCBOFGDCL-UHFFFAOYSA-N 2,2,2-trichloroacetyl isocyanate Chemical compound ClC(Cl)(Cl)C(=O)N=C=O GRNOZCCBOFGDCL-UHFFFAOYSA-N 0.000 description 1
- VBHXIMACZBQHPX-UHFFFAOYSA-N 2,2,2-trifluoroethyl prop-2-enoate Chemical compound FC(F)(F)COC(=O)C=C VBHXIMACZBQHPX-UHFFFAOYSA-N 0.000 description 1
- IJLJDZOLZATUFK-UHFFFAOYSA-N 2,2-dimethylpropyl prop-2-enoate Chemical compound CC(C)(C)COC(=O)C=C IJLJDZOLZATUFK-UHFFFAOYSA-N 0.000 description 1
- LHNAURKRXGPVDW-UHFFFAOYSA-N 2,3-diisocyanatobutane Chemical compound O=C=NC(C)C(C)N=C=O LHNAURKRXGPVDW-UHFFFAOYSA-N 0.000 description 1
- ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical group CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 1
- DZPSSIZUIOHRNG-UHFFFAOYSA-N 2,4-bis(ethenyl)pyridine Chemical compound C=CC1=CC=NC(C=C)=C1 DZPSSIZUIOHRNG-UHFFFAOYSA-N 0.000 description 1
- OLBJNSPBWLCTOT-UHFFFAOYSA-N 2,4-dichloro-1-isocyanatobenzene Chemical compound ClC1=CC=C(N=C=O)C(Cl)=C1 OLBJNSPBWLCTOT-UHFFFAOYSA-N 0.000 description 1
- OJRJDENLRJHEJO-UHFFFAOYSA-N 2,4-diethylpentane-1,5-diol Chemical compound CCC(CO)CC(CC)CO OJRJDENLRJHEJO-UHFFFAOYSA-N 0.000 description 1
- VUPXKQHLZATXTR-UHFFFAOYSA-N 2,4-diphenyl-1,3-oxazole Chemical compound C=1OC(C=2C=CC=CC=2)=NC=1C1=CC=CC=C1 VUPXKQHLZATXTR-UHFFFAOYSA-N 0.000 description 1
- SXLIFQSDMYZOBA-UHFFFAOYSA-N 2,5-bis(ethenyl)pyridine Chemical compound C=CC1=CC=C(C=C)N=C1 SXLIFQSDMYZOBA-UHFFFAOYSA-N 0.000 description 1
- NJODMNZNJKQZCB-UHFFFAOYSA-N 2,5-bis(prop-2-enoxy)bicyclo[2.2.1]heptane Chemical compound C1C2C(OCC=C)CC1C(OCC=C)C2 NJODMNZNJKQZCB-UHFFFAOYSA-N 0.000 description 1
- 150000003923 2,5-pyrrolediones Chemical class 0.000 description 1
- LRNVAYLPTLYWSI-UHFFFAOYSA-N 2-(1-adamantyl)propan-2-yl prop-2-enoate Chemical compound C1C(C2)CC3CC2CC1(C(C)(OC(=O)C=C)C)C3 LRNVAYLPTLYWSI-UHFFFAOYSA-N 0.000 description 1
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-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
- NTINFTOOVNKGIU-UHFFFAOYSA-N 2-(2-hydroxyethoxycarbonyl)benzoic acid Chemical compound OCCOC(=O)C1=CC=CC=C1C(O)=O NTINFTOOVNKGIU-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- BXPKASQEUYICBF-UHFFFAOYSA-N 2-(3-prop-2-enoyloxypropoxycarbonyl)benzoic acid Chemical compound OC(=O)C1=CC=CC=C1C(=O)OCCCOC(=O)C=C BXPKASQEUYICBF-UHFFFAOYSA-N 0.000 description 1
- WVXLLHWEQSZBLW-UHFFFAOYSA-N 2-(4-acetyl-2-methoxyphenoxy)acetic acid Chemical compound COC1=CC(C(C)=O)=CC=C1OCC(O)=O WVXLLHWEQSZBLW-UHFFFAOYSA-N 0.000 description 1
- JKWXGFNAQFDNHU-UHFFFAOYSA-N 2-(6-prop-2-enoyloxyhexoxycarbonyl)benzoic acid Chemical compound OC(=O)C1=CC=CC=C1C(=O)OCCCCCCOC(=O)C=C JKWXGFNAQFDNHU-UHFFFAOYSA-N 0.000 description 1
- XNJDQHLXEBQMDE-UHFFFAOYSA-N 2-(cyclohexyloxymethyl)oxirane Chemical compound C1OC1COC1CCCCC1 XNJDQHLXEBQMDE-UHFFFAOYSA-N 0.000 description 1
- IARGBXSVZJLGOI-UHFFFAOYSA-N 2-(ethenoxymethyl)-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COC=C IARGBXSVZJLGOI-UHFFFAOYSA-N 0.000 description 1
- UIUSRIAANRCPGF-UHFFFAOYSA-N 2-(ethenoxymethyl)oxolane Chemical compound C=COCC1CCCO1 UIUSRIAANRCPGF-UHFFFAOYSA-N 0.000 description 1
- KXZLHMICGMACLR-UHFFFAOYSA-N 2-(hydroxymethyl)-2-pentylpropane-1,3-diol Chemical compound CCCCCC(CO)(CO)CO KXZLHMICGMACLR-UHFFFAOYSA-N 0.000 description 1
- AYQKGOUDOKLLMP-UHFFFAOYSA-N 2-(naphthalene-1-carbonyl)butanoic acid Chemical compound C1=CC=C2C(C(=O)C(C(O)=O)CC)=CC=CC2=C1 AYQKGOUDOKLLMP-UHFFFAOYSA-N 0.000 description 1
- QYMQKGIGTRLDEQ-UHFFFAOYSA-N 2-(naphthalene-1-carbonyl)hexanoic acid Chemical compound C1(=CC=CC2=CC=CC=C12)C(=O)C(C(=O)O)CCCC QYMQKGIGTRLDEQ-UHFFFAOYSA-N 0.000 description 1
- JXTNDHYEIYRUCH-UHFFFAOYSA-N 2-(naphthalene-2-carbonyl)hexanoic acid Chemical compound C1=C(C=CC2=CC=CC=C12)C(=O)C(C(=O)O)CCCC JXTNDHYEIYRUCH-UHFFFAOYSA-N 0.000 description 1
- OBETXYAYXDNJHR-UHFFFAOYSA-N 2-Ethylhexanoic acid Chemical compound CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 1
- UIERETOOQGIECD-ARJAWSKDSA-M 2-Methyl-2-butenoic acid Natural products C\C=C(\C)C([O-])=O UIERETOOQGIECD-ARJAWSKDSA-M 0.000 description 1
- PZGMUSDNQDCNAG-UHFFFAOYSA-N 2-Propenyl octanoate Chemical compound CCCCCCCC(=O)OCC=C PZGMUSDNQDCNAG-UHFFFAOYSA-N 0.000 description 1
- VUDVPVOIALASLB-UHFFFAOYSA-N 2-[(2-cyano-1-hydroxypropan-2-yl)diazenyl]-3-hydroxy-2-methylpropanenitrile Chemical compound OCC(C)(C#N)N=NC(C)(CO)C#N VUDVPVOIALASLB-UHFFFAOYSA-N 0.000 description 1
- GHHRACMERDGPLU-OUKQBFOZSA-N 2-[(e)-2-naphthalen-1-ylethenyl]-1,3-benzothiazole Chemical compound C1=CC=C2SC(/C=C/C=3C4=CC=CC=C4C=CC=3)=NC2=C1 GHHRACMERDGPLU-OUKQBFOZSA-N 0.000 description 1
- HPQIRFXIDGVWBA-UHFFFAOYSA-N 2-[13,17,18,21-tetrahydroxy-7-(hydroxymethyl)-2,10,14-trioxo-5-(3,4,5-trihydroxybenzoyl)oxy-3,6,9,15-tetraoxatetracyclo[10.7.1.14,8.016,20]henicosa-1(19),16(20),17-trien-11-yl]acetic acid Chemical compound OC1C2OC(=O)C(C3=4)=CC(O)=C(O)C=4OC(=O)C(O)C3C(CC(O)=O)C(=O)OC1C(CO)OC2OC(=O)C1=CC(O)=C(O)C(O)=C1 HPQIRFXIDGVWBA-UHFFFAOYSA-N 0.000 description 1
- WMYINDVYGQKYMI-UHFFFAOYSA-N 2-[2,2-bis(hydroxymethyl)butoxymethyl]-2-ethylpropane-1,3-diol Chemical compound CCC(CO)(CO)COCC(CC)(CO)CO WMYINDVYGQKYMI-UHFFFAOYSA-N 0.000 description 1
- YIJYFLXQHDOQGW-UHFFFAOYSA-N 2-[2,4,6-trioxo-3,5-bis(2-prop-2-enoyloxyethyl)-1,3,5-triazinan-1-yl]ethyl prop-2-enoate Chemical class C=CC(=O)OCCN1C(=O)N(CCOC(=O)C=C)C(=O)N(CCOC(=O)C=C)C1=O YIJYFLXQHDOQGW-UHFFFAOYSA-N 0.000 description 1
- XRBWKWGATZNBFW-UHFFFAOYSA-N 2-[2-(2-ethenoxyethoxy)ethoxy]ethanol Chemical compound OCCOCCOCCOC=C XRBWKWGATZNBFW-UHFFFAOYSA-N 0.000 description 1
- AOBIOSPNXBMOAT-UHFFFAOYSA-N 2-[2-(oxiran-2-ylmethoxy)ethoxymethyl]oxirane Chemical compound C1OC1COCCOCC1CO1 AOBIOSPNXBMOAT-UHFFFAOYSA-N 0.000 description 1
- UTOONOCRMYRNMO-UHFFFAOYSA-N 2-[2-[2-(2-ethenoxyethoxy)ethoxy]ethoxy]ethanol Chemical compound OCCOCCOCCOCCOC=C UTOONOCRMYRNMO-UHFFFAOYSA-N 0.000 description 1
- WTYYGFLRBWMFRY-UHFFFAOYSA-N 2-[6-(oxiran-2-ylmethoxy)hexoxymethyl]oxirane Chemical compound C1OC1COCCCCCCOCC1CO1 WTYYGFLRBWMFRY-UHFFFAOYSA-N 0.000 description 1
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 1
- ZUAQCWQQTGOYKP-UHFFFAOYSA-N 2-benzoylhexanoic acid Chemical compound CCCCC(C(O)=O)C(=O)C1=CC=CC=C1 ZUAQCWQQTGOYKP-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- 125000000143 2-carboxyethyl group Chemical group [H]OC(=O)C([H])([H])C([H])([H])* 0.000 description 1
- UKTKKMZDESVUEE-UHFFFAOYSA-N 2-chloro-4-isocyanato-1-methylbenzene Chemical compound CC1=CC=C(N=C=O)C=C1Cl UKTKKMZDESVUEE-UHFFFAOYSA-N 0.000 description 1
- 125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 description 1
- OYUNTGBISCIYPW-UHFFFAOYSA-N 2-chloroprop-2-enenitrile Chemical compound ClC(=C)C#N OYUNTGBISCIYPW-UHFFFAOYSA-N 0.000 description 1
- PGYJSURPYAAOMM-UHFFFAOYSA-N 2-ethenoxy-2-methylpropane Chemical compound CC(C)(C)OC=C PGYJSURPYAAOMM-UHFFFAOYSA-N 0.000 description 1
- IZPAEFLHCVEFSX-UHFFFAOYSA-N 2-ethenoxy-4-methyl-1-propan-2-ylcyclohexane Chemical compound CC(C)C1CCC(C)CC1OC=C IZPAEFLHCVEFSX-UHFFFAOYSA-N 0.000 description 1
- KJHFNHVFNLOTEH-UHFFFAOYSA-N 2-ethenoxyadamantane Chemical compound C1C(C2)CC3CC1C(OC=C)C2C3 KJHFNHVFNLOTEH-UHFFFAOYSA-N 0.000 description 1
- BBJJJPPTYKZIJP-UHFFFAOYSA-N 2-ethenoxybenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1OC=C BBJJJPPTYKZIJP-UHFFFAOYSA-N 0.000 description 1
- VUIWJRYTWUGOOF-UHFFFAOYSA-N 2-ethenoxyethanol Chemical compound OCCOC=C VUIWJRYTWUGOOF-UHFFFAOYSA-N 0.000 description 1
- RLJPTOIWHAUUBO-UHFFFAOYSA-N 2-ethenoxyethyl acetate Chemical compound CC(=O)OCCOC=C RLJPTOIWHAUUBO-UHFFFAOYSA-N 0.000 description 1
- MASGJCHIQCNVSA-UHFFFAOYSA-N 2-ethenoxyethylcyclohexane Chemical compound C=COCCC1CCCCC1 MASGJCHIQCNVSA-UHFFFAOYSA-N 0.000 description 1
- GNUGVECARVKIPH-UHFFFAOYSA-N 2-ethenoxypropane Chemical compound CC(C)OC=C GNUGVECARVKIPH-UHFFFAOYSA-N 0.000 description 1
- BNNNAVQJVYKEHQ-UHFFFAOYSA-N 2-ethenyl-1,3-benzothiazole Chemical compound C1=CC=C2SC(C=C)=NC2=C1 BNNNAVQJVYKEHQ-UHFFFAOYSA-N 0.000 description 1
- PGMMQIGGQSIEGH-UHFFFAOYSA-N 2-ethenyl-1,3-oxazole Chemical compound C=CC1=NC=CO1 PGMMQIGGQSIEGH-UHFFFAOYSA-N 0.000 description 1
- JDCUKFVNOWJNBU-UHFFFAOYSA-N 2-ethenyl-1,3-thiazole Chemical compound C=CC1=NC=CS1 JDCUKFVNOWJNBU-UHFFFAOYSA-N 0.000 description 1
- JUKXAYLMPOWYMF-UHFFFAOYSA-N 2-ethenyl-1,4-dimethylpiperazine Chemical compound CN1CCN(C)C(C=C)C1 JUKXAYLMPOWYMF-UHFFFAOYSA-N 0.000 description 1
- ROVOJRYKKFAVMA-UHFFFAOYSA-N 2-ethenyl-1H-cinnoline Chemical compound C(=C)N1NC2=CC=CC=C2C=C1 ROVOJRYKKFAVMA-UHFFFAOYSA-N 0.000 description 1
- YRPYTFXEHXXYQW-UHFFFAOYSA-N 2-ethenyl-1h-benzimidazole Chemical compound C1=CC=C2NC(C=C)=NC2=C1 YRPYTFXEHXXYQW-UHFFFAOYSA-N 0.000 description 1
- MLMGJTAJUDSUKA-UHFFFAOYSA-N 2-ethenyl-1h-imidazole Chemical compound C=CC1=NC=CN1 MLMGJTAJUDSUKA-UHFFFAOYSA-N 0.000 description 1
- CQJLZFWJGKQGRU-UHFFFAOYSA-N 2-ethenyl-1h-pyridazine Chemical compound C=CN1NC=CC=C1 CQJLZFWJGKQGRU-UHFFFAOYSA-N 0.000 description 1
- MZNSQRLUUXWLSB-UHFFFAOYSA-N 2-ethenyl-1h-pyrrole Chemical compound C=CC1=CC=CN1 MZNSQRLUUXWLSB-UHFFFAOYSA-N 0.000 description 1
- QKPKBBFSFQAMIY-UHFFFAOYSA-N 2-ethenyl-4,4-dimethyl-1,3-oxazol-5-one Chemical compound CC1(C)N=C(C=C)OC1=O QKPKBBFSFQAMIY-UHFFFAOYSA-N 0.000 description 1
- BQBSIHIZDSHADD-UHFFFAOYSA-N 2-ethenyl-4,5-dihydro-1,3-oxazole Chemical compound C=CC1=NCCO1 BQBSIHIZDSHADD-UHFFFAOYSA-N 0.000 description 1
- ZBROKEOFSJLGFN-UHFFFAOYSA-N 2-ethenyl-5,6-dimethyl-1h-benzimidazole Chemical compound C1=C(C)C(C)=CC2=C1NC(C=C)=N2 ZBROKEOFSJLGFN-UHFFFAOYSA-N 0.000 description 1
- WMIAWAMSXLFFGM-UHFFFAOYSA-N 2-ethenyl-5-ethoxy-1,3-oxazole Chemical compound CCOc1cnc(C=C)o1 WMIAWAMSXLFFGM-UHFFFAOYSA-N 0.000 description 1
- ULQLVELTQDGZEP-UHFFFAOYSA-N 2-ethenyl-5-methyl-1h-pyrrole Chemical compound CC1=CC=C(C=C)N1 ULQLVELTQDGZEP-UHFFFAOYSA-N 0.000 description 1
- VMWGBWNAHAUQIO-UHFFFAOYSA-N 2-ethenyl-6-methylpyridine Chemical compound CC1=CC=CC(C=C)=N1 VMWGBWNAHAUQIO-UHFFFAOYSA-N 0.000 description 1
- DXARRWRGWTYQPG-UHFFFAOYSA-N 2-ethenylideneadamantane Chemical compound C1C(C2)CC3CC1C(=C=C)C2C3 DXARRWRGWTYQPG-UHFFFAOYSA-N 0.000 description 1
- IJGBQZWGRCCKFB-UHFFFAOYSA-N 2-ethenylindazole Chemical compound C1=CC=CC2=NN(C=C)C=C21 IJGBQZWGRCCKFB-UHFFFAOYSA-N 0.000 description 1
- YFVRIXYUQCYRAF-UHFFFAOYSA-N 2-ethenylpiperazine Chemical compound C=CC1CNCCN1 YFVRIXYUQCYRAF-UHFFFAOYSA-N 0.000 description 1
- ZDHWTWWXCXEGIC-UHFFFAOYSA-N 2-ethenylpyrimidine Chemical compound C=CC1=NC=CC=N1 ZDHWTWWXCXEGIC-UHFFFAOYSA-N 0.000 description 1
- JXUYHTCQKHJDBW-UHFFFAOYSA-N 2-ethenylquinazoline Chemical compound C1=CC=CC2=NC(C=C)=NC=C21 JXUYHTCQKHJDBW-UHFFFAOYSA-N 0.000 description 1
- XUGNJOCQALIQFG-UHFFFAOYSA-N 2-ethenylquinoline Chemical compound C1=CC=CC2=NC(C=C)=CC=C21 XUGNJOCQALIQFG-UHFFFAOYSA-N 0.000 description 1
- XLHFQWCMIWOPGG-UHFFFAOYSA-N 2-ethenylquinoxaline Chemical compound C1=CC=CC2=NC(C=C)=CN=C21 XLHFQWCMIWOPGG-UHFFFAOYSA-N 0.000 description 1
- VGZZAZYCLRYTNQ-UHFFFAOYSA-N 2-ethoxyethoxycarbonyloxy 2-ethoxyethyl carbonate Chemical compound CCOCCOC(=O)OOC(=O)OCCOCC VGZZAZYCLRYTNQ-UHFFFAOYSA-N 0.000 description 1
- HHKAGFTWEFVXET-UHFFFAOYSA-N 2-heptyl-2-(hydroxymethyl)propane-1,3-diol Chemical compound CCCCCCCC(CO)(CO)CO HHKAGFTWEFVXET-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
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 description 1
- JVZZUPJFERSVRN-UHFFFAOYSA-N 2-methyl-2-propylpropane-1,3-diol Chemical compound CCCC(C)(CO)CO JVZZUPJFERSVRN-UHFFFAOYSA-N 0.000 description 1
- XJUWKFZDGHHNEO-UHFFFAOYSA-N 2-methyl-3-naphthalen-1-yl-3-oxopropanoic acid Chemical compound C1=CC=C2C(C(=O)C(C(O)=O)C)=CC=CC2=C1 XJUWKFZDGHHNEO-UHFFFAOYSA-N 0.000 description 1
- NNBLEQBPONPWPV-UHFFFAOYSA-N 2-methyl-3-naphthalen-2-yl-3-oxopropanoic acid Chemical compound C1=CC=CC2=CC(C(=O)C(C(O)=O)C)=CC=C21 NNBLEQBPONPWPV-UHFFFAOYSA-N 0.000 description 1
- OVEUFHOBGCSKSH-UHFFFAOYSA-N 2-methyl-n,n-bis(oxiran-2-ylmethyl)aniline Chemical compound CC1=CC=CC=C1N(CC1OC1)CC1OC1 OVEUFHOBGCSKSH-UHFFFAOYSA-N 0.000 description 1
- HEBTZZBBPUFAFE-UHFFFAOYSA-N 2-methyl-n-(oxomethylidene)benzenesulfonamide Chemical compound CC1=CC=CC=C1S(=O)(=O)N=C=O HEBTZZBBPUFAFE-UHFFFAOYSA-N 0.000 description 1
- JGBOVFKUKBGAJQ-UHFFFAOYSA-N 2-methylidenebutanediamide Chemical compound NC(=O)CC(=C)C(N)=O JGBOVFKUKBGAJQ-UHFFFAOYSA-N 0.000 description 1
- GXRMTTBFSSTDNB-UHFFFAOYSA-N 2-methylidenebutanedinitrile Chemical compound N#CC(=C)CC#N GXRMTTBFSSTDNB-UHFFFAOYSA-N 0.000 description 1
- XEEYSDHEOQHCDA-UHFFFAOYSA-N 2-methylprop-2-ene-1-sulfonic acid Chemical compound CC(=C)CS(O)(=O)=O XEEYSDHEOQHCDA-UHFFFAOYSA-N 0.000 description 1
- AUZRCMMVHXRSGT-UHFFFAOYSA-N 2-methylpropane-1-sulfonic acid;prop-2-enamide Chemical compound NC(=O)C=C.CC(C)CS(O)(=O)=O AUZRCMMVHXRSGT-UHFFFAOYSA-N 0.000 description 1
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 1
- CWJDDCLLMRJWCQ-UHFFFAOYSA-M 2-phenylethenesulfonate;tetraethylazanium Chemical compound CC[N+](CC)(CC)CC.[O-]S(=O)(=O)C=CC1=CC=CC=C1 CWJDDCLLMRJWCQ-UHFFFAOYSA-M 0.000 description 1
- IYPBILGFFAROLA-UHFFFAOYSA-N 2-phenylethenesulfonate;trimethylazanium Chemical compound C[NH+](C)C.[O-]S(=O)(=O)C=CC1=CC=CC=C1 IYPBILGFFAROLA-UHFFFAOYSA-N 0.000 description 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- UDXXYUDJOHIIDZ-UHFFFAOYSA-N 2-phosphonooxyethyl prop-2-enoate Chemical compound OP(O)(=O)OCCOC(=O)C=C UDXXYUDJOHIIDZ-UHFFFAOYSA-N 0.000 description 1
- SIMWIZNONVKIRV-UHFFFAOYSA-N 2-prop-1-enoxybenzenesulfonic acid Chemical compound C(=CC)OC1=C(C=CC=C1)S(=O)(=O)O SIMWIZNONVKIRV-UHFFFAOYSA-N 0.000 description 1
- HCGFUIQPSOCUHI-UHFFFAOYSA-N 2-propan-2-yloxyethanol Chemical compound CC(C)OCCO HCGFUIQPSOCUHI-UHFFFAOYSA-N 0.000 description 1
- BGNWXRJWDQHCRB-UHFFFAOYSA-N 2-propan-2-ylpyrimidine Chemical group CC(C)C1=NC=CC=N1 BGNWXRJWDQHCRB-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
- QZWKEPYTBWZJJA-UHFFFAOYSA-N 3,3'-Dimethoxybenzidine-4,4'-diisocyanate Chemical compound C1=C(N=C=O)C(OC)=CC(C=2C=C(OC)C(N=C=O)=CC=2)=C1 QZWKEPYTBWZJJA-UHFFFAOYSA-N 0.000 description 1
- LVHOAHHFUNMKQA-UHFFFAOYSA-N 3,3-dihydroxy-2,2,5,5-tetramethyl-4-oxohexanoic acid Chemical compound CC(C)(C)C(=O)C(O)(O)C(C)(C)C(O)=O LVHOAHHFUNMKQA-UHFFFAOYSA-N 0.000 description 1
- KFGFVPMRLOQXNB-UHFFFAOYSA-N 3,5,5-trimethylhexanoyl 3,5,5-trimethylhexaneperoxoate Chemical compound CC(C)(C)CC(C)CC(=O)OOC(=O)CC(C)CC(C)(C)C KFGFVPMRLOQXNB-UHFFFAOYSA-N 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- WADSJYLPJPTMLN-UHFFFAOYSA-N 3-(cycloundecen-1-yl)-1,2-diazacycloundec-2-ene Chemical compound C1CCCCCCCCC=C1C1=NNCCCCCCCC1 WADSJYLPJPTMLN-UHFFFAOYSA-N 0.000 description 1
- DSSAWHFZNWVJEC-UHFFFAOYSA-N 3-(ethenoxymethyl)heptane Chemical compound CCCCC(CC)COC=C DSSAWHFZNWVJEC-UHFFFAOYSA-N 0.000 description 1
- WDGNEDMGRQQNNI-UHFFFAOYSA-N 3-(ethenoxymethyl)pentane Chemical compound CCC(CC)COC=C WDGNEDMGRQQNNI-UHFFFAOYSA-N 0.000 description 1
- MLLSDKDGPIAIPH-UHFFFAOYSA-N 3-[butyl(dimethoxy)silyl]propyl prop-2-enoate Chemical compound CCCC[Si](OC)(OC)CCCOC(=O)C=C MLLSDKDGPIAIPH-UHFFFAOYSA-N 0.000 description 1
- YDSKIYLJGKSHFX-UHFFFAOYSA-N 3-[ethyl(dimethoxy)silyl]propyl prop-2-enoate Chemical compound CC[Si](OC)(OC)CCCOC(=O)C=C YDSKIYLJGKSHFX-UHFFFAOYSA-N 0.000 description 1
- KLQJYWWHIBLKCK-UHFFFAOYSA-N 3-[ethyl(dipropoxy)silyl]propyl prop-2-enoate Chemical compound CCCO[Si](CC)(OCCC)CCCOC(=O)C=C KLQJYWWHIBLKCK-UHFFFAOYSA-N 0.000 description 1
- USICVVZOKTZACS-UHFFFAOYSA-N 3-butylpyrrole-2,5-dione Chemical compound CCCCC1=CC(=O)NC1=O USICVVZOKTZACS-UHFFFAOYSA-N 0.000 description 1
- UIZDKHDPZRCOBN-UHFFFAOYSA-N 3-dodecylpyrrole-2,5-dione Chemical compound CCCCCCCCCCCCC1=CC(=O)NC1=O UIZDKHDPZRCOBN-UHFFFAOYSA-N 0.000 description 1
- QIOWACLXWYDLPZ-UHFFFAOYSA-N 3-ethenoxyoctyl 3-oxobutanoate Chemical compound C(=C)OC(CCCCC)CCOC(CC(=O)C)=O QIOWACLXWYDLPZ-UHFFFAOYSA-N 0.000 description 1
- ZXABMDQSAABDMG-UHFFFAOYSA-N 3-ethenoxyprop-1-ene Chemical compound C=CCOC=C ZXABMDQSAABDMG-UHFFFAOYSA-N 0.000 description 1
- LANDRZNMJOEVQO-UHFFFAOYSA-N 3-ethenoxypropane-1,2-diol Chemical compound OCC(O)COC=C LANDRZNMJOEVQO-UHFFFAOYSA-N 0.000 description 1
- RXZOBWPQATUMMU-UHFFFAOYSA-N 3-ethenoxypropyl acetate Chemical compound C(=C)OCCCOC(C)=O RXZOBWPQATUMMU-UHFFFAOYSA-N 0.000 description 1
- DPZYLEIWHTWHCU-UHFFFAOYSA-N 3-ethenylpyridine Chemical compound C=CC1=CC=CN=C1 DPZYLEIWHTWHCU-UHFFFAOYSA-N 0.000 description 1
- 125000006032 3-methyl-3-butenyl group Chemical group 0.000 description 1
- YYPNJNDODFVZLE-UHFFFAOYSA-N 3-methylbut-2-enoic acid Chemical compound CC(C)=CC(O)=O YYPNJNDODFVZLE-UHFFFAOYSA-N 0.000 description 1
- JSDZSLGMRRSAHD-UHFFFAOYSA-N 3-methylbutan-2-ylcyclopropane Chemical compound CC(C)C(C)C1CC1 JSDZSLGMRRSAHD-UHFFFAOYSA-N 0.000 description 1
- ZLPORNPZJNRGCO-UHFFFAOYSA-N 3-methylpyrrole-2,5-dione Chemical compound CC1=CC(=O)NC1=O ZLPORNPZJNRGCO-UHFFFAOYSA-N 0.000 description 1
- YGCKKKCVWWRSMG-UHFFFAOYSA-N 3-naphthalen-1-yl-3-oxopropanoic acid Chemical compound C1=CC=C2C(C(=O)CC(=O)O)=CC=CC2=C1 YGCKKKCVWWRSMG-UHFFFAOYSA-N 0.000 description 1
- QZRKIGAZHXSODT-UHFFFAOYSA-N 3-naphthalen-2-yl-3-oxopropanoic acid Chemical compound C1=CC=CC2=CC(C(=O)CC(=O)O)=CC=C21 QZRKIGAZHXSODT-UHFFFAOYSA-N 0.000 description 1
- BLHDYAXSQWGYSM-UHFFFAOYSA-N 3-octadecylpyrrole-2,5-dione Chemical compound CCCCCCCCCCCCCCCCCCC1=CC(=O)NC1=O BLHDYAXSQWGYSM-UHFFFAOYSA-N 0.000 description 1
- VOYQCFMGTRPFKT-UHFFFAOYSA-N 3-octylpyrrole-2,5-dione Chemical compound CCCCCCCCC1=CC(=O)NC1=O VOYQCFMGTRPFKT-UHFFFAOYSA-N 0.000 description 1
- HXUIDZOMTRMIOE-UHFFFAOYSA-M 3-oxo-3-phenylpropionate Chemical compound [O-]C(=O)CC(=O)C1=CC=CC=C1 HXUIDZOMTRMIOE-UHFFFAOYSA-M 0.000 description 1
- IYMZEPRSPLASMS-UHFFFAOYSA-N 3-phenylpyrrole-2,5-dione Chemical compound O=C1NC(=O)C(C=2C=CC=CC=2)=C1 IYMZEPRSPLASMS-UHFFFAOYSA-N 0.000 description 1
- MDXKEHHAIMNCSW-UHFFFAOYSA-N 3-propylpyrrole-2,5-dione Chemical compound CCCC1=CC(=O)NC1=O MDXKEHHAIMNCSW-UHFFFAOYSA-N 0.000 description 1
- YFISHOAHNLGUEL-UHFFFAOYSA-N 3-tributoxysilylpropyl prop-2-enoate Chemical compound CCCCO[Si](OCCCC)(OCCCC)CCCOC(=O)C=C YFISHOAHNLGUEL-UHFFFAOYSA-N 0.000 description 1
- DCQBZYNUSLHVJC-UHFFFAOYSA-N 3-triethoxysilylpropane-1-thiol Chemical compound CCO[Si](OCC)(OCC)CCCS DCQBZYNUSLHVJC-UHFFFAOYSA-N 0.000 description 1
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 1
- KBQVDAIIQCXKPI-UHFFFAOYSA-N 3-trimethoxysilylpropyl prop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C=C KBQVDAIIQCXKPI-UHFFFAOYSA-N 0.000 description 1
- HGEKXQRHZRDGKO-UHFFFAOYSA-N 3-tripropoxysilylpropyl prop-2-enoate Chemical compound CCCO[Si](OCCC)(OCCC)CCCOC(=O)C=C HGEKXQRHZRDGKO-UHFFFAOYSA-N 0.000 description 1
- VFXXTYGQYWRHJP-UHFFFAOYSA-N 4,4'-azobis(4-cyanopentanoic acid) Chemical compound OC(=O)CCC(C)(C#N)N=NC(C)(CCC(O)=O)C#N VFXXTYGQYWRHJP-UHFFFAOYSA-N 0.000 description 1
- YNWJPOVPFGCGLE-UHFFFAOYSA-N 4,4-diethoxybut-1-enylsilane Chemical compound C(C)OC(CC=C[SiH3])OCC YNWJPOVPFGCGLE-UHFFFAOYSA-N 0.000 description 1
- UUWTZTOGLJIBDB-UHFFFAOYSA-N 4,5-bis(ethenyl)-1-methylimidazole Chemical compound CN1C=NC(=C1C=C)C=C UUWTZTOGLJIBDB-UHFFFAOYSA-N 0.000 description 1
- YRXLABUVDQYDHV-UHFFFAOYSA-N 4-(prop-2-enoylamino)butanoic acid Chemical compound OC(=O)CCCNC(=O)C=C YRXLABUVDQYDHV-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- LSEBTZWHCPGKEF-UHFFFAOYSA-N 4-[2-(4-hydroxyphenyl)propan-2-yl]-2-prop-2-enylphenol Chemical compound C=1C=C(O)C(CC=C)=CC=1C(C)(C)C1=CC=C(O)C=C1 LSEBTZWHCPGKEF-UHFFFAOYSA-N 0.000 description 1
- NXRRRCXAPUVBIA-UHFFFAOYSA-N 4-ethenoxybutyl acetate Chemical compound CC(=O)OCCCCOC=C NXRRRCXAPUVBIA-UHFFFAOYSA-N 0.000 description 1
- MQWSOHQURSXOKJ-UHFFFAOYSA-N 4-ethenyl-2-phenyl-1,3-oxazole Chemical compound C=CC1=COC(C=2C=CC=CC=2)=N1 MQWSOHQURSXOKJ-UHFFFAOYSA-N 0.000 description 1
- HZQGNQZMIHMFII-UHFFFAOYSA-N 4-ethenylbenzenesulfonohydrazide Chemical compound NNS(=O)(=O)C1=CC=C(C=C)C=C1 HZQGNQZMIHMFII-UHFFFAOYSA-N 0.000 description 1
- GEXWQYYUAINRED-UHFFFAOYSA-N 4-ethenylbenzohydrazide Chemical compound NNC(=O)C1=CC=C(C=C)C=C1 GEXWQYYUAINRED-UHFFFAOYSA-N 0.000 description 1
- IRQWEODKXLDORP-UHFFFAOYSA-N 4-ethenylbenzoic acid Chemical compound OC(=O)C1=CC=C(C=C)C=C1 IRQWEODKXLDORP-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
- DZGGGLJOCYPKHN-UHFFFAOYSA-N 4-ethenylquinoline Chemical compound C1=CC=C2C(C=C)=CC=NC2=C1 DZGGGLJOCYPKHN-UHFFFAOYSA-N 0.000 description 1
- YAXPDWVRLUOOBJ-UHFFFAOYSA-N 4-ethylhex-3-en-3-ylbenzene Chemical compound CCC(CC)=C(CC)C1=CC=CC=C1 YAXPDWVRLUOOBJ-UHFFFAOYSA-N 0.000 description 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
- UZHIMIBNVCRJIK-UHFFFAOYSA-N 4-methylbenzenesulfonate trimethyl-[3-(prop-2-enoylamino)propyl]azanium Chemical compound Cc1ccc(cc1)S([O-])(=O)=O.C[N+](C)(C)CCCNC(=O)C=C UZHIMIBNVCRJIK-UHFFFAOYSA-N 0.000 description 1
- DPOZJUIRGCAQCE-UHFFFAOYSA-M 4-methylbenzenesulfonate;trimethyl(2-prop-2-enoyloxyethyl)azanium Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1.C[N+](C)(C)CCOC(=O)C=C DPOZJUIRGCAQCE-UHFFFAOYSA-M 0.000 description 1
- UZDMJPAQQFSMMV-UHFFFAOYSA-N 4-oxo-4-(2-prop-2-enoyloxyethoxy)butanoic acid Chemical compound OC(=O)CCC(=O)OCCOC(=O)C=C UZDMJPAQQFSMMV-UHFFFAOYSA-N 0.000 description 1
- JOOXCMJARBKPKM-UHFFFAOYSA-N 4-oxopentanoic acid Chemical compound CC(=O)CCC(O)=O JOOXCMJARBKPKM-UHFFFAOYSA-N 0.000 description 1
- WNPVZANXRCPJPW-UHFFFAOYSA-N 5-[isocyano-(4-methylphenyl)sulfonylmethyl]-1,2,3-trimethoxybenzene Chemical compound COC1=C(OC)C(OC)=CC(C([N+]#[C-])S(=O)(=O)C=2C=CC(C)=CC=2)=C1 WNPVZANXRCPJPW-UHFFFAOYSA-N 0.000 description 1
- PAHSHPLLVMLCCN-UHFFFAOYSA-N 5-butyl-5-ethenylcyclohexa-1,3-diene Chemical compound CCCCC1(C=C)CC=CC=C1 PAHSHPLLVMLCCN-UHFFFAOYSA-N 0.000 description 1
- BCTDCDYHRUIHSF-UHFFFAOYSA-N 5-ethenoxypentan-1-ol Chemical compound OCCCCCOC=C BCTDCDYHRUIHSF-UHFFFAOYSA-N 0.000 description 1
- UWUHECCXEWKYFW-UHFFFAOYSA-N 5-ethenyl-2-phenyl-1,3-oxazole Chemical compound O1C(C=C)=CN=C1C1=CC=CC=C1 UWUHECCXEWKYFW-UHFFFAOYSA-N 0.000 description 1
- QUAMMXIRDIIGDJ-UHFFFAOYSA-N 5-ethenyl-4-methyl-1,3-thiazole Chemical compound CC=1N=CSC=1C=C QUAMMXIRDIIGDJ-UHFFFAOYSA-N 0.000 description 1
- SAQWCPXBLNGTCC-UHFFFAOYSA-N 6-(prop-2-enoylamino)hexanoic acid Chemical compound OC(=O)CCCCCNC(=O)C=C SAQWCPXBLNGTCC-UHFFFAOYSA-N 0.000 description 1
- ZXLYUNPVVODNRE-UHFFFAOYSA-N 6-ethenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=C)=N1 ZXLYUNPVVODNRE-UHFFFAOYSA-N 0.000 description 1
- RDJHNDDZKQCDPL-UHFFFAOYSA-N 8-ethenoxyoctan-1-ol Chemical compound OCCCCCCCCOC=C RDJHNDDZKQCDPL-UHFFFAOYSA-N 0.000 description 1
- WDJHALXBUFZDSR-UHFFFAOYSA-N Acetoacetic acid Natural products CC(=O)CC(O)=O WDJHALXBUFZDSR-UHFFFAOYSA-N 0.000 description 1
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- RMZIOVJHUJAAEY-UHFFFAOYSA-N Allyl butyrate Chemical compound CCCC(=O)OCC=C RMZIOVJHUJAAEY-UHFFFAOYSA-N 0.000 description 1
- OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical compound ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- FREHEFHMRAAAMR-UHFFFAOYSA-N C(=C)C=1C=C(C=CC=1)N(N)C(C=C)=O Chemical compound C(=C)C=1C=C(C=CC=1)N(N)C(C=C)=O FREHEFHMRAAAMR-UHFFFAOYSA-N 0.000 description 1
- RAISAQWNBJBTSG-UHFFFAOYSA-N C(=C)N1C(CCC1)=O.C(=C)N1C(=NC=C1)C=1N(C=CN1)C=C Chemical compound C(=C)N1C(CCC1)=O.C(=C)N1C(=NC=C1)C=1N(C=CN1)C=C RAISAQWNBJBTSG-UHFFFAOYSA-N 0.000 description 1
- BHAKCUHRCGNLAE-UHFFFAOYSA-N C(=C)N1CC=NC2=CC=CC=C12 Chemical compound C(=C)N1CC=NC2=CC=CC=C12 BHAKCUHRCGNLAE-UHFFFAOYSA-N 0.000 description 1
- QUMNFPDPSTXTNG-UHFFFAOYSA-N C(=C)OC(CCC)CCOC(CC(=O)C)=O Chemical compound C(=C)OC(CCC)CCOC(CC(=O)C)=O QUMNFPDPSTXTNG-UHFFFAOYSA-N 0.000 description 1
- LPPSPEYVCWWXIB-UHFFFAOYSA-N C(=C)OC1=C(C=CC=C1)S(=O)(=O)[O-].[NH4+] Chemical compound C(=C)OC1=C(C=CC=C1)S(=O)(=O)[O-].[NH4+] LPPSPEYVCWWXIB-UHFFFAOYSA-N 0.000 description 1
- PHJPQNBJTRTPNM-UHFFFAOYSA-M C(=C)OC1=C(C=CC=C1)S(=O)(=O)[O-].[Na+] Chemical compound C(=C)OC1=C(C=CC=C1)S(=O)(=O)[O-].[Na+] PHJPQNBJTRTPNM-UHFFFAOYSA-M 0.000 description 1
- HGRIMZQUGVPJLM-UHFFFAOYSA-N C(=CC1=CC=CC=C1)S(=O)(=O)[O-].C(C)[NH2+]CC Chemical compound C(=CC1=CC=CC=C1)S(=O)(=O)[O-].C(C)[NH2+]CC HGRIMZQUGVPJLM-UHFFFAOYSA-N 0.000 description 1
- KZGMQGXBHXNFKL-UHFFFAOYSA-N C(=CC1=CC=CC=C1)S(=O)(=O)[O-].C(C)[NH3+] Chemical compound C(=CC1=CC=CC=C1)S(=O)(=O)[O-].C(C)[NH3+] KZGMQGXBHXNFKL-UHFFFAOYSA-N 0.000 description 1
- QIKCPTIBVZCDNZ-UHFFFAOYSA-N C(=CC1=CC=CC=C1)S(=O)(=O)[O-].C(CC)[NH+](CCC)CCC Chemical compound C(=CC1=CC=CC=C1)S(=O)(=O)[O-].C(CC)[NH+](CCC)CCC QIKCPTIBVZCDNZ-UHFFFAOYSA-N 0.000 description 1
- JPOZDGRIMHOGHQ-UHFFFAOYSA-N C(=CC1=CC=CC=C1)S(=O)(=O)[O-].C(CC)[NH2+]CCC Chemical compound C(=CC1=CC=CC=C1)S(=O)(=O)[O-].C(CC)[NH2+]CCC JPOZDGRIMHOGHQ-UHFFFAOYSA-N 0.000 description 1
- HSBKWGUFTJKQPU-UHFFFAOYSA-N C(=CC1=CC=CC=C1)S(=O)(=O)[O-].C(CC)[NH3+] Chemical compound C(=CC1=CC=CC=C1)S(=O)(=O)[O-].C(CC)[NH3+] HSBKWGUFTJKQPU-UHFFFAOYSA-N 0.000 description 1
- YLRGBCFLWICPPS-UHFFFAOYSA-N C(=CC1=CC=CC=C1)S(=O)(=O)[O-].C(CCC)[NH3+] Chemical compound C(=CC1=CC=CC=C1)S(=O)(=O)[O-].C(CCC)[NH3+] YLRGBCFLWICPPS-UHFFFAOYSA-N 0.000 description 1
- QINKTWICOGHYSI-UHFFFAOYSA-N C(=CC1=CC=CC=C1)S(=O)(=O)[O-].C(CCCC)[NH3+] Chemical compound C(=CC1=CC=CC=C1)S(=O)(=O)[O-].C(CCCC)[NH3+] QINKTWICOGHYSI-UHFFFAOYSA-N 0.000 description 1
- KYEUSFQPVRWCOU-UHFFFAOYSA-N C(C)(C)(C)OC(=O)C(COC1=CC=C(C=C)C=C1)C Chemical compound C(C)(C)(C)OC(=O)C(COC1=CC=C(C=C)C=C1)C KYEUSFQPVRWCOU-UHFFFAOYSA-N 0.000 description 1
- BHIJJRXUVMNRAF-UHFFFAOYSA-N C(C)C1CC(OCC1)=O.C(C=C)(=O)O Chemical compound C(C)C1CC(OCC1)=O.C(C=C)(=O)O BHIJJRXUVMNRAF-UHFFFAOYSA-N 0.000 description 1
- OKEXEMTYVFJKSI-UHFFFAOYSA-N C(C)OCCO.COCCCOC(CC)O Chemical compound C(C)OCCO.COCCCOC(CC)O OKEXEMTYVFJKSI-UHFFFAOYSA-N 0.000 description 1
- HTRUCOPTVWOQLY-UHFFFAOYSA-M C(C)OS(=O)(=O)[O-].C(C=C)(=O)O[N+](CC)(C)C Chemical compound C(C)OS(=O)(=O)[O-].C(C=C)(=O)O[N+](CC)(C)C HTRUCOPTVWOQLY-UHFFFAOYSA-M 0.000 description 1
- ACFBSDQXAGAKSC-UHFFFAOYSA-N C(C)O[Si](OCC)(OCC)C=CC.CC(C(=O)O)=C Chemical compound C(C)O[Si](OCC)(OCC)C=CC.CC(C(=O)O)=C ACFBSDQXAGAKSC-UHFFFAOYSA-N 0.000 description 1
- IWWJNVPHOAEIQM-UHFFFAOYSA-N C(C1=CC=CC=C1)(=O)C(C(=O)O)CCCCCCCCCC Chemical compound C(C1=CC=CC=C1)(=O)C(C(=O)O)CCCCCCCCCC IWWJNVPHOAEIQM-UHFFFAOYSA-N 0.000 description 1
- GEZLZMFACVPSLB-UHFFFAOYSA-N C(C=C)(=O)O.C(C)C(CO)C(CCC)O Chemical compound C(C=C)(=O)O.C(C)C(CO)C(CCC)O GEZLZMFACVPSLB-UHFFFAOYSA-N 0.000 description 1
- GVUMZXBHUZZJHM-UHFFFAOYSA-N C(C=C)(=O)OC(CC)C(CC(C)=O)=O Chemical compound C(C=C)(=O)OC(CC)C(CC(C)=O)=O GVUMZXBHUZZJHM-UHFFFAOYSA-N 0.000 description 1
- ATRQEQRDOSBUJZ-UHFFFAOYSA-N C(CCC(=O)OCCCCCCCCCC1=CC=CC=C1)(=O)OC=C Chemical compound C(CCC(=O)OCCCCCCCCCC1=CC=CC=C1)(=O)OC=C ATRQEQRDOSBUJZ-UHFFFAOYSA-N 0.000 description 1
- JIURUSNJOMSBKR-UHFFFAOYSA-N C(CCC)OC(C1=CC=CC=C1)C(=C)C Chemical compound C(CCC)OC(C1=CC=CC=C1)C(=C)C JIURUSNJOMSBKR-UHFFFAOYSA-N 0.000 description 1
- MCTRWCYOGUUFLN-UHFFFAOYSA-N C(CCCC)OC(C1=CC=CC=C1)C(=C)C Chemical compound C(CCCC)OC(C1=CC=CC=C1)C(=C)C MCTRWCYOGUUFLN-UHFFFAOYSA-N 0.000 description 1
- INTKPRSTWMOVCO-UHFFFAOYSA-N C(CCCCC)OC(C1=CC=CC=C1)C(=C)C Chemical compound C(CCCCC)OC(C1=CC=CC=C1)C(=C)C INTKPRSTWMOVCO-UHFFFAOYSA-N 0.000 description 1
- SYRDCZUEIFYSQP-UHFFFAOYSA-N C(CCCCCC)OC(C1=CC=CC=C1)C(=C)C Chemical compound C(CCCCCC)OC(C1=CC=CC=C1)C(=C)C SYRDCZUEIFYSQP-UHFFFAOYSA-N 0.000 description 1
- MMOXJKNABKWXPS-UHFFFAOYSA-N C(CCCCCC)OC(C1=CC=CC=C1)C=C Chemical compound C(CCCCCC)OC(C1=CC=CC=C1)C=C MMOXJKNABKWXPS-UHFFFAOYSA-N 0.000 description 1
- RGCADROAJGAYTI-UHFFFAOYSA-N C(CCCCCCC)OC(C1=CC=CC=C1)C(=C)C Chemical compound C(CCCCCCC)OC(C1=CC=CC=C1)C(=C)C RGCADROAJGAYTI-UHFFFAOYSA-N 0.000 description 1
- OMFCEGBRHDOESA-UHFFFAOYSA-N C(CCCCCCCC)OC(C1=CC=CC=C1)C(=C)C Chemical compound C(CCCCCCCC)OC(C1=CC=CC=C1)C(=C)C OMFCEGBRHDOESA-UHFFFAOYSA-N 0.000 description 1
- HQPOBSKXZWGGOD-UHFFFAOYSA-N C(CCCCCCCC)OC(C1=CC=CC=C1)C=C Chemical compound C(CCCCCCCC)OC(C1=CC=CC=C1)C=C HQPOBSKXZWGGOD-UHFFFAOYSA-N 0.000 description 1
- UAFCOQHBLYJBSQ-UHFFFAOYSA-N C(CCCCCCCCC)(=O)OC(=O)C1=COC=C1 Chemical compound C(CCCCCCCCC)(=O)OC(=O)C1=COC=C1 UAFCOQHBLYJBSQ-UHFFFAOYSA-N 0.000 description 1
- UWXGUJPFPZEZLQ-UHFFFAOYSA-N C(CCCCCCCCC)OC(C1=CC=C(C=C1)C=C)=O Chemical compound C(CCCCCCCCC)OC(C1=CC=C(C=C1)C=C)=O UWXGUJPFPZEZLQ-UHFFFAOYSA-N 0.000 description 1
- RGFYKTZSVJYOSJ-UHFFFAOYSA-N C(CCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C Chemical compound C(CCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C RGFYKTZSVJYOSJ-UHFFFAOYSA-N 0.000 description 1
- OSGOFIMOZKGSGM-UHFFFAOYSA-N C(CCCCCCCCC)OC(C1=CC=CC=C1)C=C Chemical compound C(CCCCCCCCC)OC(C1=CC=CC=C1)C=C OSGOFIMOZKGSGM-UHFFFAOYSA-N 0.000 description 1
- LUGUZUBHPCMCGK-UHFFFAOYSA-N C(CCCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C Chemical compound C(CCCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C LUGUZUBHPCMCGK-UHFFFAOYSA-N 0.000 description 1
- NWNXGWNTMIRDPE-UHFFFAOYSA-N C(CCCCCCCCCC)OC(C1=CC=CC=C1)C=C Chemical compound C(CCCCCCCCCC)OC(C1=CC=CC=C1)C=C NWNXGWNTMIRDPE-UHFFFAOYSA-N 0.000 description 1
- AGGCDPVRDRCPNM-UHFFFAOYSA-N C(CCCCCCCCCC)OC1=C(C=CC=C1)C=C Chemical compound C(CCCCCCCCCC)OC1=C(C=CC=C1)C=C AGGCDPVRDRCPNM-UHFFFAOYSA-N 0.000 description 1
- QCPKUPIGMWINEX-UHFFFAOYSA-N C(CCCCCCCCCCC)(=O)OC(=O)C1=COC=C1 Chemical compound C(CCCCCCCCCCC)(=O)OC(=O)C1=COC=C1 QCPKUPIGMWINEX-UHFFFAOYSA-N 0.000 description 1
- MVIYDFZTDPGJDH-UHFFFAOYSA-N C(CCCCCCCCCCC)(=O)OCC1CO1.C(C=C)(=O)O Chemical compound C(CCCCCCCCCCC)(=O)OCC1CO1.C(C=C)(=O)O MVIYDFZTDPGJDH-UHFFFAOYSA-N 0.000 description 1
- HEIQLHQYCXBNCJ-UHFFFAOYSA-N C(CCCCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C Chemical compound C(CCCCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C HEIQLHQYCXBNCJ-UHFFFAOYSA-N 0.000 description 1
- PQIQNYCMAGUAPQ-UHFFFAOYSA-N C(CCCCCCCCCCC)OC1=C(C=CC=C1)C=C Chemical compound C(CCCCCCCCCCC)OC1=C(C=CC=C1)C=C PQIQNYCMAGUAPQ-UHFFFAOYSA-N 0.000 description 1
- GRARKHJXXTUAAK-UHFFFAOYSA-N C(CCCCCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C Chemical compound C(CCCCCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C GRARKHJXXTUAAK-UHFFFAOYSA-N 0.000 description 1
- ODCJJLMJFKBIDH-UHFFFAOYSA-N C(CCCCCCCCCCCC)OC(C1=CC=CC=C1)C=C Chemical compound C(CCCCCCCCCCCC)OC(C1=CC=CC=C1)C=C ODCJJLMJFKBIDH-UHFFFAOYSA-N 0.000 description 1
- SRYVVZUWVBOSCQ-UHFFFAOYSA-N C(CCCCCCCCCCCC)OC1=C(C=CC=C1)C=C Chemical compound C(CCCCCCCCCCCC)OC1=C(C=CC=C1)C=C SRYVVZUWVBOSCQ-UHFFFAOYSA-N 0.000 description 1
- RQFLKGFXDSPMAG-UHFFFAOYSA-N C(CCCCCCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C Chemical compound C(CCCCCCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C RQFLKGFXDSPMAG-UHFFFAOYSA-N 0.000 description 1
- VUGHGBCCPRVPGP-UHFFFAOYSA-N C(CCCCCCCCCCCCC)OC(C1=CC=CC=C1)C=C Chemical compound C(CCCCCCCCCCCCC)OC(C1=CC=CC=C1)C=C VUGHGBCCPRVPGP-UHFFFAOYSA-N 0.000 description 1
- HLARUGLWQQCWLJ-UHFFFAOYSA-N C(CCCCCCCCCCCCC)OC1=C(C=CC=C1)C=C Chemical compound C(CCCCCCCCCCCCC)OC1=C(C=CC=C1)C=C HLARUGLWQQCWLJ-UHFFFAOYSA-N 0.000 description 1
- FYTTWOIFBCXLPN-UHFFFAOYSA-N C(CCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C Chemical compound C(CCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C FYTTWOIFBCXLPN-UHFFFAOYSA-N 0.000 description 1
- MWNKVEZHNVQQMM-UHFFFAOYSA-N C(CCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C=C Chemical compound C(CCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C=C MWNKVEZHNVQQMM-UHFFFAOYSA-N 0.000 description 1
- KGIGSSQDRHDJLY-UHFFFAOYSA-N C(CCCCCCCCCCCCCC)OC1=C(C=CC=C1)C=C Chemical compound C(CCCCCCCCCCCCCC)OC1=C(C=CC=C1)C=C KGIGSSQDRHDJLY-UHFFFAOYSA-N 0.000 description 1
- HXOZKQVVGYJZPW-UHFFFAOYSA-N C(CCCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C Chemical compound C(CCCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C HXOZKQVVGYJZPW-UHFFFAOYSA-N 0.000 description 1
- CETHHHPDPCGXLS-UHFFFAOYSA-N C(CCCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C=C Chemical compound C(CCCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C=C CETHHHPDPCGXLS-UHFFFAOYSA-N 0.000 description 1
- YBFGMKIGOXXULM-UHFFFAOYSA-N C(CCCCCCCCCCCCCCC)OC1=C(C=CC=C1)C=C Chemical compound C(CCCCCCCCCCCCCCC)OC1=C(C=CC=C1)C=C YBFGMKIGOXXULM-UHFFFAOYSA-N 0.000 description 1
- FROLNKXKWCNEAU-UHFFFAOYSA-N C(CCCCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C Chemical compound C(CCCCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C FROLNKXKWCNEAU-UHFFFAOYSA-N 0.000 description 1
- GCNVPTXDGHWDST-UHFFFAOYSA-N C(CCCCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C=C Chemical compound C(CCCCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C=C GCNVPTXDGHWDST-UHFFFAOYSA-N 0.000 description 1
- OVZFPVRLQSCZAP-UHFFFAOYSA-N C(CCCCCCCCCCCCCCCC)OC1=C(C=CC=C1)C=C Chemical compound C(CCCCCCCCCCCCCCCC)OC1=C(C=CC=C1)C=C OVZFPVRLQSCZAP-UHFFFAOYSA-N 0.000 description 1
- CCVNCGLSSQJJPF-UHFFFAOYSA-N C(CCCCCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C Chemical compound C(CCCCCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C CCVNCGLSSQJJPF-UHFFFAOYSA-N 0.000 description 1
- OMQHAAAHBBBJTP-UHFFFAOYSA-N C(CCCCCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C=C Chemical compound C(CCCCCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C=C OMQHAAAHBBBJTP-UHFFFAOYSA-N 0.000 description 1
- IUHZJRDIYCMUIU-UHFFFAOYSA-N C(CCCCCCCCCCCCCCCCC)OC1=C(C=CC=C1)C=C Chemical compound C(CCCCCCCCCCCCCCCCC)OC1=C(C=CC=C1)C=C IUHZJRDIYCMUIU-UHFFFAOYSA-N 0.000 description 1
- DYZVRVPZAACVHI-UHFFFAOYSA-N C(CCCCCCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C Chemical compound C(CCCCCCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C DYZVRVPZAACVHI-UHFFFAOYSA-N 0.000 description 1
- CHDQJMQYBYCFOO-UHFFFAOYSA-N C(CCCCCCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C=C Chemical compound C(CCCCCCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C=C CHDQJMQYBYCFOO-UHFFFAOYSA-N 0.000 description 1
- UHCWLGJTACDELV-UHFFFAOYSA-N C(CCCCCCCCCCCCCCCCCC)OC1=C(C=CC=C1)C=C Chemical compound C(CCCCCCCCCCCCCCCCCC)OC1=C(C=CC=C1)C=C UHCWLGJTACDELV-UHFFFAOYSA-N 0.000 description 1
- LPDXHDIVOBBFSR-UHFFFAOYSA-N C(CCCCCCCCCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C Chemical class C(CCCCCCCCCCCCCCCCCCCCC)OC(C1=CC=CC=C1)C(=C)C LPDXHDIVOBBFSR-UHFFFAOYSA-N 0.000 description 1
- HPJUAANPUKDOPM-UHFFFAOYSA-N C(CCCCCCCCCCCCCCCCCCCCC)OC(C=CC)C Chemical compound C(CCCCCCCCCCCCCCCCCCCCC)OC(C=CC)C HPJUAANPUKDOPM-UHFFFAOYSA-N 0.000 description 1
- NKDJLSGXAQYVPH-UHFFFAOYSA-N C(O)C(CCC)(CO)CO.C(O)C(CCC)(CO)CO.C(C=C)(=O)O Chemical compound C(O)C(CCC)(CO)CO.C(O)C(CCC)(CO)CO.C(C=C)(=O)O NKDJLSGXAQYVPH-UHFFFAOYSA-N 0.000 description 1
- UBFPIYJGOIYUBA-UHFFFAOYSA-N C(O)C(CCCCCCC)(CO)CO.C(O)C(CCCCCCC)(CO)CO.C(C=C)(=O)O Chemical compound C(O)C(CCCCCCC)(CO)CO.C(O)C(CCCCCCC)(CO)CO.C(C=C)(=O)O UBFPIYJGOIYUBA-UHFFFAOYSA-N 0.000 description 1
- OKPVTENMJJERPX-UHFFFAOYSA-N C1(=CC=CC2=CC=CC=C12)C(=O)C(C(=O)O)CCC Chemical compound C1(=CC=CC2=CC=CC=C12)C(=O)C(C(=O)O)CCC OKPVTENMJJERPX-UHFFFAOYSA-N 0.000 description 1
- BKWZQVUEZPTJCX-UHFFFAOYSA-N C1=C(C=CC2=CC=CC=C12)C(=O)C(C(=O)O)CC Chemical compound C1=C(C=CC2=CC=CC=C12)C(=O)C(C(=O)O)CC BKWZQVUEZPTJCX-UHFFFAOYSA-N 0.000 description 1
- LBGQZKXGKLRDQP-UHFFFAOYSA-N CC(C(=O)OC=C)C(=O)C1=CC=CO1 Chemical compound CC(C(=O)OC=C)C(=O)C1=CC=CO1 LBGQZKXGKLRDQP-UHFFFAOYSA-N 0.000 description 1
- ASQDJWDHHMXJCM-UHFFFAOYSA-M CC1(C(C=CC=C1)S(=O)(=O)[O-])OC=CC.[K+] Chemical compound CC1(C(C=CC=C1)S(=O)(=O)[O-])OC=CC.[K+] ASQDJWDHHMXJCM-UHFFFAOYSA-M 0.000 description 1
- BQLRBPAJZHIJQE-UHFFFAOYSA-N CC1(C(C=CC=C1)S(=O)(=O)[O-])OC=CC.[NH4+] Chemical compound CC1(C(C=CC=C1)S(=O)(=O)[O-])OC=CC.[NH4+] BQLRBPAJZHIJQE-UHFFFAOYSA-N 0.000 description 1
- HEXSRGHNEBZMHR-UHFFFAOYSA-M CC1=CC=C(C=C1)S(=O)(=O)[O-].C(C=C)(=O)OCC[N+](CC1=CC=CC=C1)(C)C Chemical compound CC1=CC=C(C=C1)S(=O)(=O)[O-].C(C=C)(=O)OCC[N+](CC1=CC=CC=C1)(C)C HEXSRGHNEBZMHR-UHFFFAOYSA-M 0.000 description 1
- ZUFMCCIWKHFYBK-UHFFFAOYSA-N CCCCCC(=O)OC(=O)C1=COC=C1 Chemical compound CCCCCC(=O)OC(=O)C1=COC=C1 ZUFMCCIWKHFYBK-UHFFFAOYSA-N 0.000 description 1
- QPZXCTMZEMWRSS-UHFFFAOYSA-N CCCCCCCCCCCCCCCCCCC=C.CCCCCCCCCCCCCCCCCCCCC=C Chemical compound CCCCCCCCCCCCCCCCCCC=C.CCCCCCCCCCCCCCCCCCCCC=C QPZXCTMZEMWRSS-UHFFFAOYSA-N 0.000 description 1
- RKYGFBYDTLFMDB-UHFFFAOYSA-N CN.OS(=O)(=O)C=CC1=CC=CC=C1 Chemical compound CN.OS(=O)(=O)C=CC1=CC=CC=C1 RKYGFBYDTLFMDB-UHFFFAOYSA-N 0.000 description 1
- MTZNZRBCAUFELS-UHFFFAOYSA-N CO[SiH](OC)C=CC.CC(C(=O)O)=C Chemical compound CO[SiH](OC)C=CC.CC(C(=O)O)=C MTZNZRBCAUFELS-UHFFFAOYSA-N 0.000 description 1
- WPOZOGVWHJKVOX-UHFFFAOYSA-N CO[Si](OC)(OC)C=CC.CC(C(=O)O)=C Chemical compound CO[Si](OC)(OC)C=CC.CC(C(=O)O)=C WPOZOGVWHJKVOX-UHFFFAOYSA-N 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- YMOMFPVAXKZMFG-UHFFFAOYSA-M C[N+](C)(C)C.[O-]S(=O)(=O)C=CC1=CC=CC=C1 Chemical compound C[N+](C)(C)C.[O-]S(=O)(=O)C=CC1=CC=CC=C1 YMOMFPVAXKZMFG-UHFFFAOYSA-M 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229930008398 Citronellate Natural products 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- VWYIWOYBERNXLX-KTKRTIGZSA-N Glycidyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC1CO1 VWYIWOYBERNXLX-KTKRTIGZSA-N 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- HDFGOPSGAURCEO-UHFFFAOYSA-N N-ethylmaleimide Chemical compound CCN1C(=O)C=CC1=O HDFGOPSGAURCEO-UHFFFAOYSA-N 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- OXWMDCQCUNFTPO-UHFFFAOYSA-N O1CC1.C(=C)C1=CCCCC1 Chemical compound O1CC1.C(=C)C1=CCCCC1 OXWMDCQCUNFTPO-UHFFFAOYSA-N 0.000 description 1
- FHZFNOAEGYDOBX-UHFFFAOYSA-N OCC(C(=O)O)(C)C.OC(C(C(=O)O)(C)C)(O)C(C(C)(C)C)=O Chemical compound OCC(C(=O)O)(C)C.OC(C(C(=O)O)(C)C)(O)C(C(C)(C)C)=O FHZFNOAEGYDOBX-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229920000538 Poly[(phenyl isocyanate)-co-formaldehyde] Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- OLWQOPLQCXFVQA-UHFFFAOYSA-N S(=O)(=O)(C1=CC=C(C=C1)O)C1=CC=C(C=C1)O.C(C=C)(=O)O Chemical compound S(=O)(=O)(C1=CC=C(C=C1)O)C1=CC=C(C=C1)O.C(C=C)(=O)O OLWQOPLQCXFVQA-UHFFFAOYSA-N 0.000 description 1
- UTZKLAGODGTUOS-UHFFFAOYSA-N S(=O)(=O)([O-])[O-].C(C=C)(=O)NCCC[N+](CC)(CC)CC.C(C=C)(=O)NCCC[N+](CC)(CC)CC Chemical compound S(=O)(=O)([O-])[O-].C(C=C)(=O)NCCC[N+](CC)(CC)CC.C(C=C)(=O)NCCC[N+](CC)(CC)CC UTZKLAGODGTUOS-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- DPOPAJRDYZGTIR-UHFFFAOYSA-N Tetrazine Chemical compound C1=CN=NN=N1 DPOPAJRDYZGTIR-UHFFFAOYSA-N 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- GCTFWCDSFPMHHS-UHFFFAOYSA-M Tributyltin chloride Chemical compound CCCC[Sn](Cl)(CCCC)CCCC GCTFWCDSFPMHHS-UHFFFAOYSA-M 0.000 description 1
- APQHKWPGGHMYKJ-UHFFFAOYSA-N Tributyltin oxide Chemical compound CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC APQHKWPGGHMYKJ-UHFFFAOYSA-N 0.000 description 1
- 229910001297 Zn alloy Inorganic materials 0.000 description 1
- JJSCUXAFAJEQGB-QMMMGPOBSA-N [(1s)-1-isocyanatoethyl]benzene Chemical compound O=C=N[C@@H](C)C1=CC=CC=C1 JJSCUXAFAJEQGB-QMMMGPOBSA-N 0.000 description 1
- QARNHIBOPBXNSX-KRXBUXKQSA-N [(e)-prop-1-enoxy]methylbenzene Chemical compound C\C=C\OCC1=CC=CC=C1 QARNHIBOPBXNSX-KRXBUXKQSA-N 0.000 description 1
- ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 description 1
- SGDPVHRGCORYDU-UHFFFAOYSA-N [2-(hydroxymethyl)-2-methylpentyl] prop-2-enoate Chemical compound CCCC(C)(CO)COC(=O)C=C SGDPVHRGCORYDU-UHFFFAOYSA-N 0.000 description 1
- LBQFNKAHMMFVJM-UHFFFAOYSA-N [2-ethyl-2-(hydroxymethyl)butyl] prop-2-enoate Chemical compound C(C=C)(=O)OCC(CO)(CC)CC LBQFNKAHMMFVJM-UHFFFAOYSA-N 0.000 description 1
- OGUBTQJLVGOFSU-UHFFFAOYSA-N [2-ethyl-4-(hydroxymethyl)hexyl] prop-2-enoate Chemical compound CCC(CO)CC(CC)COC(=O)C=C OGUBTQJLVGOFSU-UHFFFAOYSA-N 0.000 description 1
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
- LRPWTTYFYQRYLO-UHFFFAOYSA-N [NH4+].C(=CC1=CC=CC=C1)S(=O)(=O)[O-].C(CCCCC)[NH3+].C(=CC1=CC=CC=C1)S(=O)(=O)[O-] Chemical class [NH4+].C(=CC1=CC=CC=C1)S(=O)(=O)[O-].C(CCCCC)[NH3+].C(=CC1=CC=CC=C1)S(=O)(=O)[O-] LRPWTTYFYQRYLO-UHFFFAOYSA-N 0.000 description 1
- ODRAAOWETKHDHB-UHFFFAOYSA-M [Na+].CC1(C(C=CC=C1)S(=O)(=O)[O-])OC=CC Chemical compound [Na+].CC1(C(C=CC=C1)S(=O)(=O)[O-])OC=CC ODRAAOWETKHDHB-UHFFFAOYSA-M 0.000 description 1
- KYIKRXIYLAGAKQ-UHFFFAOYSA-N abcn Chemical compound C1CCCCC1(C#N)N=NC1(C#N)CCCCC1 KYIKRXIYLAGAKQ-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- VKVOKQTWSYMEAI-UHFFFAOYSA-N acetyl 2-methylpropanoate Chemical compound CC(C)C(=O)OC(C)=O VKVOKQTWSYMEAI-UHFFFAOYSA-N 0.000 description 1
- BVQHHUQLZPXYAQ-UHFFFAOYSA-N acetyl butanoate Chemical compound CCCC(=O)OC(C)=O BVQHHUQLZPXYAQ-UHFFFAOYSA-N 0.000 description 1
- VUBTYKDZOQNADH-UHFFFAOYSA-N acetyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)=O VUBTYKDZOQNADH-UHFFFAOYSA-N 0.000 description 1
- FMZXSZBTMBNMRC-UHFFFAOYSA-N acetyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC(C)=O FMZXSZBTMBNMRC-UHFFFAOYSA-N 0.000 description 1
- KLUDQUOLAFVLOL-UHFFFAOYSA-N acetyl propanoate Chemical compound CCC(=O)OC(C)=O KLUDQUOLAFVLOL-UHFFFAOYSA-N 0.000 description 1
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 1
- 239000012345 acetylating agent Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- AUKWRHADVIQZRJ-UHFFFAOYSA-N adamantane-1,4-diol Chemical compound C1C(C2)CC3C(O)C1CC2(O)C3 AUKWRHADVIQZRJ-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 238000004378 air conditioning Methods 0.000 description 1
- 239000005456 alcohol based solvent Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000005742 alkyl ethenyl group Chemical group 0.000 description 1
- 125000005376 alkyl siloxane group Chemical group 0.000 description 1
- 150000001361 allenes Chemical class 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 150000004808 allyl alcohols Chemical class 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 230000009435 amidation Effects 0.000 description 1
- 238000007112 amidation reaction Methods 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- UIERETOOQGIECD-ARJAWSKDSA-N angelic acid Chemical compound C\C=C(\C)C(O)=O UIERETOOQGIECD-ARJAWSKDSA-N 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 125000002078 anthracen-1-yl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C([*])=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 1
- 125000000748 anthracen-2-yl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C([H])=C([*])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 1
- IPLSGZRALKDNRS-UHFFFAOYSA-N anthracen-9-ylmethyl prop-2-enoate Chemical compound C1=CC=C2C(COC(=O)C=C)=C(C=CC=C3)C3=CC2=C1 IPLSGZRALKDNRS-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- XDIJWRHVEDUFGP-UHFFFAOYSA-N azanium;2-phenylethenesulfonate Chemical compound [NH4+].[O-]S(=O)(=O)C=CC1=CC=CC=C1 XDIJWRHVEDUFGP-UHFFFAOYSA-N 0.000 description 1
- SGIAKTJHCBPGOS-UHFFFAOYSA-N azanium;ethenesulfonate Chemical compound N.OS(=O)(=O)C=C SGIAKTJHCBPGOS-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 125000005605 benzo group Chemical group 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 235000008429 bread Nutrition 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- LBQOLZVFCCPKMR-UHFFFAOYSA-N buta-1,3-diene oxirane Chemical compound C1CO1.C=CC=C LBQOLZVFCCPKMR-UHFFFAOYSA-N 0.000 description 1
- DEFMLLQRTVNBOF-UHFFFAOYSA-K butan-1-olate;trichlorotitanium(1+) Chemical compound [Cl-].[Cl-].[Cl-].CCCCO[Ti+3] DEFMLLQRTVNBOF-UHFFFAOYSA-K 0.000 description 1
- BCKTULSMISNELW-UHFFFAOYSA-N butane-1,2,4-triol;prop-2-enoic acid Chemical compound OC(=O)C=C.OCCC(O)CO BCKTULSMISNELW-UHFFFAOYSA-N 0.000 description 1
- FVURVSKYJGBCKX-UHFFFAOYSA-N butanoyl benzoate Chemical compound CCCC(=O)OC(=O)C1=CC=CC=C1 FVURVSKYJGBCKX-UHFFFAOYSA-N 0.000 description 1
- ZPVUQKUYHWTNJD-UHFFFAOYSA-N butanoyl furan-3-carboxylate Chemical compound CCCC(=O)OC(=O)C=1C=COC=1 ZPVUQKUYHWTNJD-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 238000011088 calibration curve Methods 0.000 description 1
- SHZIWNPUGXLXDT-UHFFFAOYSA-N caproic acid ethyl ester Natural products CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 description 1
- 150000001718 carbodiimides Chemical class 0.000 description 1
- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- WRJWRGBVPUUDLA-UHFFFAOYSA-N chlorosulfonyl isocyanate Chemical compound ClS(=O)(=O)N=C=O WRJWRGBVPUUDLA-UHFFFAOYSA-N 0.000 description 1
- 125000000490 cinnamyl group Chemical group C(C=CC1=CC=CC=C1)* 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- QAEKNCDIHIGLFI-UHFFFAOYSA-L cobalt(2+);2-ethylhexanoate Chemical compound [Co+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O QAEKNCDIHIGLFI-UHFFFAOYSA-L 0.000 description 1
- GAYAMOAYBXKUII-UHFFFAOYSA-L cobalt(2+);dibenzoate Chemical compound [Co+2].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 GAYAMOAYBXKUII-UHFFFAOYSA-L 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- NKKMVIVFRUYPLQ-NSCUHMNNSA-N crotononitrile Chemical compound C\C=C\C#N NKKMVIVFRUYPLQ-NSCUHMNNSA-N 0.000 description 1
- QSAWQNUELGIYBC-UHFFFAOYSA-N cyclohexane-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCCCC1C(O)=O QSAWQNUELGIYBC-UHFFFAOYSA-N 0.000 description 1
- 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 1
- KQWGXHWJMSMDJJ-UHFFFAOYSA-N cyclohexyl isocyanate Chemical compound O=C=NC1CCCCC1 KQWGXHWJMSMDJJ-UHFFFAOYSA-N 0.000 description 1
- 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 description 1
- 230000006837 decompression Effects 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
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 1
- WOWBFOBYOAGEEA-UHFFFAOYSA-N diafenthiuron Chemical compound CC(C)C1=C(NC(=S)NC(C)(C)C)C(C(C)C)=CC(OC=2C=CC=CC=2)=C1 WOWBFOBYOAGEEA-UHFFFAOYSA-N 0.000 description 1
- HEYYNPBHZQPMJJ-UHFFFAOYSA-L dibenzoyloxylead Chemical compound C=1C=CC=CC=1C(=O)O[Pb]OC(=O)C1=CC=CC=C1 HEYYNPBHZQPMJJ-UHFFFAOYSA-L 0.000 description 1
- RJGHQTVXGKYATR-UHFFFAOYSA-L dibutyl(dichloro)stannane Chemical compound CCCC[Sn](Cl)(Cl)CCCC RJGHQTVXGKYATR-UHFFFAOYSA-L 0.000 description 1
- JGFBRKRYDCGYKD-UHFFFAOYSA-N dibutyl(oxo)tin Chemical compound CCCC[Sn](=O)CCCC JGFBRKRYDCGYKD-UHFFFAOYSA-N 0.000 description 1
- JJPZOIJCDNHCJP-UHFFFAOYSA-N dibutyl(sulfanylidene)tin Chemical compound CCCC[Sn](=S)CCCC JJPZOIJCDNHCJP-UHFFFAOYSA-N 0.000 description 1
- WCRDXYSYPCEIAK-UHFFFAOYSA-N dibutylstannane Chemical compound CCCC[SnH2]CCCC WCRDXYSYPCEIAK-UHFFFAOYSA-N 0.000 description 1
- QSHZUFRQHSINTB-UHFFFAOYSA-L dibutyltin(2+);dibromide Chemical compound CCCC[Sn](Br)(Br)CCCC QSHZUFRQHSINTB-UHFFFAOYSA-L 0.000 description 1
- KIQKWYUGPPFMBV-UHFFFAOYSA-N diisocyanatomethane Chemical compound O=C=NCN=C=O KIQKWYUGPPFMBV-UHFFFAOYSA-N 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 1
- XNMQEEKYCVKGBD-UHFFFAOYSA-N dimethylacetylene Natural products CC#CC XNMQEEKYCVKGBD-UHFFFAOYSA-N 0.000 description 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
- DOWIUKUFEGKUJO-UHFFFAOYSA-N dimethylazanium 2-phenylethenesulfonate Chemical compound C(=CC1=CC=CC=C1)S(=O)(=O)[O-].C[NH2+]C DOWIUKUFEGKUJO-UHFFFAOYSA-N 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- 229960001826 dimethylphthalate Drugs 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- LQRUPWUPINJLMU-UHFFFAOYSA-N dioctyl(oxo)tin Chemical compound CCCCCCCC[Sn](=O)CCCCCCCC LQRUPWUPINJLMU-UHFFFAOYSA-N 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Natural products C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- 208000028659 discharge Diseases 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- IEAIMKJZBBZORJ-UHFFFAOYSA-N docosyl 4-ethenylbenzoate Chemical compound CCCCCCCCCCCCCCCCCCCCCCOC(=O)C1=CC=C(C=C)C=C1 IEAIMKJZBBZORJ-UHFFFAOYSA-N 0.000 description 1
- 229940069096 dodecene Drugs 0.000 description 1
- SAWZROBJJFFFHX-UHFFFAOYSA-N dodecyl 4-ethenylbenzoate Chemical compound CCCCCCCCCCCCOC(=O)C1=CC=C(C=C)C=C1 SAWZROBJJFFFHX-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 239000003759 ester based solvent Substances 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical compound NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 description 1
- XREZAPYWZGJIFS-UHFFFAOYSA-N ethenoxymethoxyethane Chemical compound CCOCOC=C XREZAPYWZGJIFS-UHFFFAOYSA-N 0.000 description 1
- MTLXSUCXWZGPKN-UHFFFAOYSA-N ethenoxymethyl acetate Chemical compound CC(=O)OCOC=C MTLXSUCXWZGPKN-UHFFFAOYSA-N 0.000 description 1
- BIUZXWXXSCLGNK-UHFFFAOYSA-N ethenoxymethylcyclohexane Chemical compound C=COCC1CCCCC1 BIUZXWXXSCLGNK-UHFFFAOYSA-N 0.000 description 1
- IYNRVIKPUTZSOR-HWKANZROSA-N ethenyl (e)-but-2-enoate Chemical compound C\C=C\C(=O)OC=C IYNRVIKPUTZSOR-HWKANZROSA-N 0.000 description 1
- YCUBDDIKWLELPD-UHFFFAOYSA-N ethenyl 2,2-dimethylpropanoate Chemical compound CC(C)(C)C(=O)OC=C YCUBDDIKWLELPD-UHFFFAOYSA-N 0.000 description 1
- ZEYMDLYHRCTNEE-UHFFFAOYSA-N ethenyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OC=C ZEYMDLYHRCTNEE-UHFFFAOYSA-N 0.000 description 1
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 description 1
- CMDXMIHZUJPRHG-UHFFFAOYSA-N ethenyl decanoate Chemical compound CCCCCCCCCC(=O)OC=C CMDXMIHZUJPRHG-UHFFFAOYSA-N 0.000 description 1
- GLVVKKSPKXTQRB-UHFFFAOYSA-N ethenyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC=C GLVVKKSPKXTQRB-UHFFFAOYSA-N 0.000 description 1
- GFJVXXWOPWLRNU-UHFFFAOYSA-N ethenyl formate Chemical compound C=COC=O GFJVXXWOPWLRNU-UHFFFAOYSA-N 0.000 description 1
- UJRIYYLGNDXVTA-UHFFFAOYSA-N ethenyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OC=C UJRIYYLGNDXVTA-UHFFFAOYSA-N 0.000 description 1
- AFSIMBWBBOJPJG-UHFFFAOYSA-N ethenyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC=C AFSIMBWBBOJPJG-UHFFFAOYSA-N 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- VEWLDLAARDMXSB-UHFFFAOYSA-N ethenyl sulfate;hydron Chemical compound OS(=O)(=O)OC=C VEWLDLAARDMXSB-UHFFFAOYSA-N 0.000 description 1
- YTUPSNLWAAEFPL-UHFFFAOYSA-N ethenyl(ethoxy)silane Chemical compound CCO[SiH2]C=C YTUPSNLWAAEFPL-UHFFFAOYSA-N 0.000 description 1
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 1
- WOXXJEVNDJOOLV-UHFFFAOYSA-N ethenyl-tris(2-methoxyethoxy)silane Chemical compound COCCO[Si](OCCOC)(OCCOC)C=C WOXXJEVNDJOOLV-UHFFFAOYSA-N 0.000 description 1
- 125000005670 ethenylalkyl group Chemical group 0.000 description 1
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
- 239000004210 ether based solvent Substances 0.000 description 1
- 229940052303 ethers for general anesthesia Drugs 0.000 description 1
- AAOWICMKJHPGAG-UHFFFAOYSA-N ethoxy(triethyl)stannane Chemical compound CCO[Sn](CC)(CC)CC AAOWICMKJHPGAG-UHFFFAOYSA-N 0.000 description 1
- WMAFNLQQGPUKCM-UHFFFAOYSA-N ethoxymethyl 2-methylprop-2-enoate Chemical compound CCOCOC(=O)C(C)=C WMAFNLQQGPUKCM-UHFFFAOYSA-N 0.000 description 1
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 description 1
- XCRHYAQWBYDRGV-JXMROGBWSA-N ethyl (e)-3-(4-propan-2-ylphenyl)prop-2-enoate Chemical compound CCOC(=O)\C=C\C1=CC=C(C(C)C)C=C1 XCRHYAQWBYDRGV-JXMROGBWSA-N 0.000 description 1
- DYSXJBCEIBVGJU-UHFFFAOYSA-N ethyl 4-ethenylbenzoate Chemical compound CCOC(=O)C1=CC=C(C=C)C=C1 DYSXJBCEIBVGJU-UHFFFAOYSA-N 0.000 description 1
- OWETXDKQWTZZAL-UHFFFAOYSA-N ethyl hexanoate;iron Chemical compound [Fe].CCCCCC(=O)OCC OWETXDKQWTZZAL-UHFFFAOYSA-N 0.000 description 1
- WUDNUHPRLBTKOJ-UHFFFAOYSA-N ethyl isocyanate Chemical compound CCN=C=O WUDNUHPRLBTKOJ-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000009501 film coating Methods 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000005021 flexible packaging material Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- 125000000755 henicosyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])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
- PSHLNTOPOCHINM-UHFFFAOYSA-N hept-1-ene-1,1-diol Chemical compound CCCCCC=C(O)O PSHLNTOPOCHINM-UHFFFAOYSA-N 0.000 description 1
- RUDVQBCFUZDOTA-UHFFFAOYSA-N hex-1-en-1-amine Chemical compound CCCCC=CN RUDVQBCFUZDOTA-UHFFFAOYSA-N 0.000 description 1
- QYZGEXRKKGDNFA-UHFFFAOYSA-N hexadecyl 4-ethenylbenzoate Chemical compound CCCCCCCCCCCCCCCCOC(=O)C1=CC=C(C=C)C=C1 QYZGEXRKKGDNFA-UHFFFAOYSA-N 0.000 description 1
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical compound FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N hexane Substances CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
- XCOLCZZTHJIBMT-UHFFFAOYSA-N hexane-1,1-diol;prop-2-enoic acid Chemical compound OC(=O)C=C.CCCCCC(O)O XCOLCZZTHJIBMT-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- SIXQKCKYEKKFRC-UHFFFAOYSA-N hexatriacont-1-ene Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC=C SIXQKCKYEKKFRC-UHFFFAOYSA-N 0.000 description 1
- XYRCGHBNOVEFGW-UHFFFAOYSA-N hexyl 4-ethenylbenzoate Chemical compound CCCCCCOC(=O)C1=CC=C(C=C)C=C1 XYRCGHBNOVEFGW-UHFFFAOYSA-N 0.000 description 1
- FAXNEIWNMFQFTC-UHFFFAOYSA-N hexyl 4-prop-1-en-2-ylbenzoate Chemical compound C(CCCCC)OC(C1=CC=C(C=C1)C(=C)C)=O FAXNEIWNMFQFTC-UHFFFAOYSA-N 0.000 description 1
- 238000007602 hot air drying Methods 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 125000000717 hydrazino group Chemical group [H]N([*])N([H])[H] 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
- 125000000336 imidazol-5-yl group Chemical group [H]N1C([H])=NC([H])=C1[*] 0.000 description 1
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Substances C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 229910052809 inorganic oxide Inorganic materials 0.000 description 1
- BJWCYHWBHZUVCU-UHFFFAOYSA-L iron(2+) 2-phenylethenesulfonate Chemical compound [Fe+2].[O-]S(=O)(=O)C=CC1=CC=CC=C1.[O-]S(=O)(=O)C=CC1=CC=CC=C1 BJWCYHWBHZUVCU-UHFFFAOYSA-L 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
- YDNLNVZZTACNJX-UHFFFAOYSA-N isocyanatomethylbenzene Chemical compound O=C=NCC1=CC=CC=C1 YDNLNVZZTACNJX-UHFFFAOYSA-N 0.000 description 1
- LADVLFVCTCHOAI-UHFFFAOYSA-N isocyanic acid;toluene Chemical compound N=C=O.CC1=CC=CC=C1 LADVLFVCTCHOAI-UHFFFAOYSA-N 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- 150000002596 lactones Chemical group 0.000 description 1
- 239000005001 laminate film Substances 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- 150000002611 lead compounds Chemical class 0.000 description 1
- GIWKOZXJDKMGQC-UHFFFAOYSA-L lead(2+);naphthalene-2-carboxylate Chemical compound [Pb+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 GIWKOZXJDKMGQC-UHFFFAOYSA-L 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 229940087305 limonene Drugs 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
- 125000005647 linker group Chemical group 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- ZKIAYSOOCAKOJR-UHFFFAOYSA-M lithium;2-phenylethenesulfonate Chemical compound [Li+].[O-]S(=O)(=O)C=CC1=CC=CC=C1 ZKIAYSOOCAKOJR-UHFFFAOYSA-M 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- GZPUKKQAJUVQHX-UHFFFAOYSA-L magnesium;2-phenylethenesulfonate Chemical compound [Mg+2].[O-]S(=O)(=O)C=CC1=CC=CC=C1.[O-]S(=O)(=O)C=CC1=CC=CC=C1 GZPUKKQAJUVQHX-UHFFFAOYSA-L 0.000 description 1
- 229920001912 maleic anhydride grafted polyethylene Polymers 0.000 description 1
- 229920001911 maleic anhydride grafted polypropylene Polymers 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000008268 mayonnaise Substances 0.000 description 1
- 235000010746 mayonnaise Nutrition 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 125000005394 methallyl group Chemical group 0.000 description 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- ZQMHJBXHRFJKOT-UHFFFAOYSA-N methyl 2-[(1-methoxy-2-methyl-1-oxopropan-2-yl)diazenyl]-2-methylpropanoate Chemical compound COC(=O)C(C)(C)N=NC(C)(C)C(=O)OC ZQMHJBXHRFJKOT-UHFFFAOYSA-N 0.000 description 1
- NUMHUJZXKZKUBN-UHFFFAOYSA-N methyl 4-ethenylbenzoate Chemical compound COC(=O)C1=CC=C(C=C)C=C1 NUMHUJZXKZKUBN-UHFFFAOYSA-N 0.000 description 1
- OVVNOSFHLSEYEP-UHFFFAOYSA-N methyl 4-prop-1-en-2-ylbenzoate Chemical compound COC(=O)C1=CC=C(C(C)=C)C=C1 OVVNOSFHLSEYEP-UHFFFAOYSA-N 0.000 description 1
- HAMGRBXTJNITHG-UHFFFAOYSA-N methyl isocyanate Chemical compound CN=C=O HAMGRBXTJNITHG-UHFFFAOYSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- PKDBSOOYVOEUQR-UHFFFAOYSA-N mucobromic acid Natural products OC1OC(=O)C(Br)=C1Br PKDBSOOYVOEUQR-UHFFFAOYSA-N 0.000 description 1
- ZAKLKBFCSHJIRI-UHFFFAOYSA-N mucochloric acid Natural products OC1OC(=O)C(Cl)=C1Cl ZAKLKBFCSHJIRI-UHFFFAOYSA-N 0.000 description 1
- YLBPOJLDZXHVRR-UHFFFAOYSA-N n'-[3-[diethoxy(methyl)silyl]propyl]ethane-1,2-diamine Chemical compound CCO[Si](C)(OCC)CCCNCCN YLBPOJLDZXHVRR-UHFFFAOYSA-N 0.000 description 1
- JAYXSROKFZAHRQ-UHFFFAOYSA-N n,n-bis(oxiran-2-ylmethyl)aniline Chemical compound C1OC1CN(C=1C=CC=CC=1)CC1CO1 JAYXSROKFZAHRQ-UHFFFAOYSA-N 0.000 description 1
- LIBWSLLLJZULCP-UHFFFAOYSA-N n-(3-triethoxysilylpropyl)aniline Chemical compound CCO[Si](OCC)(OCC)CCCNC1=CC=CC=C1 LIBWSLLLJZULCP-UHFFFAOYSA-N 0.000 description 1
- KBJFYLLAMSZSOG-UHFFFAOYSA-N n-(3-trimethoxysilylpropyl)aniline Chemical compound CO[Si](OC)(OC)CCCNC1=CC=CC=C1 KBJFYLLAMSZSOG-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- WHIVNJATOVLWBW-UHFFFAOYSA-N n-butan-2-ylidenehydroxylamine Chemical compound CCC(C)=NO WHIVNJATOVLWBW-UHFFFAOYSA-N 0.000 description 1
- HNHVTXYLRVGMHD-UHFFFAOYSA-N n-butyl isocyanate Chemical compound CCCCN=C=O HNHVTXYLRVGMHD-UHFFFAOYSA-N 0.000 description 1
- KAXILSKFDQXZPP-UHFFFAOYSA-N n-ethenyl-n-ethylnitrous amide Chemical group CCN(C=C)N=O KAXILSKFDQXZPP-UHFFFAOYSA-N 0.000 description 1
- RQAKESSLMFZVMC-UHFFFAOYSA-N n-ethenylacetamide Chemical compound CC(=O)NC=C RQAKESSLMFZVMC-UHFFFAOYSA-N 0.000 description 1
- AZDJPUNWDYYMIK-UHFFFAOYSA-N n-ethenylethanamine Chemical compound CCNC=C AZDJPUNWDYYMIK-UHFFFAOYSA-N 0.000 description 1
- ZQXSMRAEXCEDJD-UHFFFAOYSA-N n-ethenylformamide Chemical compound C=CNC=O ZQXSMRAEXCEDJD-UHFFFAOYSA-N 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- HGUZQMQXAHVIQC-UHFFFAOYSA-N n-methylethenamine Chemical compound CNC=C HGUZQMQXAHVIQC-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- FFJKAASRNUVNRT-UHFFFAOYSA-N n-trimethylsilylprop-2-en-1-amine Chemical compound C[Si](C)(C)NCC=C FFJKAASRNUVNRT-UHFFFAOYSA-N 0.000 description 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- GUSIVJZTZYXXNO-UHFFFAOYSA-N nonyl 4-ethenylbenzoate Chemical compound C(CCCCCCCC)OC(C1=CC=C(C=C1)C=C)=O GUSIVJZTZYXXNO-UHFFFAOYSA-N 0.000 description 1
- KVBNEJKPENQWOD-UHFFFAOYSA-N nonyl 4-prop-1-en-2-ylbenzoate Chemical compound C(=C)(C)C1=CC=C(C=C1)C(=O)OCCCCCCCCC KVBNEJKPENQWOD-UHFFFAOYSA-N 0.000 description 1
- UMRZSTCPUPJPOJ-KNVOCYPGSA-N norbornane Chemical compound C1C[C@H]2CC[C@@H]1C2 UMRZSTCPUPJPOJ-KNVOCYPGSA-N 0.000 description 1
- SFBTTWXNCQVIEC-UHFFFAOYSA-N o-Vinylanisole Chemical compound COC1=CC=CC=C1C=C SFBTTWXNCQVIEC-UHFFFAOYSA-N 0.000 description 1
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
- MUWJCQQULRVZIP-UHFFFAOYSA-N octadecyl 4-ethenylbenzoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C1=CC=C(C=C)C=C1 MUWJCQQULRVZIP-UHFFFAOYSA-N 0.000 description 1
- AEIJTFQOBWATKX-UHFFFAOYSA-N octane-1,2-diol Chemical compound CCCCCCC(O)CO AEIJTFQOBWATKX-UHFFFAOYSA-N 0.000 description 1
- OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 description 1
- PNGITPWPULMPMS-UHFFFAOYSA-N octatriacont-1-ene Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC=C PNGITPWPULMPMS-UHFFFAOYSA-N 0.000 description 1
- HHTOUGHLBSTKNZ-UHFFFAOYSA-N octyl 4-ethenylbenzoate Chemical compound CCCCCCCCOC(=O)C1=CC=C(C=C)C=C1 HHTOUGHLBSTKNZ-UHFFFAOYSA-N 0.000 description 1
- SFKFFKNFOUZRQL-UHFFFAOYSA-N octyl 4-prop-1-en-2-ylbenzoate Chemical compound C(CCCCCCC)OC(C1=CC=C(C=C1)C(=C)C)=O SFKFFKNFOUZRQL-UHFFFAOYSA-N 0.000 description 1
- 125000005447 octyloxy 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])O* 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- JUVGLPRIQOJMIR-UHFFFAOYSA-N oxiran-2-ylmethyl 3-phenylprop-2-enoate Chemical compound C=1C=CC=CC=1C=CC(=O)OCC1CO1 JUVGLPRIQOJMIR-UHFFFAOYSA-N 0.000 description 1
- 239000012785 packaging film Substances 0.000 description 1
- 229920006280 packaging film Polymers 0.000 description 1
- 125000001312 palmitoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- YCOFRPYSZKIPBQ-UHFFFAOYSA-N penicillic acid Natural products COC1=CC(=O)OC1(O)C(C)=C YCOFRPYSZKIPBQ-UHFFFAOYSA-N 0.000 description 1
- VOUGEZYPVGAPBB-UHFFFAOYSA-N penicillin acid Natural products OC(=O)C=C(OC)C(=O)C(C)=C VOUGEZYPVGAPBB-UHFFFAOYSA-N 0.000 description 1
- FSEKYSAWZRQAPN-UHFFFAOYSA-N pent-1-en-1-amine Chemical compound CCCC=CN FSEKYSAWZRQAPN-UHFFFAOYSA-N 0.000 description 1
- HVAMZGADVCBITI-UHFFFAOYSA-M pent-4-enoate Chemical compound [O-]C(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-M 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- BLBRUVGVLMZBOV-UHFFFAOYSA-N pentanoyl benzoate Chemical compound CCCCC(=O)OC(=O)C1=CC=CC=C1 BLBRUVGVLMZBOV-UHFFFAOYSA-N 0.000 description 1
- BFASWQMAEQIIDR-UHFFFAOYSA-N pentanoyl furan-3-carboxylate Chemical compound C(CCCC)(=O)OC(=O)C1=COC=C1 BFASWQMAEQIIDR-UHFFFAOYSA-N 0.000 description 1
- UFXWMSPXJWCWRV-UHFFFAOYSA-N pentanoyl naphthalene-2-carboxylate Chemical compound C(CCCC)(=O)OC(=O)C1=CC2=CC=CC=C2C=C1 UFXWMSPXJWCWRV-UHFFFAOYSA-N 0.000 description 1
- 125000005815 pentoxymethyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])OC([H])([H])* 0.000 description 1
- 125000005003 perfluorobutyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)* 0.000 description 1
- 125000005004 perfluoroethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- 125000005007 perfluorooctyl group Chemical group FC(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)* 0.000 description 1
- 125000005009 perfluoropropyl group Chemical group FC(C(C(F)(F)F)(F)F)(F)* 0.000 description 1
- DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical compound O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 description 1
- FAQJJMHZNSSFSM-UHFFFAOYSA-N phenylglyoxylic acid Chemical compound OC(=O)C(=O)C1=CC=CC=C1 FAQJJMHZNSSFSM-UHFFFAOYSA-N 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N phosphonic acid group Chemical group P(O)(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 125000004194 piperazin-1-yl group Chemical group [H]N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 description 1
- 238000009832 plasma treatment Methods 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000636 poly(norbornene) polymer Polymers 0.000 description 1
- 229920003050 poly-cycloolefin Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920006289 polycarbonate film Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 125000004585 polycyclic heterocycle group Chemical group 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- RWTNDBYQABFGKZ-UHFFFAOYSA-M potassium;2-ethenoxybenzenesulfonate Chemical compound [K+].[O-]S(=O)(=O)C1=CC=CC=C1OC=C RWTNDBYQABFGKZ-UHFFFAOYSA-M 0.000 description 1
- IZCABQCSROGIGG-UHFFFAOYSA-M potassium;2-methylprop-2-ene-1-sulfonate Chemical compound [K+].CC(=C)CS([O-])(=O)=O IZCABQCSROGIGG-UHFFFAOYSA-M 0.000 description 1
- QIFCIFLDTQJGHQ-UHFFFAOYSA-M potassium;2-phenylethenesulfonate Chemical compound [K+].[O-]S(=O)(=O)C=CC1=CC=CC=C1 QIFCIFLDTQJGHQ-UHFFFAOYSA-M 0.000 description 1
- YLQIJFPHMPTBGU-UHFFFAOYSA-M potassium;ethenesulfonate Chemical compound [K+].[O-]S(=O)(=O)C=C YLQIJFPHMPTBGU-UHFFFAOYSA-M 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- QVQPFHVJHZPVDM-UHFFFAOYSA-N prop-1-en-2-yl benzoate Chemical class CC(=C)OC(=O)C1=CC=CC=C1 QVQPFHVJHZPVDM-UHFFFAOYSA-N 0.000 description 1
- FZYCEURIEDTWNS-UHFFFAOYSA-N prop-1-en-2-ylbenzene Chemical compound CC(=C)C1=CC=CC=C1.CC(=C)C1=CC=CC=C1 FZYCEURIEDTWNS-UHFFFAOYSA-N 0.000 description 1
- JNLTYWDDGFTRSX-UHFFFAOYSA-N prop-1-ene-1,1-diol Chemical group CC=C(O)O JNLTYWDDGFTRSX-UHFFFAOYSA-N 0.000 description 1
- UIIIBRHUICCMAI-UHFFFAOYSA-N prop-2-ene-1-sulfonic acid Chemical compound OS(=O)(=O)CC=C UIIIBRHUICCMAI-UHFFFAOYSA-N 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- DQVOTEHORLHPRW-UHFFFAOYSA-N prop-2-enyl decanoate Chemical compound CCCCCCCCCC(=O)OCC=C DQVOTEHORLHPRW-UHFFFAOYSA-N 0.000 description 1
- ZQMAPKVSTSACQB-UHFFFAOYSA-N prop-2-enyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCC=C ZQMAPKVSTSACQB-UHFFFAOYSA-N 0.000 description 1
- BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- GHJOIQFPDMIKHT-UHFFFAOYSA-N propane-1,2,3-triol;prop-2-enoic acid Chemical compound OC(=O)C=C.OCC(O)CO GHJOIQFPDMIKHT-UHFFFAOYSA-N 0.000 description 1
- KZTMCBOPTQHICJ-UHFFFAOYSA-N propanoyl benzoate Chemical compound CCC(=O)OC(=O)C1=CC=CC=C1 KZTMCBOPTQHICJ-UHFFFAOYSA-N 0.000 description 1
- KOPQZJAYZFAPBC-UHFFFAOYSA-N propanoyl propaneperoxoate Chemical compound CCC(=O)OOC(=O)CC KOPQZJAYZFAPBC-UHFFFAOYSA-N 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- WHMDPDGBKYUEMW-UHFFFAOYSA-N pyridine-2-thiol Chemical compound SC1=CC=CC=N1 WHMDPDGBKYUEMW-UHFFFAOYSA-N 0.000 description 1
- JTDPJYXDDYUJBS-UHFFFAOYSA-N quinoline-2-carbohydrazide Chemical compound C1=CC=CC2=NC(C(=O)NN)=CC=C21 JTDPJYXDDYUJBS-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 description 1
- SZHIIIPPJJXYRY-UHFFFAOYSA-M sodium;2-methylprop-2-ene-1-sulfonate Chemical compound [Na+].CC(=C)CS([O-])(=O)=O SZHIIIPPJJXYRY-UHFFFAOYSA-M 0.000 description 1
- MNCGMVDMOKPCSQ-UHFFFAOYSA-M sodium;2-phenylethenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=CC1=CC=CC=C1 MNCGMVDMOKPCSQ-UHFFFAOYSA-M 0.000 description 1
- BWYYYTVSBPRQCN-UHFFFAOYSA-M sodium;ethenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=C BWYYYTVSBPRQCN-UHFFFAOYSA-M 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- XMRZNNGTCUALQE-UHFFFAOYSA-N tert-butyl 3-(4-ethenylphenoxy)propanoate Chemical compound CC(C)(C)OC(=O)CCOC1=CC=C(C=C)C=C1 XMRZNNGTCUALQE-UHFFFAOYSA-N 0.000 description 1
- NMOALOSNPWTWRH-UHFFFAOYSA-N tert-butyl 7,7-dimethyloctaneperoxoate Chemical compound CC(C)(C)CCCCCC(=O)OOC(C)(C)C NMOALOSNPWTWRH-UHFFFAOYSA-N 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- YQPZJBVEKZISEF-UHFFFAOYSA-N tetracont-1-ene Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC=C YQPZJBVEKZISEF-UHFFFAOYSA-N 0.000 description 1
- NPWJBNPQTPEEGC-UHFFFAOYSA-N tetradecyl 4-ethenylbenzoate Chemical compound C(CCCCCCCCCCCCC)OC(C1=CC=C(C=C1)C=C)=O NPWJBNPQTPEEGC-UHFFFAOYSA-N 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- UIERETOOQGIECD-ONEGZZNKSA-N tiglic acid Chemical compound C\C=C(/C)C(O)=O UIERETOOQGIECD-ONEGZZNKSA-N 0.000 description 1
- UAXOELSVPTZZQG-UHFFFAOYSA-N tiglic acid Natural products CC(C)=C(C)C(O)=O UAXOELSVPTZZQG-UHFFFAOYSA-N 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
- 125000005628 tolylene group Chemical group 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- YJGJRYWNNHUESM-UHFFFAOYSA-J triacetyloxystannyl acetate Chemical compound [Sn+4].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O YJGJRYWNNHUESM-UHFFFAOYSA-J 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- BDIWFCKBPZPBQT-UHFFFAOYSA-N tributyl(tributylstannylsulfanyl)stannane Chemical compound CCCC[Sn](CCCC)(CCCC)S[Sn](CCCC)(CCCC)CCCC BDIWFCKBPZPBQT-UHFFFAOYSA-N 0.000 description 1
- NXFZDTAAMQLJEC-UHFFFAOYSA-M tributyl-(2,2,2-trichloroacetyl)oxytin(1-) Chemical compound CCCC[Sn-](CCCC)(CCCC)OC(=O)C(Cl)(Cl)Cl NXFZDTAAMQLJEC-UHFFFAOYSA-M 0.000 description 1
- GQIUQDDJKHLHTB-UHFFFAOYSA-N trichloro(ethenyl)silane Chemical compound Cl[Si](Cl)(Cl)C=C GQIUQDDJKHLHTB-UHFFFAOYSA-N 0.000 description 1
- CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical compound CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-UHFFFAOYSA-N 0.000 description 1
- UMFJXASDGBJDEB-UHFFFAOYSA-N triethoxy(prop-2-enyl)silane Chemical compound CCO[Si](CC=C)(OCC)OCC UMFJXASDGBJDEB-UHFFFAOYSA-N 0.000 description 1
- NBXZNTLFQLUFES-UHFFFAOYSA-N triethoxy(propyl)silane Chemical compound CCC[Si](OCC)(OCC)OCC NBXZNTLFQLUFES-UHFFFAOYSA-N 0.000 description 1
- UDUKMRHNZZLJRB-UHFFFAOYSA-N triethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OCC)(OCC)OCC)CCC2OC21 UDUKMRHNZZLJRB-UHFFFAOYSA-N 0.000 description 1
- JXUKBNICSRJFAP-UHFFFAOYSA-N triethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCOCC1CO1 JXUKBNICSRJFAP-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- LFRDHGNFBLIJIY-UHFFFAOYSA-N trimethoxy(prop-2-enyl)silane Chemical compound CO[Si](OC)(OC)CC=C LFRDHGNFBLIJIY-UHFFFAOYSA-N 0.000 description 1
- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- NELVVTIEGZVCKM-UHFFFAOYSA-N trimethyl-[3-(prop-2-enoylamino)propyl]azanium;sulfate Chemical compound [O-]S([O-])(=O)=O.C[N+](C)(C)CCCNC(=O)C=C.C[N+](C)(C)CCCNC(=O)C=C NELVVTIEGZVCKM-UHFFFAOYSA-N 0.000 description 1
- VUWVDNLZJXLQPT-UHFFFAOYSA-N tripropoxy(propyl)silane Chemical compound CCCO[Si](CCC)(OCCC)OCCC VUWVDNLZJXLQPT-UHFFFAOYSA-N 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- UKRDPEFKFJNXQM-UHFFFAOYSA-N vinylsilane Chemical compound [SiH3]C=C UKRDPEFKFJNXQM-UHFFFAOYSA-N 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
- 238000004260 weight control Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
- IFNXAMCERSVZCV-UHFFFAOYSA-L zinc;2-ethylhexanoate Chemical compound [Zn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O IFNXAMCERSVZCV-UHFFFAOYSA-L 0.000 description 1
- CIBGZAYGXFGOFK-UHFFFAOYSA-L zinc;2-phenylethenesulfonate Chemical compound [Zn+2].[O-]S(=O)(=O)C=CC1=CC=CC=C1.[O-]S(=O)(=O)C=CC1=CC=CC=C1 CIBGZAYGXFGOFK-UHFFFAOYSA-L 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Adhesives Or Adhesive Processes (AREA)
Description
中でも、プラスチックシートラミネート鋼板として代表的なものは塩化ビニル(以下塩ビと略することがある)ラミネート鋼板が挙げられ、従来、塩ビラミネート鋼板は鋼板上に溶剤に溶解した積層シート用接着剤組成物を塗布し、200℃以上の高温で乾燥を行った直後に塩化ビニルシートをロール圧着により貼り合わせて製造されている。
イソシアネート基含有化合物(b−1)および/またはエポキシ基含有化合物(b−2)である化合物(B)と、
酸無水物基を1つ以上有する化合物(C)とを含む積層シート用接着剤組成物。
ただし、共重合体(A)は、下記(1)および(2)の条件を満たす。
(1)共重合体(A)が、α,β−不飽和化合物全量中、水酸基を有するα,β−不飽和化合物(a−1)0.01〜20重量%と、その他共重合可能なα,β−不飽和化合物(a−2)80〜99.99重量%とを共重合してなる。
(2)共重合体(A)のガラス転移点(Tg)が、20℃以上、120℃未満である。
共重合体(A)を50〜96.9重量%、
化合物(B)を3〜49.9重量%、
酸無水物基を1つ以上有する化合物(C)を0.1〜25重量%、
含有することを特徴とする請求項1記載の積層シート用接着剤組成物に関する。
本発明の共重合体(A)とは、α,β−不飽和化合物を共重合してなり、水酸基を有するα,β−不飽和化合物(a−1)およびその他共重合可能なα,β−不飽和化合物(a−2)の組成比を調整し、ガラス転移点(Tg)が20℃以上、120℃未満となる共重合体である。
0.01重量部より少ない場合は、後述の化合物(B)に含有されている官能基との硬化反応によって生じる分子量向上効果による高い凝集力が得られにくく、積層シート用接着剤組成物の硬化塗膜における凝集力が不足し、接着強度が得られない場合がある。20重量部より多い場合は、硬化反応による硬化収縮が顕著となり、十分な接着強度が得られない場合がある。尚、0.5〜10重量部の範囲が、硬化塗膜の硬化反応に伴う分子量向上効果により、エントロピー弾性を発現しうる内部凝集力を確保できるだけでなく、かつ硬化収縮を起こしにくいため、より好ましい。
このように、硬化塗膜にエントロピー弾性を持たせる事によって環境変化による基材の緩やかな伸縮運動に対して、追従させることができ、接着強度の低下を防ぐことが可能となる。
例えば、4−ビニル安息香酸メチルポリ(エチレンオキサイド)、4−ビニル安息香酸エチルポリ(エチレンオキサイド)、4−イソプロペニル安息香酸メチルポリ(プロピレンオキサイド)、4−イソプロペニル安息香酸エチルポリ(プロピレンオキサイド)などのポリアルキレンオキサイド部位を有するビニル安息香酸エステル系またはイソプロペニル安息香酸エステル系化合物類;
スチレンスルホン酸ナトリウム、スチレンスルホン酸カリウム、スチレンスルホン酸リチウム、スチレンスルホン酸マグネシウム、スチレンスルホン酸亜鉛、スチレンスルホン酸鉄等のスチレンスルホン酸の金属塩類;
ビニルオキシベンゼンスルホン酸アンモニウム、ビニルオキシベンゼンスルホン酸ナトリウム、ビニルオキシベンゼンスルホン酸カリウム等のアルケニル基含有ビニルオキシベンゼンスルホン酸の金属塩やアンモニウム塩類;
2−メチル−2−プロペニルオキシベンゼンスルホン酸アンモニウム、2−メチル−2−プロペニルオキシベンゼンスルホン酸ナトリウム、2−メチル−2−プロペニルオキシベンゼンスルホン酸カリウム等の2−メチル−2−プロペニルオキシベンゼンスルホン酸の金属塩やアンモニウム塩類;
例えば、2−メチル−2−プロペニルスルホン酸アンモニウム、2−メチル−2−プロペニルスルホン酸ナトリウム、2−メチル−2−プロペニルスルホン酸カリウム等の2−メチル−2−プロペニルスルホン酸の金属塩やアンモニウム塩類;
なお、共重合体(A)の構成成分である各単量体から形成され得るホモポリマーのTgが既知であれば、各ホモポリマーのTgと各単量体の構成比とに基づいて、共重合体(A)のTgを理論的に求めることができる。
<FOX式>1/Tg=W1/Tg1+W2/Tg2+…+Wi/Tgi+…+Wn/Tgn
〔上記FOX式は、n種の単量体からなる重合体を構成する各モノマーのホモポリマーのガラス転移温度をTgi(K)とし、各モノマーの質量分率を、Wiとしており、(W1+W2+…+Wi+…Wn=1)である。〕
本明細書では、下記の単量体の単独重合体のガラス転移点(℃)は以下のとおりとする。
(a−1) 水酸基を含有するα,β−不飽和化合物
メタクリル酸2−ヒドロキシエチル:55℃
アクリル酸4−ヒドロキシブチル:−60℃
(a−2) その他 α,β−不飽和化合物
アクリル酸ブチル:−48℃
アクリル酸2−エチルヘキシル:−50℃
メタクリル酸n-ブチル:20℃
メタクリル酸イソボルニル:110℃
メタクリル酸シクロヘキシル:66℃
スチレン:100℃
メタクリル酸メチル:105℃
メタクリル酸エチル:65℃
メタクリル酸−2−メトキシエチル:−2℃
メタクリル酸:144℃
メタクリル酸グリシジル 46℃
アクリル酸エチル −24℃
本発明における共重合体(A)は、上記したような種々のα,β−不飽和化合物(a−1)〜(a−2)の合計100重量部に対して、0.001〜20重量部の重合開始剤を用いて塊状重合、溶液重合、乳化重合、懸濁重合などの方法により合成される。好ましくは溶液重合で合成される。
次に化合物(B)について、説明する。
化合物(B)は、化合物(B)中のイソシアネート基および/またはエポキシ基が、共重合体(A)中の水酸基と硬化反応し、積層シート用接着剤組成物の硬化塗膜の分子量を向上させ、エネルギー弾性を発現する内部凝集力を向上させる役割を持つ。
また、化合物(B)は後述する基材表面との相互作用を向上させる効果も期待できる。さらには、コロナ放電処理等の物理処理、酸などで改質された化学処理のなされた基材に対しては、化合物(B)中の反応性官能基を基材と化学反応させることで、共重合体(A)と基材との間に強固な相互作用を発現させることも可能である。
このように、化合物(B)を用いる事により、強固な硬化塗膜を形成することが可能となり、急激な環境変化に伴う基材の伸縮運動を、エネルギー弾性を発現する化合物(B)により、抑制することが可能となる。
アルコール系及びラクタム系ブロック化剤は、一般には経時安定性が良好と思われるが、本発明の積層シート用樹接着剤成物を用いる場合の好ましいラミネート温度が約160〜200℃であることを考慮すると、そのラミネート温度で完全解離させるには温度差が少ないことから、オキシム系ブロック化剤が解離温度の点からは好ましい。なお、β−ジケトン系は、逆に解離温度が低すぎるため、貯蔵安定性が劣る場合がある。これらの点から、オキシム系を使用するのが好ましく、特には、メチルエチルケトンオキシムを好適に使用することができる。
錫系化合物としては、ジブチル錫ジクロライド、ジブチル錫オキサイド、ジブチル錫ジブロマイド、ジブチル錫ジマレエート、ジブチル錫ジラウレート(別名:DBTDL)、ジブチル錫ジアセテート、ジブチル錫スルファイド、トリブチル錫スルファイド、トリブチル錫オキサイド、トリブチル錫アセテート、トリエチル錫エトキサイド、トリブチル錫エトキサイド、ジオクチル錫オキサイド、トリブチル錫クロライド、トリブチル錫トリクロロアセテート、2−エチルヘキサン酸錫等が挙げられる。
非錫系化合物としては、例えばジブチルチタニウムジクロライド、テトラブチルチタネート、ブトキシチタニウムトリクロライドなどのチタン系、オレイン酸鉛、2−エチルヘキサン酸鉛、安息香酸鉛、ナフテン酸鉛などの鉛系、2−エチルヘキサン酸鉄、鉄2,4−ペンタジオネートなどの鉄系、安息香酸酸コバルト、2−エチルヘキサン酸コバルトなどのコバルト系、ナフテン酸亜鉛、2−エチルヘキサン酸亜鉛などの亜鉛系、ナフテン酸ジルコニウムなどが挙げられる。
上記触媒の中で、ジブチル錫ジラウレート(別名:DBTDL)、2−エチルヘキサン酸錫等が反応性や衛生性の点で好ましい。
当量比が1未満であると、化合物(B)の添加量が少なく、硬化反応による分子量向上効果が得られず凝集力が不足し、接着強度が低下する場合があり、当量比が8を超えると、過剰の化合物(B)が積層シート用接着剤組成物に残存し接着強度が低下する懸念があり、また、耐久性試験後に残存している化合物(B)が硬化反応を起こし、積層シート用接着剤組成物を二つの被着体の接着に使用した際に、積層シート用接着剤組成物が硬くなりすぎる等の変質を起こしてしまう場合がある。尚、当量比が1.5〜3の範囲が積層シート接着剤組成物の凝集力の制御や、化合物(B)の反応の完結が容易であることや、反応性官能基を過剰に設定し反応性官能基と基材とを化学反応させることで、共重合体(A)と基材との間に強固な相互作用が得られることから最も好ましい。
次に酸無水物基を1つ以上有する化合物(C)について、説明する。
化合物(C)は、化合物(C)中の酸無水物基が、各基材と相互作用することで、密着性を向上させることができる。金属や金属蒸着フィルムの場合特に効果が大きく、好適に利用される。また、酸無水物基は、共重合体(A)中の水酸基とも架橋反応が可能であり、各基材との密着性の向上と、積層シート用接着剤組成物の硬化塗膜の分子量を向上させ、エネルギー弾性を発現する内部凝集力を向上させる効果も期待できる。
全量100重量%中、共重合体(A)と化合物(B)が、それぞれ50重量部以上、30重量部以上であると、十分な凝集力が得られ易く耐熱性や耐水性の向上効果が期待できる。また化合物(C)が0.5重量部以上であると、基材に対して、十分な密着性を示すことが容易となる。
一方、全量100重量%中、共重合体(A)と化合物(B)が、それぞれ90重量%以下、59.5重量部以下であると、接着剤組成物の硬化収縮が低減でき、ウキ・ハガレが解消するので好ましい。また、化合物(C)が25重量部以下であると、基材として鋼板が用いられた場合には腐食が防止できる。
本発明の接着剤組成物は、本発明による効果を損なわない範囲であれば、各種添加剤を適宜配合することも可能である。例えば、硬化収縮率低減、熱膨張率低減、寸法安定性向上、弾性率向上、粘度調整、熱伝導率向上、強度向上、靭性向上、及び着色向上等の観点から、有機又は無機の充填剤を配合することができる。このような充填剤は、ポリマー、セラミックス、金属、金属酸化物、金属塩、及び染顔料等の材料から構成されるものであってよい。また、その形状については、特に限定されず、例えば、粒子状及び繊維状等であってよい。なお、上記ポリマー系の材料を配合する場合には、シランカップリング剤、チタネートカップリング剤、粘着付与剤、柔軟性付与剤、可塑剤、難燃化剤、保存安定剤、酸化防止剤、金属不活性化剤、紫外線吸収剤、チクソトロピー付与剤、レベリング剤、消泡剤、分散安定剤、流動性付与剤、及び消泡剤等の、独立した充填剤としてではなく、ポリマーブレンド又はポリマーアロイとして、接着剤組成物中に、溶解、半溶解又はミクロ分散させることも可能である。
本発明の積層シート用接着剤組成物は、上記、共重合体(A)、化合物(B)、酸無水物基を1つ以上有する化合物(C)を必須成分とし、更に、必要に応じて、シランカップリング剤やレベリング剤等のその他の成分を配合後、均一に混合することによって製造することができる。攪拌・混合する際には、減圧装置を備えた1軸または多軸エクストルーダー、ニーダー、ディソルバーのような汎用の機器を使用し攪拌・混合することにより調製してもよい。攪拌・混合する際の温度は、通常、10〜60℃に設定されるのが好ましい。調製時の設定温度が10℃未満では、粘度が高すぎて均一な撹拌・混合作業が困難になる場合があり、逆に、調製時の温度が60℃を超えると、熱による硬化反応が起きる場合があり、正常な樹脂組成物が得られない場合があるので、好ましくない。
なお、本発明における積層シート用接着剤組成物は、有機溶剤を含有して不揮発分(以下、固形分とも称す)は、10〜60重量%の範囲で使用されることが好ましい。含有される有機溶剤は、上述の共重合体(A)の重合反応時に溶媒として使用した有機溶剤が好ましく使用できるが、乾燥温度の低減等の省エネルギー性を考慮すると、沸点温度が160℃以下の有機溶剤の使用が好ましい。例えば、メタノール、エタノール、イソプロピルアルコール、アセトン、メチルエチルケトン、メチルイソブチルケトン、酢酸メチル、酢酸エチル、酢酸ブチル、エチレングリコールモノエチルエーテルアセテート、シクロヘキサン、トルエン、キシレン、エチレングリコールモノイソプロピルエーテル、その他の炭化水素系溶媒等の有機溶媒や、水が好ましく使用され、接着剤組成物の粘度を調整することもできるし、接着剤組成物を加熱して粘度を低下させることもできる。
これらの有機溶剤は単独で使用しても、2種類以上を混合して使用しても良い。溶媒の使用量は、前述した共重合体(A)の重合条件、各成分の組成、得られる共重合体(A)の粘度や濃度などを考慮して適宜決定すればよいが、化合物(C)と反応する可能性のある活性水素を有する溶剤、例えば、アルコール系溶剤、エーテル系溶剤は使用しないほうが好ましい。
塗工によって形成される上記接着層の厚さは、0.1〜10μmが好ましく、0.1μm〜6μmがより好ましい。接着層の厚さを0.1μm以上にすることによって、接着層に、十分な密着性又は接着力を得ることが容易である。一方、樹脂層の厚さが10μmを超えると、密着性又は接着力等の特性において変化は見られない場合が多い。
乾燥方法には特に制限はなく、熱風乾燥、赤外線や減圧法を利用したものが挙げられる。乾燥条件としては接着剤組成物の架橋硬化形態、膜厚や選択した有機溶剤にもよるが、通常60〜180℃程度の熱風加熱でよい。
本発明の積層シート用接着剤組成物は、プラスチックフィルム、金属板(鋼板など)、あるいはガラス板等の第1の基材(K1)に塗工され、別のプラスチックフィルム、金属板、あるいはガラス板等の第2の基材(K2)に貼着して積層体として使用され、特に、ラミネート鋼板、食品包装フィルム、自動車用内装シートあるいは太陽電池用バックシート等の用途で使用される。本実施形態において、接着剤層の膜厚、粘度、あるいは不揮発分は、積層体の用途に応じて設定される。
これらの鋼板基材には、必要な場合、防錆のために、下地処理を施すことができる。ステンレス鋼板では、下地処理を特に必要としないが、クロム酸処理により、接着剤組成物との密着性を更に向上させることができる。亜鉛めっき鋼板では、リン酸塩処理又はクロム酸処理のいずれか一方、あるいは両方の処理を施す必要がある場合もある。リン酸塩処理及びクロム酸処理については、特に制限なく、従来の一般的な方法によることができる。
また鋼板以外では、アルミニウム板、銅板、チタニウム板、真鍮、アルミニウム合金板、あるいはガルバリウム板等の金属板も用いることができる。さらに、防錆や意匠性のため塗装を施した塗装鋼板も使用することが可能である。
ラミネート鋼板は、次の2段階で製造される。まず第1段階は、接着剤組成物を、プラスチックフィルム、あるいは鋼板に塗布して、50〜200℃の任意の範囲の温度で乾燥させ、機溶剤を除去した後、乾燥状態の接着層を形成させる。この際、塗布するのは乾燥の容易性やフィルムの意匠性保持のため、鋼板側であるほうが好ましい。次に第2段階は、プラスチックフィルムと接着剤組成物が積層された鋼板を、プラスチックフィルムや接着剤組成物の種類より異なるが、例えば、圧力1.0〜5.0kg/cm2、ラミネート温度200〜220℃、及びライン速度5〜20m/分になるように加熱ロールを用いて加熱ラミネートする。ラミネートは冷却することなく乾燥直後に行うことが好ましい。この際、ラミネート時の熱により、瞬時に熱硬化が起こり、密着力が出現する。
例えば、化合物(B)として、ブロック化ポリイソシアネートを使用している場合は、熱ラミネートする際に、ブロック化剤が解離、揮発し、イソシアネート基が活性化し、共重合体(A)の水酸基と反応したり、基材と化学反応を起こしたり、空気中の水分と反応したり、イソシアネート基同士が反応したりして、フィルムと鋼板との接着強度を確保する。このようにして得られたラミネート鋼板は、意匠性、耐食性、加工密着性に優れ、多種な用途に使用できる。
[合成例1〜7]
反応槽、滴下装置、攪拌機、温度計、還流冷却器、空気導入管を備えた重合反応装置の反応槽に、下記、分子中に1個以上の水酸基を含有するα,β−不飽和二重結合基含有化合物(a−1)および分子中に水酸基を含有しないα,β−不飽和二重結合基含有化合物(a−2)、触媒及び有機溶剤をそれぞれ表1に示す比率で仕込んだ。
次に、反応槽内の空気を窒素ガスで置換した後、攪拌しながら空気雰囲気下中、80℃まで昇温し、滴下装置から表1記載の混合物を滴下開始した。2時間かけて滴下を行った後、さらに攪拌しながら6時間熟成後、酢酸エチルを加えて冷却を行い、共重合体(A−1)を含む樹脂溶液を得た。
数平均分子量(Mn)と重量平均分子量(Mw)の測定は、昭和電工社製GPC(ゲルパーミエーションクロマトグラフィー)「ShodexGPC System−21」を用いた。GPCは溶媒に溶解した物質をその分子サイズの差によって分離定量する液体クロマトグラフィーである。試料をテトラヒドロフランに溶解して、テトラヒドロフランを展開溶剤として流速を0.6ml/min、カラム温度を40℃の条件にて、測定した。標準物質としての単分散分子量のポリスチレンを使用した検量線を作成し、共重合体(A)および共重合体(B)の分子量をポリスチレン換算の数平均分子量(Mn)、重量平均分子量(Mw)を測定した。
共栓三角フラスコ中に試料、約1gを精密に量り採り、トルエン/エタノール(容量比:トルエン/エタノール=2/1)混合液100mlを加えて溶解する。更にアセチル化剤(無水酢酸25gをピリジンで溶解し、容量100mlとした溶液)を正確に5ml加え、約1時間攪拌した。これに、フェノールフタレイン試液を指示薬として加え、30秒間持続する。その後、溶液が淡紅色を呈するまで0.1Nアルコール性水酸化カリウム溶液で滴定する。
水酸基価は次式により求めた。水酸基価は樹脂の乾燥状態の数値とした(単位:mgKOH/g)。
水酸基価(mgKOH/g)=[{(b−a)×F×28.25}/S]/(不揮発分濃度/100)+D
ただし、S:試料の採取量(g)
a:0.1Nアルコール性水酸化カリウム溶液の消費量(ml)
b:空実験の0.1Nアルコール性水酸化カリウム溶液の消費量(ml)
F:0.1Nアルコール性水酸化カリウム溶液の力価
D:酸価(mgKOH/g)
・(a−1−1)メタクリル酸2−ヒドロキシエチル、
・(a−1−2)アクリル酸4−ヒドロキシブチル
・(a−2−1)アクリル酸n-ブチル
・(a−2−2)アクリル酸2−エチルヘキシル
・(a−2−3)メタクリル酸n-ブチル
・(a−2−4)メタクリル酸iso−ボルニル
・(a−2−5)メタクリル酸シクロヘキシル、
・(a−2−6)スチレン
・(a−2−7)メタクリル酸メチル
・(a−2−8)メタクリル酸エチル
・(a−2−9)メタクリル酸エトキシメチル
・(a−2−10)メタクリル酸
・重合開始剤1 アゾイソブチロニトリル
・重合開始剤2 tert−ブチルパーオキシ−2−エチルヘキサノエート
・溶剤:酢酸エチルを示す。
(合成例 比較A−1〜6)
表2に記載した原料と仕込み部を用いた以外は合成例1と同様にして合成を行い、比較合成例(比較A−1)〜(比較A−6)の樹脂溶液を得た。
・(a−2−11)メタクリル酸グリシジル
・(a−2−12)メタクリル酸アリル
・(a−2−13)アクリル酸エチル
ジメチルフタレート194g、エチレングリコール124g、ネオペンチルグリコール104g及びテトラブチルチタネート0.1gをN2ガス気流下160〜220°Cでエステル交換反応を行った。所定量のメタノール溜出後、セバシン酸202gとアジピン酸73gを加え、220〜230°Cでエステル化反応を行い、徐々に減圧して230〜260°Cで1mmHg下、3時間重縮合反応を行った。数平均分子量約6,000のポリエステルポリオールを得た。これにジブチル錫ジラウレート0.15g、イソホロンジイソシアネート100g、醋酸エチル100gを加えて、70°CでN2ガス気流下7時間反応させた。数平均分子量約10,000でOH価10のポリウレタンポリオールを得た。これにSMA1,000(スチレン/マレイン酸無水物=1/1共重合ポリマー、分子量1,600)を102g、醋酸エチル102gを加えて、70°Cで60分間反応させ、酢酸エチルにて、NV50%に調整し変性ポリエステルポリウレタン樹脂(比較A−7)を得た。特許文献5に用いられる樹脂に相当する。
酸成分としてイタコン酸、アルコール成分としてネオペンチルグリコールを用いて、常法にてポリエステルを合成したのち、イソシアネートとしてイソホロンジイソシアネート(IPDI) を用い、酸価2、水酸基当量2300の固形分4 0 % のポリウレタン樹脂(ウレタン−1)を得た。特許文献3に用いられているウレタン化合物に相当する。
[実施例1]
450ccのマヨネーズ瓶に、分子内に、共重合体(A)の樹脂溶液、化合物(B)、及び酸無水物基を1つ以上有する化合物(C)を必須成分とし、溶剤として酢酸エチルを仕込み、不揮発分20%に調整して、十分に攪拌を行い、十分に脱泡を行った後、積層シート用接着剤組成物を得た。配合は、不揮発分換算で表3に示す比率で仕込んだ。
得られた積層シート用接着剤組成物について、25℃における粘度を1時間、4時間、8時間、24時間後まで、B型粘度計(東京計器社製)を用い、20rpm、2分間回転の条件で測定し、可使時間(ポットライフ)を3段階で評価した。「△」評価以上の場合、実際の使用時に特に問題ない。
○:粘度変化がない。24時間までの粘度上昇率が2倍未満。非常に良好である。
△:若干粘度上昇が認められ、8時間までの粘度上昇率が2倍未満。使用可能である。
×:添加1時間で粘度上昇率が2倍以上。実用上問題あり。
<積層体>
表3に示した積層シート用接着剤組成物について、次の方法で各種物性(初期加工性、低温加工性、耐沸水加工性性、耐熱加工性、及び接着性)を測定し、結果を示す。
亜鉛メッキ鋼鈑(厚さ=0.5mm) に、乾燥塗膜が2μmになるようにバーコーターで積層シート用接着剤組成物を塗布した。オーブン(コンベアー付赤外線オーブン) に入れて100秒間加熱し、鋼板の温度を160℃とした工程の終了直後に、プラスチックフィルム(厚さ=150μm)をラミネーターにより、5kg/cm2の圧力でラミネートし、その直後に、水槽に入れて急冷させ、積層体を得た。
なお、積層体を安定化させるために一昼夜放置し、得られた積層体を用いて、JIS K6744に規定されるエリクセン試験を行った試料の剥離の度合いを目視にて評価した。さらに剥離をピンセットにて強制的に行い、剥離の有無を肉眼で観察し4段階で評価した。なお、「△」評価以上の場合、実際の使用時に特に問題ない。
◎:目視にて全く剥離がない、ピンセットによる強制剥離も困難。全く問題なし。
○:目視にて剥離は見られないが、ピンセットによる強制剥離は一部可能だが、問題なし。
△:目視にて剥離が見られないが、ピンセットによる強制剥離により、一部剥離可能。使用可能レベルである。
×:目視にて剥離が観察できる。実用上、使用困難。
前記積層体を、縦:3cm/横:5cmにカットし、クロスカット状にプラスチックフィルムに切り込みを入れる。この試料を0 ℃ 雰囲気中に6 時間試料を放置し0℃ 雰囲気中にて、クロスカットが中心部となるように試料をセットし、鋼板面に12mmの鉄球をのせ、鉄球上に50cmに高さから5 0 0 gの重りを落下させプラスチックフィルムが自然に剥がれる状態を肉眼で観察し、初期加工性と同等の基準にて4段階で評価した。「△」評価以上の場合、実際の使用時に特に問題ない。
◎:目視にて全く剥離がない、ピンセットによる強制剥離も困難。全く問題なし。
○:目視にて剥離は見られないが、ピンセットによる強制剥離は一部可能だが、問題なし。
△:目視にて剥離が見られないが、ピンセットによる強制剥離により、一部剥離可能。使用可能レベルである。
×:目視にて剥離が観察できる。実用上、使用困難。
前記積層体を、初期加工性評価試験と同様にエリクセン試験を行い、試験後の試料を、さらに沸騰水に3時間浸漬したあと、乾燥して初期加工性と同等の基準にて4段階で評価した。「△」評価以上の場合、実際の使用時に特に問題ない。
◎:目視にて全く剥離がない、ピンセットによる強制剥離も困難。全く問題なし。
○:目視にて剥離は見られないが、ピンセットによる強制剥離は一部可能だが、問題なし。
△:目視にて剥離が見られないが、ピンセットによる強制剥離により、一部剥離可能。使用可能レベルである。
×:目視にて剥離が観察できる。実用上、使用困難。
前記積層体を、初期加工性評価試験と同様にエリクセン試験を行い、試験後の試料を、さらに150℃雰囲気下で1時間放置した後、室温まで冷却し、初期加工性と同等の基準にて4段階で評価した。「△」評価以上の場合、実際の使用時に特に問題ない。
◎:目視にて全く剥離がない、ピンセットによる強制剥離も困難。全く問題なし。
○:目視にて剥離は見られないが、ピンセットによる強制剥離は一部可能だが、問題なし。
△:目視にて剥離が見られないが、ピンセットによる強制剥離により、一部剥離可能。使用可能レベルである。
×:目視にて剥離が観察できる。実用上、使用困難。
前記積層体を、それぞれ200mm×30mmの大きさに切断し、25℃、湿度65%の環境下で6時間静置後、ASTM−D1876−61の試験法に準じ、引張り試験機を用いて、25℃、湿度65%の環境下で、荷重速度300mm/分で180°剥離試験を行い、4段階で接着性の評価を行った。なお、「△」評価以上の場合、実際の使用時に特に問題ない。
◎:剥離不可能 接着性が非常に優れる。特に問題なし。
○:剥離強度50N/30mm以上 接着性に優れる。問題なし。
△:剥離強度20N/30mm以上、50N/30mm未満 接着性がやや足りないが、実用上、使用可能な範囲である。
×:剥離強度が20N/30mm未満で、接着性不良。実用上問題あり
表3
但し、実施例2及び7〜9は参考例である。
化合物(B)
・(b−1−1−1)1,6−ヘキサメチレンジイソシアネートのイソシアヌレート3量体−MEKオキシムブロック(住化バイエルウレタン社製「スミジュール BL3175」NCO基含有率11.2%、固形分75%)
・(b−1−1−2)トリレンジイソシアネートのトリメチロールプロパンアダクト体−MEKオキシムブロック(三井化学社製「タケネートB−830」NCO基含有率7%、固形分55.5%)
・(b−1−2)1,6−ヘキサメチレンジイソシアネートのイソシアヌレート3量体住化バイエルウレタン社製「スミジュール N3300」NCO基含有率21.8%、固形分100%)
・(b−1−3)ポリメチレンポリフェニルイソシアネートのプレポリマー(住化バイエルウレタン社製「スミジュールE22」NCO基含有率8.6%)、
・(b−2)エポキシ基含有化合物:N,N,N’,N’−テトラグリシジル−m−キシレンジアミン
・(c−1−1)スチレン−無水マレイン酸共重合体(クレイバレー社製SMA−1000 数平均分子量2800、固形分100%)
・(c−1−2)スチレン−無水マレイン酸共重合体(クレイバレー社製SMA−3000 数平均分子量5000、固形分100%)
・(c−1−3)スチレン−無水マレイン酸共重合体の一部エトキシブタノールエステル化物(クレイバレー社製SMA−1440 数平均分子量3400、固形分100%)
・(c−2)アウローレン200S(酸無水物変性ポリレフィン樹脂、日本製紙ケミカル(株)社製、数平均分子量86000、固形分15%)
・(c−3)ダイヤカルナ30(α‐オレフィン−無水マレイン酸共重合体、三菱化学社製 数平均分子量40000)
表4に記載した原料と仕込み量を用いて上記実施例1と同様の方法にて、積層シート用接着剤組成物(比較例1)〜(比較例9)を得た。実施例1と同様の評価を実施した結果を示す。
イミン化合物:(イミン−1) ポリエチレンイミン
例えば、プラスチック系素材と金属系素材との多層積層体の接合に好適に用いられる。また、優れた接着強度を有することから、建築分野(例えば、外装、内装、設備など)、電気機器分野(例えば、家電、厨房設備、空調など)、輸送器機分野(例えば、船舶、自動車など)、家具分野、雑貨分野などの各種産業分野において使用される、例えば、壁材、扉材、外板、パネル、化粧板、ケース、カバーなどの鋼板に、各種フィルムを貼着し、意匠性を付与するために、好適に用いることができる。また、160℃の低温においても、薄膜で接着強度が確保できる可能性があり、このため、エンボス加工等の施されている意匠性の高いプラスチック系フィルムを、そのエンボス加工を損なうこと無く、被着体に接着することができる。また、本発明の組成物を用いて製造したラミネート鋼板は0℃
℃付近の低温であっても、曲げ加工により端面が剥がれることがなく加工性に優れる。
本発明に係る積層シート用接着剤組成物は、特にプラスチックフィルムの表面処理層を含む積層体間で高い接着強度を示すものであるが、表面未処理フィルム(表面未処理プラスチックフィルムも含む)にも好適に適用することができる。
Claims (6)
- α,β−不飽和化合物を重合してなる共重合体(A)と、
イソシアネート基含有化合物(b−1)および/またはエポキシ基含有化合物(b−2)である化合物(B)と、
酸無水物基を1つ以上有する化合物(C)とを含む積層シート用接着剤組成物であって、
酸無水物基を1つ以上有する化合物(C)が、スチレンと、無水マレイン酸とを共重合してなる化合物(c−1)であり、
接着剤組成物全量中、不揮発分換算で、共重合体(A)を50〜96.9重量%、化合物(B)を3〜49.9重量%、化合物(C)を0.1〜25.0重量%、含有してなる積層シート用接着剤組成物。
ただし、共重合体(A)は、下記(1)および(2)の条件を満たす。
(1)共重合体(A)が、α,β−不飽和化合物全量中、水酸基を有するα,β−不飽和化合物(a−1)0.01〜20重量%と、その他共重合可能なα,β−不飽和化合物(a
−2)80〜99.99重量%とを共重合してなる。
(2)共重合体(A)のガラス転移点(Tg)が、20℃以上、120℃未満である。 - 積層シート用接着剤組成物全量中、
共重合体(A)を50〜96.9重量%、
化合物(B)を3〜49.9重量%、
酸無水物基を1つ以上有する化合物(C)を0.1〜25重量%、
含有することを特徴とする請求項1記載の積層シート用接着剤組成物。 - 酸無水物基を1つ以上有する化合物(C)が、数平均分子量500〜100000であることを特徴とする請求項1又は2記載の積層シート用接着剤組成物。
- イソシアネート基含有化合物(b−1)が、ブロックイソシアネート(b−1−1)を含有することを特徴とする請求項1〜3いずれか記載の積層シート用接着剤組成物。
- 第1の基材(K1)および第2の基材(K2)を、請求項1〜4いずれか記載の積層シート用接着剤組成物で接着してなる積層体。
- 第1の基材(K1)および/または第2の基材(K2)が、鋼板であることを特徴とする請求項5記載の積層体。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2014207901A JP6369275B2 (ja) | 2014-10-09 | 2014-10-09 | 積層シート用接着剤組成物 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2014207901A JP6369275B2 (ja) | 2014-10-09 | 2014-10-09 | 積層シート用接着剤組成物 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2016074864A JP2016074864A (ja) | 2016-05-12 |
JP6369275B2 true JP6369275B2 (ja) | 2018-08-08 |
Family
ID=55949644
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2014207901A Active JP6369275B2 (ja) | 2014-10-09 | 2014-10-09 | 積層シート用接着剤組成物 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP6369275B2 (ja) |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6083250B2 (ja) * | 2013-02-14 | 2017-02-22 | Dic株式会社 | 易接着剤組成物、積層ポリエステル樹脂フィルム及び太陽電池バックシート |
JP5888263B2 (ja) * | 2013-02-27 | 2016-03-16 | 東洋インキScホールディングス株式会社 | 積層シート接合用樹脂組成物 |
-
2014
- 2014-10-09 JP JP2014207901A patent/JP6369275B2/ja active Active
Also Published As
Publication number | Publication date |
---|---|
JP2016074864A (ja) | 2016-05-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP2017095653A (ja) | 光学フィルム用粘着剤、光学フィルム用粘着剤層、光学部材および画像表示装置 | |
EP3219769B1 (en) | Composition for powder coating material, powder coating material and coated article | |
JP6464803B2 (ja) | 活性エネルギー線重合性接着剤組成物、及びそれを用いてなる積層体 | |
JP6790865B2 (ja) | 感圧式接着剤及び接着フィルム | |
CN102115628A (zh) | 带有无机薄膜的塑料用底涂剂、带有无机薄膜的塑料以及模内成型或镶嵌成型的装饰膜 | |
TW201113343A (en) | Adhesive composition adapted for laminating polarizing plate | |
KR20140115397A (ko) | 수분산성 2액형 아크릴폴리올 수지 조성물 | |
JP2013249413A (ja) | 防曇性コーティング組成物およびそれを用いて得られる防曇性塗料 | |
JP2018044140A (ja) | 感圧式接着剤及び接着フィルム | |
JP2017019960A (ja) | 感圧式接着剤、感圧式接着フィルム、およびそれを用いた光学積層体 | |
JP2016169318A (ja) | 積層体用接着剤組成物 | |
JP2017186514A (ja) | コーティング組成物 | |
JP6369275B2 (ja) | 積層シート用接着剤組成物 | |
JP4725850B2 (ja) | 水分散性ポリイソシアネート組成物、水性硬化性組成物、水性塗料及び水性接着剤 | |
JP6432265B2 (ja) | 積層シート用接着剤組成物 | |
JP2017043725A (ja) | 感圧式接着剤、感圧式接着フィルム、およびそれを用いた光学積層体 | |
CN118119682A (zh) | 粘合剂组合物、粘合剂、粘合片以及表面保护膜 | |
JP2019026768A (ja) | 塗料用樹脂組成物、及びその製造方法 | |
JP6613818B2 (ja) | 感圧式接着剤及び感圧式接着フィルム | |
JP2016138177A (ja) | 積層シート接合用樹脂組成物 | |
JP6712891B2 (ja) | 上塗り塗料用樹脂エマルション | |
JP2016160290A (ja) | 金属基材接合用樹脂組成物 | |
JP6314679B2 (ja) | ラミネート鋼板形成用樹脂組成物、およびプラスチックフィルムラミネート鋼板。 | |
JP5957940B2 (ja) | フッ素樹脂水性分散体、水性フッ素塗料及び該塗料で塗装された物品 | |
JP6105354B2 (ja) | 積層塗膜 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20170706 |
|
A711 | Notification of change in applicant |
Free format text: JAPANESE INTERMEDIATE CODE: A711 Effective date: 20170919 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A821 Effective date: 20170919 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20180305 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20180417 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20180529 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20180612 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20180625 |
|
R151 | Written notification of patent or utility model registration |
Ref document number: 6369275 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R151 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |